# terms

id: PBO:0087744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SWI/SNF chromatin remodeling complex; regulates transcription by remodeling chromatin; required for transcription of many genes, including ADH1, ADH2, GAL1, HO, INO1 and SUC2; self-assembles to form [SWI+] prion and to alter expression pattern; human homolog ARID1A is a candidate tumor suppressor gene in breast cancer","termid":"PBO:0087744"}


id: MONDO:0000562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypomyelinating leukoencephalopathy (obsolete MONDO:0000562)","termid":"MONDO:0000562","xrefs":{"Monarch":{"xref_id":"0000562"}}}


id: PBO:0056053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LUC7 like 3 pre-mRNA splicing factor","termid":"PBO:0056053"}


id: GO:1903242
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac muscle hypertrophy in response to stress.","definition_xrefs":["GOC:BHF","GOC:TermGenie","PMID:19287093","GOC:rl","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac muscle hypertrophy","termid":"GO:0010611"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle adaptation","termid":"GO:0010612"},{"relation_name":"is_a","term_name":"regulation of response to stress","termid":"GO:0080134"},{"relation_name":"regulates","term_name":"cardiac muscle hypertrophy in response to stress","termid":"GO:0014898"}],"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 cardiac muscle hypertrophy in response to stress","termid":"GO:1903242"}


id: PBO:0005154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L17 (predicted)","termid":"PBO:0005154"}


id: PR:P87232
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrpl4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"54S ribosomal protein L4, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4G3.06c","synonyms":[{"name":"Spom972h-mrpl4","type":"exact"}],"termid":"PR:P87232"}


id: SO:0001597
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A secondary structure variant that compensate for the change made by a previous variant.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_secondary_structure_variant","termid":"SO:0001596"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"compensatory_transcript_secondary_structure_variant","synonyms":[{"name":"compensatory transcript secondary structure variant","type":"exact"}],"termid":"SO:0001597"}


id: PBO:0013469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosyltransferase Alg6","termid":"PBO:0013469"}


id: GO:0070554
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains synaptobrevin 2 (VAMP2), SNAP-25, syntaxin 3, and a complexin (or orthologs thereof).","definition_xrefs":["PMID:8824312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNARE complex","termid":"GO:0031201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"synaptobrevin 2-SNAP-25-syntaxin-3-complexin complex","synonyms":[{"name":"SNARE complex (Stx3, Snap25, Vamp2, Cplx1)","type":"narrow"},{"name":"Stx3-Snap25-Vamp2-Cplx1 complex","type":"narrow"}],"termid":"GO:0070554"}


id: PBO:0078148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 26-2","termid":"PBO:0078148"}


id: RO:0002436
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"An interaction relationship in which the two partners are molecular entities that directly physically interact with each other for example via a stable binding interaction or a brief interaction during which one modifies the other.","direct_ancestors":[{"relation_name":"is_a","term_name":"interacts_with","termid":"RO:0002434"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"molecularly_interacts_with","termid":"RO:0002436"}


id: MONDO:0004574
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Deficiency of vitamin B6. It is usually caused by alcoholism, malabsorption, or as a side effect of medications. Signs and symptoms include stomatitis, glossitis, dermatitis, peripheral neuropathy, irritability, seizures, and anemia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin B deficiency","termid":"MONDO:0042976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridoxine deficiency anemia","secondary_identifiers":["UMLS:C0272013","MESH:D026681","ICD9:281.8","MEDGEN:543733","SCTID:86448001","ICD9:266.1","NCIT:C85221","DOID:8455"],"synonyms":[{"name":"B6 deficiencies, vitamin","type":"related"},{"name":"B6 deficiency, vitamin","type":"related"},{"name":"B6 vitamin deficiencies","type":"related"},{"name":"B6 vitamin deficiency","type":"related"},{"name":"deficiencies, B6 vitamin","type":"related"},{"name":"deficiencies, vitamin B6","type":"related"},{"name":"deficiency, B6 vitamin","type":"related"},{"name":"deficiency, pyridoxine","type":"related"},{"name":"deficiency, vitamin B 6","type":"related"},{"name":"deficiency, vitamin B6","type":"related"},{"name":"pyridoxine Deficincy","type":"exact"},{"name":"pyridoxine deficiency","type":"related"},{"name":"vitamin B6 deficiencies","type":"related"},{"name":"vitamin B6 deficiency","type":"related"},{"name":"vitamin B6 deficiency syndrome","type":"exact"},{"name":"vitamin deficiencies, B6","type":"related"},{"name":"vitamin deficiency, B6","type":"related"}],"termid":"MONDO:0004574","xrefs":{"Monarch":{"xref_id":"0004574"}}}


id: GO:0015264
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the energy-independent facilitated diffusion of methylammonium through a transmembrane aqueous pore or channel. Methylammonium is CH3NH2.","definition_xrefs":["GOC:pr","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylammonium transmembrane transporter activity","termid":"GO:0015200"},{"relation_name":"is_a","term_name":"channel activity","termid":"GO:0015267"}],"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:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"methylammonium channel activity","termid":"GO:0015264"}


id: PBO:0039223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AKR7A2P pseudogene 1","termid":"PBO:0039223"}


id: PBO:0116753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF related BAF chromatin remodeling complex subunit D3","termid":"PBO:0116753"}


id: FYPO:0002629
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of galactose measured in the cell wall is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance absent from cell during vegetative growth","termid":"FYPO:0001208"},{"relation_name":"is_a","term_name":"decreased level of substance in cell wall during vegetative growth","termid":"FYPO:0002628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"galactose absent from cell wall","synonyms":[{"name":"galactose absent from cell surface","type":"related"},{"name":"galactose absent from cell wall during mitotic cell cycle","type":"related"},{"name":"galactose absent from cell wall during vegetative growth","type":"exact"}],"termid":"FYPO:0002629"}


id: GO:0036044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a protein amino acid by the addition of a malonyl (CO-CH2-CO) group.","definition_xrefs":["GOC:sp"],"gene_count":0,"genotype_count":0,"name":"obsolete protein malonylation (obsolete GO:0036044)","synonyms":[{"name":"protein malonylation","type":"exact"}],"termid":"GO:0036044"}


id: PBO:0067930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 232","termid":"PBO:0067930"}


id: GO:0050559
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: all-trans-geranylgeranyl diphosphate = (+)-copalyl diphosphate.","definition_xrefs":["EC:5.5.1.12","RHEA:24316"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular lyase activity","termid":"GO:0016872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"copalyl diphosphate synthase activity","secondary_identifiers":["KEGG_REACTION:R06298","MetaCyc:RXN-4861"],"synonyms":[{"name":"(+)-copalyl-diphosphate lyase (decyclizing)","type":"related"},{"name":"diterpene cyclase activity","type":"broad"}],"termid":"GO:0050559"}


id: CHEBI:18019
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"An L-alpha-amino acid; the L-isomer of lysine.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-lysine","termid":"CHEBI:18019"}


id: FYPO:0002828
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype in which the basal activity of a protein kinase is increased relative to normal. Basal protein kinase activity is the activity observed in the absence of a regulator. Abnormally elevated basal activity may or may not reach the levels observed in the normal activated state.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutive catalytic activity","termid":"FYPO:0000683"}],"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":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000652","FYPO:0000654","FYPO:0001985"],"is_obsolete":false,"name":"constitutive protein kinase activity","synonyms":[{"name":"constitutive protein kinase activity during mitotic cell cycle","type":"related"},{"name":"constitutive protein kinase activity during vegetative growth","type":"exact"},{"name":"constitutively active protein kinase","type":"related"}],"termid":"FYPO:0002828"}


id: PATO:0002077
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being positioned with multiple entities of the same type above and below.","definition_xrefs":["PATOC:CJM"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stacked","termid":"PATO:0002077"}


id: PBO:0078366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 10-1","termid":"PBO:0078366"}


id: PBO:0017809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitamin H transmembrane transporter Vht1","termid":"PBO:0017809"}


id: GO:0099621
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-4-deoxy-4-formamido-beta-L-arabinopyranose + ditrans,octacis-undecaprenyl phosphate = UDP + 4-deoxy-4-formamido-alpha-L-arabinopyranosyl ditrans,octacis-undecaprenyl phosphate.","definition_xrefs":["GOC:al","GOC:dos","PMID:11706007","PMID:15695810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016757","GO:0003824"],"is_obsolete":false,"name":"undecaprenyl-phosphate 4-deoxy-4-formamido-L-arabinose transferase activity","secondary_identifiers":["RHEA:27722","GO:0103019","EC:2.4.2.53","MetaCyc:RXN0-3521"],"synonyms":[{"name":"Ara4FN transferase activity","type":"exact"},{"name":"undecaprenyl phosphate-L-Ara4FN transferase activity","type":"exact"},{"name":"undecaprenyl-phosphate Ara4FN transferase activity","type":"exact"}],"termid":"GO:0099621"}


id: MONDO:0011238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant chondrodysplasia punctata","termid":"MONDO:0007321"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"chondrodysplasia punctata, brachytelephalangic, autosomal","secondary_identifiers":["OMIM:602497","UMLS:C1844853","MEDGEN:337102","GARD:15347"],"synonyms":[{"name":"brachytelephalangic chondrodysplasia punctata","type":"related"},{"name":"chondrodysplasia punctata, brachytelephalangic, autosomal","type":"exact"}],"termid":"MONDO:0011238","xrefs":{"Monarch":{"xref_id":"0011238"}}}


id: MONDO:0020837
data:
  {"annotated_genes":["SJAG_04280","SJAG_03854"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87941,87942],"is_not":false,"summary":null,"term":"MONDO:0020837"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited oocyte maturation defect","termid":"MONDO:0014769"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03854":null,"SJAG_04280":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"oocyte maturation defect 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617996","MEDGEN:1644330","UMLS:C4693865"],"synonyms":[{"name":"OOMD5","type":"exact"},{"name":"oocyte maturation defect 5","type":"exact"}],"termid":"MONDO:0020837","terms_by_termid":{"MONDO:0020837":null},"xrefs":{"Monarch":{"xref_id":"0020837"}}}


id: GO:0043027
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of a cysteine-type endopeptidase involved in the apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","PMID:14744432","Wikipedia:Caspase","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteine-type endopeptidase regulator activity involved in apoptotic process","termid":"GO:0043028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"cysteine-type endopeptidase inhibitor activity involved in apoptotic process","synonyms":[{"name":"caspase inhibitor activity","type":"broad"}],"termid":"GO:0043027"}


id: PBO:0083981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutamate decarboxylase; converts glutamate into gamma-aminobutyric acid (GABA) during glutamate catabolism; involved in response to oxidative stress","termid":"PBO:0083981"}


id: FYPO:0001483
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of alpha,alpha-trehalase activity increases normally (i.e. as in wild type) as a result of oxidative stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal alpha,alpha-trehalase activity","termid":"FYPO:0001480"},{"relation_name":"is_a","term_name":"normal cellular response to oxidative stress","termid":"FYPO:0001485"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000298","FYPO:0000002","FYPO:0000652","FYPO:0001312","FYPO:0000654"],"is_obsolete":false,"name":"normal alpha,alpha-trehalase activity increase during cellular response to oxidative stress","synonyms":[{"name":"normal alpha,alpha-trehalase activity increase during oxidative stress response","type":"exact"},{"name":"normal increase in trehalase activity in response to oxidative stress","type":"exact"},{"name":"normal neutral trehalase activity increase during cellular response to oxidative stress","type":"exact"},{"name":"normal trehalase activity increase during cellular response to oxidative stress","type":"broad"}],"termid":"FYPO:0001483"}


id: PBO:0001546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA primase catalytic subunit Spp1","termid":"PBO:0001546"}


id: GO:1905675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of adaptive immune memory response.","definition_xrefs":["GO_REF:0000058","PMID:26831526","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of adaptive immune response","termid":"GO:0002820"},{"relation_name":"is_a","term_name":"regulation of adaptive immune memory response","termid":"GO:1905674"},{"relation_name":"negatively_regulates","term_name":"adaptive immune memory response","termid":"GO:0090716"}],"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 adaptive immune memory response","synonyms":[{"name":"down regulation of adaptive immune memory response","type":"exact"},{"name":"down-regulation of adaptive immune memory response","type":"exact"},{"name":"downregulation of adaptive immune memory response","type":"exact"},{"name":"inhibition of adaptive immune memory response","type":"narrow"}],"termid":"GO:1905675"}


id: PBO:0069318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 576, pseudogene","termid":"PBO:0069318"}


id: FYPO:0004586
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to a combination of caffeine and hydroxyurea. Cells stop growing (and may die) at concentrations of caffeine and hydroxyurea that allow wild type cells to grow.","definition_xrefs":["PMID:10757807","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002683","FYPO:0000003","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to caffeine and hydroxyurea","synonyms":[{"name":"hypersensitive to caffeine and hydroxyurea","type":"exact"},{"name":"sensitive to caffeine and HU","type":"exact"},{"name":"sensitive to caffeine and hydroxyurea during mitotic cell cycle","type":"related"},{"name":"sensitive to caffeine and hydroxyurea during vegetative growth","type":"exact"},{"name":"sensitive to caffeine and hydroxyurea in combination","type":"exact"}],"termid":"FYPO:0004586"}


id: PBO:0066664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RHO family interacting cell polarization regulator 1","termid":"PBO:0066664"}


id: PBO:0000921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase, TRAMP complex subunit Mtr4","termid":"PBO:0000921"}


id: GO:1990676
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding any of the thin, flattened compartments that form the trans portion of the Golgi complex.","definition_xrefs":["PMID:16038056","PMID:24119662","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi cisterna membrane","termid":"GO:0032580"},{"relation_name":"part_of","term_name":"Golgi trans cisterna","termid":"GO:0000138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005794","GO:0005575"],"is_obsolete":false,"name":"Golgi trans cisterna membrane","synonyms":[{"name":"trans-Golgi cisterna membrane","type":"exact"}],"termid":"GO:1990676"}


id: MONDO:0019248
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of inherited lysosomal storage diseases characterized by accumulation of lipids and carbohydrates in the tissues, resulting in mental disabilities and skeletal malformations.","definition_xrefs":["NCIT:C61267"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"glycoproteinosis","termid":"MONDO:0017731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0005066"],"is_obsolete":false,"name":"mucolipidosis","secondary_identifiers":["MEDGEN:7731","GARD:18975","UMLS:C0026697","Orphanet:79212","MESH:D009081","DOID:0080488","SCTID:70528007","icd11.foundation:714623911"],"termid":"MONDO:0019248","xrefs":{"Monarch":{"xref_id":"0019248"}}}


id: MONDO:0018626
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition resembling typhoid fever that is caused by infection by Salmonella enterica serovar Parathyphi.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salmonellosis","termid":"MONDO:0000827"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paratyphoid fever","secondary_identifiers":["icd11.foundation:1780040028","EFO:0007420","ICD9:002.1","MEDGEN:18303","GARD:21855","ICD9:002.2","ICD9:002.3","NCIT:C34897","SCTID:51254007","UMLS:C0030528","Orphanet:443227","ICD9:002.9","DOID:3055","MESH:D010284"],"synonyms":[{"name":"paratyphoid","type":"related"},{"name":"paratyphoid A fever","type":"related"},{"name":"paratyphoid B fever","type":"related"},{"name":"paratyphoid C fever","type":"related"},{"name":"paratyphoid a","type":"related"},{"name":"paratyphoid b","type":"related"},{"name":"paratyphoid c","type":"related"},{"name":"paratyphoid fever A","type":"related"},{"name":"paratyphoid fever B","type":"related"},{"name":"paratyphoid fever C","type":"related"}],"termid":"MONDO:0018626","xrefs":{"Monarch":{"xref_id":"0018626"}}}


id: PBO:0030591
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_vacuolar_lysine_level","termid":"PBO:0030591"}


id: PBO:0044972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DExH-box helicase 9","termid":"PBO:0044972"}


id: PR:Q9Y7S0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC569.01c gene.","definition_xrefs":["UniProtKB:Q9Y7S0","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":"UPF0612 protein C569.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC569.01c","synonyms":[{"name":"Spom972h-SPCC569.01c","type":"exact"}],"termid":"PR:Q9Y7S0"}


id: GO:0044734
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism initiates, promotes, or enhances the activity of a pH-gated (also known as acid-sensing ion channel (ASIC)) in another organism via the action of a venom.","definition_xrefs":["GOC:fj","GOC:jl","PMID:23034652"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of pH-gated ion channel activity","termid":"GO:0044733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated activation of pH-gated ion channel activity","synonyms":[{"name":"envenomation resulting in positive regulation of ASIC channel activity in other organism","type":"exact"},{"name":"envenomation resulting in positive regulation of acid-sensing ion channel activity in another organism","type":"exact"},{"name":"envenomation resulting in positive regulation of acid-sensing ion channel activity in other organism","type":"exact"},{"name":"venom-mediated activation of acid-sensing ion channel activity","type":"related"}],"termid":"GO:0044734"}


id: MONDO:0054761
data:
  {"annotated_genes":["SJAG_00773"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87905],"is_not":false,"summary":null,"term":"MONDO:0054761"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive primary microcephaly","termid":"MONDO:0016660"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00773":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0700092"],"is_obsolete":false,"name":"microcephaly 20, primary, autosomal recessive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0051031","MEDGEN:1641618","GARD:16268","OMIM:617914","UMLS:C4693572"],"synonyms":[{"name":"MCPH20","type":"related"},{"name":"microcephaly 20, PRIMARY, autosomal recessive","type":"related"}],"termid":"MONDO:0054761","terms_by_termid":{"MONDO:0054761":null},"xrefs":{"Monarch":{"xref_id":"0054761"}}}


id: PBO:0083522
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 PEX14/YGL153W","termid":"PBO:0083522"}


id: PBO:0061898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opsin 4","termid":"PBO:0061898"}


id: GO:0047336
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2'-deoxy-5-methyl-5'-cytidylate + ATP = 5-methyldeoxycytidine diphosphate + ADP + H+.","definition_xrefs":["EC:2.7.4.19","RHEA:11396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016301","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"5-methyldeoxycytidine-5'-phosphate kinase activity","secondary_identifiers":["KEGG_REACTION:R04235","MetaCyc:2.7.4.19-RXN"],"synonyms":[{"name":"ATP:5-methyldeoxycytidine-5'-phosphate phosphotransferase activity","type":"related"}],"termid":"GO:0047336"}


id: GO:0001308
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process, which occurs as a dividing cell ages, leading to expression of genes that are typically not expressed due to silencing by regulatory proteins.","definition_xrefs":["PMID:12044934","GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of chromatin silencing involved in replicative cell aging (obsolete GO:0001308)","synonyms":[{"name":"loss of chromatin silencing during replicative cell ageing","type":"related"},{"name":"loss of chromatin silencing involved in replicative cell aging","type":"exact"}],"termid":"GO:0001308"}


id: MONDO:0975847
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune disease with susceptibility to mycobacterium tuberculosis","secondary_identifiers":["OMIM:621004"],"termid":"MONDO:0975847","xrefs":{"Monarch":{"xref_id":"0975847"}}}


id: PBO:0029188
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-enlarged_exocytic_vesicles_present_in_increased_numbers","termid":"PBO:0029188"}


id: PBO:0073146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC23 interacting protein","termid":"PBO:0073146"}


id: GO:0034080
data:
  {"annotated_genes":["SJAG_04038","SJAG_00045","SJAG_04581","SJAG_02872","SJAG_00307","SJAG_03905","SJAG_04989","SJAG_02908","SJAG_02303","SJAG_00873","SJAG_03867","SJAG_00756","SJAG_02119","SJAG_05273","SJAG_01611","SJAG_04696","SJAG_03619","SJAG_04547","SJAG_00684","SJAG_03183"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73247,81710,90817,92007,94739,96646,97422,101088,101339,104022,104861,108331,109317,115108,116220,117078,118465,119700,120836,120872],"is_not":false,"summary":null,"term":"GO:0034080"}]},"cv_name":"biological_process","definition":"The formation of chromatin containing the histone H3 variant CENP-A to form centromeric chromatin. This specialised chromatin occurs at centromeric region in point centromeres, and the central core in modular centromeres.","definition_xrefs":["GOC:mah","GOC:vw","PMID:19217403","PMID:35422390","PMID:18158900"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatin remodeling at centromere","termid":"GO:0031055"},{"relation_name":"part_of","term_name":"centromere complex assembly","termid":"GO:0034508"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00307":null,"SJAG_00684":null,"SJAG_00756":null,"SJAG_00873":null,"SJAG_01611":null,"SJAG_02119":null,"SJAG_02303":null,"SJAG_02872":null,"SJAG_02908":null,"SJAG_03183":null,"SJAG_03619":null,"SJAG_03867":null,"SJAG_03905":null,"SJAG_04038":null,"SJAG_04547":null,"SJAG_04581":null,"SJAG_04696":null,"SJAG_04989":null,"SJAG_05273":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0006325","GO:0044085"],"is_obsolete":false,"name":"CENP-A containing chromatin assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-606279","GO:0034509","GO:0061641"],"synonyms":[{"name":"CENP-A containing chromatin organization","type":"related"},{"name":"CENP-A containing nucleosome assembly","type":"related"},{"name":"CENP-A containing nucleosome assembly at centromere","type":"exact"},{"name":"CENP-A deposition","type":"related"},{"name":"CENP-A loading","type":"related"},{"name":"CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"DNA replication-independent nucleosome assembly at centromere","type":"exact"},{"name":"centromere specific nucleosome exchange","type":"related"},{"name":"centromere-specific histone exchange","type":"exact"},{"name":"centromeric DNA replication-independent nucleosome assembly","type":"exact"},{"name":"centromeric chromatin organization","type":"related"}],"termid":"GO:0034080","terms_by_termid":{"GO:0034080":null}}


id: PBO:0065072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRICKLE2 antisense RNA 1","termid":"PBO:0065072"}


id: FYPO:0005011
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone H4 acetylation occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H4 acetylation during vegetative growth","termid":"FYPO:0002364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO: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:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0002274","FYPO:0002494"],"is_obsolete":false,"name":"decreased histone H4 acetylation during vegetative growth","synonyms":[{"name":"decreased histone H4 acetylation during mitotic cell cycle","type":"related"},{"name":"reduced histone H4 acetylation during vegetative growth","type":"exact"}],"termid":"FYPO:0005011"}


id: PBO:0073791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 5 member 11","termid":"PBO:0073791"}


id: PBO:0090516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydroxy-acid dehydratase Ilv3","termid":"PBO:0090516"}


id: MONDO:0003067
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the cervical lymph nodes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphadenitis","termid":"MONDO:0002052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"cervical lymphadenitis","secondary_identifiers":["SCTID:3502005","UMLS:C0149642","MEDGEN:101763","DOID:4637","NCIT:C26937"],"synonyms":[{"name":"cervical adenitis","type":"exact"},{"name":"lymphadenitis (disease) of neck","type":"exact"},{"name":"neck lymphadenitis (disease)","type":"exact"}],"termid":"MONDO:0003067","xrefs":{"Monarch":{"xref_id":"0003067"}}}


id: MONDO:0014771
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the KIAA0556 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 26","secondary_identifiers":["GARD:16160","MEDGEN:900415","OMIM:616784","UMLS:C4084843","DOID:0110995"],"synonyms":[{"name":"JBTS26","type":"exact"},{"name":"Joubert syndrome 26","type":"exact"},{"name":"Joubert syndrome caused by mutation in KIAA0556","type":"exact"},{"name":"Joubert syndrome type 26","type":"exact"},{"name":"KIAA0556 Joubert syndrome","type":"exact"}],"termid":"MONDO:0014771","xrefs":{"Monarch":{"xref_id":"0014771"}}}


id: GO:0030695
data:
  {"annotated_genes":["SJAG_01367","SJAG_03361","SJAG_02278","SJAG_02529","SJAG_00467","SJAG_04203","SJAG_00143","SJAG_04548","SJAG_00991","SJAG_00864","SJAG_04724","SJAG_02486","SJAG_01184","SJAG_04982","SJAG_03268","SJAG_02248","SJAG_01699","SJAG_00551","SJAG_02379","SJAG_01011","SJAG_03600","SJAG_03338","SJAG_02539","SJAG_03002","SJAG_05346","SJAG_01309","SJAG_06588","SJAG_01114","SJAG_02666","SJAG_04653","SJAG_00807","SJAG_02645","SJAG_00028","SJAG_01659","SJAG_04522","SJAG_01025","SJAG_01600","SJAG_04491","SJAG_02520","SJAG_04733","SJAG_04837","SJAG_04464","SJAG_03678","SJAG_02368","SJAG_03705","SJAG_02027","SJAG_03488","SJAG_04391","SJAG_02004","SJAG_02390","SJAG_04283","SJAG_01386","SJAG_03748","SJAG_01526","SJAG_04765","SJAG_03581","SJAG_01576","SJAG_04771","SJAG_05210","SJAG_01030","SJAG_03085","SJAG_00801","SJAG_00514","SJAG_02833","SJAG_02160","SJAG_03142","SJAG_00858","SJAG_02012","SJAG_05184","SJAG_04498","SJAG_02831","SJAG_01695","SJAG_02063","SJAG_02231","SJAG_04013","SJAG_03153","SJAG_04010","SJAG_03246","SJAG_01048","SJAG_02765","SJAG_04074","SJAG_02422","SJAG_04080","SJAG_04943","SJAG_04615","SJAG_04400","SJAG_02471","SJAG_03021","SJAG_00064","SJAG_02277","SJAG_03704","SJAG_01319","SJAG_04462","SJAG_00289","SJAG_03655","SJAG_00824","SJAG_04910","SJAG_04938","SJAG_00990","SJAG_00092","SJAG_00338","SJAG_02493","SJAG_03089","SJAG_02819","SJAG_02307","SJAG_00216","SJAG_04776","SJAG_01415"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72373,77889,93040,108648,118033],"is_not":false,"summary":null,"term":"GO:0030695"},{"annotations":[73908,70467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005092"},{"annotations":[66635,97820,72548,72794,98052,80288,95271,72722,78665,79492,95279,70958,75434,95923,107255,73730,78624,81533,70122,67984,74684,76813,73131,72073,79301,73434,73512,59191,72002,76893,81097,74794,112951,67379,77523,67102,72250,75313,80146,69625,75056,78983,98507,116997,67862,60828,72083,74213,79489,89478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005096"},{"annotations":[118304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005095"},{"annotations":[80081,99257,73890,72574,96268,66056,71067,71870,99918,80473,77451,66640,73803,117535,79334,80052,80881,82290,110291,70337,94069,101057,94720,57447,67861,71913,92950,93144,61935,99674,75808,58115,62976,73332,74379,76032,75822,81989,77061,95994,108385,108967,81379,74245,118501,76556,71688,57743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005085"},{"annotations":[78017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005093"},{"annotations":[112791,77209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005094"}]},"cv_name":"molecular_function","definition":"Binds to and modulates the activity of a GTPase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside-triphosphatase regulator 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id: PBO:0070360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 36","termid":"PBO:0070360"}


id: MONDO:0013254
data:
  {"annotated_genes":["SJAG_02680"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88074],"is_not":false,"summary":null,"term":"MONDO:0013254"}]},"cv_name":"mondo","definition":"A developmental and epileptic encephalopathy characterized by microcephaly, infantile onset of seizures and developmental delay that has material basis in homozygous or compound heterozygous mutation in the PNKP gene on chromosome 19q13.","definition_xrefs":["DOID:0080457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microcephaly","termid":"MONDO:0001149"},{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02680":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"microcephaly, seizures, and developmental delay","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:462017","GARD:10933","UMLS:C3150667","Orphanet:228418","OMIM:613402"],"synonyms":[{"name":"EIEE10","type":"related"},{"name":"MCSZ","type":"related"},{"name":"early infantile epileptic encephalopathy-10","type":"related"},{"name":"epileptic encephalopathy, early infantile, 10","type":"related"},{"name":"microcephaly - seizures - developmental delay","type":"related"},{"name":"microcephaly, seizures, and developmental delay","type":"exact"}],"termid":"MONDO:0013254","terms_by_termid":{"MONDO:0013254":null},"xrefs":{"Monarch":{"xref_id":"0013254"}}}


id: GO:0033477
data:
  {"annotated_genes":["SJAG_04425"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033528"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving S-methyl-methionine (SMM). SMM can be converted to methionine by donating a methyl group to homocysteine, and concurrent operation of this reaction and that mediated by MMT sets up the SMM cycle.","definition_xrefs":["GOC:mah","PMID:12692340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04425":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006790","GO:0008150"],"is_obsolete":false,"name":"S-methylmethionine metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"S-methylmethionine metabolism","type":"exact"}],"termid":"GO:0033477","terms_by_termid":{"GO:0033528":null}}


id: GO:0102080
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phenylacetyl-CoA + glycine = H+ + phenylacetylglycine + coenzyme A.","definition_xrefs":["GOC:pz","EC:2.3.1.192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"phenylacetyl-coenzyme A:glycine N-acyltransferase activity","secondary_identifiers":["RHEA:27850","MetaCyc:RXN-10821"],"termid":"GO:0102080"}


id: PBO:0052186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium two pore domain channel subfamily K member 18","termid":"PBO:0052186"}


id: PBO:0089078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein associated with stress granule","termid":"PBO:0089078"}


id: PBO:0003738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IMP dehydrogenase Gua1 (predicted)","termid":"PBO:0003738"}


id: MONDO:0005015
data:
  {"annotated_genes":["SJAG_00092","SJAG_02426","SJAG_04394","SJAG_03247","SJAG_04206","SJAG_02000","SJAG_02012","SJAG_04495","SJAG_02013","SJAG_04334","SJAG_00214"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89293,89292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014488"},{"annotations":[89214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[87057,87056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"},{"annotations":[88332,88331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100165"},{"annotations":[89218,89216,87054,87055,87053,87052,87051,89217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0005148"}]},"cv_name":"mondo","definition":"A metabolic disorder characterized by abnormally high blood sugar levels due to diminished production of insulin or insulin resistance/desensitization.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine pancreas disorder","termid":"MONDO:0001933"},{"relation_name":"is_a","term_name":"glucose metabolism disease","termid":"MONDO:0002908"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00092":null,"SJAG_00214":null,"SJAG_02000":null,"SJAG_02012":null,"SJAG_02013":null,"SJAG_02426":null,"SJAG_03247":null,"SJAG_04206":null,"SJAG_04334":null,"SJAG_04394":null,"SJAG_04495":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"diabetes mellitus","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:E08-E13","icd11.foundation:465177735","MEDGEN:8350","ICD9:250","DOID:9351","SCTID:73211009","UMLS:C0011849","ICD10WHO:E10-E14","EFO:0000400","NANDO:2100158","HP:0000819","MESH:D003920","NCIT:C2985","NANDO:2100157"],"synonyms":[{"name":"DM","type":"exact"},{"name":"diabetes","type":"exact"},{"name":"diabetes mellitus","type":"exact"},{"name":"diabetes mellitus (disease)","type":"exact"}],"termid":"MONDO:0005015","terms_by_termid":{"MONDO:0005148":null,"MONDO:0007453":null,"MONDO:0014488":null,"MONDO:0014674":null,"MONDO:0100165":null},"xrefs":{"Monarch":{"xref_id":"0005015"}}}


id: GO:0035151
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Ensuring that an epithelial tube in an open tracheal system is of the correct length and diameter. Tracheal tubes undergo highly regulated tube-size increases during development, expanding up to 40 times their initial size by the end of larval life. Tube size appears to be controlled by regulation of apical membrane expansion and secretion, rather than by changes in cell number, size or shape.","definition_xrefs":["PMID:12930776","GOC:mtg_sensu","PMID:12973360","PMID:10887083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tube size","termid":"GO:0035150"},{"relation_name":"is_a","term_name":"regulation of tube architecture, open tracheal system","termid":"GO:0035152"}],"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 tube size, open tracheal system","synonyms":[{"name":"regulation of tracheal tube size","type":"exact"}],"termid":"GO:0035151"}


id: GO:1902548
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to vascular endothelial growth factor stimulus.","definition_xrefs":["PMID:17895370","GOC:BHF","GOC:TermGenie","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular response to growth factor stimulus","termid":"GO:0090288"},{"relation_name":"is_a","term_name":"regulation of cellular response to vascular endothelial growth factor stimulus","termid":"GO:1902547"},{"relation_name":"negatively_regulates","term_name":"cellular response to vascular endothelial growth factor stimulus","termid":"GO:0035924"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of cellular response to vascular endothelial growth factor stimulus","synonyms":[{"name":"down regulation of cellular response to VEGF","type":"exact"},{"name":"down regulation of cellular response to VEGFA","type":"narrow"},{"name":"down regulation of cellular response to VEGFB","type":"narrow"},{"name":"down regulation of cellular response to vascular endothelial growth factor","type":"exact"},{"name":"down regulation of cellular response to vascular endothelial growth factor stimulus","type":"exact"},{"name":"down-regulation of cellular response to VEGF","type":"exact"},{"name":"down-regulation of cellular response to VEGFA","type":"narrow"},{"name":"down-regulation of cellular response to VEGFB","type":"narrow"},{"name":"down-regulation of cellular response to vascular endothelial growth factor","type":"exact"},{"name":"down-regulation of cellular response to vascular endothelial growth factor stimulus","type":"exact"},{"name":"downregulation of cellular response to VEGF","type":"exact"},{"name":"downregulation of cellular response to VEGFA","type":"narrow"},{"name":"downregulation of cellular response to VEGFB","type":"narrow"},{"name":"downregulation of cellular response to vascular endothelial growth factor","type":"exact"},{"name":"downregulation of cellular response to vascular endothelial growth factor stimulus","type":"exact"},{"name":"inhibition of cellular response to VEGF","type":"narrow"},{"name":"inhibition of cellular response to VEGFA","type":"narrow"},{"name":"inhibition of cellular response to VEGFB","type":"narrow"},{"name":"inhibition of cellular response to vascular endothelial growth factor","type":"narrow"},{"name":"inhibition of cellular response to vascular endothelial growth factor stimulus","type":"narrow"},{"name":"negative regulation of cellular response to VEGF","type":"exact"},{"name":"negative regulation of cellular response to VEGFA","type":"narrow"},{"name":"negative regulation of cellular response to VEGFB","type":"narrow"},{"name":"negative regulation of cellular response to vascular endothelial growth factor","type":"exact"}],"termid":"GO:1902548"}


id: PBO:0090184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial proline metabolism regulator","termid":"PBO:0090184"}


id: MONDO:1012096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemolytic anemia, non-human animal","termid":"MONDO:1011689"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemolytic anemia, cattle","secondary_identifiers":["OMIA:000430-9913"],"termid":"MONDO:1012096","xrefs":{"Monarch":{"xref_id":"1012096"}}}


id: PBO:0048440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanylate binding protein 3","termid":"PBO:0048440"}


id: GO:0061831
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Testis-specific junction between mature spermatids and Sertoli cells at the luminal end of the Sertoli cell.","definition_xrefs":["GOC:aruk","GOC:bc","GOC:dph","PMID:23546604","PMID:22332112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell junction","termid":"GO:0005911"}],"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":"apical ectoplasmic specialization","synonyms":[{"name":"apical ES","type":"exact"}],"termid":"GO:0061831"}


id: PBO:0054475
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 1875","termid":"PBO:0054475"}


id: MONDO:0958242
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 90","secondary_identifiers":["UMLS:C5935587","MEDGEN:1853928","DOID:0070589","OMIM:620744"],"termid":"MONDO:0958242","xrefs":{"Monarch":{"xref_id":"0958242"}}}


id: RO:0002261
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c has-application-role r iff c has-role r and r is an application role (CHEBI:33232)","direct_ancestors":[{"relation_name":"is_a","term_name":"has_role","termid":"RO:0000087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_application_role","termid":"RO:0002261"}


id: PBO:0004867
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.4.16.6","termid":"PBO:0004867"}


id: FYECO:0000453
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"cells are first grown in medium containing trichostatin A, this medium is then replaced with medium containing no trichostatin A .","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping growth medium","termid":"FYECO:0000009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recovery after trichostatin A treatment","termid":"FYECO:0000453"}


id: PR:Q09130
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tif213 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09130"],"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":"eukaryotic translation initiation factor 2 subunit gamma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17G9.09","synonyms":[{"name":"Spom972h-tif213","type":"exact"},{"name":"eIF-2-gamma (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09130"}


id: MONDO:0002540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An oligodendroglioma that arises from the central nervous system and occurs during childhood.","definition_xrefs":["NCIT:C4045"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"},{"relation_name":"is_a","term_name":"oligodendroglioma","termid":"MONDO:0016695"}],"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":"childhood oligodendroglioma","secondary_identifiers":["DOID:3183","MEDGEN:76116","NANDO:2200089","UMLS:C0280475"],"synonyms":[{"name":"oligodendroglioma","type":"broad"},{"name":"oligodendroglioma of childhood","type":"exact"},{"name":"paediatric oligodendroglioma","type":"exact"},{"name":"pediatric oligodendroglioma","type":"exact"}],"termid":"MONDO:0002540","xrefs":{"Monarch":{"xref_id":"0002540"}}}


id: PBO:0083634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eIF3b subunit of the eukaryotic translation initiation factor 3 (eIF3); subunit of the core complex of eIF3; essential for translation; part of a subcomplex (Prt1p-Rpg1p-Nip1p) that stimulates binding of mRNA and tRNA(i)Met to ribosomes; eIF3 is also involved in programmed stop codon readthrough","termid":"PBO:0083634"}


id: MONDO:0011464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 11 (SCA11) is a subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the early-onset of cerebellar signs, eye movement abnormalities and pyramidal signs.","definition_xrefs":["Orphanet:98767"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type III","termid":"MONDO:0019793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"spinocerebellar ataxia type 11","secondary_identifiers":["GARD:10475","MEDGEN:346799","DOID:0050961","MESH:C565772","SCTID:719207000","UMLS:C1858351","icd11.foundation:743674840","OMIM:604432"],"synonyms":[{"name":"SCA11","type":"exact"},{"name":"spinocerebellar ataxia 11","type":"related"},{"name":"spinocerebellar ataxia type 11","type":"exact"}],"termid":"MONDO:0011464","xrefs":{"Monarch":{"xref_id":"0011464"}}}


id: PBO:0046848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acid binding protein 9","termid":"PBO:0046848"}


id: MONDO:0006229
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive, high-grade and poorly differentiated carcinoma with neuroendocrine differentiation that arises from the stomach. It is characterized by the presence of malignant small cells.","definition_xrefs":["NCIT:C6764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"gastric neuroendocrine neoplasm","termid":"MONDO:0003111"},{"relation_name":"is_a","term_name":"gastric carcinoma","termid":"MONDO:0004950"}],"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":"gastric small cell neuroendocrine carcinoma","secondary_identifiers":["EFO:1000277","MEDGEN:272664","DOID:6552","ONCOTREE:STSC","UMLS:C1333788"],"synonyms":[{"name":"Oat cell carcinoma of stomach","type":"exact"},{"name":"Oat cell carcinoma of the stomach","type":"exact"},{"name":"STSC","type":"related"},{"name":"gastric Oat cell carcinoma","type":"exact"},{"name":"gastric small cell carcinoma","type":"exact"},{"name":"gastric small cell neuroendocrine carcinoma","type":"exact"},{"name":"small cell carcinoma of stomach","type":"exact"},{"name":"small cell carcinoma of the stomach","type":"exact"},{"name":"stomach small cell carcinoma","type":"exact"}],"termid":"MONDO:0006229","xrefs":{"Monarch":{"xref_id":"0006229"}}}


id: PBO:0110466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"a master non-coding RNA antagonizing inflammation","termid":"PBO:0110466"}


id: PR:000041443
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A core histone that is a translation product of the Schizosaccharomyces pombe cnp1 gene or a 1:1 ortholog thereof.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3-like centromeric protein cnp1","synonyms":[{"name":"CENP-A","type":"broad"},{"name":"centromere protein 1","type":"exact"},{"name":"centromere protein A","type":"broad"},{"name":"cnp1","type":"exact"},{"name":"cnp1 homolog","type":"exact"},{"name":"histone H3-like centromeric protein CENP-A","type":"broad"}],"termid":"PR:000041443"}


id: GO:1901058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving p-hydroxyphenyl lignin.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignin metabolic process","termid":"GO:0009808"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"p-hydroxyphenyl lignin metabolic process","synonyms":[{"name":"H-lignin metabolic process","type":"exact"},{"name":"p-hydroxyphenyl lignin metabolism","type":"exact"}],"termid":"GO:1901058"}


id: PBO:0091054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MICOS complex subunit Mic19/25","termid":"PBO:0091054"}


id: GO:0042391
data:
  {"annotated_genes":["SJAG_01541","SJAG_02883"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68471,91463],"is_not":false,"summary":null,"term":"GO:0042391"}]},"cv_name":"biological_process","definition":"Any process that modulates the establishment or extent of a membrane potential, the electric potential existing across any membrane arising from charges in the membrane itself and from the charges present in the media on either side of the membrane.","definition_xrefs":["ISBN:0198506732","GOC:tb","GOC:jl","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01541":null,"SJAG_02883":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of membrane potential","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"termid":"GO:0042391","terms_by_termid":{"GO:0042391":null}}


id: PBO:0005592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiosis specific protein kinase Mug27/Slk1","termid":"PBO:0005592"}


id: PBO:0072509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 38","termid":"PBO:0072509"}


id: PBO:0016971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent polydeoxyribonucleotide 5'-hydroxyl-kinase activity implicated in DNA repair (predicted)","termid":"PBO:0016971"}


id: PBO:0015678
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High Copy Sterile","termid":"PBO:0015678"}


id: PBO:0030333
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_phosphoinositide_level","termid":"PBO:0030333"}


id: PBO:0027203
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_nuclear_microtubules","termid":"PBO:0027203"}


id: MONDO:0018004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute megakaryoblastic leukemia","termid":"MONDO:0018872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"acute megakaryoblastic leukemia without down syndrome","secondary_identifiers":["GARD:21490","MEDGEN:1843134","Orphanet:329469","UMLS:C5679860"],"synonyms":[{"name":"non-DS-AMKL","type":"exact"}],"termid":"MONDO:0018004","xrefs":{"Monarch":{"xref_id":"0018004"}}}


id: GO:1905902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mesoderm formation.","definition_xrefs":["GOC:BHF","GOC:rph","GOC:TermGenie","GOC:BHF_miRNA","GO_REF:0000058","PMID:23939491"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"mesoderm formation","termid":"GO:0001707"}],"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 mesoderm formation","termid":"GO:1905902"}


id: MONDO:0012405
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary mixed polyposis syndrome in which the cause of the disease is a mutation in the BMPR1A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary mixed polyposis syndrome","termid":"MONDO:0011023"}],"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":"polyposis syndrome, hereditary mixed, 2","secondary_identifiers":["UMLS:C1864730","DOID:0111686","OMIM:610069","MESH:C566451","MEDGEN:350500","GARD:18276"],"synonyms":[{"name":"BMPR1A hereditary mixed polyposis syndrome","type":"exact"},{"name":"HMPS2","type":"related"},{"name":"hereditary mixed polyposis syndrome caused by mutation in BMPR1A","type":"exact"},{"name":"polyposis syndrome, hereditary mixed, 2","type":"exact"},{"name":"polyposis syndrome, hereditary mixed, type 2","type":"exact"}],"termid":"MONDO:0012405","xrefs":{"Monarch":{"xref_id":"0012405"}}}


id: PBO:0043561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type V alpha 3 chain","termid":"PBO:0043561"}


id: MONDO:0018063
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nodular non-suppurative panniculitis, known as Weber-Christian disease (WCD), is a rare skin disorder characterized by recurring inflammation in the subcutaneous layer of fat.","definition_xrefs":["Orphanet:33577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"panniculitis","termid":"MONDO:0006591"},{"relation_name":"is_a","term_name":"subcutaneous tissue disorder","termid":"MONDO:0019296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nodular non-suppurative panniculitis","secondary_identifiers":["MedDRA:10047883","SCTID:33760009","UMLS:C0030328","MESH:D010201","MEDGEN:10559","EFO:1000742","DOID:1525","GARD:7879"],"synonyms":[{"name":"Pfeiffer-Weber-Christian syndrome","type":"exact"},{"name":"Relapsing febrile nodular nonsuppurative panniculitis","type":"exact"},{"name":"Relapsing febrile nodular panniculitis","type":"exact"},{"name":"WCD","type":"exact"},{"name":"Weber - Christian disease","type":"exact"},{"name":"Weber Christian disease","type":"related"},{"name":"Weber-Christian disease","type":"exact"},{"name":"Weber-Christian panniculitis","type":"exact"},{"name":"idiopathic lobular panniculitis","type":"exact"},{"name":"idiopathic nodular panniculitis","type":"exact"},{"name":"nodular non-suppurative febrile panniculitis","type":"exact"},{"name":"nodular nonsuppurative panniculitis","type":"exact"},{"name":"panniculitis nodular nonsuppurative","type":"related"}],"termid":"MONDO:0018063","xrefs":{"Monarch":{"xref_id":"0018063"}}}


id: FYPO:0001840
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which minichromosomes are lost at a higher frequency than normal during the vegetative growth phase of the life cycle. Minichromosome loss occurs when one or both daughter cells do not inherit copies of a minichromosome from the mother cell, and may result from failure of minichromosome replication or segregation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vegetative cell phenotype","termid":"FYPO:0001320"},{"relation_name":"is_a","term_name":"increased minichromosome loss","termid":"FYPO:0001859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased minichromosome loss during vegetative growth","synonyms":[{"name":"increased minichromosome loss during mitotic cell cycle","type":"related"},{"name":"mitotic minichromosome maintenance defect","type":"related"}],"termid":"FYPO:0001840"}


id: GO:0052110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism reduces the flow of fluid within its host's vascular system, the vessels and tissue that carry or circulate fluids, such as blood, lymph or sap, through the body of an animal or plant. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete occlusion by symbiont of host vascular system (obsolete GO:0052110)","termid":"GO:0052110"}


id: GO:0019008
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that possesses molybdopterin synthase activity. In E. coli, the complex is a heterotetramer consisting of two MoaD and two MoaE subunits.","definition_xrefs":["PMID:15709772","GOC:mah","PMID:12571227"],"gene_count":0,"genotype_count":0,"name":"obsolete molybdopterin synthase complex (obsolete GO:0019008)","synonyms":[{"name":"molybdopterin converting factor complex","type":"exact"}],"termid":"GO:0019008"}


id: GO:0045210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of fas ligand (FasL or CD95L), an antigen originally found to be expressed on the cell surface of activated human T-lymphocytes and B-lymphocytes and a variety of malignant human lymphoid cell lines.","definition_xrefs":["PMID:10637433"],"gene_count":0,"genotype_count":0,"name":"obsolete FasL biosynthetic process (obsolete GO:0045210)","synonyms":[{"name":"APT1LG1 biosynthetic process","type":"exact"},{"name":"CD178 biosynthetic process","type":"exact"},{"name":"CD95L biosynthesis","type":"exact"},{"name":"CD95L biosynthetic process","type":"exact"},{"name":"FASLG biosynthetic process","type":"exact"},{"name":"Fas-L biosynthetic process","type":"exact"},{"name":"FasL anabolism","type":"exact"},{"name":"FasL biosynthesis","type":"exact"},{"name":"FasL formation","type":"exact"},{"name":"FasL synthesis","type":"exact"},{"name":"fas ligand biosynthetic process","type":"exact"}],"termid":"GO:0045210"}


id: GO:0035950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of oligopeptide transport, by regulation of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:dgf","PMID:17005992"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of oligopeptide transport by regulation of transcription from RNA polymerase II promoter (obsolete GO:0035950)","synonyms":[{"name":"regulation of oligopeptide transport by regulation of transcription from Pol II promoter","type":"exact"}],"termid":"GO:0035950"}


id: FYPO:0001856
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription occurs to a normal (i.e. indistinguishable from wild type) extent when the cell is subject to iron ion starvation. All genes, or a specific subset of genes, may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transcription during vegetative growth","termid":"FYPO:0001855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000294","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal transcription during iron starvation","synonyms":[{"name":"normal transcription during iron depletion","type":"exact"},{"name":"normal transcription during iron deprivation","type":"exact"},{"name":"normal transcription during iron ion starvation","type":"exact"},{"name":"normal transcription during iron starvation during mitotic cell cycle","type":"related"},{"name":"normal transcription during iron starvation during vegetative growth","type":"exact"}],"termid":"FYPO:0001856"}


id: GO:0034004
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate + H2O = (1E,4S,5E,7R)-germacra-1(10),5-dien-11-ol + diphosphate.","definition_xrefs":["EC:4.2.3.22"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"germacradienol synthase activity","secondary_identifiers":["RHEA:22436"],"synonyms":[{"name":"2-trans,6-trans-farnesyl-diphosphate diphosphate-lyase [(1E,4S,5E,7R)-germacra-1(10),5-dien-11-ol-forming] activity","type":"related"}],"termid":"GO:0034004"}


id: GO:1900683
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of fumonisin biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone metabolic process","termid":"GO:0010565"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"fumonisin biosynthetic process","termid":"GO:1900541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"regulation of fumonisin biosynthetic process","synonyms":[{"name":"regulation of fumonisin anabolism","type":"exact"},{"name":"regulation of fumonisin biosynthesis","type":"exact"},{"name":"regulation of fumonisin formation","type":"exact"},{"name":"regulation of fumonisin synthesis","type":"exact"}],"termid":"GO:1900683"}


id: FYPO:0004443
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the prospore membrane is decreased during the second meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"decreased protein localization to prospore membrane","termid":"FYPO:0004442"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to prospore membrane during meiosis II","synonyms":[{"name":"decreased protein localisation to prospore membrane during meiosis II","type":"exact"},{"name":"decreased protein localization to forespore membrane during meiosis II","type":"exact"},{"name":"decreased protein localization to prospore membrane during second meiotic nuclear division","type":"exact"},{"name":"reduced protein localization to prospore membrane during meiosis II","type":"exact"}],"termid":"FYPO:0004443"}


id: MONDO:0010398
data:
  {"annotated_genes":["SJAG_04056"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89168],"is_not":false,"summary":null,"term":"MONDO:0010398"}]},"cv_name":"mondo","definition":"Any X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the UPF3B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04056":null},"genotype_count":0,"is_obsolete":false,"name":"syndromic X-linked intellectual disability 14","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060821","MEDGEN:372646","MESH:C567063","OMIM:300676","UMLS:C1970822"],"synonyms":[{"name":"MRXS14","type":"related"},{"name":"UPF3B X-linked syndromic intellectual disability","type":"exact"},{"name":"X-linked syndromic intellectual disability caused by mutation in UPF3B","type":"exact"},{"name":"intellectual developmental disorder, X-linked syndromic 14, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked, syndromic 14","type":"exact"},{"name":"intellectual disability, X-linked, syndromic type 14","type":"exact"},{"name":"mental retardation, X-linked, syndromic 14","type":"exact"},{"name":"mental retardation, X-linked, syndromic type 14","type":"exact"},{"name":"syndromic X-linked intellectual disability 14","type":"exact"},{"name":"syndromic X-linked intellectual disability type 14","type":"exact"}],"termid":"MONDO:0010398","terms_by_termid":{"MONDO:0010398":null},"xrefs":{"Monarch":{"xref_id":"0010398"}}}


id: GO:0000193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Upregulation of MAP kinase activity in the context of regulating pseudohyphal or invasive growth.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of MAPK (pseudohyphal growth) (obsolete GO:0000193)","synonyms":[{"name":"activation of MAPK (pseudohyphal growth)","type":"exact"}],"termid":"GO:0000193"}


id: MONDO:0016241
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neurodevelopmental disorder characterized by recurrent episodes of hemiplegia and paroxysmal disturbances associated with persistent developmental delay and cognitive impairment.","definition_xrefs":["Orphanet:2131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemiplegia","termid":"MONDO:0001170"},{"relation_name":"is_a","term_name":"alternating hemiplegia","termid":"MONDO:0016210"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"alternating hemiplegia of childhood","secondary_identifiers":["DOID:0050635","GARD:11","NANDO:1200525","UMLS:C0338488","icd11.foundation:301329822","MEDGEN:90925","NANDO:2200883","NCIT:C35261","NORD:758","NANDO:2100239","MESH:C536589","NANDO:2200357","OMIMPS:104290","NANDO:1200403","SCTID:230466004"],"synonyms":[{"name":"AHC","type":"exact"},{"name":"adrenal hypoplasia congenita","type":"exact"},{"name":"alternating hemiplegia","type":"related"},{"name":"alternating hemiplegia of childhood","type":"exact"},{"name":"alternating hemiplegia syndrome","type":"related"},{"name":"childhood alternating hemiplegia","type":"exact"},{"name":"congenital adrenal Hypoplasia","type":"exact"},{"name":"congenital adrenal gland hypoplasia","type":"exact"},{"name":"paediatric alternating hemiplegia","type":"exact"},{"name":"pediatric alternating hemiplegia","type":"exact"}],"termid":"MONDO:0016241","xrefs":{"Monarch":{"xref_id":"0016241"}}}


id: MONDO:0016992
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete peeling skin syndrome type B (obsolete MONDO:0016992)","termid":"MONDO:0016992","xrefs":{"Monarch":{"xref_id":"0016992"}}}


id: PBO:0036253
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PROline requiring","termid":"PBO:0036253"}


id: PBO:0075283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 24","termid":"PBO:0075283"}


id: MONDO:0014706
data:
  {"annotated_genes":["SJAG_03457","SJAG_00660"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87909,87910],"is_not":false,"summary":null,"term":"MONDO:0014706"}]},"cv_name":"mondo","definition":"An autosomal dominant cutis laxa characterized by thin skin with visible veins and wrinkles, cataract or corneal clouding, clenched fingers, pre- and postnatal growth retardation, moderate intellectual disability, and a combination of muscle hypotonia with brisk muscle reflexes that has material basis in heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.","definition_xrefs":["DOID:0070131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"autosomal dominant cutis laxa","termid":"MONDO:0019571"},{"relation_name":"is_a","term_name":"P5CS deficiency","termid":"MONDO:0100126"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00660":null,"SJAG_03457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"cutis laxa, autosomal dominant 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:899774","OMIM:616603","UMLS:C4225268","GARD:16143"],"synonyms":[{"name":"ADCL3","type":"exact"},{"name":"autosomal dominant cutis laxa 3","type":"related"},{"name":"cutis laxa, autosomal dominant 3","type":"exact"},{"name":"cutis laxa, autosomal dominant type 3","type":"exact"}],"termid":"MONDO:0014706","terms_by_termid":{"MONDO:0014706":null},"xrefs":{"Monarch":{"xref_id":"0014706"}}}


id: PBO:0018283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Med21","termid":"PBO:0018283"}


id: GO:0015928
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of fucosyl compounds, substances containing a group derived from a cyclic form of fucose or a fucose derivative.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016798"],"is_obsolete":false,"name":"fucosidase activity","termid":"GO:0015928"}


id: PBO:0049491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A.B variant histone 1","termid":"PBO:0049491"}


id: MONDO:0060556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"joint laxity, short stature, and myopia","secondary_identifiers":["Orphanet:527450","MEDGEN:1621331","OMIM:617662","UMLS:C4540020","GARD:17963"],"synonyms":[{"name":"JLSM","type":"related"},{"name":"joint laxity, short stature, and myopia","type":"exact"}],"termid":"MONDO:0060556","xrefs":{"Monarch":{"xref_id":"0060556"}}}


id: MONDO:1011067
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in domestic guinea pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, domestic guinea pig","secondary_identifiers":["OMIA:001033-10141"],"termid":"MONDO:1011067","xrefs":{"Monarch":{"xref_id":"1011067"}}}


id: GO:0016669
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a sulfur-containing group acts as a hydrogen or electron donor and reduces a cytochrome.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors","termid":"GO:0016667"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"oxidoreductase activity, acting on a sulfur group of donors, cytochrome as acceptor","secondary_identifiers":["EC:1.8.2.-"],"synonyms":[{"name":"oxidoreductase activity, acting on sulphur group of donors, cytochrome as acceptor","type":"exact"}],"termid":"GO:0016669"}


id: GO:0015069
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-amino-1-deoxy-scyllo-inositol 4-phosphate + L-arginine = 1-guanidino-1-deoxy-scyllo-inositol 4-phosphate + L-ornithine.","definition_xrefs":["RHEA:13265"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidinotransferase activity","termid":"GO:0015067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"scyllo-inosamine-4-phosphate amidinotransferase activity","secondary_identifiers":["EC:2.1.4.2","KEGG_REACTION:R03477","MetaCyc:2.1.4.2-RXN"],"synonyms":[{"name":"L-arginine:1-amino-1-deoxy-scyllo-inositol-4-phosphate amidinotransferase activity","type":"related"},{"name":"L-arginine:inosamine phosphate amidinotransferase activity","type":"related"},{"name":"L-arginine:inosamine-P-amidinotransferase activity","type":"related"},{"name":"inosamine-P amidinotransferase activity","type":"related"},{"name":"inosamine-phosphate amidinotransferase activity","type":"exact"}],"termid":"GO:0015069"}


id: PBO:0085557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein containing an N-terminal epsin-like domain; involved in clathrin recruitment and traffic between the Golgi and endosomes; associates with the clathrin adaptor Gga2p, clathrin adaptor complex AP-1, and clathrin","termid":"PBO:0085557"}


id: PBO:0087048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L22A; required for translation of long 5' UTR of IME1 mRNA and meiotic entry; required for the oxidative stress response, pseudohyphal and invasive growth; homologous to mammalian ribosomal protein L22, no bacterial homolog; RPL22A has a paralog, RPL22B, that arose from the whole genome duplication","termid":"PBO:0087048"}


id: MONDO:0019679
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brachydactyly type A7 (Smorgasbord type) is a form of brachydactyly that presents with the characteristic features of brachydactyly type A2 (shortening of the middle phalanges of the index finger and, sometimes, of the little finger) and type D (shortening of the distal phalanx of the thumb) plus various additional features.","definition_xrefs":["Orphanet:93397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly","termid":"MONDO:0021004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly type A7","secondary_identifiers":["icd11.foundation:1487696553","MEDGEN:929660","UMLS:C4303991","GARD:984","SCTID:720571006"],"synonyms":[{"name":"brachydactyly Smorgasbord type","type":"related"},{"name":"brachydactyly, Smorgasbord type","type":"exact"}],"termid":"MONDO:0019679","xrefs":{"Monarch":{"xref_id":"0019679"}}}


id: MONDO:0000485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic voice disorder characterized by momentary periods of uncontrolled spasms of the muscles of the larynx.","direct_ancestors":[{"relation_name":"is_a","term_name":"focal dystonia","termid":"MONDO:0000477"},{"relation_name":"is_a","term_name":"laryngeal disorder","termid":"MONDO:0004382"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"spasmodic dystonia","secondary_identifiers":["ICD9:478.79","UMLS:C1963946","MESH:D055154","Orphanet:93961","DOID:0050844","MEDGEN:409603","SCTID:3331000119108"],"synonyms":[{"name":"abductor spasmodic dysphonia","type":"narrow"},{"name":"adductor spasmodic dysphonia","type":"narrow"},{"name":"laryngeal dyskinesia","type":"exact"},{"name":"laryngeal dystonia","type":"exact"},{"name":"mixed spasmodic dysphonia (type)","type":"related"},{"name":"spasmodic dysphonia","type":"exact"},{"name":"spastic dysphonia","type":"exact"}],"termid":"MONDO:0000485","xrefs":{"Monarch":{"xref_id":"0000485"}}}


id: GO:0008079
data:
  {"annotated_genes":["SJAG_03232","SJAG_01518","SJAG_00308","SJAG_00338","SJAG_01696","SJAG_02189","SJAG_02601","SJAG_05221","SJAG_02812","SJAG_04283"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106668,111155,111156],"is_not":false,"summary":null,"term":"GO:0008079"},{"annotations":[118034,67696,74228,109150,70544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003747"},{"annotations":[100603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016150"},{"annotations":[75736],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016149"}]},"cv_name":"molecular_function","definition":"Functions in the termination of translation.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation factor activity","termid":"GO:0180051"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00308":null,"SJAG_00338":null,"SJAG_01518":null,"SJAG_01696":null,"SJAG_02189":null,"SJAG_02601":null,"SJAG_02812":null,"SJAG_03232":null,"SJAG_04283":null,"SJAG_05221":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"translation termination factor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0008079","terms_by_termid":{"GO:0003747":null,"GO:0008079":null,"GO:0016149":null,"GO:0016150":null}}


id: PBO:0045982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EHHADH antisense RNA 1","termid":"PBO:0045982"}


id: GO:0060229
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of a lipase, an enzyme that catalyzes of the hydrolysis of a lipid.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme activator activity","termid":"GO:0008047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0140677","GO:0098772"],"is_obsolete":false,"name":"lipase activator activity","termid":"GO:0060229"}


id: MONDO:0019970
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sinding-Larsen-Johansson disease is a type of osteochondrosis affecting the attachment of the patellar tendon to the patella and characterized by tenderness and localized swelling of the patella.","definition_xrefs":["Orphanet:97337"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrosis","termid":"MONDO:0018381"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sinding-Larsen-Johansson disease","secondary_identifiers":["GARD:19366","icd11.foundation:1733785551","MedDRA:10063585","UMLS:C1504517","MEDGEN:1672493"],"synonyms":[{"name":"Osteochondrosis of patella","type":"exact"},{"name":"aseptic necrosis of patella","type":"exact"}],"termid":"MONDO:0019970","xrefs":{"Monarch":{"xref_id":"0019970"}}}


id: GO:0019045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process required for latent viral replication in a cell.","definition_xrefs":["ISBN:0781702534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"},{"relation_name":"part_of","term_name":"viral latency","termid":"GO:0019042"}],"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":"latent virus replication","termid":"GO:0019045"}


id: GO:0034927
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: pyrene + O2 + 2 H+ + 2 e- = pyrene-1,2-oxide + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete pyrene 1,2-monooxygenase activity (obsolete GO:0034927)","termid":"GO:0034927"}


id: PBO:0053663
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 840","termid":"PBO:0053663"}


id: MONDO:0020207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare isolated myopia is a rare, genetic, refraction anomaly disorder characterized by non-syndromic severe myopia, which may be associated with cataract and vitreoretinal degeneration (retinal detachment) that may lead to blindness.","definition_xrefs":["Orphanet:98619"],"gene_count":0,"genotype_count":0,"name":"obsolete rare isolated myopia (obsolete MONDO:0020207)","termid":"MONDO:0020207","xrefs":{"Monarch":{"xref_id":"0020207"}}}


id: MONDO:0004413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A variant of cervical squamous cell carcinoma characterized by the presence of polygonal squamous cells. Intercellular bridges and cytoplasmic keratinization may be present, but keratin pearls are absent.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical squamous cell carcinoma","termid":"MONDO:0006143"}],"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":"cervical non-keratinizing squamous cell carcinoma","secondary_identifiers":["NCIT:C40188","UMLS:C1518366","DOID:7961","MEDGEN:309426"],"termid":"MONDO:0004413","xrefs":{"Monarch":{"xref_id":"0004413"}}}


id: PBO:0083418
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 ribosomal gene RPL7B","termid":"PBO:0083418"}


id: GO:0007441
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the anterior midgut (ectodermal) are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"},{"relation_name":"part_of","term_name":"ectodermal digestive tract morphogenesis","termid":"GO:0048567"}],"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":"anterior midgut (ectodermal) morphogenesis","termid":"GO:0007441"}


id: PBO:0077073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIA1 cytotoxic granule associated RNA binding protein","termid":"PBO:0077073"}


id: MONDO:0005951
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sarcocystosis (obsolete MONDO:0005951)","termid":"MONDO:0005951","xrefs":{"Monarch":{"xref_id":"0005951"}}}


id: PR:O14295
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- plr1 gene.","definition_xrefs":["UniProtKB:O14295","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":"pyridoxal reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9E9.11","synonyms":[{"name":"PL reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PL-red (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-plr1","type":"exact"}],"termid":"PR:O14295"}


id: PBO:0029568
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_small_vegetative_cell_population_(obsolete_FYPO:0002153)","termid":"PBO:0029568"}


id: PBO:0041200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BUD31 homolog","termid":"PBO:0041200"}


id: PBO:0090905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding forkhead transcription factor Fkh2","termid":"PBO:0090905"}


id: MONDO:0003932
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A glioma affecting the optic tract and occurring in childhood.","definition_xrefs":["NCIT:C7535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"optic nerve glioma","termid":"MONDO:0003235"},{"relation_name":"is_a","term_name":"childhood neoplasm","termid":"MONDO:0021079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood optic nerve glioma","secondary_identifiers":["MEDGEN:124487","DOID:6576","UMLS:C0278653"],"synonyms":[{"name":"childhood optic tract glioma","type":"exact"},{"name":"childhood visual pathway glioma","type":"exact"},{"name":"glioma of childhood visual pathway","type":"exact"},{"name":"glioma of paediatric visual pathway","type":"exact"},{"name":"glioma of pediatric visual pathway","type":"exact"},{"name":"glioma of the childhood visual pathway","type":"exact"},{"name":"glioma of the paediatric visual pathway","type":"exact"},{"name":"glioma of the pediatric visual pathway","type":"exact"},{"name":"optic nerve glioma of childhood","type":"exact"},{"name":"paediatric optic nerve glioma","type":"exact"},{"name":"paediatric optic tract glioma","type":"exact"},{"name":"paediatric visual pathway glioma","type":"exact"},{"name":"pediatric optic nerve glioma","type":"exact"},{"name":"pediatric optic tract glioma","type":"exact"},{"name":"pediatric visual pathway glioma","type":"exact"},{"name":"visual pathway and hypothalamic glioma, childhood","type":"related"},{"name":"visual pathway glioma","type":"broad"}],"termid":"MONDO:0003932","xrefs":{"Monarch":{"xref_id":"0003932"}}}


id: GO:0102352
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + a 1,2-diacyl-sn-glycerol 3-phosphate = ADP + a 1,2-diacyl-sn-glycerol 3-diphosphate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphatidate kinase activity (obsolete GO:0102352)","termid":"GO:0102352"}


id: MONDO:0010780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial myopathy","termid":"MONDO:0009637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005336","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial myopathy with reversible cytochrome C oxidase deficiency","secondary_identifiers":["MEDGEN:463248","GARD:17227","icd11.foundation:723205095","Orphanet:254864","UMLS:C3151898","OMIM:500009"],"synonyms":[{"name":"Cox deficiency myopathy, infantile, transient","type":"related"},{"name":"MMIT","type":"related"},{"name":"benign COX deficiency","type":"exact"},{"name":"infantile reversible cytochrome C oxidase deficiency myopathy","type":"exact"},{"name":"mitochondrial myopathy with reversible COX deficiency","type":"exact"},{"name":"mitochondrial myopathy with reversible complex IV deficiency","type":"exact"},{"name":"mitochondrial myopathy, infantile, transient","type":"related"},{"name":"mitochondrial myopathy, infantile, transient, due to respiratory chain deficiency","type":"related"},{"name":"respiratory chain deficiency, infantile, transient","type":"related"},{"name":"reversible infantile cytochrome C oxidase deficiency","type":"exact"},{"name":"reversible infantile respiratory chain deficiency","type":"exact"}],"termid":"MONDO:0010780","xrefs":{"Monarch":{"xref_id":"0010780"}}}


id: PATO:0000136
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphological quality pertaining to the degree to which an object contains an opening, aperture, orifice or vent.","definition_xrefs":["PATOC:GVG","PATOC:CJM"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphology","termid":"PATO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"closure","termid":"PATO:0000136"}


id: GO:0005181
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 glycopeptide hormone (obsolete GO:0005181)","synonyms":[{"name":"glycopeptide hormone","type":"exact"}],"termid":"GO:0005181"}


id: MONDO:0004544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A WHO grade II, usually recurring meningioma characterized by the predominance of tissues that are histologically similar to chordoma.","definition_xrefs":["NCIT:C6908"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"clear cell meningioma","termid":"MONDO:0002918"},{"relation_name":"is_a","term_name":"grade II meningioma","termid":"MONDO:0045056"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chordoid meningioma","secondary_identifiers":["MEDGEN:235089","UMLS:C1370510","DOID:8368","ONCOTREE:CHOM"],"synonyms":[{"name":"CHOM","type":"related"},{"name":"chordoid meningioma","type":"exact"},{"name":"meningioma, chordoid","type":"exact"},{"name":"meningioma, chordoid (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0004544","xrefs":{"Monarch":{"xref_id":"0004544"}}}


id: PBO:0034732
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromatin binding profiling","termid":"PBO:0034732"}


id: PBO:0084667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial alcohol dehydrogenase isozyme III; involved in the shuttling of mitochondrial NADH to the cytosol under anaerobic conditions and ethanol production","termid":"PBO:0084667"}


id: MONDO:0009583
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ohdo blepharophimosis syndrome (OBS) is a multiple congenital malformation syndrome characterized by blepharophimosis, ptosis, dental hypoplasia, hearing impairment and intellectual disability.","definition_xrefs":["Orphanet:2728"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ohdo syndrome and variants","termid":"MONDO:0000734"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"blepharophimosis - intellectual disability syndrome, Ohdo type","secondary_identifiers":["OMIM:249620","GARD:3348","SCTID:412787009","ICD9:525.8","UMLS:C0796094","MEDGEN:162905","ICD9:374.89"],"synonyms":[{"name":"BMRS, Ohdo type","type":"exact"},{"name":"Ohdo blepharophimosis syndrome","type":"related"},{"name":"Ohdo syndrome","type":"exact"},{"name":"Ohdo-Madokoro-Sonoda syndrome","type":"exact"},{"name":"blepharophimosis syndrome, Ohdo type","type":"exact"},{"name":"intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth","type":"related"},{"name":"mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth","type":"related"}],"termid":"MONDO:0009583","xrefs":{"Monarch":{"xref_id":"0009583"}}}


id: PBO:0050599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxy-delta-5-steroid dehydrogenase, 3 beta, pseudogene 4","termid":"PBO:0050599"}


id: GO:0018961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving pentachlorophenol, a chlorinated insecticide and fungicide used primarily to protect timber from fungal rot and wood boring insects. Pentachlorophenol is significantly toxic to mammals, plants, and many microorganisms.","definition_xrefs":["UM-BBD_pathwayID:pcp"],"gene_count":0,"genotype_count":0,"name":"obsolete pentachlorophenol metabolic process (obsolete GO:0018961)","synonyms":[{"name":"PCP metabolic process","type":"exact"},{"name":"PCP metabolism","type":"exact"},{"name":"pentachlorophenol metabolism","type":"exact"}],"termid":"GO:0018961"}


id: MONDO:0003112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell tumor that arises from the stomach. It includes choriocarcinoma and immature teratoma.","definition_xrefs":["NCIT:C5486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastric cancer","termid":"MONDO:0001056"},{"relation_name":"is_a","term_name":"extragonadal germ cell cancer","termid":"MONDO:0003113"}],"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":"malignant gastric germ cell tumor","secondary_identifiers":["DOID:4716","MEDGEN:233663","UMLS:C1334584"],"synonyms":[{"name":"germ cell tumor of the stomach","type":"exact"},{"name":"germ cell tumour of the stomach","type":"exact"},{"name":"malignant gastric germ cell neoplasm","type":"exact"},{"name":"malignant gastric germ cell tumor","type":"exact"},{"name":"malignant germ cell neoplasm of stomach","type":"exact"},{"name":"malignant germ cell neoplasm of the stomach","type":"exact"},{"name":"malignant germ cell tumor of stomach","type":"exact"},{"name":"malignant germ cell tumor of the stomach","type":"exact"},{"name":"malignant germ cell tumour of stomach","type":"exact"},{"name":"malignant germ cell tumour of the stomach","type":"exact"}],"termid":"MONDO:0003112","xrefs":{"Monarch":{"xref_id":"0003112"}}}


id: GO:0098865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or temporarily subverts the tight cell-cell junctions between cells of the host. Tight cell-cell junctions, a cell-cell junction that seals cells together in an epithelium in a way that prevents even small molecules from leaking from one side of the sheet to the other.","definition_xrefs":["PMID:24287273"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cell-cell junction","termid":"GO:0044067"}],"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 perturbation of host tight cell-cell junction","synonyms":[{"name":"disruption by symbiont of host tight cell-cell junction","type":"exact"},{"name":"disruption of host tight cell-cell junction","type":"broad"},{"name":"modification by symbiont of host bicellular tight junctions","type":"related"},{"name":"symbiont-mediated disruption of host tight cell-cell junction","type":"related"}],"termid":"GO:0098865"}


id: MONDO:1012571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cancer that occurs in domestic cats.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feline neoplasm","termid":"MONDO:0700175"},{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer, domestic cat","secondary_identifiers":["OMIA:002587-9685"],"termid":"MONDO:1012571","xrefs":{"Monarch":{"xref_id":"1012571"}}}


id: MONDO:0013992
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypogonadotropic hypogonadism","termid":"MONDO:0015770"},{"relation_name":"is_a","term_name":"inherited obesity","termid":"MONDO:0019182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"obesity due to leptin receptor gene deficiency","secondary_identifiers":["GARD:17083","OMIM:614963","NCIT:C120386","icd11.foundation:997823205","MEDGEN:767139","Orphanet:179494","NORD:109401","UMLS:C3554225"],"synonyms":[{"name":"LEPR Deficiency","type":"exact"},{"name":"leptin receptor deficiency","type":"related"},{"name":"obesity due to leptin receptor gene deficiency","type":"exact"},{"name":"obesity, morbid, due to leptin receptor deficiency","type":"exact"},{"name":"obesity, morbid, nonsyndromic 2","type":"related"}],"termid":"MONDO:0013992","xrefs":{"Monarch":{"xref_id":"0013992"}}}


id: PR:000085728
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe) that has been methylated on Lys-9 and phosphorylated on Ser-10. UniProtKB:P10651, 2-136, Lys-10, MOD:00663|Ser-11, MOD:00046.","definition_xrefs":["PMID:19362535","PRO:DAN","PomBase:VW"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe)","termid":"PR:000027598"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht3/Me(K9),Phos(S10)","pombase_gene_id":"SPBC1105.11c","synonyms":[{"name":"PRO_0000221367, Lys-10, MOD:00663|Ser-11, MOD:00046","type":"exact"},{"name":"PomBase_original_PRO_term_name: histone H3.3, initiator methionine removed K9-methylated and phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht3/InitMet-/K9MePhos:1","type":"exact"},{"name":"UniProtKB:P10651, 2-136, Lys-10, MOD:00663|Ser-11, MOD:00046","type":"exact"},{"name":"hht3/Me(K9),Phos(S10)","type":"exact"}],"termid":"PR:000085728"}


id: GO:0086023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals beginning with a G protein-coupled adrenergic cell surface receptor combining with epinephrine or norepinephrine, to activate adenylate cyclase, which contributes to a circulatory system process carried out by the heart.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylate cyclase-activating adrenergic receptor signaling pathway","termid":"GO:0071880"},{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway involved in heart process","termid":"GO:0086103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"adenylate cyclase-activating adrenergic receptor signaling pathway involved in heart process","synonyms":[{"name":"adrenergic receptor signaling pathway involved in heart process","type":"exact"},{"name":"adrenergic receptor signalling pathway involved in heart process","type":"exact"},{"name":"beta-adrenergic receptor signalling pathway involved in heart process","type":"narrow"}],"termid":"GO:0086023"}


id: GO:0004560
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an alpha-L-fucoside + H2O = an alcohol + L-fucose.","definition_xrefs":["EC:3.2.1.51"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fucosidase activity","termid":"GO:0015928"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016798"],"is_obsolete":false,"name":"alpha-L-fucosidase activity","secondary_identifiers":["MetaCyc:ALPHA-L-FUCOSIDASE-RXN","Reactome:R-HSA-5693807","RHEA:12288"],"synonyms":[{"name":"alpha-L-fucoside fucohydrolase activity","type":"related"},{"name":"alpha-fucosidase activity","type":"related"}],"termid":"GO:0004560"}


id: PBO:0055448
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 2880","termid":"PBO:0055448"}


id: MONDO:0020518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hashimoto-Pritzker histiocytosis (HPH) is a variant of Langerhans cell histiocytosis characterized by multiple disseminated skin lesions (firm, red-brown, painless papulo-nodules).","definition_xrefs":["Orphanet:99872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Langerhans cell histiocytosis specific to childhood","termid":"MONDO:0017025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"Hashimoto-Pritzker syndrome","secondary_identifiers":["GARD:2604","icd11.foundation:1011705244","ICD9:277.89","SCTID:404160007","MESH:C535843","MEDGEN:775638","UMLS:C3661439"],"synonyms":[{"name":"Hashimoto-Pritzker disease","type":"related"},{"name":"Hashimoto-Pritzker histiocytosis","type":"related"},{"name":"congenital Langerhans cell histiocytosis","type":"exact"}],"termid":"MONDO:0020518","xrefs":{"Monarch":{"xref_id":"0020518"}}}


id: GO:0052235
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism towards a lower concentration of environmental oxygen within a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative aerotaxis in other organism involved in symbiotic interaction (obsolete GO:0052235)","synonyms":[{"name":"negative aerotaxis in other organism during symbiotic interaction","type":"related"},{"name":"negative aerotaxis within other organism during symbiotic interaction","type":"exact"}],"termid":"GO:0052235"}


id: PBO:0028468
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-curved_cytoplasmic_microtubules","termid":"PBO:0028468"}


id: PBO:0083453
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 CYC8","termid":"PBO:0083453"}


id: FYPO:0000866
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 dimethylation of lysine at position 9 of histone H3 is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002494","FYPO:0001985","FYPO:0002274","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal histone H3-K9 dimethylation during vegetative growth","synonyms":[{"name":"abnormal histone H3 K9 dimethylation during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 dimethylation during mitotic cell cycle","type":"related"},{"name":"abnormal histone H3K9 dimethylation during vegetative growth","type":"exact"},{"name":"abnormal histone H3K9me2 during vegetative growth","type":"exact"},{"name":"abnormal histone lysine H3 K9 dimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000866"}


id: PBO:0072536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 66","termid":"PBO:0072536"}


id: GO:1900025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of substrate adhesion-dependent cell spreading.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell-substrate adhesion","termid":"GO:0010812"},{"relation_name":"is_a","term_name":"regulation of substrate adhesion-dependent cell spreading","termid":"GO:1900024"},{"relation_name":"negatively_regulates","term_name":"substrate adhesion-dependent cell spreading","termid":"GO:0034446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of substrate adhesion-dependent cell spreading","synonyms":[{"name":"down regulation of cell spreading during cell substrate adhesion","type":"exact"},{"name":"down regulation of substrate adhesion dependent cell spreading","type":"exact"},{"name":"down regulation of substrate adhesion-dependent cell spreading","type":"related"},{"name":"negative regulation of cell spreading during cell substrate adhesion","type":"exact"},{"name":"negative regulation of substrate adhesion dependent cell spreading","type":"exact"}],"termid":"GO:1900025"}


id: PBO:0073173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selectin E","termid":"PBO:0073173"}


id: PBO:0001451
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.26.4","termid":"PBO:0001451"}


id: PBO:0040523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-azacytidine induced 2","termid":"PBO:0040523"}


id: GO:1903248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of citrulline biosynthetic process.","definition_xrefs":["GOC:BHF","PMID:19278978","GO_REF:0000058","GOC:TermGenie","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"is_a","term_name":"regulation of amino acid biosynthetic process","termid":"GO:2000282"},{"relation_name":"regulates","term_name":"citrulline biosynthetic process","termid":"GO:0019240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"regulation of citrulline biosynthetic process","synonyms":[{"name":"regulation of citrulline anabolism","type":"exact"},{"name":"regulation of citrulline biosynthesis","type":"exact"},{"name":"regulation of citrulline formation","type":"exact"},{"name":"regulation of citrulline synthesis","type":"exact"}],"termid":"GO:1903248"}


id: GO:1903854
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of stress response to copper ion.","definition_xrefs":["GOC:TermGenie","GOC:kmv","GO_REF:0000058","PMID:23437011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of stress response to copper ion","termid":"GO:1903853"},{"relation_name":"negatively_regulates","term_name":"stress response to copper ion","termid":"GO:1990169"}],"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 stress response to copper ion","synonyms":[{"name":"down regulation of response to copper ion stress","type":"exact"},{"name":"down regulation of response to copper toxicity","type":"related"},{"name":"down regulation of stress response to copper ion","type":"exact"},{"name":"down-regulation of response to copper ion stress","type":"exact"},{"name":"down-regulation of response to copper toxicity","type":"related"},{"name":"down-regulation of stress response to copper ion","type":"exact"},{"name":"downregulation of response to copper ion stress","type":"exact"},{"name":"downregulation of response to copper toxicity","type":"related"},{"name":"downregulation of stress response to copper ion","type":"exact"},{"name":"inhibition of response to copper ion stress","type":"narrow"},{"name":"inhibition of response to copper toxicity","type":"related"},{"name":"inhibition of stress response to copper ion","type":"narrow"},{"name":"negative regulation of response to copper ion stress","type":"exact"},{"name":"negative regulation of response to copper toxicity","type":"related"}],"termid":"GO:1903854"}


id: MONDO:0011071
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The disorder is characterized by thrombocytopenia of varying severity and a predisposition to hematologic malignancies. It may be caused due to germ line variations in the RUNX1, ETV6 or ANKRD26 genes.","definition_xrefs":["PMID:28600339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"hereditary thrombocytopenia and hematologic cancer predisposition syndrome","secondary_identifiers":["NCIT:C162696","Orphanet:71290","SCTID:725034002","MESH:C563324","GARD:10352"],"synonyms":[{"name":"familial platelet syndrome with predisposition to acute myelogenous leukaemia","type":"related"},{"name":"familial thrombocytopenia with propensity to acute myelogenous leukaemia","type":"related"},{"name":"hereditary thrombocytopenia and hematologic cancer predisposition syndrome","type":"exact"},{"name":"thrombocytopenia, familial, with propensity to acute myelogenous leukaemia","type":"related"}],"termid":"MONDO:0011071","xrefs":{"Monarch":{"xref_id":"0011071"}}}


id: PBO:0081715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 641","termid":"PBO:0081715"}


id: GO:0071247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a chromate stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chromate","termid":"GO:0046687"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to chromate","termid":"GO:0071247"}


id: MONDO:0010534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia, X-linked, type 4 is characterized by ataxia, pyramidal tract signs and adult-onset dementia. It has been described in three generations of one large family. The disease manifests during early childhood with delayed walking and tremor. The pyramidal signs appear progressively and by adulthood memory problems and dementia gradually become apparent. Transmission is X-linked but the causative gene has not yet been identified. The disease is usually fatal during the sixth decade of life.","definition_xrefs":["Orphanet:85292"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked cerebellar ataxia","termid":"MONDO:0016612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"X-linked spinocerebellar ataxia type 4","secondary_identifiers":["MESH:C537316","UMLS:C1844933","DOID:0111832","OMIM:301840","icd11.foundation:1033689736","MEDGEN:337122","GARD:9980","SCTID:719818007"],"synonyms":[{"name":"SCAX4","type":"exact"},{"name":"Scax4","type":"related"},{"name":"X-linked ataxia-dementia syndrome","type":"exact"},{"name":"ataxia-dementia syndrome X-linked","type":"related"},{"name":"ataxia-dementia syndrome, X-linked","type":"related"},{"name":"spinocerebellar ataxia X-linked type 4","type":"related"},{"name":"spinocerebellar ataxia, X-linked 4","type":"related"},{"name":"spinocerebellar ataxia, X-linked type 4","type":"exact"}],"termid":"MONDO:0010534","xrefs":{"Monarch":{"xref_id":"0010534"}}}


id: PBO:0031301
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-spherical_vegetative_cell","termid":"PBO:0031301"}


id: PR:O14285
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spc34 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14285"],"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":"DASH complex subunit spc34 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8C9.17c","synonyms":[{"name":"Spom972h-spc34","type":"exact"},{"name":"outer kinetochore protein spc34 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14285"}


id: PBO:0066371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinol dehydrogenase 14","termid":"PBO:0066371"}


id: PBO:0081021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger C2HC-type containing 1C","termid":"PBO:0081021"}


id: PBO:0064603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 3 homeobox 1","termid":"PBO:0064603"}


id: GO:0140667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of oxytocin.","definition_xrefs":["PMID:25096581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene expression","termid":"GO:0010468"},{"relation_name":"regulates","term_name":"oxytocin production","termid":"GO:0036162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of oxytocin production","termid":"GO:0140667"}


id: PBO:0050561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine rich glycoprotein","termid":"PBO:0050561"}


id: PBO:0091966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase Plb5","termid":"PBO:0091966"}


id: GO:0097431
data:
  {"annotated_genes":["SJAG_02761","SJAG_02624"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[102330,120150],"is_not":false,"summary":null,"term":"GO:0097431"}]},"cv_name":"cellular_component","definition":"Either of the ends of a mitotic spindle, a spindle that forms as part of mitosis, where spindle microtubules are organized; usually contains a microtubule organizing center and accessory molecules, spindle microtubules and astral microtubules.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle pole","termid":"GO:0000922"},{"relation_name":"part_of","term_name":"mitotic spindle","termid":"GO:0072686"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02624":null,"SJAG_02761":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0072686"}],"interesting_parent_ids":["GO:0015630","GO:0072686","GO:0005575"],"is_obsolete":false,"name":"mitotic spindle pole","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0097431","terms_by_termid":{"GO:0097431":null}}


id: PBO:0054650
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 2055","termid":"PBO:0054650"}


id: MONDO:0005384
data:
  {"annotated_genes":["SJAG_02765","SJAG_00824","SJAG_01184"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024556"},{"annotations":[89083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014924"},{"annotations":[89082],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014925"}]},"cv_name":"mondo","definition":"A seizure caused by a localized disorder.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epilepsy","termid":"MONDO:0005027"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00824":null,"SJAG_01184":null,"SJAG_02765":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"focal epilepsy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:230381009","UMLS:C0014547","NCIT:C122812","DOID:2234","EFO:0004263","MEDGEN:41836","ICD9:345.50","MESH:D004828"],"synonyms":[{"name":"focal epilepsy","type":"exact"},{"name":"localisation-related epilepsy","type":"exact"},{"name":"partial epilepsy","type":"exact"}],"termid":"MONDO:0005384","terms_by_termid":{"MONDO:0014924":null,"MONDO:0014925":null,"MONDO:0024556":null},"xrefs":{"Monarch":{"xref_id":"0005384"}}}


id: PBO:0073515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain binding glutamate rich protein","termid":"PBO:0073515"}


id: GO:0010865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the stipule over time, from its formation to the mature structure. A stipule is one of (usually) a pair of appendages at the bases of leaves in many broad-leaved angiosperms.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"leaf development","termid":"GO:0048366"}],"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":"stipule development","termid":"GO:0010865"}


id: GO:1904064
data:
  {"annotated_genes":["SJAG_04551"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905665"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cation transmembrane transport.","definition_xrefs":["GO_REF:0000058","PMID:15304482","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of monoatomic ion transmembrane transport","termid":"GO:0034767"},{"relation_name":"is_a","term_name":"regulation of monoatomic cation transmembrane transport","termid":"GO:1904062"},{"relation_name":"positively_regulates","term_name":"monoatomic cation transmembrane transport","termid":"GO:0098655"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04551":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of cation transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of cation transmembrane transport","type":"narrow"},{"name":"up regulation of cation transmembrane transport","type":"exact"},{"name":"up-regulation of cation transmembrane transport","type":"exact"},{"name":"upregulation of cation transmembrane transport","type":"exact"}],"termid":"GO:1904064","terms_by_termid":{"GO:1905665":null}}


id: GO:0033698
data:
  {"annotated_genes":["SJAG_02439","SJAG_04576","SJAG_04758","SJAG_02846","SJAG_03441","SJAG_01230","SJAG_03255","SJAG_03867","SJAG_03230","SJAG_02981","SJAG_00581","SJAG_00441","SJAG_00868"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61737,63896,64679,77713,77841,78032,79226,80853,82141,91053,96588,108718,116231],"is_not":false,"summary":null,"term":"GO:0033698"}]},"cv_name":"cellular_component","definition":"A histone deacetylase complex which deacetylates histones preferentially in promoter regions. Composed of a two copies of catalytic histone deacetylase subunit (S. pombe Clr6/ S. cerevisiae Rpd3p), an Sds-3 family protein (S. pombe /S. cerevisiae Sds3(p) ), two copies of SIN3 family co-repressor (S. pombe Pst1/ S. cerevisiae Sin3p, a WD repeat protein/ histone chaperone (S. pombe Prw1/ S. cerevisiae Ume1p), and a zf- PHD finger ( S. pombe Png2/ S. cerevisiae Pho23p), plus 4 additional subunits, and associated factors.","definition_xrefs":["PMID:17450151","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Sin3-type complex","termid":"GO:0070822"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00441":null,"SJAG_00581":null,"SJAG_00868":null,"SJAG_01230":null,"SJAG_02439":null,"SJAG_02846":null,"SJAG_02981":null,"SJAG_03230":null,"SJAG_03255":null,"SJAG_03441":null,"SJAG_03867":null,"SJAG_04576":null,"SJAG_04758":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575","GO:0005654","GO:0005694"],"is_obsolete":false,"name":"Rpd3L complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0000508"],"synonyms":[{"name":"Clr6 histone deacetylase complex I/I'","type":"exact"},{"name":"Clr6L complex","type":"exact"},{"name":"Rpd3C(L)","type":"exact"},{"name":"Sin3L complex","type":"exact"}],"termid":"GO:0033698","terms_by_termid":{"GO:0033698":null}}


id: GO:0048351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of paraxial mesoderm cell fate specification.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mesodermal cell fate specification","termid":"GO:0042662"},{"relation_name":"is_a","term_name":"regulation of paraxial mesodermal cell fate specification","termid":"GO:0048349"},{"relation_name":"negatively_regulates","term_name":"paraxial mesodermal cell fate specification","termid":"GO:0048348"}],"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 paraxial mesodermal cell fate specification","synonyms":[{"name":"down regulation of paraxial mesodermal cell fate specification","type":"exact"},{"name":"down-regulation of paraxial mesodermal cell fate specification","type":"exact"},{"name":"downregulation of paraxial mesodermal cell fate specification","type":"exact"},{"name":"inhibition of paraxial mesodermal cell fate specification","type":"narrow"}],"termid":"GO:0048351"}


id: GO:0001003
data:
  {"annotated_genes":["SJAG_03354"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71701],"is_not":false,"summary":null,"term":"GO:0001003"}]},"cv_name":"molecular_function","definition":"Binding to a sequence of DNA that is a part of a type 2 promoter that controls transcription by RNA polymerase III. Type 2 promoters consist of an A box and a B box downstream of the transcription start site within the sequence within the sequence of the mature RNA. Type 2 promoters are found in many tRNA genes as well as in other small RNAs.","definition_xrefs":["PMID:12381659","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase III cis-regulatory region sequence-specific DNA binding","termid":"GO:0000992"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03354":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0000976"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0003677","GO:0005488","GO:0000976","GO:0003674"],"is_obsolete":false,"name":"RNA polymerase III type 2 promoter sequence-specific DNA binding","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0001031"],"synonyms":[{"name":"RNA polymerase III type 2 promoter DNA binding","type":"related"}],"termid":"GO:0001003","terms_by_termid":{"GO:0001003":null}}


id: PBO:0043115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic iron-sulfur assembly component 2A","termid":"PBO:0043115"}


id: PBO:0053720
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 930","termid":"PBO:0053720"}


id: MONDO:0011051
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dysplastic cortical hyperostosis","termid":"MONDO:0016357"}],"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":"lethal short-limb skeletal dysplasia, Al Gazali type","secondary_identifiers":["OMIM:601356","GARD:4827","MEDGEN:330467","MESH:C537598","Orphanet:646136","UMLS:C1832435"],"synonyms":[{"name":"dysplastic cortical hyperostosis, Al-Gazali type","type":"exact"},{"name":"lethal neonatal short limb dwarfism","type":"related"},{"name":"lethal short limb skeletal dysplasia Al Gazali type","type":"related"},{"name":"lethal short-limb skeletal dysplasia, Al Gazali type","type":"exact"}],"termid":"MONDO:0011051","xrefs":{"Monarch":{"xref_id":"0011051"}}}


id: PBO:0086510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains","termid":"PBO:0086510"}


id: GO:0097328
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 carboplatin stimulus.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to carboplatin","termid":"GO:0097328"}


id: GO:0009452
data:
  {"annotated_genes":["SJAG_01713","SJAG_01724","SJAG_04034","SJAG_04488"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77378,70376,109665,74234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006370"},{"annotations":[60622],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0106005"}]},"cv_name":"biological_process","definition":"The sequence of enzymatic reactions by which the RNA 5' cap structure, an inverted 7-methylguanosine linked via a 5'-5' triphosphate bridge (m7G(5')ppp(5')X) to the first transcribed residue, is added to a nascent transcript. Additional methylation can occur on the ribose sugars of the first and second nucleotides adjacent to the m7G nRNA cap. These methylations are often referred to as N6,2'-O-dimethyladenosine (m6,2A) and N6,2'-O-dimethylguanosine (m6,2G), respectively.","definition_xrefs":["PMID:9266685","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA capping","termid":"GO:0036260"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01713":null,"SJAG_01724":null,"SJAG_04034":null,"SJAG_04488":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"7-methylguanosine RNA capping","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"RNA capping","type":"broad"},{"name":"m(7)G RNA capping","type":"exact"}],"termid":"GO:0009452","terms_by_termid":{"GO:0006370":null,"GO:0106005":null}}


id: GO:0060300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the activity of a molecule that controls the survival, growth, differentiation and effector function of tissues and cells.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signaling receptor activity","termid":"GO:0010469"},{"relation_name":"is_a","term_name":"regulation of receptor binding","termid":"GO:1900120"}],"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 cytokine activity","termid":"GO:0060300"}


id: GO:0051174
data:
  {"annotated_genes":["SJAG_03170","SJAG_01906","SJAG_03940","SJAG_02613","SJAG_02785","SJAG_00053","SJAG_05314","SJAG_00685","SJAG_01187","SJAG_04422","SJAG_02380"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92356,59949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[78030,74975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[113365,117481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[120009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905707"},{"annotations":[114742,111715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071072"},{"annotations":[119536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902648"},{"annotations":[91641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905857"},{"annotations":[71907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006110"},{"annotations":[78029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043456"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving phosphorus or compounds containing phosphorus.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"phosphorus metabolic process","termid":"GO:0006793"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00685":null,"SJAG_01187":null,"SJAG_01906":null,"SJAG_02380":null,"SJAG_02613":null,"SJAG_02785":null,"SJAG_03170":null,"SJAG_03940":null,"SJAG_04422":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of phosphorus metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"regulation of phosphorus metabolism","type":"exact"}],"termid":"GO:0051174","terms_by_termid":{"GO:0006110":null,"GO:0043456":null,"GO:0045820":null,"GO:0071072":null,"GO:1902647":null,"GO:1902648":null,"GO:1905707":null,"GO:1905857":null,"GO:2001211":null}}


id: PBO:0054346
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 1739","termid":"PBO:0054346"}


id: PBO:0070521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L6 pseudogene 20","termid":"PBO:0070521"}


id: PBO:0077561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 268","termid":"PBO:0077561"}


id: MONDO:0008570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any thyrotoxic periodic paralysis in which the cause of the disease is a mutation in the CACNA1S gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"thyrotoxic periodic paralysis","termid":"MONDO:0019201"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyrotoxic periodic paralysis, susceptibility to, 1","secondary_identifiers":["MEDGEN:413199","OMIM:188580","UMLS:C2749982"],"synonyms":[{"name":"CACNA1S thyrotoxic periodic paralysis","type":"exact"},{"name":"TTPP1","type":"related"},{"name":"thyrotoxic periodic paralysis caused by mutation in CACNA1S","type":"exact"},{"name":"thyrotoxic periodic paralysis, susceptibility to, 1","type":"exact"},{"name":"thyrotoxic periodic paralysis, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0008570","xrefs":{"Monarch":{"xref_id":"0008570"}}}


id: PBO:0076840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TERF1 pseudogene 7","termid":"PBO:0076840"}


id: PR:Q9Y7T4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atg1 gene.","definition_xrefs":["UniProtKB:Q9Y7T4","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":"serine/threonine-protein kinase atg1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC63.08c","synonyms":[{"name":"Spom972h-atg1","type":"exact"},{"name":"autophagy-related protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"serine/threonine-protein kinase ppk36 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9Y7T4"}


id: PBO:0082931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic and mitochondrial histidine tRNA synthetase; efficient mitochondrial localization requires both a presequence and an amino-terminal sequence; mutations in human ortholog HARS2 are associated with Perrault syndrome","termid":"PBO:0082931"}


id: PBO:0080499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vexin","termid":"PBO:0080499"}


id: PBO:0078875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional repressor GATA binding 1","termid":"PBO:0078875"}


id: MONDO:0012982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Episodic ataxia type 6 (EA6) is an exceedingly rare form of hereditary episodic ataxia with varying degrees of ataxia and associated findings including slurred speech, headache, confusion and hemiplegia.","definition_xrefs":["Orphanet:209967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary episodic ataxia","termid":"MONDO:0016227"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid transport","termid":"MONDO:0019216"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"episodic ataxia type 6","secondary_identifiers":["OMIM:612656","GARD:17107","DOID:0050994","icd11.foundation:1493336901","MESH:C567207","SCTID:718753002","MEDGEN:390739","UMLS:C2675211"],"synonyms":[{"name":"EA6","type":"related"},{"name":"SLC1A3 hereditary episodic ataxia","type":"exact"},{"name":"episodic ataxia type 6","type":"exact"},{"name":"episodic ataxia, type 6","type":"related"},{"name":"hereditary episodic ataxia caused by mutation in SLC1A3","type":"exact"}],"termid":"MONDO:0012982","xrefs":{"Monarch":{"xref_id":"0012982"}}}


id: PBO:0075437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPANX family member N2","termid":"PBO:0075437"}


id: PBO:0059070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"molybdenum cofactor synthesis 1","termid":"PBO:0059070"}


id: MONDO:0037251
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic congestive enlargement of the spleen leading to the destruction of blood cells resulting in pancytopenia.","definition_xrefs":["PMID:35800794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"splenic disorder","termid":"MONDO:0002332"}],"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:0005570","MONDO:0005046"],"is_obsolete":false,"name":"congestive splenomegaly","secondary_identifiers":["MESH:C537903","MEDGEN:56339","UMLS:C0154307","GARD:5888","SCTID:19058002"],"synonyms":[{"name":"Banti syndrome","type":"exact"},{"name":"Banti's disease","type":"exact"},{"name":"Banti's spleen","type":"exact"},{"name":"Banti's syndrome","type":"exact"},{"name":"fibrocongestive splenomegaly","type":"related"},{"name":"idiopathic congestive splenomegaly","type":"related"},{"name":"idiopathic portal hypertension","type":"related"}],"termid":"MONDO:0037251","xrefs":{"Monarch":{"xref_id":"0037251"}}}


id: MONDO:0006405
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infrequent small cell carcinoma that arises from the salivary glands and is characterized by the presence of a high number of mitotic figures.","definition_xrefs":["NCIT:C35703"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"salivary gland carcinoma","termid":"MONDO:0000521"},{"relation_name":"is_a","term_name":"digestive system neuroendocrine neoplasm","termid":"MONDO:0024503"}],"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":"salivary gland small cell carcinoma","secondary_identifiers":["EFO:1000519","MEDGEN:234786","UMLS:C1335982"],"synonyms":[{"name":"anaplastic small cell carcinoma of salivary gland","type":"exact"},{"name":"anaplastic small cell carcinoma of the salivary gland","type":"exact"},{"name":"neuroendocrine carcinoma of salivary gland","type":"exact"},{"name":"neuroendocrine carcinoma of the salivary gland","type":"exact"},{"name":"saliva-secreting gland small cell carcinoma","type":"exact"},{"name":"salivary gland anaplastic small cell carcinoma","type":"exact"},{"name":"salivary gland neuroendocrine carcinoma","type":"related"},{"name":"salivary gland small cell carcinoma","type":"exact"},{"name":"small cell carcinoma of saliva-secreting gland","type":"exact"},{"name":"small cell salivary gland carcinoma","type":"exact"}],"termid":"MONDO:0006405","xrefs":{"Monarch":{"xref_id":"0006405"}}}


id: GO:0046372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving D-arabinose, the D-enantiomer of arabino-pentose. D-arabinose occurs in plant glycosides and is a constituent of arabinonucleosides.","definition_xrefs":["GOC:jsg","GOC:mah","ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete D-arabinose metabolic process (obsolete GO:0046372)","synonyms":[{"name":"D-arabinose metabolism","type":"exact"}],"termid":"GO:0046372"}


id: MONDO:0013222
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Miyoshi myopathy","termid":"MONDO:0009685"}],"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":"Miyoshi muscular dystrophy 3","secondary_identifiers":["MEDGEN:413750","DOID:0070201","MESH:C567645","OMIM:613319","Orphanet:399096","GARD:17653","UMLS:C2750076"],"synonyms":[{"name":"MMD3","type":"exact"},{"name":"Miyoshi muscular dystrophy 3","type":"exact"},{"name":"Miyoshi muscular dystrophy type 3","type":"exact"},{"name":"Miyoshi myopathy 3","type":"related"},{"name":"distal anoctaminopathy","type":"exact"}],"termid":"MONDO:0013222","xrefs":{"Monarch":{"xref_id":"0013222"}}}


id: GO:0042857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving the siderophore chrysobactin (alpha-N-(2,3-dihydroxybenzoyl)-D-lysyl-L-serine).","definition_xrefs":["GOC:jl","PMID:8837459"],"gene_count":0,"genotype_count":0,"name":"obsolete chrysobactin metabolic process (obsolete GO:0042857)","synonyms":[{"name":"chrysobactin metabolism","type":"exact"}],"termid":"GO:0042857"}


id: MONDO:0020950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections of the eye caused by minute intracellular agents. These infections may lead to severe inflammation in various parts of the eye - conjunctiva, iris, eyelids, etc. Several viruses have been identified as the causative agents. Among these are Herpesvirus, Adenovirus, Poxvirus, and Myxovirus.","definition_xrefs":["MESH:D015828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease","termid":"MONDO:0005108"},{"relation_name":"is_a","term_name":"eye infectious disorder","termid":"MONDO:0043885"}],"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":"viral eye infection","secondary_identifiers":["MEDGEN:8753","SCTID:312132001","UMLS:C0015407"],"synonyms":[{"name":"EYE INFECT VIRAL","type":"related"},{"name":"Eye Infection, Viral","type":"related"},{"name":"Eye Infections, Viral","type":"related"},{"name":"Infection, Viral Eye","type":"related"},{"name":"Infection, Viral Ocular","type":"related"},{"name":"Infections, Viral Eye","type":"related"},{"name":"Infections, Viral Ocular","type":"related"},{"name":"OCULAR INFECT VIRAL","type":"related"},{"name":"Ocular Infection, Viral","type":"related"},{"name":"Ocular Infections, Viral","type":"related"},{"name":"VIRAL EYE INFECT","type":"related"},{"name":"Viral Eye Infection","type":"related"},{"name":"Viral Eye Infections","type":"related"},{"name":"Viral Ocular Infection","type":"related"},{"name":"Viral Ocular Infections","type":"related"},{"name":"Viral eye infection","type":"related"},{"name":"viral eye infection","type":"exact"}],"termid":"MONDO:0020950","xrefs":{"Monarch":{"xref_id":"0020950"}}}


id: PBO:0072379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27a pseudogene 5","termid":"PBO:0072379"}


id: PBO:0045448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydropyrimidinase","termid":"PBO:0045448"}


id: PBO:0114500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Uridine nucleosidase (uridine-cytidine N-ribohydrolase); cleaves N-glycosidic bonds in nucleosides; dual roles in NAD+ biosynthesis and the nucleobase salvage pathway; monomeric structure unique to this class of enzymes","termid":"PBO:0114500"}


id: PBO:0031253
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_regulation_of_cytokinesis","termid":"PBO:0031253"}


id: FYPO:0007799
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a protein that is not normally found at the cell surface is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized protein during vegetative growth","termid":"FYPO:0000782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"protein mislocalized to cell surface during vegetative growth","synonyms":[{"name":"ectopic protein localization to cell surface during vegetative growth","type":"exact"},{"name":"protein mislocalised to cell surface during vegetative growth","type":"exact"},{"name":"protein mislocalized to cell surface during mitotic cell cycle","type":"related"}],"termid":"FYPO:0007799"}


id: PBO:0002083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosamine-phosphate N-acetyltransferase (predicted)","termid":"PBO:0002083"}


id: PBO:0048544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guided entry of tail-anchored proteins factor 4","termid":"PBO:0048544"}


id: GO:0140670
data:
  {"annotated_genes":["SJAG_04508","SJAG_02606"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72393,112544],"is_not":false,"summary":null,"term":"GO:0140670"}]},"cv_name":"molecular_function","definition":"Facilitating a conformational change to unload a cohesin complex from sister chromatids.","definition_xrefs":["PMID:26687354"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity, acting on DNA","termid":"GO:0140097"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02606":null,"SJAG_04508":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140097","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"cohesin unloader activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"cohesin unloading activity","type":"exact"}],"termid":"GO:0140670","terms_by_termid":{"GO:0140670":null}}


id: GO:1902296
data:
  {"annotated_genes":["SJAG_00874","SJAG_04190","SJAG_00729","SJAG_00863","SJAG_03780","SJAG_05197","SJAG_02182","SJAG_02908","SJAG_04877","SJAG_03495","SJAG_02199","SJAG_04879","SJAG_02667","SJAG_01823","SJAG_00272","SJAG_01010","SJAG_00814","SJAG_02818"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114511,69175,111928,115564,117404,72252,67093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902983"},{"annotations":[120196,97189,111088,106900,106182,104782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903459"},{"annotations":[97222,95913,97190,106901,108954,106183,109323,91523],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903460"}]},"cv_name":"biological_process","definition":"Any DNA strand elongation that is involved in cell cycle DNA replication.","definition_xrefs":["GOC:TermGenie","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA strand elongation involved in DNA replication","termid":"GO:0006271"},{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"cell cycle DNA replication","termid":"GO:0044786"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_00874":null,"SJAG_01010":null,"SJAG_01823":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02667":null,"SJAG_02818":null,"SJAG_02908":null,"SJAG_03495":null,"SJAG_03780":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_05197":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006260","GO:0007049","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"DNA strand elongation involved in cell cycle DNA replication","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"DNA replication elongation involved in cell cycle DNA replication","type":"exact"},{"name":"DNA strand elongation during DNA replication involved in cell cycle DNA replication","type":"related"}],"termid":"GO:1902296","terms_by_termid":{"GO:1902983":null,"GO:1903459":null,"GO:1903460":null}}


id: PBO:0077901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tryptase delta 1","termid":"PBO:0077901"}


id: PBO:0086371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative aryl alcohol dehydrogenase; similar to Phanerochaete chrysosporium aryl alcohol dehydrogenase; ORFs AAD6/YFL056C and AAD16/YFL057C are displaced from one another by -1 frameshift; members of the AAD gene family comprise three pairs (AAD3 + AAD15, AAD6/AAD16 + AAD4, AAD10 + AAD14) whose two genes are more related to one another than to other members of the family","termid":"PBO:0086371"}


id: PBO:0027746
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_regulation_of_sexual_differentiation_gene_mRNA_during_nitrogen_starvation","termid":"PBO:0027746"}


id: PBO:0089952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingolipid biosynthesis protein","termid":"PBO:0089952"}


id: MONDO:0024270
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections of the INTESTINES with PARASITES, commonly involving PARASITIC WORMS. Infections with roundworms (NEMATODE INFECTIONS) and tapeworms (CESTODE INFECTIONS) are also known as HELMINTHIASIS.","definition_xrefs":["MESH:D007411"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"},{"relation_name":"is_a","term_name":"parasitic infectious disease","termid":"MONDO:0005135"},{"relation_name":"is_a","term_name":"digestive system infectious disorder","termid":"MONDO:0043424"}],"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":"parasitic intestinal disorder","secondary_identifiers":["UMLS:C0021832","EFO:0009561","MEDGEN:7131"],"synonyms":[{"name":"disease, parasitic intestinal","type":"related"},{"name":"diseases, parasitic intestinal","type":"related"},{"name":"intestinal disease, parasitic","type":"related"},{"name":"intestine parasitic infection","type":"exact"},{"name":"parasitic intestinal disease","type":"exact"},{"name":"parasitic intestinal diseases","type":"related"}],"termid":"MONDO:0024270","xrefs":{"Monarch":{"xref_id":"0024270"}}}


id: PBO:0002777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromatin silencing protein Clr2","termid":"PBO:0002777"}


id: PBO:0042824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxylesterase 3","termid":"PBO:0042824"}


id: PBO:0088081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ub-like protein; Ub-like protein conjugated to phosphatidylethanolamine (PE); role in membrane fusion during autophagosome formation; membrane anchored Atg8p-PE is involved in phagophore expansion during autophagosome formation; deconjugation is also required for biogenesis; targets Atg1p to autophagosomes; binds to the Atg1p-Atg13p complex, triggers its vacuolar degradation; role in vacuolar membrane protein turnover during early stationary phase; component of autophagosomes and Cvt vesicles","termid":"PBO:0088081"}


id: MONDO:0957112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular channelopathy","termid":"MONDO:0019119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurological muscular channelopathy due to a genetic chloride channel defect","secondary_identifiers":["UMLS:C5681687","Orphanet:98739","GARD:19564","MEDGEN:1843259"],"termid":"MONDO:0957112","xrefs":{"Monarch":{"xref_id":"0957112"}}}


id: PBO:0012292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FACT complex subunit Pob3","termid":"PBO:0012292"}


id: MONDO:0019768
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Golabi-Ito-Hall syndrome is an X-linked intellectual disability syndrome (XLMR) characterized by intellectual deficiency, microcephaly and short stature. It belongs to the group of disorders collectively referred to as Renpenning syndrome.","definition_xrefs":["Orphanet:93947"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Renpenning syndrome","termid":"MONDO:0010653"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked intellectual disability, Golabi-Ito-hall type","secondary_identifiers":["UMLS:C5681614","MEDGEN:1842639","GARD:19241"],"termid":"MONDO:0019768","xrefs":{"Monarch":{"xref_id":"0019768"}}}


id: GO:0016213
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the introduction of a cis double bond at carbon 6 of acyl-CoAs, introducing a new double bond between a pre-existing double bond and the carboxyl-end of the fatty acid. Specific reactions include: (9Z,12Z)-octadecadienoyl-CoA + 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 = (6Z,9Z,12Z)-octadecatrienoyl-CoA + 2 Fe(III)-[cytochrome b5] + 2 H2O; and (9Z,12Z,15Z)-octadecatrienoyl-CoA + 2 Fe(II)-[cytochrome b5] + O2 + 2 H+ = (6Z,9Z,12Z,15Z)-octadecatetraenoyl-CoA + 2 Fe(III)-[cytochrome b5] + 2 H2O.","definition_xrefs":["PMID:7212717","EC:1.14.19.3","PMID:12713571"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA desaturase activity","termid":"GO:0016215"}],"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:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"acyl-CoA 6-desaturase activity","secondary_identifiers":["Reactome:R-HSA-2046084","MetaCyc:1.14.19.3-RXN","Reactome:R-HSA-2046097","Reactome:R-HSA-2046099","Reactome:R-HSA-2046096"],"synonyms":[{"name":"delta(6)-acyl CoA desaturase activity","type":"broad"},{"name":"delta(6)-desaturase activity","type":"broad"},{"name":"delta(6)-fatty acyl-CoA desaturase activity","type":"broad"},{"name":"delta6-acyl CoA desaturase activity","type":"related"},{"name":"delta6-desaturase activity","type":"related"},{"name":"delta6-fatty acyl-CoA desaturase activity","type":"related"},{"name":"fatty acid 6-desaturase activity","type":"broad"},{"name":"fatty acid delta(6)-desaturase activity","type":"broad"},{"name":"fatty acid delta6-desaturase activity","type":"related"},{"name":"linoleate desaturase activity","type":"related"},{"name":"linoleic acid desaturase activity","type":"related"},{"name":"linoleic desaturase activity","type":"related"},{"name":"linoleoyl CoA desaturase activity","type":"exact"},{"name":"linoleoyl-CoA desaturase activity","type":"exact"},{"name":"linoleoyl-coenzyme A desaturase activity","type":"exact"},{"name":"long-chain fatty acid delta(6)-desaturase activity","type":"broad"},{"name":"long-chain fatty acid delta6-desaturase activity","type":"related"}],"termid":"GO:0016213"}


id: MONDO:0001546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloarthropathy","termid":"MONDO:0005095"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"hypermobility of coccyx","secondary_identifiers":["ICD9:724.71","DOID:12537","icd11.foundation:588794167","MEDGEN:510502","SCTID:202809009","UMLS:C0158295"],"synonyms":[{"name":"coccygeal hypermobility syndrome","type":"exact"},{"name":"hypermobility of the coccyx","type":"exact"}],"termid":"MONDO:0001546","xrefs":{"Monarch":{"xref_id":"0001546"}}}


id: MONDO:0007947
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder of the connective tissue. Connective tissue provides strength and flexibility to structures throughout the body such as bones, ligaments, muscles, walls of blood vessels, and heart valves. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body (the aorta). It is caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Marfan syndrome is inherited in an autosomal dominant pattern. At least 25% of cases are due to a new (de novo) mutation. Treatment is based on the signs and symptoms in each person.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare disease with thoracic aortic aneurysm and aortic dissection (obsolete MONDO:0017311)","termid":"MONDO:0017311"},{"relation_name":"excluded_subClassOf","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic myopia (obsolete MONDO:0020208)","termid":"MONDO:0020208"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic keratoconus (obsolete MONDO:0020211)","termid":"MONDO:0020211"},{"relation_name":"excluded_subClassOf","term_name":"obsolete lens position anomaly (obsolete MONDO:0020236)","termid":"MONDO:0020236"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"Marfan and Marfan-related disorder","termid":"MONDO:0017310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Marfan syndrome","secondary_identifiers":["MedDRA:10026829","DOID:14323","NCIT:C34807","NORD:1403","MESH:D008382","Orphanet:558","icd11.foundation:236564145","OMIM:154700","UMLS:C0024796","MEDGEN:44287","Orphanet:284963","NANDO:1200644","NANDO:2200968","GARD:16535","SCTID:19346006","ICD9:759.82","ICD10CM:Q87.4"],"synonyms":[{"name":"MFS","type":"exact"},{"name":"MFS1","type":"exact"},{"name":"Marfan syndrome","type":"exact"},{"name":"Marfan syndrome type 1","type":"exact"},{"name":"Marfan syndrome, type 1","type":"exact"},{"name":"Marfan's syndrome","type":"exact"}],"termid":"MONDO:0007947","xrefs":{"Monarch":{"xref_id":"0007947"}}}


id: PBO:0044678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA damage inducible 1 homolog 2","termid":"PBO:0044678"}


id: GO:2001036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of tongue muscle cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of skeletal muscle fiber differentiation","termid":"GO:1902810"},{"relation_name":"is_a","term_name":"regulation of tongue muscle cell differentiation","termid":"GO:2001035"},{"relation_name":"negatively_regulates","term_name":"tongue muscle cell differentiation","termid":"GO:0035981"}],"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 tongue muscle cell differentiation","termid":"GO:2001036"}


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


id: MONDO:1012785
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cerebellar ataxia that occurs in dogs due to a mutation in the ITPR1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar ataxia, dog","termid":"MONDO:1012957"},{"relation_name":"is_a","term_name":"hereditary cerebellar ataxia, non-human animal","termid":"MONDO:1012960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinocerebellar ataxia, ITPR1-related, dog","secondary_identifiers":["OMIA:002097-9615"],"synonyms":[{"name":"SCAIS","type":"exact"},{"name":"ataxia, spinocerebellar, ITPR1-related, dog","type":"exact"}],"termid":"MONDO:1012785","xrefs":{"Monarch":{"xref_id":"1012785"}}}


id: PBO:0031469
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_glutathione_gamma-glutamylcysteinyltransferase_activity","termid":"PBO:0031469"}


id: PBO:0040352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit g pseudogene 1","termid":"PBO:0040352"}


id: PBO:0051703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INPP5B antisense RNA 1","termid":"PBO:0051703"}


id: PBO:0073539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain containing ring finger 1","termid":"PBO:0073539"}


id: MONDO:0008654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nystagmus","termid":"MONDO:0005712"},{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia","termid":"MONDO:0020380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0002039","MONDO:0002320","MONDO:0005559"],"is_obsolete":false,"name":"spinocerebellar ataxia 27A","secondary_identifiers":["MESH:C537856","OMIM:193003"],"synonyms":[{"name":"NYS4","type":"exact"},{"name":"NYSTAGMUS 4, congenital, autosomal dominant","type":"exact"},{"name":"nystagmus 4, congenital, autosomal dominant","type":"exact"},{"name":"vestibulocerebellar disorder with predominant ocular signs","type":"related"}],"termid":"MONDO:0008654","xrefs":{"Monarch":{"xref_id":"0008654"}}}


id: RO:0002085
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"during_which_starts","termid":"RO:0002088"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encompasses","termid":"RO:0002085"}


id: PBO:0001682
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"assembly at damage sites is facilitated by Swi5 independently of Rhp57","termid":"PBO:0001682"}


id: PBO:0085758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase involved in oxidative stress response; promotes pseudohyphal growth via activation of Ubp3p phosphorylation; identified as suppressor of S. pombe cell cycle checkpoint mutations; RCK1 has a paralog, RCK2, that arose from the whole genome duplication","termid":"PBO:0085758"}


id: GO:0106354
data:
  {"annotated_genes":["SJAG_01521","SJAG_03984","SJAG_01176","SJAG_03276","SJAG_03179","SJAG_04006","SJAG_01818","SJAG_04153","SJAG_01191","SJAG_00854","SJAG_04321","SJAG_04824","SJAG_16455","SJAG_04818","SJAG_03745","SJAG_02275","SJAG_01702","SJAG_04084"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96914,117542,92258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180037"},{"annotations":[76966,72167,99197,79570,109439,104043,74333,90327,73508,101568,117888,108441,117449,72512,73216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071038"}]},"cv_name":"biological_process","definition":"The set of processes involved in identifying and degrading defective or aberrant tRNAs.","definition_xrefs":["GOC:mah","PMID:32841241"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA decay","termid":"GO:0016078"},{"relation_name":"is_a","term_name":"RNA surveillance","termid":"GO:0071025"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00854":null,"SJAG_01176":null,"SJAG_01191":null,"SJAG_01521":null,"SJAG_01702":null,"SJAG_01818":null,"SJAG_02275":null,"SJAG_03179":null,"SJAG_03276":null,"SJAG_03745":null,"SJAG_03984":null,"SJAG_04006":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04321":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_16455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006399","GO:0008150"],"is_obsolete":false,"name":"tRNA surveillance","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0106354","terms_by_termid":{"GO:0071038":null,"GO:0180037":null}}


id: PBO:0011447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex subunit Sec3","termid":"PBO:0011447"}


id: GO:0034043
data:
  {"annotated_genes":["SJAG_03724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98099],"is_not":false,"summary":null,"term":"GO:0034043"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of 5-hydroxymethyluracil bases by cleaving the N-C1' glycosidic bond between the oxidized pyrimidine and the deoxyribose sugar.","definition_xrefs":["PMID:17641464","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity","termid":"GO:0000703"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140097"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0140097","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"5-hydroxymethyluracil DNA N-glycosylase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"5-hmU DNA N-glycosylase activity","type":"exact"}],"termid":"GO:0034043","terms_by_termid":{"GO:0034043":null}}


id: PBO:0003483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal lysine methyltransferase Set10","termid":"PBO:0003483"}


id: MONDO:0011688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with variable penetrance of intellectual disability and structural brain abnormalities that has material basis in homozygous or compound heterozygous mutation in the FKRP gene on chromosome 19q13.3.","definition_xrefs":["PMID:11592034","PMID:14652796","DOID:0110635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type B","termid":"MONDO:0000172"},{"relation_name":"is_a","term_name":"myopathy caused by variation in FKRP","termid":"MONDO:0700066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005066","MONDO:0024322","MONDO:0002320"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy type B5","secondary_identifiers":["MESH:C564691","OMIM:606612","MEDGEN:335764","Orphanet:52428","UMLS:C1847759"],"synonyms":[{"name":"FKRP-related congenital muscular dystrophy","type":"exact"},{"name":"MDC1C","type":"exact"},{"name":"MDDGB5","type":"exact"},{"name":"congenital muscular dystrophy 1C","type":"exact"},{"name":"congenital muscular dystrophy-FKRP related","type":"exact"},{"name":"muscular dystrophy, congenital, 1C","type":"related"},{"name":"muscular dystrophy, congenital, FKRP-related","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with or without intellectual disability), type B, 5","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5","type":"exact"}],"termid":"MONDO:0011688","xrefs":{"Monarch":{"xref_id":"0011688"}}}


id: GO:0047803
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-cysteine + sulfite = L-cysteate + sulfide.","definition_xrefs":["EC:4.4.1.10","MetaCyc:CYSTEINE-LYASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"cysteine lyase activity","secondary_identifiers":["RHEA:20916"],"synonyms":[{"name":"L-cysteine hydrogen-sulfide-lyase (adding sulfite)","type":"related"},{"name":"L-cysteine hydrogen-sulfide-lyase (adding sulfite; L-cysteate-forming)","type":"related"},{"name":"cysteine (sulfite) lyase activity","type":"related"}],"termid":"GO:0047803"}


id: GO:0000073
data:
  {"annotated_genes":["SJAG_00794","SJAG_00773","SJAG_04745"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77705,79701,97262],"is_not":false,"summary":null,"term":"GO:0000073"}]},"cv_name":"biological_process","definition":"The release of duplicated mitotic spindle pole bodies (SPBs) that begins with the nucleation of microtubules from each SPB within the nucleus, leading to V-shaped spindle microtubules. Interpolar microtubules that elongate from each pole are interconnected, forming overlapping microtubules. Capturing and antiparallel sliding apart of microtubules promotes the initial separation of the SPB.","definition_xrefs":["GOC:vw","GOC:sgd_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle pole body separation","termid":"GO:0110100"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic spindle formation (spindle phase one)","termid":"GO:0061804"},{"relation_name":"part_of","term_name":"mitotic spindle pole body organization","termid":"GO:1905047"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00773":null,"SJAG_00794":null,"SJAG_04745":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0000070"},{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007010","GO:0000070","GO:0000226","GO:0044085","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"initial mitotic spindle pole body separation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0030475"],"termid":"GO:0000073","terms_by_termid":{"GO:0000073":null}}


id: PBO:0069522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 791, pseudogene","termid":"PBO:0069522"}


id: PBO:0030652
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cell_cycle_arrest_in_mitotic_G2_phase_during_starvation","termid":"PBO:0030652"}


id: GO:0036062
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A region that surrounds the active zone of the presynaptic plasma membrane, and is specialized for the control of synaptic development.","definition_xrefs":["GOC:sart","PMID:10976048","PMID:18439406"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synaptic membrane","termid":"GO:0097060"},{"relation_name":"part_of","term_name":"presynaptic membrane","termid":"GO:0042734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"presynaptic periactive zone","synonyms":[{"name":"periactive zone","type":"exact"},{"name":"pre-synaptic periactive zone","type":"exact"}],"termid":"GO:0036062"}


id: GO:0007530
data:
  {"annotated_genes":["SJAG_02319","SJAG_01113","SJAG_02460","SJAG_03997","SJAG_02401","SJAG_02724","SJAG_00320","SJAG_01419","SJAG_01465","SJAG_05153","SJAG_03221","SJAG_01410","SJAG_00399","SJAG_01677","SJAG_01495","SJAG_01068","SJAG_01601","SJAG_01076","SJAG_00757","SJAG_02556","SJAG_06638","SJAG_00073","SJAG_02828","SJAG_02079","SJAG_02226","SJAG_03097","SJAG_03006","SJAG_00769","SJAG_00247","SJAG_00293","SJAG_05239"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95335,118207,120864,101068,118847,118535,93185,89876],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007535"},{"annotations":[99369,112288,110489,118800,89877,101069,98128,112810,91239,120783,117020,108036,91112,108603,102540],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007534"},{"annotations":[121112,121113,109021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007531"},{"annotations":[94625,101007,98599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007533"},{"annotations":[104911,61481,96028,110490],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071515"},{"annotations":[95300],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071171"}]},"cv_name":"biological_process","definition":"Any process that establishes and transmits the specification of sexual status of an individual organism.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"}],"gene_count":31,"genes_by_uniquename":{"SJAG_00073":null,"SJAG_00247":null,"SJAG_00293":null,"SJAG_00320":null,"SJAG_00399":null,"SJAG_00757":null,"SJAG_00769":null,"SJAG_01068":null,"SJAG_01076":null,"SJAG_01113":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01465":null,"SJAG_01495":null,"SJAG_01601":null,"SJAG_01677":null,"SJAG_02079":null,"SJAG_02226":null,"SJAG_02319":null,"SJAG_02401":null,"SJAG_02460":null,"SJAG_02556":null,"SJAG_02724":null,"SJAG_02828":null,"SJAG_03006":null,"SJAG_03097":null,"SJAG_03221":null,"SJAG_03997":null,"SJAG_05153":null,"SJAG_05239":null,"SJAG_06638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"sex determination","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Wikipedia:Sex-determination_system"],"termid":"GO:0007530","terms_by_termid":{"GO:0007531":null,"GO:0007533":null,"GO:0007534":null,"GO:0007535":null,"GO:0071171":null,"GO:0071515":null}}


id: PBO:0001481
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.26","termid":"PBO:0001481"}


id: PBO:0081983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and SCAN domain containing 9","termid":"PBO:0081983"}


id: PBO:0029225
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_homologous_chromosome_pairing","termid":"PBO:0029225"}


id: GO:1904342
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of colon smooth muscle contraction.","definition_xrefs":["GO_REF:0000058","PMID:24170253","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of gastro-intestinal system smooth muscle contraction","termid":"GO:1904305"},{"relation_name":"is_a","term_name":"regulation of colon smooth muscle contraction","termid":"GO:1904341"},{"relation_name":"negatively_regulates","term_name":"colon smooth muscle contraction","termid":"GO:1990765"}],"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 colon smooth muscle contraction","synonyms":[{"name":"down regulation of colon smooth muscle contraction","type":"exact"},{"name":"down-regulation of colon smooth muscle contraction","type":"exact"},{"name":"downregulation of colon smooth muscle contraction","type":"exact"},{"name":"inhibition of colon smooth muscle contraction","type":"narrow"}],"termid":"GO:1904342"}


id: PR:Q09670
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC5H10.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09670"],"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":"NADPH dehydrogenase C5H10.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5H10.04","synonyms":[{"name":"Old yellow enzyme homolog 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAC5H10.04","type":"exact"}],"termid":"PR:Q09670"}


id: FYPO:0002090
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which homologous chromosomes or sister chromatids do not move towards the spindle poles at the same time during nuclear division, but instead one or more chromosomes remain distant from the spindle pole after the bulk of the DNA has separated. Segregation may stop before completing separation of chromosomes, or may eventually be completed.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromosome segregation","termid":"FYPO:0000029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"lagging chromosomes","synonyms":[{"name":"chromosome segregation defects, lagging chromosomes","type":"exact"}],"termid":"FYPO:0002090"}


id: PBO:0082843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPII-coated vesicle protein; involved in vesicle formation and incorporation of specific secretory cargo; required for the delivery of bud-site selection protein Axl2p and Nha1p antiporter to cell surface; related to Drosophila cornichon; ERV14 has a paralog, ERV15, that arose from the whole genome duplication","termid":"PBO:0082843"}


id: PATO:0002217
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A molecular quality inhering in a bearer by virtue of the bearer's being combined, or impregnated, with nitric acid, or some of its compounds.","definition_xrefs":["neurolex:http://neurolex.org/wiki/Category:Nitrated_Molecular_Quality"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular quality","termid":"PATO:0002182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitrated","termid":"PATO:0002217"}


id: FYPO:0000112
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to sorbitol. Cells stop growing (and may die) at a concentration of sorbitol that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0002683","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to sorbitol","synonyms":[{"name":"hypersensitive to sorbitol","type":"exact"},{"name":"sensitive to glucitol","type":"exact"},{"name":"sensitive to sorbitol during mitotic cell cycle","type":"related"},{"name":"sensitive to sorbitol during vegetative growth","type":"exact"}],"termid":"FYPO:0000112"}


id: MONDO:0023152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrocartilaginous embolism (FCE) is a rare type of embolism (sudden blocking of an artery) that occurs in the spinal cord. FCE occurs when materials that are usually found within the vertebral disk of the spine enter into the nearby vascular system (veins and arteries) and block one of the spinal cord vessels. The signs and symptoms of FCE often develop after a minor or even unnoticed btriggering eventb such as lifting, straining, or falling. Symptoms of FCE may include neck and/or back pain, progressive muscle weakness, and paralysis.The exact underlying cause of FCE is poorly understood. Most cases occur sporadically in people with no family history of the disease. Diagnosis is based on imaging of the spinal cord and ruling out other causes of a blockage of the vascular system within the spinal cord. Treatment is generally focused on preventing possible complications and improving quality of life with medications and physical therapy.","definition_xrefs":["GARD:0009718"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrocartilaginous embolism","secondary_identifiers":["MEDGEN:419466","UMLS:C2931666","MESH:C537927"],"synonyms":[{"name":"embolism, fibrocartilaginous","type":"related"}],"termid":"MONDO:0023152","xrefs":{"Monarch":{"xref_id":"0023152"}}}


id: GO:0140664
data:
  {"annotated_genes":["SJAG_01410","SJAG_01419","SJAG_02708","SJAG_02748","SJAG_02267","SJAG_01620","SJAG_02187","SJAG_01807","SJAG_02226","SJAG_00757"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57291,58336,59394,60552,60933,62195,64368,65282,65958,69145],"is_not":false,"summary":null,"term":"GO:0140664"}]},"cv_name":"molecular_function","definition":"A molecule that recognises toxic DNA structures, and initiates a signaling response, driven by ATP hydrolysis.","definition_xrefs":["PMID:33510387","PMID:33302090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP-dependent activity, acting on DNA","termid":"GO:0008094"},{"relation_name":"is_a","term_name":"DNA damage sensor activity","termid":"GO:0140612"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00757":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01620":null,"SJAG_01807":null,"SJAG_02187":null,"SJAG_02226":null,"SJAG_02267":null,"SJAG_02708":null,"SJAG_02748":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140299"}],"interesting_parent_ids":["GO:0003824","GO:0140097","GO:0003674","GO:0140299","GO:0098772"],"is_obsolete":false,"name":"ATP-dependent DNA damage sensor activity","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"ATP-dependent DNA damage sensing activity","type":"exact"}],"termid":"GO:0140664","terms_by_termid":{"GO:0140664":null}}


id: FYPO:0007165
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cell cortex does not occur during the meiotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to cell cortex during vegetative growth","termid":"FYPO:0000930"},{"relation_name":"is_a","term_name":"abolished protein localization during meiotic cell cycle","termid":"FYPO:0005208"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to cell cortex during meiotic cell cycle","synonyms":[{"name":"protein absent from cell cortex during meiotic cell cycle","type":"related"},{"name":"protein localization to cell cortex abolished during meiotic cell cycle","type":"exact"}],"termid":"FYPO:0007165"}


id: MONDO:0001729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Meniere disease","termid":"MONDO:0007972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"active cochlear Meniere disease","secondary_identifiers":["DOID:13492","SCTID:194349005","UMLS:C0155497","MEDGEN:509990","ICD9:386.02"],"synonyms":[{"name":"active Meniere's disease, cochlear","type":"exact"},{"name":"active cochlear Meniere disease","type":"exact"},{"name":"active cochlear Meniere's disease","type":"exact"},{"name":"cochlear active Mnire's disease","type":"exact"}],"termid":"MONDO:0001729","xrefs":{"Monarch":{"xref_id":"0001729"}}}


id: GO:0098622
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + selenodiglutathione + NADPH = gluthathioselenol + glutathione + NADP+.","definition_xrefs":["RHEA:34927","PMID:1569062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disulfide oxidoreductase activity","termid":"GO:0015036"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor","termid":"GO:0016668"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0015036"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0015036","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"selenodiglutathione-disulfide reductase (NADPH) activity","secondary_identifiers":["Reactome:R-HSA-2408542"],"synonyms":[{"name":"selenodiglutathione-disulfide reductase (NADP) activity","type":"exact"},{"name":"selenodiglutathione-disulfide reductase activity","type":"broad"}],"termid":"GO:0098622"}


id: GO:0043682
data:
  {"annotated_genes":["SJAG_02399"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79716],"is_not":false,"summary":null,"term":"GO:0043682"}]},"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 + Cu2+(in) = ADP + phosphate + Cu2+(out).","definition_xrefs":["RHEA:10376"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper ion transmembrane transporter activity","termid":"GO:0005375"},{"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_02399":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"P-type divalent copper transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:TRANS-RXN-178","Reactome:R-HSA-6803545","GO:0004008","Reactome:R-HSA-936802","Reactome:R-HSA-3697838","EC:7.2.2.9","Reactome:R-HSA-936895"],"synonyms":[{"name":"Cu(2+)-exporting ATPase activity","type":"related"},{"name":"Cu2+-exporting ATPase activity","type":"related"},{"name":"copper exporting ATPase activity","type":"broad"},{"name":"copper transmembrane transporter activity, phosphorylative mechanism","type":"broad"},{"name":"copper-exporting ATPase activity","type":"narrow"},{"name":"copper-translocating P-type ATPase activity","type":"broad"},{"name":"copper-transporting ATPase activity","type":"broad"}],"termid":"GO:0043682","terms_by_termid":{"GO:0043682":null}}


id: MONDO:0043240
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of arthritis that affects hemophiliacs, which is characterized by bleeding into the joint space.","definition_xrefs":["NCIT:C27039"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthritic joint disease","termid":"MONDO:0005578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemophilic arthropathy","secondary_identifiers":["UMLS:C0263725","ICD10CM:M36.2","MEDGEN:120487","SCTID:80813006"],"synonyms":[{"name":"arthropathy in haemophilia","type":"related"},{"name":"arthropathy in hemophilia","type":"related"},{"name":"hemophilic arthritis","type":"exact"},{"name":"hemophilic arthropathy","type":"exact"}],"termid":"MONDO:0043240","xrefs":{"Monarch":{"xref_id":"0043240"}}}


id: GO:0009836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A fruit ripening process that involves a burst of respiration and ethylene (ethene) evolution at the onset.","definition_xrefs":["GOC:lr","ISBN:0521587840"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fruit ripening","termid":"GO:0009835"}],"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":"fruit ripening, climacteric","termid":"GO:0009836"}


id: PBO:0067733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 31","termid":"PBO:0067733"}


id: GO:0035736
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of cells, resulting in the expansion of a cell population that contributes to compound eye morphogenesis.","definition_xrefs":["GOC:sart","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"},{"relation_name":"part_of","term_name":"compound eye morphogenesis","termid":"GO:0001745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell proliferation involved in compound eye morphogenesis","termid":"GO:0035736"}


id: GO:0021876
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of an extracellular ligand to a Notch receptor on the surface of the target cell that contributes to the self renewal of neuroblasts in the forebrain.","definition_xrefs":["GOC:cls","GOC:dgh","GOC:jid","GOC:dph","PMID:16226447","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Notch signaling pathway","termid":"GO:0007219"},{"relation_name":"part_of","term_name":"forebrain neuroblast division","termid":"GO:0021873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"Notch signaling pathway involved in forebrain neuroblast division","synonyms":[{"name":"Notch signalling pathway in forebrain neuroblast division","type":"exact"}],"termid":"GO:0021876"}


id: MONDO:0019688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sulfation-related bone disorder (obsolete MONDO:0019688)","secondary_identifiers":["Orphanet:93423"],"synonyms":[{"name":"inborn error of sulphation","type":"exact"},{"name":"sulphation disorder","type":"exact"}],"termid":"MONDO:0019688","xrefs":{"Monarch":{"xref_id":"0019688"}}}


id: GO:0043970
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of an acetyl group to a lysine residue at position 9 of the histone.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K9 acetylation (obsolete GO:0043970)","synonyms":[{"name":"histone H3 acetylation at K9","type":"exact"},{"name":"histone H3K9 acetylation","type":"exact"}],"termid":"GO:0043970"}


id: PBO:0067840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 142","termid":"PBO:0067840"}


id: MONDO:1011807
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atypical myopathy, non-human animal","secondary_identifiers":["OMIA:002480"],"termid":"MONDO:1011807","xrefs":{"Monarch":{"xref_id":"1011807"}}}


id: GO:0004205
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete caspase-8 activity (obsolete GO:0004205)","synonyms":[{"name":"caspase-8 activity","type":"exact"}],"termid":"GO:0004205"}


id: GO:0106096
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 ceramide stimulus.","definition_xrefs":["PMID:18006463"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"}],"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 ceramide","termid":"GO:0106096"}


id: PBO:0038957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adipogenesis regulatory factor","termid":"PBO:0038957"}


id: PBO:0086280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with a potential role in response to iron deprivation; transcription increases during iron deprivation and during treatment with 2-(6-benzyl-2-pyridyl)quinazoline (BPQ) and copper; regulated by Aft1p and, to a lesser extent, by Aft2p; originally identified as a syntenic homolog of an Ashbya gossypii gene; localizes to nucleus and cytoplasm, and nuclear localization is enhanced under iron-replete conditions","termid":"PBO:0086280"}


id: PBO:0076408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 5","termid":"PBO:0076408"}


id: GO:0009522
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A photosystem that contains an iron-sulfur reaction center associated with accessory pigments and electron carriers. In cyanobacteria and chloroplasts, photosystem I functions as a light-dependent plastocyanin-ferredoxin oxidoreductase, transferring electrons from plastocyanin to ferredoxin; in photosynthetic bacteria that have only a single type I photosystem, such as the green sulfur bacteria, electrons can go either to ferredoxin (Fd) -> NAD+ or to menaquinone (MK) -> Cytb/FeS -> Cytc555 -> photosystem I (cyclic photophosphorylation).","definition_xrefs":["GOC:ds","GOC:mah","PMID:9821949","ISBN:0140514031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photosystem","termid":"GO:0009521"}],"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":"photosystem I","termid":"GO:0009522"}


id: PBO:0078595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 60 pseudogene 8, Y-linked","termid":"PBO:0078595"}


id: PBO:0090851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongator complex WD repeat protein Elp2","termid":"PBO:0090851"}


id: MONDO:0009889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited disorder characterized by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involvement.","definition_xrefs":["Orphanet:731"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"polycystic kidney disease","termid":"MONDO:0020642"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive polycystic kidney disease","secondary_identifiers":["ICD9:753.14","MedDRA:10036047","NORD:831","SCTID:28770003","DOID:0110861","GARD:8378","icd11.foundation:1424110943","NANDO:1200369","NCIT:C84579","MEDGEN:39076","NANDO:2200154","UMLS:C0085548"],"synonyms":[{"name":"AR-PKD","type":"exact"},{"name":"ARPKD","type":"exact"},{"name":"PKHD1","type":"related"},{"name":"autosomal recessive polycystic kidney","type":"exact"},{"name":"polycystic kidney and hepatic disease 1","type":"narrow"},{"name":"polycystic kidney disease, autosomal recessive","type":"exact"},{"name":"polycystic kidney disease, infantile type","type":"exact"},{"name":"polycystic kidney disease, infantile, type I","type":"narrow"}],"termid":"MONDO:0009889","xrefs":{"Monarch":{"xref_id":"0009889"}}}


id: GO:0010886
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate or extent of cholesterol storage. Cholesterol storage is the accumulation and maintenance in cells or tissues of cholesterol, cholest-5-en-3 beta-ol, the principal sterol of vertebrates and the precursor of many steroids, including bile acids and steroid hormones.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid storage","termid":"GO:0010884"},{"relation_name":"is_a","term_name":"regulation of cholesterol storage","termid":"GO:0010885"},{"relation_name":"positively_regulates","term_name":"cholesterol storage","termid":"GO:0010878"}],"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 cholesterol storage","synonyms":[{"name":"positive regulation of cholesterol sequestration","type":"narrow"}],"termid":"GO:0010886"}


id: PBO:0063679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piggyBac transposable element derived 4 pseudogene 3","termid":"PBO:0063679"}


id: PBO:0064997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRDM4 antisense RNA 1","termid":"PBO:0064997"}


id: PBO:0056611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malic enzyme 3","termid":"PBO:0056611"}


id: PBO:0089310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease H2 complex subunit Rnh203","termid":"PBO:0089310"}


id: PBO:0087887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional repressor encoded by the FYV5 antisense strand; negatively regulates transcription of FYV5 by binding to the promoter on the sense strand","termid":"PBO:0087887"}


id: FYPO:0005474
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutamate dehydrogenase activity using NAPD+ as a cofactor is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0000257"],"is_obsolete":false,"name":"normal glutamate dehydrogenase (NADP+) activity","synonyms":[{"name":"normal NAD(P)H-dependent glutamate dehydrogenase activity","type":"exact"},{"name":"normal NADP-GDH activity","type":"exact"}],"termid":"FYPO:0005474"}


id: MOD:01684
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to a palmitoylated-L-cysteine, such as N-palmitoyl-L-cysteine or S-palmitoyl-L-cysteine.","definition_xrefs":["OMSSA:92","Unimod:47"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"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":"palmitoylated-L-cysteine","synonyms":[{"name":"Hexadecanoylated L-cysteine","type":"exact"},{"name":"Palmitoyl","type":"related"},{"name":"Palmitoylation","type":"related"},{"name":"PamCys","type":"exact"},{"name":"palmitoylationc","type":"exact"}],"termid":"MOD:01684"}


id: MONDO:0012830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"10q22.3q23.3 microdeletion syndrome is a rare partial autosomal monosomy characterized by a mild facial dysmorphism variably including macrocephaly, broad forehead, hypertelorism or hypotelorism, deep-set eyes, upslanting or downslanting palpebral fissures, low-set ears, flat nasal bridge, smooth philtrum, thin upper lip), cleft palate, cerebellar and cardiac malformations, psychomotor development delay, and behavioral abnormalities (attention deficit hyperactivity disorder, autism). Other rare features may include congenital breast aplasia, arachnodactyly, joint hyperlaxity, club feet, feeding difficulties, failure to thrive.","definition_xrefs":["Orphanet:276413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial monosomy of the long arm of chromosome 10","termid":"MONDO:0016909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 10q23 deletion syndrome","secondary_identifiers":["DOID:0060389","MEDGEN:906099","MESH:C567385","UMLS:C4225669","GARD:17280","OMIM:612242"],"synonyms":[{"name":"10q22.3q23 microdeletion syndrome","type":"related"},{"name":"10q22.3q23.3 microdeletion syndrome","type":"related"},{"name":"Del(10)(q22.3q23.3)","type":"exact"},{"name":"chromosome 10Q22.3-q23.2 deletion syndrome","type":"related"},{"name":"chromosome 10q22.3-q23.2 deletion syndrome","type":"related"},{"name":"chromosome 10q23 deletion syndrome","type":"exact"},{"name":"deletion 10q22.3q23.3","type":"exact"},{"name":"juvenile polyposis of infancy","type":"related"},{"name":"juvenile polyposis, infantile","type":"related"},{"name":"monosomy 10q22.3q23.3","type":"exact"}],"termid":"MONDO:0012830","xrefs":{"Monarch":{"xref_id":"0012830"}}}


id: GO:0044036
data:
  {"annotated_genes":["SJAG_00667","SJAG_02278","SJAG_03057","SJAG_04327","SJAG_01288","SJAG_03082","SJAG_00876","SJAG_04184","SJAG_05285","SJAG_03646","SJAG_01021","SJAG_01264","SJAG_04771","SJAG_01171","SJAG_01835","SJAG_00598","SJAG_02519","SJAG_01276","SJAG_04906","SJAG_00816","SJAG_02916","SJAG_01290","SJAG_02192","SJAG_01255","SJAG_04668","SJAG_04483","SJAG_04770","SJAG_03587","SJAG_01017","SJAG_00218","SJAG_04236","SJAG_02222","SJAG_03123","SJAG_05001","SJAG_04864","SJAG_01787","SJAG_04462","SJAG_00424","SJAG_03705","SJAG_04659","SJAG_01028","SJAG_00610","SJAG_01453","SJAG_04666"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034413"},{"annotations":[74888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034412"},{"annotations":[73899,76703,82310,79409,89442,78860,76574,79895,81216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000032"},{"annotations":[102109,95967],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044347"},{"annotations":[73309,80651,75244,75416,72524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070600"},{"annotations":[93548,76406,77750,72952,108070,74891,115158,117818],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071970"},{"annotations":[80100,104595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070880"},{"annotations":[103900,103901,110043,97053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070879"},{"annotations":[74411,108664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071966"},{"annotations":[94368,89457],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[107880,120043,94352,92717,107309,69566,119910],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090334"},{"annotations":[91386,96891,104802,94374],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving macromolecules forming, or destined to form, part of the cell wall. A cell wall is a rigid or semi-rigid envelope lying outside the cell membrane of plant, fungal and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis.","definition_xrefs":["GOC:mah","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule metabolic process","termid":"GO:0043170"},{"relation_name":"part_of","term_name":"cell wall organization or biogenesis","termid":"GO:0071554"}],"gene_count":44,"genes_by_uniquename":{"SJAG_00218":null,"SJAG_00424":null,"SJAG_00598":null,"SJAG_00610":null,"SJAG_00667":null,"SJAG_00816":null,"SJAG_00876":null,"SJAG_01017":null,"SJAG_01021":null,"SJAG_01028":null,"SJAG_01171":null,"SJAG_01255":null,"SJAG_01264":null,"SJAG_01276":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01453":null,"SJAG_01787":null,"SJAG_01835":null,"SJAG_02192":null,"SJAG_02222":null,"SJAG_02278":null,"SJAG_02519":null,"SJAG_02916":null,"SJAG_03057":null,"SJAG_03082":null,"SJAG_03123":null,"SJAG_03587":null,"SJAG_03646":null,"SJAG_03705":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04327":null,"SJAG_04462":null,"SJAG_04483":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04770":null,"SJAG_04771":null,"SJAG_04864":null,"SJAG_04906":null,"SJAG_05001":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0071554"],"is_obsolete":false,"name":"cell wall macromolecule metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0010382"],"synonyms":[{"name":"cellular cell wall macromolecule metabolic process","type":"exact"},{"name":"cellular cell wall macromolecule metabolism","type":"exact"}],"termid":"GO:0044036","terms_by_termid":{"GO:0000032":null,"GO:0034412":null,"GO:0034413":null,"GO:0044347":null,"GO:0070600":null,"GO:0070610":null,"GO:0070879":null,"GO:0070880":null,"GO:0071966":null,"GO:0071970":null,"GO:0090334":null,"GO:0140748":null}}


id: MONDO:0003133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the glomeruli with infiltration by polymorphonuclear leukocytes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulonephritis","termid":"MONDO:0002462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"exudative glomerulonephritis","secondary_identifiers":["DOID:4777","MEDGEN:154269","NCIT:C35706","UMLS:C0546345"],"termid":"MONDO:0003133","xrefs":{"Monarch":{"xref_id":"0003133"}}}


id: MONDO:0002534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign epithelial neoplasm that arises from the fallopian tube. It is characterized by the presence of fibrovascular stalks lined by serous epithelial cells.","definition_xrefs":["NCIT:C40112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube benign neoplasm","termid":"MONDO:0000645"},{"relation_name":"is_a","term_name":"papilloma","termid":"MONDO:0002363"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fallopian tube papilloma","secondary_identifiers":["DOID:3173","UMLS:C1517123","MEDGEN:275874"],"synonyms":[{"name":"fallopian tube papilloma","type":"exact"},{"name":"fallopian tube serous papilloma","type":"exact"}],"termid":"MONDO:0002534","xrefs":{"Monarch":{"xref_id":"0002534"}}}


id: PBO:0082740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the RSC chromatin remodeling complex; essential for viability and mitotic growth; homolog of SWI/SNF subunit Swi3p, but unlike Swi3p, does not activate transcription of reporters","termid":"PBO:0082740"}


id: GO:1903157
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any iron ion transmembrane transporter activity that is involved in iron ion import into cell.","definition_xrefs":["GOC:dos","GO_REF:0000061","GOC:TermGenie","ISBN:0-8249-3695-6"],"gene_count":0,"genotype_count":0,"name":"obsolete iron ion transmembrane transporter activity involved in iron ion import into cell (obsolete GO:1903157)","synonyms":[{"name":"iron ion transmembrane transporter activity involved in iron import into cell","type":"related"},{"name":"iron ion transmembrane transporter activity involved in iron ion import into cell","type":"exact"},{"name":"iron transporter activity involved in iron import into cell","type":"related"},{"name":"iron transporter activity involved in iron ion import into cell","type":"exact"},{"name":"multicopper ferroxidase iron transport mediator activity involved in iron import into cell","type":"related"},{"name":"multicopper ferroxidase iron transport mediator activity involved in iron ion import into cell","type":"related"},{"name":"transmembrane iron ion permease activity involved in iron import into cell","type":"related"},{"name":"transmembrane iron ion permease activity involved in iron ion import into cell","type":"exact"},{"name":"transmembrane iron permease activity involved in iron import into cell","type":"related"},{"name":"transmembrane iron permease activity involved in iron ion import into cell","type":"exact"},{"name":"zinc, iron permease activity involved in iron import into cell","type":"related"},{"name":"zinc, iron permease activity involved in iron ion import into cell","type":"related"}],"termid":"GO:1903157"}


id: PBO:0045780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectodysplasin A","termid":"PBO:0045780"}


id: MONDO:0015896
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare hypoparathyroidism.","gene_count":0,"genotype_count":0,"name":"obsolete rare hypoparathyroidism (obsolete MONDO:0015896)","secondary_identifiers":["Orphanet:181405"],"synonyms":[{"name":"rare hypoparathyroidism","type":"exact"}],"termid":"MONDO:0015896","xrefs":{"Monarch":{"xref_id":"0015896"}}}


id: GO:2000523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of T cell costimulation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T cell activation","termid":"GO:0050863"},{"relation_name":"is_a","term_name":"regulation of leukocyte cell-cell adhesion","termid":"GO:1903037"},{"relation_name":"regulates","term_name":"T cell costimulation","termid":"GO:0031295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"regulation of T cell costimulation","synonyms":[{"name":"regulation of T cell co-stimulation","type":"exact"},{"name":"regulation of T lymphocyte costimulation","type":"exact"},{"name":"regulation of T-cell co-stimulation","type":"exact"},{"name":"regulation of T-cell costimulation","type":"exact"},{"name":"regulation of T-lymphocyte costimulation","type":"exact"}],"termid":"GO:2000523"}


id: SO:1000138
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A compound chromosome whereby two copies of the same chromosomal arm attached to a common centromere. The chromosome is diploid for the arm involved.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"compound_chromosome","termid":"SO:1000042"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homo_compound_chromosome","synonyms":[{"name":"homo compound chromosome","type":"exact"},{"name":"homo-compound chromosome","type":"exact"}],"termid":"SO:1000138"}


id: PR:O94416
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A general transcription factor IIF subunit 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR13011:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription initiation factor IIF subunit alpha (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.09c","secondary_identifiers":["UniProtKB:O94416"],"synonyms":[{"name":"SPCC1620.09c","type":"related"},{"name":"Spom972h-GTF2F1","type":"exact"},{"name":"TFIIF large subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TFIIF-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94416"}


id: GO:1905313
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transforming growth factor beta receptor signaling pathway that is involved in heart development.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie","GOC:rl","GOC:BHF","PMID:16140292"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor signaling pathway involved in heart development (obsolete GO:1905313)","synonyms":[{"name":"TGF-beta receptor signaling pathway involved in cardiac development","type":"related"},{"name":"TGF-beta receptor signaling pathway involved in dorsal vessel development","type":"narrow"},{"name":"TGF-beta receptor signaling pathway involved in heart development","type":"exact"},{"name":"TGF-beta receptor signalling pathway involved in cardiac development","type":"related"},{"name":"TGF-beta receptor signalling pathway involved in dorsal vessel development","type":"narrow"},{"name":"TGF-beta receptor signalling pathway involved in heart development","type":"exact"},{"name":"TGFbeta receptor signaling pathway involved in cardiac development","type":"related"},{"name":"TGFbeta receptor signaling pathway involved in dorsal vessel development","type":"narrow"},{"name":"TGFbeta receptor signaling pathway involved in heart development","type":"exact"},{"name":"TGFbeta receptor signalling pathway involved in cardiac development","type":"related"},{"name":"TGFbeta receptor signalling pathway involved in dorsal vessel development","type":"narrow"},{"name":"TGFbeta receptor signalling pathway involved in heart development","type":"exact"},{"name":"transforming growth factor beta receptor signaling pathway involved in cardiac development","type":"related"},{"name":"transforming growth factor beta receptor signaling pathway involved in dorsal vessel development","type":"narrow"},{"name":"transforming growth factor beta receptor signalling pathway involved in cardiac development","type":"related"},{"name":"transforming growth factor beta receptor signalling pathway involved in dorsal vessel development","type":"narrow"},{"name":"transforming growth factor beta receptor signalling pathway involved in heart development","type":"exact"}],"termid":"GO:1905313"}


id: MONDO:0001826
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypobetalipoproteinemia (obsolete MONDO:0001826)","termid":"MONDO:0001826","xrefs":{"Monarch":{"xref_id":"0001826"}}}


id: GO:0050024
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-galactono-1,4-lactone + O2 = L-ascorbate + H2O2 + H+.","definition_xrefs":["EC:1.3.3.12","RHEA:20617"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor","termid":"GO:0016634"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"L-galactonolactone oxidase activity","secondary_identifiers":["GO:0033733","KEGG_REACTION:R00643","MetaCyc:1.3.3.12-RXN"],"synonyms":[{"name":"L-galactono-1,4-lactone oxidase activity","type":"related"},{"name":"L-galactono-1,4-lactone:oxygen 3-oxidoreductase activity","type":"related"},{"name":"L-xylono-1,4-lactone oxidase activity","type":"related"}],"termid":"GO:0050024"}


id: PBO:0043387
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLYBL antisense RNA 1","termid":"PBO:0043387"}


id: PBO:0058854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8083","termid":"PBO:0058854"}


id: GO:0016544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process during courtship where the male insect taps the female with his frontal leg. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","PMID:11092827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male courtship behavior","termid":"GO:0008049"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"male courtship behavior, tapping to detect pheromone","synonyms":[{"name":"male courtship behavior, tapping","type":"related"},{"name":"male courtship behaviour, tapping","type":"exact"},{"name":"male courtship behaviour, tapping to detect pheromone","type":"related"}],"termid":"GO:0016544"}


id: SO:1000032
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence alteration which included an insertion and a deletion, affecting 2 or more bases.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_alteration","termid":"SO:0001059"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"delins","secondary_identifiers":["loinc:LA9659-9","http://en.wikipedia.org/wiki/Indel"],"synonyms":[{"name":"deletion-insertion","type":"exact"},{"name":"indel","type":"exact"}],"termid":"SO:1000032"}


id: PBO:0051887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITFG1 antisense RNA 1","termid":"PBO:0051887"}


id: PBO:0003670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER triose phosphate transmembrane transporter (predicted)","termid":"PBO:0003670"}


id: PBO:0091736
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heteromeric(8)","termid":"PBO:0091736"}


id: PBO:0055775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"loss of heterozygosity on chromosome 1, region 1","termid":"PBO:0055775"}


id: PBO:0057738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1468","termid":"PBO:0057738"}


id: PBO:0061155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamide nucleotide adenylyltransferase 3","termid":"PBO:0061155"}


id: MONDO:0004575
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition produced by a deficiency of choline in animals. Choline is known as a lipotropic agent because it has been shown to promote the transport of excess fat from the liver under certain conditions in laboratory animals. Combined deficiency of choline (included in the B vitamin complex) and all other methyl group donors causes liver cirrhosis in some animals. Unlike compounds normally considered as vitamins, choline does not serve as a cofactor in enzymatic reactions. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984)","definition_xrefs":["MESH:D002796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nutritional deficiency disease","termid":"MONDO:0006873"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choline deficiency disease","secondary_identifiers":["MEDGEN:930","SCTID:238113006","DOID:8456","ICD9:266.2","UMLS:C0008412"],"synonyms":[{"name":"choline deficiency","type":"exact"}],"termid":"MONDO:0004575","xrefs":{"Monarch":{"xref_id":"0004575"}}}


id: GO:2001010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of plant-type cell wall cellulose biosynthetic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellulose biosynthetic process","termid":"GO:2001007"},{"relation_name":"is_a","term_name":"regulation of plant-type cell wall cellulose biosynthetic process","termid":"GO:2001009"},{"relation_name":"negatively_regulates","term_name":"plant-type cell wall cellulose biosynthetic process","termid":"GO:0052324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"negative regulation of plant-type cell wall cellulose biosynthetic process","synonyms":[{"name":"negative regulation of cell wall cellulose biosynthesis","type":"exact"},{"name":"negative regulation of cellulose biosynthesis during cell wall biosynthesis","type":"related"}],"termid":"GO:2001010"}


id: PBO:0065501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psoriasis susceptibility 1 candidate 3","termid":"PBO:0065501"}


id: GO:0019625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of atrazine, a triazine ring-containing herbicide, into cyanuric acid.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrazine catabolic process","termid":"GO:0019381"},{"relation_name":"is_a","term_name":"cyanuric acid metabolic process","termid":"GO:0042199"}],"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":"atrazine catabolic process to cyanuric acid","synonyms":[{"name":"atrazine breakdown to cyanuric acid","type":"exact"},{"name":"atrazine degradation to cyanuric acid","type":"exact"}],"termid":"GO:0019625"}


id: PBO:0083624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E3 ubiquitin ligase; forms heterodimer with Rad6p to regulate K63 polyubiquitination in response to oxidative stress and to monoubiquinate histone H2B-K123, which is required for the subsequent methylation of histone H3-K4 and H3-K79; required for DSBR, transcription, silencing, and checkpoint control; interacts with RNA-binding protein Npl3p, linking histone ubiquitination to mRNA processing; Bre1p-dependent histone ubiquitination promotes pre-mRNA splicing","termid":"PBO:0083624"}


id: GO:1904229
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of succinate dehydrogenase activity.","definition_xrefs":["GO_REF:0000059","GOC:rl","PMID:18160053","GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of oxidoreductase activity","termid":"GO:0051341"}],"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 succinate dehydrogenase activity","synonyms":[{"name":"regulation of fumarate dehydrogenase activity","type":"exact"},{"name":"regulation of fumarate reductase activity","type":"exact"},{"name":"regulation of fumaric hydrogenase activity","type":"exact"},{"name":"regulation of succinate oxidoreductase activity","type":"exact"},{"name":"regulation of succinate:(acceptor) oxidoreductase activity","type":"exact"},{"name":"regulation of succinate:acceptor oxidoreductase activity","type":"exact"},{"name":"regulation of succinic acid dehydrogenase activity","type":"exact"},{"name":"regulation of succinic dehydrogenase activity","type":"broad"},{"name":"regulation of succinodehydrogenase activity","type":"exact"},{"name":"regulation of succinyl dehydrogenase activity","type":"exact"}],"termid":"GO:1904229"}


id: GO:0070143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of coupling alanine to alanyl-tRNA in a mitochondrion, catalyzed by alanyl-tRNA synthetase. In tRNA aminoacylation, the amino acid is first activated by linkage to AMP and then transferred to either the 2'- or the 3'-hydroxyl group of the 3'-adenosine residue of the tRNA.","definition_xrefs":["GOC:mcc","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alanyl-tRNA aminoacylation","termid":"GO:0006419"},{"relation_name":"is_a","term_name":"tRNA aminoacylation for mitochondrial protein translation","termid":"GO:0070127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0140053"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006399","GO:0140053","GO:0006520","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"mitochondrial alanyl-tRNA aminoacylation","termid":"GO:0070143"}


id: GO:0046947
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of hydroxylysine (5-hydroxy-2,6-diaminohexanoic acid), a chiral alpha-amino acid.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aspartate family amino acid biosynthetic process","termid":"GO:0009067"},{"relation_name":"is_a","term_name":"modified amino acid biosynthetic process","termid":"GO:0042398"},{"relation_name":"is_a","term_name":"hydroxylysine metabolic process","termid":"GO:0046946"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid biosynthetic process","termid":"GO:0170043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"hydroxylysine biosynthetic process","synonyms":[{"name":"hydroxylysine anabolism","type":"exact"},{"name":"hydroxylysine biosynthesis","type":"exact"},{"name":"hydroxylysine formation","type":"exact"},{"name":"hydroxylysine synthesis","type":"exact"}],"termid":"GO:0046947"}


id: PBO:0039909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc42 guanine nucleotide exchange factor 9","termid":"PBO:0039909"}


id: MONDO:0006390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroendocrine carcinoma of the prostate gland with unfavorable prognosis, composed of small cells containing neurosecretory granules. Approximately half of the cases show a mixture of small cells and adenocarcinoma cells.","definition_xrefs":["NCIT:C6766"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"prostate neuroendocrine neoplasm","termid":"MONDO:0002477"},{"relation_name":"is_a","term_name":"prostate carcinoma","termid":"MONDO:0005159"}],"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":"prostate small cell carcinoma","secondary_identifiers":["EFO:1000499","SCTID:396198006","UMLS:C1300585","MEDGEN:266251","ONCOTREE:PRSCC","DOID:7141"],"synonyms":[{"name":"Oat cell carcinoma of prostate","type":"exact"},{"name":"Oat cell carcinoma of the prostate","type":"exact"},{"name":"PRSCC","type":"related"},{"name":"prostate Oat cell carcinoma","type":"exact"},{"name":"prostate gland small cell carcinoma","type":"exact"},{"name":"prostate oat cell carcinoma","type":"exact"},{"name":"prostate small cell NEC","type":"exact"},{"name":"prostate small cell carcinoma","type":"exact"},{"name":"prostate small cell neuroendocrine carcinoma","type":"exact"},{"name":"small cell carcinoma of prostate","type":"exact"},{"name":"small cell carcinoma of prostate gland","type":"exact"},{"name":"small cell carcinoma of the prostate","type":"exact"}],"termid":"MONDO:0006390","xrefs":{"Monarch":{"xref_id":"0006390"}}}


id: GO:0033419
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CUA codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0060090","GO:0003723","GO:0005488"],"is_obsolete":false,"name":"CUA codon-amino acid adaptor activity","synonyms":[{"name":"CTA codon-amino acid adaptor activity","type":"exact"},{"name":"leucine tRNA","type":"related"}],"termid":"GO:0033419"}


id: GO:0048463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the carpel. This process pertains to the physical shaping of a rudimentary structure.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ structural organization","termid":"GO:0048450"},{"relation_name":"part_of","term_name":"carpel morphogenesis","termid":"GO:0048445"}],"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":"carpel structural organization","secondary_identifiers":["GO:0048432"],"synonyms":[{"name":"carpel structural organisation","type":"exact"}],"termid":"GO:0048463"}


id: PBO:0058010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR3936 host gene","termid":"PBO:0058010"}


id: GO:0014902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a myotube cell. Myotube differentiation starts with myoblast fusion and the appearance of specific cell markers (this is the cell development step). Then individual myotubes can fuse to form bigger myotubes and start to contract. Myotubes are multinucleated cells that are formed when proliferating myoblasts exit the cell cycle, differentiate and fuse.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striated muscle cell differentiation","termid":"GO:0051146"}],"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":"myotube differentiation","termid":"GO:0014902"}


id: MONDO:0020112
data:
  {"annotated_genes":["SJAG_03164","SJAG_00694"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87156,87155],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009797"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"megaloblastic anemia","termid":"MONDO:0001700"},{"relation_name":"is_a","term_name":"hereditary anemia","termid":"MONDO:0016624"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00694":null,"SJAG_03164":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"vitamin B12- and folate-independent constitutional megaloblastic anemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:98415","ICD10CM:D53.0","MEDGEN:1842832","UMLS:C5681710","GARD:19464"],"termid":"MONDO:0020112","terms_by_termid":{"MONDO:0009797":null},"xrefs":{"Monarch":{"xref_id":"0020112"}}}


id: MONDO:0011342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"SLC35A1-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case by repeated hemorrhagic incidents, including severe pulmonary hemorrhage.","definition_xrefs":["Orphanet:238459"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete nephropathy secondary to a storage or other metabolic disease (obsolete MONDO:0019743)","termid":"MONDO:0019743"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"},{"relation_name":"is_a","term_name":"disorder of multiple glycosylation","termid":"MONDO:0017749"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"SLC35A1-congenital disorder of glycosylation","secondary_identifiers":["DOID:0070258","GARD:12409","OMIM:603585","SCTID:723624008","MEDGEN:370234","MESH:C567040","UMLS:C1970344"],"synonyms":[{"name":"CDG IIf","type":"related"},{"name":"CDG syndrome type IIf","type":"exact"},{"name":"CDG-IIf","type":"exact"},{"name":"CDG2F","type":"exact"},{"name":"CMP-sialic acid transporter deficiency","type":"exact"},{"name":"SLC35A1-CDG","type":"exact"},{"name":"SLC35A1-CDG (CDG-IIf)","type":"related"},{"name":"SLC35A1-congenital disorder of glycosylation","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IIf","type":"exact"},{"name":"congenital disorder of glycosylation type 2f","type":"exact"},{"name":"congenital disorder of glycosylation type IIf","type":"exact"},{"name":"congenital disorder of glycosylation, type IIf","type":"related"}],"termid":"MONDO:0011342","xrefs":{"Monarch":{"xref_id":"0011342"}}}


id: PBO:0053636
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 682","termid":"PBO:0053636"}


id: MOD:00728
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a galactose group through a glycosidic bond.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylated residue","termid":"MOD:00693"}],"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":"galactosylated","synonyms":[{"name":"Gal","type":"exact"}],"termid":"MOD:00728"}


id: MONDO:0019121
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Human pneumocystosis is caused by an infectious agent, which (after recent nomenclature and taxonomy revisions) is now classed as the fungus Pneumocystis jiroveci. The prevalence is unknown. Pneumocystis jiroveci is an opportunistic infectious agent, developing in immunosuppressed patients. It is an air-borne infection, localized to the lungs. However, extrapulmonary involvement is seen in AIDS patients. The disease manifests progressively with coughing, respiratory problems (dyspnea) and fever, followed by acute respiratory insufficiency and death within a few weeks in untreated cases. The most reliable diagnostic method is bronchoalveolar lavage. The treatment of choice is cotrimoxazole.","direct_ancestors":[{"relation_name":"is_a","term_name":"opportunistic mycosis","termid":"MONDO:0002312"},{"relation_name":"is_a","term_name":"pneumonia","termid":"MONDO:0005249"},{"relation_name":"is_a","term_name":"fungal lung infectious disease","termid":"MONDO:0005766"},{"relation_name":"is_a","term_name":"Pneumocystis infectious disease","termid":"MONDO:0005923"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumocystosis","secondary_identifiers":["UMLS:C1535939","ICD10CM:B59","MEDGEN:777048","MESH:D011020","NORD:1923","GARD:4386","ICD10EXP:B59+","ICD10EXP:J17.3*","EFO:0007448","ICD9:136.3","Orphanet:723","SCTID:415125002","NCIT:C3334","DOID:11339","icd11.foundation:404370038"],"synonyms":[{"name":"PCP","type":"exact"},{"name":"PJP","type":"exact"},{"name":"Pneumocystis","type":"exact"},{"name":"Pneumocystis Pneumonia","type":"exact"},{"name":"Pneumocystis carinii pneumonia","type":"exact"},{"name":"Pneumocystis jirovecii pneumonia","type":"exact"},{"name":"Pneumocystis pneumonia","type":"exact"},{"name":"pneumocystosis","type":"exact"},{"name":"pneumocystosis pneumonia","type":"exact"},{"name":"pulmonary pneumocystosis","type":"exact"}],"termid":"MONDO:0019121","xrefs":{"Monarch":{"xref_id":"0019121"}}}


id: PBO:0059131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-phase phosphoprotein 8","termid":"PBO:0059131"}


id: GO:0036485
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of trunk neural crest cells from the neural tube, travelling dorso-laterally into the ectoderm and continuing toward the ventral midline of the belly. These migrating trunk neural crest cells become melanocytes, the melanin-forming pigment cells.","definition_xrefs":["GOC:mat","GOC:bf","PMID:2387238","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trunk neural crest cell migration","termid":"GO:0036484"}],"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":"dorsolateral trunk neural crest cell migration","synonyms":[{"name":"dorsolateral trunk NCC migration","type":"exact"}],"termid":"GO:0036485"}


id: MONDO:0010207
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":"wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome","secondary_identifiers":["MESH:C536746","Orphanet:1409","MEDGEN:98033","OMIM:278200","SCTID:239023005","UMLS:C0406718"],"synonyms":[{"name":"Salamon syndrome","type":"exact"},{"name":"woolly hair hypotrichosis everted lower lip and outstanding ears","type":"related"},{"name":"woolly hair, hypotrichosis, everted LOWER LIP, and outstanding ears","type":"related"},{"name":"wooly hair hypotrichosis everted lower lip and outstanding ears","type":"related"},{"name":"wooly hair, hypotrichosis, everted LOWER LIP, and outstanding ears","type":"related"},{"name":"wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome","type":"exact"}],"termid":"MONDO:0010207","xrefs":{"Monarch":{"xref_id":"0010207"}}}


id: PBO:0005856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexed with Cdc5 protein Cwf18","termid":"PBO:0005856"}


id: GO:0031944
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways involving glucocorticoids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucocorticoid metabolic process","termid":"GO:0031943"},{"relation_name":"is_a","term_name":"negative regulation of hormone metabolic process","termid":"GO:0032351"},{"relation_name":"is_a","term_name":"negative regulation of steroid metabolic process","termid":"GO:0045939"},{"relation_name":"negatively_regulates","term_name":"glucocorticoid metabolic process","termid":"GO:0008211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of glucocorticoid metabolic process","synonyms":[{"name":"down regulation of glucocorticoid metabolic process","type":"exact"},{"name":"down-regulation of glucocorticoid metabolic process","type":"exact"},{"name":"downregulation of glucocorticoid metabolic process","type":"exact"},{"name":"inhibition of glucocorticoid metabolic process","type":"narrow"},{"name":"negative regulation of glucocorticoid metabolism","type":"exact"}],"termid":"GO:0031944"}


id: GO:0030568
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Stops, prevents or reduces the activity of the serine endopeptidase plasmin.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete plasmin inhibitor activity (obsolete GO:0030568)","synonyms":[{"name":"plasmin inhibitor activity","type":"exact"}],"termid":"GO:0030568"}


id: PBO:0034376
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_potential_to_developmentally_contribute_to","termid":"PBO:0034376"}


id: GO:2000346
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of hepatocyte proliferation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell proliferation","termid":"GO:0050680"},{"relation_name":"is_a","term_name":"regulation of hepatocyte proliferation","termid":"GO:2000345"},{"relation_name":"negatively_regulates","term_name":"hepatocyte proliferation","termid":"GO:0072574"}],"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 hepatocyte proliferation","termid":"GO:2000346"}


id: PBO:0002840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP kinase kinase kinase Win1","termid":"PBO:0002840"}


id: GO:0042251
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The maintenance of an established polarized larval imaginal disc epithelium.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment or maintenance of polarity of larval imaginal disc epithelium","termid":"GO:0016336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007163"],"is_obsolete":false,"name":"maintenance of polarity of larval imaginal disc epithelium","termid":"GO:0042251"}


id: GO:0047141
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cystine + 2 reduced glutathione = oxidized glutathione + 2 L-cysteine.","definition_xrefs":["MetaCyc:1.8.4.4-RXN","EC:1.8.4.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"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":"glutathione-cystine transhydrogenase activity","secondary_identifiers":["RHEA:12613"],"synonyms":[{"name":"GSH-cystine transhydrogenase","type":"related"},{"name":"NADPH-dependent GSH-cystine transhydrogenase","type":"related"},{"name":"glutathione:cystine oxidoreductase","type":"related"}],"termid":"GO:0047141"}


id: GO:1903554
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway that is involved in the defense response to Gram-negative bacterium.","definition_xrefs":["GOC:kmv","PMID:25303524","GOC:TermGenie","GO_REF:0000060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"},{"relation_name":"part_of","term_name":"defense response to Gram-negative bacterium","termid":"GO:0050829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"G protein-coupled receptor signaling pathway involved in defense response to Gram-negative bacterium","synonyms":[{"name":"G protein coupled receptor protein signaling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G protein coupled receptor protein signaling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G protein coupled receptor protein signaling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G protein coupled receptor protein signaling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"G protein coupled receptor protein signaling pathway involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"G protein coupled receptor protein signalling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G protein coupled receptor protein signalling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G protein coupled receptor protein signalling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G protein coupled receptor protein signalling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"G protein coupled receptor protein signalling pathway involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"G-protein coupled receptor protein signal transduction involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G-protein coupled receptor protein signal transduction involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor protein signal transduction involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G-protein coupled receptor protein signal transduction involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor protein signal transduction involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"G-protein coupled receptor protein signaling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G-protein coupled receptor protein signaling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor protein signaling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G-protein coupled receptor protein signaling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor protein signaling pathway involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"G-protein coupled receptor signaling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G-protein coupled receptor signaling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor signaling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G-protein coupled receptor signaling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor signalling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G-protein coupled receptor signalling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor signalling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G-protein coupled receptor signalling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"G-protein coupled receptor signalling pathway involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"G-protein-coupled receptor protein signaling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G-protein-coupled receptor protein signaling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G-protein-coupled receptor protein signaling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G-protein-coupled receptor protein signaling pathway involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"G-protein-coupled receptor protein signalling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"G-protein-coupled receptor protein signalling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"G-protein-coupled receptor protein signalling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"G-protein-coupled receptor protein signalling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"G-protein-coupled receptor protein signalling pathway involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"GPCR signaling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"GPCR signaling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"GPCR signaling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"GPCR signaling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"GPCR signaling pathway involved in defense response to Gram-negative bacterium","type":"exact"},{"name":"GPCR signalling pathway involved in Gram-negative antibacterial peptide activity","type":"related"},{"name":"GPCR signalling pathway involved in defence response to Gram-negative bacteria","type":"exact"},{"name":"GPCR signalling pathway involved in defence response to Gram-negative bacterium","type":"exact"},{"name":"GPCR signalling pathway involved in defense response to Gram-negative bacteria","type":"exact"},{"name":"GPCR signalling pathway involved in defense response to Gram-negative bacterium","type":"exact"}],"termid":"GO:1903554"}


id: GO:0015939
data:
  {"annotated_genes":["SJAG_03679","SJAG_05200","SJAG_01139"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990181"},{"annotations":[74258,79551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015940"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving pantothenate, the anion of pantothenic acid, the amide of beta-alanine and pantoic acid. It is a B complex vitamin that is a constituent of coenzyme A and is distributed ubiquitously in foods.","definition_xrefs":["ISBN:0721662544","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01139":null,"SJAG_03679":null,"SJAG_05200":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"pantothenate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-199220","GO:0006770"],"synonyms":[{"name":"pantothenate metabolism","type":"exact"},{"name":"vitamin B5 metabolic process","type":"exact"},{"name":"vitamin B5 metabolism","type":"exact"}],"termid":"GO:0015939","terms_by_termid":{"GO:0015940":null,"GO:1990181":null}}


id: MONDO:0017432
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndrome with limb reduction defects (obsolete MONDO:0017432)","secondary_identifiers":["Orphanet:294955"],"termid":"MONDO:0017432","xrefs":{"Monarch":{"xref_id":"0017432"}}}


id: GO:2001159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization by the Cvt pathway.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular protein transport","termid":"GO:0033157"},{"relation_name":"is_a","term_name":"regulation of vacuolar transport","termid":"GO:1903335"},{"relation_name":"is_a","term_name":"regulation of protein targeting","termid":"GO:1903533"},{"relation_name":"regulates","term_name":"cytoplasm to vacuole targeting by the Cvt pathway","termid":"GO:0032258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0006605","GO:0008150"],"is_obsolete":false,"name":"regulation of protein localization by the Cvt pathway","synonyms":[{"name":"regulation of cytoplasm to vacuole targeting","type":"exact"},{"name":"regulation of cytoplasm-to-vacuole targeting","type":"exact"}],"termid":"GO:2001159"}


id: MONDO:0008913
data:
  {"annotated_genes":["SJAG_01519"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86921],"is_not":false,"summary":null,"term":"MONDO:0008913"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"cardiac valvular defect","termid":"MONDO:0031323"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01519":null},"genotype_count":0,"is_obsolete":false,"name":"cardiac valvular defect, developmental","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1823949","UMLS:C5774175","DOID:0080633","MESH:C565882","OMIM:212093"],"synonyms":[{"name":"CARDIAC valvular defect, developmental","type":"related"},{"name":"CVDD","type":"related"},{"name":"cardiac valvular defect, developmental","type":"exact"}],"termid":"MONDO:0008913","terms_by_termid":{"MONDO:0008913":null},"xrefs":{"Monarch":{"xref_id":"0008913"}}}


id: GO:0036396
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A RNA methyltransferase complex that catalyzes the post-transcriptional methylation of adenosine to form N6-methyladenosine (m6A). In budding yeast, the MIS complex consists of Mum2p, Ime4p and Slz1p. In vertebrates, the complex consists of METTL3, METTL14 and associated components WTAP, ZC3H13, VIRMA, CBLL1/HAKAI and in some cases of RBM15 (RBM15 or RBM15B).","definition_xrefs":["PMID:22685417","GOC:dgf","PMID:24316715","PMID:29535189","PMID:29507755","GOC:sp","PMID:24407421","PMID:29547716"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase complex","termid":"GO:0034708"}],"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":"RNA N6-methyladenosine methyltransferase complex","synonyms":[{"name":"METTL3-METTL14-WTAP methyltransferase complex","type":"related"},{"name":"MIS complex","type":"related"},{"name":"Mum2, Ime4, and Slz1 complex","type":"exact"},{"name":"WMM complex","type":"exact"},{"name":"m(6)A writer complex","type":"related"},{"name":"m6A methyltransferase complex","type":"related"}],"termid":"GO:0036396"}


id: PBO:0064681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 17","termid":"PBO:0064681"}


id: PBO:0044073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleavage stimulation factor subunit 1","termid":"PBO:0044073"}


id: PBO:0042057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 120","termid":"PBO:0042057"}


id: GO:0052605
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,3-dimethyl-6-phytyl-1,4-benzoquinone = gamma-tocopherol.","definition_xrefs":["PMID:12213958"],"gene_count":0,"genotype_count":0,"name":"obsolete gamma-tocopherol cyclase activity (obsolete GO:0052605)","termid":"GO:0052605"}


id: PBO:0033795
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_at_low_temperature","termid":"PBO:0033795"}


id: PBO:0055839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ligand dependent nuclear receptor interacting factor 1","termid":"PBO:0055839"}


id: GO:1901811
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of beta-carotene.","definition_xrefs":["MetaCyc:PWY-5943","PMID:11387982","GOC:yaf","GOC:TermGenie","UniPathway:UPA00802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid catabolic process","termid":"GO:0016118"},{"relation_name":"is_a","term_name":"carotene catabolic process","termid":"GO:0016121"},{"relation_name":"is_a","term_name":"beta-carotene metabolic process","termid":"GO:1901810"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"beta-carotene catabolic process","synonyms":[{"name":"beta-carotene breakdown","type":"exact"},{"name":"beta-carotene catabolism","type":"exact"},{"name":"beta-carotene degradation","type":"exact"}],"termid":"GO:1901811"}


id: GO:0008873
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-gluconate + NADP+ = 2-dehydro-D-gluconate + NADPH + H+.","definition_xrefs":["EC:1.1.1.215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gluconate dehydrogenase activity","termid":"GO:0008875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"gluconate 2-dehydrogenase activity","secondary_identifiers":["RHEA:16653","MetaCyc:1.1.1.215-RXN"],"synonyms":[{"name":"2-keto-D-gluconate reductase activity","type":"related"},{"name":"2-ketogluconate reductase activity","type":"related"}],"termid":"GO:0008873"}


id: MONDO:1010319
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Coloboma that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of orbital region, non-human animal","termid":"MONDO:1011315"},{"relation_name":"is_a","term_name":"disorder of visual system, non-human animal","termid":"MONDO:1011316"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coloboma, non-human animal","secondary_identifiers":["OMIA:000219"],"termid":"MONDO:1010319","xrefs":{"Monarch":{"xref_id":"1010319"}}}


id: FYPO:0001621
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-arginine measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular amino acid level","termid":"FYPO:0003985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased cellular arginine level","synonyms":[{"name":"decreased cellular L-arginine level","type":"exact"},{"name":"decreased cellular arginine level during mitotic cell cycle","type":"related"},{"name":"decreased cellular arginine level during vegetative growth","type":"exact"},{"name":"decreased level of arginine in cell","type":"exact"},{"name":"reduced cellular arginine level","type":"exact"},{"name":"reduced level of arginine in cell","type":"exact"}],"termid":"FYPO:0001621"}


id: PBO:0063717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PGM5P4 antisense RNA 1","termid":"PBO:0063717"}


id: GO:0070451
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A long, thin cell projection that contains F-actin and tubulin, with microtubules centrally located and F-actin peripherally located.","definition_xrefs":["PMID:11526084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"}],"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":"cell hair","secondary_identifiers":["Wikipedia:Membrane_nanotube"],"synonyms":[{"name":"imaginal disc-derived wing hair","type":"narrow"},{"name":"non-sensory hair","type":"exact"}],"termid":"GO:0070451"}


id: GO:0099526
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals that conveys information from the presynapse to the nucleus via cytoskeletal transport of a protein from a presynapse to the component to the nucleus where it affects biochemical processes that occur in the nucleus (e.g DNA transcription, mRNA splicing, or DNA/histone modifications).","definition_xrefs":["PMID:25652077","PMID:24317321","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"presynaptic signal transduction","termid":"GO:0098928"}],"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":"presynapse to nucleus signaling pathway","synonyms":[{"name":"presynaptic signaling to nucleus","type":"exact"}],"termid":"GO:0099526"}


id: MONDO:0010789
data:
  {"annotated_genes":["SJAG_MIT04","SJAG_MIT20","SJAG_MIT03","SJAG_MIT13"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88067,88068,88069,88070],"is_not":false,"summary":null,"term":"MONDO:0010789"}]},"cv_name":"mondo","definition":"MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations.","definition_xrefs":["Orphanet:550"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"mitochondrial encephalomyopathy","termid":"MONDO:0004675"}],"gene_count":4,"genes_by_uniquename":{"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT20":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"MELAS syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:540000","ICD10CM:E88.41","GARD:7009","DOID:3687","MESH:D017241","ICD9:277.87","SCTID:39925003","MedDRA:10053872","MEDGEN:56485","NCIT:C84885","NANDO:2200525","UMLS:C0162671","NANDO:1200176"],"synonyms":[{"name":"MELAS","type":"related"},{"name":"MELAS syndrome","type":"exact"},{"name":"mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes","type":"related"},{"name":"mitochondrial encephalomyopathy, lactic acidosis and stroke","type":"exact"},{"name":"mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes","type":"exact"},{"name":"mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes","type":"exact"},{"name":"mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes","type":"exact"}],"termid":"MONDO:0010789","terms_by_termid":{"MONDO:0010789":null},"xrefs":{"Monarch":{"xref_id":"0010789"}}}


id: PBO:0070450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L3 pseudogene 7","termid":"PBO:0070450"}


id: PBO:0117456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S43a","termid":"PBO:0117456"}


id: PBO:0074867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 51","termid":"PBO:0074867"}


id: MONDO:0003686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant sweat gland neoplasm with apocrine differentiation. Representative examples include apocrine adenoma, ceruminous adenocarcinoma, and apocrine breast carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sweat gland neoplasm","termid":"MONDO:0002381"},{"relation_name":"is_a","term_name":"apocrine sweat gland disorder","termid":"MONDO:0024467"}],"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":"apocrine sweat gland neoplasm","secondary_identifiers":["MEDGEN:272320","DOID:5876","NCIT:C6798","UMLS:C1332318"],"synonyms":[{"name":"apocrine neoplasm","type":"exact"},{"name":"apocrine neoplasm of skin","type":"exact"},{"name":"apocrine neoplasm of the skin","type":"exact"},{"name":"apocrine skin neoplasm","type":"exact"},{"name":"apocrine skin tumor","type":"exact"},{"name":"apocrine skin tumour","type":"exact"},{"name":"apocrine sweat gland neoplasm (disease)","type":"exact"},{"name":"apocrine sweat gland tumor","type":"exact"},{"name":"apocrine sweat gland tumour","type":"exact"},{"name":"apocrine tumor","type":"exact"},{"name":"apocrine tumor of skin","type":"exact"},{"name":"apocrine tumor of the skin","type":"exact"},{"name":"apocrine tumour","type":"exact"},{"name":"apocrine tumour of skin","type":"exact"},{"name":"apocrine tumour of the skin","type":"exact"},{"name":"neoplasm of apocrine sweat gland","type":"exact"},{"name":"tumor of apocrine sweat gland","type":"exact"},{"name":"tumour of apocrine sweat gland","type":"exact"}],"termid":"MONDO:0003686","xrefs":{"Monarch":{"xref_id":"0003686"}}}


id: GO:0050931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a pigmented cell, such as a melanocyte.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"developmental pigmentation","termid":"GO:0048066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pigment cell differentiation","secondary_identifiers":["GO:0043357","GO:0043358"],"synonyms":[{"name":"chromatophore differentiation","type":"exact"},{"name":"pigmented cell differentiation","type":"exact"}],"termid":"GO:0050931"}


id: PBO:0074135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 34 member 3","termid":"PBO:0074135"}


id: GO:0071416
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a tropane stimulus. Tropane is a nitrogenous bicyclic organic compound mainly known for a group of alkaloids derived from it (called tropane alkaloids), which include, among others, atropine and cocaine.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to tropane","termid":"GO:0014073"},{"relation_name":"is_a","term_name":"cellular response to alkaloid","termid":"GO:0071312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to tropane","termid":"GO:0071416"}


id: MONDO:0000268
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lymphoid interstitial pneumonia (obsolete MONDO:0000268)","termid":"MONDO:0000268","xrefs":{"Monarch":{"xref_id":"0000268"}}}


id: MONDO:0001955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dysentery that involves protozoan infection.","definition_xrefs":["DOID:14397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysentery","termid":"MONDO:0001517"},{"relation_name":"is_a","term_name":"protozoa infectious disease","termid":"MONDO:0002428"},{"relation_name":"is_a","term_name":"parasitic intestinal disorder","termid":"MONDO:0024270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"protozoal dysentery","secondary_identifiers":["ICD9:007.8","MEDGEN:1843396","UMLS:C2142761"],"termid":"MONDO:0001955","xrefs":{"Monarch":{"xref_id":"0001955"}}}


id: PBO:0066722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 19","termid":"PBO:0066722"}


id: GO:0090013
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of any TGF-beta receptor signaling pathway that contributes to the formation of the primitive streak.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transforming growth factor beta receptor signaling pathway involved in primitive streak formation (obsolete GO:0090013)","synonyms":[{"name":"regulation of transforming growth factor beta receptor signalling pathway involved in primitive streak formation","type":"exact"}],"termid":"GO:0090013"}


id: PBO:0053311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lin-54 DREAM MuvB core complex component","termid":"PBO:0053311"}


id: FYPO:0002769
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the spindle pole body is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton","termid":"FYPO:0004090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to spindle pole body","synonyms":[{"name":"abnormal protein localisation to spindle pole body","type":"exact"},{"name":"abnormal protein localization to SPB","type":"exact"}],"termid":"FYPO:0002769"}


id: GO:0046118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 7-methylguanosine, a modified nucleoside that forms a cap at the 5'-terminus of eukaryotic mRNA.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"7-methylguanosine metabolic process","termid":"GO:0008618"},{"relation_name":"is_a","term_name":"guanosine-containing compound biosynthetic process","termid":"GO:1901070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"7-methylguanosine biosynthetic process","synonyms":[{"name":"7-methylguanosine anabolism","type":"exact"},{"name":"7-methylguanosine biosynthesis","type":"exact"},{"name":"7-methylguanosine formation","type":"exact"},{"name":"7-methylguanosine synthesis","type":"exact"}],"termid":"GO:0046118"}


id: MONDO:0002287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A reactive inflammatory disorder affecting the bladder. It is characterized by the development of small cysts in the bladder wall. The cysts are lined by metaplastic glandular cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic cystitis","termid":"MONDO:0006030"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glandular cystitis","secondary_identifiers":["DOID:2392","UMLS:C0268837","NCIT:C39860","ICD9:595.89","MEDGEN:82830","SCTID:72815004"],"synonyms":[{"name":"cystitis glandularis","type":"related"}],"termid":"MONDO:0002287","xrefs":{"Monarch":{"xref_id":"0002287"}}}


id: PBO:0041580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 22 open reading frame 15","termid":"PBO:0041580"}


id: MONDO:0018680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pseudolymphoma of the skin.","definition_xrefs":["NCIT:C62776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"is_a","term_name":"immunoglobulin G4-related sclerosing disease","termid":"MONDO:0017287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"cutaneous pseudolymphoma","secondary_identifiers":["icd11.foundation:1620802923","SCTID:128862000","GARD:21889","Orphanet:451607","UMLS:C0311220","MEDGEN:81385"],"synonyms":[{"name":"lymphadenosis Benigna cutis","type":"exact"},{"name":"lymphocytoma cutis","type":"exact"},{"name":"pseudolymphoma of Spiegler","type":"exact"}],"termid":"MONDO:0018680","xrefs":{"Monarch":{"xref_id":"0018680"}}}


id: MONDO:0008802
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":"antithrombin, familial hemorrhagic diathesis due to","secondary_identifiers":["UMLS:C1859761","MEDGEN:347227","MESH:C565947","OMIM:207300"],"synonyms":[{"name":"antithrombin, familial hemorrhagic diathesis due to","type":"exact"}],"termid":"MONDO:0008802","xrefs":{"Monarch":{"xref_id":"0008802"}}}


id: MONDO:0006443
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tenosynovial giant cell tumor (obsolete MONDO:0006443)","termid":"MONDO:0006443","xrefs":{"Monarch":{"xref_id":"0006443"}}}


id: MONDO:1012148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"malignant hyperthermia, non-human animal","termid":"MONDO:1011713"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malignant hyperthermia, pig","secondary_identifiers":["OMIA:000621-9823"],"termid":"MONDO:1012148","xrefs":{"Monarch":{"xref_id":"1012148"}}}


id: PBO:0111885
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin-14 family","termid":"PBO:0111885"}


id: PBO:0027342
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_DNA_primase_activity","termid":"PBO:0027342"}


id: PBO:0110425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2D3 pseudogene 5","termid":"PBO:0110425"}


id: MONDO:0009232
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fuhrmann syndrome is mainly characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly.","definition_xrefs":["Orphanet:2854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"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":"Fuhrmann syndrome","secondary_identifiers":["MESH:C538189","UMLS:C1856728","OMIM:228930","MEDGEN:346429","SCTID:721296004","DOID:0090067","GARD:2410"],"synonyms":[{"name":"Fuhrmann syndrome","type":"exact"},{"name":"Fuhrmann-Rieger-de Sousa syndrome","type":"exact"},{"name":"bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies","type":"related"},{"name":"fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly","type":"related"},{"name":"fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome","type":"exact"}],"termid":"MONDO:0009232","xrefs":{"Monarch":{"xref_id":"0009232"}}}


id: GO:0002286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a mature or immature T cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte activation involved in immune response","termid":"GO:0002285"},{"relation_name":"is_a","term_name":"T cell activation","termid":"GO:0042110"}],"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":"T cell activation involved in immune response","synonyms":[{"name":"T cell activation during immune response","type":"related"},{"name":"T lymphocyte activation during immune response","type":"related"},{"name":"T-cell activation during immune response","type":"related"},{"name":"T-lymphocyte activation during immune response","type":"related"}],"termid":"GO:0002286"}


id: PR:O42945
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03207","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":"pre-mRNA-splicing factor ATP-dependent RNA helicase prp43 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16H5.10c","secondary_identifiers":["UniProtKB:O42945"],"synonyms":[{"name":"Spom972h-DHX15","type":"exact"}],"termid":"PR:O42945"}


id: MONDO:0012387
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by sclerosing bone dysplasia, ichthyosis vulgaris and premature ovarian failure. The bone disorder affects all metaphyseal-diaphyseal regions of the long bones, the skull, and the metacarpals.","definition_xrefs":["Orphanet:75325"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"osteosclerosis-ichthyosis-premature ovarian failure syndrome","secondary_identifiers":["SCTID:722114007","UMLS:C1864942","MEDGEN:355875","GARD:9904","OMIM:609993","MESH:C536064"],"synonyms":[{"name":"osteosclerosis with ichthyosis and POF","type":"related"},{"name":"osteosclerosis with ichthyosis and premature ovarian failure","type":"related"},{"name":"sclerosing dysplasia of bone with ichthyosis and premature ovarian failure","type":"related"},{"name":"sclerosing dysplasia of bone-ichthyosis-premature ovarian failure syndrome","type":"exact"}],"termid":"MONDO:0012387","xrefs":{"Monarch":{"xref_id":"0012387"}}}


id: PBO:0081203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger with KRAB and SCAN domains 4","termid":"PBO:0081203"}


id: GO:0102617
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oryzalexin B + NAD(P) = oryzalexin C + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oryzalexin C synthase (oryzalexin B dependent) activity (obsolete GO:0102617)","termid":"GO:0102617"}


id: MONDO:0010965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TMIE gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 6","secondary_identifiers":["DOID:0110512","MESH:C563418","OMIM:600971","UMLS:C1832992","GARD:22586","MEDGEN:322088"],"synonyms":[{"name":"DFNB6","type":"narrow"},{"name":"TMIE autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 6","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 6","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in TMIE","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 6","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 6","type":"exact"},{"name":"deafness, autosomal recessive 6","type":"narrow"},{"name":"deafness, autosomal recessive type 6","type":"narrow"},{"name":"neurosensory nonsyndromic recessive deafness 6","type":"narrow"}],"termid":"MONDO:0010965","xrefs":{"Monarch":{"xref_id":"0010965"}}}


id: PBO:0043998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorionic somatomammotropin hormone like 1","termid":"PBO:0043998"}


id: MONDO:0006525
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory skin condition caused by an immune response to direct contact between the skin and an allergen. It consists of a delayed type of allergic reaction at the affected site with resulting red, swollen, and blistered skin that may itch or leak.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atopic eczema","termid":"MONDO:0004980"},{"relation_name":"is_a","term_name":"contact dermatitis","termid":"MONDO:0005480"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"allergic contact dermatitis","secondary_identifiers":["icd11.foundation:2020673786","MEDGEN:102474","DOID:3042","ICD10WHO:L23","MESH:D017449","NCIT:C26998","SCTID:238575004","EFO:1000668","ICD9:692.9","UMLS:C0162820","ICD10CM:L23"],"synonyms":[{"name":"allergic contact dermatitis","type":"exact"},{"name":"allergic form of contact dermatitis","type":"exact"}],"termid":"MONDO:0006525","xrefs":{"Monarch":{"xref_id":"0006525"}}}


id: PBO:0079847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unc-45 myosin chaperone B","termid":"PBO:0079847"}


id: PATO:0000490
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000490 rhythym value (obsolete PATO:0000490)","termid":"PATO:0000490"}


id: MOD:01795
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue containing common isotopes to 1x(13)C,3x(2)H C(6)-labeled L-methionine.","definition_xrefs":["PubMed:15782174","PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"},{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"},{"relation_name":"is_a","term_name":"1x(13)C,3x(2)H labeled monomethylated residue","termid":"MOD:01794"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1x(13)C,3x(2)H C(6)-labeled L-methionine","synonyms":[{"name":"Methyl:2H(3)13C(1)","type":"related"}],"termid":"MOD:01795"}


id: PBO:0058957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"makorin ring finger protein 1","termid":"PBO:0058957"}


id: PBO:0052210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNQ5 antisense RNA 1","termid":"PBO:0052210"}


id: GO:0048019
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The activity of a gene product that interacts with a receptor to decrease the ability of the receptor agonist to bind and activate the receptor.","definition_xrefs":["ISBN:0198506732","GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"},{"relation_name":"is_a","term_name":"signaling receptor inhibitor activity","termid":"GO:0030547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140678","GO:0098772","GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"receptor antagonist activity","synonyms":[{"name":"receptor ligand activity","type":"broad"}],"termid":"GO:0048019"}


id: PBO:0072276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S23 pseudogene 5","termid":"PBO:0072276"}


id: PBO:0054121
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 1487","termid":"PBO:0054121"}


id: PBO:0084365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipid-binding ER protein, enriched at nucleus-vacuolar junctions (NVJ); involved in nonvesicular transfer of ceramides from ER to Golgi; may be involved in sterol metabolism or signaling at the NVJ; contains a synaptotagmin-like-mitochondrial-lipid binding protein (SMP) domain; binds phosphatidylinositols and other lipids in a large-scale study; may interact with ribosomes, based on co-purification experiments","termid":"PBO:0084365"}


id: PBO:0055330
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 2758","termid":"PBO:0055330"}


id: PBO:0030545
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_cAMP_level","termid":"PBO:0030545"}


id: GO:1905391
data:
  {"annotated_genes":["SJAG_02645"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109931],"is_not":false,"summary":null,"term":"GO:1905391"}]},"cv_name":"biological_process","definition":"Any regulation of protein localization to cell division site that is involved in cell separation after cytokinesis.","definition_xrefs":["PMID:25411334","GO_REF:0000060","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell division site","termid":"GO:1901900"},{"relation_name":"part_of","term_name":"septum digestion after cytokinesis","termid":"GO:0000920"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02645":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein localization to cell division site involved in cell separation after cytokinesis","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of protein localisation to cell division site involved in cell separation after cytokinesis","type":"exact"},{"name":"regulation of protein localisation to cell division site involved in cell separation following cytokinesis","type":"exact"},{"name":"regulation of protein localisation to cell division site involved in cytokinetic cell separation","type":"related"},{"name":"regulation of protein localisation to cell division site involved in mitotic cytokinetic cell separation","type":"exact"}],"termid":"GO:1905391","terms_by_termid":{"GO:1905391":null}}


id: PBO:0002322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial methionine-tRNA ligase (predicted)","termid":"PBO:0002322"}


id: GO:0051145
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a smooth muscle cell; smooth muscle lacks transverse striations in its constituent fibers and are almost always involuntary.","definition_xrefs":["GOC:ai","CL:0000192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle cell differentiation","termid":"GO:0042692"}],"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":"smooth muscle cell differentiation","synonyms":[{"name":"nonstriated muscle cell differentiation","type":"exact"}],"termid":"GO:0051145"}


id: MONDO:0003760
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor that arises from the ovary and occurs in children.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood germ cell tumor","termid":"MONDO:0003751"},{"relation_name":"is_a","term_name":"ovarian germ cell tumor","termid":"MONDO:0011366"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pediatric ovarian germ cell tumor","secondary_identifiers":["DOID:6084","MEDGEN:162990","NCIT:C8588","UMLS:C0796664"],"synonyms":[{"name":"childhood ovarian germ cell neoplasm","type":"exact"},{"name":"childhood ovarian germ cell tumor","type":"exact"},{"name":"childhood ovarian germ cell tumour","type":"exact"},{"name":"ovarian germ cell tumor","type":"broad"},{"name":"ovarian germ cell tumor of childhood","type":"exact"},{"name":"ovarian germ cell tumour","type":"broad"},{"name":"ovarian germ cell tumour of childhood","type":"exact"},{"name":"paediatric ovarian germ cell neoplasm","type":"exact"},{"name":"pediatric ovarian germ cell neoplasm","type":"exact"},{"name":"pediatric ovarian germ cell tumor","type":"exact"}],"termid":"MONDO:0003760","xrefs":{"Monarch":{"xref_id":"0003760"}}}


id: PBO:0060641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor coactivator 4","termid":"PBO:0060641"}


id: MONDO:0002391
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete skin sarcoma (obsolete MONDO:0002391)","termid":"MONDO:0002391","xrefs":{"Monarch":{"xref_id":"0002391"}}}


id: GO:0016180
data:
  {"annotated_genes":["SJAG_04586","SJAG_00319","SJAG_03572","SJAG_03179","SJAG_04084","SJAG_02993","SJAG_04818","SJAG_04754","SJAG_00081","SJAG_01521","SJAG_04286","SJAG_00559","SJAG_00854","SJAG_01234","SJAG_04824","SJAG_04527","SJAG_03257","SJAG_04153","SJAG_02156","SJAG_00088","SJAG_00083","SJAG_01191","SJAG_00566","SJAG_04321","SJAG_01176","SJAG_01798","SJAG_01958"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92579,110011,118050],"is_not":false,"summary":null,"term":"GO:0016180"},{"annotations":[97143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120049"},{"annotations":[117448,105778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034472"},{"annotations":[79504,108257,82173,61350,65128,59699,108194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031120"},{"annotations":[73499,73207,74324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034473"},{"annotations":[104127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034474"},{"annotations":[73208,78129,76209,78575,75439,73500,75092,79565,90328,76961,74325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034475"},{"annotations":[73501,100895,74326,73209,91927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034476"},{"annotations":[81289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034477"}]},"cv_name":"biological_process","definition":"Any process involved in the conversion of a primary small nuclear RNA (snRNA) transcript into a mature snRNA molecule. The primary function of snRNAs is processing pre-messenger RNA in the nucleus. They have also been shown to aid in the regulation of transcription factors (7SK RNA) or RNA polymerase II (B2 RNA), and maintaining the telomeres.","definition_xrefs":["PMID:31815536","PMID:15196465"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA processing","termid":"GO:0006396"},{"relation_name":"is_a","term_name":"snRNA metabolic process","termid":"GO:0016073"}],"gene_count":27,"genes_by_uniquename":{"SJAG_00081":null,"SJAG_00083":null,"SJAG_00088":null,"SJAG_00319":null,"SJAG_00559":null,"SJAG_00566":null,"SJAG_00854":null,"SJAG_01176":null,"SJAG_01191":null,"SJAG_01234":null,"SJAG_01521":null,"SJAG_01798":null,"SJAG_01958":null,"SJAG_02156":null,"SJAG_02993":null,"SJAG_03179":null,"SJAG_03257":null,"SJAG_03572":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04286":null,"SJAG_04321":null,"SJAG_04527":null,"SJAG_04586":null,"SJAG_04754":null,"SJAG_04818":null,"SJAG_04824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0016073"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0016073","GO:0008150"],"is_obsolete":false,"name":"snRNA processing","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"snRNA maturation","type":"exact"},{"name":"snRNA production","type":"exact"}],"termid":"GO:0016180","terms_by_termid":{"GO:0016180":null,"GO:0031120":null,"GO:0034472":null,"GO:0034473":null,"GO:0034474":null,"GO:0034475":null,"GO:0034476":null,"GO:0034477":null,"GO:0120049":null}}


id: SO:0000693
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes an mRNA that is recoded.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"recoded","termid":"SO:0000881"},{"relation_name":"is_a","term_name":"protein_coding_gene","termid":"SO:0001217"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene_with_recoded_mRNA","synonyms":[{"name":"gene with recoded mRNA","type":"exact"}],"termid":"SO:0000693"}


id: MONDO:1010888
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuronal ceroid lipofuscinosis that occurs in cattle due to a mutation in the CLN5 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal ceroid lipofuscinosis, cattle","termid":"MONDO:1011568"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal ceroid lipofuscinosis, CLN5-related, cattle","secondary_identifiers":["OMIA:001482-9913"],"synonyms":[{"name":"CLN5","type":"exact"},{"name":"neuronal ceroid lipofuscinosis, 5, cattle","type":"related"}],"termid":"MONDO:1010888","xrefs":{"Monarch":{"xref_id":"1010888"}}}


id: PBO:0060455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglutamate synthase","termid":"PBO:0060455"}


id: GO:0048702
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the neurocranium are generated and organized during the embryonic phase. The neurocranium is the portion of the vertebrate skull surrounding the brain.","definition_xrefs":["GOC:jid","GOC:dsf","PMID:16049113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"embryonic cranial skeleton morphogenesis","termid":"GO:0048701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"embryonic neurocranium morphogenesis","synonyms":[{"name":"embryonic braincase morphogenesis","type":"exact"},{"name":"embryonic chondrocranium morphogenesis","type":"exact"}],"termid":"GO:0048702"}


id: PBO:0091285
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LAMtor","termid":"PBO:0091285"}


id: PBO:0027987
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_without_cell_division,_cell_enlarged_around_nucleus","termid":"PBO:0027987"}


id: GO:1902462
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mesenchymal stem cell proliferation.","definition_xrefs":["PMID:18672106","GOC:pm","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal stem cell proliferation","termid":"GO:1902460"},{"relation_name":"is_a","term_name":"positive regulation of stem cell proliferation","termid":"GO:2000648"},{"relation_name":"positively_regulates","term_name":"mesenchymal stem cell proliferation","termid":"GO:0097168"}],"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 mesenchymal stem cell proliferation","synonyms":[{"name":"activation of MSC proliferation","type":"narrow"},{"name":"activation of mesenchymal stem cell proliferation","type":"narrow"},{"name":"positive regulation of MSC proliferation","type":"exact"},{"name":"up regulation of MSC proliferation","type":"exact"},{"name":"up regulation of mesenchymal stem cell proliferation","type":"exact"},{"name":"up-regulation of MSC proliferation","type":"exact"},{"name":"up-regulation of mesenchymal stem cell proliferation","type":"exact"},{"name":"upregulation of MSC proliferation","type":"exact"},{"name":"upregulation of mesenchymal stem cell proliferation","type":"exact"}],"termid":"GO:1902462"}


id: FYPO:0007004
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone exchange occurs to a lower extent than normal in regions containing protein coding genes. Histone exchange is replacement, within chromatin, of resident histones or histone subunits with alternative, sometimes variant, histones or subunits.","definition_xrefs":["PMID:26518661","GO:0005721","GO:0043486","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal chromatin organization during vegetative growth","termid":"FYPO:0001352"},{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"},{"relation_name":"is_a","term_name":"abnormal histone exchange","termid":"FYPO:0007472"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000641","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone exchange at protein coding gene during vegetative growth","synonyms":[{"name":"decreased histone exchange at protein coding gene during mitotic cell cycle","type":"related"},{"name":"reduced histone exchange at protein coding gene during vegetative growth","type":"exact"}],"termid":"FYPO:0007004"}


id: MONDO:0007722
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":"heterochromia iridis","secondary_identifiers":["UMLS:C0423318","MESH:C538115","MEDGEN:98395","HP:0001100","OMIM:142500"],"synonyms":[{"name":"heterochromia iridis","type":"exact"},{"name":"heterochromia iridis (disease)","type":"exact"}],"termid":"MONDO:0007722","xrefs":{"Monarch":{"xref_id":"0007722"}}}


id: MOD:00366
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-sulfo-L-serine.","definition_xrefs":["Unimod:40#S","PubMed:14752058","RESID:AA0361"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfated residue","termid":"MOD:00695"},{"relation_name":"is_a","term_name":"residues isobaric at 166.98-167.00 Da","termid":"MOD:00771"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-sulfo-L-serine","synonyms":[{"name":"(2S)-2-amino-3-(sulfooxy)propanoic acid","type":"exact"},{"name":"2-amino-3-hydroxypropanoic acid 3-sulfate","type":"exact"},{"name":"MOD_RES Sulfoserine","type":"exact"},{"name":"O-Sulfonation","type":"related"},{"name":"O-sulfo-L-serine","type":"exact"},{"name":"O3-sulfonoserine","type":"exact"},{"name":"O3-sulfoserine","type":"exact"},{"name":"Sulfo","type":"related"},{"name":"serine sulfate ester","type":"exact"}],"termid":"MOD:00366"}


id: MONDO:0002556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The rarest histopathologic subtype of Schwannoma. The reported cases have been located in the gastrointestinal submucosa or subcutaneous tissue. Morphologically it is characterized by the presence of a microcyst-rich network of spindle cells with minimal amount of cytoplasm and Antoni A tissue.","definition_xrefs":["NCIT:C5321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schwannoma","termid":"MONDO:0002546"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microcystic/reticular schwannoma","secondary_identifiers":["UMLS:C4054526","MEDGEN:882329"],"synonyms":[{"name":"microcystic/reticular schwannoma","type":"exact"}],"termid":"MONDO:0002556","xrefs":{"Monarch":{"xref_id":"0002556"}}}


id: PATO:0001602
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A size quality inhering in a bearer by virtue of the bearer's being abnormally expanded or increased in size.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased size","termid":"PATO:0000586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distended","synonyms":[{"name":"expanded ","type":"related"}],"termid":"PATO:0001602"}


id: GO:0033292
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level that results in the assembly, arrangement of constituent parts, or disassembly of the T-tubule. A T-tubule is an invagination of the plasma membrane of a muscle cell that extends inward from the cell surface around each myofibril.","definition_xrefs":["GOC:jl","GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane organization","termid":"GO:0061024"},{"relation_name":"part_of","term_name":"plasma membrane organization","termid":"GO:0007009"},{"relation_name":"part_of","term_name":"muscle cell development","termid":"GO:0055001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"T-tubule organization","synonyms":[{"name":"T-tubule organisation","type":"exact"},{"name":"T-tubule organization and biogenesis","type":"related"},{"name":"transverse tubule organization","type":"exact"}],"termid":"GO:0033292"}


id: MONDO:1011259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinitis pigmentosa that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa, non-human animal","termid":"MONDO:1010334"},{"relation_name":"is_a","term_name":"retinal degeneration, cattle","termid":"MONDO:1011247"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa, cattle","secondary_identifiers":["OMIA:001413-9913"],"termid":"MONDO:1011259","xrefs":{"Monarch":{"xref_id":"1011259"}}}


id: MONDO:0014830
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the SLFN14 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"platelet-type bleeding disorder 20","secondary_identifiers":["OMIM:616913","Orphanet:466806","MEDGEN:934764","DOID:0111055","UMLS:C4310797","GARD:18491"],"synonyms":[{"name":"BDPLT20","type":"exact"},{"name":"SLFN14 inherited bleeding disorder, platelet-type","type":"exact"},{"name":"autosomal dominant thrombocytopenia with platelet secretion defect","type":"exact"},{"name":"bleeding disorder, platelet-type, 20","type":"exact"},{"name":"inherited bleeding disorder, platelet-type caused by mutation in SLFN14","type":"exact"}],"termid":"MONDO:0014830","xrefs":{"Monarch":{"xref_id":"0014830"}}}


id: PBO:0001928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial matrix protein, F1F0 ATP synthase assembly factor Fmc1 (predicted)","termid":"PBO:0001928"}


id: FYPO:0001970
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 1,3-beta-D-glucan synthase activity is increased when cells are grown in medium containing aculeacin A.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased 1,3-beta-D-glucan synthase activity","termid":"FYPO:0001968"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0000707","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"increased 1,3-beta-D-glucan synthase activity during growth on aculeacin A","termid":"FYPO:0001970"}


id: PBO:0109191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi alpha-1,2-mannosyltransferase Omh4","termid":"PBO:0109191"}


id: PBO:0013775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy protein Atg11","termid":"PBO:0013775"}


id: PBO:0079102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TSBP1 and BTNL2 antisense RNA 1","termid":"PBO:0079102"}


id: PATO:0001676
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An efficiency which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"efficient","termid":"PATO:0001678"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased efficiency","synonyms":[{"name":"high efficiency","type":"exact"}],"termid":"PATO:0001676"}


id: GO:0032074
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the rate of nuclease activity, the hydrolysis of ester linkages within nucleic acids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catalytic activity","termid":"GO:0043086"},{"relation_name":"is_a","term_name":"negative regulation of nucleobase-containing compound metabolic process","termid":"GO:0045934"}],"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 nuclease activity","synonyms":[{"name":"down regulation of nuclease activity","type":"exact"},{"name":"down-regulation of nuclease activity","type":"exact"},{"name":"downregulation of nuclease activity","type":"exact"},{"name":"inhibition of nuclease activity","type":"narrow"},{"name":"nuclease inhibitor","type":"related"}],"termid":"GO:0032074"}


id: GO:0052514
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 the inflammatory response of a symbiont organism; the inflammatory response is the immediate defensive reaction (by vertebrate tissue) to infection or injury caused by chemical or physical agents. 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 positive regulation by organism of symbiont inflammatory response (obsolete GO:0052514)","synonyms":[{"name":"positive regulation by organism of symbiont inflammatory response","type":"exact"}],"termid":"GO:0052514"}


id: PATO:0002431
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality in which the bearer possesses a gradual, yet distinct, thinning from a wide starting point.","definition_xrefs":["PATOC:WC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"waisted","termid":"PATO:0002431"}


id: MONDO:0003354
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant soft tissue neoplasm that arises from the heart. The majority of cases are angiosarcomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart cancer","termid":"MONDO:0001340"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005267"],"is_obsolete":false,"name":"heart sarcoma","secondary_identifiers":["UMLS:C0238152","NCIT:C7723","DOID:5262","MEDGEN:68657"],"synonyms":[{"name":"Cardiac sarcoma","type":"exact"},{"name":"cardiac sarcoma","type":"exact"},{"name":"heart sarcoma","type":"exact"},{"name":"sarcoma of heart","type":"exact"},{"name":"sarcoma of the heart","type":"exact"}],"termid":"MONDO:0003354","xrefs":{"Monarch":{"xref_id":"0003354"}}}


id: PBO:0087315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Small subunit of the clathrin-associated adaptor complex AP-3; involved in vacuolar protein sorting; related to the sigma subunit of the mammalian clathrin AP-3 complex; suppressor of loss of casein kinase 1 function; protein abundance increases in response to DNA replication stress","termid":"PBO:0087315"}


id: PBO:0040420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V0 subunit d1","termid":"PBO:0040420"}


id: PBO:0091121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial glutamyl-tRNA amidotransferase complex subunit Gta3","termid":"PBO:0091121"}


id: MONDO:1011797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myopathy of the diaphragmatic muscles, non-human animal","secondary_identifiers":["OMIA:001319"],"termid":"MONDO:1011797","xrefs":{"Monarch":{"xref_id":"1011797"}}}


id: PBO:0064952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 4","termid":"PBO:0064952"}


id: PBO:0057381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548aw","termid":"PBO:0057381"}


id: MONDO:0003616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Formation of nodules in the isthmus of the fallopian tube due to fallopian tube diverticulosis. It may cause infertility or ectopic pregnancy.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic salpingitis","termid":"MONDO:0003617"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"salpingitis isthmica nodosa","secondary_identifiers":["DOID:5730","icd11.foundation:1586025352","MEDGEN:82840","UMLS:C0269043","NCIT:C40119","SCTID:36742000"],"termid":"MONDO:0003616","xrefs":{"Monarch":{"xref_id":"0003616"}}}


id: GO:1904902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form an ESCRT III complex.","definition_xrefs":["GOC:PARL","GO_REF:0000079","PMID:20588296","GOC:pad","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ESCRT complex assembly","termid":"GO:1904895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"ESCRT III complex assembly","synonyms":[{"name":"ESCRT III complex formation","type":"exact"}],"termid":"GO:1904902"}


id: PBO:0041642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel subunit alpha1 H","termid":"PBO:0041642"}


id: PBO:0002343
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactosialidosis","termid":"PBO:0002343"}


id: FYPO:0000540
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein transport is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal protein transport","termid":"FYPO:0005744"},{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein transport during vegetative growth","synonyms":[{"name":"abnormal protein transport during mitotic cell cycle","type":"related"},{"name":"protein transport: abnormal","type":"related"}],"termid":"FYPO:0000540"}


id: GO:0002313
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a naive B cell acquires the specialized features of a mature or memory B cell during an immune response.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell activation involved in immune response","termid":"GO:0002312"},{"relation_name":"is_a","term_name":"mature B cell differentiation","termid":"GO:0002335"}],"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":"mature B cell differentiation involved in immune response","synonyms":[{"name":"mature B cell development involved in immune response","type":"related"},{"name":"mature B cell differentiation during immune response","type":"related"},{"name":"mature B lymphocyte differentiation during immune response","type":"related"},{"name":"mature B-cell differentiation during immune response","type":"related"},{"name":"mature B-lymphocyte differentiation during immune response","type":"related"}],"termid":"GO:0002313"}


id: MONDO:0003046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the anal canal or anal margin. Representative examples of benign neoplasms include squamous papilloma and papillary hidradenoma. Representative examples of malignant neoplasms include carcinoma, lymphoma, and melanoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rectal neoplasm","termid":"MONDO:0002165"},{"relation_name":"is_a","term_name":"anus disorder","termid":"MONDO:0002519"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"anus neoplasm","secondary_identifiers":["UMLS:C0003463","EFO:0003835","DOID:4551","SCTID:126849006","NCIT:C2877","MESH:D001005","MEDGEN:360"],"synonyms":[{"name":"anal neoplasm","type":"exact"},{"name":"anal neoplasms, benign and malignant","type":"exact"},{"name":"anal tumor","type":"exact"},{"name":"anal tumors","type":"exact"},{"name":"anal tumour","type":"exact"},{"name":"anal tumours","type":"exact"},{"name":"anus neoplasm","type":"exact"},{"name":"anus neoplasm (disease)","type":"exact"},{"name":"anus tumor","type":"exact"},{"name":"anus tumour","type":"exact"},{"name":"neoplasm of anus","type":"exact"},{"name":"neoplasm of the anus","type":"exact"},{"name":"tumor of anus","type":"exact"},{"name":"tumor of the anus","type":"exact"},{"name":"tumour of anus","type":"exact"},{"name":"tumour of the anus","type":"exact"}],"termid":"MONDO:0003046","xrefs":{"Monarch":{"xref_id":"0003046"}}}


id: PBO:0002220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase Sdh1 (predicted)","termid":"PBO:0002220"}


id: MONDO:0019227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An inherited metabolic disease that is has its basis in the disruption of glycerol metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"gene_count":0,"genotype_count":0,"name":"obsolete inborn disorder of glycerol metabolism (obsolete MONDO:0019227)","secondary_identifiers":["icd11.foundation:61192754","Orphanet:79179"],"synonyms":[{"name":"disorder of glycerol metabolism","type":"related"},{"name":"inborn error of glycerol metabolic process","type":"exact"},{"name":"inborn glycerol metabolic process disorder","type":"exact"},{"name":"rare inborn error of glycerol metabolic process","type":"exact"}],"termid":"MONDO:0019227","xrefs":{"Monarch":{"xref_id":"0019227"}}}


id: GO:0016803
data:
  {"annotated_genes":["SJAG_01088"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004301"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of an ether bond, -O-.","definition_xrefs":["EC:3.3.2.-","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on ether bonds","termid":"GO:0016801"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01088":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"ether hydrolase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-8874435"],"termid":"GO:0016803","terms_by_termid":{"GO:0004301":null}}


id: GO:0002054
data:
  {"annotated_genes":["SJAG_01859"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002055"}]},"cv_name":"molecular_function","definition":"Binding to a nucleobase, any of a class of pyrmidines or purines, organic nitrogenous bases.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01859":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"nucleobase binding","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0002054","terms_by_termid":{"GO:0002055":null}}


id: PBO:0041627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel subunit alpha1 A","termid":"PBO:0041627"}


id: MONDO:0002264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete atrophy of prostate (obsolete MONDO:0002264)","secondary_identifiers":["ICD10WHO:N42.2","DOID:2301","ICD9:602.2","SCTID:29524003"],"synonyms":[{"name":"atrophic prostate","type":"related"},{"name":"atrophy of prostate","type":"exact"},{"name":"prostate atrophy","type":"related"}],"termid":"MONDO:0002264","xrefs":{"Monarch":{"xref_id":"0002264"}}}


id: PBO:0119275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial protein, implicated in regulation of proline metabolism (S. cerevisiae), and calcium import (human)","termid":"PBO:0119275"}


id: MONDO:0011279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation between D7S2453 and D7S525 in the chromosome region 7q31.","definition_xrefs":["PMID:15293785","DOID:0110472"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 17","secondary_identifiers":["GARD:22593","MESH:C566418","MEDGEN:355180","OMIM:603010","UMLS:C1864276"],"synonyms":[{"name":"DFNB17","type":"narrow"},{"name":"autosomal recessive deafness 17","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 17","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 17","type":"narrow"},{"name":"deafness, autosomal recessive 17","type":"narrow"}],"termid":"MONDO:0011279","xrefs":{"Monarch":{"xref_id":"0011279"}}}


id: MONDO:0019866
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mosaic trisomy 5 is a rare chromosomal anomaly syndrome with a variable phenotype ranging from clinically normal to patients presenting intrauterine growth retardation, congenital heart anomalies (mainly ventricular septal defect), multiple dysmorphic features (e.g. hypertelorism, prominent nasal bridge) and other congenital anomalies (incl. eventration of diaphragm, agenesis of corpus callosum, cloverleaf skull, clinodactyly, anteriorly placed anus). Psychomotor development may be normal in spite of low growth parameters being associated.","definition_xrefs":["Orphanet:96060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 5 disorder","termid":"MONDO:0700012"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mosaic trisomy 5","secondary_identifiers":["SCTID:764629008","UMLS:C2931603","MEDGEN:419849","MESH:C537762","GARD:19301"],"synonyms":[{"name":"Mosaic trisomy chromosome 5","type":"exact"},{"name":"Mosaic trisomy type 5","type":"exact"},{"name":"trisomy 5 mosaicism","type":"exact"}],"termid":"MONDO:0019866","xrefs":{"Monarch":{"xref_id":"0019866"}}}


id: MONDO:0019316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Maculopapular cutaneous mastocytosis (MCM) is a form of cutaneous mastocytosis (CM) characterized by the presence of multiple hyperpigmented macules, papules or nodules associated with abnormal accumulation of mast cells in the skin.","definition_xrefs":["Orphanet:79457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous mastocytosis","termid":"MONDO:0019023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"maculopapular cutaneous mastocytosis","secondary_identifiers":["MEDGEN:22588","NCIT:C3433","EFO:1001229","DOID:12309","GARD:16723","icd11.foundation:245322245","ICD9:708.8","ICDO:9740/1","UMLS:C0042111","MedDRA:10046752","SCTID:78745000"],"synonyms":[{"name":"Paucicellular mastocytosis","type":"related"},{"name":"UP/MPCM","type":"exact"},{"name":"telangiectasia macularis eruptive perstans","type":"related"},{"name":"telangiectatic cutaneous mastocytosis","type":"related"},{"name":"urticaria pigmentosa","type":"exact"},{"name":"urticaria pigmentosa/maculopapular cutaneous mastocytosis","type":"exact"}],"termid":"MONDO:0019316","xrefs":{"Monarch":{"xref_id":"0019316"}}}


id: GO:1904127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of convergent extension involved in somitogenesis.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:24892953","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of convergent extension involved in axis elongation","termid":"GO:1901232"},{"relation_name":"is_a","term_name":"regulation of convergent extension involved in gastrulation","termid":"GO:1904103"},{"relation_name":"regulates","term_name":"convergent extension involved in somitogenesis","termid":"GO:0090246"}],"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 convergent extension involved in somitogenesis","termid":"GO:1904127"}


id: GO:0033796
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reduction of elemental sulfur or polysulfide to hydrogen sulfide, H2 + n sulfur = H+ + hydrogen sulfide + (n-1) sulfur.","definition_xrefs":["RHEA:35591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on hydrogen as donor, with other known acceptors","termid":"GO:0046995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"sulfur reductase activity","secondary_identifiers":["MetaCyc:RXN-8269","EC:1.12.98.4"],"synonyms":[{"name":"(donor):sulfur oxidoreductase activity","type":"related"},{"name":"sulphur reductase activity","type":"exact"}],"termid":"GO:0033796"}


id: PATO:0002443
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being located at the same level as another entity.","definition_xrefs":["PATOC:NI"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"level with","termid":"PATO:0002443"}


id: PBO:0078000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAF3 interacting protein 1","termid":"PBO:0078000"}


id: MONDO:1012174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myasthenia, non-human animal","termid":"MONDO:1011849"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myasthenia, Amur tiger","secondary_identifiers":["OMIA:000684-74533"],"termid":"MONDO:1012174","xrefs":{"Monarch":{"xref_id":"1012174"}}}


id: MONDO:0003418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bile duct adenoma (obsolete MONDO:0003418)","termid":"MONDO:0003418","xrefs":{"Monarch":{"xref_id":"0003418"}}}


id: PR:P50999
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A T-complex protein 1 subunit delta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02432","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":"T-complex protein 1 subunit delta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC106.06","secondary_identifiers":["UniProtKB:P50999"],"synonyms":[{"name":"CCT-delta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CCT4","type":"exact"},{"name":"TCP-1-delta (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P50999"}


id: PBO:0040107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acylsphingosine amidohydrolase 2","termid":"PBO:0040107"}


id: PBO:0060417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-alpha-acetyltransferase 80, NatH catalytic subunit","termid":"PBO:0060417"}


id: MONDO:0004916
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0004916 (obsolete MONDO:0004916)","termid":"MONDO:0004916","xrefs":{"Monarch":{"xref_id":"0004916"}}}


id: PBO:0110490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ibosomal protein L17 pseudogene 52","termid":"PBO:0110490"}


id: PBO:0031616
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_transposition","termid":"PBO:0031616"}


id: GO:0015744
data:
  {"annotated_genes":["SJAG_01406"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098720"}]},"cv_name":"biological_process","definition":"The directed movement of succinate, the dianion of ethane dicarboxylic 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:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C4-dicarboxylate transport","termid":"GO:0015740"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01406":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"succinate transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0015744","terms_by_termid":{"GO:0098720":null}}


id: PBO:0081939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger HIT-type containing 2","termid":"PBO:0081939"}


id: GO:1902673
data:
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id: MONDO:0011882
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id: GO:0009117
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id: PBO:0084305
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id: PBO:0042941
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id: PBO:0070341
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id: PBO:0074589
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id: PBO:0070463
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id: PBO:0109617
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id: GO:0016318
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id: PBO:0047504
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id: FYPO:0002670
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id: GO:0090582
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id: PBO:0030973
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_methylation","termid":"PBO:0030973"}


id: PBO:0067746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 45","termid":"PBO:0067746"}


id: GO:0098573
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the mitochondrial membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of mitochondrial membrane (obsolete GO:0098573)","synonyms":[{"name":"intrinsic to mitochondrial membrane","type":"narrow"}],"termid":"GO:0098573"}


id: MONDO:0054725
data:
  {"annotated_genes":["SJAG_02500"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87302],"is_not":false,"summary":null,"term":"MONDO:0054725"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02500":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 21","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070163","OMIM:617644","UMLS:C4539991","MEDGEN:1617056"],"synonyms":[{"name":"SPGF21","type":"related"},{"name":"spermatogenic failure 21","type":"exact"}],"termid":"MONDO:0054725","terms_by_termid":{"MONDO:0054725":null},"xrefs":{"Monarch":{"xref_id":"0054725"}}}


id: GO:0047837
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-xylose + NADP+ = D-xylono-1,5-lactone + H+ + NADPH.","definition_xrefs":["RHEA:22000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"D-xylose 1-dehydrogenase (NADP+) activity","secondary_identifiers":["EC:1.1.1.179","KEGG_REACTION:R01430","MetaCyc:D-XYLOSE-1-DEHYDROGENASE-NADP+-RXN"],"synonyms":[{"name":"D-xylose (nicotinamide adenine dinucleotide phosphate) dehydrogenase activity","type":"related"},{"name":"D-xylose-NADP dehydrogenase activity","type":"related"},{"name":"D-xylose:NADP+ 1-oxidoreductase activity","type":"related"},{"name":"D-xylose:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047837"}


id: MONDO:1011003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polymicrogyria that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polymicrogyria, non-human animal","termid":"MONDO:1010237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymicrogyria, cattle","secondary_identifiers":["OMIA:001100-9913"],"termid":"MONDO:1011003","xrefs":{"Monarch":{"xref_id":"1011003"}}}


id: RO:HOM0000013
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Syntenic homology that involves chromosomes of different species.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_syntenic_homology_relationship_with","termid":"RO:HOM0000010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_syntenic_orthology_relationship_with","synonyms":[{"name":"syntenic orthologous to","type":"exact"}],"termid":"RO:HOM0000013"}


id: PBO:0084091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Guanine nucleotide exchange factor (GEF) for ADP ribosylation factors; involved in proliferation of the Golgi, intra-Golgi transport and ER-to-Golgi transport; found in the cytoplasm and on Golgi-associated coated vesicles","termid":"PBO:0084091"}


id: MONDO:0011755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Senior-Loken syndrome","termid":"MONDO:0017842"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005240"],"is_obsolete":false,"name":"senior-loken syndrome 3","secondary_identifiers":["MESH:C564637","MEDGEN:335569","OMIM:606995","GARD:15405","UMLS:C1846980"],"synonyms":[{"name":"SENIOR-Loken syndrome 3","type":"related"},{"name":"SLSN3","type":"exact"}],"termid":"MONDO:0011755","xrefs":{"Monarch":{"xref_id":"0011755"}}}


id: MONDO:0010220
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Young syndrome is characterized by the association of obstructive azoospermia with recurrent sinobronchial infections.","definition_xrefs":["Orphanet:3471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Young syndrome","secondary_identifiers":["MEDGEN:137934","SCTID:233666007","GARD:341","ICD9:759.89","OMIM:279000","UMLS:C0340037","icd11.foundation:1628320490","MedDRA:10063689","MESH:C536718"],"synonyms":[{"name":"Barry Perkins Young syndrome","type":"related"},{"name":"Barry-Perkins-Young syndrome","type":"related"},{"name":"azoospermia obstructive and chronic sinopulmonary infections","type":"related"},{"name":"azoospermia, obstructive, and chronic sinopulmonary infections","type":"related"},{"name":"azoospermia-sinopulmonary infections syndrome","type":"exact"},{"name":"sinusitis-infertility syndrome","type":"related"},{"name":"young syndrome","type":"exact"}],"termid":"MONDO:0010220","xrefs":{"Monarch":{"xref_id":"0010220"}}}


