# terms

id: PR:Q9URX7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein arginine N-methyltransferase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02088"],"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 arginine N-methyltransferase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC890.07c","secondary_identifiers":["UniProtKB:Q9URX7"],"synonyms":[{"name":"Spom972h-PRMT1","type":"exact"},{"name":"type I PRMT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"type I protein arginine N-methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9URX7"}


id: PBO:0000271
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromatin silencing function of H2Bub is independent of H3K4 methylation","termid":"PBO:0000271"}


id: PBO:0065495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PSMG3 antisense RNA 1 (head to head)","termid":"PBO:0065495"}


id: GO:0051352
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops or reduces the rate 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"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of ligase activity (obsolete GO:0051352)","synonyms":[{"name":"down regulation of ligase activity","type":"exact"},{"name":"down-regulation of ligase activity","type":"exact"},{"name":"downregulation of ligase activity","type":"exact"},{"name":"inhibition of ligase activity","type":"narrow"},{"name":"ligase inhibitor","type":"exact"}],"termid":"GO:0051352"}


id: PBO:0073645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIGLEC family like 1","termid":"PBO:0073645"}


id: SO:0000494
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A 9 nucleotide recombination site (e.g. ACAAAAACC), part of a 3' D-recombination signal sequence of an immunoglobulin/T-cell receptor gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"nonamer_of_recombination_feature_of_vertebrate_immune_system_gene","termid":"SO:0000562"},{"relation_name":"part_of","term_name":"three_prime_D_recombination_signal_sequence","termid":"SO:0000570"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_D_nonamer","synonyms":[{"name":"3'D-NOMAMER","type":"exact"},{"name":"three prime D nonamer","type":"exact"}],"termid":"SO:0000494"}


id: PBO:0116250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF2458 family conserved fungal protein","termid":"PBO:0116250"}


id: PBO:0029626
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_meiotic_sister_chromatid_cohesion","termid":"PBO:0029626"}


id: PBO:0049033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 20","termid":"PBO:0049033"}


id: MONDO:0015624
data:
  {"annotated_genes":["SJAG_03266","SJAG_04334","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86247,86248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011236"},{"annotations":[86576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011717"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital isolated hyperinsulinism","termid":"MONDO:0019010"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03266":null,"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0004335"],"is_obsolete":false,"name":"diazoxide-sensitive diffuse hyperinsulinism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5679570","Orphanet:165985","MEDGEN:1842739","GARD:20067"],"synonyms":[{"name":"hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form","type":"exact"}],"termid":"MONDO:0015624","terms_by_termid":{"MONDO:0011236":null,"MONDO:0011717":null},"xrefs":{"Monarch":{"xref_id":"0015624"}}}


id: GO:0005231
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of an ion by a channel that opens when a specific extracellular ligand has been bound by the channel complex or one of its constituent parts, where channel opening contributes to an increase in membrane potential.","definition_xrefs":["ISBN:0323037070","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular ligand-gated monoatomic ion channel activity","termid":"GO:0005230"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"excitatory extracellular ligand-gated monoatomic ion channel activity","secondary_identifiers":["Reactome:R-HSA-399712","Reactome:R-HSA-399711","Reactome:R-HSA-432164","Reactome:R-HSA-438037","Reactome:R-HSA-420980"],"termid":"GO:0005231"}


id: PR:O14345
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A palmitoyltransferase ZDHHC21 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02966","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":"palmitoyltransferase pfa3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2F12.15c","secondary_identifiers":["UniProtKB:O14345"],"synonyms":[{"name":"Spom972h-ZDHHC21","type":"exact"},{"name":"protein fatty acyltransferase 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14345"}


id: FYPO:0003079
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 genetic imprinting at the mating-type locus is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating type switching","termid":"FYPO:0000468"},{"relation_name":"is_a","term_name":"regulation phenotype during vegetative growth","termid":"FYPO:0001334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal genetic imprinting at mating-type locus","synonyms":[{"name":"abnormal genetic imprinting at mating-type locus during mitotic cell cycle","type":"related"},{"name":"abnormal genetic imprinting at mating-type locus during vegetative growth","type":"exact"}],"termid":"FYPO:0003079"}


id: GO:0071960
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the association between sister chromatids of a replicated chromosome along the length of the centromeric region is maintained as chromosomes condense, attach to the spindle in a bipolar orientation, and congress to the metaphase plate during a mitotic cell cycle.","definition_xrefs":["GOC:mah","PMID:1708436"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"},{"relation_name":"part_of","term_name":"mitotic sister chromatid cohesion, centromeric","termid":"GO:0071962"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"maintenance of mitotic sister chromatid cohesion, centromeric","synonyms":[{"name":"maintenance of centromeric mitotic sister chromatin cohesion","type":"exact"},{"name":"maintenance of mitotic sister chromatin cohesion at centromere","type":"exact"},{"name":"maintenance of sister chromatin cohesion at centromere at mitosis","type":"exact"}],"termid":"GO:0071960"}


id: PATO:0001420
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the bearer's disposition to rise or float in a fluid medium such as water or air.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"buoyancy","termid":"PATO:0001420"}


id: GO:0004917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-7 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:jl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"interleukin-7 receptor activity","synonyms":[{"name":"IL-7 receptor activity","type":"exact"},{"name":"IL-7R","type":"exact"}],"termid":"GO:0004917"}


id: PBO:0050105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 15","termid":"PBO:0050105"}


id: GO:0006735
data:
  {"annotated_genes":["SJAG_00605","SJAG_03373","SJAG_02369","SJAG_06621","SJAG_02191","SJAG_03828","SJAG_02107","SJAG_06622","SJAG_02135","SJAG_00839","SJAG_02796","SJAG_04334","SJAG_04495","SJAG_02945","SJAG_02154","SJAG_00461","SJAG_03903","SJAG_02009","SJAG_03660","SJAG_04192","SJAG_00027","SJAG_01310"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94868,94869],"is_not":false,"summary":null,"term":"GO:0006735"},{"annotations":[94773,105255,103427,109194,103173,109196,109195,105256,109193,109198,116159,94284,105257,105625,109197,97772,105626,77597,98051,109192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"}]},"cv_name":"biological_process","definition":"A metabolic process that generates a pool of NADH by the reduction of NAD+.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NADH metabolic process","termid":"GO:0006734"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00839":null,"SJAG_01310":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02154":null,"SJAG_02191":null,"SJAG_02369":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"NADH regeneration","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"NAD (reduced) regeneration","type":"exact"},{"name":"reduced NAD regeneration","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide regeneration","type":"exact"}],"termid":"GO:0006735","terms_by_termid":{"GO:0006735":null,"GO:0061621":null}}


id: GO:0008774
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetaldehyde + CoA + NAD+ = acetyl-CoA + NADH + H+.","definition_xrefs":["EC:1.2.1.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"acetaldehyde dehydrogenase (acetylating) activity","secondary_identifiers":["MetaCyc:ACETALD-DEHYDROG-RXN","RHEA:23288"],"synonyms":[{"name":"ADA","type":"related"},{"name":"DmpF","type":"related"},{"name":"acetaldehyde:NAD+ oxidoreductase (CoA-acetylating)","type":"related"},{"name":"acylating acetaldehyde dehydrogenase activity","type":"related"},{"name":"aldehyde dehydrogenase (acylating) activity","type":"related"}],"termid":"GO:0008774"}


id: PBO:0043208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC28 protein kinase regulatory subunit 1B pseudogene 1","termid":"PBO:0043208"}


id: PBO:0065758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyrin and HIN domain family member 1","termid":"PBO:0065758"}


id: PATO:0002274
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Multicolored quality inhering in a bearer by virtue of the bearer's being dappled with spots, patches, or blotches of different colors.","direct_ancestors":[{"relation_name":"is_a","term_name":"multi-colored","termid":"PATO:0001533"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mottled","termid":"PATO:0002274"}


id: GO:0033277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cell cycle in which mitosis is begun and progresses normally through the end of anaphase, but not completed, resulting in a cell with increased ploidy.","definition_xrefs":["PMID:9573008","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete abortive mitotic cell cycle (obsolete GO:0033277)","synonyms":[{"name":"abortive mitosis","type":"related"}],"termid":"GO:0033277"}


id: GO:0071584
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of zinc ion import.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of zinc ion transmembrane import","termid":"GO:0071581"},{"relation_name":"is_a","term_name":"negative regulation of zinc ion transmembrane transport","termid":"GO:0071583"},{"relation_name":"negatively_regulates","term_name":"zinc ion import across plasma membrane","termid":"GO:0071578"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of zinc ion transmembrane import","termid":"GO:0071584"}


id: PBO:0031052
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_trichostatin_A","termid":"PBO:0031052"}


id: MONDO:0003854
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tibial adamantinoma (obsolete MONDO:0003854)","termid":"MONDO:0003854","xrefs":{"Monarch":{"xref_id":"0003854"}}}


id: MONDO:0010425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lisch epithelial corneal dystrophy (LECD) is a very rare form of superficial corneal dystrophy characterized by feather-shaped opacities and microcysts in the corneal epithelium arranged in a band-shaped and sometimes whorled pattern, occasionally with impaired vision.","definition_xrefs":["Orphanet:98955"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial and subepithelial corneal dystrophy","termid":"MONDO:0000763"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"superficial corneal dystrophy","termid":"MONDO:0020212"}],"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":"Lisch epithelial corneal dystrophy","secondary_identifiers":["DOID:0060450","MEDGEN:411737","OMIM:620763","UMLS:C2749050","GARD:16877","icd11.foundation:1571503165","OMIM:300778","SCTID:724175002","MESH:C567588"],"synonyms":[{"name":"LECD","type":"exact"},{"name":"Lisch epithelial corneal dystrophy","type":"exact"},{"name":"band-Shaped and whorled microcystic corneal epithelial dystrophy","type":"related"},{"name":"band-shaped and whorled microcystic","type":"exact"},{"name":"band-shaped and whorled microcystic dystrophy of the corneal epithelium","type":"exact"},{"name":"corneal dystrophy, Lisch epithelial","type":"related"},{"name":"corneal dystrophy, Lisch epithelial, X-linked dominant","type":"exact"}],"termid":"MONDO:0010425","xrefs":{"Monarch":{"xref_id":"0010425"}}}


id: GO:0015818
data:
  {"annotated_genes":["SJAG_02029","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102588,109824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903714"}]},"cv_name":"biological_process","definition":"The directed movement of isoleucine, (2R*,3R*)-2-amino-3-methylpentanoic acid, 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":"branched-chain amino acid transport","termid":"GO:0015803"},{"relation_name":"is_a","term_name":"neutral amino acid transport","termid":"GO:0015804"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02029":null,"SJAG_04725":null},"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"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"isoleucine transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-isoleucine transport","type":"narrow"}],"termid":"GO:0015818","terms_by_termid":{"GO:1903714":null}}


id: GO:0050664
data:
  {"annotated_genes":["SJAG_05033","SJAG_03098"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78865,78950],"is_not":false,"summary":null,"term":"GO:0050664"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which NADH or NADPH acts as a hydrogen or electron donor and reduces an oxygen molecule.","definition_xrefs":["EC:1.6.3.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H","termid":"GO:0016651"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03098":null,"SJAG_05033":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"oxidoreductase activity, acting on NADH or NADPH, oxygen as acceptor","type":"related"}],"termid":"GO:0050664","terms_by_termid":{"GO:0050664":null}}


id: GO:0052742
data:
  {"annotated_genes":["SJAG_01863","SJAG_04537","SJAG_01571","SJAG_00114","SJAG_05330","SJAG_00638"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76241,92983,71427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004430"},{"annotations":[71147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016303"},{"annotations":[91603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052811"},{"annotations":[72244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000285"},{"annotations":[79105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016308"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + a phosphatidylinositol = ADP + a phosphatidylinositol phosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid kinase activity","termid":"GO:0001727"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00638":null,"SJAG_01571":null,"SJAG_01863":null,"SJAG_04537":null,"SJAG_05330":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016301","GO:0003824"],"is_obsolete":false,"name":"phosphatidylinositol kinase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1675773"],"synonyms":[{"name":"1-phosphatidylinositol kinase activity","type":"exact"}],"termid":"GO:0052742","terms_by_termid":{"GO:0000285":null,"GO:0004430":null,"GO:0016303":null,"GO:0016308":null,"GO:0052811":null}}


id: MONDO:0001560
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An abnormality characterized by thickening of the muscle in the wall of the pylorus. It results in the narrowing of the pyloric channel. The overlying mucosa may appear hypertrophic as well. Clinical signs and symptoms appear early in life and include projectile vomiting and dehydration.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyloric stenosis","termid":"MONDO:0001561"},{"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":"hypertrophic pyloric stenosis","secondary_identifiers":["MESH:D046248","SCTID:48644003","DOID:12638","EFO:0004707","ICD10CM:Q40.0","NCIT:C98952","ICD9:750.5"],"synonyms":[{"name":"IHPS","type":"exact"},{"name":"congenital Hypertrophy of the pylorus","type":"exact"},{"name":"congenital constriction of the pylorus","type":"exact"},{"name":"congenital hypertrophic pyloric stenosis","type":"exact"},{"name":"congenital or infantile stricture of pylorus","type":"exact"},{"name":"congenital pyloric stenosis","type":"exact"},{"name":"congenital stricture of the pylorus","type":"exact"},{"name":"infantile Hypertrophy of the pylorus","type":"exact"},{"name":"infantile constriction of the pylorus","type":"exact"},{"name":"infantile hypertrophic pyloric stenosis","type":"exact"},{"name":"infantile pyloric stenosis","type":"exact"},{"name":"infantile stricture of the pylorus","type":"exact"},{"name":"pyloric stenosis, infantile","type":"exact"}],"termid":"MONDO:0001560","xrefs":{"Monarch":{"xref_id":"0001560"}}}


id: MONDO:0015247
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Opsoclonus myoclonus syndrome (OMS) is a rare neuroinflammatory disease of paraneoplastic, parainfectious or idiopathic origin, characterized by opsoclonus, myoclonus, ataxia, and behavioral and sleep disorders.","definition_xrefs":["Orphanet:1183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"paraneoplastic neurologic syndrome","termid":"MONDO:0018215"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opsoclonus-myoclonus syndrome","secondary_identifiers":["EFO:1001383","GARD:10009","NORD:1527","MEDGEN:97955","SCTID:230350000","UMLS:C0393626","ICD9:379.59","MedDRA:10053854","MESH:D053578","NCIT:C4686"],"synonyms":[{"name":"Ataxo-opso-myoclonus syndrome","type":"exact"},{"name":"Kinsbourne syndrome","type":"exact"},{"name":"OMS","type":"exact"},{"name":"Opsoclonus-Myoclonus-Ataxia Syndrome","type":"exact"},{"name":"POMA syndrome","type":"exact"},{"name":"dancing eye syndrome","type":"exact"},{"name":"dancing eye-dancing feet syndrome","type":"exact"},{"name":"oma syndrome","type":"exact"},{"name":"opsoclonus myoclonus syndrome","type":"exact"},{"name":"opsoclonus-myoclonus-ataxia syndrome","type":"exact"},{"name":"paraneoplastic opsoclonus-myoclonus","type":"exact"},{"name":"paraneoplastic opsoclonus-myoclonus-ataxia syndrome","type":"exact"}],"termid":"MONDO:0015247","xrefs":{"Monarch":{"xref_id":"0015247"}}}


id: GO:0005675
data:
  {"annotated_genes":["SJAG_00150","SJAG_03206","SJAG_00758","SJAG_04368","SJAG_01207","SJAG_04614","SJAG_00901","SJAG_00995","SJAG_03618","SJAG_00512","SJAG_04420"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[69678,69980,74045,75981,78368,91930,108782,114635],"is_not":false,"summary":null,"term":"GO:0005675"},{"annotations":[60580,76064,111879],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070985"}]},"cv_name":"cellular_component","definition":"A complex that is capable of kinase activity directed towards the C-terminal Domain (CTD) of the largest subunit of RNA polymerase II and is essential for initiation at RNA polymerase II promoters in vitro. It is composed of the core TFIIH complex and the TFIIK complex.","definition_xrefs":["GOC:krc","PMID:14500720","GOC:ew","PMID:22572993","PMID:22308316","PMID:7813015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-terminal domain protein kinase complex","termid":"GO:0032806"},{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"},{"relation_name":"part_of","term_name":"RNA polymerase II, holoenzyme","termid":"GO:0016591"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00150":null,"SJAG_00512":null,"SJAG_00758":null,"SJAG_00901":null,"SJAG_00995":null,"SJAG_01207":null,"SJAG_03206":null,"SJAG_03618":null,"SJAG_04368":null,"SJAG_04420":null,"SJAG_04614":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0005654","GO:0032991"],"is_obsolete":false,"name":"transcription factor TFIIH holo complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"holo TFIIH complex","type":"exact"}],"termid":"GO:0005675","terms_by_termid":{"GO:0005675":null,"GO:0070985":null}}


id: GO:0003425
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cell cycle process that sets the alignment of mitotic spindle relative to other cellular structures and contributes to oriented chondrocyte division in the growth plate.","definition_xrefs":["GOC:ascb_2009","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of mitotic spindle orientation","termid":"GO:0000132"},{"relation_name":"is_a","term_name":"cytoskeleton polarization involved in growth plate cartilage chondrocyte division","termid":"GO:0003426"},{"relation_name":"is_a","term_name":"microtubule cytoskeleton organization involved in establishment of planar polarity","termid":"GO:0090176"}],"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:0000226"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0007163"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007049","GO:0007163","GO:0051179","GO:0000226","GO:0008150","GO:0007010"],"is_obsolete":false,"name":"establishment of mitotic spindle orientation involved in growth plate cartilage chondrocyte division","termid":"GO:0003425"}


id: PBO:0068342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 113B","termid":"PBO:0068342"}


id: GO:0021741
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the spinal trigeminal nucleus over time, from its formation to the mature structure.","definition_xrefs":["GOC:cls","GOC:dgh","GO_REF:0000021","GOC:curators","GOC:jid","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trigeminal sensory nucleus development","termid":"GO:0021730"}],"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":"spinal trigeminal nucleus development","termid":"GO:0021741"}


id: MONDO:1010629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chediak-Higashi syndrome that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Chediak-Higashi syndrome, non-human animal","termid":"MONDO:1010070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chediak-Higashi syndrome, domestic cat","secondary_identifiers":["OMIA:000185-9685"],"termid":"MONDO:1010629","xrefs":{"Monarch":{"xref_id":"1010629"}}}


id: GO:0047898
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: formate + ferricytochrome b1 = CO2 + ferrocytochrome b1.","definition_xrefs":["MetaCyc:FORMATE-DEHYDROGENASE-CYTOCHROME-RXN","EC:1.2.2.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, cytochrome as acceptor","termid":"GO:0016622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"formate dehydrogenase (cytochrome) activity","secondary_identifiers":["RHEA:21520"],"synonyms":[{"name":"formate:cytochrome b1 oxidoreductase activity","type":"related"},{"name":"formate:ferricytochrome-b1 oxidoreductase activity","type":"related"}],"termid":"GO:0047898"}


id: PBO:0030736
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_cycle_arrest_in_mitotic_G2_phase_during_nitrogen_starvation","termid":"PBO:0030736"}


id: MONDO:0017460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndactyly type 6 is a rare, genetic, non-syndromic, congenital limb malformation characterized by unilateral fusion of second to fifth fingers, amalgamation of distal phalanges in a knot-like structure, and second- and third-toe fusion. Some individuals present only with webbing between second and third toes, without involvement of fingers.","definition_xrefs":["Orphanet:295012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic syndactyly","termid":"MONDO:0019530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndactyly type 6","secondary_identifiers":["icd11.foundation:2105806379","GARD:21201","MEDGEN:1635950","SCTID:763624007","UMLS:C4706525"],"synonyms":[{"name":"mitten hand","type":"exact"},{"name":"syndactyly, mitten type","type":"exact"},{"name":"unilateral syndactyly of digits 2-5","type":"exact"}],"termid":"MONDO:0017460","xrefs":{"Monarch":{"xref_id":"0017460"}}}


id: PBO:0086719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; non-essential gene identified in a screen for mutants affected in mannosylphophorylation of cell wall components","termid":"PBO:0086719"}


id: PATO:0002334
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A adhesivity which is relatively low.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"},{"relation_name":"is_a","term_name":"adhesive","termid":"PATO:0002331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased adhesivity","termid":"PATO:0002334"}


id: GO:0002266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in the morphology or behavior of a follicular dendritic cell resulting from exposure to an activating factor such as a cellular or soluble ligand.","definition_xrefs":["PMID:15606789","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell activation","termid":"GO:0001775"}],"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":"follicular dendritic cell activation","termid":"GO:0002266"}


id: GO:1903034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of response to wounding.","definition_xrefs":["GOC:TermGenie","PMID:19164535","GO_REF:0000058","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to stress","termid":"GO:0080134"},{"relation_name":"regulates","term_name":"response to wounding","termid":"GO:0009611"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of response to wounding","synonyms":[{"name":"regulation of physiological response to wounding","type":"exact"}],"termid":"GO:1903034"}


id: FYPO:0004307
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the mitotic spindle is longer than normal during metaphase.","definition_xrefs":["PMID:10398680","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long mitotic spindle","termid":"FYPO:0000733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0002399"}],"interesting_parent_ids":["FYPO:0000120","FYPO:0001985","FYPO:0000054","FYPO:0000002","FYPO:0005447","FYPO:0002399","FYPO:0001320"],"is_obsolete":false,"name":"long mitotic spindle during metaphase","synonyms":[{"name":"elongated mitotic spindle during metaphase","type":"exact"},{"name":"increased mitotic spindle length during metaphase","type":"exact"},{"name":"long bipolar mitotic spindle during metaphase","type":"exact"},{"name":"long mitotic spindle during metaphase during vegetative growth","type":"exact"},{"name":"long mitotic spindles during metaphase","type":"exact"},{"name":"long spindle during metaphase of mitosis","type":"exact"},{"name":"long spindle during mitotic metaphase","type":"exact"}],"termid":"FYPO:0004307"}


id: GO:2000301
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synaptic vesicle exocytosis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of regulated secretory pathway","termid":"GO:1903306"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle exocytosis","termid":"GO:2000300"},{"relation_name":"negatively_regulates","term_name":"synaptic vesicle exocytosis","termid":"GO:0016079"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of synaptic vesicle exocytosis","termid":"GO:2000301"}


id: GO:0033688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of osteoblast proliferation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"regulates","term_name":"osteoblast proliferation","termid":"GO:0033687"}],"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 osteoblast proliferation","termid":"GO:0033688"}


id: PBO:0054300
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 1691","termid":"PBO:0054300"}


id: GO:0018575
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3,6-dichlorocatechol + O2 = 2 H+ + 2,5-dichloro-cis,cis-muconate.","definition_xrefs":["UM-BBD_reactionID:r0655"],"gene_count":0,"genotype_count":0,"name":"obsolete chlorocatechol 1,2-dioxygenase activity (obsolete GO:0018575)","termid":"GO:0018575"}


id: GO:0021886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuron located in the hypothalamus. These neurons release gonadotrophin-releasing hormone as a neural transmitter.","definition_xrefs":["GOC:cls","GOC:dph","GOC:dgh","GOC:jid","PMID:12626695","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypothalamus cell differentiation","termid":"GO:0021979"}],"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":"hypothalamus gonadotrophin-releasing hormone neuron differentiation","synonyms":[{"name":"hypothalamus gonadotropin-releasing hormone neuron differentiation","type":"exact"}],"termid":"GO:0021886"}


id: GO:0120057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of any small intestinal transit process, the migration of ingested material along the length of the small intestine.","definition_xrefs":["GOC:sl","PMID:15890336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of digestive system process","termid":"GO:0044058"},{"relation_name":"regulates","term_name":"small intestinal transit","termid":"GO:0120055"}],"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 small intestinal transit","synonyms":[{"name":"regulation of small bowel transit","type":"exact"},{"name":"regulation of small intestine transit","type":"exact"}],"termid":"GO:0120057"}


id: MONDO:1011285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any syndromic retinal atrophy in dogs due to a mutation in the BBS2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"progressive retinal atrophy, non-human animal","termid":"MONDO:1011977"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndromic retinal atrophy, BBS2-related, dog","secondary_identifiers":["OMIA:002484-9615"],"synonyms":[{"name":"Bardet-Biedl syndrome 2, dog","type":"related"}],"termid":"MONDO:1011285","xrefs":{"Monarch":{"xref_id":"1011285"}}}


id: PBO:0001637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PP2A","termid":"PBO:0001637"}


id: PBO:0042175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cellular communication network factor 5","termid":"PBO:0042175"}


id: PBO:0028998
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_cell_population_growth_on_proline_nitrogen_source","termid":"PBO:0028998"}


id: PBO:0080900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon","termid":"PBO:0080900"}


id: MONDO:0017809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Kufor-Rakeb syndrome","termid":"MONDO:0011706"},{"relation_name":"is_a","term_name":"juvenile neuronal ceroid lipofuscinosis","termid":"MONDO:0019262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0002561","MONDO:0002039","MONDO:0002525"],"is_obsolete":false,"name":"parkinsonism due to ATP13A2 deficiency","secondary_identifiers":["SCTID:789657008","Orphanet:314632","GARD:17427"],"synonyms":[{"name":"CLN12 disease","type":"exact"}],"termid":"MONDO:0017809","xrefs":{"Monarch":{"xref_id":"0017809"}}}


id: PBO:0031426
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_tert-butyl_hydroperoxide","termid":"PBO:0031426"}


id: FYPO:0008178
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 RNAs transcribed from the centromere inner repeat region are present at normal levels (i.e. indistinguishable from wild-type).","direct_ancestors":[{"relation_name":"is_a","term_name":"normal centromeric RNA level during vegetative growth","termid":"FYPO:0008177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal centromeric inner repeat transcript level","termid":"FYPO:0008178"}


id: PR:Q9USH6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- naa40 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USH6"],"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 N-acetyltransferase C825.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC825.04c","synonyms":[{"name":"Spom972h-naa40","type":"exact"}],"termid":"PR:Q9USH6"}


id: PBO:0074559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA host gene 12","termid":"PBO:0074559"}


id: MONDO:0017611
data:
  {"annotated_genes":["SJAG_03429"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm affecting the pituitary gland. The vast majority are adenomas arising from the anterior lobe of the pituitary gland.","definition_xrefs":["NCIT:C3330"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine gland neoplasm","termid":"MONDO:0002082"},{"relation_name":"is_a","term_name":"sella turcica neoplasm","termid":"MONDO:0002720"},{"relation_name":"is_a","term_name":"pituitary gland disorder","termid":"MONDO:0003381"},{"relation_name":"is_a","term_name":"reproductive system neoplasm","termid":"MONDO:0006054"},{"relation_name":"is_a","term_name":"hypothalamic neoplasm","termid":"MONDO:0006799"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03429":null},"genotype_count":0,"is_obsolete":false,"name":"pituitary tumor","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:127024001","UMLS:C0032019","GARD:21253","ICD9:239.7","MEDGEN:19326","Orphanet:304055"],"synonyms":[{"name":"neoplasm of pituitary","type":"exact"},{"name":"neoplasm of pituitary gland","type":"exact"},{"name":"neoplasm of the pituitary","type":"exact"},{"name":"neoplasm of the pituitary gland","type":"exact"},{"name":"pituitary gland neoplasm","type":"exact"},{"name":"pituitary gland tumor","type":"exact"},{"name":"pituitary gland tumour","type":"exact"},{"name":"pituitary neoplasm","type":"exact"},{"name":"pituitary tumor","type":"exact"},{"name":"tumor of pituitary","type":"exact"},{"name":"tumor of pituitary gland","type":"exact"},{"name":"tumor of the pituitary","type":"exact"},{"name":"tumor of the pituitary gland","type":"exact"},{"name":"tumour of pituitary","type":"exact"},{"name":"tumour of pituitary gland","type":"exact"},{"name":"tumour of the pituitary","type":"exact"},{"name":"tumour of the pituitary gland","type":"exact"}],"termid":"MONDO:0017611","terms_by_termid":{"MONDO:0009050":null},"xrefs":{"Monarch":{"xref_id":"0017611"}}}


id: MONDO:0006394
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually polypoid neoplasm that arises from the glandular epithelium of the rectal mucosa. It is characterized by a tubular architectural pattern. The neoplastic glandular cells have dysplastic features.","definition_xrefs":["NCIT:C96477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rectum adenoma","termid":"MONDO:0000530"},{"relation_name":"is_a","term_name":"tubular adenoma","termid":"MONDO:0024660"}],"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":"rectal tubular adenoma","secondary_identifiers":["EFO:1000504","MEDGEN:474437","UMLS:C3272804"],"synonyms":[{"name":"rectal tubular adenoma","type":"exact"}],"termid":"MONDO:0006394","xrefs":{"Monarch":{"xref_id":"0006394"}}}


id: PBO:0027296
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-tetranucleate_vegetative_cell","termid":"PBO:0027296"}


id: PBO:0001935
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates nmt1","termid":"PBO:0001935"}


id: PBO:0005670
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.1.1.12","termid":"PBO:0005670"}


id: MONDO:0800385
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A heavy metal poisoning that is caused by exposure to iron. Iron toxicity is classified as corrosive or cellular. Ingested iron can cause direct caustic injury to the gastrointestinal mucosa, resulting in nausea, vomiting, abdominal pain, and diarrhea.","definition_xrefs":["MONDO:patterns/patterns/poisoning"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heavy metal poisoning","termid":"MONDO:0023305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron poisoning","synonyms":[{"name":"iron overload","type":"exact"},{"name":"iron toxicity","type":"exact"}],"termid":"MONDO:0800385","xrefs":{"Monarch":{"xref_id":"0800385"}}}


id: PBO:0042988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHEK2 pseudogene 1","termid":"PBO:0042988"}


id: MONDO:0004418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"infiltrating bladder urothelial carcinoma","termid":"MONDO:0003890"}],"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":"microcystic variant infiltrating bladder urothelial carcinoma","secondary_identifiers":["NCIT:C39820","MEDGEN:268574","UMLS:C1512740","DOID:7971"],"synonyms":[{"name":"infiltrating bladder urothelial carcinoma, microcystic variant","type":"exact"}],"termid":"MONDO:0004418","xrefs":{"Monarch":{"xref_id":"0004418"}}}


id: PBO:0069112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 361, pseudogene","termid":"PBO:0069112"}


id: MONDO:0003057
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that occurs during childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"},{"relation_name":"is_a","term_name":"childhood neoplasm","termid":"MONDO:0021079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pediatric meningioma","secondary_identifiers":["MEDGEN:79156","NCIT:C8264","UMLS:C0280656","DOID:4593","NANDO:2200094"],"synonyms":[{"name":"childhood meningioma","type":"exact"},{"name":"childhood meningioma (disease)","type":"exact"},{"name":"meningioma","type":"broad"},{"name":"meningioma (disease) of childhood","type":"exact"},{"name":"paediatric meningioma (disease)","type":"exact"},{"name":"pediatric meningioma","type":"exact"},{"name":"pediatric meningioma (disease)","type":"exact"}],"termid":"MONDO:0003057","xrefs":{"Monarch":{"xref_id":"0003057"}}}


id: MONDO:1012019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atrial septal defect and atrial fibrillation, non-human animal","termid":"MONDO:1011640"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrial septal defect and atrial fibrillation, horse","secondary_identifiers":["OMIA:000090-9796"],"termid":"MONDO:1012019","xrefs":{"Monarch":{"xref_id":"1012019"}}}


id: MONDO:0010245
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked cone-rod dystrophy","termid":"MONDO:0021155"}],"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":"X-linked cone-rod dystrophy 2","secondary_identifiers":["MESH:C564717","DOID:0111006","GARD:1462","MEDGEN:341161","OMIM:300085","UMLS:C1848139"],"synonyms":[{"name":"COD2","type":"exact"},{"name":"CORDX2","type":"exact"},{"name":"X-linked cone dystrophy 2","type":"exact"},{"name":"X-linked cone-rod dystrophy type 2","type":"exact"},{"name":"cone dystrophy 2, X-linked","type":"exact"},{"name":"cone dystrophy X-linked 2","type":"exact"},{"name":"cone dystrophy, progressive X-linked, 2","type":"exact"},{"name":"cone-rod dystrophy X-linked 2","type":"exact"},{"name":"cone-rod dystrophy, X-linked, 2","type":"exact"}],"termid":"MONDO:0010245","xrefs":{"Monarch":{"xref_id":"0010245"}}}


id: GO:0017164
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nicotinic acetylcholine receptor-associated protein activity (obsolete GO:0017164)","synonyms":[{"name":"nicotinic acetylcholine receptor-associated protein activity","type":"exact"}],"termid":"GO:0017164"}


id: PBO:0047408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 46","termid":"PBO:0047408"}


id: MONDO:0600024
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of myositis that is caused by an inherited genomic modification in an individual, and has an unknown cause.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic inflammatory myopathy","termid":"MONDO:0600023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"familial idiopathic inflammatory myopathy","secondary_identifiers":["MESH:C000598744","MEDGEN:854861","OMIM:160750","UMLS:C3888318"],"synonyms":[{"name":"familial idiopathic myositis","type":"exact"}],"termid":"MONDO:0600024","xrefs":{"Monarch":{"xref_id":"0600024"}}}


id: PBO:0049893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HECT and RLD domain containing E3 ubiquitin protein ligase 3","termid":"PBO:0049893"}


id: MONDO:0016669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic hemoglobinopathy characterized by anemia, reticulocytosis and erythrocyte abnormalities including target cells, irreversibly sickled cells and crystal-containing cells. Clinical course is similar to sickle cell disease, but less severe and with less complications. Signs and symptoms may include acute episodes of pain, splenic infarction and splenic sequestration crisis, acute chest syndrome, focal segmental glomerulosclerosis, ischemic brain injury, peripheral retinopathy, and osteonecrosis.","definition_xrefs":["Orphanet:251365"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"sickle cell anemia","termid":"MONDO:0011382"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0006025"],"is_obsolete":false,"name":"sickle cell-hemoglobin c disease syndrome","secondary_identifiers":["MEDGEN:5496","UMLS:C0019034","GARD:6584","MedDRA:10057072"],"synonyms":[{"name":"HbSC disease","type":"exact"},{"name":"sickle cell - haemoglobin C disease","type":"related"},{"name":"sickle cell - hemoglobin C disease","type":"related"}],"termid":"MONDO:0016669","xrefs":{"Monarch":{"xref_id":"0016669"}}}


id: PBO:0112603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIN signalling inhibitor, two-component GAP Byr4","termid":"PBO:0112603"}


id: GO:0047200
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-2,3,4,5-tetrahydrodipicolinate + acetyl-CoA + H2O = L-2-acetamido-6-oxopimelate + CoA.","definition_xrefs":["RHEA:13085","EC:2.3.1.89"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetyltransferase activity","termid":"GO:0008080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"tetrahydrodipicolinate N-acetyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04364","MetaCyc:2.3.1.89-RXN"],"synonyms":[{"name":"acetyl-CoA:(S)-2,3,4,5-tetrahydrodipicolinate-2,6-dicarboxylate N2-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:(S)-2,3,4,5-tetrahydropyridine-2,6-dicarboxylate 2-N-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:L-2,3,4,5-tetrahydrodipicolinate N2-acetyltransferase activity","type":"related"},{"name":"tetrahydrodipicolinate acetylase activity","type":"related"},{"name":"tetrahydrodipicolinate:acetyl-CoA acetyltransferase activity","type":"related"}],"termid":"GO:0047200"}


id: GO:0098886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modifies the structure of a dendritic spine.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modification of postsynaptic structure","termid":"GO:0099010"}],"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":"modification of dendritic spine","termid":"GO:0098886"}


id: MONDO:0019701
data:
  {"annotated_genes":["SJAG_00702","SJAG_02855","SJAG_00326","SJAG_04810"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85087],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"},{"annotations":[85813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008974"},{"annotations":[85796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008972"},{"annotations":[85645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014743"}]},"cv_name":"mondo","definition":"A rare congenital developmental disorder characterized by the presence of stippled foci of calcification in the hyaline cartilage, joint contractions, mental retardation and ichthyosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_02855":null,"SJAG_04810":null},"genotype_count":0,"is_obsolete":false,"name":"chondrodysplasia punctata","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:3052","NANDO:2201017","SCTID:360507004","UMLS:C0008445","MESH:D002806","Orphanet:93442","NCIT:C84632","GARD:8542","icd11.foundation:1923035846","ICD10CM:Q77.3","DOID:2581","ICD9:756.59"],"synonyms":[{"name":"CDP","type":"exact"},{"name":"chondrodysplasia calcificans congenita","type":"exact"},{"name":"chondrodysplasia punctata (stippled epiphyses) Group","type":"exact"},{"name":"chondrodysplasia punctata congenita","type":"exact"}],"termid":"MONDO:0019701","terms_by_termid":{"MONDO:0008972":null,"MONDO:0008974":null,"MONDO:0010621":null,"MONDO:0014743":null},"xrefs":{"Monarch":{"xref_id":"0019701"}}}


id: PBO:0082920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytochrome c, isoform 1; also known as iso-1-cytochrome c; electron carrier of mitochondrial intermembrane space that transfers electrons from ubiquinone-cytochrome c oxidoreductase to cytochrome c oxidase during cellular respiration; CYC1 has a paralog, CYC7, that arose from the whole genome duplication; human homolog CYC1 can complement yeast null mutant; mutations in human CYC1 cause insulin-responsive hyperglycemia","termid":"PBO:0082920"}


id: GO:1902071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hypoxia-inducible factor-1alpha signaling pathway.","definition_xrefs":["GOC:TermGenie","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"hypoxia-inducible factor-1alpha signaling pathway","termid":"GO:0097411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of hypoxia-inducible factor-1alpha signaling pathway","synonyms":[{"name":"regulation of HIF1alpha pathway","type":"exact"},{"name":"regulation of hypoxia-inducible factor-1alpha signalling pathway","type":"exact"}],"termid":"GO:1902071"}


id: PBO:0041722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium/calmodulin dependent protein kinase I","termid":"PBO:0041722"}


id: PBO:0034483
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_spatial_extent_of_histone_H2B-K119_ubiquitination_at_double-strand_break_site","termid":"PBO:0034483"}


id: MONDO:0000404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cell type cancer (obsolete MONDO:0000404)","termid":"MONDO:0000404","xrefs":{"Monarch":{"xref_id":"0000404"}}}


id: GO:0019827
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which an organism or tissue maintains a population of stem cells of a single type. This can be achieved by a number of mechanisms: stem cell asymmetric division maintains stem cell numbers; stem cell symmetric division increases them; maintenance of a stem cell niche maintains the conditions for commitment to the stem cell fate for some types of stem cell; stem cells may arise de novo from other cell types.","definition_xrefs":["GOC:mah","ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"is_a","term_name":"maintenance of cell number","termid":"GO:0098727"}],"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":"stem cell population maintenance","synonyms":[{"name":"maintenance of pluripotency","type":"related"}],"termid":"GO:0019827"}


id: PBO:0084463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP kinase kinase kinase of HOG1 mitogen-activated signaling pathway; interacts with Ssk1p, leading to autophosphorylation and activation of Ssk2p which phosphorylates Pbs2p; also mediates actin cytoskeleton recovery from osmotic stress; a HOG-independent function of Ssk2p mediates the calcium-sensitive phenotype of the ptp2 msg5 double disruptant; SSK2 has a paralog, SSK22, that arose from the whole genome duplication","termid":"PBO:0084463"}


id: PBO:0088112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar aminopeptidase yscI; zinc metalloproteinase that belongs to the peptidase family M18; often used as a marker protein in studies of autophagy and cytosol to vacuole targeting (CVT) pathway; protein increases in abundance and relative distribution to cytoplasmic foci increases upon DNA replication stress","termid":"PBO:0088112"}


id: PBO:0012571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome complex subunit beta 6","termid":"PBO:0012571"}


id: GO:0052394
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of symbiont processes resulting in the thickening of its cell walls, occurring as part of the defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by organism of defense-related symbiont cell wall thickening (obsolete GO:0052394)","synonyms":[{"name":"activation by organism of symbiont defense-related cell wall thickening","type":"exact"},{"name":"activation by organism of symbiont defensive cell wall thickening","type":"exact"},{"name":"induction by organism of defense-related symbiont cell wall thickening","type":"exact"},{"name":"induction by organism of symbiont defensive cell wall thickening","type":"exact"}],"termid":"GO:0052394"}


id: PBO:0001818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b2 (L-lactate cytochrome-c oxidoreductase) (predicted)","termid":"PBO:0001818"}


id: PBO:0000287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF544 family protein","termid":"PBO:0000287"}


id: MONDO:1010361
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hyperphagia leading to hepatic steatosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"nutritional disorder, non-human animal","termid":"MONDO:1011338"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperphagia leading to hepatic steatosis, non-human animal","secondary_identifiers":["OMIA:002217"],"termid":"MONDO:1010361","xrefs":{"Monarch":{"xref_id":"1010361"}}}


id: _global:produces
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"a produces b if some process that occurs_in a has_output b, where a and b are material entities. Examples: hybridoma cell line produces monoclonal antibody reagent; chondroblast produces avascular GAG-rich matrix.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"produces","secondary_identifiers":["RO:0003000"],"termid":"_global:produces"}


id: MONDO:0004003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pancreatic solid pseudopapillary carcinoma (obsolete MONDO:0004003)","termid":"MONDO:0004003","xrefs":{"Monarch":{"xref_id":"0004003"}}}


id: GO:0046780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the splicing of host mRNA, thus interfering with normal host protein production. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:12660167","PMID:19729513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host mRNA processing","termid":"GO:0039524"}],"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":"symbiont-mediated suppression of host mRNA splicing","secondary_identifiers":["GO:0046781"],"synonyms":[{"name":"negative regulation by virus of host mRNA splicing","type":"narrow"},{"name":"suppression by virus of host mRNA splicing","type":"narrow"},{"name":"suppression by virus of host splicing factor activity","type":"exact"},{"name":"viral dispersion of host splicing factors","type":"narrow"},{"name":"viral inhibition of host mRNA splicing","type":"narrow"}],"termid":"GO:0046780"}


id: GO:0046130
data:
  {"annotated_genes":["SJAG_02959","SJAG_02580"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87330,87329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006154"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of any purine ribonucleoside, a nucleoside in which purine base is linked to a ribose (beta-D-ribofuranose) molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleoside catabolic process","termid":"GO:0006152"},{"relation_name":"is_a","term_name":"ribonucleoside catabolic process","termid":"GO:0042454"},{"relation_name":"is_a","term_name":"purine ribonucleoside metabolic process","termid":"GO:0046128"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02580":null,"SJAG_02959":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"purine ribonucleoside catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"purine ribonucleoside breakdown","type":"exact"},{"name":"purine ribonucleoside catabolism","type":"exact"},{"name":"purine ribonucleoside degradation","type":"exact"}],"termid":"GO:0046130","terms_by_termid":{"GO:0006154":null}}


id: MONDO:0007513
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":"ectodermal dysplasia with adrenal cyst","secondary_identifiers":["OMIM:129550","Orphanet:3391","MEDGEN:342106","MESH:C538015","UMLS:C1851850"],"synonyms":[{"name":"Odonto-onycho-hypohidrotic dysplasia-midline scalp defects syndrome","type":"exact"},{"name":"ectodermal dysplasia with adrenal cyst","type":"exact"}],"termid":"MONDO:0007513","xrefs":{"Monarch":{"xref_id":"0007513"}}}


id: GO:0090638
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phosphatidylcholine biosynthetic process that depends on direct conversion of the phosphatidyl-base phosphatidylethanolamine to phosphatidylcholine by successive methylations.","definition_xrefs":["MetaCyc:PWY-6825"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylcholine biosynthetic process","termid":"GO:0006656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"phosphatidylcholine biosynthesis from phosphatidylethanolamine","termid":"GO:0090638"}


id: PBO:0088256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase (Cdc14-related) Clp1/Flp1","termid":"PBO:0088256"}


id: MONDO:0859277
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":"intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects","secondary_identifiers":["UMLS:C5774199","MEDGEN:1823972","OMIM:620007"],"termid":"MONDO:0859277","xrefs":{"Monarch":{"xref_id":"0859277"}}}


id: PBO:0054753
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 2164","termid":"PBO:0054753"}


id: GO:0043225
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + inorganic anion(out) = ADP + phosphate + inorganic anion(in).","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic anion transmembrane transporter activity","termid":"GO:0015103"},{"relation_name":"is_a","term_name":"ATPase-coupled transmembrane transporter activity","termid":"GO:0042626"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"ATPase-coupled inorganic anion transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-5690340","Reactome:R-HSA-1454916"],"synonyms":[{"name":"ATP-dependent anion transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled anion transmembrane transporter activity","type":"exact"},{"name":"anion ABC transporter","type":"narrow"},{"name":"anion transmembrane-transporting ATPase activity","type":"related"},{"name":"anion-transporting ATPase activity","type":"exact"}],"termid":"GO:0043225"}


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


id: MONDO:0012263
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autoimmune disease","termid":"MONDO:0007179"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune disease, susceptibility to, 4","secondary_identifiers":["OMIM:609400","UMLS:C1836258","MEDGEN:332163"],"synonyms":[{"name":"AIS4","type":"exact"},{"name":"autoimmune disease susceptibility locus, chromosome 4-related","type":"related"},{"name":"autoimmune disease, susceptibility to, 4","type":"exact"},{"name":"vitiligo-associated multiple autoimmune disease susceptibility 5","type":"related"}],"termid":"MONDO:0012263","xrefs":{"Monarch":{"xref_id":"0012263"}}}


id: FYPO:0004548
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a protein kinase activity is normal (i.e. indistinguishable from wild type) during a cellular response to hydroxyurea.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein kinase activity","termid":"FYPO:0003075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0000257"],"is_obsolete":false,"name":"normal protein kinase activity during cellular response to hydroxyurea","synonyms":[{"name":"normal protein kinase activity during cellular response to HU","type":"exact"},{"name":"normal protein kinase activity in response to hydroxyurea","type":"related"}],"termid":"FYPO:0004548"}


id: GO:0031844
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 4 neuropeptide Y receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide Y receptor binding","termid":"GO:0031841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"type 4 neuropeptide Y receptor binding","synonyms":[{"name":"pancreatic polypeptide receptor binding","type":"exact"},{"name":"type 4 neuropeptide Y receptor ligand","type":"narrow"}],"termid":"GO:0031844"}


id: GO:0071966
data:
  {"annotated_genes":["SJAG_04327","SJAG_03587","SJAG_04236","SJAG_02278","SJAG_05001","SJAG_00424","SJAG_04864","SJAG_04771","SJAG_03057","SJAG_03646","SJAG_02192","SJAG_03123","SJAG_04483","SJAG_05285","SJAG_01171","SJAG_01290","SJAG_00876","SJAG_01835","SJAG_02916","SJAG_00218","SJAG_01453","SJAG_00610","SJAG_04666","SJAG_04184","SJAG_02222","SJAG_01028","SJAG_01288"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72184,106491],"is_not":false,"summary":null,"term":"GO:0071966"},{"annotations":[94222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034413"},{"annotations":[72696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034412"},{"annotations":[71163,72934,78431,70200,73072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070600"},{"annotations":[91352,112968,74189,72698,115628,105903,70462,75498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071970"},{"annotations":[102431,77917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070880"},{"annotations":[107866,94862,101733,101732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070879"},{"annotations":[92179,87264],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[102635,92185,94698,89186],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving the polysaccharides which make up the fungal-type cell wall.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall polysaccharide metabolic process","termid":"GO:0010383"},{"relation_name":"part_of","term_name":"fungal-type cell wall organization or biogenesis","termid":"GO:0071852"}],"gene_count":27,"genes_by_uniquename":{"SJAG_00218":null,"SJAG_00424":null,"SJAG_00610":null,"SJAG_00876":null,"SJAG_01028":null,"SJAG_01171":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01453":null,"SJAG_01835":null,"SJAG_02192":null,"SJAG_02222":null,"SJAG_02278":null,"SJAG_02916":null,"SJAG_03057":null,"SJAG_03123":null,"SJAG_03587":null,"SJAG_03646":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04327":null,"SJAG_04483":null,"SJAG_04666":null,"SJAG_04771":null,"SJAG_04864":null,"SJAG_05001":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0071554","GO:0005975","GO:0008150"],"is_obsolete":false,"name":"fungal-type cell wall polysaccharide metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0071966","terms_by_termid":{"GO:0034412":null,"GO:0034413":null,"GO:0070600":null,"GO:0070610":null,"GO:0070879":null,"GO:0070880":null,"GO:0071966":null,"GO:0071970":null,"GO:0140748":null}}


id: PBO:0088379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytokinetic formin Cdc12","termid":"PBO:0088379"}


id: GO:0046488
data:
  {"annotated_genes":["SJAG_03131","SJAG_00846","SJAG_00638","SJAG_04537","SJAG_05330","SJAG_01519","SJAG_03935","SJAG_03375","SJAG_00114","SJAG_01863","SJAG_01236","SJAG_00068","SJAG_02913","SJAG_00295","SJAG_04165","SJAG_03066","SJAG_03115","SJAG_04881","SJAG_02289","SJAG_04337","SJAG_03878","SJAG_02321","SJAG_00296","SJAG_04975","SJAG_01570","SJAG_02523","SJAG_05327","SJAG_06425","SJAG_01227","SJAG_02804","SJAG_00999","SJAG_02665","SJAG_02776","SJAG_01416","SJAG_05278","SJAG_00053","SJAG_03170","SJAG_01876","SJAG_01148","SJAG_03292","SJAG_04119","SJAG_04924","SJAG_06383","SJAG_04930","SJAG_03672","SJAG_00063","SJAG_04545","SJAG_01571","SJAG_01860","SJAG_00506","SJAG_02613","SJAG_03506","SJAG_03801","SJAG_02488","SJAG_00831"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59942,63463,95691,113361],"is_not":false,"summary":null,"term":"GO:0046488"},{"annotations":[91599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902635"},{"annotations":[76802,76108,74530,72994,77255,77252,69453,87182,71482,89300,75286,75309,77612,57993,58151,60206,72806,58040,72434,76211,77522,103560,63192,77245,62851,57640,77989,92753,62276,103498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006506"},{"annotations":[73442],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006676"},{"annotations":[90163,104165],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902647"},{"annotations":[71566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036149"},{"annotations":[92389,79945,118632,76318,116814],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006661"},{"annotations":[90974,96467,110927,111054,118274,92981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046854"},{"annotations":[62856,61424,61311,71153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036092"},{"annotations":[117345],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902648"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving phosphatidylinositol, any glycophospholipid in which a sn-glycerol 3-phosphate residue is esterified to the 1-hydroxyl group of 1D-myo-inositol.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerophospholipid metabolic process","termid":"GO:0006650"}],"gene_count":55,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00063":null,"SJAG_00068":null,"SJAG_00114":null,"SJAG_00295":null,"SJAG_00296":null,"SJAG_00506":null,"SJAG_00638":null,"SJAG_00831":null,"SJAG_00846":null,"SJAG_00999":null,"SJAG_01148":null,"SJAG_01227":null,"SJAG_01236":null,"SJAG_01416":null,"SJAG_01519":null,"SJAG_01570":null,"SJAG_01571":null,"SJAG_01860":null,"SJAG_01863":null,"SJAG_01876":null,"SJAG_02289":null,"SJAG_02321":null,"SJAG_02488":null,"SJAG_02523":null,"SJAG_02613":null,"SJAG_02665":null,"SJAG_02776":null,"SJAG_02804":null,"SJAG_02913":null,"SJAG_03066":null,"SJAG_03115":null,"SJAG_03131":null,"SJAG_03170":null,"SJAG_03292":null,"SJAG_03375":null,"SJAG_03506":null,"SJAG_03672":null,"SJAG_03801":null,"SJAG_03878":null,"SJAG_03935":null,"SJAG_04119":null,"SJAG_04165":null,"SJAG_04337":null,"SJAG_04537":null,"SJAG_04545":null,"SJAG_04881":null,"SJAG_04924":null,"SJAG_04930":null,"SJAG_04975":null,"SJAG_05278":null,"SJAG_05327":null,"SJAG_05330":null,"SJAG_06383":null,"SJAG_06425":null},"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":"phosphatidylinositol metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0030384"],"synonyms":[{"name":"PtdIns metabolic process","type":"exact"},{"name":"PtdIns metabolism","type":"exact"},{"name":"phosphatidylinositol metabolism","type":"exact"},{"name":"phosphoinositide metabolic process","type":"exact"},{"name":"phosphoinositide metabolism","type":"exact"}],"termid":"GO:0046488","terms_by_termid":{"GO:0006506":null,"GO:0006661":null,"GO:0006676":null,"GO:0036092":null,"GO:0036149":null,"GO:0046488":null,"GO:0046854":null,"GO:1902635":null,"GO:1902647":null,"GO:1902648":null}}


id: PBO:0052876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 8-1","termid":"PBO:0052876"}


id: FYPO_EXT:1000002
data:
  {"annotation_feature_type":"gene","cv_name":"fypo_extensions","definition":"FYPO extension ontology grouping term for relations relevant to penetrance","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"FYPO extension","termid":"FYPO_EXT:1000000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FYPO penetrance extension","termid":"FYPO_EXT:1000002"}


id: GO:1905813
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of motor neuron axon guidance.","definition_xrefs":["PMID:18434533","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of axon guidance","termid":"GO:1902668"},{"relation_name":"is_a","term_name":"regulation of motor neuron axon guidance","termid":"GO:1905812"},{"relation_name":"negatively_regulates","term_name":"motor neuron axon guidance","termid":"GO:0008045"}],"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 motor neuron axon guidance","synonyms":[{"name":"down regulation of motoneuron axon guidance","type":"exact"},{"name":"down regulation of motor axon guidance","type":"exact"},{"name":"down regulation of motor axon pathfinding","type":"exact"},{"name":"down regulation of motor neuron axon guidance","type":"exact"},{"name":"down-regulation of motoneuron axon guidance","type":"exact"},{"name":"down-regulation of motor axon guidance","type":"exact"},{"name":"down-regulation of motor axon pathfinding","type":"exact"},{"name":"down-regulation of motor neuron axon guidance","type":"exact"},{"name":"downregulation of motoneuron axon guidance","type":"exact"},{"name":"downregulation of motor axon guidance","type":"exact"},{"name":"downregulation of motor axon pathfinding","type":"exact"},{"name":"downregulation of motor neuron axon guidance","type":"exact"},{"name":"inhibition of motoneuron axon guidance","type":"narrow"},{"name":"inhibition of motor axon guidance","type":"narrow"},{"name":"inhibition of motor axon pathfinding","type":"narrow"},{"name":"inhibition of motor neuron axon guidance","type":"narrow"},{"name":"negative regulation of motoneuron axon guidance","type":"exact"},{"name":"negative regulation of motor axon guidance","type":"exact"},{"name":"negative regulation of motor axon pathfinding","type":"exact"}],"termid":"GO:1905813"}


id: PR:O60139
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ubiquitin carboxyl-terminal hydrolase 2 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":"ubiquitin carboxyl-terminal hydrolase 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18H10.08c","secondary_identifiers":["UniProtKB:O60139"],"synonyms":[{"name":"SPBC18H10.08c","type":"related"},{"name":"Spom972h-USP2","type":"exact"},{"name":"deubiquitinating enzyme 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin thioesterase 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-specific-processing protease 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60139"}


id: MONDO:0020174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A precancerous condition that involves the skin of eyelid.","definition_xrefs":["MONDO:patterns/location"],"gene_count":0,"genotype_count":0,"name":"obsolete precancerous lesion of palpebral epidermis (obsolete MONDO:0020174)","secondary_identifiers":["Orphanet:98583"],"synonyms":[{"name":"skin of eyelid precancerous condition","type":"exact"}],"termid":"MONDO:0020174","xrefs":{"Monarch":{"xref_id":"0020174"}}}


id: PBO:0004742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome C oxidase copper chaperone Cox17 (predicted)","termid":"PBO:0004742"}


id: GO:0097148
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A homodimeric protein complex consisting of BCL-2, a member of the Bcl-2 family of anti- and proapoptotic regulators.","definition_xrefs":["GOC:bhm","GOC:so","PMID:14634621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bcl-2 family protein complex","termid":"GO:0097136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"BCL-2 complex","termid":"GO:0097148"}


id: MONDO:0017267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Self-healing collodion baby (SHCB) is a minor variant of autosomal recessive congenital ichthyosis (ARCI) characterized by the presence of a collodion membrane at birth that heals within the first weeks of life.","definition_xrefs":["Orphanet:281122"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive congenital ichthyosis","termid":"MONDO:0017265"}],"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":"self-healing collodion baby","secondary_identifiers":["icd11.foundation:34721911","MEDGEN:383772","SCTID:718632004","MESH:C565473","UMLS:C1855789","GARD:17303"],"synonyms":[{"name":"SHCB","type":"exact"},{"name":"SICI","type":"exact"},{"name":"self-improving collodion baby","type":"related"},{"name":"self-improving congenital ichthyosis","type":"exact"}],"termid":"MONDO:0017267","xrefs":{"Monarch":{"xref_id":"0017267"}}}


id: GO:0099181
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of a presynapse.","definition_xrefs":["GOC:dos","PMID:23751498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural constituent of synapse","termid":"GO:0098918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005198"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005198"],"is_obsolete":false,"name":"structural constituent of presynapse","termid":"GO:0099181"}


id: MONDO:0002376
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant vascular neoplasm arising from the spleen.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spleen cancer","termid":"MONDO:0005966"},{"relation_name":"is_a","term_name":"angiosarcoma","termid":"MONDO:0016982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"spleen angiosarcoma","secondary_identifiers":["NCIT:C4564","MEDGEN:83426","DOID:265","ICD9:159.1","SCTID:187821001","UMLS:C0346424"],"synonyms":[{"name":"angiosarcoma (disease) of spleen","type":"exact"},{"name":"angiosarcoma of spleen","type":"exact"},{"name":"angiosarcoma of the spleen","type":"exact"},{"name":"hemangiosarcoma of spleen","type":"exact"},{"name":"hemangiosarcoma of the spleen","type":"exact"},{"name":"spleen angiosarcoma (disease)","type":"exact"},{"name":"splenic angiosarcoma","type":"exact"},{"name":"splenic hemangiosarcoma","type":"exact"}],"termid":"MONDO:0002376","xrefs":{"Monarch":{"xref_id":"0002376"}}}


id: MONDO:0017296
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Adult glycerol kinase deficiency (GKD) is an uncommon form of GKD diagnosed fortuitously and characterized by pseudohypertriglyceridemia in otherwise healthy adults.","definition_xrefs":["Orphanet:284414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated glycerol kinase deficiency","termid":"MONDO:0018459"},{"relation_name":"is_a","term_name":"disorder of gluconeogenesis","termid":"MONDO:0019225"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"glycerol kinase deficiency, adult form","secondary_identifiers":["GARD:17317","MEDGEN:1842796","UMLS:C5681013"],"termid":"MONDO:0017296","xrefs":{"Monarch":{"xref_id":"0017296"}}}


id: PBO:0045094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal-less homeobox 5","termid":"PBO:0045094"}


id: MONDO:0023013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Duker-Weiss-Siber syndrome","secondary_identifiers":["MESH:C535719","UMLS:C2930993","MEDGEN:419689"],"synonyms":[{"name":"Duker Weiss Siber syndrome","type":"related"},{"name":"microphthalmos, microencephaly, intellectual disability, agenesis of the corpus callosum, hypospadius, and cryptorchidism","type":"related"},{"name":"microphthalmos, microencephaly, mental retardation, agenesis of the corpus callosum, hypospadius, and cryptorchidism","type":"related"}],"termid":"MONDO:0023013","xrefs":{"Monarch":{"xref_id":"0023013"}}}


id: GO:0035895
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism modulates the frequency, rate or extent of blood mast cell degranulation in another organism. Mast cell degranulation is the regulated exocytosis of secretory granules containing preformed mediators such as histamine, serotonin, and neutral proteases by a mast cell.","definition_xrefs":["GOC:bf","GOC:fj","PMID:21549739"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of process of another organism","termid":"GO:0035821"},{"relation_name":"is_a","term_name":"regulation of mast cell degranulation","termid":"GO:0043304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"modulation of mast cell degranulation in another organism","synonyms":[{"name":"modulation of mast cell degranulation in other organism","type":"exact"},{"name":"regulation of mast cell degranulation in other organism","type":"exact"}],"termid":"GO:0035895"}


id: MONDO:0013795
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any fibrochondrogenesis in which the cause of the disease is a mutation in the COL11A2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrochondrogenesis","termid":"MONDO:0016068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"fibrochondrogenesis 2","secondary_identifiers":["GARD:15815","MEDGEN:482758","UMLS:C3281128","DOID:0080673","OMIM:614524"],"synonyms":[{"name":"COL11A2 fibrochondrogenesis","type":"exact"},{"name":"FBCG2","type":"related"},{"name":"fibrochondrogenesis 2","type":"exact"},{"name":"fibrochondrogenesis caused by mutation in COL11A2","type":"exact"},{"name":"fibrochondrogenesis type 2","type":"exact"}],"termid":"MONDO:0013795","xrefs":{"Monarch":{"xref_id":"0013795"}}}


id: MONDO:0009243
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":"Fraser-like syndrome","secondary_identifiers":["MESH:C565562","UMLS:C1856708","Orphanet:2051","MEDGEN:346426","OMIM:229230"],"synonyms":[{"name":"Fraser-like syndrome","type":"exact"},{"name":"Fused eyelids, airway anomalies, ovarian cysts, and digital anomalies","type":"related"}],"termid":"MONDO:0009243","xrefs":{"Monarch":{"xref_id":"0009243"}}}


id: PR:O94397
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sgf73 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94397"],"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":"SAGA-associated factor 73 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC126.04c","synonyms":[{"name":"Spom972h-sgf73","type":"exact"}],"termid":"PR:O94397"}


id: MONDO:1010753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertrichosis that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis, non-human animal","termid":"MONDO:1010130"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrichosis, cattle","secondary_identifiers":["OMIA:000513-9913"],"termid":"MONDO:1010753","xrefs":{"Monarch":{"xref_id":"1010753"}}}


id: PBO:0113488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional regulator; functions primarily as a transcriptional co-repressor with Tup1p but can also function as a transcriptional co-activator with Tup1p that recruits the SWI/SNF and SAGA complexes to promoters; target genes may be uniquely repressed by Cyc8p or Tup1p, subject to redundant repression, or in some cases de-repression of target genes in a cyc8 mutant is dependent upon TUP1 and vice versa; can form the prion [OCT+]","termid":"PBO:0113488"}


id: MONDO:0000655
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete heavy chain disease (obsolete MONDO:0000655)","termid":"MONDO:0000655","xrefs":{"Monarch":{"xref_id":"0000655"}}}


id: MONDO:0024468
data:
  {"annotated_genes":["SJAG_03429"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"}]},"cv_name":"mondo","definition":"A disease that involves the adenohypophysis.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pituitary gland disorder","termid":"MONDO:0003381"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03429":null},"genotype_count":0,"is_obsolete":false,"name":"anterior pituitary gland disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:51742006","ICD9:253.9","UMLS:C0751437","ICD9:253.4","MEDGEN:148306"],"synonyms":[{"name":"adenohypophysis disease","type":"exact"},{"name":"adenohypophysis disease or disorder","type":"exact"},{"name":"disease of adenohypophysis","type":"exact"},{"name":"disease or disorder of adenohypophysis","type":"exact"},{"name":"disorder of adenohypophysis","type":"exact"},{"name":"disorder of anterior pituitary","type":"exact"},{"name":"disorder of anterior pituitary gland","type":"related"}],"termid":"MONDO:0024468","terms_by_termid":{"MONDO:0009050":null},"xrefs":{"Monarch":{"xref_id":"0024468"}}}


id: FYPO:0003937
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which cell population growth is increased relative to normal. Increased growth may reflect an increased growth rate (i.e. faster growth), growth that occurs to a greater extent than normal, or both. Cell population growth refers to an increase in the number of cells in the population as individual cells grow and divide.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell population growth","termid":"FYPO:0000045"},{"relation_name":"is_a","term_name":"viable cell population","termid":"FYPO:0002058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000003","FYPO:0002058","FYPO:0002057","FYPO:0000139"],"is_obsolete":false,"name":"increased cell population growth","synonyms":[{"name":"fast aerobic cell population growth","type":"narrow"},{"name":"increased aerobic cell population growth","type":"narrow"},{"name":"increased growth","type":"broad"}],"termid":"FYPO:0003937"}


id: MONDO:0018519
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete squamous cell carcinoma of the anal canal (obsolete MONDO:0018519)","termid":"MONDO:0018519","xrefs":{"Monarch":{"xref_id":"0018519"}}}


id: GO:1901483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription factor catabolic process.","definition_xrefs":["GOC:TermGenie","PMID:22833559","GOC:al","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription factor catabolic process (obsolete GO:1901483)","synonyms":[{"name":"regulation of proteasome-mediated transcription factor catabolism","type":"exact"},{"name":"regulation of sequence-specific DNA binding transcription factor catabolic process","type":"exact"},{"name":"regulation of transcription factor breakdown","type":"exact"},{"name":"regulation of transcription factor catabolism","type":"exact"},{"name":"regulation of transcription factor degradation","type":"exact"}],"termid":"GO:1901483"}


id: GO:1990948
data:
  {"annotated_genes":["SJAG_01515","SJAG_04699"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98480,115367],"is_not":false,"summary":null,"term":"GO:1990948"}]},"cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of a ubiquitin ligase.","definition_xrefs":["GOC:vw","GOC:dph","PMID:21389117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-protein transferase inhibitor activity","termid":"GO:0055105"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01515":null,"SJAG_04699":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0004857","GO:0140678","GO:0030234","GO:0003674"],"is_obsolete":false,"name":"ubiquitin ligase inhibitor activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0061637","GO:0090645"],"synonyms":[{"name":"APC-Cdc20 complex inhibitor activity","type":"narrow"},{"name":"mitotic anaphase-promoting complex inhibitor activity","type":"narrow"}],"termid":"GO:1990948","terms_by_termid":{"GO:1990948":null}}


id: PBO:0056833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MGAT2 pseudogene 2","termid":"PBO:0056833"}


id: SO:0002177
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A duplication that is the result of base-calling or assembly error.","direct_ancestors":[{"relation_name":"is_a","term_name":"insertion_artifact","termid":"SO:0002175"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"duplication_artifact","synonyms":[{"name":"duplication artifact","type":"exact"}],"termid":"SO:0002177"}


id: MONDO:0012993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dyschromatosis universalis hereditaria","termid":"MONDO:0000736"}],"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":"dyschromatosis universalis hereditaria 2","secondary_identifiers":["GARD:15581","OMIM:612715","MEDGEN:382542","MESH:C567194","UMLS:C2675183"],"synonyms":[{"name":"DUH2","type":"related"},{"name":"dyschromatosis universalis hereditaria 2","type":"exact"}],"termid":"MONDO:0012993","xrefs":{"Monarch":{"xref_id":"0012993"}}}


id: PBO:0042759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 41","termid":"PBO:0042759"}


id: MONDO:1012612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A liver disorder characterized by chronic conjugated hyperbilirubinemia and abundant intrahepatic pigment in a centrilobular and midzonal distribution that occurs in golden lion tamarins.","definition_xrefs":["PMID:8116141"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver disorder, non-human animal","termid":"MONDO:1012967"},{"relation_name":"is_a","term_name":"hyperbilirubinemia, non-human animal","termid":"MONDO:1012974"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conjugated hyperbilirubinemia, golden lion tamarin","secondary_identifiers":["OMIA:000498-30588"],"synonyms":[{"name":"Dubin-Johnson syndrome, golden lion tamarin","type":"related"},{"name":"hyperbilirubinaemia II-like, golden lion tamarin","type":"related"}],"termid":"MONDO:1012612","xrefs":{"Monarch":{"xref_id":"1012612"}}}


id: GO:0042887
data:
  {"annotated_genes":["SJAG_03497","SJAG_02139","SJAG_01660","SJAG_00922","SJAG_03503","SJAG_05175","SJAG_02029","SJAG_02779","SJAG_02125","SJAG_04725","SJAG_02780","SJAG_03577","SJAG_04325","SJAG_01344","SJAG_01983","SJAG_03452","SJAG_05182","SJAG_02602"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015421"},{"annotations":[96825,118017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044604"},{"annotations":[59391],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008521"},{"annotations":[71489,79032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015225"},{"annotations":[70154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015228"},{"annotations":[71488,79031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901604"},{"annotations":[71584,118157,118158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071916"},{"annotations":[73563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008517"},{"annotations":[112939,95286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034634"},{"annotations":[102590,109826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015182"},{"annotations":[72143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015233"},{"annotations":[107785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901584"},{"annotations":[71582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042937"},{"annotations":[70272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015204"}]},"cv_name":"molecular_function","definition":"Enables the transfer of an amide, any compound containing one, two, or three acyl groups attached to a nitrogen atom, from one side of a membrane to the other.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00922":null,"SJAG_01344":null,"SJAG_01660":null,"SJAG_01983":null,"SJAG_02029":null,"SJAG_02125":null,"SJAG_02139":null,"SJAG_02602":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_03452":null,"SJAG_03497":null,"SJAG_03503":null,"SJAG_03577":null,"SJAG_04325":null,"SJAG_04725":null,"SJAG_05175":null,"SJAG_05182":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"amide transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"amine/amide/polyamine channel activity","type":"narrow"}],"termid":"GO:0042887","terms_by_termid":{"GO:0008517":null,"GO:0008521":null,"GO:0015182":null,"GO:0015204":null,"GO:0015225":null,"GO:0015228":null,"GO:0015233":null,"GO:0015421":null,"GO:0034634":null,"GO:0042937":null,"GO:0044604":null,"GO:0071916":null,"GO:1901584":null,"GO:1901604":null}}


id: PBO:0086005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; similar to uncharacterized proteins from other fungi","termid":"PBO:0086005"}


id: PBO:0090357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein Hsp16-family","termid":"PBO:0090357"}


id: PBO:0045558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 8 pseudogene 2","termid":"PBO:0045558"}


id: SO:0000185
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript that in its initial state requires modification to be functional.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary_transcript","secondary_identifiers":["http://en.wikipedia.org/wiki/Primary_transcript"],"synonyms":[{"name":"INSDC_feature:precursor_RNA","type":"exact"},{"name":"INSDC_feature:prim_transcript","type":"exact"},{"name":"precursor RNA","type":"exact"},{"name":"primary transcript","type":"exact"}],"termid":"SO:0000185"}


id: GO:0019035
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A nucleoprotein complex containing viral genetic material and the viral integrase, required for genome integration into the host's genome. May contain other proteins.","definition_xrefs":["PMID:2721960","PMID:29900498","PMID:21037296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"host cell","termid":"GO:0043657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"viral integration complex","secondary_identifiers":["Wikipedia:Pre-integration_complex"],"synonyms":[{"name":"PIC","type":"broad"},{"name":"pre-integration complex","type":"exact"}],"termid":"GO:0019035"}


id: PBO:0002553
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.51","termid":"PBO:0002553"}


id: MONDO:0100426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A characteristic of a diseae which results from diagnostic and therapeutic procedures undertaken on a patient.","definition_xrefs":["PMID:27407693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iatrogenic or non-iatrogenic","termid":"MONDO:0100369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iatrogenic","secondary_identifiers":["icd11.foundation:4953745"],"termid":"MONDO:0100426","xrefs":{"Monarch":{"xref_id":"0100426"}}}


id: GO:0047074
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: benzene-1,2,4-triol + O2 = maleylacetate + 2 H+.","definition_xrefs":["RHEA:35595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"4-hydroxycatechol 1,2-dioxygenase activity","secondary_identifiers":["MetaCyc:RXN-10137","EC:1.13.11.37"],"termid":"GO:0047074"}


id: PBO:0028607
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_serine_phosphorylation_during_vegetative_growth","termid":"PBO:0028607"}


id: GO:1900087
data:
  {"annotated_genes":["SJAG_02404","SJAG_01825","SJAG_03591","SJAG_04140","SJAG_03699","SJAG_02723","SJAG_02810","SJAG_03048","SJAG_01401","SJAG_03681","SJAG_01311","SJAG_01210"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102162,105615,105770,106454,108987,116880],"is_not":false,"summary":null,"term":"GO:1900087"},{"annotations":[115713,74559,108697,115148,91503,76469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007089"}]},"cv_name":"biological_process","definition":"Any signaling pathway that increases or activates a cell cycle cyclin-dependent protein kinase to modulate the switch from G1 phase to S phase of the mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mitotic cell cycle phase transition","termid":"GO:1901992"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle G1/S phase transition","termid":"GO:1902808"},{"relation_name":"is_a","term_name":"regulation of G1/S transition of mitotic cell cycle","termid":"GO:2000045"},{"relation_name":"positively_regulates","term_name":"G1/S transition of mitotic cell cycle","termid":"GO:0000082"}],"gene_count":12,"genes_by_uniquename":{"SJAG_01210":null,"SJAG_01311":null,"SJAG_01401":null,"SJAG_01825":null,"SJAG_02404":null,"SJAG_02723":null,"SJAG_02810":null,"SJAG_03048":null,"SJAG_03591":null,"SJAG_03681":null,"SJAG_03699":null,"SJAG_04140":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0044772"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0044772"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0044772"],"is_obsolete":false,"name":"positive regulation of G1/S transition of mitotic cell cycle","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"activation of G1/S transition of mitotic cell cycle","type":"narrow"},{"name":"up regulation of G1/S transition of mitotic cell cycle","type":"exact"},{"name":"up-regulation of G1/S transition of mitotic cell cycle","type":"exact"},{"name":"upregulation of G1/S transition of mitotic cell cycle","type":"exact"}],"termid":"GO:1900087","terms_by_termid":{"GO:0007089":null,"GO:1900087":null}}


id: PBO:0040108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acylsphingosine amidohydrolase 2B","termid":"PBO:0040108"}


id: GO:0102067
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (E)-3,7,11,15-tetramethylhexadec-2-en-1-yl diphosphate + 3 NADP = 2-trans,6-trans,10-trans-geranylgeranyl diphosphate + 3 NADPH + 3 H+.","definition_xrefs":["GOC:pz","EC:1.3.1.83"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"geranylgeranyl diphosphate reductase activity","secondary_identifiers":["MetaCyc:RXN-10625","RHEA:26229"],"termid":"GO:0102067"}


id: GO:1990909
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multiprotein protein complex containing membrane-localized Wnt receptors and cytosolic protein complexes, which is capable of transmitting the Wnt signal. Contains at least a Wnt protein, LRP5 or LRP6, a member of the Frizzled (Fz) family, Axin and and a Dishevelled (DVL) protein.","definition_xrefs":["PMID:25336320","GOC:bf","GOC:PARL","PMID:22899650"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Wnt signalosome","synonyms":[{"name":"LRP5/6 signalosome","type":"exact"},{"name":"LRP6 signalosome","type":"narrow"},{"name":"Wnt signalosome complex","type":"exact"},{"name":"Wnt-LRP5/6 signalosome","type":"exact"}],"termid":"GO:1990909"}


id: MONDO:1012003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corneal sequestra, non-human animal","secondary_identifiers":["OMIA:002574"],"termid":"MONDO:1012003","xrefs":{"Monarch":{"xref_id":"1012003"}}}


id: PBO:0061564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5' nucleotidase, ecto-like, pseudogene","termid":"PBO:0061564"}


id: MONDO:0022608
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"brittle bone disorder","termid":"MONDO:0011375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"brittle bone syndrome lethal type","secondary_identifiers":["GARD:1018"],"termid":"MONDO:0022608","xrefs":{"Monarch":{"xref_id":"0022608"}}}


id: FYPO:0003971
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell of that undergoes two or more rounds of cell division in which cells do not completely separate upon cytokinesis, form septa that are thicker than normal, and then die.","definition_xrefs":["PomBase:mah","PomBase:vw","PMID:9046095"],"direct_ancestors":[{"relation_name":"has_part","term_name":"increased septum thickness","termid":"FYPO:0001406"},{"relation_name":"has_part","term_name":"abnormal cell separation after cytokinesis resulting in septated cell","termid":"FYPO:0001972"},{"relation_name":"is_a","term_name":"abnormal cell separation after cytokinesis","termid":"FYPO:0000164"},{"relation_name":"is_a","term_name":"increased septum thickness","termid":"FYPO:0001406"},{"relation_name":"is_a","term_name":"inviable after spore germination, multiple cell divisions, with abnormal septation","termid":"FYPO:0006878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000004","FYPO:0000032","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, multiple cell divisions, with abnormal cytokinetic cell separation and increased septum thickness","synonyms":[{"name":"inviable after spore germination, multiple cell divisions, with abnormal cytokinetic cell separation and thick septa","type":"exact"},{"name":"inviable following spore germination, multiple cell divisions, with abnormal cytokinetic cell separation and increased septum thickness","type":"exact"},{"name":"inviable germinated spore, multiple cell divisions, with abnormal cytokinetic cell separation and increased septum thickness","type":"exact"},{"name":"lethal after spore germination, multiple cell divisions, with abnormal cytokinetic cell separation and increased septum thickness","type":"exact"}],"termid":"FYPO:0003971"}


id: PBO:0090636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S4","termid":"PBO:0090636"}


id: PBO:0110464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTR2 pseudogene 2","termid":"PBO:0110464"}


id: GO:0018529
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nitrilotriacetate + FMNH2 + O2 = aminodiacetate + FMN + glyoxylate + H2O.","definition_xrefs":["RHEA:31359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"nitrilotriacetate monooxygenase activity","secondary_identifiers":["MetaCyc:RXN-9508","KEGG_REACTION:R09798","UM-BBD_reactionID:r0587","EC:1.14.14.10"],"termid":"GO:0018529"}


id: PBO:0083769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential non-ATPase regulatory subunit of the 26S proteasome lid; similar to the p58 subunit of the human 26S proteasome; temperature-sensitive alleles cause metaphase arrest, suggesting a role for the proteasome in cell cycle control","termid":"PBO:0083769"}


id: PBO:0057537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 653","termid":"PBO:0057537"}


id: PBO:0046052
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","termid":"PBO:0046052"}


id: PBO:0074270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schlafen family member 12","termid":"PBO:0074270"}


id: GO:0035462
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of the diencephalon with respect to the left and right halves.","definition_xrefs":["PMID:15084459","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"determination of left/right asymmetry in nervous system","termid":"GO:0035545"},{"relation_name":"part_of","term_name":"diencephalon development","termid":"GO:0021536"}],"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":"determination of left/right asymmetry in diencephalon","termid":"GO:0035462"}


id: PBO:0083365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the verified gene TRM5/YHR070W","termid":"PBO:0083365"}


id: MONDO:0009119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"digestive system disorder","termid":"MONDO:0004335"}],"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":"diverticulosis, small-intestinal","secondary_identifiers":["MESH:C565620","MEDGEN:341730","UMLS:C1857228","OMIM:223320"],"synonyms":[{"name":"diverticulosis, small-intestinal","type":"exact"}],"termid":"MONDO:0009119","xrefs":{"Monarch":{"xref_id":"0009119"}}}


id: PBO:0001743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial fusion and transport protein Ugo1 (predicted)","termid":"PBO:0001743"}


id: GO:0141212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An intracellular signaling cassette that starts with activation of phospholipase C (PLC) activity and ends with the activation of protein kinase C (PKC). PLC produces inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG). IP3 regulates the opening of calcium channels in intracellular calcium store, leading to the release of calcium into the cytosol. Calcium and DAG activate protein kinase C (PKC), which in turn activates downstream effectors. This cassette is often part of the phospholipase C-activating G protein-coupled receptor signaling pathway.","definition_xrefs":["PMID:26605346"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signaling cassette","termid":"GO:0141124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"phospholipase C/protein kinase C signal transduction","synonyms":[{"name":"PLC/PKC signaling","type":"exact"},{"name":"PLC/PKC/PKD signaling","type":"exact"}],"termid":"GO:0141212"}


id: PBO:0071251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 92","termid":"PBO:0071251"}


id: PBO:0025521
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is not functionally complemented by S. cerevisiae KIN28","termid":"PBO:0025521"}


id: MONDO:0008750
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microcephaly - albinism - digital anomalies syndrome is a very rare syndrome associating microcephaly, micrognathia, oculocutaneous albinism, hypoplasia of the distal phalanx of fingers and agenesia of the distal end of the right big toe.","definition_xrefs":["Orphanet:2513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microcephaly-albinism-digital anomalies syndrome","secondary_identifiers":["GARD:3604","MEDGEN:395372","MESH:C537322","SCTID:719377004","OMIM:203340","UMLS:C1859910"],"synonyms":[{"name":"Castro Gago-Pombo-Novo syndrome","type":"exact"},{"name":"albinism-microcephaly digital anomalies syndrome","type":"related"},{"name":"albinism-microcephaly-digital anomalies syndrome","type":"related"},{"name":"microcephaly-albinism-digital anomalies syndrome","type":"exact"}],"termid":"MONDO:0008750","xrefs":{"Monarch":{"xref_id":"0008750"}}}


id: GO:0004985
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an opioid (any narcotic derived from or resembling opium), and transmitting the signal across the membrane by activating an associated G-protein.","definition_xrefs":["PMID:20494127","GOC:ai","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"G protein-coupled opioid receptor activity","synonyms":[{"name":"opioid receptor activity","type":"broad"}],"termid":"GO:0004985"}


id: PBO:0001285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal recognition particle subunit Srp21 (predicted)","termid":"PBO:0001285"}


id: GO:0007238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of Pbs2 (obsolete GO:0007238)","synonyms":[{"name":"activation of Pbs2","type":"exact"}],"termid":"GO:0007238"}


id: GO:0005108
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete transmembrane ephrin (obsolete GO:0005108)","synonyms":[{"name":"transmembrane ephrin","type":"exact"}],"termid":"GO:0005108"}


id: MONDO:0032875
data:
  {"annotated_genes":["SJAG_02513"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86546],"is_not":false,"summary":null,"term":"MONDO:0032875"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02513":null},"genotype_count":0,"is_obsolete":false,"name":"short stature and microcephaly with genital anomalies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618702","UMLS:C5231467","MEDGEN:1684791"],"synonyms":[{"name":"SHORT STATURE AND MICROCEPHALY WITH GENITAL ANOMALIES","type":"related"},{"name":"SSMGA","type":"related"}],"termid":"MONDO:0032875","terms_by_termid":{"MONDO:0032875":null},"xrefs":{"Monarch":{"xref_id":"0032875"}}}


id: MONDO:0034971
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare eyelid malposition disorder characterized by congenital abnormal inversion of the eyelid towards the globe, potentially causing mechanical irritation of the ocular surface by the eyelashes, which may lead to corneal abrasion and scarring with visual impairment. Typical initial symptoms are foreign body sensation, redness, tearing, and ocular discharge.","definition_xrefs":["Orphanet:519386"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital entropion","termid":"MONDO:0020159"}],"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":"isolated congenital entropion","secondary_identifiers":["GARD:22123","icd11.foundation:1290880184"],"termid":"MONDO:0034971","xrefs":{"Monarch":{"xref_id":"0034971"}}}


id: GO:0050611
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + arsenite + 2 oxidized azurin = 2 H+ + 2 reduced azurin + arsenate.","definition_xrefs":["EC:1.20.9.1","MetaCyc:1.20.98.1-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on phosphorus or arsenic in donors, with a copper protein as acceptor","termid":"GO:0052882"}],"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:0016491","GO:0003824"],"is_obsolete":false,"name":"arsenate reductase (azurin) activity","secondary_identifiers":["UM-BBD_reactionID:r0634","RHEA:18701","GO:0018691"],"synonyms":[{"name":"arsenite oxidase activity","type":"related"},{"name":"arsenite:azurin oxidoreductase activity","type":"related"}],"termid":"GO:0050611"}


id: MONDO:0002837
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A poorly differentiated transitional cell carcinoma characterized by the presence of malignant cells with spindle cell morphologic features.","definition_xrefs":["NCIT:C4120"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sarcomatoid carcinoma","termid":"MONDO:0006406"},{"relation_name":"is_a","term_name":"transitional cell carcinoma","termid":"MONDO:0006474"}],"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":"sarcomatoid transitional cell carcinoma","secondary_identifiers":["MEDGEN:83120","DOID:4014","ICDO:8122/3","UMLS:C0334271"],"synonyms":[{"name":"sarcomatoid transitional cell carcinoma","type":"exact"},{"name":"transitional cell carcinoma, sarcomatoid","type":"exact"},{"name":"transitional cell spindle cell carcinoma","type":"exact"},{"name":"transitional spindle cell carcinoma","type":"exact"}],"termid":"MONDO:0002837","xrefs":{"Monarch":{"xref_id":"0002837"}}}


id: GO:0090715
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any immunological memory process that can contribute to the formation of immunological memory.","definition_xrefs":["PMID:26086132","PMID:26831526","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunological memory process","termid":"GO:0090713"}],"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":"immunological memory formation process","termid":"GO:0090715"}


id: GO:0061285
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mesonephric capsule over time, from its formation to the mature structure. The mesonephric capsule is the tough fibrous layer surrounding the mesonephros, covered in a thick layer of perinephric adipose tissue.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal capsule development","termid":"GO:0072127"},{"relation_name":"part_of","term_name":"mesonephros development","termid":"GO:0001823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric capsule development","termid":"GO:0061285"}


id: GO:1903525
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of membrane tubulation.","definition_xrefs":["GOC:TermGenie","PMID:18388313","GO_REF:0000058","GOC:pm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of plasma membrane organization","termid":"GO:1903729"},{"relation_name":"regulates","term_name":"plasma membrane tubulation","termid":"GO:0097320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"regulation of membrane tubulation","synonyms":[{"name":"regulation of plasma membrane tubulation","type":"exact"},{"name":"regulation of vesicle scission","type":"related"}],"termid":"GO:1903525"}


id: GO:1900707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tensidol A biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone biosynthetic process","termid":"GO:0010566"},{"relation_name":"is_a","term_name":"regulation of amide metabolic process","termid":"GO:0034248"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"tensidol A biosynthetic process","termid":"GO:1900605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"regulation of tensidol A biosynthetic process","synonyms":[{"name":"regulation of tensidol A anabolism","type":"exact"},{"name":"regulation of tensidol A biosynthesis","type":"exact"},{"name":"regulation of tensidol A formation","type":"exact"},{"name":"regulation of tensidol A synthesis","type":"exact"}],"termid":"GO:1900707"}


id: GO:1900493
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of [4Fe-4S] cluster assembly.","definition_xrefs":["GOC:pr","GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of [4Fe-4S] cluster assembly","termid":"GO:1900491"},{"relation_name":"is_a","term_name":"positive regulation of iron-sulfur cluster assembly","termid":"GO:1903331"},{"relation_name":"positively_regulates","term_name":"[4Fe-4S] cluster assembly","termid":"GO:0044572"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0016226"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016226"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0016226"],"is_obsolete":false,"name":"positive regulation of [4Fe-4S] cluster assembly","synonyms":[{"name":"activation of 4Fe-4S cluster assembly","type":"narrow"},{"name":"activation of [4Fe-4S] cluster assembly","type":"narrow"},{"name":"activation of [4Fe-4S] cluster biosynthetic process","type":"related"},{"name":"positive regulation of 4Fe-4S cluster assembly","type":"exact"},{"name":"positive regulation of [4Fe-4S] cluster biosynthetic process","type":"related"},{"name":"up regulation of 4Fe-4S cluster assembly","type":"exact"},{"name":"up regulation of [4Fe-4S] cluster assembly","type":"exact"},{"name":"up regulation of [4Fe-4S] cluster biosynthetic process","type":"related"},{"name":"up-regulation of 4Fe-4S cluster assembly","type":"exact"},{"name":"up-regulation of [4Fe-4S] cluster assembly","type":"exact"},{"name":"up-regulation of [4Fe-4S] cluster biosynthetic process","type":"related"},{"name":"upregulation of 4Fe-4S cluster assembly","type":"exact"},{"name":"upregulation of [4Fe-4S] cluster assembly","type":"exact"},{"name":"upregulation of [4Fe-4S] cluster biosynthetic process","type":"related"}],"termid":"GO:1900493"}


id: FYPO:0003889
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 fungal-type cell wall is thinner than normal at the old end of the cell.","definition_xrefs":["PomBase:mah","PMID:10547441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cell wall thickness at cell tip during vegetative growth","termid":"FYPO:0006746"}],"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"},{"rel_name":"is_a","termid":"FYPO:0002946"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0002946"],"is_obsolete":false,"name":"decreased cell wall thickness at old end during vegetative growth","synonyms":[{"name":"decreased cell wall thickness at growing end during vegetative growth","type":"related"},{"name":"decreased cell wall thickness at old end during mitotic cell cycle","type":"related"},{"name":"reduced cell wall thickness at old end during vegetative growth","type":"exact"},{"name":"thin cell wall at old end during vegetative growth","type":"exact"}],"termid":"FYPO:0003889"}


id: GO:0000148
data:
  {"annotated_genes":["SJAG_03587","SJAG_05285","SJAG_01288","SJAG_01453","SJAG_02222"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[59774,62602,63914,69027,102424],"is_not":false,"summary":null,"term":"GO:0000148"}]},"cv_name":"cellular_component","definition":"A protein complex that catalyzes the transfer of a glucose group from UDP-glucose to a (1->3)-beta-D-glucan chain.","definition_xrefs":["PMID:7983071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01288":null,"SJAG_01453":null,"SJAG_02222":null,"SJAG_03587":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"1,3-beta-D-glucan synthase complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"(1->3)-beta-glucan synthase complex","type":"exact"},{"name":"1,3-beta-glucan synthase complex","type":"exact"}],"termid":"GO:0000148","terms_by_termid":{"GO:0000148":null}}


id: GO:0140833
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + RNA polymerase II large subunit CTD heptapeptide repeat (consensus YSPTSPS) = ADP + H+ + RNA polymerase II large subunit phosphotyrosine (position 1).","definition_xrefs":["PMID:28248323"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II CTD heptapeptide repeat kinase activity","termid":"GO:0008353"}],"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:0004672"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016740","GO:0016301","GO:0140096","GO:0003674","GO:0003824","GO:0004672"],"is_obsolete":false,"name":"RNA polymerase II CTD heptapeptide repeat Y1 kinase activity","synonyms":[{"name":"RNA polymerase II C-terminal domain Y1 kinase activity","type":"exact"}],"termid":"GO:0140833"}


id: PBO:0035714
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-K9_dimethylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0035714"}


id: GO:0102510
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: pelargonidin 3-O-beta-D-glucoside + 1-O-vanilloyl-beta-D-glucose = anthocyanidin 3,5-di-O-beta-D-glucoside + vanillate + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete pelargonidin 3-O-glucoside 5-O-glucosyltransferase (acyl-glucose dependent) activity (obsolete GO:0102510)","termid":"GO:0102510"}


id: PBO:0060434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAC alpha domain containing","termid":"PBO:0060434"}


id: GO:0032391
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the photoreceptor cell cilium linking the photoreceptor inner and outer segments. It's considered to be equivalent to the ciliary transition zone.","definition_xrefs":["PMID:22653444","GOC:cilia","PMID:8718680","PMID:15917207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary transition zone","termid":"GO:0035869"},{"relation_name":"part_of","term_name":"photoreceptor cell cilium","termid":"GO:0097733"}],"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":"photoreceptor connecting cilium","synonyms":[{"name":"photoreceptor cilium","type":"related"}],"termid":"GO:0032391"}


id: PBO:0073671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal regulatory protein alpha pseudogene 1","termid":"PBO:0073671"}


id: GO:1990233
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex capable of catalyzing the transfer of a phosphate group from one position to another within a single molecule.","definition_xrefs":["GOC:bhm","PMID:16540464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005829","GO:0032991"],"is_obsolete":false,"name":"intramolecular phosphotransferase complex","termid":"GO:1990233"}


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":["PRO:DNx","UniProtKB:P36579"],"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: MONDO:0009002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coloboma","termid":"MONDO:0001476"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"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":"coloboma, ocular, autosomal recessive","secondary_identifiers":["UMLS:C4011974","MEDGEN:860411","OMIM:216820"],"synonyms":[{"name":"coloboma, ocular, autosomal recessive","type":"exact"}],"termid":"MONDO:0009002","xrefs":{"Monarch":{"xref_id":"0009002"}}}


id: PBO:0052788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 27","termid":"PBO:0052788"}


id: PBO:0029756
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_modification","termid":"PBO:0029756"}


id: FYPO:0000001
data:
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id: MOD:01902
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-isoleucine residue and an L-serine residue to form L-cysteine oxazole-4-carboxylic acid.","definition_xrefs":["PubMed:21568297","RESID:AA0573","PubMed:21950656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxazole/oxazoline ring crosslinked residues (Ser)","termid":"MOD:01421"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"},{"relation_name":"is_a","term_name":"crosslinked L-isoleucine residue","termid":"MOD:02049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-isoleucine oxazole-4-carboxylic acid","synonyms":[{"name":"2-[(1S,2S)-1-amino-2-methylbutyl]-1,3-oxazole-4-carboxylic acid","type":"exact"},{"name":"2-[(1S,2S)-1-azanyl-2-methylbutyl]-1,3-oxazole-4-carboxylic acid","type":"exact"},{"name":"CROSSLNK Oxazole-4-carboxylic acid (Ile-Ser)","type":"exact"},{"name":"L-isoleucine oxazole-4-carboxylic acid","type":"exact"}],"termid":"MOD:01902"}


id: MOD:01956
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to (3R)-3-hydroxy-L-arginine.","definition_xrefs":["PubMed:786730","PubMed:10094780","PubMed:23103944","RESID:AA0601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydroxylated arginine","termid":"MOD:00682"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(3R)-3-hydroxy-L-arginine","synonyms":[{"name":"(2S,3R)-2-amino-5-[(diaminomethylidene)amino]-3-hydroxypentanoic acid","type":"exact"},{"name":"(3R)-3-hydroxy-L-arginine","type":"exact"},{"name":"2-amino-5-(carbamimidamido)-3-hydroxypentanoic acid [tautomer]","type":"exact"},{"name":"2-amino-5-[(aminoiminomethyl)amino]-3-hydroxypentanoic acid [tautomer]","type":"exact"},{"name":"2-amino-5-guanidino-3-hydroxypentanoic acid","type":"exact"},{"name":"C(beta)-hydroxyarginine","type":"exact"},{"name":"MOD_RES (3R)-3-hydroxyarginine","type":"exact"},{"name":"beta-hydroxyarginine","type":"exact"}],"termid":"MOD:01956"}


id: PBO:0036029
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transcription_during_cellular_response_to_heat","termid":"PBO:0036029"}


id: MONDO:0006118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Breast fibrocystic change characterized by the prominence of fibrotic changes in the parenchyma.","definition_xrefs":["NCIT:C3660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"non-proliferative fibrocystic change of the breast","termid":"MONDO:0003724"},{"relation_name":"is_a","term_name":"breast neoplasm","termid":"MONDO:0021100"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibrosis","secondary_identifiers":["MEDGEN:57627","UMLS:C0156318","ICD10CM:N60.3","ICD9:610.3","SCTID:29070004","EFO:1000145","DOID:10353"],"synonyms":[{"name":"breast fibrosclerosis","type":"exact"},{"name":"breast fibrosis","type":"exact"},{"name":"fibrosclerosis of breast","type":"exact"},{"name":"fibrosclerosis of the breast","type":"exact"},{"name":"fibrosis of breast","type":"exact"},{"name":"fibrosis of the breast","type":"exact"}],"termid":"MONDO:0006118","xrefs":{"Monarch":{"xref_id":"0006118"}}}


id: PBO:0083509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF CRN1","termid":"PBO:0083509"}


id: PATO:0001309
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A process quality inhering in a bearer by virtue of the bearer's magnitude of the temporal extent between the starting and ending point.","definition_xrefs":["PATOC:mellybelly"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality of a process","termid":"PATO:0002062"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"duration","secondary_identifiers":["PATO:0000081"],"synonyms":[{"name":"period","type":"exact"},{"name":"time","type":"related"}],"termid":"PATO:0001309"}


id: PBO:0043751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COX7B pseudogene 6","termid":"PBO:0043751"}


id: GO:0030229
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a very-low-density lipoprotein particle and delivering the very-low-density lipoprotein into the cell via endocytosis.","definition_xrefs":["GOC:bf","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle receptor activity","termid":"GO:0030228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038024"}],"interesting_parent_ids":["GO:0003674","GO:0038024"],"is_obsolete":false,"name":"very-low-density lipoprotein particle receptor activity","secondary_identifiers":["Wikipedia:VLDL_receptor"],"synonyms":[{"name":"VLDL receptor","type":"exact"},{"name":"apolipoprotein E receptor activity","type":"related"},{"name":"very-low-density lipoprotein receptor activity","type":"exact"}],"termid":"GO:0030229"}


id: PBO:0086974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulatory subunit of protein phosphatase PP4; presence of Psy4p in the PP4 complex (along with catalytic subunit Pph3p and Psy2p) is required for dephosphorylation of the histone variant H2AX, but not for dephosphorylation of Rad53p, during recovery from the DNA damage checkpoint; localization is cell-cycle dependent and regulated by Cdc28p phosphorylation; required for cisplatin resistance; homolog of mammalian R2","termid":"PBO:0086974"}


id: GO:0047186
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acetylneuraminate + acetyl-CoA = N-acetyl-7-O(or 9-O)-acetylneuraminate + CoA.","definition_xrefs":["EC:2.3.1.45","MetaCyc:2.3.1.45-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"N-acetylneuraminate 7-O(or 9-O)-acetyltransferase activity","secondary_identifiers":["RHEA:20808"],"synonyms":[{"name":"N-acetylneuraminate 7(8)-O-acetyltransferase activity","type":"related"},{"name":"N-acetylneuraminate 7,8-O-acetyltransferase activity","type":"related"},{"name":"N-acetylneuraminate O7-(or O9-)acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:N-acetylneuraminate 7-O(or 9-O)-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:N-acetylneuraminate-7- and/or 8-O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:N-acetylneuraminate-7- or 8-O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:N-acetylneuraminate-9(7)-O-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:N-acetylneuraminate-9(or 7)-O-acetyltransferase activity","type":"related"},{"name":"glycoprotein 7(9)-O-acetyltransferase activity","type":"related"},{"name":"sialate O-acetyltransferase","type":"broad"}],"termid":"GO:0047186"}


id: PBO:0049822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine decarboxylase","termid":"PBO:0049822"}


id: FYPO:0000032
data:
  {"alleles_by_uniquename":{"SJAG_00118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00118","name":"mid2delta","uniquename":"SJAG_00118:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_03596:allele-1":{"allele_type":"amino_acid_mutation","description":"L264P,P442T","gene_uniquename":"SJAG_03596","name":"cdc15-A","uniquename":"SJAG_03596:allele-1"},"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[119031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[119188],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"},{"annotations":[119027],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0000118"}],"single_locus_phenotype":[{"annotations":[119019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[118956,119174],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"},{"annotations":[119052],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0002026"},{"annotations":[119122,119020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[119189],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"},{"annotations":[119016,119017],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0000118"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which cytokinesis is abnormal. 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id: PBO:0046882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 8 member A7, pseudogene","termid":"PBO:0046882"}


id: PBO:0070708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 13","termid":"PBO:0070708"}


id: PBO:0046804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coagulation factor VIII associated 2","termid":"PBO:0046804"}


id: PBO:0051990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"janus kinase and microtubule interacting protein 2","termid":"PBO:0051990"}


id: MONDO:0017431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic limb overgrowth (obsolete MONDO:0017431)","secondary_identifiers":["Orphanet:294953"],"synonyms":[{"name":"limb overgrowth","type":"related"}],"termid":"MONDO:0017431","xrefs":{"Monarch":{"xref_id":"0017431"}}}


id: RO:0000085
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"a relation between an independent continuant (the bearer) and a function, in which the function specifically depends on the bearer for its existence","direct_ancestors":[{"relation_name":"is_a","term_name":"bearer_of","termid":"RO:0000053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_function","termid":"RO:0000085"}


id: PBO:0073972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 22 member 23","termid":"PBO:0073972"}


id: PBO:0079154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspanin 14","termid":"PBO:0079154"}


id: PBO:0060034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 22","termid":"PBO:0060034"}


id: PBO:0066755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 53","termid":"PBO:0066755"}


id: MONDO:0800066
data:
  {"annotated_genes":["SJAG_01213"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86489],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010408"}]},"cv_name":"mondo","definition":"Any skeletal dysplasia that is characterizedby polydactyly, syndactyly and triphalangism, where a digit has three phalanges instead of two.","definition_xrefs":["PMID:31633310","PMID:19125433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"relation_name":"is_a","term_name":"syndactyly","termid":"MONDO:0021002"},{"relation_name":"is_a","term_name":"polydactyly","termid":"MONDO:0021003"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01213":null},"genotype_count":0,"is_obsolete":false,"name":"polydactyly-syndactyly-triphalangism","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0800066","terms_by_termid":{"MONDO:0010408":null},"xrefs":{"Monarch":{"xref_id":"0800066"}}}


id: PBO:0087804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tail-anchored type II integral peroxisomal membrane protein; required for peroxisome biogenesis; cells lacking Pex15p mislocalize peroxisomal matrix proteins to cytosol; overexpression results in impaired peroxisome assembly","termid":"PBO:0087804"}


id: GO:0106064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving cobalamin (vitamin B12), a water-soluble vitamin characterized by possession of a corrin nucleus containing a cobalt atom.","definition_xrefs":["PMID:29056341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vitamin metabolic process","termid":"GO:0030656"},{"relation_name":"is_a","term_name":"regulation of tetrapyrrole metabolic process","termid":"GO:1901401"},{"relation_name":"regulates","term_name":"cobalamin metabolic process","termid":"GO:0009235"}],"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:0033013"},{"rel_name":"regulates","termid":"GO:0006766"}],"interesting_parent_ids":["GO:0006766","GO:0033013","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"regulation of cobalamin metabolic process","termid":"GO:0106064"}


id: PR:C6Y4A8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC23D3.16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4A8"],"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 C23D3.16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23D3.16","synonyms":[{"name":"Spom972h-SPAC23D3.16","type":"exact"}],"termid":"PR:C6Y4A8"}


id: PBO:0070697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9","termid":"PBO:0070697"}


id: GO:0098028
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The tube of the non-contractile tails of some viruses.","definition_xrefs":["GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"virion component","termid":"GO:0044423"},{"relation_name":"part_of","term_name":"virus tail","termid":"GO:0098015"}],"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":"virus tail, shaft","synonyms":[{"name":"bacteriophage tail shaft","type":"narrow"}],"termid":"GO:0098028"}


id: PBO:0054022
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 1353","termid":"PBO:0054022"}


id: GO:0051839
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism modulates the frequency, rate or extent of the cytolysis by that organism of cells in its symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation by host of cytolysis of symbiont cells (obsolete GO:0051839)","termid":"GO:0051839"}


id: GO:0032632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-3 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"interleukin-3 production","secondary_identifiers":["GO:0042223","GO:0072601"],"synonyms":[{"name":"IL-3 production","type":"exact"},{"name":"interleukin-3 biosynthetic process","type":"narrow"},{"name":"interleukin-3 secretion","type":"narrow"}],"termid":"GO:0032632"}


id: PBO:0087847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Topoisomerase II; relieves torsional strain in DNA by cleaving and re-sealing phosphodiester backbone of both positively and negatively supercoiled DNA; cleaves complementary strands; localizes to axial cores in meiosis; required for replication slow zone (RSZ) breakage following Mec1p inactivation; human homolog TOP2A implicated in cancers, and can complement yeast null mutant","termid":"PBO:0087847"}


id: PR:Q9UUE1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pyruvate carboxylase, 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":"pyruvate carboxylase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17G9.11c","secondary_identifiers":["UniProtKB:Q9UUE1"],"synonyms":[{"name":"PCB (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBC17G9.11c","type":"related"},{"name":"Spom972h-PC","type":"exact"},{"name":"pyruvic carboxylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UUE1"}


id: MONDO:0968977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral striopallidodentate calcinosis","termid":"MONDO:0008947"}],"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":"basal ganglia calcification, idiopathic, 9, autosomal recessive","secondary_identifiers":["MEDGEN:1854926","UMLS:C5935607","OMIM:620786"],"termid":"MONDO:0968977","xrefs":{"Monarch":{"xref_id":"0968977"}}}


id: GO:0017074
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of the N-propeptide of collagen chain alpha-1(I) at Pro-Gln and of alpha-1(II) and alpha-2(I) chains at Ala-Gln.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete procollagen N-endopeptidase activity (obsolete GO:0017074)","synonyms":[{"name":"aminoprocollagen peptidase activity","type":"related"},{"name":"aminoterminal procollagen peptidase activity","type":"related"},{"name":"procollagen N-endopeptidase activity","type":"exact"},{"name":"procollagen N-proteinase activity","type":"related"},{"name":"procollagen N-terminal peptidase activity","type":"related"},{"name":"procollagen N-terminal proteinase activity","type":"related"},{"name":"procollagen aminopeptidase activity","type":"related"},{"name":"procollagen aminoterminal protease activity","type":"related"},{"name":"type I/II procollagen N-proteinase activity","type":"related"},{"name":"type III procollagen","type":"related"}],"termid":"GO:0017074"}


id: PBO:0112562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-demethoxyubiquinol 3-hydroxylase Coq7","termid":"PBO:0112562"}


id: PBO:0084251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Inositol 1,3,4,5,6-pentakisphosphate 2-kinase; nuclear protein required for synthesis of 1,2,3,4,5,6-hexakisphosphate (phytate), which is integral to cell function; has 2 motifs conserved in other fungi; ipk1 gle1 double mutant is inviable; human IPPK can complement ipk1 null mutant","termid":"PBO:0084251"}


id: GO:0044701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A response to a stimulus that involves only one organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete response to stimulus by single organism (obsolete GO:0044701)","synonyms":[{"name":"response to stimulus by single organism","type":"exact"}],"termid":"GO:0044701"}


id: PBO:0051537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 5","termid":"PBO:0051537"}


id: MONDO:0033483
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial polycythemia in which the cause of the disease is a mutation in the EPO gene.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial polycythemia","termid":"MONDO:0001115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"erythrocytosis, familial, 5","secondary_identifiers":["OMIM:617907","MEDGEN:1638941","UMLS:C4693552","DOID:0080290"],"synonyms":[{"name":"ECYT5","type":"related"},{"name":"EPO familial polycythemia","type":"exact"},{"name":"erythrocytosis, familial, 5","type":"exact"},{"name":"familial erythrocytosis 5","type":"related"},{"name":"familial polycythemia caused by mutation in EPO","type":"exact"}],"termid":"MONDO:0033483","xrefs":{"Monarch":{"xref_id":"0033483"}}}


id: PBO:0075590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine peptidase inhibitor, Kunitz type 2","termid":"PBO:0075590"}


id: GO:0032451
data:
  {"annotated_genes":["SJAG_03286","SJAG_03664","SJAG_03041","SJAG_03997","SJAG_03635","SJAG_02401","SJAG_00892","SJAG_03750"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87137,70047],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051864"},{"annotations":[66598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140680"},{"annotations":[69646,74548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034647"},{"annotations":[70042,117571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032454"},{"annotations":[103019,93843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140683"},{"annotations":[88223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008398"},{"annotations":[102887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990984"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of a methyl group from a substrate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity","termid":"GO:0003824"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00892":null,"SJAG_02401":null,"SJAG_03041":null,"SJAG_03286":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03750":null,"SJAG_03997":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"demethylase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0032451","terms_by_termid":{"GO:0008398":null,"GO:0032454":null,"GO:0034647":null,"GO:0051864":null,"GO:0140680":null,"GO:0140683":null,"GO:1990984":null}}


id: GO:1902261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of delayed rectifier potassium channel activity.","definition_xrefs":["GOC:BHF","GOC:TermGenie","PMID:11299204","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of delayed rectifier potassium channel activity","termid":"GO:1902259"},{"relation_name":"is_a","term_name":"positive regulation of voltage-gated potassium channel activity","termid":"GO:1903818"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of delayed rectifier potassium channel activity","synonyms":[{"name":"activation of delayed rectifier potassium channel activity","type":"narrow"},{"name":"up regulation of delayed rectifier potassium channel activity","type":"exact"},{"name":"up-regulation of delayed rectifier potassium channel activity","type":"exact"},{"name":"upregulation of delayed rectifier potassium channel activity","type":"exact"}],"termid":"GO:1902261"}


id: PBO:0088786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial matrix Lon protease","termid":"PBO:0088786"}


id: GO:0001779
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a natural killer cell.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte differentiation","termid":"GO:0030098"},{"relation_name":"is_a","term_name":"natural killer cell activation","termid":"GO:0030101"}],"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":"natural killer cell differentiation","synonyms":[{"name":"NK cell differentiation","type":"exact"},{"name":"natural killer cell development","type":"related"}],"termid":"GO:0001779"}


id: GO:0009119
data:
  {"annotated_genes":["SJAG_06634","SJAG_00694","SJAG_02580","SJAG_03881","SJAG_02959","SJAG_03771","SJAG_03096","SJAG_00044","SJAG_01859","SJAG_00134","SJAG_02582","SJAG_01673","SJAG_01070"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046086"},{"annotations":[87330,87329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006154"},{"annotations":[90299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046085"},{"annotations":[116646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006169"},{"annotations":[69565,69404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009972"},{"annotations":[69550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006190"},{"annotations":[61545,66242,73201,93515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006166"},{"annotations":[73074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046132"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving any ribonucleoside, a nucleoside in which purine or pyrimidine base is linked to a ribose (beta-D-ribofuranose) molecule.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside metabolic process","termid":"GO:0009116"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00134":null,"SJAG_00694":null,"SJAG_01070":null,"SJAG_01673":null,"SJAG_01859":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02959":null,"SJAG_03096":null,"SJAG_03771":null,"SJAG_03881":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"ribonucleoside metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"synonyms":[{"name":"ribonucleoside metabolism","type":"exact"}],"termid":"GO:0009119","terms_by_termid":{"GO:0006154":null,"GO:0006166":null,"GO:0006169":null,"GO:0006190":null,"GO:0009972":null,"GO:0046085":null,"GO:0046086":null,"GO:0046132":null}}


id: PBO:0029119
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mononucleate_cell_with_increased_DNA_content_during_stationary_phase","termid":"PBO:0029119"}


id: PBO:0028082
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_total_nuclear_polyadenylated_mRNA_level_during_vegetative_growth","termid":"PBO:0028082"}


id: GO:0051738
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to xanthophylls, any of several neutral yellow to orange carotenoid pigments containing oxygen.","definition_xrefs":["ISBN:0122146743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid binding","termid":"GO:0019840"},{"relation_name":"is_a","term_name":"pigment binding","termid":"GO:0031409"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0008289","GO:0005488"],"is_obsolete":false,"name":"xanthophyll binding","termid":"GO:0051738"}


id: MOD:00759
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod N-linked glycosylation","definition_xrefs":["Unimod:307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N4-glycosyl-L-asparagine","termid":"MOD:00160"},{"relation_name":"is_a","term_name":"complex glycosylation","termid":"MOD:00725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"fucosylated biantennary (-1 galactose) N4-glycosylated asparagine","synonyms":[{"name":"Fucosylated biantennary (-1 galactose)","type":"related"},{"name":"dHex(1)Hex(4)HexNAc(4)","type":"related"}],"termid":"MOD:00759"}


id: PBO:0029210
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_dTTP_level","termid":"PBO:0029210"}


id: PR:Q9USQ5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spa1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USQ5"],"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":"ornithine decarboxylase antizyme (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC577.14c","synonyms":[{"name":"ODC-Az (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spa1","type":"exact"}],"termid":"PR:Q9USQ5"}


id: PBO:0062980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PABPN1 pseudogene 2","termid":"PBO:0062980"}


id: GO:0070208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a protein heterotrimer, a macromolecular structure consisting of three noncovalently associated subunits, of which not all are identical.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein heterooligomerization","termid":"GO:0051291"},{"relation_name":"is_a","term_name":"protein trimerization","termid":"GO:0070206"}],"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":"protein heterotrimerization","synonyms":[{"name":"protein heterotrimer assembly","type":"exact"},{"name":"protein heterotrimer biosynthesis","type":"exact"},{"name":"protein heterotrimer biosynthetic process","type":"exact"},{"name":"protein heterotrimer formation","type":"exact"}],"termid":"GO:0070208"}


id: PBO:0033823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic APC activator Mfr1","termid":"PBO:0033823"}


id: PBO:0045935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongation factor like GTPase 1 pseudogene 2","termid":"PBO:0045935"}


id: GO:0099054
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a presynapse.","definition_xrefs":["GOC:PARL","GOC:dos","GOC:bf","PMID:24449494"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"presynapse organization","termid":"GO:0099172"},{"relation_name":"part_of","term_name":"synapse assembly","termid":"GO:0007416"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"presynapse assembly","synonyms":[{"name":"presynapse biogenesis","type":"exact"},{"name":"presynaptic terminal assembly","type":"exact"}],"termid":"GO:0099054"}


id: MONDO:0002810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant epithelial neoplasm that is usually cystic and arises from the exocrine pancreas. It is characterized by the presence of neoplastic epithelial cells that produce fluid similar to serum. Representative examples include serous cystadenoma and serous cystadenocarcinoma.","definition_xrefs":["NCIT:C41248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic exocrine neoplasm","termid":"MONDO:0021076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"pancreatic serous cystic neoplasm","secondary_identifiers":["DOID:3919","MEDGEN:274122","UMLS:C1518875"],"synonyms":[{"name":"pancreatic serous cystic neoplasm","type":"exact"},{"name":"pancreatic serous neoplasm","type":"exact"}],"termid":"MONDO:0002810","xrefs":{"Monarch":{"xref_id":"0002810"}}}


id: PBO:0044280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X-C motif chemokine receptor 3","termid":"PBO:0044280"}


id: GO:0170048
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed import of D-alanine from the extracellular region across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:25425233","PMID:22418438"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-alanine transmembrane transport","termid":"GO:0042941"}],"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:0051179","GO:0008150"],"is_obsolete":false,"name":"D-alanine import across plasma membrane","synonyms":[{"name":"D-alanine import","type":"broad"},{"name":"D-alanine import into cell","type":"exact"},{"name":"D-alanine uptake","type":"exact"}],"termid":"GO:0170048"}


id: PBO:0073824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 7 member 3","termid":"PBO:0073824"}


id: FYPO:0006025
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of a protein to one or more actin filaments does not occur. The affected protein 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 protein complex binding","termid":"FYPO:0003591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000652","FYPO:0000702"],"is_obsolete":false,"name":"abolished actin filament binding","synonyms":[{"name":"abolished F-actin binding","type":"exact"},{"name":"abolished filamentous actin binding","type":"exact"},{"name":"actin filament binding abolished","type":"exact"}],"termid":"FYPO:0006025"}


id: MONDO:0023539
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0023539 (obsolete MONDO:0023539)","termid":"MONDO:0023539","xrefs":{"Monarch":{"xref_id":"0023539"}}}


id: PBO:0001628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIID complex subunit Taf3 (predicted)","termid":"PBO:0001628"}


id: PBO:0049003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol-3-phosphate dehydrogenase 1 like","termid":"PBO:0049003"}


id: GO:1905887
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which (2R,4S)-2-methyltetrahydrofuran-2,3,3,4-tetrol (autoinducer AI-2) is transported across a membrane. AI-2 is produced by prokaryotes and is believed to play a role in quorum sensing.","definition_xrefs":["GOC:TermGenie","PMID:15601708","GO_REF:0000069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyol transmembrane transport","termid":"GO:0015791"}],"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:0055085","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"autoinducer AI-2 transmembrane transport","synonyms":[{"name":"(2R,4S)-2-methyltetrahydrofuran-2,3,3,4-tetrol transmembrane transport","type":"exact"},{"name":"AI-2 transmembrane transport","type":"exact"},{"name":"autoinducer 2 transmembrane transport","type":"exact"}],"termid":"GO:1905887"}


id: MONDO:0005994
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection by roundworms of the superfamily trichostrongyloidea, including the genera trichostrongylus; ostertagia; Cooperia, haemonchus; Nematodirus, Hyostrongylus, and dictyocaulus.","definition_xrefs":["MESH:D014252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"helminthiasis","termid":"MONDO:0004664"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trichostrongyloidiasis","secondary_identifiers":["UMLS:C0040947","DOID:1255","MEDGEN:11907"],"synonyms":[{"name":"Trichostrongyloidea caused disease or disorder","type":"exact"},{"name":"Trichostrongyloidea disease or disorder","type":"exact"},{"name":"Trichostrongyloidea infectious disease","type":"exact"}],"termid":"MONDO:0005994","xrefs":{"Monarch":{"xref_id":"0005994"}}}


id: GO:1990509
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Protein complex involved in the disassembly of Mago-Y14 from the spliced mRNA during first round of translation, independently of the translational machinery. Conserved from fission yeast to humans.","definition_xrefs":["PMID:14968132","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"PYM-mago-Y14 complex","synonyms":[{"name":"PYM-mago-RNA-binding protein 8A complex","type":"exact"},{"name":"wibg-mago-tsu complex","type":"exact"}],"termid":"GO:1990509"}


id: PBO:0089260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane hydrolase, implicted in protein catabolism or lipid metabolism","termid":"PBO:0089260"}


id: FYPO:0005068
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 number of sites of double-strand breaks in DNA is greater than normal during S phase of the mitotic cell cycle.","definition_xrefs":["PMID:18180284","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased number of double-strand break sites during vegetative growth","termid":"FYPO:0000455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased number of double-strand break sites during mitotic S phase","synonyms":[{"name":"accumulation of DNA damage foci during mitotic S phase","type":"related"},{"name":"accumulation of double-strand break sites during mitotic S phase","type":"exact"},{"name":"increased number of DNA damage foci during mitotic S phase","type":"related"},{"name":"increased number of double-strand break sites during S phase during vegetative growth","type":"exact"},{"name":"increased number of double-strand break sites during S phase of mitotic cell cycle","type":"exact"}],"termid":"FYPO:0005068"}


id: MONDO:0001212
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A otitis media which involves transudation of fluid in the middle ear without pus formation.","definition_xrefs":["DOID:11180"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otitis media","termid":"MONDO:0005441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-suppurative otitis media","secondary_identifiers":["ICD9:381.4","MEDGEN:543351","UMLS:C0271446","SCTID:275481002"],"synonyms":[{"name":"nonsuppurative otitis media","type":"exact"}],"termid":"MONDO:0001212","xrefs":{"Monarch":{"xref_id":"0001212"}}}


id: GO:0000720
data:
  {"annotated_genes":["SJAG_00500","SJAG_03613"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116501,116502],"is_not":false,"summary":null,"term":"GO:0000720"}]},"cv_name":"biological_process","definition":"The repair of UV-induced T-T, C-T, and C-C dimers by the recognition and removal of the damaged DNA strand from the DNA helix as an oligonucleotide. The small gap left in the DNA helix is filled in by the sequential action of DNA polymerase and DNA ligase.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-excision repair","termid":"GO:0006289"},{"relation_name":"is_a","term_name":"pyrimidine dimer repair","termid":"GO:0006290"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00500":null,"SJAG_03613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006281","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"pyrimidine dimer repair by nucleotide-excision repair","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000720","terms_by_termid":{"GO:0000720":null}}


id: PBO:0084275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral membrane protein; required for the fusion of ER-derived COPII transport vesicles with the Golgi; interacts with Yip1p and Yos1p; localizes to the Golgi, the ER, and COPII vesicles; homolog of human YIPF3","termid":"PBO:0084275"}


id: PBO:0071977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 pseudogene 5","termid":"PBO:0071977"}


id: PBO:0028234
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_methionine_and_purine","termid":"PBO:0028234"}


id: FYPO:0005097
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is abnormally arrested during G1 phase. Arrest may either occur under conditions where arrest is not a normal occurrence, or may progress differently from normal under conditions where arrest normally does take place.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle arrest in mitotic G1 phase","termid":"FYPO:0000445"},{"relation_name":"is_a","term_name":"abnormal cell cycle arrest in mitotic interphase","termid":"FYPO:0001028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"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:0000631","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal cell cycle arrest in mitotic G1 phase","synonyms":[{"name":"abnormal cell cycle arrest in G1 phase during mitotic cell cycle","type":"exact"},{"name":"abnormal cell cycle arrest in mitotic G1 phase during vegetative growth","type":"exact"},{"name":"abnormal mitotic cell cycle arrest in G1 phase","type":"exact"}],"termid":"FYPO:0005097"}


id: SO:0000842
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a gene that has a specific function.","direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"},{"relation_name":"part_of","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene_component_region","synonyms":[{"name":"gene component region","type":"exact"}],"termid":"SO:0000842"}


id: PBO:0051204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 4-30-4","termid":"PBO:0051204"}


id: MONDO:0020697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lung carcinoma arising within the bronchi or bronchial tubes. It is characterized by the presence of myoepithelial cells, spindle cells, clear cells, and duct-forming epithelial cells. Surgical resection may be curative.","definition_xrefs":["NCIT:C45545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial-myoepithelial carcinoma","termid":"MONDO:0003389"},{"relation_name":"is_a","term_name":"lung carcinoma","termid":"MONDO:0005138"}],"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":"lung epithelial-myoepithelial carcinoma","secondary_identifiers":["UMLS:C1708770","MEDGEN:353868"],"synonyms":[{"name":"lung epithelial-myoepithelial cancer","type":"exact"},{"name":"lung epithelial-myoepithelial carcinoma","type":"exact"}],"termid":"MONDO:0020697","xrefs":{"Monarch":{"xref_id":"0020697"}}}


id: GO:0033078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a T cell via a differentiation pathway independent of the thymus.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell differentiation","termid":"GO:0030217"}],"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":"extrathymic T cell differentiation","synonyms":[{"name":"extrathymic T cell development","type":"related"}],"termid":"GO:0033078"}


id: PBO:0011508
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactic acidosis and hyperpyruvatemia","termid":"PBO:0011508"}


id: MONDO:0011019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism.","definition_xrefs":["Orphanet:1014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia","termid":"MONDO:0004907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome","secondary_identifiers":["SCTID:720981000","OMIM:601217","MEDGEN:321990","MESH:C563370","GARD:16553","UMLS:C1832593"],"synonyms":[{"name":"Devriendt-Vandenberghe-Fryns syndrome","type":"exact"},{"name":"alopecia-intellectual disability syndrome with convulsions and hypergonadotropic hypogonadism","type":"related"},{"name":"alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism","type":"related"}],"termid":"MONDO:0011019","xrefs":{"Monarch":{"xref_id":"0011019"}}}


id: GO:0048836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the number of petals produced in a developing flower.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of petal number","termid":"GO:0048834"}],"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":"specification of increased petal number","termid":"GO:0048836"}


id: PATO:0001136
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001136 ig e concentration (obsolete PATO:0001136)","termid":"PATO:0001136"}


id: GO:0000913
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form the preprophase band, a dense band of microtubules that marks the position in the cell where cytokinesis will occur in cells that perform cytokinesis by cell plate formation.","definition_xrefs":["GOC:clt","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"part_of","term_name":"cytokinesis by cell plate formation","termid":"GO:0000911"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"preprophase band assembly","synonyms":[{"name":"preprophase band formation","type":"related"}],"termid":"GO:0000913"}


id: GO:0005590
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(VII) chains; type VII collagen triple helices form antiparallel dimer, which in turn associate laterally to form anchoring fibrils that connect type IV collagen in the basal lamina to plaques in the underlying connective tissue. It binds laminin.","definition_xrefs":["ISBN:0721639976","PMID:19693541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anchoring collagen complex","termid":"GO:0030934"},{"relation_name":"part_of","term_name":"collagen type VII anchoring fibril","termid":"GO:0098652"}],"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":"collagen type VII trimer","termid":"GO:0005590"}


id: PBO:0064815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 6","termid":"PBO:0064815"}


id: PBO:0045438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dpy-19 like C-mannosyltransferase 3","termid":"PBO:0045438"}


id: MONDO:0012795
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":"hypophosphatemic rickets and hyperparathyroidism","secondary_identifiers":["MEDGEN:383131","OMIM:612089","UMLS:C2677524","MESH:C567423"],"synonyms":[{"name":"hypophosphatemic rickets and hyperparathyroidism","type":"exact"}],"termid":"MONDO:0012795","xrefs":{"Monarch":{"xref_id":"0012795"}}}


id: PBO:0075511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal peptidase complex subunit 2 pseudogene 2","termid":"PBO:0075511"}


id: PBO:0050048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class I, K (pseudogene)","termid":"PBO:0050048"}


id: GO:0034074
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: oxidosqualene = marneral.","definition_xrefs":["PMID:18033581","PMID:16425307","GOC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidosqualene cyclase activity","termid":"GO:0031559"}],"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:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"marneral synthase activity","secondary_identifiers":["RHEA:31875","MetaCyc:RXN-9664"],"termid":"GO:0034074"}


id: PBO:0005777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U5 snRNP-associated protein Prp18 (predicted)","termid":"PBO:0005777"}


id: GO:0060801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transforming growth factor signaling process that decreases the rate, frequency, or extent of trophoblast stem cells differentiating into the more mature cells of the trophoblast.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sdb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of trophoblast cell differentiation by transforming growth factor beta signaling pathway (obsolete GO:0060801)","synonyms":[{"name":"negative regulation of trophoblast cell differentiation by transforming growth factor beta signalling pathway","type":"exact"}],"termid":"GO:0060801"}


id: MONDO:0032013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disorder with homogeneous therapeutic possibilities, regardless of the pathophysiological mechanism involved.","definition_xrefs":["Orphanet:377792"],"gene_count":0,"genotype_count":0,"name":"obsolete clinical syndrome (obsolete MONDO:0032013)","termid":"MONDO:0032013","xrefs":{"Monarch":{"xref_id":"0032013"}}}


id: PBO:0064888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPP2R2B intronic transcript 1","termid":"PBO:0064888"}


id: GO:0019436
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sophorosyloxydocosanoate, 13-sophorosyloxydocosanoate 6',6''-diacetate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolipid catabolic process","termid":"GO:0019377"},{"relation_name":"is_a","term_name":"sophorosyloxydocosanoate metabolic process","termid":"GO:0019434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"sophorosyloxydocosanoate catabolic process","secondary_identifiers":["MetaCyc:SOPHOROSYLOXYDOCOSANOATE-DEG-PWY"],"synonyms":[{"name":"sophorosyloxydocosanoate breakdown","type":"exact"},{"name":"sophorosyloxydocosanoate catabolism","type":"exact"},{"name":"sophorosyloxydocosanoate degradation","type":"exact"}],"termid":"GO:0019436"}


id: PBO:0057109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 199a-1","termid":"PBO:0057109"}


id: GO:1902326
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chlorophyll biosynthetic process.","definition_xrefs":["PMID:23555952","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chlorophyll biosynthetic process","termid":"GO:0010380"},{"relation_name":"is_a","term_name":"positive regulation of tetrapyrrole biosynthetic process","termid":"GO:1901465"},{"relation_name":"positively_regulates","term_name":"chlorophyll biosynthetic process","termid":"GO:0015995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0033013"},{"rel_name":"positively_regulates","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"positive regulation of chlorophyll biosynthetic process","synonyms":[{"name":"activation of chlorophyll anabolism","type":"narrow"},{"name":"activation of chlorophyll biosynthesis","type":"narrow"},{"name":"activation of chlorophyll biosynthetic process","type":"narrow"},{"name":"activation of chlorophyll formation","type":"narrow"},{"name":"activation of chlorophyll synthesis","type":"narrow"},{"name":"positive regulation of chlorophyll anabolism","type":"exact"},{"name":"positive regulation of chlorophyll biosynthesis","type":"exact"},{"name":"positive regulation of chlorophyll formation","type":"exact"},{"name":"positive regulation of chlorophyll synthesis","type":"exact"},{"name":"up regulation of chlorophyll anabolism","type":"exact"},{"name":"up regulation of chlorophyll biosynthesis","type":"exact"},{"name":"up regulation of chlorophyll biosynthetic process","type":"exact"},{"name":"up regulation of chlorophyll formation","type":"exact"},{"name":"up regulation of chlorophyll synthesis","type":"exact"},{"name":"up-regulation of chlorophyll anabolism","type":"exact"},{"name":"up-regulation of chlorophyll biosynthesis","type":"exact"},{"name":"up-regulation of chlorophyll biosynthetic process","type":"exact"},{"name":"up-regulation of chlorophyll formation","type":"exact"},{"name":"up-regulation of chlorophyll synthesis","type":"exact"},{"name":"upregulation of chlorophyll anabolism","type":"exact"},{"name":"upregulation of chlorophyll biosynthesis","type":"exact"},{"name":"upregulation of chlorophyll biosynthetic process","type":"exact"},{"name":"upregulation of chlorophyll formation","type":"exact"},{"name":"upregulation of chlorophyll synthesis","type":"exact"}],"termid":"GO:1902326"}


id: GO:0004139
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-deoxy-D-ribose 5-phosphate = D-glyceraldehyde 3-phosphate + acetaldehyde.","definition_xrefs":["RHEA:12821","EC:4.1.2.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"deoxyribose-phosphate aldolase activity","secondary_identifiers":["KEGG_REACTION:R01066","MetaCyc:DEOXYRIBOSE-P-ALD-RXN","Reactome:R-HSA-6787321"],"synonyms":[{"name":"2-deoxy-D-ribose-5-phosphate acetaldehyde-lyase (D-glyceraldehyde-3-phosphate-forming)","type":"related"},{"name":"2-deoxy-D-ribose-5-phosphate acetaldehyde-lyase activity","type":"related"},{"name":"2-deoxyribose-5-phosphate aldolase activity","type":"related"},{"name":"deoxyriboaldolase activity","type":"related"},{"name":"deoxyribose-5-phosphate aldolase activity","type":"related"},{"name":"phosphodeoxyriboaldolase activity","type":"related"}],"termid":"GO:0004139"}


id: GO:1902878
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of BMP signaling pathway involved in spinal cord association neuron specification.","definition_xrefs":["GO_REF:0000058","PMID:21730158","GOC:mr","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of BMP signaling pathway involved in spinal cord association neuron specification (obsolete GO:1902878)","synonyms":[{"name":"regulation of BMP signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"regulation of bone morphogenetic protein signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"regulation of bone morphogenetic protein signalling pathway involved in spinal cord association neuron specification","type":"exact"}],"termid":"GO:1902878"}


id: PBO:0091485
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long tco1 transcript produced under low-oxygen conditions is not translated","termid":"PBO:0091485"}


id: RO:0003306
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between an entity (e.g. a genotype, genetic variation, chemical, or environmental exposure) and a condition (a phenotype or disease), where the entity influences the frequency of the condition in a population.","direct_ancestors":[{"relation_name":"is_a","term_name":"contributes_to_condition","termid":"RO:0003304"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contributes_to_frequency_of_condition","termid":"RO:0003306"}


id: FYPO:0001878
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is viable but is elongated and has an abnormally low thickness or diameter.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable elongated vegetative cell","termid":"FYPO:0001492"},{"relation_name":"is_a","term_name":"viable thin vegetative cell","termid":"FYPO:0001877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000002","FYPO:0001985","FYPO:0000004","FYPO:0001320"],"is_obsolete":false,"name":"viable thin, elongated vegetative cell","synonyms":[{"name":"thin, elongated viable cell during vegetative growth","type":"exact"},{"name":"thin, elongated viable vegetative cell","type":"exact"},{"name":"viable elongated vegetative cell with decreased cell diameter","type":"exact"},{"name":"viable elongated vegetative cell with decreased cell thickness","type":"exact"},{"name":"viable elongated vegetative cell with decreased cell width","type":"exact"},{"name":"viable thin, elongated vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001878"}


id: GO:0036510
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of an alpha-1,2-linked mannose from the C-chain of a glycoprotein oligosaccharide in the endoplasmic reticulum.","definition_xrefs":["PMID:20065073","GOC:bf","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum mannose trimming","termid":"GO:1904380"}],"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":"trimming of terminal mannose on C branch","synonyms":[{"name":"conversion of (Man)9(GlcNAc)2 to (Man)8C(GlcNAc)2","type":"related"},{"name":"conversion of M9 to M8C","type":"related"},{"name":"glycoprotein mannose trimming on C branch","type":"exact"}],"termid":"GO:0036510"}


id: MOD:01958
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts four L-cysteine residues and a two-iron two-sulfur cluster to bis-L-cysteinyl bisglutathion-S-yl diiron disulfide.","definition_xrefs":["RESID:AA0603","PubMed:17121859"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron-sulfur cluster containing modification","termid":"MOD:00739"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"}],"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":"bis-L-cysteinyl bisglutathion-S-yl diiron disulfide","synonyms":[{"name":"bis-L-cysteinyl bisglutathion-S-yl diiron disulfide","type":"exact"},{"name":"di-mu-sulfido-bis(cysteinato)-1kappaS,2kappaS-bis(glutathionato)-1kappaS,2kappaS-diiron","type":"exact"},{"name":"mitochondrial glutaredoxin 2 dimer iron-sulfur cluster","type":"exact"},{"name":"plant glutaredoxin C1 dimer iron-sulfur cluster","type":"exact"}],"termid":"MOD:01958"}


id: MONDO:0020558
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy.","definition_xrefs":["Orphanet:99944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"autosomal dominant Charcot-Marie-Tooth disease type 2K","secondary_identifiers":["NCIT:C133886","MEDGEN:334294","GARD:9199","SCTID:719512003","UMLS:C1842984"],"synonyms":[{"name":"CMT2K","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 2K","type":"exact"}],"termid":"MONDO:0020558","xrefs":{"Monarch":{"xref_id":"0020558"}}}


id: FYPO:0001825
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 export of sodium ions out of a cell occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal sodium export","termid":"FYPO:0001721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"increased sodium export","synonyms":[{"name":"increased cellular sodium export","type":"exact"},{"name":"increased sodium export during mitotic cell cycle","type":"related"},{"name":"increased sodium export during vegetative growth","type":"exact"},{"name":"increased sodium export from cell","type":"exact"},{"name":"increased sodium ion export","type":"exact"}],"termid":"FYPO:0001825"}


id: PBO:0083466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene NAP1","termid":"PBO:0083466"}


id: MONDO:0022293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder that affects the blood vessels of the penis. Representative examples include atherosclerosis, venous leak, and hemangioma.","definition_xrefs":["NCIT:C35218"],"direct_ancestors":[{"relation_name":"is_a","term_name":"penile disorder","termid":"MONDO:0002036"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular disorder of penis","secondary_identifiers":["UMLS:C0156307","ICD9:607.82","MEDGEN:102349","SCTID:198029003"],"synonyms":[{"name":"Penile Vascular Disorder","type":"related"},{"name":"Penile vascular disorder","type":"related"},{"name":"Penis vascular disorder","type":"related"},{"name":"Vascular disorder of penis","type":"related"},{"name":"penile vascular disorder","type":"exact"}],"termid":"MONDO:0022293","xrefs":{"Monarch":{"xref_id":"0022293"}}}


id: MONDO:0015664
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic pulmonary artery dilatation is a rare developmental defect during embryogenesis characterized by the dilatation of the main pulmonary artery, with or without dilatation of the right and left pulmonary artery branches, and not attributed to any other cardiac, pulmonary and/or arterial wall disease. It may present with exertional dyspnea, fatigue, cough, hemoptysis, palpitation and chest pain, but may also be asymptomatic. In serious cases, trachea constriction due to postural changes may lead to attacks of cyanosis with severe dyspnea. Sudden cardiac death has been reported in some cases.","definition_xrefs":["Orphanet:1676"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital anomaly of the great arteries","termid":"MONDO:0020292"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic pulmonary artery dilatation","secondary_identifiers":["MEDGEN:1842555","GARD:6757","UMLS:C1384816"],"synonyms":[{"name":"idiopathic dilatation of the pulmonary artery","type":"related"}],"termid":"MONDO:0015664","xrefs":{"Monarch":{"xref_id":"0015664"}}}


id: GO:0008189
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The function held by products which directly block any step in the process of apoptosis.","definition_xrefs":["GOC:hb"],"gene_count":0,"genotype_count":0,"name":"obsolete apoptosis inhibitor activity (obsolete GO:0008189)","synonyms":[{"name":"apoptosis inhibitor activity","type":"exact"}],"termid":"GO:0008189"}


id: PBO:0045564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 12 pseudogene 1","termid":"PBO:0045564"}


id: FYPO:0000562
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 cellular respiration does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular respiration","termid":"FYPO:0000078"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abolished cellular respiration","synonyms":[{"name":"abolished cellular respiration during mitotic cell cycle","type":"related"},{"name":"absent respiratory metabolism","type":"exact"},{"name":"cellular respiration abolished","type":"exact"},{"name":"cellular respiration abolished during vegetative growth","type":"exact"},{"name":"respiration abolished","type":"broad"},{"name":"respiratory metabolism abolished","type":"exact"},{"name":"respiratory metabolism: absent","type":"related"}],"termid":"FYPO:0000562"}


id: MONDO:0012790
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the TARDBP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"},{"relation_name":"is_a","term_name":"frontotemporal dementia with motor neuron disease","termid":"MONDO:0017161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"amyotrophic lateral sclerosis type 10","secondary_identifiers":["GARD:15540","UMLS:C2677565","MESH:C567429","MEDGEN:383137","DOID:0060201","OMIM:612069"],"synonyms":[{"name":"ALS10","type":"exact"},{"name":"Ftld-TDP, Tardbp-related","type":"related"},{"name":"TARDBP amyotrophic lateral sclerosis","type":"exact"},{"name":"TARDBP-related frontotemporal lobar degeneration with Tdp43 inclusions","type":"exact"},{"name":"amyotrophic lateral sclerosis 10","type":"exact"},{"name":"amyotrophic lateral sclerosis 10 with or without frontotemporal dementia","type":"related"},{"name":"amyotrophic lateral sclerosis 10, with or without FTD","type":"exact"},{"name":"amyotrophic lateral sclerosis 10, with or without frontotemporal dementia","type":"exact"},{"name":"amyotrophic lateral sclerosis caused by mutation in TARDBP","type":"exact"},{"name":"amyotrophic lateral sclerosis type 10","type":"exact"},{"name":"frontotemporal dementia with Tdp43 inclusions, Tardbp-related","type":"related"},{"name":"frontotemporal lobar Degeneration with Tdp43 inclusions, Tardbp-related","type":"related"},{"name":"frontotemporal lobar degeneration, TARDBP-related","type":"exact"}],"termid":"MONDO:0012790","xrefs":{"Monarch":{"xref_id":"0012790"}}}


id: GO:1904722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of mRNA endonucleolytic cleavage involved in unfolded protein response.","definition_xrefs":["GOC:PARL","PMID:20625543","GO_REF:0000058","GOC:TermGenie","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of mRNA endonucleolytic cleavage involved in unfolded protein response (obsolete GO:1904722)","synonyms":[{"name":"activation of HAC1 mRNA cleavage","type":"narrow"},{"name":"activation of HAC1-type intron splice site recognition and cleavage","type":"narrow"},{"name":"activation of IRE1-mediated XBP-1 mRNA cleavage","type":"narrow"},{"name":"activation of XBP1 mRNA cleavage","type":"narrow"},{"name":"activation of mRNA endonucleolytic cleavage involved in unfolded protein response","type":"narrow"},{"name":"positive regulation of HAC1 mRNA cleavage","type":"narrow"},{"name":"positive regulation of HAC1-type intron splice site recognition and cleavage","type":"narrow"},{"name":"positive regulation of IRE1-mediated XBP-1 mRNA cleavage","type":"narrow"},{"name":"positive regulation of XBP1 mRNA cleavage","type":"narrow"},{"name":"up regulation of HAC1 mRNA cleavage","type":"narrow"},{"name":"up regulation of HAC1-type intron splice site recognition and cleavage","type":"narrow"},{"name":"up regulation of IRE1-mediated XBP-1 mRNA cleavage","type":"narrow"},{"name":"up regulation of XBP1 mRNA cleavage","type":"narrow"},{"name":"up regulation of mRNA endonucleolytic cleavage involved in unfolded protein response","type":"exact"},{"name":"up-regulation of HAC1 mRNA cleavage","type":"narrow"},{"name":"up-regulation of HAC1-type intron splice site recognition and cleavage","type":"narrow"},{"name":"up-regulation of IRE1-mediated XBP-1 mRNA cleavage","type":"narrow"},{"name":"up-regulation of XBP1 mRNA cleavage","type":"narrow"},{"name":"up-regulation of mRNA endonucleolytic cleavage involved in unfolded protein response","type":"exact"},{"name":"upregulation of HAC1 mRNA cleavage","type":"narrow"},{"name":"upregulation of HAC1-type intron splice site recognition and cleavage","type":"narrow"},{"name":"upregulation of IRE1-mediated XBP-1 mRNA cleavage","type":"narrow"},{"name":"upregulation of XBP1 mRNA cleavage","type":"narrow"},{"name":"upregulation of mRNA endonucleolytic cleavage involved in unfolded protein response","type":"exact"}],"termid":"GO:1904722"}


id: PBO:0000448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF complex subunit Snf5","termid":"PBO:0000448"}


id: PBO:0073409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET pseudogene 12","termid":"PBO:0073409"}


id: PBO:0040334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit c locus 2","termid":"PBO:0040334"}


id: GO:0004319
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: acyl-[acyl-carrier protein] + NADP+ = trans-2,3-dehydroacyl-[acyl-carrier protein] + NADPH + H+.","definition_xrefs":["EC:1.3.1.10"],"gene_count":0,"genotype_count":0,"name":"obsolete enoyl-[acyl-carrier-protein] reductase (NADPH, B-specific) activity (obsolete GO:0004319)","synonyms":[{"name":"NADPH 2-enoyl Co A reductase activity","type":"related"},{"name":"acyl-acyl-carrier-protein:NADP+ oxidoreductase (B-specific)","type":"related"},{"name":"enoyl acyl-carrier-protein reductase activity","type":"related"},{"name":"enoyl-ACP reductase (NADPH, B-specific) activity","type":"exact"},{"name":"enoyl-[acyl-carrier protein] reductase (NADPH, B-specific) activity","type":"exact"},{"name":"enoyl-acyl-carrier-protein reductase (NADPH, B-specific)","type":"related"},{"name":"enoyl-acyl-carrier-protein reductase (NADPH2, B-specific)","type":"related"},{"name":"reductase, enoyl-acyl carrier protein (reduced nicotinamide adenine dinucleotide phosphate)","type":"related"}],"termid":"GO:0004319"}


id: GO:1902287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any semaphorin-plexin signaling pathway that is involved in axon guidance.","definition_xrefs":["GOC:TermGenie","GOC:rl","PMID:22790009","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"semaphorin-plexin signaling pathway involved in neuron projection guidance","termid":"GO:1902285"},{"relation_name":"part_of","term_name":"axon guidance","termid":"GO:0007411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"semaphorin-plexin signaling pathway involved in axon guidance","synonyms":[{"name":"semaphorin-plexin signaling pathway involved in axon chemotaxis","type":"related"},{"name":"semaphorin-plexin signaling pathway involved in axon growth cone guidance","type":"narrow"},{"name":"semaphorin-plexin signaling pathway involved in axon pathfinding","type":"exact"},{"name":"semaphorin-plexin signalling pathway involved in axon chemotaxis","type":"related"},{"name":"semaphorin-plexin signalling pathway involved in axon growth cone guidance","type":"narrow"},{"name":"semaphorin-plexin signalling pathway involved in axon guidance","type":"exact"},{"name":"semaphorin-plexin signalling pathway involved in axon pathfinding","type":"exact"}],"termid":"GO:1902287"}


id: GO:0043302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of leukocyte degranulation.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune effector process","termid":"GO:0002699"},{"relation_name":"is_a","term_name":"regulation of leukocyte degranulation","termid":"GO:0043300"},{"relation_name":"is_a","term_name":"positive regulation of regulated secretory pathway","termid":"GO:1903307"},{"relation_name":"positively_regulates","term_name":"leukocyte degranulation","termid":"GO:0043299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of leukocyte degranulation","synonyms":[{"name":"activation of leukocyte degranulation","type":"narrow"},{"name":"positive regulation of immune cell degranulation","type":"exact"},{"name":"positive regulation of leucocyte degranulation","type":"exact"},{"name":"stimulation of leukocyte degranulation","type":"narrow"},{"name":"up regulation of leukocyte degranulation","type":"exact"},{"name":"up-regulation of leukocyte degranulation","type":"exact"},{"name":"upregulation of leukocyte degranulation","type":"exact"}],"termid":"GO:0043302"}


id: GO:0010518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of phospholipase activity, the hydrolysis of a phospholipid.","definition_xrefs":["GOC:BHF","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phospholipase activity","termid":"GO:0010517"},{"relation_name":"is_a","term_name":"positive regulation of lipase activity","termid":"GO:0060193"}],"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 phospholipase activity","termid":"GO:0010518"}


id: GO:0001049
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to RNA polymerase V core enzyme, a multisubunit eukaryotic nuclear RNA polymerase found in plants and involved in production of noncoding transcripts at target loci for silencing.","definition_xrefs":["GOC:txnOH","PMID:19110459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase core enzyme binding","termid":"GO:0043175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"RNA polymerase V core binding","termid":"GO:0001049"}


id: PATO:0000880
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000880 fertility value (obsolete PATO:0000880)","termid":"PATO:0000880"}


id: GO:0060266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of a phase of elevated metabolic activity, during which oxygen consumption increases made as a defense response ; this leads to the production, by an NADH dependent system, of hydrogen peroxide (H2O2), superoxide anions and hydroxyl radicals.","definition_xrefs":["GOC:dph","GOC:BHF","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immune effector process","termid":"GO:0002698"},{"relation_name":"is_a","term_name":"negative regulation of innate immune response","termid":"GO:0045824"},{"relation_name":"is_a","term_name":"negative regulation of inflammatory response","termid":"GO:0050728"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of respiratory burst involved in inflammatory response","termid":"GO:0060264"},{"relation_name":"is_a","term_name":"negative regulation of respiratory burst","termid":"GO:0060268"},{"relation_name":"is_a","term_name":"regulation of cell development","termid":"GO:0060284"},{"relation_name":"negatively_regulates","term_name":"respiratory burst involved in inflammatory response","termid":"GO:0002536"}],"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 respiratory burst involved in inflammatory response","synonyms":[{"name":"negative regulation of respiratory burst involved in acute inflammatory response","type":"broad"}],"termid":"GO:0060266"}


id: PBO:0040741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCR pseudogene 7","termid":"PBO:0040741"}


id: PATO:0000902
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000902 chinsurah boro type value (obsolete PATO:0000902)","termid":"PATO:0000902"}


id: MONDO:0004808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"breast disorder","termid":"MONDO:0002657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign mammary dysplasia","secondary_identifiers":["DOID:9504","MEDGEN:726820","UMLS:C1305934","ICD9:610.9","ICD9:610.8","SCTID:57993004"],"synonyms":[{"name":"benign dysplasia of breast","type":"related"},{"name":"benign mammary dysplasia","type":"exact"}],"termid":"MONDO:0004808","xrefs":{"Monarch":{"xref_id":"0004808"}}}


id: PBO:0045634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 46 (pseudogene)","termid":"PBO:0045634"}


id: GO:0006053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of N-acetylmannosamine, the acetylated derivative of mannosamine, 2-amino-2-deoxymannose.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetylmannosamine metabolic process","termid":"GO:0006051"},{"relation_name":"is_a","term_name":"mannosamine catabolic process","termid":"GO:0046346"}],"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":"N-acetylmannosamine catabolic process","synonyms":[{"name":"N-acetylmannosamine breakdown","type":"exact"},{"name":"N-acetylmannosamine catabolism","type":"exact"},{"name":"N-acetylmannosamine degradation","type":"exact"}],"termid":"GO:0006053"}


id: GO:0061032
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the visceral serous pericardium from its formation to the mature structure. The visceral serous pericardium is the inner layer of the pericardium.","definition_xrefs":["GOC:yaf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"pericardium development","termid":"GO:0060039"}],"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":"visceral serous pericardium development","synonyms":[{"name":"epicardium development","type":"exact"}],"termid":"GO:0061032"}


id: MONDO:0003754
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brown-Sequard syndrome is a rare neurological condition that results from an injury or damage to one side of the spinal cord. This condition results in weakness or paralysis on one side of the body (hemiparaplegia) and a loss of sensation on the opposite side (hemianesthesia). Brown-Sequard syndrome most commonly occurs in the the thoracic spine (upper and middle back). There are several causes of Brown-Sequard syndrome, including: a spinal cord tumor, trauma (such as a puncture wound to the neck or back), infectious or inflammatory diseases (tuberculosis or multiple sclerosis), and disk herniation. Treatment for this condition varies depending on the underlying cause.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"paraplegia","termid":"MONDO:0003757"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Brown-Sequard syndrome","secondary_identifiers":["SCTID:27982003","DOID:606","EFO:1001279","UMLS:C0242644","MEDGEN:69225","ICD10CM:G83.81","NCIT:C84601","MESH:D018437"],"synonyms":[{"name":"Brown-Squard syndrome","type":"exact"},{"name":"Hemicord syndrome","type":"related"},{"name":"Hemiparaplegic syndrome","type":"related"},{"name":"Hemispinal cord syndrome","type":"related"}],"termid":"MONDO:0003754","xrefs":{"Monarch":{"xref_id":"0003754"}}}


id: GO:0008504
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of monoamines, organic compounds that contain one amino group that is connected to an aromatic ring by an ethylene group (-CH2-CH2-), from one side of a membrane to the other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"active transmembrane transporter activity","termid":"GO:0022804"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"monoamine transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-380586","Reactome:R-HSA-380620","Reactome:R-HSA-5660706","Reactome:R-HSA-444160","GO:0015201","Reactome:R-HSA-372542","Reactome:R-HSA-379393"],"termid":"GO:0008504"}


id: GO:1901563
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 camptothecin stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alkaloid","termid":"GO:0043279"},{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"}],"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 camptothecin","synonyms":[{"name":"response to CPT","type":"exact"}],"termid":"GO:1901563"}


id: GO:0045490
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of pectin, a polymer containing a backbone of alpha-1,4-linked D-galacturonic acid residues.","definition_xrefs":["GOC:go_curators","PMID:11931668"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide catabolic process","termid":"GO:0000272"},{"relation_name":"is_a","term_name":"pectin metabolic process","termid":"GO:0045488"}],"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":"pectin catabolic process","synonyms":[{"name":"pectin breakdown","type":"exact"},{"name":"pectin catabolism","type":"exact"},{"name":"pectin degradation","type":"exact"}],"termid":"GO:0045490"}


id: PBO:0043598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type XXVII alpha 1 chain","termid":"PBO:0043598"}


id: MONDO:0030407
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disease with Cushing syndrome as a major feature (obsolete MONDO:0030407)","termid":"MONDO:0030407","xrefs":{"Monarch":{"xref_id":"0030407"}}}


id: GO:0061114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the branches of the pancreas are generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of a branching epithelium","termid":"GO:0061138"},{"relation_name":"part_of","term_name":"pancreas morphogenesis","termid":"GO:0061113"}],"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":"branching involved in pancreas morphogenesis","termid":"GO:0061114"}


id: PBO:0013121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic chromosome segregation protein Dbl2","termid":"PBO:0013121"}


id: GO:0038194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by thyroid-stimulating hormone (thyrotropin) binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:10809230","GOC:gap"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"thyroid-stimulating hormone signaling pathway","synonyms":[{"name":"TSH signaling pathway","type":"exact"},{"name":"thyrotropin signaling pathway","type":"exact"}],"termid":"GO:0038194"}


id: MONDO:0003391
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An alveolar soft part sarcoma arising from the vulva.","definition_xrefs":["NCIT:C40320"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vulva sarcoma","termid":"MONDO:0005214"},{"relation_name":"is_a","term_name":"alveolar soft part sarcoma","termid":"MONDO:0011655"}],"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":"vulvar alveolar soft part sarcoma","secondary_identifiers":["UMLS:C1520069","DOID:5313","MEDGEN:276988"],"termid":"MONDO:0003391","xrefs":{"Monarch":{"xref_id":"0003391"}}}


id: GO:0008556
data:
  {"annotated_genes":["SJAG_04167"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008900"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + K+(out) = ADP + phosphate + K+(in).","definition_xrefs":["RHEA:16777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium ion transmembrane transporter activity","termid":"GO:0015079"},{"relation_name":"is_a","term_name":"P-type ion transporter activity","termid":"GO:0015662"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04167":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"P-type potassium transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0015618","MetaCyc:TRANS-RXN-2","EC:7.2.2.6"],"synonyms":[{"name":"ATP phosphohydrolase (K+-importing)","type":"related"},{"name":"ATP-dependent potassium transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled potassium transmembrane transporter activity","type":"related"},{"name":"K(+)-importing ATPase activity","type":"narrow"},{"name":"K(+)-transporting ATPase activity","type":"related"},{"name":"K+-importing ATPase activity","type":"related"},{"name":"K+-transporting ATPase activity","type":"exact"},{"name":"potassium ABC transporter","type":"narrow"},{"name":"potassium transmembrane transporter activity, phosphorylative mechanism","type":"exact"},{"name":"potassium transporting ATPase activity","type":"exact"},{"name":"potassium-importing ATPase activity","type":"narrow"},{"name":"potassium-transporting ATPase activity","type":"exact"},{"name":"potassium-uptake-ATPase activity","type":"exact"}],"termid":"GO:0008556","terms_by_termid":{"GO:0008900":null}}


id: PBO:0048475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosaminyl (N-acetyl) transferase 1, core 2 pseudogene 2","termid":"PBO:0048475"}


id: FYPO:0009066
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 amorolfine than normal.","definition_xrefs":["PomBase:mlr"],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000003","FYPO:0002682","FYPO:0000139"],"is_obsolete":false,"name":"resistance to amorolfine","synonyms":[{"name":"resistance to amorolfine during mitotic cell cycle","type":"related"},{"name":"resistance to amorolfine during vegetative growth","type":"exact"},{"name":"resistant to amorolfine","type":"exact"}],"termid":"FYPO:0009066"}


id: PBO:0028523
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_acetylation","termid":"PBO:0028523"}


id: PBO:0065588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prothymosin alpha pseudogene 4","termid":"PBO:0065588"}


id: GO:0160202
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structural component of the microsporidian spore's invasion apparatus that is located at the anterior end of the spore and serves to attach the polar tube to the inside of the spore wall.","definition_xrefs":["PMID:16005007","PMID:19673893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"polar tube anchoring disc","termid":"GO:0160202"}


id: PBO:0072797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spalt like transcription factor 4 pseudogene 3","termid":"PBO:0072797"}


id: MONDO:0030537
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"central hypoventilation syndrome, congenital","termid":"MONDO:0800031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central hypoventilation syndrome, congenital, 2, and autonomic dysfunction","secondary_identifiers":["UMLS:C5561963","MEDGEN:1794173","OMIM:619482"],"synonyms":[{"name":"CCHS2","type":"exact"},{"name":"central hypoventilation syndrome, congenital, 2, and autonomic dysfunction","type":"exact"}],"termid":"MONDO:0030537","xrefs":{"Monarch":{"xref_id":"0030537"}}}


id: MONDO:0016191
data:
  {"annotated_genes":["SJAG_00185"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009709"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00185":null},"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of titin","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5680843","GARD:20430","MEDGEN:1843244","Orphanet:209053"],"termid":"MONDO:0016191","terms_by_termid":{"MONDO:0009709":null},"xrefs":{"Monarch":{"xref_id":"0016191"}}}


id: MONDO:0015665
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scleromyxedema is a rare, severe skin disorder. Signs and symptoms include abnormal accumulation of mucin in the skin (mucinosis), causing papular and sclerodermoid bumps; increased production of fibroblasts (connective tissue cells) in the absence of a thyroid disorder; and monoclonal gammopathy (abnormal proteins in the blood). It often involves internal organs and may affect various body systems. The cause of scleromyxedema is not known. There is no standard treatment. Management may involve the use of intravenous immunoglobulin (IVIG), plasmapheresis, thalidomide and corticoids, or more aggressive interventions, such as autologous bone marrow transplantation.","direct_ancestors":[{"relation_name":"is_a","term_name":"lichen myxedematosus","termid":"MONDO:0018432"}],"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":"scleromyxedema","secondary_identifiers":["GARD:7615","MedDRA:10055046","UMLS:C0263390","NCIT:C85061","Orphanet:167635","ICD9:701.8","MESH:D053718","MEDGEN:120476","SCTID:402468007"],"synonyms":[{"name":"Arndt-Gottron disease","type":"exact"},{"name":"Scleromyxedema","type":"exact"},{"name":"generalised lichenoid papular eruption","type":"exact"},{"name":"generalised papular and sclerodermoid","type":"related"},{"name":"generalised papular and sclerodermoid lichen myxedematosus","type":"exact"},{"name":"generalized lichenoid papular eruption","type":"exact"},{"name":"generalized papular and sclerodermoid","type":"related"},{"name":"generalized papular and sclerodermoid lichen myxedematosus","type":"exact"},{"name":"lichen myxedematosus","type":"related"},{"name":"mucinosis, papular","type":"related"},{"name":"myxedematosus, lichen","type":"related"},{"name":"papular mucinosis","type":"related"},{"name":"scleromyxoedema","type":"exact"}],"termid":"MONDO:0015665","xrefs":{"Monarch":{"xref_id":"0015665"}}}


id: GO:1905326
data:
  {"annotated_genes":["SJAG_04259"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113589],"is_not":false,"summary":null,"term":"GO:1905326"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the meiosis I spindle assembly checkpoint.","definition_xrefs":["GO_REF:0000058","PMID:26483559","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"is_a","term_name":"positive regulation of spindle checkpoint","termid":"GO:0090232"},{"relation_name":"is_a","term_name":"regulation of meiosis I spindle assembly checkpoint","termid":"GO:1905325"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"meiosis I spindle assembly checkpoint signaling","termid":"GO:1905318"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0140013"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0140013","GO:0023052"],"is_obsolete":false,"name":"positive regulation of meiosis I spindle assembly checkpoint","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of meiosis I spindle assembly checkpoint","type":"narrow"},{"name":"up regulation of meiosis I spindle assembly checkpoint","type":"exact"},{"name":"up-regulation of meiosis I spindle assembly checkpoint","type":"exact"},{"name":"upregulation of meiosis I spindle assembly checkpoint","type":"exact"}],"termid":"GO:1905326","terms_by_termid":{"GO:1905326":null}}


id: PBO:0058535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6080","termid":"PBO:0058535"}


id: PBO:0063140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAS domain containing serine/threonine kinase","termid":"PBO:0063140"}


id: MONDO:1010589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial goiter that occurs in goat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial goiter, non-human animal","termid":"MONDO:1010053"},{"relation_name":"is_a","term_name":"congenital hypothyroidism, goat","termid":"MONDO:1010605"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial goiter, goat","secondary_identifiers":["OMIA:000424-9925"],"termid":"MONDO:1010589","xrefs":{"Monarch":{"xref_id":"1010589"}}}


id: GO:1901899
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of relaxation of cardiac muscle.","definition_xrefs":["GOC:rl","GOC:TermGenie","PMID:19708671","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of relaxation of muscle","termid":"GO:1901079"},{"relation_name":"is_a","term_name":"regulation of relaxation of cardiac muscle","termid":"GO:1901897"},{"relation_name":"positively_regulates","term_name":"relaxation of cardiac muscle","termid":"GO:0055119"}],"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 relaxation of cardiac muscle","synonyms":[{"name":"activation of relaxation of cardiac muscle","type":"narrow"},{"name":"up regulation of relaxation of cardiac muscle","type":"exact"},{"name":"up-regulation of relaxation of cardiac muscle","type":"exact"},{"name":"upregulation of relaxation of cardiac muscle","type":"exact"}],"termid":"GO:1901899"}


id: PBO:0017584
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae RTS1","termid":"PBO:0017584"}


id: PBO:0063316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphorylated CTD interacting factor 1","termid":"PBO:0063316"}


id: MONDO:0003075
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinoblastoma involving both eyes. This occurs in the majority of patients with the inherited variant. A minority of patient with bilateral retinoblastoma were found to have involvement of the pineal gland as well.","definition_xrefs":["NCIT:C8713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinoblastoma","termid":"MONDO:0008380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"bilateral retinoblastoma","secondary_identifiers":["DOID:4650","MEDGEN:163163","NANDO:2201038","UMLS:C0854914"],"termid":"MONDO:0003075","xrefs":{"Monarch":{"xref_id":"0003075"}}}


id: GO:0070636
data:
  {"annotated_genes":["SJAG_00957"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90411],"is_not":false,"summary":null,"term":"GO:0070636"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: nicotinic acid riboside + H2O = nicotinic acid + D-ribose.","definition_xrefs":["GOC:mah","PMID:19001417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing N-glycosyl compounds","termid":"GO:0016799"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00957":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"nicotinic acid riboside hydrolase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"D-ribosylnicotinate hydrolase activity","type":"exact"},{"name":"D-ribosylnicotinic acid hydrolase activity","type":"exact"},{"name":"nicotinate ribonucleoside hydrolase activity","type":"exact"},{"name":"nicotinate riboside hydrolase activity","type":"exact"},{"name":"nicotinic acid ribonucleoside hydrolase activity","type":"exact"}],"termid":"GO:0070636","terms_by_termid":{"GO:0070636":null}}


id: PBO:0113353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for pheromone-induced projection (shmoo) formation; regulates septin architecture during mating; has an RVXF motif that mediates targeting of Glc7p to mating projections; also detected in peroxisomes; interacts with Cdc12p; AFR1 has a paralog, YER158C, that arose from the whole genome duplication","termid":"PBO:0113353"}


id: FYPO:0006582
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of bis(5'-nucleosyl)-tetraphosphatase (asymmetrical) activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal bis(5'-nucleosyl)-tetraphosphatase (asymmetrical) activity","termid":"FYPO:0004644"}],"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:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000652","FYPO:0000707","FYPO:0000661","FYPO:0001985"],"is_obsolete":false,"name":"decreased bis(5'-nucleosyl)-tetraphosphatase (asymmetrical) activity","synonyms":[{"name":"reduced bis(5'-nucleosyl)-tetraphosphatase (asymmetrical) activity","type":"exact"}],"termid":"FYPO:0006582"}


id: PBO:0001499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome regulatory particle, gankyrin (predicted)","termid":"PBO:0001499"}


id: MONDO:0013162
data:
  {"annotated_genes":["SJAG_04053","SJAG_04316"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86420,86421],"is_not":false,"summary":null,"term":"MONDO:0013162"}]},"cv_name":"mondo","definition":"Autosomal recessive limb-girdle muscular dystrophy type 2N (LGMD2N) is a form of limb-girdle muscular dystrophy characterized by proximal weakness (manifesting as slowness in running) presenting in infancy, along with calf hypertrophy, mild lordosis, scapular winging and normal intelligence or mild intellectual disability.","definition_xrefs":["Orphanet:206559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type C","termid":"MONDO:0000173"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of protein O-mannosyltransferase 2","termid":"MONDO:0016185"},{"relation_name":"is_a","term_name":"myopathy caused by variation in POMT2","termid":"MONDO:0700071"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04053":null,"SJAG_04316":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005336","MONDO:0006025","MONDO:0005066","MONDO:0002320"],"is_obsolete":false,"name":"autosomal recessive limb-girdle muscular dystrophy type 2N","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:461768","OMIM:613158","DOID:0110298","UMLS:C3150418","GARD:12539"],"synonyms":[{"name":"LGMD-POMT2 related","type":"exact"},{"name":"LGMD2N","type":"exact"},{"name":"MDDGC2","type":"exact"},{"name":"POMT2 autosomal recessive limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT2","type":"exact"},{"name":"limb-girdle muscular dystrophy type 2N","type":"related"},{"name":"muscular dystrophy, limb-girdle, type 2N","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-related","type":"related"}],"termid":"MONDO:0013162","terms_by_termid":{"MONDO:0013162":null},"xrefs":{"Monarch":{"xref_id":"0013162"}}}


id: MONDO:0024521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial abdominal aortic aneurysm","termid":"MONDO:0007031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic aneurysm, familial abdominal, 1","secondary_identifiers":["GARD:16491","MEDGEN:339961","OMIM:100070","UMLS:C1853365"],"synonyms":[{"name":"AAA1","type":"exact"},{"name":"abdominal aortic aneurysm","type":"related"},{"name":"aneurysm, abdominal aortic","type":"related"},{"name":"aortic aneurysm, familial abdominal 1","type":"exact"},{"name":"aortic aneurysm, familial abdominal, 1","type":"exact"}],"termid":"MONDO:0024521","xrefs":{"Monarch":{"xref_id":"0024521"}}}


id: PR:P21537
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atp9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P21537"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase subunit 9, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPMIT.10","synonyms":[{"name":"Spom972h-atp9","type":"exact"},{"name":"lipid-binding protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P21537"}


id: GO:1901796
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of signal transduction by p53 class mediator.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"signal transduction by p53 class mediator","termid":"GO:0072331"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of signal transduction by p53 class mediator","secondary_identifiers":["Reactome:R-HSA-5633007"],"termid":"GO:1901796"}


id: PBO:0073074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndecan binding protein pseudogene 3","termid":"PBO:0073074"}


id: MONDO:0005008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most common type of colorectal carcinoma. It is characterized by the presence of malignant glandular epithelial cells invading through the muscularis mucosa into the submucosa. Histologic variants include mucinous adenocarcinoma, signet ring cell carcinoma, medullary carcinoma, serrated adenocarcinoma, cribriform comedo-type adenocarcinoma, and micropapillary adenocarcinoma.","definition_xrefs":["NCIT:C5105"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"colorectal carcinoma","termid":"MONDO:0024331"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"colorectal adenocarcinoma","secondary_identifiers":["DOID:0050861","EFO:0000365","MEDGEN:230816","SCTID:408645001","UMLS:C1319315","ONCOTREE:COADREAD","DOID:0050913","SCTID:269533000"],"synonyms":[{"name":"adenocarcinoma of large bowel","type":"exact"},{"name":"adenocarcinoma of large intestine","type":"exact"},{"name":"adenocarcinoma of the large bowel","type":"exact"},{"name":"adenocarcinoma of the large intestine","type":"exact"},{"name":"colorectal (colon or rectal) adenocarcinoma","type":"exact"},{"name":"colorectal adenocarcinoma","type":"exact"},{"name":"colorectum adenocarcinoma","type":"exact"},{"name":"large bowel adenocarcinoma","type":"exact"},{"name":"large intestine adenocarcinoma","type":"exact"}],"termid":"MONDO:0005008","xrefs":{"Monarch":{"xref_id":"0005008"}}}


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: PBO:0088822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase S6K family Psk1","termid":"PBO:0088822"}


id: PBO:0047126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 169 member A","termid":"PBO:0047126"}


id: FYPO:0007795
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is arrested in G1 phase after the cells have undergone two rounds of cell division under nutrient-replete conditions. This arrest resembles that of wild-type cells under conditions of nitrogen starvation.","definition_xrefs":["PMID:28476936","PMID:17121544","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell cycle arrest in mitotic G1 phase","termid":"FYPO:0005097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"two cell divisions prior to cell cycle arrest in mitotic G1 phase without nutrient starvation","synonyms":[{"name":"two cell divisions prior to mitotic G1 arrest without nutrient starvation","type":"exact"},{"name":"two cell divisions prior to mitotic cell cycle arrest in G1 phase without nutrient starvation","type":"exact"}],"termid":"FYPO:0007795"}


id: PBO:0051591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IL20RB antisense RNA 1","termid":"PBO:0051591"}


id: MONDO:0100111
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Mendelian diseases characterized by global developmental delay and renal dysfunction manifest as proteinuria and nephrotic syndrome apparent from infancy or early childhood. Some patients present with renal disease, whereas others present with developmental delay and develop renal disease later in childhood. Renal biopsy shows focal segmental glomerulosclerosis (FSGS), but the course of the disease is variable: some patients have transient proteinuria and others require renal transplant. Neurodevelopmental features are also variable, with some patients having only mildly impaired intellectual development, and others having a severe developmental disorder associated with early-onset refractory seizures or epileptic encephalopathy. Additional features, including feeding difficulties, poor overall growth, and nonspecific dysmorphic facial features, are commonly observed.","definition_xrefs":["OMIM:619428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"focal segmental glomerulosclerosis and neurodevelopmental syndrome","secondary_identifiers":["UMLS:C5561938","MEDGEN:1794148"],"synonyms":[{"name":"FSGSNEDS","type":"exact"}],"termid":"MONDO:0100111","xrefs":{"Monarch":{"xref_id":"0100111"}}}


id: PATO:0001357
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A convex 3-D shape quality inhering in a bearer by virtue of the bearer's being shaped like a cushion or has a marked convex cushion-like form.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"convex 3-D shape","termid":"PATO:0002007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulvinate","termid":"PATO:0001357"}


id: PBO:0057456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 575","termid":"PBO:0057456"}


id: PBO:0002059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane alkali metal cation/H+ antiporter Sod22","termid":"PBO:0002059"}


id: GO:0102272
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: glutathionate + a poly gamma-glutamylcysteine-beta-alanine = glycine + a poly gamma-glutamylcysteine-beta-alanine.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete homophytochelatin synthase activity (polymer-forming) (obsolete GO:0102272)","termid":"GO:0102272"}


id: GO:1904356
data:
  {"annotated_genes":["SJAG_02194"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032210"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of telomere maintenance via telomere lengthening.","definition_xrefs":["GO_REF:0000058","GOC:nc","PMID:23959892","GOC:BHF_telomere","GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of telomere maintenance","termid":"GO:0032204"},{"relation_name":"regulates","term_name":"telomere maintenance via telomere lengthening","termid":"GO:0010833"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02194":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0032200"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0032200","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"regulation of telomere maintenance via telomere lengthening","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:1904356","terms_by_termid":{"GO:0032210":null}}


id: GO:0033119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of RNA splicing.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of gene expression","termid":"GO:0010629"},{"relation_name":"is_a","term_name":"regulation of RNA splicing","termid":"GO:0043484"},{"relation_name":"negatively_regulates","term_name":"RNA splicing","termid":"GO:0008380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of RNA splicing","termid":"GO:0033119"}


id: MONDO:0012251
data:
  {"annotated_genes":["SJAG_00379"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84945],"is_not":false,"summary":null,"term":"MONDO:0012251"}]},"cv_name":"mondo","definition":"MEDNIK syndrome, previously known as Erythrokeratodermia Variabilis type 3 (EKV3), is characterized by intellectual deficit, enteropathy, sensorineural hearing loss, peripheral neuropathy, lamellar and erythrodermic ichthyosis, and keratodermia (MEDNIK stands for Mental retardation, Enteropathy, Deafness, peripheral Neuropathy, Ichtyosis, Keratodermia).","definition_xrefs":["Orphanet:171851"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"disorder of copper metabolism","termid":"MONDO:0017762"},{"relation_name":"is_a","term_name":"erythrokeratoderma","termid":"MONDO:0019270"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00379":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"MEDNIK syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:609313","DOID:0060483","GARD:17072","SCTID:722035007","MEDGEN:322893","UMLS:C1836330","MESH:C563739"],"synonyms":[{"name":"MEDNIK","type":"related"},{"name":"erythrokeratodermia variabilis 3","type":"exact"},{"name":"erythrokeratodermia variabilis, Kamouraska type","type":"exact"},{"name":"intellectual disability, enteropathy, deafness, neuropathy, ichthyosis, keratodermia","type":"exact"},{"name":"intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma","type":"related"},{"name":"intellectual disability-enteropathy-deafness-peripheral neuropathy-ichthyosis-keratodermia syndrome","type":"exact"},{"name":"mental retardation, enteropathy, deafness, neuropathy, ichthyosis, keratodermia","type":"exact"},{"name":"mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma","type":"related"}],"termid":"MONDO:0012251","terms_by_termid":{"MONDO:0012251":null},"xrefs":{"Monarch":{"xref_id":"0012251"}}}


id: GO:1905144
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 acetylcholine stimulus.","definition_xrefs":["PMID:21238497","GO_REF:0000071","GOC:TermGenie"],"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 acetylcholine","termid":"GO:1905144"}


id: PBO:0072013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S7 pseudogene 15","termid":"PBO:0072013"}


id: SO:1000078
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variation that decreases the rate a which transcription of the sequence occurs.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000078 sequence_variant_decreasing_rate_of_transcription (obsolete SO:1000078)","synonyms":[{"name":"mutation decreasing rate of transcription","type":"related"},{"name":"sequence variation decreasing rate of transcription","type":"exact"}],"termid":"SO:1000078"}


id: GO:0003830
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + beta-D-mannosyl-R = UDP + 4-(N-acetyl-beta-D-glucosaminyl)-beta-D-mannosyl-R.","definition_xrefs":["EC:2.4.1.144"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a glycoprotein","termid":"GO:0140103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016757","GO:0140096","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"beta-1,4-mannosylglycoprotein 4-beta-N-acetylglucosaminyltransferase activity","secondary_identifiers":["Reactome:R-HSA-975926","MetaCyc:2.4.1.144-RXN","RHEA:15509"],"synonyms":[{"name":"GnTIII activity","type":"related"},{"name":"N-acetylglucosaminyltransferase III activity","type":"related"},{"name":"N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase III activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine:beta-D-mannosyl-glycoprotein 4-beta-N-acetyl-D-glucosaminyltransferase activity","type":"related"},{"name":"beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase activity","type":"related"},{"name":"beta-1,4-mannosyl-glycoprotein beta-1,4-N-acetylglucosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-glycopeptide beta-4-acetylglucosaminyltransferase III activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-glycopeptide beta4-acetylglucosaminyltransferase III","type":"related"}],"termid":"GO:0003830"}


id: GO:0006128
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidized glutathione reduction (obsolete GO:0006128)","synonyms":[{"name":"oxidized glutathione reduction","type":"exact"}],"termid":"GO:0006128"}


id: PBO:0050791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxytryptamine receptor 3D","termid":"PBO:0050791"}


id: PBO:0065739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal membrane protein 4","termid":"PBO:0065739"}


id: PR:O94396
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pus1 gene.","definition_xrefs":["UniProtKB:O94396","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":"tRNA pseudouridine synthase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC126.03","synonyms":[{"name":"Spom972h-pus1","type":"exact"},{"name":"tRNA pseudouridylate synthase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tRNA-uridine isomerase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94396"}


id: PBO:0059533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded tRNA-Glu (GAA/G)","termid":"PBO:0059533"}


id: MONDO:0000332
data:
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id: GO:0006839
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id: PBO:0070326
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id: GO:1902614
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id: PBO:0050746
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id: PBO:0082383
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id: FYPO:0001526
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id: PBO:0080022
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id: PBO:0047421
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id: GO:2000958
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id: MONDO:0007466
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id: PBO:0087863
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id: GO:1903078
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