# terms

id: GO:0072020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the proximal straight tubule over time, from its formation to the mature structure. The proximal straight tubule is the part of the descending limb that extends from the proximal convoluted tubule to the descending thin tubule.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron tubule development","termid":"GO:0072080"},{"relation_name":"part_of","term_name":"proximal tubule development","termid":"GO:0072014"}],"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":"proximal straight tubule development","synonyms":[{"name":"S3 development","type":"exact"}],"termid":"GO:0072020"}


id: PBO:0000892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase Spg1","termid":"PBO:0000892"}


id: PBO:0003304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human COMT homolog 1","termid":"PBO:0003304"}


id: PBO:0117193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPB41L3 antisense RNA 1","termid":"PBO:0117193"}


id: MONDO:0000027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epilepsy, absence (obsolete MONDO:0000027)","termid":"MONDO:0000027","xrefs":{"Monarch":{"xref_id":"0000027"}}}


id: PR:O74875
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC330.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74875"],"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 heme-binding protein C330.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC330.03c","synonyms":[{"name":"Spom972h-SPCC330.03c","type":"exact"}],"termid":"PR:O74875"}


id: PBO:0071554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 19","termid":"PBO:0071554"}


id: GO:0033694
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a CH-NH group acts as a hydrogen or electron donor and reduces an iron-sulfur protein.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors","termid":"GO:0016645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"oxidoreductase activity, acting on the CH-NH group of donors, iron-sulfur protein as acceptor","secondary_identifiers":["EC:1.5.7.-"],"termid":"GO:0033694"}


id: PBO:0005750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucear export factor Sac3 (predicted)","termid":"PBO:0005750"}


id: GO:1905660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a mitotic checkpoint complex.","definition_xrefs":["PMID:26882497","GO_REF:0000079","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"mitotic checkpoint complex assembly","synonyms":[{"name":"MCC assembly","type":"exact"},{"name":"MCC formation","type":"exact"},{"name":"mitotic checkpoint complex formation","type":"exact"}],"termid":"GO:1905660"}


id: MONDO:0034981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare ophthalmic disorder characterized by a usually congenital and unilateral round or oval, gray, white, or yellowish depression in the optic disk. There may be more than one pit present in one eye, and the anomaly is most commonly found in the inferotemporal region of the optic disk, although any sector may be involved. Patients are often asymptomatic, or may present with visual field defects, in particular paracentral arcuate scotoma connected to an enlarged blind spot. A number of patients develop serous macular detachment, with loss of vision typically becoming apparent in the third or fourth decade of life. [Orphanet:519404]","definition_xrefs":["Orphanet:519404"],"gene_count":0,"genotype_count":0,"name":"obsolete optic disk pit (obsolete MONDO:0034981)","secondary_identifiers":["ICD10CM:Q14.2"],"termid":"MONDO:0034981","xrefs":{"Monarch":{"xref_id":"0034981"}}}


id: MONDO:0017528
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"polydactyly of an index finger","termid":"MONDO:0008271"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polydactyly of an index finger, bilateral","secondary_identifiers":["icd11.foundation:806174152","MEDGEN:1727346","Orphanet:295154","UMLS:C5438861"],"synonyms":[{"name":"preaxial polydactyly type 3, bilateral","type":"exact"}],"termid":"MONDO:0017528","xrefs":{"Monarch":{"xref_id":"0017528"}}}


id: PBO:0068888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 129, pseudogene","termid":"PBO:0068888"}


id: PBO:0087633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the EGO/GSE complex; the vacuolar/endosomal membrane associated EGO/GSE complex regulates exit from rapamycin-induced growth arrest, stimulating microautophagy and sorting of Gap1p from the endosome to the plasma membrane; identified by homology to Ashbya gossypii; EGO2 has a paralog, EGO4, that arose from the whole genome duplication","termid":"PBO:0087633"}


id: PBO:0001320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"helix-hairpin-helix","termid":"PBO:0001320"}


id: PBO:0047829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FOXP1 divergent transcript","termid":"PBO:0047829"}


id: PBO:0076838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TERF1 pseudogene 5","termid":"PBO:0076838"}


id: PR:O14297
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC9E9.15 gene.","definition_xrefs":["UniProtKB:O14297","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 C9E9.15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9E9.15","synonyms":[{"name":"Spom972h-SPAC9E9.15","type":"exact"}],"termid":"PR:O14297"}


id: PBO:0085666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in nucleolar integrity and processing of pre-rRNA; has a role in processing rRNA for the 60S ribosome subunit; transcript is induced in response to cytotoxic stress but not genotoxic stress; relocalizes from nucleus to nucleolus upon DNA replication stress","termid":"PBO:0085666"}


id: MONDO:0021008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An antiphospholipid syndrome that occurs alongside another autoimmune disorder.","direct_ancestors":[{"relation_name":"is_a","term_name":"antiphospholipid syndrome","termid":"MONDO:8000010"}],"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":"secondary antiphospholipid syndrome","secondary_identifiers":["ICD9:795.79","UMLS:C0409983","icd11.foundation:138987181","MEDGEN:592743","SCTID:239895006"],"termid":"MONDO:0021008","xrefs":{"Monarch":{"xref_id":"0021008"}}}


id: GO:0050274
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: salicyl alcohol + UDP-D-glucose = H+ + salicin + UDP.","definition_xrefs":["EC:2.4.1.172","RHEA:11512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"salicyl-alcohol beta-D-glucosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R03558","MetaCyc:SALICYL-ALCOHOL-GLUCOSYLTRANSFERASE-RXN"],"synonyms":[{"name":"UDP-glucose:salicyl-alcohol beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:salicyl alcohol phenyl-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:salicyl-alcohol beta-D-glucosyltransferase activity","type":"related"},{"name":"salicyl-alcohol b-D-glucosyltransferase activity","type":"exact"},{"name":"salicyl-alcohol glucosyltransferase activity","type":"exact"},{"name":"uridine diphosphoglucose-salicyl alcohol 2-glucosyltransferase activity","type":"related"}],"termid":"GO:0050274"}


id: PBO:0035772
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K14_acetylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0035772"}


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


id: GO:0080145
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A homeostatic process involved in the maintenance of a steady state level of cysteine within a cell.","definition_xrefs":["PMID:19955263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular amino acid homeostasis","termid":"GO:0080144"}],"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":"intracellular cysteine homeostasis","synonyms":[{"name":"cellular cysteine homeostasis","type":"exact"},{"name":"cysteine homeostasis","type":"exact"}],"termid":"GO:0080145"}


id: MONDO:0022513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrophoderma of Pierini and Pasini is thought to possibly represent a late stage of morphea a type of localized scleroderma. Signs and symptoms ofatrophoderma of Pierini and Pasini include multiple oval, darkened (hyperpigmented) plaques in which tissue under the skin breaks downso that there is a depression (dent) within the skin. Some findings suggest that atrophoderma of Pierini and Pasini may be associated with B burgdorferi, a bacteria that causesLyme disease, in some cases.","definition_xrefs":["GARD:0005866"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"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":"atrophoderma of Pierini and Pasini","secondary_identifiers":["SCTID:711524008","GARD:5866","UMLS:C3887897","ICD10CM:L90.3","MEDGEN:854615","Orphanet:658810"],"synonyms":[{"name":"congenital atrophoderma of Pasini and Pierini","type":"related"},{"name":"idiopathic atrophoderma of Pasini and Pierini","type":"related"}],"termid":"MONDO:0022513","xrefs":{"Monarch":{"xref_id":"0022513"}}}


id: GO:2001156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of L-proline catabolic process to L-glutamate.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"is_a","term_name":"regulation of glutamate metabolic process","termid":"GO:2000211"},{"relation_name":"is_a","term_name":"regulation of L-proline metabolic process","termid":"GO:2000214"},{"relation_name":"regulates","term_name":"L-proline catabolic process to L-glutamate","termid":"GO:0010133"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"regulation of L-proline catabolic process to L-glutamate","synonyms":[{"name":"regulation of proline breakdown to glutamate","type":"exact"},{"name":"regulation of proline catabolic process to glutamate","type":"broad"},{"name":"regulation of proline degradation to glutamate","type":"exact"},{"name":"regulation of proline oxidation","type":"related"}],"termid":"GO:2001156"}


id: PBO:0044578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diazepam binding inhibitor-like 5 pseudogene 2","termid":"PBO:0044578"}


id: GO:0018169
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the posttranslational transfer of one or more glutamic acid residues to the C-terminus of ribosomal protein S6.","definition_xrefs":["PMID:2570347","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-glutamic acid ligase activity","termid":"GO:0070739"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ribosomal S6-glutamic acid ligase activity","termid":"GO:0018169"}


id: MONDO:0012775
data:
  {"annotated_genes":["SJAG_02744"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88093],"is_not":false,"summary":null,"term":"MONDO:0012775"}]},"cv_name":"mondo","definition":"Any thrombocytopenia in which the cause of the disease is a mutation in the CYCS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited thrombocytopenia","termid":"MONDO:0100241"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02744":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombocytopenia 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:394329","MESH:C567438","UMLS:C2677608","OMIM:612004","GARD:18289"],"synonyms":[{"name":"CYCS thrombocytopenia","type":"exact"},{"name":"THC4","type":"related"},{"name":"thrombocytopenia 4","type":"exact"},{"name":"thrombocytopenia caused by mutation in CYCS","type":"exact"},{"name":"thrombocytopenia type 4","type":"exact"},{"name":"thrombocytopenia, autosomal dominant, 4","type":"related"}],"termid":"MONDO:0012775","terms_by_termid":{"MONDO:0012775":null},"xrefs":{"Monarch":{"xref_id":"0012775"}}}


id: PBO:0074836
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 31","termid":"PBO:0074836"}


id: GO:0051669
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of terminal, non-reducing 2,1- and 2,6-linked beta-D-fructofuranose residues in fructans.","definition_xrefs":["EC:3.2.1.80"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"fructan beta-fructosidase activity","secondary_identifiers":["MetaCyc:3.2.1.80-RXN"],"synonyms":[{"name":"beta-D-fructan fructohydrolase activity","type":"related"},{"name":"exo-beta-D-fructosidase activity","type":"exact"},{"name":"exo-beta-fructosidase activity","type":"exact"},{"name":"fructan b-fructosidase activity","type":"exact"},{"name":"fructan exohydrolase activity","type":"exact"},{"name":"fructanase activity","type":"related"},{"name":"polysaccharide beta-fructofuranosidase activity","type":"exact"}],"termid":"GO:0051669"}


id: PBO:0047396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 36","termid":"PBO:0047396"}


id: PBO:0084388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low-affinity phosphate transporter; acts upstream of Pho81p in regulation of the PHO pathway; deletion of pho84, pho87, pho89, pho90, and pho91 causes synthetic lethality; transcription independent of Pi and Pho4p activity; overexpression results in vigorous growth; PHO90 has a paralog, PHO87, that arose from the whole genome duplication","termid":"PBO:0084388"}


id: GO:0150189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of interleukin-32 production.","definition_xrefs":["PMID:23729669","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-32 production","termid":"GO:0072637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-32 production","secondary_identifiers":["GO:0150192"],"synonyms":[{"name":"regulation of interleukin-32 biosynthetic process","type":"narrow"},{"name":"regulation of interleukin-32 secretion","type":"narrow"}],"termid":"GO:0150189"}


id: MONDO:0000713
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Balo concentric sclerosis (obsolete MONDO:0000713)","termid":"MONDO:0000713","xrefs":{"Monarch":{"xref_id":"0000713"}}}


id: PBO:0081934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zn regulated GTPase metalloprotein activator 1D, pseudogene","termid":"PBO:0081934"}


id: PR:O74394
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 39S ribosomal protein L33, mitochondrial 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":"54S ribosomal protein L39, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.08c","secondary_identifiers":["UniProtKB:O74394"],"synonyms":[{"name":"SPBC4F6.08c","type":"related"},{"name":"Spom972h-MRPL33","type":"exact"}],"termid":"PR:O74394"}


id: PBO:0046300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EMX2 opposite strand/antisense RNA","termid":"PBO:0046300"}


id: PBO:0004105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F0-ATPase subunit D (predicted)","termid":"PBO:0004105"}


id: PBO:0049750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemoglobin subunit zeta pseudogene 1","termid":"PBO:0049750"}


id: MOD:01324
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other -","definition_xrefs":["Unimod:254#H","PubMed:7744761"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetaldehyde +26","termid":"MOD:00577"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetaldehyde +26 - site H","synonyms":[{"name":"Acetaldehyde +26","type":"related"},{"name":"Delta:H(2)C(2)","type":"related"}],"termid":"MOD:01324"}


id: GO:0075079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism activates, maintains or increases the frequency, rate or extent of receptor-mediated signal transduction in the symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by host of symbiont receptor-mediated signal transduction (obsolete GO:0075079)","termid":"GO:0075079"}


id: PBO:0045857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 47","termid":"PBO:0045857"}


id: FYPO:0006453
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate or other catalytic property of a histone acetyltransferase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin organization","termid":"FYPO:0000642"},{"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:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000661","FYPO:0000654","FYPO:0000002","FYPO:0000652","FYPO:0005447","FYPO:0000641"],"is_obsolete":false,"name":"abnormal histone acetyltransferase activity","synonyms":[{"name":"abnormal histone acetylase activity","type":"exact"}],"termid":"FYPO:0006453"}


id: GO:1990645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of phosphorylases by removal of phosphate groups.","definition_xrefs":["PMID:8602837"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphorylase dephosphorylation (obsolete GO:1990645)","synonyms":[{"name":"phosphorylase dephosphorylation","type":"exact"}],"termid":"GO:1990645"}


id: PBO:0054037
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 1372","termid":"PBO:0054037"}


id: PBO:0074582
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 2A","termid":"PBO:0074582"}


id: MONDO:0010545
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by the association in male patients of congenital cataracts with microcornea, dental anomalies and facial dysmorphism.","definition_xrefs":["Orphanet:627"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nance-Horan syndrome","secondary_identifiers":["UMLS:C0796085","NORD:1489","MESH:C538336","DOID:0060599","GARD:7161","MEDGEN:208665","OMIM:302350","SCTID:445257004","icd11.foundation:938299000","ICD9:759.89"],"synonyms":[{"name":"Mesiodens cataract syndrome","type":"related"},{"name":"Mesiodens-cataract syndrome","type":"related"},{"name":"NHS","type":"related"},{"name":"Nance-Horan syndrome","type":"exact"},{"name":"cataract X-linked with Hutchinsonian teeth","type":"related"},{"name":"cataract dental syndrome","type":"related"},{"name":"cataract, X-linked, with Hutchinsonian teeth","type":"related"},{"name":"cataract-dental syndrome","type":"related"},{"name":"nance-horan syndrome, X-linked dominant","type":"exact"}],"termid":"MONDO:0010545","xrefs":{"Monarch":{"xref_id":"0010545"}}}


id: PBO:0071152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 17","termid":"PBO:0071152"}


id: PR:P36579
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- arf1 gene.","definition_xrefs":["UniProtKB:P36579","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":"ADP-ribosylation factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.18c","synonyms":[{"name":"Spom972h-arf1","type":"exact"}],"termid":"PR:P36579"}


id: FYPO:0003066
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A sporulation phenotype in which asci that contain one, two, or three spores form following conjugation and subsequent sporulation.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal sporulation resulting in formation of ascus with more or fewer than four spores","termid":"FYPO:0001894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000121","FYPO:0000631","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal sporulation resulting in formation of ascus with fewer than four spores","synonyms":[{"name":"abnormal ascospore formation resulting in formation of asci with fewer than four spores","type":"exact"},{"name":"abnormal sporulation resulting in formation of asci with fewer than four spores","type":"exact"}],"termid":"FYPO:0003066"}


id: MONDO:0001851
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal apparatus disorder","termid":"MONDO:0001854"}],"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":"primary lacrimal atrophy","secondary_identifiers":["DOID:1399","ICD9:375.13","MEDGEN:509859","SCTID:17093002","UMLS:C0155229"],"termid":"MONDO:0001851","xrefs":{"Monarch":{"xref_id":"0001851"}}}


id: GO:0048281
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of inflorescences are generated and organized. An inflorescence is the part of a seed plant body that is usually above ground and that can bear flowers.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"shoot system morphogenesis","termid":"GO:0010016"},{"relation_name":"is_a","term_name":"post-embryonic plant morphogenesis","termid":"GO:0090698"},{"relation_name":"part_of","term_name":"inflorescence development","termid":"GO:0010229"}],"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":"inflorescence morphogenesis","termid":"GO:0048281"}


id: PBO:0073932
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 5","termid":"PBO:0073932"}


id: PBO:0053706
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 908","termid":"PBO:0053706"}


id: PBO:0089986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,3-galactosyltransferase Otg3","termid":"PBO:0089986"}


id: PBO:0076315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SYNM antisense RNA 1","termid":"PBO:0076315"}


id: PBO:0027146
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_farnesyltranstransferase_activity","termid":"PBO:0027146"}


id: FYPO:0002610
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone H2A phosphorylation is normal at centromeric outer repeat regions. All histone H2A phosphorylation may be assayed, or phosphorylation of specific sites on histone H2A may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H2A phosphorylation during vegetative growth","termid":"FYPO:0002601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal histone H2A phosphorylation at centromere outer repeat during vegetative growth","synonyms":[{"name":"abnormal histone H2A phosphorylation at centromere otr during vegetative growth","type":"exact"},{"name":"abnormal histone H2A phosphorylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"abnormal histone H2A phosphorylation at pericentric region during vegetative growth","type":"related"},{"name":"abnormal histone H2A phosphorylation at pericentromeric region during vegetative growth","type":"related"},{"name":"normal histone H2A phosphorylation at centromere outer repeat during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002610"}


id: GO:0031228
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the Golgi membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of Golgi membrane (obsolete GO:0031228)","synonyms":[{"name":"intrinsic to Golgi membrane","type":"narrow"}],"termid":"GO:0031228"}


id: PBO:0062505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily G member 7 pseudogene","termid":"PBO:0062505"}


id: PBO:0062780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 56 subfamily B member 2 pseudogene","termid":"PBO:0062780"}


id: PBO:0004056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane protein involved in cytochrome oxidase biogenesis Cmc1 (predicted)","termid":"PBO:0004056"}


id: GO:0000722
data:
  {"annotated_genes":["SJAG_05173","SJAG_00640","SJAG_05105","SJAG_02079","SJAG_05353","SJAG_01677","SJAG_06642","SJAG_06597"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81965,97999,113586,114800,114801,114802,114803,114804],"is_not":false,"summary":null,"term":"GO:0000722"}]},"cv_name":"biological_process","definition":"Any recombinational process that contributes to the maintenance of proper telomeric length.","definition_xrefs":["GOC:elh","PMID:11850777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere maintenance","termid":"GO:0000723"},{"relation_name":"is_a","term_name":"mitotic recombination","termid":"GO:0006312"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00640":null,"SJAG_01677":null,"SJAG_02079":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05353":null,"SJAG_06597":null,"SJAG_06642":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0032200"},{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006310","GO:0032200","GO:0006259"],"is_obsolete":false,"name":"telomere maintenance via recombination","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"telomerase-independent telomere maintenance","type":"related"}],"termid":"GO:0000722","terms_by_termid":{"GO:0000722":null}}


id: FYPO:0001536
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 copper 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:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal cellular copper level","synonyms":[{"name":"normal cellular copper accumulation","type":"related"},{"name":"normal cellular copper ion level","type":"exact"},{"name":"normal cellular copper level during mitotic cell cycle","type":"related"},{"name":"normal cellular copper level during vegetative growth","type":"exact"}],"termid":"FYPO:0001536"}


id: GO:0021703
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the locus ceruleus over time, from its formation to the mature structure. The locus ceruleus is a dense cluster of neurons within the dorsorostral pons. This nucleus is the major location of neurons that release norepinephrine throughout the brain, and is responsible for physiological responses to stress and panic.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:dph","ISBN:0838580343","GO_REF:0000021","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"pons development","termid":"GO:0021548"}],"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":"locus ceruleus development","synonyms":[{"name":"locus caeruleus development","type":"exact"},{"name":"locus coeruleus development","type":"exact"}],"termid":"GO:0021703"}


id: RO:0002376
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x tributary_of y if and only if x a channel for the flow of a substance into y, where y is larger than x. If x and y are hydrographic features, then y is the main stem of a river, or a lake or bay, but not the sea or ocean. If x and y are anatomical, then y is a vein.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_branching_relationship_with","termid":"RO:0002375"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tributary_of","termid":"RO:0002376"}


id: PBO:0069044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 289, pseudogene","termid":"PBO:0069044"}


id: MONDO:0030476
data:
  {"annotated_genes":["SJAG_04700"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87826],"is_not":false,"summary":null,"term":"MONDO:0030476"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Galloway-Mowat syndrome","termid":"MONDO:0009627"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04700":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Galloway-Mowat syndrome 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1794230","UMLS:C5562020","OMIM:619609"],"synonyms":[{"name":"GAMOS10","type":"exact"}],"termid":"MONDO:0030476","terms_by_termid":{"MONDO:0030476":null},"xrefs":{"Monarch":{"xref_id":"0030476"}}}


id: MOD:00394
data:
  {"annotated_genes":["SJAG_00733","SJAG_02522"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[82376,82426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00050"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with an acetyl group.","definition_xrefs":["PubMed:11857757","DeltaMass:0","PubMed:11999733","PubMed:14730666","PubMed:12175151","PubMed:15350136","Unimod:1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylated residue","termid":"MOD:00649"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00733":null,"SJAG_02522":null},"genotype_count":0,"is_obsolete":false,"name":"acetylated residue","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"AcRes","type":"exact"},{"name":"Acetyl","type":"related"},{"name":"Acetylation","type":"related"},{"name":"Acetylation (N terminus, N epsilon of Lysine, O of Serine) (Ac)","type":"exact"}],"termid":"MOD:00394","terms_by_termid":{"MOD:00050":null}}


id: MONDO:0014886
data:
  {"annotated_genes":["SJAG_02978"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87908],"is_not":false,"summary":null,"term":"MONDO:0014886"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02978":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617051","MEDGEN:934712","UMLS:C4310745","GARD:17895","Orphanet:488627"],"synonyms":[{"name":"MRT55","type":"exact"},{"name":"intellectual disability, autosomal recessive 55","type":"exact"},{"name":"intellectual disability, autosomal recessive type 55","type":"exact"},{"name":"mental retardation, autosomal recessive 55","type":"exact"},{"name":"mental retardation, autosomal recessive type 55","type":"exact"},{"name":"neurodevelopmental disorder with microcephaly and gray sclerae","type":"exact"},{"name":"neurodevelopmental disorder with microcephaly and grey sclerae","type":"exact"}],"termid":"MONDO:0014886","terms_by_termid":{"MONDO:0014886":null},"xrefs":{"Monarch":{"xref_id":"0014886"}}}


id: MONDO:0003930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Stage 0 includes: 0a (Ta, N0, M0); 0is (Tis, N0, M0). Ta: Noninvasive papillary carcinoma. Tis: Carcinoma in situ: \\\"flat tumor\\\". N0: No regional lymph node metastasis. M0: No distant metastasis. (AJCC 6th and 7th eds.)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder transitional cell carcinoma","termid":"MONDO:0005611"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"non-invasive bladder urothelial carcinoma","secondary_identifiers":["UMLS:C1336089","NCIT:C6188","MEDGEN:233466","DOID:6571"],"synonyms":[{"name":"non-invasive bladder urothelial carcinoma","type":"exact"},{"name":"stage 0 bladder urothelial cancer","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma aJCC v6","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma aJCC v6 and v7","type":"exact"},{"name":"stage 0 bladder urothelial carcinoma aJCC v7","type":"exact"},{"name":"stage 0 transitional cell carcinoma of bladder","type":"exact"},{"name":"stage 0 transitional cell carcinoma of the bladder","type":"exact"},{"name":"stage 0 transitional cell carcinoma of the urinary bladder","type":"exact"},{"name":"stage 0 transitional cell carcinoma of urinary bladder","type":"exact"},{"name":"stage 0 urinary bladder transitional cell carcinoma","type":"exact"}],"termid":"MONDO:0003930","xrefs":{"Monarch":{"xref_id":"0003930"}}}


id: GO:0045226
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of polysaccharides used in extracellular structures.","definition_xrefs":["GOC:go_curators","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete extracellular polysaccharide biosynthetic process (obsolete GO:0045226)","synonyms":[{"name":"extracellular polysaccharide anabolism","type":"exact"},{"name":"extracellular polysaccharide biosynthesis","type":"exact"},{"name":"extracellular polysaccharide formation","type":"exact"},{"name":"extracellular polysaccharide synthesis","type":"exact"}],"termid":"GO:0045226"}


id: GO:0014736
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of muscle atrophy.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle atrophy","termid":"GO:0014735"},{"relation_name":"is_a","term_name":"negative regulation of muscle adaptation","termid":"GO:0014745"},{"relation_name":"negatively_regulates","term_name":"muscle atrophy","termid":"GO:0014889"}],"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 muscle atrophy","termid":"GO:0014736"}


id: GO:0015909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a long-chain fatty acid into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. A long-chain fatty acid has an aliphatic tail containing 13 to 22 carbons.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid transport","termid":"GO:0015908"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"long-chain fatty acid transport","secondary_identifiers":["Reactome:R-HSA-804914"],"termid":"GO:0015909"}


id: PBO:0116810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DTNBP1 antisense RNA 1","termid":"PBO:0116810"}


id: FYPO:0001934
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which a cell population does not grow in a medium containing glycerol as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cell population growth on glycerol carbon source","termid":"FYPO:0000684"},{"relation_name":"is_a","term_name":"abolished vegetative cell population growth","termid":"FYPO:0001575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0002060","FYPO:0002058","FYPO:0000003","FYPO:0005447","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"abolished cell population growth on glycerol carbon source","synonyms":[{"name":"abolished glycerol utilization","type":"related"},{"name":"abolished growth on glycerol carbon source","type":"broad"},{"name":"abolished vegetative cell population growth on glycerol carbon source","type":"exact"},{"name":"cell population growth on glycerol carbon source abolished","type":"exact"}],"termid":"FYPO:0001934"}


id: GO:0050296
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + stipitatonate = CO2 + H+ + stipitatate.","definition_xrefs":["EC:4.1.1.60","RHEA:13885"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"stipitatonate decarboxylase activity","secondary_identifiers":["KEGG_REACTION:R03739","MetaCyc:STIPITATONATE-DECARBOXYLASE-RXN"],"synonyms":[{"name":"stipitatonate carboxy-lyase (decyclizing)","type":"related"},{"name":"stipitatonate carboxy-lyase (decyclizing, stipitatate-forming)","type":"related"}],"termid":"GO:0050296"}


id: PBO:0027572
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_nuclear_envelope_morphology_during_mitotic_interphase","termid":"PBO:0027572"}


id: MONDO:0015355
data:
  {"annotated_genes":["SJAG_02695"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011879"}]},"cv_name":"mondo","definition":"Distal hereditary motor neuropathy type 7 is a rare, slowly progressive genetic peripheral neuropathy characterized by distal atrophy and weakness affecting the upper limbs (with a predilection for the thenar eminence) and subsequently the lower limbs, associated with uni- or bilateral vocal cord paresis leading to hoarse voice and breathing difficulties, and facial weakness.","definition_xrefs":["Orphanet:139589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, autosomal dominant","termid":"MONDO:0015362"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02695":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0005559","MONDO:0000426"],"is_obsolete":false,"name":"distal hereditary motor neuropathy type 7","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111199","icd11.foundation:80361835","MEDGEN:1662655","GARD:16960","UMLS:C4749653"],"synonyms":[{"name":"dHMN7","type":"exact"},{"name":"distal spinal muscular atrophy with vocal cord paralysis","type":"exact"}],"termid":"MONDO:0015355","terms_by_termid":{"MONDO:0011879":null},"xrefs":{"Monarch":{"xref_id":"0015355"}}}


id: GO:0015301
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: anion A(out) + anion B(in) = anion A(in) + anion B(out).","definition_xrefs":["GOC:ai","GOC:mtg_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete anion:anion antiporter activity (obsolete GO:0015301)","synonyms":[{"name":"anion exchanger activity","type":"exact"},{"name":"bicarbonate:chloride antiporter","type":"narrow"}],"termid":"GO:0015301"}


id: GO:1901844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell communication by electrical coupling involved in cardiac conduction.","definition_xrefs":["GOC:rl","GOC:TermGenie","PMID:17130302","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication by electrical coupling","termid":"GO:0010649"},{"relation_name":"regulates","term_name":"cell communication by electrical coupling involved in cardiac conduction","termid":"GO:0086064"}],"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 cell communication by electrical coupling involved in cardiac conduction","termid":"GO:1901844"}


id: PBO:0078339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (CTC) 5-1","termid":"PBO:0078339"}


id: PBO:0040494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AU RNA binding methylglutaconyl-CoA hydratase","termid":"PBO:0040494"}


id: PBO:0050215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosome binding domain 1 pseudogene 32","termid":"PBO:0050215"}


id: PBO:0072312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S25 pseudogene 9","termid":"PBO:0072312"}


id: GO:0016402
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2S)-pristanoyl-CoA + O2 = (2E)-pristenoyl-CoA + H2O2.","definition_xrefs":["RHEA:40459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA oxidase activity","termid":"GO:0003997"}],"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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"pristanoyl-CoA oxidase activity","secondary_identifiers":["Reactome:R-HSA-389889","Reactome:R-HSA-389891"],"termid":"GO:0016402"}


id: GO:2000573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of DNA biosynthetic process.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macromolecule biosynthetic process","termid":"GO:0010557"},{"relation_name":"is_a","term_name":"positive regulation of DNA metabolic process","termid":"GO:0051054"},{"relation_name":"is_a","term_name":"regulation of DNA biosynthetic process","termid":"GO:2000278"},{"relation_name":"positively_regulates","term_name":"DNA biosynthetic process","termid":"GO:0071897"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"positive regulation of DNA biosynthetic process","synonyms":[{"name":"positive regulation of DNA anabolism","type":"exact"},{"name":"positive regulation of DNA biosynthesis","type":"exact"},{"name":"positive regulation of DNA formation","type":"exact"},{"name":"positive regulation of DNA synthesis","type":"exact"}],"termid":"GO:2000573"}


id: GO:0075258
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of teliospore formation, which is the formation of a thick-walled resting or overwintering spore produced by the rust fungi (Uredinales) and smut fungi (Ustilaginales) in which karyogamy occurs.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043944"},{"relation_name":"is_a","term_name":"regulation of teliospore formation","termid":"GO:0075256"},{"relation_name":"negatively_regulates","term_name":"teliospore formation","termid":"GO:0075255"}],"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 teliospore formation","termid":"GO:0075258"}


id: PBO:0001865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome small subunit biogenesis protein (predicted)","termid":"PBO:0001865"}


id: MONDO:0800145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any non-severe combined immunodeficiency in which the cause of the disease is variation in the POLD1/POLD2 gene.","definition_xrefs":["PMID:31449058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"}],"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":"non-severe combined immunodeficiency due to polymerase delta deficiency","termid":"MONDO:0800145","xrefs":{"Monarch":{"xref_id":"0800145"}}}


id: PBO:0043181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDGSH iron sulfur domain 1 pseudogene 1","termid":"PBO:0043181"}


id: PBO:0084993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADPH-dependent medium chain alcohol dehydrogenase; has broad substrate specificity; member of the cinnamyl family of alcohol dehydrogenases; may be involved in fusel alcohol synthesis or in aldehyde tolerance; protein abundance increases in response to DNA replication stress","termid":"PBO:0084993"}


id: GO:0044693
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: trehalose(out) + H+(out) = trehalose(in) + H+(in).","definition_xrefs":["PMID:11136464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate:proton symporter activity","termid":"GO:0005351"},{"relation_name":"is_a","term_name":"trehalose transmembrane transporter activity","termid":"GO:0015574"}],"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:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"trehalose:proton symporter activity","synonyms":[{"name":"trehalose:hydrogen symporter activity","type":"exact"}],"termid":"GO:0044693"}


id: PBO:0074545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sushi, nidogen and EGF like domains 1","termid":"PBO:0074545"}


id: MONDO:0002975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanoma that arises usually from the breast skin and less often from the breast glandular tissue. Primary breast melanomas are rare.","definition_xrefs":["NCIT:C8410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanoma","termid":"MONDO:0005105"},{"relation_name":"is_a","term_name":"breast cancer","termid":"MONDO:0007254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant breast melanoma","secondary_identifiers":["MEDGEN:138069","DOID:4364","UMLS:C0346787","SCTID:188050009"],"synonyms":[{"name":"breast melanoma","type":"exact"},{"name":"breast melanoma (disease)","type":"exact"},{"name":"malignant breast melanoma","type":"exact"},{"name":"malignant melanoma of breast","type":"exact"},{"name":"malignant melanoma of the breast","type":"exact"},{"name":"melanoma (disease) of breast","type":"exact"}],"termid":"MONDO:0002975","xrefs":{"Monarch":{"xref_id":"0002975"}}}


id: MONDO:0014323
data:
  {"annotated_genes":["SJAG_05342","SJAG_02946","SJAG_02150","SJAG_04296","SJAG_04637","SJAG_02955","SJAG_01998","SJAG_02947","SJAG_03827"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88381,88382,88383,88384,88385,88386,88387,88388,88389],"is_not":false,"summary":null,"term":"MONDO:0014323"}]},"cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the SLC7A14 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":9,"genes_by_uniquename":{"SJAG_01998":null,"SJAG_02150":null,"SJAG_02946":null,"SJAG_02947":null,"SJAG_02955":null,"SJAG_03827":null,"SJAG_04296":null,"SJAG_04637":null,"SJAG_05342":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 68","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16004","MEDGEN:816710","DOID:0110374","OMIM:615725","ICD10CM:H35.5","UMLS:C3810380"],"synonyms":[{"name":"RP68","type":"exact"},{"name":"SLC7A14 retinitis pigmentosa","type":"exact"},{"name":"retinitis pigmentosa 68","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in SLC7A14","type":"exact"},{"name":"retinitis pigmentosa type 68","type":"exact"}],"termid":"MONDO:0014323","terms_by_termid":{"MONDO:0014323":null},"xrefs":{"Monarch":{"xref_id":"0014323"}}}


id: FYPO:0001416
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of sulfide:quinone oxidoreductase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased oxidoreductase activity","termid":"FYPO:0000690"},{"relation_name":"is_a","term_name":"abnormal sulfide:quinone oxidoreductase activity","termid":"FYPO:0001415"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0001985","FYPO:0000661","FYPO:0000654"],"is_obsolete":false,"name":"decreased sulfide:quinone oxidoreductase activity","synonyms":[{"name":"decreased sulfide-quinone reductase activity","type":"exact"},{"name":"decreased sulfide:quinone reductase activity","type":"exact"},{"name":"decreased sulphide:quinone oxidoreductase activity","type":"exact"},{"name":"reduced sulfide:quinone oxidoreductase activity","type":"exact"}],"termid":"FYPO:0001416"}


id: PBO:0035723
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_glycosylation_during_vegetative_growth","termid":"PBO:0035723"}


id: PBO:0081677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 598, E3 ubiquitin ligase","termid":"PBO:0081677"}


id: GO:0080028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a nitrile, an organic compound containing trivalent nitrogen attached to one carbon atom.","definition_xrefs":["PMID:18987211"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"nitrile metabolic process","termid":"GO:0050898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"nitrile biosynthetic process","termid":"GO:0080028"}


id: MONDO:0016238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Solitary fibrous tumor (SFT) represents a diverse group of ubiquitous rare spindle cell neoplasms that may be benign or malignant and that most frequently arises from the pleura and peritoneum and rarely from other sites such as head and neck, liver and skeletal muscle. SFT may be clinically asymptomatic or may present with enlarging mass, compressive effects depending on the site involved and rarely with paraneoplastic manifestations (osteoarthropathy or hypoglycemia).","definition_xrefs":["Orphanet:2126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblastic neoplasm","termid":"MONDO:0006209"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solitary fibrous tumor","secondary_identifiers":["NCIT:C7634","UMLS:C1266119","ICDO:8815/1","MEDGEN:224764","ICDO:9051/0","ONCOTREE:SFT","MESH:D006393","GARD:15014","ICD9:238.1","MedDRA:10018825","ICDO:8815/0","MESH:D054364"],"synonyms":[{"name":"SFT","type":"exact"},{"name":"hemangiopericytoma","type":"related"},{"name":"localised fibrous mesothelioma","type":"exact"},{"name":"localised fibrous tumour","type":"exact"},{"name":"localized fibrous mesothelioma","type":"exact"},{"name":"localized fibrous tumor","type":"exact"},{"name":"solitary fibrous tumor","type":"exact"},{"name":"solitary fibrous tumor/hemangiopericytoma","type":"related"},{"name":"submesothelial fibroma","type":"exact"}],"termid":"MONDO:0016238","xrefs":{"Monarch":{"xref_id":"0016238"}}}


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


id: PBO:0079803
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 B24, pseudogene","termid":"PBO:0079803"}


id: MOD:01615
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue by a dithioester bond to form glycyl cysteine dithioester.","definition_xrefs":["PubMed:11438688","PubMed:16388576","RESID:AA0512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thioester crosslinked residues","termid":"MOD:00395"},{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"glycyl cysteine dithioester","synonyms":[{"name":"(2R)-2-amino-3-[(aminoacetyl)disulfanyl]propanoic acid","type":"exact"},{"name":"2-(glycyldithio)alanine","type":"exact"},{"name":"S-glycyl cysteine persulfide","type":"exact"},{"name":"S-glycyl thiocysteine","type":"exact"},{"name":"glycyl cysteine dithioester","type":"exact"},{"name":"thioglycine cysteine disulfide","type":"exact"}],"termid":"MOD:01615"}


id: PBO:0038412
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-acts_upstream_of,_positive_effect","termid":"PBO:0038412"}


id: GO:0046665
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Maintenance of the amnioserosa, an epithelium that occupies a hole in the embryonic dorsal epidermis.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue homeostasis","termid":"GO:0001894"},{"relation_name":"part_of","term_name":"embryonic development via the syncytial blastoderm","termid":"GO:0001700"}],"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":"amnioserosa maintenance","termid":"GO:0046665"}


id: PBO:0078032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 22","termid":"PBO:0078032"}


id: MONDO:0017534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"postaxial polydactyly type B","termid":"MONDO:0019674"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly type B, bilateral","secondary_identifiers":["Orphanet:295169","icd11.foundation:921497168"],"termid":"MONDO:0017534","xrefs":{"Monarch":{"xref_id":"0017534"}}}


id: PBO:0031678
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_cell_cycle_arrest_in_response_to_pheromone","termid":"PBO:0031678"}


id: PBO:0067895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 197","termid":"PBO:0067895"}


id: GO:0031894
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a V1A vasopressin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasopressin receptor binding","termid":"GO:0031893"}],"gene_count":0,"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:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"V1A vasopressin receptor binding","synonyms":[{"name":"V1A vasopressin receptor ligand","type":"narrow"}],"termid":"GO:0031894"}


id: PBO:0075420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated antigen 6","termid":"PBO:0075420"}


id: GO:1902117
data:
  {"annotated_genes":["SJAG_00718","SJAG_01837","SJAG_02332","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91466,118535,104196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905561"},{"annotations":[113289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110161"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of organelle assembly.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"positive regulation of cellular component biogenesis","termid":"GO:0044089"},{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"positively_regulates","term_name":"organelle assembly","termid":"GO:0070925"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00718":null,"SJAG_01837":null,"SJAG_02332":null,"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"positive regulation of organelle assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of organelle assembly","type":"narrow"},{"name":"up regulation of organelle assembly","type":"exact"},{"name":"up-regulation of organelle assembly","type":"exact"},{"name":"upregulation of organelle assembly","type":"exact"}],"termid":"GO:1902117","terms_by_termid":{"GO:0110161":null,"GO:1905561":null}}


id: PBO:0067529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 673, pseudogene","termid":"PBO:0067529"}


id: GO:0031628
data:
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id: PBO:0026794
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id: GO:1903080
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id: MONDO:1011918
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id: GO:0005198
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id: PBO:0041184
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id: FYPO:0003282
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id: PBO:0054087
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id: MONDO:0032821
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id: GO:0140670
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id: MONDO:0021535
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id: PBO:0043079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic alpha 9 subunit","termid":"PBO:0043079"}


id: MONDO:0044347
data:
  {"annotated_genes":["SJAG_00988","SJAG_01351","SJAG_00839","SJAG_00235","SJAG_04217","SJAG_04495","SJAG_03929","SJAG_01162","SJAG_02297","SJAG_04334","SJAG_02796"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010480"},{"annotations":[87691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009259"},{"annotations":[88000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009284"},{"annotations":[87972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013275"},{"annotations":[88662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019531"},{"annotations":[87774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009606"},{"annotations":[87320,87321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009605"},{"annotations":[88254,88255],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009340"},{"annotations":[87383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009950"}]},"cv_name":"mondo","definition":"A disease or disorder that involves the erythrocyte.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder","termid":"MONDO:0005570"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00235":null,"SJAG_00839":null,"SJAG_00988":null,"SJAG_01162":null,"SJAG_01351":null,"SJAG_02297":null,"SJAG_02796":null,"SJAG_03929":null,"SJAG_04217":null,"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"erythrocyte disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:526127","UMLS:C0221016","SCTID:38292009","ICD9:289.9"],"synonyms":[{"name":"disease of erythrocyte","type":"exact"},{"name":"disease or disorder of erythrocyte","type":"exact"},{"name":"disorder of erythrocyte","type":"exact"},{"name":"erythrocyte disease","type":"exact"},{"name":"erythrocyte disease or disorder","type":"exact"},{"name":"red blood cell disease","type":"exact"},{"name":"red blood cell disorder","type":"exact"}],"termid":"MONDO:0044347","terms_by_termid":{"MONDO:0009259":null,"MONDO:0009284":null,"MONDO:0009340":null,"MONDO:0009605":null,"MONDO:0009606":null,"MONDO:0009950":null,"MONDO:0010480":null,"MONDO:0013275":null,"MONDO:0019531":null},"xrefs":{"Monarch":{"xref_id":"0044347"}}}


id: PBO:0070165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 79 pseudogene","termid":"PBO:0070165"}


id: GO:0031126
data:
  {"annotated_genes":["SJAG_04321","SJAG_04754","SJAG_00943","SJAG_00854","SJAG_02350","SJAG_03179","SJAG_04942","SJAG_01521","SJAG_04153","SJAG_01191","SJAG_03745"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61649],"is_not":false,"summary":null,"term":"GO:0031126"},{"annotations":[112044,75023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000494"},{"annotations":[82035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000495"},{"annotations":[76818,74949,77988,72364,76066,79429,117308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071051"}]},"cv_name":"biological_process","definition":"Any process involved in forming the mature 3' end of a snoRNA family molecule, also referred to as an sRNA in Archaea.","definition_xrefs":["GOC:krc","GOC:mah","PMID:17284456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA 3'-end processing","termid":"GO:0031123"},{"relation_name":"is_a","term_name":"sno(s)RNA processing","termid":"GO:0043144"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00854":null,"SJAG_00943":null,"SJAG_01191":null,"SJAG_01521":null,"SJAG_02350":null,"SJAG_03179":null,"SJAG_03745":null,"SJAG_04153":null,"SJAG_04321":null,"SJAG_04754":null,"SJAG_04942":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016074"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0016074"],"is_obsolete":false,"name":"sno(s)RNA 3'-end processing","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"sRNA 3'-end processing","type":"narrow"},{"name":"sno(s)RNA 3' end processing","type":"exact"},{"name":"snoRNA 3'-end processing","type":"narrow"}],"termid":"GO:0031126","terms_by_termid":{"GO:0000494":null,"GO:0000495":null,"GO:0031126":null,"GO:0071051":null}}


id: GO:1902270
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which (R)-carnitine is transported across a membrane.","definition_xrefs":["PMID:23755272","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(R)-carnitine transport","termid":"GO:1900749"},{"relation_name":"is_a","term_name":"carnitine transmembrane transport","termid":"GO:1902603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"(R)-carnitine transmembrane transport","termid":"GO:1902270"}


id: PBO:0066653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIO kinase 1","termid":"PBO:0066653"}


id: PBO:0044025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"casein kinase 2 beta","termid":"PBO:0044025"}


id: PBO:0048079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin light chain","termid":"PBO:0048079"}


id: PBO:0056219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member C2","termid":"PBO:0056219"}


id: PBO:0058685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6813","termid":"PBO:0058685"}


id: GO:0047944
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-glutamate + ATP = alpha-L-glutamyl phosphate + ADP + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete glutamate 1-kinase activity (obsolete GO:0047944)","synonyms":[{"name":"ATP:L-glutamate 1-phosphotransferase activity","type":"related"}],"termid":"GO:0047944"}


id: PBO:0048143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FXYD6 antisense RNA 1","termid":"PBO:0048143"}


id: PBO:0072996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scm polycomb group protein like 4","termid":"PBO:0072996"}


id: MONDO:0044223
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete radin blood group antigen (obsolete MONDO:0044223)","secondary_identifiers":["OMIM:111620"],"synonyms":[{"name":"RADIN blood group antigen","type":"related"},{"name":"RD","type":"related"},{"name":"blood Group--Radin antigen","type":"related"},{"name":"blood group, Radin","type":"exact"}],"termid":"MONDO:0044223","xrefs":{"Monarch":{"xref_id":"0044223"}}}


id: PBO:0117036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP2K7 antisense RNA 1","termid":"PBO:0117036"}


id: GO:0051341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of oxidoreductase activity, the catalysis of an oxidation-reduction (redox) reaction, a reversible chemical reaction in which the oxidation state of an atom or atoms within a molecule is altered. One substrate acts as a hydrogen or electron donor and becomes oxidized, while the other acts as hydrogen or electron acceptor and becomes reduced.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catalytic activity","termid":"GO:0050790"}],"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 oxidoreductase activity","synonyms":[{"name":"oxidoreductase regulator","type":"exact"}],"termid":"GO:0051341"}


id: MONDO:0100269
data:
  {"annotated_genes":["SJAG_03440"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013942"},{"annotations":[89044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013943"}]},"cv_name":"mondo","definition":"Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX16 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Zellweger spectrum disorders","termid":"MONDO:0019609"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03440":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019053"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0006025","MONDO:0019053","MONDO:0005559","MONDO:0005066"],"is_obsolete":false,"name":"peroxisome biogenesis disorder due to PEX16 defect","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"PEX16 related Zellweger spectrum disorder","type":"exact"},{"name":"peroxisome biogenesis disorder due to PEX16 defect","type":"exact"}],"termid":"MONDO:0100269","terms_by_termid":{"MONDO:0013942":null,"MONDO:0013943":null},"xrefs":{"Monarch":{"xref_id":"0100269"}}}


id: PBO:0039296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG10 alpha-1,2-glucosyltransferase B","termid":"PBO:0039296"}


id: PBO:0031185
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_thiamine_level","termid":"PBO:0031185"}


id: GO:0045953
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of natural killer mediated cytotoxicity.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte mediated cytotoxicity","termid":"GO:0001911"},{"relation_name":"is_a","term_name":"negative regulation of natural killer cell mediated immunity","termid":"GO:0002716"},{"relation_name":"is_a","term_name":"regulation of natural killer cell mediated cytotoxicity","termid":"GO:0042269"},{"relation_name":"negatively_regulates","term_name":"natural killer cell mediated cytotoxicity","termid":"GO:0042267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of natural killer cell mediated cytotoxicity","synonyms":[{"name":"down regulation of natural killer cell mediated cytotoxicity","type":"exact"},{"name":"down-regulation of natural killer cell mediated cytotoxicity","type":"exact"},{"name":"downregulation of natural killer cell mediated cytotoxicity","type":"exact"},{"name":"inhibition of natural killer cell mediated cytotoxicity","type":"narrow"},{"name":"negative regulation of NK cell mediated cell death","type":"exact"},{"name":"negative regulation of NK cell mediated cell killing","type":"exact"},{"name":"negative regulation of NK cell mediated cytolysis","type":"related"},{"name":"negative regulation of NK cell mediated cytotoxicity","type":"exact"},{"name":"negative regulation of natural killer cell mediated cell death","type":"exact"},{"name":"negative regulation of natural killer cell mediated cell killing","type":"exact"},{"name":"negative regulation of natural killer cell mediated cytolysis","type":"related"}],"termid":"GO:0045953"}


id: PBO:0070609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 77","termid":"PBO:0070609"}


id: MONDO:0600008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome that occurs after therapeutic infusion of antibodies into the blood and is characterized by nausea, headache, tachycardia, hypotension, rash, and shortness of breath. It is caused by the release of cytokines from the cells that are targeted by the antibodies. Most patients experience a mild to moderate reaction; however, the reaction may be severe and life-threatening.","definition_xrefs":["PMID:24876563","NCIT:C78251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"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":"cytokine release syndrome","secondary_identifiers":["ICD10CM:D89.83","MEDGEN:215297","MESH:D000080424","UMLS:C0948245"],"synonyms":[{"name":"CRS","type":"exact"},{"name":"cytokine storm","type":"exact"},{"name":"cytokine-associated toxicity","type":"exact"}],"termid":"MONDO:0600008","xrefs":{"Monarch":{"xref_id":"0600008"}}}


id: PBO:0081586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 513","termid":"PBO:0081586"}


id: MONDO:0017254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete posterior uveitis (obsolete MONDO:0017254)","synonyms":[{"name":"obsolete posterior uveitis (disease)","type":"exact"}],"termid":"MONDO:0017254","xrefs":{"Monarch":{"xref_id":"0017254"}}}


id: GO:0001983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The increase in nerve impulses from baroreceptors as a result of increased pressure on an artery that results in an inhibition of sympathetic nerve impulses to peripheral blood vessels.","definition_xrefs":["GOC:mtg_cardio","ISBN:0323031951","ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure by carotid sinus baroreceptor feedback","termid":"GO:0001978"},{"relation_name":"is_a","term_name":"negative regulation of systemic arterial blood pressure","termid":"GO:0003085"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"baroreceptor response to increased systemic arterial blood pressure","termid":"GO:0001983"}


id: MONDO:0015582
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of pregnancy disorder that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare disorder related with pregnancy, childbirth and puerperium (obsolete MONDO:0015582)","secondary_identifiers":["Orphanet:163637"],"synonyms":[{"name":"rare pregnancy disorder","type":"exact"}],"termid":"MONDO:0015582","xrefs":{"Monarch":{"xref_id":"0015582"}}}


id: FYPO:0004722
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 morphology of nuclear microtubules is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"}],"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:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal nuclear microtubules","synonyms":[{"name":"normal nuclear microtubule morphology","type":"exact"},{"name":"normal nuclear microtubule structure","type":"narrow"},{"name":"normal nuclear microtubules during mitotic cell cycle","type":"related"},{"name":"normal nuclear microtubules during vegetative growth","type":"exact"}],"termid":"FYPO:0004722"}


id: PBO:0084588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged open reading frame; does not encode a discrete protein; YDL038C was originally annotated as an independent ORF, but as a result of a sequence correction, was merged with adjacent ORF PRM7/YDL039C into a single open reading frame","termid":"PBO:0084588"}


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


id: GO:0044560
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism alters or subverts the activity of an ion channel in another organism via the action of a venom.","definition_xrefs":["GOC:fj","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of biological process","termid":"GO:0035738"}],"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":"venom-mediated perturbation of ion channel activity","synonyms":[{"name":"envenomation resulting in modulation of ion channel activity in another organism","type":"exact"},{"name":"envenomation resulting in modulation of ion channel activity in other organism","type":"exact"},{"name":"envenomation resulting in regulation of ion channel activity in other organism","type":"exact"}],"termid":"GO:0044560"}


id: MONDO:0007419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Darwinian tubercle of pinna (obsolete MONDO:0007419)","termid":"MONDO:0007419","xrefs":{"Monarch":{"xref_id":"0007419"}}}


id: GO:0001559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the size of the nucleus with respect to the cytoplasm modulates the frequency, rate or extent of cell growth, the irreversible increase in size of a cell over time.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cell growth by detection of nuclear:cytoplasmic ratio (obsolete GO:0001559)","synonyms":[{"name":"detection of nuclear:cytoplasmic ratio to regulate cell growth","type":"exact"},{"name":"interpretation of nuclear:cytoplasmic ratio to regulate cell growth","type":"exact"},{"name":"regulation of cell growth by nuclear:cytoplasmic ratio","type":"exact"},{"name":"regulation of cell growth by sensing of nuclear:cytoplasmic ratio","type":"exact"}],"termid":"GO:0001559"}


id: GO:0071608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of macrophage inflammatory protein 1 alpha due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:rv","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine production","termid":"GO:0032602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"macrophage inflammatory protein-1 alpha production","synonyms":[{"name":"CCL3 production","type":"exact"},{"name":"MIP-1a production","type":"exact"},{"name":"chemokine (C-C motif) ligand 3 production","type":"exact"},{"name":"macrophage inflammatory protein production","type":"broad"}],"termid":"GO:0071608"}


id: GO:0061864
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of molecules that form the basement membrane, including carbohydrates and glycoproteins by a cell.","definition_xrefs":["PMID:26610918","PMID:28228250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix constituent secretion","termid":"GO:0070278"}],"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:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"basement membrane constituent secretion","termid":"GO:0061864"}


id: PBO:0091426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-xylose 1-dehydrogenase (NADP+)","termid":"PBO:0091426"}


id: PBO:0030763
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_response_to_zinc_ion","termid":"PBO:0030763"}


id: PBO:0070228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 164 pseudogene","termid":"PBO:0070228"}


id: PBO:0062878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orthodenticle homeobox 2","termid":"PBO:0062878"}


id: GO:0001914
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of T cell mediated cytotoxicity.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte mediated cytotoxicity","termid":"GO:0001910"},{"relation_name":"is_a","term_name":"regulation of T cell mediated immunity","termid":"GO:0002709"},{"relation_name":"regulates","term_name":"T cell mediated cytotoxicity","termid":"GO:0001913"}],"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 T cell mediated cytotoxicity","synonyms":[{"name":"regulation of T cell mediated apoptosis","type":"exact"},{"name":"regulation of T cell mediated cell death","type":"exact"},{"name":"regulation of T cell mediated cell killing","type":"exact"},{"name":"regulation of T cell mediated cytolysis","type":"related"},{"name":"regulation of T lymphocyte mediated cytotoxicity","type":"exact"},{"name":"regulation of T-cell mediated apoptosis","type":"exact"},{"name":"regulation of T-cell mediated cell death","type":"exact"},{"name":"regulation of T-cell mediated cell killing","type":"exact"},{"name":"regulation of T-cell mediated cytolysis","type":"related"},{"name":"regulation of T-cell mediated cytotoxicity","type":"exact"},{"name":"regulation of T-lymphocyte mediated cytotoxicity","type":"exact"}],"termid":"GO:0001914"}


id: FYPO:0005089
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which RNA polymerase II carboxy-terminal domain kinase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein kinase activity","termid":"FYPO:0001384"},{"relation_name":"is_a","term_name":"abnormal regulation of transcription","termid":"FYPO:0004526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0005447","FYPO:0000707","FYPO:0000654","FYPO:0000661","FYPO:0006551","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abolished RNA polymerase II carboxy-terminal domain kinase activity","synonyms":[{"name":"RNA polymerase II carboxy-terminal domain kinase activity abolished","type":"exact"}],"termid":"FYPO:0005089"}


id: GO:0002639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of immunoglobulin production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of immunoglobulin production","termid":"GO:0002637"},{"relation_name":"is_a","term_name":"positive regulation of production of molecular mediator of immune response","termid":"GO:0002702"},{"relation_name":"positively_regulates","term_name":"immunoglobulin production","termid":"GO:0002377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of immunoglobulin production","secondary_identifiers":["GO:0002642","GO:0051024"],"synonyms":[{"name":"activation of immunoglobulin production","type":"narrow"},{"name":"positive regulation of immunoglobulin biosynthetic process","type":"narrow"},{"name":"positive regulation of immunoglobulin secretion","type":"narrow"},{"name":"stimulation of immunoglobulin production","type":"narrow"},{"name":"up regulation of immunoglobulin production","type":"exact"},{"name":"up-regulation of immunoglobulin production","type":"exact"},{"name":"upregulation of immunoglobulin production","type":"exact"}],"termid":"GO:0002639"}


id: PBO:0055542
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 2978","termid":"PBO:0055542"}


id: GO:0031983
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane or protein that forms a vesicle.","definition_xrefs":["GOC:vesicles","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle lumen","termid":"GO:0043233"},{"relation_name":"part_of","term_name":"vesicle","termid":"GO:0031982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"vesicle lumen","secondary_identifiers":["NIF_Subcellular:sao797538226"],"termid":"GO:0031983"}


id: PBO:0057763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR2052 host gene","termid":"PBO:0057763"}


id: GO:1903352
data:
  {"annotated_genes":["SJAG_00543"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990575"}]},"cv_name":"biological_process","definition":"The directed movement of L-ornithine across a membrane.","definition_xrefs":["PMID:8195186","GOC:krc","GO_REF:0000069","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ornithine transport","termid":"GO:0015822"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00543":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"L-ornithine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1903352","terms_by_termid":{"GO:1990575":null}}


id: PBO:0066003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ral GTPase activating protein catalytic subunit alpha 2","termid":"PBO:0066003"}


id: GO:1902125
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of (+)-pinoresinol.","definition_xrefs":["GOC:TermGenie","PMID:8910615","PMID:9872995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"lignan catabolic process","termid":"GO:0046273"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"},{"relation_name":"is_a","term_name":"(+)-pinoresinol metabolic process","termid":"GO:1902124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"(+)-pinoresinol catabolic process","synonyms":[{"name":"(+)-pinoresinol breakdown","type":"exact"},{"name":"(+)-pinoresinol catabolism","type":"exact"},{"name":"(+)-pinoresinol degradation","type":"exact"}],"termid":"GO:1902125"}


id: PR:Q9P5N4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC359.01 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P5N4"],"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 amino-acid permease C359.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC359.01","synonyms":[{"name":"Spom972h-SPBC359.01","type":"exact"}],"termid":"PR:Q9P5N4"}


id: PBO:0036054
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_O-linked_glycosylation_during_vegetative_growth","termid":"PBO:0036054"}


id: FYPO:0007834
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 distribution of a protein localized to chromatin along the length of genes that can be transcribed by RNA polymerase II is altered such that more of the protein is present at the 3' end, and less at the 5' end, than normal.","definition_xrefs":["PomBase:mah","PMID:31837996"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein distribution along RNA polymerase II-transcribed genes","termid":"FYPO:0006020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"protein displaced from 5' end to 3' end of RNA polymerase II-transcribed genes","synonyms":[{"name":"decreased protein localization to chromatin at 5' end of RNA polymerase II-transcribed genes with increased localization towards 3' end","type":"exact"},{"name":"protein displaced from 5' end to 3' end of RNA polymerase II-transcribed genes during mitotic cell cycle","type":"related"},{"name":"protein displaced from 5' end to 3' end of RNA polymerase II-transcribed genes during vegetative growth","type":"exact"}],"termid":"FYPO:0007834"}


id: FYPO:0004128
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a cysteine-type peptidase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal peptidase activity","termid":"FYPO:0000666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0000661","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"abnormal cysteine-type peptidase activity","synonyms":[{"name":"abnormal caspase activity","type":"narrow"},{"name":"abnormal cysteine protease activity","type":"exact"}],"termid":"FYPO:0004128"}


id: GO:0051351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ligase activity, the catalysis of the ligation of two substances with concomitant breaking of a diphosphate linkage, usually in a nucleoside triphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catalytic activity","termid":"GO:0043085"}],"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 ligase activity","synonyms":[{"name":"activation of ligase activity","type":"narrow"},{"name":"ligase activator","type":"exact"},{"name":"stimulation of ligase activity","type":"narrow"},{"name":"up regulation of ligase activity","type":"exact"},{"name":"up-regulation of ligase activity","type":"exact"},{"name":"upregulation of ligase activity","type":"exact"}],"termid":"GO:0051351"}


id: PBO:0052539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kallikrein related peptidase 12","termid":"PBO:0052539"}


id: SO:0002369
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A scaRNA possessing a box C/D sequence motif, guiding the methylation of snRNAs.","definition_xrefs":["PMID:17099227","PMID:24659245"],"direct_ancestors":[{"relation_name":"is_a","term_name":"scaRNA","termid":"SO:0002095"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C_D_box_scaRNA","synonyms":[{"name":"C/D scaRNA","type":"exact"}],"termid":"SO:0002369"}


id: GO:0060642
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a preadipocyte acquires specialized features of a white adipocyte of the mammary gland. White adipocytes have cytoplasmic lipids arranged in a unique vacuole.","definition_xrefs":["GOC:dph","PMID:12558599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"white fat cell differentiation","termid":"GO:0050872"},{"relation_name":"part_of","term_name":"mammary gland fat development","termid":"GO:0060611"}],"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":"white fat cell differentiation involved in mammary gland fat development","termid":"GO:0060642"}


id: GO:0071839
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The apoptotic process in cells in the bone marrow.","definition_xrefs":["GOC:mah","GOC:mtg_apoptosis","PMID:17063141"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"}],"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":"apoptotic process in bone marrow cell","synonyms":[{"name":"apoptosis in bone marrow","type":"narrow"},{"name":"bone marrow cell apoptosis","type":"exact"},{"name":"bone marrow cell programmed cell death by apoptosis","type":"exact"},{"name":"killing of bone marrow cells","type":"exact"},{"name":"programmed cell death of bone marrow cells by apoptosis","type":"exact"},{"name":"programmed cell death, bone marrow cells","type":"exact"}],"termid":"GO:0071839"}


id: GO:0000028
data:
  {"annotated_genes":["SJAG_04524","SJAG_04746","SJAG_03617","SJAG_01296","SJAG_03798","SJAG_04998","SJAG_02340","SJAG_02749","SJAG_02479","SJAG_01169","SJAG_02184","SJAG_02335","SJAG_00572","SJAG_03424","SJAG_02803","SJAG_01548"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71724,73460,74985,75132,76265,76335,76459,76487,76979,78396,78409,78987,96576,120488],"is_not":false,"summary":null,"term":"GO:0000028"},{"annotations":[114926,74653],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034462"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of constituent RNAs and proteins to form the small ribosomal subunit.","definition_xrefs":["PMID:30467428","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-RNA complex assembly","termid":"GO:0022618"},{"relation_name":"part_of","term_name":"ribosome assembly","termid":"GO:0042255"},{"relation_name":"part_of","term_name":"ribosomal small subunit biogenesis","termid":"GO:0042274"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00572":null,"SJAG_01169":null,"SJAG_01296":null,"SJAG_01548":null,"SJAG_02184":null,"SJAG_02335":null,"SJAG_02340":null,"SJAG_02479":null,"SJAG_02749":null,"SJAG_02803":null,"SJAG_03424":null,"SJAG_03617":null,"SJAG_03798":null,"SJAG_04524":null,"SJAG_04746":null,"SJAG_04998":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150","GO:0042254"],"is_obsolete":false,"name":"ribosomal small subunit assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"30S ribosomal subunit assembly","type":"narrow"},{"name":"40S ribosomal subunit assembly","type":"narrow"}],"termid":"GO:0000028","terms_by_termid":{"GO:0000028":null,"GO:0034462":null}}


id: GO:0042480
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of eye photoreceptor development.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell development","termid":"GO:0010721"},{"relation_name":"is_a","term_name":"regulation of eye photoreceptor cell development","termid":"GO:0042478"},{"relation_name":"negatively_regulates","term_name":"eye photoreceptor cell development","termid":"GO:0042462"}],"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 eye photoreceptor cell development","synonyms":[{"name":"down regulation of eye photoreceptor cell development","type":"exact"},{"name":"down-regulation of eye photoreceptor cell development","type":"exact"},{"name":"downregulation of eye photoreceptor cell development","type":"exact"},{"name":"inhibition of eye photoreceptor cell development","type":"narrow"},{"name":"negative regulation of eye photoreceptor development","type":"exact"}],"termid":"GO:0042480"}


id: GO:0043696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a specialized structure (cell, tissue or organ) loses structural or functional features that characterize it in the mature organism, or some other relatively stable phase of the organism's life history. Under certain conditions, these structures can revert back to the features of their ancestors.","definition_xrefs":["GOC:dph","GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process","termid":"GO:0032502"}],"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":"dedifferentiation","secondary_identifiers":["Wikipedia:Cellular_differentiation#Dedifferentiation"],"termid":"GO:0043696"}


id: PBO:0005281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-specific DNA binding protein Spt2 (predicted)","termid":"PBO:0005281"}


id: PBO:0089156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GATA-like domain protein","termid":"PBO:0089156"}


id: MONDO:1011650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pentalogy of Fallot, non-human animal","secondary_identifiers":["OMIA:001857"],"termid":"MONDO:1011650","xrefs":{"Monarch":{"xref_id":"1011650"}}}


id: PBO:0061616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nudix hydrolase 2","termid":"PBO:0061616"}


id: GO:0016563
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any transcription regulator activity required for initiation or upregulation of transcription.","definition_xrefs":["ISBN:0124325653","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription activator activity (obsolete GO:0016563)","synonyms":[{"name":"transcription activating factor","type":"narrow"},{"name":"transcription activator activity","type":"exact"},{"name":"transcriptional activator activity","type":"exact"}],"termid":"GO:0016563"}


id: PBO:0057881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3185","termid":"PBO:0057881"}


id: GO:0052145
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism on or near its host organism towards a lower level of a physical stimulus involved in energy generation, such as light, oxygen, and oxidizable substrates. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative energy taxis on or near host (obsolete GO:0052145)","termid":"GO:0052145"}


id: PBO:0053853
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 1122","termid":"PBO:0053853"}


id: GO:0018450
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: myrtenol + O2 + 2 H+ + 2 e- = 2 H2O + myrtenal.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete myrtenol dehydrogenase activity (obsolete GO:0018450)","termid":"GO:0018450"}


id: PBO:0034263
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_synaptic_terminal_in","termid":"PBO:0034263"}


id: PBO:0055003
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 2418","termid":"PBO:0055003"}


id: PBO:0082831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Conserved ribosomal protein P0 of the ribosomal stalk; involved in interaction between translational elongation factors and the ribosome; phosphorylated on serine 302; homologous to mammalian ribosomal protein LP0 and bacterial L10","termid":"PBO:0082831"}


id: PBO:0052077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"katanin regulatory subunit B1 like 1 pseudogene 2","termid":"PBO:0052077"}


id: PR:P36209
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sts1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P36209"],"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":"delta(24(24(1)))-sterol reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20G4.07c","synonyms":[{"name":"C-24(28) sterol reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-sts1","type":"exact"},{"name":"sterol Delta(24(28))-reductase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P36209"}


id: PR:P87120
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ribonuclease P protein subunit p30 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00574","PANTHER:PTHR13031:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease P protein subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A12.04c","secondary_identifiers":["UniProtKB:P87120"],"synonyms":[{"name":"Spom972h-RPP30","type":"exact"}],"termid":"PR:P87120"}


id: GO:0018993
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The determination of sex and sexual phenotypes in an organism's soma.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sex determination","termid":"GO:0007530"},{"relation_name":"part_of","term_name":"multicellular organism development","termid":"GO:0007275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"somatic sex determination","termid":"GO:0018993"}


id: PBO:0060843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurofilament medium chain","termid":"PBO:0060843"}


id: FYPO:0004474
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the mitotic cell cycle DNA replication checkpoint is normal (i.e. indistinguishable from wild type). The mitotic DNA replication checkpoint normally prevents the initiation of mitosis until DNA replication is complete.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic cell cycle checkpoint","termid":"FYPO:0001703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257","FYPO:0000298"],"is_obsolete":false,"name":"normal mitotic cell cycle DNA replication checkpoint","synonyms":[{"name":"normal DNA replication checkpoint during mitotic cell cycle","type":"exact"},{"name":"normal DNA replication checkpoint during vegetative growth","type":"exact"},{"name":"normal mitotic DNA replication checkpoint activation","type":"exact"}],"termid":"FYPO:0004474"}


id: PBO:0054502
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 1902","termid":"PBO:0054502"}


id: GO:0031040
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bounded organelle of ciliated protozoan cells that contains a diploid copy of the cell's complete genome. Sections of contiguous sequence in the macronucleus are often interrupted by internal eliminated sequences (IES), and may be permuted, in micronuclei. Genic transcription is not found in micronuclei. Some ciliate species may contain multiple micronuclei per cell.","definition_xrefs":["GOC:ns"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"micronucleus","secondary_identifiers":["Wikipedia:Micronucleus"],"termid":"GO:0031040"}


id: PBO:0082283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP4A phosphorylase; bifunctional diadenosine 5',5'''-P1,P4-tetraphosphate phosphorylase and ADP sulfurylase involved in catabolism of bis(5'-nucleosidyl) tetraphosphates; catalyzes phosphorolysis of dinucleoside oligophosphates, cleaving substrates' alpha/beta-anhydride bond and introducing Pi into the beta-position of the corresponding NDP formed; protein abundance increases under DNA replication stress; APA1 has a paralog, APA2, that arose from the whole genome duplication","termid":"PBO:0082283"}


id: PBO:0029675
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_elongated_multinucleate_aseptate_vegetative_cell","termid":"PBO:0029675"}


id: PBO:0083074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dinucleoside triphosphate hydrolase; has similarity to the tumor suppressor FHIT and belongs to the histidine triad (HIT) superfamily of nucleotide-binding proteins","termid":"PBO:0083074"}


id: GO:2000825
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of androgen receptor activity.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transcription by RNA polymerase II","termid":"GO:0006357"},{"relation_name":"is_a","term_name":"regulation of signaling receptor activity","termid":"GO:0010469"},{"relation_name":"is_a","term_name":"positive regulation of DNA-binding transcription factor activity","termid":"GO:0051091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006351","GO:0006355","GO:0010467","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of androgen receptor activity","termid":"GO:2000825"}


id: PBO:0034112
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-immediately_precedes","termid":"PBO:0034112"}


id: PBO:0000590
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates pmc1","termid":"PBO:0000590"}


id: PBO:0078506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tribbles pseudokinase 3","termid":"PBO:0078506"}


id: GO:0016727
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a CH2 group acts as a hydrogen or electron donor and reduces an oxygen molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups","termid":"GO:0016725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on CH or CH2 groups, oxygen as acceptor","secondary_identifiers":["EC:1.17.3.-"],"termid":"GO:0016727"}


id: FYPO:0001144
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 Man8GlcNAc2 measured in a cell is lower than normal. Man8GlcNAc2 is any N-glycan that consists of a branched ten-membered mannooligosaccharide containing eight D-mannosyl residues and two N-acetylglucosamine residues.","definition_xrefs":["PomBase:mah","CHEBI:64052","CHEBI:64048","PMID:12686557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased polysaccharide level during vegetative growth","termid":"FYPO:0001080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased Man8GlcNAc level","synonyms":[{"name":"decreased Man8GlcNAc accumulation","type":"related"},{"name":"decreased Man8GlcNAc level during mitotic cell cycle","type":"related"},{"name":"decreased Man8GlcNAc level during vegetative growth","type":"exact"},{"name":"decreased Man8GlcNAc2 level","type":"exact"},{"name":"decreased cellular Man8GlcNAc level","type":"exact"},{"name":"reduced Man8GlcNAc level","type":"exact"}],"termid":"FYPO:0001144"}


id: PBO:0052770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 62","termid":"PBO:0052770"}


id: MONDO:0000157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete episodic pain syndrome, familial (obsolete MONDO:0000157)","termid":"MONDO:0000157","xrefs":{"Monarch":{"xref_id":"0000157"}}}


id: MONDO:0018774
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete erythrokeratodermia-cardiomyopathy syndrome (obsolete MONDO:0018774)","secondary_identifiers":["GARD:21950"],"termid":"MONDO:0018774","xrefs":{"Monarch":{"xref_id":"0018774"}}}


id: PR:C6Y4C2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4C2"],"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":"sporulation-specific protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16C6.14","synonyms":[{"name":"Spom972h-spo2","type":"exact"}],"termid":"PR:C6Y4C2"}


id: PBO:0045798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endothelin 2","termid":"PBO:0045798"}


id: FYPO:0003439
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 a cell forms a septum that has branches. For example, the septum may be Y-shaped.","definition_xrefs":["PMID:24798735","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal septum morphology during vegetative growth","termid":"FYPO:0002023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000032"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000032"],"is_obsolete":false,"name":"branched septum","synonyms":[{"name":"branched septum during mitotic cell cycle","type":"related"},{"name":"branched septum during vegetative growth","type":"exact"}],"termid":"FYPO:0003439"}


id: FYPO:0008002
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype observed during mating in which a cell lyses, i.e. the plasma membrane ruptures and cytoplasm is lost, during the process of cell fusion that occurs during mating. Note that in fission yeast cell lysis, the integrity of the cell wall is also compromised.","definition_xrefs":["PMID:35673994","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell lysis","termid":"FYPO:0002488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"cell lysis during mating","synonyms":[{"name":"cell lysis during cell fusion","type":"related"},{"name":"cell lysis during cellular fusion","type":"related"}],"termid":"FYPO:0008002"}


id: PBO:0000207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxidoreductase (predicted)","termid":"PBO:0000207"}


id: PBO:0067505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 645, pseudogene","termid":"PBO:0067505"}


id: PBO:0052797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 37","termid":"PBO:0052797"}


id: GO:0048613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring during the embryonic phase, by which the anatomical structures of the ectodermal digestive tract are generated and organized.","definition_xrefs":["GOC:jid","GOC:rc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"embryonic digestive tract morphogenesis","termid":"GO:0048557"},{"relation_name":"part_of","term_name":"ectodermal digestive tract morphogenesis","termid":"GO:0048567"},{"relation_name":"part_of","term_name":"embryonic ectodermal digestive tract development","termid":"GO:0048611"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"embryonic ectodermal digestive tract morphogenesis","synonyms":[{"name":"embryonic ectodermal gut morphogenesis","type":"related"}],"termid":"GO:0048613"}


id: PBO:0072913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-phase cyclin A associated protein in the ER","termid":"PBO:0072913"}


id: PBO:0074497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNAP25 antisense RNA 1","termid":"PBO:0074497"}


id: GO:0060903
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of meiosis I, a cell cycle process comprising the steps by which a cell progresses through the first phase of meiosis, in which cells divide and homologous chromosomes are paired and segregated from each other, producing two daughter cells.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of meiotic nuclear division","termid":"GO:0045836"},{"relation_name":"is_a","term_name":"regulation of meiosis I","termid":"GO:0060631"},{"relation_name":"positively_regulates","term_name":"meiosis I","termid":"GO:0007127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0140013"},{"rel_name":"positively_regulates","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0140013","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"positive regulation of meiosis I","termid":"GO:0060903"}


id: PBO:0038541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 14B","termid":"PBO:0038541"}


id: PBO:0044457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 36, pseudogene","termid":"PBO:0044457"}


id: GO:0031545
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: peptidyl L-proline + 2-oxoglutarate + O2 = peptidyl trans-4-hydroxy-L-proline + succinate + CO2.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-proline dioxygenase activity","termid":"GO:0031543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"peptidyl-proline 4-dioxygenase activity","secondary_identifiers":["Reactome:R-HSA-1234165","Reactome:R-HSA-1234177","Reactome:R-HSA-1234166","Reactome:R-HSA-1234179","Reactome:R-HSA-1234181","Reactome:R-HSA-1234173","RHEA:63484"],"synonyms":[{"name":"HIF-type prolyl 4-hydroxylase","type":"narrow"},{"name":"prolyl 4-hydroxylase","type":"broad"}],"termid":"GO:0031545"}


id: MONDO:0014102
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the SPRY4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kallmann syndrome","termid":"MONDO:0018800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 17 with or without anosmia","secondary_identifiers":["GARD:15928","DOID:0090079","ICD10CM:E23.0","OMIM:615266","MEDGEN:815301","UMLS:C3808971"],"synonyms":[{"name":"HH17","type":"related"},{"name":"SPRY4 hypogonadotropic hypogonadism","type":"exact"},{"name":"hypogonadotropic hypogonadism 17 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in SPRY4","type":"exact"}],"termid":"MONDO:0014102","xrefs":{"Monarch":{"xref_id":"0014102"}}}


id: PBO:0001588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterotrimeric G protein alpha-2 subunit Gpa2","termid":"PBO:0001588"}


id: GO:0000242
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A network of small fibers that surrounds the centrioles in cells; contains the microtubule nucleating activity of the centrosome.","definition_xrefs":["GOC:clt","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"centrosome","termid":"GO:0005813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005575","GO:0015630"],"is_obsolete":false,"name":"pericentriolar material","termid":"GO:0000242"}


id: PBO:0070496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 31","termid":"PBO:0070496"}


id: MONDO:0001991
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant germ cell tumor that arises from the pericardium.","definition_xrefs":["NCIT:C5371"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart cancer","termid":"MONDO:0001340"},{"relation_name":"is_a","term_name":"extragonadal germ cell cancer","termid":"MONDO:0003113"},{"relation_name":"is_a","term_name":"cardiac germ cell tumor","termid":"MONDO:0020589"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0004992"],"is_obsolete":false,"name":"malignant cardiac germ cell tumor","secondary_identifiers":["UMLS:C1334566","DOID:14535","MEDGEN:233143"],"synonyms":[{"name":"malignant Cardiac germ cell neoplasm","type":"exact"},{"name":"malignant Cardiac germ cell tumor","type":"exact"},{"name":"malignant Cardiac germ cell tumour","type":"exact"},{"name":"malignant germ cell neoplasm of heart","type":"exact"},{"name":"malignant germ cell neoplasm of the heart","type":"exact"},{"name":"malignant germ cell tumor of heart","type":"exact"},{"name":"malignant germ cell tumor of the heart","type":"exact"},{"name":"malignant germ cell tumour of heart","type":"exact"},{"name":"malignant germ cell tumour of the heart","type":"exact"},{"name":"malignant heart germ cell neoplasm","type":"exact"},{"name":"malignant heart germ cell tumor","type":"exact"},{"name":"malignant heart germ cell tumour","type":"exact"}],"termid":"MONDO:0001991","xrefs":{"Monarch":{"xref_id":"0001991"}}}


id: MONDO:0000194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Otofaciocervical syndrome (obsolete MONDO:0000194)","termid":"MONDO:0000194","xrefs":{"Monarch":{"xref_id":"0000194"}}}


id: PR:C6Y4A4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC688.16 gene.","definition_xrefs":["UniProtKB:C6Y4A4","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 membrane protein C688.16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC688.16","synonyms":[{"name":"Spom972h-SPAC688.16","type":"exact"}],"termid":"PR:C6Y4A4"}


id: GO:0035373
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a chondroitin sulfate proteoglycan, any proteoglycan containing chondroitin sulfate as the glycosaminoglycan carbohydrate unit.","definition_xrefs":["GOC:kmv","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteoglycan binding","termid":"GO:0043394"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"chondroitin sulfate proteoglycan binding","termid":"GO:0035373"}


id: MONDO:0015183
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Short bowel syndrome is an intestinal failure due to either a congenital defect, intestinal infarction or extensive surgical resection of the intestinal tract that results in a functional small intestine of less than 200cm in length and is characterized by diarrhea, nutrient malabsoption, bowel dilation and dysmobility.","definition_xrefs":["Orphanet:104008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"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":"short bowel syndrome","secondary_identifiers":["DOID:10605","ICD9:579.3","NANDO:2100274","MESH:D012778","UMLS:C0036992","icd11.foundation:780637678","GARD:1502","MedDRA:10049416","NCIT:C99059","NORD:1708","NANDO:2200944","SCTID:26629001","MEDGEN:19966"],"synonyms":[{"name":"acquired short bowel syndrome","type":"exact"},{"name":"short gut syndrome","type":"exact"}],"termid":"MONDO:0015183","xrefs":{"Monarch":{"xref_id":"0015183"}}}


id: PATO:0001407
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A nucleate quality inhering in a bearer by virtue of the bearer's having one nucleus.","definition_xrefs":["Biology-online:Biology-online"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleated","termid":"PATO:0002505"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mononucleate","termid":"PATO:0001407"}


id: PBO:0044225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortexin domain containing 2","termid":"PBO:0044225"}


id: GO:0007136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle phase which is the first stage of meiosis II and during which chromosomes condense and the two daughter centrioles and their asters migrate toward the poles of the cell.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prophase","termid":"GO:0051324"},{"relation_name":"is_a","term_name":"meiosis II cell cycle phase","termid":"GO:0098765"}],"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":"meiotic prophase II","termid":"GO:0007136"}


id: PBO:0084137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity copper transporter of the plasma membrane; acts as a trimer; gene is disrupted by a Ty2 transposon insertion in many laboratory strains of S. cerevisiae","termid":"PBO:0084137"}


id: MONDO:1012264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"androgen insensitivity syndrome, non-human animal","termid":"MONDO:1011919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"androgen insensitivity syndrome, dog","secondary_identifiers":["OMIA:000991-9615"],"synonyms":[{"name":"AIS, dog","type":"exact"}],"termid":"MONDO:1012264","xrefs":{"Monarch":{"xref_id":"1012264"}}}


id: PBO:0042666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule 22, pseudogene","termid":"PBO:0042666"}


id: GO:0006997
data:
  {"annotated_genes":["SJAG_00810","SJAG_01467","SJAG_02210","SJAG_00900","SJAG_03219","SJAG_01050","SJAG_01422","SJAG_04271","SJAG_00840","SJAG_01242","SJAG_01370","SJAG_04039","SJAG_05207","SJAG_03892","SJAG_03891","SJAG_01075","SJAG_02778","SJAG_01356","SJAG_03982","SJAG_04883","SJAG_01906","SJAG_03200","SJAG_03783","SJAG_04936","SJAG_02286","SJAG_04509","SJAG_04578","SJAG_02763","SJAG_01613","SJAG_02737","SJAG_01579","SJAG_03844","SJAG_03313","SJAG_01745","SJAG_02045","SJAG_03593","SJAG_00934","SJAG_00416","SJAG_01834","SJAG_03182","SJAG_03491","SJAG_03073","SJAG_01460","SJAG_01833","SJAG_04464","SJAG_03449","SJAG_00680","SJAG_04972","SJAG_04319","SJAG_04489","SJAG_03592","SJAG_01263","SJAG_03940"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89573,92806,93198,101033,80387,118809,113318],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000742"},{"annotations":[95649,103260],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140515"},{"annotations":[89708,99498,100166,111757,94869,112169],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0101026"},{"annotations":[112309],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007077"},{"annotations":[121102,121058,121061],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0101024"},{"annotations":[99770,104967,121335,97779,102709,108394,121337,93156,121338,121336],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007084"},{"annotations":[105480],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0140516"},{"annotations":[93550,121066,114604,79912],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006998"},{"annotations":[72284,93157],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071765"},{"annotations":[80389],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048288"},{"annotations":[109554,105277,93761,111577,121263,107786],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071763"},{"annotations":[73854],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031468"},{"annotations":[109598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051292"},{"annotations":[75747,77810,82089,78694,77900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006999"},{"annotations":[74157,72692,93890,105911,109998,113962,115151],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000183"}]},"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 the nucleus.","definition_xrefs":["GOC:jl","GOC:dph","GOC:mah","GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle organization","termid":"GO:0006996"}],"gene_count":53,"genes_by_uniquename":{"SJAG_00416":null,"SJAG_00680":null,"SJAG_00810":null,"SJAG_00840":null,"SJAG_00900":null,"SJAG_00934":null,"SJAG_01050":null,"SJAG_01075":null,"SJAG_01242":null,"SJAG_01263":null,"SJAG_01356":null,"SJAG_01370":null,"SJAG_01422":null,"SJAG_01460":null,"SJAG_01467":null,"SJAG_01579":null,"SJAG_01613":null,"SJAG_01745":null,"SJAG_01833":null,"SJAG_01834":null,"SJAG_01906":null,"SJAG_02045":null,"SJAG_02210":null,"SJAG_02286":null,"SJAG_02737":null,"SJAG_02763":null,"SJAG_02778":null,"SJAG_03073":null,"SJAG_03182":null,"SJAG_03200":null,"SJAG_03219":null,"SJAG_03313":null,"SJAG_03449":null,"SJAG_03491":null,"SJAG_03592":null,"SJAG_03593":null,"SJAG_03783":null,"SJAG_03844":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03940":null,"SJAG_03982":null,"SJAG_04039":null,"SJAG_04271":null,"SJAG_04319":null,"SJAG_04464":null,"SJAG_04489":null,"SJAG_04509":null,"SJAG_04578":null,"SJAG_04883":null,"SJAG_04936":null,"SJAG_04972":null,"SJAG_05207":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"nucleus organization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"PMID:21802294":null,"PMID:24184107":null,"PMID:26774782":null,"PMID:28954740":null,"PMID:32243490":null},"secondary_identifiers":["GO:0048287"],"synonyms":[{"name":"nuclear morphology","type":"related"},{"name":"nuclear organisation","type":"exact"},{"name":"nuclear organization","type":"exact"},{"name":"nuclear organization and biogenesis","type":"related"},{"name":"nucleus organization and biogenesis","type":"related"}],"termid":"GO:0006997","terms_by_termid":{"GO:0000183":null,"GO:0000742":null,"GO:0006998":null,"GO:0006999":null,"GO:0007077":null,"GO:0007084":null,"GO:0031468":null,"GO:0048288":null,"GO:0051292":null,"GO:0071763":null,"GO:0071765":null,"GO:0101024":null,"GO:0101026":null,"GO:0140515":null,"GO:0140516":null}}


id: MONDO:0004036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0004036 (obsolete MONDO:0004036)","termid":"MONDO:0004036","xrefs":{"Monarch":{"xref_id":"0004036"}}}


id: MONDO:0003947
data:
  {"annotated_genes":["SJAG_02528"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011971"}]},"cv_name":"mondo","definition":"A primary immune deficiency disorder characterized by defective CD40 signaling; via B cells affecting class switch recombination (CSR) and somatic hypermutation.","definition_xrefs":["Wikipedia:Hyper_IgM_syndrome"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperimmunoglobulin syndrome","termid":"MONDO:0002468"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02528":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":"hyper-IgM syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C3990","MESH:D053306","NCIT:C84783","OMIMPS:308230","NANDO:2200718","UMLS:C0272236","SCTID:82286005","ICD9:279.05","DOID:0080544","MEDGEN:124420","NANDO:1200345"],"synonyms":[{"name":"hyperimmunoglobulin M syndrome","type":"related"},{"name":"immunodeficiency with hyper-IgM","type":"exact"}],"termid":"MONDO:0003947","terms_by_termid":{"MONDO:0011971":null},"xrefs":{"Monarch":{"xref_id":"0003947"}}}


id: PBO:0045467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dopamine receptor D4","termid":"PBO:0045467"}


id: PBO:0046055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit F pseudogene 3","termid":"PBO:0046055"}


id: MONDO:0024297
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A collective term for nutritional disorders resulting from poor absorption or nutritional imbalance, and metabolic disorders resulting from defects in biosynthesis (ANABOLISM) or breakdown (CATABOLISM) of endogenous substances.","definition_xrefs":["MESH:D009750"],"gene_count":0,"genotype_count":0,"name":"obsolete nutritional or metabolic disease (obsolete MONDO:0024297)","secondary_identifiers":["ICD10CM:E00-E90"],"termid":"MONDO:0024297","xrefs":{"Monarch":{"xref_id":"0024297"}}}


id: PR:Q9UR09
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- psu1 gene.","definition_xrefs":["UniProtKB:Q9UR09","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":"secreted beta-glucosidase PSU1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1002.13c","synonyms":[{"name":"Spom972h-psu1","type":"exact"},{"name":"cell wall synthesis protein psu1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UR09"}


id: FYECO:0000093
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which lithium ions were added to the assay buffer in excess compared to standard assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ ions","termid":"FYECO:0000030"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ Li ions","synonyms":[{"name":"lithium ions added","type":"exact"}],"termid":"FYECO:0000093"}


id: MONDO:0024271
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A parasitic helminthiasis infectious disease that involves the intestine.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"helminthiasis","termid":"MONDO:0004664"},{"relation_name":"is_a","term_name":"parasitic intestinal disorder","termid":"MONDO:0024270"}],"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":"intestinal helminthiasis","secondary_identifiers":["MEDGEN:87591","MESH:C531698","UMLS:C0348287","SCTID:26249004"],"synonyms":[{"name":"intestine parasitic helminthiasis infectious disease","type":"exact"}],"termid":"MONDO:0024271","xrefs":{"Monarch":{"xref_id":"0024271"}}}


id: GO:0001324
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.) occurring in non-dividing cells as they age as a result of oxidative stress, where the change varies according to the age of the cell or organism.","definition_xrefs":["GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete age-dependent response to oxidative stress involved in chronological cell aging (obsolete GO:0001324)","synonyms":[{"name":"age-dependent response to oxidative stress during chronological cell ageing","type":"related"},{"name":"age-dependent response to oxidative stress during chronological cell aging","type":"related"}],"termid":"GO:0001324"}


id: PBO:0000930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho guanine nucleotide exchange factor (predicted)","termid":"PBO:0000930"}


id: GO:0044101
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (3R)-citramalyl-CoA = pyruvate + acetyl-CoA.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxo-acid-lyase activity","termid":"GO:0016833"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"(3R)-citramalyl-CoA lyase activity","secondary_identifiers":["EC:4.1.3.46","MetaCyc:RXN-13231","RHEA:38275"],"synonyms":[{"name":"Ccl","type":"related"},{"name":"R-citramalyl-CoA lyase activity","type":"exact"}],"termid":"GO:0044101"}


id: PBO:0091003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF4451 family conserved fungal protein","termid":"PBO:0091003"}


id: PBO:0085221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Palmitoyltransferase with autoacylation activity; required for palmitoylation of amino acid permeases containing a C-terminal Phe-Trp-Cys site; required for modification of Chs3p; member of the DHHC family of putative palmitoyltransferases","termid":"PBO:0085221"}


id: PBO:0005032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase Gem1 (predicted)","termid":"PBO:0005032"}


id: GO:0033574
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 testosterone stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"relation_name":"is_a","term_name":"response to ketone","termid":"GO:1901654"}],"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 testosterone","synonyms":[{"name":"response to testosterone stimulus","type":"exact"}],"termid":"GO:0033574"}


id: GO:1990899
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process following clipping in double-strand break processing of SPO11 induced breaks, where long-tract single-stranded 3'-end DNA is generated from naked (SPO11 has been removed) 5' ends.","definition_xrefs":["PMID:26130711"],"gene_count":0,"genotype_count":0,"name":"obsolete meiotic DNA double-strand break resectioning (obsolete GO:1990899)","termid":"GO:1990899"}


id: SO:0000101
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transposon or insertion sequence. An element that can insert in a variety of DNA sequences.","direct_ancestors":[{"relation_name":"is_a","term_name":"integrated_mobile_genetic_element","termid":"SO:0001039"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transposable_element","secondary_identifiers":["http://en.wikipedia.org/wiki/Transposable_element"],"synonyms":[{"name":"transposable element","type":"exact"},{"name":"transposon","type":"exact"}],"termid":"SO:0000101"}


id: GO:0014916
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that modulates the force with which blood travels through the lungs. The process is controlled by a balance of processes that increase pressure and decrease pressure.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of blood pressure","termid":"GO:0008217"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of lung blood pressure","synonyms":[{"name":"regulation of pulmonary blood pressure","type":"exact"}],"termid":"GO:0014916"}


id: PBO:0039529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD33B pseudogene 10","termid":"PBO:0039529"}


id: MONDO:0014815
data:
  {"annotated_genes":["SJAG_01991"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87600],"is_not":false,"summary":null,"term":"MONDO:0014815"}]},"cv_name":"mondo","definition":"Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LMAN2L gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01991":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0006025","MONDO:0037792"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 52","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:616887","GARD:22572","DOID:0081215","MEDGEN:903181","UMLS:C4225168"],"synonyms":[{"name":"LMAN2L autosomal recessive non-syndromic intellectual disability","type":"exact"},{"name":"MRT52","type":"exact"},{"name":"autosomal recessive non-syndromic intellectual disability caused by mutation in LMAN2L","type":"exact"},{"name":"intellectual developmental disorder, autosomal recessive 52","type":"exact"},{"name":"intellectual disability, autosomal recessive 52","type":"exact"},{"name":"intellectual disability, autosomal recessive type 52","type":"exact"},{"name":"mental retardation, autosomal recessive 52","type":"exact"},{"name":"mental retardation, autosomal recessive type 52","type":"exact"}],"termid":"MONDO:0014815","terms_by_termid":{"MONDO:0014815":null},"xrefs":{"Monarch":{"xref_id":"0014815"}}}


id: PBO:0064553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POM121 transmembrane nucleoporin like 15, pseudogene","termid":"PBO:0064553"}


id: PBO:0089401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage and polyadenylation factor complex RNA-binding subunit Pcf11","termid":"PBO:0089401"}


id: PBO:0051844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iroquois homeobox 1","termid":"PBO:0051844"}


id: GO:1990576
data:
  {"annotated_genes":["SJAG_01699"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[117395],"is_not":false,"summary":null,"term":"GO:1990576"}]},"cv_name":"molecular_function","definition":"Combining with an extracellular glucose molecule 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:15667320"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01699":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled glucose receptor activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"G-protein coupled glucose receptor activity","type":"exact"}],"termid":"GO:1990576","terms_by_termid":{"GO:1990576":null}}


id: MONDO:0016283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leiomyosarcoma of the cervix uteri is a rare, malignant mesenchymal tumor of smooth muscle origin, macroscopically appearing as a large, poorly circumscribed mass, often protruding from the cervical canal or expanding it circumferentially. The most common presenting symptoms are vaginal discharge or bleeding, pain in the lower abdomen and a bulky cervical mass. There is a reported tendency to metastatsize hematogenously, especially to the lungs, peritoneum, bones and the liver.","definition_xrefs":["Orphanet:213807"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyosarcoma","termid":"MONDO:0005058"},{"relation_name":"is_a","term_name":"sarcoma of cervix uteri","termid":"MONDO:0016280"}],"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":"leiomyosarcoma of the cervix uteri","secondary_identifiers":["GARD:20495","ONCOTREE:CELI","SCTID:763771009","UMLS:C4289817","NCIT:C128047","ICD10CM:C53.0","MEDGEN:927349"],"synonyms":[{"name":"CELI","type":"related"},{"name":"cervical leiomyosarcoma","type":"exact"},{"name":"leiomyosarcoma of uterine cervix","type":"exact"},{"name":"uterine cervix leiomyosarcoma","type":"exact"}],"termid":"MONDO:0016283","xrefs":{"Monarch":{"xref_id":"0016283"}}}


id: PBO:0043881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CREB/ATF bZIP transcription factor","termid":"PBO:0043881"}


id: PBO:0072208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S18 pseudogene 7","termid":"PBO:0072208"}


id: GO:0086098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An angiotensin receptor signaling pathway which contributes to a circulatory system process carried out by the heart.","definition_xrefs":["PMID:17376402","GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiotensin-activated signaling pathway","termid":"GO:0038166"},{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway involved in heart process","termid":"GO:0086103"}],"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":"angiotensin-activated signaling pathway involved in heart process","synonyms":[{"name":"angiotensin receptor signaling pathway involved in heart process","type":"exact"},{"name":"angiotensin receptor signalling pathway involved in heart process","type":"exact"},{"name":"angiotensin-mediated signaling pathway involved in heart process","type":"related"}],"termid":"GO:0086098"}


id: GO:0046214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of enterobactin, a catechol-derived siderochrome of Enterobacteria; enterobactin (N',N',N''-(2,6,10-trioxo-1,5,9-triacyclodecane-3,7,11-triyl)tris(2,3-dihydroxy)benzamide) is a self-triester of 2,3-dihydroxy-N-benzoyl-L-serine and a product of the shikimate pathway.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enterobactin metabolic process","termid":"GO:0009238"},{"relation_name":"is_a","term_name":"catechol-containing compound catabolic process","termid":"GO:0019614"},{"relation_name":"is_a","term_name":"polyketide catabolic process","termid":"GO:0030640"},{"relation_name":"is_a","term_name":"siderophore catabolic process","termid":"GO:0046215"},{"relation_name":"is_a","term_name":"lactone catabolic process","termid":"GO:1901335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"enterobactin catabolic process","synonyms":[{"name":"enterobactin breakdown","type":"exact"},{"name":"enterobactin catabolism","type":"exact"},{"name":"enterobactin degradation","type":"exact"}],"termid":"GO:0046214"}


id: PBO:0044929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol kinase eta","termid":"PBO:0044929"}


id: PBO:0090084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly protein Cox11","termid":"PBO:0090084"}


id: GO:0070369
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains beta-catenin and TCF7L2 (TCF4), binds to the TCF DNA motif within a promoter element, and is involved in the regulation of WNT target gene transcription.","definition_xrefs":["GOC:BHF","PMID:9065402","GOC:rl","PMID:9065401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catenin-TCF7L2 complex","termid":"GO:0071664"},{"relation_name":"is_a","term_name":"beta-catenin-TCF complex","termid":"GO:1990907"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"beta-catenin-TCF7L2 complex","synonyms":[{"name":"beta-catenin-TCF4 complex","type":"exact"}],"termid":"GO:0070369"}


id: GO:1990080
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the biogenic amine 2-phenylethylamine to initiate a change in cell activity.","definition_xrefs":["PMID:16878137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled amine receptor activity","termid":"GO:0008227"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"2-phenylethylamine receptor activity","synonyms":[{"name":"beta-phenylethylamine receptor activity","type":"exact"}],"termid":"GO:1990080"}


id: MONDO:0024460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Herpesviridae infections (obsolete MONDO:0024460)","termid":"MONDO:0024460","xrefs":{"Monarch":{"xref_id":"0024460"}}}


id: PBO:0050453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homer scaffold protein 1","termid":"PBO:0050453"}


id: PBO:0062648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 12 subfamily D member 2","termid":"PBO:0062648"}


id: GO:0015528
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: lactose(out) + H+(out) = lactose(in) + H+(in).","definition_xrefs":["TC:2.A.1.1.9","TC:2.A.1.5.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate:proton symporter activity","termid":"GO:0005351"},{"relation_name":"is_a","term_name":"lactose transmembrane transporter activity","termid":"GO:0015155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"lactose:proton symporter activity","synonyms":[{"name":"lactose, galactose:hydrogen symporter activity","type":"broad"},{"name":"lactose:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015528"}


id: PBO:0084086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Guanine nucleotide exchange factor for Gpa1p; amplifies G protein signaling; functions as a chaperone under ATP-depleted oxidative stress conditions; subunit of GET complex, involved in ATP dependent Golgi to ER trafficking and insertion of tail-anchored (TA) proteins into ER membrane under non-stress conditions; binds as dimer to transmembrane domain (TMD) cargo, shielding TMDs from aqueous solvent; protein abundance increases under DNA replication stress","termid":"PBO:0084086"}


id: PBO:0113188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low-affinity inorganic phosphate (Pi) transporter; acts upstream of Pho81p in regulation of PHO pathway; targeted to vacuole via AP-3 pathway; expression is independent of Pi concentration and Pho4p activity; contains 12 membrane-spanning segments; PHO87 has a paralog, PHO90, that arose from the whole genome duplication","termid":"PBO:0113188"}


id: FYPO:0006656
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the unwinding of G-quadruplex DNA structures occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromosome organization","termid":"FYPO:0000641"},{"relation_name":"is_a","term_name":"abnormal cellular component organization during vegetative growth","termid":"FYPO:0001353"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000641","FYPO:0005447","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased G-quadruplex DNA unwinding","synonyms":[{"name":"decreased G-quadruplex DNA unwinding during mitotic cell cycle","type":"related"},{"name":"decreased G-quadruplex DNA unwinding during vegetative growth","type":"exact"},{"name":"decreased G-quartet DNA unwinding","type":"exact"},{"name":"decreased G4 DNA unwinding","type":"exact"},{"name":"reduced G-quadruplex DNA unwinding","type":"exact"}],"termid":"FYPO:0006656"}


id: PBO:0085742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in translation inhibition and nonsense-mediated decay; interacts with cap binding protein Cdc33p and with Nam7p; localizes to P-bodies upon glucose starvation; mRNA abundance regulated by mRNA decay factors; EBS1 has a paralog, EST1, that arose from the whole genome duplication","termid":"PBO:0085742"}


id: MONDO:0009148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare congenital ectodermal dysplasia syndrome with a range of signs and symptoms including cleft lip or palate, mental retardation and various forms of ectodermal dysplasia. Additional symptoms may include fused eyelids, absent nails, delayed bone growth and dry skin. It is believed that this syndrome follows an autosomal dominant pattern of inheritance with incomplete penetrance, and caused by a mutation affecting the TP63 gene","definition_xrefs":["Wikipedia:Rosselli%E2%80%93Gulienetti_syndrome"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","termid":"MONDO:0007124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0005093"],"is_obsolete":false,"name":"Rosselli-Gulienetti syndrome","secondary_identifiers":["UMLS:C0796139","icd11.foundation:1430451924","MEDGEN:163221","MESH:C563117","Orphanet:90339","OMIM:225000"],"synonyms":[{"name":"Rosselli-Gulienetti syndrome","type":"exact"}],"termid":"MONDO:0009148","xrefs":{"Monarch":{"xref_id":"0009148"}}}


id: PBO:0113274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"[PIN(+)] prion, named for [PSI+] INducibility; an infectious protein conformation that is generally an ordered protein aggregate","termid":"PBO:0113274"}


id: PBO:0070458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L4 pseudogene 1","termid":"PBO:0070458"}


id: GO:0071152
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex formed by the association of the guanine nucleotide exchange factor synembrin with the alpha(q) subunit of a heterotrimeric G protein.","definition_xrefs":["PMID:12509430","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"part_of","term_name":"intracellular anatomical structure","termid":"GO:0005622"}],"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":"G-protein alpha(q)-synembrin complex","synonyms":[{"name":"Ric-8A G(q) alpha subunit complex","type":"narrow"}],"termid":"GO:0071152"}


id: GO:0097086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whereby a relatively unspecialized cell acquires specialized features of an amniotic stem cell. An amniotic stem cell is a mesenchymal stem cell extracted from amniotic fluid. Amniotic stem cells are able to differentiate into various tissue types such as skin, cartilage, cardiac tissue, nerves, muscle, and bone.","definition_xrefs":["GOC:yaf","PMID:20942606","Wikipedia:Amniotic_stem_cells","CL:0002639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchymal stem cell differentiation","termid":"GO:0072497"}],"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":"amniotic stem cell differentiation","termid":"GO:0097086"}


id: GO:0046304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 2-nitropropane, a clear, colorless liquid with a mild, fruity odor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-nitropropane metabolic process","termid":"GO:0018938"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"2-nitropropane catabolic process","synonyms":[{"name":"2-nitropropane breakdown","type":"exact"},{"name":"2-nitropropane catabolism","type":"exact"},{"name":"2-nitropropane degradation","type":"exact"}],"termid":"GO:0046304"}


id: PBO:0061902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opioid related nociceptin receptor 1","termid":"PBO:0061902"}


id: MONDO:0000731
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete peeling skin syndrome (obsolete MONDO:0000731)","termid":"MONDO:0000731","xrefs":{"Monarch":{"xref_id":"0000731"}}}


id: PBO:0090331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"candidate S. pombe Csi1 ortholog, syntenic position, intrinsically disordered protein","termid":"PBO:0090331"}


id: GO:0036508
data:
  {"annotated_genes":["SJAG_01858"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904380"}]},"cv_name":"biological_process","definition":"The removal of one or more alpha 1,2-linked mannose residues from a mannosylated protein.","definition_xrefs":["PMID:21062743","PMID:25092655","GOC:PARL","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein demannosylation","termid":"GO:0036507"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01858":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein alpha-1,2-demannosylation","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"glycoprotein mannose trimming","type":"related"},{"name":"mannose trimming","type":"broad"}],"termid":"GO:0036508","terms_by_termid":{"GO:1904380":null}}


id: MONDO:0011801
data:
  {"annotated_genes":["SJAG_04418"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87385],"is_not":false,"summary":null,"term":"MONDO:0011801"}]},"cv_name":"mondo","definition":"Spinocerebellar ataxia with axonal neuropathy type 1 is a rare, genetic neurological disorder characterized by a late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations in upper and lower extremities. Gaze nystagmus, cerebellar dysarthria, peripheral neuropathy, stepagge gait and pes cavus develop as disease progresses. Cerebellar atrophy (especially of the vermis) is present in all affected individuals. Additional reported manifestations include seizures, mild brain atrophy, mild hypercholesterolemia and borderline hypoalbuminemia.","definition_xrefs":["Orphanet:94124"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy","termid":"MONDO:0020771"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04418":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0005559","MONDO:0006025","MONDO:0021190","MONDO:0005066"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:607250","NORD:1730","UMLS:C4759870","GARD:10000","MESH:C537313","MEDGEN:1683470","DOID:0090115","SCTID:765091006"],"synonyms":[{"name":"SCAN1","type":"exact"},{"name":"Spinocerebellar Ataxia with Axonal Neuropathy","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia with axonal neuropathy","type":"broad"},{"name":"spinocerebellar ataxia autosomal recessive with axonal neuropathy","type":"related"},{"name":"spinocerebellar ataxia type 1 with axonal neuropathy","type":"exact"},{"name":"spinocerebellar ataxia with axonal neuropathy","type":"related"},{"name":"spinocerebellar ataxia with axonal neuropathy type 1","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy","type":"broad"},{"name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1","type":"exact"}],"termid":"MONDO:0011801","terms_by_termid":{"MONDO:0011801":null},"xrefs":{"Monarch":{"xref_id":"0011801"}}}


id: FYECO:0000190
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which DAPI was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000190 DAPI added (obsolete FYECO:0000190)","synonyms":[{"name":"4',6-diamidino-2-phenylindole added","type":"exact"}],"termid":"FYECO:0000190"}


id: MONDO:0013481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Monosomy 13q14 is a rare chromosomal anomaly syndrome, resulting from a partial deletion of the long arm of chromosome 13, characterized by developmental delay, variable degrees of intellectual disability, retinoblastoma and craniofacial dysmorphism (incl. micro/dolichocephaly, high and broad forehead, prominent eyebrows, thick, anteverted ear lobes, short nose with a broad nasal bridge and bulbous tip, prominent philtrum, large mouth with thin upper lip and thick, everted lower lip). Other features reported include high birth weight, macrocephaly, pinealoma, hepatomegaly, inguinal hernia and cryptorchidism.","definition_xrefs":["Orphanet:1587"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete chromosomal anomaly with cataract (obsolete MONDO:0020226)","termid":"MONDO:0020226"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 13","termid":"MONDO:0016911"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 13q14 deletion syndrome","secondary_identifiers":["MESH:C535484","NCIT:C36421","OMIM:613884","UMLS:C3151302","DOID:0060391","GARD:16570","MEDGEN:462652"],"synonyms":[{"name":"Del(13)(q14)","type":"exact"},{"name":"chromosome 13Q deletion syndrome","type":"related"},{"name":"chromosome 13q14 deletion syndrome","type":"exact"},{"name":"chromosome 13q14 deletion syndrome, isolated cases","type":"exact"},{"name":"del(13q14)","type":"exact"},{"name":"deletion 13q14","type":"exact"},{"name":"monosomy 13q14","type":"related"},{"name":"monosomy type 13q14","type":"exact"}],"termid":"MONDO:0013481","xrefs":{"Monarch":{"xref_id":"0013481"}}}


id: PR:Q9P6K6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- erv14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6K6"],"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":"ER-derived vesicles protein erv14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC30C2.05","synonyms":[{"name":"Spom972h-erv14","type":"exact"}],"termid":"PR:Q9P6K6"}


id: GO:0071330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a trehalose-6-phosphate stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to disaccharide stimulus","termid":"GO:0071324"},{"relation_name":"is_a","term_name":"response to trehalose-6-phosphate","termid":"GO:0080094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to trehalose-6-phosphate stimulus","termid":"GO:0071330"}


id: GO:0006065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of UDP-glucuronate, a substance composed of glucuronic acid in glycosidic linkage with uridine diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"},{"relation_name":"is_a","term_name":"UDP-glucuronate metabolic process","termid":"GO:0046398"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"UDP-glucuronate biosynthetic process","synonyms":[{"name":"UDP-glucuronate anabolism","type":"exact"},{"name":"UDP-glucuronate biosynthesis","type":"exact"},{"name":"UDP-glucuronate formation","type":"exact"},{"name":"UDP-glucuronate synthesis","type":"exact"}],"termid":"GO:0006065"}


id: FYPO:0002635
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the ubiquitination of one or more specific proteins, or of specific protein sites, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein modification during vegetative growth","termid":"FYPO:0000549"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal protein ubiquitination during vegetative growth","synonyms":[{"name":"normal protein ubiquitination during mitotic cell cycle","type":"related"},{"name":"normal protein ubiquitinylation during vegetative growth","type":"exact"},{"name":"normal protein ubiquitylation during vegetative growth","type":"exact"},{"name":"normal protein/peptide ubiquitination during vegetative growth","type":"exact"}],"termid":"FYPO:0002635"}


id: MONDO:1010827
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndactyly that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndactyly, non-human animal","termid":"MONDO:1010160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndactyly, cattle","secondary_identifiers":["OMIA:000963-9913"],"termid":"MONDO:1010827","xrefs":{"Monarch":{"xref_id":"1010827"}}}


id: GO:0035609
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of a C-terminal, gene-encoded glutamate residue from a protein.","definition_xrefs":["GOC:sp","PMID:21074048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-terminal protein amino acid modification","termid":"GO:0018410"},{"relation_name":"is_a","term_name":"protein deglutamylation","termid":"GO:0035608"}],"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":"C-terminal protein deglutamylation","synonyms":[{"name":"protein primary sequence deglutamylation","type":"exact"}],"termid":"GO:0035609"}


id: MONDO:1010278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent Mullerian duct syndrome that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"difference of sexual differentiation, non-human animal","termid":"MONDO:0700105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent Mullerian duct syndrome, non-human animal","secondary_identifiers":["OMIA:000791"],"termid":"MONDO:1010278","xrefs":{"Monarch":{"xref_id":"1010278"}}}


id: PBO:0043375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clustered mitochondria homolog pseudogene 5","termid":"PBO:0043375"}


id: PBO:0040682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCAS2 pre-mRNA processing factor","termid":"PBO:0040682"}


id: PBO:0084564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Membrane-embedded ubiquitin-protein ligase and retrotranslocase; ER and inner nuclear membrane localized RING-CH domain E3 ligase involved in ER-associated protein degradation (ERAD); aids Cdc48p in the extraction of faulty membrane proteins; targets misfolded cytosolic/nucleoplasmic domains of soluble and membrane embedded proteins (ERAD-C) and Sbh2p, a transmembrane domain-containing substrate (ERAD-M); C-terminal element, conserved in human ortholog MARCH6, determines substrate selectivity","termid":"PBO:0084564"}


id: FYPO:0005001
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein having high molecular mass due to polyubiquitin conjugation is lower than normal.","definition_xrefs":["PMID:10082519","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased cellular HMW ubiquitin conjugate level","synonyms":[{"name":"decreased cellular HMW ubiquitin conjugate level during mitotic cell cycle","type":"related"},{"name":"decreased cellular HMW ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"decreased cellular high molecular mass ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"decreased cellular high molecular weight ubiquitin conjugate level during vegetative growth","type":"exact"},{"name":"reduced cellular HMW ubiquitin conjugate level","type":"exact"}],"termid":"FYPO:0005001"}


id: PBO:0005006
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cullin-associated Methyltransferase complex subunit","termid":"PBO:0005006"}


id: MONDO:0009093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatoleukodystrophy is characterized by the association of a progressive leukodystrophy marked by generalized mental and motor impairment with the presence of thickened and wrinkled skin. It has been described in a Japanese brother and sister born to healthy parents. Both patients died in early childhood.","definition_xrefs":["Orphanet:1659"],"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":"dermatoleukodystrophy","secondary_identifiers":["MESH:C538220","OMIM:221790","SCTID:733044009","UMLS:C1857314","MEDGEN:387794","GARD:1813"],"synonyms":[{"name":"Dermatoleukodystrophy","type":"exact"}],"termid":"MONDO:0009093","xrefs":{"Monarch":{"xref_id":"0009093"}}}


id: PBO:0084754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial matrix GTPase; associates with mitochondrial ribosomes; important for translation under temperature and nutrient stress; may have a role in translational fidelity; similar to bacterial LepA elongation factor","termid":"PBO:0084754"}


id: GO:0005750
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex located in the mitochondrial inner membrane that forms part of the mitochondrial respiratory chain. Contains about 10 polypeptide subunits including four redox centers: cytochrome b/b6, cytochrome c1 and an 2Fe-2S cluster. Catalyzes the oxidation of ubiquinol by oxidized cytochrome c1.","definition_xrefs":["GOC:mtg_sensu","ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial respiratory chain complex III (obsolete GO:0005750)","synonyms":[{"name":"mitochondrial coenzyme Q-cytochrome c oxidoreductase complex","type":"exact"},{"name":"mitochondrial coenzyme Q-cytochrome c reductase complex","type":"exact"},{"name":"mitochondrial complex III","type":"exact"},{"name":"mitochondrial cytochrome bc(1) complex","type":"exact"},{"name":"mitochondrial cytochrome bc1 complex","type":"exact"},{"name":"mitochondrial electron transport complex III","type":"related"},{"name":"mitochondrial ubiquinol-cytochrome c oxidoreductase complex","type":"exact"},{"name":"mitochondrial ubiquinol-cytochrome-c reductase complex","type":"exact"}],"termid":"GO:0005750"}


id: RO:0002248
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship that holds between a substance and a chemical entity, if the chemical entity is part of the substance, and the chemical entity forms the biologically active component of the substance.","direct_ancestors":[{"relation_name":"is_a","term_name":"has_part","termid":"BFO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_active_ingredient","synonyms":[{"name":"has active pharmaceutical ingredient","type":"related"},{"name":"has active substance","type":"exact"}],"termid":"RO:0002248"}


id: PBO:0050419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein F","termid":"PBO:0050419"}


id: PBO:0008485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PP2A-type phosphatase inhibitor Sds23/Moc1","termid":"PBO:0008485"}


id: PomGeneEx:0000022
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneExProt","definition":"A gene expression qualifier that indicates that a protein is not detectable under a given set of conditions or at an indicated time.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"absent","termid":"PomGeneEx:0000006"},{"relation_name":"is_a","term_name":"protein expression level","termid":"PomGeneEx:0000010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein absent","synonyms":[{"name":"protein expression absent","type":"exact"}],"termid":"PomGeneEx:0000022"}


id: FYPO:0007175
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 plasma membrane surrounding the cell division site is abolished during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to plasma membrane at cell division site during vegetative growth","termid":"FYPO:0006936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to plasma membrane at cell division site during mitotic interphase","synonyms":[{"name":"abolished protein localisation to plasma membrane at cell division site during mitotic interphase","type":"exact"},{"name":"abolished protein localization in plasma membrane at cell division site during mitotic interphase","type":"exact"},{"name":"abolished protein localization to cell membrane at cell division site during mitotic interphase","type":"exact"},{"name":"abolished protein localization to plasma membrane at cell division site during interphase during vegetative growth","type":"exact"},{"name":"abolished protein localization to plasma membrane at cell division site during interphase of mitotic cell cycle","type":"exact"},{"name":"protein localization to plasma membrane at cell division site abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007175"}


id: PBO:0071829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 24","termid":"PBO:0071829"}


id: PBO:0050466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HORMAD2 and MTMR3 antisense RNA 1","termid":"PBO:0050466"}


id: GO:0042565
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex which usually consists of three components, e.g. in Xenopus and yeast, the export receptor CRM1 (also known as exportin 1), the Ran protein and any RNA with a nuclear export sequence (NES). The complex acts to export RNA molecules with a NES from the nucleus through a nuclear pore.","definition_xrefs":["GOC:jl","PMID:9323123"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleocytoplasmic transport complex","termid":"GO:0031074"}],"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":"RNA nuclear export complex","termid":"GO:0042565"}


id: SO:0000688
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A set of subregions selected from sequence contigs which when concatenated form a nonredundant linear sequence.","definition_xrefs":["SO:ls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_assembly","termid":"SO:0000353"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golden_path","synonyms":[{"name":"golden path","type":"exact"}],"termid":"SO:0000688"}


id: MONDO:0044965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease or disorder that involves the abdominal segment of trunk.","definition_xrefs":["MONDO:design_pattern"],"gene_count":0,"genotype_count":0,"name":"obsolete abdominal and pelvic region disorder (obsolete MONDO:0044965)","secondary_identifiers":["SCTID:609618002"],"synonyms":[{"name":"abdominal segment of trunk disease","type":"exact"},{"name":"abdominal segment of trunk disease or disorder","type":"exact"},{"name":"disease of abdominal segment of trunk","type":"exact"},{"name":"disease or disorder of abdominal segment of trunk","type":"exact"},{"name":"disorder of abdominal segment of trunk","type":"exact"}],"termid":"MONDO:0044965","xrefs":{"Monarch":{"xref_id":"0044965"}}}


id: GO:0032556
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a pyrimidine deoxyribonucleotide, any compound consisting of a pyrimidine deoxyribonucleoside that is esterified with (ortho)phosphate or an oligophosphate at any hydroxyl group on the deoxyribose moiety.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleotide binding","termid":"GO:0019103"},{"relation_name":"is_a","term_name":"deoxyribonucleotide binding","termid":"GO:0032552"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"pyrimidine deoxyribonucleotide binding","termid":"GO:0032556"}


id: PBO:0082025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger ZZ-type and EF-hand domain containing 1","termid":"PBO:0082025"}


id: GO:1903077
data:
  {"annotated_genes":["SJAG_03970","SJAG_04597","SJAG_02392"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97670],"is_not":false,"summary":null,"term":"GO:1903077"},{"annotations":[89903],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042997"},{"annotations":[96221],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140325"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to plasma membrane.","definition_xrefs":["GOC:TermGenie","GOC:rl","GO_REF:0000058","GOC:BHF","PMID:11602640"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to plasma membrane","termid":"GO:1903076"},{"relation_name":"is_a","term_name":"negative regulation of protein localization to cell periphery","termid":"GO:1904376"},{"relation_name":"is_a","term_name":"negative regulation of protein localization to membrane","termid":"GO:1905476"},{"relation_name":"negatively_regulates","term_name":"protein localization to plasma membrane","termid":"GO:0072659"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02392":null,"SJAG_03970":null,"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein localization to plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0090005","GO:1905964"],"synonyms":[{"name":"down regulation of protein localisation in plasma membrane","type":"exact"},{"name":"down regulation of protein localization in plasma membrane","type":"exact"},{"name":"down regulation of protein localization to plasma membrane","type":"exact"},{"name":"down regulation of protein targeting to plasma membrane","type":"related"},{"name":"down regulation of protein-plasma membrane targeting","type":"related"},{"name":"down-regulation of protein localisation in plasma membrane","type":"exact"},{"name":"down-regulation of protein localization in plasma membrane","type":"exact"},{"name":"down-regulation of protein localization to plasma membrane","type":"exact"},{"name":"down-regulation of protein targeting to plasma membrane","type":"related"},{"name":"down-regulation of protein-plasma membrane targeting","type":"related"},{"name":"downregulation of protein localisation in plasma membrane","type":"exact"},{"name":"downregulation of protein localization in plasma membrane","type":"exact"},{"name":"downregulation of protein localization to plasma membrane","type":"exact"},{"name":"downregulation of protein targeting to plasma membrane","type":"related"},{"name":"downregulation of protein-plasma membrane targeting","type":"related"},{"name":"inhibition of protein localisation in plasma membrane","type":"narrow"},{"name":"inhibition of protein localization in plasma membrane","type":"narrow"},{"name":"inhibition of protein localization to plasma membrane","type":"narrow"},{"name":"inhibition of protein targeting to plasma membrane","type":"narrow"},{"name":"inhibition of protein-plasma membrane targeting","type":"narrow"},{"name":"negative regulation of establishment of protein localisation in plasma membrane","type":"related"},{"name":"negative regulation of establishment of protein localization in plasma membrane","type":"related"},{"name":"negative regulation of establishment of protein localization to plasma membrane","type":"related"},{"name":"negative regulation of protein localisation in plasma membrane","type":"related"},{"name":"negative regulation of protein localization in plasma membrane","type":"exact"},{"name":"negative regulation of protein targeting to plasma membrane","type":"related"},{"name":"negative regulation of protein-plasma membrane targeting","type":"related"}],"termid":"GO:1903077","terms_by_termid":{"GO:0042997":null,"GO:0140325":null,"GO:1903077":null}}


id: PBO:0046606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K9, member 8","termid":"PBO:0046606"}


id: GO:0061476
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 anticoagulant stimulus.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to anticoagulant","termid":"GO:0061476"}


id: GO:0030790
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + trichlorophenol = S-adenosyl-L-homocysteine + trichloroanisole.","definition_xrefs":["EC:2.1.1.136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"chlorophenol O-methyltransferase activity","secondary_identifiers":["MetaCyc:2.1.1.136-RXN","RHEA:18909"],"synonyms":[{"name":"S-adenosyl-L-methionine:trichlorophenol O-methyltransferase activity","type":"related"},{"name":"halogenated phenol O-methyltransferase activity","type":"broad"},{"name":"trichlorophenol O-methyltransferase activity","type":"related"}],"termid":"GO:0030790"}


id: MONDO:0011986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tropical pancreatitis is a rare pancreatic disease of juvenile onset occurring mainly in tropical developing countries and characterized by chronic non-alcoholic pancreatitis manifesting with abdominal pain, steatorrhea and fibrocalculous pancreatopathy. It is also commonly associated with the development of pancreatic calculi and pancreatic cancer at a much higher frequency than seen in ordinary chronic pancreatitis.","definition_xrefs":["Orphanet:103918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary chronic pancreatitis","termid":"MONDO:0008185"}],"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":"tropical pancreatitis","secondary_identifiers":["GARD:16946","MEDGEN:334069","UMLS:C1842402","SCTID:724540009","icd11.foundation:1645607956","OMIM:608189","MESH:C564276"],"synonyms":[{"name":"TCP","type":"exact"},{"name":"fibrocalculous pancreatic diabetes, susceptibility to","type":"related"},{"name":"tropical calcific chronic pancreatitis","type":"exact"},{"name":"tropical calcific pancreatitis","type":"related"}],"termid":"MONDO:0011986","xrefs":{"Monarch":{"xref_id":"0011986"}}}


id: GO:1904920
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of MAPK cascade involved in axon regeneration.","definition_xrefs":["GOC:kmv","GOC:TermGenie","PMID:20203177","GO_REF:0000058"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of MAPK cascade involved in axon regeneration (obsolete GO:1904920)","synonyms":[{"name":"regulation of ERK/MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"regulation of MAP kinase cascade involved in axon regeneration","type":"exact"},{"name":"regulation of MAP kinase kinase kinase cascade involved in axon regeneration","type":"exact"},{"name":"regulation of MAPK signal transduction involved in axon regeneration","type":"exact"},{"name":"regulation of MAPK signaling involved in axon regeneration","type":"related"},{"name":"regulation of MAPK signalling involved in axon regeneration","type":"related"},{"name":"regulation of MAPKKK cascade during sporulation involved in axon regeneration","type":"narrow"},{"name":"regulation of MAPKKK cascade involved in axon regeneration","type":"exact"},{"name":"regulation of mitogen-activated protein kinase cascade involved in axon regeneration","type":"exact"}],"termid":"GO:1904920"}


id: PBO:0040382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP6AP1 divergent transcript","termid":"PBO:0040382"}


id: PBO:0085949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; null mutant displays reduced respiratory growth and elevated frequency of mitochondrial genome loss; the authentic, non-tagged protein is detected in purified mitochondria in high-throughput studies","termid":"PBO:0085949"}


id: GO:0009657
data:
  {"annotation_feature_type":"gene","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 a plastid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle organization","termid":"GO:0006996"}],"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":"plastid organization","synonyms":[{"name":"plastid organisation","type":"exact"},{"name":"plastid organization and biogenesis","type":"related"}],"termid":"GO:0009657"}


id: PR:O94400
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pbr1 gene.","definition_xrefs":["UniProtKB:O94400","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":"PHD and RING finger domain-containing protein C126.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC126.07c","synonyms":[{"name":"Spom972h-pbr1","type":"exact"}],"termid":"PR:O94400"}


id: GO:1905439
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 chondroitin 6'-sulfate stimulus.","definition_xrefs":["GOC:TermGenie","PMID:22365850","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to chondroitin 6'-sulfate","termid":"GO:1905439"}


id: PBO:0091408
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"assembly at damage sites is facilitated by Rad57 independently of Swi5","termid":"PBO:0091408"}


id: GO:0046082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of 5-methylcytosine, a methylated base of DNA.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 5-methylcytosine biosynthetic process (obsolete GO:0046082)","synonyms":[{"name":"5-methylcytosine anabolism","type":"exact"},{"name":"5-methylcytosine biosynthesis","type":"exact"},{"name":"5-methylcytosine formation","type":"exact"},{"name":"5-methylcytosine synthesis","type":"exact"}],"termid":"GO:0046082"}


id: PBO:0085771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein localized to COPII-coated vesicles; forms a complex with Erv41p; involved in the membrane fusion stage of transport","termid":"PBO:0085771"}


id: GO:0072544
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to L-DOPA, the modified amino acid (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid binding","termid":"GO:0016597"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"modified amino acid binding","termid":"GO:0072341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"L-DOPA binding","termid":"GO:0072544"}


id: GO:0062159
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A non-membrane-bounded organelle of eukaryotic cells, especially Protozoa, that fills with water from the cytoplasm and then discharges this externally. One of its functions is osmoregulatory.","definition_xrefs":["PMID:23890380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"contractile vacuole complex","synonyms":[{"name":"CVC","type":"related"}],"termid":"GO:0062159"}


id: PBO:0062271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily H member 2","termid":"PBO:0062271"}


id: GO:0043613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of isoprene, C5H8.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprene metabolic process","termid":"GO:0043611"},{"relation_name":"is_a","term_name":"terpene catabolic process","termid":"GO:0046247"},{"relation_name":"is_a","term_name":"olefinic compound catabolic process","termid":"GO:0120256"}],"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:0008150","GO:0006629"],"is_obsolete":false,"name":"isoprene catabolic process","synonyms":[{"name":"2-methyl-1,3-butadiene catabolic process","type":"exact"},{"name":"2-methyl-1,3-butadiene catabolism","type":"exact"},{"name":"hemiterpene catabolic process","type":"exact"},{"name":"hemiterpene catabolism","type":"exact"}],"termid":"GO:0043613"}


id: GO:0102278
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: n H2O + chitin = N,N'-diacetylchitobiose.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete N,N'-diacetylchitobiose synthase activity (obsolete GO:0102278)","termid":"GO:0102278"}


id: PBO:0114862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box/WD repeat protein, probable hydrogen sulfide sensing ubiquitin ligase adaptor Pof1","termid":"PBO:0114862"}


id: FYPO:0005369
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which a cell population does not grow at low temperatures.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished vegetative cell population growth","termid":"FYPO:0001575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0002060","FYPO:0002057","FYPO:0002058","FYPO:0000139"],"is_obsolete":false,"name":"abolished cell population growth at low temperature","synonyms":[{"name":"abolished cell population growth at low temperature during mitotic cell cycle","type":"related"},{"name":"abolished growth at low temperature","type":"broad"},{"name":"abolished vegetative cell population growth at low temperature","type":"exact"},{"name":"cell population growth at low temperature abolished","type":"exact"},{"name":"cold sensitive","type":"related"},{"name":"hypersensitive to low temperature","type":"related"},{"name":"sensitive to cold","type":"related"},{"name":"sensitive to low temperature","type":"related"},{"name":"sensitive to low temperature during vegetative growth","type":"related"},{"name":"temperature sensitive","type":"related"}],"termid":"FYPO:0005369"}


id: PBO:0109833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex, phosphatidylinositol pseudokinase subunit Tra1","termid":"PBO:0109833"}


id: GO:0019649
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pathways in which formaldehyde is processed and used as a carbon source for the cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formaldehyde metabolic process","termid":"GO:0046292"}],"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":"formaldehyde assimilation","termid":"GO:0019649"}


id: PR:O13732
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A trafficking protein particle complex subunit 2-like protein 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":"uncharacterized protein C15A10.12c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC15A10.12c","secondary_identifiers":["UniProtKB:O13732"],"synonyms":[{"name":"Spom972h-TRAPPC2L","type":"exact"}],"termid":"PR:O13732"}


id: MONDO:1011737
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dystrophic epidermolysis bullosa, non-human animal","secondary_identifiers":["OMIA:000341"],"termid":"MONDO:1011737","xrefs":{"Monarch":{"xref_id":"1011737"}}}


id: MONDO:0004537
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cervical mucinous adenocarcinoma that resembles the large intestinal adenocarcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical mucinous adenocarcinoma","termid":"MONDO:0002742"},{"relation_name":"is_a","term_name":"intestinal type adenocarcinoma","termid":"MONDO:0006254"}],"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":"intestinal variant cervical mucinous adenocarcinoma","secondary_identifiers":["UMLS:C1516422","DOID:8339","NCIT:C40203","MEDGEN:273124","ONCOTREE:ICEMU"],"synonyms":[{"name":"cervical mucinous adenocarcinoma, intestinal variant","type":"exact"},{"name":"cervical mucinous adenocarcinoma, intestinal-type","type":"exact"},{"name":"intestinal type mucinous carcinoma","type":"related"}],"termid":"MONDO:0004537","xrefs":{"Monarch":{"xref_id":"0004537"}}}


id: PBO:0069276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 532, pseudogene","termid":"PBO:0069276"}


id: PBO:0058069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4288","termid":"PBO:0058069"}


id: MONDO:0007148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"appendicitis, proneness to","secondary_identifiers":["MEDGEN:400099","OMIM:107700","UMLS:C1862632"],"synonyms":[{"name":"appendicitis, proneness to","type":"exact"},{"name":"appendicitis, susceptibility","type":"related"}],"termid":"MONDO:0007148","xrefs":{"Monarch":{"xref_id":"0007148"}}}


id: MONDO:0002406
data:
  {"annotated_genes":["SJAG_03850","SJAG_04109"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008296"},{"annotations":[88322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008218"}]},"cv_name":"mondo","definition":"An inflammatory process affecting the skin. Signs include red rash, itching, and blister formation. Representative examples are contact dermatitis, atopic dermatitis, and seborrheic dermatitis.","definition_xrefs":["NCIT:C2983"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03850":null,"SJAG_04109":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"dermatitis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:849741","MESH:D003872","ICD9:692.9","UMLS:C3875321","DOID:2723","SCTID:43116000"],"synonyms":[{"name":"inflammation of skin","type":"exact"},{"name":"inflammation of the skin","type":"exact"},{"name":"inflammation of zone of skin","type":"exact"},{"name":"inflammatory skin disease","type":"exact"},{"name":"skin inflammation","type":"exact"},{"name":"zone of skin inflammation","type":"exact"}],"termid":"MONDO:0002406","terms_by_termid":{"MONDO:0008218":null,"MONDO:0008296":null},"xrefs":{"Monarch":{"xref_id":"0002406"}}}


id: PBO:0068568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 19, pseudogene","termid":"PBO:0068568"}


id: FYPO:0000441
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of antimycin than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0005447","FYPO:0002682","FYPO:0000139"],"is_obsolete":false,"name":"resistance to antimycin A","synonyms":[{"name":"resistance to antimycin A during mitotic cell cycle","type":"related"},{"name":"resistance to antimycin A during vegetative growth","type":"exact"},{"name":"resistant to antimycin A","type":"exact"}],"termid":"FYPO:0000441"}


id: RO:0002230
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x ends with y if and only if x has part y and the time point at which x ends is equivalent to the time point at which y ends. Formally: α(y) > α(x) ∧ ω(y) = ω(x), where α is a function that maps a process to a start point, and ω is a function that maps a process to an end point.","direct_ancestors":[{"relation_name":"is_a","term_name":"has_part","termid":"BFO:0000051"},{"relation_name":"is_a","term_name":"temporally_related_to","termid":"RO:0002222"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ends_with","termid":"RO:0002230"}


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


id: MOD:00134
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-lysine residue and a glycine residue by an isopeptide bond to form N6-glycyl-L-lysine.","definition_xrefs":["ChEBI:21885","RESID:AA0125"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isopeptide crosslinked residues","termid":"MOD:00688"},{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"},{"relation_name":"is_a","term_name":"crosslinked L-lysine residue","termid":"MOD:02051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"N6-glycyl-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-[(aminoacetyl)amino]hexanoic acid","type":"exact"},{"name":"CROSSLNK Glycyl lysine isopeptide (Gly-Lys) (interchain with K-...)","type":"exact"},{"name":"CROSSLNK Glycyl lysine isopeptide (Lys-Gly) (interchain with G-...)","type":"exact"},{"name":"N6-(glycyl)-L-lysine","type":"exact"},{"name":"N6-glycyllysine","type":"exact"},{"name":"XLNK-N6Lys-1Gly","type":"exact"}],"termid":"MOD:00134"}


id: GO:0021949
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The early migration of a precerebellar neuronal precursor in which a cell move from the rhombic lip, orthogonal to the direction of radial migration and ultimately reside in the brainstem.","definition_xrefs":["GO_REF:0000021","GOC:jid","GOC:cls","GOC:dgh","PMID:15157725","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hindbrain tangential cell migration","termid":"GO:0021934"}],"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":"brainstem precerebellar neuron precursor migration","termid":"GO:0021949"}


id: PBO:0034117
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-supplies","termid":"PBO:0034117"}


id: PBO:0024475
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human USB1","termid":"PBO:0024475"}


id: FYPO:0004918
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 positive regulation of a protein kinase activity does not occur.","definition_xrefs":["PMID:11402029","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of catalytic activity","termid":"FYPO:0004916"},{"relation_name":"is_a","term_name":"abolished biological process","termid":"FYPO:0005448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abolished positive regulation of protein kinase activity","synonyms":[{"name":"abolished activation of protein kinase activity","type":"narrow"},{"name":"abolished positive regulation of protein kinase activity during mitotic cell cycle","type":"related"},{"name":"abolished positive regulation of protein kinase activity during vegetative growth","type":"exact"},{"name":"positive regulation of protein kinase activity abolished","type":"exact"}],"termid":"FYPO:0004918"}


id: GO:0032781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the rate of an ATP-dependent activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ATP-dependent activity","termid":"GO:0043462"},{"relation_name":"is_a","term_name":"positive regulation of molecular function","termid":"GO:0044093"}],"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 ATP-dependent activity","synonyms":[{"name":"activation of ATPase activity","type":"narrow"},{"name":"positive regulation of ATPase activity","type":"exact"},{"name":"positive regulation of adenosinetriphosphatase activity","type":"exact"},{"name":"stimulation of ATPase activity","type":"narrow"},{"name":"up regulation of ATPase activity","type":"exact"},{"name":"up-regulation of ATPase activity","type":"exact"},{"name":"upregulation of ATPase activity","type":"exact"}],"termid":"GO:0032781"}


id: PBO:0060925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurofibromin 1 pseudogene 12","termid":"PBO:0060925"}


id: MONDO:0700273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary cancer predisposition due to variation(s) in the RAD51C gene. Pathogenic germline variation in RAD51C confers an autosomal dominant predisposition to tumor formation at multiple primary sites, including ovarian cancer, triple negative breast cancer and ER negative breast cancer.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD51C-related cancer predisposition","termid":"MONDO:0700273","xrefs":{"Monarch":{"xref_id":"0700273"}}}


id: GO:0031385
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the end of mating projection formation by unicellular fungi.","definition_xrefs":["PMID:14734532"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mating projection assembly","termid":"GO:0031383"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"regulation of termination of mating projection growth","termid":"GO:0031385"}


id: GO:0008692
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-hydroxybutanoyl-CoA = (R)-3-hydroxybutanoyl-CoA.","definition_xrefs":["EC:5.1.2.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on hydroxy acids and derivatives","termid":"GO:0016856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"3-hydroxybutyryl-CoA epimerase activity","secondary_identifiers":["RHEA:21760","MetaCyc:OHBUTYRYL-COA-EPIM-RXN"],"synonyms":[{"name":"3-hydroxyacyl-CoA epimerase activity","type":"related"},{"name":"3-hydroxybutanoyl-CoA 3-epimerase activity","type":"related"},{"name":"3-hydroxybutyryl coenzyme A epimerase activity","type":"related"}],"termid":"GO:0008692"}


id: GO:0061126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of directed movement of a motile cell or organism up a concentration gradient of 3',5'-cAMP by the action of DIF-1. DIF-1 is a chlorinated alkylphenone.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of positive chemotaxis to cAMP by DIF-1","termid":"GO:0061120"},{"relation_name":"is_a","term_name":"positive regulation of positive chemotaxis to cAMP by chlorinated alkylphenone","termid":"GO:0061124"}],"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 positive chemotaxis to cAMP by DIF-1","termid":"GO:0061126"}


id: MONDO:0012551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia, isolated","termid":"MONDO:0000005"},{"relation_name":"is_a","term_name":"alopecia totalis","termid":"MONDO:0019080"}],"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":"alopecia areata 2","secondary_identifiers":["UMLS:C1853104","GARD:15496","MEDGEN:343971","MESH:C565186","OMIM:610753"],"synonyms":[{"name":"AA2","type":"exact"},{"name":"alopecia areata 2","type":"exact"}],"termid":"MONDO:0012551","xrefs":{"Monarch":{"xref_id":"0012551"}}}


id: PBO:0053213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galectin 9C","termid":"PBO:0053213"}


id: PBO:0035970
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H4_acetylation_during_vegetative_growth","termid":"PBO:0035970"}


id: MONDO:0007318
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alagille (AGS) syndrome is variably characterized by chronic cholestasis due to paucity of intrahepatic bile ducts, peripheral pulmonary artery stenosis, vertebrae segmentation anomalies, characteristic facies, posterior embryotoxon/anterior segment abnormalities, pigmentary retinopathy, and dysplastic kidneys.","definition_xrefs":["Orphanet:52"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"biliary tract disorder","termid":"MONDO:0004868"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004335","MONDO:0005267","MONDO:0002515"],"is_obsolete":false,"name":"Alagille syndrome","secondary_identifiers":["SCTID:31742004","DOID:9245","OMIMPS:118450","NORD:748","NANDO:2200931","ICD9:759.89","MEDGEN:39014","GARD:804","icd11.foundation:1249656206","NANDO:1200918","MESH:D016738","NANDO:1200919","NCIT:C35139","MedDRA:10053870","UMLS:C0085280"],"synonyms":[{"name":"Alagille syndrome","type":"exact"},{"name":"Alagille-Watson syndrome","type":"exact"},{"name":"Arteriohepatic dysplasia","type":"exact"},{"name":"Cardiovertebral syndrome","type":"related"},{"name":"Hepatofacioneurocardiovertebral syndrome","type":"related"},{"name":"Watson Alagille syndrome","type":"related"},{"name":"Watson-Miller syndrome","type":"related"},{"name":"hepatic ductular hypoplasia","type":"related"},{"name":"paucity of interlobular bile ducts","type":"related"},{"name":"syndromic bile duct paucity","type":"exact"}],"termid":"MONDO:0007318","xrefs":{"Monarch":{"xref_id":"0007318"}}}


id: PBO:0036363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, human HGH1 ortholog","termid":"PBO:0036363"}


id: GO:2000653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of genetic imprinting.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of genetic imprinting (obsolete GO:2000653)","synonyms":[{"name":"regulation of DNA imprinting","type":"exact"}],"termid":"GO:2000653"}


id: GO:0008684
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-hydroxy-2-oxopentanoate = 2-oxopent-4-enoate + H2O.","definition_xrefs":["EC:4.2.1.80"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"2-oxopent-4-enoate hydratase activity","secondary_identifiers":["GO:0018821","UM-BBD_enzymeID:r0101","MetaCyc:2-OXOPENT-4-ENOATE-HYDRATASE-RXN","RHEA:22580"],"synonyms":[{"name":"2-keto-4-pentenoate (vinylpyruvate)hydratase activity","type":"related"},{"name":"2-keto-4-pentenoate hydratase activity","type":"related"},{"name":"4-hydroxy-2-oxopentanoate hydro-lyase (2-oxopent-4-enoate-forming)","type":"related"},{"name":"4-hydroxy-2-oxopentanoate hydro-lyase activity","type":"related"},{"name":"OEH activity","type":"related"}],"termid":"GO:0008684"}


id: PR:O94590
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94590"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein transport protein sec1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC584.05","synonyms":[{"name":"Spom972h-sec1","type":"exact"}],"termid":"PR:O94590"}


id: PBO:0072239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 14","termid":"PBO:0072239"}


id: PBO:0077474
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 196","termid":"PBO:0077474"}


id: GO:0014816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a satellite cell.","definition_xrefs":["GOC:mtg_muscle","GOC:ef","PMID:16607119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal muscle cell differentiation","termid":"GO:0035914"}],"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 differentiation","termid":"GO:0014816"}


id: MONDO:0016513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. This term refers to a group of diseases characterized by alpha-thalassemia and an associated disorder. Three conditions are included in this group: alpha thalassemia - X-linked intellectual deficit (or ATR-X syndrome), alpha-thalassemia-intellectual deficit syndrome (or ATR-16 syndrome) and alpha-thalassemia-myelodysplastic disease (or ATMDS).*","definition_xrefs":["Orphanet:232288"],"gene_count":0,"genotype_count":0,"name":"obsolete alpha-thalassemia-related diseases (obsolete MONDO:0016513)","secondary_identifiers":["ICD10CM:D56.0"],"termid":"MONDO:0016513","xrefs":{"Monarch":{"xref_id":"0016513"}}}


id: GO:0031873
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 2 proteinase activated receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteinase activated receptor binding","termid":"GO:0031871"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"type 2 proteinase activated receptor binding","synonyms":[{"name":"type 2 proteinase activated receptor ligand","type":"narrow"}],"termid":"GO:0031873"}


id: PBO:0000616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Prh1 (predicted)","termid":"PBO:0000616"}


id: GO:1903246
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of adrenergic receptor signaling pathway involved in positive regulation of heart rate.","definition_xrefs":["GOC:BHF","PMID:17242280","GOC:TermGenie","GOC:mtg_cardiac_conduct_nov11","GO_REF:0000058","GOC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of adrenergic receptor signaling pathway involved in positive regulation of heart rate (obsolete GO:1903246)","synonyms":[{"name":"down regulation of Gs-coupled adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"down regulation of If activation by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"down regulation of activation of funny current by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"down regulation of adenylate cyclase-activating cardiac adrenergic receptor signaling pathway","type":"related"},{"name":"down regulation of adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"down regulation of adrenergic receptor signalling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"down regulation of beta adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"narrow"},{"name":"down-regulation of Gs-coupled adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"down-regulation of If activation by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"down-regulation of activation of funny current by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"down-regulation of adenylate cyclase-activating cardiac adrenergic receptor signaling pathway","type":"related"},{"name":"down-regulation of adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"down-regulation of adrenergic receptor signalling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"down-regulation of beta adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"narrow"},{"name":"downregulation of Gs-coupled adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"downregulation of If activation by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"downregulation of activation of funny current by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"downregulation of adenylate cyclase-activating cardiac adrenergic receptor signaling pathway","type":"related"},{"name":"downregulation of adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"downregulation of adrenergic receptor signalling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"downregulation of beta adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"narrow"},{"name":"inhibition of Gs-coupled adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"narrow"},{"name":"inhibition of If activation by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"inhibition of activation of funny current by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"inhibition of adenylate cyclase-activating cardiac adrenergic receptor signaling pathway","type":"related"},{"name":"inhibition of adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"narrow"},{"name":"inhibition of adrenergic receptor signalling pathway involved in positive regulation of heart rate","type":"narrow"},{"name":"inhibition of beta adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"narrow"},{"name":"negative regulation of Gs-coupled adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"negative regulation of If activation by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"negative regulation of activation of funny current by beta-adrenergic receptor signaling pathway","type":"related"},{"name":"negative regulation of adenylate cyclase-activating cardiac adrenergic receptor signaling pathway","type":"related"},{"name":"negative regulation of adrenergic receptor signalling pathway involved in positive regulation of heart rate","type":"exact"},{"name":"negative regulation of beta adrenergic receptor signaling pathway involved in positive regulation of heart rate","type":"narrow"}],"termid":"GO:1903246"}


id: GO:0018021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The methylation of peptidyl-L-histidine to form peptidyl-L-1'-methyl-L-histidine (otherwise known as tau-methylhistidine, tele-methylhistidine) or peptidyl-L-3'-methyl-L-histidine (otherwise known as pi-methylhistidine, pros-methylhistidine).","definition_xrefs":["RESID:AA0073","RESID:AA0317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein methylation","termid":"GO:0006479"},{"relation_name":"is_a","term_name":"peptidyl-histidine modification","termid":"GO:0018202"}],"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":"peptidyl-histidine methylation","termid":"GO:0018021"}


id: FYPO:0001762
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 tRNA modification, the covalent alteration of one or more nucleotides within a tRNA molecule, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["GO:0006400","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA processing","termid":"FYPO:0001980"},{"relation_name":"is_a","term_name":"normal RNA metabolic process","termid":"FYPO:0004850"}],"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:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal tRNA modification","synonyms":[{"name":"normal tRNA modification during mitotic cell cycle","type":"related"},{"name":"normal tRNA modification during vegetative growth","type":"exact"}],"termid":"FYPO:0001762"}


id: PBO:0036201
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-short_microtubule_bundle","termid":"PBO:0036201"}


id: PR:P36630
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A G2/mitotic-specific cyclin-B2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01138","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":"G2/mitotic-specific cyclin cig2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB2B4.03","secondary_identifiers":["UniProtKB:P36630"],"synonyms":[{"name":"Spom972h-CCNB2","type":"exact"}],"termid":"PR:P36630"}


id: GO:0010647
data:
  {"annotated_genes":["SJAG_02135","SJAG_01199","SJAG_00027","SJAG_01150","SJAG_00209","SJAG_06588","SJAG_04551","SJAG_01181","SJAG_00318","SJAG_00561","SJAG_01787","SJAG_01805","SJAG_03405","SJAG_04910","SJAG_00143","SJAG_02424","SJAG_00781","SJAG_00845","SJAG_01587","SJAG_03453","SJAG_04666","SJAG_03371","SJAG_01632","SJAG_05030","SJAG_06622","SJAG_03907","SJAG_03705","SJAG_06592","SJAG_04776","SJAG_02945","SJAG_03568","SJAG_03089","SJAG_00082","SJAG_02486","SJAG_03903","SJAG_02682","SJAG_02231","SJAG_00424","SJAG_06621","SJAG_00457","SJAG_00610","SJAG_02605","SJAG_03828","SJAG_01978","SJAG_01837","SJAG_04259","SJAG_02183","SJAG_03048","SJAG_03969","SJAG_03936","SJAG_05184","SJAG_04496"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103963,112830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050850"},{"annotations":[92580,89898,119768,69407,94230,91252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903139"},{"annotations":[115646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905326"},{"annotations":[118536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090267"},{"annotations":[97074,110782,110784,110783,110781,119235,113672,110786,110780,114336,110785,120158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900745"},{"annotations":[89957,116482,117450,105521,92659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062038"},{"annotations":[89344,104206,112374,95620,91817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031031"},{"annotations":[80170,115296,115294,62292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000640"},{"annotations":[74749,70914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032008"},{"annotations":[90125,75740,96129,114718,74274,77136,78524,77646,112390,78186,97916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904263"},{"annotations":[93007,99559,108827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904515"}]},"cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of cell communication. Cell communication is the process that mediates interactions between a cell and its surroundings. Encompasses interactions such as signaling or attachment between one cell and another cell, between a cell and an extracellular matrix, or between a cell and any other aspect of its environment.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell communication","termid":"GO:0010646"},{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"positively_regulates","term_name":"cell communication","termid":"GO:0007154"}],"gene_count":52,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00082":null,"SJAG_00143":null,"SJAG_00209":null,"SJAG_00318":null,"SJAG_00424":null,"SJAG_00457":null,"SJAG_00561":null,"SJAG_00610":null,"SJAG_00781":null,"SJAG_00845":null,"SJAG_01150":null,"SJAG_01181":null,"SJAG_01199":null,"SJAG_01587":null,"SJAG_01632":null,"SJAG_01787":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01978":null,"SJAG_02135":null,"SJAG_02183":null,"SJAG_02231":null,"SJAG_02424":null,"SJAG_02486":null,"SJAG_02605":null,"SJAG_02682":null,"SJAG_02945":null,"SJAG_03048":null,"SJAG_03089":null,"SJAG_03371":null,"SJAG_03405":null,"SJAG_03453":null,"SJAG_03568":null,"SJAG_03705":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_03907":null,"SJAG_03936":null,"SJAG_03969":null,"SJAG_04259":null,"SJAG_04496":null,"SJAG_04551":null,"SJAG_04666":null,"SJAG_04776":null,"SJAG_04910":null,"SJAG_05030":null,"SJAG_05184":null,"SJAG_06588":null,"SJAG_06592":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cell communication","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0010647","terms_by_termid":{"GO:0031031":null,"GO:0032008":null,"GO:0050850":null,"GO:0062038":null,"GO:0090267":null,"GO:1900745":null,"GO:1903139":null,"GO:1904263":null,"GO:1904515":null,"GO:1905326":null,"GO:2000640":null}}


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


id: PBO:0039577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and sterile alpha motif domain containing 6","termid":"PBO:0039577"}


id: PBO:0006200
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-directly_localizes","termid":"PBO:0006200"}


id: PBO:0081621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 550","termid":"PBO:0081621"}


id: GO:0010079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism retains a population of vegetative meristem cells, preventing the commitment of all stem cell progeny to a differentiated cell fate.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of meristem identity","termid":"GO:0010074"}],"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":"maintenance of vegetative meristem identity","termid":"GO:0010079"}


id: GO:0009541
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A three dimensional regular lattice found in etioplasts. It is composed of a continuous system of tubules but when exposed to light the symmetrical arrangement is rapidly lost as tubules become pinched off into two dimensional sections of lattice. These for perforated sheets of membrane that move apart, extend and increase, finally establishing the typical granal and intergranal lamellae of the mature chloroplast.","definition_xrefs":["ISBN:0140514031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"etioplast","termid":"GO:0009513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"etioplast prolamellar body","termid":"GO:0009541"}


id: PBO:0043442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calponin 2 pseudogene 2","termid":"PBO:0043442"}


id: SO:0001096
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A binding site that, in the polypeptide molecule, interacts selectively and non-covalently with copper ions.","definition_xrefs":["SO:cb","EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_metal_contact","termid":"SO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_copper_ion_contact_site","secondary_identifiers":["BS:00146"],"synonyms":[{"name":"Cu_contact_site","type":"exact"},{"name":"polypeptide copper ion contact site","type":"exact"}],"termid":"SO:0001096"}


id: GO:0097432
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a hippocampal pyramidal neuron, a pyramidal cell of the hippocampus.","definition_xrefs":["CL:1001571","GOC:jc","PMID:19342486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyramidal neuron differentiation","termid":"GO:0021859"},{"relation_name":"is_a","term_name":"cerebral cortex neuron differentiation","termid":"GO:0021895"}],"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":"hippocampal pyramidal neuron differentiation","termid":"GO:0097432"}


id: GO:0001567
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: AH2 + cholesterol + O2 = 25-hydroxycholesterol + A + H2O.","definition_xrefs":["RHEA:21104"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hydroxylase activity","termid":"GO:0008395"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"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:0016491","GO:0003824"],"is_obsolete":false,"name":"cholesterol 25-hydroxylase activity","secondary_identifiers":["EC:1.14.99.38","KEGG_REACTION:R07218","MetaCyc:1.14.99.38-RXN"],"synonyms":[{"name":"cholesterol 25-monooxygenase activity","type":"related"},{"name":"cholesterol,hydrogen-donor:oxygen oxidoreductase (25-hydroxylating) activity","type":"related"}],"termid":"GO:0001567"}


id: GO:1903634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of leucine-tRNA ligase activity.","definition_xrefs":["PMID:2280766","GOC:TermGenie","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of leucine-tRNA ligase activity (obsolete GO:1903634)","synonyms":[{"name":"down regulation of L-leucine:tRNALeu ligase (AMP-forming)","type":"exact"},{"name":"down regulation of leucine translase activity","type":"exact"},{"name":"down regulation of leucine-tRNA ligase activity","type":"exact"},{"name":"down regulation of leucine-tRNA synthetase activity","type":"exact"},{"name":"down regulation of leucyl-tRNA synthetase activity","type":"exact"},{"name":"down regulation of leucyl-transfer RNA synthetase activity","type":"exact"},{"name":"down regulation of leucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"down regulation of leucyl-transfer ribonucleic acid synthetase activity","type":"exact"},{"name":"down-regulation of L-leucine:tRNALeu ligase (AMP-forming)","type":"exact"},{"name":"down-regulation of leucine translase activity","type":"exact"},{"name":"down-regulation of leucine-tRNA ligase activity","type":"exact"},{"name":"down-regulation of leucine-tRNA synthetase activity","type":"exact"},{"name":"down-regulation of leucyl-tRNA synthetase activity","type":"exact"},{"name":"down-regulation of leucyl-transfer RNA synthetase activity","type":"exact"},{"name":"down-regulation of leucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"down-regulation of leucyl-transfer ribonucleic acid synthetase activity","type":"exact"},{"name":"downregulation of L-leucine:tRNALeu ligase (AMP-forming)","type":"exact"},{"name":"downregulation of leucine translase activity","type":"exact"},{"name":"downregulation of leucine-tRNA ligase activity","type":"exact"},{"name":"downregulation of leucine-tRNA synthetase activity","type":"exact"},{"name":"downregulation of leucyl-tRNA synthetase activity","type":"exact"},{"name":"downregulation of leucyl-transfer RNA synthetase activity","type":"exact"},{"name":"downregulation of leucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"downregulation of leucyl-transfer ribonucleic acid synthetase activity","type":"exact"},{"name":"inhibition of L-leucine:tRNALeu ligase (AMP-forming)","type":"narrow"},{"name":"inhibition of leucine translase activity","type":"narrow"},{"name":"inhibition of leucine-tRNA ligase activity","type":"narrow"},{"name":"inhibition of leucine-tRNA synthetase activity","type":"narrow"},{"name":"inhibition of leucyl-tRNA synthetase activity","type":"narrow"},{"name":"inhibition of leucyl-transfer RNA synthetase activity","type":"narrow"},{"name":"inhibition of leucyl-transfer ribonucleate synthetase activity","type":"narrow"},{"name":"inhibition of leucyl-transfer ribonucleic acid synthetase activity","type":"narrow"},{"name":"negative regulation of L-leucine:tRNALeu ligase (AMP-forming)","type":"exact"},{"name":"negative regulation of leucine translase activity","type":"exact"},{"name":"negative regulation of leucine-tRNA synthetase activity","type":"exact"},{"name":"negative regulation of leucyl-tRNA synthetase activity","type":"exact"},{"name":"negative regulation of leucyl-transfer RNA synthetase activity","type":"exact"},{"name":"negative regulation of leucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"negative regulation of leucyl-transfer ribonucleic acid synthetase activity","type":"exact"}],"termid":"GO:1903634"}


id: PBO:0027882
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H4-K20_dimethylation","termid":"PBO:0027882"}


id: PR:000050502
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the dis1 gene in Schizosaccharomyces pombe.","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":"TOG/XMAP215 microtubule plus end tracking polymerase Dis1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPCC736.14","synonyms":[{"name":"SPCC736.14","type":"related"},{"name":"Spom-dis1","type":"exact"},{"name":"dis1","type":"related"},{"name":"phosphoprotein p99","type":"exact"}],"termid":"PR:000050502"}


id: GO:0035702
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of monocytes such that the total number of monocytes within a whole or part of an organism is stable over time in the absence of an outside stimulus.","definition_xrefs":["PMID:18832716","GOC:BHF","CL:0000576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte homeostasis","termid":"GO:0001776"},{"relation_name":"is_a","term_name":"myeloid cell homeostasis","termid":"GO:0002262"}],"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":"monocyte homeostasis","termid":"GO:0035702"}


id: MONDO:0019939
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"schizophrenia","termid":"MONDO:0005090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039"],"is_obsolete":false,"name":"early-onset schizophrenia","secondary_identifiers":["GARD:19352","Orphanet:96369","UMLS:C1656427","MEDGEN:1800824"],"termid":"MONDO:0019939","xrefs":{"Monarch":{"xref_id":"0019939"}}}


id: MONDO:1012567
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osseous choristoma of the ciliary body, non-human animal","termid":"MONDO:1012004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osseous choristoma of the ciliary body, domestic guinea pig","secondary_identifiers":["OMIA:002576-10141"],"termid":"MONDO:1012567","xrefs":{"Monarch":{"xref_id":"1012567"}}}


id: MONDO:0014940
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset","secondary_identifiers":["UMLS:C4310693","OMIM:617145","DOID:0081364","MEDGEN:934660"],"synonyms":[{"name":"NADGP","type":"exact"},{"name":"neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset","type":"exact"},{"name":"neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset; NADGP","type":"exact"}],"termid":"MONDO:0014940","xrefs":{"Monarch":{"xref_id":"0014940"}}}


id: GO:0051275
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of beta-glucans.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucan catabolic process","termid":"GO:0009251"},{"relation_name":"is_a","term_name":"beta-glucan metabolic process","termid":"GO:0051273"}],"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":"beta-glucan catabolic process","synonyms":[{"name":"beta-glucan breakdown","type":"exact"},{"name":"beta-glucan catabolism","type":"exact"},{"name":"beta-glucan degradation","type":"exact"}],"termid":"GO:0051275"}


id: PBO:0065411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit alpha 8","termid":"PBO:0065411"}


id: MONDO:0013083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuroblastoma in which the cause of the disease is a mutation in the ALK gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"neuroblastoma","termid":"MONDO:0005072"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroblastoma, susceptibility to, 3","secondary_identifiers":["OMIM:613014","MEDGEN:414083","UMLS:C2751681"],"synonyms":[{"name":"ALK neuroblastoma","type":"exact"},{"name":"NBLST3","type":"related"},{"name":"neuroblastoma caused by mutation in ALK","type":"exact"},{"name":"neuroblastoma, susceptibility to, 3","type":"exact"},{"name":"neuroblastoma, susceptibility to, type 3","type":"exact"},{"name":"susceptibility to neuroblastoma 3","type":"related"}],"termid":"MONDO:0013083","xrefs":{"Monarch":{"xref_id":"0013083"}}}


id: MONDO:0000113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cerebellar ataxia, mental retardation, and dysequilibrium syndrome (obsolete MONDO:0000113)","termid":"MONDO:0000113","xrefs":{"Monarch":{"xref_id":"0000113"}}}


id: MONDO:0009433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypoplastic left heart syndrome in which the cause of the disease is a mutation in the GJA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypoplastic left heart syndrome","termid":"MONDO:0004933"}],"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":"hypoplastic left heart syndrome 1","secondary_identifiers":["MEDGEN:1646779","UMLS:C4551854","OMIM:241550"],"synonyms":[{"name":"GJA1 hypoplastic left heart syndrome","type":"exact"},{"name":"HLHS","type":"broad"},{"name":"HLHS1","type":"related"},{"name":"hypoplastic left heart syndrome 1","type":"exact"},{"name":"hypoplastic left heart syndrome caused by mutation in GJA1","type":"exact"},{"name":"hypoplastic left heart syndrome type 1","type":"exact"}],"termid":"MONDO:0009433","xrefs":{"Monarch":{"xref_id":"0009433"}}}


id: GO:0006856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of eye pigment precursors, the inactive forms of visual pigments, 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":"transport","termid":"GO:0006810"},{"relation_name":"part_of","term_name":"developmental pigmentation","termid":"GO:0048066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"eye pigment precursor transport","termid":"GO:0006856"}


id: MONDO:0018244
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited obesity","termid":"MONDO:0019182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"obesity due to SIM1 deficiency","secondary_identifiers":["GARD:21580","Orphanet:369873","UMLS:C5191050","MEDGEN:1680592"],"termid":"MONDO:0018244","xrefs":{"Monarch":{"xref_id":"0018244"}}}


id: GO:0160225
data:
  {"annotated_genes":["SJAG_03780"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[114388],"is_not":false,"summary":null,"term":"GO:0160225"}]},"cv_name":"molecular_function","definition":"Unwinding G-quadruplex structures in nucleic acids. A G-quadruplex is a specialized structure formed in DNA/RNA when sequences rich in guanine (G) assemble into a unique four-stranded arrangement.","definition_xrefs":["PMID:34113828","PMID:1324186","PMID:26883636"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity, acting on a nucleic acid","termid":"GO:0140640"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03780":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"G-quadruplex unwinding activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"G-quadruplex resolving activity","type":"exact"},{"name":"G4 unwinding activity","type":"exact"}],"termid":"GO:0160225","terms_by_termid":{"GO:0160225":null}}


id: PBO:0056845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial genome maintenance exonuclease 1","termid":"PBO:0056845"}


id: GO:1902037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of hematopoietic stem cell differentiation.","definition_xrefs":["GOC:TermGenie","PMID:23403623"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hematopoietic progenitor cell differentiation","termid":"GO:1901533"},{"relation_name":"is_a","term_name":"regulation of hematopoietic stem cell differentiation","termid":"GO:1902036"},{"relation_name":"is_a","term_name":"negative regulation of stem cell differentiation","termid":"GO:2000737"},{"relation_name":"negatively_regulates","term_name":"hematopoietic stem cell differentiation","termid":"GO:0060218"}],"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 hematopoietic stem cell differentiation","synonyms":[{"name":"down regulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"down regulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"down regulation of hematopoietic stem cell differentiation","type":"exact"},{"name":"down regulation of hemopoietic stem cell differentiation","type":"exact"},{"name":"down-regulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"down-regulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"down-regulation of hematopoietic stem cell differentiation","type":"exact"},{"name":"down-regulation of hemopoietic stem cell differentiation","type":"exact"},{"name":"downregulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"downregulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"downregulation of hematopoietic stem cell differentiation","type":"exact"},{"name":"downregulation of hemopoietic stem cell differentiation","type":"exact"},{"name":"inhibition of haematopoietic stem cell differentiation","type":"narrow"},{"name":"inhibition of haemopoietic stem cell differentiation","type":"narrow"},{"name":"inhibition of hematopoietic stem cell differentiation","type":"narrow"},{"name":"inhibition of hemopoietic stem cell differentiation","type":"narrow"},{"name":"negative regulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"negative regulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"negative regulation of hemopoietic stem cell differentiation","type":"exact"}],"termid":"GO:1902037"}


id: PATO:0001423
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A reflectivity quality inhering in the bearer by virtue of the bearer's ability to refract light.","definition_xrefs":["biology-online:biology-online"],"direct_ancestors":[{"relation_name":"is_a","term_name":"refractivity","termid":"PATO:0001372"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"refractile","termid":"PATO:0001423"}


id: SO:0001294
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"N4_N4_2_prime_O_trimethylcytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N4_N4_2_prime_O_trimethylcytidine","secondary_identifiers":["RNAMOD:107"],"synonyms":[{"name":"N4,N4,2'-O-trimethylcytidine","type":"exact"},{"name":"m42Cm","type":"exact"}],"termid":"SO:0001294"}


id: PR:Q9P5M9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P5M9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 14 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC359.06","synonyms":[{"name":"Spom972h-mug14","type":"exact"}],"termid":"PR:Q9P5M9"}


id: PR:O13650
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sfc9 gene.","definition_xrefs":["UniProtKB:O13650","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":"transcription factor tau subunit sfc9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC8D2.07c","synonyms":[{"name":"Spom972h-sfc9","type":"exact"},{"name":"TFIIIC subunit sfc9 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"transcription factor C subunit 9 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13650"}


id: GO:0005850
data:
  {"annotated_genes":["SJAG_05003","SJAG_03629","SJAG_00466"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73133,79364,79758],"is_not":false,"summary":null,"term":"GO:0005850"}]},"cv_name":"cellular_component","definition":"Complex of three heterogeneous polypeptide chains, that form a ternary complex with initiator methionyl-tRNA and GTP. This ternary complex binds to free 40S subunit, which subsequently binds the 5' end of mRNA.","definition_xrefs":["PMID:10216940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00466":null,"SJAG_03629":null,"SJAG_05003":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"eukaryotic translation initiation factor 2 complex","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Wikipedia:EIF-2"],"synonyms":[{"name":"eIF-2","type":"exact"},{"name":"eIF2","type":"exact"}],"termid":"GO:0005850","terms_by_termid":{"GO:0005850":null}}


id: MONDO:0030335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital diarrhea","termid":"MONDO:0000824"}],"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":"diarrhea 12, with microvillus atrophy","secondary_identifiers":["OMIM:619445","MEDGEN:1794152","UMLS:C5561942"],"synonyms":[{"name":"DIAR12","type":"exact"},{"name":"diarrhea 12, with microvillus atrophy","type":"exact"},{"name":"microvillus inclusion disease 2","type":"exact"}],"termid":"MONDO:0030335","xrefs":{"Monarch":{"xref_id":"0030335"}}}


id: RO:0002354
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"output_of","termid":"RO:0002353"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formed_as_result_of","termid":"RO:0002354"}


id: GO:0001546
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Increase in size of follicles surrounded by two or more layers of granulosa cells up to the onset of antrum formation.","direct_ancestors":[{"relation_name":"is_a","term_name":"ovulation cycle process","termid":"GO:0022602"},{"relation_name":"is_a","term_name":"developmental growth","termid":"GO:0048589"},{"relation_name":"part_of","term_name":"ovarian follicle development","termid":"GO:0001541"},{"relation_name":"part_of","term_name":"multi-layer follicle stage","termid":"GO:0048162"}],"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":"preantral ovarian follicle growth","termid":"GO:0001546"}


id: PATO:0002012
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A texture quality that exists through a liquid cover on the surface of the bearer.","definition_xrefs":["Wikipedia:Wikipedia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"texture","termid":"PATO:0000150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coating","termid":"PATO:0002012"}


id: MONDO:0014352
data:
  {"annotated_genes":["SJAG_04980"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88197],"is_not":false,"summary":null,"term":"MONDO:0014352"}]},"cv_name":"mondo","definition":"Any metabolic syndrome in which the cause of the disease is a mutation in the DYRK1B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abdominal obesity-metabolic syndrome","termid":"MONDO:0000816"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04980":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"abdominal obesity-metabolic syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4014361","OMIM:615812","DOID:0060612","MEDGEN:862798"],"synonyms":[{"name":"AOMS3","type":"related"},{"name":"DYRK1B metabolic syndrome","type":"exact"},{"name":"abdominal obesity-metabolic syndrome 3","type":"exact"},{"name":"abdominal obesity-metabolic syndrome type 3","type":"exact"},{"name":"central obesity, type 2 diabetes, hypertension, and early-onset coronary artery disease","type":"related"},{"name":"metabolic syndrome caused by mutation in DYRK1B","type":"exact"}],"termid":"MONDO:0014352","terms_by_termid":{"MONDO:0014352":null},"xrefs":{"Monarch":{"xref_id":"0014352"}}}


id: PR:Q09679
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gmh1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09679"],"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":"alpha-1,2-galactosyltransferase gmh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5H10.11","synonyms":[{"name":"Spom972h-gmh1","type":"exact"}],"termid":"PR:Q09679"}


id: PBO:0063118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(ADP-ribose) polymerase family member 4","termid":"PBO:0063118"}


id: PR:O60161
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cirhin that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03817","PRO:DNx","PANTHER:PTHR22841:SF4"],"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":"U3 small nucleolar RNA-associated protein 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19F5.02c","secondary_identifiers":["UniProtKB:O60161"],"synonyms":[{"name":"Spom972h-CIRH1A","type":"exact"},{"name":"U3 protein 4 required for transcription (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"U3 snoRNA-associated protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60161"}


id: MONDO:0022406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete aksu von stockhausen syndrome (obsolete MONDO:0022406)","termid":"MONDO:0022406","xrefs":{"Monarch":{"xref_id":"0022406"}}}


id: FYPO:0003372
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA measured in a cell is too low to detect during one or both meiotic nuclear divisions. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA absent from cell during meiotic cell cycle","termid":"FYPO:0006975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"RNA absent from cell during meiosis","synonyms":[{"name":"RNA absent from cell during meiotic nuclear division","type":"exact"},{"name":"transcripts absent from cell during meiosis","type":"exact"},{"name":"undetectable cellular RNA level during meiosis","type":"exact"}],"termid":"FYPO:0003372"}


id: MONDO:0004063
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Iris melanoma characterized by the presence of intermediate cells which are similar to but smaller than epithelioid cells.","definition_xrefs":["NCIT:C6101"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate cell type uveal melanoma","termid":"MONDO:0004062"},{"relation_name":"is_a","term_name":"iris melanoma","termid":"MONDO:0004064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"intermediate cell type iris melanoma","secondary_identifiers":["DOID:6993","MEDGEN:233564","UMLS:C1334210"],"synonyms":[{"name":"Intermediate cell type iris melanoma","type":"exact"},{"name":"intermediate cell type uveal melanoma of iris","type":"exact"},{"name":"iris intermediate cell type uveal melanoma","type":"exact"},{"name":"iris mixed cell melanoma","type":"related"}],"termid":"MONDO:0004063","xrefs":{"Monarch":{"xref_id":"0004063"}}}


id: MONDO:0008929
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cataract-intellectual disability-hypogonadism syndrome (obsolete MONDO:0008929)","termid":"MONDO:0008929","xrefs":{"Monarch":{"xref_id":"0008929"}}}


id: PBO:0065153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRMT5 antisense RNA 1","termid":"PBO:0065153"}


id: PBO:0078256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 30","termid":"PBO:0078256"}


id: GO:0005367
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: myo-inositol(out) + Na+(out) = myo-inositol(in) + Na+(in).","definition_xrefs":["TC:2.A.21.4.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myo-inositol transmembrane transporter activity","termid":"GO:0005365"},{"relation_name":"is_a","term_name":"solute:sodium symporter activity","termid":"GO:0015370"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"myo-inositol:sodium symporter activity","secondary_identifiers":["Reactome:R-HSA-429663"],"synonyms":[{"name":"myo-inositol-sodium cotransporter activity","type":"broad"}],"termid":"GO:0005367"}


id: MONDO:0800453
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic epilepsy with onset occurring around puberty. Juvenile absence epilepsy is characterized by sporadic occurrence of absence seizures, frequently associated with a long-life prevalence of generalized tonic-clonic seizures (GTCS) and sporadic myoclonic jerks.","definition_xrefs":["Orphanet:1941"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete adolescent/adult-onset epilepsy syndrome (obsolete MONDO:0100030)","termid":"MONDO:0100030"},{"relation_name":"is_a","term_name":"variable-age onset idiopathic generalized epilepsy syndrome","termid":"MONDO:0800487"}],"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":"juvenile absence epilepsy","secondary_identifiers":["UMLS:C4317339","DOID:0060172","icd11.foundation:519416529","MEDGEN:1388059","GARD:2162","SCTID:230413002","NCIT:C129868"],"synonyms":[{"name":"JAE","type":"exact"},{"name":"epilepsy juvenile absence","type":"related"}],"termid":"MONDO:0800453","xrefs":{"Monarch":{"xref_id":"0800453"}}}


id: GO:0032189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an actomyosin contractile ring is maintained in a location and prevented from moving elsewhere.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete maintenance of actomyosin contractile ring localization (obsolete GO:0032189)","synonyms":[{"name":"cytokinetic ring anchoring","type":"related"},{"name":"maintenance of contractile ring localisation involved in cell cycle cytokinesis","type":"exact"},{"name":"maintenance of contractile ring localization involved in cell cycle cytokinesis","type":"exact"},{"name":"maintenance of contractile ring localization involved in cytokinesis during cell cycle","type":"related"}],"termid":"GO:0032189"}


id: PBO:0016046
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snu3 and snu32 RNAs present at similar levels","termid":"PBO:0016046"}


id: PBO:0057971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3689d-1","termid":"PBO:0057971"}


id: GO:0051503
data:
  {"annotated_genes":["SJAG_00612","SJAG_02050","SJAG_03334","SJAG_04328"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76454],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015866"},{"annotations":[103180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990554"},{"annotations":[103181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990553"},{"annotations":[59189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140021"},{"annotations":[59188,104677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990544"},{"annotations":[94718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990549"}]},"cv_name":"biological_process","definition":"The directed movement of adenine nucleotides, ATP, ADP, and/or AMP, 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":"purine nucleotide transport","termid":"GO:0015865"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00612":null,"SJAG_02050":null,"SJAG_03334":null,"SJAG_04328":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"adenine nucleotide transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0051503","terms_by_termid":{"GO:0015866":null,"GO:0140021":null,"GO:1990544":null,"GO:1990549":null,"GO:1990553":null,"GO:1990554":null}}


id: PR:O74508
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spf1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74508"],"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":"set1 complex component spp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC594.05c","synonyms":[{"name":"COMPASS component spp1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Set1C component spp1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spf1","type":"exact"},{"name":"complex proteins associated with set1 protein spp1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74508"}


id: GO:0032287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structure and material content of mature peripheral nervous system myelin is kept in a functional state.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myelin maintenance","termid":"GO:0043217"},{"relation_name":"part_of","term_name":"myelination in peripheral nervous system","termid":"GO:0022011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"peripheral nervous system myelin maintenance","synonyms":[{"name":"myelin maintenance in peripheral nervous system","type":"exact"},{"name":"peripheral nervous system myelin sheath maintenance","type":"exact"}],"termid":"GO:0032287"}


id: GO:1990943
data:
  {"annotated_genes":["SJAG_00073"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95166],"is_not":false,"summary":null,"term":"GO:1990943"}]},"cv_name":"molecular_function","definition":"Binding to the replication fork barrier found in the mating type region of fission yeast.","definition_xrefs":["PMID:18723894"],"direct_ancestors":[{"relation_name":"is_a","term_name":"replication fork barrier binding","termid":"GO:0031634"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00073":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0003674","GO:0003677","GO:0005488"],"is_obsolete":false,"name":"mating type region replication fork barrier binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"RTS1 barrier binding","type":"exact"},{"name":"RTS1 element binding","type":"exact"}],"termid":"GO:1990943","terms_by_termid":{"GO:1990943":null}}


id: PBO:0017692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine hydroxymethyltransferase Shm1 (predicted)","termid":"PBO:0017692"}


id: PATO:0000462
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality denoting the lack of an entity.","definition_xrefs":["thefreedictionary.:thefreedictionary."],"direct_ancestors":[{"relation_name":"is_a","term_name":"amount","termid":"PATO:0000070"},{"relation_name":"reciprocal_of","term_name":"lacking processual parts","termid":"PATO:0001558"},{"relation_name":"reciprocal_of","term_name":"lacks all parts of type","termid":"PATO:0002000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"absent","secondary_identifiers":["PATO:0001996"],"synonyms":[{"name":"absence","type":"exact"},{"name":"absent from organism","type":"exact"}],"termid":"PATO:0000462"}


id: MONDO:0011982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune thyroid disease, susceptibility to","termid":"MONDO:0000162"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune thyroid disease, susceptibility to, 3","secondary_identifiers":["MEDGEN:374932","UMLS:C1842444","OMIM:608175"],"synonyms":[{"name":"AITD3","type":"related"},{"name":"autoimmune thyroid disease, susceptibility to, 3","type":"exact"},{"name":"autoimmune thyroid disease, susceptibility to, type 3","type":"exact"}],"termid":"MONDO:0011982","xrefs":{"Monarch":{"xref_id":"0011982"}}}


id: GO:0045542
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 cholesterol.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cholesterol biosynthetic process","termid":"GO:0045540"},{"relation_name":"is_a","term_name":"positive regulation of cholesterol metabolic process","termid":"GO:0090205"},{"relation_name":"is_a","term_name":"positive regulation of sterol biosynthetic process","termid":"GO:0106120"},{"relation_name":"is_a","term_name":"positive regulation of alcohol biosynthetic process","termid":"GO:1902932"},{"relation_name":"positively_regulates","term_name":"cholesterol biosynthetic process","termid":"GO:0006695"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cholesterol biosynthetic process","synonyms":[{"name":"activation of cholesterol biosynthetic process","type":"narrow"},{"name":"positive regulation of cholesterol anabolism","type":"exact"},{"name":"positive regulation of cholesterol biosynthesis","type":"exact"},{"name":"positive regulation of cholesterol formation","type":"exact"},{"name":"positive regulation of cholesterol synthesis","type":"exact"},{"name":"stimulation of cholesterol biosynthetic process","type":"narrow"},{"name":"up regulation of cholesterol biosynthetic process","type":"exact"},{"name":"up-regulation of cholesterol biosynthetic process","type":"exact"},{"name":"upregulation of cholesterol biosynthetic process","type":"exact"}],"termid":"GO:0045542"}


id: PATO:0000972
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000972 relative permeability (obsolete PATO:0000972)","termid":"PATO:0000972"}


id: GO:0032601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of connective tissue growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"connective tissue growth factor production","synonyms":[{"name":"CCN2 production","type":"exact"},{"name":"CTGF production","type":"exact"},{"name":"Fisp12 production","type":"exact"},{"name":"Hcs24 production","type":"exact"},{"name":"IGFBP8 production","type":"exact"},{"name":"hypertrophic chondrocyte-specific gene product 24 production","type":"exact"}],"termid":"GO:0032601"}


id: GO:0016131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving brassinosteroids, any of a group of steroid derivatives that occur at very low concentrations in plant tissues and may have hormone-like effects.","definition_xrefs":["ISBN:0192801023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phytosteroid metabolic process","termid":"GO:0016128"},{"relation_name":"is_a","term_name":"hormone metabolic process","termid":"GO:0042445"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"brassinosteroid metabolic process","synonyms":[{"name":"brassinosteroid metabolism","type":"exact"}],"termid":"GO:0016131"}


id: GO:0072550
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: triferuloyl spermidine + NADPH + O2 = diferuloyl mono-(hydroxyferuloyl) spermidine + NADP+ + H2O.","definition_xrefs":["GOC:kad","PMID:19779199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tri-(feruloyl or hydroxyferuloyl) spermidine meta-hydroxylase activity","termid":"GO:0072532"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"triferuloylspermidine meta-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-11262"],"synonyms":[{"name":"triferuloyl spermidine meta-hydroxylase activity","type":"exact"}],"termid":"GO:0072550"}


id: PBO:0109634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin alpha 14 (pseudogene)","termid":"PBO:0109634"}


id: GO:0035781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of CD86, a CD marker that occurs on antigen presenting cells that provides co-stimulatory signals necessary for T cell activation and survival.","definition_xrefs":["GOC:BHF","GOC:ebc"],"gene_count":0,"genotype_count":0,"name":"obsolete CD86 biosynthetic process (obsolete GO:0035781)","synonyms":[{"name":"CD86 anabolism","type":"exact"},{"name":"CD86 biosynthesis","type":"exact"},{"name":"CD86 formation","type":"exact"},{"name":"CD86 synthesis","type":"exact"}],"termid":"GO:0035781"}


id: GO:0050226
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phosphoadenosine 5'-phosphosulfate + galactosylsphingosine = adenosine 3',5'-bisphosphate + psychosine sulfate.","definition_xrefs":["EC:2.8.2.13","MetaCyc:PSYCHOSINE-SULFOTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfotransferase activity","termid":"GO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016782"}],"interesting_parent_ids":["GO:0003674","GO:0016782","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"psychosine sulfotransferase activity","secondary_identifiers":["RHEA:14137"],"synonyms":[{"name":"3'-phosphoadenosine 5'-phosphosulfate-psychosine sulphotransferase activity","type":"related"},{"name":"3'-phosphoadenylyl-sulfate:galactosylsphingosine sulfotransferase activity","type":"related"},{"name":"PAPS:psychosine sulphotransferase activity","type":"related"},{"name":"psychosine sulphotransferase activity","type":"exact"}],"termid":"GO:0050226"}


id: PBO:0071694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L38","termid":"PBO:0071694"}


id: MONDO:0956995
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An IDH-mutant anaplastic astrocytoma that is characterized by the presence of increased mitotic activity and anaplastic features.","definition_xrefs":["DOID:0081257"],"direct_ancestors":[{"relation_name":"is_a","term_name":"IDH-mutant anaplastic astrocytoma","termid":"MONDO:0850332"}],"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":"astrocytoma, IDH-mutant, grade 3","secondary_identifiers":["MEDGEN:927513","NCIT:C129290","UMLS:C4289981"],"termid":"MONDO:0956995","xrefs":{"Monarch":{"xref_id":"0956995"}}}


id: MONDO:0008511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Proximal symphalangism is a very rare, genetic bone disorder characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients.","definition_xrefs":["Orphanet:3250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symphalangism","termid":"MONDO:0000151"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"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":"proximal symphalangism","secondary_identifiers":["MEDGEN:348856","MESH:C536223","GARD:8182","icd11.foundation:49802338","OMIMPS:185800","DOID:0050788","HP:0100264","UMLS:C1861385"],"synonyms":[{"name":"Cushing's symphalangism","type":"exact"},{"name":"Strasburger-Hawkins-Eldridge syndrome","type":"related"},{"name":"Strasburger-Hawkins-Eldridge-Hargrave-McKusick syndrome","type":"related"},{"name":"hereditary absence of proximal interphalangeal joints","type":"related"},{"name":"hereditary absence of the proximal interphalangeal joints","type":"related"},{"name":"proximal symphalangism","type":"exact"},{"name":"proximal symphalangism (disease)","type":"exact"},{"name":"symphalangism, Cushing type","type":"exact"},{"name":"vessel’s syndrome","type":"related"}],"termid":"MONDO:0008511","xrefs":{"Monarch":{"xref_id":"0008511"}}}


id: PBO:0090334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane guanine and adenine transmembrane transporter","termid":"PBO:0090334"}


id: GO:0048390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the intermediate mesoderm are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesoderm morphogenesis","termid":"GO:0048332"},{"relation_name":"part_of","term_name":"intermediate mesoderm development","termid":"GO:0048389"}],"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":"intermediate mesoderm morphogenesis","termid":"GO:0048390"}


id: MONDO:0044256
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete skin/hair/eye pigmentation, variation in, 5 (obsolete MONDO:0044256)","secondary_identifiers":["OMIM:227240"],"synonyms":[{"name":"SHEP5","type":"related"},{"name":"skin/hair/eye pigmentation 5, Black/nonblack hair","type":"related"},{"name":"skin/hair/eye pigmentation 5, black/nonblack hair","type":"exact"},{"name":"skin/hair/eye pigmentation 5, dark/fair skin","type":"exact"},{"name":"skin/hair/eye pigmentation 5, dark/light eyes","type":"exact"},{"name":"skin/hair/eye pigmentation, variation IN, 5","type":"related"}],"termid":"MONDO:0044256","xrefs":{"Monarch":{"xref_id":"0044256"}}}


id: PBO:0029161
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_resistance_to_chemical","termid":"PBO:0029161"}


id: PBO:0091219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sub-telomeric 5Tm protein family Ftm2","termid":"PBO:0091219"}


id: GO:0033600
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of mammary gland epithelial cell proliferation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mammary gland epithelial cell proliferation","termid":"GO:0033599"},{"relation_name":"is_a","term_name":"negative regulation of epithelial cell proliferation","termid":"GO:0050680"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"mammary gland epithelial cell proliferation","termid":"GO:0033598"}],"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 mammary gland epithelial cell proliferation","synonyms":[{"name":"down regulation of mammary gland epithelial cell proliferation","type":"exact"},{"name":"down-regulation of mammary gland epithelial cell proliferation","type":"exact"},{"name":"downregulation of mammary gland epithelial cell proliferation","type":"exact"},{"name":"inhibition of mammary gland epithelial cell proliferation","type":"narrow"}],"termid":"GO:0033600"}


id: PBO:0117415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zDHHC palmitoyltransferase 11","termid":"PBO:0117415"}


id: PBO:0064026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 60","termid":"PBO:0064026"}


id: GO:0046258
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 2,4,6-trinitrotoluene, 1-methyl-2,4,6-trinitrobenzene, a highly explosive pale yellow crystalline solid, in the absence of oxygen.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anaerobic 2,4,6-trinitrotoluene metabolic process","termid":"GO:0018975"},{"relation_name":"is_a","term_name":"2,4,6-trinitrotoluene catabolic process","termid":"GO:0046256"}],"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":"anaerobic 2,4,6-trinitrotoluene catabolic process","synonyms":[{"name":"anaerobic 2,4,6-trinitrotoluene breakdown","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene catabolism","type":"exact"},{"name":"anaerobic 2,4,6-trinitrotoluene degradation","type":"exact"}],"termid":"GO:0046258"}


id: GO:0021932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The radially directed movement of a cell along radial glial cells in the hindbrain. Radial migration refers to a directed movement from the internal ventricular area to the outer surface of the hindbrain.","definition_xrefs":["GOC:dgh","GOC:jid","GOC:dph","PMID:15157725","GO_REF:0000021","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration in hindbrain","termid":"GO:0021535"}],"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":"hindbrain radial glia guided cell migration","termid":"GO:0021932"}


id: PBO:0031254
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_spindle_assembly","termid":"PBO:0031254"}


id: PBO:0044101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis antigen family 47 member A9","termid":"PBO:0044101"}


id: PBO:0031615
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transposition","termid":"PBO:0031615"}


id: MONDO:0014133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A developmental and epileptic encephalopathy characterized by seizure onset in the first weeks or months of life, delayed or regression of psychomotor development, and hypotonia that has material basis in homozygous or compound heterozygous mutation in the TBC1D24 gene on chromosome 16p13.","definition_xrefs":["DOID:0080449"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant migrating partial seizures of infancy","termid":"MONDO:0017385"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 16","secondary_identifiers":["MEDGEN:815503","UMLS:C3809173","OMIM:615338","GARD:15945"],"synonyms":[{"name":"DEE16","type":"exact"},{"name":"EIEE16","type":"exact"},{"name":"developmental and epileptic encephalopathy 16","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 16","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 16","type":"exact"}],"termid":"MONDO:0014133","xrefs":{"Monarch":{"xref_id":"0014133"}}}


id: PBO:0091064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-3-methyladenine glycosylase Mag2","termid":"PBO:0091064"}


id: PBO:0000338
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae MAC1","termid":"PBO:0000338"}


id: MONDO:1011830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"audiogenic seizure, non-human animal","secondary_identifiers":["OMIA:000093"],"termid":"MONDO:1011830","xrefs":{"Monarch":{"xref_id":"1011830"}}}


id: PBO:0031062
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,_without_cell_division,_with_elongated,_septated_germ_tube","termid":"PBO:0031062"}


id: PBO:0076011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stress induced phosphoprotein 1 pseudogene 2","termid":"PBO:0076011"}


id: PBO:0113001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha subunit of translation initiation factor eIF2B (eIF2Bα); guanine-nucleotide exchange factor for eIF2; mutations in eIF2Bα alter localization of eIF2B; activity regulated by phosphorylated eIF2; positive regulator of GCN4 expression; mutations in human ortholog EIF2B2 cause fatal brain disease childhood ataxia with central nervous system hypomyelination (CACH); human ortholog EIF2B1 can complement yeast null mutant","termid":"PBO:0113001"}


id: MONDO:0018501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare stomach carcinoma.","gene_count":0,"genotype_count":0,"name":"obsolete rare carcinoma of stomach (obsolete MONDO:0018501)","secondary_identifiers":["Orphanet:423771"],"synonyms":[{"name":"rare gastric carcinoma","type":"exact"},{"name":"rare stomach carcinoma","type":"exact"}],"termid":"MONDO:0018501","xrefs":{"Monarch":{"xref_id":"0018501"}}}


id: PBO:0017062
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"~37 copies of a 7-10 repeat consensus 'PMEEITTMTI' and a S/N rich C terminal region","termid":"PBO:0017062"}


id: MONDO:0015340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterized by a generalized skin rash, fever, eosinophilia, lymphocytosis and visceral involvement (hepatitis, nephritis, pneumonitis, pericarditis and myocarditis) and, in some patients, reactivation of human herpes virus 6.","definition_xrefs":["Orphanet:139402"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"urticaria","termid":"MONDO:0005492"},{"relation_name":"is_a","term_name":"severe cutaneous adverse reaction","termid":"MONDO:0005594"},{"relation_name":"is_a","term_name":"toxic dermatosis","termid":"MONDO:0017396"}],"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":"drug rash with eosinophilia and systemic symptoms","secondary_identifiers":["ICD10CM:D72.12","UMLS:C3541994","GARD:13629","MedDRA:10058919","MEDGEN:762193","MESH:D063926","SCTID:702809001","icd11.foundation:516577496","NCIT:C112208"],"synonyms":[{"name":"DHS","type":"exact"},{"name":"DRESS","type":"exact"},{"name":"DRESS syndrome","type":"exact"},{"name":"Drug hypersensitivity syndrome","type":"exact"},{"name":"Drug reaction with eosinophilia and Systemic symptoms","type":"exact"},{"name":"dress","type":"exact"},{"name":"drug reaction eosinophilic systemic syndrome","type":"exact"}],"termid":"MONDO:0015340","xrefs":{"Monarch":{"xref_id":"0015340"}}}


id: GO:0070418
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that is involved in the repair of DNA double-strand breaks and, in mammals, V(D)J recombination events. It consists of the DNA-dependent protein kinase catalytic subunit (DNA-PKcs) and the DNA end-binding heterodimer Ku.","definition_xrefs":["PMID:10854421","PMID:12235392","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"is_a","term_name":"serine/threonine protein kinase complex","termid":"GO:1902554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"DNA-dependent protein kinase complex","synonyms":[{"name":"DNA-PK complex","type":"exact"},{"name":"DNA-PK-Ku antigen complex","type":"exact"},{"name":"DNA-dependent protein kinase, DNA-end-binding complex","type":"narrow"}],"termid":"GO:0070418"}


id: MONDO:0027068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any mitochondrial complex 1 deficiency, mitochondrial type 1, in which the cause of the disease is a mutation in the MTND3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"disease","termid":"MONDO:0000001"},{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, mitochondrial type","termid":"MONDO:0100134"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, mitochondrial type 1","secondary_identifiers":["UMLS:C4746992","OMIM:500014","MEDGEN:1648371","DOID:0112101"],"synonyms":[{"name":"MC1DM1","type":"exact"},{"name":"mitochondrial complex I deficiency, mitochondrial type 1","type":"exact"}],"termid":"MONDO:0027068","xrefs":{"Monarch":{"xref_id":"0027068"}}}


id: PBO:0073216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEMA5A antisense RNA 1","termid":"PBO:0073216"}


id: PR:Q9Y704
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mok14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y704"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall alpha-1,3-glucan synthase mok14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC63.04","synonyms":[{"name":"Spom972h-mok14","type":"exact"}],"termid":"PR:Q9Y704"}


id: PBO:0088432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EKC/KEOPS complex associated ATPase Bud32","termid":"PBO:0088432"}


id: GO:1990791
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a dorsal root ganglion over time, from its formation to the mature structure.","definition_xrefs":["PMID:18583150"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ganglion development","termid":"GO:0061548"}],"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 root ganglion development","synonyms":[{"name":"DRG development","type":"exact"}],"termid":"GO:1990791"}


id: GO:0034821
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: citronellol + NAD+ = citronellal + NADH + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete citronellol dehydrogenase activity (obsolete GO:0034821)","termid":"GO:0034821"}


id: PBO:0042486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 11","termid":"PBO:0042486"}


id: PBO:0067310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 396, pseudogene","termid":"PBO:0067310"}


id: PBO:0042332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD58 molecule","termid":"PBO:0042332"}


id: PBO:0002667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"medial ring protein Mid2","termid":"PBO:0002667"}


id: FYPO:0001611
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 L-histidine measured in the vacuole is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular histidine level","termid":"FYPO:0001562"},{"relation_name":"is_a","term_name":"decreased level of substance in vacuole","termid":"FYPO:0001602"}],"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:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased vacuolar histidine level","synonyms":[{"name":"decreased level of histidine in vacuole","type":"exact"},{"name":"decreased vacuolar L-histidine level","type":"exact"},{"name":"decreased vacuolar histidine level during mitotic cell cycle","type":"related"},{"name":"decreased vacuolar histidine level during vegetative growth","type":"exact"},{"name":"reduced level of histidine in vacuole","type":"exact"},{"name":"reduced vacuolar histidine level","type":"exact"}],"termid":"FYPO:0001611"}


id: GO:0033409
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UAU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003723","GO:0060090","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"UAU codon-amino acid adaptor activity","synonyms":[{"name":"TAT codon-amino acid adaptor activity","type":"exact"},{"name":"tyrosine tRNA","type":"related"}],"termid":"GO:0033409"}


id: PBO:0069955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1248, pseudogene","termid":"PBO:0069955"}


id: MONDO:0014462
data:
  {"annotated_genes":["SJAG_01143","SJAG_00118"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88675,88676],"is_not":false,"summary":null,"term":"MONDO:0014462"}]},"cv_name":"mondo","definition":"Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the ANLN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited focal segmental glomerulosclerosis","termid":"MONDO:0005363"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_01143":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"focal segmental glomerulosclerosis 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4014993","MEDGEN:863430","OMIM:616032","DOID:0111133","GARD:16051"],"synonyms":[{"name":"ANLN focal segmental glomerulosclerosis","type":"exact"},{"name":"FSGS8","type":"exact"},{"name":"focal segmental glomerulosclerosis 8","type":"exact"},{"name":"focal segmental glomerulosclerosis caused by mutation in ANLN","type":"exact"},{"name":"focal segmental glomerulosclerosis type 8","type":"exact"},{"name":"glomerulosclerosis, focal segmental, 8","type":"related"}],"termid":"MONDO:0014462","terms_by_termid":{"MONDO:0014462":null},"xrefs":{"Monarch":{"xref_id":"0014462"}}}


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


id: GO:0090487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of secondary metabolites, the compounds that are not necessarily required for growth and maintenance of cells, and are often unique to a taxon.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"secondary metabolite catabolic process","synonyms":[{"name":"secondary metabolite breakdown","type":"exact"},{"name":"secondary metabolite catabolism","type":"exact"},{"name":"secondary metabolite degradation","type":"exact"}],"termid":"GO:0090487"}


id: PBO:0067110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 152, pseudogene","termid":"PBO:0067110"}


id: PBO:0080591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 18","termid":"PBO:0080591"}


id: GO:1905219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of platelet formation.","definition_xrefs":["GOC:TermGenie","PMID:10606160","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell morphogenesis","termid":"GO:0022604"},{"relation_name":"is_a","term_name":"regulation of myeloid cell differentiation","termid":"GO:0045637"},{"relation_name":"regulates","term_name":"platelet formation","termid":"GO:0030220"}],"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 platelet formation","synonyms":[{"name":"regulation of platelet extrusion","type":"exact"}],"termid":"GO:1905219"}


id: MONDO:0958333
data:
  {"annotated_genes":["SJAG_01784","SJAG_03818","SJAG_02951"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88963,88964,88965],"is_not":false,"summary":null,"term":"MONDO:0958333"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited thrombocytopenia","termid":"MONDO:0100241"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01784":null,"SJAG_02951":null,"SJAG_03818":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombocytopenia 13, syndromic","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1856296","OMIM:620776","UMLS:C5935599"],"termid":"MONDO:0958333","terms_by_termid":{"MONDO:0958333":null},"xrefs":{"Monarch":{"xref_id":"0958333"}}}


id: MONDO:0012032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Braddock syndrome is a rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, that is characterized by VACTERL -like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect.","definition_xrefs":["Orphanet:52047"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary hypertension","termid":"MONDO:0005149"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Braddock syndrome","secondary_identifiers":["UMLS:C1842082","GARD:16652","OMIM:608406","SCTID:720575002","MESH:C564244","MEDGEN:333986"],"synonyms":[{"name":"VATER-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency","type":"related"},{"name":"Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency","type":"exact"}],"termid":"MONDO:0012032","xrefs":{"Monarch":{"xref_id":"0012032"}}}


id: PR:O14170
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pop2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat-containing protein pop2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.03","synonyms":[{"name":"Spom972h-pop2","type":"exact"},{"name":"proteolysis factor sud1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14170"}


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


id: PBO:0012268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carboxylate transporter (predicted)","termid":"PBO:0012268"}


id: PBO:0111870
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B-type cyclin","termid":"PBO:0111870"}


id: PBO:0066311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBPJ pseudogene 5","termid":"PBO:0066311"}


id: MONDO:0019015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterized by a large hernia of the abdominal wall, centered on the umbilical cord, in which the protruding viscera are protected by a sac.","definition_xrefs":["Orphanet:660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abdominal wall malformation","termid":"MONDO:0100298"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"omphalocele","secondary_identifiers":["UMLS:C0795690","MedDRA:10030308","MESH:D006554","SCTID:396347007","DOID:0060327","GARD:16540","HP:0001539","NCIT:C98997","SCTID:18735004","ICD9:756.72","icd11.foundation:1168696429","MEDGEN:162756"],"synonyms":[{"name":"congenital omphalocele","type":"exact"},{"name":"eventration","type":"broad"},{"name":"exomphalos","type":"exact"},{"name":"omphalocele","type":"exact"},{"name":"omphalocele (disease)","type":"exact"},{"name":"omphalocoele","type":"exact"}],"termid":"MONDO:0019015","xrefs":{"Monarch":{"xref_id":"0019015"}}}


id: PBO:0049327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIE subunit 1","termid":"PBO:0049327"}


id: PBO:0030653
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_methylamine","termid":"PBO:0030653"}


id: GO:0045750
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of S phase of mitotic cell cycle activity.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of S phase of mitotic cell cycle (obsolete GO:0045750)","synonyms":[{"name":"activation of S phase of mitotic cell cycle","type":"narrow"},{"name":"positive regulation of S phase of mitotic cell cycle","type":"exact"},{"name":"positive regulation of S-phase of mitotic cell cycle","type":"exact"},{"name":"stimulation of S phase of mitotic cell cycle","type":"narrow"},{"name":"up regulation of S phase of mitotic cell cycle","type":"exact"},{"name":"up-regulation of S phase of mitotic cell cycle","type":"exact"},{"name":"upregulation of S phase of mitotic cell cycle","type":"exact"}],"termid":"GO:0045750"}


id: GO:0106176
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a clathrin-coated endocytic vesicle.","definition_xrefs":["PMID:2516741","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocytic vesicle lumen","termid":"GO:0071682"},{"relation_name":"part_of","term_name":"clathrin-coated endocytic vesicle","termid":"GO:0045334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"clathrin-coated endocytic vesicle lumen","termid":"GO:0106176"}


id: PBO:0076092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STUB1 pseudogene 1","termid":"PBO:0076092"}


id: PATO:0001413
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the rate of the bearer's angular movement about an axis; the angle rotated in a given time.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Angular_velocity"],"direct_ancestors":[{"relation_name":"is_a","term_name":"velocity","termid":"PATO:0002242"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angular velocity","termid":"PATO:0001413"}


id: PBO:0060172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTUS1 divergent transcript","termid":"PBO:0060172"}


id: MONDO:0007842
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of Ehlers-Danlos syndrome characterized by generalized joint hypermobility often complicated by dislocation of major joints, particularly the shoulder but in some cases the kneecap. Congenital hip dislocation has also been frequently reported. The syndrome has been described in several families. It is transmitted as an autosomal dominant trait, with high penetrance.","definition_xrefs":["Orphanet:2295"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"joint laxity, familial","secondary_identifiers":["GARD:3054","OMIM:147900","MEDGEN:120629","UMLS:C0268349","SCTID:71322004","MESH:C535884"],"synonyms":[{"name":"EDS 11 (formerly)","type":"related"},{"name":"EDS XI","type":"exact"},{"name":"EDS Xi","type":"related"},{"name":"EDS Xi, formerly","type":"related"},{"name":"EDS11","type":"related"},{"name":"EDS11, formerly","type":"related"},{"name":"Ehlers-Danlos syndrome type 11, formerly","type":"exact"},{"name":"Ehlers-Danlos syndrome, type 11 (formerly)","type":"related"},{"name":"Ehlers-Danlos syndrome, type Xi","type":"related"},{"name":"Ehlers-Danlos syndrome, type Xi, formerly","type":"related"},{"name":"Joint instability syndrome","type":"exact"},{"name":"articular hypermobility syndrome","type":"related"},{"name":"familial joint instability syndrome","type":"exact"},{"name":"familial joint laxity","type":"exact"},{"name":"joint laxity, familial","type":"exact"}],"termid":"MONDO:0007842","xrefs":{"Monarch":{"xref_id":"0007842"}}}


id: PBO:0078500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon TAT) 2-3","termid":"PBO:0078500"}


id: MONDO:0012392
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare organic aciduria characterized by impaired isoleucine degradation with increased plasma or whole blood C5 acylcarnitine levels (typically observed in newborn screening) and increased urinary excretion of N-methylbutyrylglycine. The condition is usually clinically asymptomatic, although patients with muscular hypotonia, developmental delay, and seizures (among others) have been reported.","definition_xrefs":["Orphanet:79157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"classic organic aciduria","termid":"MONDO:0019215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"2-methylbutyryl-CoA dehydrogenase deficiency","secondary_identifiers":["MEDGEN:355324","MESH:C566487","NCIT:C98863","UMLS:C1864912","OMIM:610006","GARD:10322"],"synonyms":[{"name":"2-methylbutyric aciduria","type":"exact"},{"name":"2-methylbutyryl Glycinuria","type":"related"},{"name":"2-methylbutyryl-CoA dehydrogenase deficiency","type":"exact"},{"name":"2-methylbutyrylglycinuria","type":"exact"},{"name":"SBCAD deficiency","type":"exact"},{"name":"butyryl-CoA dehydrogenase deficiency","type":"exact"},{"name":"developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency","type":"exact"},{"name":"short branched-chain acyl-CoA dehydrogenase deficiency","type":"related"},{"name":"short/branched-chain acyl-Coa dehydrogenase deficiency","type":"related"},{"name":"short/branched-chain acyl-coA dehydrogenase deficiency","type":"exact"}],"termid":"MONDO:0012392","xrefs":{"Monarch":{"xref_id":"0012392"}}}


id: MONDO:1012651
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary hypothyroidism and primary cortisol-deficient hypoadrenocorticism with increased serum concentrations of thyroglobulin autoantibodies and 21-hydroxylase autoantibodies that occurs in dogs.","definition_xrefs":["PMID:27487017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypoadrenocorticism, dog","termid":"MONDO:1012109"},{"relation_name":"is_a","term_name":"primary hypothyroidism, dog","termid":"MONDO:1012121"},{"relation_name":"is_a","term_name":"autoimmune disease, non-human animal","termid":"MONDO:1012985"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune polyendocrinopathy, dog","secondary_identifiers":["OMIA:001179-9615"],"synonyms":[{"name":"polyglandular autoimmune syndrome, type II, dog","type":"related"}],"termid":"MONDO:1012651","xrefs":{"Monarch":{"xref_id":"1012651"}}}


id: SO:0000973
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A terminal_inverted_repeat_element that is bacterial and only encodes the functions required for its transposition between these inverted repeats.","definition_xrefs":["SO:as"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insertion_sequence","secondary_identifiers":["http://en.wikipedia.org/wiki/Insertion_sequence"],"synonyms":[{"name":"IS","type":"related"},{"name":"insertion sequence","type":"exact"}],"termid":"SO:0000973"}


id: GO:0003118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of reductions in the diameter of blood vessels as a result of norepinephrine released by nerve endings.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vasoconstriction by norepinephrine","termid":"GO:0003116"}],"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 vasoconstriction by neuronal norepinephrine","synonyms":[{"name":"regulation of vasoconstriction by neuronal noradrenaline","type":"exact"}],"termid":"GO:0003118"}


id: PBO:0077697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tankyrase 1 binding protein 1","termid":"PBO:0077697"}


id: MONDO:0023530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypertensive disorder","termid":"MONDO:0005044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kallikrein hypertension","secondary_identifiers":["UMLS:C1171349","MEDGEN:257936","HGNC:6357","MESH:C537707"],"synonyms":[{"name":"kallikrein attenuated hypertension","type":"related"}],"termid":"MONDO:0023530","xrefs":{"Monarch":{"xref_id":"0023530"}}}


id: FYPO:0003633
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which U1 snRNP binding by a gene product does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction","termid":"FYPO:0000705"},{"relation_name":"is_a","term_name":"abnormal ribonucleoprotein complex binding","termid":"FYPO:0003632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0001985","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"abolished U1 snRNP binding","synonyms":[{"name":"U1 snRNP binding abolished","type":"exact"}],"termid":"FYPO:0003633"}


id: GO:0032143
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a double-stranded DNA region containing a single thymine insertion or a deletion that results in an unpaired thymine.","definition_xrefs":["GOC:mah","GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"single base insertion or deletion binding","termid":"GO:0032138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0003677","GO:0005488"],"is_obsolete":false,"name":"single thymine insertion binding","termid":"GO:0032143"}


id: GO:0004756
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O + hydrogen selenide = AMP + 3 H+ + phosphate + selenophosphorate.","definition_xrefs":["EC:2.7.9.3","RHEA:18737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, paired acceptors","termid":"GO:0016781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"selenide, water dikinase activity","secondary_identifiers":["MetaCyc:2.7.9.3-RXN","UM-BBD_reactionID:r0833","KEGG_REACTION:R03595","Reactome:R-HSA-8959510"],"synonyms":[{"name":"ATP:selenide, water phosphotransferase activity","type":"related"},{"name":"selenide,water dikinase activity","type":"related"},{"name":"selenium donor protein activity","type":"related"},{"name":"selenophosphate synthase activity","type":"exact"},{"name":"selenophosphate synthetase activity","type":"related"}],"termid":"GO:0004756"}


id: GO:0080017
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = alpha-humulene + diphosphate.","definition_xrefs":["PMID:9442047","PMID:12566586","RHEA:31895"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclase activity","termid":"GO:0009975"},{"relation_name":"is_a","term_name":"sesquiterpene synthase activity","termid":"GO:0010334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0009975"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824","GO:0009975"],"is_obsolete":false,"name":"alpha-humulene synthase activity","secondary_identifiers":["EC:4.2.3.104","MetaCyc:RXN-8415"],"termid":"GO:0080017"}


id: PBO:0076232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Suv3 like RNA helicase","termid":"PBO:0076232"}


id: MONDO:1012822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital myopathy that occurs in pigs due to a mutation in the SPTBN4 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy, non-human animal","termid":"MONDO:1010196"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital myopathy, SPTBN4-related, pig","secondary_identifiers":["OMIA:002232-9823"],"termid":"MONDO:1012822","xrefs":{"Monarch":{"xref_id":"1012822"}}}


id: PBO:0073996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 3 pseudogene 3","termid":"PBO:0073996"}


id: GO:0060848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involved in cell fate commitment of an endothelial cell. Once determination has taken place, a cell becomes committed to differentiate down a particular pathway regardless of its environment.","definition_xrefs":["GOC:dph","GOC:tb","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate determination","termid":"GO:0001709"},{"relation_name":"part_of","term_name":"endothelial cell fate commitment","termid":"GO:0060839"}],"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":"endothelial cell fate determination","termid":"GO:0060848"}


id: PBO:0057133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 216b","termid":"PBO:0057133"}


id: PBO:0082582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chromatin associated high mobility group (HMG) family member; involved in compacting, bending, bridging and looping DNA; rDNA-binding component that regulates transcription from RNA polymerase I promoters; regulates start site selection of ribosomal protein genes via RNA polymerase II promoters; role in genome maintenance; associates with a 5'-3' DNA helicase and Fpr1p, a prolyl isomerase; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082582"}


id: PBO:0083315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps ORF DAP2/YHR028C","termid":"PBO:0083315"}


id: MONDO:0013068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"},{"relation_name":"is_a","term_name":"presbycusis","termid":"MONDO:0043765"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"age-related hearing impairment 2","secondary_identifiers":["UMLS:C2751814","MEDGEN:416639","OMIM:612976","MESH:C567834"],"synonyms":[{"name":"ARHI2","type":"exact"},{"name":"age-related hearing impairment 2","type":"exact"},{"name":"presbycusis 2","type":"related"}],"termid":"MONDO:0013068","xrefs":{"Monarch":{"xref_id":"0013068"}}}


id: MONDO:0032692
data:
  {"annotated_genes":["SJAG_04148"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87867],"is_not":false,"summary":null,"term":"MONDO:0032692"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Galloway-Mowat syndrome","termid":"MONDO:0009627"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04148":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Galloway-Mowat syndrome 7","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16344","OMIM:618348","UMLS:C5193044","MEDGEN:1679283"],"synonyms":[{"name":"GALLOWAY-MOWAT SYNDROME 7","type":"related"},{"name":"GAMOS7","type":"related"}],"termid":"MONDO:0032692","terms_by_termid":{"MONDO:0032692":null},"xrefs":{"Monarch":{"xref_id":"0032692"}}}


id: MONDO:0010757
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":"widow's peak syndrome","secondary_identifiers":["MESH:C564040","OMIM:314570","UMLS:C1839112","MEDGEN:374133"],"synonyms":[{"name":"widow's peak syndrome","type":"exact"},{"name":"widow's peak, ptosis, and skeletal anomalies","type":"related"}],"termid":"MONDO:0010757","xrefs":{"Monarch":{"xref_id":"0010757"}}}


id: PBO:0053920
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 1217","termid":"PBO:0053920"}


id: SO:0000184
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A major type of spliceosomal intron spliced by the U2 spliceosome, that includes U1, U2, U4/U6 and U5 snRNAs.","definition_xrefs":["PMID:9428511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal_intron","termid":"SO:0000662"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2_intron","synonyms":[{"name":"U2 intron","type":"exact"}],"termid":"SO:0000184"}


id: GO:1903330
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of iron-sulfur cluster assembly.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"regulation of iron-sulfur cluster assembly","termid":"GO:1903329"},{"relation_name":"negatively_regulates","term_name":"iron-sulfur cluster assembly","termid":"GO:0016226"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0016226"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0016226"}],"interesting_parent_ids":["GO:0008150","GO:0016226","GO:0044085"],"is_obsolete":false,"name":"negative regulation of iron-sulfur cluster assembly","synonyms":[{"name":"down regulation of iron-sulfur cluster assembly","type":"exact"},{"name":"down regulation of iron-sulfur cluster biosynthesis","type":"related"},{"name":"down regulation of iron-sulphur cluster assembly","type":"exact"},{"name":"down-regulation of iron-sulfur cluster assembly","type":"exact"},{"name":"down-regulation of iron-sulfur cluster biosynthesis","type":"related"},{"name":"down-regulation of iron-sulphur cluster assembly","type":"exact"},{"name":"downregulation of iron-sulfur cluster assembly","type":"exact"},{"name":"downregulation of iron-sulfur cluster biosynthesis","type":"related"},{"name":"downregulation of iron-sulphur cluster assembly","type":"exact"},{"name":"inhibition of iron-sulfur cluster assembly","type":"narrow"},{"name":"inhibition of iron-sulfur cluster biosynthesis","type":"related"},{"name":"inhibition of iron-sulphur cluster assembly","type":"narrow"},{"name":"negative regulation of iron-sulfur cluster biosynthesis","type":"related"},{"name":"negative regulation of iron-sulphur cluster assembly","type":"exact"}],"termid":"GO:1903330"}


id: GO:1905278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of epithelial tube formation.","definition_xrefs":["GO_REF:0000058","GOC:bhm","GOC:TermGenie","PMID:25745997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of epithelial tube formation","termid":"GO:1905276"},{"relation_name":"is_a","term_name":"positive regulation of morphogenesis of an epithelium","termid":"GO:1905332"},{"relation_name":"positively_regulates","term_name":"epithelial tube formation","termid":"GO:0072175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of epithelial tube formation","synonyms":[{"name":"activation of epithelial tube formation","type":"narrow"},{"name":"up regulation of epithelial tube formation","type":"exact"},{"name":"up-regulation of epithelial tube formation","type":"exact"},{"name":"upregulation of epithelial tube formation","type":"exact"}],"termid":"GO:1905278"}


id: PBO:0085237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peptidyl-prolyl cis/trans-isomerase; activator of the phosphotyrosyl phosphatase activity of PP2A; involved in G1 phase progression, microtubule dynamics, bud morphogenesis and DNA repair; required for rapid reduction of Sgs1p levels in response to rapamycin; subunit of the Tap42p-Sit4p-Rrd1p complex; protein increases in abundance and relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0085237"}


id: FYPO:0002316
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 squalene 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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal cellular squalene level","synonyms":[{"name":"normal cellular squalene accumulation","type":"related"},{"name":"normal cellular squalene level during mitotic cell cycle","type":"related"},{"name":"normal cellular squalene level during vegetative growth","type":"exact"}],"termid":"FYPO:0002316"}


id: PBO:0073950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 20 member 1 pseudogene 3","termid":"PBO:0073950"}


id: GO:0061807
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of DNA recombination at the centromere.","definition_xrefs":["GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA recombination","termid":"GO:0045911"},{"relation_name":"is_a","term_name":"regulation of DNA recombination at centromere","termid":"GO:0061806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"positively_regulates","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0006310"],"is_obsolete":false,"name":"positive regulation of DNA recombination at centromere","synonyms":[{"name":"positive regulation of centromeric recombination","type":"exact"}],"termid":"GO:0061807"}


id: FYPO:0006923
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype in which the frequency of DNA recombination is normal (i.e. indistinguishable from wild type) at DNA replication fork barriers.","definition_xrefs":["PMID:31149897","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"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 DNA recombination frequency at mitotic DNA replication fork barriers","synonyms":[{"name":"normal DNA recombination frequency at mitotic DNA replication fork barriers during mitotic cell cycle","type":"related"},{"name":"normal DNA recombination frequency at mitotic DNA replication fork barriers during vegetative growth","type":"exact"}],"termid":"FYPO:0006923"}


id: GO:0032295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which satellite glial cells isolate neuronal cell bodies.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ensheathment of neurons","termid":"GO:0007272"}],"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":"ensheathment of neuronal cell bodies","termid":"GO:0032295"}


id: MONDO:0007348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete colchicine resistance (obsolete MONDO:0007348)","secondary_identifiers":["OMIM:120080"],"synonyms":[{"name":"colchicine resistance","type":"exact"},{"name":"colchicine sensitivity","type":"related"}],"termid":"MONDO:0007348","xrefs":{"Monarch":{"xref_id":"0007348"}}}


id: MOD:01840
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to L-allo-isoleucine.","definition_xrefs":["ChEBI:43433","PubMed:20805503","RESID:AA0546"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stereoisomerized residue","termid":"MOD:00664"},{"relation_name":"is_a","term_name":"modified L-isoleucine residue","termid":"MOD:00910"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-allo-isoleucine","synonyms":[{"name":"(2S,3R)-2-amino-3-methylpentanoic acid","type":"exact"},{"name":"2-azanyl-3-methylpentanoic acid","type":"exact"},{"name":"3-methyl-norvaline","type":"exact"},{"name":"L-allo-isoleucine","type":"exact"},{"name":"L-threo-isoleucine","type":"exact"},{"name":"MOD_RES L-allo-isoleucine","type":"exact"},{"name":"allo-L-isoleucine","type":"exact"},{"name":"alpha-amino-beta-methylvaleric acid","type":"exact"}],"termid":"MOD:01840"}


id: MONDO:0021107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sleep disorder characterized by a tendency for excessive sleepiness during the day which occurs even after adequate sleep in the nighttime. The persons who suffer from this condition experience fatigue and may fall asleep at inappropriate times during the day.","definition_xrefs":["NCIT:C84489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sleep-wake disorder","termid":"MONDO:0003406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"narcolepsy","secondary_identifiers":["MESH:D009290","DOID:8986","GARD:22460","icd11.foundation:1201727099","SCTID:60380001","ICD10CM:G47.41","UMLS:C0027404","Orphanet:619284","MEDGEN:45001"],"synonyms":[{"name":"narcolepsy with or without cataplexy","type":"exact"},{"name":"narcolepsy, without cataplexy","type":"narrow"},{"name":"paroxysmal sleep","type":"exact"}],"termid":"MONDO:0021107","xrefs":{"Monarch":{"xref_id":"0021107"}}}


id: PBO:0001121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI inositol deacylase (predicted)","termid":"PBO:0001121"}


id: PBO:0068225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 532","termid":"PBO:0068225"}


id: GO:0060780
data:
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