# terms

id: PBO:0079809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP glycosyltransferase family 3 member A1","termid":"PBO:0079809"}


id: MONDO:0018743
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete immune-mediated acquired neuromuscular junction disease (obsolete MONDO:0018743)","secondary_identifiers":["Orphanet:464764"],"termid":"MONDO:0018743","xrefs":{"Monarch":{"xref_id":"0018743"}}}


id: PBO:0028387
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_methylglyoxal","termid":"PBO:0028387"}


id: FYPO:0009057
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process in which catastrophe rate (i.e. the frequency of transition from pause or growth to shrinkage) of microtubules is lower than normal as part of centromere clustering during meiotic prophase I.","definition_xrefs":["PMID:36435910"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased microtubule depolymerisation involved in meitotic centromere clustering during meiotic prophase I","termid":"FYPO:0009058"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000054"],"is_obsolete":false,"name":"decreased rate of microtubule catastrophe involved in meitotic centromere clustering during meiotic prophase I","termid":"FYPO:0009057"}


id: PBO:0049262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gasdermin A","termid":"PBO:0049262"}


id: GO:0099076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Vesicle-mediated transport of cargo from the mitochondrion to the peroxisome, mediated by a mitochondrion-derived vesicle.","definition_xrefs":["GOC:pad","GOC:PARL-UCL","PMID:20619655","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrion-derived vesicle mediated transport","termid":"GO:0099075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"mitochondrion to peroxisome vesicle-mediated transport","synonyms":[{"name":"mitochondrion to peroxisome transport","type":"exact"}],"termid":"GO:0099076"}


id: PBO:0079879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UPK1A antisense RNA 1","termid":"PBO:0079879"}


id: MONDO:0700136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital metabolic disorder characterized by a deficiency in the enzyme ferrochelatase, which occurs in cattle.","definition_xrefs":["NCIT:C131472"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bovine neoplasm","termid":"MONDO:0700134"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bovine protoporphyria","termid":"MONDO:0700136","xrefs":{"Monarch":{"xref_id":"0700136"}}}


id: MONDO:0012310
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital fibrosis of extraocular muscles","termid":"MONDO:0007614"}],"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":"fibrosis of extraocular muscles, congenital, with synergistic divergence","secondary_identifiers":["MEDGEN:351285","MESH:C566508","GARD:15466","UMLS:C1865040","OMIM:609612"],"synonyms":[{"name":"congenital fibrosis syndrome with synergistic divergence","type":"related"},{"name":"external ophthalmoplegia with synergistic divergence","type":"related"},{"name":"external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation","type":"related"},{"name":"fibrosis of extraocular muscles, congenital, with synergistic divergence","type":"exact"}],"termid":"MONDO:0012310","xrefs":{"Monarch":{"xref_id":"0012310"}}}


id: GO:1990767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the uptake of a prostaglandin receptor into an endocytic vesicle.","definition_xrefs":["PMID:15937517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor internalization","termid":"GO:0002031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"prostaglandin receptor internalization","termid":"GO:1990767"}


id: MONDO:0010744
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":"thrombocytopenia with elevated serum IgA and renal disease","secondary_identifiers":["OMIM:314000","MESH:C564051","MEDGEN:374149","UMLS:C1839162"],"synonyms":[{"name":"thrombocytopenia with elevated serum IgA and renal disease","type":"exact"}],"termid":"MONDO:0010744","xrefs":{"Monarch":{"xref_id":"0010744"}}}


id: GO:0099616
data:
  {"annotated_genes":["SJAG_00852","SJAG_01249"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[100452,103763],"is_not":false,"summary":null,"term":"GO:0099616"}]},"cv_name":"cellular_component","definition":"The component of the matrix side of the mitochondrial inner membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of mitochondrial inner membrane","termid":"GO:0031314"},{"relation_name":"part_of","term_name":"matrix side of mitochondrial inner membrane","termid":"GO:0099617"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00852":null,"SJAG_01249":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005739"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005739"],"is_obsolete":false,"name":"extrinsic component of matrix side of mitochondrial inner membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0099616","terms_by_termid":{"GO:0099616":null}}


id: MONDO:0013709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0006025"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 28","secondary_identifiers":["MEDGEN:482175","GARD:22562","DOID:0081199","OMIM:614347","UMLS:C3280545"],"synonyms":[{"name":"MRT28","type":"exact"},{"name":"intellectual disability, autosomal recessive 28","type":"exact"},{"name":"mental retardation, autosomal recessive 28","type":"related"}],"termid":"MONDO:0013709","xrefs":{"Monarch":{"xref_id":"0013709"}}}


id: PBO:0005899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Cysteine, mitochondrial","termid":"PBO:0005899"}


id: FYPO:0001495
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is viable, is elongated, and contains more than one nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated multinucleate vegetative cell","termid":"FYPO:0000133"},{"relation_name":"is_a","term_name":"viable elongated vegetative cell","termid":"FYPO:0001492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001320","FYPO:0005447","FYPO:0000032","FYPO:0001985","FYPO:0000004","FYPO:0000005","FYPO:0000002"],"is_obsolete":false,"name":"viable elongated multinucleate vegetative cell","synonyms":[{"name":"elongated multinucleate viable cell during vegetative growth","type":"exact"},{"name":"elongated multinucleate viable vegetative cell","type":"exact"},{"name":"viable elongated multinucleate vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001495"}


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


id: PR:Q9P7Q1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC186.02c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7Q1"],"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":"2-hydroxyacid dehydrogenase homolog 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC186.02c","synonyms":[{"name":"Spom972h-SPAC186.02c","type":"exact"}],"termid":"PR:Q9P7Q1"}


id: PBO:0063213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCCA antisense RNA 1","termid":"PBO:0063213"}


id: PBO:0044489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 46 subfamily A member 1","termid":"PBO:0044489"}


id: PBO:0090067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI-anchor transamidase complex subunit Gaa1","termid":"PBO:0090067"}


id: GO:0170021
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of an ion by a channel that opens when a soluble compound has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["PMID:36828965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"taste receptor activity","termid":"GO:0008527"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic ion channel activity","termid":"GO:0015276"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0038023","GO:0022857"],"is_obsolete":false,"name":"ionotropic taste receptor activity","termid":"GO:0170021"}


id: GO:1905254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of epidermal growth factor receptor signaling pathway that is involved in heart process.","definition_xrefs":["GO_REF:0000060","GOC:bc","GOC:BHF","GOC:TermGenie","GOC:BHF_miRNA","PMID:23069713"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of epidermal growth factor receptor signaling pathway involved in heart process (obsolete GO:1905254)","synonyms":[{"name":"activation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"activation of epidermal growth factor receptor signaling pathway involved in heart process","type":"narrow"},{"name":"positive regulation of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"positive regulation of EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"positive regulation of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"positive regulation of EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"positive regulation of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"positive regulation of EGFR signaling pathway involved in heart process","type":"exact"},{"name":"positive regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"stimulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"stimulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"narrow"},{"name":"up regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"up regulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"},{"name":"up-regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"up-regulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"},{"name":"upregulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"upregulation of epidermal growth factor receptor signaling pathway involved in heart process","type":"exact"}],"termid":"GO:1905254"}


id: MONDO:0010069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spondylocostal dysostosis-anal and genitourinary malformations syndrome is characterized by the association of spondylocostal dysostosis with anal and genitourinary malformations (anal atresia and agenesis of external and internal genitalia). To date, only four cases have been described in the literature. Autosomal recessive inheritance has been suggested.","definition_xrefs":["Orphanet:94095"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"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":"spondylocostal dysostosis-anal and genitourinary malformations syndrome","secondary_identifiers":["MESH:C564799","UMLS:C1849069","MEDGEN:341373","OMIM:271520"],"synonyms":[{"name":"CMn syndrome","type":"related"},{"name":"Casamassima-Morton-Nance syndrome","type":"exact"},{"name":"spondylocostal dysostosis with anal atresia and urogenital anomalies","type":"related"},{"name":"spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome","type":"related"}],"termid":"MONDO:0010069","xrefs":{"Monarch":{"xref_id":"0010069"}}}


id: PBO:0076185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small ubiquitin like modifier 1","termid":"PBO:0076185"}


id: PBO:0116805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEPDC1 antisense RNA 2","termid":"PBO:0116805"}


id: GO:1900103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of endoplasmic reticulum unfolded protein response.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of endoplasmic reticulum unfolded protein response","termid":"GO:1900101"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"is_a","term_name":"positive regulation of response to endoplasmic reticulum stress","termid":"GO:1905898"},{"relation_name":"positively_regulates","term_name":"endoplasmic reticulum unfolded protein response","termid":"GO:0030968"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of endoplasmic reticulum unfolded protein response","synonyms":[{"name":"activation of ER unfolded protein response","type":"exact"},{"name":"activation of SREBP-mediated signalling pathway","type":"related"},{"name":"activation of endoplasmic reticulum unfolded protein response","type":"narrow"},{"name":"activation of erUPR","type":"exact"},{"name":"positive regulation of ER unfolded protein response","type":"exact"},{"name":"positive regulation of SREBP-mediated signalling pathway","type":"related"},{"name":"positive regulation of erUPR","type":"exact"},{"name":"up regulation of ER unfolded protein response","type":"exact"},{"name":"up regulation of SREBP-mediated signalling pathway","type":"related"},{"name":"up regulation of endoplasmic reticulum unfolded protein response","type":"exact"},{"name":"up regulation of erUPR","type":"exact"},{"name":"up-regulation of ER unfolded protein response","type":"exact"},{"name":"up-regulation of SREBP-mediated signalling pathway","type":"related"},{"name":"up-regulation of endoplasmic reticulum unfolded protein response","type":"exact"},{"name":"up-regulation of erUPR","type":"exact"},{"name":"upregulation of ER unfolded protein response","type":"exact"},{"name":"upregulation of SREBP-mediated signalling pathway","type":"related"},{"name":"upregulation of endoplasmic reticulum unfolded protein response","type":"exact"},{"name":"upregulation of erUPR","type":"exact"}],"termid":"GO:1900103"}


id: GO:0018063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The linkage of cytochromes and other heme proteins to heme.","definition_xrefs":["RESID:AA0135","RESID:AA0134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-heme linkage","termid":"GO:0017003"},{"relation_name":"is_a","term_name":"cytochrome complex assembly","termid":"GO:0017004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"cytochrome c-heme linkage","synonyms":[{"name":"cytochrome c-haem linkage","type":"exact"}],"termid":"GO:0018063"}


id: PBO:0064348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plexin B2","termid":"PBO:0064348"}


id: SO:0000391
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"U1 is a small nuclear RNA (snRNA) component of the spliceosome (involved in pre-mRNA splicing). Its 5' end forms complementary base pairs with the 5' splice junction, thus defining the 5' donor site of an intron. There are significant differences in sequence and secondary structure between metazoan and yeast U1 snRNAs, the latter being much longer (568 nucleotides as compared to 164 nucleotides in human). Nevertheless, secondary structure predictions suggest that all U1 snRNAs share a 'common core' consisting of helices I, II, the proximal region of III, and IV.","direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA","termid":"SO:0000274"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U1_snRNA","secondary_identifiers":["http://en.wikipedia.org/wiki/U1_snRNA"],"synonyms":[{"name":"U1 small nuclear RNA","type":"exact"},{"name":"U1 snRNA","type":"exact"},{"name":"small nuclear RNA U1","type":"exact"},{"name":"snRNA U1","type":"exact"}],"termid":"SO:0000391"}


id: PBO:0090477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ornithine N5 monooxygenase","termid":"PBO:0090477"}


id: PBO:0031800
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_at_mitotic_G2/M_phase_transition","termid":"PBO:0031800"}


id: PBO:0056314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase kinase 1","termid":"PBO:0056314"}


id: PBO:0086171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for synthesis of diphthamide; required along with Dph2p, Kti11p, Jjj3p, and Dph5p; diphthamide is a modified histidine residue of translation elongation factor 2 (Eft1p or Eft2p); forms a complex with Dph2p that catalyzes the first step of diphthamide biosynthesis","termid":"PBO:0086171"}


id: PBO:0089046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Mug130","termid":"PBO:0089046"}


id: GO:0003957
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADPH + NAD+ = NADP+ + NADH.","definition_xrefs":["RHEA:11692"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H as acceptor","termid":"GO:0016652"}],"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:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"NAD(P)+ transhydrogenase (Si-specific) activity","secondary_identifiers":["EC:1.6.1.1","Reactome:R-HSA-450971"],"synonyms":[{"name":"H+-thase","type":"broad"},{"name":"NAD transhydrogenase","type":"broad"},{"name":"NAD(P) transhydrogenase (B-specific) activity","type":"exact"},{"name":"NAD(P)+ transhydrogenase (B-specific) activity","type":"exact"},{"name":"NADH transhydrogenase","type":"broad"},{"name":"NADH-NADP-transhydrogenase","type":"broad"},{"name":"NADPH-NAD oxidoreductase","type":"broad"},{"name":"NADPH-NAD transhydrogenase","type":"broad"},{"name":"NADPH:NAD+ oxidoreductase (B-specific)","type":"related"},{"name":"NADPH:NAD+ transhydrogenase","type":"broad"},{"name":"nicotinamide adenine dinucleotide (phosphate) transhydrogenase","type":"broad"},{"name":"nicotinamide nucleotide transhydrogenase activity","type":"broad"},{"name":"non-energy-linked transhydrogenase activity","type":"related"},{"name":"pyridine nucleotide transferase","type":"broad"},{"name":"pyridine nucleotide transhydrogenase activity","type":"broad"}],"termid":"GO:0003957"}


id: PBO:0091494
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hal3 N-term functionally complements S. cerevisiae HAL3","termid":"PBO:0091494"}


id: PBO:0075959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"steroidogenic acute regulatory protein","termid":"PBO:0075959"}


id: GO:0033163
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a microneme.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bounding membrane of organelle","termid":"GO:0098588"},{"relation_name":"part_of","term_name":"microneme","termid":"GO:0020009"}],"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":"microneme membrane","termid":"GO:0033163"}


id: GO:0019593
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mannitol, the alditol derived from D-mannose by reduction of the aldehyde group.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexitol biosynthetic process","termid":"GO:0019406"},{"relation_name":"is_a","term_name":"mannitol metabolic process","termid":"GO:0019594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"mannitol biosynthetic process","secondary_identifiers":["MetaCyc:PWY-3881"],"synonyms":[{"name":"mannitol anabolism","type":"exact"},{"name":"mannitol biosynthesis","type":"exact"},{"name":"mannitol formation","type":"exact"},{"name":"mannitol synthesis","type":"exact"}],"termid":"GO:0019593"}


id: PBO:0004669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-ZNF_U1","termid":"PBO:0004669"}


id: MONDO:0006946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormalities of bone mineral metabolism associated with chronic kidney disease.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary hyperparathyroidism of renal origin","termid":"MONDO:0001530"},{"relation_name":"is_a","term_name":"rickets","termid":"MONDO:0005520"}],"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":"renal osteodystrophy","secondary_identifiers":["EFO:1001152","MEDGEN:20524","MESH:D012080","MedDRA:10038489","ICD10CM:N25.0","SCTID:16726004","DOID:13068","UMLS:C0035086","ICD9:588.0"],"synonyms":[{"name":"Osteodystrophies, renal","type":"related"},{"name":"osteodystrophy, renal","type":"related"},{"name":"renal Osteodystrophies","type":"related"},{"name":"renal rickets","type":"exact"},{"name":"rickets, renal","type":"related"}],"termid":"MONDO:0006946","xrefs":{"Monarch":{"xref_id":"0006946"}}}


id: SO:0001385
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_amino_acid_feature","synonyms":[{"name":"modified amino acid feature","type":"exact"}],"termid":"SO:0001385"}


id: MONDO:0018349
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"MAN1B1-CDG is a form of congenital disorders of N-linked glycosylation characterized by intellectual disability, delayed motor development, hypotonia and truncal obesity. Additional features include slight facial dysmorphism (hypertelorism, downslanting palpebral fissures, large, low-set ears, hypoplastic nasolabial fold, thin upper lip), hypermobility of the joints and skin laxity. The disease is caused by mutations in the gene MAN1B1 (9q34.3).","definition_xrefs":["Orphanet:397941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"MAN1B1-congenital disorder of glycosylation","secondary_identifiers":["GARD:12417","MEDGEN:1375785","SCTID:733450008","UMLS:C4518783"],"synonyms":[{"name":"MAN1B1-CDG","type":"exact"},{"name":"MAN1B1-congenital disorder of glycosylation","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency","type":"exact"},{"name":"congenital disorder of glycosylation type 2 due to MAN1B1 deficiency","type":"exact"},{"name":"congenital disorder of glycosylation type II due to MAN1B1 deficiency","type":"exact"},{"name":"intellectual disability-truncal obesity syndrome","type":"exact"}],"termid":"MONDO:0018349","xrefs":{"Monarch":{"xref_id":"0018349"}}}


id: PBO:0085705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in secretion and cell wall organization; localizes to plasma membrane microdomains called MCCs (membrane compartment occupied by Can1); GFP-fusion protein localizes to the cell periphery and vacuole; Sur7/PalI family transmembrane domain (TMD) containing protein; TOS7 has a paralog, DCV1, that arose from the whole genome duplication","termid":"PBO:0085705"}


id: PBO:0085084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear-enriched ubiquitin-like polyubiquitin-binding protein; required for spindle pole body (SPB) duplication and for transit through the G2/M phase of the cell cycle; involved in proteolysis; interacts with the proteasome; protein abundance increases in response to DNA replication stress","termid":"PBO:0085084"}


id: PBO:0027062
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_negative_regulation_of_premeiotic_DNA_replication_initiation_resulting_in_partial_rereplication","termid":"PBO:0027062"}


id: PBO:0045774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ecm29 proteasome adaptor and scaffold","termid":"PBO:0045774"}


id: PBO:0065635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPN11 pseudogene 4","termid":"PBO:0065635"}


id: GO:0031166
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the vacuolar membrane consisting of gene products and protein complexes that have some part that penetrates at least one leaflet of the membrane bilayer. May also refer to the state of being buried in the bilayer with no exposure outside the bilayer.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of vacuolar membrane (obsolete GO:0031166)","synonyms":[{"name":"integral to vacuolar membrane","type":"narrow"}],"termid":"GO:0031166"}


id: FYPO:0007515
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which RNA stability is decreased during a cellular response to oxidative stress. RNA molecules are more likely to degrade over a given time period than in wild type. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah","PMID:14633985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA stability","termid":"FYPO:0003038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased RNA stability during cellular response to oxidative stress","synonyms":[{"name":"decreased RNA stability during cellular response to oxidative stress during mitotic cell cycle","type":"related"},{"name":"decreased RNA stability during cellular response to oxidative stress during vegetative growth","type":"exact"},{"name":"decreased RNA stability in response to oxidative stress","type":"exact"},{"name":"reduced RNA stability during cellular response to oxidative stress","type":"exact"}],"termid":"FYPO:0007515"}


id: FYECO:0000027
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiment was performed in the presence of mating pheromone.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000027 presence of mating pheromone (obsolete FYECO:0000027)","termid":"FYECO:0000027"}


id: FYPO:0004438
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the mitotic spindle is longer than normal during anaphase.","definition_xrefs":["PMID:17352737","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long mitotic spindle","termid":"FYPO:0000733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002399"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0000120","FYPO:0005447","FYPO:0002399","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"long mitotic spindle during anaphase","synonyms":[{"name":"elongated mitotic spindle during anaphase","type":"exact"},{"name":"increased mitotic spindle length during anaphase","type":"exact"},{"name":"long bipolar mitotic spindle during anaphase","type":"exact"},{"name":"long mitotic spindle during anaphase during vegetative growth","type":"exact"},{"name":"long mitotic spindles during anaphase","type":"exact"},{"name":"long spindle during anaphase of mitosis","type":"exact"},{"name":"long spindle during mitotic anaphase","type":"exact"}],"termid":"FYPO:0004438"}


id: PBO:0047016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A19","termid":"PBO:0047016"}


id: PBO:0052047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KN motif and ankyrin repeat domains 3","termid":"PBO:0052047"}


id: PATO:0002173
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An alignment quality inhering in a bearer by virtue of the bearer's being in a improper spatial positioning towards an additional entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"misaligned with","termid":"PATO:0001654"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"misaligned towards","termid":"PATO:0002173"}


id: PBO:0074292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STE20 like kinase","termid":"PBO:0074292"}


id: SO:0000931
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a guide_RNA that base-pairs to a target mRNA.","definition_xrefs":["SO:jk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guide_RNA_region","termid":"SO:0000930"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anchor_region","synonyms":[{"name":"anchor region","type":"exact"}],"termid":"SO:0000931"}


id: GO:0048562
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Morphogenesis, during the embryonic phase, of a tissue or tissues that work together to perform a specific function or functions. Morphogenesis is the process in which anatomical structures are generated and organized. Organs are commonly observed as visibly distinct structures, but may also exist as loosely associated clusters of cells that work together to perform a specific function or functions.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"embryonic organ development","termid":"GO:0048568"}],"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 organ morphogenesis","termid":"GO:0048562"}


id: MONDO:0011266
data:
  {"annotated_genes":["SJAG_02043"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86207],"is_not":false,"summary":null,"term":"MONDO:0011266"}]},"cv_name":"mondo","definition":"Myotonic dystrophy type 2 (MD2), also known as proximal myotonic myopathy, is a very rare genetic multi-system disorder of late childhood or adult-onset characterized by mild myotonia, muscle weakness, and rarely cardiac conduction disorders.","definition_xrefs":["Orphanet:606"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myotonic dystrophy","termid":"MONDO:0016107"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02043":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myotonic dystrophy type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:41574007","UMLS:C2931689","GARD:9728","icd11.foundation:1005849639","OMIM:602668","NCIT:C122789","ICD9:359.2","NCIT:C122790","DOID:0050759","MEDGEN:419137","NCIT:C84680"],"synonyms":[{"name":"CNBP myotonic dystrophy","type":"exact"},{"name":"DM2","type":"related"},{"name":"PROMM","type":"related"},{"name":"dystrophia myotonica 2","type":"related"},{"name":"dystrophia myotonica type 2","type":"related"},{"name":"myotonic dystrophy 2","type":"related"},{"name":"myotonic dystrophy caused by mutation in CNBP","type":"exact"},{"name":"myotonic dystrophy type 2","type":"exact"},{"name":"myotonic myopathy, proximal","type":"related"},{"name":"proximal myotonic dystrophy","type":"exact"},{"name":"proximal myotonic myopathy","type":"exact"},{"name":"ricker disease","type":"exact"},{"name":"ricker syndrome","type":"exact"}],"termid":"MONDO:0011266","terms_by_termid":{"MONDO:0011266":null},"xrefs":{"Monarch":{"xref_id":"0011266"}}}


id: PBO:0083982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutamine-dependent NAD(+) synthetase; essential for the formation of NAD(+) from nicotinic acid adenine dinucleotide","termid":"PBO:0083982"}


id: PBO:0083077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dipeptidyl aminopeptidase; synthesized as a glycosylated precursor; localizes to the vacuolar membrane; similar to Ste13p","termid":"PBO:0083077"}


id: PBO:0051956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol 1,4,5-trisphosphate receptor type 3","termid":"PBO:0051956"}


id: PATO:0001732
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a plant by virtue of the bearer's disposition to not shed any body part.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shedability","termid":"PATO:0001729"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-deciduous (any body part)","termid":"PATO:0001732"}


id: PBO:0113519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-like protein conjugated to phosphatidylethanolamine (PE); role in membrane fusion and 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; targeted to vacuole via AP-3 pathway","termid":"PBO:0113519"}


id: RO:0002000
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"a relation between a 2D immaterial entity (the boundary) and a material entity, in which the boundary delimits the material entity","direct_ancestors":[{"relation_name":"is_a","term_name":"mereotopologically_related_to","termid":"RO:0002323"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2D_boundary_of","termid":"RO:0002000"}


id: PBO:0002854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase I upstream activation factor complex subunit Rrn5","termid":"PBO:0002854"}


id: GO:1900855
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of fumitremorgin B biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of fumitremorgin B biosynthetic process (obsolete GO:1900855)","synonyms":[{"name":"regulation of Lanosulin anabolism","type":"related"},{"name":"regulation of Lanosulin biosynthesis","type":"related"},{"name":"regulation of Lanosulin biosynthetic process","type":"related"},{"name":"regulation of Lanosulin formation","type":"related"},{"name":"regulation of Lanosulin synthesis","type":"related"},{"name":"regulation of fumitremorgin B anabolism","type":"exact"},{"name":"regulation of fumitremorgin B biosynthesis","type":"exact"},{"name":"regulation of fumitremorgin B formation","type":"exact"},{"name":"regulation of fumitremorgin B synthesis","type":"exact"}],"termid":"GO:1900855"}


id: PBO:0065348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRXL2C pseudogene 1","termid":"PBO:0065348"}


id: GO:0021684
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the cerebellar granule layer. This process pertains to the initial formation of a structure from unspecified parts. The granular layer is the innermost layer of the cerebellar cortex. This layer contains densely packed small neurons, mostly granule cells. Some Golgi cells are found at the outer border. Granule neurons send parallel fibers to the upper molecular layer, where they synapse with Purkinje cell dendrites. Mossy fibers from the pontine nuclei in the white matter synapse with granule cell axons, Golgi cell axons and unipolar brush interneuron axons at cerebellar glomeruli in the granule cell layer.","definition_xrefs":["ISBN:0838580343","GOC:cls","GO_REF:0000021","GOC:dph","GOC:jid","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"cerebellar granular layer morphogenesis","termid":"GO:0021683"},{"relation_name":"part_of","term_name":"cerebellar cortex formation","termid":"GO:0021697"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebellar granular layer formation","termid":"GO:0021684"}


id: MONDO:0005261
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pervasive developmental disorder - not otherwise specified (obsolete MONDO:0005261)","termid":"MONDO:0005261","xrefs":{"Monarch":{"xref_id":"0005261"}}}


id: PR:O74507
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC594.04c gene.","definition_xrefs":["UniProtKB:O74507","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C594.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC594.04c","synonyms":[{"name":"Spom972h-SPCC594.04c","type":"exact"}],"termid":"PR:O74507"}


id: GO:0019547
data:
  {"annotated_genes":["SJAG_03398"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70336],"is_not":false,"summary":null,"term":"GO:0019547"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of arginine into other compounds, including ornithine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arginine catabolic process","termid":"GO:0006527"},{"relation_name":"is_a","term_name":"ornithine metabolic process","termid":"GO:0006591"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03398":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281","GO:0044248"],"is_obsolete":false,"name":"arginine catabolic process to ornithine","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"arginine breakdown to ornithine","type":"exact"},{"name":"arginine degradation to ornithine","type":"exact"}],"termid":"GO:0019547","terms_by_termid":{"GO:0019547":null}}


id: PBO:0032745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF2B delta subunit","termid":"PBO:0032745"}


id: FYPO:0003309
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of IMP cyclohydrolase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000707","FYPO:0001985","FYPO:0000652","FYPO:0000661"],"is_obsolete":false,"name":"abnormal IMP cyclohydrolase activity","termid":"FYPO:0003309"}


id: MONDO:0012335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pro-opiomelanocortin (POMC) deficiency is a form of monogenic obesity resulting in severe early-onset obesity, adrenal insufficiency, red hair and pale skin.","definition_xrefs":["Orphanet:71526"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited obesity","termid":"MONDO:0019182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"obesity due to pro-opiomelanocortin deficiency","secondary_identifiers":["MESH:C565726","SCTID:702949005","ICD9:255.5","GARD:10823","icd11.foundation:530374033","NORD:110450","OMIM:609734","UMLS:C1857854","MEDGEN:341863"],"synonyms":[{"name":"OBAIRH","type":"related"},{"name":"POMC Deficiency","type":"exact"},{"name":"POMC deficiency","type":"exact"},{"name":"PROOPIOMELANOCORTIN deficiency","type":"related"},{"name":"obesity, adrenal insufficiency, and red hair due to POMC deficiency","type":"exact"},{"name":"obesity, early-onset, adrenal insufficiency, and Red hair","type":"related"},{"name":"obesity, early-onset, with adrenal insufficiency and RED hair","type":"related"},{"name":"obesity, early-onset, with adrenal insufficiency and Red hair","type":"related"}],"termid":"MONDO:0012335","xrefs":{"Monarch":{"xref_id":"0012335"}}}


id: GO:0021572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of rhombomere 6 over time, from its formation to the mature structure. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in anterior to posterior order.","definition_xrefs":["GOC:dph","GOC:curators","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere development","termid":"GO:0021546"}],"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":"rhombomere 6 development","termid":"GO:0021572"}


id: MONDO:0000692
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Kleine-Levin syndrome (obsolete MONDO:0000692)","termid":"MONDO:0000692","xrefs":{"Monarch":{"xref_id":"0000692"}}}


id: MONDO:0005648
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dysfunction of the aortic valve characterized by incomplete valve closure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aortic valve disorder","termid":"MONDO:0003803"},{"relation_name":"is_a","term_name":"vascular insufficiency disorder","termid":"MONDO:0020674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"aortic valve insufficiency","secondary_identifiers":["MEDGEN:8153","NANDO:2200307","SCTID:78031003","DOID:57","MESH:D001022","UMLS:C0003504","icd11.foundation:1548485475","ICD10CM:I06.1","ICD9:395.1","NCIT:C51223","ICD9:396.3","EFO:0007148"],"synonyms":[{"name":"Corrigan's disease","type":"related"},{"name":"aortic incompetence","type":"exact"},{"name":"aortic insufficiency","type":"exact"},{"name":"aortic regurgitation","type":"exact"},{"name":"rheumatic aortic insufficiency","type":"exact"},{"name":"rheumatic aortic regurgitation","type":"exact"},{"name":"rheumatic aortic valve insufficiency","type":"exact"},{"name":"rheumatic aortic valve regurgitation","type":"exact"}],"termid":"MONDO:0005648","xrefs":{"Monarch":{"xref_id":"0005648"}}}


id: GO:0090736
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a meprin and TRAF homology (MATH) domain.","definition_xrefs":["PMID:22621901","InterPro:IPR002083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"MATH domain binding","termid":"GO:0090736"}


id: GO:0050184
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a (9Z)-octadecenoyl-containing glycerolipid + 2 Fe(II)-[cytochrome b5] + 2 H+ + O2 = a (9Z,12Z)-octadecadienoyl-containing glycerolipid + 2 Fe(III)-[cytochrome b5] + 2 H2O.","definition_xrefs":["RHEA:46332"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water","termid":"GO:0016717"}],"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:0003674","GO:0003824"],"is_obsolete":false,"name":"acyl-lipid omega-6 desaturase (cytochrome b5) activity","secondary_identifiers":["GO:0102855","GO:0102857","GO:0102861","KEGG_REACTION:R03475","MetaCyc:RXN-9669","GO:0102860","EC:1.14.19.22","GO:0102871"],"synonyms":[{"name":"1-16:0-2-18:1-phosphatidylcholine desaturase activity","type":"narrow"},{"name":"1-18:1-2-18:2-phosphatidylcholine desaturase activity","type":"narrow"},{"name":"1-18:1-2-18:2-phosphatidylcholine synthase activity","type":"narrow"},{"name":"1-18:1-2-18:3-phosphatidylcholinedesaturase activity","type":"narrow"},{"name":"1-18:2-2-18:1-phosphatidylcholine desaturase activity (SN2-18:2 forming)","type":"narrow"},{"name":"1-acyl-2-oleoyl-sn-glycero-3-phosphocholine:NAD+ delta12-oxidoreductase activity","type":"related"},{"name":"linoleate synthase activity","type":"related"},{"name":"oleate desaturase activity","type":"related"},{"name":"oleoyl-CoA desaturase activity","type":"related"},{"name":"oleoylphosphatidylcholine desaturase activity","type":"related"},{"name":"phosphatidylcholine desaturase activity","type":"related"}],"termid":"GO:0050184"}


id: MONDO:0001558
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, lethal congenital malformation characterized by bilateral renal agenesis and the absence or decreased volume of amniotic fluid (oligohydramnios). The presence of oligohydramnios gives rise to congenital anomalies that include hypoplastic lungs, lower extremities abnormalities, and characteristic facial features (low-set ears, widely separated eyes, nose flattening, and receding chin). Newborn infants usually die of respiratory failure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"oligohydramnios","termid":"MONDO:0005881"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Potter sequence","secondary_identifiers":["MEDGEN:472617","UMLS:C0178426","DOID:12594","NCIT:C40435","ICD10CM:Q60.6","NANDO:2200157","SCTID:41962002"],"synonyms":[{"name":"Potter syndrome","type":"exact"},{"name":"Potter's sequence","type":"exact"},{"name":"Potter's syndrome","type":"exact"},{"name":"oligohydramnios sequence","type":"exact"}],"termid":"MONDO:0001558","xrefs":{"Monarch":{"xref_id":"0001558"}}}


id: PR:Q9C105
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone deacetylase complex subunit SAP130 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitinase-like protein PB1E7.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB1E7.04c","secondary_identifiers":["UniProtKB:Q9C105"],"synonyms":[{"name":"Spom972h-SAP130","type":"exact"}],"termid":"PR:Q9C105"}


id: MONDO:0001096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A ganglioneuroblastoma arising from the mediastinum.","definition_xrefs":["NCIT:C6627"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mediastinal cancer","termid":"MONDO:0005843"},{"relation_name":"is_a","term_name":"mediastinum neuroblastoma","termid":"MONDO:0001095"},{"relation_name":"is_a","term_name":"peripheral ganglioneuroblastoma","termid":"MONDO:0003327"}],"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":"mediastinum ganglioneuroblastoma","secondary_identifiers":["DOID:10661","UMLS:C1334653","MEDGEN:235308"],"synonyms":[{"name":"ganglioneuroblastoma (disease) of mediastinum","type":"exact"},{"name":"ganglioneuroblastoma of mediastinum","type":"exact"},{"name":"ganglioneuroblastoma of the mediastinum","type":"exact"},{"name":"mediastinal ganglioneuroblastoma","type":"exact"},{"name":"mediastinum ganglioneuroblastoma (disease)","type":"exact"}],"termid":"MONDO:0001096","xrefs":{"Monarch":{"xref_id":"0001096"}}}


id: MONDO:1012311
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"motor neuron disease, non-human animal","termid":"MONDO:1011868"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"motor neuron disease, dog","secondary_identifiers":["OMIA:001165-9615"],"termid":"MONDO:1012311","xrefs":{"Monarch":{"xref_id":"1012311"}}}


id: PBO:0072637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ras suppressor protein 1 pseudogene 3","termid":"PBO:0072637"}


id: FYECO:0000368
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which tamoxifen was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ tamoxifen","termid":"FYECO:0000368"}


id: FYPO:0000144
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing is abnormal. Chromatin silencing is the observed effect of processes that repress transcription in a region of the genome that is normally assembled into heterochromatin or CENP-A-containing chromatin (the latter is found at the centromere central core).","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal gene silencing","termid":"FYPO:0000574"},{"relation_name":"is_a","term_name":"abnormal negative regulation of transcription during vegetative growth","termid":"FYPO:0000624"}],"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:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0006551","FYPO:0001320"],"is_obsolete":false,"name":"abnormal chromatin silencing","synonyms":[{"name":"abnormal chromatin silencing during mitotic cell cycle","type":"related"},{"name":"abnormal chromatin silencing during vegetative growth","type":"exact"}],"termid":"FYPO:0000144"}


id: PBO:0005502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbohydrate kinase domain family protein","termid":"PBO:0005502"}


id: PBO:0078819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Pro (anticodon AGG) 2-2","termid":"PBO:0078819"}


id: MONDO:0006183
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign process that affects the peritoneal cavity and is characterized by the formation of multiple small nodules that are composed of well differentiated smooth muscle. It usually affects adults in their late reproductive years. Most patients are asymptomatic. The tumor nodules may regress spontaneously.","definition_xrefs":["NCIT:C3958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peritoneal benign neoplasm","termid":"MONDO:0000650"},{"relation_name":"is_a","term_name":"leiomyomatosis","termid":"MONDO:0003295"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disseminated peritoneal leiomyomatosis","secondary_identifiers":["Orphanet:71274","UMLS:C0267785","MEDGEN:78634","SCTID:62557001","DOID:5728","EFO:1000220","GARD:12843"],"synonyms":[{"name":"DPL","type":"exact"},{"name":"LPD","type":"exact"},{"name":"diffuse peritoneal leiomyomatosis","type":"exact"},{"name":"disseminated peritoneal leiomyomatosis","type":"exact"},{"name":"leiomyomatosis peritonealis disseminata","type":"exact"},{"name":"leiomyomatosis peritonealis disseminate","type":"exact"}],"termid":"MONDO:0006183","xrefs":{"Monarch":{"xref_id":"0006183"}}}


id: PR:O59778
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A biotin synthase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04215"],"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":"biotin synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.02","secondary_identifiers":["UniProtKB:O59778"],"synonyms":[{"name":"Spom972h-bioB","type":"exact"}],"termid":"PR:O59778"}


id: PBO:0049949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIF1A antisense RNA 2","termid":"PBO:0049949"}


id: PBO:0041600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbonic anhydrase 11","termid":"PBO:0041600"}


id: PBO:0029112
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiotic_cell_cycle_process","termid":"PBO:0029112"}


id: PBO:0004368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF3f","termid":"PBO:0004368"}


id: GO:0046962
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + Na+(in) -> ADP + phosphate + Na+(out), by a rotational mechanism.","definition_xrefs":["PMID:30791207","RHEA:58157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium ion transmembrane transporter activity","termid":"GO:0015081"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"},{"relation_name":"is_a","term_name":"ATPase activity, coupled to transmembrane movement of ions, rotational mechanism","termid":"GO:0044769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"sodium-transporting ATPase activity, rotational mechanism","secondary_identifiers":["EC:7.2.2.1"],"synonyms":[{"name":"ATP phosphohydrolase (Na+-transporting) activity","type":"related"},{"name":"ATP synthase, sodium ion specific activity","type":"related"},{"name":"Na(+)-translocating ATPase activity","type":"broad"},{"name":"Na(+)-transporting two-sector ATPase activity","type":"related"},{"name":"Na+-translocating ATPase activity","type":"related"},{"name":"Na+-translocating F1Fo-ATPase","type":"narrow"},{"name":"Na+-transporting two-sector ATPase","type":"narrow"},{"name":"sodium transporting ATPase activity, rotational mechanism","type":"exact"},{"name":"sodium-translocating F-type ATPase activity","type":"narrow"},{"name":"sodium-translocating V-type ATPase activity","type":"narrow"},{"name":"sodium-transporting two-sector ATPase activity","type":"narrow"},{"name":"vacuolar-type Na+-ATPase","type":"narrow"},{"name":"vacuolar-type Na+-translocating ATPase","type":"narrow"}],"termid":"GO:0046962"}


id: GO:0032995
data:
  {"annotated_genes":["SJAG_00661","SJAG_04666","SJAG_02684","SJAG_04551","SJAG_02278","SJAG_04771","SJAG_00610","SJAG_00424"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92679,100179,102154],"is_not":false,"summary":null,"term":"GO:0032995"},{"annotations":[92389,87472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"},{"annotations":[94910,89394,92395,102850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"Any process that modulates the process in which a cell wall is synthesized, aggregates, and bonds together. The fungal-type cell wall contains beta-glucan and may contain chitin.","definition_xrefs":["GOC:tb","GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"is_a","term_name":"regulation of cell wall organization or biogenesis","termid":"GO:1903338"},{"relation_name":"regulates","term_name":"fungal-type cell wall biogenesis","termid":"GO:0009272"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00424":null,"SJAG_00610":null,"SJAG_00661":null,"SJAG_02278":null,"SJAG_02684":null,"SJAG_04551":null,"SJAG_04666":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0071554","GO:0044085"],"is_obsolete":false,"name":"regulation of fungal-type cell wall biogenesis","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of chitin- and beta-glucan-containing cell wall biogenesis","type":"related"}],"termid":"GO:0032995","terms_by_termid":{"GO:0032995":null,"GO:0070610":null,"GO:0140748":null}}


id: GO:0097379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the migration of an axon growth cone of a dorsal spinal cord interneuron is directed to a specific target site in the posterior direction along the anterior-posterior body axis in response to a combination of attractive and repulsive cues. The anterior-posterior axis is defined by a line that runs from the head or mouth of an organism to the tail or opposite end of the organism.","definition_xrefs":["GOC:yaf","PMID:19545367"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior/posterior axon guidance","termid":"GO:0033564"},{"relation_name":"is_a","term_name":"dorsal spinal cord interneuron axon guidance","termid":"GO:0097378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"dorsal spinal cord interneuron posterior axon guidance","synonyms":[{"name":"dorsal interneuron caudal axon projection","type":"related"}],"termid":"GO:0097379"}


id: PR:O13905
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC22A12.14c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13905"],"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":"BSD domain-containing protein C22A12.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22A12.14c","synonyms":[{"name":"Spom972h-SPAC22A12.14c","type":"exact"}],"termid":"PR:O13905"}


id: PBO:0046160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E74 like ETS transcription factor 2","termid":"PBO:0046160"}


id: PBO:0029738
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_DNA_topoisomerase_II_activity","termid":"PBO:0029738"}


id: PBO:0072424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 29","termid":"PBO:0072424"}


id: GO:0010819
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of T cell chemotaxis. T cell chemotaxis is the directed movement of a T cell in response to an external stimulus.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lymphocyte chemotaxis","termid":"GO:1901623"},{"relation_name":"is_a","term_name":"regulation of T cell migration","termid":"GO:2000404"},{"relation_name":"regulates","term_name":"T cell chemotaxis","termid":"GO:0010818"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of T cell chemotaxis","termid":"GO:0010819"}


id: PBO:0028663
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_gross_chromosomal_rearrangement_during_replication_fork_processing","termid":"PBO:0028663"}


id: PBO:0074836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 31","termid":"PBO:0074836"}


id: GO:0015446
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + arsenite(in) = ADP + phosphate + arsenite(out).","definition_xrefs":["RHEA:11348","PMID:10970874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase-coupled transmembrane transporter activity","termid":"GO:0042626"},{"relation_name":"is_a","term_name":"arsenate ion transmembrane transporter activity","termid":"GO:1901683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"ATPase-coupled arsenite transmembrane transporter activity","secondary_identifiers":["EC:7.3.2.7","MetaCyc:3.6.3.16-RXN","TC:3.A.4.1.1"],"synonyms":[{"name":"arsenical pump-driving ATPase activity","type":"related"},{"name":"arsenical resistance ATPase activity","type":"related"},{"name":"arsenical resistance efflux pump","type":"related"},{"name":"arsenite ABC transporter","type":"narrow"},{"name":"arsenite transporting ATPase activity","type":"exact"},{"name":"arsenite-translocating ATPase activity","type":"related"},{"name":"arsenite-transmembrane transporting ATPase activity","type":"related"},{"name":"arsenite-transporting ATPase activity","type":"related"}],"termid":"GO:0015446"}


id: GO:0039568
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces STAT1-dependent gene transcription, by preventing STAT1 from binding to promoter sites in the nucleus.","definition_xrefs":["PMID:17287281"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host STAT1 activity by inhibition of DNA binding (obsolete GO:0039568)","synonyms":[{"name":"inhibition of DNA binding of STAT1","type":"exact"},{"name":"suppression by virus of host STAT1 activity by negative regulation of DNA binding","type":"exact"}],"termid":"GO:0039568"}


id: PBO:0063821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology like domain family B member 3","termid":"PBO:0063821"}


id: PR:Q9UT25
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC9.02c gene.","definition_xrefs":["UniProtKB:Q9UT25","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized N-acetyltransferase C9.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9.02c","synonyms":[{"name":"Spom972h-SPAC9.02c","type":"exact"}],"termid":"PR:Q9UT25"}


id: PBO:0030775
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_sorbitol","termid":"PBO:0030775"}


id: MONDO:0018163
data:
  {"annotated_genes":["SJAG_00516"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87041],"is_not":false,"summary":null,"term":"MONDO:0018163"},{"annotations":[85567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010208"}]},"cv_name":"mondo","definition":"An autosomal recessive cutis laxa type II classic type that has material basis in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24.","definition_xrefs":["DOID:0070134"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metabolic disease","termid":"MONDO:0005066"},{"relation_name":"excluded_subClassOf","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"},{"relation_name":"excluded_subClassOf","term_name":"defect in V-ATPase","termid":"MONDO:0017752"},{"relation_name":"excluded_subClassOf","term_name":"obsolete congenital disorder of glycosylation-related bone disorder (obsolete MONDO:0018292)","termid":"MONDO:0018292"},{"relation_name":"excluded_subClassOf","term_name":"obsolete neurometabolic disease (obsolete MONDO:0019058)","termid":"MONDO:0019058"},{"relation_name":"is_a","term_name":"autosomal recessive cutis laxa type 2","termid":"MONDO:0019573"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"},{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005093","MONDO:0005328","MONDO:0004736","MONDO:0005497","MONDO:0005066"],"is_obsolete":false,"name":"autosomal recessive cutis laxa type 2A","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:357058","GARD:1638","UMLS:C0268355","OMIM:219200","MEDGEN:82795"],"synonyms":[{"name":"ARCL2A","type":"exact"},{"name":"autosomal recessive cutis laxa type 2A","type":"exact"},{"name":"autosomal recessive cutis laxa type IIA","type":"exact"},{"name":"cutis laxa with Joint laxity and retarded development","type":"exact"},{"name":"cutis laxa with bone dystrophy","type":"exact"},{"name":"cutis laxa with congenital disorder of glycosylation","type":"exact"},{"name":"cutis laxa with growth and developmental delay","type":"exact"},{"name":"cutis laxa, autosomal recessive type 2A","type":"exact"},{"name":"cutis laxa, autosomal recessive, type 2A","type":"exact"},{"name":"cutis laxa, autosomal recessive, type IIA","type":"exact"},{"name":"cutis laxa, debre type","type":"exact"}],"termid":"MONDO:0018163","terms_by_termid":{"MONDO:0010208":null,"MONDO:0018163":null},"xrefs":{"Monarch":{"xref_id":"0018163"}}}


id: PBO:0049406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanylate cyclase activator 2B","termid":"PBO:0049406"}


id: GO:0008539
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Stops, prevents or reduces the activity of the proteasome complex. The proteasome complex performs regulated ubiquitin-dependent cytosolic and nuclear proteolysis.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete proteasome inhibitor activity (obsolete GO:0008539)","synonyms":[{"name":"PI-31","type":"narrow"},{"name":"proteasome inhibitor activity","type":"exact"}],"termid":"GO:0008539"}


id: PBO:0108569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rpd3L histone deacetylase complex subunit, Sds3-like family protein Dep1","termid":"PBO:0108569"}


id: MOD:00829
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-phenylalanine residue and an L-serine residue by an ester bond to form S-(L-phenylalaninyl)-L-serine.","definition_xrefs":["RESID:AA0418","PubMed:12591958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ester crosslinked residues","termid":"MOD:00885"},{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"crosslinked L-phenylalanine residue","termid":"MOD:02053"},{"relation_name":"is_a","term_name":"crosslinked L-serine residue","termid":"MOD:02055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-(L-phenylalanyl)-L-serine","synonyms":[{"name":"(2S)-2-amino-3-([(2S)-2-amino-3-phenylpropanoyl]oxy)propanoic acid","type":"exact"},{"name":"CROSSLNK Phenylalanyl serine ester (Ser-Phe)","type":"exact"},{"name":"O-(2-amino-3-phenylpropanoyl)serine","type":"exact"},{"name":"O-(L-phenylalanyl)-L-serine","type":"exact"},{"name":"XLNK1PheOSer","type":"exact"},{"name":"phenylalanine serine ester","type":"exact"}],"termid":"MOD:00829"}


id: GO:0006161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of deoxyguanosine, a nucleoside consisting of the base guanine and the sugar deoxyribose.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyguanosine metabolic process","termid":"GO:0042453"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside catabolic process","termid":"GO:0046124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"deoxyguanosine catabolic process","synonyms":[{"name":"deoxyguanosine breakdown","type":"exact"},{"name":"deoxyguanosine catabolism","type":"exact"},{"name":"deoxyguanosine degradation","type":"exact"}],"termid":"GO:0006161"}


id: MOD:01751
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-129 reagent acylated residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"TMT6plex-129 reporter+balance reagent acylated residue","termid":"MOD:01744"},{"relation_name":"derives_from","term_name":"cysTMT6plex-129 reporter+balance reagent cysteine disulfide","termid":"MOD:01826"},{"relation_name":"is_a","term_name":"TMT6plex reporter fragment","termid":"MOD:01716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMT6plex-129 reporter fragment","synonyms":[{"name":"2,6-dimethyl-1-methylidenepiperidinium","type":"exact"},{"name":"Sixplex Tandem Mass Tag(TM)","type":"related"},{"name":"TMT6plex","type":"related"},{"name":"cysTMT6plex-129 reporter fragment","type":"exact"}],"termid":"MOD:01751"}


id: MONDO:0010484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any X-linked nonsyndromic deafness in which the cause of the disease is a mutation in the COL4A6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked nonsyndromic hearing loss","termid":"MONDO:0019586"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497"],"is_obsolete":false,"name":"hearing loss, X-linked 6","secondary_identifiers":["UMLS:C3806737","OMIM:300914","GARD:18097","MEDGEN:813067","DOID:0111740"],"synonyms":[{"name":"COL4A6 X-linked nonsyndromic deafness","type":"narrow"},{"name":"DFNX6","type":"narrow"},{"name":"X-linked nonsyndromic deafness caused by mutation in COL4A6","type":"narrow"},{"name":"deafness, X-linked 6","type":"narrow"},{"name":"deafness, X-linked 6, X-linked recessive","type":"narrow"},{"name":"deafness, X-linked type 6","type":"narrow"},{"name":"hearing loss, X-linked 6","type":"exact"}],"termid":"MONDO:0010484","xrefs":{"Monarch":{"xref_id":"0010484"}}}


id: MONDO:0016202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant form of rhegmatogenous retinal detachment.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Stickler syndrome, type I, nonsyndromic ocular","termid":"MONDO:0012287"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"rhegmatogenous retinal detachment","termid":"MONDO:0005464"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant rhegmatogenous retinal detachment","secondary_identifiers":["Orphanet:209867","MEDGEN:322821","UMLS:C1836081","icd11.foundation:1308905567","GARD:17104"],"synonyms":[{"name":"DRRD","type":"exact"},{"name":"rhegmatogenous retinal detachment, autosomal dominant","type":"exact"}],"termid":"MONDO:0016202","xrefs":{"Monarch":{"xref_id":"0016202"}}}


id: PR:O59751
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- klp6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59751"],"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":"kinesin-like protein 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1685.15c","synonyms":[{"name":"Spom972h-klp6","type":"exact"}],"termid":"PR:O59751"}


id: PBO:0055725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lamin tail domain containing 2","termid":"PBO:0055725"}


id: GO:0010085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process resulting in the establishment of polarity along the proximal/distal axis.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of axis polarity","termid":"GO:0065001"},{"relation_name":"part_of","term_name":"proximal/distal axis specification","termid":"GO:0009946"}],"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":"polarity specification of proximal/distal axis","termid":"GO:0010085"}


id: MONDO:0007208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Boomerang dysplasia (BD) is a rare lethal skeletal dysplasia characterized by severe short-limbed dwarfism, dislocated joints, club feet, distinctive facies and diagnostic x-ray findings of underossified and dysplastic long tubular bones, with a boomerang-like bowing.","definition_xrefs":["Orphanet:1263"],"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":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"filamin-related bone disorder","termid":"MONDO:0019690"}],"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":"Boomerang dysplasia","secondary_identifiers":["GARD:933","icd11.foundation:423736259","ICD9:756.9","UMLS:C0432201","DOID:0050680","OMIM:112310","SCTID:254054000","MESH:C536573","MEDGEN:96579"],"synonyms":[{"name":"Boomerang dysplasia","type":"exact"},{"name":"Boomerang-like skeletal dysplasia","type":"related"},{"name":"dwarfism with short, bowed, rigid limbs and characteristic facies","type":"related"}],"termid":"MONDO:0007208","xrefs":{"Monarch":{"xref_id":"0007208"}}}


id: PBO:0039561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 54","termid":"PBO:0039561"}


id: MONDO:0004981
data:
  {"annotated_genes":["SJAG_02757","SJAG_00228"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014340"},{"annotations":[86976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015001"}]},"cv_name":"mondo","definition":"A disorder characterized by an electrocardiographic finding of a supraventricular arrhythmia characterized by the replacement of consistent P waves by rapid oscillations or fibrillatory waves that vary in size, shape and timing and are accompanied by an irregular ventricular response. (CDISC)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac rhythm disease","termid":"MONDO:0007263"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00228":null,"SJAG_02757":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial fibrillation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D001281","NCIT:C50466","SCTID:49436004","DOID:0060224","icd11.foundation:171698302","NANDO:2100051","MEDGEN:445","ICD9:427.31","EFO:0000275","NANDO:2200226","HP:0005110","UMLS:C0004238"],"synonyms":[{"name":"A-fib","type":"exact"},{"name":"AF","type":"exact"},{"name":"AFib","type":"exact"},{"name":"atrial fibrillation","type":"exact"},{"name":"atrial fibrillation (disease)","type":"exact"}],"termid":"MONDO:0004981","terms_by_termid":{"MONDO:0014340":null,"MONDO:0015001":null},"xrefs":{"Monarch":{"xref_id":"0004981"}}}


id: PBO:0046793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coagulation factor II, thrombin","termid":"PBO:0046793"}


id: MONDO:0030676
data:
  {"annotated_genes":["SJAG_04840"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87067],"is_not":false,"summary":null,"term":"MONDO:0030676"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"parkinsonism-dystonia, infantile","termid":"MONDO:0013150"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04840":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"parkinsonism-dystonia 3, childhood-onset","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5676913","MEDGEN:1808365","OMIM:619738"],"synonyms":[{"name":"PKDYS3","type":"exact"},{"name":"parkinsonism-dystonia 3, childhood-onset","type":"exact"}],"termid":"MONDO:0030676","terms_by_termid":{"MONDO:0030676":null},"xrefs":{"Monarch":{"xref_id":"0030676"}}}


id: GO:1901964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell proliferation involved in outflow tract morphogenesis.","definition_xrefs":["GOC:TermGenie","GOC:dph","PMID:21419760","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell proliferation involved in outflow tract morphogenesis","termid":"GO:1901963"},{"relation_name":"is_a","term_name":"positive regulation of cell proliferation involved in heart morphogenesis","termid":"GO:2000138"},{"relation_name":"positively_regulates","term_name":"cell proliferation involved in outflow tract morphogenesis","termid":"GO:0061325"}],"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 cell proliferation involved in outflow tract morphogenesis","synonyms":[{"name":"activation of cell proliferation involved in outflow tract morphogenesis","type":"narrow"},{"name":"up regulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"},{"name":"up-regulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"},{"name":"upregulation of cell proliferation involved in outflow tract morphogenesis","type":"exact"}],"termid":"GO:1901964"}


id: PBO:0076788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trans-2,3-enoyl-CoA reductase pseudogene 2","termid":"PBO:0076788"}


id: GO:0106161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of small RNA loading onto RISC.","definition_xrefs":["GOC:ha","PMID:29775584"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of small RNA loading onto RISC (obsolete GO:0106161)","termid":"GO:0106161"}


id: PBO:0027699
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_rDNA_separation","termid":"PBO:0027699"}


id: RO:0002615
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Inverse of is-model-of","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_model","termid":"RO:0002615"}


id: PBO:0051720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INSM transcriptional repressor 1","termid":"PBO:0051720"}


id: PBO:0073540
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 2","termid":"PBO:0073540"}


id: GO:0031235
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of a plasma membrane consisting of gene products and protein complexes that have some covalently attached part (e.g. peptide sequence or GPI anchor) which is embedded in the cytoplasmic side of the plasma membrane only.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of the cytoplasmic side of the plasma membrane (obsolete GO:0031235)","synonyms":[{"name":"intrinsic to cytoplasmic side of plasma membrane","type":"narrow"},{"name":"intrinsic to internal leaflet of plasma membrane","type":"exact"},{"name":"intrinsic to internal side of plasma membrane","type":"exact"}],"termid":"GO:0031235"}


id: PATO:0000054
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000054 absolute number (obsolete PATO:0000054)","termid":"PATO:0000054"}


id: PBO:0087528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of NuA4, an essential histone acetyltransferase complex; positions Piccolo NuA4 for efficient acetylation of histone H4 or histone H2A; relocalizes to the cytosol in response to hypoxia; similar to human tumor suppressor ING1 and its isoforms ING4 and ING5","termid":"PBO:0087528"}


id: MONDO:0018064
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait.","definition_xrefs":["Orphanet:3365"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"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":"trigonocephaly-broad thumbs syndrome","secondary_identifiers":["MEDGEN:930637","UMLS:C4304968","SCTID:719949001","GARD:2756"],"synonyms":[{"name":"Hunter Rudd Hoffmann syndrome","type":"related"},{"name":"Hunter-Rudd-Hoffmann syndrome","type":"exact"}],"termid":"MONDO:0018064","xrefs":{"Monarch":{"xref_id":"0018064"}}}


id: GO:0031356
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the chloroplast inner 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","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of chloroplast inner membrane (obsolete GO:0031356)","synonyms":[{"name":"intrinsic to chloroplast inner membrane","type":"narrow"}],"termid":"GO:0031356"}


id: MONDO:0035466
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete nephrotic syndrome without extrarenal manifestations (obsolete MONDO:0035466)","secondary_identifiers":["Orphanet:567564"],"termid":"MONDO:0035466","xrefs":{"Monarch":{"xref_id":"0035466"}}}


id: MONDO:0003568
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that involves the optic chiasma.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disorder of optic chiasm","secondary_identifiers":["UMLS:C0155307","DOID:5655","ICD9:377.5","ICD10CM:H47.4","ICD9:377.63","SCTID:70476006","icd11.foundation:927459952","MEDGEN:509905"],"synonyms":[{"name":"chiasma syndrome","type":"exact"},{"name":"chiasmal syndrome","type":"exact"},{"name":"disease of optic chiasma","type":"exact"},{"name":"disease or disorder of optic chiasma","type":"exact"},{"name":"disorder of optic chiasm","type":"exact"},{"name":"disorder of optic chiasma","type":"exact"},{"name":"optic chiasma disease","type":"exact"},{"name":"optic chiasma disease or disorder","type":"exact"}],"termid":"MONDO:0003568","xrefs":{"Monarch":{"xref_id":"0003568"}}}


id: GO:0030125
data:
  {"annotated_genes":["SJAG_02805","SJAG_02282","SJAG_00104","SJAG_04565","SJAG_02177","SJAG_00800","SJAG_04517","SJAG_04644","SJAG_00379","SJAG_04609","SJAG_01167","SJAG_01809"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73708,79719],"is_not":false,"summary":null,"term":"GO:0030125"},{"annotations":[112798,62100,113013,77734],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030121"},{"annotations":[108345,78053,58393,74283],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030122"},{"annotations":[65377,58639],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030130"}]},"cv_name":"cellular_component","definition":"A clathrin coat found on a vesicle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin coat","termid":"GO:0030118"},{"relation_name":"is_a","term_name":"vesicle coat","termid":"GO:0030120"},{"relation_name":"part_of","term_name":"clathrin-coated vesicle membrane","termid":"GO:0030665"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00379":null,"SJAG_00800":null,"SJAG_01167":null,"SJAG_01809":null,"SJAG_02177":null,"SJAG_02282":null,"SJAG_02805":null,"SJAG_04517":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_04644":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0031410","GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"clathrin vesicle coat","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0030125","terms_by_termid":{"GO:0030121":null,"GO:0030122":null,"GO:0030125":null,"GO:0030130":null}}


id: MONDO:1010027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Endocardial fibroelastosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder, non-human animal","termid":"MONDO:1012982"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endocardial fibroelastosis, non-human animal","secondary_identifiers":["OMIA:001803"],"termid":"MONDO:1010027","xrefs":{"Monarch":{"xref_id":"1010027"}}}


id: MONDO:0005909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with viruses of the genus pestivirus, family flaviviridae.","definition_xrefs":["MESH:D018182"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Flaviviridae infectious disease","termid":"MONDO:0005763"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pestivirus infectious disease","secondary_identifiers":["EFO:0007432","UMLS:C0206611","MEDGEN:60191"],"synonyms":[{"name":"Pestivirus caused disease or disorder","type":"exact"},{"name":"Pestivirus disease or disorder","type":"exact"},{"name":"Pestivirus infection","type":"related"},{"name":"Pestivirus infectious disease","type":"exact"},{"name":"infection, Pestivirus","type":"related"},{"name":"infections, Pestivirus","type":"related"}],"termid":"MONDO:0005909","xrefs":{"Monarch":{"xref_id":"0005909"}}}


id: PBO:0050559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine rich carboxyl terminus 1","termid":"PBO:0050559"}


id: PBO:0047657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 9","termid":"PBO:0047657"}


id: MONDO:1012154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Megaesophagus that occurs in domestic ferret.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"megaesophagus, non-human animal","termid":"MONDO:1011660"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megaesophagus, domestic ferret","secondary_identifiers":["OMIA:000631-9669"],"termid":"MONDO:1012154","xrefs":{"Monarch":{"xref_id":"1012154"}}}


id: PBO:0059924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 10","termid":"PBO:0059924"}


id: MOD:01487
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group.","definition_xrefs":["OMSSA:168","Unimod:532#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ4plex-114 reporter+balance reagent acylated residue","termid":"MOD:01485"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent N-acylated residue","termid":"MOD:01709"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"iTRAQ4plex-114 reporter+balance reagent N6-acylated lysine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Accurate mass for 114","type":"related"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"iTRAQ114","type":"related"},{"name":"iTRAQ114K","type":"exact"},{"name":"iTRAQ4plex114","type":"related"}],"termid":"MOD:01487"}


id: PBO:0012889
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"quant_gene_ex_cell_distribution","termid":"PBO:0012889"}


id: PBO:0038400
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-relation_between_physical_entity_and_a_process_or_stage","termid":"PBO:0038400"}


id: PBO:0061789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outer dynein arm docking complex subunit 1","termid":"PBO:0061789"}


id: FYPO:0001943
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of microtubule binding by a gene product (usually a protein) in a mutant is abnormal. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-protein interaction","termid":"FYPO:0000704"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000652","FYPO:0000702"],"is_obsolete":false,"name":"abnormal microtubule binding","termid":"FYPO:0001943"}


id: GO:0045353
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Blocks the binding of interleukin-1 to interleukin-1 type II receptors.","definition_xrefs":["GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-1 receptor antagonist activity","termid":"GO:0005152"}],"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:0003674"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0098772","GO:0140678","GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"interleukin-1 type II receptor antagonist activity","synonyms":[{"name":"IL-1ra type II","type":"exact"}],"termid":"GO:0045353"}


id: PBO:0052333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1958","termid":"PBO:0052333"}


id: GO:0002710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of T cell mediated immunity.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lymphocyte mediated immunity","termid":"GO:0002707"},{"relation_name":"is_a","term_name":"regulation of T cell mediated immunity","termid":"GO:0002709"},{"relation_name":"is_a","term_name":"negative regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains","termid":"GO:0002823"},{"relation_name":"negatively_regulates","term_name":"T cell mediated immunity","termid":"GO:0002456"}],"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 T cell mediated immunity","synonyms":[{"name":"down regulation of T cell mediated immunity","type":"exact"},{"name":"down-regulation of T cell mediated immunity","type":"exact"},{"name":"downregulation of T cell mediated immunity","type":"exact"},{"name":"inhibition of T cell mediated immunity","type":"narrow"},{"name":"negative regulation of T lymphocyte mediated immunity","type":"exact"},{"name":"negative regulation of T-cell mediated immunity","type":"exact"},{"name":"negative regulation of T-lymphocyte mediated immunity","type":"exact"}],"termid":"GO:0002710"}


id: PBO:0057991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3915","termid":"PBO:0057991"}


id: PBO:0080025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 17 like family member 11","termid":"PBO:0080025"}


id: PR:Q9UTM5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1420.01c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTM5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1420.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1420.01c","synonyms":[{"name":"Spom972h-SPAC1420.01c","type":"exact"}],"termid":"PR:Q9UTM5"}


id: GO:1900244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of synaptic vesicle endocytosis.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endocytosis","termid":"GO:0045807"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle endocytosis","termid":"GO:1900242"},{"relation_name":"is_a","term_name":"positive regulation of synaptic vesicle recycling","termid":"GO:1903423"},{"relation_name":"positively_regulates","term_name":"synaptic vesicle endocytosis","termid":"GO:0048488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"positive regulation of synaptic vesicle endocytosis","synonyms":[{"name":"activation of synaptic vesicle endocytosis","type":"narrow"},{"name":"activation of synaptic vesicle retrieval","type":"related"},{"name":"positive regulation of synaptic vesicle retrieval","type":"related"},{"name":"up regulation of synaptic vesicle endocytosis","type":"exact"},{"name":"up regulation of synaptic vesicle retrieval","type":"related"},{"name":"up-regulation of synaptic vesicle endocytosis","type":"exact"},{"name":"up-regulation of synaptic vesicle retrieval","type":"related"},{"name":"upregulation of synaptic vesicle endocytosis","type":"exact"},{"name":"upregulation of synaptic vesicle retrieval","type":"related"}],"termid":"GO:1900244"}


id: PBO:0112996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribosylation factor; GTPase of the Ras superfamily that regulates coated vesicle formation during intracellular trafficking within the Golgi; regulates mitochondrial fission, fusion and function, controlling the flow of fatty acids and metabolites from lipid droplets to peroxisomes and mitochondria; localizes to the Golgi apparatus and the active form to ER and lipid droplets; arf1 arf2 double null mutation is complemented by human ARF1, ARF4, ARF5, or ARF6","termid":"PBO:0112996"}


id: PBO:0058798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7704","termid":"PBO:0058798"}


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


id: PBO:0074635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 29","termid":"PBO:0074635"}


id: GO:0002618
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of macrophage antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of antigen processing and presentation","termid":"GO:0002579"},{"relation_name":"is_a","term_name":"regulation of macrophage antigen processing and presentation","termid":"GO:0002616"},{"relation_name":"positively_regulates","term_name":"macrophage antigen processing and presentation","termid":"GO:0002472"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of macrophage antigen processing and presentation","synonyms":[{"name":"activation of macrophage antigen processing and presentation","type":"narrow"},{"name":"stimulation of macrophage antigen processing and presentation","type":"narrow"},{"name":"up regulation of macrophage antigen processing and presentation","type":"exact"},{"name":"up-regulation of macrophage antigen processing and presentation","type":"exact"},{"name":"upregulation of macrophage antigen processing and presentation","type":"exact"}],"termid":"GO:0002618"}


id: PBO:0079839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UNC5C antisense RNA 1","termid":"PBO:0079839"}


id: PBO:0064533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit K pseudogene 1","termid":"PBO:0064533"}


id: PBO:0041385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 5 open reading frame 34","termid":"PBO:0041385"}


id: GO:0006191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that generates deoxyinosine from derivatives of it, without de novo synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine deoxyribonucleoside salvage","termid":"GO:0043098"},{"relation_name":"is_a","term_name":"deoxyinosine biosynthetic process","termid":"GO:0046095"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"deoxyinosine salvage","termid":"GO:0006191"}


id: PBO:0075409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm acrosome associated 6","termid":"PBO:0075409"}


id: GO:0036106
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a class II peroxisomal membrane targeting sequence, any of several sequences of amino acids within a protein that can act as a signal for the localization of the protein into the peroxisome membrane in a PEX19-independent manner.","definition_xrefs":["PMID:14709540","PMID:17020786","GOC:pm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisome membrane targeting sequence binding","termid":"GO:0033328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005048"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005048","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"peroxisome membrane class-2 targeting sequence binding","synonyms":[{"name":"PEX19-independent mPTS binding","type":"related"},{"name":"class 2 mPTS binding","type":"exact"}],"termid":"GO:0036106"}


id: SO:0001950
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 4th residue (a lysine), from the start of the H4 protein is tri-methylated.","definition_xrefs":["EBI:nj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_methylation_site","termid":"SO:0001701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H4K4_trimethylation_site","synonyms":[{"name":" H4K4me3","type":"exact"},{"name":"H4K4 trimethylation site","type":"exact"}],"termid":"SO:0001950"}


id: MONDO:0030492
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 59","secondary_identifiers":["OMIM:619645","UMLS:C5562034","DOID:0112357","MEDGEN:1794244"],"synonyms":[{"name":"SPGF59","type":"exact"}],"termid":"MONDO:0030492","xrefs":{"Monarch":{"xref_id":"0030492"}}}


id: GO:0046540
data:
  {"annotated_genes":["SJAG_03460","SJAG_03469","SJAG_02843","SJAG_02279","SJAG_01819","SJAG_05240","SJAG_04222","SJAG_04538","SJAG_02455","SJAG_01634","SJAG_03954","SJAG_04405","SJAG_03070","SJAG_03410","SJAG_01301","SJAG_04433","SJAG_00531","SJAG_02469","SJAG_00147","SJAG_01870","SJAG_01308","SJAG_02295","SJAG_01327","SJAG_00989","SJAG_03369","SJAG_04529","SJAG_04497","SJAG_00414","SJAG_02304","SJAG_00643"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61911,63184,70318,70537,71382,72612,74144,75561,76221,77276,77310,77390,77414,78279,78442,78744,79196,79998,93083,95151,98003,100632,105849,105891,108552,110082,110641,111150,114882,116429],"is_not":false,"summary":null,"term":"GO:0046540"}]},"cv_name":"cellular_component","definition":"A ribonucleoprotein complex that is formed by the association of the U4/U6 and U5 snRNPs.","definition_xrefs":["GOC:krc","GOC:pr","ISBN:0879695897","PMID:11867543"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal tri-snRNP complex","termid":"GO:0097526"}],"gene_count":30,"genes_by_uniquename":{"SJAG_00147":null,"SJAG_00414":null,"SJAG_00531":null,"SJAG_00643":null,"SJAG_00989":null,"SJAG_01301":null,"SJAG_01308":null,"SJAG_01327":null,"SJAG_01634":null,"SJAG_01819":null,"SJAG_01870":null,"SJAG_02279":null,"SJAG_02295":null,"SJAG_02304":null,"SJAG_02455":null,"SJAG_02469":null,"SJAG_02843":null,"SJAG_03070":null,"SJAG_03369":null,"SJAG_03410":null,"SJAG_03460":null,"SJAG_03469":null,"SJAG_03954":null,"SJAG_04222":null,"SJAG_04405":null,"SJAG_04433":null,"SJAG_04497":null,"SJAG_04529":null,"SJAG_04538":null,"SJAG_05240":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"U4/U6 x U5 tri-snRNP complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"U4/U6.U5 snRNP complex","type":"exact"}],"termid":"GO:0046540","terms_by_termid":{"GO:0046540":null}}


id: PBO:0060143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myotrophin","termid":"PBO:0060143"}


id: PR:O13950
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A signal recognition particle receptor subunit beta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR19326:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal recognition particle receptor subunit beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23H4.07c","secondary_identifiers":["UniProtKB:O13950"],"synonyms":[{"name":"SPAC23H4.07c","type":"related"},{"name":"SR-beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SRPRB","type":"exact"}],"termid":"PR:O13950"}


id: SO:0000396
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"U6 snRNA is a component of the spliceosome which is involved in splicing pre-mRNA. The putative secondary structure consensus base pairing is confined to a short 5' stem loop, but U6 snRNA is thought to form extensive base-pair interactions with U4 snRNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA","termid":"SO:0000274"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U6_snRNA","secondary_identifiers":["http://en.wikipedia.org/wiki/U6_snRNA"],"synonyms":[{"name":"U6 small nuclear RNA","type":"exact"},{"name":"U6 snRNA","type":"exact"},{"name":"small nuclear RNA U6","type":"exact"},{"name":"snRNA U6","type":"exact"}],"termid":"SO:0000396"}


id: MONDO:0700018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 11 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 11 disorder","termid":"MONDO:0700018","xrefs":{"Monarch":{"xref_id":"0700018"}}}


id: FYPO:0001422
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular metabolism phenotype observed in the vegetative growth phase of the life cycle in which the observed occurrence of protein processing is decreased.","definition_xrefs":["PMID:19520858","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein processing during vegetative growth","termid":"FYPO:0001421"},{"relation_name":"is_a","term_name":"decreased proteolysis during vegetative growth","termid":"FYPO:0005443"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002494","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0002274","FYPO:0006551"],"is_obsolete":false,"name":"decreased protein processing during vegetative growth","synonyms":[{"name":"decreased Sre1 cleavage","type":"narrow"},{"name":"decreased protein cleavage during vegetative growth","type":"related"},{"name":"decreased protein maturation by peptide bond cleavage during vegetative growth","type":"exact"},{"name":"decreased protein maturation by peptide bond hydrolysis during vegetative growth","type":"exact"},{"name":"decreased protein processing during mitotic cell cycle","type":"related"},{"name":"reduced protein processing during vegetative growth","type":"exact"}],"termid":"FYPO:0001422"}


id: PBO:0084059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase activating protein (GAP) for Rho3p, involved in cell polarity green fluorescent protein (GFP)-fusion protein localizes to the cell periphery and cytoplasm; relocalizes from bud neck to cytoplasm upon DNA replication stress","termid":"PBO:0084059"}


id: MONDO:0000593
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autoimmune disease of skin and connective tissue (obsolete MONDO:0000593)","termid":"MONDO:0000593","xrefs":{"Monarch":{"xref_id":"0000593"}}}


id: MONDO:0005149
data:
  {"annotated_genes":["SJAG_02977"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013458"}]},"cv_name":"mondo","definition":"Increased pressure within the pulmonary circulation due to lung or heart disorder.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertensive disorder","termid":"MONDO:0005044"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02977":null},"genotype_count":0,"is_obsolete":false,"name":"pulmonary hypertension","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:6432","MEDGEN:9376","icd11.foundation:1496633964","MedDRA:10037400","MESH:D006976","SCTID:70995007","UMLS:C0020542"],"termid":"MONDO:0005149","terms_by_termid":{"MONDO:0013458":null},"xrefs":{"Monarch":{"xref_id":"0005149"}}}


id: PBO:0027226
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-monoseptate_vegetative_cell_with_binucleate_and_anucleate_compartments","termid":"PBO:0027226"}


id: PBO:0043173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corepressor interacting with RBPJ, CIR1","termid":"PBO:0043173"}


id: GO:2000544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endothelial cell chemotaxis to fibroblast growth factor.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell chemotaxis to fibroblast growth factor","termid":"GO:1904847"},{"relation_name":"is_a","term_name":"regulation of endothelial cell chemotaxis","termid":"GO:2001026"},{"relation_name":"regulates","term_name":"endothelial cell chemotaxis to fibroblast growth factor","termid":"GO:0035768"}],"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 endothelial cell chemotaxis to fibroblast growth factor","termid":"GO:2000544"}


id: GO:0048721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the clypeus are generated and organized.","definition_xrefs":["GOC:rc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"clypeo-labral disc morphogenesis","termid":"GO:0007453"},{"relation_name":"part_of","term_name":"clypeus development","termid":"GO:0048723"}],"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":"clypeus morphogenesis","termid":"GO:0048721"}


id: PBO:0071834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 29","termid":"PBO:0071834"}


id: GO:0008939
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,6-dimethylbenzimidazole + nicotinate D-ribonucleotide = alpha-ribazole 5'-phosphate + H+ + nicotinate.","definition_xrefs":["RHEA:11196","EC:2.4.2.21"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"nicotinate-nucleotide-dimethylbenzimidazole phosphoribosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04148","MetaCyc:DMBPPRIBOSYLTRANS-RXN"],"synonyms":[{"name":"CobT","type":"related"},{"name":"N(1)-alpha-phosphoribosyltransferase activity","type":"related"},{"name":"N1-alpha-phosphoribosyltransferase activity","type":"related"},{"name":"nicotinate mononucleotide (NaMN):5,6-dimethylbenzimidazole phosphoribosyltransferase activity","type":"related"},{"name":"nicotinate mononucleotide-dimethylbenzimidazole phosphoribosyltransferase activity","type":"related"},{"name":"nicotinate ribonucleotide:benzimidazole (adenine) phosphoribosyltransferase activity","type":"related"},{"name":"nicotinate-nucleotide:5,6-dimethylbenzimidazole phospho-D-ribosyltransferase activity","type":"related"},{"name":"nicotinate-nucleotide:dimethylbenzimidazole phospho-D-ribosyltransferase activity","type":"related"}],"termid":"GO:0008939"}


id: PBO:0077261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 10 pseudogene 1","termid":"PBO:0077261"}


id: MONDO:0015703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"T-B+ severe combined immunodeficiency","termid":"MONDO:0044200"}],"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":"T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta","secondary_identifiers":["Orphanet:169160","MEDGEN:1842819","GARD:17053","UMLS:C5679578"],"synonyms":[{"name":"T-B+ SCID due to CD3delta/CD3epsilon/CD3zeta","type":"exact"}],"termid":"MONDO:0015703","xrefs":{"Monarch":{"xref_id":"0015703"}}}


id: PBO:0042152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine ligand 14","termid":"PBO:0042152"}


id: GO:0033192
data:
  {"annotated_genes":["SJAG_03631"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79498],"is_not":false,"summary":null,"term":"GO:0033192"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: protein serine/threonine phosphate + H2O = protein serine/threonine + phosphate, dependent on the presence of calcium-bound calmodulin.","definition_xrefs":["GOC:mah","PMID:15359118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium-dependent protein serine/threonine phosphatase activity","termid":"GO:0004723"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03631":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0016787","GO:0140096","GO:0003674","GO:0004721"],"is_obsolete":false,"name":"calmodulin-dependent protein phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-2730849","Reactome:R-HSA-4551451"],"synonyms":[{"name":"Ca2+/CaM-dependent protein phosphatase activity","type":"related"},{"name":"calcineurin activity","type":"narrow"},{"name":"calcium- and calmodulin-dependent protein phosphatase activity","type":"exact"},{"name":"calcium/calmodulin-dependent protein phosphatase activity","type":"exact"}],"termid":"GO:0033192","terms_by_termid":{"GO:0033192":null}}


id: GO:0070393
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of teichoic acid, which is a major component of the cell wall of Gram-positive bacteria and typically consists of a polymer of glycerol-phosphate or ribitol-phosphate to which are attached glycosyl and D-alanyl ester residues.","definition_xrefs":["PMID:14665680","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule catabolic process","termid":"GO:0009057"},{"relation_name":"is_a","term_name":"teichoic acid metabolic process","termid":"GO:0046374"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"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":"teichoic acid catabolic process","synonyms":[{"name":"teichoic acid breakdown","type":"exact"},{"name":"teichoic acid catabolism","type":"exact"},{"name":"teichoic acid degradation","type":"exact"}],"termid":"GO:0070393"}


id: PBO:0048754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerate kinase","termid":"PBO:0048754"}


id: GO:0070801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of conidiophore stalk development, a process that leads to the formation of a conidiophore stalk. The conidiophore stalk is part of a specialized hypha that extends aerially from the growth substrate and supports structures from which conidia, or asexual spores, develop.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of conidiophore development","termid":"GO:0070795"},{"relation_name":"is_a","term_name":"regulation of conidiophore stalk development","termid":"GO:0070799"},{"relation_name":"positively_regulates","term_name":"conidiophore stalk development","termid":"GO:0070788"}],"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 conidiophore stalk development","termid":"GO:0070801"}


id: PBO:0046638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group W member 19","termid":"PBO:0046638"}


id: PBO:0090927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation elongation factor G Mef2","termid":"PBO:0090927"}


id: GO:0034028
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-amino-1-(5-phospho-D-ribosyl)imidazole + ATP + bicarbonate = 5-carboxyamino-1-(5-phospho-D-ribosyl)imidazole + ADP + 3 H+ + phosphate.","definition_xrefs":["RHEA:19317","EC:6.3.4.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"5-(carboxyamino)imidazole ribonucleotide synthase activity","secondary_identifiers":["KEGG_REACTION:R07404","MetaCyc:RXN0-742"],"synonyms":[{"name":"5-amino-1-(5-phospho-D-ribosyl)imidazole:carbon-dioxide ligase (ADP-forming) activity","type":"related"},{"name":"N5-CAIR synthetase activity","type":"related"},{"name":"N5-carboxyaminoimidazole ribonucleotide synthetase activity","type":"related"},{"name":"PurK","type":"related"}],"termid":"GO:0034028"}


id: GO:0160138
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: uridine(2604) in 23S rRNA = pseudouridine(2604) in 23S rRNA.","definition_xrefs":["EC:5.4.99.21","RHEA:38875"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA pseudouridine synthase activity","termid":"GO:0120159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"23S rRNA pseudouridine(2604) synthase activity","termid":"GO:0160138"}


id: GO:0060058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cell death by apoptotic process of mammary epithelial cells during mammary gland involution.","definition_xrefs":["PMID:15282149","GOC:dph","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of apoptotic process involved in morphogenesis","termid":"GO:1902339"},{"relation_name":"positively_regulates","term_name":"apoptotic process involved in mammary gland involution","termid":"GO:0060057"}],"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 apoptotic process involved in mammary gland involution","synonyms":[{"name":"positive regulation of apoptosis involved in mammary gland involution","type":"narrow"}],"termid":"GO:0060058"}


id: GO:0060839
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of a cell to an endothelial cell fate and its capacity to differentiate into an endothelial cell.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell fate commitment","termid":"GO:0072148"},{"relation_name":"part_of","term_name":"endothelial cell differentiation","termid":"GO:0045446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"endothelial cell fate commitment","termid":"GO:0060839"}


id: MONDO:0009385
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":"hyperleucine-Isoleucinemia","secondary_identifiers":["UMLS:C0268574","MEDGEN:82821","OMIM:238340","MESH:C562674","SCTID:7046009"],"synonyms":[{"name":"hyperleucine-Isoleucinemia","type":"exact"}],"termid":"MONDO:0009385","xrefs":{"Monarch":{"xref_id":"0009385"}}}


id: GO:0061891
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of calcium ions (Ca2+).","definition_xrefs":["PMID:17020874","PMID:28151650","PMID:16005298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal ion sensor activity","termid":"GO:0140784"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0098772","GO:0003674","GO:0140299"],"is_obsolete":false,"name":"calcium ion sensor activity","termid":"GO:0061891"}


id: GO:0033008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of mast cell activation as part of an immune response.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mast cell activation","termid":"GO:0033005"},{"relation_name":"is_a","term_name":"regulation of mast cell activation involved in immune response","termid":"GO:0033006"},{"relation_name":"is_a","term_name":"positive regulation of immune response","termid":"GO:0050778"},{"relation_name":"positively_regulates","term_name":"mast cell activation involved in immune response","termid":"GO:0002279"}],"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 mast cell activation involved in immune response","synonyms":[{"name":"positive regulation of mast cell activation during immune response","type":"related"}],"termid":"GO:0033008"}


id: MONDO:0019368
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Florid cemento-osseous dysplasia (FCOD) is a rare fibro-osseous lesion in the jaw that predominantly affects middle-aged women of African descent. It is generally asymptomatic or may manifest with pain and gingival swelling. Radiologically, it is characterized by multiple dense lobulated bone lesions, often symmetrically located in various regions of the jaw.","definition_xrefs":["Orphanet:83451"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mouth disorder","termid":"MONDO:0006858"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"florid cemento-osseous dysplasia","secondary_identifiers":["MESH:C537063","ICDO:9275/0","MEDGEN:107519","icd11.foundation:2031259585","NCIT:C8381","ICD10CM:D16.5","GARD:10173","SCTID:715634002","UMLS:C0555197"],"synonyms":[{"name":"Gigantiform cementoma","type":"related"},{"name":"florid osseous dysplasia","type":"exact"},{"name":"focal cemento-osseous dysplasia","type":"exact"}],"termid":"MONDO:0019368","xrefs":{"Monarch":{"xref_id":"0019368"}}}


id: PBO:0066028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAN binding protein 17","termid":"PBO:0066028"}


id: MOD:00050
data:
  {"annotated_genes":["SJAG_00733","SJAG_02522"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[80489,80696],"is_not":false,"summary":null,"term":"MOD:00050"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-alanine residue to N-acetyl-L-alanine.","definition_xrefs":["PubMed:4700463","PubMed:363452","RESID:AA0041"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-alanine residue","termid":"MOD:00901"},{"relation_name":"is_a","term_name":"alpha-amino acetylated residue","termid":"MOD:01458"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00733":null,"SJAG_02522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00408"}],"interesting_parent_ids":["MOD:00408"],"is_obsolete":false,"name":"N-acetyl-L-alanine","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"(2S)-2-(acetamido)propanoic acid","type":"exact"},{"name":"2-(acetylamino)propanoic acid","type":"exact"},{"name":"2-(acetylazanyl)propanoic acid","type":"exact"},{"name":"AcAla","type":"exact"},{"name":"MOD_RES N-acetylalanine","type":"exact"},{"name":"N-acetyl-L-alanine","type":"exact"},{"name":"N-acetylated L-alanine","type":"exact"},{"name":"acetylalanine","type":"exact"}],"termid":"MOD:00050","terms_by_termid":{"MOD:00050":null}}


id: PBO:0057443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 561","termid":"PBO:0057443"}


id: GO:0106267
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (3-chloro-2,4,6-trihydroxyphenyl)hexan-1-one + chloride + FADH2 + O2 = (3,5-dichloro-2,4,6-trihydroxyphenyl)hexan-1-one + FAD + 2 H2O.","definition_xrefs":["RHEA:64360","PMID:20231486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"3,5 dichloro-THPH synthase activity","termid":"GO:0106267"}


id: PBO:0065074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRICKLE2 antisense RNA 3","termid":"PBO:0065074"}


id: PBO:0076763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosyl-DNA phosphodiesterase 2","termid":"PBO:0076763"}


id: GO:0140403
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process mediated by a molecule secreted by a symbiont that results in the suppression of a host innate immune response. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:30584105","PMID:21467214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host innate immune response","termid":"GO:0052170"},{"relation_name":"is_a","term_name":"effector-mediated perturbation of host innate immune response by symbiont","termid":"GO:0140404"},{"relation_name":"is_a","term_name":"effector-mediated suppression of host defense response","termid":"GO:0140590"}],"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":"effector-mediated suppression of host innate immune response","synonyms":[{"name":"effector dependent suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector triggered suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector-dependent suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector-mediated suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector-mediated suppression of host innate immune response by symbiont","type":"exact"},{"name":"effector-mediated suppression of host innate immunity","type":"exact"},{"name":"effector-triggered suppression of host immune innate response by symbiont","type":"exact"}],"termid":"GO:0140403"}


id: MONDO:0012725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic dyslipidemia","termid":"MONDO:0015905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"lipoprotein glomerulopathy","secondary_identifiers":["UMLS:C2673196","ICD9:593.89","GARD:17504","MEDGEN:382034","OMIM:611771","SCTID:446923008","icd11.foundation:69778702","MESH:C567089","ICD9:272.8","NANDO:2200134","Orphanet:329481"],"synonyms":[{"name":"LPG","type":"exact"},{"name":"lipoprotein glomerulopathy","type":"exact"}],"termid":"MONDO:0012725","xrefs":{"Monarch":{"xref_id":"0012725"}}}


id: MONDO:0022729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chondrodysplasia","termid":"MONDO:0022723"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondrodysplasia punctata with steroid sulfatase deficiency","termid":"MONDO:0022729","xrefs":{"Monarch":{"xref_id":"0022729"}}}


id: PBO:0090711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamidase Pnc1","termid":"PBO:0090711"}


id: PBO:0027284
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_nucleus_during_cellular_response_to_salt_stress","termid":"PBO:0027284"}


id: GO:1905741
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any mitochondrial calcium release that is involved in positive regulation of presynaptic cytosolic calcium concentration.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie","PMID:26644474"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"is_a","term_name":"calcium export from the mitochondrion","termid":"GO:0099093"},{"relation_name":"part_of","term_name":"positive regulation of presynaptic cytosolic calcium concentration","termid":"GO:0099533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"calcium export from the mitochondrion involved in positive regulation of presynaptic cytosolic calcium concentration","synonyms":[{"name":"calcium ion transmembrane export from mitochondrion involved in positive regulation of presynaptic cytosolic calcium concentration","type":"exact"},{"name":"mitochondrial calcium release involved in positive regulation of presynaptic cytosolic calcium concentration","type":"exact"}],"termid":"GO:1905741"}


id: PBO:0113253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pantothenate kinase, ATP:D-pantothenate 4'-phosphotransferase; cytoplasmic enzyme that catalyzes the first committed step in the universal biosynthetic pathway for coenzyme A (CoA) synthesis; transcription is regulated by Upc2p via a sterol response element; overexpressed human homologs, PANK1 and PANK3, complement yeast hypomorphic alleles, while PANK2, a gene implicated in pantothenate-kinase associated neurodegeneration, partially complements after the mitochondrial transit peptide is removed","termid":"PBO:0113253"}


id: GO:0009450
data:
  {"annotated_genes":["SJAG_03293","SJAG_00674"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87394,88375],"is_not":false,"summary":null,"term":"GO:0009450"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of gamma-aminobutyric acid (GABA, 4-aminobutyrate), an amino acid which acts as a neurotransmitter in some organisms.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid catabolic process","termid":"GO:0009063"},{"relation_name":"is_a","term_name":"gamma-aminobutyric acid metabolic process","termid":"GO:0009448"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid catabolic process","termid":"GO:0170044"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00674":null,"SJAG_03293":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044248","GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"gamma-aminobutyric acid catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-916853","MetaCyc:4AMINOBUTMETAB-PWY"],"synonyms":[{"name":"4-aminobutanoate catabolic process","type":"exact"},{"name":"4-aminobutanoate catabolism","type":"exact"},{"name":"4-aminobutyrate catabolic process","type":"exact"},{"name":"4-aminobutyrate catabolism","type":"exact"},{"name":"GABA catabolic process","type":"exact"},{"name":"GABA catabolism","type":"exact"},{"name":"gamma-aminobutyric acid breakdown","type":"exact"},{"name":"gamma-aminobutyric acid catabolism","type":"exact"},{"name":"gamma-aminobutyric acid degradation","type":"exact"}],"termid":"GO:0009450","terms_by_termid":{"GO:0009450":null}}


id: MONDO:0012689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ovarian failure in which the cause of the disease is a mutation in the NOBOX gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"premature ovarian failure 5","secondary_identifiers":["DOID:0080862","MEDGEN:409743","UMLS:C1969060","OMIM:611548","MESH:C566921"],"synonyms":[{"name":"NOBOX primary ovarian failure","type":"exact"},{"name":"Pof5","type":"related"},{"name":"premature ovarian failure 5","type":"exact"},{"name":"premature ovarian failure type 5","type":"exact"},{"name":"primary ovarian failure caused by mutation in NOBOX","type":"exact"}],"termid":"MONDO:0012689","xrefs":{"Monarch":{"xref_id":"0012689"}}}


id: PBO:0075349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sclerostin domain containing 1","termid":"PBO:0075349"}


id: PBO:0084149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity maltose transporter (alpha-glucoside transporter); inducible; encoded in the MAL1 complex locus; broad substrate specificity that includes maltotriose; required for isomaltose utilization","termid":"PBO:0084149"}


id: PBO:0003406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extender of the chronological lifespan protein Ecl2","termid":"PBO:0003406"}


id: PBO:0035932
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_trimethylation_at_centromere_during_vegetative_growth","termid":"PBO:0035932"}


id: GO:0050967
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events that contribute to the perception of pain in which an electrical stimulus is received and converted into a molecular signal.","definition_xrefs":["GOC:ai","GOC:dph","GOC:tb","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of electrical stimulus involved in sensory perception","termid":"GO:0050963"},{"relation_name":"is_a","term_name":"detection of stimulus involved in sensory perception of pain","termid":"GO:0062149"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of electrical stimulus involved in sensory perception of pain","synonyms":[{"name":"detection of electrical stimulus during sensory perception of pain","type":"related"},{"name":"perception of pain, detection of electrical stimulus","type":"exact"},{"name":"perception of pain, sensory detection of electrical stimulus","type":"exact"},{"name":"perception of pain, sensory transduction of electrical stimulus","type":"exact"},{"name":"sensory detection of electrical stimulus during perception of pain","type":"related"},{"name":"sensory transduction of electrical stimulus during perception of pain","type":"related"}],"termid":"GO:0050967"}


id: PBO:0111067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA, antisense cyp7, readthrough snd301","termid":"PBO:0111067"}


id: PBO:0016055
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mating type Auxiliary Plus","termid":"PBO:0016055"}


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


id: PBO:0040329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit c locus 1 pseudogene 4","termid":"PBO:0040329"}


id: GO:1900966
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of methanophenazine metabolic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of metabolic process","termid":"GO:0009892"},{"relation_name":"is_a","term_name":"regulation of methanophenazine metabolic process","termid":"GO:1900965"},{"relation_name":"negatively_regulates","term_name":"methanophenazine metabolic process","termid":"GO:1900629"}],"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 methanophenazine metabolic process","synonyms":[{"name":"down regulation of methanophenazine metabolic process","type":"exact"},{"name":"down regulation of methanophenazine metabolism","type":"exact"},{"name":"down-regulation of methanophenazine metabolic process","type":"exact"},{"name":"down-regulation of methanophenazine metabolism","type":"exact"},{"name":"downregulation of methanophenazine metabolic process","type":"exact"},{"name":"downregulation of methanophenazine metabolism","type":"exact"},{"name":"inhibition of methanophenazine metabolic process","type":"narrow"},{"name":"inhibition of methanophenazine metabolism","type":"exact"},{"name":"negative regulation of methanophenazine metabolism","type":"exact"}],"termid":"GO:1900966"}


id: GO:0004021
data:
  {"annotated_genes":["SJAG_04145"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111250],"is_not":false,"summary":null,"term":"GO:0004021"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + L-alanine = L-glutamate + pyruvate.","definition_xrefs":["RHEA:19453"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alanine-oxo-acid transaminase activity","termid":"GO:0047635"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04145":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016769","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"L-alanine:2-oxoglutarate aminotransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:ALANINE-AMINOTRANSFERASE-RXN","Reactome:R-HSA-507775","KEGG_REACTION:R00258","Reactome:R-HSA-507749","Reactome:R-HSA-70523","Reactome:R-HSA-70524","EC:2.6.1.2"],"synonyms":[{"name":"ALT","type":"related"},{"name":"GPT","type":"related"},{"name":"L-alanine aminotransferase activity","type":"broad"},{"name":"L-alanine transaminase activity","type":"broad"},{"name":"L-alanine-alpha-ketoglutarate aminotransferase activity","type":"related"},{"name":"alanine aminotransferase activity","type":"broad"},{"name":"alanine transaminase activity","type":"broad"},{"name":"alanine-alpha-ketoglutarate aminotransferase activity","type":"related"},{"name":"alanine-pyruvate aminotransferase activity","type":"related"},{"name":"beta-alanine aminotransferase","type":"broad"},{"name":"glutamic acid-pyruvic acid transaminase activity","type":"related"},{"name":"glutamic--alanine transaminase activity","type":"related"},{"name":"glutamic--pyruvic transaminase activity","type":"related"},{"name":"glutamic-pyruvic aminotransferase activity","type":"related"},{"name":"pyruvate transaminase activity","type":"broad"},{"name":"pyruvate-alanine aminotransferase activity","type":"related"},{"name":"pyruvate-glutamate transaminase activity","type":"related"}],"termid":"GO:0004021","terms_by_termid":{"GO:0004021":null}}


id: FYPO:0007466
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which methylation of lysine at position 9 of histone H3 is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone methylation","termid":"FYPO:0006870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0000002"],"is_obsolete":false,"name":"abnormal histone H3-K9 methylation","synonyms":[{"name":"abnormal histone H3 K9 methylation","type":"exact"},{"name":"abnormal histone H3K9me","type":"exact"},{"name":"abnormal histone lysine H3 K9 methylation","type":"exact"}],"termid":"FYPO:0007466"}


id: GO:0033979
data:
  {"annotated_genes":["SJAG_04754"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000495"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving box H/ACA type small nucleolar RNA.","definition_xrefs":["GOC:krc","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sno(s)RNA metabolic process","termid":"GO:0016074"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016074"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016074","GO:0008150"],"is_obsolete":false,"name":"box H/ACA sno(s)RNA metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"box H/ACA sRNA metabolic process","type":"narrow"},{"name":"box H/ACA snoRNA metabolic process","type":"narrow"}],"termid":"GO:0033979","terms_by_termid":{"GO:0000495":null}}


id: MONDO:0018638
data:
  {"annotated_genes":["SJAG_04335"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013782"}]},"cv_name":"mondo","definition":"An inherited or acquired disorder of electrolyte metabolism, characterized by the inability of the renal tubules to respond to aldosterone. It is manifested by hyperkalemic metabolic acidosis, urinary salt wasting, normal or increased aldosterone secretion and normal glomerular filtration rate.","definition_xrefs":["NCIT:C85034"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal tubular transport disease","termid":"MONDO:0006510"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"pseudohypoaldosteronism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:77098009","ICD9:255.8","MEDGEN:18721","DOID:4479","UMLS:C0033805","MESH:D011546","NANDO:2200367","GARD:21861","Orphanet:444916","NANDO:2100133"],"termid":"MONDO:0018638","terms_by_termid":{"MONDO:0013782":null},"xrefs":{"Monarch":{"xref_id":"0018638"}}}


id: PBO:0043712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6B1","termid":"PBO:0043712"}


id: SO:0000810
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A cDNA clone invalidated because it is chimeric.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"invalidated_by_chimeric_cDNA","termid":"SO:0000362"},{"relation_name":"is_a","term_name":"invalidated_cDNA_clone","termid":"SO:0000809"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chimeric_cDNA_clone","synonyms":[{"name":"chimeric cDNA clone","type":"exact"}],"termid":"SO:0000810"}


id: GO:0006477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of a sulfate group as an ester to a protein amino acid.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"},{"relation_name":"is_a","term_name":"sulfation","termid":"GO:0051923"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0006790"],"is_obsolete":false,"name":"protein sulfation","synonyms":[{"name":"protein amino acid sulfation","type":"exact"},{"name":"protein amino acid sulphation","type":"exact"}],"termid":"GO:0006477"}


id: MONDO:0007052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"growth hormone-producing pituitary gland adenoma","termid":"MONDO:0006238"},{"relation_name":"is_a","term_name":"familial isolated pituitary adenoma","termid":"MONDO:0017824"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth hormone secreting pituitary adenoma 1","secondary_identifiers":["DOID:0112009","OMIM:102200","MEDGEN:1618709","UMLS:C4538355"],"synonyms":[{"name":"PAGH1","type":"related"},{"name":"PITA1","type":"related"},{"name":"Somatotrophinoma, familial","type":"related"},{"name":"acromegaly due to pituitary adenoma 1","type":"related"},{"name":"familial isolated pituitary adenoma syndrome","type":"related"},{"name":"isolated familial somatotropinoma","type":"related"},{"name":"pituitary adenoma 1, multiple types","type":"related"},{"name":"pituitary adenoma 1, multiple types, autosomal dominant, somatic mutation","type":"exact"},{"name":"pituitary adenoma predisposition","type":"related"},{"name":"pituitary adenoma predisposition, autosomal dominant, somatic mutation","type":"exact"},{"name":"pituitary adenoma, familial isolated","type":"related"},{"name":"pituitary adenoma, growth hormone-secreting, 1","type":"related"},{"name":"pituitary adenoma, growth hormone-secreting, type 1","type":"exact"},{"name":"somatotropinoma, familial isolated","type":"related"}],"termid":"MONDO:0007052","xrefs":{"Monarch":{"xref_id":"0007052"}}}


id: FYPO:0002403
data:
  {"alleles_by_uniquename":{"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"},"SJAG_01906:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01906","name":"nem1delta","uniquename":"SJAG_01906:allele-1"},"SJAG_02763:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02763","name":"ned1delta","uniquename":"SJAG_02763:allele-1"},"SJAG_02763:allele-2":{"allele_type":"amino_acid_mutation","description":"D422E,D424E","gene_uniquename":"SJAG_02763","name":"ned1cat","synonyms":[{"name":"Catalytic mutant","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-2"},"SJAG_02763:allele-4":{"allele_type":"amino_acid_mutation","description":"S235E; S651E","gene_uniquename":"SJAG_02763","name":"ned1S235E/S651E","synonyms":[{"name":"phosphomimetic","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-4"},"SJAG_02763:allele-5":{"allele_type":"amino_acid_mutation","description":"S499E; S538E; T620E; T638E; S651E","gene_uniquename":"SJAG_02763","name":"ned1-5E","uniquename":"SJAG_02763:allele-5"},"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"},"SJAG_03940:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03940","name":"nem2delta","uniquename":"SJAG_03940:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119613,119217,119606,119611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003779"},{"annotations":[119635,119627,119631,119628,119643,119640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001556"},{"annotations":[119128],"is_not":false,"rel_names":["is_a","has_part"],"summary":null,"term":"FYPO:0003976"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, or morphology of all or part of the nucleus is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01745":null,"SJAG_01906":null,"SJAG_02763":null,"SJAG_03449":null,"SJAG_03940":null,"SJAG_04464":null},"genotype_count":11,"genotypes_by_uniquename":{"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Man1DHEH(man1DHEH)","display_uniquename":"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-2","expression":"Not assayed or wild type"}]}]},"lem2delta":{"display_name":"lem2delta","display_uniquename":"lem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01745:allele-1","expression":"Null"}]}]},"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type":{"display_name":"man1-1-488(aa)","display_uniquename":"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-3","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]},"ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ned1-5E(S499E; S538E; T620E; T638E; S651E aa)","display_uniquename":"ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-5","expression":"Not assayed or wild type"}]}]},"ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ned1S235E/S651E(S235E; S651E aa)","display_uniquename":"ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-4","expression":"Not assayed or wild type"}]}]},"ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ned1cat(D422E,D424E aa)","display_uniquename":"ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-2","expression":"Not assayed or wild type"}]}]},"ned1delta":{"display_name":"ned1delta","display_uniquename":"ned1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02763:allele-1","expression":"Null"}]}]},"nem1delta":{"display_name":"nem1delta","display_uniquename":"nem1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01906:allele-1","expression":"Null"}]}]},"nem2delta":{"display_name":"nem2delta","display_uniquename":"nem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03940:allele-1","expression":"Null"}]}]},"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]}},"in_subsets":["fypo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal nucleus","references_by_uniquename":{"PMID:21802294":null,"PMID:24184107":null,"PMID:26774782":null,"PMID:28954740":null},"single_locus_annotated_genes":["SJAG_03449","SJAG_02763","SJAG_01745","SJAG_03940","SJAG_01906","SJAG_04464"],"single_locus_genotype_uniquenames":["ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","nem2delta","ned1delta","lem2delta","ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","man1delta","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type","pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","nem1delta"],"synonyms":[{"name":"abnormal nucleus physical object quality","type":"exact"}],"termid":"FYPO:0002403","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000162":null,"FYPO:0001556":null,"FYPO:0003779":null,"FYPO:0003976":null,"FYPO_EXT:0000001":null}}


id: PATO:0001775
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's location of features or characteristics along the dorsal-ventral axis.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positional polarity","termid":"PATO:0001769"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dorsal-ventral polarity","termid":"PATO:0001775"}


id: PBO:0041087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain and PHD finger containing 3","termid":"PBO:0041087"}


id: RO:HOM0000046
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Historical homology that involves not recombining and subsequently differentiated sex chromosomes.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_chromosomal_homology_relationship_with","termid":"RO:HOM0000047"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_gametology_relationship_with","synonyms":[{"name":"gametologous to","type":"exact"}],"termid":"RO:HOM0000046"}


id: MONDO:0002205
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually pigmented, nodular or polypoid malignant neoplasm that originates from melanocytes and arises from the vulva. It presents with bleeding and dysuria.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vulva cancer","termid":"MONDO:0001528"},{"relation_name":"is_a","term_name":"non-cutaneous melanoma","termid":"MONDO:0006320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"vulvar melanoma","secondary_identifiers":["HP:0030418","SCTID:254896002","DOID:2093","NCIT:C40329","UMLS:C0241989","MEDGEN:66040"],"synonyms":[{"name":"malignant melanoma of vulva","type":"exact"},{"name":"mammalian vulva melanoma","type":"exact"},{"name":"mammalian vulva melanoma (disease)","type":"exact"},{"name":"melanoma (disease) of mammalian vulva","type":"exact"},{"name":"vulvar melanoma","type":"exact"},{"name":"vulvar melanoma (disease)","type":"exact"}],"termid":"MONDO:0002205","xrefs":{"Monarch":{"xref_id":"0002205"}}}


id: MONDO:0100441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A retinopathy caused by a heterozygous gain of function or dominant-negative variant or in the GUCY2D gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"GUCY2D retinopathy","termid":"MONDO:0100454"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005328"],"is_obsolete":false,"name":"GUCY2D-related dominant retinopathy","synonyms":[{"name":"CACD1","type":"narrow"},{"name":"CORD6","type":"narrow"},{"name":"GUCY2D central areolar choroidal dystrophy","type":"narrow"},{"name":"GUCY2D cone-rod dystrophy","type":"narrow"},{"name":"RCD2","type":"narrow"},{"name":"central areolar choroidal dystrophy caused by mutation in GUCY2D","type":"narrow"},{"name":"choroidal dystrophy, central areolar","type":"narrow"},{"name":"choroidal dystrophy, central areolar, 1","type":"narrow"},{"name":"choroidal sclerosis","type":"narrow"},{"name":"cone-rod dystrophy 6","type":"narrow"},{"name":"cone-rod dystrophy caused by mutation in GUCY2D","type":"narrow"},{"name":"cone-rod dystrophy type 6","type":"narrow"},{"name":"dominant GUCY2D retinopathy","type":"exact"},{"name":"retinal cone dystrophy 2","type":"narrow"}],"termid":"MONDO:0100441","xrefs":{"Monarch":{"xref_id":"0100441"}}}


id: GO:0047207
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [(1->2)-beta-D-fructosyl](n) + [(1->2)-beta-D-fructosyl](m) = [(1->2)-beta-D-fructosyl](n+1) + [(1->2)-beta-D-fructosyl](m-1).","definition_xrefs":["EC:2.4.1.100","MetaCyc:2.4.1.100-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fructosyltransferase activity","termid":"GO:0050738"}],"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:0016757"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016757"],"is_obsolete":false,"name":"1,2-beta-fructan 1F-fructosyltransferase activity","synonyms":[{"name":"1,2-beta-D-fructan 1(F)-fructosyltransferase activity","type":"related"},{"name":"1,2-beta-D-fructan 1F-fructosyltransferase activity","type":"related"},{"name":"1,2-beta-D-fructan:1,2-beta-D-fructan 1(F)-beta-D-fructosyltransferase activity","type":"related"},{"name":"1,2-beta-D-fructan:1,2-beta-D-fructan 1F-beta-D-fructosyltransferase activity","type":"related"},{"name":"1,2-beta-fructan 1(F)-fructosyltransferase activity","type":"related"},{"name":"2,1-beta-D-fructan:2,1-beta-D-fructan 1-beta-D-fructosyltransferase activity","type":"related"},{"name":"2,1-fructan:2,1-fructan 1-fructosyltransferase activity","type":"related"},{"name":"FFT activity","type":"related"},{"name":"fructan:fructan fructosyl transferase activity","type":"related"}],"termid":"GO:0047207"}


id: MONDO:1011048
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nephrotic syndrome that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrotic syndrome, non-human animal","termid":"MONDO:1010261"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nephrotic syndrome, domestic cat","secondary_identifiers":["OMIA:000712-9685"],"termid":"MONDO:1011048","xrefs":{"Monarch":{"xref_id":"1011048"}}}


id: PR:O74184
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A target of rapamycin complex subunit LST8 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02946","PANTHER:PTHR19842:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat-containing protein wat1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21B10.05c","secondary_identifiers":["UniProtKB:O74184"],"synonyms":[{"name":"Spom972h-MLST8","type":"exact"},{"name":"WD repeat-containing protein pop3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74184"}


id: PBO:0046137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 5A2 pseudogene 1","termid":"PBO:0046137"}


id: MONDO:0016140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Deficiencies or mutations in the genes for the sarcoglycan complex subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency.","definition_xrefs":["MESH:D058088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sarcoglycanopathy","secondary_identifiers":["GARD:20389","UMLS:C2936331","MEDGEN:424705","Orphanet:207052"],"synonyms":[{"name":"qualitative or quantitative defects of sarcoglycan","type":"exact"}],"termid":"MONDO:0016140","xrefs":{"Monarch":{"xref_id":"0016140"}}}


id: FYPO:0002355
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the dimethylation of lysine at position 9 of histone H3 in silent mating-type cassettes occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone H3-K9 dimethylation during vegetative growth","termid":"FYPO:0000876"},{"relation_name":"is_a","term_name":"abnormal histone methylation at silent mating-type cassette during vegetative growth","termid":"FYPO:0007373"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0002274","FYPO:0002494","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H3-K9 dimethylation at silent mating-type cassette during vegetative growth","synonyms":[{"name":"decreased histone H3 K9 dimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 dimethylation at mating-type region heterochromatin during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 dimethylation at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K9 dimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"decreased histone H3K9me2 at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K9 dimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"decreased silent mating-type cassette histone H3-K9 dimethylation during vegetative growth","type":"exact"},{"name":"reduced histone H3-K9 dimethylation at silent mating-type cassette during vegetative growth","type":"exact"}],"termid":"FYPO:0002355"}


id: SO:0000097
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene from nucleomorph sequence.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"nucleomorphic_sequence","termid":"SO:0000739"},{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleomorph_gene","synonyms":[{"name":"nucleomorph gene","type":"exact"}],"termid":"SO:0000097"}


id: GO:0032824
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of natural killer cell differentiation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of natural killer cell activation","termid":"GO:0032815"},{"relation_name":"is_a","term_name":"regulation of natural killer cell differentiation","termid":"GO:0032823"},{"relation_name":"is_a","term_name":"negative regulation of lymphocyte differentiation","termid":"GO:0045620"},{"relation_name":"negatively_regulates","term_name":"natural killer cell differentiation","termid":"GO:0001779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of natural killer cell differentiation","synonyms":[{"name":"down regulation of natural killer cell differentiation","type":"exact"},{"name":"down-regulation of natural killer cell differentiation","type":"exact"},{"name":"downregulation of natural killer cell differentiation","type":"exact"},{"name":"inhibition of natural killer cell differentiation","type":"narrow"},{"name":"negative regulation of NK cell differentiation","type":"exact"},{"name":"negative regulation of natural killer cell development","type":"related"}],"termid":"GO:0032824"}


id: PBO:0075162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide C pseudogene 18","termid":"PBO:0075162"}


id: MONDO:0006490
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma arising from the vagina. Human papillomavirus infection is associated with the development of vaginal intraepithelial neoplasia and invasive squamous cell carcinoma. Signs and symptoms include painless bleeding, postcoital bleeding, and urinary tract symptoms. Morphologically it resembles squamous cell carcinomas in other anatomic sites. Radiation therapy is the preferred treatment for most cases. The prognosis is related to the stage of the disease.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal squamous tumor","termid":"MONDO:0001806"},{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"vaginal carcinoma","termid":"MONDO:0015867"}],"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":"vaginal squamous cell carcinoma","secondary_identifiers":["EFO:1000620","NCIT:C180915","ONCOTREE:VSC","NCIT:C7736","SCTID:105121000119102","UMLS:C0238518","MEDGEN:66775"],"synonyms":[{"name":"carcinoma of vagina squamous cell","type":"exact"},{"name":"epidermoid carcinoma of the vagina","type":"exact"},{"name":"epidermoid carcinoma of vagina","type":"exact"},{"name":"epidermoid cell carcinoma of the vagina","type":"exact"},{"name":"epidermoid cell carcinoma of vagina","type":"exact"},{"name":"squamous cell carcinoma of the vagina","type":"exact"},{"name":"squamous cell carcinoma of the vulva/vagina","type":"related"},{"name":"squamous cell carcinoma of vagina","type":"exact"},{"name":"vagina epidermoid carcinoma","type":"exact"},{"name":"vagina epidermoid cell carcinoma","type":"exact"},{"name":"vagina squamous cell carcinoma","type":"exact"},{"name":"vaginal epidermoid carcinoma","type":"exact"},{"name":"vaginal epidermoid cell carcinoma","type":"exact"},{"name":"vaginal squamous cell cancer","type":"exact"},{"name":"vaginal squamous cell cancer, NOS","type":"exact"},{"name":"vaginal squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0006490","xrefs":{"Monarch":{"xref_id":"0006490"}}}


id: PBO:0080845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 1 pseudogene 9","termid":"PBO:0080845"}


id: GO:1903997
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of non-membrane spanning protein tyrosine kinase activity.","definition_xrefs":["GOC:nc","GO_REF:0000059","PMID:10518561","GOC:TermGenie","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of non-membrane spanning protein tyrosine kinase activity (obsolete GO:1903997)","synonyms":[{"name":"activation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"narrow"},{"name":"activation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"activation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"activation of focal adhesion kinase activity","type":"narrow"},{"name":"activation of janus kinase 1 activity","type":"narrow"},{"name":"activation of janus kinase 2 activity","type":"narrow"},{"name":"activation of janus kinase 3 activity","type":"narrow"},{"name":"activation of non-membrane spanning protein tyrosine kinase activity","type":"narrow"},{"name":"activation of non-specific protein-tyrosine kinase activity","type":"narrow"},{"name":"activation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"positive regulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"positive regulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"positive regulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"positive regulation of focal adhesion kinase activity","type":"narrow"},{"name":"positive regulation of janus kinase 1 activity","type":"narrow"},{"name":"positive regulation of janus kinase 2 activity","type":"narrow"},{"name":"positive regulation of janus kinase 3 activity","type":"narrow"},{"name":"positive regulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"positive regulation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"up regulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"up regulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"up regulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"up regulation of focal adhesion kinase activity","type":"narrow"},{"name":"up regulation of janus kinase 1 activity","type":"narrow"},{"name":"up regulation of janus kinase 2 activity","type":"narrow"},{"name":"up regulation of janus kinase 3 activity","type":"narrow"},{"name":"up regulation of non-membrane spanning protein tyrosine kinase activity","type":"exact"},{"name":"up regulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"up regulation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"up-regulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"up-regulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"up-regulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"up-regulation of focal adhesion kinase activity","type":"narrow"},{"name":"up-regulation of janus kinase 1 activity","type":"narrow"},{"name":"up-regulation of janus kinase 2 activity","type":"narrow"},{"name":"up-regulation of janus kinase 3 activity","type":"narrow"},{"name":"up-regulation of non-membrane spanning protein tyrosine kinase activity","type":"exact"},{"name":"up-regulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"up-regulation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"upregulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"upregulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"upregulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"upregulation of focal adhesion kinase activity","type":"narrow"},{"name":"upregulation of janus kinase 1 activity","type":"narrow"},{"name":"upregulation of janus kinase 2 activity","type":"narrow"},{"name":"upregulation of janus kinase 3 activity","type":"narrow"},{"name":"upregulation of non-membrane spanning protein tyrosine kinase activity","type":"exact"},{"name":"upregulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"upregulation of p60c-src protein tyrosine kinase activity","type":"narrow"}],"termid":"GO:1903997"}


id: PBO:0072479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 8","termid":"PBO:0072479"}


id: PBO:0029202
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_micafungin","termid":"PBO:0029202"}


id: PBO:0029020
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_protein_phosphorylation_during_mitotic_M_phase","termid":"PBO:0029020"}


id: GO:0060942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a neural crest cell acquires the specialized structural and/or functional features of a cardiac fibroblast. A cardiac fibroblast is a connective tissue cell in the heart which secretes an extracellular matrix rich in collagen and other macromolecules.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac fibroblast cell differentiation","termid":"GO:0060935"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural crest-derived cardiac fibroblast cell differentiation","termid":"GO:0060942"}


id: MONDO:0011939
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy of childhood","termid":"MONDO:0957408"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spondyloenchondrodysplasia with immune dysregulation","secondary_identifiers":["OMIM:607944","MESH:C564307","Orphanet:1855","Orphanet:50816","SCTID:703523004","OMIM:271550","NANDO:2200744","GARD:4978","MEDGEN:375009","ICD9:759.89","SCTID:254079002","MESH:C535782","ICD9:756.9","UMLS:C1842763"],"synonyms":[{"name":"Roifman Immunoskeletal syndrome","type":"exact"},{"name":"SEM","type":"related"},{"name":"SPENCD","type":"exact"},{"name":"SPENCDI","type":"exact"},{"name":"Spondyloenchondrodysplasia with immune dysregulation","type":"exact"},{"name":"combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia","type":"exact"},{"name":"spondyloenchondrodysplasia","type":"exact"},{"name":"spondyloenchondrodysplasia with immune dysregulation","type":"exact"},{"name":"spondyloenchondromatosis","type":"exact"},{"name":"spondylometaphyseal dysplasia with combined immunodeficiency","type":"exact"},{"name":"spondylometaphyseal dysplasia with enchondromatous changes","type":"exact"}],"termid":"MONDO:0011939","xrefs":{"Monarch":{"xref_id":"0011939"}}}


id: MONDO:0003390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon, usually aggressive adenocarcinoma of the breast characterized by the presence of clear cells that contain glycogen.","definition_xrefs":["NCIT:C40368"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invasive ductal breast carcinoma","termid":"MONDO:0004953"},{"relation_name":"is_a","term_name":"clear cell adenocarcinoma","termid":"MONDO:0005004"},{"relation_name":"is_a","term_name":"glycogen-rich carcinoma","termid":"MONDO:0045055"}],"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":"glycogen-rich clear cell breast carcinoma","secondary_identifiers":["UMLS:C2012261","DOID:5310","ICDO:8315/3","MEDGEN:1785052"],"synonyms":[{"name":"glycogen-rich carcinoma","type":"broad"},{"name":"glycogen-rich carcinoma (morphologic abnormality)","type":"broad"},{"name":"glycogen-rich, clear cell breast carcinoma","type":"exact"}],"termid":"MONDO:0003390","xrefs":{"Monarch":{"xref_id":"0003390"}}}


id: SO:0000065
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome structure variation whereby an arm exists as an individual chromosome element.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome_structure_variation","termid":"SO:1000183"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"free_chromosome_arm","synonyms":[{"name":"free chromosome arm","type":"exact"}],"termid":"SO:0000065"}


id: MONDO:0017618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital sucrase-isomaltase deficiency","termid":"MONDO:0009114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"congenital sucrase-isomaltase deficiency with starch intolerance","secondary_identifiers":["Orphanet:306436"],"synonyms":[{"name":"CSID with starch intolerance","type":"exact"},{"name":"congenital sucrase-isomaltose malabsorption with starch intolerance","type":"exact"},{"name":"congenital sucrose intolerance with starch intolerance","type":"exact"},{"name":"disaccharide intolerance with starch intolerance","type":"exact"}],"termid":"MONDO:0017618","xrefs":{"Monarch":{"xref_id":"0017618"}}}


id: GO:0033427
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CAA 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:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003723","GO:0005488","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"CAA codon-amino acid adaptor activity","synonyms":[{"name":"glutamine tRNA","type":"related"}],"termid":"GO:0033427"}


id: PBO:0057149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 297","termid":"PBO:0057149"}


id: PBO:0046247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELOVL fatty acid elongase 3","termid":"PBO:0046247"}


id: PBO:0111750
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc20/Fizzy subfamily","termid":"PBO:0111750"}


id: GO:1901334
data:
  {"annotated_genes":["SJAG_00265"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070485"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving lactone.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00265":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lactone metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"lactone metabolism","type":"exact"}],"termid":"GO:1901334","terms_by_termid":{"GO:0070485":null}}


id: FYPO:0006262
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is inviable and has two nuclei, and the cell diameter is larger than normal and the cell length is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"binucleate vegetative cell","termid":"FYPO:0001222"},{"relation_name":"is_a","term_name":"binucleate vegetative cell","termid":"FYPO:0001222"},{"relation_name":"is_a","term_name":"inviable stubby multinucleate vegetative cell","termid":"FYPO:0006199"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000005","FYPO:0001985","FYPO:0000004"],"is_obsolete":false,"name":"inviable stubby binucleate vegetative cell","synonyms":[{"name":"inviable stubby binucleate cell during vegetative growth","type":"exact"},{"name":"inviable stubby binucleate vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable watermelon-shaped binucleate vegetative cell","type":"exact"},{"name":"lethal; stubby binucleate vegetative cell","type":"exact"},{"name":"stubby binucleate inviable vegetative cell","type":"exact"}],"termid":"FYPO:0006262"}


id: GO:0019826
data:
  {"annotated_genes":["SJAG_02135","SJAG_02945","SJAG_06621","SJAG_00642","SJAG_03828","SJAG_03903","SJAG_00027","SJAG_06622"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108982,108983,108984,108985,108986,108987,108988,111732],"is_not":false,"summary":null,"term":"GO:0019826"}]},"cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of oxygen (O2).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular sensor activity","termid":"GO:0140299"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00642":null,"SJAG_02135":null,"SJAG_02945":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0098772","GO:0140299"],"is_obsolete":false,"name":"oxygen sensor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0019826","terms_by_termid":{"GO:0019826":null}}


id: PBO:0064628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPAN-P2RY11 readthrough","termid":"PBO:0064628"}


id: GO:2000950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of xyloglucan metabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macromolecule metabolic process","termid":"GO:0010604"},{"relation_name":"is_a","term_name":"positive regulation of carbohydrate metabolic process","termid":"GO:0045913"},{"relation_name":"is_a","term_name":"regulation of xyloglucan metabolic process","termid":"GO:2000948"},{"relation_name":"positively_regulates","term_name":"xyloglucan metabolic process","termid":"GO:0010411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"positive regulation of xyloglucan metabolic process","synonyms":[{"name":"positive regulation of xyloglucan metabolism","type":"exact"}],"termid":"GO:2000950"}


id: GO:0030210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of heparin proteoglycans, which have glycosaminoglycan repeats consisting predominantly of alternating alpha-(1->4)-linked D-galactose and N-acetyl-D-glucosamine-6-sulfate residues.","definition_xrefs":["GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteoglycan biosynthetic process","termid":"GO:0030166"},{"relation_name":"is_a","term_name":"heparin proteoglycan metabolic process","termid":"GO:0030202"}],"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":"heparin proteoglycan biosynthetic process","synonyms":[{"name":"heparan sulfate biosynthetic process","type":"related"},{"name":"heparin anabolism","type":"exact"},{"name":"heparin biosynthesis","type":"exact"},{"name":"heparin formation","type":"exact"},{"name":"heparin synthesis","type":"exact"}],"termid":"GO:0030210"}


id: PBO:0081421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 277","termid":"PBO:0081421"}


id: MONDO:0003895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intermediate grade malignant bone-forming mesenchymal neoplasm with chondroblastic differentiation. It arises from the surface of the bone and affects the diaphysis or diaphyseal- metaphyseal portion of the long bones. A painless mass or swelling is the most common clinical sign. It is associated with a better prognosis than conventional osteosarcoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral osteosarcoma","termid":"MONDO:0002628"}],"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":"periosteal osteogenic sarcoma","secondary_identifiers":["UMLS:C1377843","NCIT:C8970","MEDGEN:234607","DOID:6489","ONCOTREE:PEOS","ICDO:9193/3"],"synonyms":[{"name":"PEOS","type":"related"},{"name":"juxtacortical chondroblastic osteosarcoma","type":"exact"},{"name":"periosteal osteogenic sarcoma","type":"exact"},{"name":"periosteal osteosarcoma","type":"exact"},{"name":"periosteal osteosarcoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003895","xrefs":{"Monarch":{"xref_id":"0003895"}}}


id: GO:2000510
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of dendritic cell chemotaxis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte chemotaxis","termid":"GO:0002690"},{"relation_name":"is_a","term_name":"positive regulation of mononuclear cell migration","termid":"GO:0071677"},{"relation_name":"is_a","term_name":"regulation of dendritic cell chemotaxis","termid":"GO:2000508"},{"relation_name":"positively_regulates","term_name":"dendritic cell chemotaxis","termid":"GO:0002407"}],"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 dendritic cell chemotaxis","termid":"GO:2000510"}


id: PBO:0002785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"checkpoint clamp complex protein Rad1","termid":"PBO:0002785"}


id: GO:0035441
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a cell from one site to another that will contribute to the differentiation of an endothelial cell that will form de novo blood vessels and tubes.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"vasculogenesis","termid":"GO:0001570"}],"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 migration involved in vasculogenesis","termid":"GO:0035441"}


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


id: GO:0002691
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of cellular extravasation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte migration","termid":"GO:0002685"},{"relation_name":"regulates","term_name":"cellular extravasation","termid":"GO:0045123"}],"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 cellular extravasation","termid":"GO:0002691"}


id: GO:0004453
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: methyl (2E,6E)-(10R,11S)-10,11-epoxy-3,7,11-trimethyltrideca-2,6-dienoate + H2O = (2E,6E)-(10R,11S)-10,11-epoxy-3,7,11-trimethyltrideca-2,6-dienoate + methanol. A carboxylesterase that hydrolyzes the ester linkage of juvenile hormone.","definition_xrefs":["PMID:11267890","RHEA:16393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0016788","GO:0003674"],"is_obsolete":false,"name":"juvenile-hormone esterase activity","secondary_identifiers":["MetaCyc:JUVENILE-HORMONE-ESTERASE-RXN","EC:3.1.1.59"],"synonyms":[{"name":"JH esterase activity","type":"related"},{"name":"JH-esterase activity","type":"related"},{"name":"juvenile hormone analog esterase activity","type":"related"},{"name":"juvenile hormone carboxyesterase activity","type":"related"},{"name":"methyl-(2E,6E)-(10R,11S)-10,11-epoxy-3,7,11-trimethyltrideca-2,6-dienoate acylhydrolase activity","type":"related"}],"termid":"GO:0004453"}


id: PBO:0114357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA splicing surveillance factor, RNA-binding protein Hrb1","termid":"PBO:0114357"}


id: GO:1903339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell wall organization or biogenesis.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"regulation of cell wall organization or biogenesis","termid":"GO:1903338"},{"relation_name":"negatively_regulates","term_name":"cell wall organization or biogenesis","termid":"GO:0071554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0071554"],"is_obsolete":false,"name":"negative regulation of cell wall organization or biogenesis","synonyms":[{"name":"down regulation of cell wall organisation or biogenesis","type":"exact"},{"name":"down regulation of cell wall organization or biogenesis","type":"exact"},{"name":"down regulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"down regulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"down regulation of cellular cell wall organization or biogenesis","type":"exact"},{"name":"down-regulation of cell wall organisation or biogenesis","type":"exact"},{"name":"down-regulation of cell wall organization or biogenesis","type":"exact"},{"name":"down-regulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"down-regulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"down-regulation of cellular cell wall organization or biogenesis","type":"exact"},{"name":"downregulation of cell wall organisation or biogenesis","type":"exact"},{"name":"downregulation of cell wall organization or biogenesis","type":"exact"},{"name":"downregulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"downregulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"downregulation of cellular cell wall organization or biogenesis","type":"exact"},{"name":"inhibition of cell wall organisation or biogenesis","type":"narrow"},{"name":"inhibition of cell wall organization or biogenesis","type":"narrow"},{"name":"inhibition of cell wall organization or biogenesis at cellular level","type":"narrow"},{"name":"inhibition of cellular cell wall organisation or biogenesis","type":"narrow"},{"name":"inhibition of cellular cell wall organization or biogenesis","type":"narrow"},{"name":"negative regulation of cell wall organisation or biogenesis","type":"exact"},{"name":"negative regulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"negative regulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"negative regulation of cellular cell wall organization or biogenesis","type":"exact"}],"termid":"GO:1903339"}


id: MONDO:0035940
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality","termid":"MONDO:0035605"}],"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":"B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)","secondary_identifiers":["Orphanet:585909","GARD:22342","MEDGEN:1842992","DOID:0080643","NCIT:C80331","icd11.foundation:381281608","UMLS:C5680319"],"synonyms":[{"name":"B-ALL with t(9;22)(q34.1;q11.2)","type":"exact"},{"name":"BCR-ABL1-like B-ALL","type":"exact"},{"name":"Philadelphia chromosome-like B-ALL","type":"exact"}],"termid":"MONDO:0035940","xrefs":{"Monarch":{"xref_id":"0035940"}}}


id: GO:0034713
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type I transforming growth factor beta receptor.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transforming growth factor beta receptor binding","termid":"GO:0005160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"type I transforming growth factor beta receptor binding","secondary_identifiers":["GO:0005103","GO:0005120","GO:0005116"],"synonyms":[{"name":"TGF-beta type I binding","type":"exact"},{"name":"babo binding","type":"narrow"},{"name":"babo ligand","type":"narrow"},{"name":"baboon binding","type":"narrow"},{"name":"baboon ligand","type":"narrow"},{"name":"baboon receptor ligand","type":"narrow"},{"name":"sax binding","type":"narrow"},{"name":"sax ligand","type":"narrow"},{"name":"saxophone binding","type":"narrow"},{"name":"saxophone ligand","type":"narrow"},{"name":"thickveins binding","type":"narrow"},{"name":"thickveins ligand","type":"narrow"},{"name":"tkv binding","type":"narrow"},{"name":"tkv ligand","type":"narrow"},{"name":"transforming growth factor beta ligand binding to type I receptor","type":"related"},{"name":"transforming growth factor beta receptor type I binding","type":"exact"},{"name":"type I TGF-beta binding","type":"exact"}],"termid":"GO:0034713"}


id: MONDO:0009576
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"corneal disorder","termid":"MONDO:0000942"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"megalocornea","secondary_identifiers":["UMLS:C0344530","DOID:0060305","MESH:C562829","HP:0007660","MEDGEN:138008","HP:0000485","OMIM:249300","SCTID:268158009","icd11.foundation:58849242"],"synonyms":[{"name":"anterior megalophthalmos","type":"exact"},{"name":"megalocornea","type":"exact"},{"name":"megalocornea (disease)","type":"exact"}],"termid":"MONDO:0009576","xrefs":{"Monarch":{"xref_id":"0009576"}}}


id: PR:O94721
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An RWD domain-containing protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12292:SF2","OMA:SCHPO04459","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":"RWD domain-containing protein C1393.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1393.09c","secondary_identifiers":["UniProtKB:O94721"],"synonyms":[{"name":"Spom972h-RWDD1","type":"exact"}],"termid":"PR:O94721"}


id: MONDO:0023167
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":"focal alopecia congenital megalencephaly","termid":"MONDO:0023167","xrefs":{"Monarch":{"xref_id":"0023167"}}}


id: GO:0061625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of fructose into pyruvate through a fructose-1-phosphate intermediate, with the concomitant production of ATP and NADH.","definition_xrefs":["GOC:dph","ISBN:0201090910"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fructose catabolic process","termid":"GO:0006001"},{"relation_name":"is_a","term_name":"glycolytic process","termid":"GO:0006096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086","GO:0005975","GO:0006091"],"is_obsolete":false,"name":"glycolytic process through fructose-1-phosphate","secondary_identifiers":["MetaCyc:PWY-8404"],"termid":"GO:0061625"}


id: PBO:0081226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger MYM-type containing 5","termid":"PBO:0081226"}


id: GO:0000053
data:
  {"annotated_genes":["SJAG_04577"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70273],"is_not":false,"summary":null,"term":"GO:0000053"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving argininosuccinate, 2-(N(omega)-arginino)succinate, an intermediate in the ornithine-urea cycle, where it is synthesized from citrulline and aspartate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"tricarboxylic acid metabolic process","termid":"GO:0072350"},{"relation_name":"is_a","term_name":"L-amino acid metabolic process","termid":"GO:0170033"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid metabolic process","termid":"GO:0170041"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04577":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"argininosuccinate metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"argininosuccinate metabolism","type":"exact"}],"termid":"GO:0000053","terms_by_termid":{"GO:0000053":null}}


id: PBO:0113093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic seryl-tRNA synthetase; class II aminoacyl-tRNA synthetase that aminoacylates tRNA(Ser), displays tRNA-dependent amino acid recognition which enhances discrimination of the serine substrate; copurifies with Abp140p in an RNA-dependent manner and stimulates 3-methylcytidine (m3C) modification of residue 32 of the tRNA anticodon loop of tRNA-Ser; interacts with peroxin Pex21p","termid":"PBO:0113093"}


id: FYPO:0000523
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 peroxisomal transport does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal peroxisomal transport","termid":"FYPO:0000522"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abolished peroxisomal transport","synonyms":[{"name":"abolished peroxisomal transport during mitotic cell cycle","type":"related"},{"name":"absent peroxisomal transport","type":"exact"},{"name":"peroxisomal transport abolished","type":"exact"},{"name":"peroxisomal transport abolished during vegetative growth","type":"exact"},{"name":"peroxisomal transport: absent","type":"related"}],"termid":"FYPO:0000523"}


id: PBO:0039087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiotensin II receptor type 1","termid":"PBO:0039087"}


id: MONDO:0018495
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome is a rare genetic neurometabolic disease characterized by severe intellectual disability, spastic quadraparesis, Leber´s congenital amaurosis and diabetes insipidus. Additional manifestations include facial dysmorphy (dolichocephalic skull, hypertelorism, deep-set eyes, hypoplastic nares, low-set ears), short stature, truncal hypotonia and axial hypertonia. Brain anomalies (e.g. thin corpus callosum with lack of isthmus and tapered splenium, hypoplasia or atrophy of the optic chiasm, prominent lateral ventricles, diminished white matter), described on magnetic resonance imaging, have been reported. High prenatal α-fetoprotein and intrauterine growth restriction is observed in routine pregnancy examination.","definition_xrefs":["Orphanet:423479"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"},{"relation_name":"is_a","term_name":"inborn disorder of purine metabolism","termid":"MONDO:0019236"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005328","MONDO:0019254"],"is_obsolete":false,"name":"X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome","secondary_identifiers":["UMLS:C4517296","MEDGEN:1374000","GARD:21752"],"termid":"MONDO:0018495","xrefs":{"Monarch":{"xref_id":"0018495"}}}


id: MONDO:0013209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Metabolic dysfunction-associated steatotic liver disease (MASLD, formerly known as nonalcoholic fatty liver disease or NAFLD) is a type of liver disease that is not caused by alcohol. It typically does not cause symptoms in the early stages, but it can cause health problems due to fat accumulation, inflammation, and scarring in the liver.","direct_ancestors":[{"relation_name":"is_a","term_name":"fatty liver disease","termid":"MONDO:0004790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"metabolic dysfunction-associated steatotic liver disease","secondary_identifiers":["UMLS:C0400966","ICD9:571.8","MEDGEN:96033","MESH:D065626","DOID:0080546","DOID:0080208","NCIT:C84444","EFO:0003095","MedDRA:10029530","Orphanet:33271","SCTID:197315008"],"synonyms":[{"name":"MASLD","type":"exact"},{"name":"NAFLD","type":"exact"},{"name":"NAFLD - nonalcoholic fatty liver disease","type":"exact"},{"name":"NAFLD1","type":"related"},{"name":"fatty liver disease, nonalcoholic","type":"exact"},{"name":"fatty liver disease, nonalcoholic, susceptibility to, 1","type":"related"},{"name":"liver disease, alcoholic, susceptibility to, 1","type":"related"},{"name":"non-alcoholic fatty liver","type":"exact"},{"name":"non-alcoholic fatty liver disease","type":"exact"},{"name":"nonalcoholic fatty liver disease","type":"exact"}],"termid":"MONDO:0013209","xrefs":{"Monarch":{"xref_id":"0013209"}}}


id: PR:Q9P772
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gua2 gene.","definition_xrefs":["UniProtKB:Q9P772","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":"GMP synthase [glutamine-hydrolyzing] (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP7G5.02c","synonyms":[{"name":"GMP synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gua2","type":"exact"},{"name":"glutamine amidotransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P772"}


id: GO:0009635
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 herbicide stimulus. Herbicides are chemicals used to kill or control the growth of plants.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to toxic substance","termid":"GO:0009636"}],"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 herbicide","synonyms":[{"name":"herbicide susceptibility/resistance","type":"related"}],"termid":"GO:0009635"}


id: PBO:0116796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CRK antisense RNA 1","termid":"PBO:0116796"}


id: GO:1905393
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the plant organ. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:TermGenie","GOC:tb","GO_REF:0000081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"}],"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":"plant organ formation","termid":"GO:1905393"}


id: PBO:0079558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBA domain containing 2","termid":"PBO:0079558"}


id: MONDO:0019972
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"arteriovenous hemangioma/malformation","termid":"MONDO:0001256"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dural sinus malformation","secondary_identifiers":["MEDGEN:824993","Orphanet:97339","GARD:19368","icd11.foundation:454640405","UMLS:C3839148"],"synonyms":[{"name":"cranial dural arteriovenous fistula","type":"exact"},{"name":"cranial dural arteriovenous malformations","type":"exact"}],"termid":"MONDO:0019972","xrefs":{"Monarch":{"xref_id":"0019972"}}}


id: PBO:0029709
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_low_pH","termid":"PBO:0029709"}


id: FYPO:0000032
data:
  {"alleles_by_uniquename":{"SJAG_00118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00118","name":"mid2delta","uniquename":"SJAG_00118:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_03596:allele-1":{"allele_type":"amino_acid_mutation","description":"L264P,P442T","gene_uniquename":"SJAG_03596","name":"cdc15-A","uniquename":"SJAG_03596:allele-1"},"SJAG_04280:allele-1":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-1"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[119281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[119437],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"},{"annotations":[119277],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0000118"}],"single_locus_phenotype":[{"annotations":[119269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000231"},{"annotations":[119380,119452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002998"},{"annotations":[119302],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0002026"},{"annotations":[119270,119582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000729"},{"annotations":[119438],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0001369"},{"annotations":[119266,119267],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0000118"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which cytokinesis is abnormal. Cytokinesis is part of the cell cycle and results in the division of the cytoplasm of a cell and its separation into two daughter cells.","definition_xrefs":["PomBase:mah","GO:0000281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell division","termid":"FYPO:0000186"},{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle process","termid":"FYPO:0002737"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_01143":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_03596":null,"SJAG_04280":null,"SJAG_04522":null},"genotype_count":10,"genotypes_by_uniquename":{"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cdc15-A(L264P,P442T aa)","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]}]},"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta":{"display_name":"cdc15-A(L264P,P442T aa) mid1delta","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__mid2delta":{"display_name":"mid1delta mid2delta","display_uniquename":"mid1delta__mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"mid2delta":{"display_name":"mid2delta","display_uniquename":"mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"in_subsets":["fypo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03596","SJAG_00118","SJAG_01143","SJAG_02392","SJAG_04522","SJAG_04280"],"name":"abnormal cytokinesis","references_by_uniquename":{"PMID:25866389":null,"PMID:27059155":null,"PMID:30664646":null,"PMID:32915139":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_04522","SJAG_00118","SJAG_03596","SJAG_02392","SJAG_02592","SJAG_01143"],"single_locus_genotype_uniquenames":["mid2delta","cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","pom1delta","mid1delta","rga4delta","sty1delta"],"synonyms":[{"name":"abnormal cell cycle cytokinesis","type":"exact"},{"name":"abnormal cytokinesis during mitotic cell cycle","type":"related"},{"name":"abnormal cytokinesis during vegetative growth","type":"exact"},{"name":"abnormal mitotic cytokinesis","type":"exact"},{"name":"cytokinesis defects","type":"exact"},{"name":"cytokinesis: abnormal","type":"related"}],"termid":"FYPO:0000032","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000248":null,"FYECO:0000338":null,"FYPO:0000118":null,"FYPO:0000231":null,"FYPO:0000729":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0002998":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: GO:0001698
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of gastric acid induced by the interaction of gastrin with its receptor.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastric acid secretion","termid":"GO:0001696"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"gastrin-induced gastric acid secretion","termid":"GO:0001698"}


id: PBO:0002201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic cohesin complex associated protein Moa1","termid":"PBO:0002201"}


id: GO:0048889
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuromast support cell. Support cells are non-sensory cells of the neuromast that extend between the sensory hair cells from the basement membrane to the apical surface; they are surrounded by mantle cells.","definition_xrefs":["ISBN:0125296509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"neuromast development","termid":"GO:0048884"}],"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":"neuromast support cell differentiation","termid":"GO:0048889"}


id: MONDO:0001661
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An early stage of diabetic retinopathy that is characterized by retinal hemorrhage and exudate, but without proliferation of the blood vessels.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetic retinopathy","termid":"MONDO:0005266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"background diabetic retinopathy","secondary_identifiers":["ICD9:362.03","SCTID:390834004","UMLS:C0004606","NCIT:C35668","MEDGEN:2531","DOID:13208","ICD9:362.01"],"synonyms":[{"name":"non proliferative diabetic retinopathy","type":"exact"},{"name":"non-proliferative diabetic retinopathy","type":"exact"}],"termid":"MONDO:0001661","xrefs":{"Monarch":{"xref_id":"0001661"}}}


id: GO:0007521
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell fate determination process in which a cell becomes capable of differentiating autonomously into a muscle cell regardless of its environment; upon determination, the cell fate cannot be reversed.","definition_xrefs":["CL:0000187","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate determination","termid":"GO:0001709"},{"relation_name":"part_of","term_name":"muscle cell fate commitment","termid":"GO:0042693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"muscle cell fate determination","termid":"GO:0007521"}


id: PBO:0117079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLIN3 antisense RNA 1","termid":"PBO:0117079"}


id: GO:0018266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a C-terminal peptidyl-aspartic acid ethanolamide-linked glycosylphosphatidylinositol (GPI) anchor following hydrolysis of a aspartyl-peptide bond in the carboxy-terminal region of a membrane-associated protein.","definition_xrefs":["RESID:AA0159"],"gene_count":0,"genotype_count":0,"name":"obsolete GPI anchor biosynthetic process via N-aspartyl-glycosylphosphatidylinositolethanolamine (obsolete GO:0018266)","termid":"GO:0018266"}


id: PBO:0052693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 16 pseudogene 1","termid":"PBO:0052693"}


id: PBO:0058959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MKRN2 opposite strand","termid":"PBO:0058959"}


id: CHEBI:52646
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A leptomycin having a (2E,10E,12E,16Z,18E)-double bond configuration as well as an ethyl substituent at position 17.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leptomycin B","termid":"CHEBI:52646"}


id: GO:0097476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a spinal cord motor neuron from one site to another. A spinal cord motor neuron is a motor neuron that passes from the spinal cord toward or to a muscle and conducts an impulse that causes movement.","definition_xrefs":["PMID:20711475","CL:0011001","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"motor neuron migration","termid":"GO:0097475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"spinal cord motor neuron migration","termid":"GO:0097476"}


id: MONDO:0000443
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete adenylosuccinase lyase deficiency (obsolete MONDO:0000443)","termid":"MONDO:0000443","xrefs":{"Monarch":{"xref_id":"0000443"}}}


id: GO:0031752
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a D5 dopamine receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dopamine receptor binding","termid":"GO:0050780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"D5 dopamine receptor binding","synonyms":[{"name":"D1B dopamine receptor binding","type":"exact"},{"name":"D5 dopamine receptor ligand","type":"narrow"}],"termid":"GO:0031752"}


id: MONDO:0020474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cheirospondyloenchondromatosis is an extremely rare type of enchondromatosis of very early onset (from neonatal period to infancy) characterized by symmetrical multiple enchondromas with metacarpal and phalangeal involvement resulting in short hands and feet, platyspondyly, mild to moderate short stature and intellectual disability.","definition_xrefs":["Orphanet:99647"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cheirospondyloenchondromatosis","secondary_identifiers":["icd11.foundation:1707937102","GARD:19682","SCTID:725104005"],"synonyms":[{"name":"generalised enchondromatosis with platyspondyly","type":"exact"},{"name":"generalized enchondromatosis with platyspondyly","type":"exact"}],"termid":"MONDO:0020474","xrefs":{"Monarch":{"xref_id":"0020474"}}}


id: GO:0047243
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a flavanone + UDP-D-glucose = a flavanone 7-O-beta-D-glucoside + UDP.","definition_xrefs":["MetaCyc:2.4.1.185-RXN","EC:2.4.1.185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"flavanone 7-O-beta-glucosyltransferase activity","synonyms":[{"name":"UDP-glucose:flavanone 7-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:flavanone 7-O-beta-D-glucosyltransferase activity","type":"related"},{"name":"hesperetin 7-O-glucosyl-transferase activity","type":"related"},{"name":"naringenin 7-O-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-flavanone 7-O-glucosyltransferase activity","type":"related"}],"termid":"GO:0047243"}


id: MONDO:0019697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mesomelic and rhizo-mesomelic dysplasia (obsolete MONDO:0019697)","secondary_identifiers":["icd11.foundation:533702276","Orphanet:93438"],"termid":"MONDO:0019697","xrefs":{"Monarch":{"xref_id":"0019697"}}}


id: PBO:0043893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine rich protein 1","termid":"PBO:0043893"}


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


id: PBO:0065476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, non-ATPase 13","termid":"PBO:0065476"}


id: MONDO:0012243
data:
  {"annotated_genes":["SJAG_03567"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85119],"is_not":false,"summary":null,"term":"MONDO:0012243"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03567":null},"genotype_count":0,"is_obsolete":false,"name":"B-cell immunodeficiency, distal limb anomalies, and urogenital malformations","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:567502","OMIM:609296","MEDGEN:332208","MESH:C563745","UMLS:C1836437"],"synonyms":[{"name":"B-cell immunodeficiency, distal limb anomalies, and urogenital malformations","type":"exact"},{"name":"B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome","type":"exact"},{"name":"BILU syndrome","type":"exact"},{"name":"Hoffman syndrome","type":"exact"}],"termid":"MONDO:0012243","terms_by_termid":{"MONDO:0012243":null},"xrefs":{"Monarch":{"xref_id":"0012243"}}}


id: MONDO:0011369
data:
  {"annotated_genes":["SJAG_02432","SJAG_01072","SJAG_04785"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86467,86468,86469],"is_not":false,"summary":null,"term":"MONDO:0011369"}]},"cv_name":"mondo","definition":"Any familial hypercholesterolemia in which the cause of the disease is a mutation in the PCSK9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypercholesterolemia","termid":"MONDO:0005439"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01072":null,"SJAG_02432":null,"SJAG_04785":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"hypercholesterolemia, autosomal dominant, 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:603776","MESH:C566337","MEDGEN:355007","UMLS:C1863551"],"synonyms":[{"name":"Fh3","type":"related"},{"name":"HCHOLA3","type":"related"},{"name":"PCSK9 familial hypercholesterolemia","type":"exact"},{"name":"familial hypercholesterolemia caused by mutation in PCSK9","type":"exact"},{"name":"hypercholesterolemia, autosomal dominant, 3","type":"exact"},{"name":"hypercholesterolemia, autosomal dominant, type 3","type":"exact"},{"name":"hypercholesterolemia, familial, 3","type":"exact"},{"name":"low density lipoprotein cholesterol level QTL 1","type":"exact"},{"name":"low density lipoprotein cholesterol level quantitative trait locus 1","type":"related"}],"termid":"MONDO:0011369","terms_by_termid":{"MONDO:0011369":null},"xrefs":{"Monarch":{"xref_id":"0011369"}}}


id: MONDO:0100104
data:
  {"annotated_genes":["SJAG_01065"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86091],"is_not":false,"summary":null,"term":"MONDO:0100104"}]},"cv_name":"mondo","definition":"Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the NUP88 gene.","definition_xrefs":["OMIM:618393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fetal akinesia deformation sequence","termid":"MONDO:0008824"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01065":null},"genotype_count":0,"is_obsolete":false,"name":"fetal akinesia deformation sequence 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111379","MEDGEN:1675450","UMLS:C4760578","GARD:16497"],"synonyms":[{"name":"FADS4","type":"exact"}],"termid":"MONDO:0100104","terms_by_termid":{"MONDO:0100104":null},"xrefs":{"Monarch":{"xref_id":"0100104"}}}


id: PBO:0082184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alanine transaminase (glutamic pyruvic transaminase); involved in alanine biosynthesis and catabolism; TOR1-independent role in determining chronological lifespan; expression is induced in the presence of alanine; repression is mediated by Nrg1p; ALT1 has a paralog, ALT2, that arose from the whole genome duplication; Alt2p is catalytically inactive","termid":"PBO:0082184"}


id: PBO:0043034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"charged multivesicular body protein 4C","termid":"PBO:0043034"}


id: MONDO:0043112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"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":"lachiewicz sibley syndrome","secondary_identifiers":["UMLS:C2931742","MESH:C538131","MEDGEN:419151"],"synonyms":[{"name":"hereditary renal disease and preauricular pits","type":"related"}],"termid":"MONDO:0043112","xrefs":{"Monarch":{"xref_id":"0043112"}}}


id: GO:0003911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD+ + deoxyribonucleotide(n) + deoxyribonucleotide(m) = AMP + nicotinamide nucleotide + deoxyribonucleotide(n+m).","definition_xrefs":["EC:6.5.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA ligase activity","termid":"GO:0003909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874","GO:0140097"],"is_obsolete":false,"name":"DNA ligase (NAD+) activity","secondary_identifiers":["MetaCyc:DNA-LIGASE-NAD+-RXN"],"synonyms":[{"name":"DNA joinase activity","type":"broad"},{"name":"DNA ligase (NAD)","type":"related"},{"name":"DNA repair enzyme activity","type":"related"},{"name":"DNA-joining enzyme","type":"related"},{"name":"deoxyribonucleate ligase","type":"broad"},{"name":"deoxyribonucleic acid joinase","type":"broad"},{"name":"deoxyribonucleic acid ligase","type":"broad"},{"name":"deoxyribonucleic joinase","type":"broad"},{"name":"deoxyribonucleic ligase","type":"broad"},{"name":"deoxyribonucleic repair enzyme","type":"related"},{"name":"deoxyribonucleic-joining enzyme","type":"related"},{"name":"poly(deoxyribonucleotide):poly(deoxyribonucleotide) ligase (AMP-forming, NMN-forming)","type":"related"},{"name":"polydeoxyribonucleotide synthase (NAD(+)) activity","type":"related"},{"name":"polydeoxyribonucleotide synthase (NAD)","type":"related"},{"name":"polydeoxyribonucleotide synthase (NAD+) activity","type":"related"},{"name":"polynucleotide ligase","type":"broad"},{"name":"polynucleotide ligase (NAD(+)) activity","type":"related"},{"name":"polynucleotide ligase (NAD)","type":"related"},{"name":"polynucleotide ligase (NAD+) activity","type":"related"},{"name":"polynucleotide ligase (nicotinamide adenine dinucleotide)","type":"related"},{"name":"polynucleotide synthetase (nicotinamide adenine dinucleotide)","type":"related"},{"name":"polynucleotide synthetase activity","type":"related"}],"termid":"GO:0003911"}


id: PBO:0056724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylphosphate capping enzyme","termid":"PBO:0056724"}


id: PBO:0001839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine decarboxylase T subunit (predicted)","termid":"PBO:0001839"}


id: PR:Q09709
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An RNA pseudouridylate synthase domain-containing protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C18B11.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC18B11.02c","secondary_identifiers":["UniProtKB:Q09709"],"synonyms":[{"name":"Spom972h-RPUSD2","type":"exact"}],"termid":"PR:Q09709"}


id: PBO:0076665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-box transcription factor T","termid":"PBO:0076665"}


id: GO:0034661
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of non-coding RNA transcripts (ncRNAs). Includes the breakdown of cryptic unstable transcripts (CUTs).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete ncRNA catabolic process (obsolete GO:0034661)","termid":"GO:0034661"}


id: PBO:0056179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAF bZIP transcription factor B","termid":"PBO:0056179"}


id: MONDO:1010628
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chediak-Higashi syndrome that occurs in Arctic fox.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Chediak-Higashi syndrome, non-human animal","termid":"MONDO:1010070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chediak-Higashi syndrome, Arctic fox","secondary_identifiers":["OMIA:000185-494514"],"termid":"MONDO:1010628","xrefs":{"Monarch":{"xref_id":"1010628"}}}


id: PBO:0056029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lanosterol synthase","termid":"PBO:0056029"}


id: GO:0031332
data:
  {"annotated_genes":["SJAG_02621","SJAG_03042","SJAG_04061","SJAG_03706","SJAG_02594","SJAG_03916"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[64650],"is_not":false,"summary":null,"term":"GO:0031332"},{"annotations":[62844,88729,118112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033167"},{"annotations":[91234,118118,112222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030958"}]},"cv_name":"cellular_component","definition":"Any protein complex that mediates the effects of small interfering RNAs on gene expression. Most known examples contain one or more members of the Argonaute family of proteins.","definition_xrefs":["GOC:mah","PMID:14704433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoprotein complex","termid":"GO:1990904"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02594":null,"SJAG_02621":null,"SJAG_03042":null,"SJAG_03706":null,"SJAG_03916":null,"SJAG_04061":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"RNAi effector complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"termid":"GO:0031332","terms_by_termid":{"GO:0030958":null,"GO:0031332":null,"GO:0033167":null}}


id: PBO:0057821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3141","termid":"PBO:0057821"}


id: SO:0000584
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tmRNA liberates a mRNA from a stalled ribosome. To accomplish this part of the tmRNA is used as a reading frame that ends in a translation stop signal. The broken mRNA is replaced in the ribosome by the tmRNA and translation of the tmRNA leads to addition of a proteolysis tag to the incomplete protein enabling recognition by a protease. Recently a number of permuted tmRNAs genes have been found encoded in two parts. TmRNAs have been identified in eubacteria and some chloroplasts but are absent from archeal and Eukaryote nuclear genomes.","direct_ancestors":[{"relation_name":"is_a","term_name":"small_regulatory_ncRNA","termid":"SO:0000370"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tmRNA","secondary_identifiers":["http://en.wikipedia.org/wiki/TmRNA"],"synonyms":[{"name":"10Sa RNA","type":"related"},{"name":"INSDC_feature:tmRNA","type":"exact"},{"name":"ssrA","type":"related"}],"termid":"SO:0000584"}


id: PBO:0053523
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 518","termid":"PBO:0053523"}


id: PBO:0082219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-adaptin; large subunit of the clathrin associated protein complex (AP-2); involved in vesicle mediated transport","termid":"PBO:0082219"}


id: PBO:0072697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RUN and SH3 domain containing 2","termid":"PBO:0072697"}


id: PBO:0057664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1255b-2","termid":"PBO:0057664"}


id: GO:0140721
data:
  {"annotated_genes":["SJAG_02594"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060698"}]},"cv_name":"molecular_function","definition":"Binds to and modulates the activity of a nuclease.","definition_xrefs":["PMID:30046034","PMID:28785032","PMID:29554913"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02594":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0004857","GO:0003674","GO:0140678"],"is_obsolete":false,"name":"nuclease inhibitor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140721","terms_by_termid":{"GO:0060698":null}}


id: GO:0051846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any mechanism of immune avoidance that directly affects the symbiont immune system, e.g. blocking any stage in symbiont MHC class I and II presentation. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:12439615"],"gene_count":0,"genotype_count":0,"name":"obsolete active evasion of symbiont immune response (obsolete GO:0051846)","synonyms":[{"name":"active evasion of symbiont immune response","type":"exact"},{"name":"active immune evasion","type":"broad"}],"termid":"GO:0051846"}


id: PBO:0053255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM homeobox 8","termid":"PBO:0053255"}


id: MONDO:1010766
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vitiligo that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitiligo, non-human animal","termid":"MONDO:1010136"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitiligo, domestic cat","secondary_identifiers":["OMIA:001055-9685"],"termid":"MONDO:1010766","xrefs":{"Monarch":{"xref_id":"1010766"}}}


id: GO:1904144
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of phosphatidylinositol phosphate phosphatase activity.","definition_xrefs":["GOC:TermGenie","PMID:12525165","GO_REF:0000088","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase complex","termid":"GO:1903293"}],"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":"phosphatidylinositol phosphate phosphatase complex","synonyms":[{"name":"prostatic acid phosphatase complex","type":"narrow"}],"termid":"GO:1904144"}


id: GO:0075067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The increase in size or mass of symbiont, or the progression of the symbiont from an initial condition to a later condition, occurring in its host's intercellular space. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete growth or development of symbiont in host intercellular space (obsolete GO:0075067)","synonyms":[{"name":"growth or development of symbiont in host intercellular space","type":"exact"}],"termid":"GO:0075067"}


id: MONDO:0006005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition caused by infection by the Venezuelan equine encephalitis virus, which is characterized by headache, fever, myalgia, nausea, and vomiting.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"encephalomyelitis","termid":"MONDO:0005156"},{"relation_name":"is_a","term_name":"Alphavirus infectious disease","termid":"MONDO:0005643"},{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"},{"relation_name":"is_a","term_name":"viral infection of central nervous system","termid":"MONDO:0024318"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Venezuelan equine encephalitis","secondary_identifiers":["ICD10CM:A92.2","GARD:6355","icd11.foundation:608978790","EFO:0007534","MEDGEN:4036","MESH:D004685","ICD9:066.2","NCIT:C35121","SCTID:417067005","DOID:9584","UMLS:C0014078"],"synonyms":[{"name":"Venezuelan equine encephalitis virus caused disease or disorder","type":"exact"},{"name":"Venezuelan equine encephalitis virus disease or disorder","type":"exact"},{"name":"Venezuelan equine encephalitis virus infectious disease","type":"exact"},{"name":"Venezuelan equine fever","type":"related"}],"termid":"MONDO:0006005","xrefs":{"Monarch":{"xref_id":"0006005"}}}


id: FYPO:0006960
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 adenosine measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular adenosine level","synonyms":[{"name":"increased adenosine accumulation","type":"related"},{"name":"increased cellular adenosine level during mitotic cell cycle","type":"related"},{"name":"increased cellular adenosine level during vegetative growth","type":"exact"}],"termid":"FYPO:0006960"}


id: FYPO:0004664
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the duration of protein phosphorylation on tyrosine residues is longer than normal during a cellular response to salt stress. All protein tyrosine phosphorylation may be affected, or tyrosine residues in one or more specific proteins, or at specific protein sites, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete increased duration of protein tyrosine phosphorylation during cellular response to salt stress (obsolete FYPO:0004664)","synonyms":[{"name":"increased duration of protein tyrosine phosphorylation during cellular response to salt stress during mitotic cell cycle","type":"related"},{"name":"increased duration of protein tyrosine phosphorylation during cellular response to salt stress during vegetative growth","type":"exact"},{"name":"prolonged protein tyrosine phosphorylation during cellular response to salt stress","type":"exact"}],"termid":"FYPO:0004664"}


id: MONDO:0020694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from the salivary glands, most often the parotid gland. It presents as a slow growing and painless mass. It is characterized by the presence of duct-like structures lined by two layers of cells, an inner layer composed of epithelial-type cells and an outer layer composed of clear, myoepithelial-type cells.","definition_xrefs":["NCIT:C35701"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland carcinoma","termid":"MONDO:0000521"},{"relation_name":"is_a","term_name":"epithelial-myoepithelial carcinoma","termid":"MONDO:0003389"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"salivary gland epithelial myoepithelial carcinoma","secondary_identifiers":["MEDGEN:234769","UMLS:C1335900"],"synonyms":[{"name":"salivary gland epithelial myoepithelial carcinoma","type":"exact"}],"termid":"MONDO:0020694","xrefs":{"Monarch":{"xref_id":"0020694"}}}


id: GO:2000255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of male germ cell proliferation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of germ cell proliferation","termid":"GO:1905937"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"is_a","term_name":"regulation of male germ cell proliferation","termid":"GO:2000254"},{"relation_name":"negatively_regulates","term_name":"male germ cell proliferation","termid":"GO:0002176"}],"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 male germ cell proliferation","termid":"GO:2000255"}


id: PBO:0080670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1","termid":"PBO:0080670"}


id: SO:0000540
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA in rearranged configuration including at least one D-J-GENE, one J-GENE and one C-GENE.","direct_ancestors":[{"relation_name":"has_part","term_name":"J_gene_segment","termid":"SO:0000470"},{"relation_name":"has_part","term_name":"C_gene_segment","termid":"SO:0000478"},{"relation_name":"has_part","term_name":"DJ_gene_segment","termid":"SO:0000572"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","termid":"SO:0000938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DJ_J_C_cluster","synonyms":[{"name":"(DJ)-J-C-CLUSTER","type":"exact"},{"name":"DJ J C cluster","type":"exact"}],"termid":"SO:0000540"}


id: GO:0016217
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: deethylsimazine + H2O = N-ethylammeline + chloride + H+.","definition_xrefs":["MetaCyc:R465-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid halide bonds, in C-halide compounds","termid":"GO:0019120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"N-ethylammeline chlorohydrolase activity","termid":"GO:0016217"}


id: MONDO:0019848
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Posterior hypospadias is a rare, non-syndromic, urogenital tract malformation characterized by an ectopic urethral meatus opening located in the posterior penis, the penoscrotal junction, the scrotum or the perineum, which often appears stenotic. The scrotum might appear bifid in severe cases and micropenis is not commonly associated. Urinary tract malformations, such as ureteropelvic junction obstruction, vesicoureteric reflux, pelvic or horseshoe kidney, crossed renal ectopia, renal agenesis, may be observed.","definition_xrefs":["Orphanet:95706"],"direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"posterior hypospadias","secondary_identifiers":["GARD:16840","UMLS:C5231010","MEDGEN:1684864"],"synonyms":[{"name":"perineal, scrotal or penoscrotal hypospadias","type":"exact"}],"termid":"MONDO:0019848","xrefs":{"Monarch":{"xref_id":"0019848"}}}


id: MONDO:0014957
data:
  {"annotated_genes":["SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87146],"is_not":false,"summary":null,"term":"MONDO:0014957"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03081":null},"genotype_count":0,"is_obsolete":false,"name":"language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:934645","OMIM:617182","UMLS:C4310678"],"synonyms":[{"name":"LADCI","type":"exact"},{"name":"language delay and ADHD/cognitive impairment with or without cardiac arrhythmia","type":"exact"},{"name":"language delay and attention Deficit-hyperactivity disorder/cognitive impairment with or without Cardiac arrhythmia","type":"exact"},{"name":"language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia; LADCI","type":"exact"}],"termid":"MONDO:0014957","terms_by_termid":{"MONDO:0014957":null},"xrefs":{"Monarch":{"xref_id":"0014957"}}}


id: PBO:0063943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 4","termid":"PBO:0063943"}


id: GO:0031990
data:
  {"annotated_genes":["SJAG_01584"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73066],"is_not":false,"summary":null,"term":"GO:0031990"}]},"cv_name":"biological_process","definition":"The directed movement of mRNA from the nucleus to the cytoplasm during a heat stimulus, a temperature stimulus above the optimal temperature for the organism; in particular, a process that enables an organism withstand exposure to temperatures that would otherwise lethally impair poly(A)+ mRNA-nucleus export.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA export from nucleus","termid":"GO:0006406"},{"relation_name":"is_a","term_name":"cellular response to heat","termid":"GO:0034605"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01584":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006913"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006913","GO:0051179","GO:0010467","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"mRNA export from nucleus in response to heat stress","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"mRNA export from cell nucleus during heat stress","type":"exact"},{"name":"mRNA export from nucleus during heat stress","type":"related"}],"termid":"GO:0031990","terms_by_termid":{"GO:0031990":null}}


id: GO:0090554
data:
  {"annotated_genes":["SJAG_00669","SJAG_02897","SJAG_01731"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94400,97924,100195],"is_not":false,"summary":null,"term":"GO:0090554"}]},"cv_name":"molecular_function","definition":"Catalysis of the movement of phosphatidylcholine from the cytosolic to the exoplasmic leaflet of a membrane, using energy from the hydrolysis of ATP.","definition_xrefs":["GOC:ab","RHEA:38583","PMID:16452632"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylcholine transporter activity","termid":"GO:0008525"},{"relation_name":"is_a","term_name":"floppase activity","termid":"GO:0140328"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00669":null,"SJAG_01731":null,"SJAG_02897":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0140303"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0140303"],"is_obsolete":false,"name":"phosphatidylcholine floppase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ATP-dependent phosphatidylcholine transporter activity","type":"broad"},{"name":"ATPase-coupled phosphatidylcholine transporter activity","type":"broad"},{"name":"phosphatidylcholine floppase activity (cytosolic to exoplasmic leaflet)","type":"exact"},{"name":"phosphatidylcholine-translocating ATPase activity","type":"broad"}],"termid":"GO:0090554","terms_by_termid":{"GO:0090554":null}}


id: GO:0002470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a plasmacytoid dendritic cell expresses antigen (peptide or lipid) on its cell surface in association with an MHC protein complex.","definition_xrefs":["GOC:add","ISBN:0781735149","PMID:15771591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendritic cell antigen processing and presentation","termid":"GO:0002468"}],"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":"plasmacytoid dendritic cell antigen processing and presentation","termid":"GO:0002470"}


id: GO:0072190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the urothelium of the ureter over time, from its formation to the mature structure. The urothelium is an epithelium that makes up the epithelial tube of the ureter.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelium development","termid":"GO:0060429"},{"relation_name":"part_of","term_name":"ureter development","termid":"GO:0072189"}],"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":"ureter urothelium development","synonyms":[{"name":"ureter epithelium development","type":"exact"}],"termid":"GO:0072190"}


id: GO:0033078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a T cell via a differentiation pathway independent of the thymus.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell differentiation","termid":"GO:0030217"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"extrathymic T cell differentiation","synonyms":[{"name":"extrathymic T cell development","type":"related"}],"termid":"GO:0033078"}


id: MONDO:0014664
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the KIAA0586 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 23","secondary_identifiers":["UMLS:C4084822","GARD:16124","OMIM:616490","DOID:0110992","MEDGEN:900119"],"synonyms":[{"name":"JBTS23","type":"exact"},{"name":"Joubert syndrome 23","type":"exact"},{"name":"Joubert syndrome caused by mutation in KIAA0586","type":"exact"},{"name":"Joubert syndrome type 23","type":"exact"},{"name":"KIAA0586 Joubert syndrome","type":"exact"}],"termid":"MONDO:0014664","xrefs":{"Monarch":{"xref_id":"0014664"}}}


id: MONDO:0004482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic soft tissue disorder characterized by the localized formation of reactive fibrous and bone tissues. It usually occurs in the subcutaneous tissue of the proximal phalanx. Less frequently, it involves the toe. It presents with swelling and pain of the affected area. The prognosis is excellent. However, incomplete excision may lead to the re-growth of the lesion.","definition_xrefs":["NCIT:C6573"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"bone benign neoplasm","termid":"MONDO:0000631"},{"relation_name":"is_a","term_name":"benign soft tissue neoplasm","termid":"MONDO:0044335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroosseous pseudotumor of the digits","secondary_identifiers":["MEDGEN:232507","ICD9:215.9","SCTID:403991009","UMLS:C1333612","DOID:8153"],"synonyms":[{"name":"fibroosseous digital pseudotumor","type":"exact"},{"name":"fibroosseous pseudotumor of digits","type":"exact"},{"name":"fibroosseous pseudotumor of the digits","type":"exact"}],"termid":"MONDO:0004482","xrefs":{"Monarch":{"xref_id":"0004482"}}}


id: MONDO:0018172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Malignant sex cord stromal tumor (SCST) of ovary is a rare ovarian cancer arising from granulosa, theca, sertoli and leydig cells or stromal fibroblasts, occurring at any age and presenting with abdominal or pelvic mass, and characterized (with the exception of fibroma) by the production of sex steroids resulting in manifestations of hormone excess, with a relatively favorable prognosis.","definition_xrefs":["Orphanet:35808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant non-epithelial tumor of ovary","termid":"MONDO:0018365"},{"relation_name":"is_a","term_name":"ovarian sex cord-stromal tumor","termid":"MONDO:0021657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant sex cord stromal tumor of ovary","secondary_identifiers":["GARD:18816","MEDGEN:233667","NCIT:C8053","UMLS:C1334609"],"synonyms":[{"name":"malignant Sex cord-stromal tumor of ovary","type":"exact"},{"name":"malignant Sex cord-stromal tumor of the ovary","type":"exact"},{"name":"malignant Sex cord-stromal tumour of ovary","type":"exact"},{"name":"malignant Sex cord-stromal tumour of the ovary","type":"exact"},{"name":"malignant ovarian SCST","type":"exact"},{"name":"malignant ovarian Sex cord-stromal neoplasm","type":"exact"},{"name":"malignant ovarian Sex cord-stromal tumor","type":"exact"},{"name":"malignant ovarian Sex cord-stromal tumour","type":"exact"},{"name":"malignant ovarian sex cord-stromal tumor","type":"exact"},{"name":"malignant ovarian sex cord-stromal tumour","type":"exact"},{"name":"ovarian sex cord-stromal tumor, malignant","type":"exact"}],"termid":"MONDO:0018172","xrefs":{"Monarch":{"xref_id":"0018172"}}}


id: SO:0001314
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"1,2'-O-dimethyladenosine is a modified adenosine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_adenosine","termid":"SO:0001273"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"one_two_prime_O_dimethyladenosine","secondary_identifiers":["RNAMOD:097"],"synonyms":[{"name":"1,2'-O-dimethyladenosine","type":"exact"},{"name":"m1Am","type":"exact"},{"name":"one two prime O dimethyladenosine","type":"exact"}],"termid":"SO:0001314"}


id: GO:0051652
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a chromosome is maintained in a specific location within a cell and prevented from moving elsewhere.","definition_xrefs":["GOC:dph","GOC:ai","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome localization","termid":"GO:0050000"},{"relation_name":"is_a","term_name":"maintenance of organelle location","termid":"GO:0051657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"maintenance of chromosome location","synonyms":[{"name":"maintenance of chromosome localization","type":"related"}],"termid":"GO:0051652"}


id: GO:0051767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a nitric-oxide synthase, an enzyme which catalyzes the reaction L-arginine + n NADPH + n H+ + m O2 = citrulline + nitric oxide + n NADP+.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nitric-oxide synthase biosynthetic process (obsolete GO:0051767)","synonyms":[{"name":"NO synthase biosynthesis","type":"exact"},{"name":"NO synthase biosynthetic process","type":"exact"},{"name":"NOS biosynthesis","type":"exact"},{"name":"NOS biosynthetic process","type":"exact"},{"name":"NOS1 biosynthesis","type":"narrow"},{"name":"NOS2 biosynthesis","type":"narrow"},{"name":"NOS2 synthase biosynthesis","type":"narrow"},{"name":"NOS2 synthase biosynthetic process","type":"narrow"},{"name":"NOS3 biosynthesis","type":"narrow"},{"name":"brain nitric-oxide synthase biosynthetic process","type":"narrow"},{"name":"endothelial nitric-oxide synthase biosynthetic process","type":"narrow"},{"name":"inducible nitric-oxide synthase biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase (type 2) biosynthesis","type":"narrow"},{"name":"nitric-oxide synthase (type 2) biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase (type II) biosynthesis","type":"narrow"},{"name":"nitric-oxide synthase (type II) biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase 2 biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase-1 biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase-2 biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase-3 biosynthetic process","type":"narrow"}],"termid":"GO:0051767"}


id: MONDO:0042724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations (obsolete MONDO:0042724)","termid":"MONDO:0042724","xrefs":{"Monarch":{"xref_id":"0042724"}}}


id: MONDO:0004501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign, asymptomatic neoplasm that arises from the fallopian tube. The tumors are round and solitary and contain connective tissue and cystic structures lined by serous-type epithelium. The majority of cases are incidental findings during operation for an unrelated gynecologic disorder.","definition_xrefs":["NCIT:C40114"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube serous adenofibroma","termid":"MONDO:0003461"},{"relation_name":"is_a","term_name":"cystadenofibroma","termid":"MONDO:0003464"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fallopian tube cystadenofibroma","secondary_identifiers":["UMLS:C1517111","DOID:8211","MEDGEN:273292"],"synonyms":[{"name":"cystadenofibroma of fallopian tube","type":"exact"},{"name":"fallopian tube cystadenofibroma","type":"exact"},{"name":"fallopian tube serous cystadenofibroma","type":"exact"}],"termid":"MONDO:0004501","xrefs":{"Monarch":{"xref_id":"0004501"}}}


id: PBO:0059992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 12","termid":"PBO:0059992"}


id: PBO:0054698
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 2107","termid":"PBO:0054698"}


id: MONDO:1012641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any von Willebrand disease that occurs in pigs and is characterized by low plasma vWF concentrations and mild to moderate bleeding symptoms.","definition_xrefs":["OMIA:001057-9823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Von Willebrand disease, pig","termid":"MONDO:1011615"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Willebrand disease I, pig","termid":"MONDO:1012641","xrefs":{"Monarch":{"xref_id":"1012641"}}}


id: FYPO:0002859
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the non-growing cell tip is abolished. The new cell tip formed upon cell division does not grow until after new end take-off.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to cell tip during vegetative growth","termid":"FYPO:0001585"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to non-growing cell tip","synonyms":[{"name":"abolished protein localisation to non-growing cell tip","type":"exact"},{"name":"abolished protein localization to new cell end","type":"related"},{"name":"abolished protein localization to new cell tip","type":"related"},{"name":"abolished protein localization to new non-growing cell tip","type":"exact"},{"name":"abolished protein localization to non-growing cell end","type":"exact"},{"name":"abolished protein localization to non-growing cell tip during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to non-growing cell tip during vegetative growth","type":"exact"},{"name":"protein localization to non-growing cell tip abolished","type":"exact"}],"termid":"FYPO:0002859"}


id: GO:0031105
data:
  {"annotated_genes":["SJAG_00663","SJAG_03374","SJAG_04375","SJAG_01769","SJAG_04470","SJAG_01277","SJAG_03688"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[94470,100109,106021,115993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032152"},{"annotations":[97886,100961,100112,103921],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032151"}]},"cv_name":"cellular_component","definition":"A protein complex containing septins. Typically, these complexes contain multiple septins and are oligomeric.","definition_xrefs":["GOC:mah","PMID:15385632"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cell cortex","termid":"GO:0005938"},{"relation_name":"part_of","term_name":"septin cytoskeleton","termid":"GO:0032156"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00663":null,"SJAG_01277":null,"SJAG_01769":null,"SJAG_03374":null,"SJAG_03688":null,"SJAG_04375":null,"SJAG_04470":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005938"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005938","GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"septin complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0031105","terms_by_termid":{"GO:0032151":null,"GO:0032152":null}}


id: GO:0008617
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving guanine, guanine riboside, a nucleoside with a wide species distribution.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanosine-containing compound metabolic process","termid":"GO:1901068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"guanosine metabolic process","synonyms":[{"name":"guanosine metabolism","type":"exact"}],"termid":"GO:0008617"}


id: GO:0002503
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The binding of a peptide to the antigen binding groove of an MHC class II protein complex.","definition_xrefs":["PMID:15771591","GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide antigen assembly with MHC protein complex","termid":"GO:0002501"},{"relation_name":"part_of","term_name":"MHC class II protein complex assembly","termid":"GO:0002399"},{"relation_name":"part_of","term_name":"antigen processing and presentation of peptide antigen via MHC class II","termid":"GO:0002495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"peptide antigen assembly with MHC class II protein complex","termid":"GO:0002503"}


id: GO:0090692
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The site on the mitochondrial membrane where the separation of a single continuous mitochondrial membrane into two membranes occurs as a final step in mitochondrial fission.","definition_xrefs":["GOC:bc","PMID:26618722","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"mitochondrial membrane","termid":"GO:0031966"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005739"}],"interesting_parent_ids":["GO:0005739","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"mitochondrial membrane scission site","termid":"GO:0090692"}


id: PBO:0057027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 124-3","termid":"PBO:0057027"}


id: PBO:0027290
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_glutathione_peroxidase_activity","termid":"PBO:0027290"}


id: GO:1904543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of free ubiquitin chain polymerization.","definition_xrefs":["GOC:pad","GO_REF:0000058","PMID:24660806","GOC:TermGenie","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein polymerization","termid":"GO:0032272"},{"relation_name":"is_a","term_name":"regulation of free ubiquitin chain polymerization","termid":"GO:1904542"},{"relation_name":"negatively_regulates","term_name":"free ubiquitin chain polymerization","termid":"GO:0010994"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"negative regulation of free ubiquitin chain polymerization","synonyms":[{"name":"down regulation of free ubiquitin chain polymerization","type":"exact"},{"name":"down-regulation of free ubiquitin chain polymerization","type":"exact"},{"name":"downregulation of free ubiquitin chain polymerization","type":"exact"},{"name":"inhibition of free ubiquitin chain polymerization","type":"narrow"}],"termid":"GO:1904543"}


id: GO:0045469
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or prevents the correct R8 cell spacing pattern in a compound eye.","definition_xrefs":["PMID:11880339","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of R8 cell spacing in compound eye","termid":"GO:0045468"}],"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 R8 cell spacing in compound eye","synonyms":[{"name":"down regulation of R8 spacing","type":"exact"},{"name":"down-regulation of R8 spacing","type":"exact"},{"name":"downregulation of R8 spacing","type":"exact"},{"name":"inhibition of R8 spacing","type":"narrow"}],"termid":"GO:0045469"}


id: GO:1903673
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any cleavage furrow formation that is involved in mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle","GO_REF:0000060","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleavage furrow formation","termid":"GO:0036089"},{"relation_name":"is_a","term_name":"mitotic cytokinetic process","termid":"GO:1902410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0000281"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0000281","GO:0061024"],"is_obsolete":false,"name":"mitotic cleavage furrow formation","synonyms":[{"name":"cleavage furrow positioning involved in mitotic cell cycle","type":"narrow"}],"termid":"GO:1903673"}


id: PBO:0034727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orthologous to S. cereviaie YER035W and YGL222C","termid":"PBO:0034727"}


id: PBO:0030680
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_spore","termid":"PBO:0030680"}


id: SO:0002103
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A pseudogenic variable region which closely resembles a known functional T receptor variable gene but in which the coding region has stop codons, frameshift mutations or a mutation that effects the initiation codon that rearranges at the DNA level and codes the variable region of an immunoglobulin chain.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html","IGMT:http://www.imgt.org/IMGTScientificChart/SequenceDescription/Keywords.php"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T_cell_receptor_pseudogene","termid":"SO:0002099"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TR_V_pseudogene","synonyms":[{"name":"T cell receptor V pseudogene","type":"exact"},{"name":"T cell receptor Variable pseudogene","type":"exact"},{"name":"TR V pseudogene","type":"exact"},{"name":"T_cell_receptor_V_pseudogene","type":"exact"},{"name":"T_cell_receptor_Variable_pseudogene","type":"exact"}],"termid":"SO:0002103"}


id: PBO:0056823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major facilitator superfamily domain containing 14A","termid":"PBO:0056823"}


id: MONDO:1010701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyruvate kinase deficiency of erythrocyte that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate kinase deficiency of erythrocyte, non-human animal","termid":"MONDO:1010099"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate kinase deficiency of erythrocyte, dog","secondary_identifiers":["OMIA:000844-9615"],"termid":"MONDO:1010701","xrefs":{"Monarch":{"xref_id":"1010701"}}}


id: PBO:0062373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily A member 15 pseudogene","termid":"PBO:0062373"}


id: PBO:0072307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S25 pseudogene 4","termid":"PBO:0072307"}


id: PBO:0082035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-acyl-sn-glycerol-3-phosphate acyltransferase; catalyzes the acylation of lysophosphatidic acid to form phosphatidic acid, a key intermediate in lipid metabolism; enzymatic activity detected in lipid particles and microsomes","termid":"PBO:0082035"}


id: GO:0090682
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A G protein-coupled receptor activity that is responsible for the sense of bitter taste.","definition_xrefs":["GOC:hat","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bitter taste receptor activity","termid":"GO:0033038"},{"relation_name":"is_a","term_name":"GPCR taste receptor activity","termid":"GO:0090681"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"GPCR bitter taste receptor activity","synonyms":[{"name":"G protein-coupled receptor bitter taste receptor activity","type":"exact"},{"name":"G-protein coupled receptor bitter taste receptor activity","type":"exact"}],"termid":"GO:0090682"}


id: PBO:0047906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(8)(q24.1)","termid":"PBO:0047906"}


id: PR:Q9P6H9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- reb1 gene.","definition_xrefs":["UniProtKB:Q9P6H9","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":"DNA-binding protein reb1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.11c","synonyms":[{"name":"Spom972h-reb1","type":"exact"}],"termid":"PR:Q9P6H9"}


id: PATO:0001759
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A composition quality inhering in a bearer by virtue of the bearer's containing granules.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"composition","termid":"PATO:0000025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"granular","termid":"PATO:0001759"}


id: PBO:0031117
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_nuclear_protein_level_during_vegetative_growth","termid":"PBO:0031117"}


id: PBO:0063583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PET100 cytochrome c oxidase chaperone","termid":"PBO:0063583"}


id: MONDO:0001812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"blepharitis","termid":"MONDO:0004785"},{"relation_name":"is_a","term_name":"parasitic eye infection","termid":"MONDO:0020947"}],"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":"parasitic eyelid infestation","secondary_identifiers":["SCTID:193922006","DOID:13823","ICD9:373.6","MEDGEN:509836","UMLS:C0155183"],"synonyms":[{"name":"parasitic eyelid infestation","type":"exact"},{"name":"parasitic infestation of eyelid","type":"exact"}],"termid":"MONDO:0001812","xrefs":{"Monarch":{"xref_id":"0001812"}}}


id: MONDO:0957462
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary tuberculosis","termid":"MONDO:0006052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary pulmonary tuberculosis","secondary_identifiers":["icd11.foundation:882244568","Orphanet:645814"],"termid":"MONDO:0957462","xrefs":{"Monarch":{"xref_id":"0957462"}}}


id: PBO:0061667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUP50 divergent transcript","termid":"PBO:0061667"}


id: FYPO:0002027
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell forms an actomyosin contractile ring that is not perpendicular to the long axis of the cell.","definition_xrefs":["PMID:8834798","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized actomyosin contractile ring","termid":"FYPO:0001369"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000032","FYPO:0001985","FYPO:0004803","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"angled actomyosin contractile ring","synonyms":[{"name":"actomyosin contractile ring not orthogonal to long axis of cell","type":"exact"},{"name":"actomyosin contractile ring not perpendicular to long axis of cell","type":"related"},{"name":"angled actomyosin contractile ring during mitotic cell cycle","type":"related"},{"name":"angled actomyosin contractile ring during vegetative growth","type":"exact"},{"name":"angled cytokinetic contractile ring","type":"exact"},{"name":"angled mitotic contractile ring","type":"exact"},{"name":"tilted actomyosin contractile ring","type":"exact"}],"termid":"FYPO:0002027"}


id: GO:0042447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of any hormone, naturally occurring substances secreted by specialized cells that affects the metabolism or behavior of other cells possessing functional receptors for the hormone.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"hormone metabolic process","termid":"GO:0042445"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hormone catabolic process","synonyms":[{"name":"hormone breakdown","type":"exact"},{"name":"hormone catabolism","type":"exact"},{"name":"hormone degradation","type":"exact"}],"termid":"GO:0042447"}


id: MONDO:0007472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has material basis in mutations in the CFH gene on chromosome 1q31.3.","definition_xrefs":["PMID:18252232","PMID:5448127","DOID:0060746"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal dystrophies primarily involving Bruch's membrane","termid":"MONDO:0001666"},{"relation_name":"is_a","term_name":"retinal drusen","termid":"MONDO:0006949"}],"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":"basal laminar drusen","secondary_identifiers":["MEDGEN:152676","ICD10CM:H35.5","OMIM:126700","GARD:15060","UMLS:C0730295","MESH:C563034"],"synonyms":[{"name":"basal laminar drusen","type":"exact"},{"name":"cuticular drusen","type":"exact"},{"name":"drusen of Bruch membrane","type":"exact"},{"name":"drusen, cuticular","type":"related"},{"name":"drusen, early adult-onset, grouped","type":"related"},{"name":"early adult-onset grouped drusen","type":"exact"}],"termid":"MONDO:0007472","xrefs":{"Monarch":{"xref_id":"0007472"}}}


id: PBO:0039158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate kinase 4 pseudogene 5","termid":"PBO:0039158"}


id: PBO:0060200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucin 20, cell surface associated pseudogene 1","termid":"PBO:0060200"}


id: PBO:0085164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nudix hydrolase family member with ADP-ribose pyrophosphatase activity; shown to metabolize O-acetyl-ADP-ribose to AMP and acetylated ribose 5'-phosphate","termid":"PBO:0085164"}


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


id: MONDO:0012033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bradyopsia is characterized by prolonged electroretinal response suppression leading to difficulties adjusting to changes in luminance, normal to subnormal acuity and photophobia.","definition_xrefs":["Orphanet:75374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"bradyopsia","secondary_identifiers":["DOID:0050335","icd11.foundation:1497247503","GARD:12299","ICD9:368.8","MESH:C564243","MEDGEN:331206","OMIMPS:608415","SCTID:711163009","UMLS:C1842073"],"synonyms":[{"name":"PERRS","type":"exact"},{"name":"bradyopsia","type":"exact"},{"name":"prolonged electroretinal response suppression","type":"exact"}],"termid":"MONDO:0012033","xrefs":{"Monarch":{"xref_id":"0012033"}}}


id: PBO:0000065
data:
  {"annotation_feature_type":"gene","cv_name":"sequence_feature","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein N-terminal signal sequence","termid":"PBO:0000065"}


id: PBO:0089206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin-related substrate adaptor Aly3","termid":"PBO:0089206"}


id: PBO:0089569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ctf18 RFC-like complex subunit Ctf8","termid":"PBO:0089569"}


id: SO:0001993
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Intronic positions associated with cis-splicing. Contains the first and second positions immediately before the exon and the first, second and fifth positions immediately after.","definition_xrefs":["SANGER:am"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cis_splice_site","termid":"SO:0001419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extended_cis_splice_site","synonyms":[{"name":"extended cis splice site","type":"exact"}],"termid":"SO:0001993"}


id: PBO:0030119
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_protein_level_during_cellular_response_to_hypoxia","termid":"PBO:0030119"}


id: MONDO:0014419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome is a rare neuro-ophthalmological disease characterized by nonprogressive cerebellar ataxia, delayed motor and language development, and intellectual disability in addition to ophthalmological abnormalities (e.g. oculomotor apraxia, strabismus, amblyopia, retinal dystrophy, and myopia). Cerebellar cysts, cerebellar dysplasia and cerebellar vermis hypoplasia, seen on magnetic resonance imaging, are also characteristic of the disease.","definition_xrefs":["Orphanet:370022"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome","secondary_identifiers":["GARD:17597","OMIM:615960","UMLS:C4014821","MEDGEN:863258"],"synonyms":[{"name":"PORETTI-Boltshauser syndrome","type":"related"},{"name":"PTBHS","type":"related"},{"name":"Poretti-Boltshauser syndrome","type":"exact"},{"name":"ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome","type":"exact"}],"termid":"MONDO:0014419","xrefs":{"Monarch":{"xref_id":"0014419"}}}


id: FYPO:0002283
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of tyrosine residues in one or more specific proteins, or of specific protein sites, does not occur during a cellular response to heat.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete abolished protein tyrosine phosphorylation during cellular response to heat (obsolete FYPO:0002283)","synonyms":[{"name":"abolished protein tyrosine phosphorylation during cellular response to heat during mitotic cell cycle","type":"related"},{"name":"abolished protein tyrosine phosphorylation during cellular response to heat during vegetative growth","type":"exact"},{"name":"abolished protein tyrosine phosphorylation during cellular response to heat shock","type":"narrow"},{"name":"protein phosphorylation abolished during cellular response to heat","type":"exact"}],"termid":"FYPO:0002283"}


id: RO:0002428
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c involved in regulation of p if c is involved in some 'p' and p' regulates some p","direct_ancestors":[{"relation_name":"is_a","term_name":"acts_upstream_of","termid":"RO:0002263"},{"relation_name":"is_a","term_name":"involved_in_or_involved_in_regulation_of","termid":"RO:0002431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"involved_in_regulation_of","termid":"RO:0002428"}


id: PBO:0059156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallophosphoesterase 1 pseudogene 1","termid":"PBO:0059156"}


id: PR:Q9UUH6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC630.06c gene.","definition_xrefs":["UniProtKB:Q9UUH6","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized nucleolar protein C630.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC630.06c","synonyms":[{"name":"Spom972h-SPAC630.06c","type":"exact"}],"termid":"PR:Q9UUH6"}


id: GO:0070763
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of homodimer of the Notch ligand Delta1.","definition_xrefs":["PMID:12794186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Delta1 complex","synonyms":[{"name":"Delta1 homodimer complex","type":"exact"}],"termid":"GO:0070763"}


id: PBO:0016105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine-dependent NAD(+) synthetase Qns1 (predicted)","termid":"PBO:0016105"}


id: FYPO:0006894
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of inositol hexakisphosphate kinase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal inositol hexakisphosphate kinase activity","termid":"FYPO:0006891"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000707","FYPO:0000661","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"increased inositol hexakisphosphate kinase activity","termid":"FYPO:0006894"}


id: PBO:0048909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A8 family member D, pseudogene","termid":"PBO:0048909"}


id: PBO:0058847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8076","termid":"PBO:0058847"}


id: PBO:0046796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coagulation factor II thrombin receptor like 2","termid":"PBO:0046796"}


id: GO:0015856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of cytosine, 4-amino-2-hydroxypyrimidine, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase transport","termid":"GO:0015855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"cytosine transport","synonyms":[{"name":"cytosine transmembrane transport","type":"exact"}],"termid":"GO:0015856"}


id: GO:0006631
data:
  {"annotated_genes":["SJAG_03198","SJAG_01271","SJAG_03313","SJAG_02885","SJAG_03526","SJAG_03553","SJAG_04107","SJAG_03130","SJAG_01402","SJAG_00221","SJAG_01396","SJAG_03943","SJAG_01356","SJAG_03909","SJAG_00706","SJAG_01238","SJAG_02763","SJAG_00902","SJAG_04972","SJAG_02007","SJAG_00305","SJAG_01458","SJAG_04007","SJAG_03180","SJAG_04570","SJAG_00102","SJAG_03972","SJAG_00099","SJAG_04913","SJAG_03471","SJAG_01300","SJAG_01946","SJAG_00630","SJAG_00947","SJAG_02769","SJAG_00734","SJAG_02717"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72248,76720,77596,93486,101646],"is_not":false,"summary":null,"term":"GO:0006631"},{"annotations":[73076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001561"},{"annotations":[107487,77307,69999,91406,108729,94980,67499,76963,63863,102057],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006633"},{"annotations":[71156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009062"},{"annotations":[73563,111337,79629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030497"},{"annotations":[91910,77583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034625"},{"annotations":[77580,91911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019367"},{"annotations":[97152,74936,97854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009107"},{"annotations":[72050,104324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042759"},{"annotations":[113779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042758"},{"annotations":[77225,78922,108381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001676"},{"annotations":[70618],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045717"},{"annotations":[97675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900535"},{"annotations":[75039],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010510"},{"annotations":[75082,70137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006636"},{"annotations":[73560,72442,77581,91914,103475],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042761"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving fatty acids, aliphatic monocarboxylic acids liberated from naturally occurring fats and oils by hydrolysis.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid metabolic process","termid":"GO:0006629"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00099":null,"SJAG_00102":null,"SJAG_00221":null,"SJAG_00305":null,"SJAG_00630":null,"SJAG_00706":null,"SJAG_00734":null,"SJAG_00902":null,"SJAG_00947":null,"SJAG_01238":null,"SJAG_01271":null,"SJAG_01300":null,"SJAG_01356":null,"SJAG_01396":null,"SJAG_01402":null,"SJAG_01458":null,"SJAG_01946":null,"SJAG_02007":null,"SJAG_02717":null,"SJAG_02763":null,"SJAG_02769":null,"SJAG_02885":null,"SJAG_03130":null,"SJAG_03180":null,"SJAG_03198":null,"SJAG_03313":null,"SJAG_03471":null,"SJAG_03526":null,"SJAG_03553":null,"SJAG_03909":null,"SJAG_03943":null,"SJAG_03972":null,"SJAG_04007":null,"SJAG_04107":null,"SJAG_04570":null,"SJAG_04913":null,"SJAG_04972":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"fatty acid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-211935","Reactome:R-HSA-8978868","Wikipedia:Fatty_acid_metabolism","Reactome:R-HSA-434313"],"synonyms":[{"name":"fatty acid metabolism","type":"exact"}],"termid":"GO:0006631","terms_by_termid":{"GO:0001561":null,"GO:0001676":null,"GO:0006631":null,"GO:0006633":null,"GO:0006636":null,"GO:0009062":null,"GO:0009107":null,"GO:0010510":null,"GO:0019367":null,"GO:0030497":null,"GO:0034625":null,"GO:0042758":null,"GO:0042759":null,"GO:0042761":null,"GO:0045717":null,"GO:1900535":null}}


id: SO:0000819
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome originating in a mitochondria.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_origin","term_name":"mitochondrial_sequence","termid":"SO:0000737"},{"relation_name":"is_a","term_name":"chromosome","termid":"SO:0000340"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial_chromosome","synonyms":[{"name":"mitochondrial chromosome","type":"exact"}],"termid":"SO:0000819"}


id: GO:0160226
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An oligosaccharyltransferase complex that contains STT3A as the catalytic subunit.","definition_xrefs":["PMID:31831667","PMID:39509507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharyltransferase complex","termid":"GO:0008250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005789"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005789","GO:0005575","GO:0005783"],"is_obsolete":false,"name":"oligosaccharyltransferase complex A","synonyms":[{"name":"OST-A","type":"exact"}],"termid":"GO:0160226"}


id: MONDO:0011507
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":"diabetes mellitus, congenital autoimmune","secondary_identifiers":["OMIM:605026","UMLS:C1857958","MESH:C565730","MEDGEN:347586"],"synonyms":[{"name":"diabetes mellitus, congenital autoimmune","type":"exact"}],"termid":"MONDO:0011507","xrefs":{"Monarch":{"xref_id":"0011507"}}}


id: PR:P36617
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA repair endonuclease XPF that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10150:SF0","OMA:SCHPO04346","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":"DNA repair protein rad16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC970.01","secondary_identifiers":["UniProtKB:P36617"],"synonyms":[{"name":"Spom972h-ERCC4","type":"exact"}],"termid":"PR:P36617"}


id: MONDO:0033282
data:
  {"annotated_genes":["SJAG_03701"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85321],"is_not":false,"summary":null,"term":"MONDO:0033282"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fatal multiple mitochondrial dysfunctions syndrome","termid":"MONDO:0017338"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03701":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"multiple mitochondrial dysfunctions syndrome 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617613","MEDGEN:1623132","Orphanet:569274","UMLS:C4539919","GARD:22305","DOID:0080274"],"synonyms":[{"name":"MMDS5","type":"related"},{"name":"multiple mitochondrial dysfunctions syndrome 5","type":"exact"}],"termid":"MONDO:0033282","terms_by_termid":{"MONDO:0033282":null},"xrefs":{"Monarch":{"xref_id":"0033282"}}}


id: PBO:0045819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 9","termid":"PBO:0045819"}


id: PBO:0066170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBIS pseudogene 3","termid":"PBO:0066170"}


id: GO:0098863
data:
  {"annotated_genes":["SJAG_03835","SJAG_03673","SJAG_02509","SJAG_04387","SJAG_02737","SJAG_04003","SJAG_03073"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70542,74874,101447,107443,109624,113966,116972],"is_not":false,"summary":null,"term":"GO:0098863"}]},"cv_name":"biological_process","definition":"The directed movement of the nucleus by pushing forces exerted by polymerization of backward-extending microtubules.","definition_xrefs":["GOC:vw","PMID:16611238","PMID:11309419"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear migration","termid":"GO:0007097"},{"relation_name":"is_a","term_name":"microtubule polymerization based movement","termid":"GO:0099098"},{"relation_name":"is_a","term_name":"microtubule-based transport","termid":"GO:0099111"}],"gene_count":7,"genes_by_uniquename":{"SJAG_02509":null,"SJAG_02737":null,"SJAG_03073":null,"SJAG_03673":null,"SJAG_03835":null,"SJAG_04003":null,"SJAG_04387":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"nuclear migration by microtubule mediated pushing forces","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0098863","terms_by_termid":{"GO:0098863":null}}


id: MONDO:0012868
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant form of hereditary thrombophilia due to congenital protein S deficiency.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete thrombotic disorder due to an acquired coagulation factors defect (obsolete MONDO:0016634)","termid":"MONDO:0016634"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hereditary thrombophilia due to congenital protein S deficiency","termid":"MONDO:0019144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0000426"],"is_obsolete":false,"name":"thrombophilia due to protein S deficiency, autosomal dominant","secondary_identifiers":["GARD:18568","Orphanet:26349","MESH:C567077","OMIM:612336","MEDGEN:479841","DOID:0111900","UMLS:C3278211","MedDRA:10068370"],"synonyms":[{"name":"THPH5","type":"related"},{"name":"autosomal dominant hereditary thrombophilia due to congenital protein S deficiency","type":"exact"},{"name":"hereditary thrombophilia due to congenital protein S deficiency, autosomal dominant","type":"exact"},{"name":"protein S acquired deficiency","type":"related"},{"name":"thrombophilia 5 due to protein S deficiency, autosomal dominant","type":"exact"},{"name":"thrombophilia due to protein S deficiency, autosomal dominant","type":"exact"}],"termid":"MONDO:0012868","xrefs":{"Monarch":{"xref_id":"0012868"}}}


id: GO:0044618
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. OBSOLETE. The process in which an organism effects a change in the relaxation of smooth muscle in the uterus of a second organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete obsolete modulation of relaxation of uterine smooth muscle in another organism (obsolete GO:0044618)","synonyms":[{"name":"modulation of relaxation of uterine smooth muscle in other organism","type":"exact"},{"name":"regulation of relaxation of uterine smooth muscle in other organism","type":"exact"}],"termid":"GO:0044618"}


id: PBO:0060948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFIB antisense RNA 1","termid":"PBO:0060948"}


id: GO:0103015
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (Kdo)2-lipid A + 2 4-amino-4-deoxy-alpha-L-arabinopyranosyl di-trans,poly-cis-undecaprenyl phosphate = (beta-L-Ara4N)2-(KDO)2-lipid A + 2 ditrans,polycis-undecaprenyl phosphate.","definition_xrefs":["GOC:pz","EC:2.4.2.43"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"4-amino-4-deoxy-L-arabinose transferase activity","secondary_identifiers":["MetaCyc:RXN0-2001","RHEA:35371"],"termid":"GO:0103015"}


id: GO:0010037
data:
  {"annotated_genes":["SJAG_06611"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071244"}]},"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 carbon dioxide (CO2) stimulus.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":1,"genes_by_uniquename":{"SJAG_06611":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to carbon dioxide","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0010037","terms_by_termid":{"GO:0071244":null}}


id: MONDO:0007680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multinodular goiter - cystic kidney - polydactyly syndrome is a very rare syndrome characterized by the association of multinodular goiter, cystic renal disease and digital anomalies.","definition_xrefs":["Orphanet:2091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multinodular goiter-cystic kidney-polydactyly syndrome","secondary_identifiers":["MESH:C535986","SCTID:723409007","MEDGEN:333929","OMIM:138790","GARD:1671","UMLS:C1841853"],"synonyms":[{"name":"Daneman Davy Mancer syndrome","type":"related"},{"name":"Daneman-Davy-Mancer syndrome","type":"exact"},{"name":"MNG/CRD/Da","type":"related"},{"name":"goiter, multinodular, cystic renal disease, and digital anomalies","type":"related"},{"name":"multinodular goiter - cystic kidney - polydactyly","type":"related"},{"name":"multinodular goiter, cystic renal disease, and digital anomalies","type":"related"},{"name":"multinodular goiter/cystic renal disease/digital anomalies","type":"related"},{"name":"multinodular goitre - cystic kidney - polydactyly","type":"related"},{"name":"thyroid-renal-digital anomalies","type":"exact"}],"termid":"MONDO:0007680","xrefs":{"Monarch":{"xref_id":"0007680"}}}


id: GO:0000456
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Dimethylation of the N6 amino groups of two consecutive adenosine residues near the 3'-end of the SSU rRNA. This process has been conserved from bacteria to eukaryotes.","definition_xrefs":["GOC:curators","GOC:tb","ISBN:1555811337","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete dimethylation involved in SSU-rRNA maturation (obsolete GO:0000456)","termid":"GO:0000456"}


id: PATO:0002539
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's having a shape like a ring (a circular shape enclosing a space).","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring shaped","termid":"PATO:0002539"}


id: PBO:0075939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 and cysteine rich domain 2","termid":"PBO:0075939"}


id: PBO:0005344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Sum3","termid":"PBO:0005344"}


id: MONDO:0014247
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, autosomal dominant disorder caused by mutation in the SCN11A gene. It is characterized by intense episodic pain mainly affecting the distal lower extremities in early childhood. The pain diminishes with age.","definition_xrefs":["NCIT:C125390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"familial episodic pain syndrome","termid":"MONDO:0018319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"familial episodic pain syndrome with predominantly lower limb involvement","secondary_identifiers":["MEDGEN:816229","Orphanet:391392","DOID:0111731","UMLS:C3809899","OMIM:615552","GARD:17619"],"synonyms":[{"name":"FEPS3","type":"related"},{"name":"episodic pain syndrome, familial, 3","type":"related"},{"name":"episodic pain syndrome, familial, type 3","type":"exact"}],"termid":"MONDO:0014247","xrefs":{"Monarch":{"xref_id":"0014247"}}}


id: PATO:0001812
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A relaxation which is relatively low.","definition_xrefs":["PATOC:GVG"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001812 decreased relaxation (obsolete PATO:0001812)","synonyms":[{"name":"low relaxation","type":"exact"}],"termid":"PATO:0001812"}


id: PR:O13951
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- iwr1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II nuclear localization protein iwr1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23H4.08","synonyms":[{"name":"Spom972h-iwr1","type":"exact"}],"termid":"PR:O13951"}


id: MONDO:0016571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macrocephaly-short stature-paraplegia syndrome is characterized by macrocephaly and midface hypoplasia, intellectual deficit, short stature, spastic paraplegia and severe central nervous system anomalies (hydrocephalus and Dandy-Walker malformation). It has been described in two unrelated adults.","definition_xrefs":["Orphanet:2427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0020022"],"is_obsolete":false,"name":"macrocephaly-short stature-paraplegia syndrome","secondary_identifiers":["MEDGEN:419845","SCTID:722033000","GARD:172","MESH:C537718","UMLS:C2931595"],"synonyms":[{"name":"Volcke Soekarman syndrome","type":"exact"},{"name":"Volcke-Soekarman syndrome","type":"exact"},{"name":"macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations","type":"exact"}],"termid":"MONDO:0016571","xrefs":{"Monarch":{"xref_id":"0016571"}}}


id: MOD:00413
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that is produced by reaction of a cysteine residue with biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine.","definition_xrefs":["Unimod:20#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"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":"biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine derivatized cysteine","synonyms":[{"name":"Biotinyl-iodoacetamidyl-3,6-dioxaoctanediamine","type":"related"},{"name":"PEO-Iodoacetyl-LC-Biotin","type":"related"}],"termid":"MOD:00413"}


id: GO:0051402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in a neuron, the basic cellular unit of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the nervous system.","definition_xrefs":["CL:0000540","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neuron apoptotic process","synonyms":[{"name":"apoptosis of neuronal cells","type":"exact"},{"name":"apoptosis of neurons","type":"exact"},{"name":"neuron apoptosis","type":"narrow"},{"name":"neuron programmed cell death by apoptosis","type":"exact"},{"name":"neuronal cell apoptosis","type":"exact"},{"name":"neuronal cell programmed cell death by apoptosis","type":"exact"},{"name":"programmed cell death of neuronal cells by apoptosis","type":"exact"},{"name":"programmed cell death of neurons by apoptosis","type":"exact"},{"name":"programmed cell death, neuronal cells","type":"exact"},{"name":"programmed cell death, neurons","type":"exact"}],"termid":"GO:0051402"}


id: GO:0071332
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 fructose stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to fructose","termid":"GO:0009750"},{"relation_name":"is_a","term_name":"cellular response to hexose stimulus","termid":"GO:0071331"}],"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 fructose stimulus","termid":"GO:0071332"}


id: GO:0046435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 3-(3-hydroxy)phenylpropionate, a hydroxylated derivative of phenylpropionate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol metabolic process","termid":"GO:0006066"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"3-(3-hydroxy)phenylpropionate metabolic process","synonyms":[{"name":"3-(3-hydroxy)phenylpropionate metabolism","type":"exact"}],"termid":"GO:0046435"}


id: MONDO:1011120
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Orchitis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orchitis, non-human animal","termid":"MONDO:1010277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orchitis, dog","secondary_identifiers":["OMIA:000745-9615"],"termid":"MONDO:1011120","xrefs":{"Monarch":{"xref_id":"1011120"}}}


id: GO:0031224
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of a membrane consisting of the gene products having some covalently attached portion, for example part of a peptide sequence or some other covalently attached group such as a GPI anchor, which spans or is embedded in one or both leaflets of the membrane.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of membrane (obsolete GO:0031224)","synonyms":[{"name":"intrinsic to membrane","type":"narrow"}],"termid":"GO:0031224"}


id: PBO:0062020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily M member 1 pseudogene","termid":"PBO:0062020"}


id: PBO:0090723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spore wall 1,3-beta-glucanosyltransferase Gas4","termid":"PBO:0090723"}


id: GO:0006977
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cascade of processes induced by the cell cycle regulator phosphoprotein p53, or an equivalent protein, in response to the detection of DNA damage and resulting in the stopping or reduction in rate of the cell cycle.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest (obsolete GO:0006977)","secondary_identifiers":["Reactome:R-HSA-6791312","Reactome:R-HSA-69563"],"synonyms":[{"name":"positive regulation of cell cycle arrest by p53-mediated DNA damage response","type":"exact"}],"termid":"GO:0006977"}


id: MONDO:0018532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete adenocarcinoma of liver and intrahepatic biliary tract (obsolete MONDO:0018532)","secondary_identifiers":["Orphanet:424943"],"synonyms":[{"name":"adenocarcinoma of liver and IBT","type":"exact"},{"name":"adenocarcinoma of the liver and IBT","type":"exact"},{"name":"adenocarcinoma of the liver and intrahepatic biliary tract","type":"exact"}],"termid":"MONDO:0018532","xrefs":{"Monarch":{"xref_id":"0018532"}}}


id: PBO:0091572
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae RPB9","termid":"PBO:0091572"}


id: MONDO:0003747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A glomus tumor characterized by huge vascular channel formations.","definition_xrefs":["NCIT:C5345"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous glomangioma","termid":"MONDO:0002298"}],"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":"telangiectatic glomangioma","secondary_identifiers":["MEDGEN:236998","UMLS:C1336699","DOID:6048"],"synonyms":[{"name":"telangiectatic glomangioma","type":"exact"}],"termid":"MONDO:0003747","xrefs":{"Monarch":{"xref_id":"0003747"}}}


id: MONDO:0035408
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"furuncular myiasis","termid":"MONDO:0018941"}],"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":"furuncular myiasis due to Cordylobia rodhaini","secondary_identifiers":["Orphanet:563690","MEDGEN:1685143","UMLS:C5231033","GARD:22261","ICD10CM:B87.0"],"synonyms":[{"name":"furunculoid myiasis due to Cordylobia rodhaini","type":"exact"},{"name":"furunculous myiasis due to Cordylobia rodhaini","type":"exact"}],"termid":"MONDO:0035408","xrefs":{"Monarch":{"xref_id":"0035408"}}}


id: MONDO:0010857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Semantic dementia (SD) is a form of frontotemporal dementia (FTD), characterized by the progressive, amodal and profound loss of semantic knowledge (combination of visual associative agnosia, anomia, surface dyslexia or dysgraphia and disrupted comprehension of word meaning) and behavioral abnormalities, attributable to the degeneration of the anterior temporal lobes.","definition_xrefs":["Orphanet:100069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive non-fluent aphasia","termid":"MONDO:0015059"},{"relation_name":"is_a","term_name":"behavioral variant of frontotemporal dementia","termid":"MONDO:0017160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"semantic dementia","secondary_identifiers":["DOID:0081391","UMLS:C0338462","GARD:10792","NANDO:1200550","OMIM:600274","MEDGEN:83268"],"synonyms":[{"name":"FTD","type":"related"},{"name":"Ftdp17","type":"related"},{"name":"Ftld with Tau inclusions","type":"related"},{"name":"Pallidopontonigral Degeneration","type":"related"},{"name":"Pick Complex","type":"related"},{"name":"Wilhelmsen-Lynch disease","type":"related"},{"name":"dementia, frontotemporal","type":"exact"},{"name":"dementia, frontotemporal, with Parkinsonism","type":"related"},{"name":"dementia, frontotemporal, with or without parkinsonism","type":"exact"},{"name":"disinhibition-dementia-Parkinsonism-amyotrophy Complex","type":"related"},{"name":"frontotemporal dementia","type":"related"},{"name":"frontotemporal dementia with Parkinsonism","type":"related"},{"name":"frontotemporal lobar Degeneration with Tau inclusions","type":"related"},{"name":"frontotemporal lobe dementia","type":"related"},{"name":"multiple system tauopathy with presenile dementia","type":"related"},{"name":"semantic primary progressive aphasia","type":"exact"},{"name":"semantic variant PPA","type":"exact"}],"termid":"MONDO:0010857","xrefs":{"Monarch":{"xref_id":"0010857"}}}


id: MONDO:0010948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYBA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset non-syndromic cataract","termid":"MONDO:0011060"}],"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":"cataract 10 multiple types","secondary_identifiers":["MESH:C563435","UMLS:C1833229","OMIM:600881","DOID:0110258","MEDGEN:318817"],"synonyms":[{"name":"CCZS","type":"narrow"},{"name":"CRYBA1 early-onset non-syndromic cataract","type":"exact"},{"name":"CTRCT10","type":"exact"},{"name":"cataract 10, multiple types","type":"related"},{"name":"cataract, congenital zonular, with sutural opacities","type":"related"},{"name":"congenital zonular cataract with sutural opacities","type":"narrow"},{"name":"early-onset non-syndromic cataract caused by mutation in CRYBA1","type":"exact"}],"termid":"MONDO:0010948","xrefs":{"Monarch":{"xref_id":"0010948"}}}


id: GO:0047867
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-3,3-dimethylmalate + NAD+ = 3-methyl-2-oxobutanoate + CO2 + NADH.","definition_xrefs":["EC:1.1.1.84","RHEA:13321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"dimethylmalate dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R01211","MetaCyc:DIMETHYLMALATE-DEHYDROGENASE-RXN"],"synonyms":[{"name":"(R)-3,3-dimethylmalate:NAD+ oxidoreductase (decarboxylating)","type":"related"},{"name":"beta,beta-dimethylmalate dehydrogenase activity","type":"related"}],"termid":"GO:0047867"}


id: PBO:0043803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexin 3","termid":"PBO:0043803"}


id: GO:0047345
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 5-phosphate + ADP + H+ = ADP-ribose + phosphate.","definition_xrefs":["RHEA:14529","EC:2.7.7.35"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"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:0016779"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016779"],"is_obsolete":false,"name":"ribose-5-phosphate adenylyltransferase activity","secondary_identifiers":["MetaCyc:2.7.7.35-RXN","KEGG_REACTION:R01052"],"synonyms":[{"name":"ADP ribose phosphorylase activity","type":"related"},{"name":"ADP-ribose phosphorylase activity","type":"related"},{"name":"ADP:D-ribose-5-phosphate adenylyltransferase activity","type":"related"},{"name":"ADP:ribose-5-phosphate adenylyltransferase activity","type":"exact"},{"name":"adenosine diphosphoribose phosphorylase activity","type":"related"}],"termid":"GO:0047345"}


id: PBO:0074017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 11","termid":"PBO:0074017"}


id: PBO:0081184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc fingers and homeoboxes 1","termid":"PBO:0081184"}


id: PBO:0047236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 230 member H","termid":"PBO:0047236"}


id: GO:1905275
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a Rohon-Beard neuron.","definition_xrefs":["GO_REF:0000086","ZFIN:ZDB-PUB-120807-45","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system neuron differentiation","termid":"GO:0021953"}],"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":"Rohon-Beard neuron differentiation","termid":"GO:1905275"}


id: PBO:0078557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 45","termid":"PBO:0078557"}


id: GO:0042103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the rate or extent of resting T cell proliferation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of T cell proliferation","termid":"GO:0042102"},{"relation_name":"is_a","term_name":"regulation of T cell homeostatic proliferation","termid":"GO:0046013"},{"relation_name":"positively_regulates","term_name":"T cell homeostatic proliferation","termid":"GO:0001777"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"positive regulation of T cell homeostatic proliferation","synonyms":[{"name":"activation of T cell homeostatic proliferation","type":"narrow"},{"name":"positive regulation of T lymphocyte homeostatic proliferation","type":"exact"},{"name":"positive regulation of T-cell homeostatic proliferation","type":"exact"},{"name":"positive regulation of T-lymphocyte homeostatic proliferation","type":"exact"},{"name":"positive regulation of resting T cell proliferation","type":"exact"},{"name":"stimulation of T cell homeostatic proliferation","type":"narrow"},{"name":"up regulation of T cell homeostatic proliferation","type":"exact"},{"name":"up-regulation of T cell homeostatic proliferation","type":"exact"},{"name":"upregulation of T cell homeostatic proliferation","type":"exact"}],"termid":"GO:0042103"}


id: PBO:0051219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 7-27 (pseudogene)","termid":"PBO:0051219"}


id: PBO:0060083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 30","termid":"PBO:0060083"}


id: MONDO:0032805
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":"hypopigmentation, organomegaly, and delayed myelination and development","secondary_identifiers":["MEDGEN:1684826","OMIM:618541","UMLS:C5203300"],"synonyms":[{"name":"HOD","type":"related"},{"name":"HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT","type":"related"}],"termid":"MONDO:0032805","xrefs":{"Monarch":{"xref_id":"0032805"}}}


id: PBO:0045362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double PHD fingers 2","termid":"PBO:0045362"}


id: PBO:0038980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribosylserine hydrolase","termid":"PBO:0038980"}


id: PBO:0040472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATR interacting protein","termid":"PBO:0040472"}


id: MONDO:0005472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital heart malformation (obsolete MONDO:0005472)","termid":"MONDO:0005472","xrefs":{"Monarch":{"xref_id":"0005472"}}}


id: PBO:0062609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily S member 1","termid":"PBO:0062609"}


id: PBO:0048697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GLIS3 antisense RNA 2","termid":"PBO:0048697"}


id: PBO:0071684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37 pseudogene 16","termid":"PBO:0071684"}


id: GO:0141174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont inhibits or disrupts anti-inflammatory cytokine signaling in the host organism, either by disruption of production, sequesteration, or destruction of at least one component of the signaling pathway.  Anti-inflammatory cytokines include: interleukin (IL)-1, IL-4, IL-6, IL-10, IL-11, and IL-13. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:29720526","PMID:19168731","PMID:32754056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host receptor-mediated signal transduction","termid":"GO:0075109"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host anti-inflammatory cytokine signaling","synonyms":[{"name":"negative regulation by symbiont of host anti-inflammatory cytokine production","type":"exact"},{"name":"suppression by symbiont of host anti-inflammatory cytokine production","type":"exact"},{"name":"suppression by symbiont of host anti-inflammatory cytokine secretion","type":"related"},{"name":"symbiont-mediated degradation of host anti-inflammatory cytokine","type":"narrow"},{"name":"symbiont-mediated sequestering of host anti-inflammatory cytokine","type":"related"},{"name":"symbiont-mediated suppression of host anti-inflammatory cytokine production","type":"related"}],"termid":"GO:0141174"}


id: MONDO:0003999
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pilocytic astrocytoma that occurs during adolescence.","definition_xrefs":["NCIT:C27081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood pilocytic astrocytoma","termid":"MONDO:0004000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"juvenile pilocytic astrocytoma","secondary_identifiers":["MEDGEN:128890","Orphanet:673580","DOID:6811","UMLS:C0280783"],"synonyms":[{"name":"juvenile pilocytic astrocytoma","type":"exact"}],"termid":"MONDO:0003999","xrefs":{"Monarch":{"xref_id":"0003999"}}}


id: GO:0002253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that initiates an immune response.","definition_xrefs":["GO_REF:0000022","GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system process","termid":"GO:0002376"},{"relation_name":"is_a","term_name":"positive regulation of immune response","termid":"GO:0050778"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"activation of immune response","termid":"GO:0002253"}


id: PR:P87306
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- srb4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87306"],"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":"mediator of RNA polymerase II transcription subunit 17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC31F10.04c","synonyms":[{"name":"Spom972h-srb4","type":"exact"},{"name":"mediator complex subunit 17 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"suppressor of RNA polymerase B 4 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87306"}


id: PBO:0005551
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.34","termid":"PBO:0005551"}


id: FYPO:0001546
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to zinc ion is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0006551"],"is_obsolete":false,"name":"decreased RNA level during cellular response to zinc ion","synonyms":[{"name":"decreased RNA accumulation during cellular response to zinc ion","type":"related"},{"name":"decreased RNA level during cellular response to zinc","type":"exact"},{"name":"decreased RNA level during cellular response to zinc ion during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to zinc ion during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to zinc ion","type":"narrow"},{"name":"decreased transcript level during cellular response to zinc ion","type":"exact"},{"name":"reduced RNA level during cellular response to zinc ion","type":"exact"}],"termid":"FYPO:0001546"}


id: PBO:0079086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (anticodon GTA) 3-1","termid":"PBO:0079086"}


id: PBO:0061758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2'-5'-oligoadenylate synthetase 1","termid":"PBO:0061758"}


id: PR:Q10366
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phosphatidylinositol 4-kinase beta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02103","PRO:DNx","PANTHER:PTHR10048:SF22"],"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":"phosphatidylinositol 4-kinase pik1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22E12.16c","secondary_identifiers":["UniProtKB:Q10366"],"synonyms":[{"name":"PI4-kinase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PtdIns-4-kinase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PI4KB","type":"exact"}],"termid":"PR:Q10366"}


id: MONDO:0015036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lissencephaly with cerebellar hypoplasia type C (LCHc) is a severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death.","definition_xrefs":["Orphanet:100013"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly with cerebellar hypoplasia","termid":"MONDO:0019450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"lissencephaly with cerebellar hypoplasia type C","secondary_identifiers":["MEDGEN:900624","UMLS:C4274992","GARD:19733","icd11.foundation:1837040262","SCTID:715820004"],"termid":"MONDO:0015036","xrefs":{"Monarch":{"xref_id":"0015036"}}}


id: PBO:0087040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L19B; rpl19a and rpl19b single null mutations result in slow growth, while the double null mutation is lethal; homologous to mammalian ribosomal protein L19, no bacterial homolog; RPL19B has a paralog, RPL19A, that arose from the whole genome duplication","termid":"PBO:0087040"}


id: PBO:0030917
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vegetative_cell_morphology","termid":"PBO:0030917"}


id: FYPO:0003050
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which homologous chromosome pairing during meiosis (synapsis) is normal (i.e. indistinguishable from wild type). Synapsis is the process in which the side by side pairing and physical juxtaposition of homologous chromosomes is established and maintained. Pairing may be assayed globally or at one or more specific loci.","definition_xrefs":["PomBase:mah","GO:0007129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal homologous chromosome pairing","synonyms":[{"name":"normal homologous chromosome pairing at meiosis","type":"exact"},{"name":"normal synapsis","type":"exact"}],"termid":"FYPO:0003050"}


id: GO:0042173
data:
  {"annotated_genes":["SJAG_04140","SJAG_04853","SJAG_02169","SJAG_00993"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[102294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[90691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[92156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of spore formation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sporulation","termid":"GO:0043937"},{"relation_name":"regulates","term_name":"sporulation resulting in formation of a cellular spore","termid":"GO:0030435"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00993":null,"SJAG_02169":null,"SJAG_04140":null,"SJAG_04853":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 sporulation resulting in formation of a cellular spore","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0042173","terms_by_termid":{"GO:0034307":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


id: PBO:0030526
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_localization_to_chromatin","termid":"PBO:0030526"}


id: PBO:0075982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal transducer and activator of transcription 6","termid":"PBO:0075982"}


id: GO:1903421
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synaptic vesicle recycling.","definition_xrefs":["GO_REF:0000058","PMID:22745285","GOC:PARL","GOC:TermGenie","GOC:pad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"synaptic vesicle recycling","termid":"GO:0036465"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of synaptic vesicle recycling","synonyms":[{"name":"regulation of kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"regulation of kiss-and-stay synaptic vesicle recycling","type":"narrow"}],"termid":"GO:1903421"}


id: PBO:0027683
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_number_of_Rad54_foci_during_cellular_response_to_doxorubicin","termid":"PBO:0027683"}


id: PBO:0081446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 304","termid":"PBO:0081446"}


id: PBO:0062504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily G member 5","termid":"PBO:0062504"}


id: MONDO:0003866
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteosarcoma arising from the liver.","definition_xrefs":["NCIT:C5833"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver sarcoma","termid":"MONDO:0002397"},{"relation_name":"is_a","term_name":"extraosseous osteosarcoma","termid":"MONDO:0002621"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515","MONDO:0004992"],"is_obsolete":false,"name":"liver extraskeletal osteosarcoma","secondary_identifiers":["MEDGEN:232597","DOID:6370","UMLS:C1333974"],"synonyms":[{"name":"hepatic extraskeletal osteosarcoma","type":"exact"},{"name":"hepatic osteogenic sarcoma","type":"exact"},{"name":"hepatic osteosarcoma","type":"exact"},{"name":"liver extraskeletal osteosarcoma","type":"exact"},{"name":"liver osteogenic sarcoma","type":"exact"},{"name":"liver osteosarcoma","type":"exact"},{"name":"liver osteosarcoma (disease)","type":"exact"},{"name":"osteogenic sarcoma of liver","type":"exact"},{"name":"osteogenic sarcoma of the liver","type":"exact"},{"name":"osteosarcoma of liver","type":"exact"},{"name":"osteosarcoma of the liver","type":"exact"}],"termid":"MONDO:0003866","xrefs":{"Monarch":{"xref_id":"0003866"}}}


id: PBO:0027314
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_carbendazim","termid":"PBO:0027314"}


id: MONDO:0700088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paroxysmal non-kinesigenic dyskinesia (PNKD) is a form of paroxysmal dyskinesia, characterized by attacks of dystonic or choreathetotic movements precipitated by stress, fatigue, coffee or alcohol intake or menstruation.","definition_xrefs":["Orphanet:98810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paroxysmal dyskinesia","termid":"MONDO:0015427"}],"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":"paroxysmal nonkinesigenic dyskinesia","secondary_identifiers":["UMLS:C1869117","MEDGEN:401504","GARD:8722"],"synonyms":[{"name":"DYT-MR-1","type":"related"},{"name":"Paroxysomal nonkinesigenic dyskinesia","type":"related"},{"name":"Paroxystic non-kinesigenic choreoathetosis","type":"exact"},{"name":"paroxysmal non-kinesigenic dyskinesia","type":"related"}],"termid":"MONDO:0700088","xrefs":{"Monarch":{"xref_id":"0700088"}}}


id: CHEBI:32035
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium hydroxide","termid":"CHEBI:32035"}


id: PBO:0058647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6776","termid":"PBO:0058647"}


id: PBO:0059964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 9","termid":"PBO:0059964"}


id: GO:0050267
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (cis-prenyl)n-diphosphate + isopentenyl diphosphate = (cis-prenyl)(n+1)-diphosphate + diphosphate.","definition_xrefs":["RHEA:18801"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyl diphosphate synthase activity","termid":"GO:0120531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016765","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"rubber cis-polyprenylcistransferase activity","secondary_identifiers":["MetaCyc:2.5.1.20-RXN","EC:2.5.1.20"],"synonyms":[{"name":"cis-prenyl transferase activity","type":"related"},{"name":"isopentenyl pyrophosphate cis-1,4-polyisoprenyl transferase activity","type":"related"},{"name":"poly-cis-polyprenyl-diphosphate:isopentenyl-diphosphate polyprenylcistransferase activity","type":"related"},{"name":"rubber allyltransferase activity","type":"related"},{"name":"rubber polymerase activity","type":"related"},{"name":"rubber prenyltransferase activity","type":"related"},{"name":"rubber transferase activity","type":"broad"}],"termid":"GO:0050267"}


id: PBO:0063990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 24","termid":"PBO:0063990"}


id: PBO:0070600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 67","termid":"PBO:0070600"}


id: FYPO:0004536
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a mitotic cell cycle arrest that normally occurs in response to mitotic cell cycle spindle assembly checkpoint signaling is abnormal (does not occur, or occurs abnormally). Abnormal arrest may result from a problem with detection of conditions that normally trigger a checkpoint, transduction of the checkpoint signal, or the response to the checkpoint signal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal response to mitotic cell cycle checkpoint signaling","termid":"FYPO:0002517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000298","FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal response to mitotic cell cycle spindle assembly checkpoint signaling","synonyms":[{"name":"abnormal mitotic cell cycle spindle assembly checkpoint arrest","type":"related"},{"name":"abnormal occurrence of mitotic cell cycle arrest resulting from spindle assembly checkpoint activation","type":"related"},{"name":"abnormal occurrence of mitotic cell cycle arrest resulting from spindle assembly defective checkpoint activation","type":"related"},{"name":"abnormal response to mitotic spindle assembly checkpoint signaling","type":"exact"}],"termid":"FYPO:0004536"}


id: PBO:0059432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane spanning 4-domains A3","termid":"PBO:0059432"}


id: GO:0016327
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The apical end of the lateral plasma membrane of epithelial cells.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"}],"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":"apicolateral plasma membrane","synonyms":[{"name":"apical lateral plasma membrane","type":"exact"}],"termid":"GO:0016327"}


id: GO:0050780
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a dopamine receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"dopamine receptor binding","termid":"GO:0050780"}


id: SO:0002206
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Identifies the biological source of the specified span of the sequence","definition_xrefs":["NCBI:tm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_attribute","termid":"SO:0000400"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence_source","synonyms":[{"name":"INSDC_feature:source","type":"exact"},{"name":"sequence source","type":"exact"}],"termid":"SO:0002206"}


id: GO:2000348
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of signaling via the CD40 signaling pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"CD40 signaling pathway","termid":"GO:0023035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of CD40 signaling pathway","synonyms":[{"name":"regulation of CD40 signalling pathway","type":"exact"}],"termid":"GO:2000348"}


id: PBO:0108543
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneExRNA","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternative transcripts, alternative mRNA processing","termid":"PBO:0108543"}


id: PBO:0028642
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-branched,_elongated_cell_with_branch_forming_adjacent_to_septum","termid":"PBO:0028642"}


id: PBO:0030280
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_microtubule_cytoskeleton_morphology_during_vegetative_growth","termid":"PBO:0030280"}


id: PBO:0004055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing protein 1, Bdc1","termid":"PBO:0004055"}


id: MONDO:0024645
data:
  {"annotated_genes":["SJAG_01895","SJAG_00260","SJAG_01671"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[85596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[85805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the retroperitoneum.","definition_xrefs":["NCIT:C3357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01671":null,"SJAG_01895":null},"genotype_count":0,"is_obsolete":false,"name":"retroperitoneal neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:48439","UMLS:C0035358"],"synonyms":[{"name":"neoplasm of retroperitoneal space","type":"exact"},{"name":"retroperitoneal neoplasm","type":"exact"},{"name":"retroperitoneal space neoplasm","type":"exact"},{"name":"retroperitoneal space tumor","type":"exact"},{"name":"retroperitoneal space tumour","type":"exact"},{"name":"tumor of retroperitoneal space","type":"exact"},{"name":"tumour of retroperitoneal space","type":"exact"}],"termid":"MONDO:0024645","terms_by_termid":{"MONDO:0007273":null,"MONDO:0011121":null,"MONDO:0013602":null},"xrefs":{"Monarch":{"xref_id":"0024645"}}}


id: PBO:0046466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoplasmic reticulum aminopeptidase 2","termid":"PBO:0046466"}


id: GO:0010466
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the rate of peptidase activity, the hydrolysis of peptide bonds within proteins.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of proteolysis","termid":"GO:0045861"},{"relation_name":"is_a","term_name":"negative regulation of hydrolase activity","termid":"GO:0051346"},{"relation_name":"is_a","term_name":"regulation of peptidase activity","termid":"GO:0052547"}],"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 peptidase activity","termid":"GO:0010466"}


id: MONDO:0021113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The significant impairment of gas exchange within the lungs resulting in hypoxia, hypercarbia, or both, to the extent that organ tissue perfusion is severely compromised. Causes include chronic obstructive pulmonary disease, asthma, emphysema, acute respiratory distress syndrome, pneumonia, pulmonary edema, pneumothorax, and congestive heart failure. Treatment requires intubation and mechanical ventilation until the time the lungs recover sufficient function.","definition_xrefs":["NCIT:C26872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung disorder","termid":"MONDO:0005275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"respiratory failure","secondary_identifiers":["MEDGEN:257837","EFO:0009686","MESH:D012131","UMLS:C1145670","icd11.foundation:370028006","ICD9:518.83","SCTID:39871006","ICD9:518.81","DOID:11162"],"synonyms":[{"name":"acute and chronic respiratory failure","type":"related"},{"name":"acute respiratory failure","type":"narrow"},{"name":"acute-on-chronic respiratory failure","type":"related"},{"name":"chronic respiratory failure","type":"narrow"},{"name":"failure, respiratory","type":"exact"},{"name":"respiratory failure","type":"exact"},{"name":"respiratory insufficiency/failure","type":"exact"}],"termid":"MONDO:0021113","xrefs":{"Monarch":{"xref_id":"0021113"}}}


id: PBO:0075830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal sequence receptor subunit 4 pseudogene 1","termid":"PBO:0075830"}


id: GO:0015911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a long-chain fatty acid from outside of a cell, across the plasma membrane and into the cytosol. A long-chain fatty acid has an aliphatic tail containing 13 to 22 carbons.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid import into cell","termid":"GO:0044539"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"fatty acid transmembrane transport","termid":"GO:1902001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"long-chain fatty acid import across plasma membrane","synonyms":[{"name":"plasma membrane long-chain fatty acid transport","type":"exact"}],"termid":"GO:0015911"}


id: PBO:0050468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOXA transcript antisense RNA, myeloid-specific 1","termid":"PBO:0050468"}


id: PR:Q9P6J8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An adenosine deaminase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02335"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized deaminase C1683.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1683.02","secondary_identifiers":["UniProtKB:Q9P6J8"],"synonyms":[{"name":"Spom972h-ADA","type":"exact"}],"termid":"PR:Q9P6J8"}


id: PBO:0038982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenoceptor alpha 1B","termid":"PBO:0038982"}


id: PBO:0076681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A3","termid":"PBO:0076681"}


id: PBO:0004891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA export factor, nucleoporin Rae1","termid":"PBO:0004891"}


id: PBO:0069633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 910, pseudogene","termid":"PBO:0069633"}


id: PBO:0048903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A7","termid":"PBO:0048903"}


id: GO:0080109
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: indole-3-acetonitrile + H2O = indole-3-acetamide.","definition_xrefs":["MetaCyc:RXN-7567","PMID:12430025","PMID:11607511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrile hydratase activity","termid":"GO:0018822"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"indole-3-acetonitrile nitrile hydratase activity","secondary_identifiers":["KEGG_REACTION:R04020"],"termid":"GO:0080109"}


