# terms

id: PBO:0052017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"jumonji domain containing 7","termid":"PBO:0052017"}


id: MONDO:0013229
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hot water reflex epilepsy is a rare neurologic disease characterized by the onset of generalized or focal seizures following immersion of the head in hot water, or with hot water being poured over the head. Primary generalized tonic-clonic seizures have been reported in rare cases.","definition_xrefs":["Orphanet:166412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited reflex epilepsy","termid":"MONDO:0023224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"hot water reflex epilepsy","secondary_identifiers":["UMLS:C4706506","GARD:17028","OMIMPS:613339","ICD9:345.10","MEDGEN:1631373","DOID:0081104","SCTID:230454005"],"synonyms":[{"name":"bathing epilepsy","type":"related"},{"name":"epilepsy, hot water","type":"exact"},{"name":"hot water epilepsy","type":"exact"},{"name":"water immersion epilepsy","type":"related"}],"termid":"MONDO:0013229","xrefs":{"Monarch":{"xref_id":"0013229"}}}


id: PBO:0053320
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 102","termid":"PBO:0053320"}


id: PBO:0084303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Iron-regulated transcriptional activator; activates genes involved in intracellular iron use and required for iron homeostasis and resistance to oxidative stress; AFT2 has a paralog, AFT1, that arose from the whole genome duplication","termid":"PBO:0084303"}


id: MONDO:0030717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive complex immunologic disorder with variable features. Affected individuals present in the first decade of life with inflammatory interstitial lung disease or colitis due to abnormal tissue infiltration by activated T cells. Patients develop autoimmune cytopenias and may have lymphadenopathy; 1 reported patient had features of hemophagocytic lymphohistiocytosis (HLH). Some patients may have recurrent infections associated with mild lymphopenia, hypogammaglobulinemia, and NK cell dysfunction. Immunologic workup indicates signs of significant immune dysregulation with elevation of inflammatory serum markers, variable immune cell defects involving neutrophils, NK cells, and myeloid cells, and disrupted levels of T regulatory cells (Tregs). Two unrelated patients have been reported.","definition_xrefs":["OMIM:619802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"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":"immunodeficiency 97 with autoinflammation","secondary_identifiers":["UMLS:C5676946","MEDGEN:1802936"],"synonyms":[{"name":"IMD97","type":"exact"},{"name":"immunodeficiency 97 with autoinflammation","type":"exact"}],"termid":"MONDO:0030717","xrefs":{"Monarch":{"xref_id":"0030717"}}}


id: GO:0032340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the regulated release of inhibin from a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inhibin secretion","termid":"GO:0032338"},{"relation_name":"is_a","term_name":"positive regulation of hormone secretion","termid":"GO:0046887"},{"relation_name":"positively_regulates","term_name":"inhibin secretion","termid":"GO:0032334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of inhibin secretion","synonyms":[{"name":"activation of inhibin secretion","type":"narrow"},{"name":"stimulation of inhibin secretion","type":"narrow"},{"name":"up regulation of inhibin secretion","type":"exact"},{"name":"up-regulation of inhibin secretion","type":"exact"},{"name":"upregulation of inhibin secretion","type":"exact"}],"termid":"GO:0032340"}


id: GO:0035520
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of the ubiquitin group from a monoubiquitinated protein.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein deubiquitination","termid":"GO:0016579"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"monoubiquitinated protein deubiquitination","synonyms":[{"name":"monoubiquitinated protein deubiquitinylation","type":"exact"},{"name":"monoubiquitinated protein deubiquitylation","type":"exact"}],"termid":"GO:0035520"}


id: GO:0061412
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of deprivation of amino acids.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to amino acid starvation (obsolete GO:0061412)","termid":"GO:0061412"}


id: MONDO:0043786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of a serous membrane.","definition_xrefs":["NCIT:C70428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serositis","secondary_identifiers":["MEDGEN:20711","SCTID:370469003","MESH:D012700","UMLS:C0036749"],"synonyms":[{"name":"Serositides","type":"related"},{"name":"inflammation of serous membrane","type":"exact"},{"name":"serositis","type":"exact"},{"name":"serous membrane inflammation","type":"exact"}],"termid":"MONDO:0043786","xrefs":{"Monarch":{"xref_id":"0043786"}}}


id: PBO:0077516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM231 pseudogene 1","termid":"PBO:0077516"}


id: MONDO:0013660
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":"arthrogryposis, Perthes disease, and upward gaze palsy","secondary_identifiers":["UMLS:C3280309","OMIM:614262","MEDGEN:481939"],"synonyms":[{"name":"APUG","type":"related"},{"name":"arthrogryposis, Perthes disease, and upward gaze palsy","type":"exact"}],"termid":"MONDO:0013660","xrefs":{"Monarch":{"xref_id":"0013660"}}}


id: PR:Q9Y7I4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01102","PANTHER:PTHR12646:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC7D4.06c","secondary_identifiers":["UniProtKB:Q9Y7I4"],"synonyms":[{"name":"Dol-P-Man-dependent alpha(1-3)-mannosyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ALG3","type":"exact"},{"name":"asparagine-linked glycosylation protein 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"dolichyl-phosphate-mannose--glycolipid alpha-mannosyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9Y7I4"}


id: PBO:0001282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein","termid":"PBO:0001282"}


id: PBO:0069106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 354, pseudogene","termid":"PBO:0069106"}


id: PBO:0073680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sirtuin 2","termid":"PBO:0073680"}


id: FYPO:0005165
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 spatio-temporal pattern of localization of replication forks into nuclear foci is abnormal. Normally, replication forks appear organized into foci outside the nucleolus in early S phase. As S phase progresses, the number of foci first increases, then decreases, and the remaining foci concentrate within the nucleolus or at the nucleolar periphery. The last replication foci remaining at the end of S phase are one or two large spots at the nucleolar border.","definition_xrefs":["PomBase:mah","PMID:17304223"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abnormal spatio-temporal regulation of replication fork localization","synonyms":[{"name":"abnormal replication foci dynamics","type":"related"},{"name":"abnormal replication focus organization","type":"related"},{"name":"abnormal spatio-temporal regulation of replication fork localisation","type":"exact"},{"name":"abnormal spatio-temporal regulation of replication fork localization during mitotic cell cycle","type":"related"},{"name":"abnormal spatio-temporal regulation of replication fork localization during vegetative growth","type":"exact"},{"name":"abnormal spatio-temporal replication fork organization","type":"related"}],"termid":"FYPO:0005165"}


id: PBO:0070586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 52","termid":"PBO:0070586"}


id: PBO:0082284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Apyrase with wide substrate specificity; helps prevent inhibition of glycosylation by hydrolyzing nucleoside tri- and diphosphates that inhibit glycotransferases; partially redundant with Gda1p; mediates adenovirus E4orf4-induced toxicity","termid":"PBO:0082284"}


id: PBO:0111617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLRC complex subunit, cullin 4","termid":"PBO:0111617"}


id: PBO:0001439
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expression induced by hydrogen peroxide","termid":"PBO:0001439"}


id: PBO:0051877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isochorismatase domain containing 2","termid":"PBO:0051877"}


id: PBO:0012520
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_output_o_product_of","termid":"PBO:0012520"}


id: PBO:0028982
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_rate_of_mitotic_spindle_elongation","termid":"PBO:0028982"}


id: PBO:0059987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 7","termid":"PBO:0059987"}


id: MONDO:0006873
data:
  {"annotated_genes":["SJAG_04459","SJAG_01881","SJAG_05230","SJAG_04042","SJAG_04425","SJAG_03069","SJAG_01199"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015005"},{"annotations":[85505],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009666"},{"annotations":[84474,84473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009354"},{"annotations":[85085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009609"},{"annotations":[85905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"},{"annotations":[84724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012407"}]},"cv_name":"mondo","definition":"A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed)","definition_xrefs":["MESH:D003677"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nutritional disorder","termid":"MONDO:0005137"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01199":null,"SJAG_01881":null,"SJAG_03069":null,"SJAG_04042":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_05230":null},"genotype_count":0,"is_obsolete":false,"name":"nutritional deficiency disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:269.9","UMLS:C4761312","DOID:5113","ICD10CM:E40-E46","ICD9:269.8","EFO:1001067","NCIT:C3669","MedDRA:10046058","SCTID:70241007","SCTID:363246002","MEDGEN:1677627"],"synonyms":[{"name":"malnourished","type":"exact"},{"name":"malnutrition","type":"exact"}],"termid":"MONDO:0006873","terms_by_termid":{"MONDO:0009354":null,"MONDO:0009609":null,"MONDO:0009666":null,"MONDO:0010184":null,"MONDO:0012407":null,"MONDO:0015005":null},"xrefs":{"Monarch":{"xref_id":"0006873"}}}


id: PBO:0063299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma constant","termid":"PBO:0063299"}


id: MONDO:0013460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SP7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"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":"osteogenesis imperfecta type 12","secondary_identifiers":["MEDGEN:462783","GARD:15722","OMIM:613849","UMLS:C3151433","DOID:0110348"],"synonyms":[{"name":"OI, type 12","type":"related"},{"name":"OI12","type":"exact"},{"name":"SP7 osteogenesis imperfecta","type":"exact"},{"name":"osteogenesis imperfecta caused by mutation in SP7","type":"exact"},{"name":"osteogenesis imperfecta type XII","type":"exact"},{"name":"osteogenesis imperfecta, type 12","type":"related"},{"name":"osteogenesis imperfecta, type XII","type":"related"}],"termid":"MONDO:0013460","xrefs":{"Monarch":{"xref_id":"0013460"}}}


id: MONDO:0010628
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":"immunoglobulin M, level of","secondary_identifiers":["UMLS:C1839966","OMIM:308250","MEDGEN:327005"],"synonyms":[{"name":"immunoglobulin M, level of","type":"exact"}],"termid":"MONDO:0010628","xrefs":{"Monarch":{"xref_id":"0010628"}}}


id: GO:0035653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of a macromolecular complex between proteins of the AP-1 adaptor complex and proteins and/or lipoproteins that are going to be transported by a clathrin-coated vesicle. The AP-1 adaptor protein complex is a component of the cytoplasmic coat found on clathrin-coated vesicles, and binds to sorting signals of cargo to facilitate their trafficking.","definition_xrefs":["PMID:16162817","PMID:12802059","GOC:lb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-coated vesicle cargo loading","termid":"GO:0035652"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"clathrin-coated vesicle cargo loading, AP-1-mediated","synonyms":[{"name":"cargo loading into clathrin-coated vesicle, AP-1-mediated","type":"exact"}],"termid":"GO:0035653"}


id: GO:0009050
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycopeptides, a compound in which carbohydrate is covalently attached to an oligopeptide composed of residues of L and/or D-amino acids. The term usually denotes a product of proteolytic degradation of a glycoprotein but includes glycated peptide.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"},{"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":"glycopeptide catabolic process","synonyms":[{"name":"glycopeptide breakdown","type":"exact"},{"name":"glycopeptide catabolism","type":"exact"},{"name":"glycopeptide degradation","type":"exact"}],"termid":"GO:0009050"}


id: MONDO:0030935
data:
  {"annotated_genes":["SJAG_07005"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84812],"is_not":false,"summary":null,"term":"MONDO:0030935"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex II deficiency, nuclear type","termid":"MONDO:0031230"}],"gene_count":1,"genes_by_uniquename":{"SJAG_07005":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex 2 deficiency, nuclear type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1742371","OMIM:619166","UMLS:C5436933","GARD:16429"],"synonyms":[{"name":"MC2DN2","type":"exact"},{"name":"mitochondrial complex 2 deficiency, nuclear type 2","type":"exact"},{"name":"mitochondrial complex II deficiency, nuclear type 2","type":"exact"}],"termid":"MONDO:0030935","terms_by_termid":{"MONDO:0030935":null},"xrefs":{"Monarch":{"xref_id":"0030935"}}}


id: FYPO:0002846
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which all cells in a population are inviable, and the population includes a mixture of ungerminated spores, germinated spores and small vegetative cells. The spheroid cells arise from division of some of the germinated spores, and may form a microcolony of up to 64 cells.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population including spores, germinated spores and small cells (obsolete FYPO:0002846)","termid":"FYPO:0002846"}


id: PBO:0048846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglucosamine-1-phosphate transferase subunits alpha and beta","termid":"PBO:0048846"}


id: PBO:0029341
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_nickel","termid":"PBO:0029341"}


id: GO:0018452
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-exo-hydroxycamphor + NAD+ = NADH + H+ + 2,5-diketocamphane.","definition_xrefs":["UM-BBD_reactionID:r0427"],"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:0003674","GO:0003824"],"is_obsolete":false,"name":"5-exo-hydroxycamphor dehydrogenase activity","secondary_identifiers":["EC:1.1.1.327","MetaCyc:R542-RXN","RHEA:32879"],"termid":"GO:0018452"}


id: PBO:0005361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formin For3","termid":"PBO:0005361"}


id: GO:0140837
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + RNA polymerase II large subunit CTD heptapeptide repeat (consensus YSPTSPS) = ADP + H+ + RNA polymerase II large subunit phosphoserine (position 7).","definition_xrefs":["PMID:28248323"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II CTD heptapeptide repeat kinase activity","termid":"GO:0008353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016301","GO:0004672","GO:0016740","GO:0003824","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"RNA polymerase II CTD heptapeptide repeat S7 kinase activity","synonyms":[{"name":"RNA polymerase II C-terminal domain S7 kinase activity","type":"exact"}],"termid":"GO:0140837"}


id: PBO:0048046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"follistatin like 4","termid":"PBO:0048046"}


id: GO:1903106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of insulin receptor signaling pathway involved in determination of adult lifespan.","definition_xrefs":["GOC:kmv","GO_REF:0000058","GOC:TermGenie","PMID:19853560"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of insulin receptor signaling pathway involved in determination of adult lifespan (obsolete GO:1903106)","synonyms":[{"name":"activation of daf-2 receptor signaling pathway of determination of adult lifespan","type":"narrow"},{"name":"activation of insulin receptor signaling pathway involved in determination of adult lifespan","type":"narrow"},{"name":"activation of insulin receptor signaling pathway of determination of adult lifespan","type":"narrow"},{"name":"activation of insulin receptor signalling pathway of determination of adult lifespan","type":"narrow"},{"name":"positive regulation of daf-2 receptor signaling pathway of determination of adult lifespan","type":"narrow"},{"name":"positive regulation of insulin receptor signaling pathway of determination of adult lifespan","type":"exact"},{"name":"positive regulation of insulin receptor signalling pathway of determination of adult lifespan","type":"exact"},{"name":"up regulation of daf-2 receptor signaling pathway of determination of adult lifespan","type":"narrow"},{"name":"up regulation of insulin receptor signaling pathway involved in determination of adult lifespan","type":"exact"},{"name":"up regulation of insulin receptor signaling pathway of determination of adult lifespan","type":"exact"},{"name":"up regulation of insulin receptor signalling pathway of determination of adult lifespan","type":"exact"},{"name":"up-regulation of daf-2 receptor signaling pathway of determination of adult lifespan","type":"narrow"},{"name":"up-regulation of insulin receptor signaling pathway involved in determination of adult lifespan","type":"exact"},{"name":"up-regulation of insulin receptor signaling pathway of determination of adult lifespan","type":"exact"},{"name":"up-regulation of insulin receptor signalling pathway of determination of adult lifespan","type":"exact"},{"name":"upregulation of daf-2 receptor signaling pathway of determination of adult lifespan","type":"narrow"},{"name":"upregulation of insulin receptor signaling pathway involved in determination of adult lifespan","type":"exact"},{"name":"upregulation of insulin receptor signaling pathway of determination of adult lifespan","type":"exact"},{"name":"upregulation of insulin receptor signalling pathway of determination of adult lifespan","type":"exact"}],"termid":"GO:1903106"}


id: MONDO:0018066
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy X is a sex chromosome anomaly with a variable phenotype caused by the presence of an extra X chromosome in females (47,XXX instead of 46,XX).","definition_xrefs":["Orphanet:3375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"},{"relation_name":"is_a","term_name":"chromosome X disorder","termid":"MONDO:0700027"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"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":"trisomy X","secondary_identifiers":["GARD:5672","NCIT:C129718","icd11.foundation:423644907","NORD:1798","MEDGEN:113140","SCTID:35111009","UMLS:C0221033","MESH:C535318"],"synonyms":[{"name":"47 XXX syndrome","type":"related"},{"name":"47,XXX","type":"exact"},{"name":"47,XXX syndrome","type":"exact"},{"name":"Triplo X syndrome","type":"related"},{"name":"Triplo-X syndrome","type":"exact"},{"name":"XXX syndrome","type":"exact"},{"name":"triple X syndrome","type":"exact"},{"name":"triple-X chromosome syndrome","type":"related"},{"name":"triple-X female","type":"related"},{"name":"trisomy X","type":"exact"},{"name":"trisomy type X","type":"exact"}],"termid":"MONDO:0018066","xrefs":{"Monarch":{"xref_id":"0018066"}}}


id: MONDO:0009742
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Elejalde syndrome (ES) is characterized by silvery to leaden hair, bronze skin color in sun-exposed areas and severe neurological impairment.","definition_xrefs":["Orphanet:33445"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"excluded_subClassOf","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"},{"relation_name":"excluded_subClassOf","term_name":"overgrowth syndrome","termid":"MONDO:0019716"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroectodermal melanolysosomal disease","secondary_identifiers":["SCTID:724091002","MEDGEN:348553","UMLS:C1860157","OMIM:256710","GARD:16630","icd11.foundation:771734461","MESH:C536203"],"synonyms":[{"name":"ELEJALDE disease","type":"related"},{"name":"Elejalde disease","type":"exact"},{"name":"neuroectodermal melanolysosomal disease","type":"exact"}],"termid":"MONDO:0009742","xrefs":{"Monarch":{"xref_id":"0009742"}}}


id: GO:0008503
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with benzodiazepines, a class of drugs with hypnotic, anxiolytic, anticonvulsive, amnestic and myorelaxant properties, to initiate a change in cell activity.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter receptor activity","termid":"GO:0030594"}],"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":"benzodiazepine receptor activity","termid":"GO:0008503"}


id: PBO:0059178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannose receptor C-type 1","termid":"PBO:0059178"}


id: GO:0090650
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 the deprivation of oxygen and glucose.","definition_xrefs":["GOC:sl","PMID:21525936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to nutrient levels","termid":"GO:0031669"},{"relation_name":"is_a","term_name":"cellular response to decreased oxygen levels","termid":"GO:0036294"},{"relation_name":"is_a","term_name":"response to oxygen-glucose deprivation","termid":"GO:0090649"}],"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 oxygen-glucose deprivation","synonyms":[{"name":"cellular response to OGD","type":"exact"}],"termid":"GO:0090650"}


id: MONDO:0012833
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Crouzon syndrome with acanthosis nigricans (CAN) is a very rare, clinically heterogeneous form of faciocraniostenosis with Crouzon-like features and premature synostosis of cranial sutures (Crouzon disease), associated with acanthosis nigricans (AN).","definition_xrefs":["Orphanet:93262"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"inherited focal segmental glomerulosclerosis","termid":"MONDO:0005363"},{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"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"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0000426"],"is_obsolete":false,"name":"Crouzon syndrome-acanthosis nigricans syndrome","secondary_identifiers":["OMIM:612247","MESH:C567382","NCIT:C38145","DOID:0111161","GARD:16810","UMLS:C2677099","SCTID:702361006","MEDGEN:394201"],"synonyms":[{"name":"CAN","type":"exact"},{"name":"Chronic kidney allograft nephropathy","type":"exact"},{"name":"Crouzon syndrome with acanthosis nigricans","type":"related"},{"name":"Crouzon-dermoskeletal syndrome","type":"exact"},{"name":"Crouzonodermoskeletal syndrome","type":"exact"},{"name":"can","type":"related"},{"name":"chronic allograft nephropathy","type":"exact"}],"termid":"MONDO:0012833","xrefs":{"Monarch":{"xref_id":"0012833"}}}


id: PBO:0080500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WW domain containing adaptor with coiled-coil","termid":"PBO:0080500"}


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


id: GO:0071626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of biting and mashing food with the teeth prior to swallowing.","definition_xrefs":["GOC:gvg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system process","termid":"GO:0022600"}],"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":"mastication","synonyms":[{"name":"chewing","type":"exact"}],"termid":"GO:0071626"}


id: FYPO:0002697
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of methylenetetrahydrofolate reductase (NADPH) activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased oxidoreductase activity","termid":"FYPO:0000690"},{"relation_name":"is_a","term_name":"abnormal methylenetetrahydrofolate reductase (NADPH) activity","termid":"FYPO:0002695"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0000661","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"decreased methylenetetrahydrofolate reductase (NADPH) activity","synonyms":[{"name":"reduced methylenetetrahydrofolate reductase (NADPH) activity","type":"exact"}],"termid":"FYPO:0002697"}


id: GO:0140505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of microlipophagy, the microautophagy-mediated direct internalization of lipid droplets into a lysosome-like vacuole during nutrient depletion.","definition_xrefs":["PMID:28394250","PMID:29601311"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of autophagy","termid":"GO:0010506"},{"relation_name":"regulates","term_name":"microlipophagy","termid":"GO:0140504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0008150","GO:0006914"],"is_obsolete":false,"name":"regulation of microlipophagy","termid":"GO:0140505"}


id: PBO:0002047
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N syndrome","termid":"PBO:0002047"}


id: PBO:0086418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative GTPase; member of the Obg family; peripheral protein of the mitochondrial inner membrane that associates with the large ribosomal subunit; required for mitochondrial translation, possibly via a role in ribosome assembly","termid":"PBO:0086418"}


id: GO:0023040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which information is sent from one location to another, within a living organism or between living organisms, via ionic flux.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signaling via ionic flux (obsolete GO:0023040)","synonyms":[{"name":"signaling via ionic flux","type":"exact"},{"name":"signalling via ionic flux","type":"exact"}],"termid":"GO:0023040"}


id: SO:0000195
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An exon whereby at least one base is part of a codon (here, 'codon' is inclusive of the stop_codon).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exon","termid":"SO:0000147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coding_exon","synonyms":[{"name":"coding exon","type":"exact"}],"termid":"SO:0000195"}


id: GO:0039505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont inhibits or disrupts the normal processing and presentation of a peptide antigen on its cell surface in association with an MHC class II protein complex.","definition_xrefs":["GOC:add","VZ:820","PMID:27832589","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host antigen processing and presentation","termid":"GO:0039588"}],"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 antigen processing and presentation of peptide antigen via MHC class II","synonyms":[{"name":"inhibition of host MHC class II molecule presentation by virus","type":"narrow"},{"name":"suppression by virus of host antigen processing and presentation of peptide antigen via MHC class II","type":"narrow"}],"termid":"GO:0039505"}


id: PBO:0080459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-set and transmembrane domain containing 2 like","termid":"PBO:0080459"}


id: PBO:0028470
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_methotrexate","termid":"PBO:0028470"}


id: GO:0006039
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of cell wall chitin, a linear polysaccharide consisting of beta-(1->4)-linked N-acetyl-D-glucosamine residues, found in the walls of cells.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cell wall chitin catabolic process (obsolete GO:0006039)","synonyms":[{"name":"cell wall chitin breakdown","type":"exact"},{"name":"cell wall chitin catabolism","type":"exact"},{"name":"cell wall chitin degradation","type":"exact"}],"termid":"GO:0006039"}


id: GO:0046451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving diaminopimelate, the anion of the dicarboxylic acid 2,6-diaminoheptanedioic acid. It is an intermediate in lysine biosynthesis and as a component (as meso-diaminopimelate) of the peptidoglycan of Gram-negative bacterial cell walls.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolic process","termid":"GO:0006520"},{"relation_name":"is_a","term_name":"dicarboxylic acid metabolic process","termid":"GO:0043648"},{"relation_name":"is_a","term_name":"fatty acid derivative metabolic process","termid":"GO:1901568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520","GO:0006629"],"is_obsolete":false,"name":"diaminopimelate metabolic process","synonyms":[{"name":"diaminopimelate metabolism","type":"exact"}],"termid":"GO:0046451"}


id: GO:0070464
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphav-beta3 integrin complex bound to the alpha3 chain of type VI collagen; the integrin binds most strongly to unfolded collagen.","definition_xrefs":["PMID:8387021"],"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:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"alphav-beta3 integrin-collagen alpha3(VI) complex","termid":"GO:0070464"}


id: FYPO:0003756
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 has more than one mitotic spindle, and mitotic sister chromatid separation does not occur.","definition_xrefs":["PMID:8978688","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished mitotic sister chromatid separation","termid":"FYPO:0001946"},{"relation_name":"is_a","term_name":"multiple mitotic spindles","termid":"FYPO:0003754"},{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype","termid":"FYPO:0003755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000631","FYPO:0002399","FYPO:0000337","FYPO:0000002","FYPO:0000120","FYPO:0001985","FYPO:0000054","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"multiple mitotic spindles with abolished sister chromatid separation","synonyms":[{"name":"multiple mitotic spindles with abolished chromosome separation","type":"exact"},{"name":"multiple mitotic spindles with abolished sister chromatid segregation","type":"related"},{"name":"multiple mitotic spindles with abolished sister chromatid separation during mitotic cell cycle","type":"related"},{"name":"multiple mitotic spindles with abolished sister chromatid separation during vegetative growth","type":"exact"}],"termid":"FYPO:0003756"}


id: MONDO:1011802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital merosin-deficient muscular dystrophy, non-human animal","secondary_identifiers":["OMIA:001619"],"termid":"MONDO:1011802","xrefs":{"Monarch":{"xref_id":"1011802"}}}


id: MONDO:0030020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation deficiency 44","secondary_identifiers":["MEDGEN:1718899","OMIM:618855","UMLS:C5394293","DOID:0070424"],"synonyms":[{"name":"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 44","type":"exact"},{"name":"COXPD44","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 44","type":"exact"}],"termid":"MONDO:0030020","xrefs":{"Monarch":{"xref_id":"0030020"}}}


id: GO:0015364
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: dicarboxylate(out) + phosphate(in) = dicarboxylate(in) +  phosphate(out).","definition_xrefs":["TC:2.A.29.2.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transmembrane transporter activity","termid":"GO:0005310"},{"relation_name":"is_a","term_name":"phosphate transmembrane transporter activity","termid":"GO:0005315"},{"relation_name":"is_a","term_name":"solute:inorganic anion antiporter activity","termid":"GO:0005452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"dicarboxylate:phosphate antiporter activity","synonyms":[{"name":"dicarboxylate:inorganic phosphate antiporter activity","type":"exact"}],"termid":"GO:0015364"}


id: MONDO:0007911
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":"lipoprotein, variant of beta","secondary_identifiers":["MEDGEN:322642","OMIM:152400","UMLS:C1835357"],"synonyms":[{"name":"Beta-lipoprotein, Double","type":"related"},{"name":"lipoprotein, variant of beta","type":"exact"}],"termid":"MONDO:0007911","xrefs":{"Monarch":{"xref_id":"0007911"}}}


id: MONDO:0003206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma that is not present at birth but develops later in life.","definition_xrefs":["NCIT:C27018"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acquired hemangioma","secondary_identifiers":["UMLS:C0856897","DOID:492","MEDGEN:208988"],"synonyms":[{"name":"acquired hemangioma","type":"exact"}],"termid":"MONDO:0003206","xrefs":{"Monarch":{"xref_id":"0003206"}}}


id: PBO:0062344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily K member 3","termid":"PBO:0062344"}


id: MONDO:0022545
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":"Barnicoat Baraitser syndrome","synonyms":[{"name":"Barnicoat-Baraitser syndrome","type":"related"},{"name":"polysyndactyly overgrowth syndrome","type":"related"}],"termid":"MONDO:0022545","xrefs":{"Monarch":{"xref_id":"0022545"}}}


id: MONDO:0006820
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Death of cells in the kidney cortex, a common final result of various renal injuries including hypoxia; ischemia; and drug toxicity.","definition_xrefs":["MESH:D007673"],"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":"kidney cortex necrosis","secondary_identifiers":["MedDRA:10023414","UMLS:C0022656","MEDGEN:9634","ICD9:583.6","SCTID:444691002","DOID:2973"],"synonyms":[{"name":"renal cortical necrosis","type":"exact"}],"termid":"MONDO:0006820","xrefs":{"Monarch":{"xref_id":"0006820"}}}


id: GO:0051158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-arabitol, the pentitol derived from arabinose or lyxose by reduction of the aldehyde group.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arabitol catabolic process","termid":"GO:0051157"},{"relation_name":"is_a","term_name":"L-arabitol metabolic process","termid":"GO:0051162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"L-arabitol catabolic process","synonyms":[{"name":"L-arabitol breakdown","type":"exact"},{"name":"L-arabitol catabolism","type":"exact"},{"name":"L-arabitol degradation","type":"exact"}],"termid":"GO:0051158"}


id: FYPO:0001600
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 isoleucine import into the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal amino acid import","termid":"FYPO:0001596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal isoleucine import","synonyms":[{"name":"normal L-isoleucine import","type":"exact"},{"name":"normal L-isoleucine import across plasma membrane","type":"exact"},{"name":"normal isoleucine import during mitotic cell cycle","type":"related"},{"name":"normal isoleucine import during vegetative growth","type":"exact"},{"name":"normal isoleucine import into cell","type":"exact"},{"name":"normal isoleucine uptake","type":"exact"}],"termid":"FYPO:0001600"}


id: MONDO:0800155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder of amino acid metabolism that has its basis in the disruption of the metabolism of glycine and/or serine.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of serine family metabolism","termid":"MONDO:0019239"},{"relation_name":"is_a","term_name":"glycine metabolism disease","termid":"MONDO:0045020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"inborn disorder of glycine and serine metabolism","termid":"MONDO:0800155","xrefs":{"Monarch":{"xref_id":"0800155"}}}


id: PBO:0032731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfite reductase beta subunit Sir1","termid":"PBO:0032731"}


id: PATO:0000947
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spheroid quality inhering in a bearer by virtue of the bearer's being oval with two axes of symmetry, as produced by a conical section.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"superelliptic","termid":"PATO:0002318"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elliptic","synonyms":[{"name":"ellipse-shaped","type":"exact"},{"name":"ellipsoid","type":"exact"},{"name":"elliptical","type":"exact"},{"name":"oval","type":"related"},{"name":"ovoid","type":"related"}],"termid":"PATO:0000947"}


id: MONDO:0016872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 7 disorder","termid":"MONDO:0700014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 7","secondary_identifiers":["GARD:20795","MEDGEN:1825962","UMLS:C5679655","Orphanet:261796"],"synonyms":[{"name":"partial deletion of chromosome type 7","type":"exact"},{"name":"partial monosomy of chromosome 7","type":"exact"}],"termid":"MONDO:0016872","xrefs":{"Monarch":{"xref_id":"0016872"}}}


id: GO:0016202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of striated muscle development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle organ development","termid":"GO:0048634"},{"relation_name":"is_a","term_name":"regulation of muscle tissue development","termid":"GO:1901861"},{"relation_name":"regulates","term_name":"striated muscle tissue development","termid":"GO:0014706"}],"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 striated muscle tissue development","termid":"GO:0016202"}


id: PBO:0001572
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.3.-","termid":"PBO:0001572"}


id: MONDO:0003033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant vascular neoplasm arising from the prostate.","definition_xrefs":["NCIT:C5528"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostate sarcoma","termid":"MONDO:0002854"},{"relation_name":"is_a","term_name":"angiosarcoma","termid":"MONDO:0016982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"prostate angiosarcoma","secondary_identifiers":["UMLS:C1335504","DOID:4524","MEDGEN:235498"],"synonyms":[{"name":"angiosarcoma (disease) of prostate gland","type":"exact"},{"name":"angiosarcoma of prostate","type":"exact"},{"name":"angiosarcoma of the prostate","type":"exact"},{"name":"hemangiosarcoma of prostate","type":"exact"},{"name":"hemangiosarcoma of the prostate","type":"exact"},{"name":"prostate angiosarcoma","type":"exact"},{"name":"prostate gland angiosarcoma (disease)","type":"exact"},{"name":"prostate hemangiosarcoma","type":"exact"},{"name":"prostatic angiosarcoma","type":"exact"},{"name":"prostatic hemangiosarcoma","type":"exact"}],"termid":"MONDO:0003033","xrefs":{"Monarch":{"xref_id":"0003033"}}}


id: PBO:0089499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pumilio family RNA-binding protein Nop9","termid":"PBO:0089499"}


id: MONDO:0001659
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0001659 (obsolete MONDO:0001659)","termid":"MONDO:0001659","xrefs":{"Monarch":{"xref_id":"0001659"}}}


id: GO:0003093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glomerular filtration. Glomerular filtration is the process in which blood is filtered by the glomerulus into the renal tubule.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal system process involved in regulation of blood volume","termid":"GO:0001977"},{"relation_name":"is_a","term_name":"regulation of renal system process","termid":"GO:0098801"},{"relation_name":"regulates","term_name":"glomerular filtration","termid":"GO:0003094"}],"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 glomerular filtration","termid":"GO:0003093"}


id: GO:0019647
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pathway in which formaldehyde is used as a carbon source in the ribulose monophosphate cycle. Methanotrophic bacteria produce formaldehyde from the oxidation of methane and methanol, and then assimilate it via the ribulose monophosphate cycle to form intermediates of the central metabolic routes that are subsequently used for biosynthesis of cell material. Three molecules of formaldehyde are assimilated, forming a three-carbon intermediate of central metabolism; in this pathway, all cellular carbon is assimilated at the oxidation level of formaldehyde.","definition_xrefs":["MetaCyc:PWY-1861"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formaldehyde assimilation","termid":"GO:0019649"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"formaldehyde assimilation via ribulose monophosphate cycle","synonyms":[{"name":"formaldehyde assimilation via RuMP cycle","type":"exact"},{"name":"ribulose monophosphate cycle","type":"broad"}],"termid":"GO:0019647"}


id: MONDO:0013869
data:
  {"annotated_genes":["SJAG_01859"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85379],"is_not":false,"summary":null,"term":"MONDO:0013869"}]},"cv_name":"mondo","definition":"Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive (AR) disorder characterized by the formation and hyperexcretion of 2,8-dihydroxyadenine (2,8-DHA) in urine, causing urolithiasis and crystalline nephropathy.","definition_xrefs":["Orphanet:976"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete nephropathy secondary to a storage or other metabolic disease (obsolete MONDO:0019743)","termid":"MONDO:0019743"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid metabolism","termid":"MONDO:0004736"},{"relation_name":"is_a","term_name":"inborn disorder of purine metabolism","termid":"MONDO:0019236"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01859":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0019254"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"adenine phosphoribosyltransferase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:753682703","GARD:546","NANDO:2200587","DOID:0060350","MESH:C538228","NCIT:C121564","OMIM:614723","SCTID:124274002","MEDGEN:82772","UMLS:C0268120"],"synonyms":[{"name":"2,8-dihydroxyadenine urolithiasis","type":"exact"},{"name":"2,8-dihydroxyadeninuria disease","type":"exact"},{"name":"APRT deficiency","type":"exact"},{"name":"APRTD","type":"related"},{"name":"Dihydroxyadeninuria","type":"related"},{"name":"adenine phosphoribosyltransferase deficiency","type":"exact"},{"name":"nephrolithiasis, Dha","type":"related"},{"name":"urolithiasis, 2,8-dihydroxyadenine","type":"related"},{"name":"urolithiasis, Dha","type":"related"}],"termid":"MONDO:0013869","terms_by_termid":{"MONDO:0013869":null},"xrefs":{"Monarch":{"xref_id":"0013869"}}}


id: PBO:0040293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP2A1 antisense RNA 1","termid":"PBO:0040293"}


id: PBO:0050286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H6 family homeobox 3","termid":"PBO:0050286"}


id: PBO:0045197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member B8","termid":"PBO:0045197"}


id: PBO:0063206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCBP2 pseudogene 2","termid":"PBO:0063206"}


id: PBO:0003050
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by CCAAT complex","termid":"PBO:0003050"}


id: FYPO:0003973
data:
  {"alleles_by_uniquename":{"SJAG_01374:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01374","name":"nup132delta","uniquename":"SJAG_01374:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118668],"is_not":false,"summary":null,"term":"FYPO:0003973"}]},"cv_name":"fission_yeast_phenotype","definition":"A localization phenotype observed in the vegetative growth phase of the life cycle in which nuclear pore localization is abnormal, resulting in an abnormal spatial arrangement of nuclear pores within the nuclear envelope.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nucleus organization","termid":"FYPO:0000810"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01374":null},"genotype_count":1,"genotypes_by_uniquename":{"nup132delta":{"display_name":"nup132delta","display_uniquename":"nup132delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01374:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal nuclear pore localization","references_by_uniquename":{"PMID:33495454":null},"single_locus_annotated_genes":["SJAG_01374"],"single_locus_genotype_uniquenames":["nup132delta"],"synonyms":[{"name":"abnormal NPC localization","type":"exact"},{"name":"abnormal nuclear pore complex localization","type":"exact"},{"name":"abnormal nuclear pore distribution","type":"exact"},{"name":"abnormal nuclear pore localisation","type":"exact"},{"name":"abnormal nuclear pore localization during mitotic cell cycle","type":"related"},{"name":"abnormal nuclear pore localization during vegetative growth","type":"exact"}],"termid":"FYPO:0003973","terms_by_termid":{"FYPO:0003973":null}}


id: PBO:0024847
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"origin binding by Cdc13 and Mcm4 is mutually exclusive","termid":"PBO:0024847"}


id: PBO:0040319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase F1 subunit gamma pseudogene 1","termid":"PBO:0040319"}


id: MONDO:0013923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CEP152 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive primary microcephaly","termid":"MONDO:0016660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0700092"],"is_obsolete":false,"name":"microcephaly 9, primary, autosomal recessive","secondary_identifiers":["MEDGEN:766800","OMIM:614852","UMLS:C3553886","DOID:0070292","GARD:15855"],"synonyms":[{"name":"CEP152 autosomal recessive primary microcephaly","type":"exact"},{"name":"MCPH9","type":"related"},{"name":"autosomal recessive primary microcephaly caused by mutation in CEP152","type":"exact"},{"name":"microcephaly 9, primary, autosomal recessive","type":"exact"}],"termid":"MONDO:0013923","xrefs":{"Monarch":{"xref_id":"0013923"}}}


id: MONDO:0004700
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the parotid gland. Representative examples include carcinoma, malignant mixed tumor, and non-Hodgkin lymphoma.","definition_xrefs":["NCIT:C3525"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parotid gland neoplasm","termid":"MONDO:0021243"},{"relation_name":"is_a","term_name":"major salivary gland cancer","termid":"MONDO:0044743"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"parotid gland cancer","secondary_identifiers":["ICD9:142.0","MEDGEN:152885","MESH:D010307","DOID:9036","UMLS:C0747273","SCTID:363379000"],"synonyms":[{"name":"cancer of parotid","type":"exact"},{"name":"cancer of parotid gland","type":"exact"},{"name":"cancer of the parotid","type":"exact"},{"name":"cancer of the parotid gland","type":"exact"},{"name":"malignant neoplasm of parotid","type":"exact"},{"name":"malignant neoplasm of parotid gland","type":"exact"},{"name":"malignant neoplasm of the parotid","type":"exact"},{"name":"malignant neoplasm of the parotid gland","type":"exact"},{"name":"malignant parotid gland neoplasm","type":"exact"},{"name":"malignant parotid gland tumor","type":"exact"},{"name":"malignant parotid gland tumour","type":"exact"},{"name":"malignant parotid neoplasm","type":"exact"},{"name":"malignant parotid tumor","type":"exact"},{"name":"malignant parotid tumour","type":"exact"},{"name":"malignant tumor of parotid","type":"exact"},{"name":"malignant tumor of parotid gland","type":"exact"},{"name":"malignant tumor of the parotid","type":"exact"},{"name":"malignant tumor of the parotid gland","type":"exact"},{"name":"malignant tumour of parotid","type":"exact"},{"name":"malignant tumour of parotid gland","type":"exact"},{"name":"malignant tumour of the parotid","type":"exact"},{"name":"malignant tumour of the parotid gland","type":"exact"},{"name":"parotid cancer","type":"exact"},{"name":"parotid gland cancer","type":"exact"}],"termid":"MONDO:0004700","xrefs":{"Monarch":{"xref_id":"0004700"}}}


id: PBO:0077414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 150B","termid":"PBO:0077414"}


id: GO:0001167
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to a specific DNA sequence in order to modulate transcription by RNA polymerase I. The transcription factor may or may not also interact selectively with a protein or macromolecular complex.","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA polymerase I transcription factor activity, sequence-specific DNA binding (obsolete GO:0001167)","synonyms":[{"name":"sequence-specific DNA binding RNA polymerase I transcription factor activity","type":"exact"}],"termid":"GO:0001167"}


id: PBO:0072854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretion associated Ras related GTPase 1A pseudogene 4","termid":"PBO:0072854"}


id: MONDO:0004614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (myeloid progenitor cells) in the bone marrow and other sites.","definition_xrefs":["MESH:D007951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic leukemia","termid":"MONDO:0001014"},{"relation_name":"is_a","term_name":"monocytic leukemia","termid":"MONDO:0004600"}],"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":"chronic monocytic leukemia","secondary_identifiers":["MEDGEN:9729","DOID:8593","ICD9:206.1","NCIT:C34774","ICD9:206.11","UMLS:C0023466","ICD9:206.10","SCTID:188745007"],"synonyms":[{"name":"monocytic leukemia, chronic","type":"exact"}],"termid":"MONDO:0004614","xrefs":{"Monarch":{"xref_id":"0004614"}}}


id: GO:1901261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of sorocarp spore cell differentiation.","definition_xrefs":["GOC:TermGenie","GOC:rjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sorocarp development","termid":"GO:0031156"},{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"regulates","term_name":"sorocarp spore cell differentiation","termid":"GO:0044671"}],"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 sorocarp spore cell differentiation","termid":"GO:1901261"}


id: MONDO:0001629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"Jaccoud syndrome","secondary_identifiers":["ICD9:714.4","UMLS:C0152084","SCTID:84801008","DOID:13080","MEDGEN:508877"],"synonyms":[{"name":"Jaccoud syndrome","type":"exact"},{"name":"Jaccoud's syndrome","type":"exact"}],"termid":"MONDO:0001629","xrefs":{"Monarch":{"xref_id":"0001629"}}}


id: PBO:0045610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 21 (pseudogene)","termid":"PBO:0045610"}


id: MONDO:0800347
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"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":"cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction","synonyms":[{"name":"CMH23","type":"exact"}],"termid":"MONDO:0800347","xrefs":{"Monarch":{"xref_id":"0800347"}}}


id: GO:0033367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a secretory granule in a mast cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to secretory granule","termid":"GO:0033366"},{"relation_name":"part_of","term_name":"mast cell secretory granule organization","termid":"GO:0033364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to mast cell secretory granule","synonyms":[{"name":"protein localisation in mast cell secretory granule","type":"exact"},{"name":"protein localization in mast cell secretory granule","type":"exact"}],"termid":"GO:0033367"}


id: MOD:01471
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to (Z)-dehydrobutyrine.","definition_xrefs":["RESID:AA0182","DeltaMass:0","PubMed:1547888","PubMed:3769923"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dehydrobutyrine (Thr)","termid":"MOD:00190"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(Z)-dehydrobutyrine (Thr)","synonyms":[{"name":"(2Z)-2-aminobut-2-enoic acid","type":"exact"},{"name":"(Z)-2-amino-2-butenoic acid","type":"exact"},{"name":"(Z)-2-aminobutenoic acid","type":"exact"},{"name":"(Z)-dehydrobutyrine","type":"exact"},{"name":"(Z)dHAbu","type":"exact"},{"name":"2,3-didehydrobutyrine","type":"exact"},{"name":"3-methyldehydroalanine","type":"exact"},{"name":"Dehydrated","type":"related"},{"name":"Dehydration","type":"related"},{"name":"Dehydroamino butyric acid","type":"exact"},{"name":"Dhb","type":"exact"},{"name":"MOD_RES (Z)-2,3-didehydrobutyrine","type":"exact"},{"name":"alpha,beta-dehydroaminobutyric acid","type":"exact"},{"name":"anhydrothreonine","type":"exact"},{"name":"methyl-dehydroalanine","type":"exact"}],"termid":"MOD:01471"}


id: GO:0001951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Uptake of D-glucose into the blood by absorption from the small intestine.","definition_xrefs":["GOC:mgi_curators","PMID:5601832"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal hexose absorption","termid":"GO:0106001"}],"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":"intestinal D-glucose absorption","termid":"GO:0001951"}


id: PBO:0077812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor protein p53 binding protein 2 pseudogene 1","termid":"PBO:0077812"}


id: PBO:0004050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex subunit Sgf29","termid":"PBO:0004050"}


id: GO:0047789
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: creatinine + H2O = creatine.","definition_xrefs":["EC:3.5.2.10","RHEA:14533"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides","termid":"GO:0016812"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016810"],"is_obsolete":false,"name":"creatininase activity","secondary_identifiers":["KEGG_REACTION:R01884","MetaCyc:CREATININASE-RXN"],"synonyms":[{"name":"creatinine amidohydrolase activity","type":"related"},{"name":"creatinine hydrolase","type":"broad"}],"termid":"GO:0047789"}


id: MONDO:0020277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ectodermal malformation syndrome associated with ocular features (obsolete MONDO:0020277)","termid":"MONDO:0020277","xrefs":{"Monarch":{"xref_id":"0020277"}}}


id: PBO:0039485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 20 family member A8, pseudogene","termid":"PBO:0039485"}


id: GO:0042841
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of D-glucuronate, the D-enantiomer of glucuronate.","definition_xrefs":["GOC:mah","GOC:jsg","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-glucuronate metabolic process","termid":"GO:0042839"},{"relation_name":"is_a","term_name":"glucuronate biosynthetic process","termid":"GO:0046399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"D-glucuronate biosynthetic process","synonyms":[{"name":"D-glucuronate anabolism","type":"exact"},{"name":"D-glucuronate biosynthesis","type":"exact"},{"name":"D-glucuronate formation","type":"exact"},{"name":"D-glucuronate synthesis","type":"exact"}],"termid":"GO:0042841"}


id: GO:0019718
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Vesicular particles formed from disrupted endoplasmic reticulum membranes and studded with ribosomes on the outside.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete rough microsome (obsolete GO:0019718)","synonyms":[{"name":"rough microsome","type":"exact"}],"termid":"GO:0019718"}


id: SOFP:sp_status
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sp_status","termid":"SOFP:sp_status"}


id: FYPO:0005394
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which vegetative cell population growth is slower than normal for several generations, with the population growth rate decreasing over successive generations, after which the population resumes growing at a normal or near-normal rate.","definition_xrefs":["PMID:12196391","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"progressively decreasing vegetative cell population growth rate","termid":"FYPO:0005393"},{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0002058"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0002060","FYPO:0002057","FYPO:0000003","FYPO:0001985","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"progressively decreasing vegetative cell population growth rate followed by return to normal growth rate","synonyms":[{"name":"emergence of telomerase-deficient survivors","type":"related"},{"name":"progressively decreasing cell population growth rate followed by return to normal growth rate during vegetative growth","type":"exact"},{"name":"progressively decreasing cell population proliferation followed by return to normal proliferation","type":"related"},{"name":"progressively decreasing cell proliferation followed by return to normal proliferation","type":"related"},{"name":"progressively reduced cell proliferation followed by return to normal proliferation","type":"related"},{"name":"progressively reduced vegetative cell population growth rate followed by return to normal growth rate","type":"exact"}],"termid":"FYPO:0005394"}


id: GO:0021550
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the medulla oblongata over time, from its formation to the mature structure. The medulla oblongata lies directly above the spinal cord and controls vital autonomic functions such as digestion, breathing and the control of heart rate.","definition_xrefs":["GOC:jid","GOC:cls","ISBN:0838580343","GOC:dph","GO_REF:0000021","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"hindbrain development","termid":"GO:0030902"}],"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":"medulla oblongata development","synonyms":[{"name":"medulla development","type":"related"},{"name":"myelencephalon development","type":"related"}],"termid":"GO:0021550"}


id: GO:0061844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An immune response against microbes mediated by anti-microbial peptides in body fluid.","definition_xrefs":["PMID:15761415","PMID:24287494"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antimicrobial humoral response","termid":"GO:0019730"}],"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":"antimicrobial humoral immune response mediated by antimicrobial peptide","synonyms":[{"name":"antimicrobial peptide-mediated antimicrobial humoral response","type":"exact"},{"name":"peptide-mediated antimicrobial humoral response","type":"broad"}],"termid":"GO:0061844"}


id: PBO:0076245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sushi domain containing 6","termid":"PBO:0076245"}


id: MONDO:0010475
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An X-linked recessive syndrome caused by loss-of-function mutation(s) in IGSF1, encoding immunoglobulin superfamily member 1. This condition can result in central hypothyroidism, macroorchidism, delayed puberty, and variable prolactin deficiency.","definition_xrefs":["NCIT:C130989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"central congenital hypothyroidism","termid":"MONDO:0016410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked central congenital hypothyroidism with late-onset testicular enlargement","secondary_identifiers":["GARD:17499","DOID:0111140","Orphanet:329235","OMIM:300888","MEDGEN:763877","UMLS:C3550963"],"synonyms":[{"name":"CHTE","type":"exact"},{"name":"IGSF1 deficiency syndrome","type":"exact"},{"name":"Immunoglobulin superfamily member 1 deficiency syndrome","type":"exact"},{"name":"X-linked central congenital hypothyroidism with late-onset macroorchidism","type":"exact"},{"name":"X-linked central congenital hypothyroidism with late-onset testicular enlargement","type":"exact"},{"name":"central hypothyroidism and testicular enlargement","type":"exact"},{"name":"hypothyroidism Central and testicular enlargement","type":"exact"},{"name":"hypothyroidism, central, and testicular enlargement","type":"related"},{"name":"hypothyroidism, central, and testicular enlargement, X-linked recessive","type":"exact"}],"termid":"MONDO:0010475","xrefs":{"Monarch":{"xref_id":"0010475"}}}


id: PBO:0088654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab GTPase binding involved in ER to Golgi vesicle transport Yip3","termid":"PBO:0088654"}


id: GO:0090383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces the pH of the phagosome, measured by the concentration of the hydrogen ion.","definition_xrefs":["GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular pH reduction","termid":"GO:0051452"},{"relation_name":"part_of","term_name":"phagosome maturation","termid":"GO:0090382"}],"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":"phagosome acidification","synonyms":[{"name":"phagosomal acidification","type":"exact"}],"termid":"GO:0090383"}


id: PBO:0072674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RTRAF pseudogene 1","termid":"PBO:0072674"}


id: MOD:00773
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Natural or modified residues with a mass of 181.00-181.02 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.01 Da","termid":"MOD:00770"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 181.00-181.02 Da","termid":"MOD:00773"}


id: MONDO:0016438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Linear focal elastosis is a rare, acquired, dermis elastic tissue disorder characterized by asymptomatic, palpable, hypertrophic or atrophic, yellowish or red, indurated, horizontal, striae-like linear plaques distributed symmetrically across the mid and lower back. No systemic involvement has been described. Skin biopsy reveals a focal increase in abnormal elastic tissue with abundant, wavy, fragmented and aggregated, basophilic elastic fibers in the reticular dermis.","definition_xrefs":["Orphanet:228236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"linear focal dermal elastosis","secondary_identifiers":["GARD:20579","UMLS:C4751166","MEDGEN:1666729"],"synonyms":[{"name":"Elastotic striae","type":"exact"},{"name":"linear focal elastosis","type":"related"}],"termid":"MONDO:0016438","xrefs":{"Monarch":{"xref_id":"0016438"}}}


id: PBO:0113392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; null mutant shows improved incorporation efficiency of noncanonical amino acids in place of amber stop codon","termid":"PBO:0113392"}


id: GO:1905875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of postsynaptic density organization.","definition_xrefs":["PMID:21887379","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organelle organization","termid":"GO:0010639"},{"relation_name":"is_a","term_name":"regulation of postsynaptic density organization","termid":"GO:1905874"},{"relation_name":"negatively_regulates","term_name":"postsynaptic density organization","termid":"GO:0097106"}],"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 postsynaptic density organization","synonyms":[{"name":"down regulation of PSD organization","type":"exact"},{"name":"down regulation of post synaptic density organization","type":"exact"},{"name":"down regulation of post-synaptic density organization","type":"exact"},{"name":"down regulation of postsynaptic density organisation","type":"exact"},{"name":"down regulation of postsynaptic density organization","type":"exact"},{"name":"down-regulation of PSD organization","type":"exact"},{"name":"down-regulation of post synaptic density organization","type":"exact"},{"name":"down-regulation of post-synaptic density organization","type":"exact"},{"name":"down-regulation of postsynaptic density organisation","type":"exact"},{"name":"down-regulation of postsynaptic density organization","type":"exact"},{"name":"downregulation of PSD organization","type":"exact"},{"name":"downregulation of post synaptic density organization","type":"exact"},{"name":"downregulation of post-synaptic density organization","type":"exact"},{"name":"downregulation of postsynaptic density organisation","type":"exact"},{"name":"downregulation of postsynaptic density organization","type":"exact"},{"name":"inhibition of PSD organization","type":"narrow"},{"name":"inhibition of post synaptic density organization","type":"narrow"},{"name":"inhibition of post-synaptic density organization","type":"narrow"},{"name":"inhibition of postsynaptic density organisation","type":"narrow"},{"name":"inhibition of postsynaptic density organization","type":"narrow"},{"name":"negative regulation of PSD organization","type":"exact"},{"name":"negative regulation of post synaptic density organization","type":"exact"},{"name":"negative regulation of post-synaptic density organization","type":"exact"},{"name":"negative regulation of postsynaptic density organisation","type":"exact"}],"termid":"GO:1905875"}


id: PBO:0082930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic and mitochondrial glycyl-tRNA synthase; ligates glycine to the cognate anticodon-bearing tRNA; transcription termination factor that may interact with the 3'-end of pre-mRNA to promote 3'-end formation; GRS1 has a paralog, GRS2, that arose from the whole genome duplication; human homolog GARS implicated in Charcot-Marie-Tooth disease, can complement yeast null mutant","termid":"PBO:0082930"}


id: PBO:0030741
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-tapered_cell_during_nitrogen_starvation","termid":"PBO:0030741"}


id: PATO:0001288
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of red and brown hue and low brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"red brown","termid":"PATO:0001287"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dark red brown","termid":"PATO:0001288"}


id: PR:O14273
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC8C9.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14273"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated protein C8C9.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8C9.04","synonyms":[{"name":"Spom972h-SPAC8C9.04","type":"exact"}],"termid":"PR:O14273"}


id: GO:0015504
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: cytosine(out) + H+(out) = cytosine(in) + H+(in).","definition_xrefs":["TC:2.A.39.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytosine transmembrane transporter activity","termid":"GO:0015209"},{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"},{"relation_name":"is_a","term_name":"nucleobase:monoatomic cation symporter activity","termid":"GO:0015391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"cytosine:proton symporter activity","synonyms":[{"name":"cytosine permease activity","type":"related"},{"name":"cytosine:hydrogen ion symporter activity","type":"exact"}],"termid":"GO:0015504"}


id: PBO:0045878
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 delta pseudogene 2","termid":"PBO:0045878"}


id: GO:0102477
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 6C-glucosyl-2,5,7-trihydroxyflavanone = H+ + 6C-hexosyl chrysin + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,5,7-trihydroxyflavanone 6C-glucoside dehydratase activity (obsolete GO:0102477)","termid":"GO:0102477"}


id: MONDO:0005721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A heterogeneous group of infections produced by coxsackieviruses, including herpangina, aseptic meningitis (meningitis, aseptic), a common-cold-like syndrome, a non-paralytic poliomyelitis-like syndrome, epidemic pleurodynia (pleurodynia, epidemic) and a serious myocarditis.","definition_xrefs":["MESH:D003384"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enterovirus infectious disease","termid":"MONDO:0005747"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coxsackievirus infectious disease","secondary_identifiers":["DOID:10545","UMLS:C0010246","MEDGEN:1159","EFO:0007226"],"termid":"MONDO:0005721","xrefs":{"Monarch":{"xref_id":"0005721"}}}


id: PBO:0089173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G-patch RNA-binding protein, involved in splicing","termid":"PBO:0089173"}


id: PBO:0038806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 10","termid":"PBO:0038806"}


id: PBO:0000961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis ATPase (predicted)","termid":"PBO:0000961"}


id: MONDO:0005569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Softening and degeneration of the CARTILAGE. Pathological processes involving the chondral tissue (CARTILAGE).","definition_xrefs":["EFO:0005802"],"gene_count":0,"genotype_count":0,"name":"obsolete cartilage disease (obsolete MONDO:0005569)","secondary_identifiers":["ICD9:733.99","DOID:1222","SCTID:50927007","MESH:D002357"],"synonyms":[{"name":"cartilage disorder","type":"exact"},{"name":"cartilage tissue disease","type":"exact"},{"name":"cartilage tissue disease or disorder","type":"exact"},{"name":"chondropathy","type":"exact"},{"name":"disease of cartilage tissue","type":"exact"},{"name":"disease or disorder of cartilage tissue","type":"exact"},{"name":"disorder of cartilage tissue","type":"exact"}],"termid":"MONDO:0005569","xrefs":{"Monarch":{"xref_id":"0005569"}}}


id: MONDO:0060622
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A complex neurodevelopmental disorder caused by variation in DHX30. Individuals with variants in DHX30 have been found to have variable presentations including intellectual development, delayed or absent speech development, delayed motor development, hypotonia, feeding difficulties, and ataxic gait or the inability to walk. Other phenotypic features commonly reported include sleep disorders, autistic features, seizures, and joint hypermobility","definition_xrefs":["PMID:29100085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex neurodevelopmental disorder","termid":"MONDO:0100038"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with severe motor impairment and absent language","secondary_identifiers":["Orphanet:647788","UMLS:C4540496","OMIM:617804","GARD:13608","MEDGEN:1622162"],"synonyms":[{"name":"DHX30-related complex neurodevelopmental disorder","type":"exact"},{"name":"NEDMIAL","type":"related"},{"name":"neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome","type":"exact"},{"name":"neurodevelopmental disorder with severe motor impairment and absent language","type":"exact"}],"termid":"MONDO:0060622","xrefs":{"Monarch":{"xref_id":"0060622"}}}


id: GO:0085019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of a symbiont-induced complex organelle that comprises of multiple protein and lipid domains for the purpose of obtaining nutrients from its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formation of specialized structure for nutrient acquisition","termid":"GO:0052093"}],"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":"formation of tubovesicular network for nutrient acquisition","synonyms":[{"name":"formation by symbiont of a tubovesicular network for nutrient acquisition from host","type":"related"},{"name":"formation of a symbiont- induced tubovesicular network for nutrient acquisition from host","type":"exact"}],"termid":"GO:0085019"}


id: PBO:0090319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sec14 cytosolic factor family, phospholipid-intermembrane transfer protein Csr102","termid":"PBO:0090319"}


id: GO:0097686
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A horn-shaped dinoflagellate apex found in thecate species.","definition_xrefs":["PMID:7002229","GOC:at"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dinoflagellate apex","termid":"GO:0097683"}],"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":"dinoflagellate apical horn","termid":"GO:0097686"}


id: MONDO:1011539
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypokalaemic periodic paralysis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypokalaemic periodic paralysis, non-human animal","termid":"MONDO:1011434"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypokalaemic periodic paralysis, domestic cat","secondary_identifiers":["OMIA:001759-9685"],"termid":"MONDO:1011539","xrefs":{"Monarch":{"xref_id":"1011539"}}}


id: PBO:0071149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 13","termid":"PBO:0071149"}


id: PBO:0081305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 90","termid":"PBO:0081305"}


id: MONDO:0001465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"keratitis","termid":"MONDO:0003085"}],"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":"superficial keratitis","secondary_identifiers":["DOID:12196","ICD9:370.20","MEDGEN:509771","SCTID:27019000","UMLS:C0155074"],"termid":"MONDO:0001465","xrefs":{"Monarch":{"xref_id":"0001465"}}}


id: FYECO:0000223
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 1NM-PP1 was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 1-NM-PP1","synonyms":[{"name":"+ 1NM-PP1","type":"exact"}],"termid":"FYECO:0000223"}


id: PBO:0091716
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Multistep PhosphoRelay","termid":"PBO:0091716"}


id: GO:0047287
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: beta-D-galactoside + CMP-N-acetyl-beta-neuraminate = an N-acetyl-alpha-neuraminyl-(2->6)-beta-D-galactosyl derivative + CMP + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete lactosylceramide alpha-2,6-N-sialyltransferase activity (obsolete GO:0047287)","termid":"GO:0047287"}


id: GO:0008051
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A complex that possesses farnesyl-diphosphate farnesyl transferase activity.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete farnesyl-diphosphate farnesyl transferase complex (obsolete GO:0008051)","synonyms":[{"name":"farnesyl-diphosphate farnesyl transferase complex","type":"exact"}],"termid":"GO:0008051"}


id: FYPO:0001131
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"}]},"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 heterochromatin is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to chromatin during vegetative growth","termid":"FYPO:0000452"},{"relation_name":"is_a","term_name":"abnormal protein localization to heterochromatin","termid":"FYPO:0004718"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null,"SJAG_03892":null},"genotype_count":1,"genotypes_by_uniquename":{"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03892","SJAG_01050"],"name":"abnormal protein localization to heterochromatin during vegetative growth","references_by_uniquename":{"PMID:32109380":null},"synonyms":[{"name":"abnormal protein localisation to heterochromatin during vegetative growth","type":"exact"},{"name":"abnormal protein localization to heterochromatin during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001131","terms_by_termid":{"FYPO:0001132":null,"FYPO_EXT:0000001":null}}


id: PBO:0004996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UCS-domain protein Rng3","termid":"PBO:0004996"}


id: MONDO:0003822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papillary neoplasm of the urinary bladder in which the transitional cells form papillae. The papillary structures exhibit minimal architectural distortion and minimal atypia. Mitoses are infrequent. Patients are at an increased risk of developing new papillary lesions. Occasionally, the new lesions are urothelial carcinomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder papillary urothelial neoplasm","termid":"MONDO:0003442"},{"relation_name":"is_a","term_name":"urinary tract non-invasive transitional cell neoplasm","termid":"MONDO:0003755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-invasive bladder papillary urothelial neoplasm","secondary_identifiers":["DOID:6239","MEDGEN:309424","UMLS:C1518358","NCIT:C39831"],"synonyms":[{"name":"bladder PUNLMP","type":"exact"},{"name":"bladder papillary neoplasm of low malignant potential","type":"exact"},{"name":"non-invasive bladder papillary urothelial neoplasm","type":"exact"},{"name":"papillary urothelial neoplasm of low malignant potential","type":"exact"}],"termid":"MONDO:0003822","xrefs":{"Monarch":{"xref_id":"0003822"}}}


id: GO:0030994
data:
  {"annotated_genes":["SJAG_00667","SJAG_01774"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88940,99334,99335],"is_not":false,"summary":null,"term":"GO:0030994"}]},"cv_name":"biological_process","definition":"Dissolution of the primary septum during cell separation.","definition_xrefs":["PMID:12665550"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component disassembly","termid":"GO:0022411"},{"relation_name":"part_of","term_name":"septum digestion after cytokinesis","termid":"GO:0000920"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00667":null,"SJAG_01774":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"primary cell septum disassembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"hydrolysis of primary cell septum","type":"exact"},{"name":"primary cell septum hydrolysis","type":"exact"},{"name":"primary septum hydrolysis","type":"broad"}],"termid":"GO:0030994","terms_by_termid":{"GO:0030994":null}}


id: PBO:0052695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 16 pseudogene 3","termid":"PBO:0052695"}


id: GO:0045477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nurse cell apoptotic process.","definition_xrefs":["PMID:11973306","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process involved in development","termid":"GO:1904748"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"nurse cell apoptotic process","termid":"GO:0045476"}],"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 nurse cell apoptotic process","synonyms":[{"name":"regulation of nurse cell apoptosis","type":"narrow"}],"termid":"GO:0045477"}


id: PBO:0054105
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 1470","termid":"PBO:0054105"}


id: GO:0044162
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a host cell cytoplasmic vesicle.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell membrane","termid":"GO:0033644"},{"relation_name":"is_a","term_name":"host cell cytoplasm part","termid":"GO:0033655"},{"relation_name":"part_of","term_name":"host cell cytoplasmic vesicle","termid":"GO:0044161"}],"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":"host cell cytoplasmic vesicle membrane","termid":"GO:0044162"}


id: PR:O14075
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A glyoxylate/hydroxypyruvate reductase B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01215"],"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 UNK4.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPACUNK4.10","secondary_identifiers":["UniProtKB:O14075"],"synonyms":[{"name":"Spom972h-ghrB","type":"exact"}],"termid":"PR:O14075"}


id: PBO:0048868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A4","termid":"PBO:0048868"}


id: GO:0090502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving the hydrolysis of internal 3',5'-phosphodiester bonds in one or two strands of ribonucleotides.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA phosphodiester bond hydrolysis, endonucleolytic (obsolete GO:0090502)","termid":"GO:0090502"}


id: PBO:0053130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LCT antisense RNA 1","termid":"PBO:0053130"}


id: MONDO:0016634
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of rare thrombotic disorder due to a coagulation factors defect that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"gene_count":0,"genotype_count":0,"name":"obsolete thrombotic disorder due to an acquired coagulation factors defect (obsolete MONDO:0016634)","secondary_identifiers":["Orphanet:248365"],"synonyms":[{"name":"acquired rare thrombotic disorder due to a coagulation factors defect","type":"exact"}],"termid":"MONDO:0016634","xrefs":{"Monarch":{"xref_id":"0016634"}}}


id: PBO:0043632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic obstructive pulmonary disease associated lncRNA 1","termid":"PBO:0043632"}


id: PBO:0090142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2-type precatalytic spliceosome WW domain-binding protein Wbp4","termid":"PBO:0090142"}


id: GO:0070356
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains synaptotagmin, synaptobrevin 2 (VAMP2), SNAP-25, syntaxin 1a, syntaxin1b, and Rab3a (or orthologs thereof).","definition_xrefs":["PMID:7654227"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNARE complex","termid":"GO:0031201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"synaptotagmin-synaptobrevin 2-SNAP-25-syntaxin-1a-syntaxin-1b-Rab3a complex","synonyms":[{"name":"SNARE complex (STX1a, STX1b, SNAP25, RAB3a, SYT1, VAMP2)","type":"narrow"},{"name":"STX1a-STX1b-SNAP25-RAB3a-SYT1-VAMP2 complex","type":"narrow"}],"termid":"GO:0070356"}


id: PBO:0040602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAG cochaperone 6","termid":"PBO:0040602"}


id: GO:0036397
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: formate + a quinone = CO2 + a quinol.","definition_xrefs":["GOC:bhm","RHEA:48592"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups, quinone or similar compound as acceptor","termid":"GO:0033695"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"formate dehydrogenase (quinone) activity","secondary_identifiers":["KEGG_REACTION:R09494","MetaCyc:FORMATEDEHYDROG-RXN","EC:1.17.5.3"],"synonyms":[{"name":"Fdh-N activity","type":"related"},{"name":"formate dehydrogenase-N activity","type":"related"},{"name":"formate:quinone oxidoreductase activity","type":"related"}],"termid":"GO:0036397"}


id: MOD:01331
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to 6x(13)C labeled L-arginine.","definition_xrefs":["PubMed:12716131","OMSSA:136","Unimod:188#R"],"direct_ancestors":[{"relation_name":"is_a","term_name":"6x(13)C labeled residue","termid":"MOD:00544"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled L-arginine","synonyms":[{"name":"13C(6) Silac label","type":"related"},{"name":"Label:13C(6)","type":"related"},{"name":"arg-13c6","type":"exact"}],"termid":"MOD:01331"}


id: PBO:0111691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 QL1","termid":"PBO:0111691"}


id: PBO:0045429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dpy-19 like C-mannosyltransferase 1","termid":"PBO:0045429"}


id: MONDO:0008855
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Immunodeficiency by defective expression of HLA class 2 is a rare primary genetic immunodeficiency disorder characterized by partial or complete absence of human leukocyte antigen class 2 expression resulting in severe defect in both cellular and humoral immune response to antigens. The disorder presents clinically as marked susceptibility to infections, severe malabsorption and failure to thrive and is often fatal in early childhood.","definition_xrefs":["Orphanet:572"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"severe combined immunodeficiency","termid":"MONDO:0015974"},{"relation_name":"is_a","term_name":"familial severe combined immunodeficiency","termid":"MONDO:0031520"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"MHC class II deficiency","secondary_identifiers":["NCIT:C176823","UMLS:C2931418","MESH:C537079","DOID:5812","MEDGEN:444051","SCTID:71904008","GARD:824","icd11.foundation:2021339495","OMIMPS:209920","NANDO:1200329","NCIT:C3895","NANDO:2200702","MESH:D016511"],"synonyms":[{"name":"BARE lymphocyte syndrome","type":"related"},{"name":"BARE lymphocyte syndrome, type II","type":"related"},{"name":"BARE lymphocyte syndrome, type II, complementation group B, included","type":"related"},{"name":"BARE lymphocyte syndrome, type II, complementation group C, included","type":"related"},{"name":"BARE lymphocyte syndrome, type II, complementation group D, included","type":"related"},{"name":"BARE lymphocyte syndrome, type II, complementation group E, included","type":"related"},{"name":"BLS","type":"related"},{"name":"BLS 2","type":"related"},{"name":"BLS type II","type":"related"},{"name":"BLS, type II","type":"related"},{"name":"BLSII","type":"related"},{"name":"Bare lymphocyte syndrome","type":"related"},{"name":"Bare lymphocyte syndrome 2","type":"related"},{"name":"Bare lymphocyte syndrome type 2","type":"related"},{"name":"Bare lymphocyte syndrome, type 2","type":"related"},{"name":"Bare lymphocyte syndrome, type II","type":"related"},{"name":"Bare lymphocyte syndrome, type II, complementation group A","type":"related"},{"name":"Bare lymphocyte syndrome, type II, complementation group B","type":"related"},{"name":"Bare lymphocyte syndrome, type II, complementation group C","type":"related"},{"name":"Bare lymphocyte syndrome, type II, complementation group D","type":"related"},{"name":"Bare lymphocyte syndrome, type II, complementation group E","type":"related"},{"name":"Bls, type 2","type":"related"},{"name":"HLA class 2-negative SCID","type":"exact"},{"name":"HLA class 2-negative severe combined immunodeficiency","type":"exact"},{"name":"MHC class II expression deficiency","type":"exact"},{"name":"SCID due to absent class II HLA antigens","type":"exact"},{"name":"SCID, HLA CLASS II-NEGATIVE BARE lymphocyte syndrome, type II, complementation group A, included","type":"related"},{"name":"SCID, HLA Class 2-negative","type":"related"},{"name":"SCID, HLA Class II-negative","type":"related"},{"name":"bare lymphocyte syndrome type II","type":"related"},{"name":"immunodeficiency by defective expression of HLA class 2","type":"related"},{"name":"immunodeficiency by defective expression of HLA class type 2","type":"exact"},{"name":"major histocompatibility complex class II expression deficiency","type":"exact"},{"name":"severe combined immunodeficiency, HLA Class II-negative","type":"related"},{"name":"severe combined immunodeficiency, HLA class ii-negative","type":"related"}],"termid":"MONDO:0008855","xrefs":{"Monarch":{"xref_id":"0008855"}}}


id: PBO:0054826
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 2239","termid":"PBO:0054826"}


id: GO:0150137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-37 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["PMID:30362558","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"interleukin-37 production","synonyms":[{"name":"interleukin-37 biosynthetic process","type":"narrow"}],"termid":"GO:0150137"}


id: GO:1904910
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment of RNA localization to telomere.","definition_xrefs":["GOC:BHF_telomere","GOC:rph","GOC:TermGenie","PMID:26586433","GOC:BHF","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"regulates","term_name":"establishment of RNA localization to telomere","termid":"GO:0097694"}],"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 establishment of RNA localization to telomere","synonyms":[{"name":"regulation of establishment of RNA localisation to telomere","type":"exact"}],"termid":"GO:1904910"}


id: PBO:0002388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation elongation factor eIF5A (predicted)","termid":"PBO:0002388"}


id: MONDO:0018645
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of endocrine system","termid":"MONDO:0000569"},{"relation_name":"is_a","term_name":"autoimmune disorder of gastrointestinal tract","termid":"MONDO:0000588"},{"relation_name":"is_a","term_name":"IgG4-related disease","termid":"MONDO:0017287"},{"relation_name":"is_a","term_name":"sclerosing cholangitis","termid":"MONDO:0018646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"IgG4-related sclerosing cholangitis","secondary_identifiers":["icd11.foundation:1676971795","SCTID:722870008","NANDO:1200928","MEDGEN:927778","UMLS:C4302109","Orphanet:447764","GARD:21867"],"termid":"MONDO:0018645","xrefs":{"Monarch":{"xref_id":"0018645"}}}


id: MONDO:0009354
data:
  {"annotated_genes":["SJAG_04042","SJAG_04459"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84473,84474],"is_not":false,"summary":null,"term":"MONDO:0009354"}]},"cv_name":"mondo","definition":"An autosomal recessive condition caused by mutation(s) in the MTRR gene, encoding methionine synthase reductase. It is characterized by homocystinuria and megaloblastic anemia.","definition_xrefs":["NCIT:C142173"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"methylmalonic acidemia","termid":"MONDO:0002012"},{"relation_name":"is_a","term_name":"homocystinuria without methylmalonic aciduria","termid":"MONDO:0018964"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04042":null,"SJAG_04459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005570","MONDO:0005066","MONDO:0004736","MONDO:0002280"],"is_obsolete":false,"name":"methylcobalamin deficiency type cblE","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:3576","MESH:C565510","NANDO:2201109","OMIM:236270","DOID:0112255","UMLS:C1856057","Orphanet:2169","MEDGEN:344640","DOID:0050732"],"synonyms":[{"name":"HMAE","type":"related"},{"name":"functional methionine synthase deficiency type cblE","type":"exact"},{"name":"homocystinuria due to defect in methylation Cbl e","type":"related"},{"name":"homocystinuria-megaloblastic Anaemia due to defect in cobalamin metabolism, cblE complementation type","type":"related"},{"name":"homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblE complementation type","type":"related"},{"name":"homocystinuria-megaloblastic anemia, cbl e type","type":"exact"},{"name":"homocystinuria-megaloblastic anemia, cblE complementation type","type":"related"},{"name":"methylcobalamin deficiency type cblE","type":"exact"},{"name":"methylcobalamin deficiency, cblE type","type":"related"},{"name":"methylmalonic aciduria and homocystinuria type cblE","type":"related"},{"name":"vitamin B12-responsive homocystinuria, cblE type","type":"related"}],"termid":"MONDO:0009354","terms_by_termid":{"MONDO:0009354":null},"xrefs":{"Monarch":{"xref_id":"0009354"}}}


id: PBO:0085639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in inserting tail-anchored proteins into ER membranes; forms a complex with Mdy2p; highly conserved across species and homologous to human gene C7orf20","termid":"PBO:0085639"}


id: MONDO:0850285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intrinsic asthma that is characterized by exposure to tobacco smoke and other inflammatory gasses or particulate matter.","definition_xrefs":["DOID:0080819"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrinsic asthma","termid":"MONDO:0004765"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"environmental induced asthma","termid":"MONDO:0850285","xrefs":{"Monarch":{"xref_id":"0850285"}}}


id: FYPO:0007304
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the mitotic spindle is shorter than normal during anaphase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"short bipolar mitotic spindle","termid":"FYPO:0000732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0002399","FYPO:0001985","FYPO:0000054","FYPO:0000120"],"is_obsolete":false,"name":"short bipolar mitotic spindle during anaphase","synonyms":[{"name":"decreased mitotic spindle length during anaphase","type":"exact"},{"name":"short mitotic spindle during anaphase","type":"exact"},{"name":"short mitotic spindle during anaphase during vegetative growth","type":"exact"},{"name":"short mitotic spindles during anaphase","type":"exact"},{"name":"short spindle during mitotic anaphase","type":"exact"}],"termid":"FYPO:0007304"}


id: PBO:0063250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin alpha subfamily C, 1","termid":"PBO:0063250"}


id: PBO:0061550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-nucleotidase, cytosolic IIIA","termid":"PBO:0061550"}


id: MONDO:0968947
data:
  {"annotated_genes":["SJAG_04936"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86386],"is_not":false,"summary":null,"term":"MONDO:0968947"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04936":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder plus optic atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620784"],"termid":"MONDO:0968947","terms_by_termid":{"MONDO:0968947":null},"xrefs":{"Monarch":{"xref_id":"0968947"}}}


id: GO:0071629
data:
  {"annotated_genes":["SJAG_01556","SJAG_02341","SJAG_00173","SJAG_00552","SJAG_02419"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107160,108793,108896,109479,112753],"is_not":false,"summary":null,"term":"GO:0071629"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of misfolded proteins in the cytoplasm, which are targeted to cytoplasmic proteasomes for degradation.","definition_xrefs":["GOC:mah","GOC:rb","PMID:20080635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome-mediated ubiquitin-dependent protein catabolic process","termid":"GO:0043161"},{"relation_name":"is_a","term_name":"cytoplasm protein quality control","termid":"GO:0140455"},{"relation_name":"part_of","term_name":"cellular response to misfolded protein","termid":"GO:0071218"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00173":null,"SJAG_00552":null,"SJAG_01556":null,"SJAG_02341":null,"SJAG_02419":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0030163"},{"rel_name":"part_of","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"cytoplasm protein quality control by the ubiquitin-proteasome system","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cytoplasm-associated proteasomal ubiquitin-dependent protein breakdown","type":"exact"},{"name":"cytoplasm-associated proteasomal ubiquitin-dependent protein catabolism","type":"exact"},{"name":"cytoplasm-associated proteasomal ubiquitin-dependent protein degradation","type":"exact"},{"name":"ubiquitin-dependent catabolism of misfolded proteins by cytoplasm-associated proteasome","type":"exact"}],"termid":"GO:0071629","terms_by_termid":{"GO:0071629":null}}


id: PBO:0056625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 6 pseudogene 1","termid":"PBO:0056625"}


id: PBO:0073835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 7 member 11","termid":"PBO:0073835"}


id: PBO:0040195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"argininosuccinate synthetase 1 pseudogene 8","termid":"PBO:0040195"}


id: GO:0015344
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: siderophore-iron(ferrioxamine)(out) + H+(out) = siderophore-iron(ferrioxamine)(in) + H+(in).","definition_xrefs":["TC:2.A.1.16.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore-iron transmembrane transporter activity","termid":"GO:0015343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"siderophore uptake transmembrane transporter activity","synonyms":[{"name":"ferrioxamine uptake transmembrane transporter activity","type":"related"},{"name":"siderochrome-iron (ferrioxamine) uptake transporter","type":"narrow"},{"name":"siderophore-iron uptake transmembrane transporter activity","type":"related"}],"termid":"GO:0015344"}


id: PBO:0044959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase/reductase 4 like 1 (pseudogene)","termid":"PBO:0044959"}


id: GO:0046263
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of nitrotoluene, any methylbenzene molecule with NO2 group(s) attached.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrotoluene metabolic process","termid":"GO:0019326"},{"relation_name":"is_a","term_name":"toluene-containing compound catabolic process","termid":"GO:0072491"}],"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":"nitrotoluene catabolic process","synonyms":[{"name":"nitrotoluene breakdown","type":"exact"},{"name":"nitrotoluene catabolism","type":"exact"},{"name":"nitrotoluene degradation","type":"exact"}],"termid":"GO:0046263"}


id: GO:0061034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the olfactory bulb mitral cell layer over time from its initial formation until its mature state. The mitral cell layer is composed of pyramidal neurons whose cell bodies are located between the granule cell layer and the plexiform layer.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"olfactory bulb development","termid":"GO:0021772"}],"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":"olfactory bulb mitral cell layer development","termid":"GO:0061034"}


id: GO:0003926
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: GTP + H2O = GDP + phosphate.","definition_xrefs":["EC:3.6.1.47"],"gene_count":0,"genotype_count":0,"name":"obsolete ARF small monomeric GTPase activity (obsolete GO:0003926)","synonyms":[{"name":"ARF small monomeric GTPase activity","type":"exact"}],"termid":"GO:0003926"}


id: PBO:0000131
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.1.1.1","termid":"PBO:0000131"}


id: PBO:0059510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded conserved sequence block III","termid":"PBO:0059510"}


id: MONDO:0957408
data:
  {"annotated_genes":["SJAG_05239","SJAG_01884","SJAG_03805","SJAG_04118","SJAG_03151","SJAG_04380","SJAG_04969","SJAG_04290","SJAG_04541","SJAG_04569","SJAG_02039","SJAG_00400"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012429"},{"annotations":[84401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012471"},{"annotations":[84404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012472"},{"annotations":[84490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014007"},{"annotations":[86499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014629"},{"annotations":[85971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054698"},{"annotations":[85782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054700"},{"annotations":[84654,84655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054699"},{"annotations":[85656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024541"},{"annotations":[85507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013818"},{"annotations":[84873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010523"}]},"cv_name":"mondo","definition":"A type 1 interferonopathy that occurs during childhood.","definition_xrefs":["MONDO:patterns/childhood"],"direct_ancestors":[{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome of childhood","termid":"MONDO:0957018"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00400":null,"SJAG_01884":null,"SJAG_02039":null,"SJAG_03151":null,"SJAG_03805":null,"SJAG_04118":null,"SJAG_04290":null,"SJAG_04380":null,"SJAG_04541":null,"SJAG_04569":null,"SJAG_04969":null,"SJAG_05239":null},"genotype_count":0,"is_obsolete":false,"name":"type 1 interferonopathy of childhood","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1843010","GARD:21986","UMLS:C5681250","Orphanet:481671"],"termid":"MONDO:0957408","terms_by_termid":{"MONDO:0010523":null,"MONDO:0012429":null,"MONDO:0012471":null,"MONDO:0012472":null,"MONDO:0013818":null,"MONDO:0014007":null,"MONDO:0014629":null,"MONDO:0024541":null,"MONDO:0054698":null,"MONDO:0054699":null,"MONDO:0054700":null},"xrefs":{"Monarch":{"xref_id":"0957408"}}}


id: GO:0036391
data:
  {"annotated_genes":["SJAG_03374","SJAG_00118","SJAG_04375","SJAG_03703","SJAG_00663","SJAG_01277","SJAG_01658","SJAG_02645","SJAG_04703","SJAG_04566"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[97010,97086,99295,100143,100950,103092,107110,111905,116997,117759],"is_not":false,"summary":null,"term":"GO:0036391"}]},"cv_name":"cellular_component","definition":"A ring-shaped structure that forms at the medial cortex of a symmetrically dividing cell at the onset of cytokinesis; composed of members of the conserved family of filament forming proteins called septins as well as septin-associated proteins.","definition_xrefs":["GOC:vw","PMID:16009555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin ring","termid":"GO:0005940"},{"relation_name":"is_a","term_name":"cleavage apparatus septin structure","termid":"GO:0032161"},{"relation_name":"part_of","term_name":"medial cortex","termid":"GO:0031097"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_00663":null,"SJAG_01277":null,"SJAG_01658":null,"SJAG_02645":null,"SJAG_03374":null,"SJAG_03703":null,"SJAG_04375":null,"SJAG_04566":null,"SJAG_04703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005938"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005938","GO:0005737"],"is_obsolete":false,"name":"medial cortex septin ring","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0036391","terms_by_termid":{"GO:0036391":null}}


id: PBO:0073721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLAIN motif family member 1","termid":"PBO:0073721"}


id: MONDO:0012779
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"celiac disease","termid":"MONDO:0005130"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"celiac disease, susceptibility to, 10","secondary_identifiers":["MEDGEN:394326","OMIM:612008","UMLS:C2677604"],"synonyms":[{"name":"CELIAC10","type":"exact"},{"name":"celiac disease, susceptibility to, 10","type":"exact"},{"name":"gluten-sensitive enteropathy, susceptibility to, 10","type":"related"}],"termid":"MONDO:0012779","xrefs":{"Monarch":{"xref_id":"0012779"}}}


id: PBO:0083055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Diadenosine and diphosphoinositol polyphosphate phosphatase; hydrolyzes diphosphorylated inositol polyphosphates and diadenosine polyphosphates; high specificity for diadenosine hexa- and pentaphosphates; contains endopolyphosphatase activity with a high affinity for polyphosphates, an activity also observed for its human DIPP homologs; possesses mRNA decapping activity; nudix hydrolase family member; protein abundance increases in response to DNA replication stress","termid":"PBO:0083055"}


id: PBO:0072083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 13","termid":"PBO:0072083"}


id: PBO:0078285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 18-1","termid":"PBO:0078285"}


id: PBO:0073876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 10 member 4","termid":"PBO:0073876"}


id: PBO:0076368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trace amine associated receptor 5","termid":"PBO:0076368"}


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


id: GO:0098923
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell-cell signaling from postsynapse to presynapse, across the synaptic cleft, mediated by an soluble gas ligand.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retrograde trans-synaptic signaling","termid":"GO:0098917"},{"relation_name":"is_a","term_name":"trans-synaptic signaling by soluble gas","termid":"GO:0099543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"retrograde trans-synaptic signaling by soluble gas","termid":"GO:0098923"}


id: MONDO:0011214
data:
  {"annotated_genes":["SJAG_03363"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84769],"is_not":false,"summary":null,"term":"MONDO:0011214"}]},"cv_name":"mondo","definition":"Progressive familial intrahepatic cholestasis type 3 (PFIC3), a type of progressive familial intrahepatic cholestasis (PFIC), is a late-onset hereditary disorder in bile formation that is hepatocellular in origin. Onset may occur from infancy to young adulthood.","definition_xrefs":["Orphanet:79305"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive familial intrahepatic cholestasis","termid":"MONDO:0015762"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03363":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515","MONDO:0005066"],"is_obsolete":false,"name":"progressive familial intrahepatic cholestasis type 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1276600959","UMLS:C1865643","NORD:1416","MEDGEN:356333","NANDO:1201045","GARD:1289","OMIM:602347","DOID:0070223","MESH:C535935"],"synonyms":[{"name":"ABCB4 progressive familial intrahepatic cholestasis","type":"exact"},{"name":"MDR3 Deficiency","type":"exact"},{"name":"Mdr3 deficiency","type":"related"},{"name":"PFIC3","type":"exact"},{"name":"cholestasis, progressive familial intrahepatic 3","type":"exact"},{"name":"cholestasis, progressive familial intrahepatic, 3","type":"related"},{"name":"cholestasis, progressive familial intrahepatic, type 3","type":"exact"},{"name":"cholestasis, progressive familial intrahepatic, with elevated serum gamma-glutamyltransferase","type":"related"},{"name":"progressive familial intrahepatic cholestasis caused by mutation in ABCB4","type":"exact"},{"name":"progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase","type":"related"}],"termid":"MONDO:0011214","terms_by_termid":{"MONDO:0011214":null},"xrefs":{"Monarch":{"xref_id":"0011214"}}}


id: FYPO:0000555
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which re-entry into the mitotic cell cycle after pheromone arrest is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype","termid":"FYPO:0000145"},{"relation_name":"is_a","term_name":"abnormal response to pheromone","termid":"FYPO:0000302"},{"relation_name":"is_a","term_name":"abnormal cell cycle process","termid":"FYPO:0002734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0005447","FYPO:0000002","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"abnormal re-entry into mitotic cell cycle after pheromone arrest","synonyms":[{"name":"abnormal recovery from pheromone-induced cell cycle arrest","type":"exact"},{"name":"recovery from pheromone-induced cell cycle arrest: abnormal","type":"related"}],"termid":"FYPO:0000555"}


id: GO:0106146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sideretin.","definition_xrefs":["PMID:29581584","GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coumarin biosynthetic process","termid":"GO:0009805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"sideretin biosynthesis","termid":"GO:0106146"}


id: PBO:0057303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 514b","termid":"PBO:0057303"}


id: MONDO:0016412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Peripheral hypothyroidism is a type of permanent congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth, that results from peripheral defects in thyroid hormone metabolism.","definition_xrefs":["Orphanet:226310"],"direct_ancestors":[{"relation_name":"is_a","term_name":"permanent congenital hypothyroidism","termid":"MONDO:0016408"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peripheral hypothyroidism","secondary_identifiers":["UMLS:C5704669","MEDGEN:1843430"],"termid":"MONDO:0016412","xrefs":{"Monarch":{"xref_id":"0016412"}}}


id: GO:0034137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of toll-like receptor 2 signaling pathway.","definition_xrefs":["PMID:16551253","GOC:add","PMID:17328678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of toll-like receptor 2 signaling pathway","termid":"GO:0034135"},{"relation_name":"is_a","term_name":"positive regulation of pattern recognition receptor signaling pathway","termid":"GO:0062208"},{"relation_name":"positively_regulates","term_name":"toll-like receptor 2 signaling pathway","termid":"GO:0034134"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of toll-like receptor 2 signaling pathway","synonyms":[{"name":"positive regulation of TLR2 signaling pathway","type":"exact"},{"name":"positive regulation of toll-like receptor 2 signalling pathway","type":"exact"}],"termid":"GO:0034137"}


id: GO:1902951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dendritic spine maintenance.","definition_xrefs":["PMID:24328732","GO_REF:0000058","GOC:TermGenie","GOC:sjp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell projection organization","termid":"GO:0031345"},{"relation_name":"is_a","term_name":"regulation of dendritic spine maintenance","termid":"GO:1902950"},{"relation_name":"negatively_regulates","term_name":"dendritic spine maintenance","termid":"GO:0097062"}],"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 dendritic spine maintenance","synonyms":[{"name":"down regulation of dendritic spine maintenance","type":"exact"},{"name":"down-regulation of dendritic spine maintenance","type":"exact"},{"name":"downregulation of dendritic spine maintenance","type":"exact"},{"name":"inhibition of dendritic spine maintenance","type":"narrow"}],"termid":"GO:1902951"}


id: RO:0002388
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x has potential to directly develop into y iff x directly develops into y or x is capable of directly developing into y","direct_ancestors":[{"relation_name":"is_a","term_name":"has_potential_to_develop_into","termid":"RO:0002387"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_potential_to_directly_develop_into","termid":"RO:0002388"}


id: PBO:0113229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglucosamine (GlcNAc) kinase; requires a divalent cation and a broad range of NTPs as phosphoryl donor to generate GlcNAc-6-phosphate, a substrate for glycan biosynthesis; promotes UDP-GlcNAc biosynthesis a precursor for chitin production; phylogenically distinct from known GlcNAc kinases and hexokinases; transcript is upregulated during sporulation and the unfolded protein response; contains a hexokinase-like ATPase domain; non-essential gene","termid":"PBO:0113229"}


id: PBO:0066069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RARB antisense RNA 1","termid":"PBO:0066069"}


id: GO:0060335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of an interferon-gamma-mediated signaling pathway.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine-mediated signaling pathway","termid":"GO:0001961"},{"relation_name":"is_a","term_name":"positive regulation of response to type II interferon","termid":"GO:0060332"},{"relation_name":"is_a","term_name":"regulation of type II interferon-mediated signaling pathway","termid":"GO:0060334"},{"relation_name":"positively_regulates","term_name":"type II interferon-mediated signaling pathway","termid":"GO:0060333"}],"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:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of type II interferon-mediated signaling pathway","synonyms":[{"name":"positive regulation of gamma-interferon-mediated signaling pathway","type":"related"},{"name":"positive regulation of immune interferon-mediated signaling pathway","type":"exact"},{"name":"positive regulation of interferon-gamma-mediated signaling pathway","type":"broad"},{"name":"positive regulation of interferon-gamma-mediated signalling pathway","type":"exact"},{"name":"positive regulation of type II IFN-mediated pathway","type":"broad"}],"termid":"GO:0060335"}


id: PBO:0075861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family member 9, pseudogene","termid":"PBO:0075861"}


id: GO:0018030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a myristoyl group to the N6 nitrogen atom on a lysine residue of a peptide or protein molecule.","definition_xrefs":["PMID:1402651","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myristoyltransferase activity","termid":"GO:0019107"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016740","GO:0140096","GO:0003824","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"peptidyl-lysine N6-myristoyltransferase activity","termid":"GO:0018030"}


id: MONDO:0100493
data:
  {"annotated_genes":["SJAG_00185"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009709"}]},"cv_name":"mondo","definition":"Autosomal recessive form of TTN-related myopathy.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"TTN-related myopathy","termid":"MONDO:0100175"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00185":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"autosomal recessive titinopathy","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"TTN-related myopathy, autosomal recessive","type":"exact"}],"termid":"MONDO:0100493","terms_by_termid":{"MONDO:0009709":null},"xrefs":{"Monarch":{"xref_id":"0100493"}}}


id: MONDO:0060712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete developmental delay, intellectual disability, obesity, and dysmorphic features (obsolete MONDO:0060712)","termid":"MONDO:0060712","xrefs":{"Monarch":{"xref_id":"0060712"}}}


id: GO:0015669
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of substances that are gaseous in normal living conditions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"gas transport","termid":"GO:0015669"}


id: MONDO:0019800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Chronic hepatic porphyrias represent a sub-group of porphyrias. They are characterized by bullous photodermatitis caused by a deficiency of uroporphyrinogen decarboxylase (URO-D; the fifth enzyme in the heme biosynthesis pathway). Chronic hepatic porphyria encompasses two diseases: porphyria cutanea tarda and hepatoerythropoietic porphyria (extremely rare).","definition_xrefs":["Orphanet:95161"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"inherited porphyria","termid":"MONDO:0019142"}],"gene_count":0,"genotype_count":0,"name":"obsolete chronic hepatic porphyria (obsolete MONDO:0019800)","synonyms":[{"name":"acute hepatic porphyria, chronic","type":"exact"},{"name":"chronic acute hepatic porphyria","type":"exact"}],"termid":"MONDO:0019800","xrefs":{"Monarch":{"xref_id":"0019800"}}}


id: MONDO:0008718
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases.","definition_xrefs":["Orphanet:83467"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular channelopathy","termid":"MONDO:0019119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Morvan syndrome","secondary_identifiers":["MEDGEN:1632829","SCTID:763803004","EFO:1001897","GARD:9766","UMLS:C3854373"],"synonyms":[{"name":"Morvan's fibrillary chorea","type":"exact"},{"name":"limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome","type":"exact"}],"termid":"MONDO:0008718","xrefs":{"Monarch":{"xref_id":"0008718"}}}


id: FYPO:0004974
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which telomere localization, a process in which a telomere is transported to, and/or maintained in, a specific location, is normal (i.e. indistinguishable from wild type) during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal telomere localization","termid":"FYPO:0004973"}],"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:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal telomere localization during mitotic interphase","synonyms":[{"name":"normal telomere localisation during mitotic interphase","type":"exact"},{"name":"normal telomere localization during interphase of mitotic cell cycle","type":"exact"},{"name":"normal telomere localization during mitotic interphase during vegetative growth","type":"exact"},{"name":"normal telomere tethering to nuclear periphery during mitotic interphase","type":"exact"}],"termid":"FYPO:0004974"}


id: PBO:0063539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PEAK family member 3","termid":"PBO:0063539"}


id: GO:1902376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any protein denaturation that is involved in proteasomal ubiquitin-dependent protein catabolic process.","definition_xrefs":["GOC:TermGenie","PMID:21091378"],"gene_count":0,"genotype_count":0,"name":"obsolete protein denaturation involved in proteasomal ubiquitin-dependent protein catabolic process (obsolete GO:1902376)","synonyms":[{"name":"protein denaturation involved in proteasomal pathway","type":"exact"},{"name":"protein denaturation involved in proteasomal processing","type":"related"},{"name":"protein denaturation involved in proteasomal ubiquitin-dependent protein breakdown","type":"exact"},{"name":"protein denaturation involved in proteasomal ubiquitin-dependent protein catabolism","type":"exact"},{"name":"protein denaturation involved in proteasomal ubiquitin-dependent protein degradation","type":"exact"},{"name":"protein denaturation involved in proteasome pathway","type":"related"}],"termid":"GO:1902376"}


id: GO:1990644
data:
  {"annotated_genes":["SJAG_00207","SJAG_00646"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87219,110829],"is_not":false,"summary":null,"term":"GO:1990644"}]},"cv_name":"molecular_function","definition":"The binding activity of a molecule that attaches the spindle microtubules to the kinetochore.","definition_xrefs":["PMID:20723757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-macromolecule adaptor activity","termid":"GO:0030674"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00207":null,"SJAG_00646":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0030674"}],"interesting_parent_ids":["GO:0003674","GO:0060090","GO:0030674"],"is_obsolete":false,"name":"microtubule site clamp","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990644","terms_by_termid":{"GO:1990644":null}}


id: GO:0042052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly and arrangement of a rhabdomere within a cell. The rhabdomere is the organelle on the apical surface of a photoreceptor cell that contains the visual pigments.","definition_xrefs":["PMID:3937883","PMID:3076112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle organization","termid":"GO:0006996"},{"relation_name":"part_of","term_name":"compound eye photoreceptor development","termid":"GO:0042051"}],"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":"rhabdomere development","synonyms":[{"name":"rhabdomere organization","type":"exact"}],"termid":"GO:0042052"}


id: MONDO:0003956
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloarthropathy","termid":"MONDO:0005095"},{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Baastrup syndrome","secondary_identifiers":["UMLS:C0158248","DOID:6643","MEDGEN:510482","SCTID:82304009","ICD9:721.5"],"synonyms":[{"name":"Baastrup syndrome","type":"exact"},{"name":"Baastrup's syndrome","type":"exact"},{"name":"kissing spine","type":"exact"}],"termid":"MONDO:0003956","xrefs":{"Monarch":{"xref_id":"0003956"}}}


id: MONDO:0018851
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple familial keratoacanthoma (KA) of Witten and Zak is a rare a rare inherited skin cancer syndrome and is characterized by the coexistence of features characteristic of both multiple KA, Ferguson Smith type and generalized eruptive keratoacanthoma, such as multiple small miliary-type lesions, larger self-healing lesions, and nodulo-ulcerative lesions. Lesions do not have a predilection for the mucosal surfaces. Transmission is autosomal dominant.","definition_xrefs":["Orphanet:493"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"is_a","term_name":"keratoacanthoma","termid":"MONDO:0002527"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"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":"familial keratoacanthoma","secondary_identifiers":["UMLS:C5848325","SCTID:716774008","GARD:18693","MEDGEN:1843863"],"synonyms":[{"name":"hereditary keratoacanthoma","type":"exact"},{"name":"multiple keratoacanthoma","type":"exact"}],"termid":"MONDO:0018851","xrefs":{"Monarch":{"xref_id":"0018851"}}}


id: PBO:0046915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 30 member B","termid":"PBO:0046915"}


id: PBO:0031111
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_response_to_reactive_oxygen_species_during_G0_phase","termid":"PBO:0031111"}


id: MONDO:0010406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome Xp11.22 duplication syndrome","secondary_identifiers":["UMLS:C0796238","MEDGEN:208679","DOID:0112037","GARD:22683","OMIM:300705","DECIPHER:90"],"synonyms":[{"name":"Xp11.22 microduplication syndrome","type":"exact"},{"name":"Xp11.22-linked intellectual disability","type":"exact"},{"name":"chromosome Xp11.22 duplication syndrome","type":"exact"},{"name":"intellectual disability, X-linked 17","type":"related"},{"name":"intellectual disability, X-linked 31","type":"related"},{"name":"mental retardation, X-linked 17","type":"related"},{"name":"mental retardation, X-linked 31","type":"related"}],"termid":"MONDO:0010406","xrefs":{"Monarch":{"xref_id":"0010406"}}}


id: PBO:0065021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxiredoxin 3","termid":"PBO:0065021"}


id: GO:0001797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of type IIa hypersensitivity, a type of inflammatory response.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of type IIa hypersensitivity","termid":"GO:0001796"},{"relation_name":"is_a","term_name":"negative regulation of type II hypersensitivity","termid":"GO:0002893"},{"relation_name":"negatively_regulates","term_name":"type IIa hypersensitivity","termid":"GO:0001794"}],"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 type IIa hypersensitivity","synonyms":[{"name":"down regulation of type IIa hypersensitivity","type":"exact"},{"name":"down-regulation of type IIa hypersensitivity","type":"exact"},{"name":"downregulation of type IIa hypersensitivity","type":"exact"},{"name":"inhibition of type IIa hypersensitivity","type":"narrow"}],"termid":"GO:0001797"}


id: PBO:0076707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor 7 like 1","termid":"PBO:0076707"}


id: MONDO:0000887
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hepatic veno-occlusive disease (obsolete MONDO:0000887)","termid":"MONDO:0000887","xrefs":{"Monarch":{"xref_id":"0000887"}}}


id: PBO:0082372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Basic leucine zipper (bZIP) transcription factor; physically interacts with the Tup1-Cyc8 complex and recruits Tup1p to its targets; overexpression increases sodium and lithium tolerance; computational analysis suggests a role in regulation of expression of genes involved in carbohydrate metabolism; YAP6 has a paralog, CIN5, that arose from the whole genome duplication","termid":"PBO:0082372"}


id: PBO:0084056
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 Cin4p; tubulin folding factor C involved in beta-tubulin (Tub2p) folding; mutants display increased chromosome loss and benomyl sensitivity; human homolog RP2 complements yeast null mutant","termid":"PBO:0084056"}


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


id: SO:0001356
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Uridine_5_oxyacetic_acid is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine_five_oxyacetic_acid","secondary_identifiers":["RNAMOD:064"],"synonyms":[{"name":"cmo5U","type":"exact"},{"name":"uridine 5-oxyacetic acid","type":"exact"},{"name":"uridine five oxyacetic acid","type":"exact"}],"termid":"SO:0001356"}


id: MONDO:0019649
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic steroid-sensitive nephrotic syndrome","termid":"MONDO:0019067"}],"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":"idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis","secondary_identifiers":["Orphanet:93206"],"synonyms":[{"name":"idiopathic steroid-sensitive nephrotic syndrome with focal segmental glomerulosclerosis","type":"exact"}],"termid":"MONDO:0019649","xrefs":{"Monarch":{"xref_id":"0019649"}}}


id: MONDO:0022060
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coloboma","termid":"MONDO:0001476"},{"relation_name":"is_a","term_name":"amenorrhea","termid":"MONDO:0001836"},{"relation_name":"is_a","term_name":"corpus callosum, agenesis of","termid":"MONDO:0009022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002320"],"is_obsolete":false,"name":"calloso-genital dysplasia","secondary_identifiers":["MESH:C537962","UMLS:C2931677","MEDGEN:419867"],"synonyms":[{"name":"primary amenorrhoea with coloboma and total agenesis of the corpus callosum","type":"related"}],"termid":"MONDO:0022060","xrefs":{"Monarch":{"xref_id":"0022060"}}}


id: FYECO:0000410
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which 3,4-dihydrocoumarin was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ 3,4-dihydrocoumarin","synonyms":[{"name":"3,4-dihydrocoumarin added","type":"exact"}],"termid":"FYECO:0000410"}


id: MONDO:1012960
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Herediatary cerebellar ataxia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar ataxia, non-human animal","termid":"MONDO:1012956"},{"relation_name":"is_a","term_name":"hereditary ataxia, non-human animal","termid":"MONDO:1012959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary cerebellar ataxia, non-human animal","termid":"MONDO:1012960","xrefs":{"Monarch":{"xref_id":"1012960"}}}


id: GO:0014062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of serotonin.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of monoatomic ion transport","termid":"GO:0043269"},{"relation_name":"is_a","term_name":"regulation of secretion by cell","termid":"GO:1903530"},{"relation_name":"regulates","term_name":"serotonin secretion","termid":"GO:0001820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of serotonin secretion","synonyms":[{"name":"regulation of serotonin release","type":"related"}],"termid":"GO:0014062"}


id: PBO:0075624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPRING1 pseudogene 1","termid":"PBO:0075624"}


id: FYPO:0005357
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 site-specific DNA replication termination at RTS1 barrier in the mating type region occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal site-specific DNA replication termination at RTS1 barrier","termid":"FYPO:0005355"}],"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:0000293"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000293","FYPO:0001985"],"is_obsolete":false,"name":"decreased site-specific DNA replication termination at RTS1 barrier","synonyms":[{"name":"decreased site-specific DNA replication termination at RTS1 barrier during mitotic cell cycle","type":"related"},{"name":"decreased site-specific DNA replication termination at RTS1 barrier during vegetative growth","type":"exact"},{"name":"reduced site-specific DNA replication termination at RTS1 barrier","type":"exact"}],"termid":"FYPO:0005357"}


id: FYPO:0002359
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 telomeric regions is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H3-K9 methylation during vegetative growth","termid":"FYPO:0003232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal histone H3-K9 dimethylation at telomere during vegetative growth","synonyms":[{"name":"normal histone H3-K9 dimethylation at telomere during mitotic cell cycle","type":"related"},{"name":"normal histone H3K9me2 at telomere during vegetative growth","type":"exact"},{"name":"normal telomeric histone H3-K9 dimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002359"}


id: GO:0001533
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A type of plasma membrane that has been modified through addition of distinct intracellular and extracellular components, including ceramide, found in cornifying epithelial cells (corneocytes).","definition_xrefs":["GOC:add","PMID:15803139","PMID:11112355","PMID:11590230"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane","termid":"GO:0005886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"cornified envelope","termid":"GO:0001533"}


id: GO:0022605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A reproductive process that is a step in the formation and maturation of an ovum or female gamete from a primordial female germ cell.","definition_xrefs":["GOC:mtg_sensu","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal reproductive process","termid":"GO:0048609"},{"relation_name":"part_of","term_name":"oogenesis","termid":"GO:0048477"}],"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":"mammalian oogenesis stage","synonyms":[{"name":"mammalian oogenesis process","type":"exact"}],"termid":"GO:0022605"}


id: PBO:0043609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COMM domain containing 2","termid":"PBO:0043609"}


id: PBO:0073221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semaphorin 6B","termid":"PBO:0073221"}


id: GO:0051436
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of ubiquitin ligase activity that contributes to the mitotic cell cycle.","definition_xrefs":["GOC:ai","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle (obsolete GO:0051436)","synonyms":[{"name":"APC inhibition during mitotic cell cycle","type":"narrow"},{"name":"anaphase promoting complex inhibition during mitotic cell cycle","type":"narrow"},{"name":"anaphase-promoting complex inhibition during mitotic cell cycle","type":"narrow"},{"name":"down regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"down-regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"downregulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"inhibition of ubiquitin ligase activity during mitotic cell cycle","type":"narrow"},{"name":"mitotic APC inhibition","type":"narrow"},{"name":"mitotic APC inhibitor","type":"narrow"},{"name":"mitotic SCF complex inhibitor","type":"narrow"},{"name":"mitotic anaphase promoting complex inhibition","type":"narrow"},{"name":"mitotic anaphase promoting complex inhibitor","type":"narrow"},{"name":"mitotic anaphase-promoting complex inhibition","type":"narrow"},{"name":"mitotic anaphase-promoting complex inhibitor","type":"narrow"},{"name":"mitotic ubiquitin ligase inhibitor","type":"narrow"},{"name":"negative regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"negative regulation of ubiquitin-protein ligase activity during mitotic cell cycle","type":"related"}],"termid":"GO:0051436"}


id: MONDO:0010224
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Corpus callosum agenesis-abnormal genitalia syndrome is a rare, genetic developmental defect during embryogenesis syndrome characterized by agenesis of the corpus callosum, mild to severe neurological manifestations (intellectual disability, developmental delay, epilepsy, dystonia), and urogenital anomalies (hypospadias, cryptorchidism, renal dysplasia, ambiguous genitalia). Additionally, skeletal anomalies (limb contractures, scoliosis), dysmorphic facial features (large eyes, prominent supraorbital ridges, synophris) and optic atrophy have been observed.","definition_xrefs":["Orphanet:2508"],"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":0,"genotype_count":0,"is_obsolete":false,"name":"corpus callosum agenesis-abnormal genitalia syndrome","secondary_identifiers":["SCTID:763797003","UMLS:C0796124","OMIM:300004","MESH:C563110","MEDGEN:163217","DOID:0112151","GARD:4528"],"synonyms":[{"name":"ACC with abnormal genitalia","type":"related"},{"name":"ACC-abnormal genitalia syndrome","type":"exact"},{"name":"New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum","type":"related"},{"name":"Proud Levine Carpenter syndrome","type":"related"},{"name":"Proud syndrome","type":"exact"},{"name":"Proud-Levine-Carpenter syndrome","type":"exact"},{"name":"corpus callosum, agenesis of, with abnormal genitalia","type":"related"},{"name":"microcephaly-corpus callosum agenesis-abnormal genitalia syndrome","type":"exact"}],"termid":"MONDO:0010224","xrefs":{"Monarch":{"xref_id":"0010224"}}}


id: MONDO:0001002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pulmonary siderosis (obsolete MONDO:0001002)","termid":"MONDO:0001002","xrefs":{"Monarch":{"xref_id":"0001002"}}}


id: PBO:0085661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in negative regulation of iron regulon transcription; forms an iron independent complex with Fra2p, Grx3p, and Grx4p; cytosolic; mutant fails to repress transcription of iron regulon and is defective in spore formation","termid":"PBO:0085661"}


id: MONDO:0000301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An myiasis caused by infection with Oestrus ovis.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypodermyiasis","termid":"MONDO:0005805"}],"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":"ophthalmomyiasis","secondary_identifiers":["DOID:0050268","SCTID:48216006","UMLS:C0027034","MEDGEN:507965"],"synonyms":[{"name":"Oestrus ovis caused myiasis","type":"exact"},{"name":"Oestrus ovis myiasis","type":"exact"},{"name":"ophthalmic myiasis","type":"exact"},{"name":"ophthalmomyiasis","type":"exact"}],"termid":"MONDO:0000301","xrefs":{"Monarch":{"xref_id":"0000301"}}}


id: GO:0030430
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The cytoplasm of a host cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host intracellular part","termid":"GO:0033646"}],"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":"host cell cytoplasm","secondary_identifiers":["GO:0097679"],"synonyms":[{"name":"other organism cytoplasm","type":"related"}],"termid":"GO:0030430"}


id: PATO:0001076
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001076 relative momentum (obsolete PATO:0001076)","termid":"PATO:0001076"}


id: GO:0047429
data:
  {"annotated_genes":["SJAG_03676","SJAG_03797","SJAG_01651","SJAG_00705","SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110980,113097],"is_not":false,"summary":null,"term":"GO:0047429"},{"annotations":[96299,117727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106379"},{"annotations":[98187,117728],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035870"},{"annotations":[96300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036218"},{"annotations":[98188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004170"},{"annotations":[117729],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036220"},{"annotations":[96301],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036221"},{"annotations":[117730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036222"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a nucleoside triphosphate + H2O = a nucleotide + H+ + diphosphate.","definition_xrefs":["EC:3.6.1.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00705":null,"SJAG_01651":null,"SJAG_03676":null,"SJAG_03797":null,"SJAG_04487":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"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:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"nucleoside triphosphate diphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:NUCLEOTIDE-PYROPHOSPHATASE-RXN","Reactome:R-HSA-9755030"],"synonyms":[{"name":"nucleoside-triphosphate diphosphatase activity","type":"exact"},{"name":"nucleoside-triphosphate diphosphohydrolase activity","type":"exact"},{"name":"nucleoside-triphosphate pyrophosphatase activity","type":"exact"}],"termid":"GO:0047429","terms_by_termid":{"GO:0004170":null,"GO:0035870":null,"GO:0036218":null,"GO:0036220":null,"GO:0036221":null,"GO:0036222":null,"GO:0047429":null,"GO:0106379":null}}


id: PBO:0000528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U4/U6 x U5 tri-snRNP complex subunit Snu23 (predicted)","termid":"PBO:0000528"}


id: MONDO:1010873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lysosomal storage disease characterised by impaired unesterified cholesterol and sphingomyelin transport and metabolism, resulting in the accumulation of un-esterified cholesterol and glycosphingolipids within late endosomes and lysosomes that occurs in dogs. Affected animals present with hepatosplenomegaly, neurological degeneration and premature death.","definition_xrefs":["OMIA:000725-9615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease, dog","termid":"MONDO:1010860"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Niemann-Pick disease, type C, dog","synonyms":[{"name":"Niemann-Pick disease, type C1, dog","type":"related"}],"termid":"MONDO:1010873","xrefs":{"Monarch":{"xref_id":"1010873"}}}


id: MONDO:0054802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial polycythemia","termid":"MONDO:0001115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"erythrocytosis, familial, 7","secondary_identifiers":["DOID:0111631","UMLS:C4693823","MEDGEN:1642594","OMIM:617981"],"synonyms":[{"name":"ECYT7","type":"related"},{"name":"erythrocytosis 7","type":"exact"},{"name":"erythrocytosis, Alpha-globin type","type":"related"},{"name":"erythrocytosis, FAMILIAL, 7","type":"related"},{"name":"polycythemia, Alpha-globin type","type":"related"}],"termid":"MONDO:0054802","xrefs":{"Monarch":{"xref_id":"0054802"}}}


id: FYPO:0007591
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitophagy, i.e. autophagic degradation of the mitochondria, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","GO:0000422"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"}],"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 mitophagy","synonyms":[{"name":"normal autophagy of mitochondrion","type":"exact"}],"termid":"FYPO:0007591"}


id: PBO:0060619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NCF4 antisense RNA 1","termid":"PBO:0060619"}


id: GO:0010901
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of very-low-density lipoprotein particle remodeling. Very-low-density lipoprotein particle remodeling is the acquisition, loss or modification of a protein or lipid within a very-low-density lipoprotein particle, including the hydrolysis of triglyceride by hepatic lipase or lipoprotein lipase and the subsequent loss of free fatty acid.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"very-low-density lipoprotein particle remodeling","termid":"GO:0034372"}],"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 very-low-density lipoprotein particle remodeling","synonyms":[{"name":"regulation of VLDL remodeling","type":"exact"},{"name":"regulation of VLDL remodelling","type":"exact"},{"name":"regulation of very-low-density lipoprotein particle remodelling","type":"exact"}],"termid":"GO:0010901"}


id: PBO:0090005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial holo-[acyl-carrier-protein] synthase Ppt2","termid":"PBO:0090005"}


id: PBO:0067448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 570, pseudogene","termid":"PBO:0067448"}


id: PBO:0083358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the verified gene REV1; null mutant displays increased resistance to antifungal agents gliotoxin, cycloheximide and H2O2","termid":"PBO:0083358"}


id: GO:0102754
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + chlorophyllide b + (E)-3,7,11,15-tetramethylhexadec-2-en-1-yl diphosphate = chlorophyll b + diphosphoric acid.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete chlorophyllide-b:phytyl-diphosphate phytyltransferase activity (obsolete GO:0102754)","termid":"GO:0102754"}


id: GO:0010038
data:
  {"annotated_genes":["SJAG_00988","SJAG_02599","SJAG_01803","SJAG_01344","SJAG_03879","SJAG_03631","SJAG_01351","SJAG_03799","SJAG_02858","SJAG_01233","SJAG_04403","SJAG_04454","SJAG_03497","SJAG_00044","SJAG_04516","SJAG_01078"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92503,96563,107584,96246,117326,96208],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0098849"},{"annotations":[96209,92504,96564,88091,107585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071276"},{"annotations":[112489,113811,115262,100179,109311,97304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071277"},{"annotations":[92332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071248"},{"annotations":[113812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035865"},{"annotations":[96565],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010273"},{"annotations":[92963,92962],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010312"}]},"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 metal ion stimulus.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00988":null,"SJAG_01078":null,"SJAG_01233":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_01803":null,"SJAG_02599":null,"SJAG_02858":null,"SJAG_03497":null,"SJAG_03631":null,"SJAG_03799":null,"SJAG_03879":null,"SJAG_04403":null,"SJAG_04454":null,"SJAG_04516":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 metal ion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"heavy metal sensitivity/resistance","type":"related"},{"name":"response to heavy metal","type":"narrow"},{"name":"response to metal","type":"exact"}],"termid":"GO:0010038","terms_by_termid":{"GO:0010273":null,"GO:0010312":null,"GO:0035865":null,"GO:0071248":null,"GO:0071276":null,"GO:0071277":null,"GO:0098849":null}}


id: FYPO:0004050
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutathione transferase activity is decreased in a cell culture in stationary phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased glutathione transferase activity","termid":"FYPO:0004034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0001985","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"decreased glutathione transferase activity during stationary phase","synonyms":[{"name":"decreased glutathione transferase activity in stationary phase","type":"exact"},{"name":"reduced glutathione transferase activity during stationary phase","type":"exact"}],"termid":"FYPO:0004050"}


id: PBO:0028390
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_glyoxalase_III_activity","termid":"PBO:0028390"}


id: PBO:0060869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative elongation factor complex member A","termid":"PBO:0060869"}


id: MONDO:1011663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"displaced abomasum, non-human animal","secondary_identifiers":["OMIA:001119"],"termid":"MONDO:1011663","xrefs":{"Monarch":{"xref_id":"1011663"}}}


id: PR:Q10328
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- phx1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10328"],"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":"homeobox transcription factor phx1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC32A11.03c","synonyms":[{"name":"Spom972h-phx1","type":"exact"}],"termid":"PR:Q10328"}


id: GO:0007218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by a neuropeptide binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process.","definition_xrefs":["GOC:mah","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"neuropeptide signaling pathway","synonyms":[{"name":"neuropeptide signalling pathway","type":"exact"}],"termid":"GO:0007218"}


id: GO:0070395
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lipoteichoic acid, which is a major component of the cell wall of gram-positive bacteria and typically consists of a chain of glycerol-phosphate repeating units linked to a glycolipid anchor.","definition_xrefs":["PMID:16020688","GOC:add","PMID:14665680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teichoic acid biosynthetic process","termid":"GO:0019350"},{"relation_name":"is_a","term_name":"lipoteichoic acid metabolic process","termid":"GO:0070394"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0044085","GO:0071554"],"is_obsolete":false,"name":"lipoteichoic acid biosynthetic process","synonyms":[{"name":"LTA biosynthetic process","type":"broad"},{"name":"lipoteichoic acid anabolism","type":"exact"},{"name":"lipoteichoic acid biosynthesis","type":"exact"},{"name":"lipoteichoic acid formation","type":"exact"},{"name":"lipoteichoic acid synthesis","type":"exact"}],"termid":"GO:0070395"}


id: PBO:0066999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA component of signal recognition particle 7SL3","termid":"PBO:0066999"}


id: MONDO:0023134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Febrile ulceronecrotic Mucha-Habermann disease (FUMHD) is a rare and severe form of pityriasis lichenoides et varioliformis acuta (PLEVA). PLEVA is characterized by skin lesions that ulcerate, breakdown, form open sores, then form a red-brown crust. FUMHD often begins as PLEVA, but then rapidly and suddenly progresses to large, destructive ulcers. There may be fever and extensive, painful loss of skin tissue as well as secondary infection of the ulcers. Diagnosis of FUMHD is confirmed by biopsy of skin lesions. FUMHD occurs more frequently in children, peaking at age 5 to 10. Males tend to be affected more often than females. While some cases of FUMHD have resolved without therapy, others have resulted in death. Early diagnosis and prompt treatment may help to reduce morbidity and death.","definition_xrefs":["GARD:0009516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute lichenoid pityriasis","termid":"MONDO:0024250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"febrile ulceronecrotic Mucha-Habermann disease","secondary_identifiers":["MESH:C537077","SCTID:402860008","UMLS:C1274297","MEDGEN:266145","GARD:9516","icd11.foundation:1408299147"],"synonyms":[{"name":"A severe variant of pityriasis lichenoides et varioliformis acuta (PLEVA)","type":"related"},{"name":"FUMHD","type":"related"},{"name":"febrile ulceronecrotic Mucha-Habermann disease","type":"exact"},{"name":"febrile ulceronecrotic pityriasis lichenoides acuta","type":"exact"},{"name":"ulceronecrotic Mucha-Habermann disease","type":"related"},{"name":"variant of Mucha-Habermann disease","type":"related"}],"termid":"MONDO:0023134","xrefs":{"Monarch":{"xref_id":"0023134"}}}


id: PR:O59703
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo9 gene.","definition_xrefs":["UniProtKB:O59703","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":"geranylgeranyl pyrophosphate synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC36.06c","synonyms":[{"name":"(2E,6E)-farnesyl diphosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Dimethylallyltranstransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Farnesyltranstransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GGPP synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GGPPSase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Geranyltranstransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spo9","type":"exact"},{"name":"farnesyl diphosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"geranylgeranyl diphosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sporulation-specific protein 9 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O59703"}


id: PBO:0004809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homoserine O-acetyltransferase Met6","termid":"PBO:0004809"}


id: PBO:0072804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"senescence associated long non-coding RNA 3","termid":"PBO:0072804"}


id: MONDO:0019298
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare urticaria.","gene_count":0,"genotype_count":0,"name":"obsolete rare urticaria (obsolete MONDO:0019298)","secondary_identifiers":["Orphanet:79384"],"synonyms":[{"name":"rare hives","type":"exact"},{"name":"rare urticaria","type":"exact"},{"name":"rare urticaria (disease)","type":"exact"}],"termid":"MONDO:0019298","xrefs":{"Monarch":{"xref_id":"0019298"}}}


id: MONDO:0003351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant smooth muscle neoplasm that arises from the colon. It is characterized by a proliferation of neoplastic spindle cells.","definition_xrefs":["NCIT:C5494"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon sarcoma","termid":"MONDO:0003352"},{"relation_name":"is_a","term_name":"leiomyosarcoma","termid":"MONDO:0005058"}],"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":"colon leiomyosarcoma","secondary_identifiers":["MEDGEN:232380","DOID:5259","UMLS:C1333093"],"synonyms":[{"name":"colon leiomyosarcoma","type":"exact"},{"name":"colonic leiomyosarcoma","type":"exact"},{"name":"leiomyosarcoma of colon","type":"exact"},{"name":"leiomyosarcoma of the colon","type":"exact"}],"termid":"MONDO:0003351","xrefs":{"Monarch":{"xref_id":"0003351"}}}


id: PBO:0052268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 4B","termid":"PBO:0052268"}


id: MONDO:0021355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the esophagus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"},{"relation_name":"is_a","term_name":"digestive system neoplasm","termid":"MONDO:0021223"},{"relation_name":"is_a","term_name":"neoplasm of thorax","termid":"MONDO:0021350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"neoplasm of esophagus","secondary_identifiers":["NCIT:C3028","SCTID:126817006","UMLS:C0014859","MEDGEN:4547"],"synonyms":[{"name":"esophageal neoplasm","type":"exact"},{"name":"esophageal neoplasms, benign and malignant","type":"exact"},{"name":"esophageal tumor","type":"exact"},{"name":"esophageal tumors","type":"exact"},{"name":"esophageal tumour","type":"exact"},{"name":"esophageal tumours","type":"exact"},{"name":"esophagus neoplasm","type":"exact"},{"name":"esophagus neoplasm (disease)","type":"exact"},{"name":"esophagus tumor","type":"exact"},{"name":"neoplasm of esophagus","type":"exact"},{"name":"neoplasm of the esophagus","type":"exact"},{"name":"neoplasm of the oesophagus","type":"exact"},{"name":"oesophagus neoplasm","type":"exact"},{"name":"oesophagus neoplasm (disease)","type":"exact"},{"name":"oesophagus tumour","type":"exact"},{"name":"tumor of esophagus","type":"exact"},{"name":"tumor of the esophagus","type":"exact"},{"name":"tumour of oesophagus","type":"exact"},{"name":"tumour of the oesophagus","type":"exact"}],"termid":"MONDO:0021355","xrefs":{"Monarch":{"xref_id":"0021355"}}}


id: FYPO:0007105
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which sites at which the protein Rad52 accumulates remain present for a longer time than normal during the meiotic cell cycle. Normally, Rad52 foci form during prophase I but disappear before metaphase I.","definition_xrefs":["PMID:22292001","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype","termid":"FYPO:0004638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased duration of Rad52 focus presence during meiotic cell cycle","termid":"FYPO:0007105"}


id: MONDO:0020349
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute motor axonal neuropathy (AMAN) is a pure motor axonal form of Guillain-Barre syndrome (GBS).","definition_xrefs":["Orphanet:98918"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Guillain-Barre syndrome, familial","termid":"MONDO:0007691"},{"relation_name":"is_a","term_name":"Guillain-Barre syndrome","termid":"MONDO:0016218"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"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":"acute motor axonal neuropathy","secondary_identifiers":["SCTID:715770009","icd11.foundation:745197078","UMLS:C3890941","GARD:19602","NCIT:C116929","MEDGEN:855842"],"synonyms":[{"name":"AMAN","type":"exact"},{"name":"acute pure motor GBS","type":"exact"},{"name":"acute pure motor Guillain-Barre syndrome","type":"exact"},{"name":"acute pure motor Guillain-Barré syndrome","type":"exact"}],"termid":"MONDO:0020349","xrefs":{"Monarch":{"xref_id":"0020349"}}}


id: GO:0052176
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism involving glucans within the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete metabolism by symbiont of host glucan (obsolete GO:0052176)","termid":"GO:0052176"}


id: GO:0031436
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric complex comprising BRCA1 and BARD1, which possesses ubiquitin ligase activity and is involved in genome maintenance, possibly by functioning in surveillance for DNA damage.","definition_xrefs":["PMID:12787778"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear ubiquitin ligase complex","termid":"GO:0000152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"BRCA1-BARD1 complex","termid":"GO:0031436"}


id: PBO:0082005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger SWIM-type containing 5 pseudogene 1","termid":"PBO:0082005"}


id: MONDO:0007497
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":"ear antitragus, tag at base of","secondary_identifiers":["MEDGEN:343680","OMIM:128290","UMLS:C1851905"],"synonyms":[{"name":"ear antitragus, tag at base of","type":"exact"}],"termid":"MONDO:0007497","xrefs":{"Monarch":{"xref_id":"0007497"}}}


id: PBO:0047296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fatty acyl-CoA reductase 2 pseudogene 3","termid":"PBO:0047296"}


id: PBO:0054207
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 1587","termid":"PBO:0054207"}


id: PR:O14355
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC30D10.09c gene.","definition_xrefs":["UniProtKB:O14355","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized membrane protein C30D10.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC30D10.09c","synonyms":[{"name":"Spom972h-SPBC30D10.09c","type":"exact"}],"termid":"PR:O14355"}


id: PBO:0076614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 32","termid":"PBO:0076614"}


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


id: FYPO:0007497
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 fewer, larger nuclear exosome foci are present than normal. Nuclear exosome foci, also called Mmi1 foci, are small structures that form within the nucleus, and contain proteins involved in degrading meiosis-specific RNAs during the mitotic cell cycle, such as Mmi1, Iss10, and Red1.","definition_xrefs":["PomBase:mah","PMID:24920274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to nucleus during vegetative growth","termid":"FYPO:0001129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"aggregated nuclear exosome foci","synonyms":[{"name":"Mmi1 nuclear foci present in decreased numbers","type":"related"},{"name":"aggregated Mmi1 nuclear foci","type":"exact"},{"name":"aggregated nuclear exosome foci during mitotic cell cycle","type":"related"},{"name":"aggregated nuclear exosome foci during vegetative growth","type":"exact"},{"name":"nuclear exosome foci present in decreased numbers","type":"related"}],"termid":"FYPO:0007497"}


id: PBO:0089204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial heat shock protein Hsp10","termid":"PBO:0089204"}


id: MONDO:0002134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Physiological disturbances in normal sexual performance in either the male or the female.","definition_xrefs":["MESH:D012735"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"sexual and gender identity disorders","termid":"MONDO:0000595"},{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"physiological sexual disorder","secondary_identifiers":["UMLS:C0237873","DOID:1876","MEDGEN:66756"],"synonyms":[{"name":"Sex disorders","type":"broad"},{"name":"physiological sexual disorder","type":"exact"},{"name":"physiological sexual disorders","type":"related"},{"name":"physiological sexual dysfunction","type":"exact"},{"name":"physiological sexual dysfunctions","type":"related"},{"name":"sexual disorder, physiological","type":"related"},{"name":"sexual disorders, physiological","type":"related"},{"name":"sexual dysfunction","type":"broad"},{"name":"sexual dysfunctions, physiological","type":"related"}],"termid":"MONDO:0002134","xrefs":{"Monarch":{"xref_id":"0002134"}}}


id: PBO:0016902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA U3","termid":"PBO:0016902"}


id: GO:0043990
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H2A by the addition of an phosphate group to a serine residue at position 1 of the histone.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H2A-S1 phosphorylation (obsolete GO:0043990)","synonyms":[{"name":"histone H2A phosphorylation at S1","type":"exact"},{"name":"histone H2AS1 phosphorylation","type":"exact"}],"termid":"GO:0043990"}


id: FYPO:0003939
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of m7G(5')pppN diphosphatase 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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000661","FYPO:0000654"],"is_obsolete":false,"name":"abnormal m7G(5')pppN diphosphatase activity","synonyms":[{"name":"abnormal mRNA decapping activity","type":"related"}],"termid":"FYPO:0003939"}


id: MONDO:0008030
data:
  {"annotated_genes":["SJAG_02396"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85378],"is_not":false,"summary":null,"term":"MONDO:0008030"}]},"cv_name":"mondo","definition":"Any facioscapulohumeral muscular dystrophy in which the cause of the disease is a mutation in the FRG1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"facioscapulohumeral muscular dystrophy","termid":"MONDO:0001347"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02396":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0019303","MONDO:0005336"],"is_obsolete":false,"name":"facioscapulohumeral muscular dystrophy 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111192","NCIT:C172704","GARD:15087","MESH:C536391","OMIM:158900","MEDGEN:1727901","UMLS:C5399970"],"synonyms":[{"name":"FMD","type":"broad"},{"name":"FRG1 facioscapulohumeral muscular dystrophy","type":"exact"},{"name":"FSHD","type":"broad"},{"name":"FSHD1","type":"related"},{"name":"FSHD1A","type":"related"},{"name":"FSHMD1A","type":"related"},{"name":"Landouzy-Dejerine muscular dystrophy","type":"related"},{"name":"Landouzy-Dejerine muscular dystrophy facioscapulohumeral muscular dystrophy, infantile, included","type":"related"},{"name":"facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles","type":"related"},{"name":"facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles, included","type":"related"},{"name":"facioscapulohumeral muscular dystrophy","type":"broad"},{"name":"facioscapulohumeral muscular dystrophy 1","type":"exact"},{"name":"facioscapulohumeral muscular dystrophy 1A","type":"related"},{"name":"facioscapulohumeral muscular dystrophy caused by mutation in FRG1","type":"exact"},{"name":"facioscapulohumeral muscular dystrophy type 1","type":"exact"},{"name":"facioscapulohumeral muscular dystrophy, infantile","type":"related"},{"name":"muscular dystrophy, facioscapulohumeral","type":"related"},{"name":"muscular dystrophy, facioscapulohumeral, type 1","type":"related"},{"name":"muscular dystrophy, facioscapulohumeral, type 1A","type":"narrow"}],"termid":"MONDO:0008030","terms_by_termid":{"MONDO:0008030":null},"xrefs":{"Monarch":{"xref_id":"0008030"}}}


id: MONDO:0042498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"intellectual disability","termid":"MONDO:0001071"},{"relation_name":"excluded_subClassOf","term_name":"ichthyosis","termid":"MONDO:0019269"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ruzicka-Goerz-Anton syndrome","secondary_identifiers":["MESH:C537192","MEDGEN:444055","UMLS:C2931438"],"synonyms":[{"name":"Ruzicka Goerz Anton syndrome","type":"exact"},{"name":"ichthyosis congenita, neurosensory deafness, oligophrenia, dental aplasia, brachydactyly, clinodactyly, accessory cervical ribs and thyroid carcinoma","type":"related"},{"name":"ichthyosis deafness intellectual disability skeletal anomalies","type":"related"},{"name":"ichthyosis deafness mental retardation skeletal anomalies","type":"related"}],"termid":"MONDO:0042498","xrefs":{"Monarch":{"xref_id":"0042498"}}}


id: PBO:0003294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NatC N-acetyltransferase non catalytic Sm-like domain subunit Naa38 (predicted)","termid":"PBO:0003294"}


id: MONDO:0005775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An X-linked genetic condition caused by alterations in the gene G6PD that result in moderately to severely decreased activity levels of the enzyme glucose-6-phosphate dehydrogenase. Most individuals with G6PD deficiency are asymptomatic throughout their life. Individuals with G6PD variants that cause G6PD deficiency are at risk for severe neonatal jaundice. These individuals are also at risk for acute hemolytic anemia in response to certain medication exposures, chemical exposures, infections, or consumption of fava beans.","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn carbohydrate metabolic disorder","termid":"MONDO:0019214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"G6PD deficiency","secondary_identifiers":["UMLS:C2939465","NANDO:2200627","NCIT:C98933","MESH:D005955","SCTID:62403005","EFO:0007287","MEDGEN:473706","DOID:2862"],"synonyms":[{"name":"G-6-PD variant enzyme deficiency Anaemia","type":"exact"},{"name":"G-6-PD variant enzyme deficiency Anemia","type":"exact"},{"name":"G6PD","type":"exact"},{"name":"G6PD deficiency","type":"exact"},{"name":"deficiency of G-6PD","type":"exact"},{"name":"glucose-6-phosphate dehydrogenase deficiency","type":"exact"},{"name":"glucosephosphate dehydrogenase deficiency","type":"exact"},{"name":"inborn error of glucose-6-phosphate dehydrogenase activity","type":"exact"},{"name":"inborn glucose-6-phosphate dehydrogenase activity disorder","type":"exact"},{"name":"rare inborn error of glucose-6-phosphate dehydrogenase activity","type":"exact"}],"termid":"MONDO:0005775","xrefs":{"Monarch":{"xref_id":"0005775"}}}


id: GO:0009574
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A dense band of microtubules, 1-3 pm wide, that appears just beneath the cell membrane before the start of cell division in the cells of higher plants. It precedes the onset of prophase and then disappears as mitosis begins, yet it somehow determines the plane of orientation of the new cell plate forming in late telophase and marks the zone of the parental cell wall where fusion with the growing cell plate ultimately occurs.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"},{"relation_name":"part_of","term_name":"microtubule cytoskeleton","termid":"GO:0015630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0015630"],"is_obsolete":false,"name":"preprophase band","secondary_identifiers":["Wikipedia:Preprophase_band"],"termid":"GO:0009574"}


id: MONDO:0002799
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete nodular medulloblastoma (obsolete MONDO:0002799)","termid":"MONDO:0002799","xrefs":{"Monarch":{"xref_id":"0002799"}}}


id: MONDO:0014879
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete patent ductus arteriosus 3 (obsolete MONDO:0014879)","termid":"MONDO:0014879","xrefs":{"Monarch":{"xref_id":"0014879"}}}


id: PATO:0025000
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the bearer's disposition to being fit to be used as a safe means of hydration.","definition_xrefs":["Wikipedia:https://en.wikipedia.org/wiki/Drinking_water"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potability","synonyms":[{"name":"drinkability","type":"exact"}],"termid":"PATO:0025000"}


id: PBO:0072151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 28","termid":"PBO:0072151"}


id: PBO:0027631
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_acetylation_at_subtelomere","termid":"PBO:0027631"}


id: PBO:0080961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 4","termid":"PBO:0080961"}


id: GO:0010572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate or frequency of platelet activation. Platelet activation is a series of progressive, overlapping events triggered by exposure of the platelets to subendothelial tissue.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of platelet activation","termid":"GO:0010543"},{"relation_name":"is_a","term_name":"positive regulation of cell activation","termid":"GO:0050867"},{"relation_name":"positively_regulates","term_name":"platelet activation","termid":"GO:0030168"}],"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 platelet activation","termid":"GO:0010572"}


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


id: 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: SO:0001692
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A site where restriction enzymes can cleave that will produce an overhang or 'sticky end'.","direct_ancestors":[{"relation_name":"is_a","term_name":"restriction_enzyme_recognition_site","termid":"SO:0001687"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sticky_end_restriction_enzyme_cleavage_site","synonyms":[{"name":"sticky end restriction enzyme cleavage site","type":"related"}],"termid":"SO:0001692"}


id: GO:0034247
data:
  {"annotated_genes":["SJAG_03112"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102201],"is_not":false,"summary":null,"term":"GO:0034247"}]},"cv_name":"biological_process","definition":"The process of removing sections of a primary snoRNA transcript to remove sequences not present in the mature form of the snoRNA and joining the remaining sections to form the mature form of the snoRNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA splicing","termid":"GO:0008380"},{"relation_name":"is_a","term_name":"sno(s)RNA processing","termid":"GO:0043144"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03112":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0016074"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0016074"],"is_obsolete":false,"name":"snoRNA splicing","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0034247","terms_by_termid":{"GO:0034247":null}}


id: PBO:0066472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger and FYVE like domain containing E3 ubiquitin protein ligase","termid":"PBO:0066472"}


id: PBO:0075969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"StAR related lipid transfer domain containing 9","termid":"PBO:0075969"}


id: PBO:0089301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH/NADPH-dependent indole-3-acetaldehyde reductase, implicated in cellular detoxification","termid":"PBO:0089301"}


id: MONDO:0007810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ichthyosis vulgaris is a common skin disorder passed down through families that leads to dry, scaly skin. It often begins in early childhood. Treatment may include heavy duty moisturizers which contain chemicals that help the skin to shed normally, including lactic acid, salicylic acid, and urea. Ichthyosis vulgaris can be a nuisance, but it rarely affects overall health. The condition usually disappears during adulthood, but may return in later years. This condition is inherited in an autosomal dominant pattern.","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"ichthyosis vulgaris","termid":"MONDO:0024304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant ichthyosis vulgaris","secondary_identifiers":["NCIT:C84778","Orphanet:462","UMLS:C0432300","MEDGEN:609440","SCTID:254157005","ICD10CM:Q80.0","OMIM:146700","DOID:1702"],"synonyms":[{"name":"autosomal dominant ichthyosis vulgaris","type":"exact"},{"name":"dominant congenital ichthyosiform erythroderma","type":"exact"},{"name":"dominant ichthyosis vulgaris","type":"related"},{"name":"ichthyosis simplex","type":"related"},{"name":"ichthyosis vulgaris","type":"related"},{"name":"ichthyosis vulgaris, autosomal dominant","type":"exact"}],"termid":"MONDO:0007810","xrefs":{"Monarch":{"xref_id":"0007810"}}}


id: MONDO:0971032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acquired metabolic disease that is characterized by ethanol fermentation in the bladder and the absence of alcoholic intoxication.","definition_xrefs":["DOID:0081456"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"bladder fermentation syndrome","termid":"MONDO:0971032","xrefs":{"Monarch":{"xref_id":"0971032"}}}


id: PBO:0029536
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_microcolony,_small_cells_(obsolete_FYPO:0002186)","termid":"PBO:0029536"}


id: PATO:0002631
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An occurrence of a process during which time there is an inability to change the course, extent, or repetition of the process.","definition_xrefs":["PATO:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"occurrence","termid":"PATO:0000057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"refractory","termid":"PATO:0002631"}


id: GO:0035482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The spontaneous peristaltic movements of the stomach that aid in digestion, moving food through the stomach and out through the pyloric sphincter into the duodenum.","definition_xrefs":["ISBN:9781416032458","GOC:cy","PMID:16139031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system process","termid":"GO:0022600"}],"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":"gastric motility","termid":"GO:0035482"}


id: PBO:0081190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zic family member 3","termid":"PBO:0081190"}


id: MONDO:0017178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare bone disease characterized by an acquired idiopathic necrotic lesion of subchondral bone with the formation of a sequestrum, which may detach to form loose bodies in joints. OCD mainly affects the knee, ankle and elbow joints and can lead to pain, functional limitations and secondary osteoarthritis.","definition_xrefs":["Orphanet:2764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteonecrosis of genetic origin","termid":"MONDO:0018383"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteochondritis dissecans","secondary_identifiers":["UMLS:C0029421","HP:0010886","ICD9:732.7","NCIT:C34878","GARD:12703","DOID:84","MESH:D010008","SCTID:82562007","MEDGEN:10494","icd11.foundation:467851106","NORD:111730","MedDRA:10031231"],"synonyms":[{"name":"Koenig disease","type":"exact"},{"name":"Konig disease","type":"exact"},{"name":"König disease","type":"exact"},{"name":"OCD","type":"exact"},{"name":"OD","type":"exact"},{"name":"SSOAOD","type":"related"},{"name":"familial osteochondritis dissecans","type":"narrow"},{"name":"osteochondritis dissecans","type":"exact"},{"name":"osteochondritis dissecans (disease)","type":"exact"},{"name":"osteochondritis dissecans and short stature","type":"related"},{"name":"osteochondritis dissecans, short stature, and early-onset osteoarthritis","type":"related"},{"name":"short stature and advanced bone Age, with or without early-onset osteoarthritis and/Or osteochondritis Dissecans","type":"related"}],"termid":"MONDO:0017178","xrefs":{"Monarch":{"xref_id":"0017178"}}}


id: PBO:0000093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short chain dehydrogenase (predicted)","termid":"PBO:0000093"}


id: GO:0005368
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of taurine from one side of a membrane to the other. Taurine (2-aminoethanesulfonic acid) is a sulphur-containing amino acid derivative which is important in the metabolism of fats.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic acid transmembrane transporter activity","termid":"GO:0005342"},{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"sulfur compound transmembrane transporter activity","termid":"GO:1901682"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"taurine transmembrane transporter activity","termid":"GO:0005368"}


id: PATO:0002143
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"sloped","termid":"PATO:0001481"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sloped downward","termid":"PATO:0002143"}


id: PBO:0054978
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 2392","termid":"PBO:0054978"}


id: FYECO:0000252
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which glycerol was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ glycerol","synonyms":[{"name":"glycerol added","type":"exact"}],"termid":"FYECO:0000252"}


id: PBO:0083761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential kinetochore protein; component of the CBF3 complex that binds the CDEIII region of the centromere; contains an N-terminal Zn2Cys6 type zinc finger domain, a C-terminal acidic domain, and a putative coiled coil dimerization domain","termid":"PBO:0083761"}


id: GO:0036346
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 L-cysteine stimulus. L-cysteine is an optically active form of cysteine having L-configuration.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amino acid stimulus","termid":"GO:0071230"},{"relation_name":"is_a","term_name":"response to L-cysteine","termid":"GO:1901367"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to L-cysteine","termid":"GO:0036346"}


id: PBO:0046201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin A3, pseudogene","termid":"PBO:0046201"}


id: PBO:0063283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma subfamily A, 9","termid":"PBO:0063283"}


id: PBO:0062929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolyl 3-hydroxylase 2","termid":"PBO:0062929"}


id: FYPO:0002469
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells that are longer than normal and taper at one end to a diameter smaller than the other. Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:vw","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, elongated tapered cells (obsolete FYPO:0002469)","synonyms":[{"name":"inviable microcolony, elongated bottle/skittle cells","type":"exact"},{"name":"inviable microcolony, elongated skittle-shaped cells","type":"exact"},{"name":"inviable microcolony, elongated tapered vegetative cells","type":"exact"}],"termid":"FYPO:0002469"}


id: MONDO:0002154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection that is caused by Trichomonas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protozoa infectious disease","termid":"MONDO:0002428"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trichomoniasis","secondary_identifiers":["ICD10CM:A59","icd11.foundation:1220564554","MEDGEN:52838","SCTID:56335008","NCIT:C35720","DOID:1947","ICD9:131","ICD9:131.8","UMLS:C0040921","MESH:D014245","ICD9:131.9"],"synonyms":[{"name":"Trichomonas infection","type":"exact"},{"name":"infections, Trichomonas","type":"related"}],"termid":"MONDO:0002154","xrefs":{"Monarch":{"xref_id":"0002154"}}}


id: PBO:0083688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Enolase II, a phosphopyruvate hydratase; catalyzes conversion of 2-phosphoglycerate to phosphoenolpyruvate during glycolysis and the reverse reaction during gluconeogenesis; expression induced in response to glucose; ENO2 has a paralog, ENO1, that arose from the whole genome duplication","termid":"PBO:0083688"}


id: PBO:0036362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E4 involved in splicing Prp19","termid":"PBO:0036362"}


id: GO:1905721
data:
  {"annotated_genes":["SJAG_02695"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[96168],"is_not":false,"summary":null,"term":"GO:1905721"}]},"cv_name":"cellular_component","definition":"Any microtubule end that is part of a mitotic spindle astral microtubule.","definition_xrefs":["GO_REF:0000064","PMID:11007487","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule end","termid":"GO:1990752"},{"relation_name":"part_of","term_name":"mitotic spindle astral microtubule","termid":"GO:0061673"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02695":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:0015630"},{"rel_name":"part_of","termid":"GO:0072686"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0072686","GO:0015630"],"is_obsolete":false,"name":"mitotic spindle astral microtubule end","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitotic spindle astral microtubule tip","type":"exact"}],"termid":"GO:1905721","terms_by_termid":{"GO:1905721":null}}


id: PBO:0084650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Minor isoform of large subunit of ribonucleotide-diphosphate reductase; the RNR complex catalyzes rate-limiting step in dNTP synthesis, regulated by DNA replication and DNA damage checkpoint pathways via localization of small subunits; RNR3 has a paralog, RNR1, that arose from the whole genome duplication","termid":"PBO:0084650"}


id: PATO:0001462
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a cell's plasma membrane by virtue of the electrical potential difference across it.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Membrane_potential"],"direct_ancestors":[{"relation_name":"is_a","term_name":"electric potential","termid":"PATO:0001464"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane potential","termid":"PATO:0001462"}


id: GO:0099574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates synaptic transmission by regulating protein degradation at the synapse.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of chemical synaptic transmission","termid":"GO:0050804"},{"relation_name":"is_a","term_name":"regulation protein catabolic process at synapse","termid":"GO:0140250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of protein catabolic process at synapse, modulating synaptic transmission","termid":"GO:0099574"}


id: GO:0048363
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the pectin component of mucilage.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pectin metabolic process","termid":"GO:0045488"},{"relation_name":"part_of","term_name":"mucilage metabolic process","termid":"GO:0010191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"mucilage pectin metabolic process","synonyms":[{"name":"mucilage pectin metabolism","type":"exact"}],"termid":"GO:0048363"}


id: GO:0035804
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of an egg coat. An egg coat is a specialized extracellular matrix that surrounds the ovum of animals. The egg coat provides structural support and can play an essential role in oogenesis, fertilization and early development.","definition_xrefs":["PMID:17163408","PMID:16944418"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix structural constituent","termid":"GO:0005201"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005198"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005198","GO:0003674"],"is_obsolete":false,"name":"structural constituent of egg coat","synonyms":[{"name":"structural constituent of vitelline envelope","type":"narrow"},{"name":"structural constituent of zona pellucida","type":"narrow"}],"termid":"GO:0035804"}


id: PBO:0081759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 689","termid":"PBO:0081759"}


id: GO:0042621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly(3-hydroxyalkanoates), polyesters of 3-hydroxyacids produced as intracellular granules by a large variety of bacteria.","definition_xrefs":["GOC:jl","PMID:9925580"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"poly(3-hydroxyalkanoate) metabolic process","termid":"GO:0042620"}],"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":"poly(3-hydroxyalkanoate) biosynthetic process","synonyms":[{"name":"PHA biosynthesis","type":"broad"},{"name":"PHA biosynthetic process","type":"broad"},{"name":"poly(3-hydroxyalkanoate) anabolism","type":"exact"},{"name":"poly(3-hydroxyalkanoate) biosynthesis","type":"exact"},{"name":"poly(3-hydroxyalkanoate) formation","type":"exact"},{"name":"poly(3-hydroxyalkanoate) synthesis","type":"exact"}],"termid":"GO:0042621"}


id: PBO:0073252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEPTIN4 antisense RNA 1","termid":"PBO:0073252"}


id: MONDO:0002101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm involving a facial nerve.","definition_xrefs":["MONDO:patterns/neoplasm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"facial nerve disorder","termid":"MONDO:0002098"},{"relation_name":"is_a","term_name":"cranial nerve neoplasm","termid":"MONDO:0002633"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"facial nerve neoplasm","secondary_identifiers":["UMLS:C1263899","SCTID:126973004","DOID:1760","ICD9:239.7","NCIT:C5827","MEDGEN:224733"],"synonyms":[{"name":"VIIth cranial nerve neoplasms","type":"exact"},{"name":"VIIth cranial nerve tumors","type":"exact"},{"name":"VIIth cranial nerve tumours","type":"exact"},{"name":"facial nerve neoplasm","type":"exact"},{"name":"facial nerve neoplasm (disease)","type":"exact"},{"name":"facial nerve neoplasms","type":"exact"},{"name":"facial nerve tumor","type":"exact"},{"name":"facial nerve tumors","type":"exact"},{"name":"facial nerve tumour","type":"exact"},{"name":"facial nerve tumours","type":"exact"},{"name":"neoplasm of Facial nerve","type":"exact"},{"name":"neoplasm of facial nerve","type":"exact"},{"name":"neoplasm of seventh cranial nerve","type":"exact"},{"name":"neoplasm of the Facial nerve","type":"exact"},{"name":"neoplasm of the seventh cranial nerve","type":"exact"},{"name":"seventh cranial nerve neoplasm","type":"exact"},{"name":"seventh cranial nerve neoplasms","type":"exact"},{"name":"seventh cranial nerve tumor","type":"exact"},{"name":"seventh cranial nerve tumors","type":"exact"},{"name":"seventh cranial nerve tumour","type":"exact"},{"name":"seventh cranial nerve tumours","type":"exact"},{"name":"tumor of Facial nerve","type":"exact"},{"name":"tumor of facial nerve","type":"exact"},{"name":"tumor of seventh cranial nerve","type":"exact"},{"name":"tumor of the Facial nerve","type":"exact"},{"name":"tumor of the seventh cranial nerve","type":"exact"},{"name":"tumour of Facial nerve","type":"exact"},{"name":"tumour of facial nerve","type":"exact"},{"name":"tumour of seventh cranial nerve","type":"exact"},{"name":"tumour of the Facial nerve","type":"exact"},{"name":"tumour of the seventh cranial nerve","type":"exact"}],"termid":"MONDO:0002101","xrefs":{"Monarch":{"xref_id":"0002101"}}}


id: FYPO:0004542
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 chromatin silencing at subtelomeric regions is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin silencing at subtelomere","termid":"FYPO:0000169"},{"relation_name":"is_a","term_name":"increased gene silencing","termid":"FYPO:0000577"},{"relation_name":"is_a","term_name":"increased chromatin silencing","termid":"FYPO:0004540"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0006551"],"is_obsolete":false,"name":"increased chromatin silencing at subtelomere","secondary_identifiers":["FYPO:0006367"],"synonyms":[{"name":"increased chromatin silencing at subtelomere during mitotic cell cycle","type":"related"},{"name":"increased chromatin silencing at subtelomere during vegetative growth","type":"exact"},{"name":"increased chromatin silencing at telomere","type":"related"}],"termid":"FYPO:0004542"}


id: PBO:0058899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 12117","termid":"PBO:0058899"}


id: FYPO:0006677
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of DNA binding at double-strand break sites by a gene product is decreased, when a gene or the bound DNA sequence is mutated. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PMID:30104346","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased DNA binding","termid":"FYPO:0000658"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000653"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000653"],"is_obsolete":false,"name":"decreased DNA binding at double-strand break","synonyms":[{"name":"decreased DNA binding at site of double-strand break","type":"exact"},{"name":"decreased double-stranded DNA break binding","type":"exact"},{"name":"reduced DNA binding at double-strand break","type":"exact"}],"termid":"FYPO:0006677"}


id: PATO:0000268
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000268 absolute visual threshold (obsolete PATO:0000268)","termid":"PATO:0000268"}


id: MONDO:1010609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Exocrine pancreatic insufficiency that occurs in tiger.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocrine pancreatic insufficiency, non-human animal","termid":"MONDO:1010058"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocrine pancreatic insufficiency, tiger","secondary_identifiers":["OMIA:000765-9694"],"termid":"MONDO:1010609","xrefs":{"Monarch":{"xref_id":"1010609"}}}


id: GO:0071701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the directed movement of a MAP kinase from the nucleus to the cytoplasm.","definition_xrefs":["GOC:dgf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of MAPK export from nucleus (obsolete GO:0071701)","synonyms":[{"name":"regulation of MAPK export from cell nucleus","type":"exact"},{"name":"regulation of MAPK export out of nucleus","type":"exact"},{"name":"regulation of MAPK transport from nucleus to cytoplasm","type":"exact"},{"name":"regulation of MAPK-nucleus export","type":"exact"},{"name":"regulation of cytoplasmic translocation of MAP kinase","type":"exact"},{"name":"regulation of cytoplasmic translocation of mitogen-activated protein kinase","type":"exact"}],"termid":"GO:0071701"}


id: PBO:0084950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Multigene complex, polymeric locus for maltose fermentation; encodes the MAL63 trans-acting MAL-activator, MAL61 maltose permease, and MAL62 maltase; on the left arm of Chromosome VIII, but not in strain S288C","termid":"PBO:0084950"}


id: _global:regulates_o_results_in_division_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"This is the combination of the regulates relation with the results_in_division_of relation.","definition_xrefs":["GOC:mtg_berkeley_2013"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_division_of","secondary_identifiers":["GOREL:0001024"],"termid":"_global:regulates_o_results_in_division_of"}


id: GO:0101003
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a ficolin-1-rich granule.","definition_xrefs":["PMID:23650620","GOC:mec"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule membrane","termid":"GO:0030667"},{"relation_name":"part_of","term_name":"tertiary granule","termid":"GO:0070820"},{"relation_name":"part_of","term_name":"ficolin-1-rich granule","termid":"GO:0101002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"ficolin-1-rich granule membrane","termid":"GO:0101003"}


id: MONDO:0012045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopia","termid":"MONDO:0001384"}],"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":"myopia 5, autosomal dominant","secondary_identifiers":["MEDGEN:324913","MESH:C563922","UMLS:C1837972","OMIM:608474"],"synonyms":[{"name":"MYP5","type":"exact"},{"name":"myopia 5, autosomal dominant","type":"exact"}],"termid":"MONDO:0012045","xrefs":{"Monarch":{"xref_id":"0012045"}}}


id: PBO:0083107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ-like chaperone required for nuclear membrane fusion during mating; localizes to the ER membrane; exhibits genetic interactions with KAR2","termid":"PBO:0083107"}


id: MONDO:0011057
data:
  {"annotated_genes":["SJAG_03145"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013542"}]},"cv_name":"mondo","definition":"A disorder resulting from inadequate blood flow in the vessels that supply the brain. Representative examples include cerebrovascular ischemia, cerebral embolism, and cerebral infarction.","definition_xrefs":["NCIT:C2938"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"arterial disorder","termid":"MONDO:0000473"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03145":null},"genotype_count":0,"is_obsolete":false,"name":"cerebrovascular disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:434.91","MESH:D002561","ICD10CM:I60-I69","MEDGEN:858","SCTID:62914000","ICD9:437.8","EFO:0003763","ICD9:430-438.99","UMLS:C0007820","ICD9:437.9","DOID:6713"],"synonyms":[{"name":"CVA","type":"narrow"},{"name":"CVA (cerebral vascular accident)","type":"narrow"},{"name":"cerebral infarction","type":"narrow"},{"name":"cerebrovascular accident","type":"narrow"},{"name":"cerebrovascular disease","type":"exact"},{"name":"cerebrovascular disorder","type":"exact"},{"name":"stroke","type":"narrow"}],"termid":"MONDO:0011057","terms_by_termid":{"MONDO:0013542":null},"xrefs":{"Monarch":{"xref_id":"0011057"}}}


id: PBO:0018079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly protein Isa2","termid":"PBO:0018079"}


id: GO:0006425
data:
  {"annotated_genes":["SJAG_04482"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108446],"is_not":false,"summary":null,"term":"GO:0006425"}]},"cv_name":"biological_process","definition":"The process of coupling glutamine to glutaminyl-tRNA, catalyzed by glutaminyl-tRNA synthetase. The glutaminyl-tRNA synthetase is a class-I synthetase. The activated amino acid is transferred to the 2'-OH group of a glutamine-accetping tRNA. The 2'-O-aminoacyl-tRNA will ultimately migrate to the 3' position via transesterification.","definition_xrefs":["ISBN:0716730510","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA aminoacylation for protein translation","termid":"GO:0006418"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04482":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0010467","GO:0006399","GO:0008150"],"is_obsolete":false,"name":"glutaminyl-tRNA aminoacylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0006425","terms_by_termid":{"GO:0006425":null}}


id: GO:0018609
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,3-unsubstituted benzenoid + O2 + NAD(P)H + H+ = 2,3-cis-dihydroxydihydrobenzenoid + NAD(P)+. Substrates include 1,4-dichlorobenzene (forms 3,6-dichloro-cis-1,2-dihydroxycyclohexa-3,5-diene), 1,2,3,4-tetrachlorobenzene (forms cis-chlorobenzene dihydrodiol) and 1,2,4-trichlorobenzene (forms 3,4,6-trichloro-cis-1,2-dihydroxycyclohexa-3,5-diene).","definition_xrefs":["UM-BBD_enzymeID:e0062"],"gene_count":0,"genotype_count":0,"name":"obsolete chlorobenzene dioxygenase activity (obsolete GO:0018609)","termid":"GO:0018609"}


id: PBO:0000275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"related to neuronal calcium sensor Ncs1","termid":"PBO:0000275"}


id: MONDO:0014838
data:
  {"annotated_genes":["SJAG_03576"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84846],"is_not":false,"summary":null,"term":"MONDO:0014838"}]},"cv_name":"mondo","definition":"Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCE1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Coffin-Siris syndrome","termid":"MONDO:0015452"},{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03576":null},"genotype_count":0,"is_obsolete":false,"name":"Coffin-Siris syndrome 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:616938","GARD:16170","DOID:0112368","MEDGEN:934755","UMLS:C4310788"],"synonyms":[{"name":"COFFIN-SIRIS syndrome 5","type":"related"},{"name":"CSS5","type":"related"},{"name":"Coffin-Siris syndrome 5","type":"exact"},{"name":"Coffin-Siris syndrome caused by mutation in SMARCE1","type":"exact"},{"name":"Coffin-Siris syndrome type 5","type":"exact"},{"name":"SMARCE1 Coffin-Siris syndrome","type":"exact"}],"termid":"MONDO:0014838","terms_by_termid":{"MONDO:0014838":null},"xrefs":{"Monarch":{"xref_id":"0014838"}}}


id: FYECO:0000295
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"A sequential growth condition in which cells are first grown at a low temperature, transferred to standard, and then to high temperature.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping sequential growth conditions","termid":"FYECO:0000094"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"two-step temperature shift, low to standard, standard to high","termid":"FYECO:0000295"}


id: MONDO:0020525
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Transient neonatal diabetes mellitus (TNDM) is a genetically heterogeneous form of neonatal diabetes (NDM) characterized by hyperglycemia presenting in the neonatal period that remits during infancy but recurs in later life in most patients.","definition_xrefs":["Orphanet:99886"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal diabetes mellitus","termid":"MONDO:0016391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005015"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005015","MONDO:0004335"],"is_obsolete":false,"name":"transient neonatal diabetes mellitus","secondary_identifiers":["DOID:0060334","icd11.foundation:1596856936","HP:0008255","NCIT:C114899","SCTID:237603002","UMLS:C0342273","MEDGEN:449530"],"synonyms":[{"name":"TNDM","type":"exact"},{"name":"chromosome 6-associated transient diabetes mellitus","type":"related"},{"name":"diabetes mellitus, 6q24-related transient neonatal","type":"related"},{"name":"diabetes mellitus, transient neonatal","type":"related"},{"name":"transient neonatal diabetes mellitus","type":"exact"},{"name":"transient neonatal diabetes mellitus (disease)","type":"exact"}],"termid":"MONDO:0020525","xrefs":{"Monarch":{"xref_id":"0020525"}}}


id: PBO:0078925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon ACG) 2-1","termid":"PBO:0078925"}


id: MONDO:0008400
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Presence of small calculi in the terminal salivary ducts (salivary sand), or stones (larger calculi) found in the larger ducts.","definition_xrefs":["MESH:D012465"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"salivary duct calculi","secondary_identifiers":["MEDGEN:19865","OMIM:181010","UMLS:C0036089"],"synonyms":[{"name":"parotid duct calculi","type":"related"},{"name":"salivary duct calculi","type":"exact"},{"name":"submandibular duct calculi","type":"related"}],"termid":"MONDO:0008400","xrefs":{"Monarch":{"xref_id":"0008400"}}}


id: PBO:0029772
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_spore_shape","termid":"PBO:0029772"}


id: GO:0050104
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-gulonate + NAD+ = 3-dehydro-L-gulonate + H+ + NADH.","definition_xrefs":["RHEA:12889","EC:1.1.1.45"],"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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"L-gulonate 3-dehydrogenase activity","secondary_identifiers":["Reactome:R-HSA-5661290","MetaCyc:L-GULONATE-3-DEHYDROGENASE-RXN","KEGG_REACTION:R02640"],"synonyms":[{"name":"L-3-aldonate dehydrogenase activity","type":"related"},{"name":"L-3-aldonic dehydrogenase activity","type":"related"},{"name":"L-3-hydroxyacid dehydrogenase activity","type":"related"},{"name":"L-beta-hydroxy-acid-NAD-oxidoreductase activity","type":"related"},{"name":"L-beta-hydroxyacid dehydrogenase activity","type":"related"},{"name":"L-gulonate:NAD+ 3-oxidoreductase activity","type":"related"},{"name":"L-gulonic acid dehydrogenase activity","type":"related"}],"termid":"GO:0050104"}


id: PBO:0075083
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 133","termid":"PBO:0075083"}


id: PBO:0074873
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 56","termid":"PBO:0074873"}


id: MONDO:0968983
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"proteosome-associated autoinflammatory syndrome","termid":"MONDO:0009726"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0006025"],"is_obsolete":false,"name":"proteasome-associated autoinflammatory syndrome 6","secondary_identifiers":["OMIM:620796"],"termid":"MONDO:0968983","xrefs":{"Monarch":{"xref_id":"0968983"}}}


id: GO:0046512
data:
  {"annotated_genes":["SJAG_01057","SJAG_02706","SJAG_04178","SJAG_00880","SJAG_02305","SJAG_02429"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91980,96098,96855,104700,105148,108867],"is_not":false,"summary":null,"term":"GO:0046512"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sphingosine (sphing-4-enine), trans-D-erytho-2-amino-octadec-4-ene-1,3-diol, a long chain amino diol sphingoid base that occurs in most sphingolipids in animal tissues.","definition_xrefs":["ISBN:0198506732","GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphingosine metabolic process","termid":"GO:0006670"},{"relation_name":"is_a","term_name":"diol biosynthetic process","termid":"GO:0034312"},{"relation_name":"is_a","term_name":"sphingoid biosynthetic process","termid":"GO:0046520"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00880":null,"SJAG_01057":null,"SJAG_02305":null,"SJAG_02429":null,"SJAG_02706":null,"SJAG_04178":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"sphingosine biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"sphingosine anabolism","type":"exact"},{"name":"sphingosine biosynthesis","type":"exact"},{"name":"sphingosine formation","type":"exact"},{"name":"sphingosine synthesis","type":"exact"}],"termid":"GO:0046512","terms_by_termid":{"GO:0046512":null}}


id: MONDO:0034054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"severe combined immunodeficiency","termid":"MONDO:0015974"},{"relation_name":"is_a","term_name":"lymphoproliferative syndrome","termid":"MONDO:0016537"}],"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":"severe combined immunodeficiency due to CD70 deficiency","secondary_identifiers":["Orphanet:538958","UMLS:C5568559","MEDGEN:1799982","GARD:17978","OMIM:618261"],"synonyms":[{"name":"lymphoproliferative syndrome 3","type":"exact"}],"termid":"MONDO:0034054","xrefs":{"Monarch":{"xref_id":"0034054"}}}


id: GO:0071229
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 stimulus by the chemical structure of the anion portion of the dissociated acid (rather than the acid acting as a proton donor). The acid chemical may be in gaseous, liquid or solid form.","definition_xrefs":["GOC:mah","Wikipedia:Acid","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to acid chemical","termid":"GO:0001101"},{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"}],"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 acid chemical","synonyms":[{"name":"cellular response to acid","type":"broad"},{"name":"cellular response to acid anion","type":"related"},{"name":"cellular response to oxoanion","type":"related"}],"termid":"GO:0071229"}


id: PBO:0080188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular endothelial growth factor A","termid":"PBO:0080188"}


id: PBO:0005394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol 1,3,4,5,6-pentakisphosphate (IP5) kinase","termid":"PBO:0005394"}


id: GO:0086004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac muscle cell contraction.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac muscle contraction","termid":"GO:0055117"},{"relation_name":"is_a","term_name":"regulation of actin filament-based movement","termid":"GO:1903115"},{"relation_name":"regulates","term_name":"cardiac muscle cell contraction","termid":"GO:0086003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cardiac muscle cell contraction","termid":"GO:0086004"}


id: GO:0001596
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"An angiotensin receptor activity that acts via Gq-mediated activation of phospholipase C followed by phosphoinositide hydrolysis and Ca2+ signaling, and may act via additional signaling mechanisms.","definition_xrefs":["PMID:10977869","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiotensin receptor activity","termid":"GO:0001595"}],"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:0038023","GO:0003674"],"is_obsolete":false,"name":"angiotensin type I receptor activity","synonyms":[{"name":"PLC-activating angiotensin receptor activity","type":"exact"}],"termid":"GO:0001596"}


id: PR:G2TRN9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC11D3.11c gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRN9"],"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 transcriptional regulatory protein C11D3.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11D3.11c","synonyms":[{"name":"Spom972h-SPAC11D3.11c","type":"exact"}],"termid":"PR:G2TRN9"}


id: MONDO:0019479
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant neoplasm with a poor response to therapy, usually presenting as stage III/IV disease. It is characterized by the presence of neoplastic cells with morphologic and immunophenotypic characteristics similar to those seen in mature histiocytes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histiocytic and dendritic cell neoplasm","termid":"MONDO:0006247"}],"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":"histiocytic sarcoma","secondary_identifiers":["SCTID:109988003","UMLS:C0334663","MESH:D054747","GARD:19080","ICD10CM:C96.A","DOID:0080915","icd11.foundation:1925254893","icd11.foundation:911785965","ICD9:171.9","ICDO:9755/3","ONCOTREE:HS","Orphanet:86896","NCIT:C27349","MEDGEN:137793"],"synonyms":[{"name":"histiocytic sarcoma","type":"exact"},{"name":"sarcoma, histiocytic, malignant","type":"exact"}],"termid":"MONDO:0019479","xrefs":{"Monarch":{"xref_id":"0019479"}}}


id: PBO:0069285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 541, pseudogene","termid":"PBO:0069285"}


id: PBO:0087364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sporulation-specific exo-1,3-beta-glucanase; contributes to ascospore thermoresistance; SPR1 has a paralog, EXG1, that arose from the whole genome duplication","termid":"PBO:0087364"}


id: MOD:01226
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to an L-fluorotryptophan.","definition_xrefs":["Unimod:127#W","PubMed:8069568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fluorinated residue","termid":"MOD:00498"},{"relation_name":"is_a","term_name":"halogenated tryptophan","termid":"MOD:01068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monofluorinated L-tryptophan","synonyms":[{"name":"Fluoro","type":"related"},{"name":"fluorophenylalanine replacement of phenylalanine","type":"related"}],"termid":"MOD:01226"}


id: MONDO:0005411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the gall bladder","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"biliary tract cancer","termid":"MONDO:0003060"},{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"},{"relation_name":"is_a","term_name":"gallbladder neoplasm","termid":"MONDO:0021253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"gallbladder cancer","secondary_identifiers":["ICD9:156.0","ICD9:156.8","SCTID:363353009","UMLS:C0153452","DOID:3121","MEDGEN:57784","NCIT:C7481","ONCOTREE:GBC"],"synonyms":[{"name":"cancer of gall bladder","type":"exact"},{"name":"gall bladder cancer","type":"exact"},{"name":"gallbladder Ca","type":"exact"},{"name":"gallbladder neoplasm","type":"broad"},{"name":"localised malignant gallbladder neoplasm","type":"narrow"},{"name":"localized malignant gallbladder neoplasm","type":"narrow"},{"name":"malignant gall bladder neoplasm","type":"exact"},{"name":"malignant gallbladder neoplasm","type":"exact"},{"name":"malignant gallbladder tumor","type":"exact"},{"name":"malignant gallbladder tumour","type":"exact"},{"name":"malignant neoplasm of gall bladder","type":"exact"},{"name":"malignant neoplasm of gallbladder","type":"exact"},{"name":"malignant neoplasm of the gallbladder","type":"exact"},{"name":"malignant tumor of gallbladder","type":"exact"},{"name":"malignant tumor of the gallbladder","type":"exact"},{"name":"malignant tumour of gallbladder","type":"exact"},{"name":"malignant tumour of the gallbladder","type":"exact"},{"name":"tumor of the gallbladder","type":"broad"},{"name":"tumour of the gallbladder","type":"broad"}],"termid":"MONDO:0005411","xrefs":{"Monarch":{"xref_id":"0005411"}}}


id: PBO:0005455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear export mediator factor NEMF","termid":"PBO:0005455"}


id: GO:0075318
data:
  {"annotated_genes":["SJAG_03501"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075319"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ascus development, a process that leads to the formation of basidium, a sac-like structure produced by fungi of the phylum Ascomycota (sac fungi) in which sexually produced spores (ascospores), usually four or eight in number, are formed.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of spore-bearing organ development","termid":"GO:0075260"},{"relation_name":"regulates","term_name":"ascus development","termid":"GO:0075317"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03501":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 ascus development","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0075318","terms_by_termid":{"GO:0075319":null}}


id: MONDO:0009721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nathalie syndrome is characterized by deafness, cataract, muscular atrophy, skeletal abnormalities, growth retardation, underdeveloped secondary sexual characteristics, and electrocardiographic abnormalities. It has been described in a Dutch family: in three sisters (one named Nathalie) and their brother.","definition_xrefs":["Orphanet:2663"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nathalie syndrome","secondary_identifiers":["GARD:3929","MEDGEN:338087","OMIM:255990","MESH:C538342","SCTID:716170005","UMLS:C1850626"],"synonyms":[{"name":"Nathalie syndrome","type":"exact"},{"name":"deafness, cataract, muscular atrophy, skeletal abnormalities, growth retardation, underdeveloped secondary sexual characteristics","type":"related"},{"name":"deafness-cataract-skeletal anomalies syndrome","type":"exact"},{"name":"deafness-cataracts-skeletal anomalies syndrome","type":"exact"},{"name":"sensorineural hearing loss-cataract-skeletal anomalies-cardiomyopathy syndrome","type":"exact"}],"termid":"MONDO:0009721","xrefs":{"Monarch":{"xref_id":"0009721"}}}


id: MONDO:0005910
data:
  {"annotated_genes":["SJAG_04743"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010600"}]},"cv_name":"mondo","definition":"Disorders in which phagocytic cells cannot kill ingested bacteria; characterized by frequent recurring infection with formulation of granulomas.","definition_xrefs":["MESH:D010585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"leukocyte disorder","termid":"MONDO:0004805"},{"relation_name":"is_a","term_name":"phagocytic cell dysfunction","termid":"MONDO:0024627"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04743":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"phagocyte bactericidal dysfunction","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:14713","UMLS:C0031306","EFO:0007433","DOID:3262"],"synonyms":[{"name":"phagocytic dysfunction","type":"exact"}],"termid":"MONDO:0005910","terms_by_termid":{"MONDO:0010600":null},"xrefs":{"Monarch":{"xref_id":"0005910"}}}


id: PBO:0004948
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translocase of the Inner Membrane","termid":"PBO:0004948"}


id: PBO:0046664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"estrogen receptor 2","termid":"PBO:0046664"}


id: PBO:0059709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO2 pseudogene 17","termid":"PBO:0059709"}


id: MONDO:0007845
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kaposi sarcoma, susceptibility to","secondary_identifiers":["MEDGEN:761233","UMLS:C3538945","OMIM:148000"],"synonyms":[{"name":"Kaposi sarcoma, susceptibility to","type":"exact"},{"name":"multicentric Castleman disease, susceptibility to","type":"related"},{"name":"multiple idiopathic pigmented hemangiosarcoma, susceptibility to","type":"related"},{"name":"susceptibility to Kaposi sarcoma","type":"related"}],"termid":"MONDO:0007845","xrefs":{"Monarch":{"xref_id":"0007845"}}}


id: PBO:0062536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily G member 1","termid":"PBO:0062536"}


id: PBO:0050744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family E (Hsp10) member 1 pseudogene 6","termid":"PBO:0050744"}


id: GO:1904192
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cholangiocyte apoptotic process.","definition_xrefs":["GO_REF:0000058","PMID:24498161","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell apoptotic process","termid":"GO:1904035"},{"relation_name":"regulates","term_name":"cholangiocyte apoptotic process","termid":"GO:1902488"}],"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 cholangiocyte apoptotic process","synonyms":[{"name":"regulation of cholangiocyte apoptosis","type":"narrow"},{"name":"regulation of epithelial cell of bile duct apoptosis","type":"narrow"},{"name":"regulation of epithelial cell of bile duct apoptotic process","type":"exact"}],"termid":"GO:1904192"}


id: GO:1903782
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of sodium ion import across the plasma membrane.","definition_xrefs":["GOC:nc","PMID:19376779","GOC:mtg_cardiac_conduct_nov11","GOC:TermGenie","GO_REF:0000058","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sodium ion transmembrane transport","termid":"GO:1902305"},{"relation_name":"regulates","term_name":"sodium ion import across plasma membrane","termid":"GO:0098719"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of sodium ion import across plasma membrane","termid":"GO:1903782"}


id: PBO:0053433
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 378","termid":"PBO:0053433"}


id: GO:1904016
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 Thyroglobulin triiodothyronine stimulus.","definition_xrefs":["PMID:7531505","GOC:TermGenie","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to Thyroglobulin triiodothyronine","termid":"GO:1904016"}


id: PBO:0065126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKD3 divergent transcript","termid":"PBO:0065126"}


id: GO:0102122
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A34 + S-adenosyl-L-methionine = gibberellin A34 methyl ester + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A34 carboxyl methyltransferase activity (obsolete GO:0102122)","termid":"GO:0102122"}


id: FYPO:0000578
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 gene silencing is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal gene silencing","synonyms":[{"name":"normal gene silencing during mitotic cell cycle","type":"related"},{"name":"normal gene silencing during vegetative growth","type":"exact"},{"name":"silencing: normal","type":"related"}],"termid":"FYPO:0000578"}


id: PBO:0073822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 7 member 2","termid":"PBO:0073822"}


id: GO:0090356
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the chemical reactions and pathways involving auxins, plant hormones that regulate aspects of plant growth.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hormone metabolic process","termid":"GO:0032351"},{"relation_name":"is_a","term_name":"regulation of auxin metabolic process","termid":"GO:0090354"},{"relation_name":"negatively_regulates","term_name":"auxin metabolic process","termid":"GO:0009850"}],"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 auxin metabolic process","synonyms":[{"name":"negative regulation of auxin metabolism","type":"exact"}],"termid":"GO:0090356"}


id: PBO:0085770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase with similarity to mammalian PDK1 and yeast Pkh1p/Phk2p; yeast Pkh1p and Pkh2p are two redundant upstream activators of Pkc1p; identified as a multicopy suppressor of a pkh1 pkh2 double mutant","termid":"PBO:0085770"}


id: GO:0031365
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The alteration of the N-terminal amino acid residue in a protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"N-terminal protein amino acid modification","secondary_identifiers":["GO:0018409"],"synonyms":[{"name":"peptide or protein amino-terminal blocking","type":"related"},{"name":"peptide/protein amino-terminal blocking","type":"related"}],"termid":"GO:0031365"}


id: MONDO:0018293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital disorder of glycosylation with skin involvement (obsolete MONDO:0018293)","secondary_identifiers":["Orphanet:371200"],"synonyms":[{"name":"CDG with skin involvement","type":"exact"}],"termid":"MONDO:0018293","xrefs":{"Monarch":{"xref_id":"0018293"}}}


id: PBO:0082333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-binding cassette (ABC) transporter; multidrug transporter involved in multiple drug resistance; mediates sterol uptake when sterol biosynthesis is compromised; regulated by Pdr1p; required for anaerobic growth; PDR11 has a paralog, AUS1, that arose from the whole genome duplication","termid":"PBO:0082333"}


id: GO:0034397
data:
  {"annotated_genes":["SJAG_01263","SJAG_00756","SJAG_03685","SJAG_03287","SJAG_01777","SJAG_03299","SJAG_01601","SJAG_01584","SJAG_05196","SJAG_05226","SJAG_01837","SJAG_05260","SJAG_03092","SJAG_01067","SJAG_01538","SJAG_03680","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115801],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0120110"},{"annotations":[88970,105113],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070197"},{"annotations":[99110,88971,101999,104265,86616],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032121"},{"annotations":[116825,105114,116687,95911,115078,86617],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045141"},{"annotations":[105115,113119],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044821"},{"annotations":[104266,98324,88972,105116,116003],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0044820"},{"annotations":[101554],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1904537"},{"annotations":[88220,115556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034398"}]},"cv_name":"biological_process","definition":"Any process in which a telomere is transported to, and/or maintained in, a specific location.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome localization","termid":"GO:0050000"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00756":null,"SJAG_01067":null,"SJAG_01263":null,"SJAG_01538":null,"SJAG_01584":null,"SJAG_01601":null,"SJAG_01777":null,"SJAG_01837":null,"SJAG_03048":null,"SJAG_03092":null,"SJAG_03287":null,"SJAG_03299":null,"SJAG_03680":null,"SJAG_03685":null,"SJAG_05196":null,"SJAG_05226":null,"SJAG_05260":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"telomere localization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"telomere localisation","type":"exact"}],"termid":"GO:0034397","terms_by_termid":{"GO:0032121":null,"GO:0034398":null,"GO:0044820":null,"GO:0044821":null,"GO:0045141":null,"GO:0070197":null,"GO:0120110":null,"GO:1904537":null}}


id: PATO:0001236
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality which inheres in an process.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"quality","termid":"PATO:0000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"process quality","secondary_identifiers":["PATO:0001240","PATO:0001239"],"synonyms":[{"name":"quality of a process","type":"exact"},{"name":"quality of occurrent","type":"exact"},{"name":"quality of process","type":"exact"},{"name":"relational quality of occurrent","type":"exact"}],"termid":"PATO:0001236"}


id: PBO:0075700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SREK1 interacting protein 1","termid":"PBO:0075700"}


id: GO:1904202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of iodide transport.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:20392814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of monoatomic anion transport","termid":"GO:1903792"},{"relation_name":"is_a","term_name":"regulation of iodide transport","termid":"GO:1904201"},{"relation_name":"negatively_regulates","term_name":"iodide transport","termid":"GO:0015705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of iodide transport","synonyms":[{"name":"down regulation of iodide transport","type":"exact"},{"name":"down-regulation of iodide transport","type":"exact"},{"name":"downregulation of iodide transport","type":"exact"},{"name":"inhibition of iodide transport","type":"narrow"}],"termid":"GO:1904202"}


id: PBO:0017777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABC transmembrane transporter Ybt1","termid":"PBO:0017777"}


id: GO:1900613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of F-9775B.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"polyketide catabolic process","termid":"GO:0030640"},{"relation_name":"is_a","term_name":"F-9775B metabolic process","termid":"GO:1900612"},{"relation_name":"is_a","term_name":"organic heteropentacyclic compound catabolic process","termid":"GO:1901377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"F-9775B catabolic process","synonyms":[{"name":"F-9775B breakdown","type":"exact"},{"name":"F-9775B catabolism","type":"exact"},{"name":"F-9775B degradation","type":"exact"}],"termid":"GO:1900613"}


id: PATO:0000221
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000221 urination (obsolete PATO:0000221)","termid":"PATO:0000221"}


id: MONDO:0010658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked intellectual disability, Wilson type is characterized by severe intellectual deficit with mutism, epilepsy, growth retardation and recurrent infections. It has been described in three males from three generations of one family. The causative gene has been localized to the 11p region of the X chromosome.","definition_xrefs":["Orphanet:85290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndromic X-linked intellectual disability 12","secondary_identifiers":["MEDGEN:333405","SCTID:719009006","UMLS:C1839792","MESH:C564106","DOID:0060804","GARD:16747","OMIM:309545"],"synonyms":[{"name":"MRXS12","type":"related"},{"name":"X-linked intellectual disability, Wilson type","type":"exact"},{"name":"intellectual disability, X-linked, syndromic 12","type":"exact"},{"name":"mental retardation, X-linked, syndromic 12","type":"exact"},{"name":"syndromic X-linked intellectual disability type 12","type":"exact"}],"termid":"MONDO:0010658","xrefs":{"Monarch":{"xref_id":"0010658"}}}


id: GO:0004226
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: peptidyl-Gly-Xaa + H2O = peptidyl-Gly + Xaa.","definition_xrefs":["EC:3.4.17.4"],"gene_count":0,"genotype_count":0,"name":"obsolete Gly-X carboxypeptidase activity (obsolete GO:0004226)","synonyms":[{"name":"Gly-X carboxypeptidase activity","type":"exact"},{"name":"Gly-Xaa carboxypeptidase activity","type":"related"},{"name":"carboxypeptidase S activity","type":"related"},{"name":"carboxypeptidase a","type":"related"},{"name":"glycine carboxypeptidase activity","type":"related"},{"name":"peptidase alpha","type":"related"},{"name":"yeast carboxypeptidase activity","type":"related"}],"termid":"GO:0004226"}


id: MONDO:0005456
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete avian influenza (obsolete MONDO:0005456)","termid":"MONDO:0005456","xrefs":{"Monarch":{"xref_id":"0005456"}}}


id: GO:0005163
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nerve growth factor receptor.","definition_xrefs":["GOC:ai","PMID:15654015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"death receptor binding","termid":"GO:0005123"},{"relation_name":"is_a","term_name":"neurotrophin receptor binding","termid":"GO:0005165"}],"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:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"nerve growth factor receptor binding","synonyms":[{"name":"NGF receptor binding","type":"exact"},{"name":"nerve growth factor receptor ligand","type":"narrow"},{"name":"neurotrophin","type":"narrow"}],"termid":"GO:0005163"}


id: GO:0060084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of communication from a neuron to a smooth muscle in the bladder that contributes to the expulsion of urine from the body.","definition_xrefs":["PMID:15827347","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuromuscular synaptic transmission","termid":"GO:0007274"},{"relation_name":"part_of","term_name":"micturition","termid":"GO:0060073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"synaptic transmission involved in micturition","synonyms":[{"name":"synaptic transmission involved in urination","type":"related"}],"termid":"GO:0060084"}


id: PBO:0074471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"smoothelin","termid":"PBO:0074471"}


id: GO:0001066
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nucleoside triphosphate + RNA(n) = diphosphate + RNA(n+1). Utilizes a DNA template that contains a single subunit type plastid RNA polymerase specific promoter to direct initiation and catalyses DNA-template-directed extension of the 3'-end of an RNA strand by one nucleotide at a time. Can initiate a chain 'de novo'.","definition_xrefs":["PMID:20701995","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"single subunit type RNA polymerase activity","termid":"GO:0001064"}],"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:0140098"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0140098","GO:0016740","GO:0016779"],"is_obsolete":false,"name":"plastid single subunit type RNA polymerase activity","termid":"GO:0001066"}


id: GO:0047825
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-2-O-sulfolactate + H2O = (R)-lactate + H+ + sulfate.","definition_xrefs":["EC:3.1.6.17","RHEA:20337"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfuric ester hydrolase activity","termid":"GO:0008484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"D-lactate-2-sulfatase activity","secondary_identifiers":["MetaCyc:D-LACTATE-2-SULFATASE-RXN","KEGG_REACTION:R01448"],"synonyms":[{"name":"(S)-2-O-sulfolactate 2-sulfohydrolase activity","type":"related"},{"name":"D-lactate-2-sulphatase activity","type":"exact"}],"termid":"GO:0047825"}


id: MONDO:0008115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.","definition_xrefs":["Orphanet:391641"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Feingold syndrome","termid":"MONDO:0015267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Feingold syndrome type 1","secondary_identifiers":["MEDGEN:1637716","UMLS:C4551774","ICD9:759.89","GARD:17624","OMIM:164280","SCTID:702431004"],"synonyms":[{"name":"Brunner-Winter syndrome type 1","type":"exact"},{"name":"FGLDS1","type":"exact"},{"name":"FS1","type":"exact"},{"name":"Feingold syndrome","type":"related"},{"name":"Feingold syndrome 1","type":"related"},{"name":"Feingold syndrome caused by mutation in MYCN","type":"exact"},{"name":"Feingold syndrome type 1","type":"exact"},{"name":"MMT type 1","type":"exact"},{"name":"MODED syndrome type 1","type":"exact"},{"name":"MYCN Feingold syndrome","type":"exact"},{"name":"Mmt syndrome","type":"related"},{"name":"ODED syndrome type 1","type":"exact"},{"name":"Oded syndrome","type":"related"},{"name":"digital anomalies with short palpebral fissures and atresia of esophagus or duodenum","type":"related"},{"name":"digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1","type":"exact"},{"name":"digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum","type":"related"},{"name":"digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1","type":"exact"},{"name":"microcephaly and digital abnormalities with normal intelligence","type":"related"},{"name":"microcephaly, intellectual disability, and tracheoesophageal fistula syndrome","type":"related"},{"name":"microcephaly, mental retardation, and tracheoesophageal fistula syndrome","type":"related"},{"name":"microcephaly-digital anomalies-normal intelligence syndrome type 1","type":"exact"},{"name":"microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1","type":"exact"},{"name":"microcephaly-oculo-digito-esophageal-duodenal syndrome","type":"related"},{"name":"microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1","type":"exact"},{"name":"oculo-digito-esophageal-duodenal syndrome type 1","type":"exact"},{"name":"oculodigitoesophagoduodenal syndrome","type":"related"}],"termid":"MONDO:0008115","xrefs":{"Monarch":{"xref_id":"0008115"}}}


id: PBO:0053865
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 1140","termid":"PBO:0053865"}


id: PBO:0017578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-glycosylation protein Eos1 (predicted)","termid":"PBO:0017578"}


id: MONDO:0009700
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Carey-Fineman-Ziter syndrome (obsolete MONDO:0009700)","termid":"MONDO:0009700","xrefs":{"Monarch":{"xref_id":"0009700"}}}


id: MONDO:0007590
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemifacial hyperplasia is a rare morphological anomaly of the maxillofacial region characterized by unilateral overgrowth of all facial structures (bone, soft tissues, teeth), called true hemifacial hypertrophy, or overgrowth of one or more but not all facial structures, called partial hemifacial hypertrophy. It may be isolated or related to some syndromes (e.g. Beckwith-Wiedemann, Proteus, Klippel-Trenaunay-Weber, McCune-Albright syndrome, Neurofibromatosis type 1). It may be associated with airway obstruction, sensorineural hearing loss or swallowing difficulties.","definition_xrefs":["Orphanet:141145"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"macroglossia","termid":"MONDO:0015496"},{"relation_name":"is_a","term_name":"overgrowth syndrome","termid":"MONDO:0019716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemifacial hypertrophy","secondary_identifiers":["OMIM:133900","MEDGEN:452987","UMLS:C1399354","icd11.foundation:2090544963","GARD:16971"],"synonyms":[{"name":"facial asymmetry","type":"related"},{"name":"facial hemihypertrophy","type":"related"},{"name":"hemifacial hyperplasia","type":"related"},{"name":"hemifacial hypertrophy","type":"exact"}],"termid":"MONDO:0007590","xrefs":{"Monarch":{"xref_id":"0007590"}}}


id: PBO:0005247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H4-like TAF Taf6, SAGA complex subunit","termid":"PBO:0005247"}


id: PBO:0053535
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 537","termid":"PBO:0053535"}


id: GO:0006971
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 detection of, or exposure to, a hypotonic environment, i.e. an environment with a lower concentration of solutes than the organism or cell.","definition_xrefs":["GOC:jl","PMID:12598593"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to osmotic stress","termid":"GO:0006970"}],"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":"hypotonic response","synonyms":[{"name":"hypo-osmotic response","type":"exact"}],"termid":"GO:0006971"}


id: MONDO:0015824
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculomaxillofacial dysostosis is a rare, genetic bone developmental disorder characterized by short stature, orbital region and ocular abnormalities (e.g. asymmetric orbits, anophthalmia, down-slanted and S-shaped palpebral fissures, sparse eyebrows/eyelashes, abnormal eyelids, ectropion, symblepharon, corneal leukoma), abnormal nose (e.g. broad and abnormally modeled nasal root, bridge and tip, lateral deviation), malar hypoplasia, cleft lip/palate, and oblique facial clefts. Intellectual disability, microcephaly, micrognathia and limb anomalies (e.g. hemimelia, abnormal scapular girdle, brachydactyly, syndactyly, broad halluces) have also been reported.","definition_xrefs":["Orphanet:1794"],"direct_ancestors":[{"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":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"disorder of facial skeleton","termid":"MONDO:0023369"}],"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":"oculomaxillofacial dysostosis","secondary_identifiers":["MESH:C537736","MEDGEN:333072","SCTID:763830009","GARD:4046","UMLS:C1838348","icd11.foundation:921026296"],"synonyms":[{"name":"Richieri Costa Gorlin syndrome","type":"related"},{"name":"Richieri-Costa-Gorlin syndrome","type":"exact"},{"name":"oblique facial clefts","type":"related"},{"name":"oculomaxillofacial dysplasia with oblique facial clefts","type":"related"}],"termid":"MONDO:0015824","xrefs":{"Monarch":{"xref_id":"0015824"}}}


id: PBO:0044300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b5 type A pseudogene 3","termid":"PBO:0044300"}


id: GO:1905498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of triplex DNA binding.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:26503245"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA binding","termid":"GO:0043388"},{"relation_name":"is_a","term_name":"regulation of triplex DNA binding","termid":"GO:1905496"}],"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 triplex DNA binding","synonyms":[{"name":"activation of triplex DNA binding","type":"narrow"},{"name":"up regulation of triplex DNA binding","type":"exact"},{"name":"up-regulation of triplex DNA binding","type":"exact"},{"name":"upregulation of triplex DNA binding","type":"exact"}],"termid":"GO:1905498"}


id: GO:0033449
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a GUU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003723","GO:0005488","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"GUU codon-amino acid adaptor activity","synonyms":[{"name":"GTT codon-amino acid adaptor activity","type":"exact"},{"name":"valine tRNA","type":"related"}],"termid":"GO:0033449"}


id: GO:0050476
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + acetylenedicarboxylate = CO2 + pyruvate.","definition_xrefs":["EC:4.1.1.78"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"acetylenedicarboxylate decarboxylase activity","secondary_identifiers":["RHEA:17733","MetaCyc:4.1.1.78-RXN"],"synonyms":[{"name":"acetylenedicarboxylate carboxy-lyase (pyruvate-forming)","type":"related"},{"name":"acetylenedicarboxylate carboxy-lyase activity","type":"related"},{"name":"acetylenedicarboxylate hydrase activity","type":"related"},{"name":"acetylenedicarboxylate hydratase activity","type":"related"}],"termid":"GO:0050476"}


id: PBO:0003826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPII vesicle coat component Erp5/Erp6 (predicted)","termid":"PBO:0003826"}


id: PBO:0089933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L36","termid":"PBO:0089933"}


id: MONDO:0850289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Human betaherpesvirus 5.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent","DOID:0080827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease","termid":"MONDO:0005108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human betaherpesvirus 5 infectious disease","synonyms":[{"name":"human cytomegalovirus infection","type":"broad"}],"termid":"MONDO:0850289","xrefs":{"Monarch":{"xref_id":"0850289"}}}


id: MONDO:0020640
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the brain secondary to an immune response triggered by the body itself.","definition_xrefs":["NCIT:C122414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of central nervous system","termid":"MONDO:0000568"},{"relation_name":"is_a","term_name":"encephalitis","termid":"MONDO:0019956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune encephalitis","secondary_identifiers":["SCTID:95643007","UMLS:C5671289","icd11.foundation:241281019","NANDO:2200902","GARD:11979","MEDGEN:1804547","NANDO:2100248","Orphanet:622014"],"synonyms":[{"name":"autoimmune encephalitis","type":"exact"}],"termid":"MONDO:0020640","xrefs":{"Monarch":{"xref_id":"0020640"}}}


id: GO:1990497
data:
  {"annotated_genes":["SJAG_03869","SJAG_04383","SJAG_02072","SJAG_00690","SJAG_04873","SJAG_00786","SJAG_01942","SJAG_00169","SJAG_02592"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108826,92011,114749,93566,98528,91715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"},{"annotations":[94418,102505,103139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990611"}]},"cv_name":"biological_process","definition":"Modulation of the frequency, rate or extent of cytoplasmic translation as a result of a stimulus indicating the organism is under stress. The stress is usually, but not necessarily, exogenous (e.g. temperature, humidity, ionizing radiation).","definition_xrefs":["GOC:vw","PMID:16278445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation in response to stress","termid":"GO:0043555"},{"relation_name":"is_a","term_name":"regulation of cytoplasmic translation","termid":"GO:2000765"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00690":null,"SJAG_00786":null,"SJAG_01942":null,"SJAG_02072":null,"SJAG_02592":null,"SJAG_03869":null,"SJAG_04383":null,"SJAG_04873":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0002181"}],"interesting_parent_ids":["GO:0010467","GO:0002181","GO:0008150"],"is_obsolete":false,"name":"regulation of cytoplasmic translation in response to stress","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990497","terms_by_termid":{"GO:1990611":null,"GO:1990625":null}}


id: PBO:0001212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane transporter (predicted)","termid":"PBO:0001212"}


id: GO:0010193
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 ozone stimulus.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to reactive oxygen species","termid":"GO:0000302"}],"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 ozone","termid":"GO:0010193"}


id: PBO:0067560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 713, pseudogene","termid":"PBO:0067560"}


id: PBO:0049185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"grainyhead like transcription factor 2","termid":"PBO:0049185"}


id: MONDO:0017344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Epstein-Barr virus-related tumor","termid":"MONDO:0017342"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Epstein-Barr virus-associated carcinoma","secondary_identifiers":["Orphanet:289651","GARD:21148","UMLS:C5679940","MEDGEN:1842328"],"synonyms":[{"name":"EBV-associated carcinoma","type":"exact"}],"termid":"MONDO:0017344","xrefs":{"Monarch":{"xref_id":"0017344"}}}


id: MONDO:0007977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mesomelic dysplasia Kantaputra type (MDK) is a rare skeletal disease characterized by symmetric shortening of the middle segments of limbs and short stature.","definition_xrefs":["Orphanet:1836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"relation_name":"is_a","term_name":"mesomelic dysplasia","termid":"MONDO:0023599"}],"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":"mesomelic dysplasia, Kantaputra type","secondary_identifiers":["MEDGEN:331880","GARD:3074","OMIM:156232","SCTID:719397009","MESH:C535547","UMLS:C1835009"],"synonyms":[{"name":"Kantaputra mesomelic dysplasia","type":"exact"},{"name":"MDK","type":"exact"},{"name":"MMDK","type":"related"},{"name":"Mdk","type":"related"},{"name":"mesomelic dysplasia Kantaputra type","type":"related"},{"name":"mesomelic dysplasia Thai type","type":"related"},{"name":"mesomelic dysplasia with ankle carpal and tarsal synostosis","type":"related"},{"name":"mesomelic dysplasia with ankle, carpal, and tarsal synostosis","type":"related"},{"name":"mesomelic dysplasia, Kantaputra type","type":"exact"},{"name":"mesomelic dysplasia, Thai type","type":"exact"}],"termid":"MONDO:0007977","xrefs":{"Monarch":{"xref_id":"0007977"}}}


id: PBO:0003286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone promoter control protein Hip4","termid":"PBO:0003286"}


id: GO:0033820
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of an alpha-D-glucosyl residue from UDP-glucose to a hydroxymethylcytosine residue in DNA.","definition_xrefs":["EC:2.4.1.26"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosyltransferase activity","termid":"GO:0046527"},{"relation_name":"is_a","term_name":"catalytic activity, acting on DNA","termid":"GO:0140097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140097"}],"interesting_parent_ids":["GO:0140097","GO:0003824","GO:0016740","GO:0003674","GO:0016757"],"is_obsolete":false,"name":"DNA alpha-glucosyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.26-RXN"],"synonyms":[{"name":"T2-HMC-alpha-glucosyl transferase activity","type":"related"},{"name":"T4-HMC-alpha-glucosyl transferase activity","type":"related"},{"name":"T6-HMC-alpha-glucosyl transferase activity","type":"related"},{"name":"UDP-glucose:DNA alpha-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose-DNA alpha-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-deoxyribonucleate alpha-glucosyltransferase activity","type":"related"}],"termid":"GO:0033820"}


id: PBO:0070664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 35","termid":"PBO:0070664"}


id: MONDO:0003963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This is usually an oligoclonal CD8+ lymphocytic infiltration of various organs.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diffuse infiltrative lymphocytosis syndrome","secondary_identifiers":["NCIT:C35699","UMLS:C1333292","SCTID:449784008","DOID:6677","MEDGEN:232428"],"synonyms":[{"name":"diffuse infiltra. lymph. sydrome","type":"exact"},{"name":"diffuse infiltra. lymph. syndrome","type":"exact"}],"termid":"MONDO:0003963","xrefs":{"Monarch":{"xref_id":"0003963"}}}


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


id: PBO:0065360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoserine aminotransferase 1 pseudogene 1","termid":"PBO:0065360"}


id: PR:Q9P7Y4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mediator of RNA polymerase II transcription subunit 14 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12809:SF2","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":"mediator of RNA polymerase II transcription subunit 14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1A4.10c","secondary_identifiers":["UniProtKB:Q9P7Y4"],"synonyms":[{"name":"SPBC1A4.10c","type":"related"},{"name":"Spom972h-MED14","type":"exact"},{"name":"mediator complex subunit 14 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"mediator of RNA polymerase II complex subunit pmc1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"pmc1","type":"related"}],"termid":"PR:Q9P7Y4"}


id: PBO:0116275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic gamma-glutamyl phosphate reductase; catalyzes the second step in proline biosynthesis","termid":"PBO:0116275"}


id: FYPO:0007680
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 more ribonucleotides than normal are incorporated into one or both strands during mitotic DNA replication.","definition_xrefs":["PomBase:mah","PMID:33568651"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic DNA replication","termid":"FYPO:0001343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000293","FYPO:0005447","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"name":"increased ribonucleotide incorporation into DNA","termid":"FYPO:0007680"}


id: PBO:0112311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGF-beta induced lncRNA activating myofibroblasts","termid":"PBO:0112311"}


id: FYPO:0006452
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed processivity of a histone H3 acetyltransferase activity is lower than normal. Processivity refers to the number of methylation reactions catalyzed (methyl residues added) per histone binding event.","definition_xrefs":["PomBase:mah","PMID:26401015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone acetyltransferase activity","termid":"FYPO:0006453"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000654","FYPO:0001985","FYPO:0000002","FYPO:0000652","FYPO:0005447","FYPO:0000641","FYPO:0000707"],"is_obsolete":false,"name":"decreased histone H3 acetyltransferase processivity","synonyms":[{"name":"decreased H3 histone acetyltransferase processivity","type":"exact"},{"name":"reduced histone H3 acetyltransferase processivity","type":"exact"}],"termid":"FYPO:0006452"}


id: PBO:0049089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 143 pseudogene","termid":"PBO:0049089"}


id: GO:0047816
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabinose + NAD+ = D-arabinono-1,4-lactone + NADH.","definition_xrefs":["RHEA:20457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-arabinose 1-dehydrogenase [NAD(P)+] activity","termid":"GO:0045290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"D-arabinose 1-dehydrogenase (NAD+) activity","secondary_identifiers":["EC:1.1.1.116","MetaCyc:D-ARABINOSE-1-DEHYDROGENASE-RXN"],"synonyms":[{"name":"D-arabinose:NAD+ 1-oxidoreductase activity","type":"related"},{"name":"NAD-pentose-dehydrogenase activity","type":"related"},{"name":"arabinose(fucose)dehydrogenase activity","type":"related"}],"termid":"GO:0047816"}


id: PBO:0088418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF4050 family protein, conserved in fungi and plants","termid":"PBO:0088418"}


id: GO:0070449
data:
  {"annotated_genes":["SJAG_03211","SJAG_00540"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104663,107046],"is_not":false,"summary":null,"term":"GO:0070449"}]},"cv_name":"cellular_component","definition":"A transcription elongation factor complex that suppresses RNA polymerase II pausing, and may act by promoting proper alignment of the 3'-end of nascent transcripts with the polymerase catalytic site. Consists of a transcriptionally active Elongin A subunit (about 100 kDa) and two smaller Elongin B (about 18 kDa) and Elongin C (about 15 kDa) subunits.","definition_xrefs":["PMID:12676794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription elongation factor complex","termid":"GO:0008023"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00540":null,"SJAG_03211":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0005654","GO:0032991"],"is_obsolete":false,"name":"elongin complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"elongin (SIII) complex","type":"exact"},{"name":"transcription elongation factor SIII complex","type":"exact"},{"name":"transcription factor B (SIII) complex","type":"exact"}],"termid":"GO:0070449","terms_by_termid":{"GO:0070449":null}}


id: GO:0072680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a thymocyte through distinct intrathymic niches (e.g. medulla, cortex), where it receives a unique set of developmental cues required for T-cell development, dependent on extracellular matrix components including fibronectin, collagen and laminin.","definition_xrefs":["CL:0000893","GOC:BHF","GOC:mah","PMID:20856819"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substrate-dependent cell migration","termid":"GO:0006929"},{"relation_name":"is_a","term_name":"thymocyte migration","termid":"GO:0072679"}],"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":"extracellular matrix-dependent thymocyte migration","synonyms":[{"name":"extracellular matrix-dependent immature T cell migration","type":"related"},{"name":"extracellular matrix-dependent immature T lymphocyte migration","type":"related"},{"name":"extracellular matrix-dependent immature T-cell migration","type":"related"},{"name":"extracellular matrix-dependent immature T-lymphocyte migration","type":"related"},{"name":"extracellular matrix-dependent thymic lymphocyte migration","type":"exact"}],"termid":"GO:0072680"}


id: PBO:0059831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metal regulatory transcription factor 1","termid":"PBO:0059831"}


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:0030051
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_mitotic_anaphase_A","termid":"PBO:0030051"}


id: MONDO:0032891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intracranial berry aneurysm","termid":"MONDO:0016483"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneurysm, intracranial berry, 12","secondary_identifiers":["UMLS:C5231484","DOID:0080975","MEDGEN:1684660","OMIM:618734","GARD:18330"],"synonyms":[{"name":"ANEURYSM, INTRACRANIAL BERRY, 12","type":"related"},{"name":"ANIB12","type":"related"}],"termid":"MONDO:0032891","xrefs":{"Monarch":{"xref_id":"0032891"}}}


id: MONDO:0003108
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"infratentorial cancer","termid":"MONDO:0003107"},{"relation_name":"is_a","term_name":"spinal cord neoplasm","termid":"MONDO:0021234"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervicomedullary junction neoplasm","secondary_identifiers":["DOID:4707","UMLS:C1332923","MEDGEN:272453","NCIT:C5423"],"synonyms":[{"name":"cervicomedullary junction neoplasms","type":"exact"},{"name":"cervicomedullary junction tumor","type":"exact"},{"name":"cervicomedullary junction tumour","type":"exact"},{"name":"neoplasm of cervicomedullary junction","type":"exact"},{"name":"neoplasm of the cervicomedullary junction","type":"exact"},{"name":"tumor of cervicomedullary junction","type":"exact"},{"name":"tumor of the cervicomedullary junction","type":"exact"},{"name":"tumour of cervicomedullary junction","type":"exact"},{"name":"tumour of the cervicomedullary junction","type":"exact"}],"termid":"MONDO:0003108","xrefs":{"Monarch":{"xref_id":"0003108"}}}


id: GO:0098561
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transmembrane protein complex that consists of multiple methyl-accepting chemoreceptor protein subunits, a histidine kinase and a connector protein and which functions in the regulation of flagellar rotary motor activity in response to an external chemical stimulus.","definition_xrefs":["GOC:dos","PMID:15802240","PMID:1326408"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"methyl accepting chemotaxis protein complex","termid":"GO:0098561"}


id: MONDO:0005190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Macroglobulinemia is the presence of increased levels of macroglobulins in the circulating blood. It is a Plasma cell dyscrasia, resembling leukemia, with cells of lymphocytic, plasmacytic, or intermediate morphology, which secrete a monoclonal immunoglobulin M component. There is diffuse infiltration by the malignant cells of the bone marrow and also, in many cases, of the spleen, liver, or lymph nodes. The circulating macroglobulin can produce symptoms of hyperviscosity syndrome: weakness, fatigue, bleeding disorders, and visual disturbances. Peak incidence of macroglobulinemia is in the sixth and seventh decades of life.","definition_xrefs":["EFO:0002616"],"gene_count":0,"genotype_count":0,"name":"obsolete macroglobulinemia (obsolete MONDO:0005190)","secondary_identifiers":["MESH:D008258","DOID:9080","SCTID:190817009","NCIT:C80307","NCIT:C3212","Wikipedia:Macroglobulinemia","ICD10CM:C88.0","ICD9:273.3"],"synonyms":[{"name":"primary macroglobulinemia","type":"exact"}],"termid":"MONDO:0005190","xrefs":{"Monarch":{"xref_id":"0005190"}}}


id: PBO:0062480
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 L member 1 pseudogene","termid":"PBO:0062480"}


id: GO:0009622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete resistance to pathogenic fungi (obsolete GO:0009622)","synonyms":[{"name":"resistance to pathogenic fungi","type":"exact"}],"termid":"GO:0009622"}


id: MONDO:0002964
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-Langerhans-cell histiocytosis (obsolete MONDO:0002964)","termid":"MONDO:0002964","xrefs":{"Monarch":{"xref_id":"0002964"}}}


id: MONDO:0019343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mixed connective tissue disease (obsolete MONDO:0019343)","termid":"MONDO:0019343","xrefs":{"Monarch":{"xref_id":"0019343"}}}


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


id: PATO:0001760
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"semi-fertile","termid":"PATO:0001767"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"female semi-fertile","termid":"PATO:0001760"}


id: MONDO:0007952
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":"maxillofacial dysostosis","secondary_identifiers":["OMIM:155000","MESH:C563599","UMLS:C1835088","MEDGEN:320517"],"synonyms":[{"name":"maxillofacial dysostosis","type":"exact"}],"termid":"MONDO:0007952","xrefs":{"Monarch":{"xref_id":"0007952"}}}


id: MONDO:0013458
data:
  {"annotated_genes":["SJAG_02977"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86136],"is_not":false,"summary":null,"term":"MONDO:0013458"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary hypertension","termid":"MONDO:0005149"},{"relation_name":"is_a","term_name":"inherited renal tubular disease","termid":"MONDO:0015962"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02977":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005240","MONDO:0005066"],"is_obsolete":false,"name":"hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:462559","OMIM:613845","Orphanet:363694","UMLS:C3151209","GARD:17569"],"synonyms":[{"name":"HUPRA syndrome","type":"exact"},{"name":"HUPRAS","type":"related"},{"name":"Hupra syndrome","type":"related"},{"name":"hyperuricemia, pulmonary hypertension, renal failure, and alkalosis","type":"exact"},{"name":"hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome","type":"related"}],"termid":"MONDO:0013458","terms_by_termid":{"MONDO:0013458":null},"xrefs":{"Monarch":{"xref_id":"0013458"}}}


id: PBO:0075547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPECC1 pseudogene 1","termid":"PBO:0075547"}


id: PBO:0040844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bleomycin hydrolase","termid":"PBO:0040844"}


id: GO:1902890
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of root hair elongation.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:22329353","GOC:als"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell growth","termid":"GO:0001558"},{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","term_name":"root hair elongation","termid":"GO:0048767"}],"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 root hair elongation","termid":"GO:1902890"}


id: MONDO:0005388
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary biliary cholangitis (PBC) is a chronic and slowly progressive cholestatic liver disease of autoimmune etiology characterized by injury of the intrahepatic bile ducts that may eventually lead to liver failure.","definition_xrefs":["Orphanet:186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biliary tract disorder","termid":"MONDO:0004868"},{"relation_name":"is_a","term_name":"cirrhosis, familial","termid":"MONDO:0007329"}],"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:0019303"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0019303","MONDO:0002515"],"is_obsolete":false,"name":"primary biliary cholangitis","secondary_identifiers":["MedDRA:10019137","ICD9:571.6","MedDRA:10004661","GARD:7459","NANDO:1200439","DOID:12236","MESH:D008105","EFO:1001486","NCIT:C27167","UMLS:C0008312","SCTID:31712002","MEDGEN:3035","NORD:1604","OMIMPS:109720","icd11.foundation:649193479"],"synonyms":[{"name":"Hanot syndrome","type":"exact"},{"name":"PBC","type":"exact"},{"name":"biliary cirrhosis, primary","type":"related"},{"name":"biliary liver cirrhosis","type":"exact"},{"name":"cholestatic cirrhosis","type":"exact"},{"name":"chronic non-suppurative destructive cholangitis","type":"exact"},{"name":"chronic nonsuppurative destructive cholangitis","type":"exact"},{"name":"familial primary biliary cirrhosis","type":"related"},{"name":"primary Bilary cirrhosis (PBC)","type":"exact"},{"name":"primary biliary cirrhosis","type":"exact"}],"termid":"MONDO:0005388","xrefs":{"Monarch":{"xref_id":"0005388"}}}


id: MONDO:0014831
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progeroid and marfanoid aspect-lipodystrophy syndrome","secondary_identifiers":["UMLS:C4310796","OMIM:616914","Orphanet:300382","MEDGEN:934763","GARD:17371"],"synonyms":[{"name":"MFLS","type":"related"},{"name":"Marfan lipodystrophy syndrome","type":"exact"},{"name":"Marfan-progeroid-lipodystrophy syndrome","type":"related"},{"name":"Marfanoid-progeroid syndrome","type":"related"}],"termid":"MONDO:0014831","xrefs":{"Monarch":{"xref_id":"0014831"}}}


id: PBO:0082127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Aconitase; required for the tricarboxylic acid (TCA) cycle and also independently required for mitochondrial genome maintenance; component of the mitochondrial nucleoid; mutation leads to glutamate auxotrophy; mutation in human homolog ACO2 is associated with dominant optic nerve atrophy; human homolog ACO2 can complement yeast null mutant","termid":"PBO:0082127"}


id: MONDO:0011101
data:
  {"annotated_genes":["SJAG_02619"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86412],"is_not":false,"summary":null,"term":"MONDO:0011101"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"peroxisome biogenesis disorder","termid":"MONDO:0019234"},{"relation_name":"is_a","term_name":"peroxisome biogenesis disorder due to PEX1 defect","termid":"MONDO:0100259"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02619":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0019053","MONDO:0005244","MONDO:0005559","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"peroxisome biogenesis disorder 1B","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081240","MEDGEN:79470","UMLS:C0282527","NCIT:C155749","OMIM:601539"],"synonyms":[{"name":"PBD1B","type":"related"},{"name":"Refsum disease, infantile","type":"related"},{"name":"adrenoleukodystrophy, autosomal neonatal","type":"related"},{"name":"infantile phytanic acid storage disease","type":"related"},{"name":"peroxisome biogenesis disorder (NALD/Ird)","type":"related"},{"name":"peroxisome biogenesis disorder (neonatal adrenoleukodystrophy/infantile Refsum disease)","type":"related"},{"name":"peroxisome biogenesis disorder 1B","type":"exact"},{"name":"peroxisome biogenesis disorder 1B (NALD/IRD)","type":"exact"},{"name":"peroxisome biogenesis disorder type 1B","type":"exact"}],"termid":"MONDO:0011101","terms_by_termid":{"MONDO:0011101":null},"xrefs":{"Monarch":{"xref_id":"0011101"}}}


id: PBO:0079659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2V1 pseudogene 7","termid":"PBO:0079659"}


id: GO:1901708
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (+)-3'-hydroxylarreatricin.","definition_xrefs":["GOC:TermGenie","PMID:12960376"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan biosynthetic process","termid":"GO:0009807"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"(+)-3'-hydroxylarreatricin biosynthetic process","synonyms":[{"name":"(+)-3'-hydroxylarreatricin anabolism","type":"exact"},{"name":"(+)-3'-hydroxylarreatricin biosynthesis","type":"exact"},{"name":"(+)-3'-hydroxylarreatricin formation","type":"exact"},{"name":"(+)-3'-hydroxylarreatricin synthesis","type":"exact"}],"termid":"GO:1901708"}


id: MONDO:0016592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"cerebellar ataxia","termid":"MONDO:0000437"}],"gene_count":0,"genotype_count":0,"name":"obsolete non-hereditary degenerative ataxia (obsolete MONDO:0016592)","secondary_identifiers":["icd11.foundation:1257393361","Orphanet:247239"],"termid":"MONDO:0016592","xrefs":{"Monarch":{"xref_id":"0016592"}}}


id: MONDO:0005206
data:
  {"annotated_genes":["SJAG_01144","SJAG_03787","SJAG_03677","SJAG_00440","SJAG_02231"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"},{"annotations":[85385],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0003789"},{"annotations":[86003,86004,86005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007763"}]},"cv_name":"mondo","definition":"A carcinoma arising from the epithelium of the renal parenchyma or the renal pelvis. The majority are renal cell carcinomas. Kidney carcinomas usually affect middle aged and elderly adults. Hematuria, abdominal pain, and a palpable mass are common symptoms.","definition_xrefs":["NCIT:C9384"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney cancer","termid":"MONDO:0002367"},{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00440":null,"SJAG_01144":null,"SJAG_02231":null,"SJAG_03677":null,"SJAG_03787":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"renal carcinoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:4451","UMLS:C1378703","MEDGEN:235133","EFO:0002890","icd11.foundation:1075394530"],"synonyms":[{"name":"carcinoma of kidney","type":"exact"},{"name":"kidney (including renal cell) cancer","type":"broad"},{"name":"kidney (renal) cancer","type":"broad"},{"name":"kidney cancer","type":"broad"},{"name":"kidney carcinoma","type":"exact"},{"name":"renal cancer","type":"broad"},{"name":"renal carcinoma","type":"exact"}],"termid":"MONDO:0005206","terms_by_termid":{"MONDO:0003789":null,"MONDO:0007763":null,"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0005206"}}}


id: SO:0001027
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A genotype is a variant genome, complete or incomplete.","definition_xrefs":["SO:immuno_workshop"],"direct_ancestors":[{"relation_name":"is_a","term_name":"variant_collection","termid":"SO:0001507"},{"relation_name":"variant_of","term_name":"genome","termid":"SO:0001026"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genotype","secondary_identifiers":["http://en.wikipedia.org/wiki/Genotype"],"termid":"SO:0001027"}


id: PBO:0065954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD21 antisense RNA 1","termid":"PBO:0065954"}


id: PR:O42645
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A secretion-regulating guanine nucleotide exchange factor that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00488","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":"RCC1 repeat-containing protein C10F6.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC10F6.04","secondary_identifiers":["UniProtKB:O42645"],"synonyms":[{"name":"Spom972h-SERGEF","type":"exact"}],"termid":"PR:O42645"}


id: FYPO:0007936
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the number of sites of  DNA breakpoint junctions is greater than normal.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased DNA damage","termid":"FYPO:0003546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"increased number of DNA breakpoint junctions","termid":"FYPO:0007936"}


id: MONDO:0006763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A painful inflammatory process leads to a mechanical block in active and passive range of motion (ROM) of the shoulder. Adhesive capsulitis of the shoulder is characterized by functional loss of passive and active shoulder motion. This inflammatory process results in fibroblastic proliferation and extensive scar tissue formation. Fibroblastic proliferation, a late phase of the inflammatory process involved in tissue repair, leads to thickening, fibrosis, and adhesion of the capsule to itself and the humerus.","definition_xrefs":["PMID:34772852"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"muscle tissue disorder","termid":"MONDO:0003939"},{"relation_name":"is_a","term_name":"arthropathy","termid":"MONDO:0006816"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frozen shoulder","secondary_identifiers":["SCTID:399114005","DOID:14188","EFO:1000941","MESH:D002062","ICD9:726.0","UMLS:C0311223","ICD10CM:M75.0","MedDRA:10017391","MEDGEN:90227"],"synonyms":[{"name":"adhesions-capsulitis,shoulder","type":"exact"},{"name":"adhesive capsulitis","type":"exact"},{"name":"adhesive capsulitis of shoulder","type":"exact"}],"termid":"MONDO:0006763","xrefs":{"Monarch":{"xref_id":"0006763"}}}


id: BFO:0000060
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"obsolete_preceded_by","termid":"BFO:0000060"}


id: MONDO:0001050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An otitis externa which involves infection of the external ear that has spread to involve the skull bone containing part of the ear canal, the middle ear, and the inner ear. It is caused by the bacteria Pseudomonas. This is common in people with weakened immune systems and in older people with diabetes.","definition_xrefs":["DOID:10516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otitis externa","termid":"MONDO:0004795"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malignant otitis externa","secondary_identifiers":["ICD9:380.14","MEDGEN:509950","icd11.foundation:984580942","SCTID:94146005","UMLS:C0155395","ICD10CM:H60.2"],"termid":"MONDO:0001050","xrefs":{"Monarch":{"xref_id":"0001050"}}}


id: PBO:0039150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AK3 pseudogene 5","termid":"PBO:0039150"}


id: MONDO:0001777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of gonococcal cystitis.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute cystitis","termid":"MONDO:0001650"},{"relation_name":"is_a","term_name":"gonococcal cystitis","termid":"MONDO:0021160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute gonococcal cystitis","secondary_identifiers":["UMLS:C0153191","MEDGEN:509193","ICD9:098.11","SCTID:24868007","DOID:13690"],"synonyms":[{"name":"acute gonorrhea of bladder","type":"exact"},{"name":"acute gonorrhoea of bladder","type":"exact"},{"name":"gonococcal cystitis (acute)","type":"exact"},{"name":"gonococcal cystitis, acute","type":"exact"}],"termid":"MONDO:0001777","xrefs":{"Monarch":{"xref_id":"0001777"}}}


id: GO:0120285
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 tyrosine.","definition_xrefs":["PMID:31498992","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid sensor activity","termid":"GO:0140785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140299","GO:0098772"],"is_obsolete":false,"name":"tyrosine sensor activity","synonyms":[{"name":"tyrosine sensing activity","type":"exact"}],"termid":"GO:0120285"}


id: PBO:0063416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDE2A antisense RNA 1","termid":"PBO:0063416"}


id: PBO:0051051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 2-8","termid":"PBO:0051051"}


id: PBO:0085659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in mRNA splicing; contains a consensus nuclear export signal (NES) sequence similar to the consensus sequence recognized by Crm1p; interacts genetically with Prp40p and Tgs1p; contains WD40 repeats","termid":"PBO:0085659"}


id: GO:0046183
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-idonate, the anion of idonic acid, an aldonic acid derived from L-idose, an aldohexose which is epimeric with D-glucose.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate catabolic process","termid":"GO:0016052"},{"relation_name":"is_a","term_name":"L-idonate metabolic process","termid":"GO:0019523"},{"relation_name":"is_a","term_name":"aldonic acid catabolic process","termid":"GO:0046176"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"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:0008150","GO:0005975","GO:0044248","GO:0044281"],"is_obsolete":false,"name":"L-idonate catabolic process","synonyms":[{"name":"L-idonate breakdown","type":"exact"},{"name":"L-idonate catabolism","type":"exact"},{"name":"L-idonate degradation","type":"exact"}],"termid":"GO:0046183"}


id: PBO:0071101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 103","termid":"PBO:0071101"}


id: FYPO:0004011
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 occurrence of degradation of one or more ribosomal proteins is increased.","definition_xrefs":["PomBase:mah","PMID:2839305"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein degradation during vegetative growth","termid":"FYPO:0000847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased degradation of ribosomal proteins during vegetative growth","synonyms":[{"name":"increased degradation of ribosomal proteins during mitotic cell cycle","type":"related"},{"name":"increased ribosomal protein breakdown during vegetative growth","type":"exact"},{"name":"increased ribosomal protein catabolic process during vegetative growth","type":"exact"},{"name":"increased ribosomal protein catabolism during vegetative growth","type":"exact"},{"name":"increased ribosomal protein degradation cycle during vegetative growth","type":"related"}],"termid":"FYPO:0004011"}


id: PBO:0028469
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_interphase_microtubule_nucleation","termid":"PBO:0028469"}


id: PBO:0056529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanoma cell adhesion molecule","termid":"PBO:0056529"}


id: PR:O13793
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC17G6.15c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13793"],"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":"mitochondrial transport protein fsf1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.15c","synonyms":[{"name":"Spom972h-SPAC17G6.15c","type":"exact"},{"name":"fungal sideroflexin-1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13793"}


id: PR:Q9UUJ0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pvg5 gene.","definition_xrefs":["UniProtKB:Q9UUJ0","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":"pyruvylated Gal-beta-1,3-epitope synthesis protein 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22F8.02c","synonyms":[{"name":"PvGal synthesis protein 5 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-pvg5","type":"exact"},{"name":"meiotically up-regulated gene 50 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UUJ0"}


id: MONDO:0012967
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemolytic anemia due to adenylate kinase deficiency is a rare hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by moderate to severe chronic nonspherocytic hemolytic anemia that may require regular blood transfusions and/or splenectomy and may be associated with psychomotor impairment.","definition_xrefs":["Orphanet:86817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hemolytic anemia","termid":"MONDO:0003689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"hemolytic anemia due to adenylate kinase deficiency","secondary_identifiers":["MESH:C567228","UMLS:C2675459","GARD:16760","MEDGEN:390802","OMIM:612631","SCTID:766982000"],"synonyms":[{"name":"ADENYLATE KINASE deficiency, hemolytic anaemia due to","type":"related"},{"name":"ADENYLATE KINASE deficiency, hemolytic anemia due to","type":"related"}],"termid":"MONDO:0012967","xrefs":{"Monarch":{"xref_id":"0012967"}}}


id: GO:1902399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any detection of stimulus that is involved in G1 DNA damage checkpoint.","definition_xrefs":["GOC:TermGenie","GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in G1 DNA damage checkpoint (obsolete GO:1902399)","synonyms":[{"name":"detection of stimulus involved in G1/S DNA damage checkpoint","type":"exact"},{"name":"perception of stimulus involved in G1 DNA damage checkpoint","type":"related"},{"name":"perception of stimulus involved in G1/S DNA damage checkpoint","type":"related"},{"name":"stimulus detection involved in G1 DNA damage checkpoint","type":"exact"},{"name":"stimulus detection involved in G1/S DNA damage checkpoint","type":"exact"},{"name":"stimulus sensing involved in G1 DNA damage checkpoint","type":"related"},{"name":"stimulus sensing involved in G1/S DNA damage checkpoint","type":"related"}],"termid":"GO:1902399"}


id: PBO:0052907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 12-4","termid":"PBO:0052907"}


id: PBO:0028356
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_phosphatase_activity","termid":"PBO:0028356"}


id: MONDO:0033552
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blood group, lewis system (obsolete MONDO:0033552)","secondary_identifiers":["OMIM:618983"],"synonyms":[{"name":"BLOOD GROUP, LEWIS SYSTEM","type":"related"},{"name":"LE","type":"related"},{"name":"Lewis Blood Group System","type":"related"},{"name":"Lewis-Negative Phenotype","type":"related"},{"name":"blood group, Lewis","type":"exact"}],"termid":"MONDO:0033552","xrefs":{"Monarch":{"xref_id":"0033552"}}}


id: GO:0097109
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a member of the neuroligin protein family, neuronal cell surface proteins that mediate synapse formation.","definition_xrefs":["GOC:BHF","GOC:sjp","GOC:pr","PMID:21424692"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"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":"neuroligin family protein binding","termid":"GO:0097109"}


id: GO:0021888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a hypothalamus gonadotrophin-releasing hormone neuron over time, from initial commitment of its fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:cls","GOC:dgh","GOC:dph","GO_REF:0000021","GOC:jid","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"forebrain neuron development","termid":"GO:0021884"},{"relation_name":"part_of","term_name":"hypothalamus gonadotrophin-releasing hormone neuron differentiation","termid":"GO:0021886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hypothalamus gonadotrophin-releasing hormone neuron development","synonyms":[{"name":"hypothalamus gonadotropin-releasing hormone neuron development","type":"related"}],"termid":"GO:0021888"}


id: PBO:0052678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 46","termid":"PBO:0052678"}


id: MONDO:1012456
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple autoimmune diseases syndrome, non-human animal","termid":"MONDO:1011731"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple autoimmune diseases syndrome, dog","secondary_identifiers":["OMIA:001808-9615"],"termid":"MONDO:1012456","xrefs":{"Monarch":{"xref_id":"1012456"}}}


id: MONDO:0033643
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"inflammatory bowel disease 30","secondary_identifiers":["UMLS:C5436750","MEDGEN:1737985","DOID:0112154","OMIM:619079"],"synonyms":[{"name":"IBD30","type":"exact"},{"name":"inflammatory bowel disease (Crohn disease) 30","type":"exact"}],"termid":"MONDO:0033643","xrefs":{"Monarch":{"xref_id":"0033643"}}}


id: GO:0047451
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (3R)-3-hydroxyoctanoyl-[acyl-carrier protein] = H2O + (2E)-octenoyl-[acyl-carrier protein].","definition_xrefs":["PMID:8910376"],"gene_count":0,"genotype_count":0,"name":"obsolete (3R)-3-hydroxyoctanoyl-[acyl-carrier-protein] dehydratase activity (obsolete GO:0047451)","synonyms":[{"name":"(3R)-3-hydroxyoctanoyl-[acyl-carrier-protein] hydro-lyase activity","type":"related"},{"name":"3-hydroxyoctanoyl-ACP dehydratase activity","type":"exact"},{"name":"3-hydroxyoctanoyl-[acyl-carrier protein] dehydratase activity","type":"exact"},{"name":"3-hydroxyoctanoyl-[acyl-carrier-protein] dehydratase activity","type":"broad"}],"termid":"GO:0047451"}


id: GO:0005332
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: gamma-aminobutyric acid(out) + Na+(out) + Cl-(out) = gamma-aminobutyric acid(in) + Na+(in) + Cl(in).","definition_xrefs":["PMID:7861179","PMID:7589472"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid:sodium symporter activity","termid":"GO:0005283"},{"relation_name":"is_a","term_name":"gamma-aminobutyric acid transmembrane transporter activity","termid":"GO:0015185"},{"relation_name":"is_a","term_name":"sodium:chloride symporter activity","termid":"GO:0015378"},{"relation_name":"is_a","term_name":"monocarboxylate:sodium symporter activity","termid":"GO:0140161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"gamma-aminobutyric acid:sodium:chloride symporter activity","secondary_identifiers":["Reactome:R-HSA-444007","TC:2.A.22.3.2"],"synonyms":[{"name":"4-aminobutanoate:sodium symporter activity","type":"exact"},{"name":"4-aminobutyrate:sodium symporter activity","type":"exact"},{"name":"GABA:sodium symporter activity","type":"exact"},{"name":"betaine/GABA:sodium symporter activity","type":"exact"},{"name":"gamma-aminobutyric acid:sodium symporter activity","type":"exact"},{"name":"sodium/chloride-dependent GABA transporter activity","type":"broad"}],"termid":"GO:0005332"}


id: MONDO:0045046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of thyroid hormone metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland disorder","termid":"MONDO:0003240"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"inherited thyroid metabolism disease","secondary_identifiers":["MEDGEN:543589","UMLS:C0271824","ICD9:246.8","SCTID:36985004"],"synonyms":[{"name":"inborn error of thyroid hormone metabolic process","type":"exact"},{"name":"inborn thyroid hormone metabolic process disorder","type":"exact"},{"name":"inherited disorder of thyroid metabolism","type":"exact"},{"name":"rare inborn error of thyroid hormone metabolic process","type":"exact"}],"termid":"MONDO:0045046","xrefs":{"Monarch":{"xref_id":"0045046"}}}


id: GO:0000174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Downregulation of MAP kinase activity in the context of transduction of mating pheromone signal, as described for Saccharomyces.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete inactivation of MAPK (mating sensu Saccharomyces) (obsolete GO:0000174)","synonyms":[{"name":"inactivation of MAPK (mating sensu Saccharomyces)","type":"exact"}],"termid":"GO:0000174"}


id: PR:O13693
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC11E3.14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13693"],"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 C11E3.14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11E3.14","synonyms":[{"name":"Spom972h-SPAC11E3.14","type":"exact"}],"termid":"PR:O13693"}


id: GO:1902966
data:
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