# terms

id: GO:1904445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of establishment of Sertoli cell barrier.","definition_xrefs":["PMID:18057314","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell development","termid":"GO:0010721"},{"relation_name":"is_a","term_name":"negative regulation of epithelial cell differentiation","termid":"GO:0030857"},{"relation_name":"is_a","term_name":"regulation of establishment of Sertoli cell barrier","termid":"GO:1904444"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_regulates","term_name":"establishment of Sertoli cell barrier","termid":"GO:0097368"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of establishment of Sertoli cell barrier","synonyms":[{"name":"down regulation of establishment of BTB","type":"exact"},{"name":"down regulation of establishment of SCB","type":"exact"},{"name":"down regulation of establishment of Sertoli cell barrier","type":"exact"},{"name":"down regulation of establishment of blood-testis barrier","type":"exact"},{"name":"down-regulation of establishment of BTB","type":"exact"},{"name":"down-regulation of establishment of SCB","type":"exact"},{"name":"down-regulation of establishment of Sertoli cell barrier","type":"exact"},{"name":"down-regulation of establishment of blood-testis barrier","type":"exact"},{"name":"downregulation of establishment of BTB","type":"exact"},{"name":"downregulation of establishment of SCB","type":"exact"},{"name":"downregulation of establishment of Sertoli cell barrier","type":"exact"},{"name":"downregulation of establishment of blood-testis barrier","type":"exact"},{"name":"inhibition of establishment of BTB","type":"narrow"},{"name":"inhibition of establishment of SCB","type":"narrow"},{"name":"inhibition of establishment of Sertoli cell barrier","type":"narrow"},{"name":"inhibition of establishment of blood-testis barrier","type":"narrow"},{"name":"negative regulation of establishment of BTB","type":"exact"},{"name":"negative regulation of establishment of SCB","type":"exact"},{"name":"negative regulation of establishment of blood-testis barrier","type":"exact"}],"termid":"GO:1904445"}


id: PBO:0074847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 37","termid":"PBO:0074847"}


id: PBO:0053743
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 970","termid":"PBO:0053743"}


id: GO:0050422
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3alpha(S)-strictosidine + H2O = D-glucose + strictosidine aglycone.","definition_xrefs":["EC:3.2.1.105","RHEA:12917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-glucosidase activity","termid":"GO:0008422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016798","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"strictosidine beta-glucosidase activity","secondary_identifiers":["KEGG_REACTION:R03820","MetaCyc:STRICTOSIDINE-BETA-GLUCOSIDASE-RXN"],"synonyms":[{"name":"strictosidine b-glucosidase activity","type":"exact"},{"name":"strictosidine beta-D-glucohydrolase activity","type":"related"}],"termid":"GO:0050422"}


id: GO:0043452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving an alkyne, any acyclic branched or unbranched hydrocarbon (compound composed only of carbon and hydrogen) having a carbon-carbon triple bond and the general formula CnH2n-2, as carried out by individual cells.","definition_xrefs":["GOC:krc","Wikipedia:Alkyne","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylenic compound metabolic process","termid":"GO:0120246"},{"relation_name":"is_a","term_name":"hydrocarbon metabolic process","termid":"GO:0120252"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"alkyne metabolic process","synonyms":[{"name":"alkyne metabolism","type":"exact"}],"termid":"GO:0043452"}


id: PBO:0000377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic suppressor protein Ste7","termid":"PBO:0000377"}


id: PBO:0063652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate mutase 1 pseudogene 9","termid":"PBO:0063652"}


id: MONDO:0033558
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":"autoinflammation, immune dysregulation, and eosinophilia","secondary_identifiers":["OMIM:618999","UMLS:C5436572","MEDGEN:1750270"],"synonyms":[{"name":"AIIDE","type":"related"},{"name":"AUTOINFLAMMATION, IMMUNE DYSREGULATION, AND EOSINOPHILIA","type":"related"},{"name":"Atopic Dermatitis, Enteritis, Colitis, and Eosinophilia","type":"related"}],"termid":"MONDO:0033558","xrefs":{"Monarch":{"xref_id":"0033558"}}}


id: PBO:0052739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 31","termid":"PBO:0052739"}


id: PBO:0054842
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 2256","termid":"PBO:0054842"}


id: GO:0048692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of axon extension involved in regeneration.","definition_xrefs":["GOC:dph","GOC:dgh","GOC:lm","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of axon extension","termid":"GO:0030517"},{"relation_name":"is_a","term_name":"negative regulation of sprouting of injured axon","termid":"GO:0048688"},{"relation_name":"is_a","term_name":"regulation of axon extension involved in regeneration","termid":"GO:0048690"},{"relation_name":"negatively_regulates","term_name":"axon extension involved in regeneration","termid":"GO:0048677"}],"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 axon extension involved in regeneration","synonyms":[{"name":"down regulation of axon extension involved in regeneration","type":"exact"},{"name":"down-regulation of axon extension involved in regeneration","type":"exact"},{"name":"downregulation of axon extension involved in regeneration","type":"exact"},{"name":"inhibition of axon extension involved in regeneration","type":"narrow"}],"termid":"GO:0048692"}


id: GO:1903409
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of reactive oxygen species, any molecules or ions formed by the incomplete one-electron reduction of oxygen.","definition_xrefs":["GOC:PARL","PMID:24252804","GO_REF:0000068","GOC:bf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"reactive oxygen species metabolic process","termid":"GO:0072593"}],"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":"reactive oxygen species biosynthetic process","synonyms":[{"name":"ROS formation","type":"related"},{"name":"ROS generation","type":"related"},{"name":"reactive oxygen species anabolism","type":"exact"},{"name":"reactive oxygen species biosynthesis","type":"exact"},{"name":"reactive oxygen species formation","type":"exact"},{"name":"reactive oxygen species generation","type":"related"},{"name":"reactive oxygen species synthesis","type":"exact"}],"termid":"GO:1903409"}


id: GO:0033056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving D-ornithine, the D-enantiomer of the amino acid ornithine, i.e. (2R)-2,5-diaminopentanoic acid.","definition_xrefs":["GOC:jsg","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete D-ornithine metabolic process (obsolete GO:0033056)","synonyms":[{"name":"D-ornithine metabolism","type":"exact"}],"termid":"GO:0033056"}


id: GO:0050237
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pyridoxine + O2 = pyridoxal + H2O2.","definition_xrefs":["EC:1.1.3.12","MetaCyc:PYRIDOXINE-4-OXIDASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"pyridoxine 4-oxidase activity","secondary_identifiers":["RHEA:15033"],"synonyms":[{"name":"pyridoxin 4-oxidase activity","type":"related"},{"name":"pyridoxine:oxygen 4-oxidoreductase activity","type":"related"},{"name":"pyridoxol 4-oxidase activity","type":"related"}],"termid":"GO:0050237"}


id: GO:0000049
data:
  {"annotated_genes":["SJAG_03626","SJAG_00325","SJAG_03461","SJAG_00358","SJAG_03071","SJAG_04856","SJAG_04175","SJAG_02661","SJAG_03545","SJAG_02637","SJAG_00936","SJAG_00169","SJAG_04680","SJAG_02288","SJAG_02099","SJAG_01074","SJAG_02352","SJAG_03932","SJAG_04409","SJAG_04285","SJAG_04756","SJAG_01797","SJAG_04762","SJAG_03629","SJAG_04993","SJAG_04181","SJAG_01877","SJAG_00195","SJAG_02615","SJAG_01704","SJAG_04582","SJAG_00488","SJAG_02042","SJAG_01314","SJAG_01248","SJAG_03584","SJAG_04700","SJAG_02263","SJAG_02977","SJAG_00466","SJAG_00886","SJAG_01302","SJAG_03788","SJAG_00579"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58612,59406,59629,61261,61532,61830,62218,62881,64129,64641,65445,68199,69292,69767,70771,71022,72487,73034,73693,74083,74219,74273,74353,74863,75426,75504,78679,79420,80834,81344,81427,89685,96429,96663,100436,104222,104846,107748,111660,114146,114866,119930],"is_not":false,"summary":null,"term":"GO:0000049"},{"annotations":[99176,107386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990856"}]},"cv_name":"molecular_function","definition":"Binding to a transfer RNA.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":44,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00195":null,"SJAG_00325":null,"SJAG_00358":null,"SJAG_00466":null,"SJAG_00488":null,"SJAG_00579":null,"SJAG_00886":null,"SJAG_00936":null,"SJAG_01074":null,"SJAG_01248":null,"SJAG_01302":null,"SJAG_01314":null,"SJAG_01704":null,"SJAG_01797":null,"SJAG_01877":null,"SJAG_02042":null,"SJAG_02099":null,"SJAG_02263":null,"SJAG_02288":null,"SJAG_02352":null,"SJAG_02615":null,"SJAG_02637":null,"SJAG_02661":null,"SJAG_02977":null,"SJAG_03071":null,"SJAG_03461":null,"SJAG_03545":null,"SJAG_03584":null,"SJAG_03626":null,"SJAG_03629":null,"SJAG_03788":null,"SJAG_03932":null,"SJAG_04175":null,"SJAG_04181":null,"SJAG_04285":null,"SJAG_04409":null,"SJAG_04582":null,"SJAG_04680":null,"SJAG_04700":null,"SJAG_04756":null,"SJAG_04762":null,"SJAG_04856":null,"SJAG_04993":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"tRNA binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0000946","Reactome:R-HSA-2408509"],"synonyms":[{"name":"base pairing with tRNA","type":"narrow"}],"termid":"GO:0000049","terms_by_termid":{"GO:0000049":null,"GO:1990856":null}}


id: PBO:0039648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adaptor related protein complex 1 subunit gamma 2","termid":"PBO:0039648"}


id: PBO:0079526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-yW synthesizing protein 1 homolog","termid":"PBO:0079526"}


id: SO:0000578
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that can be transcribed into a small nucleolar RNA (snoRNA).","direct_ancestors":[{"relation_name":"is_a","term_name":"non_protein_coding","termid":"SO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snoRNA_encoding","synonyms":[{"name":"snoRNA encoding","type":"exact"}],"termid":"SO:0000578"}


id: PBO:0083924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fructose 1,6-bisphosphate aldolase; required for glycolysis and gluconeogenesis; catalyzes conversion of fructose 1,6 bisphosphate to glyceraldehyde-3-P and dihydroxyacetone-P; locates to mitochondrial outer surface upon oxidative stress; N-terminally propionylated in vivo","termid":"PBO:0083924"}


id: PBO:0081717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 646","termid":"PBO:0081717"}


id: GO:0006829
data:
  {"annotated_genes":["SJAG_04185","SJAG_00328","SJAG_01078","SJAG_03528","SJAG_00222","SJAG_01803","SJAG_01990","SJAG_02968"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140147"},{"annotations":[106130,115207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071578"},{"annotations":[95720,95721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140209"},{"annotations":[106270,76631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904257"},{"annotations":[80189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071577"}]},"cv_name":"biological_process","definition":"The directed movement of zinc (Zn II) ions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transport","termid":"GO:0000041"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00222":null,"SJAG_00328":null,"SJAG_01078":null,"SJAG_01803":null,"SJAG_01990":null,"SJAG_02968":null,"SJAG_03528":null,"SJAG_04185":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"zinc ion transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"zinc II ion transport","type":"exact"},{"name":"zinc transport","type":"exact"}],"termid":"GO:0006829","terms_by_termid":{"GO:0071577":null,"GO:0071578":null,"GO:0140147":null,"GO:0140209":null,"GO:1904257":null}}


id: PBO:0079808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP glucuronosyltransferase family 2 member B29, pseudogene","termid":"PBO:0079808"}


id: PBO:0047419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and WD repeat domain containing 10","termid":"PBO:0047419"}


id: PBO:0084177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone acetyltransferase; critical for cell survival in presence of DNA damage during S phase, required for recovery after DSB repair; acetylates H3K56, H3K9; H3K56 acetylation activity required for expression homeostasis, buffering of mRNA synthesis rate against changes in gene dosage during S phase; involved in non-homologous end joining and regulation of Ty1 transposition; prevents hyper-amplification of rDNA; interacts physically with Vps75p","termid":"PBO:0084177"}


id: MOD:00960
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a carboxylic acid group with a hydrogen atom.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decarboxylated residue","termid":"MOD:00960"}


id: PBO:0030135
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_zinc_starvation","termid":"PBO:0030135"}


id: MONDO:0008327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant disorder caused by mutations in the LOXL1 gene, encoding lysyl oxidase homolog 1. The condition is characterized by abnormal fibrillar extracellular material in anterior segment tissues, and may lead to glaucoma.","definition_xrefs":["NCIT:C129025"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phacogenic glaucoma","termid":"MONDO:0001554"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"iris disorder","termid":"MONDO:0002289"},{"relation_name":"is_a","term_name":"hereditary glaucoma","termid":"MONDO:0018174"}],"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":"exfoliation syndrome","secondary_identifiers":["UMLS:C0206368","SCTID:111514006","EFO:0004235","DOID:13641","MESH:D017889","ICD9:365.52","MEDGEN:60133","Orphanet:529819"],"synonyms":[{"name":"XFG","type":"exact"},{"name":"XFS","type":"exact"},{"name":"pseudoexfoliation glaucoma","type":"exact"},{"name":"pseudoexfoliation syndrome","type":"exact"}],"termid":"MONDO:0008327","xrefs":{"Monarch":{"xref_id":"0008327"}}}


id: PBO:0091105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THO complex subunit Tho3","termid":"PBO:0091105"}


id: PBO:0080441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VRK serine/threonine kinase 2","termid":"PBO:0080441"}


id: GO:0047310
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,4,6/3,5-pentahydroxycyclohexanone + L-glutamine = 1-amino-1-deoxy-scyllo-inositol + 2-oxoglutaramate.","definition_xrefs":["RHEA:22920","EC:2.6.1.50"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-glutamine aminotransferase activity","termid":"GO:0070548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016769","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"glutamine-scyllo-inositol transaminase activity","secondary_identifiers":["MetaCyc:2.6.1.50-RXN","KEGG_REACTION:R02781"],"synonyms":[{"name":"L-glutamine-keto-scyllo-inositol aminotransferase activity","type":"related"},{"name":"L-glutamine-scyllo-inosose transaminase activity","type":"related"},{"name":"L-glutamine:2,4,6/3,5-pentahydroxycyclohexanone aminotransferase activity","type":"related"},{"name":"glutamine scyllo-inosose aminotransferase activity","type":"related"},{"name":"glutamine--scyllo-inosose aminotransferase activity","type":"related"},{"name":"glutamine--scyllo-inosose transaminase activity","type":"related"},{"name":"glutamine-scyllo-inosose aminotransferase activity","type":"exact"},{"name":"glutamine-scyllo-inosose transaminase activity","type":"exact"}],"termid":"GO:0047310"}


id: MONDO:0004390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormally low intraocular pressure often related to chronic inflammation (uveitis).","definition_xrefs":["MESH:D015814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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":"ocular hypotension","secondary_identifiers":["ICD9:360.3","SCTID:19721008","MEDGEN:10424","DOID:790","UMLS:C0028841","ICD9:360.30","ICD10CM:H44.4"],"synonyms":[{"name":"hypotony of eye","type":"exact"}],"termid":"MONDO:0004390","xrefs":{"Monarch":{"xref_id":"0004390"}}}


id: FYPO:0000695
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of DNA-1,N6-ethenoadenine N-glycosylase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA-1,N6-ethenoadenine N-glycosylase activity","termid":"FYPO:0000692"},{"relation_name":"is_a","term_name":"increased DNA N-glycosylase activity","termid":"FYPO:0008217"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"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"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000661","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"increased DNA-1,N6-ethenoadenine N-glycosylase activity","termid":"FYPO:0000695"}


id: GO:0032572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a menaquinone (vitamin K2) stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to vitamin K","termid":"GO:0032571"}],"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 menaquinone","synonyms":[{"name":"response to menatetrenone","type":"exact"},{"name":"response to vitamin K2","type":"exact"}],"termid":"GO:0032572"}


id: GO:2000800
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocardial cushion to mesenchymal transition involved in heart valve formation.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of endocardial cushion to mesenchymal transition","termid":"GO:0140049"},{"relation_name":"regulates","term_name":"endocardial cushion to mesenchymal transition involved in heart valve formation","termid":"GO:0003199"}],"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 endocardial cushion to mesenchymal transition involved in heart valve formation","synonyms":[{"name":"regulation of endocardial cushion to mesenchymal transition involved in valve formation","type":"exact"}],"termid":"GO:2000800"}


id: PBO:0066466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication factor C 3 pseudogene 1","termid":"PBO:0066466"}


id: GO:0007169
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by an extracellular ligand binding to a receptor on the surface of the target cell where the receptor possesses tyrosine kinase activity, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme-linked receptor protein signaling pathway","termid":"GO:0007167"}],"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":"cell surface receptor protein tyrosine kinase signaling pathway","secondary_identifiers":["Reactome:R-HSA-187015"],"synonyms":[{"name":"transmembrane receptor protein serine/threonine kinase signaling pathway","type":"broad"},{"name":"transmembrane receptor protein tyrosine kinase signalling pathway","type":"exact"}],"termid":"GO:0007169"}


id: MONDO:0020437
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrioventricular septal defect with communication at the atrial level only.","definition_xrefs":["PMID:34304616"],"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, ostium primum type","secondary_identifiers":["GARD:10695","Orphanet:99106","SCTID:17718000","icd11.foundation:1159570489","MESH:C548006","MEDGEN:1825952","UMLS:C5680294","MESH:D006344"],"synonyms":[{"name":"ASD ostium primum type","type":"exact"},{"name":"ASD, ostium primum type","type":"exact"},{"name":"PAVC","type":"exact"},{"name":"PAVSD","type":"exact"},{"name":"atrial septal defect ostium primum","type":"exact"},{"name":"atrioventricular defect with atrial shunting only","type":"exact"},{"name":"incomplete atrioventricular canal defect with isolated atrial component","type":"exact"},{"name":"incomplete atrioventricular septal defect with isolated atrial component","type":"exact"},{"name":"ostium primum ASD","type":"exact"},{"name":"partial atrioventricular canal defect with isolated atrial component","type":"exact"},{"name":"partial atrioventricular septal defect","type":"exact"},{"name":"partial atrioventricular septal defect: ostium primum type","type":"exact"},{"name":"primum atrial septal defect","type":"exact"}],"termid":"MONDO:0020437","xrefs":{"Monarch":{"xref_id":"0020437"}}}


id: PBO:0068669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 50, pseudogene","termid":"PBO:0068669"}


id: MONDO:0021812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign sweat gland neoplasm usually occurring in the scalp or the face. It may present as solitary or multiple papular or nodular lesions. It may be a sporadic lesion or part of Brooke-Spiegler syndrome. It arises from the dermis and has a multinodular, circumscribed appearance. The nodules contain basaloid cells with small, dark nuclei. Complete excision is usually curative.","definition_xrefs":["NCIT:C27094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm of sweat gland","termid":"MONDO:0021489"}],"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":"adnexal spiradenoma/cylindroma of a sweat gland","secondary_identifiers":["ICDO:8200/0","SCTID:274903001"],"synonyms":[{"name":"adnexal sweat gland spiradenoma/cylindroma","type":"related"},{"name":"cylindroma","type":"exact"},{"name":"cylindroma of skin","type":"exact"},{"name":"cylindroma of the skin","type":"exact"},{"name":"dermal cylindroma","type":"exact"}],"termid":"MONDO:0021812","xrefs":{"Monarch":{"xref_id":"0021812"}}}


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


id: GO:2001123
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a maltoheptaose.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide catabolic process","termid":"GO:0009313"},{"relation_name":"is_a","term_name":"maltoheptaose metabolic process","termid":"GO:2001122"}],"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":"maltoheptaose catabolic process","synonyms":[{"name":"maltoheptaose catabolism","type":"exact"}],"termid":"GO:2001123"}


id: PBO:0000311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerate kinase (predicted)","termid":"PBO:0000311"}


id: PBO:0035728
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_methylation_at_subtelomeric_heterochromatin_during_vegetative_growth","termid":"PBO:0035728"}


id: GO:1901260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any peptidyl-lysine hydroxylation that is involved in bacterial-type EF-P lysine modification.","definition_xrefs":["GOC:TermGenie","GOC:imk","PMID:22706199"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-lysine hydroxylation involved in bacterial-type EF-P lysine modification (obsolete GO:1901260)","synonyms":[{"name":"EF-P lysine hydroxylation","type":"related"}],"termid":"GO:1901260"}


id: GO:0033195
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 alkyl hydroperoxide stimulus. Alkyl hydroperoxides are monosubstitution products of hydrogen peroxide, HOOH, where the substituent is an alkyl group.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to hydroperoxide","termid":"GO:0033194"}],"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 alkyl hydroperoxide","termid":"GO:0033195"}


id: MONDO:0023045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"ectodermal dysplasia arthrogryposis diabetes mellitus","secondary_identifiers":["GARD:2042"],"termid":"MONDO:0023045","xrefs":{"Monarch":{"xref_id":"0023045"}}}


id: GO:0003921
data:
  {"annotated_genes":["SJAG_04634"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76599],"is_not":false,"summary":null,"term":"GO:0003921"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + XMP + NH4(+) = AMP + diphosphate + GMP + 2H+.","definition_xrefs":["RHEA:18301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"},{"relation_name":"part_of","term_name":"GMP synthase (glutamine-hydrolyzing) activity","termid":"GO:0003922"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"part_of","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"part_of","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"GMP synthase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:GMP-SYN-NH3-RXN"],"termid":"GO:0003921","terms_by_termid":{"GO:0003921":null}}


id: PBO:0058460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5189","termid":"PBO:0058460"}


id: PBO:0089022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shelterin complex subunit Tpz1","termid":"PBO:0089022"}


id: PBO:0053208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galectin 7B","termid":"PBO:0053208"}


id: MONDO:0033569
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":"combined oxidative phosphorylation deficiency 49","secondary_identifiers":["MEDGEN:1762338","UMLS:C5436616","DOID:0112110","OMIM:619024"],"synonyms":[{"name":"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49","type":"related"},{"name":"COXPD49","type":"related"}],"termid":"MONDO:0033569","xrefs":{"Monarch":{"xref_id":"0033569"}}}


id: FYPO:0007462
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of filamentous actin measured the cell is higher than normal when the cell is in the vegetative growth phase of the life cycle. The total actin level (globular and filamentous actin) may be normal or abnormal.","definition_xrefs":["PomBase:mah"],"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":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0006551","FYPO:0001985"],"is_obsolete":false,"name":"increased filamentous actin level","synonyms":[{"name":"increased F-actin level","type":"exact"},{"name":"increased accumulation of filamentous actin in cell","type":"related"},{"name":"increased cellular F-actin level","type":"exact"},{"name":"increased cellular filamentous actin level","type":"exact"},{"name":"increased filamentous actin level during mitotic cell cycle","type":"related"},{"name":"increased filamentous actin level during vegetative growth","type":"exact"}],"termid":"FYPO:0007462"}


id: PBO:0040407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V1 subunit G2","termid":"PBO:0040407"}


id: FYPO:0004607
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of the spindle pole body is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"}],"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":"abnormal spindle pole body morphology","synonyms":[{"name":"abnormal SPB morphology","type":"exact"},{"name":"abnormal spindle pole body structure","type":"narrow"}],"termid":"FYPO:0004607"}


id: PBO:0026805
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_meiotic_DNA_double-strand_break_formation","termid":"PBO:0026805"}


id: MONDO:0016007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of clinical signs observed in newborns exposed in utero to cocaine, a short-acting central nervous system stimulant used as a recreational drug through inhalation of the powder or intravenous injection. Cocaine use during pregnancy is associated with intrauterine growth restriction, low birth weight, seizures, respiratory distress (decreased apnea density and periodic breathing), feeding difficulties, irritability and lability of state, decreased behavioral and autonomic regulation, poor alertness and orientation and cognitive impairment (impaired auditory information processing , visual-spatial delay and subtle language delay) in the offspring.","definition_xrefs":["Orphanet:1911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxic or drug-related embryofetopathy","termid":"MONDO:0016677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cocaine embryofetopathy","secondary_identifiers":["GARD:1413","ICD9:760.75","icd11.foundation:1604796846","MEDGEN:140937","SCTID:254250002","UMLS:C0432371"],"synonyms":[{"name":"cocaine antenatal exposure","type":"related"},{"name":"cocaine fetopathy","type":"related"},{"name":"fetal cocaine syndrome","type":"exact"},{"name":"foetal cocaine syndrome","type":"exact"},{"name":"prenatal cocaine exposure","type":"related"}],"termid":"MONDO:0016007","xrefs":{"Monarch":{"xref_id":"0016007"}}}


id: GO:1905018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of methionine-tRNA ligase activity.","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","PMID:1665486"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of methionine-tRNA ligase activity (obsolete GO:1905018)","synonyms":[{"name":"regulation of L-methionine:tRNAMet ligase (AMP-forming)","type":"exact"},{"name":"regulation of MetRS activity","type":"exact"},{"name":"regulation of methionine translase activity","type":"exact"},{"name":"regulation of methionyl-tRNA synthetase activity","type":"exact"},{"name":"regulation of methionyl-transfer RNA synthetase activity","type":"exact"},{"name":"regulation of methionyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"regulation of methionyl-transfer ribonucleic acid synthetase activity","type":"exact"}],"termid":"GO:1905018"}


id: GO:2001229
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of response to gamma radiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of response to gamma radiation","termid":"GO:2001228"},{"relation_name":"negatively_regulates","term_name":"response to gamma radiation","termid":"GO:0010332"}],"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 response to gamma radiation","synonyms":[{"name":"negative regulation of response to gamma ray","type":"related"},{"name":"negative regulation of response to gamma-ray photon","type":"related"}],"termid":"GO:2001229"}


id: MONDO:0004710
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma in situ involving a uterus.","definition_xrefs":["MONDO:patterns/carcinoma_in_situ"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"},{"relation_name":"is_a","term_name":"uterine carcinoma","termid":"MONDO:0005213"}],"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":"uterus carcinoma in situ","secondary_identifiers":["SCTID:92788005","DOID:9108","MEDGEN:673127","UMLS:C0686237","ICD9:233.2"],"synonyms":[{"name":"carcinoma in situ of uterus","type":"exact"},{"name":"stage 0 uterus carcinoma","type":"exact"},{"name":"uterus in situ carcinoma","type":"exact"}],"termid":"MONDO:0004710","xrefs":{"Monarch":{"xref_id":"0004710"}}}


id: PBO:0040164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adipocyte associated metabolic related lncRNA 2","termid":"PBO:0040164"}


id: PBO:0013106
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"csx1-related protein 1","termid":"PBO:0013106"}


id: MONDO:0045014
data:
  {"annotated_genes":["SJAG_03275","SJAG_03098"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012994"},{"annotations":[86960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007495"},{"annotations":[87338],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100186"}]},"cv_name":"mondo","definition":"A disease that has its basis in the disruption of tetrahydrobiopterin metabolic process.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of phenylalanine metabolism","termid":"MONDO:0017306"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03098":null,"SJAG_03275":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"tetrahydrobiopterin metabolic process disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:237913008","MEDGEN:575174","UMLS:C0342676"],"synonyms":[{"name":"disorder of tetrahydrobiopterin metabolic process","type":"exact"},{"name":"disorder of tetrahydrobiopterin metabolism","type":"exact"},{"name":"tetrahydrobiopterin metabolism disease","type":"exact"}],"termid":"MONDO:0045014","terms_by_termid":{"MONDO:0007495":null,"MONDO:0012994":null,"MONDO:0100186":null},"xrefs":{"Monarch":{"xref_id":"0045014"}}}


id: SO:0001969
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript variant occurring within an intron of a coding transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intron_variant","termid":"SO:0001627"},{"relation_name":"is_a","term_name":"coding_transcript_variant","termid":"SO:0001968"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coding_transcript_intron_variant","synonyms":[{"name":"Jannovar:coding_transcript_intron_variant","type":"exact"},{"name":"coding sequence intron variant","type":"exact"}],"termid":"SO:0001969"}


id: MONDO:0013671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any complete hydatidiform mole in which the cause of the disease is a mutation in the KHDC3L gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"coronary artery disorder","termid":"MONDO:0005010"},{"relation_name":"is_a","term_name":"complete hydatidiform mole","termid":"MONDO:0016785"},{"relation_name":"is_a","term_name":"gestational trophoblastic neoplasm","termid":"MONDO:0018944"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydatidiform mole, recurrent, 2","secondary_identifiers":["UMLS:C3280352","MEDGEN:481982","GARD:18366","OMIM:614293"],"synonyms":[{"name":"HYDM2","type":"related"},{"name":"KHDC3L complete hydatidiform mole","type":"exact"},{"name":"complete hydatidiform mole caused by mutation in KHDC3L","type":"exact"},{"name":"hydatidiform MOLE, recurrent, 2","type":"related"},{"name":"hydatidiform Mole, complete","type":"related"},{"name":"hydatidiform Mole, recurrent, type 2","type":"exact"},{"name":"hydatidiform mole, recurrent, 2","type":"exact"}],"termid":"MONDO:0013671","xrefs":{"Monarch":{"xref_id":"0013671"}}}


id: GO:0007206
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A phospholipase C-activating G protein-coupled receptor signaling pathway initiated by glutamate binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:mah","GOC:signaling","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase C-activating G protein-coupled receptor signaling pathway","termid":"GO:0007200"},{"relation_name":"is_a","term_name":"G protein-coupled glutamate receptor signaling pathway","termid":"GO:0007216"}],"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":"phospholipase C-activating G protein-coupled glutamate receptor signaling pathway","synonyms":[{"name":"activation of phospholipase C activity by G-protein coupled glutamate receptor signaling pathway","type":"related"},{"name":"activation of phospholipase C activity by metabotropic glutamate receptor signaling pathway","type":"related"},{"name":"activation of phospholipase C activity by metabotropic glutamate receptor signalling pathway","type":"related"},{"name":"metabotropic glutamate receptor, phospholipase C activating pathway","type":"related"},{"name":"phospholipase C-activating G-protein coupled glutamate receptor signaling pathway","type":"related"}],"termid":"GO:0007206"}


id: PBO:0073937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 17 member 9","termid":"PBO:0073937"}


id: PBO:0086347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PtdIns-3-P binding protein that tethers the ER to vacuoles at NVJs; anchored in the ER membrane at nucleus-vacuole junctions and binds phosphatidylinositol 3-phosphate (PtdIns-3-P) in the vacuolar membrane via its Phox homology (PX) domain; expressed predominantly in late G1 to early S phase of the cell cycle; mutation affects nuclear and mitochondrial transmission to daughter buds; similar to 4 human genes, one of which (SNX14) is associated with neurological disease","termid":"PBO:0086347"}


id: PBO:0048838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein nucleolar 3 like pseudogene 1","termid":"PBO:0048838"}


id: PBO:0062194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily R member 3 pseudogene","termid":"PBO:0062194"}


id: PBO:0086627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and to the nucleus","termid":"PBO:0086627"}


id: PBO:0017460
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-host_of","termid":"PBO:0017460"}


id: PBO:0075096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 145","termid":"PBO:0075096"}


id: MONDO:0007186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic disorder characterized by reflux of the gastric and/or duodenal contents into the distal esophagus. It is usually caused by incompetence of the lower esophageal sphincter. Symptoms include heartburn and acid indigestion. It may cause injury to the esophageal mucosa.","definition_xrefs":["NCIT:C26781"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"stomach disorder","termid":"MONDO:0004298"}],"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":"gastroesophageal reflux disease","secondary_identifiers":["SCTID:235595009","ICD9:530.81","EFO:0003948","DOID:8534","UMLS:C0017168","OMIM:109350","MEDGEN:6553","MESH:D005764"],"synonyms":[{"name":"GERD","type":"exact"},{"name":"GERD - gastro-esophageal reflux disease","type":"exact"},{"name":"Gastresophageal reflux","type":"exact"},{"name":"acid reflux","type":"exact"},{"name":"gastro-esophageal reflux","type":"exact"},{"name":"gastroesophageal reflux","type":"exact"},{"name":"gastroesophageal reflux disease","type":"exact"},{"name":"gastroesophageal reflux, paediatric","type":"related"},{"name":"gastroesophageal reflux, pediatric","type":"related"},{"name":"ger","type":"related"}],"termid":"MONDO:0007186","xrefs":{"Monarch":{"xref_id":"0007186"}}}


id: GO:0047819
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glutamate + H2O + O2 = 2-oxoglutarate + NH3 + H2O2, and D-aspartate + H2O + O2 = oxaloacetate + NH3 + H2O2.","definition_xrefs":["EC:1.4.3.15"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-amino-acid oxidase activity","termid":"GO:0003884"}],"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":"D-glutamate(D-aspartate) oxidase activity","synonyms":[{"name":"D-glutamate(D-aspartate):oxygen oxidoreductase (deaminating)","type":"related"},{"name":"D-glutamic-aspartic oxidase activity","type":"related"},{"name":"D-monoaminodicarboxylic acid oxidase activity","type":"related"}],"termid":"GO:0047819"}


id: PBO:0044340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 24","termid":"PBO:0044340"}


id: GO:0042846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycol, a diol in which the two hydroxy groups are on different carbon atoms, usually but not necessarily adjacent.","definition_xrefs":["Wikipedia:Ethylene_glycol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diol catabolic process","termid":"GO:0034313"},{"relation_name":"is_a","term_name":"glycol metabolic process","termid":"GO:0042844"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"glycol catabolic process","synonyms":[{"name":"dihydric alcohol catabolic process","type":"broad"},{"name":"dihydric alcohol catabolism","type":"broad"},{"name":"glycol breakdown","type":"exact"},{"name":"glycol catabolism","type":"exact"},{"name":"glycol degradation","type":"exact"}],"termid":"GO:0042846"}


id: GO:0102358
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-dihydroxycoumarin + S-adenosyl-L-methionine = 7-hydroxy-8-methoxycoumarin + H+ + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:68960"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"daphnetin-8-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-13448"],"termid":"GO:0102358"}


id: PATO:0000566
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000566 width value (obsolete PATO:0000566)","synonyms":[{"name":":breadth","type":"related"}],"termid":"PATO:0000566"}


id: PBO:0015219
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae SEC14","termid":"PBO:0015219"}


id: MONDO:0004166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fallopian tube carcinoma that has developed in relatives of patients that have a history of fallopian tube carcinoma.","definition_xrefs":["NCIT:C40455"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"fallopian tube carcinoma","termid":"MONDO:0006206"}],"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":"hereditary fallopian tube carcinoma","secondary_identifiers":["DOID:7266","UMLS:C1512418","MEDGEN:307556"],"synonyms":[{"name":"familial fallopian tube carcinoma","type":"exact"},{"name":"familiar fallopian tube carcinoma","type":"related"},{"name":"hereditary fallopian tube cancer","type":"exact"},{"name":"hereditary fallopian tube carcinoma","type":"exact"}],"termid":"MONDO:0004166","xrefs":{"Monarch":{"xref_id":"0004166"}}}


id: GO:1903126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of centriole-centriole cohesion.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:als","PMID:24554434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"regulation of centriole-centriole cohesion","termid":"GO:0030997"},{"relation_name":"negatively_regulates","term_name":"centriole-centriole cohesion","termid":"GO:0010457"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0007010","GO:0000226"],"is_obsolete":false,"name":"negative regulation of centriole-centriole cohesion","synonyms":[{"name":"down regulation of centriole-centriole cohesion","type":"exact"},{"name":"down-regulation of centriole-centriole cohesion","type":"exact"},{"name":"downregulation of centriole-centriole cohesion","type":"exact"},{"name":"inhibition of centriole-centriole cohesion","type":"narrow"}],"termid":"GO:1903126"}


id: GO:0061620
data:
  {"annotated_genes":["SJAG_04192","SJAG_03903","SJAG_03660","SJAG_00027","SJAG_03828","SJAG_02135","SJAG_02009","SJAG_02107","SJAG_00605","SJAG_06622","SJAG_02945","SJAG_00839","SJAG_04334","SJAG_04495","SJAG_02369","SJAG_01310","SJAG_00461","SJAG_03373","SJAG_06621","SJAG_02796"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111380,111374,107419,96474,100213,107418,105336,111377,111379,107788,107787,107417,111376,105593,74323,79726,99942,111378,118347,111375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a carbohydrate into pyruvate, occurring through a glucose-6-phosphate intermediate, with the concomitant production of a small amount of ATP.","definition_xrefs":["GOC:dph","ISBN:0201090910","ISBN:0879010479"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolytic process through fructose-6-phosphate","termid":"GO:0061615"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00839":null,"SJAG_01310":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02369":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006091","GO:0005975","GO:0055086"],"is_obsolete":false,"name":"glycolytic process through glucose-6-phosphate","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0061620","terms_by_termid":{"GO:0061621":null}}


id: PBO:0043610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COMM domain containing 3","termid":"PBO:0043610"}


id: PBO:0004246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"condensin complex subunit Cut14","termid":"PBO:0004246"}


id: PBO:0087321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Snf1p-related nutrient-responsive protein kinase; overexpression increases sodium and lithium tolerance, whereas gene disruption increases cation and low pH sensitivity and impairs potassium uptake, suggesting a role in regulation of Trk1p and/or Trk2p transporters; HAL5 has a paralog, KKQ8, that arose from the whole genome duplication","termid":"PBO:0087321"}


id: PBO:0074662
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 50B","termid":"PBO:0074662"}


id: MOD:01976
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O3-(poly-3-hydroxybutyrate)-L-serine.","definition_xrefs":["PubMed:17659252","PubMed:20004640","RESID:AA0618"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acylated residue","termid":"MOD:00671"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O3-(poly-3-hydroxybutyrate)-L-serine","synonyms":[{"name":"(2S)-2-amino-3-[([(3R)-3-hydroxybutanoyl]oxy)-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)]propanoic acid","type":"exact"},{"name":"MOD_RES O3-poly(beta-hydroxybutyryl)lysine","type":"exact"},{"name":"O3-(poly-3-hydroxybutyrate)-L-serine","type":"exact"},{"name":"O3-poly(3-hydroxybutanoate)serine","type":"exact"},{"name":"O3-poly(3-hydroxybutanoic acid)serine","type":"exact"},{"name":"O3-poly(3-hydroxybutyrate)serine","type":"exact"},{"name":"O3-poly(3-hydroxybutyric acid)serine","type":"exact"},{"name":"O3-poly(beta-hydroxybutyrate)serine","type":"exact"},{"name":"O3-poly[(R)-3-hydroxybutyrate]serine","type":"exact"}],"termid":"MOD:01976"}


id: PBO:0048030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fascin actin-bundling protein 1 pseudogene 1","termid":"PBO:0048030"}


id: PBO:0047261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 242 member D","termid":"PBO:0047261"}


id: GO:0043135
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-phospho-alpha-D-ribose 1-diphosphate + H2O = ribose 1,5 bisphosphate + phosphate + H+.","definition_xrefs":["PMID:12370170","MetaCyc:RXN-10969"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"5-phosphoribosyl 1-pyrophosphate pyrophosphatase activity","synonyms":[{"name":"PRPP pyrophosphatase activity","type":"exact"}],"termid":"GO:0043135"}


id: GO:0048650
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which individuals, having the potential to develop any of several distinct developmental paths, have their individual developmental fate determined in response to environmental cues. Individuals with distinct developmental fates perform different functions in a colony of social insects.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"caste determination","termid":"GO:0048648"},{"relation_name":"is_a","term_name":"polyphenic determination, influence by environmental factors","termid":"GO:0048651"}],"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":"caste determination, influence by environmental factors","termid":"GO:0048650"}


id: GO:1901816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving beta-zeacarotene.","definition_xrefs":["PMID:3710717","GOC:yaf","GOC:TermGenie","UniPathway:UPA00805"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid metabolic process","termid":"GO:0016116"},{"relation_name":"is_a","term_name":"carotene metabolic process","termid":"GO:0016119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"beta-zeacarotene metabolic process","synonyms":[{"name":"beta-zeacarotene metabolism","type":"exact"}],"termid":"GO:1901816"}


id: MONDO:0037255
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant epithelial tumor of the ovary characterized by the presence of neoplastic epithelial cells that, in well differentiated tumors, resemble the epithelial cells of the fallopian tube and, in poorly differentiated tumors, show anaplastic features. Approximately thirty to fifty percent of the tumors are bilateral. Grossly, the better differentiated tumors consist of cystic masses, usually unilocular, containing a clear but sometimes viscous fluid. Papillary formations are often present. The more malignant tumors tend to be solid and invasive, with areas of necrosis and hemorrhage.","definition_xrefs":["NCIT:C8431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian epithelial tumor","termid":"MONDO:0002229"},{"relation_name":"is_a","term_name":"serous neoplasm","termid":"MONDO:0037256"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian serous tumor","secondary_identifiers":["UMLS:C0476122","MEDGEN:141653"],"synonyms":[{"name":"ovarian serous neoplasm","type":"exact"},{"name":"ovarian serous tumor","type":"exact"},{"name":"serous neoplasm of ovary","type":"exact"},{"name":"serous neoplasm of the ovary","type":"exact"},{"name":"serous tumor of ovary","type":"exact"},{"name":"serous tumor of the ovary","type":"exact"},{"name":"serous tumour of ovary","type":"exact"},{"name":"serous tumour of the ovary","type":"exact"}],"termid":"MONDO:0037255","xrefs":{"Monarch":{"xref_id":"0037255"}}}


id: PBO:0043148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 16","termid":"PBO:0043148"}


id: MONDO:0008223
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypokalemic periodic paralysis (hypoPP) is characterized by episodes of muscle paralysis lasting from a few to 24-48 hours and associated with a fall in blood potassium levels.","definition_xrefs":["Orphanet:681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial periodic paralysis","termid":"MONDO:0000995"},{"relation_name":"is_a","term_name":"potassium deficiency disease","termid":"MONDO:0003019"}],"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":"hypokalemic periodic paralysis","secondary_identifiers":["NANDO:1200503","SCTID:82732003","MEDGEN:116058","DOID:14452","NCIT:C84775","GARD:6729","icd11.foundation:1494773635","MESH:D020514","UMLS:C0238358"],"synonyms":[{"name":"HKPP","type":"exact"},{"name":"HOKPP","type":"exact"},{"name":"HypoPP","type":"exact"},{"name":"Westphall disease","type":"exact"},{"name":"familial hypokalemic periodic paralysis","type":"exact"},{"name":"familial periodic paralysis (& [hypokalaemic])","type":"exact"},{"name":"hypokalemic familial periodic paralysis","type":"exact"},{"name":"hypokalemic periodic paralysis","type":"exact"},{"name":"periodic hypokalemic paralysis","type":"exact"},{"name":"periodic paralysis I","type":"narrow"}],"termid":"MONDO:0008223","xrefs":{"Monarch":{"xref_id":"0008223"}}}


id: PBO:0083964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Geranylgeranyl diphosphate synthase (GGPPS); increases the intracellular pool of geranylgeranyl diphosphate, suppressor of bet2 mutation that causes defective geranylgeranylation of small GTP-binding proteins that mediate vesicular traffic","termid":"PBO:0083964"}


id: MONDO:0016654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 5 syndrome is a rare chromosomal anomaly syndrome, with high phenotypic variability, principally characterized by a neonatal mewing cry, severe developmental delay and intellectual disability, short stature, hypotonia, dysmorphic features (incl. microcephaly, facial asymmetry, hypertelorism, epicanthal folds, abnormal ears, micro/retrognathia), congenital cardiac anomalies (such as atrial and ventricular septal defect, tricuspid insufficiency, hypoplastic aorta) and skeletal abnormalities (e.g. hypoplastic thumbs, anomalous ulna/radius, dysplastic metacarpals and phalanges).","definition_xrefs":["Orphanet:251043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 5 disorder","termid":"MONDO:0700012"},{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 5","secondary_identifiers":["UMLS:C4050064","SCTID:765487008","NCIT:C121984","GARD:10841","MEDGEN:881956"],"synonyms":[{"name":"R5","type":"related"},{"name":"Ring 5","type":"related"},{"name":"Ring chromosome 5 syndrome","type":"related"},{"name":"Ring chromosome type 5","type":"exact"},{"name":"chromosome 5 ring","type":"related"},{"name":"rose cluster 5","type":"exact"}],"termid":"MONDO:0016654","xrefs":{"Monarch":{"xref_id":"0016654"}}}


id: FYPO:0004934
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during G1 phase of the mitotic cell cycle 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"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased RNA level during mitotic G1 phase","synonyms":[{"name":"increased RNA accumulation during mitotic G1 phase","type":"related"},{"name":"increased RNA level during G1 phase of mitotic cell cycle","type":"exact"},{"name":"increased RNA level during mitotic G1 phase during vegetative growth","type":"exact"},{"name":"increased mRNA level during mitotic G1 phase","type":"narrow"},{"name":"increased transcript level during mitotic G1 phase","type":"exact"}],"termid":"FYPO:0004934"}


id: PBO:0086691
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; induced by treatment with 8-methoxypsoralen and UVA irradiation","termid":"PBO:0086691"}


id: GO:0120274
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a virus component, and in cooperation with a nearby primary receptor, initiating a change in cell activity.","definition_xrefs":["PMID:16051304","GOC:krc","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exogenous protein binding","termid":"GO:0140272"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"virus coreceptor activity","synonyms":[{"name":"viral coreceptor activity","type":"exact"}],"termid":"GO:0120274"}


id: MONDO:0014262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Loeys-Dietz syndrome-5 (LDS5), also known as Rienhoff (pronounced REENhoff) syndrome, is characterized by syndromic presentation of aortic aneurysms involving the thoracic and/or abdominal aorta, with risk of dissection and rupture. Other systemic features include cleft palate, bifid uvula, mitral valve disease, skeletal overgrowth, cervical spine instability, and clubfoot deformity; however, not all clinical features occur in all patients. In contrast to other forms of LDS, no striking aortic or arterial tortuosity is present in these patients, and there is no strong evidence for early aortic dissection.","definition_xrefs":["EFO:1000012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"Loeys-Dietz syndrome","termid":"MONDO:0018954"}],"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":"Rienhoff syndrome","secondary_identifiers":["DOID:0070236","GARD:12356","MEDGEN:816342","OMIM:615582","UMLS:C3810012"],"synonyms":[{"name":"LDS5","type":"related"},{"name":"Loeys-Dietz syndrome 5","type":"related"},{"name":"Loeys-Dietz syndrome type 5","type":"exact"},{"name":"Rienhoff syndrome","type":"exact"}],"termid":"MONDO:0014262","xrefs":{"Monarch":{"xref_id":"0014262"}}}


id: GO:0090216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of the catalysis of the reaction: ATP + 1-phosphatidyl-1D-myo-inositol 4-phosphate = ADP + 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of 1-phosphatidylinositol-4-phosphate 5-kinase activity (obsolete GO:0090216)","termid":"GO:0090216"}


id: FYPO:0003093
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which small RNA molecules physically associated with the Argonaute protein (Ago1) are longer than normal.","definition_xrefs":["PomBase:mah","PMID:24095277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985"],"is_obsolete":false,"name":"increased Argonaute-associated RNA length","synonyms":[{"name":"increased Argonaute-associated priRNA length","type":"narrow"},{"name":"increased Argonaute-associated siRNA length","type":"narrow"},{"name":"increased length of Ago1-associated RNA","type":"narrow"},{"name":"increased length of Argonaute-associated RNA","type":"exact"},{"name":"increased length of Argonaute-associated small RNA","type":"exact"}],"termid":"FYPO:0003093"}


id: GO:0030710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that regulates the frequency, rate or extent of border cell delamination.","definition_xrefs":["PMID:10822261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-cell adhesion","termid":"GO:0022407"},{"relation_name":"regulates","term_name":"border follicle cell delamination","termid":"GO:0030709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"regulation of border follicle cell delamination","synonyms":[{"name":"regulation of border cell delamination","type":"broad"}],"termid":"GO:0030710"}


id: PBO:0029837
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-single_microtubule_bundle","termid":"PBO:0029837"}


id: PBO:0078874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transient receptor potential cation channel subfamily M member 8","termid":"PBO:0078874"}


id: GO:1904373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a kainic acid stimulus.","definition_xrefs":["PMID:17443789","GO_REF:0000071","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to amino acid","termid":"GO:0043200"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to kainic acid","termid":"GO:1904373"}


id: GO:0120242
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-iminobutanoate + H2O = 2-oxobutanoate + NH4(+).","definition_xrefs":["RHEA:39975"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-iminobutanoate/2-iminopropanoate deaminase","termid":"GO:0120241"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016810","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"2-iminobutanoate deaminase activity","secondary_identifiers":["Reactome:R-HSA-9014641","KEGG_REACTION:R11098","MetaCyc:RXN-15123"],"synonyms":[{"name":"2-iminobutanoate/2-iminopropanoate deaminase","type":"broad"}],"termid":"GO:0120242"}


id: GO:0009437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving carnitine (hydroxy-trimethyl aminobutyric acid), a compound that participates in the transfer of acyl groups across the inner mitochondrial membrane.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine metabolic process","termid":"GO:0006577"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"carnitine metabolic process","synonyms":[{"name":"carnitine metabolism","type":"exact"},{"name":"vitamin Bt metabolic process","type":"exact"},{"name":"vitamin Bt metabolism","type":"exact"}],"termid":"GO:0009437"}


id: MONDO:0015984
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare genetic immune system disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic immune disease (obsolete MONDO:0015984)","secondary_identifiers":["Orphanet:183770"],"synonyms":[{"name":"rare genetic immune system disease","type":"exact"}],"termid":"MONDO:0015984","xrefs":{"Monarch":{"xref_id":"0015984"}}}


id: GO:0097075
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An interferon regulatory factor complex that consists of a heterodimer of interferon regulatory factor 3 and interferon regulatory factor 7.","definition_xrefs":["GOC:cna","PMID:18068231"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interferon regulatory factor complex","termid":"GO:0097071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"interferon regulatory factor 3-interferon regulatory factor 7 complex","synonyms":[{"name":"IRF3:IRF7 complex","type":"exact"}],"termid":"GO:0097075"}


id: FYPO:0006054
data:
  {"alleles_by_uniquename":{"SJAG_02763:allele-4":{"allele_type":"amino_acid_mutation","description":"S235E; S651E","gene_uniquename":"SJAG_02763","name":"ned1S235E/S651E","synonyms":[{"name":"phosphomimetic","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-4"},"SJAG_02763:allele-5":{"allele_type":"amino_acid_mutation","description":"S499E; S538E; T620E; T638E; S651E","gene_uniquename":"SJAG_02763","name":"ned1-5E","uniquename":"SJAG_02763:allele-5"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121433,121436],"is_not":false,"summary":null,"term":"FYPO:0006054"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of lipid droplet formation is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"lipid droplets present in decreased numbers","termid":"FYPO:0002552"},{"relation_name":"is_a","term_name":"abnormal lipid droplet formation","termid":"FYPO:0008430"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02763":null},"genotype_count":2,"genotypes_by_uniquename":{"ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ned1-5E(S499E; S538E; T620E; T638E; S651E aa)","display_uniquename":"ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-5","expression":"Not assayed or wild type"}]}]},"ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ned1S235E/S651E(S235E; S651E aa)","display_uniquename":"ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-4","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased lipid droplet formation","references_by_uniquename":{"PMID:26774782":null},"single_locus_annotated_genes":["SJAG_02763"],"single_locus_genotype_uniquenames":["ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"decreased lipid droplet assembly","type":"exact"},{"name":"decreased lipid particle formation","type":"exact"},{"name":"reduced lipid droplet formation","type":"exact"}],"termid":"FYPO:0006054","terms_by_termid":{"FYPO:0006054":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0049714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAUS augmin like complex subunit 1 pseudogene 2","termid":"PBO:0049714"}


id: GO:0051115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transient uridylylation of peptidyl-histidine to form 1'-(phospho-5'-uridine)-L-histidine (otherwise known as tau-UMP-histidine, tele-UMP-histidine).","definition_xrefs":["RESID:AA0372"],"gene_count":0,"genotype_count":0,"name":"obsolete enzyme active site formation via 1'-(phospho-5'-uridine)-L-histidine (obsolete GO:0051115)","termid":"GO:0051115"}


id: FYPO:0003319
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell adhesion phenotype observed in the vegetative growth phase of the life cycle in which mannose-specific flocculation is increased. Mannose-specific flocculation is the non-sexual aggregation of cells, mediated via the binding of cell wall proteins on one cell to mannose residues on the other, and when it is increased cells adhere to each other more strongly or to a greater extent than normal.","definition_xrefs":["PomBase:mah","GO:0036350"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cell-cell adhesion","termid":"FYPO:0005760"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased mannose-specific flocculation","synonyms":[{"name":"increased cell-cell adhesion involved in mannose-specific flocculation","type":"exact"},{"name":"increased mannose-specific flocculation during mitotic cell cycle","type":"related"},{"name":"increased mannose-specific flocculation during vegetative growth","type":"exact"}],"termid":"FYPO:0003319"}


id: PBO:0049942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxyisobutyryl-CoA hydrolase","termid":"PBO:0049942"}


id: GO:0045007
data:
  {"annotated_genes":["SJAG_02261"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96818],"is_not":false,"summary":null,"term":"GO:0045007"}]},"cv_name":"biological_process","definition":"The disruption of the bond between the sugar in the backbone and the A or G base, causing the base to be removed and leaving a depurinated sugar.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"base-excision repair, AP site formation","termid":"GO:0006285"},{"relation_name":"is_a","term_name":"DNA modification","termid":"GO:0006304"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006281"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0006281"],"is_obsolete":false,"name":"depurination","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Depurination","Reactome:R-HSA-73927"],"termid":"GO:0045007","terms_by_termid":{"GO:0045007":null}}


id: PBO:0075538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"speedy/RINGO cell cycle regulator family member E18","termid":"PBO:0075538"}


id: PBO:0012844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ski complex interacting GTPase Ski7","termid":"PBO:0012844"}


id: MONDO:0014018
data:
  {"annotated_genes":["SJAG_04506","SJAG_04292","SJAG_00199"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87200,87201,87202],"is_not":false,"summary":null,"term":"MONDO:0014018"}]},"cv_name":"mondo","definition":"A rare, complex form of hereditary spastic paraplegia characterized by the onset in early childhood of progressive spastic paraplegia associated with cerebellar signs, short stature, delayed psychomotor development, intellectual disability and, less commonly, foot contractures, dysarthria, dysphagia, strabismus and optic hypoplasia. SPG54 is caused by mutations in the DDHD2 gene (8p11.23) encoding phospholipase DDHD2.","definition_xrefs":["Orphanet:320380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00199":null,"SJAG_04292":null,"SJAG_04506":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 54","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110806","GARD:17475","OMIM:615033","MEDGEN:761341","SCTID:723824005","UMLS:C3539495"],"synonyms":[{"name":"DDHD2 autosomal recessive complex spastic paraplegia","type":"exact"},{"name":"SPG54","type":"exact"},{"name":"autosomal recessive complex spastic paraplegia caused by mutation in DDHD2","type":"exact"},{"name":"autosomal recessive spastic paraplegia 54","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 54","type":"exact"},{"name":"hereditary spastic paraplegia type 54","type":"exact"},{"name":"spastic paraplegia 54, autosomal recessive","type":"related"}],"termid":"MONDO:0014018","terms_by_termid":{"MONDO:0014018":null},"xrefs":{"Monarch":{"xref_id":"0014018"}}}


id: SO:0002183
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes a sense overlap long non-coding RNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"lncRNA_gene","termid":"SO:0002127"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sense_overlap_lncRNA_gene","synonyms":[{"name":"sense overlap lncRNA gene","type":"exact"},{"name":"sense overlap ncRNA gene","type":"exact"},{"name":"sense_overlap_lncRNA_gene","type":"exact"}],"termid":"SO:0002183"}


id: FYPO:0000920
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of aconitate hydratase (also known as aconitase) activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000654","FYPO:0000661"],"is_obsolete":false,"name":"abnormal aconitate hydratase activity","synonyms":[{"name":"abnormal aconitase activity","type":"exact"}],"termid":"FYPO:0000920"}


id: MONDO:0005808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the conjunctiva in a newborn due to Chlamydia trachomatis which was acquired during labor and delivery.","definition_xrefs":["NCIT:C116817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlamydia trachomatis infectious disease","termid":"MONDO:0005701"},{"relation_name":"is_a","term_name":"bacterial conjunctivitis","termid":"MONDO:0006668"}],"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":"inclusion conjunctivitis","secondary_identifiers":["ICD9:077.0","ICD9:077.98","SCTID:231861005","EFO:0007324","ICD10CM:A74.0","DOID:13800","MEDGEN:1095","MESH:D003235","UMLS:C0009770"],"synonyms":[{"name":"Chlamydial conjunctivitis","type":"exact"},{"name":"Paratrachoma","type":"related"},{"name":"Trachoma","type":"exact"},{"name":"adult inclusion conjunctivitis","type":"exact"},{"name":"inclusion blennorrhoea","type":"exact"},{"name":"inclusion blenorrhea","type":"exact"},{"name":"neonatal Chlamydia conjunctivitis","type":"exact"}],"termid":"MONDO:0005808","xrefs":{"Monarch":{"xref_id":"0005808"}}}


id: FYPO:0002798
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of protein degradation is decreased when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"increased protein level during cellular response to nitrogen starvation","termid":"FYPO:0001219"},{"relation_name":"is_a","term_name":"abnormal protein degradation during nitrogen starvation","termid":"FYPO:0002796"},{"relation_name":"is_a","term_name":"decreased protein degradation","termid":"FYPO:0002797"}],"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:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0002274"],"is_obsolete":false,"name":"decreased protein degradation during nitrogen starvation","synonyms":[{"name":"decreased protein catabolic process during nitrogen starvation","type":"exact"},{"name":"decreased protein catabolism during nitrogen starvation","type":"exact"},{"name":"decreased protein degradation during nitrogen depletion","type":"exact"},{"name":"decreased protein degradation during nitrogen deprivation","type":"exact"},{"name":"reduced protein degradation during nitrogen starvation","type":"exact"}],"termid":"FYPO:0002798"}


id: PBO:0058367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4739","termid":"PBO:0058367"}


id: MONDO:0015945
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Polymalformative genetic syndrome with increased risk of developing cancer (PGSIRC) comprises a wide range of syndromes characterized by congenital malformations with a high risk of developing tumors including up to 50 different rare diseases.","definition_xrefs":["Orphanet:183422"],"gene_count":0,"genotype_count":0,"name":"obsolete polymalformative genetic syndrome with increased risk of developing cancer (obsolete MONDO:0015945)","synonyms":[{"name":"PGSIRC","type":"exact"}],"termid":"MONDO:0015945","xrefs":{"Monarch":{"xref_id":"0015945"}}}


id: PBO:0047425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fc alpha receptor","termid":"PBO:0047425"}


id: PBO:0039462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD11 pseudogene 2","termid":"PBO:0039462"}


id: PBO:0066397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regenerating family member 1 alpha","termid":"PBO:0066397"}


id: GO:0004488
data:
  {"annotated_genes":["SJAG_04156","SJAG_01126","SJAG_00106"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58082,77587,78473],"is_not":false,"summary":null,"term":"GO:0004488"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,10-methylenetetrahydrofolate + NADP+ = 5,10-methenyltetrahydrofolate + NADPH.","definition_xrefs":["EC:1.5.1.5","RHEA:22812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_01126":null,"SJAG_04156":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"methylenetetrahydrofolate dehydrogenase (NADP+) activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-200718","MetaCyc:METHYLENETHFDEHYDROG-NADP-RXN","Reactome:R-HSA-200644","KEGG_REACTION:R01220"],"synonyms":[{"name":"5,10-methylenetetrahydrofolate:NADP oxidoreductase activity","type":"related"},{"name":"5,10-methylenetetrahydrofolate:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0004488","terms_by_termid":{"GO:0004488":null}}


id: PBO:0003426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2AF large subunit (U2AF-59)","termid":"PBO:0003426"}


id: GO:0008868
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: galactitol-1-phosphate + NAD+ = D-tagatose 6-phosphate + NADH + H+.","definition_xrefs":["EC:1.1.1.251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"galactitol-1-phosphate 5-dehydrogenase activity","secondary_identifiers":["MetaCyc:1.1.1.251-RXN","RHEA:15137"],"synonyms":[{"name":"galactitol-1-phosphate:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0008868"}


id: MONDO:0018710
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"macrocephaly, dysmorphic facies, and psychomotor retardation","termid":"MONDO:0014863"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"overgrowth syndrome","termid":"MONDO:0019716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megalencephaly-severe kyphoscoliosis-overgrowth syndrome","secondary_identifiers":["UMLS:C5681123","Orphanet:457359","GARD:17805","MEDGEN:1814470"],"termid":"MONDO:0018710","xrefs":{"Monarch":{"xref_id":"0018710"}}}


id: PBO:0055316
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 2744","termid":"PBO:0055316"}


id: PBO:0000507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin-dependent kinase activating kinase Csk1","termid":"PBO:0000507"}


id: PBO:0058131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4432 host gene","termid":"PBO:0058131"}


id: SO:0000436
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence that can autonomously replicate, as a plasmid, when transformed into a bacterial host.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"origin_of_replication","termid":"SO:0000296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARS","synonyms":[{"name":"autonomously replicating sequence","type":"exact"}],"termid":"SO:0000436"}


id: PBO:0045239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 7","termid":"PBO:0045239"}


id: GO:1903123
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of thioredoxin peroxidase activity.","definition_xrefs":["GOC:PARL","GO_REF:0000059","GOC:bf","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of thioredoxin peroxidase activity (obsolete GO:1903123)","synonyms":[{"name":"regulation of TPx activity","type":"exact"},{"name":"regulation of TrxPx activity","type":"exact"},{"name":"regulation of thiol peroxidase activity","type":"exact"}],"termid":"GO:1903123"}


id: PBO:0082268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ammonium permease involved in regulation of pseudohyphal growth; belongs to Mep-Amt-Rh family of well-conserved ammonium (NH4+) transporters that includes human Rh factors; expression is under the nitrogen catabolite repression regulation; activity is controlled by phospho-silencing; phosphorylation of Mep2 mediated by Npr1; dephosphorylation involves Psr1p and Psr2p","termid":"PBO:0082268"}


id: PBO:0078105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPPC12 antisense RNA 1","termid":"PBO:0078105"}


id: PBO:0072725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RYK pseudogene 1","termid":"PBO:0072725"}


id: GO:0004394
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phosphoadenosine 5'-phosphosulfate + heparan sulfate = adenosine 3',5'-bisphosphate + heparan sulfate 2-O-sulfate; results in 2-O-sulfation of iduronic acid residues in heparan sulfate.","definition_xrefs":["PMID:9153262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heparan sulfate sulfotransferase activity","termid":"GO:0034483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016782","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"heparan sulfate 2-sulfotransferase activity","secondary_identifiers":["MetaCyc:RXN-11558","Reactome:R-HSA-2076508"],"synonyms":[{"name":"heparan sulfate 2-O-sulfotransferase activity","type":"exact"},{"name":"heparan-sulfate 2-O-sulphotransferase activity","type":"exact"},{"name":"heparin 2-sulfotransferase activity","type":"related"},{"name":"heparin-sulphate 2-sulphotransferase activity","type":"related"}],"termid":"GO:0004394"}


id: GO:0019182
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the energy-independent facilitated diffusion of a chloride ion through a transmembrane channel that opens when bound to histamine.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chloride channel activity","termid":"GO:0005254"}],"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:0022857","GO:0005215"],"is_obsolete":false,"name":"histamine-gated chloride channel activity","termid":"GO:0019182"}


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: PBO:0011522
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dfp1 half-life 30-45 minutes in S and G2 phases","termid":"PBO:0011522"}


id: PBO:0090617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eIF4E-associated protein Eap1","termid":"PBO:0090617"}


id: GO:0002204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which immunoglobulin genes are formed through recombination of the germline genetic elements, also known as immunoglobulin gene segments, within a single locus following the induction of and contributing to an immune response.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immunoglobulins involved in immune response","termid":"GO:0002208"},{"relation_name":"is_a","term_name":"somatic recombination of immunoglobulin gene segments","termid":"GO:0016447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006259","GO:0010467","GO:0006310","GO:0008150"],"is_obsolete":false,"name":"somatic recombination of immunoglobulin genes involved in immune response","synonyms":[{"name":"somatic recombination of antibody genes during immune response","type":"related"},{"name":"somatic recombination of immunoglobulin genes during immune response","type":"related"}],"termid":"GO:0002204"}


id: MOD:00640
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6-N-biotinylaminohexyl isopropyl phosphorofluoridate","synonyms":[{"name":"6-N-biotinylaminohexyl isopropyl phosphate","type":"related"},{"name":"Can-FP-biotin","type":"related"}],"termid":"MOD:00640"}


id: SO:0001921
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A contig of mitochondria derived sequences.","definition_xrefs":["GMOD:ea"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"mitochondrial_sequence","termid":"SO:0000737"},{"relation_name":"is_a","term_name":"contig","termid":"SO:0000149"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial_contig","synonyms":[{"name":"mitochondrial contig","type":"exact"}],"termid":"SO:0001921"}


id: MONDO:0859347
data:
  {"annotated_genes":["SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87532],"is_not":false,"summary":null,"term":"MONDO:0859347"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00134":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620191","UMLS:C5774285","MEDGEN:1824058"],"termid":"MONDO:0859347","terms_by_termid":{"MONDO:0859347":null},"xrefs":{"Monarch":{"xref_id":"0859347"}}}


id: MONDO:1011473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Amyloidosis that occurs in Japanese quail.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"amyloidosis, non-human animal","termid":"MONDO:1011415"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloidosis, Japanese quail","secondary_identifiers":["OMIA:000037-93934"],"termid":"MONDO:1011473","xrefs":{"Monarch":{"xref_id":"1011473"}}}


id: PBO:0061304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NPEPPS pseudogene 1","termid":"PBO:0061304"}


id: PATO:0001924
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being positioned towards the middle of an organism.","definition_xrefs":["PATOC:mb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalised","termid":"PATO:0000628"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mislocalised medially","termid":"PATO:0001924"}


id: GO:0038070
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the phosphorylation and activation of a MAP kinase kinase (MAPKK), as part of a MAPK signaling cascade that contributes to cell wall organization or biogenesis.","definition_xrefs":["GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete MAP kinase kinase kinase activity involved in cell wall organization or biogenesis (obsolete GO:0038070)","synonyms":[{"name":"MAP kinase kinase kinase activity involved in cell wall biogenesis","type":"exact"},{"name":"MAP3K activity involved in cell wall integrity","type":"exact"},{"name":"MAPKKK activity involved in cell wall integrity","type":"exact"}],"termid":"GO:0038070"}


id: PBO:0030569
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_glutamine_level","termid":"PBO:0030569"}


id: PBO:0086138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for mismatch repair in mitosis and meiosis; forms a complex with Msh2p to repair both single-base & insertion-deletion mispairs; also involved in interstrand cross-link repair; potentially phosphorylated by Cdc28p; contains PIP motif that binds PCNA (Pol30p) and Rev1p","termid":"PBO:0086138"}


id: PBO:0029805
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_mixed_population_including_germinated_spores_and_cells_with_abnormal_shape_(obsolete_FYPO:0002432)","termid":"PBO:0029805"}


id: FYPO:0006338
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the divided nuclei are located near the cell tips (instead of at the midpoint of the long axis of each daughter cell) during telophase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah","PMID:15937127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized nucleus during mitotic telophase","termid":"FYPO:0009105"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"nucleus mislocalized towards cell tip during mitotic telophase","synonyms":[{"name":"nuclear displacement towards cell tip during mitotic telophase","type":"exact"},{"name":"nucleus displaced towards cell tip during mitotic telophase","type":"exact"},{"name":"nucleus mislocalised to cell tip during mitotic telophase","type":"exact"},{"name":"nucleus mislocalized towards cell end during mitotic telophase","type":"exact"},{"name":"nucleus mislocalized towards cell tip during mitotic telophase during mitotic cell cycle","type":"related"},{"name":"nucleus mislocalized towards cell tip during mitotic telophase during vegetative growth","type":"exact"},{"name":"telophase nucleus mislocalized to cell tip","type":"exact"}],"termid":"FYPO:0006338"}


id: PBO:0028157
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-branched,_curved,_elongated,_multiseptate_vegetative_cell","termid":"PBO:0028157"}


id: PBO:0043209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC28 protein kinase regulatory subunit 1B pseudogene 2","termid":"PBO:0043209"}


id: GO:0102713
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A25 + 2-oxoglutarate(2-) + O2 = gibberellin A46 + succinate(2-) + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A25 hydroxylase activity (obsolete GO:0102713)","termid":"GO:0102713"}


id: PBO:0089187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial Mpv17/PMP22 family protein 1","termid":"PBO:0089187"}


id: PBO:0090245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-type ATPase inhibitor and disassembly protein linked to MTOR","termid":"PBO:0090245"}


id: PBO:0083659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endonuclease that cleaves pre-rRNA at site A2 for 18S rRNA biogenesis; subunit of U3-containing 90S preribosome processome complex involved in small ribosomal subunit assembly; stimulates Bms1p GTPase and U3 binding activity; similar to RNA cyclase-like proteins but no cyclase activity detected","termid":"PBO:0083659"}


id: MONDO:0008176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bone Paget disease","termid":"MONDO:0005382"},{"relation_name":"is_a","term_name":"SQSTM1-related multisystem proteinopathy","termid":"MONDO:0800464"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"Paget disease of bone 3","secondary_identifiers":["DOID:0081366","OMIM:167250","UMLS:C4085252","MEDGEN:895927"],"synonyms":[{"name":"PDB3","type":"related"},{"name":"Paget disease of bone 3","type":"exact"},{"name":"Paget disease of bone type 3","type":"exact"},{"name":"Paget disease of bone, familial","type":"related"},{"name":"familial Paget disease of bone","type":"related"}],"termid":"MONDO:0008176","xrefs":{"Monarch":{"xref_id":"0008176"}}}


id: PBO:0050986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intraflagellar transport 70A","termid":"PBO:0050986"}


id: PBO:0079222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetratricopeptide repeat domain 1","termid":"PBO:0079222"}


id: GO:0052013
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the breakdown of macromolecules within the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by symbiont of host macromolecule (obsolete GO:0052013)","synonyms":[{"name":"catabolism by organism of host macromolecule","type":"exact"}],"termid":"GO:0052013"}


id: GO:0021826
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process where neuronal precursors migrate tangentially in the telencephalon, primarily guided by interactions that do not require cell-cell contact.","definition_xrefs":["GOC:dph","PMID:12626695","GOC:jid","GOC:dgh","GO_REF:0000021","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telencephalon cell migration","termid":"GO:0022029"}],"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":"substrate-independent telencephalic tangential migration","termid":"GO:0021826"}


id: GO:0038182
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an extracellular bile acid and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["PMID:12524422","PMID:35415765","PMID:36409000","PMID:32480317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled bile acid receptor activity","secondary_identifiers":["Wikipedia:G_protein-coupled_bile_acid_receptor"],"synonyms":[{"name":"G-protein coupled bile acid receptor activity","type":"exact"},{"name":"cell surface bile acid receptor","type":"broad"},{"name":"lithocholic acid receptor activity","type":"broad"},{"name":"membrane bile acid receptor activity","type":"broad"}],"termid":"GO:0038182"}


id: PBO:0047429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCF1 rRNA-processing protein","termid":"PBO:0047429"}


id: GO:0061510
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a protein is transported to, or maintained to the new mitotic spindle pole body resulting in its being distributed asymmetrically.","definition_xrefs":["GOC:dph","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete asymmetric protein localization to new mitotic spindle pole body (obsolete GO:0061510)","termid":"GO:0061510"}


id: PBO:0073942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 18 member B1","termid":"PBO:0073942"}


id: GO:0021701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroblasts acquire specialized structural and/or functional features that characterize the mature cerebellar Golgi cell. Differentiation includes the processes involved in commitment of a neuroblast to a Golgi cell fate. A cerebellar Golgi cell is an inhibitory GABAergic interneuron found in the cerebellar cortex.","definition_xrefs":["GOC:jid","GOC:dph","PMID:15157725","GOC:cls","GO_REF:0000021","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation in hindbrain","termid":"GO:0021533"},{"relation_name":"is_a","term_name":"central nervous system neuron differentiation","termid":"GO:0021953"},{"relation_name":"is_a","term_name":"GABAergic neuron differentiation","termid":"GO:0097154"},{"relation_name":"part_of","term_name":"cerebellar granular layer formation","termid":"GO:0021684"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebellar Golgi cell differentiation","termid":"GO:0021701"}


id: PBO:0017597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein Ssz1 (predicted)","termid":"PBO:0017597"}


id: PBO:0091007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, stationary phase-specific Phx1","termid":"PBO:0091007"}


id: GO:0038190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by vascular endothelial growth factor (VEGF) binding to a neuropilin protein on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:BHF","GOC:rl","PMID:12852851"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular endothelial growth factor signaling pathway","termid":"GO:0038084"},{"relation_name":"is_a","term_name":"neuropilin signaling pathway","termid":"GO:0038189"}],"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":"VEGF-activated neuropilin signaling pathway","synonyms":[{"name":"VEGF-Npn-1 signaling","type":"exact"},{"name":"vascular endothelial growth factor-activated neuropilin signaling pathway","type":"exact"}],"termid":"GO:0038190"}


id: GO:0035605
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a nitric oxide (NO) group to a sulphur atom within a cysteine residue of a protein.","definition_xrefs":["PMID:20972426","GOC:sp","PMID:20972425"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring nitrogenous groups","termid":"GO:0016769"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0140096","GO:0016769","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"peptidyl-cysteine S-nitrosylase activity","synonyms":[{"name":"S-nitrosylase activity","type":"exact"},{"name":"protein nitrosylase activity","type":"related"}],"termid":"GO:0035605"}


id: PBO:0063723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progesterone receptor membrane component 1","termid":"PBO:0063723"}


id: MONDO:0012316
data:
  {"annotated_genes":["SJAG_02763"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87805],"is_not":false,"summary":null,"term":"MONDO:0012316"}]},"cv_name":"mondo","definition":"Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis.","definition_xrefs":["Orphanet:77297"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic recurrent multifocal osteomyelitis","termid":"MONDO:0009813"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02763":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"Majeed syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C537839","SCTID:703540008","ICD9:759.89","MEDGEN:351273","NANDO:2200453","NCIT:C119058","UMLS:C1864997","GARD:10088","icd11.foundation:1316564349","MedDRA:10072223","OMIM:609628"],"synonyms":[{"name":"CDA and CRMO","type":"related"},{"name":"MAJEED syndrome","type":"related"},{"name":"MJDS","type":"related"},{"name":"Majeed syndrome","type":"exact"},{"name":"chronic recurrent multifocal osteomyelitis, congenital","type":"related"},{"name":"chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic Anemia, and neutrophilic dermatosis","type":"related"},{"name":"chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome","type":"exact"},{"name":"congenital dyserythropoietic anaemia and chronic recurrent multifocal osteomyelitis","type":"related"},{"name":"congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis","type":"related"},{"name":"dyserythropoietic anemia, and neutrophilic dermatosis","type":"related"}],"termid":"MONDO:0012316","terms_by_termid":{"MONDO:0012316":null},"xrefs":{"Monarch":{"xref_id":"0012316"}}}


id: MOD:00700
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct with a compound containing a tetrapyrrole group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetrapyrrole modified residue","synonyms":[{"name":"TetrapyrRes","type":"exact"}],"termid":"MOD:00700"}


id: PBO:0086346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P subunit of the mitochondrial glycine decarboxylase complex; glycine decarboxylase is required for the catabolism of glycine to 5,10-methylene-THF; expression is regulated by levels of 5,10-methylene-THF in the cytoplasm","termid":"PBO:0086346"}


id: GO:0006936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within muscle tissue, resulting in a change in muscle geometry. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis.","definition_xrefs":["GOC:ef","GOC:mtg_muscle","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle system process","termid":"GO:0003012"}],"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":"muscle contraction","secondary_identifiers":["Reactome:R-HSA-445355","Wikipedia:Muscle_contraction"],"termid":"GO:0006936"}


id: GO:0044732
data:
  {"annotated_genes":["SJAG_04498","SJAG_00104","SJAG_03843","SJAG_04551","SJAG_01224","SJAG_05309","SJAG_05290","SJAG_01790","SJAG_00229","SJAG_04931","SJAG_04461","SJAG_01371","SJAG_01620","SJAG_03048","SJAG_04239","SJAG_03592","SJAG_01760","SJAG_00910","SJAG_05264","SJAG_01756","SJAG_00773","SJAG_03216","SJAG_04841","SJAG_03116","SJAG_03351","SJAG_03501","SJAG_01422","SJAG_04609","SJAG_00317","SJAG_04745","SJAG_01785","SJAG_03615","SJAG_02246","SJAG_01370","SJAG_03200","SJAG_03695","SJAG_01146","SJAG_00719","SJAG_00907","SJAG_04558","SJAG_02332","SJAG_03376","SJAG_03026","SJAG_01775","SJAG_01799","SJAG_01242","SJAG_07018","SJAG_02186","SJAG_03681","SJAG_01232","SJAG_03810","SJAG_02336","SJAG_00646","SJAG_06270","SJAG_04140","SJAG_02795","SJAG_04455","SJAG_00082","SJAG_00800","SJAG_04595","SJAG_01805","SJAG_03062","SJAG_02624","SJAG_05266","SJAG_00356","SJAG_02886","SJAG_05978","SJAG_05196","SJAG_00472","SJAG_04597","SJAG_05315","SJAG_01297","SJAG_02444","SJAG_03936","SJAG_02104","SJAG_02761","SJAG_02724","SJAG_02058","SJAG_00666","SJAG_00918","SJAG_03612","SJAG_04943","SJAG_03508","SJAG_03259","SJAG_01082","SJAG_02542","SJAG_00807","SJAG_01546","SJAG_00333","SJAG_03891","SJAG_01386","SJAG_02921","SJAG_05207","SJAG_02609","SJAG_02737","SJAG_01330","SJAG_01401","SJAG_04653","SJAG_00982","SJAG_04280","SJAG_01538","SJAG_04468","SJAG_01215","SJAG_02514","SJAG_04901","SJAG_02550","SJAG_01464","SJAG_02169","SJAG_05205","SJAG_03544","SJAG_02266","SJAG_03835","SJAG_02616","SJAG_05185","SJAG_03602","SJAG_00724","SJAG_03264","SJAG_00526","SJAG_01188","SJAG_02232","SJAG_03540","SJAG_03342","SJAG_01745","SJAG_03287","SJAG_02098","SJAG_04980","SJAG_02556","SJAG_02045","SJAG_03052","SJAG_04457","SJAG_01563","SJAG_04884","SJAG_02923","SJAG_03491","SJAG_00142","SJAG_02299","SJAG_00856","SJAG_03708"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[66885,70328,72435,72635,76566,89339,90899,91187,91559,91593,91691,91936,92071,92665,92924,92934,93127,93281,93327,93703,94238,94471,94872,95204,95403,95682,95740,95824,95885,96172,96199,96346,96354,96720,98224,98276,98333,98343,98421,98661,98714,99221,99398,99749,99975,100375,100566,101552,102041,102096,102161,102331,102478,102494,102556,103226,103575,104095,104274,105002,105666,105770,105842,106534,107143,107443,108281,108322,108413,108599,108814,109475,110226,110313,110716,110731,111003,111535,111886,111944,112153,112161,112912,113042,113490,113672,114466,114760,114996,115660,116680,116794,116910,116947,117289,117897,118000,118510,118707,119019,119193,119205,119279,119299,120234,120777,121257,121259,121269],"is_not":false,"summary":null,"term":"GO:0044732"},{"annotations":[96930,99888,104952,107347,116987,118411],"is_not":true,"summary":null,"term":"GO:0044732"},{"annotations":[101804,98807,100218],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061493"},{"annotations":[118937,110821,114631,112566,117118,114833,111581],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061496"},{"annotations":[102943,110822,112567,113421,104760,111582],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061497"},{"annotations":[109112,104306,104766,101808,108352,93084,112509,107318,113182,102902],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071958"},{"annotations":[104309,114837,104769,111587,110828,108353,112570,94787,97587,112511,109512,101618,113188,116491,107007],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071957"},{"annotations":[110829,109068,118942],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061499"},{"annotations":[94788,117471],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0160065"}]},"cv_name":"cellular_component","definition":"The microtubule organizing center that forms as part of the mitotic cell cycle; functionally homologous to the animal cell centrosome.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle pole body","termid":"GO:0005816"}],"gene_count":138,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00093":null,"SJAG_00104":null,"SJAG_00142":null,"SJAG_00229":null,"SJAG_00317":null,"SJAG_00333":null,"SJAG_00356":null,"SJAG_00471":null,"SJAG_00472":null,"SJAG_00526":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00719":null,"SJAG_00724":null,"SJAG_00773":null,"SJAG_00800":null,"SJAG_00807":null,"SJAG_00856":null,"SJAG_00907":null,"SJAG_00910":null,"SJAG_00918":null,"SJAG_00982":null,"SJAG_01065":null,"SJAG_01082":null,"SJAG_01146":null,"SJAG_01188":null,"SJAG_01215":null,"SJAG_01224":null,"SJAG_01232":null,"SJAG_01242":null,"SJAG_01293":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01386":null,"SJAG_01401":null,"SJAG_01422":null,"SJAG_01464":null,"SJAG_01538":null,"SJAG_01546":null,"SJAG_01563":null,"SJAG_01584":null,"SJAG_01620":null,"SJAG_01745":null,"SJAG_01756":null,"SJAG_01760":null,"SJAG_01775":null,"SJAG_01785":null,"SJAG_01790":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_02045":null,"SJAG_02058":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02169":null,"SJAG_02186":null,"SJAG_02232":null,"SJAG_02246":null,"SJAG_02266":null,"SJAG_02274":null,"SJAG_02299":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02444":null,"SJAG_02514":null,"SJAG_02542":null,"SJAG_02550":null,"SJAG_02556":null,"SJAG_02609":null,"SJAG_02616":null,"SJAG_02624":null,"SJAG_02724":null,"SJAG_02737":null,"SJAG_02761":null,"SJAG_02795":null,"SJAG_02886":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03052":null,"SJAG_03062":null,"SJAG_03116":null,"SJAG_03200":null,"SJAG_03216":null,"SJAG_03259":null,"SJAG_03264":null,"SJAG_03287":null,"SJAG_03342":null,"SJAG_03351":null,"SJAG_03376":null,"SJAG_03491":null,"SJAG_03501":null,"SJAG_03508":null,"SJAG_03540":null,"SJAG_03544":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03612":null,"SJAG_03615":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03708":null,"SJAG_03810":null,"SJAG_03835":null,"SJAG_03843":null,"SJAG_03891":null,"SJAG_03936":null,"SJAG_04140":null,"SJAG_04239":null,"SJAG_04280":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04468":null,"SJAG_04498":null,"SJAG_04551":null,"SJAG_04558":null,"SJAG_04595":null,"SJAG_04597":null,"SJAG_04609":null,"SJAG_04653":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04884":null,"SJAG_04901":null,"SJAG_04931":null,"SJAG_04943":null,"SJAG_04980":null,"SJAG_05185":null,"SJAG_05196":null,"SJAG_05205":null,"SJAG_05207":null,"SJAG_05264":null,"SJAG_05266":null,"SJAG_05290":null,"SJAG_05309":null,"SJAG_05315":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005816"}],"interesting_parent_ids":["GO:0005816","GO:0005575","GO:0015630"],"is_obsolete":false,"name":"mitotic spindle pole body","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:32243490":null},"termid":"GO:0044732","terms_by_termid":{"GO:0044732":null,"GO:0061493":null,"GO:0061496":null,"GO:0061497":null,"GO:0061499":null,"GO:0071957":null,"GO:0071958":null,"GO:0160065":null}}


id: MONDO:0000725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Simpson-Golabi-Behmel syndrome (obsolete MONDO:0000725)","termid":"MONDO:0000725","xrefs":{"Monarch":{"xref_id":"0000725"}}}


id: GO:0030154
data:
  {"annotated_genes":["SJAG_03688","SJAG_02529","SJAG_02712","SJAG_03587","SJAG_02248","SJAG_03581","SJAG_00486","SJAG_03483","SJAG_02320","SJAG_00993","SJAG_04236","SJAG_01769","SJAG_01483","SJAG_04615","SJAG_03090","SJAG_01321","SJAG_04080","SJAG_04238","SJAG_04781","SJAG_00663","SJAG_03250","SJAG_02392","SJAG_01531","SJAG_00821","SJAG_04010","SJAG_00405","SJAG_00514","SJAG_01662","SJAG_03057","SJAG_04859","SJAG_03915","SJAG_00971","SJAG_02241","SJAG_04140","SJAG_03536","SJAG_04853","SJAG_04470","SJAG_00826","SJAG_05309","SJAG_04184","SJAG_04275","SJAG_03557","SJAG_04483","SJAG_03013","SJAG_00974","SJAG_04868","SJAG_03746","SJAG_00114","SJAG_04901","SJAG_04271","SJAG_02169","SJAG_04922"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96527,91813,97796],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0051519"},{"annotations":[107089,114706,98884,102685,98469,113503],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030437"},{"annotations":[96413],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034413"},{"annotations":[90157,90647,92193,93722],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030476"},{"annotations":[74888],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034412"},{"annotations":[119783,119791,116078,111051,106125],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070591"},{"annotations":[106941,74890,93449],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031321"},{"annotations":[112100,115926,120554,120855,99501,107253,121038,97323,100780,103667,99538,93238,101859,109358],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032120"},{"annotations":[106083,98818,99502,115927,94239,101788,109689,108803,104874,101789],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031322"},{"annotations":[113191],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0075297"},{"annotations":[92671],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0051517"},{"annotations":[104242],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0075296"},{"annotations":[92673],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903024"},{"annotations":[94135],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0034307"},{"annotations":[102078,101791,96454,101790,117969,107980],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070583"}]},"cv_name":"biological_process","definition":"The cellular developmental process in which a relatively unspecialized cell, e.g. embryonic or regenerative cell, acquires specialized structural and/or functional features that characterize a specific cell. Differentiation includes the processes involved in commitment of a cell to a specific fate and its subsequent development to the mature state.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"}],"gene_count":52,"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_00993":null,"SJAG_01321":null,"SJAG_01483":null,"SJAG_01531":null,"SJAG_01662":null,"SJAG_01769":null,"SJAG_02169":null,"SJAG_02241":null,"SJAG_02248":null,"SJAG_02320":null,"SJAG_02392":null,"SJAG_02529":null,"SJAG_02712":null,"SJAG_03013":null,"SJAG_03057":null,"SJAG_03090":null,"SJAG_03250":null,"SJAG_03483":null,"SJAG_03536":null,"SJAG_03557":null,"SJAG_03581":null,"SJAG_03587":null,"SJAG_03688":null,"SJAG_03746":null,"SJAG_03915":null,"SJAG_04010":null,"SJAG_04080":null,"SJAG_04140":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04271":null,"SJAG_04275":null,"SJAG_04470":null,"SJAG_04483":null,"SJAG_04615":null,"SJAG_04781":null,"SJAG_04853":null,"SJAG_04859":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"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell differentiation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Cellular_differentiation"],"termid":"GO:0030154","terms_by_termid":{"GO:0030437":null,"GO:0030476":null,"GO:0031321":null,"GO:0031322":null,"GO:0032120":null,"GO:0034307":null,"GO:0034412":null,"GO:0034413":null,"GO:0051517":null,"GO:0051519":null,"GO:0070583":null,"GO:0070591":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


id: PR:O14000
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A methionyl-tRNA synthetase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11946:SF1","OMA:SCHPO01668"],"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, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27E2.06c","secondary_identifiers":["UniProtKB:O14000"],"synonyms":[{"name":"MtMetRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MARS2","type":"exact"},{"name":"mitochondrial methionyl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14000"}


id: GO:0031428
data:
  {"annotated_genes":["SJAG_03410","SJAG_02377","SJAG_02350","SJAG_00744","SJAG_00943"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72676,75175,77321,78292,112180],"is_not":false,"summary":null,"term":"GO:0031428"}]},"cv_name":"cellular_component","definition":"A ribonucleoprotein complex containing a box C/D type RNA that is capable of ribose-2'-O-methylation of target RNAs. Box C/D type RNAs are widespread in eukaryotes and in Archaea, suggesting that an RNA-based guide mechanism for directing specific RNA 2'-O-ribose methylations was present in the common ancestor of Archaea and Eukarya.","definition_xrefs":["PMID:17284456","ISBN:0879695897","PMID:11842104"],"direct_ancestors":[{"relation_name":"is_a","term_name":"box C/D RNP complex","termid":"GO:0170049"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00744":null,"SJAG_00943":null,"SJAG_02350":null,"SJAG_02377":null,"SJAG_03410":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"box C/D methylation guide snoRNP complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"box C/D sRNP complex","type":"narrow"},{"name":"box C/D small nucleolar ribonucleoprotein complex","type":"narrow"},{"name":"box C/D snoRNP complex","type":"narrow"},{"name":"box C/D snoRNP ribose 2'-O methylase complex","type":"exact"},{"name":"box C/D snoRNP ribose-2'-O-methyltransferase complex","type":"narrow"}],"termid":"GO:0031428","terms_by_termid":{"GO:0031428":null}}


id: MONDO:0030846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 48","secondary_identifiers":["OMIM:619108","UMLS:C5436823","MEDGEN:1761843","GARD:16420","DOID:0112176"],"synonyms":[{"name":"SPGF48","type":"exact"},{"name":"spermatogenic failure 48","type":"exact"}],"termid":"MONDO:0030846","xrefs":{"Monarch":{"xref_id":"0030846"}}}


id: PBO:0026757
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_septated_cell_with_condensed_chromatin","termid":"PBO:0026757"}


id: MONDO:0100614
data:
  {"annotated_genes":["SJAG_03145","SJAG_03764","SJAG_03703","SJAG_02431","SJAG_04901","SJAG_04781"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013261"},{"annotations":[88091,88092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013262"},{"annotations":[87337,87336],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014548"},{"annotations":[87335,87334],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014550"},{"annotations":[88631,88630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032915"},{"annotations":[89307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013367"}]},"cv_name":"mondo","definition":"Congenital heart disease with co-occurrence of other extracardiac congenital anomalies, or well characterized genetic conditions.","definition_xrefs":["PMID:30571578"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital heart disease","termid":"MONDO:0005453"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02431":null,"SJAG_03145":null,"SJAG_03703":null,"SJAG_03764":null,"SJAG_04781":null,"SJAG_04901":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"syndromic congenital heart disease","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0100614","terms_by_termid":{"MONDO:0013261":null,"MONDO:0013262":null,"MONDO:0013367":null,"MONDO:0014548":null,"MONDO:0014550":null,"MONDO:0032915":null},"xrefs":{"Monarch":{"xref_id":"0100614"}}}


id: PR:P17477
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpp102 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P17477"],"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":"60S acidic ribosomal protein P1-alpha 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B9.13c","synonyms":[{"name":"A3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rpp102","type":"exact"}],"termid":"PR:P17477"}


id: GO:0015009
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving corrin, C19H22N4, the fundamental heterocyclic skeleton of the corrinoids. It consists of four reduced pyrrole rings joined into a macrocyclic ring. Corrin is the core of the vitamin B12 molecule.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete corrin metabolic process (obsolete GO:0015009)","synonyms":[{"name":"corrin metabolism","type":"exact"}],"termid":"GO:0015009"}


id: GO:0052404
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents, or reduces the frequency, rate or extent of symbiont protease activity, the catalysis of the hydrolysis of peptide bonds in a protein. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:tb","GOC:dph","GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by host of symbiont peptidase activity (obsolete GO:0052404)","synonyms":[{"name":"down regulation by host of symbiont protease activity","type":"narrow"},{"name":"down-regulation by host of symbiont protease activity","type":"narrow"},{"name":"downregulation by host of symbiont protease activity","type":"narrow"},{"name":"inhibition by host of symbiont protease activity","type":"narrow"},{"name":"inhibition of symbiont protease activity","type":"narrow"},{"name":"negative regulation by host of symbiont protease activity","type":"narrow"}],"termid":"GO:0052404"}


id: PBO:0028178
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_vanadate","termid":"PBO:0028178"}


id: GO:1903771
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of beta-galactosidase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","GOC:nc","PMID:11927518","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of hydrolase activity","termid":"GO:0051345"}],"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 beta-galactosidase activity","synonyms":[{"name":"activation of S 2107","type":"related"},{"name":"activation of beta-D-galactanase activity","type":"narrow"},{"name":"activation of beta-D-galactoside galactohydrolase activity","type":"narrow"},{"name":"activation of beta-D-lactosidase activity","type":"narrow"},{"name":"activation of beta-galactosidase activity","type":"narrow"},{"name":"activation of beta-lactosidase activity","type":"narrow"},{"name":"activation of exo-(1->4)-beta-D-galactanase activity","type":"narrow"},{"name":"activation of hydrolact","type":"related"},{"name":"activation of lactose hydrolysis","type":"related"},{"name":"activation of lactozym","type":"related"},{"name":"activation of maxilact","type":"related"},{"name":"activation of oryzatym","type":"related"},{"name":"activation of sumiklat","type":"related"},{"name":"activation of trilactase activity","type":"narrow"},{"name":"positive regulation of S 2107","type":"related"},{"name":"positive regulation of beta-D-galactanase activity","type":"exact"},{"name":"positive regulation of beta-D-galactoside galactohydrolase activity","type":"exact"},{"name":"positive regulation of beta-D-lactosidase activity","type":"exact"},{"name":"positive regulation of beta-lactosidase activity","type":"exact"},{"name":"positive regulation of exo-(1->4)-beta-D-galactanase activity","type":"exact"},{"name":"positive regulation of hydrolact","type":"related"},{"name":"positive regulation of lactose hydrolysis","type":"related"},{"name":"positive regulation of lactozym","type":"related"},{"name":"positive regulation of maxilact","type":"related"},{"name":"positive regulation of oryzatym","type":"related"},{"name":"positive regulation of sumiklat","type":"related"},{"name":"positive regulation of trilactase activity","type":"exact"},{"name":"up regulation of S 2107","type":"related"},{"name":"up regulation of beta-D-galactanase activity","type":"exact"},{"name":"up regulation of beta-D-galactoside galactohydrolase activity","type":"exact"},{"name":"up regulation of beta-D-lactosidase activity","type":"exact"},{"name":"up regulation of beta-galactosidase activity","type":"exact"},{"name":"up regulation of beta-lactosidase activity","type":"exact"},{"name":"up regulation of exo-(1->4)-beta-D-galactanase activity","type":"exact"},{"name":"up regulation of hydrolact","type":"related"},{"name":"up regulation of lactose hydrolysis","type":"related"},{"name":"up regulation of lactozym","type":"related"},{"name":"up regulation of maxilact","type":"related"},{"name":"up regulation of oryzatym","type":"related"},{"name":"up regulation of sumiklat","type":"related"},{"name":"up regulation of trilactase activity","type":"exact"},{"name":"up-regulation of S 2107","type":"related"},{"name":"up-regulation of beta-D-galactanase activity","type":"exact"},{"name":"up-regulation of beta-D-galactoside galactohydrolase activity","type":"exact"},{"name":"up-regulation of beta-D-lactosidase activity","type":"exact"},{"name":"up-regulation of beta-galactosidase activity","type":"exact"},{"name":"up-regulation of beta-lactosidase activity","type":"exact"},{"name":"up-regulation of exo-(1->4)-beta-D-galactanase activity","type":"exact"},{"name":"up-regulation of hydrolact","type":"related"},{"name":"up-regulation of lactose hydrolysis","type":"related"},{"name":"up-regulation of lactozym","type":"related"},{"name":"up-regulation of maxilact","type":"related"},{"name":"up-regulation of oryzatym","type":"related"},{"name":"up-regulation of sumiklat","type":"related"},{"name":"up-regulation of trilactase activity","type":"exact"},{"name":"upregulation of S 2107","type":"related"},{"name":"upregulation of beta-D-galactanase activity","type":"exact"},{"name":"upregulation of beta-D-galactoside galactohydrolase activity","type":"exact"},{"name":"upregulation of beta-D-lactosidase activity","type":"exact"},{"name":"upregulation of beta-galactosidase activity","type":"exact"},{"name":"upregulation of beta-lactosidase activity","type":"exact"},{"name":"upregulation of exo-(1->4)-beta-D-galactanase activity","type":"exact"},{"name":"upregulation of hydrolact","type":"related"},{"name":"upregulation of lactose hydrolysis","type":"related"},{"name":"upregulation of lactozym","type":"related"},{"name":"upregulation of maxilact","type":"related"},{"name":"upregulation of oryzatym","type":"related"},{"name":"upregulation of sumiklat","type":"related"},{"name":"upregulation of trilactase activity","type":"exact"}],"termid":"GO:1903771"}


id: PBO:0062398
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 21 pseudogene","termid":"PBO:0062398"}


id: GO:1904361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of spore germination.","definition_xrefs":["PMID:14718564","GO_REF:0000058","GOC:TermGenie","PMID:8798577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of spore germination","termid":"GO:1904359"},{"relation_name":"positively_regulates","term_name":"spore germination","termid":"GO:0009847"}],"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 spore germination","secondary_identifiers":["GO:0075007"],"synonyms":[{"name":"activation of spore germination","type":"narrow"},{"name":"positive regulation of spore germination on or near host","type":"narrow"},{"name":"up regulation of spore germination","type":"exact"},{"name":"up-regulation of spore germination","type":"exact"},{"name":"upregulation of spore germination","type":"exact"}],"termid":"GO:1904361"}


id: MONDO:0010841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg syndrome type 2","termid":"MONDO:0019517"}],"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":"Waardenburg syndrome type 2B","secondary_identifiers":["GARD:5522","MEDGEN:373973","MESH:C536465","OMIM:600193","DOID:0110947","UMLS:C1838447"],"synonyms":[{"name":"WS2B","type":"exact"},{"name":"Waardenburg syndrome type IIB","type":"exact"},{"name":"Waardenburg syndrome, type 2B","type":"related"}],"termid":"MONDO:0010841","xrefs":{"Monarch":{"xref_id":"0010841"}}}


id: GO:0002287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of an alpha-beta T cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell activation involved in immune response","termid":"GO:0002286"},{"relation_name":"is_a","term_name":"alpha-beta T cell activation","termid":"GO:0046631"}],"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":"alpha-beta T cell activation involved in immune response","synonyms":[{"name":"alpha-beta T cell activation during immune response","type":"related"},{"name":"alpha-beta T lymphocyte activation during immune response","type":"related"},{"name":"alpha-beta T-cell activation during immune response","type":"related"},{"name":"alpha-beta T-lymphocyte activation during immune response","type":"related"}],"termid":"GO:0002287"}


id: GO:0075031
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of symbiont germ tube hook structure formation.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"modulation of formation of symbiont germ tube hook structure for appressorium development","termid":"GO:0075030"},{"relation_name":"positively_regulates","term_name":"formation of appressorium germ tube hook structure","termid":"GO:0075029"}],"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 formation of symbiont germ tube hook structure for appressorium development","synonyms":[{"name":"positive regulation of formation of symbiont germ tube hook structure on or near host","type":"exact"},{"name":"positive regulation of germ tube tip of symbiont on or near the exterior of host","type":"exact"},{"name":"positive regulation of symbiont germ tube hook structure formation on or near host","type":"related"}],"termid":"GO:0075031"}


id: MONDO:0017109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated cerebellar vermis agenesis","termid":"MONDO:0017107"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"isolated partial cerebellar vermis agenesis","secondary_identifiers":["UMLS:C5680780","GARD:20992","MEDGEN:1842645","Orphanet:269209"],"termid":"MONDO:0017109","xrefs":{"Monarch":{"xref_id":"0017109"}}}


id: MONDO:0800489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neonatal/infantile-onset self-limited familial syndrome characterized by the presence of febrile seizures in an individual with a family history of seizures/epilepsy. Febrile seizures may be typical febrile seizures or 'febrile seizures plus' (FS+) may occur, where febrile seizures continue past 6 years of age and/or are accompanied by afebrile seizures which may be generalized or focal. FS+ and GEFS+ are distinguished on the basis of family history. A number of dominantly inherited genes have been linked to both GEFS+ and FS+, with implications for specific genetic counselling, due to the variable severity of the epilepsy in different family members. Although febrile seizures are the hallmark of this familial syndrome, not all individuals in a family may have these.","direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal/infantile-onset self-limited epilepsy syndrome","termid":"MONDO:0800488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"genetic epilepsy with febrile seizures plus spectrum","synonyms":[{"name":"GEFS+","type":"exact"}],"termid":"MONDO:0800489","xrefs":{"Monarch":{"xref_id":"0800489"}}}


id: GO:1901195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of formation of translation preinitiation complex.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of formation of translation preinitiation complex","termid":"GO:1901193"},{"relation_name":"positively_regulates","term_name":"formation of translation preinitiation complex","termid":"GO:0001731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0002181"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0002181","GO:0044085","GO:0010467","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"positive regulation of formation of translation preinitiation complex","synonyms":[{"name":"activation of formation of translation pre-initiation complex","type":"exact"},{"name":"activation of formation of translation preinitiation complex","type":"narrow"},{"name":"activation of translation preinitiation complex assembly","type":"exact"},{"name":"positive regulation of formation of translation pre-initiation complex","type":"exact"},{"name":"positive regulation of translation preinitiation complex assembly","type":"exact"},{"name":"up regulation of formation of translation pre-initiation complex","type":"exact"},{"name":"up regulation of formation of translation preinitiation complex","type":"exact"},{"name":"up regulation of translation preinitiation complex assembly","type":"exact"},{"name":"up-regulation of formation of translation pre-initiation complex","type":"exact"},{"name":"up-regulation of formation of translation preinitiation complex","type":"exact"},{"name":"up-regulation of translation preinitiation complex assembly","type":"exact"},{"name":"upregulation of formation of translation pre-initiation complex","type":"exact"},{"name":"upregulation of formation of translation preinitiation complex","type":"exact"},{"name":"upregulation of translation preinitiation complex assembly","type":"exact"}],"termid":"GO:1901195"}


id: PBO:0084374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Long-chain base-1-phosphate phosphatase; specific for dihydrosphingosine-1-phosphate, regulates ceramide and long-chain base phosphates levels, involved in incorporation of exogenous long chain bases in sphingolipids; LCB3 has a paralog, YSR3, that arose from the whole genome duplication","termid":"PBO:0084374"}


id: FYPO:0001596
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 amino acid import into the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transport","termid":"FYPO:0001071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000138","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal amino acid import","synonyms":[{"name":"normal amino acid import across plasma membrane","type":"exact"},{"name":"normal amino acid import during mitotic cell cycle","type":"related"},{"name":"normal amino acid import during vegetative growth","type":"exact"},{"name":"normal amino acid import into cell","type":"exact"},{"name":"normal amino acid uptake","type":"exact"}],"termid":"FYPO:0001596"}


id: GO:0061766
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that increases the force with which blood travels through the lungs.","definition_xrefs":["GOC:bc","GOC:BHF_miRNA","GOC:BHF","PMID:22161164"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lung blood pressure","termid":"GO:0014916"}],"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 lung blood pressure","synonyms":[{"name":"positive regulation of pulmonary blood pressure","type":"exact"}],"termid":"GO:0061766"}


id: FYECO:0000397
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which micafungin was added to the medium or assay buffer in excess compared to standard medium or assay buffers at lethal dose for the assayed cell density.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ micafungin","termid":"FYECO:0000395"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ micafungin LD","termid":"FYECO:0000397"}


id: PBO:0033760
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_duration_of_meiosis_I","termid":"PBO:0033760"}


id: GO:2000277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of oxidative phosphorylation uncoupler activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmembrane transporter activity","termid":"GO:0022898"},{"relation_name":"is_a","term_name":"positive regulation of transporter activity","termid":"GO:0032411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"positive regulation of oxidative phosphorylation uncoupler activity","synonyms":[{"name":"positive regulation of mitochondrial uncoupling protein activity","type":"related"},{"name":"positive regulation of uncoupling protein activity","type":"related"}],"termid":"GO:2000277"}


id: GO:0050376
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucosamine = UDP-galactosamine.","definition_xrefs":["EC:5.1.3.16","MetaCyc:UDP-GLUCOSAMINE-EPIMERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on carbohydrates and derivatives","termid":"GO:0016857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"UDP-glucosamine 4-epimerase activity","secondary_identifiers":["RHEA:23492"],"synonyms":[{"name":"UDP-glucosamine epimerase activity","type":"exact"},{"name":"UDPglucosamine 4-epimerase activity","type":"related"}],"termid":"GO:0050376"}


id: GO:0008458
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-carnitine + octanoyl-CoA = CoA + O-octanoyl-(R)-carnitine.","definition_xrefs":["RHEA:17177"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carnitine O-acyltransferase activity","termid":"GO:0016406"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"carnitine O-octanoyltransferase activity","secondary_identifiers":["EC:2.3.1.137","KEGG_REACTION:R03779","Reactome:R-HSA-390281","MetaCyc:CARNITINE-O-OCTANOYLTRANSFERASE-RXN"],"synonyms":[{"name":"carnitine medium-chain acyltransferase activity","type":"related"},{"name":"easily solubilized mitochondrial carnitine palmitoyltransferase","type":"narrow"},{"name":"medium-chain/long-chain carnitine acyltransferase activity","type":"related"},{"name":"octanoyl-CoA:L-carnitine O-octanoyltransferase activity","type":"related"},{"name":"overt mitochondrial carnitine palmitoyltransferase","type":"narrow"}],"termid":"GO:0008458"}


id: MONDO:0008585
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A life-threatening condition that can potentially complicate pregnancy. It is named for 3 features of the condition: H emolysis, E levated L iver enzyme levels, and L ow P latelet levels. It typically occurs in the last 3 months of pregnancy (the third trimester) but can also start soon after delivery. A wide range of non-specific symptoms may be present in women with HELLP syndrome. Symptoms may include fatigue; malaise; fluid retention and excess weight gain; headache; nausea and vomiting; pain in the upper right or middle of the abdomen; blurry vision; and rarely, nosebleed or seizures. The cause of HELLP syndrome is not known, but certain risk factors have been associated with the condition. It is most common in women with preeclampsia or eclampsia. If not diagnosed and treated quickly, HELLP syndrome can lead to serious complications for the mother and baby.The main treatment is to deliver the baby as soon as possible, even if premature. Treatment may also include medications needed for the mother or baby, and blood transfusion for severe bleeding problems.","direct_ancestors":[{"relation_name":"is_a","term_name":"severe pre-eclampsia","termid":"MONDO:0001641"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HELLP syndrome","secondary_identifiers":["MedDRA:10049058","ICD10CM:O14.2","MEDGEN:58162","NCIT:C84750","DOID:13133","Orphanet:244242","EFO:0007297","icd11.foundation:1748922908","UMLS:C0162739","GARD:8528","MESH:D017359"],"synonyms":[{"name":"PEE1","type":"related"},{"name":"PREECLAMPSIA/eclampsia 1","type":"related"},{"name":"PREG1","type":"related"},{"name":"hemolysis, elevated liver enzymes, and low platelet count","type":"related"},{"name":"hemolysis, elevated liver enzymes, low platelets in pregnancy","type":"exact"},{"name":"hemolysis, elevated liver enzymes, lowered platelets","type":"related"},{"name":"hemolysis-elevated liver enzymes-low platelet count syndrome","type":"exact"},{"name":"hemolysis-elevated liver enzymes-low platelets syndrome","type":"exact"},{"name":"hypertension, pregnancy-induced","type":"related"},{"name":"toxaemia of pregnancy","type":"related"},{"name":"toxemia of pregnancy","type":"related"}],"termid":"MONDO:0008585","xrefs":{"Monarch":{"xref_id":"0008585"}}}


id: MONDO:0009878
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the PROP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"panhypopituitarism","termid":"MONDO:0019591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"pituitary hormone deficiency, combined, 2","secondary_identifiers":["UMLS:C0878683","MEDGEN:209236","DOID:0061020","GARD:15222","MESH:C563172","OMIM:262600"],"synonyms":[{"name":"CPHD2","type":"related"},{"name":"Hanhart dwarfism","type":"related"},{"name":"PROP1 combined pituitary hormone deficiencies, genetic form","type":"exact"},{"name":"ateliotic dwarfism with hypogonadism","type":"related"},{"name":"combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1","type":"exact"},{"name":"panhypopituitarism","type":"related"},{"name":"pituitary dwarfism 3","type":"related"},{"name":"pituitary hormone deficiency, combined, 2","type":"exact"},{"name":"pituitary hormone deficiency, combined, type 2","type":"exact"}],"termid":"MONDO:0009878","xrefs":{"Monarch":{"xref_id":"0009878"}}}


id: MONDO:0021307
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0021307 (obsolete MONDO:0021307)","termid":"MONDO:0021307","xrefs":{"Monarch":{"xref_id":"0021307"}}}


id: PBO:0087305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ski complex component and TPR protein; mediates 3'-5' RNA degradation by the cytoplasmic exosome; null mutants have superkiller phenotype of increased viral dsRNAs and are synthetic lethal with mutations in 5'-3' mRNA decay; mutations in the human ortholog, TTC37, causes Syndromic diarrhea/Trichohepatoenteric (SD/THE) syndrome","termid":"PBO:0087305"}


id: MONDO:0003394
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the dental pulp.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"connective tissue disorder","termid":"MONDO:0003900"},{"relation_name":"is_a","term_name":"tooth disorder","termid":"MONDO:0006999"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dental pulp disorder","secondary_identifiers":["NCIT:C34530","DOID:5330","ICD9:522.9","MESH:D003788","SCTID:57203004","UMLS:C0011405","EFO:0009540","MEDGEN:8305"],"synonyms":[{"name":"dental pulp disease","type":"exact"},{"name":"dental pulp disease or disorder","type":"exact"},{"name":"dental pulp disorder","type":"exact"},{"name":"disease of dental pulp","type":"exact"},{"name":"disease or disorder of dental pulp","type":"exact"},{"name":"disorder of dental pulp","type":"exact"},{"name":"disorder of pulp of tooth","type":"exact"},{"name":"pulp disorder","type":"exact"}],"termid":"MONDO:0003394","xrefs":{"Monarch":{"xref_id":"0003394"}}}


id: PBO:0084419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Major exo-1,3-beta-glucanase of the cell wall; involved in cell wall beta-glucan assembly; exists as three differentially glycosylated isoenzymes; EXG1 has a paralog, SPR1, that arose from the whole genome duplication","termid":"PBO:0084419"}


id: MONDO:0017051
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Classic maple syrup urine disease (classic MSUD) is the most severe and probably common form of MSUD characterized by a maple syrup odor in the cerumen at birth, poor feeding, lethargy and focal dystonia, followed by progressive encephalopathy and central respiratory failure if untreated.","definition_xrefs":["Orphanet:268145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maple syrup urine disease","termid":"MONDO:0009563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"classic maple syrup urine disease","secondary_identifiers":["NANDO:2201078","MEDGEN:78689","UMLS:C0268568","GARD:17263"],"synonyms":[{"name":"classic BCKD deficiency","type":"exact"},{"name":"classic MSUD","type":"exact"},{"name":"classic branched-chain 2-ketoacid dehydrogenase deficiency","type":"exact"},{"name":"classic branched-chain alpha-ketoacid dehydrogenase deficiency","type":"exact"},{"name":"classic branched-chain ketoaciduria","type":"exact"},{"name":"classic maple syrup urine disease","type":"exact"}],"termid":"MONDO:0017051","xrefs":{"Monarch":{"xref_id":"0017051"}}}


id: PR:000028197
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cdc8 gene or a 1:1 ortholog thereof.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin cdc8","synonyms":[{"name":"cdc8","type":"exact"}],"termid":"PR:000028197"}


id: MONDO:0013216
data:
  {"annotated_genes":["SJAG_04695","SJAG_02904"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88213,88214],"is_not":false,"summary":null,"term":"MONDO:0013216"}]},"cv_name":"mondo","definition":"Any Diamond-Blackfan anemia in which the cause of the disease is a mutation in the RPS10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia","termid":"MONDO:0015253"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02904":null,"SJAG_04695":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"Diamond-Blackfan anemia 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C567650","MEDGEN:412874","GARD:15644","NCIT:C176918","UMLS:C2750081","DOID:0111884","OMIM:613308"],"synonyms":[{"name":"DBA9","type":"related"},{"name":"Diamond-Blackfan Anaemia type 9","type":"exact"},{"name":"Diamond-Blackfan Anemia type 9","type":"exact"},{"name":"Diamond-Blackfan anaemia caused by mutation in RPS10","type":"exact"},{"name":"Diamond-Blackfan anemia 9","type":"exact"},{"name":"Diamond-Blackfan anemia caused by mutation in RPS10","type":"exact"},{"name":"RPS10 Diamond-Blackfan anaemia","type":"exact"},{"name":"RPS10 Diamond-Blackfan anemia","type":"exact"}],"termid":"MONDO:0013216","terms_by_termid":{"MONDO:0013216":null},"xrefs":{"Monarch":{"xref_id":"0013216"}}}


id: SO:0002126
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variable gene that rearranges at the DNA level and codes the variable region of the variable domain of an Immunoglobulin chain.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html","IGMT:http://www.imgt.org/IMGTScientificChart/SequenceDescription/Keywords.php"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin_gene","termid":"SO:0002122"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IG_V_gene","synonyms":[{"name":"IGV_gene","type":"exact"},{"name":"IG_variable_gene","type":"exact"},{"name":"Immunoglobulin_variable_gene","type":"exact"}],"termid":"SO:0002126"}


id: MONDO:1011116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cryptorchidism that occurs in goat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cryptorchidism, non-human animal","termid":"MONDO:1010275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryptorchidism, goat","secondary_identifiers":["OMIA:000243-9925"],"termid":"MONDO:1011116","xrefs":{"Monarch":{"xref_id":"1011116"}}}


id: PBO:0075614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secreted phosphoprotein 2","termid":"PBO:0075614"}


id: PBO:0064716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 52","termid":"PBO:0064716"}


id: PBO:0076695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A N-terminal and central domain containing 2","termid":"PBO:0076695"}


id: RO:0002505
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"p has intermediate c if and only if p has parts p1, p2 and p1 has output c, and p2 has input c","direct_ancestors":[{"relation_name":"is_a","term_name":"has_participant","termid":"RO:0000057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_intermediate","termid":"RO:0002505"}


id: PBO:0077392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane 131 like","termid":"PBO:0077392"}


id: PBO:0083763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential kinetochore protein associated with microtubules and SPBs; component of the kinetochore sub-complex COMA (Ctf19p, Okp1p, Mcm21p, Ame1p); involved in spindle checkpoint maintenance; orthologous to human centromere constitutive-associated network (CCAN) subunit CENP-U and fission yeast Mis17; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0083763"}


id: GO:0098538
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the transport vesicle membrane that faces the lumen.","definition_xrefs":["GOC:ab"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lumenal side of membrane","termid":"GO:0098576"},{"relation_name":"part_of","term_name":"transport vesicle membrane","termid":"GO:0030658"}],"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:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"lumenal side of transport vesicle membrane","synonyms":[{"name":"internal side of transport vesicle membrane","type":"exact"}],"termid":"GO:0098538"}


id: FYPO:0007291
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 UDP-galactose measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular UDP-galactose level","synonyms":[{"name":"decreased cellular UDP-galactose level during mitotic cell cycle","type":"related"},{"name":"decreased cellular UDP-galactose level during vegetative growth","type":"exact"},{"name":"idecreased cellular UDP-D-galactose level","type":"exact"},{"name":"reduced cellular UDP-galactose level","type":"exact"}],"termid":"FYPO:0007291"}


id: PBO:0082394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Beta subunit of cytoplasmic phenylalanyl-tRNA synthetase; forms a tetramer with Frs2p to generate active enzyme; able to hydrolyze mis-aminoacylated tRNA-Phe, which could contribute to translational quality control","termid":"PBO:0082394"}


id: FYPO:0000178
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which regulation of cytokinesis is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype during vegetative growth","termid":"FYPO:0001334"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal regulation of cytokinesis","synonyms":[{"name":"abnormal regulation of cytokinesis during mitotic cell cycle","type":"related"},{"name":"abnormal regulation of cytokinesis during vegetative growth","type":"exact"},{"name":"abnormal regulation of mitotic cytokinesis","type":"exact"}],"termid":"FYPO:0000178"}


id: PBO:0087342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spermidine synthase; involved in biosynthesis of spermidine and also in biosynthesis of pantothenic acid; spermidine is required for growth of wild-type cells","termid":"PBO:0087342"}


id: GO:0033326
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of cerebrospinal fluid (CSF) from the choroid plexus of the lateral, third and fourth ventricles. The cerebrospinal fluid is a clear liquid that located within the ventricles, spinal canal, and subarachnoid spaces.","definition_xrefs":["GOC:ln","PMID:10716451"],"direct_ancestors":[{"relation_name":"is_a","term_name":"body fluid secretion","termid":"GO:0007589"},{"relation_name":"is_a","term_name":"secretion by tissue","termid":"GO:0032941"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"cerebrospinal fluid secretion","synonyms":[{"name":"CSF secretion","type":"exact"}],"termid":"GO:0033326"}


id: GO:0010514
data:
  {"annotated_genes":["SJAG_03735","SJAG_04009","SJAG_03501","SJAG_03802","SJAG_01699","SJAG_03081","SJAG_03067","SJAG_01254","SJAG_02785","SJAG_01113","SJAG_03346","SJAG_05153","SJAG_02444","SJAG_00526","SJAG_02723","SJAG_02592","SJAG_01718","SJAG_06638","SJAG_02730","SJAG_00975","SJAG_01311","SJAG_02066","SJAG_04026","SJAG_00600","SJAG_00256","SJAG_00781","SJAG_04312","SJAG_03486","SJAG_02266","SJAG_03309","SJAG_04206","SJAG_00472","SJAG_02472","SJAG_04813","SJAG_01084","SJAG_02773","SJAG_00210"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89973,91159,108242,118140,118481,120238],"is_not":false,"summary":null,"term":"GO:0010514"},{"annotations":[100366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031141"},{"annotations":[117587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031142"},{"annotations":[116467,102499,106458,94875,96316,108621,93356,96175,118068,117533,107774,108467,108817,110993,107871,90150,103806],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0010515"},{"annotations":[103349,89798,118275,121115,109022,102457,121114,106398,110551,110784,101451,105318],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900237"}]},"cv_name":"biological_process","definition":"The process in which a cell initiates conjugation with cellular fusion. Conjugation with cellular fusion is the process that results in the union of cellular and genetic information from compatible mating types.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of conjugation with cellular fusion","termid":"GO:0031139"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00210":null,"SJAG_00256":null,"SJAG_00472":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_00781":null,"SJAG_00975":null,"SJAG_01084":null,"SJAG_01113":null,"SJAG_01254":null,"SJAG_01311":null,"SJAG_01699":null,"SJAG_01718":null,"SJAG_02066":null,"SJAG_02266":null,"SJAG_02444":null,"SJAG_02472":null,"SJAG_02592":null,"SJAG_02723":null,"SJAG_02730":null,"SJAG_02773":null,"SJAG_02785":null,"SJAG_03067":null,"SJAG_03081":null,"SJAG_03309":null,"SJAG_03346":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03735":null,"SJAG_03802":null,"SJAG_04009":null,"SJAG_04026":null,"SJAG_04206":null,"SJAG_04312":null,"SJAG_04813":null,"SJAG_05153":null,"SJAG_06638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0000747"},{"rel_name":"positively_regulates","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0000747"],"is_obsolete":false,"name":"induction of conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010514","terms_by_termid":{"GO:0010514":null,"GO:0010515":null,"GO:0031141":null,"GO:0031142":null,"GO:1900237":null}}


id: MONDO:1010472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent truncus arteriosus that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"persistent truncus arteriosus, non-human animal","termid":"MONDO:1010018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent truncus arteriosus, domestic cat","secondary_identifiers":["OMIA:000795-9685"],"termid":"MONDO:1010472","xrefs":{"Monarch":{"xref_id":"1010472"}}}


id: GO:0061783
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A catalytic activity that contributes to the degradation of peptidoglycan.","definition_xrefs":["GOC:jh","GOC:dph","PMID:22748813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity","termid":"GO:0003824"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"peptidoglycan muralytic activity","termid":"GO:0061783"}


id: MONDO:0005066
data:
  {"annotated_genes":["SJAG_03066","SJAG_01174","SJAG_01461","SJAG_01422","SJAG_00183","SJAG_01630","SJAG_04449","SJAG_03506","SJAG_03672","SJAG_00866","SJAG_00092","SJAG_00846","SJAG_03147","SJAG_04394","SJAG_04785","SJAG_05950","SJAG_02163","SJAG_04885","SJAG_03813","SJAG_04529","SJAG_04882","SJAG_04203","SJAG_03311","SJAG_02693","SJAG_02006","SJAG_03396","SJAG_03865","SJAG_00995","SJAG_04499","SJAG_02788","SJAG_03296","SJAG_03774","SJAG_02353","SJAG_04114","SJAG_01416","SJAG_05180","SJAG_00325","SJAG_00413","SJAG_00281","SJAG_01351","SJAG_03188","SJAG_03099","SJAG_02828","SJAG_02068","SJAG_03316","SJAG_03292","SJAG_06383","SJAG_00115","SJAG_00412","SJAG_00120","SJAG_01851","SJAG_05342","SJAG_03371","SJAG_03150","SJAG_04843","SJAG_05271","SJAG_01903","SJAG_06022","SJAG_01526","SJAG_02716","SJAG_00459","SJAG_01004","SJAG_02274","SJAG_04637","SJAG_02428","SJAG_MIT13","SJAG_00531","SJAG_02876","SJAG_02158","SJAG_02398","SJAG_04316","SJAG_03923","SJAG_01413","SJAG_01043","SJAG_04323","SJAG_03069","SJAG_00885","SJAG_00601","SJAG_MIT15","SJAG_02426","SJAG_00319","SJAG_00947","SJAG_00747","SJAG_02313","SJAG_02463","SJAG_00611","SJAG_04378","SJAG_02211","SJAG_02399","SJAG_04277","SJAG_04300","SJAG_02518","SJAG_02013","SJAG_04094","SJAG_00898","SJAG_02388","SJAG_04665","SJAG_03811","SJAG_04410","SJAG_02599","SJAG_04821","SJAG_01616","SJAG_03671","SJAG_01007","SJAG_01165","SJAG_02539","SJAG_00255","SJAG_01207","SJAG_04362","SJAG_04295","SJAG_07003","SJAG_03669","SJAG_01063","SJAG_03556","SJAG_03797","SJAG_01152","SJAG_02656","SJAG_02783","SJAG_04978","SJAG_00997","SJAG_02796","SJAG_00516","SJAG_04096","SJAG_01069","SJAG_02384","SJAG_01820","SJAG_02480","SJAG_01841","SJAG_03827","SJAG_04645","SJAG_03660","SJAG_02139","SJAG_01183","SJAG_04980","SJAG_05278","SJAG_04348","SJAG_02504","SJAG_03024","SJAG_01077","SJAG_04183","SJAG_02855","SJAG_02619","SJAG_00857","SJAG_00070","SJAG_02000","SJAG_04810","SJAG_04704","SJAG_01589","SJAG_01625","SJAG_00839","SJAG_01826","SJAG_04109","SJAG_04000","SJAG_02229","SJAG_00944","SJAG_00217","SJAG_04790","SJAG_01647","SJAG_04127","SJAG_01991","SJAG_01303","SJAG_04157","SJAG_03275","SJAG_04816","SJAG_02302","SJAG_03552","SJAG_00721","SJAG_02997","SJAG_04553","SJAG_01612","SJAG_00212","SJAG_01071","SJAG_04495","SJAG_03400","SJAG_03018","SJAG_03881","SJAG_00358","SJAG_05373","SJAG_01190","SJAG_04859","SJAG_03712","SJAG_04823","SJAG_01072","SJAG_02658","SJAG_03064","SJAG_01634","SJAG_02295","SJAG_04296","SJAG_01405","SJAG_00702","SJAG_01865","SJAG_05218","SJAG_04397","SJAG_00605","SJAG_03659","SJAG_03440","SJAG_03818","SJAG_02951","SJAG_04728","SJAG_05175","SJAG_05230","SJAG_MIT03","SJAG_04473","SJAG_05327","SJAG_04367","SJAG_01465","SJAG_02148","SJAG_00694","SJAG_04459","SJAG_00886","SJAG_02523","SJAG_02297","SJAG_03011","SJAG_03322","SJAG_01924","SJAG_02012","SJAG_01671","SJAG_00464","SJAG_00554","SJAG_01524","SJAG_02042","SJAG_02265","SJAG_00339","SJAG_03162","SJAG_03596","SJAG_04146","SJAG_02324","SJAG_01859","SJAG_02226","SJAG_00461","SJAG_05305","SJAG_02305","SJAG_04791","SJAG_00495","SJAG_04053","SJAG_04697","SJAG_01410","SJAG_02107","SJAG_06046","SJAG_01471","SJAG_02453","SJAG_01503","SJAG_04588","SJAG_00133","SJAG_05194","SJAG_00154","SJAG_02084","SJAG_04363","SJAG_02334","SJAG_02977","SJAG_02548","SJAG_00755","SJAG_03475","SJAG_01459","SJAG_02180","SJAG_03553","SJAG_00379","SJAG_04763","SJAG_00354","SJAG_03293","SJAG_00797","SJAG_04321","SJAG_01575","SJAG_03781","SJAG_01597","SJAG_01797","SJAG_01866","SJAG_00636","SJAG_02643","SJAG_00891","SJAG_05283","SJAG_03782","SJAG_01236","SJAG_01887","SJAG_03588","SJAG_04334","SJAG_03173","SJAG_05277","SJAG_02009","SJAG_03861","SJAG_02785","SJAG_01960","SJAG_02804","SJAG_01466","SJAG_00108","SJAG_01036","SJAG_01950","SJAG_01537","SJAG_00043","SJAG_05219","SJAG_02615","SJAG_00643","SJAG_03052","SJAG_03014","SJAG_03398","SJAG_01355","SJAG_01640","SJAG_01344","SJAG_02242","SJAG_03149","SJAG_01474","SJAG_00964","SJAG_04952","SJAG_03098","SJAG_MIT20","SJAG_01577","SJAG_03290","SJAG_04119","SJAG_04497","SJAG_01356","SJAG_00260","SJAG_00933","SJAG_03992","SJAG_02850","SJAG_02050","SJAG_03222","SJAG_00978","SJAG_02339","SJAG_01216","SJAG_00924","SJAG_00831","SJAG_00852","SJAG_04608","SJAG_04757","SJAG_02464","SJAG_03509","SJAG_02913","SJAG_MIT04","SJAG_02119","SJAG_00222","SJAG_03641","SJAG_03258","SJAG_04881","SJAG_02641","SJAG_01957","SJAG_02896","SJAG_03584","SJAG_01868","SJAG_04954","SJAG_00308","SJAG_04042","SJAG_04654","SJAG_01432","SJAG_03490","SJAG_03164","SJAG_03866","SJAG_02949","SJAG_04084","SJAG_03032","SJAG_03447","SJAG_01940","SJAG_02369","SJAG_01677","SJAG_02131","SJAG_02564","SJAG_01417","SJAG_00938","SJAG_01162","SJAG_02748","SJAG_01147","SJAG_01407","SJAG_01490","SJAG_01059","SJAG_04540","SJAG_02848","SJAG_03363","SJAG_04077","SJAG_04425","SJAG_03656","SJAG_03550","SJAG_00214","SJAG_01049","SJAG_05213","SJAG_04549","SJAG_16456","SJAG_04165","SJAG_03332","SJAG_03333","SJAG_00088","SJAG_04016","SJAG_00326","SJAG_04206","SJAG_04019","SJAG_04568","SJAG_00068","SJAG_04862","SJAG_03375","SJAG_03104","SJAG_02903","SJAG_04149","SJAG_04418","SJAG_01872","SJAG_04263","SJAG_00737","SJAG_02031","SJAG_00295","SJAG_02397","SJAG_03557","SJAG_03448","SJAG_04178","SJAG_00103","SJAG_03560","SJAG_02885","SJAG_00946","SJAG_02102","SJAG_00522","SJAG_00570","SJAG_03960","SJAG_02016","SJAG_04738","SJAG_04577","SJAG_02432","SJAG_00894","SJAG_03785","SJAG_03434","SJAG_00653","SJAG_03961","SJAG_01199","SJAG_01070","SJAG_02946","SJAG_02712","SJAG_04560","SJAG_03824","SJAG_03071","SJAG_03773","SJAG_03795","SJAG_06514","SJAG_04849","SJAG_00084","SJAG_03153","SJAG_01784","SJAG_02696","SJAG_07005","SJAG_00674","SJAG_02895","SJAG_03804","SJAG_04639","SJAG_02954","SJAG_03158","SJAG_01570","SJAG_05199","SJAG_00041","SJAG_05182","SJAG_04358","SJAG_01491","SJAG_01702","SJAG_04944","SJAG_01649","SJAG_01372","SJAG_03286","SJAG_03206","SJAG_02056","SJAG_04317","SJAG_02007","SJAG_01061","SJAG_00437","SJAG_00334","SJAG_02271","SJAG_03362","SJAG_00835","SJAG_03056","SJAG_06603","SJAG_02556","SJAG_02099","SJAG_01998","SJAG_04865","SJAG_04706","SJAG_00080","SJAG_00158","SJAG_02201","SJAG_01179","SJAG_03934","SJAG_04285","SJAG_00695","SJAG_00717","SJAG_03115","SJAG_02646","SJAG_01359","SJAG_03155","SJAG_02901","SJAG_01209","SJAG_03585","SJAG_03227","SJAG_03457","SJAG_02947","SJAG_03635","SJAG_03114","SJAG_04681","SJAG_02805","SJAG_02721","SJAG_00359","SJAG_02150","SJAG_02769","SJAG_00582","SJAG_03266","SJAG_00906","SJAG_04975","SJAG_02717","SJAG_04260","SJAG_04110","SJAG_01620","SJAG_02955","SJAG_04934","SJAG_03310","SJAG_01995","SJAG_02235","SJAG_03046","SJAG_01881","SJAG_04640","SJAG_02791","SJAG_00513","SJAG_01164","SJAG_01368","SJAG_00186","SJAG_03701","SJAG_00660","SJAG_02187","SJAG_00634","SJAG_01298","SJAG_04856","SJAG_03461","SJAG_02117","SJAG_03994","SJAG_02648","SJAG_02433","SJAG_00635","SJAG_01890","SJAG_04270","SJAG_03592","SJAG_03054","SJAG_00640","SJAG_00404","SJAG_04192","SJAG_03247","SJAG_04231","SJAG_02306","SJAG_00547","SJAG_05560","SJAG_02763","SJAG_04190","SJAG_02708","SJAG_01941","SJAG_02452","SJAG_00988","SJAG_03723","SJAG_00392","SJAG_03563","SJAG_04819","SJAG_03324","SJAG_06634","SJAG_01536","SJAG_01918","SJAG_00578"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011614"},{"annotations":[87633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009603"},{"annotations":[88857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009787"},{"annotations":[87265],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012435"},{"annotations":[88943,88944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044723"},{"annotations":[87204],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044724"},{"annotations":[87577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009825"},{"annotations":[88328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014352"},{"annotations":[87883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013571"},{"annotations":[87115,87116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010966"},{"annotations":[87448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013111"},{"annotations":[87232],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008294"},{"annotations":[88072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013869"},{"annotations":[87549],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100255"},{"annotations":[87380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007068"},{"annotations":[88225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009958"},{"annotations":[88523],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[86962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012282"},{"annotations":[87035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014648"},{"annotations":[89179,89180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009053"},{"annotations":[87547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012052"},{"annotations":[88997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013349"},{"annotations":[87662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011783"},{"annotations":[88802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011933"},{"annotations":[88425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010998"},{"annotations":[87150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011291"},{"annotations":[86976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011969"},{"annotations":[88358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012117"},{"annotations":[87088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012221"},{"annotations":[87091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012222"},{"annotations":[87489],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011790"},{"annotations":[89164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971004"},{"annotations":[87161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010480"},{"annotations":[87098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009025"},{"annotations":[87623],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008814"},{"annotations":[87486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008815"},{"annotations":[88455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008822"},{"annotations":[87332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008842"},{"annotations":[87270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024557"},{"annotations":[88192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014399"},{"annotations":[88665,88664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009727"},{"annotations":[87731],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014248"},{"annotations":[87681],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008134"},{"annotations":[88227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012784"},{"annotations":[86916,86917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014702"},{"annotations":[89023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018163"},{"annotations":[87079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013051"},{"annotations":[88740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0027462"},{"annotations":[88739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0027451"},{"annotations":[87112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012248"},{"annotations":[88590,88591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[87860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014142"},{"annotations":[87407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011422"},{"annotations":[87804],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008858"},{"annotations":[88715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011559"},{"annotations":[88962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008760"},{"annotations":[86956,86957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009376"},{"annotations":[87273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011451"},{"annotations":[87026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014051"},{"annotations":[87005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014667"},{"annotations":[87003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014668"},{"annotations":[87611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012557"},{"annotations":[88794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014455"},{"annotations":[88790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008955"},{"annotations":[87599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012553"},{"annotations":[86911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014696"},{"annotations":[87600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012554"},{"annotations":[88352,88353],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008083"},{"annotations":[88810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014467"},{"annotations":[89007,89006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011534"},{"annotations":[87854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014733"},{"annotations":[88105,88104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010699"},{"annotations":[87248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"},{"annotations":[88568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013761"},{"annotations":[87089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010221"},{"annotations":[88980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013995"},{"annotations":[88913,88914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030810"},{"annotations":[87790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031040"},{"annotations":[87249,87251,87250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019149"},{"annotations":[89199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009528"},{"annotations":[89004],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008988"},{"annotations":[87876],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009258"},{"annotations":[87243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009352"},{"annotations":[87955],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019569"},{"annotations":[87992],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019570"},{"annotations":[88369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011829"},{"annotations":[88219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013838"},{"annotations":[87784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033615"},{"annotations":[88690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012637"},{"annotations":[88109],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013281"},{"annotations":[88976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013325"},{"annotations":[88374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013810"},{"annotations":[88870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012635"},{"annotations":[87573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013661"},{"annotations":[89142,89143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013969"},{"annotations":[88978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013986"},{"annotations":[88977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013987"},{"annotations":[87841,87840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014190"},{"annotations":[87895],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012510"},{"annotations":[88193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014397"},{"annotations":[88194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014398"},{"annotations":[88654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014525"},{"annotations":[87333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014547"},{"annotations":[87154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014636"},{"annotations":[87015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014684"},{"annotations":[87774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012534"},{"annotations":[89188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013306"},{"annotations":[87882],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013570"},{"annotations":[88379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013811"},{"annotations":[87571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014269"},{"annotations":[88814],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020727"},{"annotations":[87849,87850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014775"},{"annotations":[87134,87135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054677"},{"annotations":[87017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054741"},{"annotations":[87016],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054742"},{"annotations":[87912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054781"},{"annotations":[88033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032712"},{"annotations":[88055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032726"},{"annotations":[87425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030006"},{"annotations":[87426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030007"},{"annotations":[87430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030008"},{"annotations":[87437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030017"},{"annotations":[87283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033533"},{"annotations":[87285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033534"},{"annotations":[87284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033537"},{"annotations":[88488],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030311"},{"annotations":[89053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859228"},{"annotations":[87630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859323"},{"annotations":[87514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859337"},{"annotations":[87980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957992"},{"annotations":[89194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013310"},{"annotations":[87394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012393"},{"annotations":[87450,87451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013116"},{"annotations":[86923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800044"},{"annotations":[88348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012123"},{"annotations":[88058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014904"},{"annotations":[87831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026729"},{"annotations":[88280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957540"},{"annotations":[88160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957820"},{"annotations":[88819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054559"},{"annotations":[87473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859356"},{"annotations":[87472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859357"},{"annotations":[89036],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859223"},{"annotations":[87372,87371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009134"},{"annotations":[87515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012071"},{"annotations":[87009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010020"},{"annotations":[88566,88567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013760"},{"annotations":[87745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014258"},{"annotations":[87206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014023"},{"annotations":[87889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012518"},{"annotations":[87327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014543"},{"annotations":[87324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014542"},{"annotations":[88938,88939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009114"},{"annotations":[87482,87483],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011503"},{"annotations":[87376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[87909,87910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014706"},{"annotations":[86938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009058"},{"annotations":[87065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014072"},{"annotations":[87396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024554"},{"annotations":[88990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013345"},{"annotations":[88345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013789"},{"annotations":[89209,86928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010799"},{"annotations":[88218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013837"},{"annotations":[88309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014392"},{"annotations":[87173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014593"},{"annotations":[87183,87184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014598"},{"annotations":[87147,87146,87145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014625"},{"annotations":[87927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014719"},{"annotations":[88815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010472"},{"annotations":[89099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014933"},{"annotations":[87031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014647"},{"annotations":[87348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033364"},{"annotations":[88923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032808"},{"annotations":[88947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032822"},{"annotations":[89292,89293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014488"},{"annotations":[88716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007205"},{"annotations":[88096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012803"},{"annotations":[88720,88721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009107"},{"annotations":[87602],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012556"},{"annotations":[87366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012994"},{"annotations":[86908],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010155"},{"annotations":[86942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011964"},{"annotations":[87076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013049"},{"annotations":[87221,87220,87222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009380"},{"annotations":[86960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007495"},{"annotations":[88956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015003"},{"annotations":[89008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012873"},{"annotations":[87948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014139"},{"annotations":[87444,87443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013726"},{"annotations":[88216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013840"},{"annotations":[88964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015005"},{"annotations":[88525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010526"},{"annotations":[87392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010926"},{"annotations":[87123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010080"},{"annotations":[87632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008296"},{"annotations":[88215],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[88237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013248"},{"annotations":[88667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013499"},{"annotations":[86922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014108"},{"annotations":[88941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014986"},{"annotations":[88945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014987"},{"annotations":[88942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014985"},{"annotations":[87886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012512"},{"annotations":[87884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018346"},{"annotations":[88882],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007620"},{"annotations":[87293,87292,87294,87295,87296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010027"},{"annotations":[87342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011730"},{"annotations":[88599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013166"},{"annotations":[87950,87952,87951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009257"},{"annotations":[87389,87390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009737"},{"annotations":[88147,88146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009285"},{"annotations":[87821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009259"},{"annotations":[89197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009890"},{"annotations":[87694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009947"},{"annotations":[88131],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009284"},{"annotations":[86909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958179"},{"annotations":[88319],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958192"},{"annotations":[87072,87071,87073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013046"},{"annotations":[89182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010392"},{"annotations":[87756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009865"},{"annotations":[87143,87144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009290"},{"annotations":[87595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009295"},{"annotations":[89163,89162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013291"},{"annotations":[86995],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060627"},{"annotations":[86996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0040500"},{"annotations":[88458],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060724"},{"annotations":[88286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0029140"},{"annotations":[87977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008974"},{"annotations":[88971,88970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008962"},{"annotations":[87747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014261"},{"annotations":[87338],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100186"},{"annotations":[87375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012999"},{"annotations":[87331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030048"},{"annotations":[87424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011417"},{"annotations":[89013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009113"},{"annotations":[88103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013275"},{"annotations":[88793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019531"},{"annotations":[87356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012191"},{"annotations":[87782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007369"},{"annotations":[87257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009238"},{"annotations":[87845],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013584"},{"annotations":[88230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012787"},{"annotations":[87199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014020"},{"annotations":[88038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014882"},{"annotations":[88409,88410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011006"},{"annotations":[88040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014885"},{"annotations":[87894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011997"},{"annotations":[88198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009666"},{"annotations":[87188,87187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009353"},{"annotations":[88006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014869"},{"annotations":[86952,86953],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009377"},{"annotations":[88428,88426,88427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011369"},{"annotations":[87125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012465"},{"annotations":[88459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044330"},{"annotations":[88675,88674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009849"},{"annotations":[87481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859362"},{"annotations":[88412,88411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011236"},{"annotations":[88748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011717"},{"annotations":[87362,87361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009388"},{"annotations":[88846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013404"},{"annotations":[88243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009398"},{"annotations":[88082],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013882"},{"annotations":[88511],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014318"},{"annotations":[88801],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014457"},{"annotations":[87682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014780"},{"annotations":[88662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009400"},{"annotations":[88620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009401"},{"annotations":[88844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013458"},{"annotations":[87436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100058"},{"annotations":[88681,88682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011174"},{"annotations":[87509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859328"},{"annotations":[88086],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010299"},{"annotations":[88145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009448"},{"annotations":[88329,88330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014353"},{"annotations":[88365,88366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013802"},{"annotations":[87874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014162"},{"annotations":[87634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033572"},{"annotations":[88187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032662"},{"annotations":[87964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032665"},{"annotations":[88891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032789"},{"annotations":[89034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030533"},{"annotations":[88322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957288"},{"annotations":[89035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958204"},{"annotations":[88407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013173"},{"annotations":[87859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013528"},{"annotations":[88317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014348"},{"annotations":[88206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014409"},{"annotations":[89026,89027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012613"},{"annotations":[87036],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014649"},{"annotations":[87730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014815"},{"annotations":[87520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014832"},{"annotations":[89090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014930"},{"annotations":[88954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014996"},{"annotations":[88787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015020"},{"annotations":[88617],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044313"},{"annotations":[88260,88261,88259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020850"},{"annotations":[89028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012615"},{"annotations":[88062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013898"},{"annotations":[88868,88869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"},{"annotations":[87465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0006065"},{"annotations":[88539,88540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011816"},{"annotations":[87463,87462,87464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010788"},{"annotations":[88085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010298"},{"annotations":[88156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009867"},{"annotations":[88930],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014976"},{"annotations":[87531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009953"},{"annotations":[88850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012622"},{"annotations":[89148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013971"},{"annotations":[88031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958023"},{"annotations":[88570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013762"},{"annotations":[87359],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014576"},{"annotations":[88569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012074"},{"annotations":[87038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014057"},{"annotations":[89214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[87057,87056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"},{"annotations":[87105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012251"},{"annotations":[88267],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011246"},{"annotations":[88070,88068,88069,88067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010789"},{"annotations":[87367],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010651"},{"annotations":[87885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009607"},{"annotations":[87165,87164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009354"},{"annotations":[87772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009609"},{"annotations":[88604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"},{"annotations":[86975,86974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012481"},{"annotations":[87701],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014793"},{"annotations":[87008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008787"},{"annotations":[88881],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010159"},{"annotations":[87691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030840"},{"annotations":[87692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030841"},{"annotations":[87610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030843"},{"annotations":[88164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032617"},{"annotations":[88170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032630"},{"annotations":[88172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032631"},{"annotations":[88158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032609"},{"annotations":[88161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032612"},{"annotations":[87501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030935"},{"annotations":[87502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030937"},{"annotations":[87474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030974"},{"annotations":[88621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032909"},{"annotations":[87631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859321"},{"annotations":[87656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033639"},{"annotations":[87658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033645"},{"annotations":[87657],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033649"},{"annotations":[87669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033651"},{"annotations":[87663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033653"},{"annotations":[87665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033654"},{"annotations":[87666],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033655"},{"annotations":[87648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033635"},{"annotations":[87645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033636"},{"annotations":[87654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033637"},{"annotations":[87655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033638"},{"annotations":[88272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020858"},{"annotations":[88803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032869"},{"annotations":[88120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100294"},{"annotations":[88390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007415"},{"annotations":[87047],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014063"},{"annotations":[87048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014064"},{"annotations":[87046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014065"},{"annotations":[87050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014066"},{"annotations":[87848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014194"},{"annotations":[88338],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014356"},{"annotations":[88344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014364"},{"annotations":[88624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014496"},{"annotations":[89157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0700250"},{"annotations":[88464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859160"},{"annotations":[88500],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859520"},{"annotations":[87024],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014091"},{"annotations":[87411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011421"},{"annotations":[88472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957254"},{"annotations":[88471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957255"},{"annotations":[87045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014062"},{"annotations":[87276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011283"},{"annotations":[89136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014959"},{"annotations":[87828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014175"},{"annotations":[87742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014820"},{"annotations":[89123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014943"},{"annotations":[88936,88937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032815"},{"annotations":[87414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032932"},{"annotations":[86994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0976132"},{"annotations":[88994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008758"},{"annotations":[88996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013350"},{"annotations":[87554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009747"},{"annotations":[88240],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012792"},{"annotations":[89166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009504"},{"annotations":[88239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012791"},{"annotations":[88065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013865"},{"annotations":[87606],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020714"},{"annotations":[87179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044714"},{"annotations":[87852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010779"},{"annotations":[88080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013877"},{"annotations":[88507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011629"},{"annotations":[88247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011257"},{"annotations":[88763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015012"},{"annotations":[87878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013563"},{"annotations":[88828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010466"},{"annotations":[87873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014165"},{"annotations":[87667,87668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009189"},{"annotations":[87060],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011582"},{"annotations":[88779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0975806"},{"annotations":[87587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013675"},{"annotations":[87940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014132"},{"annotations":[87208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014611"},{"annotations":[87274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033282"},{"annotations":[87913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054785"},{"annotations":[88265],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957382"},{"annotations":[88935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971174"},{"annotations":[87767,87765,87766],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009364"},{"annotations":[87853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014140"},{"annotations":[88584,88585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013154"},{"annotations":[87166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033556"},{"annotations":[88589],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013159"},{"annotations":[87858],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014141"},{"annotations":[88587,88588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013160"},{"annotations":[88995],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009992"},{"annotations":[87635],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033619"},{"annotations":[88824,88825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024553"},{"annotations":[89191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013307"},{"annotations":[87978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0034121"},{"annotations":[86918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010794"},{"annotations":[87350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014562"},{"annotations":[87395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009736"},{"annotations":[88811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014466"},{"annotations":[88854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010476"},{"annotations":[87551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014290"},{"annotations":[87676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033642"},{"annotations":[87320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030037"},{"annotations":[88022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032705"},{"annotations":[87746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009744"},{"annotations":[87757],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008767"},{"annotations":[88877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008086"},{"annotations":[88981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013337"},{"annotations":[88852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009756"},{"annotations":[88121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011871"},{"annotations":[88114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011873"},{"annotations":[89195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009623"},{"annotations":[87452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013118"},{"annotations":[88385,88386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009340"},{"annotations":[87339],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009515"},{"annotations":[89037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010572"},{"annotations":[89171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010645"},{"annotations":[89019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011683"},{"annotations":[87059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014070"},{"annotations":[87381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008133"},{"annotations":[89005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009796"},{"annotations":[88975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010703"},{"annotations":[87155,87156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009797"},{"annotations":[88951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008759"},{"annotations":[87365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012992"},{"annotations":[88842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010438"},{"annotations":[87875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014166"},{"annotations":[88332,88331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100165"},{"annotations":[89184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013948"},{"annotations":[88813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054549"},{"annotations":[89185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013949"},{"annotations":[89183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013950"},{"annotations":[89186],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013951"},{"annotations":[89187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013952"},{"annotations":[89145,89144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013967"},{"annotations":[88773],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008953"},{"annotations":[89135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011101"},{"annotations":[88761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008954"},{"annotations":[89046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008736"},{"annotations":[89167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013927"},{"annotations":[89169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013930"},{"annotations":[89170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013931"},{"annotations":[89172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013936"},{"annotations":[89174],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013937"},{"annotations":[89175],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013938"},{"annotations":[89173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013939"},{"annotations":[89178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013942"},{"annotations":[89176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013943"},{"annotations":[89181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013945"},{"annotations":[88222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009959"},{"annotations":[89147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013972"},{"annotations":[87920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014126"},{"annotations":[86959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0976232"},{"annotations":[89141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013968"},{"annotations":[88853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011152"},{"annotations":[89189,89190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010395"},{"annotations":[86920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008907"},{"annotations":[88652,88653],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014526"},{"annotations":[88229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013853"},{"annotations":[87231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012683"},{"annotations":[88834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014485"},{"annotations":[87377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013000"},{"annotations":[87812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014754"},{"annotations":[87580,87581],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009824"},{"annotations":[88967],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013382"},{"annotations":[88454],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024528"},{"annotations":[87078],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012238"},{"annotations":[87449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013117"},{"annotations":[88266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009783"},{"annotations":[87040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014656"},{"annotations":[88337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020845"},{"annotations":[87979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957993"},{"annotations":[88845],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011156"},{"annotations":[87458],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011214"},{"annotations":[87068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008319"},{"annotations":[88444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012596"},{"annotations":[86910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011301"},{"annotations":[87855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013531"},{"annotations":[87347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044726"},{"annotations":[88405],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013171"},{"annotations":[87413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012407"},{"annotations":[87677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009949"},{"annotations":[88359],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010717"},{"annotations":[87839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013580"},{"annotations":[88701],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009502"},{"annotations":[87127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009529"},{"annotations":[88702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009503"},{"annotations":[88357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012120"},{"annotations":[87516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009950"},{"annotations":[89126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007067"},{"annotations":[87717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013624"},{"annotations":[88057],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011268"},{"annotations":[88244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008379"},{"annotations":[87993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010828"},{"annotations":[88133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010806"},{"annotations":[88049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011075"},{"annotations":[89127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010723"},{"annotations":[88598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012363"},{"annotations":[86968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012477"},{"annotations":[88683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013468"},{"annotations":[87382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013516"},{"annotations":[87759,87760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013611"},{"annotations":[87743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014256"},{"annotations":[88517,88519,88516,88518,88515,88512,88513,88520,88514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014323"},{"annotations":[88197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014400"},{"annotations":[88762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015013"},{"annotations":[88637,88636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044320"},{"annotations":[88159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032604"},{"annotations":[88228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012783"},{"annotations":[87958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008972"},{"annotations":[87803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014743"},{"annotations":[88573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012073"},{"annotations":[87281,87279,87278,87277,87280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011449"},{"annotations":[88839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010013"},{"annotations":[87603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008922"},{"annotations":[88351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011835"},{"annotations":[88199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014402"},{"annotations":[87925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018767"},{"annotations":[88843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010437"},{"annotations":[87714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014804"},{"annotations":[88093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020747"},{"annotations":[88795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020748"},{"annotations":[88855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010478"},{"annotations":[89165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010035"},{"annotations":[87406],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012664"},{"annotations":[89002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013354"},{"annotations":[88592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013776"},{"annotations":[87713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014803"},{"annotations":[87099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012450"},{"annotations":[88209,88210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014417"},{"annotations":[87518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011801"},{"annotations":[88536,88537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018996"},{"annotations":[88663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010075"},{"annotations":[87227,87228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019666"},{"annotations":[87067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009593"},{"annotations":[89015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012885"},{"annotations":[88041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014889"},{"annotations":[87572],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014270"},{"annotations":[87575],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014271"},{"annotations":[87107,87108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010083"},{"annotations":[88469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009492"},{"annotations":[87476],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030982"},{"annotations":[88073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013870"},{"annotations":[87697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014790"},{"annotations":[88538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011624"},{"annotations":[88032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014881"},{"annotations":[88958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011125"},{"annotations":[87210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014615"},{"annotations":[87211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014619"},{"annotations":[87705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014221"},{"annotations":[87054,87055,87053,87052,89217,87051,89218,89216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0005148"},{"annotations":[88691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010909"},{"annotations":[88208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013829"},{"annotations":[87651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008297"},{"annotations":[88301],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957577"},{"annotations":[88083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009910"},{"annotations":[89078],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010200"},{"annotations":[87508,87506,87507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019148"},{"annotations":[87519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010208"},{"annotations":[88645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010420"},{"annotations":[88643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020721"},{"annotations":[88574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010210"},{"annotations":[87771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012531"},{"annotations":[88595,88594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010211"},{"annotations":[88603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010212"},{"annotations":[88562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010215"},{"annotations":[88510],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010216"},{"annotations":[88547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010214"}]},"cv_name":"mondo","definition":"A congenital disorder (due to inherited enzyme abnormality) or acquired (due to failure of a metabolically important organ) disorder resulting from an abnormal metabolic process.","definition_xrefs":["NCIT:C3235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":553,"genes_by_uniquename":{"SJAG_00041":null,"SJAG_00043":null,"SJAG_00068":null,"SJAG_00070":null,"SJAG_00080":null,"SJAG_00084":null,"SJAG_00088":null,"SJAG_00092":null,"SJAG_00103":null,"SJAG_00108":null,"SJAG_00115":null,"SJAG_00120":null,"SJAG_00133":null,"SJAG_00154":null,"SJAG_00158":null,"SJAG_00183":null,"SJAG_00186":null,"SJAG_00212":null,"SJAG_00214":null,"SJAG_00217":null,"SJAG_00222":null,"SJAG_00255":null,"SJAG_00260":null,"SJAG_00281":null,"SJAG_00295":null,"SJAG_00308":null,"SJAG_00319":null,"SJAG_00325":null,"SJAG_00326":null,"SJAG_00334":null,"SJAG_00339":null,"SJAG_00354":null,"SJAG_00358":null,"SJAG_00359":null,"SJAG_00379":null,"SJAG_00392":null,"SJAG_00404":null,"SJAG_00412":null,"SJAG_00413":null,"SJAG_00437":null,"SJAG_00459":null,"SJAG_00461":null,"SJAG_00464":null,"SJAG_00495":null,"SJAG_00513":null,"SJAG_00516":null,"SJAG_00522":null,"SJAG_00531":null,"SJAG_00547":null,"SJAG_00554":null,"SJAG_00570":null,"SJAG_00578":null,"SJAG_00582":null,"SJAG_00601":null,"SJAG_00605":null,"SJAG_00611":null,"SJAG_00634":null,"SJAG_00635":null,"SJAG_00636":null,"SJAG_00640":null,"SJAG_00643":null,"SJAG_00653":null,"SJAG_00660":null,"SJAG_00674":null,"SJAG_00694":null,"SJAG_00695":null,"SJAG_00702":null,"SJAG_00717":null,"SJAG_00721":null,"SJAG_00737":null,"SJAG_00747":null,"SJAG_00755":null,"SJAG_00797":null,"SJAG_00831":null,"SJAG_00835":null,"SJAG_00839":null,"SJAG_00846":null,"SJAG_00852":null,"SJAG_00857":null,"SJAG_00866":null,"SJAG_00885":null,"SJAG_00886":null,"SJAG_00891":null,"SJAG_00894":null,"SJAG_00898":null,"SJAG_00906":null,"SJAG_00924":null,"SJAG_00933":null,"SJAG_00938":null,"SJAG_00944":null,"SJAG_00946":null,"SJAG_00947":null,"SJAG_00964":null,"SJAG_00978":null,"SJAG_00988":null,"SJAG_00995":null,"SJAG_00997":null,"SJAG_01004":null,"SJAG_01007":null,"SJAG_01036":null,"SJAG_01043":null,"SJAG_01049":null,"SJAG_01059":null,"SJAG_01061":null,"SJAG_01063":null,"SJAG_01069":null,"SJAG_01070":null,"SJAG_01071":null,"SJAG_01072":null,"SJAG_01077":null,"SJAG_01147":null,"SJAG_01152":null,"SJAG_01162":null,"SJAG_01164":null,"SJAG_01165":null,"SJAG_01174":null,"SJAG_01179":null,"SJAG_01183":null,"SJAG_01190":null,"SJAG_01199":null,"SJAG_01207":null,"SJAG_01209":null,"SJAG_01216":null,"SJAG_01236":null,"SJAG_01298":null,"SJAG_01303":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_01355":null,"SJAG_01356":null,"SJAG_01359":null,"SJAG_01368":null,"SJAG_01372":null,"SJAG_01405":null,"SJAG_01407":null,"SJAG_01410":null,"SJAG_01413":null,"SJAG_01416":null,"SJAG_01417":null,"SJAG_01422":null,"SJAG_01432":null,"SJAG_01459":null,"SJAG_01461":null,"SJAG_01465":null,"SJAG_01466":null,"SJAG_01471":null,"SJAG_01474":null,"SJAG_01490":null,"SJAG_01491":null,"SJAG_01503":null,"SJAG_01524":null,"SJAG_01526":null,"SJAG_01536":null,"SJAG_01537":null,"SJAG_01570":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01589":null,"SJAG_01597":null,"SJAG_01612":null,"SJAG_01616":null,"SJAG_01620":null,"SJAG_01625":null,"SJAG_01630":null,"SJAG_01634":null,"SJAG_01640":null,"SJAG_01647":null,"SJAG_01649":null,"SJAG_01671":null,"SJAG_01677":null,"SJAG_01702":null,"SJAG_01784":null,"SJAG_01797":null,"SJAG_01820":null,"SJAG_01826":null,"SJAG_01841":null,"SJAG_01851":null,"SJAG_01859":null,"SJAG_01865":null,"SJAG_01866":null,"SJAG_01868":null,"SJAG_01872":null,"SJAG_01881":null,"SJAG_01887":null,"SJAG_01890":null,"SJAG_01903":null,"SJAG_01918":null,"SJAG_01924":null,"SJAG_01940":null,"SJAG_01941":null,"SJAG_01950":null,"SJAG_01957":null,"SJAG_01960":null,"SJAG_01991":null,"SJAG_01995":null,"SJAG_01998":null,"SJAG_02000":null,"SJAG_02006":null,"SJAG_02007":null,"SJAG_02009":null,"SJAG_02012":null,"SJAG_02013":null,"SJAG_02016":null,"SJAG_02031":null,"SJAG_02042":null,"SJAG_02050":null,"SJAG_02056":null,"SJAG_02068":null,"SJAG_02084":null,"SJAG_02099":null,"SJAG_02102":null,"SJAG_02107":null,"SJAG_02117":null,"SJAG_02119":null,"SJAG_02131":null,"SJAG_02139":null,"SJAG_02148":null,"SJAG_02150":null,"SJAG_02158":null,"SJAG_02163":null,"SJAG_02180":null,"SJAG_02187":null,"SJAG_02201":null,"SJAG_02211":null,"SJAG_02226":null,"SJAG_02229":null,"SJAG_02235":null,"SJAG_02242":null,"SJAG_02265":null,"SJAG_02271":null,"SJAG_02274":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02302":null,"SJAG_02305":null,"SJAG_02306":null,"SJAG_02313":null,"SJAG_02324":null,"SJAG_02334":null,"SJAG_02339":null,"SJAG_02353":null,"SJAG_02369":null,"SJAG_02384":null,"SJAG_02388":null,"SJAG_02397":null,"SJAG_02398":null,"SJAG_02399":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02432":null,"SJAG_02433":null,"SJAG_02452":null,"SJAG_02453":null,"SJAG_02463":null,"SJAG_02464":null,"SJAG_02480":null,"SJAG_02504":null,"SJAG_02518":null,"SJAG_02523":null,"SJAG_02539":null,"SJAG_02548":null,"SJAG_02556":null,"SJAG_02564":null,"SJAG_02599":null,"SJAG_02615":null,"SJAG_02619":null,"SJAG_02641":null,"SJAG_02643":null,"SJAG_02646":null,"SJAG_02648":null,"SJAG_02656":null,"SJAG_02658":null,"SJAG_02693":null,"SJAG_02696":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02716":null,"SJAG_02717":null,"SJAG_02721":null,"SJAG_02748":null,"SJAG_02763":null,"SJAG_02769":null,"SJAG_02783":null,"SJAG_02785":null,"SJAG_02788":null,"SJAG_02791":null,"SJAG_02796":null,"SJAG_02804":null,"SJAG_02805":null,"SJAG_02828":null,"SJAG_02848":null,"SJAG_02850":null,"SJAG_02855":null,"SJAG_02876":null,"SJAG_02885":null,"SJAG_02895":null,"SJAG_02896":null,"SJAG_02901":null,"SJAG_02903":null,"SJAG_02913":null,"SJAG_02946":null,"SJAG_02947":null,"SJAG_02949":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_02955":null,"SJAG_02977":null,"SJAG_02997":null,"SJAG_03011":null,"SJAG_03014":null,"SJAG_03018":null,"SJAG_03024":null,"SJAG_03032":null,"SJAG_03046":null,"SJAG_03052":null,"SJAG_03054":null,"SJAG_03056":null,"SJAG_03064":null,"SJAG_03066":null,"SJAG_03069":null,"SJAG_03071":null,"SJAG_03098":null,"SJAG_03099":null,"SJAG_03104":null,"SJAG_03114":null,"SJAG_03115":null,"SJAG_03147":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_03153":null,"SJAG_03155":null,"SJAG_03158":null,"SJAG_03162":null,"SJAG_03164":null,"SJAG_03173":null,"SJAG_03188":null,"SJAG_03206":null,"SJAG_03222":null,"SJAG_03227":null,"SJAG_03247":null,"SJAG_03258":null,"SJAG_03266":null,"SJAG_03275":null,"SJAG_03286":null,"SJAG_03290":null,"SJAG_03292":null,"SJAG_03293":null,"SJAG_03296":null,"SJAG_03310":null,"SJAG_03311":null,"SJAG_03316":null,"SJAG_03322":null,"SJAG_03324":null,"SJAG_03332":null,"SJAG_03333":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03375":null,"SJAG_03396":null,"SJAG_03398":null,"SJAG_03400":null,"SJAG_03434":null,"SJAG_03440":null,"SJAG_03447":null,"SJAG_03448":null,"SJAG_03457":null,"SJAG_03461":null,"SJAG_03475":null,"SJAG_03490":null,"SJAG_03506":null,"SJAG_03509":null,"SJAG_03550":null,"SJAG_03552":null,"SJAG_03553":null,"SJAG_03556":null,"SJAG_03557":null,"SJAG_03560":null,"SJAG_03563":null,"SJAG_03584":null,"SJAG_03585":null,"SJAG_03588":null,"SJAG_03592":null,"SJAG_03596":null,"SJAG_03635":null,"SJAG_03641":null,"SJAG_03656":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03669":null,"SJAG_03671":null,"SJAG_03672":null,"SJAG_03701":null,"SJAG_03712":null,"SJAG_03723":null,"SJAG_03773":null,"SJAG_03774":null,"SJAG_03781":null,"SJAG_03782":null,"SJAG_03785":null,"SJAG_03795":null,"SJAG_03797":null,"SJAG_03804":null,"SJAG_03811":null,"SJAG_03813":null,"SJAG_03818":null,"SJAG_03824":null,"SJAG_03827":null,"SJAG_03861":null,"SJAG_03865":null,"SJAG_03866":null,"SJAG_03881":null,"SJAG_03923":null,"SJAG_03934":null,"SJAG_03960":null,"SJAG_03961":null,"SJAG_03992":null,"SJAG_03994":null,"SJAG_04000":null,"SJAG_04016":null,"SJAG_04019":null,"SJAG_04042":null,"SJAG_04053":null,"SJAG_04077":null,"SJAG_04084":null,"SJAG_04094":null,"SJAG_04096":null,"SJAG_04109":null,"SJAG_04110":null,"SJAG_04114":null,"SJAG_04119":null,"SJAG_04127":null,"SJAG_04146":null,"SJAG_04149":null,"SJAG_04157":null,"SJAG_04165":null,"SJAG_04178":null,"SJAG_04183":null,"SJAG_04190":null,"SJAG_04192":null,"SJAG_04203":null,"SJAG_04206":null,"SJAG_04231":null,"SJAG_04260":null,"SJAG_04263":null,"SJAG_04270":null,"SJAG_04277":null,"SJAG_04285":null,"SJAG_04295":null,"SJAG_04296":null,"SJAG_04300":null,"SJAG_04316":null,"SJAG_04317":null,"SJAG_04321":null,"SJAG_04323":null,"SJAG_04334":null,"SJAG_04348":null,"SJAG_04358":null,"SJAG_04362":null,"SJAG_04363":null,"SJAG_04367":null,"SJAG_04378":null,"SJAG_04394":null,"SJAG_04397":null,"SJAG_04410":null,"SJAG_04418":null,"SJAG_04425":null,"SJAG_04449":null,"SJAG_04459":null,"SJAG_04473":null,"SJAG_04495":null,"SJAG_04497":null,"SJAG_04499":null,"SJAG_04529":null,"SJAG_04540":null,"SJAG_04549":null,"SJAG_04553":null,"SJAG_04560":null,"SJAG_04568":null,"SJAG_04577":null,"SJAG_04588":null,"SJAG_04608":null,"SJAG_04637":null,"SJAG_04639":null,"SJAG_04640":null,"SJAG_04645":null,"SJAG_04654":null,"SJAG_04665":null,"SJAG_04681":null,"SJAG_04697":null,"SJAG_04704":null,"SJAG_04706":null,"SJAG_04728":null,"SJAG_04738":null,"SJAG_04757":null,"SJAG_04763":null,"SJAG_04785":null,"SJAG_04790":null,"SJAG_04791":null,"SJAG_04810":null,"SJAG_04816":null,"SJAG_04819":null,"SJAG_04821":null,"SJAG_04823":null,"SJAG_04843":null,"SJAG_04849":null,"SJAG_04856":null,"SJAG_04859":null,"SJAG_04862":null,"SJAG_04865":null,"SJAG_04881":null,"SJAG_04882":null,"SJAG_04885":null,"SJAG_04934":null,"SJAG_04944":null,"SJAG_04952":null,"SJAG_04954":null,"SJAG_04975":null,"SJAG_04978":null,"SJAG_04980":null,"SJAG_05175":null,"SJAG_05180":null,"SJAG_05182":null,"SJAG_05194":null,"SJAG_05199":null,"SJAG_05213":null,"SJAG_05218":null,"SJAG_05219":null,"SJAG_05230":null,"SJAG_05271":null,"SJAG_05277":null,"SJAG_05278":null,"SJAG_05283":null,"SJAG_05305":null,"SJAG_05327":null,"SJAG_05342":null,"SJAG_05373":null,"SJAG_05560":null,"SJAG_05950":null,"SJAG_06022":null,"SJAG_06046":null,"SJAG_06383":null,"SJAG_06514":null,"SJAG_06603":null,"SJAG_06634":null,"SJAG_07003":null,"SJAG_07005":null,"SJAG_16456":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT15":null,"SJAG_MIT20":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"is_obsolete":false,"name":"metabolic disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0000589","MESH:D008659","UMLS:C0025517","ICD9:277.8","ICD9:277.9","DOID:0014667","NANDO:1100002","SCTID:75934005","ICD10CM:E70-E88","MEDGEN:44376","ICD10WHO:E70-E90"],"synonyms":[{"name":"disease of metabolism","type":"related"},{"name":"disorder of metabolic process","type":"exact"},{"name":"metabolic disease","type":"exact"},{"name":"metabolic disorder","type":"exact"},{"name":"metabolic process disease","type":"exact"}],"termid":"MONDO:0005066","terms_by_termid":{"MONDO:0005148":null,"MONDO:0006065":null,"MONDO:0007067":null,"MONDO:0007068":null,"MONDO:0007205":null,"MONDO:0007369":null,"MONDO:0007415":null,"MONDO:0007453":null,"MONDO:0007495":null,"MONDO:0007620":null,"MONDO:0008083":null,"MONDO:0008086":null,"MONDO:0008133":null,"MONDO:0008134":null,"MONDO:0008294":null,"MONDO:0008296":null,"MONDO:0008297":null,"MONDO:0008319":null,"MONDO:0008379":null,"MONDO:0008736":null,"MONDO:0008758":null,"MONDO:0008759":null,"MONDO:0008760":null,"MONDO:0008767":null,"MONDO:0008787":null,"MONDO:0008814":null,"MONDO:0008815":null,"MONDO:0008822":null,"MONDO:0008842":null,"MONDO:0008858":null,"MONDO:0008907":null,"MONDO:0008922":null,"MONDO:0008953":null,"MONDO:0008954":null,"MONDO:0008955":null,"MONDO:0008962":null,"MONDO:0008972":null,"MONDO:0008974":null,"MONDO:0008988":null,"MONDO:0009025":null,"MONDO:0009053":null,"MONDO:0009058":null,"MONDO:0009107":null,"MONDO:0009113":null,"MONDO:0009114":null,"MONDO:0009134":null,"MONDO:0009189":null,"MONDO:0009238":null,"MONDO:0009257":null,"MONDO:0009258":null,"MONDO:0009259":null,"MONDO:0009284":null,"MONDO:0009285":null,"MONDO:0009290":null,"MONDO:0009295":null,"MONDO:0009340":null,"MONDO:0009352":null,"MONDO:0009353":null,"MONDO:0009354":null,"MONDO:0009364":null,"MONDO:0009376":null,"MONDO:0009377":null,"MONDO:0009380":null,"MONDO:0009388":null,"MONDO:0009398":null,"MONDO:0009400":null,"MONDO:0009401":null,"MONDO:0009448":null,"MONDO:0009492":null,"MONDO:0009502":null,"MONDO:0009503":null,"MONDO:0009504":null,"MONDO:0009515":null,"MONDO:0009528":null,"MONDO:0009529":null,"MONDO:0009593":null,"MONDO:0009603":null,"MONDO:0009607":null,"MONDO:0009609":null,"MONDO:0009623":null,"MONDO:0009666":null,"MONDO:0009727":null,"MONDO:0009736":null,"MONDO:0009737":null,"MONDO:0009744":null,"MONDO:0009747":null,"MONDO:0009756":null,"MONDO:0009783":null,"MONDO:0009787":null,"MONDO:0009796":null,"MONDO:0009797":null,"MONDO:0009824":null,"MONDO:0009825":null,"MONDO:0009849":null,"MONDO:0009865":null,"MONDO:0009867":null,"MONDO:0009890":null,"MONDO:0009902":null,"MONDO:0009910":null,"MONDO:0009947":null,"MONDO:0009949":null,"MONDO:0009950":null,"MONDO:0009953":null,"MONDO:0009958":null,"MONDO:0009959":null,"MONDO:0009992":null,"MONDO:0010013":null,"MONDO:0010020":null,"MONDO:0010027":null,"MONDO:0010035":null,"MONDO:0010075":null,"MONDO:0010080":null,"MONDO:0010083":null,"MONDO:0010155":null,"MONDO:0010159":null,"MONDO:0010184":null,"MONDO:0010200":null,"MONDO:0010208":null,"MONDO:0010210":null,"MONDO:0010211":null,"MONDO:0010212":null,"MONDO:0010214":null,"MONDO:0010215":null,"MONDO:0010216":null,"MONDO:0010221":null,"MONDO:0010298":null,"MONDO:0010299":null,"MONDO:0010392":null,"MONDO:0010395":null,"MONDO:0010420":null,"MONDO:0010437":null,"MONDO:0010438":null,"MONDO:0010466":null,"MONDO:0010472":null,"MONDO:0010476":null,"MONDO:0010478":null,"MONDO:0010480":null,"MONDO:0010526":null,"MONDO:0010572":null,"MONDO:0010621":null,"MONDO:0010645":null,"MONDO:0010651":null,"MONDO:0010699":null,"MONDO:0010703":null,"MONDO:0010717":null,"MONDO:0010723":null,"MONDO:0010779":null,"MONDO:0010788":null,"MONDO:0010789":null,"MONDO:0010794":null,"MONDO:0010799":null,"MONDO:0010806":null,"MONDO:0010828":null,"MONDO:0010909":null,"MONDO:0010926":null,"MONDO:0010966":null,"MONDO:0010998":null,"MONDO:0011006":null,"MONDO:0011075":null,"MONDO:0011101":null,"MONDO:0011125":null,"MONDO:0011152":null,"MONDO:0011156":null,"MONDO:0011174":null,"MONDO:0011214":null,"MONDO:0011236":null,"MONDO:0011246":null,"MONDO:0011257":null,"MONDO:0011268":null,"MONDO:0011283":null,"MONDO:0011291":null,"MONDO:0011301":null,"MONDO:0011369":null,"MONDO:0011417":null,"MONDO:0011421":null,"MONDO:0011422":null,"MONDO:0011449":null,"MONDO:0011451":null,"MONDO:0011503":null,"MONDO:0011534":null,"MONDO:0011559":null,"MONDO:0011582":null,"MONDO:0011614":null,"MONDO:0011624":null,"MONDO:0011629":null,"MONDO:0011683":null,"MONDO:0011706":null,"MONDO:0011717":null,"MONDO:0011730":null,"MONDO:0011783":null,"MONDO:0011790":null,"MONDO:0011801":null,"MONDO:0011816":null,"MONDO:0011829":null,"MONDO:0011835":null,"MONDO:0011871":null,"MONDO:0011873":null,"MONDO:0011933":null,"MONDO:0011964":null,"MONDO:0011969":null,"MONDO:0011997":null,"MONDO:0012052":null,"MONDO:0012071":null,"MONDO:0012073":null,"MONDO:0012074":null,"MONDO:0012099":null,"MONDO:0012117":null,"MONDO:0012120":null,"MONDO:0012123":null,"MONDO:0012191":null,"MONDO:0012221":null,"MONDO:0012222":null,"MONDO:0012238":null,"MONDO:0012248":null,"MONDO:0012251":null,"MONDO:0012282":null,"MONDO:0012363":null,"MONDO:0012393":null,"MONDO:0012407":null,"MONDO:0012435":null,"MONDO:0012450":null,"MONDO:0012465":null,"MONDO:0012477":null,"MONDO:0012481":null,"MONDO:0012510":null,"MONDO:0012512":null,"MONDO:0012518":null,"MONDO:0012531":null,"MONDO:0012534":null,"MONDO:0012553":null,"MONDO:0012554":null,"MONDO:0012556":null,"MONDO:0012557":null,"MONDO:0012596":null,"MONDO:0012613":null,"MONDO:0012615":null,"MONDO:0012622":null,"MONDO:0012635":null,"MONDO:0012637":null,"MONDO:0012664":null,"MONDO:0012683":null,"MONDO:0012783":null,"MONDO:0012784":null,"MONDO:0012787":null,"MONDO:0012791":null,"MONDO:0012792":null,"MONDO:0012803":null,"MONDO:0012873":null,"MONDO:0012885":null,"MONDO:0012992":null,"MONDO:0012994":null,"MONDO:0012999":null,"MONDO:0013000":null,"MONDO:0013046":null,"MONDO:0013049":null,"MONDO:0013051":null,"MONDO:0013111":null,"MONDO:0013116":null,"MONDO:0013117":null,"MONDO:0013118":null,"MONDO:0013154":null,"MONDO:0013159":null,"MONDO:0013160":null,"MONDO:0013162":null,"MONDO:0013166":null,"MONDO:0013171":null,"MONDO:0013173":null,"MONDO:0013248":null,"MONDO:0013275":null,"MONDO:0013281":null,"MONDO:0013291":null,"MONDO:0013306":null,"MONDO:0013307":null,"MONDO:0013310":null,"MONDO:0013325":null,"MONDO:0013337":null,"MONDO:0013345":null,"MONDO:0013349":null,"MONDO:0013350":null,"MONDO:0013354":null,"MONDO:0013382":null,"MONDO:0013404":null,"MONDO:0013458":null,"MONDO:0013468":null,"MONDO:0013499":null,"MONDO:0013516":null,"MONDO:0013528":null,"MONDO:0013531":null,"MONDO:0013563":null,"MONDO:0013570":null,"MONDO:0013571":null,"MONDO:0013580":null,"MONDO:0013584":null,"MONDO:0013611":null,"MONDO:0013624":null,"MONDO:0013661":null,"MONDO:0013675":null,"MONDO:0013726":null,"MONDO:0013760":null,"MONDO:0013761":null,"MONDO:0013762":null,"MONDO:0013776":null,"MONDO:0013789":null,"MONDO:0013802":null,"MONDO:0013810":null,"MONDO:0013811":null,"MONDO:0013829":null,"MONDO:0013836":null,"MONDO:0013837":null,"MONDO:0013838":null,"MONDO:0013840":null,"MONDO:0013853":null,"MONDO:0013865":null,"MONDO:0013869":null,"MONDO:0013870":null,"MONDO:0013877":null,"MONDO:0013882":null,"MONDO:0013898":null,"MONDO:0013927":null,"MONDO:0013930":null,"MONDO:0013931":null,"MONDO:0013936":null,"MONDO:0013937":null,"MONDO:0013938":null,"MONDO:0013939":null,"MONDO:0013942":null,"MONDO:0013943":null,"MONDO:0013945":null,"MONDO:0013948":null,"MONDO:0013949":null,"MONDO:0013950":null,"MONDO:0013951":null,"MONDO:0013952":null,"MONDO:0013967":null,"MONDO:0013968":null,"MONDO:0013969":null,"MONDO:0013971":null,"MONDO:0013972":null,"MONDO:0013986":null,"MONDO:0013987":null,"MONDO:0013995":null,"MONDO:0014020":null,"MONDO:0014023":null,"MONDO:0014051":null,"MONDO:0014057":null,"MONDO:0014062":null,"MONDO:0014063":null,"MONDO:0014064":null,"MONDO:0014065":null,"MONDO:0014066":null,"MONDO:0014070":null,"MONDO:0014072":null,"MONDO:0014091":null,"MONDO:0014108":null,"MONDO:0014126":null,"MONDO:0014132":null,"MONDO:0014139":null,"MONDO:0014140":null,"MONDO:0014141":null,"MONDO:0014142":null,"MONDO:0014162":null,"MONDO:0014165":null,"MONDO:0014166":null,"MONDO:0014175":null,"MONDO:0014190":null,"MONDO:0014194":null,"MONDO:0014221":null,"MONDO:0014248":null,"MONDO:0014256":null,"MONDO:0014258":null,"MONDO:0014261":null,"MONDO:0014269":null,"MONDO:0014270":null,"MONDO:0014271":null,"MONDO:0014290":null,"MONDO:0014318":null,"MONDO:0014323":null,"MONDO:0014348":null,"MONDO:0014352":null,"MONDO:0014353":null,"MONDO:0014356":null,"MONDO:0014364":null,"MONDO:0014392":null,"MONDO:0014397":null,"MONDO:0014398":null,"MONDO:0014399":null,"MONDO:0014400":null,"MONDO:0014402":null,"MONDO:0014409":null,"MONDO:0014417":null,"MONDO:0014455":null,"MONDO:0014457":null,"MONDO:0014466":null,"MONDO:0014467":null,"MONDO:0014485":null,"MONDO:0014488":null,"MONDO:0014496":null,"MONDO:0014525":null,"MONDO:0014526":null,"MONDO:0014542":null,"MONDO:0014543":null,"MONDO:0014547":null,"MONDO:0014562":null,"MONDO:0014576":null,"MONDO:0014593":null,"MONDO:0014598":null,"MONDO:0014611":null,"MONDO:0014615":null,"MONDO:0014619":null,"MONDO:0014625":null,"MONDO:0014636":null,"MONDO:0014647":null,"MONDO:0014648":null,"MONDO:0014649":null,"MONDO:0014656":null,"MONDO:0014667":null,"MONDO:0014668":null,"MONDO:0014674":null,"MONDO:0014684":null,"MONDO:0014696":null,"MONDO:0014702":null,"MONDO:0014706":null,"MONDO:0014719":null,"MONDO:0014733":null,"MONDO:0014743":null,"MONDO:0014754":null,"MONDO:0014775":null,"MONDO:0014780":null,"MONDO:0014790":null,"MONDO:0014793":null,"MONDO:0014803":null,"MONDO:0014804":null,"MONDO:0014815":null,"MONDO:0014820":null,"MONDO:0014832":null,"MONDO:0014869":null,"MONDO:0014881":null,"MONDO:0014882":null,"MONDO:0014885":null,"MONDO:0014889":null,"MONDO:0014904":null,"MONDO:0014930":null,"MONDO:0014933":null,"MONDO:0014943":null,"MONDO:0014959":null,"MONDO:0014976":null,"MONDO:0014985":null,"MONDO:0014986":null,"MONDO:0014987":null,"MONDO:0014996":null,"MONDO:0015003":null,"MONDO:0015005":null,"MONDO:0015012":null,"MONDO:0015013":null,"MONDO:0015020":null,"MONDO:0018163":null,"MONDO:0018346":null,"MONDO:0018767":null,"MONDO:0018996":null,"MONDO:0019148":null,"MONDO:0019149":null,"MONDO:0019531":null,"MONDO:0019569":null,"MONDO:0019570":null,"MONDO:0019666":null,"MONDO:0020714":null,"MONDO:0020721":null,"MONDO:0020727":null,"MONDO:0020747":null,"MONDO:0020748":null,"MONDO:0020845":null,"MONDO:0020850":null,"MONDO:0020858":null,"MONDO:0024528":null,"MONDO:0024553":null,"MONDO:0024554":null,"MONDO:0024557":null,"MONDO:0026729":null,"MONDO:0027451":null,"MONDO:0027462":null,"MONDO:0029140":null,"MONDO:0030006":null,"MONDO:0030007":null,"MONDO:0030008":null,"MONDO:0030017":null,"MONDO:0030037":null,"MONDO:0030048":null,"MONDO:0030311":null,"MONDO:0030533":null,"MONDO:0030810":null,"MONDO:0030840":null,"MONDO:0030841":null,"MONDO:0030843":null,"MONDO:0030935":null,"MONDO:0030937":null,"MONDO:0030974":null,"MONDO:0030982":null,"MONDO:0031040":null,"MONDO:0032604":null,"MONDO:0032609":null,"MONDO:0032612":null,"MONDO:0032617":null,"MONDO:0032630":null,"MONDO:0032631":null,"MONDO:0032662":null,"MONDO:0032665":null,"MONDO:0032705":null,"MONDO:0032712":null,"MONDO:0032726":null,"MONDO:0032789":null,"MONDO:0032808":null,"MONDO:0032815":null,"MONDO:0032822":null,"MONDO:0032869":null,"MONDO:0032909":null,"MONDO:0032932":null,"MONDO:0033282":null,"MONDO:0033364":null,"MONDO:0033533":null,"MONDO:0033534":null,"MONDO:0033537":null,"MONDO:0033556":null,"MONDO:0033572":null,"MONDO:0033615":null,"MONDO:0033619":null,"MONDO:0033635":null,"MONDO:0033636":null,"MONDO:0033637":null,"MONDO:0033638":null,"MONDO:0033639":null,"MONDO:0033642":null,"MONDO:0033645":null,"MONDO:0033649":null,"MONDO:0033651":null,"MONDO:0033653":null,"MONDO:0033654":null,"MONDO:0033655":null,"MONDO:0034121":null,"MONDO:0040500":null,"MONDO:0044313":null,"MONDO:0044320":null,"MONDO:0044330":null,"MONDO:0044714":null,"MONDO:0044723":null,"MONDO:0044724":null,"MONDO:0044726":null,"MONDO:0054549":null,"MONDO:0054559":null,"MONDO:0054677":null,"MONDO:0054741":null,"MONDO:0054742":null,"MONDO:0054781":null,"MONDO:0054785":null,"MONDO:0060627":null,"MONDO:0060724":null,"MONDO:0100058":null,"MONDO:0100165":null,"MONDO:0100186":null,"MONDO:0100255":null,"MONDO:0100294":null,"MONDO:0700250":null,"MONDO:0800044":null,"MONDO:0859160":null,"MONDO:0859223":null,"MONDO:0859228":null,"MONDO:0859321":null,"MONDO:0859323":null,"MONDO:0859328":null,"MONDO:0859337":null,"MONDO:0859356":null,"MONDO:0859357":null,"MONDO:0859362":null,"MONDO:0859520":null,"MONDO:0957254":null,"MONDO:0957255":null,"MONDO:0957288":null,"MONDO:0957382":null,"MONDO:0957540":null,"MONDO:0957577":null,"MONDO:0957820":null,"MONDO:0957992":null,"MONDO:0957993":null,"MONDO:0958023":null,"MONDO:0958179":null,"MONDO:0958192":null,"MONDO:0958204":null,"MONDO:0971004":null,"MONDO:0971174":null,"MONDO:0975806":null,"MONDO:0976132":null,"MONDO:0976232":null},"xrefs":{"Monarch":{"xref_id":"0005066"}}}


id: MONDO:0007064
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of SCID characterized by profound lymphopenia and very low immunoglobulin levels of all isotypes resulting in severe and recurrent opportunistic infections.","definition_xrefs":["Orphanet:277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T-B- severe combined immunodeficiency","termid":"MONDO:0017855"},{"relation_name":"is_a","term_name":"inborn disorder of purine metabolism","termid":"MONDO:0019236"},{"relation_name":"is_a","term_name":"familial severe combined immunodeficiency","termid":"MONDO:0031520"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0005046","MONDO:0005066"],"is_obsolete":false,"name":"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency","secondary_identifiers":["MEDGEN:354935","DOID:5810","OMIM:102700","SCTID:44940001","NCIT:C3962","UMLS:C1863236","CSP:1560-6660","NANDO:1200323","ICD9:277.2","MedDRA:10066367","NANDO:2200696","GARD:5748","MESH:C531816"],"synonyms":[{"name":"ADA","type":"exact"},{"name":"ADA deficiency","type":"exact"},{"name":"ADA-SCID","type":"exact"},{"name":"SCID due to ADA deficiency","type":"exact"},{"name":"SCID due to ADA deficiency, delayed onset","type":"related"},{"name":"SCID due to ADA deficiency, early-onset","type":"exact"},{"name":"SCID due to ADA deficiency, late-onset","type":"related"},{"name":"SCID due to adenosine deaminase deficiency","type":"exact"},{"name":"adenosine deaminase deficiency","type":"exact"},{"name":"adenosine deaminase deficiency, partial","type":"related"},{"name":"adenosine deaminase deficiency, partial, Autosomal recessive, Somatic mosaicism","type":"exact"},{"name":"adenosine deaminase deficient severe combined immunodeficiency","type":"exact"},{"name":"partial ADA deficiency","type":"related"},{"name":"severe combined immunodeficiency due to ADA deficiency","type":"related"},{"name":"severe combined immunodeficiency due to ADA deficiency, Autosomal recessive, Somatic mosaicism","type":"exact"},{"name":"severe combined immunodeficiency due to adenosine deaminase deficiency","type":"related"},{"name":"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency","type":"exact"}],"termid":"MONDO:0007064","xrefs":{"Monarch":{"xref_id":"0007064"}}}


id: PBO:0061808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"odr-4 GPCR localization factor homolog","termid":"PBO:0061808"}


id: PBO:0016899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule binding protein Mcp1","termid":"PBO:0016899"}


id: MONDO:0001849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disease of orbital part of eye adnexa","termid":"MONDO:0004751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic orbital inflammation","secondary_identifiers":["UMLS:C0155261","ICD9:376.1","SCTID:44729001","DOID:1397","ICD9:376.10","MEDGEN:509880"],"synonyms":[{"name":"chronic inflammation of orbit","type":"exact"}],"termid":"MONDO:0001849","xrefs":{"Monarch":{"xref_id":"0001849"}}}


id: PBO:0079462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TVP23B pseudogene 2","termid":"PBO:0079462"}


id: GO:0002865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of an acute inflammatory response to an antigenic stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of acute inflammatory response","termid":"GO:0002674"},{"relation_name":"is_a","term_name":"negative regulation of inflammatory response to antigenic stimulus","termid":"GO:0002862"},{"relation_name":"is_a","term_name":"regulation of acute inflammatory response to antigenic stimulus","termid":"GO:0002864"},{"relation_name":"negatively_regulates","term_name":"acute inflammatory response to antigenic stimulus","termid":"GO:0002438"}],"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 acute inflammatory response to antigenic stimulus","synonyms":[{"name":"down regulation of acute inflammatory response to antigenic stimulus","type":"exact"},{"name":"down-regulation of acute inflammatory response to antigenic stimulus","type":"exact"},{"name":"downregulation of acute inflammatory response to antigenic stimulus","type":"exact"},{"name":"inhibition of acute inflammatory response to antigenic stimulus","type":"narrow"}],"termid":"GO:0002865"}


id: MONDO:0006929
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the genus proteus.","definition_xrefs":["MESH:D011512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Proteus infectious disease","secondary_identifiers":["MEDGEN:46164","SCTID:186437007","UMLS:C0033700"],"synonyms":[{"name":"Proteus <enterobacteria> caused disease or disorder","type":"exact"},{"name":"Proteus <enterobacteria> disease or disorder","type":"exact"},{"name":"Proteus <enterobacteria> infectious disease","type":"exact"},{"name":"Proteus infection","type":"related"},{"name":"infection, Proteus","type":"related"},{"name":"infections, Proteus","type":"related"}],"termid":"MONDO:0006929","xrefs":{"Monarch":{"xref_id":"0006929"}}}


id: GO:0007570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete age dependent accumulation of genetic damage (obsolete GO:0007570)","synonyms":[{"name":"age dependent accumulation of genetic damage","type":"exact"}],"termid":"GO:0007570"}


id: GO:0021868
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The unequal mitotic division of a forebrain radial glial cell that gives rise to a radial glial cell and a ventricular zone cell.","definition_xrefs":["GOC:cls","GOC:jid","PMID:16226447","GOC:dph","GOC:dgh","GO_REF:0000021"],"gene_count":0,"genotype_count":0,"name":"obsolete ventricular zone cell-producing asymmetric radial glial cell division in forebrain (obsolete GO:0021868)","termid":"GO:0021868"}


id: GO:0048479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the style over time, from its formation to the mature structure. The style is an elongated part of a carpel, or group of fused carpels, and it lies between the ovary and the stigma.","definition_xrefs":["GOC:jid","PO:0009074"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"carpel development","termid":"GO:0048440"}],"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":"style development","termid":"GO:0048479"}


id: GO:0072257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the cells of the metanephric nephron tubule as it progresses from its formation to the mature state.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron tubule epithelial cell differentiation","termid":"GO:0072160"},{"relation_name":"is_a","term_name":"cell differentiation involved in metanephros development","termid":"GO:0072202"},{"relation_name":"part_of","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 nephron tubule epithelial cell differentiation","termid":"GO:0072257"}


id: PBO:0085733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in thiamine and pyridoxine biosynthesis; member of a stationary phase-induced gene family where transcriptional induction precedes the diauxic shift; induced in the absence of thiamin in a Thi2/3p-dependent manner and repressed in its presence; forms a co-regulated gene pair with SNO2; interacts with Thi11p; paralog of SNZ1 and SNZ3","termid":"PBO:0085733"}


id: MONDO:0019454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A myelodysplastic syndrome characterized by the presence of 5-19% myeloblasts in the bone marrow or 2-19% blasts in the peripheral blood. It includes two categories: myelodysplastic syndrome with excess blasts-1 and myelodysplastic syndrome with excess blasts-2.","definition_xrefs":["NCIT:C7506"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myelodysplastic syndrome","termid":"MONDO:0018881"},{"relation_name":"is_a","term_name":"hematopoietic and lymphoid cell neoplasm","termid":"MONDO:0044881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"myelodysplastic syndrome with excess blasts","secondary_identifiers":["MedDRA:10038270","MEDGEN:8066","EFO:0003811","GARD:19070","ICDO:9983/3","UMLS:C0002894","MESH:D000754","Orphanet:86839","SCTID:398623004"],"synonyms":[{"name":"MDS-EB","type":"exact"},{"name":"RAEB","type":"exact"},{"name":"myelodysplastic syndrome with Excess blasts","type":"exact"},{"name":"refractory Anaemia with Excess blasts","type":"exact"},{"name":"refractory Anaemia with an Excess of blasts","type":"exact"},{"name":"refractory Anemia with Excess blasts","type":"exact"},{"name":"refractory Anemia with an Excess of blasts","type":"exact"}],"termid":"MONDO:0019454","xrefs":{"Monarch":{"xref_id":"0019454"}}}


id: MONDO:0011227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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 otorhinolaryngologic disease","termid":"MONDO:0018751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome","secondary_identifiers":["GARD:17633","OMIM:602471","Orphanet:397623","SCTID:417081007","UMLS:C1865361","MESH:C566544","MEDGEN:355971"],"synonyms":[{"name":"SAMS","type":"related"},{"name":"SAMS syndrome","type":"exact"},{"name":"short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities","type":"related"},{"name":"short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities","type":"exact"}],"termid":"MONDO:0011227","xrefs":{"Monarch":{"xref_id":"0011227"}}}


id: PBO:0082632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of cytosolic iron-sulfur protein assembly (CIA) machinery; acts at late step of Fe-S cluster assembly; forms CIA targeting complex with Cia2p and Met18p that directs Fe-S cluster incorporation and maturation of a subset of cytosolic and nuclear proteins involved in methionine biosynthesis, DNA replication and repair, transcription and telomere maintenance; contains WD40 repeats; human homolog CIAO1 complements the yeast cia1 null mutant","termid":"PBO:0082632"}


id: PR:O74814
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A regulation of nuclear pre-mRNA domain-containing protein 1A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UPF0400 protein C337.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC337.03","secondary_identifiers":["UniProtKB:O74814"],"synonyms":[{"name":"Spom972h-RPRD1A","type":"exact"}],"termid":"PR:O74814"}


id: PR:O14329
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- zrg17 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14329"],"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":"zinc transporter zrg17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16E9.14c","synonyms":[{"name":"Spom972h-zrg17","type":"exact"}],"termid":"PR:O14329"}


id: GO:0045725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of glycogen.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glycogen biosynthetic process","termid":"GO:0005979"},{"relation_name":"is_a","term_name":"positive regulation of macromolecule biosynthetic process","termid":"GO:0010557"},{"relation_name":"is_a","term_name":"positive regulation of glycogen metabolic process","termid":"GO:0070875"},{"relation_name":"positively_regulates","term_name":"glycogen biosynthetic process","termid":"GO:0005978"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0005975"},{"rel_name":"positively_regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0044281","GO:0005975","GO:0008150"],"is_obsolete":false,"name":"positive regulation of glycogen biosynthetic process","synonyms":[{"name":"activation of glycogen biosynthetic process","type":"narrow"},{"name":"positive regulation of glycogen anabolism","type":"exact"},{"name":"positive regulation of glycogen biosynthesis","type":"exact"},{"name":"positive regulation of glycogen formation","type":"exact"},{"name":"positive regulation of glycogen synthesis","type":"exact"},{"name":"stimulation of glycogen biosynthetic process","type":"narrow"},{"name":"up regulation of glycogen biosynthetic process","type":"exact"},{"name":"up-regulation of glycogen biosynthetic process","type":"exact"},{"name":"upregulation of glycogen biosynthetic process","type":"exact"}],"termid":"GO:0045725"}


id: PBO:0043254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"claudin 12","termid":"PBO:0043254"}


id: PBO:0069042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 287, pseudogene","termid":"PBO:0069042"}


id: MOD:01708
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 an isotope tagged reagent acyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-amino acylated residue","termid":"MOD:01696"},{"relation_name":"is_a","term_name":"isotope tagged reagent acylated residue","termid":"MOD:01705"},{"relation_name":"is_a","term_name":"isotope tagged reagent N-acylated residue","termid":"MOD:01706"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isotope tagged reagent alpha-amino acylated residue","termid":"MOD:01708"}


id: PBO:0005176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial conserved eukaryotic protein (predicted)","termid":"PBO:0005176"}


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: GO:1990637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a prolactin stimulus. The anterior pituitary hormone prolactin has a number of roles including being essential for lactation.","definition_xrefs":["PMID:7760850"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to peptide hormone","termid":"GO:0043434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to prolactin","termid":"GO:1990637"}


id: GO:0102378
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: steviolmonoside + UDP-alpha-D-glucose = rubusoside + UDP.","definition_xrefs":["RHEA:61736"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"steviolmonoside glucosyltransferase activity","secondary_identifiers":["MetaCyc:RXN-13512"],"termid":"GO:0102378"}


id: PBO:0056381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase 11","termid":"PBO:0056381"}


id: PBO:0059997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 17","termid":"PBO:0059997"}


id: PBO:0039338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkaline phosphatase, placental","termid":"PBO:0039338"}


id: MONDO:0024455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant Robinow syndrome in which the cause of the disease is a mutation in the WNT5A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant Robinow syndrome","termid":"MONDO:0008389"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant Robinow syndrome 1","secondary_identifiers":["UMLS:C4551475","GARD:2013","DOID:0060766","MEDGEN:1641736","OMIM:180700"],"synonyms":[{"name":"DRS1","type":"exact"},{"name":"Robinow dwarfism","type":"related"},{"name":"Robinow syndrome, autosomal dominant 1","type":"exact"},{"name":"WNT5A autosomal dominant Robinow syndrome","type":"exact"},{"name":"acral dysostosis with Facial and genital abnormalities","type":"related"},{"name":"autosomal dominant Robinow syndrome caused by mutation in WNT5A","type":"exact"},{"name":"dysostosis acral with facial and genital abnormalities","type":"exact"},{"name":"fetal face syndrome","type":"related"},{"name":"foetal face syndrome","type":"related"}],"termid":"MONDO:0024455","xrefs":{"Monarch":{"xref_id":"0024455"}}}


id: MOD:00645
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue sulfanyl group with an acetylsulfanyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylated residue","termid":"MOD:00394"},{"relation_name":"is_a","term_name":"S-acylated residue","termid":"MOD:00672"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-acetylated residue","synonyms":[{"name":"SAcRes","type":"exact"}],"termid":"MOD:00645"}


id: PBO:0087823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFIID subunit (67 kDa); involved in RNA polymerase II transcription initiation","termid":"PBO:0087823"}


id: PBO:0087074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L36B; binds to 5.8 S rRNA; homologous to mammalian ribosomal protein L36, no bacterial homolog; RPL36B has a paralog, RPL36A, that arose from the whole genome duplication","termid":"PBO:0087074"}


id: PBO:0083425
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 uncharacterized ORF YAL027W and the verified gene DRS2","termid":"PBO:0083425"}


id: GO:0090521
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a podocyte from one site to another, often during the development of a multicellular organism or multicellular structure. A podocyte is a specialized kidney epithelial cell.","definition_xrefs":["GOC:pm","PMID:21402783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell migration","termid":"GO:0010631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"podocyte cell migration","synonyms":[{"name":"glomerular visceral epithelial cell migration","type":"exact"}],"termid":"GO:0090521"}


id: PBO:0069326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 584, pseudogene","termid":"PBO:0069326"}


id: PBO:0077637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMX2-CTNND1 readthrough (NMD candidate)","termid":"PBO:0077637"}


id: PBO:0066173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBIS pseudogene 6","termid":"PBO:0066173"}


id: GO:1902888
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 an astral microtubule.","definition_xrefs":["PMID:16054030","GO_REF:0000087","GOC:kmv","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to spindle microtubule","termid":"GO:1902889"},{"relation_name":"is_a","term_name":"protein localization to cytoplasmic microtubule","termid":"GO:1905755"}],"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:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to astral microtubule","synonyms":[{"name":"protein localisation in astral microtubule","type":"exact"},{"name":"protein localisation to astral microtubule","type":"exact"},{"name":"protein localization in astral microtubule","type":"exact"}],"termid":"GO:1902888"}


id: GO:0015486
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: (glycoside, pentoside or hexuronide)(out) + monovalent cation(out) = (glycoside, pentoside or hexuronide)(in) + monovalent cation(in). The cation is Na+, Li+ or H+.","definition_xrefs":["TC:2.A.2.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate:monoatomic cation symporter activity","termid":"GO:0005402"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"glycoside-pentoside-hexuronide:cation symporter activity","termid":"GO:0015486"}


id: FYPO:0008259
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 cell surface is decreased, and the localizatiion to the endosomal structure is increased. The cell surface refers to the external part of the cell wall and/or plasma membrane.","definition_xrefs":["PMID:22848669"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to cell surface","termid":"FYPO:0008258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to cell surface with increased localization to endosomal structures","termid":"FYPO:0008259"}


id: PR:O94460
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A queuine tRNA-ribosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00369","PRO:DNx","PANTHER:PTHR11962:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"queuine tRNA-ribosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.19c","secondary_identifiers":["UniProtKB:O94460"],"synonyms":[{"name":"Spom972h-QTRT1","type":"exact"},{"name":"guanine insertion enzyme (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tRNA-guanine transglycosylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94460"}


id: MONDO:0014745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the COL13A1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"postsynaptic congenital myasthenic syndrome","termid":"MONDO:0020344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital myasthenic syndrome 19","secondary_identifiers":["GARD:16153","DOID:0110673","MEDGEN:897962","UMLS:C4225235","OMIM:616720"],"synonyms":[{"name":"CMS19","type":"exact"},{"name":"COL13A1 congenital myasthenic syndrome","type":"exact"},{"name":"congenital myasthenic syndrome caused by mutation in COL13A1","type":"exact"},{"name":"congenital myasthenic syndrome type 19","type":"exact"},{"name":"myasthenic syndrome, congenital, 19","type":"exact"},{"name":"myasthenic syndrome, congenital, type 19","type":"exact"}],"termid":"MONDO:0014745","xrefs":{"Monarch":{"xref_id":"0014745"}}}


id: MONDO:0030487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylometaphyseal dysplasia, pagnamenta type","secondary_identifiers":["OMIM:619638","UMLS:C5562030","MEDGEN:1794240"],"synonyms":[{"name":"SMDP","type":"exact"}],"termid":"MONDO:0030487","xrefs":{"Monarch":{"xref_id":"0030487"}}}


id: GO:0061574
data:
  {"annotated_genes":["SJAG_05926","SJAG_00888"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[77635,116353],"is_not":false,"summary":null,"term":"GO:0061574"}]},"cv_name":"cellular_component","definition":"A protein complex involved in regulation of mRNA processing and apoptosis. It binds to RNA in a sequence-independent manner and is recruited to the EJC prior to or during the splicing process. In humans the core proteins are RNPS1, SAP18 and ACIN1.","definition_xrefs":["GOC:dph","PMID:16314458","PMID:22388736","PMID:12665594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00888":null,"SJAG_05926":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"ASAP complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0061574","terms_by_termid":{"GO:0061574":null}}


id: GO:1902093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of flagellated sperm motility.","definition_xrefs":["GOC:krc","GOC:cilia","GOC:jh2","GOC:TermGenie","PMID:7513657"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cilium movement","termid":"GO:0003353"},{"relation_name":"is_a","term_name":"regulation of flagellated sperm motility","termid":"GO:1901317"},{"relation_name":"is_a","term_name":"positive regulation of cilium-dependent cell motility","termid":"GO:2000155"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"flagellated sperm motility","termid":"GO:0030317"}],"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 flagellated sperm motility","synonyms":[{"name":"activation of sperm motility","type":"narrow"},{"name":"activation of sperm movement","type":"broad"},{"name":"positive regulation of sperm motility","type":"broad"},{"name":"positive regulation of sperm movement","type":"broad"},{"name":"up regulation of sperm motility","type":"broad"},{"name":"up regulation of sperm movement","type":"broad"},{"name":"up-regulation of sperm motility","type":"broad"},{"name":"up-regulation of sperm movement","type":"broad"},{"name":"upregulation of sperm motility","type":"broad"},{"name":"upregulation of sperm movement","type":"broad"}],"termid":"GO:1902093"}


id: FYPO:0005769
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone H2A phosphorylation occurs to a greater extent than normal in regions containing G-quartet (G4) motifs. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be increased.","definition_xrefs":["PomBase:mah","PMID:27611590","PMID:25471935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H2A phosphorylation during vegetative growth","termid":"FYPO:0002596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0002274","FYPO:0002494","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H2A phosphorylation at G4 motif during vegetative growth","synonyms":[{"name":"increased histone H2A phosphorylation at G-quadruplex during vegetative growth","type":"exact"},{"name":"increased histone H2A phosphorylation at G-quartet during vegetative growth","type":"exact"},{"name":"increased histone H2A phosphorylation at G4 motif during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005769"}


id: FYPO:0004351
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 nucleus is increased during a cellular response to methylglyoxal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to nucleus during vegetative growth","termid":"FYPO:0001130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"increased protein localization to nucleus during cellular response to methylglyoxal","synonyms":[{"name":"increased protein localisation to nucleus during cellular response to methylglyoxal","type":"exact"},{"name":"increased protein localization to nucleus during cellular response to methylglyoxal during mitotic cell cycle","type":"related"},{"name":"increased protein localization to nucleus during cellular response to methylglyoxal during vegetative growth","type":"exact"}],"termid":"FYPO:0004351"}


id: PBO:0083174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps ORF TRM5/YHR070W","termid":"PBO:0083174"}


id: GO:0097646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by an extracellular member of the calcitonin family (e.g. adrenomedullin, adrenomedullin 2 (intermedin), amylin, calcitonin and calcitonin gene-related peptides (CGRPs)) binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process.","definition_xrefs":["PMID:18687416","GOC:bhm","PMID:10871296","PMID:12037140"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"}],"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":"calcitonin family receptor signaling pathway","synonyms":[{"name":"calcitonin family receptor signalling pathway","type":"exact"}],"termid":"GO:0097646"}


id: GO:0019345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cysteine, via the intermediate S-sulfo-L-cysteine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteine biosynthetic process","termid":"GO:0019344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"cysteine biosynthetic process via S-sulfo-L-cysteine","synonyms":[{"name":"cysteine anabolism via S-sulfo-L-cysteine","type":"exact"},{"name":"cysteine biosynthesis via S-sulpho-L-cysteine","type":"exact"},{"name":"cysteine biosynthetic process via S-sulpho-L-cysteine","type":"exact"},{"name":"cysteine formation via S-sulfo-L-cysteine","type":"exact"},{"name":"cysteine synthesis via S-sulfo-L-cysteine","type":"exact"}],"termid":"GO:0019345"}


id: GO:0005516
data:
  {"annotated_genes":["SJAG_02249","SJAG_04498","SJAG_01851","SJAG_03631","SJAG_02180","SJAG_02858"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67622,70803,75164,77094,79302,81436],"is_not":false,"summary":null,"term":"GO:0005516"}]},"cv_name":"molecular_function","definition":"Binding to calmodulin, a calcium-binding protein with many roles, both in the calcium-bound and calcium-free states.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01851":null,"SJAG_02180":null,"SJAG_02249":null,"SJAG_02858":null,"SJAG_03631":null,"SJAG_04498":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"calmodulin binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-202110"],"termid":"GO:0005516","terms_by_termid":{"GO:0005516":null}}


id: MONDO:0013159
data:
  {"annotated_genes":["SJAG_01491"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88589],"is_not":false,"summary":null,"term":"MONDO:0013159"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type B","termid":"MONDO:0000172"},{"relation_name":"is_a","term_name":"myopathy caused by variation in POMT1","termid":"MONDO:0700070"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01491":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002320","MONDO:0005336","MONDO:0024322"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:613155","DOID:0050588","UMLS:C5436962","MEDGEN:1774807"],"synonyms":[{"name":"MDDGB1","type":"related"},{"name":"congenital muscular dystrophy-POMT1 related","type":"exact"},{"name":"muscular dystrophy, congenital, Pomt1-related","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 1","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1","type":"related"}],"termid":"MONDO:0013159","terms_by_termid":{"MONDO:0013159":null},"xrefs":{"Monarch":{"xref_id":"0013159"}}}


id: MONDO:0007355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Uveal coloboma-cleft lip and palate-intellectual disability is characterized by coloboma of the iris, bilateral cleft lip and palate, and intellectual deficiency of varying degree. A wide variability in clinical expression is observed. Some patients also present with microphthalmia, cataract, glaucoma, ptosis, sensorineural hearing loss and haematuria. To date, 12 cases have been described from three generations of a single family. Transmission is autosomal dominant.","definition_xrefs":["Orphanet:1473"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"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":"uveal coloboma-cleft lip and palate-intellectual disability","secondary_identifiers":["DOID:0111249","MESH:C535971","OMIM:120433","UMLS:C3805432","GARD:1440","MEDGEN:811762"],"synonyms":[{"name":"COB1","type":"related"},{"name":"coloboma, cleft lip/palate and intellectual disability syndrome","type":"related"},{"name":"coloboma, cleft lip/palate and mental retardation syndrome","type":"related"},{"name":"coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or intellectual disability","type":"related"},{"name":"coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation","type":"related"},{"name":"coloboma-microphthalmos syndrome","type":"related"},{"name":"coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate","type":"related"},{"name":"uveal coloboma-cleft lip and palate-intellectual disability","type":"exact"},{"name":"uveal coloboma-cleft lip/palate-intellectual disability syndrome","type":"related"},{"name":"uveal coloboma-cleft lip/palate-mental retardation syndrome","type":"related"}],"termid":"MONDO:0007355","xrefs":{"Monarch":{"xref_id":"0007355"}}}


id: PBO:0031080
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cytoskeleton_organization_phenotype","termid":"PBO:0031080"}


id: PR:C6Y4C8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vma21 gene.","definition_xrefs":["UniProtKB:C6Y4C8","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":"vacuolar ATPase assembly integral membrane protein vma21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.16","synonyms":[{"name":"Spom972h-vma21","type":"exact"}],"termid":"PR:C6Y4C8"}


id: GO:0036167
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A reversible switch of a cell from one phenotype to another that occurs upon infection of a host or host cell. For example, Candida albicans switches from a unicellular form to an invasive multicellular filamentous form upon infection of host tissue. Phenotypic switching begins with changes in cell morphology and altered gene expression patterns and ends when the morphology of a population of cells has reverted back to the default state, accompanied by altered expression patterns.","definition_xrefs":["PMID:16696644","Wikipedia:Phenotypic_switching","GOC:di"],"gene_count":0,"genotype_count":0,"name":"obsolete phenotypic switching in response to host (obsolete GO:0036167)","termid":"GO:0036167"}


id: GO:0039582
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the frequency, rate or extent of host PKR (protein kinase regulated by RNA) activity by promoting the localization of PKR in the nucleus. For example, human cytomegalovirus (HMCV) gene products directly interact with PKR and inhibit its activation by sequestering it in the nucleus, away from both its activator (cytoplasmic dsRNA) and its substrate, (eIF2alpha).","definition_xrefs":["PMID:16987971"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host PKR activity by positive regulation of PKR nuclear localization (obsolete GO:0039582)","synonyms":[{"name":"suppression by virus of host PKR activity by nuclear sequestration of PKR","type":"exact"},{"name":"suppression by virus of host PKR activity by positive regulation of PKR localization to nucleus","type":"exact"},{"name":"suppression by virus of host PKR activity by sequestering of PKR in nucleus","type":"exact"}],"termid":"GO:0039582"}


id: _global:is_kinase_activity
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_interaction_relation_helper_property","termid":"_global:molecular_interaction_relation_helper_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_kinase_activity","secondary_identifiers":["RO:0002481"],"termid":"_global:is_kinase_activity"}


id: PBO:0040683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCAS2 pseudogene 1","termid":"PBO:0040683"}


id: GO:1902059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of sporocarp development involved in sexual reproduction.","definition_xrefs":["PMID:23480775","GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of spore-bearing organ development","termid":"GO:0075262"},{"relation_name":"is_a","term_name":"regulation of sporocarp development involved in sexual reproduction","termid":"GO:1902058"},{"relation_name":"negatively_regulates","term_name":"sporocarp development involved in sexual reproduction","termid":"GO:0000909"}],"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 sporocarp development involved in sexual reproduction","synonyms":[{"name":"down regulation of ascus development","type":"narrow"},{"name":"down regulation of fruiting body development involved in sexual reproduction","type":"broad"},{"name":"down regulation of fruiting body formation involved in sexual reproduction","type":"broad"},{"name":"down regulation of perfect stage fruiting body development","type":"narrow"},{"name":"down regulation of sporocarp development involved in sexual reproduction","type":"exact"},{"name":"down-regulation of ascus development","type":"narrow"},{"name":"down-regulation of fruiting body development involved in sexual reproduction","type":"broad"},{"name":"down-regulation of fruiting body formation involved in sexual reproduction","type":"broad"},{"name":"down-regulation of perfect stage fruiting body development","type":"narrow"},{"name":"down-regulation of sporocarp development involved in sexual reproduction","type":"exact"},{"name":"downregulation of ascus development","type":"narrow"},{"name":"downregulation of fruiting body development involved in sexual reproduction","type":"broad"},{"name":"downregulation of fruiting body formation involved in sexual reproduction","type":"broad"},{"name":"downregulation of perfect stage fruiting body development","type":"narrow"},{"name":"downregulation of sporocarp development involved in sexual reproduction","type":"exact"},{"name":"inhibition of ascus development","type":"narrow"},{"name":"inhibition of fruiting body development involved in sexual reproduction","type":"broad"},{"name":"inhibition of fruiting body formation involved in sexual reproduction","type":"broad"},{"name":"inhibition of perfect stage fruiting body development","type":"narrow"},{"name":"inhibition of sporocarp development involved in sexual reproduction","type":"narrow"},{"name":"negative regulation of ascus development","type":"narrow"},{"name":"negative regulation of fruiting body development involved in sexual reproduction","type":"broad"},{"name":"negative regulation of fruiting body formation involved in sexual reproduction","type":"broad"},{"name":"negative regulation of perfect stage fruiting body development","type":"narrow"}],"termid":"GO:1902059"}


id: GO:0033875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a ribonucleoside bisphosphate, a compound consisting of a nucleobase linked to a ribose sugar esterified with one phosphate group attached to each of two different hydroxyl groups on the sugar.","definition_xrefs":["GOC:pde","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside bisphosphate metabolic process","termid":"GO:0033865"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"ribonucleoside bisphosphate metabolic process","synonyms":[{"name":"ribonucleoside bisphosphate metabolism","type":"exact"}],"termid":"GO:0033875"}


id: MONDO:0859311
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"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":"Charcot-Marie-Tooth disease, demyelinating, type 1J","secondary_identifiers":["UMLS:C5774249","MEDGEN:1824022","OMIM:620111"],"termid":"MONDO:0859311","xrefs":{"Monarch":{"xref_id":"0859311"}}}


id: PBO:0061800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outer dense fiber of sperm tails 2","termid":"PBO:0061800"}


id: PBO:0004686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2 domain protein Git1","termid":"PBO:0004686"}


id: PBO:0068922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 165, pseudogene","termid":"PBO:0068922"}


id: MONDO:0850053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F12-associated cold autoinflammatory syndrome","secondary_identifiers":["GARD:22454","MEDGEN:1843368","Orphanet:617919","UMLS:C5681829"],"termid":"MONDO:0850053","xrefs":{"Monarch":{"xref_id":"0850053"}}}


id: PBO:0028446
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_localization_to_mitotic_spindle_midzone_during_anaphase_B","termid":"PBO:0028446"}


id: MONDO:0000464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Stargardt disease (obsolete MONDO:0000464)","termid":"MONDO:0000464","xrefs":{"Monarch":{"xref_id":"0000464"}}}


id: PATO:0000608
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphological quality inhering in a bearer by virtue of the bearer's affording blocked passage or view.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"closure","termid":"PATO:0000136"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"closed","synonyms":[{"name":"blocked","type":"related"}],"termid":"PATO:0000608"}


id: PBO:0116468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HHE domain cation binding protein, implicated in the repair of iron-sulfur clusters damaged by oxidative and nitrosative stress","termid":"PBO:0116468"}


id: PBO:0038385
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_parasitoid","termid":"PBO:0038385"}


id: PBO:0034694
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:0034694"}


id: PBO:0111736
data:
  {"annotation_feature_type":"gene","cv_name":"feature_relationshipprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter_gene","termid":"PBO:0111736"}


id: GO:0007060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which genetic material, in the form of chromosomes, is organized and then physically separated and apportioned to two or more sets during the meiotic cell cycle in a male.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic chromosome segregation","termid":"GO:0045132"},{"relation_name":"part_of","term_name":"male meiotic nuclear division","termid":"GO:0007140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0140013","GO:0007049"],"is_obsolete":false,"name":"male meiosis chromosome segregation","termid":"GO:0007060"}


id: PBO:0001490
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.32","termid":"PBO:0001490"}


id: PBO:0058382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4754","termid":"PBO:0058382"}


id: PBO:0056870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MICALL2 divergent transcript","termid":"PBO:0056870"}


id: MONDO:1012042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar abiotrophy, non-human animal","termid":"MONDO:1011834"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar abiotrophy, goat","secondary_identifiers":["OMIA:000175-9925"],"termid":"MONDO:1012042","xrefs":{"Monarch":{"xref_id":"1012042"}}}


id: MONDO:0003485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete colon squamous cell carcinoma (obsolete MONDO:0003485)","termid":"MONDO:0003485","xrefs":{"Monarch":{"xref_id":"0003485"}}}


id: MONDO:0002220
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth disorder","termid":"MONDO:0006999"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth hard tissue disease","secondary_identifiers":["SCTID:46557008","UMLS:C0155926","ICD9:521.89","DOID:214","ICD9:521.8","MEDGEN:510140","ICD10CM:K03"],"synonyms":[{"name":"disorder of hard tissues of teeth","type":"exact"},{"name":"teeth hard tissue disease","type":"related"},{"name":"teeth hard tissue diseases","type":"related"}],"termid":"MONDO:0002220","xrefs":{"Monarch":{"xref_id":"0002220"}}}


id: GO:0032185
data:
  {"annotated_genes":["SJAG_01143","SJAG_00514","SJAG_00118","SJAG_03146","SJAG_01658","SJAG_02683","SJAG_04375","SJAG_00663"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112679],"is_not":false,"summary":null,"term":"GO:0032185"},{"annotations":[74276,61273,105875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000921"},{"annotations":[99768,119039,103725,72040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031106"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures comprising septin complexes and their associated proteins.","definition_xrefs":["GOC:mah","GOC:dph","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoskeleton organization","termid":"GO:0007010"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_00514":null,"SJAG_00663":null,"SJAG_01143":null,"SJAG_01658":null,"SJAG_02683":null,"SJAG_03146":null,"SJAG_04375":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0008150","GO:0007010"],"is_obsolete":false,"name":"septin cytoskeleton organization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"septin cytoskeleton organisation","type":"exact"},{"name":"septin cytoskeleton organization and biogenesis","type":"related"}],"termid":"GO:0032185","terms_by_termid":{"GO:0000921":null,"GO:0031106":null,"GO:0032185":null}}


id: PR:Q10207
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC17D1.01 gene.","definition_xrefs":["UniProtKB:Q10207","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C17D1.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17D1.01","synonyms":[{"name":"Spom972h-SPBC17D1.01","type":"exact"}],"termid":"PR:Q10207"}


id: MONDO:0016246
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete adenocarcinoma of ovary (obsolete MONDO:0016246)","termid":"MONDO:0016246","xrefs":{"Monarch":{"xref_id":"0016246"}}}


id: GO:1990051
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that initiates the activity of the inactive enzyme protein kinase C.","definition_xrefs":["PMID:3156004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activation of protein kinase activity","termid":"GO:0032147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"activation of protein kinase C activity","synonyms":[{"name":"PKC activation","type":"exact"},{"name":"protein kinase C activation","type":"exact"}],"termid":"GO:1990051"}


id: _global:mereotopologically_related_to
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"A mereological relationship or a topological relationship","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mereotopologically_related_to","secondary_identifiers":["RO:0002323"],"termid":"_global:mereotopologically_related_to"}


id: MONDO:1030002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A developmental disorder affecting the growth and development of the proximal end of the femur (thigh bone) near the hip joint characterized by avascular necrosis of the femoral head, cystic changes of the femoral head, and/or sclerosis of the femoral head. It is a relatively milder form of the other skeletal disorders associated with COL2A1.","direct_ancestors":[{"relation_name":"is_a","term_name":"type 2 collagenopathy","termid":"MONDO:0022800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysplasia of the proximal femoral epiphyses","secondary_identifiers":["MEDGEN:481394","UMLS:C3279764"],"termid":"MONDO:1030002","xrefs":{"Monarch":{"xref_id":"1030002"}}}


id: PBO:0029159
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_phlorizin_during_spore_germination","termid":"PBO:0029159"}


id: GO:0031247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of actin rods, a cellular structure consisting of parallel, hexagonally arranged actin tubules.","definition_xrefs":["GOC:pg","PMID:14706699"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament bundle assembly","termid":"GO:0051017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0007010","GO:0030036"],"is_obsolete":false,"name":"actin rod assembly","synonyms":[{"name":"actin rod formation","type":"related"}],"termid":"GO:0031247"}


id: PBO:0063919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma","termid":"PBO:0063919"}


id: MONDO:0003986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0003986 (obsolete MONDO:0003986)","termid":"MONDO:0003986","xrefs":{"Monarch":{"xref_id":"0003986"}}}


id: PBO:0088172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xylitol dehydrogenase; converts xylitol to D-xylulose; expression induced by xylose, even though this pentose sugar is not well utilized by S. cerevisiae; null mutant has cell wall defect","termid":"PBO:0088172"}


id: PBO:0067696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5.8S ribosomal pseudogene 4","termid":"PBO:0067696"}


id: PR:Q9P6J9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An inner membrane metabolite transport protein YgcS that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02334","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":"inorganic phosphate transporter C1683.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1683.01","secondary_identifiers":["UniProtKB:Q9P6J9"],"synonyms":[{"name":"Spom972h-ygcS","type":"exact"}],"termid":"PR:Q9P6J9"}


id: GO:0030218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a myeloid precursor cell acquires specializes features of an erythrocyte.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid cell differentiation","termid":"GO:0030099"},{"relation_name":"part_of","term_name":"erythrocyte homeostasis","termid":"GO:0034101"}],"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":"erythrocyte differentiation","secondary_identifiers":["Wikipedia:Erythropoiesis"],"synonyms":[{"name":"RBC differentiation","type":"exact"},{"name":"erythrocyte cell differentiation","type":"exact"},{"name":"erythropoiesis","type":"exact"},{"name":"red blood cell differentiation","type":"exact"}],"termid":"GO:0030218"}


id: MONDO:0019438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AL Amyloidosis is a plasma cell disorder characterized by the aggregation and deposition of insoluble amyloid fibrils derived from misfolding of monoclonal immunoglobulin light chains usually produced by a plasma cell tumor. It usually presents as primary systemic amyloidosis (PSA) with multiple organ involvement and less frequently as primary localized amyloidosis (PLA) restricted to a single organ.","definition_xrefs":["Orphanet:85443"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"},{"relation_name":"is_a","term_name":"non-familial hypertrophic cardiomyopathy","termid":"MONDO:0016330"},{"relation_name":"is_a","term_name":"non-familial restrictive cardiomyopathy","termid":"MONDO:0016345"},{"relation_name":"is_a","term_name":"amyloidosis","termid":"MONDO:0019065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"AL amyloidosis","secondary_identifiers":["NANDO:1200211","NCIT:C158963","DOID:0080933","icd11.foundation:113043090","UMLS:C0268381","GARD:5797","icd11.foundation:1061366491","MedDRA:10036673","MEDGEN:75674","MESH:C531616"],"synonyms":[{"name":"Light chain amyloidosis","type":"related"},{"name":"Light-chain amyloidosis","type":"exact"},{"name":"amyloidosis AL","type":"related"},{"name":"amyloidosis primary systemic","type":"related"},{"name":"primary AL amyloidosis","type":"related"},{"name":"primary amyloidosis","type":"exact"},{"name":"primary systemic AL amyloidosis","type":"related"},{"name":"primary systemic amyloidosis","type":"related"},{"name":"systemic AL amyloidsis","type":"related"}],"termid":"MONDO:0019438","xrefs":{"Monarch":{"xref_id":"0019438"}}}


id: PBO:0041007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BLOC-1 related complex subunit 8","termid":"PBO:0041007"}


id: PBO:0081367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 205","termid":"PBO:0081367"}


id: PBO:0071017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 19","termid":"PBO:0071017"}


id: PBO:0076190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO1 pseudogene 5","termid":"PBO:0076190"}


id: PBO:0002824
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds HSE 5'-NGAANNTTCNNGAAN-3'","termid":"PBO:0002824"}


id: MONDO:0015161
data:
  {"annotated_genes":["SJAG_02708","SJAG_05180","SJAG_02556","SJAG_02879","SJAG_01444","SJAG_02339","SJAG_02618","SJAG_02200","SJAG_00612","SJAG_04222","SJAG_00539","SJAG_04995","SJAG_01065","SJAG_01644","SJAG_00611","SJAG_00504","SJAG_01410","SJAG_03847","SJAG_00322","SJAG_01677","SJAG_02855","SJAG_03578","SJAG_01213","SJAG_00197","SJAG_01863","SJAG_02539","SJAG_00984","SJAG_00640","SJAG_00731","SJAG_01615","SJAG_03703","SJAG_03396","SJAG_03153","SJAG_00288","SJAG_02349","SJAG_02431"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"},{"annotations":[87530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012064"},{"annotations":[88946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010879"},{"annotations":[88628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007204"},{"annotations":[87358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014573"},{"annotations":[89104,89105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020746"},{"annotations":[87642,87641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958175"},{"annotations":[88906,88907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011911"},{"annotations":[87709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014801"},{"annotations":[88237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013248"},{"annotations":[88667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013499"},{"annotations":[86922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014108"},{"annotations":[88941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014986"},{"annotations":[88945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014987"},{"annotations":[88942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014985"},{"annotations":[88047],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100104"},{"annotations":[89200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012853"},{"annotations":[89122,89121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008675"},{"annotations":[88101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009670"},{"annotations":[87399],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012656"},{"annotations":[88569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012074"},{"annotations":[87094],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007943"},{"annotations":[89195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009623"},{"annotations":[87452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013118"},{"annotations":[87319],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009903"},{"annotations":[87478,87479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009955"},{"annotations":[87124],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009998"},{"annotations":[88659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010408"},{"annotations":[88969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013385"},{"annotations":[87596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009558"},{"annotations":[87272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030067"},{"annotations":[87433],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030077"},{"annotations":[88238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013252"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome","termid":"MONDO:0019042"}],"gene_count":36,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00288":null,"SJAG_00322":null,"SJAG_00504":null,"SJAG_00539":null,"SJAG_00611":null,"SJAG_00612":null,"SJAG_00640":null,"SJAG_00731":null,"SJAG_00984":null,"SJAG_01065":null,"SJAG_01213":null,"SJAG_01410":null,"SJAG_01444":null,"SJAG_01615":null,"SJAG_01644":null,"SJAG_01677":null,"SJAG_01863":null,"SJAG_02200":null,"SJAG_02339":null,"SJAG_02349":null,"SJAG_02431":null,"SJAG_02539":null,"SJAG_02556":null,"SJAG_02618":null,"SJAG_02708":null,"SJAG_02855":null,"SJAG_02879":null,"SJAG_03153":null,"SJAG_03396":null,"SJAG_03578":null,"SJAG_03703":null,"SJAG_03847":null,"SJAG_04222":null,"SJAG_04995":null,"SJAG_05180":null},"genotype_count":0,"is_obsolete":false,"name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:19833","MEDGEN:1842829","UMLS:C5680373","Orphanet:102285"],"synonyms":[{"name":"MCA without intellectual disability","type":"exact"},{"name":"multiple congenital anomalies without intellectual disability with or without dysmorphism","type":"exact"}],"termid":"MONDO:0015161","terms_by_termid":{"MONDO:0007204":null,"MONDO:0007943":null,"MONDO:0008675":null,"MONDO:0009558":null,"MONDO:0009623":null,"MONDO:0009670":null,"MONDO:0009903":null,"MONDO:0009955":null,"MONDO:0009998":null,"MONDO:0010408":null,"MONDO:0010621":null,"MONDO:0010879":null,"MONDO:0011911":null,"MONDO:0012064":null,"MONDO:0012074":null,"MONDO:0012656":null,"MONDO:0012853":null,"MONDO:0013118":null,"MONDO:0013248":null,"MONDO:0013252":null,"MONDO:0013385":null,"MONDO:0013499":null,"MONDO:0014108":null,"MONDO:0014573":null,"MONDO:0014801":null,"MONDO:0014985":null,"MONDO:0014986":null,"MONDO:0014987":null,"MONDO:0020746":null,"MONDO:0030067":null,"MONDO:0030077":null,"MONDO:0100104":null,"MONDO:0958175":null},"xrefs":{"Monarch":{"xref_id":"0015161"}}}


id: PBO:0038963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenomedullin 2","termid":"PBO:0038963"}


id: FYPO:0007178
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 medial cortex of a cell is abolished during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to medial cortex during vegetative growth","termid":"FYPO:0002555"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to medial cortex during mitosis","synonyms":[{"name":"abolished protein localisation to medial cortex during mitosis","type":"exact"},{"name":"abolished protein localization to medial cortex during mitosis during vegetative growth","type":"exact"},{"name":"abolished protein localization to medial cortex during mitotic M phase","type":"related"},{"name":"abolished protein localization to medial cortex during mitotic nuclear division","type":"exact"},{"name":"abolished protein localization to medial ring during mitosis","type":"exact"},{"name":"protein localization to medial cortex abolished during mitosis","type":"exact"}],"termid":"FYPO:0007178"}


id: FYPO:0006712
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 acetyl-CoA measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular acetyl-CoA level","synonyms":[{"name":"decreased cellular acetyl-CoA level during mitotic cell cycle","type":"related"},{"name":"decreased cellular acetyl-CoA level during vegetative growth","type":"exact"},{"name":"reduced cellular acetyl-CoA level","type":"exact"}],"termid":"FYPO:0006712"}


id: MONDO:0020122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An umbrella term for diseases which have chronic muscle inflammation and weakness of unknown etiology. The types of idiopathic inflammatory myopathy are further defined by either clinicopathologic criteria or by the presence of certain autoantibodies.","definition_xrefs":["NCIT:C116796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired skeletal muscle disease","termid":"MONDO:0016105"},{"relation_name":"is_a","term_name":"idiopathic inflammatory myopathy","termid":"MONDO:0600023"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"acquired idiopathic inflammatory myopathy","secondary_identifiers":["GARD:9128","Orphanet:98482","icd11.foundation:464294586","ICD9:359.79"],"synonyms":[{"name":"IIm","type":"exact"},{"name":"IMM","type":"exact"},{"name":"idiopathic inflammatory myopathies","type":"exact"},{"name":"idiopathic inflammatory myopathy, familial","type":"related"},{"name":"idiopathic inflammatory myositis","type":"exact"}],"termid":"MONDO:0020122","xrefs":{"Monarch":{"xref_id":"0020122"}}}


id: MONDO:0000674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An agnosia that is a loss of the ability to acknowledge objects in the neglected field that are visible when a mirror reflects the object visible in the non-neglected field.","definition_xrefs":["DOID:0060144"],"direct_ancestors":[{"relation_name":"is_a","term_name":"agnosia","termid":"MONDO:0005638"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mirror agnosia","termid":"MONDO:0000674","xrefs":{"Monarch":{"xref_id":"0000674"}}}


id: GO:0035053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of dorsal vessel cardioblast cells to a heart proper cell fate and their capacity to differentiate into heart cells. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["PMID:12397110","GOC:mtg_sensu","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate commitment involved in pattern specification","termid":"GO:0060581"},{"relation_name":"is_a","term_name":"cardiac cell fate commitment","termid":"GO:0060911"},{"relation_name":"part_of","term_name":"embryonic heart tube anterior/posterior pattern specification","termid":"GO:0035054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"dorsal vessel heart proper cell fate commitment","termid":"GO:0035053"}


id: PBO:0002487
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.101","termid":"PBO:0002487"}


id: PR:O94717
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ers1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-silencing factor ers1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1393.05","synonyms":[{"name":"Spom972h-ers1","type":"exact"}],"termid":"PR:O94717"}


id: PBO:0049036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 25","termid":"PBO:0049036"}


id: GO:0035391
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The maintenance of chromatin in a transcriptionally silent state such as heterochromatin at silent mating-type loci.","definition_xrefs":["GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete maintenance of chromatin silencing at silent mating-type cassette (obsolete GO:0035391)","termid":"GO:0035391"}


id: PBO:0072137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 14","termid":"PBO:0072137"}


id: GO:1900122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of a protein or other molecule binding to a receptor.","definition_xrefs":["GOC:TermGenie","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein binding","termid":"GO:0032092"},{"relation_name":"is_a","term_name":"regulation of receptor binding","termid":"GO:1900120"}],"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 receptor binding","synonyms":[{"name":"activation of receptor binding","type":"narrow"},{"name":"up regulation of receptor binding","type":"exact"},{"name":"upregulation of receptor binding","type":"exact"}],"termid":"GO:1900122"}


id: FYPO:0005513
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the kinetochore of a chromosome is increased during one or both meiotic nuclear divisions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore during meiosis","termid":"FYPO:0004762"},{"relation_name":"is_a","term_name":"increased protein localization to centromere during meiotic cell cycle","termid":"FYPO:0005598"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to kinetochore during meiosis","synonyms":[{"name":"increased protein localisation to kinetochore during meiosis","type":"exact"},{"name":"increased protein localization to kinetochore during meiotic nuclear division","type":"exact"},{"name":"increased protein localization to meiotic kinetochore","type":"exact"}],"termid":"FYPO:0005513"}


id: PBO:0067285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 368, pseudogene","termid":"PBO:0067285"}


id: PBO:0068163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 470","termid":"PBO:0068163"}


id: GO:1901769
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of carbapenem.","definition_xrefs":["UniPathway:UPA00182","GOC:TermGenie","GOC:yaf","PMID:9402024"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-lactam antibiotic biosynthetic process","termid":"GO:0030654"},{"relation_name":"is_a","term_name":"carbapenem metabolic process","termid":"GO:1901767"}],"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":"carbapenem biosynthetic process","synonyms":[{"name":"carbapenem anabolism","type":"exact"},{"name":"carbapenem biosynthesis","type":"exact"},{"name":"carbapenem formation","type":"exact"},{"name":"carbapenem synthesis","type":"exact"}],"termid":"GO:1901769"}


id: GO:0098617
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + adenylylselenate => ADP + 3'-phosphoadenylylselenate.","definition_xrefs":["PMID:2537056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"adenylylselenate kinase activity","secondary_identifiers":["Reactome:R-HSA-2408540"],"termid":"GO:0098617"}


id: GO:2001060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a D-glycero-D-manno-heptose 7-phosphate.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"},{"relation_name":"is_a","term_name":"organophosphate metabolic process","termid":"GO:0019637"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"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":"D-glycero-D-manno-heptose 7-phosphate metabolic process","synonyms":[{"name":"D-glycero-D-manno-heptose 7-phosphate metabolism","type":"exact"}],"termid":"GO:2001060"}


id: MONDO:0044624
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"gastritis","termid":"MONDO:0004966"}],"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":"pediatric collagenous gastritis","secondary_identifiers":["GARD:21998","Orphanet:487809","UMLS:C5680109","MEDGEN:1805938"],"synonyms":[{"name":"childhood-onset collagenous gastritis","type":"exact"}],"termid":"MONDO:0044624","xrefs":{"Monarch":{"xref_id":"0044624"}}}


id: MONDO:0015940
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of rheumatologic disorder that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare rheumatologic disease (obsolete MONDO:0015940)","secondary_identifiers":["Orphanet:182231"],"synonyms":[{"name":"rare rheumatologic disorder","type":"exact"},{"name":"rare rheumatological disease","type":"exact"}],"termid":"MONDO:0015940","xrefs":{"Monarch":{"xref_id":"0015940"}}}


id: FYPO:0008244
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein does not localize to, and is therefore absent from the prospore wall.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization during meiotic cell cycle","termid":"FYPO:0005208"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to prospore wall","termid":"FYPO:0008244"}


id: MONDO:0000400
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of cerebral palsy characterized by both the tight muscle tone of spastic cerebral palsy and the writhing, involuntary muscle movements of athetoid cerebral palsy.","definition_xrefs":["NCIT:C97177"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral palsy","termid":"MONDO:0006497"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mixed cerebral palsy","secondary_identifiers":["MEDGEN:148218","SCTID:702318008","ICD9:343.8","UMLS:C0751024","DOID:0050673"],"termid":"MONDO:0000400","xrefs":{"Monarch":{"xref_id":"0000400"}}}


id: GO:0047509
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-4-dehydropantoate + H2O + NAD+ = (R)-3,3-dimethylmalate + 2 H+ + NADH.","definition_xrefs":["RHEA:19349","EC:1.2.1.33"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"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":"(R)-dehydropantoate dehydrogenase activity","secondary_identifiers":["MetaCyc:R-DEHYDROPANTOATE-DEHYDROGENASE-RXN","KEGG_REACTION:R03198"],"synonyms":[{"name":"(R)-4-dehydropantoate:NAD+ 4-oxidoreductase activity","type":"related"},{"name":"D-2-hydroxy-3,3-dimethyl-3-formylpropionate:diphosphopyridine nucleotide (DPN+) oxidoreductase activity","type":"related"},{"name":"D-aldopantoate dehydrogenase activity","type":"related"}],"termid":"GO:0047509"}


id: GO:2000632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of pre-microRNA processing.","definition_xrefs":["GOC:dph","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of miRNA processing","termid":"GO:1903799"},{"relation_name":"is_a","term_name":"regulation of pre-miRNA processing","termid":"GO:2000631"},{"relation_name":"negatively_regulates","term_name":"pre-miRNA processing","termid":"GO:0031054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of pre-miRNA processing","synonyms":[{"name":"negative regulation of miRNA maturation","type":"exact"},{"name":"negative regulation of pre-microRNA processing","type":"exact"}],"termid":"GO:2000632"}


id: PBO:0054769
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 2181","termid":"PBO:0054769"}


id: PBO:0062958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) binding protein cytoplasmic 1 pseudogene 1","termid":"PBO:0062958"}


id: PBO:0046627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group W member 8","termid":"PBO:0046627"}


id: GO:0051890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardioblast differentiation, the process in which a relatively unspecialized mesodermal cell acquires the specialized structural and/or functional features of a cardioblast. A cardioblast is a cardiac precursor cell. It is a cell that has been committed to a cardiac fate, but will undergo more cell division rather than terminally differentiating.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiocyte differentiation","termid":"GO:1905207"},{"relation_name":"is_a","term_name":"regulation of stem cell differentiation","termid":"GO:2000736"},{"relation_name":"regulates","term_name":"cardioblast differentiation","termid":"GO:0010002"}],"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 cardioblast differentiation","termid":"GO:0051890"}


id: PBO:0056049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lung adenocarcinoma associated transcript 1","termid":"PBO:0056049"}


id: MONDO:0006738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare cutaneous tumor of eccrine sweat gland origin. It is most commonly found on the extremities and is usually benign. There is no indication that heredity or external agents cause these tumors.","definition_xrefs":["MESH:D018250"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eccrine sweat gland cancer","termid":"MONDO:0005506"},{"relation_name":"is_a","term_name":"benign neoplasm of sweat gland","termid":"MONDO:0021489"}],"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":"eccrine acrospiroma","secondary_identifiers":["ONCOTREE:PORO","NCIT:C7568","NCIT:C27273","SCTID:253020008","UMLS:C0206671","MEDGEN:104915","DOID:5442","SCTID:400099008","EFO:1000912"],"synonyms":[{"name":"Hidradenomas","type":"related"},{"name":"Hidradenomas, solid-cystic","type":"related"},{"name":"Hidradrenoma, clear-cell","type":"related"},{"name":"Hidradrenoma, nodular","type":"related"},{"name":"Hidradrenomas, clear-cell","type":"related"},{"name":"Hidradrenomas, nodular","type":"related"},{"name":"acrospiroma, eccrine","type":"related"},{"name":"acrospiromas","type":"related"},{"name":"acrospiromas, eccrine","type":"related"},{"name":"clear cell Hidradrenoma","type":"related"},{"name":"clear-cell Hidradrenoma","type":"related"},{"name":"clear-cell Hidradrenomas","type":"related"},{"name":"eccrine Acrospiromas","type":"related"},{"name":"eccrine acrospiroma","type":"exact"},{"name":"eccrine hidradenoma","type":"exact"},{"name":"eccrine hidradenoma of skin","type":"exact"},{"name":"eccrine poroma","type":"exact"},{"name":"hidradenoma","type":"related"},{"name":"hidradenoma, solid-cystic","type":"related"},{"name":"nodular Hidradrenoma","type":"related"},{"name":"nodular Hidradrenomas","type":"related"},{"name":"poroma","type":"exact"},{"name":"poroma (acrospiroma)","type":"exact"},{"name":"poroma/acrospiroma","type":"related"},{"name":"solid cystic hidradenoma","type":"related"},{"name":"solid-cystic Hidradenomas","type":"related"},{"name":"solid-cystic hidradenoma","type":"related"}],"termid":"MONDO:0006738","xrefs":{"Monarch":{"xref_id":"0006738"}}}


id: PBO:0078754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA methyltransferase 61A","termid":"PBO:0078754"}


id: FYPO:0001541
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 molybdenum ion measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"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:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal cellular molybdenum level","synonyms":[{"name":"normal cellular molybdenum accumulation","type":"related"},{"name":"normal cellular molybdenum ion level","type":"exact"},{"name":"normal cellular molybdenum level during mitotic cell cycle","type":"related"},{"name":"normal cellular molybdenum level during vegetative growth","type":"exact"}],"termid":"FYPO:0001541"}


id: GO:0043841
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (S)-lactate + GTP = 2-phospho-(S)-lactate + GDP.","definition_xrefs":["PMID:11535063"],"gene_count":0,"genotype_count":0,"name":"obsolete (S)-lactate 2-kinase activity (obsolete GO:0043841)","synonyms":[{"name":"lactate 2-kinase activity","type":"exact"}],"termid":"GO:0043841"}


id: GO:0014834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process by which the number of skeletal muscle satellite cells in a skeletal muscle is maintained during muscle regeneration. There are at least three mechanisms by which this is achieved. Skeletal muscle satellite stem cell asymmetric division ensures satellite stem cell numbers are kept constant. Symmetric division of these cells amplifies the number of skeletal muscle satellite stem cells. Some adult skeletal muscle myoblasts (descendants of activated satellite cells) can develop back into quiescent satellite cells, replenishing the overall pool of satellite cells.","definition_xrefs":["PMID:23303905","GOC:dph","GOC:ef","GOC:mtg_muscle","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of cell number","termid":"GO:0098727"},{"relation_name":"part_of","term_name":"skeletal muscle tissue regeneration","termid":"GO:0043403"}],"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":"skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration","synonyms":[{"name":"satellite cell compartment self-renewal involved in skeletal muscle regeneration","type":"exact"},{"name":"satellite cell population maintenance","type":"exact"},{"name":"satellite cell self-renewal","type":"broad"}],"termid":"GO:0014834"}


id: GO:1904456
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of neuronal action potential.","definition_xrefs":["PMID:25126967","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of action potential","termid":"GO:0045759"},{"relation_name":"is_a","term_name":"negative regulation of transmission of nerve impulse","termid":"GO:0051970"},{"relation_name":"is_a","term_name":"regulation of neuronal action potential","termid":"GO:0098908"},{"relation_name":"negatively_regulates","term_name":"neuronal action potential","termid":"GO:0019228"}],"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 neuronal action potential","synonyms":[{"name":"down regulation of generation of action potential","type":"related"},{"name":"down regulation of neuronal action potential","type":"exact"},{"name":"down-regulation of generation of action potential","type":"related"},{"name":"down-regulation of neuronal action potential","type":"exact"},{"name":"downregulation of generation of action potential","type":"related"},{"name":"downregulation of neuronal action potential","type":"exact"},{"name":"inhibition of generation of action potential","type":"related"},{"name":"inhibition of neuronal action potential","type":"narrow"},{"name":"negative regulation of generation of action potential","type":"related"}],"termid":"GO:1904456"}


id: PBO:0048631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GIT ArfGAP 2","termid":"PBO:0048631"}


id: PBO:0113118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Epsin-like protein involved in endocytosis and actin patch assembly; K63-specific Ub chain binding protein that functions as an endocytic adaptor; binds clathrin via a clathrin-binding domain motif at C-terminus; contains two ubiquitin-interacting motifs (UIMs); functionally redundant with Ent2p; relocalizes from bud neck to cytoplasm upon DNA replication stress; ENT1 has a paralog, ENT2, that arose from the whole genome duplication","termid":"PBO:0113118"}


id: PBO:0052430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIZ antisense RNA 1","termid":"PBO:0052430"}


id: PBO:0068801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 38, pseudogene","termid":"PBO:0068801"}


id: PBO:0052498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 10","termid":"PBO:0052498"}


id: GO:0000191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Upregulation of MAPKKK activity in the context of regulating pseudohyphal or invasive growth.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of MAPKKK (pseudohyphal growth) (obsolete GO:0000191)","synonyms":[{"name":"activation of MAPKKK (pseudohyphal growth)","type":"exact"}],"termid":"GO:0000191"}


id: MONDO:0859167
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":"hypokalemic tubulopathy and deafness","secondary_identifiers":["OMIM:619406","UMLS:C5543621","MEDGEN:1785163"],"termid":"MONDO:0859167","xrefs":{"Monarch":{"xref_id":"0859167"}}}


id: PBO:0059224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maestro heat like repeat family member 6","termid":"PBO:0059224"}


id: PBO:0085706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in septin-ER tethering; interacts with ER membrane protein, Scs2p, and Shs1p, a septin ring component, at bud neck to create ER diffusion barrier; GFP-fusion protein localizes to the cell periphery, cytoplasm, bud, and bud neck; interacts with Crm1p in two-hybrid assay; YMR124W has a paralog, YLR031W, that arose from the whole genome duplication","termid":"PBO:0085706"}


id: GO:0034233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of cell wall chitin.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cell wall chitin catabolic process (obsolete GO:0034233)","synonyms":[{"name":"regulation of cell wall chitin breakdown","type":"exact"},{"name":"regulation of cell wall chitin catabolism","type":"exact"},{"name":"regulation of cell wall chitin degradation","type":"exact"}],"termid":"GO:0034233"}


id: MONDO:0014843
data:
  {"annotated_genes":["SJAG_04114"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87539],"is_not":false,"summary":null,"term":"MONDO:0014843"}]},"cv_name":"mondo","definition":"Any primary ovarian failure in which the cause of the disease is a mutation in the ERCC6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04114":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"premature ovarian failure 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080869","UMLS:C4310783","MEDGEN:934750","OMIM:616946","DOID:0080868"],"synonyms":[{"name":"ERCC6 primary ovarian failure","type":"exact"},{"name":"POF11","type":"exact"},{"name":"premature ovarian failure 11","type":"exact"},{"name":"premature ovarian failure 11; POF11","type":"exact"},{"name":"premature ovarian failure type 11","type":"exact"},{"name":"primary ovarian failure caused by mutation in ERCC6","type":"exact"}],"termid":"MONDO:0014843","terms_by_termid":{"MONDO:0014843":null},"xrefs":{"Monarch":{"xref_id":"0014843"}}}


id: FYPO:0007394
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the structure of one or more RNA molecules differs from normal.","definition_xrefs":["PomBase:mah","PMID:24793650"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985"],"is_obsolete":false,"name":"abnormal RNA structure","synonyms":[{"name":"abnormal RNA secondary structure","type":"narrow"}],"termid":"FYPO:0007394"}


id: MONDO:0015348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leukoencephalopathy with bilateral anterior temporal lobe cysts is a nonprogressive neurological disorder marked by intellectual deficit, spasticity and motor retardation associated with characteristic MRI findings of anterior bilateral temporal lobe cysts and multilobar leukoencephalopathy. So far, around 30 cases have been reported in the literature. Onset occurs in the first few months of life. Sensorineural deafness and microcephaly have also been reported. The etiology is unknown but an autosomal recessive mode of inheritance has been suggested.","definition_xrefs":["Orphanet:139444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukoencephalopathy with bilateral anterior temporal lobe cysts","secondary_identifiers":["icd11.foundation:138159250","UMLS:C4304744","GARD:19917","MEDGEN:930413"],"termid":"MONDO:0015348","xrefs":{"Monarch":{"xref_id":"0015348"}}}


id: PBO:0083572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps verified ORF RRP9","termid":"PBO:0083572"}


id: MONDO:0002977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by the degeneration of the nervous system due to autoimmunity. Representative examples include multiple sclerosis, Guillain-Barre syndrome, and myasthenia gravis.","definition_xrefs":["NCIT:C99383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune disorder of the nervous system","secondary_identifiers":["UMLS:C0751871","DOID:438","MEDGEN:155946","MESH:D020274"],"synonyms":[{"name":"autoimmune disease of nervous system","type":"exact"},{"name":"autoimmune disease, neurologic","type":"exact"},{"name":"autoimmune diseases, nervous system","type":"exact"},{"name":"autoimmune diseases, neurologic","type":"exact"},{"name":"autoimmune disorders of the nervous system","type":"exact"},{"name":"autoimmune disorders, nervous system","type":"exact"},{"name":"autoimmune nervous system diseases","type":"exact"},{"name":"autoimmune nervous system disorder","type":"exact"},{"name":"disease, neurologic autoimmune","type":"exact"},{"name":"diseases, neurologic autoimmune","type":"exact"},{"name":"immune diseases, nervous system","type":"exact"},{"name":"immune disorders, nervous system","type":"exact"},{"name":"nervous system autoimmune disease","type":"exact"},{"name":"nervous system autoimmune diseases","type":"exact"},{"name":"nervous system hypersensitivity reaction type II disease","type":"exact"},{"name":"nervous system immune diseases","type":"exact"},{"name":"nervous system immune disorders","type":"exact"},{"name":"neurologic autoimmune disease","type":"exact"},{"name":"neurologic autoimmune diseases","type":"exact"}],"termid":"MONDO:0002977","xrefs":{"Monarch":{"xref_id":"0002977"}}}


id: GO:0035616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A histone deubiquitination process in which a ubiquitin monomer is removed from a conserved lysine residue in the C-terminus of histone H2B. The conserved lysine residue is K119 in fission yeast, K123 in budding yeast, or K120 in mammals.","definition_xrefs":["GOC:vw","GOC:bf","PMID:15657442"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H2B conserved C-terminal lysine deubiquitination (obsolete GO:0035616)","synonyms":[{"name":"budding yeast H2B K123 deubiquitination","type":"narrow"},{"name":"fission yeast H2B K119 deubiquitination","type":"narrow"},{"name":"mammalian H2B K120 deubiquitination","type":"narrow"}],"termid":"GO:0035616"}


id: GO:0002927
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involved in the biosynthesis of archaeosine, an archaea-specific modified base found at position 15 in the D-loop of certain archaeal tRNAs.","definition_xrefs":["GOC:hjd","PMID:20129918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA modification","termid":"GO:0006400"},{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006399","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"archaeosine-tRNA biosynthetic process","termid":"GO:0002927"}


id: MONDO:1011805
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exercise induced metabolic myopathy, non-human animal","secondary_identifiers":["OMIA:002140"],"termid":"MONDO:1011805","xrefs":{"Monarch":{"xref_id":"1011805"}}}


id: PR:Q10233
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerase III subunit RPC2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00937","PANTHER:PTHR20856:SF8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase III subunit RPC2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4G9.08c","secondary_identifiers":["UniProtKB:Q10233"],"synonyms":[{"name":"C128 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"DNA-directed RNA polymerase III 130 kDa polypeptide (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase III subunit 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerase III subunit C2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RPC130 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLR3B","type":"exact"}],"termid":"PR:Q10233"}


id: GO:0033709
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabinitol + NADP+ = D-ribulose + NADPH + H+. Can also produce D-ribulose.","definition_xrefs":["EC:1.1.1.287"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"D-arabinitol dehydrogenase (NADP+) activity","synonyms":[{"name":"ARD1p","type":"related"},{"name":"D-arabinitol dehydrogenase 1 activity","type":"broad"},{"name":"D-arabinitol dehydrogenase, D-ribulose forming (NADP+) activity","type":"related"},{"name":"D-arabinitol dehydrogenase, D-xylulose forming (NADP+) activity","type":"related"},{"name":"D-arabinitol:NADP+ dehydrogenase activity","type":"broad"},{"name":"NADP+-dependent D-arabinitol dehydrogenase activity","type":"broad"}],"termid":"GO:0033709"}


id: GO:1990366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an organic acid.","definition_xrefs":["PMID:23356676","GOC:mengo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete response to organic acid (obsolete GO:1990366)","synonyms":[{"name":"response to organic acid","type":"exact"}],"termid":"GO:1990366"}


id: GO:0008413
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 8-oxo-7,8-dihydroguanosine triphosphate (8-oxo-GTP) + H2O = 8-oxo-7,8-dihydroguanosine diphosphate (8-oxo-GDP) + phosphate. 8-oxo-7,8-dihydroguanosine triphosphate (8-oxo-GTP) is the oxidised form of the free guanine nucleotide and can act as a potent mutagenic substrate for transcription.","definition_xrefs":["PMID:15878881","RHEA:60032"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate diphosphatase activity","termid":"GO:0047429"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0047429"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0047429","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity","secondary_identifiers":["EC:3.6.1.69"],"synonyms":[{"name":"7,8-dihydro-8-oxoguanine-triphosphatase activity","type":"exact"},{"name":"8-oxo-7,8-dihydroguanine triphosphatase activity","type":"exact"},{"name":"8-oxo-7,8-dihydroguanosine triphosphatase activity","type":"exact"},{"name":"8-oxo-GTPase activity","type":"exact"}],"termid":"GO:0008413"}


id: GO:0160165
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of CD8-positive alpha-beta T cells such that the total number of CD8-positive alpha-beta T cells within a whole or part of an organism is stable over time in the absence of an outside stimulus.","definition_xrefs":["PMID:33815406","PMID:30650357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell homeostasis","termid":"GO:0043029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"CD8-positive, alpha-beta T cell homeostasis","synonyms":[{"name":"CD8+ T cell homeostasis","type":"broad"},{"name":"CD8-positive T cell homeostasis","type":"broad"}],"termid":"GO:0160165"}


id: PBO:0028873
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_poly(A)_tail_length","termid":"PBO:0028873"}


id: PBO:0043065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor muscarinic 1","termid":"PBO:0043065"}


id: PBO:0044646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dendrocyte expressed seven transmembrane protein","termid":"PBO:0044646"}


id: MONDO:0015163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary glomerular disease (obsolete MONDO:0015163)","secondary_identifiers":["Orphanet:102373"],"termid":"MONDO:0015163","xrefs":{"Monarch":{"xref_id":"0015163"}}}


