# terms

id: MONDO:0016264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hepatitis caused by autoantibodies. Drugs, infections, and toxins may trigger the production of the autoantibodies against the liver parenchyma.","definition_xrefs":["NCIT:C27029"],"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 exocrine system","termid":"MONDO:0000586"},{"relation_name":"is_a","term_name":"autoimmune disorder of gastrointestinal tract","termid":"MONDO:0000588"},{"relation_name":"is_a","term_name":"hepatitis","termid":"MONDO:0002251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"autoimmune hepatitis","secondary_identifiers":["NANDO:1200441","DOID:2048","NANDO:1200442","NORD:1897","icd11.foundation:1235727122","SCTID:408335007","UMLS:C4721555","MESH:D019693","ICD9:571.42","ICD10CM:K75.4","MEDGEN:1666753","EFO:0005676","NANDO:2100264","GARD:5871","MedDRA:10003827","Orphanet:2137"],"synonyms":[{"name":"AIH","type":"related"},{"name":"autoimmune chronic active hepatitis","type":"narrow"},{"name":"autoimmune chronic hepatitis","type":"related"},{"name":"autoimmune hepatitis","type":"exact"},{"name":"autoimmune hepatitis with centrilobular necrosis","type":"narrow"},{"name":"autoimmune liver disease","type":"broad"},{"name":"chronic autoimmune hepatitis","type":"narrow"}],"termid":"MONDO:0016264","xrefs":{"Monarch":{"xref_id":"0016264"}}}


id: PBO:0054834
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 2248","termid":"PBO:0054834"}


id: FYPO:0001524
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of L-thialysine than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002682","FYPO:0000139","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"resistance to L-thialysine","synonyms":[{"name":"resistance to L-thialysine during mitotic cell cycle","type":"related"},{"name":"resistance to L-thialysine during vegetative growth","type":"exact"},{"name":"resistance to thialysine","type":"broad"},{"name":"resistant to L-thialysine","type":"exact"}],"termid":"FYPO:0001524"}


id: GO:0045803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the organization, biogenesis or maintenance of the cytoskeleton.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cytoskeleton (obsolete GO:0045803)","synonyms":[{"name":"positive regulation of cytoskeleton","type":"exact"}],"termid":"GO:0045803"}


id: GO:0033639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism modulates a change in state or activity of a host cell or organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a water stimulus. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by symbiont of host response to water (obsolete GO:0033639)","termid":"GO:0033639"}


id: PBO:0071568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 34","termid":"PBO:0071568"}


id: MONDO:0021309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the endocervix.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant neoplasm of endocervix","secondary_identifiers":["MEDGEN:56309","NCIT:C3553","SCTID:372097009","ICD9:180.0","ICD10CM:C53.0","UMLS:C0153569"],"synonyms":[{"name":"cancer of endocervix","type":"exact"},{"name":"endocervix cancer","type":"exact"},{"name":"malignant endocervical neoplasm","type":"exact"},{"name":"malignant endocervical tumor","type":"exact"},{"name":"malignant endocervical tumour","type":"exact"},{"name":"malignant endocervix neoplasm","type":"exact"},{"name":"malignant endocervix tumor","type":"exact"},{"name":"malignant endocervix tumour","type":"exact"},{"name":"malignant neoplasm of endocervix","type":"exact"},{"name":"malignant neoplasm of the endocervix","type":"exact"},{"name":"malignant neoplasm of the uterine endocervix","type":"exact"},{"name":"malignant neoplasm of uterine endocervix","type":"exact"},{"name":"malignant tumor of endocervix","type":"exact"},{"name":"malignant tumor of the endocervix","type":"exact"},{"name":"malignant tumor of the uterine endocervix","type":"exact"},{"name":"malignant tumor of uterine endocervix","type":"exact"},{"name":"malignant tumour of endocervix","type":"exact"},{"name":"malignant tumour of the endocervix","type":"exact"},{"name":"malignant tumour of the uterine endocervix","type":"exact"},{"name":"malignant tumour of uterine endocervix","type":"exact"},{"name":"malignant uterine endocervix neoplasm","type":"exact"},{"name":"malignant uterine endocervix tumor","type":"exact"},{"name":"malignant uterine endocervix tumour","type":"exact"}],"termid":"MONDO:0021309","xrefs":{"Monarch":{"xref_id":"0021309"}}}


id: PBO:0045611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 22 (pseudogene)","termid":"PBO:0045611"}


id: PBO:0048874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A5 pseudogene 1","termid":"PBO:0048874"}


id: FYECO:0000008
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"The expression level of the gene was decreased compared to expressing it from its endogenous promoter in the genome.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000008 knockdown (obsolete FYECO:0000008)","termid":"FYECO:0000008"}


id: PBO:0043468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4-NOT transcription complex subunit 7","termid":"PBO:0043468"}


id: PBO:0074204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 39 member 13","termid":"PBO:0074204"}


id: PBO:0078276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 9-4","termid":"PBO:0078276"}


id: MONDO:0013401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4E1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 51","secondary_identifiers":["OMIM:613744","MEDGEN:462406","GARD:13737","UMLS:C3151056","DOID:0110803","NORD:1990"],"synonyms":[{"name":"AP4E1 hereditary spastic paraplegia","type":"exact"},{"name":"CPSQ4","type":"exact"},{"name":"SPG51","type":"exact"},{"name":"Spastic Paraplegia 51","type":"exact"},{"name":"autosomal dominant spastic paraplegia 51","type":"exact"},{"name":"cerebral palsy, spastic quadriplegic, 4","type":"related"},{"name":"cerebral palsy, spastic quadriplegic, 4, formerly","type":"related"},{"name":"hereditary spastic paraplegia caused by mutation in AP4E1","type":"exact"},{"name":"hereditary spastic paraplegia type 51","type":"exact"},{"name":"spastic paraplegia 51, autosomal recessive","type":"related"},{"name":"spastic quadriplegic cerebral palsy 4","type":"exact"}],"termid":"MONDO:0013401","xrefs":{"Monarch":{"xref_id":"0013401"}}}


id: MONDO:0013570
data:
  {"annotated_genes":["SJAG_01797"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87704],"is_not":false,"summary":null,"term":"MONDO:0013570"}]},"cv_name":"mondo","definition":"Combined oxidative phosphorylation defect type 8 is a mitochondrial disease due to a defect in mitochondrial protein synthesis resulting in deficiency of respiratory chain complexes I, III and IV in the cardiac and skeletal muscle and brain characterized by severe hypertrophic cardiomyopathy, pulmonary hypoplasia, generalized muscle weakness and neurological involvement.","definition_xrefs":["Orphanet:319504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01797":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111479","MEDGEN:1377817","GARD:17452","UMLS:C4518839","OMIM:614096","SCTID:733600007"],"synonyms":[{"name":"AARS2 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"COXPD8","type":"exact"},{"name":"cardiomyopathy, hypertrophic mitochondrial, fatal infantile","type":"related"},{"name":"combined oxidative phosphorylation deficiency 8","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in AARS2","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 8","type":"exact"}],"termid":"MONDO:0013570","terms_by_termid":{"MONDO:0013570":null},"xrefs":{"Monarch":{"xref_id":"0013570"}}}


id: MONDO:0012806
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia and immune deficiency","termid":"MONDO:0010293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"ectodermal dysplasia and immunodeficiency 2","secondary_identifiers":["OMIM:612132","MESH:C567411","UMLS:C2677481","DOID:0081079","GARD:15542","MEDGEN:394295","NCIT:C176826"],"synonyms":[{"name":"EPAID2","type":"exact"},{"name":"ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant","type":"exact"}],"termid":"MONDO:0012806","xrefs":{"Monarch":{"xref_id":"0012806"}}}


id: PBO:0001885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sec14 cytosolic factor family (predicted)","termid":"PBO:0001885"}


id: PBO:0069869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1156, pseudogene","termid":"PBO:0069869"}


id: MONDO:0032928
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":"T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant","secondary_identifiers":["OMIM:618806","MEDGEN:1712366","Orphanet:676039","UMLS:C5394133"],"synonyms":[{"name":"T-CELL LYMPHOPENIA, INFANTILE, WITH OR WITHOUT NAIL DYSTROPHY, AUTOSOMAL DOMINANT","type":"related"},{"name":"TLIND","type":"related"}],"termid":"MONDO:0032928","xrefs":{"Monarch":{"xref_id":"0032928"}}}


id: PBO:0074671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 57","termid":"PBO:0074671"}


id: MONDO:0002313
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the cornea that is seasonal in nature.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic conjunctivitis","termid":"MONDO:0002314"}],"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":"vernal conjunctivitis","secondary_identifiers":["ICD9:372.13","UMLS:C0009773","DOID:2474","ICD10CM:H10.44","icd11.foundation:1653249836","MEDGEN:3211","NCIT:C34508","SCTID:318316003"],"termid":"MONDO:0002313","xrefs":{"Monarch":{"xref_id":"0002313"}}}


id: MONDO:0000141
data:
  {"annotated_genes":["SJAG_03436","SJAG_04699","SJAG_02795","SJAG_04884","SJAG_00213","SJAG_01082"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859575"},{"annotations":[87348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859576"},{"annotations":[88530,88529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009759"},{"annotations":[87664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013582"},{"annotations":[87346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859346"}]},"cv_name":"mondo","definition":"Mosaic variegated aneuploidy (MVA) syndrome is a chromosomal anomaly characterized by multiple mosaic aneuploidies that leads to a variety of phenotypic abnormalities and cancer predisposition.","definition_xrefs":["Orphanet:1052"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"chromosomal disorder","termid":"MONDO:0019040"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00213":null,"SJAG_01082":null,"SJAG_02795":null,"SJAG_03436":null,"SJAG_04699":null,"SJAG_04884":null},"genotype_count":0,"is_obsolete":false,"name":"mosaic variegated aneuploidy syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080688","OMIMPS:257300","UMLS:C4551972","MESH:C536987","GARD:3007","MEDGEN:1641418","SCTID:700056005","icd11.foundation:398235351","ICD9:758.89"],"synonyms":[{"name":"Warburton-Anyane-Yeboa syndrome","type":"exact"}],"termid":"MONDO:0000141","terms_by_termid":{"MONDO:0009759":null,"MONDO:0013582":null,"MONDO:0859346":null,"MONDO:0859575":null,"MONDO:0859576":null},"xrefs":{"Monarch":{"xref_id":"0000141"}}}


id: PBO:0043379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clustered mitochondria homolog pseudogene 9","termid":"PBO:0043379"}


id: GO:0060283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate or extent of the process whose specific outcome is the progression of an oocyte over time, from initial commitment of the cell to its specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell development","termid":"GO:0010721"},{"relation_name":"is_a","term_name":"regulation of oocyte development","termid":"GO:0060281"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_regulates","term_name":"oocyte development","termid":"GO:0048599"}],"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 oocyte development","termid":"GO:0060283"}


id: PBO:0085672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in outer spore wall assembly; possible role in assembly of the dityrosine layer; similar to adjacent ORF, LOH1; irc18 loh1 double mutant exhibits reduced dityrosine fluorescence relative to single mutants; SWAT-GFP fusion protein localizes to the ER and vacuole, while mCherry fusion localizes to the vacuole; expression induced in respiratory-deficient cells and carbon-limited chemostat culture; null mutant displays increased levels of spontaneous Rad52p foci","termid":"PBO:0085672"}


id: PBO:0049545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B clustered histone 8","termid":"PBO:0049545"}


id: GO:0048392
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an intermediate mesoderm cell.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesodermal cell differentiation","termid":"GO:0048333"},{"relation_name":"part_of","term_name":"intermediate mesoderm formation","termid":"GO:0048391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"intermediate mesodermal cell differentiation","synonyms":[{"name":"intermediate mesoderm cell differentiation","type":"exact"}],"termid":"GO:0048392"}


id: MONDO:1012797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteogenesis imperfecta that occurs in dogs due to a mutation in the COL1A1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta, dog","termid":"MONDO:1011581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteogenesis imperfecta, type III, COL1A1-related, dog","secondary_identifiers":["OMIA:002126-9615"],"synonyms":[{"name":"osteogenesis imperfecta, type III, COL1A1-related, dog","type":"exact"}],"termid":"MONDO:1012797","xrefs":{"Monarch":{"xref_id":"1012797"}}}


id: PBO:0072195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17 pseudogene 12","termid":"PBO:0072195"}


id: PBO:0062179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily M member 2B","termid":"PBO:0062179"}


id: PBO:0091459
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"I:g.3197528_3197529insG","termid":"PBO:0091459"}


id: PBO:0078734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Met (anticodon CAT) 6-1","termid":"PBO:0078734"}


id: PBO:0047326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAU pseudogene 4","termid":"PBO:0047326"}


id: PBO:0109838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NuA4 histone acetyltransferase core complex-Piccolo HAT module linker protein Epl1","termid":"PBO:0109838"}


id: PBO:0076518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 20","termid":"PBO:0076518"}


id: PBO:0058325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4698","termid":"PBO:0058325"}


id: GO:0046870
data:
  {"annotated_genes":["SJAG_04516"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[99146],"is_not":false,"summary":null,"term":"GO:0046870"}]},"cv_name":"molecular_function","definition":"Binding to a cadmium ion (Cd).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion binding","termid":"GO:0046914"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0046872"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0046872"],"is_obsolete":false,"name":"cadmium ion binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Cd ion binding","type":"exact"},{"name":"cadmium binding","type":"exact"},{"name":"copper/cadmium binding","type":"broad"}],"termid":"GO:0046870","terms_by_termid":{"GO:0046870":null}}


id: MONDO:0025420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition of chronic gastroenteritis in adult pigs and fatal gastroenteritis in piglets caused by a coronavirus.","definition_xrefs":["MESH:D005761"],"direct_ancestors":[{"relation_name":"is_a","term_name":"swine disease","termid":"MONDO:0024990"},{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gastroenteritis, transmissible, of swine","synonyms":[{"name":"Gastroenteritides, porcine transmissible","type":"related"},{"name":"Gastroenteritides, swine transmissible","type":"related"},{"name":"Gastroenteritides, transmissible porcine","type":"related"},{"name":"gastroenteritis, porcine transmissible","type":"related"},{"name":"gastroenteritis, swine transmissible","type":"related"},{"name":"gastroenteritis, transmissible porcine","type":"related"},{"name":"gastroenteritis, transmissible, porcine","type":"related"},{"name":"porcine Gastroenteritides, transmissible","type":"related"},{"name":"porcine gastroenteritis, transmissible","type":"related"},{"name":"porcine transmissible Gastroenteritides","type":"related"},{"name":"porcine transmissible gastroenteritis","type":"related"},{"name":"swine transmissible Gastroenteritides","type":"related"},{"name":"swine transmissible gastroenteritis","type":"related"},{"name":"transmissible Gastroenteritides, porcine","type":"related"},{"name":"transmissible Gastroenteritides, swine","type":"related"},{"name":"transmissible gastroenteritis of swine","type":"related"},{"name":"transmissible gastroenteritis, porcine","type":"related"},{"name":"transmissible gastroenteritis, swine","type":"related"},{"name":"transmissible porcine Gastroenteritides","type":"related"},{"name":"transmissible porcine gastroenteritis","type":"related"}],"termid":"MONDO:0025420","xrefs":{"Monarch":{"xref_id":"0025420"}}}


id: PBO:0075673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine palmitoyltransferase small subunit A","termid":"PBO:0075673"}


id: GO:0005176
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a protein-tyrosine kinase receptor Neu/ErbB-2/HER2.","definition_xrefs":["GOC:jl"],"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:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"ErbB-2 class receptor binding","synonyms":[{"name":"ErbB-2 class receptor ligand","type":"narrow"},{"name":"HER2 receptor binding","type":"exact"},{"name":"HER2 receptor ligand","type":"narrow"},{"name":"Neu receptor binding","type":"exact"},{"name":"Neu receptor ligand","type":"narrow"}],"termid":"GO:0005176"}


id: MONDO:0009665
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A late-onset form of multiple carboxylase deficiency, an inborn error of biotin metabolism that, if untreated, is characterized by seizures, breathing difficulties, hypotonia, skin rash, alopecia, hearing loss and delayed development.","definition_xrefs":["Orphanet:79241"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metabolic epilepsy","termid":"MONDO:0100033"},{"relation_name":"is_a","term_name":"multiple carboxylase deficiency","termid":"MONDO:0015454"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0004736","MONDO:0005244"],"is_obsolete":false,"name":"biotinidase deficiency","secondary_identifiers":["MedDRA:10071434","DOID:856","MESH:D028921","ICD10CM:D81.810","NORD:857","NANDO:1200822","GARD:894","OMIM:253260","UMLS:C0220754","MEDGEN:66323","NCIT:C84598","ICD9:277.6","SCTID:8808004"],"synonyms":[{"name":"BTD deficiency","type":"exact"},{"name":"biotin deficiency","type":"related"},{"name":"biotinidase deficiency","type":"exact"},{"name":"deficiency of biotinidase","type":"exact"},{"name":"juvenile-onset multiple carboxylase deficiency","type":"exact"},{"name":"late-onset biotin-responsive multiple carboxylase deficiency","type":"related"},{"name":"late-onset multiple carboxylase deficiency","type":"exact"},{"name":"multiple carboxylase deficiency, juvenile-onset","type":"related"},{"name":"multiple carboxylase deficiency, late-onset","type":"related"}],"termid":"MONDO:0009665","xrefs":{"Monarch":{"xref_id":"0009665"}}}


id: GO:0003873
data:
  {"annotated_genes":["SJAG_03336","SJAG_00039","SJAG_02596","SJAG_02713"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75041,76697,80508,81972],"is_not":false,"summary":null,"term":"GO:0003873"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-D-fructose 6-phosphate + ATP = beta-D-fructose 2,6-bisphosphate + ADP + 2 H+.","definition_xrefs":["RHEA:15653","EC:2.7.1.105"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphofructokinase activity","termid":"GO:0008443"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00039":null,"SJAG_02596":null,"SJAG_02713":null,"SJAG_03336":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"6-phosphofructo-2-kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R02732","MetaCyc:6-PHOSPHOFRUCTO-2-KINASE-RXN","Reactome:R-HSA-71802"],"synonyms":[{"name":"6-phosphofructo-2-kinase (phosphorylating)","type":"related"},{"name":"6-phosphofructose 2-kinase activity","type":"related"},{"name":"ATP:D-fructose-6-phosphate 2-phosphotransferase activity","type":"related"},{"name":"ATP:beta-D-fructose-6-phosphate 2-phosphotransferase activity","type":"related"},{"name":"fructose 6-phosphate 2-kinase activity","type":"related"},{"name":"phosphofructokinase 2 activity","type":"related"}],"termid":"GO:0003873","terms_by_termid":{"GO:0003873":null}}


id: PATO:0002088
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structure quality inhering in a bearer by virtue of the bearer's body consisting of one sac.","definition_xrefs":["mondofacto:mondofacto"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cystic","termid":"PATO:0001673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monocystic","termid":"PATO:0002088"}


id: MONDO:0011616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.","definition_xrefs":["PMID:11343300","DOID:0110874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"holoprosencephaly","termid":"MONDO:0016296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"holoprosencephaly 6","secondary_identifiers":["MESH:C565274","MEDGEN:342979","OMIM:605934","UMLS:C1853830"],"synonyms":[{"name":"HPE6","type":"exact"},{"name":"holoprosencephaly 6","type":"exact"},{"name":"holoprosencephaly type 6","type":"exact"}],"termid":"MONDO:0011616","xrefs":{"Monarch":{"xref_id":"0011616"}}}


id: GO:0034889
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: endosulfan hemisulfate + H2O = endosulfan monoalcohol + 2 H+ + sulfate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete endosulfan hemisulfate sulfatase activity (obsolete GO:0034889)","termid":"GO:0034889"}


id: PR:Q9P6J0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1683.12 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6J0"],"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 transporter C1683.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1683.12","synonyms":[{"name":"Spom972h-SPBC1683.12","type":"exact"}],"termid":"PR:Q9P6J0"}


id: FYPO:0001035
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the fungal-type cell wall is thicker than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell wall thickness during vegetative growth","termid":"FYPO:0006745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002946"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0002946","FYPO:0001985"],"is_obsolete":false,"name":"increased cell wall thickness during vegetative growth","synonyms":[{"name":"increased cell wall thickness during mitotic cell cycle","type":"related"},{"name":"thickened cell wall during vegetative growth","type":"exact"}],"termid":"FYPO:0001035"}


id: PBO:0053861
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 1134","termid":"PBO:0053861"}


id: PBO:0053997
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 1320","termid":"PBO:0053997"}


id: PBO:0080226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"viral integration site 1","termid":"PBO:0080226"}


id: GO:1901292
data:
  {"annotated_genes":["SJAG_00461","SJAG_06622","SJAG_04334","SJAG_03676","SJAG_04487","SJAG_00027","SJAG_00839","SJAG_02945","SJAG_02785","SJAG_03373","SJAG_03977","SJAG_02369","SJAG_04048","SJAG_01310","SJAG_01974","SJAG_04870","SJAG_02107","SJAG_03828","SJAG_01595","SJAG_02009","SJAG_02796","SJAG_02481","SJAG_02135","SJAG_00605","SJAG_02247","SJAG_03797","SJAG_05314","SJAG_04169","SJAG_06621","SJAG_03903","SJAG_04192","SJAG_01055","SJAG_04495","SJAG_03660","SJAG_03091","SJAG_00685","SJAG_04939"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901911"},{"annotations":[118220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006198"},{"annotations":[111218,111219,99776,105179,118191,107628,107260,107259,105436,111215,107258,111216,111214,107629,74116,79530,111213,100047,96301,111217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[79720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015938"},{"annotations":[77461,70426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009159"},{"annotations":[62607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009204"},{"annotations":[80957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901909"},{"annotations":[80956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901907"},{"annotations":[113281,118937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015964"},{"annotations":[100772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"},{"annotations":[81188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"},{"annotations":[90375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[74075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019677"},{"annotations":[74076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006742"},{"annotations":[74768,77826],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045820"},{"annotations":[72194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009134"},{"annotations":[71694],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006110"},{"annotations":[115150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009191"},{"annotations":[78139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006256"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a nucleoside phosphate.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside phosphate metabolic process","termid":"GO:0006753"},{"relation_name":"is_a","term_name":"nucleobase-containing compound catabolic process","termid":"GO:0034655"},{"relation_name":"is_a","term_name":"organophosphate catabolic process","termid":"GO:0046434"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00685":null,"SJAG_00839":null,"SJAG_01055":null,"SJAG_01310":null,"SJAG_01595":null,"SJAG_01974":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02247":null,"SJAG_02369":null,"SJAG_02481":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03091":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03676":null,"SJAG_03797":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_03977":null,"SJAG_04048":null,"SJAG_04169":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04487":null,"SJAG_04495":null,"SJAG_04870":null,"SJAG_04939":null,"SJAG_05314":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"nucleoside phosphate catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"nucleoside phosphate breakdown","type":"exact"},{"name":"nucleoside phosphate catabolism","type":"exact"},{"name":"nucleoside phosphate degradation","type":"exact"}],"termid":"GO:1901292","terms_by_termid":{"GO:0006110":null,"GO:0006198":null,"GO:0006256":null,"GO:0006742":null,"GO:0009134":null,"GO:0009159":null,"GO:0009191":null,"GO:0009204":null,"GO:0015938":null,"GO:0015964":null,"GO:0019677":null,"GO:0035863":null,"GO:0045820":null,"GO:0046081":null,"GO:0061613":null,"GO:0061621":null,"GO:1901907":null,"GO:1901909":null,"GO:1901911":null}}


id: PBO:0113014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Autophagy receptor; highly enriched in autophagic body fractions of both rapamycin-treated and nitrogen-starved cells; binds directly to forming isolation membranes during bulk autophagy; small protein of 144 amino acid residues without any identifiable membrane-spanning regions; N-terminal 42 amino acid region contains an amphipathic helix and an Atg8-family interacting motif","termid":"PBO:0113014"}


id: PBO:0004431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex bromodomain subunit Spt7","termid":"PBO:0004431"}


id: PBO:0038443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adipogenesis associated Mth938 domain containing","termid":"PBO:0038443"}


id: MONDO:0019041
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic inherited tumor (obsolete MONDO:0019041)","secondary_identifiers":["Orphanet:68336"],"synonyms":[{"name":"rare genetic tumor","type":"related"}],"termid":"MONDO:0019041","xrefs":{"Monarch":{"xref_id":"0019041"}}}


id: GO:0030108
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a MHC class I molecule of the HLA-A subclass to mediate signaling that activates a lymphocyte.","definition_xrefs":["GOC:add","PMID:11929129","GOC:mah","PMID:9368779"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activating MHC class I receptor activity","termid":"GO:0032397"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"HLA-A specific activating MHC class I receptor activity","termid":"GO:0030108"}


id: PBO:0060383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myelin transcription factor 1","termid":"PBO:0060383"}


id: MONDO:0011034
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Odontomicronychial dysplasia is a rare, hereditary ectodermal dysplasia syndrome characterized by involvement of teeth and nails - precocious eruption and shedding of deciduous dentition, precocious eruption of secondary dentition with short, rhomboid roots, and short, thin, slow growing nails.","definition_xrefs":["Orphanet:1811"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"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":"odontomicronychial dysplasia","secondary_identifiers":["GARD:4053","MESH:C537741","OMIM:601319","MEDGEN:371336","UMLS:C1832473"],"synonyms":[{"name":"ectodermal dysplasia, nail/Tooth type","type":"related"},{"name":"odonto-micronychial dysplasia","type":"related"},{"name":"odontomicronychial dysplasia","type":"exact"}],"termid":"MONDO:0011034","xrefs":{"Monarch":{"xref_id":"0011034"}}}


id: GO:0045480
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-galactose + O2 = D-galacto-hexodialdose + hydrogen peroxide.","definition_xrefs":["EC:1.1.3.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"galactose oxidase activity","secondary_identifiers":["MetaCyc:GALACTOSE-OXIDASE-RXN","RHEA:24160"],"synonyms":[{"name":"D-galactose oxidase activity","type":"related"},{"name":"D-galactose:oxygen 6-oxidoreductase activity","type":"related"},{"name":"beta-galactose oxidase activity","type":"related"}],"termid":"GO:0045480"}


id: MONDO:0017689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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:0005066","MONDO:0037792"],"is_obsolete":false,"name":"disorder of fructose metabolism","secondary_identifiers":["UMLS:C0342744","GARD:21307","SCTID:39452003","Orphanet:308463","icd11.foundation:596254627","MEDGEN:575202"],"termid":"MONDO:0017689","xrefs":{"Monarch":{"xref_id":"0017689"}}}


id: GO:0032722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of chemokine production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine production","termid":"GO:0001819"},{"relation_name":"is_a","term_name":"regulation of chemokine production","termid":"GO:0032642"},{"relation_name":"positively_regulates","term_name":"chemokine production","termid":"GO:0032602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of chemokine production","secondary_identifiers":["GO:0090197","GO:0045080"],"synonyms":[{"name":"activation of chemokine production","type":"narrow"},{"name":"positive regulation of chemokine biosynthetic process","type":"narrow"},{"name":"positive regulation of chemokine secretion","type":"narrow"},{"name":"stimulation of chemokine production","type":"narrow"},{"name":"up regulation of chemokine production","type":"exact"},{"name":"up-regulation of chemokine production","type":"exact"},{"name":"upregulation of chemokine production","type":"exact"}],"termid":"GO:0032722"}


id: PBO:0069257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 512, pseudogene","termid":"PBO:0069257"}


id: PBO:0048455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRIP and coiled-coil domain containing 2","termid":"PBO:0048455"}


id: PBO:0016916
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Septum Promoting GTPase","termid":"PBO:0016916"}


id: PBO:0062891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovo like zinc finger 3","termid":"PBO:0062891"}


id: PBO:0040089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arylsulfatase family member I","termid":"PBO:0040089"}


id: MONDO:0007574
data:
  {"annotated_genes":["SJAG_01356","SJAG_02885"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87379,87380],"is_not":false,"summary":null,"term":"MONDO:0007574"}]},"cv_name":"mondo","definition":"A subtype of autosomal dominant cerebellar ataxia type I (ADCA type I), characterized by papulosquamous, ichthyosiform plaques on the limbs appearing shortly after birth and later manifestations including progressive ataxia, dysarthria, nystagmus and decreased reflexes.","definition_xrefs":["Orphanet:1955"],"direct_ancestors":[{"relation_name":"is_a","term_name":"erythrokeratoderma","termid":"MONDO:0019270"},{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type I","termid":"MONDO:0019792"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01356":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005093","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"spinocerebellar ataxia type 34","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:59","SCTID:719255000","DOID:0050981","MESH:C535738","UMLS:C1851481","OMIM:133190","MEDGEN:338703","NORD:1105"],"synonyms":[{"name":"Erythrokeratodermia with Ataxia","type":"exact"},{"name":"Giroux Barbeau syndrome","type":"related"},{"name":"SCA34","type":"exact"},{"name":"erythrokeratodermia - ataxia","type":"related"},{"name":"erythrokeratodermia with ataxia","type":"exact"},{"name":"spinocerebellar ataxia 34","type":"related"},{"name":"spinocerebellar ataxia and erythrokeratodermia","type":"exact"},{"name":"spinocerebellar ataxia type 34","type":"exact"}],"termid":"MONDO:0007574","terms_by_termid":{"MONDO:0007574":null},"xrefs":{"Monarch":{"xref_id":"0007574"}}}


id: PBO:0014256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome quality control complex (RQC) complex subunit Rqc1 (predicted)","termid":"PBO:0014256"}


id: PBO:0091480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosamine-phosphate N-acetyltransferase","termid":"PBO:0091480"}


id: PBO:0060582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBPF member 19","termid":"PBO:0060582"}


id: MOD:00999
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00404. Remap to MOD:00404.","definition_xrefs":["DeltaMass:90"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:00999 homoseryl lactone (obsolete MOD:00999)","termid":"MOD:00999"}


id: PBO:0071490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 31","termid":"PBO:0071490"}


id: GO:0120219
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of a polarized cell that is just below the apical region. For example, in a polarized epithelial cell, the apical region has an exposed surface and lies opposite to the basal lamina that separates the epithelium from other tissue so the subapical region is further from the exposed surface and closer to the basal lamina.","definition_xrefs":["PMID:29891944","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"subapical part of cell","synonyms":[{"name":"subapical region of cell","type":"exact"}],"termid":"GO:0120219"}


id: GO:1903301
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hexokinase activity.","definition_xrefs":["GO_REF:0000059","GOC:mr","PMID:15804508","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of kinase activity","termid":"GO:0033674"}],"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 hexokinase activity","synonyms":[{"name":"activation of ATP-dependent hexokinase activity","type":"narrow"},{"name":"activation of ATP:D-hexose 6-phosphotransferase activity","type":"narrow"},{"name":"activation of glucose ATP phosphotransferase activity","type":"narrow"},{"name":"activation of hexokinase (phosphorylating)","type":"narrow"},{"name":"activation of hexokinase D","type":"related"},{"name":"activation of hexokinase activity","type":"narrow"},{"name":"activation of hexokinase type I activity","type":"narrow"},{"name":"activation of hexokinase type II activity","type":"narrow"},{"name":"activation of hexokinase type III activity","type":"narrow"},{"name":"activation of hexokinase type IV","type":"related"},{"name":"activation of hexokinase type IV (glucokinase) activity","type":"narrow"},{"name":"activation of hexokinase type IV glucokinase activity","type":"narrow"},{"name":"positive regulation of ATP-dependent hexokinase activity","type":"exact"},{"name":"positive regulation of ATP:D-hexose 6-phosphotransferase activity","type":"exact"},{"name":"positive regulation of glucose ATP phosphotransferase activity","type":"exact"},{"name":"positive regulation of hexokinase (phosphorylating)","type":"exact"},{"name":"positive regulation of hexokinase D","type":"related"},{"name":"positive regulation of hexokinase type I activity","type":"narrow"},{"name":"positive regulation of hexokinase type II activity","type":"narrow"},{"name":"positive regulation of hexokinase type III activity","type":"narrow"},{"name":"positive regulation of hexokinase type IV","type":"related"},{"name":"positive regulation of hexokinase type IV (glucokinase) activity","type":"narrow"},{"name":"positive regulation of hexokinase type IV glucokinase activity","type":"exact"},{"name":"up regulation of ATP-dependent hexokinase activity","type":"exact"},{"name":"up regulation of ATP:D-hexose 6-phosphotransferase activity","type":"exact"},{"name":"up regulation of glucose ATP phosphotransferase activity","type":"exact"},{"name":"up regulation of hexokinase (phosphorylating)","type":"exact"},{"name":"up regulation of hexokinase D","type":"related"},{"name":"up regulation of hexokinase activity","type":"exact"},{"name":"up regulation of hexokinase type I activity","type":"narrow"},{"name":"up regulation of hexokinase type II activity","type":"narrow"},{"name":"up regulation of hexokinase type III activity","type":"narrow"},{"name":"up regulation of hexokinase type IV","type":"related"},{"name":"up regulation of hexokinase type IV (glucokinase) activity","type":"narrow"},{"name":"up regulation of hexokinase type IV glucokinase activity","type":"exact"},{"name":"up-regulation of ATP-dependent hexokinase activity","type":"exact"},{"name":"up-regulation of ATP:D-hexose 6-phosphotransferase activity","type":"exact"},{"name":"up-regulation of glucose ATP phosphotransferase activity","type":"exact"},{"name":"up-regulation of hexokinase (phosphorylating)","type":"exact"},{"name":"up-regulation of hexokinase D","type":"related"},{"name":"up-regulation of hexokinase activity","type":"exact"},{"name":"up-regulation of hexokinase type I activity","type":"narrow"},{"name":"up-regulation of hexokinase type II activity","type":"narrow"},{"name":"up-regulation of hexokinase type III activity","type":"narrow"},{"name":"up-regulation of hexokinase type IV","type":"related"},{"name":"up-regulation of hexokinase type IV (glucokinase) activity","type":"narrow"},{"name":"up-regulation of hexokinase type IV glucokinase activity","type":"exact"},{"name":"upregulation of ATP-dependent hexokinase activity","type":"exact"},{"name":"upregulation of ATP:D-hexose 6-phosphotransferase activity","type":"exact"},{"name":"upregulation of glucose ATP phosphotransferase activity","type":"exact"},{"name":"upregulation of hexokinase (phosphorylating)","type":"exact"},{"name":"upregulation of hexokinase D","type":"related"},{"name":"upregulation of hexokinase activity","type":"exact"},{"name":"upregulation of hexokinase type I activity","type":"narrow"},{"name":"upregulation of hexokinase type II activity","type":"narrow"},{"name":"upregulation of hexokinase type III activity","type":"narrow"},{"name":"upregulation of hexokinase type IV","type":"related"},{"name":"upregulation of hexokinase type IV (glucokinase) activity","type":"narrow"},{"name":"upregulation of hexokinase type IV glucokinase activity","type":"exact"}],"termid":"GO:1903301"}


id: PBO:0004606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vac7 ortholog (predicted)","termid":"PBO:0004606"}


id: MONDO:0044303
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":"congenital heart defects and ectodermal dysplasia","secondary_identifiers":["UMLS:C4479250","MEDGEN:1387409","OMIM:617364"],"synonyms":[{"name":"CHDED","type":"related"},{"name":"congenital heart defects and ectodermal dysplasia","type":"exact"}],"termid":"MONDO:0044303","xrefs":{"Monarch":{"xref_id":"0044303"}}}


id: GO:0000379
data:
  {"annotated_genes":["SJAG_01260","SJAG_00754","SJAG_04907","SJAG_03328"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73146,74583,75626,80662],"is_not":false,"summary":null,"term":"GO:0000379"}]},"cv_name":"biological_process","definition":"RNA processing that begins when the tertiary structure of a tRNA type intron is recognized, and ends when the endonucleolytic cleavage of the RNA at both the 5' and 3' splice sites occurs.","definition_xrefs":["GOC:mah","ISBN:0879695897","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA processing","termid":"GO:0006396"},{"relation_name":"part_of","term_name":"tRNA splicing, via endonucleolytic cleavage and ligation","termid":"GO:0006388"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00754":null,"SJAG_01260":null,"SJAG_03328":null,"SJAG_04907":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0006399","GO:0010467"],"is_obsolete":false,"name":"tRNA-type intron splice site recognition and cleavage","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0000379","terms_by_termid":{"GO:0000379":null}}


id: GO:0048784
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a pigment, contributing to the process in which a membrane-bounded organelle develops into a pigment granule. Maturation is a developmental process, independent of morphogenetic (shape) change, that is required for a cell or structure to attain its fully functional state.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pigment metabolic process involved in developmental pigmentation","termid":"GO:0043324"},{"relation_name":"is_a","term_name":"pigment biosynthetic process involved in pigment accumulation","termid":"GO:0043477"},{"relation_name":"part_of","term_name":"pigment granule maturation","termid":"GO:0048757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"pigment biosynthetic process involved in pigment granule maturation","synonyms":[{"name":"pigment biosynthetic process during pigment granule maturation","type":"related"}],"termid":"GO:0048784"}


id: PBO:0034695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene characterisation status","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved_unknown","termid":"PBO:0034695"}


id: PBO:0001991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA snR91","termid":"PBO:0001991"}


id: MOD:01896
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by trifluoroacetic acid forming an adduct, either a salt or a hydrogen bonded carboxylic acid dimer, with an amino acid residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fluorinated residue","termid":"MOD:00498"},{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trifluoroacetic acid adduct","synonyms":[{"name":"TFA","type":"exact"}],"termid":"MOD:01896"}


id: GO:0018827
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-chloro-2,2-bis(4-chlorophenyl)ethane = HCl + unsym-bis(4-chlorophenyl)ethene. 1-chloro-2,2-bis(4-chlorophenyl)ethane is also known as DDMS; unsym-bis(4-chlorophenyl)ethene is also known as DDNU.","definition_xrefs":["UM-BBD_reactionID:r0515"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-chloro-2,2-bis(4-chlorophenyl)ethane dehydrochlorinase activity (obsolete GO:0018827)","synonyms":[{"name":"DDMS dehydrochlorinase activity","type":"exact"}],"termid":"GO:0018827"}


id: GO:0043592
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outermost layer of a bacterial endospore, which is loosely attached and located outside of the endospore coat. It is generally composed of protein, carbohydrate, and perhaps lipid.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"endospore external encapsulating structure","termid":"GO:0043591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005618"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005618"],"is_obsolete":false,"name":"exosporium","synonyms":[{"name":"epispore","type":"related"},{"name":"exospore","type":"related"},{"name":"perispore","type":"related"}],"termid":"GO:0043592"}


id: MONDO:0017589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Follicular cholangitis and pancreatitis is a rare pancreatobiliary disease characterized by marked duct-centered lymphoid follicular inflammation that develops in both biliary and pancreatic ductal systems, mainly affecting the hilar bile ducts and the pancreatic head. Patients present with jaundice, abdominal pain, liver dysfunction, pruritus and/or weight loss. Histology shows lymphoplasmacytic infiltration with formation of numerous, large lymphpoid follicles around the affected bile and pancreatic ducts.","definition_xrefs":["Orphanet:300552"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreas disorder","termid":"MONDO:0002356"},{"relation_name":"is_a","term_name":"biliary tract disorder","termid":"MONDO:0004868"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"follicular cholangitis and pancreatitis","secondary_identifiers":["MEDGEN:1667817","GARD:21236","UMLS:C4749906"],"synonyms":[{"name":"follicular pancreatocholangitis","type":"exact"}],"termid":"MONDO:0017589","xrefs":{"Monarch":{"xref_id":"0017589"}}}


id: PBO:0078640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triple QxxK/R motif containing","termid":"PBO:0078640"}


id: FYPO:0003549
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype that affects the localization of a protein in a cell during one or both meiotic nuclear divisions. A protein may be observed in a place where it is not normally found, absent from a place where it is normally found, or both.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiotic cell cycle","termid":"FYPO:0004094"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization during meiosis","synonyms":[{"name":"abnormal cellular protein localisation during meiosis","type":"exact"},{"name":"abnormal cellular protein localization during meiosis","type":"exact"},{"name":"abnormal protein localisation during meiosis","type":"exact"},{"name":"abnormal protein localization during meiotic nuclear division","type":"exact"}],"termid":"FYPO:0003549"}


id: GO:2000438
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of monocyte extravasation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular extravasation","termid":"GO:0002692"},{"relation_name":"is_a","term_name":"negative regulation of mononuclear cell migration","termid":"GO:0071676"},{"relation_name":"is_a","term_name":"regulation of monocyte extravasation","termid":"GO:2000437"},{"relation_name":"negatively_regulates","term_name":"monocyte extravasation","termid":"GO:0035696"}],"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 monocyte extravasation","termid":"GO:2000438"}


id: MONDO:0014163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any left ventricular noncompaction in which the cause of the disease is a mutation in the MYBPC3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"left ventricular noncompaction","termid":"MONDO:0018901"},{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"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":"left ventricular noncompaction 10","secondary_identifiers":["OMIM:615396","GARD:15956","MEDGEN:811617","UMLS:C3715165"],"synonyms":[{"name":"LVNC10","type":"related"},{"name":"MYBPC3 left ventricular noncompaction","type":"exact"},{"name":"cardiomyopathy, dilated, 1Mm","type":"related"},{"name":"left ventricular noncompaction 10","type":"exact"},{"name":"left ventricular noncompaction caused by mutation in MYBPC3","type":"exact"},{"name":"left ventricular noncompaction type 10","type":"exact"}],"termid":"MONDO:0014163","xrefs":{"Monarch":{"xref_id":"0014163"}}}


id: PR:O43030
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fes1 gene.","definition_xrefs":["UniProtKB:O43030","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":"hsp70 nucleotide exchange factor fes1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B9.01","synonyms":[{"name":"Spom972h-fes1","type":"exact"}],"termid":"PR:O43030"}


id: GO:0006082
data:
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id: PBO:0039684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloid beta precursor protein binding family B member 1 interacting protein","termid":"PBO:0039684"}


id: MONDO:0025294
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bacterial, viral, or parasitic diseases transmitted to humans and animals by the bite of infected ticks. The families Ixodidae and Argasidae contain many bloodsucking species that are important pests of man and domestic birds and mammals and probably exceed all other arthropods in the number and variety of disease agents they transmit. Many of the tick-borne diseases are zoonotic.","definition_xrefs":["MESH:D017282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tick-borne infectious disease","secondary_identifiers":["MEDGEN:56488","UMLS:C0162700"],"synonyms":[{"name":"Tick borne diseases","type":"related"},{"name":"Tick borne infections","type":"related"},{"name":"Tick-borne disease","type":"related"},{"name":"Tick-borne infection","type":"related"},{"name":"Tick-borne infections","type":"related"},{"name":"disease, Tick-borne","type":"related"},{"name":"diseases, Tick-borne","type":"related"},{"name":"infection, Tick-borne","type":"related"},{"name":"infections, Tick borne","type":"related"},{"name":"infections, Tick-borne","type":"related"}],"termid":"MONDO:0025294","xrefs":{"Monarch":{"xref_id":"0025294"}}}


id: PBO:0066494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ret finger protein like 4A pseudogene 5","termid":"PBO:0066494"}


id: PBO:0066689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of MON1-CCZ1","termid":"PBO:0066689"}


id: MONDO:0019417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked intellectual disability-precocious puberty-obesity syndrome is characterized by moderate intellectual deficit and precocious puberty. It has been described in three males from two generations of one Australian family. Morbid obesity was noted in the mothers of the patients. Transmission is X-linked.","definition_xrefs":["Orphanet:85318"],"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":"X-linked intellectual disability-precocious puberty-obesity syndrome","termid":"MONDO:0019417","xrefs":{"Monarch":{"xref_id":"0019417"}}}


id: PBO:0091290
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LEM-like Enriched in Stalks","termid":"PBO:0091290"}


id: PBO:0078309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asp (GTC) 5-1","termid":"PBO:0078309"}


id: PBO:0088126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar membrane polyphosphate polymerase; subunit of the vacuolar transporter chaperone (VTC) complex involved in synthesis and transfer of polyP to the vacuole; regulates membrane trafficking; role in non-autophagic vacuolar fusion; protein abundance increases in response to DNA replication stress","termid":"PBO:0088126"}


id: PBO:0017921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial FAD transmembrane transporter (predicted)","termid":"PBO:0017921"}


id: PBO:0060312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYLK antisense RNA 2","termid":"PBO:0060312"}


id: FYPO:0004308
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 CENP-A-containing chromatin organization is abnormal.","definition_xrefs":["PMID:9230309","GO:0061641","PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin organization during vegetative growth","termid":"FYPO:0001352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000641","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal CENP-A containing chromatin organization","synonyms":[{"name":"abnormal CENP-A containing chromatin organisation","type":"exact"},{"name":"abnormal CENP-A containing chromatin organization during mitotic cell cycle","type":"related"},{"name":"abnormal CENP-A containing chromatin organization during vegetative growth","type":"exact"},{"name":"abnormal chromatin organization at centromere central core","type":"related"}],"termid":"FYPO:0004308"}


id: GO:0000766
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"In organisms that undergo pheromone-induced unidirectional conjugation, the process involved in desensitization following exposure to pheromone stimulus that acts to down-regulate further stimulation or block initial conjugation responses.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative adaptation of signaling pathway","termid":"GO:0022401"},{"relation_name":"part_of","term_name":"response to pheromone regulating pheromone-induced unidirectional conjugation","termid":"GO:0000765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative adaptation of signaling pathway by response to pheromone involved in pheromone-induced unidirectional conjugation","synonyms":[{"name":"adaptation to pheromone during pheromone-induced unidirectional conjugation","type":"related"},{"name":"desensitization to pheromone during pheromone-induced unidirectional conjugation","type":"exact"},{"name":"negative adaptation of signalling pathway by response to pheromone involved in pheromone-induced unidirectional conjugation","type":"exact"}],"termid":"GO:0000766"}


id: MONDO:1040020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A bacterial infectious disease caused by methicillin-susceptible staphylococcus aureus.","definition_xrefs":["PMID:33144192","MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"staphylococcus aureus infection","termid":"MONDO:0005545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methicillin-susceptible staphylococcus aureus infectious disease","termid":"MONDO:1040020","xrefs":{"Monarch":{"xref_id":"1040020"}}}


id: GO:0030671
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a clathrin-coated phagocytic vesicle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-coated endocytic vesicle membrane","termid":"GO:0030669"},{"relation_name":"is_a","term_name":"phagocytic vesicle membrane","termid":"GO:0030670"},{"relation_name":"part_of","term_name":"clathrin-coated phagocytic vesicle","termid":"GO:0045336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"clathrin-coated phagocytic vesicle membrane","termid":"GO:0030671"}


id: FYPO:0003503
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell has a normal length.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell size","termid":"FYPO:0001124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal vegetative cell length","synonyms":[{"name":"normal cell length during vegetative growth","type":"exact"},{"name":"normal vegetative cell length during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003503"}


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


id: PBO:0046165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E74 like ETS transcription factor 3","termid":"PBO:0046165"}


id: PBO:0071972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 kinase like 1","termid":"PBO:0071972"}


id: GO:0034863
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,4,4-trimethyl-1-pentanol = 2,4,4-trimethylpentanal + 2 H+ + 2 e-.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,4,4-trimethyl-1-pentanol dehydrogenase activity (obsolete GO:0034863)","termid":"GO:0034863"}


id: GO:1903591
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of lysozyme activity.","definition_xrefs":["GOC:mr","GOC:TermGenie","PMID:23954697","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of lysozyme activity (obsolete GO:1903591)","synonyms":[{"name":"down regulation of 1,4-N-acetylmuramidase activity","type":"exact"},{"name":"down regulation of L-7001","type":"related"},{"name":"down regulation of N,O-diacetylmuramidase activity","type":"exact"},{"name":"down regulation of PR1-lysozyme","type":"related"},{"name":"down regulation of globulin G","type":"related"},{"name":"down regulation of globulin G1","type":"related"},{"name":"down regulation of lysozyme activity","type":"exact"},{"name":"down regulation of lysozyme g","type":"related"},{"name":"down regulation of mucopeptide N-acetylmuramoylhydrolase activity","type":"exact"},{"name":"down regulation of mucopeptide glucohydrolase activity","type":"exact"},{"name":"down regulation of muramidase activity","type":"exact"},{"name":"down regulation of peptidoglycan N-acetylmuramoylhydrolase activity","type":"exact"},{"name":"down-regulation of 1,4-N-acetylmuramidase activity","type":"exact"},{"name":"down-regulation of L-7001","type":"related"},{"name":"down-regulation of N,O-diacetylmuramidase activity","type":"exact"},{"name":"down-regulation of PR1-lysozyme","type":"related"},{"name":"down-regulation of globulin G","type":"related"},{"name":"down-regulation of globulin G1","type":"related"},{"name":"down-regulation of lysozyme activity","type":"exact"},{"name":"down-regulation of lysozyme g","type":"related"},{"name":"down-regulation of mucopeptide N-acetylmuramoylhydrolase activity","type":"exact"},{"name":"down-regulation of mucopeptide glucohydrolase activity","type":"exact"},{"name":"down-regulation of muramidase activity","type":"exact"},{"name":"down-regulation of peptidoglycan N-acetylmuramoylhydrolase activity","type":"exact"},{"name":"downregulation of 1,4-N-acetylmuramidase activity","type":"exact"},{"name":"downregulation of L-7001","type":"related"},{"name":"downregulation of N,O-diacetylmuramidase activity","type":"exact"},{"name":"downregulation of PR1-lysozyme","type":"related"},{"name":"downregulation of globulin G","type":"related"},{"name":"downregulation of globulin G1","type":"related"},{"name":"downregulation of lysozyme activity","type":"exact"},{"name":"downregulation of lysozyme g","type":"related"},{"name":"downregulation of mucopeptide N-acetylmuramoylhydrolase activity","type":"exact"},{"name":"downregulation of mucopeptide glucohydrolase activity","type":"exact"},{"name":"downregulation of muramidase activity","type":"exact"},{"name":"downregulation of peptidoglycan N-acetylmuramoylhydrolase activity","type":"exact"},{"name":"inhibition of 1,4-N-acetylmuramidase activity","type":"narrow"},{"name":"inhibition of L-7001","type":"related"},{"name":"inhibition of N,O-diacetylmuramidase activity","type":"narrow"},{"name":"inhibition of PR1-lysozyme","type":"related"},{"name":"inhibition of globulin G","type":"related"},{"name":"inhibition of globulin G1","type":"related"},{"name":"inhibition of lysozyme activity","type":"narrow"},{"name":"inhibition of lysozyme g","type":"related"},{"name":"inhibition of mucopeptide N-acetylmuramoylhydrolase activity","type":"narrow"},{"name":"inhibition of mucopeptide glucohydrolase activity","type":"narrow"},{"name":"inhibition of muramidase activity","type":"narrow"},{"name":"inhibition of peptidoglycan N-acetylmuramoylhydrolase activity","type":"narrow"},{"name":"negative regulation of 1,4-N-acetylmuramidase activity","type":"exact"},{"name":"negative regulation of L-7001","type":"related"},{"name":"negative regulation of N,O-diacetylmuramidase activity","type":"exact"},{"name":"negative regulation of PR1-lysozyme","type":"related"},{"name":"negative regulation of globulin G","type":"related"},{"name":"negative regulation of globulin G1","type":"related"},{"name":"negative regulation of lysozyme g","type":"related"},{"name":"negative regulation of mucopeptide N-acetylmuramoylhydrolase activity","type":"exact"},{"name":"negative regulation of mucopeptide glucohydrolase activity","type":"exact"},{"name":"negative regulation of muramidase activity","type":"exact"},{"name":"negative regulation of peptidoglycan N-acetylmuramoylhydrolase activity","type":"exact"}],"termid":"GO:1903591"}


id: PBO:0054321
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 1713","termid":"PBO:0054321"}


id: PBO:0036206
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H3-K4_methylation_during_vegetative_growth","termid":"PBO:0036206"}


id: GO:1902447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of shade avoidance.","definition_xrefs":["GOC:TermGenie","PMID:23763263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of shade avoidance","termid":"GO:1902446"},{"relation_name":"negatively_regulates","term_name":"shade avoidance","termid":"GO:0009641"}],"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 shade avoidance","synonyms":[{"name":"down regulation of shade avoidance","type":"exact"},{"name":"down-regulation of shade avoidance","type":"exact"},{"name":"downregulation of shade avoidance","type":"exact"},{"name":"inhibition of shade avoidance","type":"narrow"}],"termid":"GO:1902447"}


id: MONDO:0019442
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital toxoplasmosis (obsolete MONDO:0019442)","termid":"MONDO:0019442","xrefs":{"Monarch":{"xref_id":"0019442"}}}


id: GO:1901173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phytoene.","definition_xrefs":["GOC:yaf","UniPathway:UPA00799","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotene catabolic process","termid":"GO:0016121"},{"relation_name":"is_a","term_name":"phytoene metabolic process","termid":"GO:1901172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"phytoene catabolic process","synonyms":[{"name":"phytoene breakdown","type":"exact"},{"name":"phytoene catabolism","type":"exact"},{"name":"phytoene degradation","type":"exact"}],"termid":"GO:1901173"}


id: GO:0035448
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of a thylakoid membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:bf","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of membrane","termid":"GO:0019898"},{"relation_name":"part_of","term_name":"thylakoid membrane","termid":"GO:0042651"}],"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":"extrinsic component of thylakoid membrane","synonyms":[{"name":"extrinsic to thylakoid membrane","type":"narrow"},{"name":"peripheral to thylakoid membrane","type":"exact"}],"termid":"GO:0035448"}


id: MONDO:0006012
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the lung parenchyma that is caused by a viral infection.","definition_xrefs":["MESH:D011024"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumonia","termid":"MONDO:0005249"},{"relation_name":"is_a","term_name":"viral respiratory tract infection","termid":"MONDO:0024352"},{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"viral pneumonia","secondary_identifiers":["ICD9:480.8","icd11.foundation:1024154490","ICD9:480","SCTID:75570004","DOID:10533","ICD9:480.9","MEDGEN:45974","EFO:0007541","UMLS:C0032310"],"synonyms":[{"name":"Viruses caused pneumonia","type":"exact"},{"name":"Viruses pneumonia","type":"exact"}],"termid":"MONDO:0006012","xrefs":{"Monarch":{"xref_id":"0006012"}}}


id: PBO:0041918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBR1 antisense RNA 1","termid":"PBO:0041918"}


id: MONDO:0002196
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal perforation","termid":"MONDO:0006807"}],"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":"perinatal intestinal perforation","secondary_identifiers":["UMLS:C0159006","DOID:2073","ICD10CM:P78.0","ICD9:777.6","SCTID:65390006","MEDGEN:510691"],"termid":"MONDO:0002196","xrefs":{"Monarch":{"xref_id":"0002196"}}}


id: MONDO:0015616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic intestinal disease (obsolete MONDO:0015616)","secondary_identifiers":["Orphanet:165655"],"synonyms":[{"name":"genetic intestinal disease","type":"exact"}],"termid":"MONDO:0015616","xrefs":{"Monarch":{"xref_id":"0015616"}}}


id: MONDO:1010420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Narcolepsy that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"narcolepsy, non-human animal","termid":"MONDO:1010003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"narcolepsy, horse","secondary_identifiers":["OMIA:000703-9796"],"termid":"MONDO:1010420","xrefs":{"Monarch":{"xref_id":"1010420"}}}


id: PBO:0074355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structural maintenance of chromosomes 3","termid":"PBO:0074355"}


id: PBO:0081182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger CCCH-type and G-patch domain containing","termid":"PBO:0081182"}


id: PATO:0001770
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A viability quality inhering in a population by virtue of some of it's members' ability to survive.","definition_xrefs":["PATOC:CVC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viability","termid":"PATO:0000169"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semi-viable","termid":"PATO:0001770"}


id: GO:0060190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of protein desumoylation. Protein desumoylation is the process in which a SUMO protein (small ubiquitin-related modifier) is cleaved from its target protein.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein desumoylation","termid":"GO:0060188"},{"relation_name":"is_a","term_name":"negative regulation of protein modification by small protein conjugation or removal","termid":"GO:1903321"},{"relation_name":"negatively_regulates","term_name":"protein desumoylation","termid":"GO:0016926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein desumoylation","termid":"GO:0060190"}


id: PBO:0004890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA specific adenosine deaminase (predicted)","termid":"PBO:0004890"}


id: PBO:0012230
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"switching","termid":"PBO:0012230"}


id: GO:2000519
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of T-helper 1 cell activation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of CD4-positive, alpha-beta T cell activation","termid":"GO:2000516"},{"relation_name":"is_a","term_name":"regulation of T-helper 1 cell activation","termid":"GO:2000517"},{"relation_name":"positively_regulates","term_name":"T-helper 1 cell activation","termid":"GO:0035711"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"positive regulation of T-helper 1 cell activation","synonyms":[{"name":"positive regulation of Th1 cell activation","type":"exact"}],"termid":"GO:2000519"}


id: MONDO:0019968
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Osgood-Schlatter disease (obsolete MONDO:0019968)","termid":"MONDO:0019968","xrefs":{"Monarch":{"xref_id":"0019968"}}}


id: FYPO:0002828
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype in which the basal activity of a protein kinase is increased relative to normal. Basal protein kinase activity is the activity observed in the absence of a regulator. Abnormally elevated basal activity may or may not reach the levels observed in the normal activated state.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutive catalytic activity","termid":"FYPO:0000683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000652","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"constitutive protein kinase activity","synonyms":[{"name":"constitutive protein kinase activity during mitotic cell cycle","type":"related"},{"name":"constitutive protein kinase activity during vegetative growth","type":"exact"},{"name":"constitutively active protein kinase","type":"related"}],"termid":"FYPO:0002828"}


id: GO:0120154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ERBB4 signaling pathway.","definition_xrefs":["PMID:15219672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of ERBB signaling pathway","termid":"GO:1901185"},{"relation_name":"negatively_regulates","term_name":"ERBB4 signaling pathway","termid":"GO:0038130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of ERBB4 signaling pathway","termid":"GO:0120154"}


id: GO:0098953
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which a membrane receptor, diffusing freely within the plasma membeane, becomes trapped in some plasma membrane region. This can happen when a receptor bind, directly or indirectly, to some component of the underlying matrix.","definition_xrefs":["PMID:18832033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization within membrane","termid":"GO:0051668"}],"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:0008150","GO:0051179"],"is_obsolete":false,"name":"receptor diffusion trapping","termid":"GO:0098953"}


id: GO:0010110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of photosynthesis dark reaction.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of photosynthesis","termid":"GO:0010109"},{"relation_name":"is_a","term_name":"regulation of carbohydrate biosynthetic process","termid":"GO:0043255"},{"relation_name":"regulates","term_name":"photosynthesis, dark reaction","termid":"GO:0019685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"regulation of photosynthesis, dark reaction","termid":"GO:0010110"}


id: GO:1904084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of epiboly.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24892953"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of epiboly (obsolete GO:1904084)","synonyms":[{"name":"down regulation of epiboly","type":"exact"},{"name":"down-regulation of epiboly","type":"exact"},{"name":"downregulation of epiboly","type":"exact"},{"name":"inhibition of epiboly","type":"narrow"},{"name":"negative regulation of epiboly","type":"exact"}],"termid":"GO:1904084"}


id: MONDO:0005982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A skin infection caused by a fungus.","definition_xrefs":["NCIT:C112181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous mycosis","termid":"MONDO:0000254"},{"relation_name":"is_a","term_name":"skin infection","termid":"MONDO:0021201"}],"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":"tinea infection","secondary_identifiers":["DOID:12404","EFO:0007510","MEDGEN:52757","UMLS:C0040247"],"synonyms":[{"name":"Tinea","type":"exact"},{"name":"Tinea caused disease or disorder","type":"exact"},{"name":"Tinea disease or disorder","type":"exact"},{"name":"Tinea infection","type":"exact"},{"name":"Tinea infectious disease","type":"exact"},{"name":"ringworm","type":"related"}],"termid":"MONDO:0005982","xrefs":{"Monarch":{"xref_id":"0005982"}}}


id: PBO:0060368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myocardin-induced smooth muscle lncRNA, inducer of differentiation","termid":"PBO:0060368"}


id: PBO:0042015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 71 like","termid":"PBO:0042015"}


id: PBO:0028139
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cytosolic_small_ribosomal_subunit_level","termid":"PBO:0028139"}


id: FYPO:0008372
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 cell surface is normal (i.e. indistinguishable from wild-type.","definition_xrefs":["PomBase:pb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during vegetative growth","termid":"FYPO:0000644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to cell surface during vegetative growth","termid":"FYPO:0008372"}


id: GO:0002586
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of antigen processing and presentation of peptide antigen via MHC class II.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation of peptide or polysaccharide antigen via MHC class II","termid":"GO:0002580"},{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation of peptide antigen","termid":"GO:0002583"},{"relation_name":"regulates","term_name":"antigen processing and presentation of peptide antigen via MHC class II","termid":"GO:0002495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of antigen processing and presentation of peptide antigen via MHC class II","synonyms":[{"name":"regulation of peptide antigen processing and presentation via MHC class II","type":"exact"}],"termid":"GO:0002586"}


id: PBO:0046441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epsin 2","termid":"PBO:0046441"}


id: GO:2000498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of induction of apoptosis in response to chemical stimulus.","definition_xrefs":["GOC:mtg_apoptosis","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of induction of apoptosis in response to chemical stimulus (obsolete GO:2000498)","synonyms":[{"name":"regulation of induction of apoptosis in response to chemical stimulus","type":"exact"},{"name":"regulation of induction of apoptosis in response to chemical substance","type":"exact"}],"termid":"GO:2000498"}


id: PR:O74359
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC28E12.02 gene.","definition_xrefs":["UniProtKB:O74359","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":"meiotically up-regulated gene 60 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC28E12.02","synonyms":[{"name":"Spom972h-SPBC28E12.02","type":"exact"}],"termid":"PR:O74359"}


id: MONDO:0000958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuroretinitis is an inflammation of the neural retina and optic nerve. Pathology: Direct invasion or autoimmune activation against the optic nerve may cause optic nerve vascular inflammation with secondary inflammation and edema in the nerve fiber layer of the retina.","direct_ancestors":[{"relation_name":"is_a","term_name":"neuritis","termid":"MONDO:0002122"},{"relation_name":"is_a","term_name":"retinal nerve fiber layer disorder","termid":"MONDO:0003579"},{"relation_name":"is_a","term_name":"optic papillitis","termid":"MONDO:0006879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0005328"],"is_obsolete":false,"name":"neuroretinitis","secondary_identifiers":["UMLS:C0154874","DOID:10176","ICD9:363.05","MESH:D012173","icd11.foundation:418437487","MEDGEN:57826"],"synonyms":[{"name":"Juxtapapillary focal retinitis and retinochoroiditis","type":"narrow"},{"name":"focal retinitis and retinochoroiditis, juxtapapillary","type":"narrow"},{"name":"papilloretinitis","type":"narrow"}],"termid":"MONDO:0000958","xrefs":{"Monarch":{"xref_id":"0000958"}}}


id: PBO:0077407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 141","termid":"PBO:0077407"}


id: PBO:0027118
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_zygotic_meiosis_II","termid":"PBO:0027118"}


id: PBO:0077456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM183A pseudogene 6","termid":"PBO:0077456"}


id: MONDO:0001544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mononeuritis of lower limb","termid":"MONDO:0004797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"tibial nerve palsy","secondary_identifiers":["MEDGEN:509643","SCTID:365258000","ICD9:355.8","DOID:12529","UMLS:C0154751"],"termid":"MONDO:0001544","xrefs":{"Monarch":{"xref_id":"0001544"}}}


id: GO:0048717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the anterior cibarial plate are generated and organized.","definition_xrefs":["GOC:rc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"clypeo-labral disc morphogenesis","termid":"GO:0007453"},{"relation_name":"part_of","term_name":"anterior cibarial plate development","termid":"GO:0048722"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"anterior cibarial plate morphogenesis","termid":"GO:0048717"}


id: GO:0010108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which a glutamine stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:sm"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of glutamine (obsolete GO:0010108)","synonyms":[{"name":"glutamine detection","type":"exact"},{"name":"glutamine perception","type":"related"},{"name":"glutamine sensing","type":"related"}],"termid":"GO:0010108"}


id: PBO:0073362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family F member 2","termid":"PBO:0073362"}


id: GO:0008936
data:
  {"annotated_genes":["SJAG_04467"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111441],"is_not":false,"summary":null,"term":"GO:0008936"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: nicotinamide + H2O = nicotinate + NH4+.","definition_xrefs":["RHEA:14545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidase activity","termid":"GO:0004040"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04467":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787","GO:0016810"],"is_obsolete":false,"name":"nicotinamidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:3.5.1.19","MetaCyc:NICOTINAMID-RXN"],"synonyms":[{"name":"NAMase activity","type":"related"},{"name":"YNDase activity","type":"related"},{"name":"nicotinamide amidase activity","type":"related"},{"name":"nicotinamide amidohydrolase activity","type":"related"},{"name":"nicotinamide deaminase activity","type":"related"},{"name":"nicotine deamidase activity","type":"related"}],"termid":"GO:0008936","terms_by_termid":{"GO:0008936":null}}


id: GO:1905934
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell fate determination.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:25793578","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate commitment","termid":"GO:0010454"},{"relation_name":"is_a","term_name":"regulation of cell fate determination","termid":"GO:1905933"},{"relation_name":"negatively_regulates","term_name":"cell fate determination","termid":"GO:0001709"}],"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 cell fate determination","synonyms":[{"name":"down regulation of cell fate determination","type":"exact"},{"name":"down-regulation of cell fate determination","type":"exact"},{"name":"downregulation of cell fate determination","type":"exact"},{"name":"inhibition of cell fate determination","type":"narrow"}],"termid":"GO:1905934"}


id: PBO:0053963
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 1271","termid":"PBO:0053963"}


id: GO:2000179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neural precursor cell proliferation.","definition_xrefs":["GOC:yaf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell population proliferation","termid":"GO:0008284"},{"relation_name":"is_a","term_name":"regulation of neural precursor cell proliferation","termid":"GO:2000177"},{"relation_name":"positively_regulates","term_name":"neural precursor cell proliferation","termid":"GO:0061351"}],"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 neural precursor cell proliferation","termid":"GO:2000179"}


id: PBO:0064822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 3D","termid":"PBO:0064822"}


id: PBO:0051406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IgLON family member 5","termid":"PBO:0051406"}


id: MONDO:0000608
data:
  {"annotated_genes":["SJAG_02208","SJAG_02330"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87866,87867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014891"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02208":null,"SJAG_02330":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"familial juvenile hyperuricemic nephropathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:162000","MESH:C537696","DOID:0060062","NANDO:2100014","UMLS:C0268113","NANDO:2200139","SCTID:46785007","MEDGEN:75651"],"synonyms":[{"name":"FJHN","type":"exact"},{"name":"familial juvenile gouty nephropathy","type":"exact"},{"name":"familial juvenile hyperuricemic nephropathy","type":"exact"},{"name":"familial nephropathy associated with hyperuricemia","type":"exact"},{"name":"familial nephropathy with gout","type":"exact"},{"name":"gouty nephropathy, familial","type":"related"},{"name":"gouty nephropathy, familial juvenile","type":"exact"},{"name":"juvenile gout","type":"exact"},{"name":"juvenile gouty nephropathy","type":"exact"},{"name":"nephropathy, familial, with gout","type":"exact"},{"name":"tubulointerstitial kidney disease","type":"exact"}],"termid":"MONDO:0000608","terms_by_termid":{"MONDO:0014891":null},"xrefs":{"Monarch":{"xref_id":"0000608"}}}


id: GO:1902176
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of an oxidative stress-induced intrinsic apoptotic signaling pathway.","definition_xrefs":["GOC:BHF","GOC:TermGenie","GOC:mtg_apoptosis","PMID:11672522"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of oxidative stress-induced intrinsic apoptotic signaling pathway","termid":"GO:1902175"},{"relation_name":"is_a","term_name":"negative regulation of intrinsic apoptotic signaling pathway","termid":"GO:2001243"},{"relation_name":"negatively_regulates","term_name":"intrinsic apoptotic signaling pathway in response to oxidative stress","termid":"GO:0008631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway","synonyms":[{"name":"down regulation of intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"},{"name":"down-regulation of intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"},{"name":"downregulation of intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"},{"name":"inhibition of intrinsic apoptotic signaling pathway in response to oxidative stress","type":"narrow"},{"name":"negative regulation of intrinsic apoptotic signaling pathway in response to oxidative stress","type":"exact"}],"termid":"GO:1902176"}


id: GO:0072349
data:
  {"annotated_genes":["SJAG_03577","SJAG_05175","SJAG_03503","SJAG_01660"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008517"},{"annotations":[114972,97308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034634"},{"annotations":[74148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015233"}]},"cv_name":"molecular_function","definition":"Enables the transfer of modified amino acids from one side of a membrane to the other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01660":null,"SJAG_03503":null,"SJAG_03577":null,"SJAG_05175":null},"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:0003674","GO:0022857"],"is_obsolete":false,"name":"modified amino acid transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"amino acid derivative transmembrane transporter activity","type":"exact"},{"name":"modified amino acid transporter activity","type":"broad"}],"termid":"GO:0072349","terms_by_termid":{"GO:0008517":null,"GO:0015233":null,"GO:0034634":null}}


id: PBO:0091878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PI31 proteasome regulator Fub2","termid":"PBO:0091878"}


id: PBO:0064675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 10","termid":"PBO:0064675"}


id: PBO:0084040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI-anchored protein involved in efficient glucose uptake; possible role in apical bud growth; GPI-anchoring on the plasma membrane crucial to function; phosphorylated in mitochondria; similar to Sps2p; ECM33 has a paralog, PST1, that arose from the whole genome duplication","termid":"PBO:0084040"}


id: MONDO:0007261
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":"Carabelli anomaly of maxillary molar teeth","secondary_identifiers":["OMIM:114700","MEDGEN:396243","MESH:C566175","UMLS:C1861897"],"synonyms":[{"name":"Carabelli anomaly of maxillary molar teeth","type":"exact"}],"termid":"MONDO:0007261","xrefs":{"Monarch":{"xref_id":"0007261"}}}


id: PBO:0045948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidermal growth factor","termid":"PBO:0045948"}


id: PBO:0049266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gasdermin E","termid":"PBO:0049266"}


id: GO:0061159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification and formation of bipolar intracellular organization or cell growth patterns that contribute to cell morphogenesis. Bipolar organization is the organization that is a mirror image along an axis from a plane.","definition_xrefs":["GOC:dph","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of bipolar cell polarity","termid":"GO:0061171"},{"relation_name":"part_of","term_name":"cell morphogenesis","termid":"GO:0000902"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"establishment of bipolar cell polarity involved in cell morphogenesis","termid":"GO:0061159"}


id: GO:0035961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of ergosterol biosynthesis by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:dgf","PMID:11533229"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of ergosterol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0035961)","synonyms":[{"name":"positive regulation of ergosterol anabolism by positive regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of ergosterol anabolism by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol anabolism by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol anabolism by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol anabolism by upregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol biosynthesis by positive regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of ergosterol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol biosynthesis by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol biosynthesis by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol biosynthesis by upregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol biosynthetic process by activation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol biosynthetic process by positive regulation of transcription from Pol II promoter","type":"related"},{"name":"positive regulation of ergosterol biosynthetic process by stimulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol biosynthetic process by up regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol biosynthetic process by up-regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol biosynthetic process by upregulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol formation by positive regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of ergosterol formation by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol formation by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol formation by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol formation by upregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol synthesis by positive regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of ergosterol synthesis by positive regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of ergosterol synthesis by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol synthesis by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of ergosterol synthesis by upregulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0035961"}


id: PR:Q9P7H8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proteasome-associated protein ECM29 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome component ecm29 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1782.01","secondary_identifiers":["UniProtKB:Q9P7H8"],"synonyms":[{"name":"SPAC1782.01","type":"related"},{"name":"Spom972h-ECM29","type":"exact"}],"termid":"PR:Q9P7H8"}


id: GO:0097226
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The tightly packed helical sheath of ATP-producing mitochondria restricted to the midpiece of the sperm flagellum.","definition_xrefs":["PMID:32791035","MP:0009832","GOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"sperm midpiece","termid":"GO:0097225"}],"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":"sperm mitochondrial sheath","termid":"GO:0097226"}


id: PBO:0054459
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 1856","termid":"PBO:0054459"}


id: PBO:0001504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase epsilon subunit Dpb3","termid":"PBO:0001504"}


id: GO:0034193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-galactonate, the anion of L-galactonic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"galactonate metabolic process","termid":"GO:0019583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"L-galactonate metabolic process","synonyms":[{"name":"L-galactonate metabolism","type":"exact"}],"termid":"GO:0034193"}


id: PBO:0004868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosome subunit Rrp42 (predicted)","termid":"PBO:0004868"}


id: PBO:0039898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGEF2 antisense RNA 2","termid":"PBO:0039898"}


id: PBO:0059653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 19","termid":"PBO:0059653"}


id: PBO:0043740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 7A1","termid":"PBO:0043740"}


id: MONDO:1011792
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":"subacute progressive myopathy, non-human animal","secondary_identifiers":["OMIA:000696"],"termid":"MONDO:1011792","xrefs":{"Monarch":{"xref_id":"1011792"}}}


id: PBO:0047029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 91 member A4, pseudogene","termid":"PBO:0047029"}


id: GO:0044211
data:
  {"annotated_genes":["SJAG_00533","SJAG_03708"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69538,94743],"is_not":false,"summary":null,"term":"GO:0044211"}]},"cv_name":"biological_process","definition":"Any process which produces cytidine 5'-triphosphate (CTP) from derivatives of it, without de novo synthesis.","definition_xrefs":["PMID:10501935","GOC:jl","GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CTP biosynthetic process","termid":"GO:0006241"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide salvage","termid":"GO:0010138"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00533":null,"SJAG_03708":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"CTP salvage","references_by_uniquename":{"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"CTP biosynthetic process via salvage pathway","type":"exact"},{"name":"cytidine 5'-triphosphate salvage","type":"exact"}],"termid":"GO:0044211","terms_by_termid":{"GO:0044211":null}}


id: PBO:0053287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain containing 1","termid":"PBO:0053287"}


id: PBO:0049788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 23","termid":"PBO:0049788"}


id: GO:1901697
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of olivetolic acid.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide biosynthetic process","termid":"GO:0030639"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"olivetolic acid biosynthetic process","synonyms":[{"name":"olivetolic acid anabolism","type":"exact"},{"name":"olivetolic acid biosynthesis","type":"exact"},{"name":"olivetolic acid formation","type":"exact"},{"name":"olivetolic acid synthesis","type":"exact"}],"termid":"GO:1901697"}


id: GO:0034183
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the extent to which the association between sister chromatids of a replicated chromosome is maintained during a mitotic cell cycle.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of maintenance of sister chromatid cohesion","termid":"GO:0034092"},{"relation_name":"is_a","term_name":"regulation of maintenance of mitotic sister chromatid cohesion","termid":"GO:0034182"},{"relation_name":"negatively_regulates","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of maintenance of mitotic sister chromatid cohesion","termid":"GO:0034183"}


id: PBO:0084468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPKK involved in the protein kinase C signaling pathway; involved in control of cell integrity; upon activation by Bck1p phosphorylates downstream target, Slt2p; functionally redundant with Mkk2p; MKK1 has a paralog, MKK2, that arose from the whole genome duplication","termid":"PBO:0084468"}


id: MONDO:0031071
data:
  {"annotated_genes":["SJAG_01621"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87505],"is_not":false,"summary":null,"term":"MONDO:0031071"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia","termid":"MONDO:0015253"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"Diamond-Blackfan anemia 21","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620072","UMLS:C5774230","MEDGEN:1824003"],"synonyms":[{"name":"DBA21","type":"exact"},{"name":"diamond-blackfan anaemia 21","type":"exact"},{"name":"diamond-blackfan anemia 21","type":"exact"}],"termid":"MONDO:0031071","terms_by_termid":{"MONDO:0031071":null},"xrefs":{"Monarch":{"xref_id":"0031071"}}}


id: MONDO:0015748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"White sponge nevus (WSN) is a rare and autosomal dominant genetic disease in which the oral mucosa is white or grayish, thickened, folded, and spongy. The onset is early in life, and both sexes are affected equally. Other common sites include the tongue, floor of the mouth, and alveolar mucosa.","definition_xrefs":["Orphanet:171723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"},{"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":"hereditary mucosal leukokeratosis","secondary_identifiers":["MEDGEN:328433","GARD:8501","MESH:D053529","NCIT:C84760","OMIMPS:193900","DOID:0050448","ICD9:528.6","SCTID:389203001","UMLS:C1721005"],"synonyms":[{"name":"White sponge nevus of Cannon","type":"exact"},{"name":"hereditary mucosal leukokeratosis","type":"exact"},{"name":"white sponge nevus","type":"exact"},{"name":"white sponge nevus of Cannon","type":"exact"}],"termid":"MONDO:0015748","xrefs":{"Monarch":{"xref_id":"0015748"}}}


id: GO:0102343
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (R)-3-hydroxyicosanoyl-CoA = trans-2-icosenoyl-CoA + H2O.","definition_xrefs":["EC:4.2.1.134","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-hydroxy-arachidoyl-CoA dehydratase activity (obsolete GO:0102343)","termid":"GO:0102343"}


id: PBO:0001181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L1 (predicted)","termid":"PBO:0001181"}


id: MONDO:0026193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic thrombotic microangiopathy (obsolete MONDO:0026193)","secondary_identifiers":["Orphanet:183589"],"termid":"MONDO:0026193","xrefs":{"Monarch":{"xref_id":"0026193"}}}


id: GO:0000113
data:
  {"annotated_genes":["SJAG_04147","SJAG_00500","SJAG_03612","SJAG_03613"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[113074,118530,118531,118552],"is_not":false,"summary":null,"term":"GO:0000113"}]},"cv_name":"cellular_component","definition":"One of several protein complexes involved in nucleotide-excision repair; possesses DNA damage recognition and DNA-dependent ATPase activities. In S. cerevisiae, it is composed of Rad7p and Rad16p.","definition_xrefs":["PMID:10915862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-excision repair complex","termid":"GO:0000109"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00500":null,"SJAG_03612":null,"SJAG_03613":null,"SJAG_04147":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"nucleotide-excision repair factor 4 complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"NEF4 complex","type":"exact"}],"termid":"GO:0000113","terms_by_termid":{"GO:0000113":null}}


id: PBO:0080989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZBTB20 antisense RNA 5","termid":"PBO:0080989"}


id: PBO:0048038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrous sheath interacting protein 1","termid":"PBO:0048038"}


id: PBO:0036118
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_modification_during_vegetative_growth","termid":"PBO:0036118"}


id: GO:0047160
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-alkyl-sn-glycerol 3-phosphate + acetyl-CoA = 1-alkyl-2-acetyl-sn-glycerol 3-phosphate + CoA.","definition_xrefs":["EC:2.3.1.105","RHEA:18557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016746"],"is_obsolete":false,"name":"alkylglycerophosphate 2-O-acetyltransferase activity","secondary_identifiers":["MetaCyc:2.3.1.105-RXN","KEGG_REACTION:R03455"],"synonyms":[{"name":"acetyl-CoA:1-alkyl-sn-glycero-3-phosphate 2-O-acetyltransferase activity","type":"related"},{"name":"alkyllyso-GP:acetyl-CoA acetyltransferase activity","type":"related"}],"termid":"GO:0047160"}


id: PBO:0056850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microsomal glutathione S-transferase 2","termid":"PBO:0056850"}


id: PATO:0001894
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"biological sex","termid":"PATO:0000047"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenotypic sex","termid":"PATO:0001894"}


id: PBO:0042416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle 27","termid":"PBO:0042416"}


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


id: MONDO:0007837
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Johnson neuroectodermal syndrome is characterized by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism.","definition_xrefs":["Orphanet:2316"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"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":"Johnson neuroectodermal syndrome","secondary_identifiers":["GARD:378","MEDGEN:167092","icd11.foundation:1480597785","MESH:C535882","UMLS:C0796002","OMIM:147770","SCTID:721584005"],"synonyms":[{"name":"Aadh syndrome","type":"related"},{"name":"Johnson neuroectodermal syndrome","type":"exact"},{"name":"Johnson-McMillin syndrome","type":"exact"},{"name":"alopecia anosmia deafness hypogonadism syndrome","type":"related"},{"name":"alopecia-anosmia-conductive hearing loss-hypogonadism syndrome","type":"exact"},{"name":"alopecia-anosmia-deafness-hypogonadism syndrome","type":"exact"}],"termid":"MONDO:0007837","xrefs":{"Monarch":{"xref_id":"0007837"}}}


id: PBO:0080407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS37A subunit of ESCRT-I","termid":"PBO:0080407"}


id: PBO:0052754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 46","termid":"PBO:0052754"}


id: MONDO:0019006
data:
  {"annotated_genes":["SJAG_00933","SJAG_01185","SJAG_04148","SJAG_03182","SJAG_03361","SJAG_04000","SJAG_04621","SJAG_00093"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[86830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011303"},{"annotations":[87638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014752"},{"annotations":[87561,87562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014817"},{"annotations":[87560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014818"},{"annotations":[86732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014099"},{"annotations":[87566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014257"}]},"cv_name":"mondo","definition":"Familial idiopathic steroid-resistant nephrotic syndrome is characterized by a nephrotic syndrome with often early onset.","definition_xrefs":["Orphanet:656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial nephrotic syndrome","termid":"MONDO:0002350"},{"relation_name":"is_a","term_name":"idiopathic nephrotic syndrome","termid":"MONDO:0018170"},{"relation_name":"is_a","term_name":"steroid-resistant nephrotic syndrome","termid":"MONDO:0044765"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00093":null,"SJAG_00933":null,"SJAG_01185":null,"SJAG_03182":null,"SJAG_03361":null,"SJAG_04000":null,"SJAG_04148":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"familial idiopathic steroid-resistant nephrotic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4273714","MEDGEN:902527","SCTID:718141008","GARD:3946","icd11.foundation:1385860879"],"synonyms":[{"name":"familial idiopathic nephrotic syndrome","type":"exact"}],"termid":"MONDO:0019006","terms_by_termid":{"MONDO:0011303":null,"MONDO:0013836":null,"MONDO:0014099":null,"MONDO:0014257":null,"MONDO:0014752":null,"MONDO:0014817":null,"MONDO:0014818":null},"xrefs":{"Monarch":{"xref_id":"0019006"}}}


id: PBO:0013819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin family protein Art1","termid":"PBO:0013819"}


id: MONDO:0023006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiomyopathy","termid":"MONDO:0004994"}],"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":"doxorubicin induced cardiomyopathy","secondary_identifiers":["GARD:6285"],"termid":"MONDO:0023006","xrefs":{"Monarch":{"xref_id":"0023006"}}}


id: FYPO:0006361
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which dimethylation of lysine at position 9 of histone H3 in heterochromatin at subtelomeric regions occurs to a greater extent than normal.","definition_xrefs":["PMID:26438724","PMID:29214404","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 dimethylation during vegetative growth","termid":"FYPO:0000873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002494","FYPO:0002274","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H3-K9 dimethylation at subtelomeric heterochromatin during vegetative growth","synonyms":[{"name":"increased histone H3 K9 dimethylation at subtelomeric heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 dimethylation at subtelomeres during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 dimethylation at subtelomeric heterochromatin during mitotic cell cycle","type":"related"},{"name":"increased histone H3-K9 dimethylation at telomeric heterochromatin during vegetative growth","type":"related"},{"name":"increased histone H3K9me2 at subtelomeric heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 dimethylation at subtelomeric heterochromatin during vegetative growth","type":"exact"}],"termid":"FYPO:0006361"}


id: PBO:0057484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 602","termid":"PBO:0057484"}


id: PBO:0042140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCL3 antisense RNA 1","termid":"PBO:0042140"}


id: GO:0071586
data:
  {"annotated_genes":["SJAG_03396","SJAG_00730"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71759,76584],"is_not":false,"summary":null,"term":"GO:0071586"}]},"cv_name":"biological_process","definition":"The second process in a series of specific posttranslational modifications to the CAAX box region of CAAX box proteins, in which the last three amino acids of the protein (AAX) are removed by proteolysis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein processing","termid":"GO:0016485"},{"relation_name":"part_of","term_name":"CAAX-box protein maturation","termid":"GO:0080120"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00730":null,"SJAG_03396":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0010467","GO:0051604","GO:0008150"],"is_obsolete":false,"name":"CAAX-box protein processing","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0071586","terms_by_termid":{"GO:0071586":null}}


id: PBO:0080943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zygote arrest 1 like","termid":"PBO:0080943"}


id: GO:0005381
data:
  {"annotated_genes":["SJAG_04867","SJAG_04675","SJAG_04737","SJAG_04260","SJAG_02968","SJAG_02473"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67488,115051,115633],"is_not":false,"summary":null,"term":"GO:0005381"},{"annotations":[71946,105591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015093"},{"annotations":[94222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061840"}]},"cv_name":"molecular_function","definition":"Enables the transfer of iron (Fe) ions from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transmembrane transporter activity","termid":"GO:0046915"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02473":null,"SJAG_02968":null,"SJAG_04260":null,"SJAG_04675":null,"SJAG_04737":null,"SJAG_04867":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"iron ion transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-904830","Reactome:R-HSA-917936","GO:0097689","GO:0005382","Reactome:R-HSA-435349","GO:0016033","Reactome:R-HSA-5623558","Reactome:R-HSA-5655733"],"synonyms":[{"name":"iron cation channel activity","type":"exact"},{"name":"iron channel activity","type":"exact"},{"name":"iron transporter activity","type":"exact"},{"name":"multicopper ferroxidase iron transport mediator activity","type":"related"},{"name":"transmembrane iron ion permease activity","type":"exact"},{"name":"transmembrane iron permease activity","type":"exact"},{"name":"zinc, iron permease activity","type":"related"}],"termid":"GO:0005381","terms_by_termid":{"GO:0005381":null,"GO:0015093":null,"GO:0061840":null}}


id: GO:0032115
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucitol + NADP+ = L-sorbose + H+ + NADPH. The reaction may occur, to a minor extent, in the reverse direction.","definition_xrefs":["EC:1.1.1.289","RHEA:14609"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"sorbose reductase activity","secondary_identifiers":["KEGG_REACTION:R07346","MetaCyc:1.1.1.289-RXN"],"synonyms":[{"name":"D-glucitol:NADP+ oxidoreductase activity","type":"related"},{"name":"Sou1p","type":"related"}],"termid":"GO:0032115"}


id: PR:O60102
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-binding cassette sub-family E member 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04015"],"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":"translation initiation factor rli1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC14F5.06","secondary_identifiers":["UniProtKB:O60102"],"synonyms":[{"name":"ATP-binding cassette sub-family E member rli1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNase L inhibitor (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ABCE1","type":"exact"}],"termid":"PR:O60102"}


id: FYPO:0009092
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is decreased relative to normal in a medium containing lysine and serine as nitrogen sources.","direct_ancestors":[{"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:0002058"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0002058","FYPO:0001985","FYPO:0002057","FYPO:0005447","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"decreased cell population growth on lysine and serine nitrogen source","synonyms":[{"name":"decreased vegetative cell growth on lysine and serine nitrogen source","type":"exact"}],"termid":"FYPO:0009092"}


id: FYECO:0000245
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which phosphate was added to the medium or assay buffer in excess.","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":"+ phosphate","termid":"FYECO:0000245"}


id: FYPO:0005836
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein transport along microtubules to the cell tip does not occur. Transport of all proteins or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to cell tip during vegetative growth","termid":"FYPO:0001585"},{"relation_name":"is_a","term_name":"abnormal protein transport along microtubule to cell tip during vegetative growth","termid":"FYPO:0005831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein transport along microtubule to cell tip during vegetative growth","synonyms":[{"name":"abolished protein movement along microtubule to cell tip during vegetative growth","type":"exact"},{"name":"abolished protein transport during mitotic cell cycle","type":"related"},{"name":"protein transport along microtubule to cell tip abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0005836"}


id: PBO:0075415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermadhesin family member","termid":"PBO:0075415"}


id: PBO:0083655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endonuclease I-SceII; encoded by a mobile group I intron within the mitochondrial COX1 gene; intron is normally spliced by the BI4p maturase but AI4p can mutate to acquire the same maturase activity","termid":"PBO:0083655"}


id: GO:0047519
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (-)-quinate + pyrroloquinoline-quinone = (-)-3-dehydroquinate + pyrroloquinoline-quinol.","definition_xrefs":["RHEA:23672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor","termid":"GO:0016901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"quinate dehydrogenase (quinone) activity","secondary_identifiers":["MetaCyc:1.1.99.25-RXN","KEGG_REACTION:R01873","EC:1.1.5.8"],"synonyms":[{"name":"NAD(P)-independent quinate dehydrogenase activity","type":"related"},{"name":"quinate:pyrroloquinoline-quinone 5-oxidoreductase activity","type":"related"},{"name":"quinate:quinone 3-oxidoreductase activity","type":"exact"}],"termid":"GO:0047519"}


id: MONDO:0007993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by the association of microgastria with a limb reduction defect.","definition_xrefs":["Orphanet:2538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microgastria-limb reduction defect syndrome","secondary_identifiers":["GARD:3640","UMLS:C1834929","MEDGEN:322532","MESH:C537554","OMIM:156810"],"synonyms":[{"name":"MLRD","type":"related"},{"name":"congenital microgastria and limb reduction defects","type":"related"},{"name":"microgastria limb reduction defect","type":"related"},{"name":"microgastria-limb reduction defects association","type":"related"}],"termid":"MONDO:0007993","xrefs":{"Monarch":{"xref_id":"0007993"}}}


id: GO:0007147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which the second meiotic division occurs in the female germline.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiosis II","termid":"GO:0007135"},{"relation_name":"is_a","term_name":"female meiotic nuclear division","termid":"GO:0007143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0140013","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"female meiosis II","synonyms":[{"name":"female meiosis II nuclear division","type":"exact"}],"termid":"GO:0007147"}


id: GO:0044474
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism inhibits or disrupts the activity of a voltage-gated calcium channel in another organism via the action of a venom.","definition_xrefs":["GOC:jl","PMID:20920515","GOC:fj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated inhibition of calcium channel activity","termid":"GO:0044473"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"venom-mediated inhibition of voltage-gated calcium channel activity","synonyms":[{"name":"envenomation resulting in negative regulation of voltage-gated calcium channel activity in another organism","type":"exact"},{"name":"envenomation resulting in negative regulation of voltage-gated calcium channel activity in other organism","type":"exact"}],"termid":"GO:0044474"}


id: MONDO:0011626
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":"acromegaloid features, overgrowth, cleft palate, and hernia","secondary_identifiers":["MEDGEN:340050","MESH:C535656","OMIM:606049","UMLS:C1853757"],"synonyms":[{"name":"Aoch","type":"related"},{"name":"acromegaloid features, overgrowth, cleft palate and hernia","type":"related"},{"name":"acromegaloid features, overgrowth, cleft palate, and hernia","type":"exact"}],"termid":"MONDO:0011626","xrefs":{"Monarch":{"xref_id":"0011626"}}}


id: MONDO:0013455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"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":"hypertrophic cardiomyopathy 16","secondary_identifiers":["DOID:0110322","UMLS:C3151204","OMIM:613838","MEDGEN:462554"],"synonyms":[{"name":"CMH16","type":"exact"},{"name":"MYOZ2 hypertrophic cardiomyopathy","type":"exact"},{"name":"cardiomyopathy familial hypertrophic 16","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 16","type":"related"},{"name":"cardiomyopathy, familial hypertrophic, type 16","type":"exact"},{"name":"cardiomyopathy, hypertrophic, 16","type":"exact"},{"name":"hypertrophic cardiomyopathy caused by mutation in MYOZ2","type":"exact"},{"name":"hypertrophic cardiomyopathy type 16","type":"exact"}],"termid":"MONDO:0013455","xrefs":{"Monarch":{"xref_id":"0013455"}}}


id: SO:0001067
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence motif is a short (up to 20 amino acids) region of biological interest. Such motifs, although they are too short to constitute functional domains, share sequence similarities and are conserved in different proteins. They display a common function (protein-binding, subcellular location etc.).","definition_xrefs":["EBIBS:GAR","UniProt:curation_manual"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_conserved_region","termid":"SO:0100021"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_motif","secondary_identifiers":["BS:00032"],"synonyms":[{"name":"motif","type":"broad"},{"name":"polypeptide motif","type":"exact"}],"termid":"SO:0001067"}


id: GO:0044208
data:
  {"annotated_genes":["SJAG_02850","SJAG_00044"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78671,80656],"is_not":false,"summary":null,"term":"GO:0044208"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of adenosine monophosphate (AMP) from inosine 5'-monophosphate (IMP).","definition_xrefs":["GOC:ecd","PMID:10888601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AMP biosynthetic process","termid":"GO:0006167"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_02850":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"'de novo' AMP biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0044208","terms_by_termid":{"GO:0044208":null}}


id: PBO:0030012
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_phosphorylation_during_salt_stress","termid":"PBO:0030012"}


id: PBO:0053818
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 1079","termid":"PBO:0053818"}


id: PR:G2TRU1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC18.20 gene.","definition_xrefs":["UniProtKB:G2TRU1","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C18.20 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18.20","synonyms":[{"name":"Spom972h-SPCC18.20","type":"exact"}],"termid":"PR:G2TRU1"}


id: MONDO:0004738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete histidine metabolism disease (obsolete MONDO:0004738)","termid":"MONDO:0004738","xrefs":{"Monarch":{"xref_id":"0004738"}}}


id: PBO:0113475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of tRNA-specific adenosine-34 deaminase; forms a heterodimer with Tad2p that converts adenosine to inosine at the wobble position of several tRNAs; localizes to cytosol, nucleus and peroxisomes","termid":"PBO:0113475"}


id: PBO:0039086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP/GTP binding carboxypeptidase 1","termid":"PBO:0039086"}


id: GO:0046644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of gamma-delta T cell activation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gamma-delta T cell activation","termid":"GO:0046643"},{"relation_name":"is_a","term_name":"negative regulation of T cell activation","termid":"GO:0050868"},{"relation_name":"negatively_regulates","term_name":"gamma-delta T cell activation","termid":"GO:0046629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of gamma-delta T cell activation","synonyms":[{"name":"down regulation of gamma-delta T cell activation","type":"exact"},{"name":"down-regulation of gamma-delta T cell activation","type":"exact"},{"name":"downregulation of gamma-delta T cell activation","type":"exact"},{"name":"inhibition of gamma-delta T cell activation","type":"narrow"},{"name":"negative regulation of gamma-delta T lymphocyte activation","type":"exact"},{"name":"negative regulation of gamma-delta T-cell activation","type":"exact"},{"name":"negative regulation of gamma-delta T-lymphocyte activation","type":"exact"}],"termid":"GO:0046644"}


id: GO:0004442
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: D-myo-inositol 1,3-bisphosphate + H2O = D-myo-inositol 1-monophosphate + phosphate.","definition_xrefs":["EC:3.1.3.65","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete inositol-1,4,-bisphosphate 3-phosphatase (obsolete GO:0004442)","synonyms":[{"name":"inositol-1,4,-bisphosphate 3-phosphatase","type":"exact"}],"termid":"GO:0004442"}


id: PBO:0070209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 137 pseudogene","termid":"PBO:0070209"}


id: MONDO:1011074
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Urolithiasis that occurs in Dusky leaf-monkey.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urolithiasis, Dusky leaf-monkey","secondary_identifiers":["OMIA:001033-54181"],"termid":"MONDO:1011074","xrefs":{"Monarch":{"xref_id":"1011074"}}}


id: GO:0019470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of trans-4-hydroxy-L-proline, C5H9NO3, a derivative of the amino acid proline.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-hydroxyproline metabolic process","termid":"GO:0019471"},{"relation_name":"is_a","term_name":"modified amino acid catabolic process","termid":"GO:0042219"},{"relation_name":"is_a","term_name":"L-amino acid catabolic process","termid":"GO:0170035"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid catabolic process","termid":"GO:0170044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"trans-4-hydroxy-L-proline catabolic process","secondary_identifiers":["MetaCyc:HYDROXYPRODEG-PWY"],"synonyms":[{"name":"4-hydroxyproline breakdown","type":"exact"},{"name":"4-hydroxyproline catabolism","type":"exact"},{"name":"4-hydroxyproline degradation","type":"exact"}],"termid":"GO:0019470"}


id: PBO:0077230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane channel like 6","termid":"PBO:0077230"}


id: MOD:01549
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of a residue with the Applied Biosystems iTRAQ8plex-116 reporter+balance group.","definition_xrefs":["Unimod:730"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(13)C isotope tagged reagent","termid":"MOD:01428"},{"relation_name":"is_a","term_name":"(15)N isotope tagged reagent","termid":"MOD:01429"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent acylated residue","termid":"MOD:01526"},{"relation_name":"is_a","term_name":"modifications with monoisotopic mass differences that are nominally equal at 304.205359 Da","termid":"MOD:01591"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-116 reporter+balance reagent acylated residue","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"Representative mass and accurate mass for 113, 114, 116 & 117","type":"related"},{"name":"iTRAQ8plex","type":"related"},{"name":"iTRAQ8plex:13C(7)15N(1)","type":"related"}],"termid":"MOD:01549"}


id: PBO:0120031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-specific trancription factor Pc OR mating-type transcription factor (Pc-like)","termid":"PBO:0120031"}


id: CHEBI:57643
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1,2-diacyl-sn-glycero-3-phosphocholine","termid":"CHEBI:57643"}


id: GO:1901120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of tobramycin.","definition_xrefs":["UniPathway:UPA00971","GOC:yaf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoside catabolic process","termid":"GO:0016139"},{"relation_name":"is_a","term_name":"polyol catabolic process","termid":"GO:0046174"},{"relation_name":"is_a","term_name":"tobramycin metabolic process","termid":"GO:1901119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"tobramycin catabolic process","synonyms":[{"name":"tobramycin breakdown","type":"exact"},{"name":"tobramycin catabolism","type":"exact"},{"name":"tobramycin degradation","type":"exact"}],"termid":"GO:1901120"}


id: PBO:0050157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 13","termid":"PBO:0050157"}


id: PBO:0081241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF8-ERVK3-1 readthrough (NMD candidate)","termid":"PBO:0081241"}


id: MONDO:0020118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dense granule disease (obsolete MONDO:0020118)","secondary_identifiers":["icd11.foundation:1930060978","Orphanet:98456"],"synonyms":[{"name":"Delta granule disease","type":"exact"}],"termid":"MONDO:0020118","xrefs":{"Monarch":{"xref_id":"0020118"}}}


id: GO:0016798
data:
  {"annotated_genes":["SJAG_04789","SJAG_01883","SJAG_02590","SJAG_04859","SJAG_03824","SJAG_02179","SJAG_01171","SJAG_04363","SJAG_02076","SJAG_01781","SJAG_04851","SJAG_04301","SJAG_02261","SJAG_02131","SJAG_02649","SJAG_03646","SJAG_02718","SJAG_01029","SJAG_05001","SJAG_00620","SJAG_05272","SJAG_02192","SJAG_03280","SJAG_00485","SJAG_03295","SJAG_01119","SJAG_02799","SJAG_01971","SJAG_03444","SJAG_01858","SJAG_04927","SJAG_03724","SJAG_02478","SJAG_00310","SJAG_02528","SJAG_01888","SJAG_00096","SJAG_04238","SJAG_00667","SJAG_04864","SJAG_02435","SJAG_02446","SJAG_01974","SJAG_04850","SJAG_02949","SJAG_01017","SJAG_02711","SJAG_03032","SJAG_04327","SJAG_00957"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034042"},{"annotations":[77460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070694"},{"annotations":[97930],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034043"},{"annotations":[75978,97931,75244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034039"},{"annotations":[73160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004555"},{"annotations":[103396,103395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004558"},{"annotations":[68814,60598,67775,62084,59965,64795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004556"},{"annotations":[69548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004557"},{"annotations":[90073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004559"},{"annotations":[117470,89211,110213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008422"},{"annotations":[79864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004568"},{"annotations":[103376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052820"},{"annotations":[103377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008725"},{"annotations":[103378],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043916"},{"annotations":[62665,70966],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052861"},{"annotations":[89141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106407"},{"annotations":[80480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004573"},{"annotations":[60482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004339"},{"annotations":[70037,57942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051118"},{"annotations":[75775,79598,81765],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042973"},{"annotations":[74948,103744,103745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046557"},{"annotations":[74945,96887,72166,72269,78747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004338"},{"annotations":[76861,78488],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015926"},{"annotations":[77704,90463,64126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004553"},{"annotations":[98713,58176,64028,57945,57559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008496"},{"annotations":[68112,80459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004571"},{"annotations":[92424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070635"},{"annotations":[92425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070636"},{"annotations":[114006,76946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008477"},{"annotations":[75248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000701"},{"annotations":[100372,100371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106432"},{"annotations":[78492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004575"},{"annotations":[79986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004844"},{"annotations":[92427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045437"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any glycosyl bond.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase 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activity, acting on glycosyl bonds","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-2065233","EC:3.2.-.-","Reactome:R-HSA-1793176","Reactome:R-HSA-5333609"],"synonyms":[{"name":"N-glycosylase","type":"narrow"},{"name":"glycosidase 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id: PBO:0111380
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific, implicated in rRNA processing","termid":"PBO:0111380"}


id: PBO:0048465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate-cysteine ligase catalytic subunit","termid":"PBO:0048465"}


id: GO:0052602
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-chloronitrobenzene + NADPH + H+ = 1-chloro-4-nitrosobenzene + NADP+ + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-chloronitrobenzene nitroreductase activity (obsolete GO:0052602)","termid":"GO:0052602"}


id: PBO:0053984
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 1300","termid":"PBO:0053984"}


id: GO:0021982
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the pineal gland over time from its initial formation until its mature state. The pineal gland is an endocrine gland that secretes melatonin and is involved in circadian rhythms.","definition_xrefs":["GO_REF:0000021","GOC:dph","GOC:jid","GOC:dgh","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gland development","termid":"GO:0048732"},{"relation_name":"part_of","term_name":"diencephalon development","termid":"GO:0021536"},{"relation_name":"part_of","term_name":"endocrine system development","termid":"GO:0035270"}],"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":"pineal gland development","synonyms":[{"name":"epiphysis development","type":"exact"}],"termid":"GO:0021982"}


id: PBO:0108700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RanGAP Sbp1","termid":"PBO:0108700"}


id: GO:0042425
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of choline (2-hydroxyethyltrimethylammonium), an amino alcohol that occurs widely in living organisms as a constituent of certain types of phospholipids and in the neurotransmitter acetylcholine.","definition_xrefs":["ISBN:0192801023","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choline metabolic process","termid":"GO:0019695"},{"relation_name":"is_a","term_name":"biogenic amine biosynthetic process","termid":"GO:0042401"}],"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":"choline biosynthetic process","secondary_identifiers":["MetaCyc:PWY-4762"],"synonyms":[{"name":"choline anabolism","type":"exact"},{"name":"choline biosynthesis","type":"exact"},{"name":"choline formation","type":"exact"},{"name":"choline synthesis","type":"exact"}],"termid":"GO:0042425"}


id: FYPO:0005529
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 chromatin at the IRC1L boundary element is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:25972440","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin during vegetative growth","termid":"FYPO:0001509"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to chromatin at boundary element IRC1L","synonyms":[{"name":"normal protein localisation to chromatin at boundary element IRC1L","type":"exact"},{"name":"normal protein localization to centromeric boundary element IRC1L","type":"exact"},{"name":"normal protein localization to chromatin at boundary element IRC1L during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at boundary element IRC1L during vegetative growth","type":"exact"}],"termid":"FYPO:0005529"}


id: MONDO:0100017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of skin conditions that cause constant inflammation and scaling of the skin. People with PRP have reddish, scaly patches that may occur everywhere on the body, or only on certain areas. Some people with PRP also develop thickened skin on the underside of the hands and feet (palmoplantar keratoderma), various nail abnormalities, and/or thinning of the hair. There are several types of PRP classified by age when symptoms begin, body areas involved, and whether other conditions are present. This condition occurs in adults (adult onset PRP) as well as children (juvenile onset PRP).","definition_xrefs":["GARD:0007401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exanthem","termid":"MONDO:0006547"},{"relation_name":"is_a","term_name":"erythrokeratoderma","termid":"MONDO:0019270"}],"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":"pityriasis rubra pilaris","secondary_identifiers":["ICD9:696.4","DOID:9212","GARD:7401","icd11.foundation:2048594962","MEDGEN:45939","ICD10CM:L44.0","UMLS:C0032027","MESH:D010916","NCIT:C85014","NORD:1582","SCTID:3755001"],"termid":"MONDO:0100017","xrefs":{"Monarch":{"xref_id":"0100017"}}}


id: PR:Q9P7X0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13337:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP23A10.16","secondary_identifiers":["UniProtKB:Q9P7X0"],"synonyms":[{"name":"CybS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBP23A10.16","type":"related"},{"name":"Spom972h-SDHD","type":"exact"},{"name":"succinate-ubiquinone reductase membrane anchor subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tim18","type":"related"}],"termid":"PR:Q9P7X0"}


id: PBO:0087725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SAS complex (Sas2p, Sas4p, Sas5p); acetylates free histones and nucleosomes and regulates transcriptional silencing; required for the HAT activity of Sas2p","termid":"PBO:0087725"}


id: MOD:01638
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces a glycine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified glycine residue","termid":"MOD:00908"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue removal","termid":"MOD:01651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine removal","termid":"MOD:01638"}


id: PBO:0042692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDH13 antisense oligodendrocyte and neuron associated lncRNA","termid":"PBO:0042692"}


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


id: GO:0018865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving acrylonitrile, a colorless, volatile liquid with a pungent odor. Acrylonitrile is used in the production of acrylic fibers, plastics, and synthetic rubbers.","definition_xrefs":["PMID:1390687","PMID:3830164"],"gene_count":0,"genotype_count":0,"name":"obsolete acrylonitrile metabolic process (obsolete GO:0018865)","synonyms":[{"name":"acrylonitrile metabolism","type":"broad"}],"termid":"GO:0018865"}


id: MONDO:0006465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete thyroid gland oncocytic follicular carcinoma (obsolete MONDO:0006465)","secondary_identifiers":["EFO:1000592"],"termid":"MONDO:0006465","xrefs":{"Monarch":{"xref_id":"0006465"}}}


id: PBO:0114111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"REX family exonuclease, implicated in rDNA metabolism or ribosome biogenesis, potential human ISG20L2 ortholog","termid":"PBO:0114111"}


id: MOD:00856
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-alanine residue to an L-alaninium (protonated L-alanine).","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-alanine residue","termid":"MOD:00901"},{"relation_name":"is_a","term_name":"alpha-amino protonated residue","termid":"MOD:01700"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protonated L-alanine (L-alaninium) residue","termid":"MOD:00856"}


id: GO:0033581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of a galactose unit to a protein amino acid in any compartment of the Golgi apparatus.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete protein galactosylation in Golgi (obsolete GO:0033581)","synonyms":[{"name":"protein amino acid galactosylation in Golgi","type":"exact"}],"termid":"GO:0033581"}


id: MONDO:0007745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary hyperbilirubinemia","termid":"MONDO:0002408"}],"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":"Gilbert syndrome","secondary_identifiers":["ICD10CM:E80.4","NCIT:C84729","DOID:2739","MESH:D005878","MEDGEN:4891","OMIM:143500","SCTID:27503000","Orphanet:357","UMLS:C0017551","icd11.foundation:1947520963","EFO:0005556"],"synonyms":[{"name":"Gilbert disease","type":"exact"},{"name":"Gilbert syndrome","type":"exact"},{"name":"Gilbert's disease","type":"exact"},{"name":"Gilbert's syndrome","type":"exact"},{"name":"Gilbert-Meulengracht syndrome","type":"exact"},{"name":"constitutional hyperbilirubinemia","type":"exact"},{"name":"familial cholemia","type":"exact"},{"name":"hereditary nonhemolytic jaundice","type":"exact"},{"name":"hyperbilirubinemia 1","type":"related"},{"name":"hyperbilirubinemia type 1","type":"exact"},{"name":"hyperbilirubinemia, Arias type","type":"related"},{"name":"hyperbilirubinemia, Gilbert type","type":"related"}],"termid":"MONDO:0007745","xrefs":{"Monarch":{"xref_id":"0007745"}}}


id: PBO:0063575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline and glutamate rich with coiled coil 1","termid":"PBO:0063575"}


id: GO:0098723
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A myofibril of a skeletal muscle fiber.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myofibril","termid":"GO:0030016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"skeletal muscle myofibril","termid":"GO:0098723"}


id: GO:1902318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any synthesis of RNA primer that is involved in nuclear cell cycle DNA replication.","definition_xrefs":["GOC:mtg_cell_cycle","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete synthesis of RNA primer involved in nuclear cell cycle DNA replication (obsolete GO:1902318)","synonyms":[{"name":"DNA replication, synthesis of RNA primer involved in DNA replication during S phase","type":"related"},{"name":"DNA replication, synthesis of RNA primer involved in DNA replication involved in S phase","type":"exact"},{"name":"DNA replication, synthesis of RNA primer involved in DNA replication involved in S-phase","type":"exact"},{"name":"replication priming involved in DNA replication during S phase","type":"related"},{"name":"replication priming involved in DNA replication involved in S phase","type":"related"},{"name":"replication priming involved in DNA replication involved in S-phase","type":"related"},{"name":"replication priming involved in nuclear cell cycle DNA replication","type":"related"}],"termid":"GO:1902318"}


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","OMIM:608474","UMLS:C1837972"],"synonyms":[{"name":"MYP5","type":"exact"},{"name":"myopia 5, autosomal dominant","type":"exact"}],"termid":"MONDO:0012045","xrefs":{"Monarch":{"xref_id":"0012045"}}}


id: PBO:0079962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 9 Y-linked","termid":"PBO:0079962"}


id: SO:0000349
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A match against a protein sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"match","termid":"SO:0000343"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein_match","synonyms":[{"name":"protein match","type":"exact"}],"termid":"SO:0000349"}


id: PBO:0088349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexitol dehydrogenase","termid":"PBO:0088349"}


id: MONDO:0002288
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ovarian cancer (obsolete MONDO:0002288)","termid":"MONDO:0002288","xrefs":{"Monarch":{"xref_id":"0002288"}}}


id: SO:0000961
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Structural unit composed of a self-replicating, RNA molecule.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"RNA","termid":"SO:0000356"},{"relation_name":"is_a","term_name":"chromosome","termid":"SO:0000340"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA_chromosome","synonyms":[{"name":"RNA chromosome","type":"exact"}],"termid":"SO:0000961"}


id: PBO:0089944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prospore membrane alpha-1,3-glucan synthase Mok12","termid":"PBO:0089944"}


id: GO:0102545
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 1,2-diacyl-sn-glycero-3-phosphocholine + 2 H2O = sn-glycerol 3-phosphocholine + 2 a carboxylate + 2 H+.","definition_xrefs":["RHEA:32907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase activity","termid":"GO:0004620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"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:0016788","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"phospholipase B activity","secondary_identifiers":["MetaCyc:RXN-14899"],"synonyms":[{"name":"phosphatidyl phospholipase B activity","type":"exact"}],"termid":"GO:0102545"}


id: PATO:0002124
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's processing the form of a thin plate sheet or layer.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laminar","termid":"PATO:0002124"}


id: PBO:0114475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tandem fusion lysine methyltransferase/ citidine deaminase involved in riboflavin biosynthesis","termid":"PBO:0114475"}


id: GO:0006173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dADP, deoxyadenosine diphosphate (2'-deoxyadenosine 5'-diphosphate).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine deoxyribonucleotide biosynthetic process","termid":"GO:0009153"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside diphosphate biosynthetic process","termid":"GO:0009183"},{"relation_name":"is_a","term_name":"dADP metabolic process","termid":"GO:0046056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"dADP biosynthetic process","synonyms":[{"name":"dADP anabolism","type":"exact"},{"name":"dADP biosynthesis","type":"exact"},{"name":"dADP formation","type":"exact"},{"name":"dADP synthesis","type":"exact"}],"termid":"GO:0006173"}


id: MONDO:0002398
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign adenofibroma characterized by the presence of epithelial cells which contain intracytoplasmic mucin and a fibrotic stroma. A representative example is the ovarian mucinous adenofibroma. Cases with epithelial atypia described in the ovary lacking stromal invasion are designated as borderline mucinous adenofibromas and have a low grade malignant potential.","definition_xrefs":["NCIT:C8978"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenofibroma","termid":"MONDO:0006071"},{"relation_name":"is_a","term_name":"mucinous neoplasm","termid":"MONDO:0024338"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucinous adenofibroma","secondary_identifiers":["DOID:2700","MEDGEN:83158","UMLS:C0334499","ICDO:9015/0"],"synonyms":[{"name":"mucinous adenofibroma","type":"exact"}],"termid":"MONDO:0002398","xrefs":{"Monarch":{"xref_id":"0002398"}}}


id: PBO:0068737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U5A small nuclear 8, pseudogene","termid":"PBO:0068737"}


id: FYPO:0004335
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to another does not occur during a cellular response to hydrogen peroxide. The relevant proteins may include the one encoded by the mutated gene, or may both be encoded by different genes.","definition_xrefs":["PomBase:mah","PMID:22139357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction during cellular response to rapamycin","termid":"FYPO:0003425"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000702"],"is_obsolete":false,"name":"abolished protein-protein interaction during cellular response to hydrogen peroxide","synonyms":[{"name":"abolished protein binding cellular response to hydrogen peroxide","type":"exact"},{"name":"abolished protein-protein interaction during cellular response to H2O2","type":"exact"},{"name":"protein-protein interaction abolished during cellular response to hydrogen peroxide","type":"exact"}],"termid":"FYPO:0004335"}


id: MONDO:0012177
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Posterior column ataxia - retinitis pigmentosa is characterized by the association of progressive sensory ataxia and retinitis pigmentosa.","definition_xrefs":["Orphanet:88628"],"direct_ancestors":[{"relation_name":"is_a","term_name":"FLVCR1-related retinopathy with or without ataxia","termid":"MONDO:0100449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559","MONDO:0005328"],"is_obsolete":false,"name":"posterior column ataxia-retinitis pigmentosa syndrome","secondary_identifiers":["MESH:C536343","OMIM:609033","UMLS:C1836916","GARD:9898","SCTID:724065003","MEDGEN:324636"],"synonyms":[{"name":"AXPC1","type":"related"},{"name":"PCARP","type":"exact"},{"name":"POSTERIOR column ataxia with retinitis pigmentosa","type":"related"},{"name":"Pcarp","type":"related"},{"name":"ataxia, posterior column, with retinitis pigmentosa","type":"exact"},{"name":"autosomal recessive posterior column ataxia and retinitis pigmentosa","type":"exact"}],"termid":"MONDO:0012177","xrefs":{"Monarch":{"xref_id":"0012177"}}}


id: PBO:0075089
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 139","termid":"PBO:0075089"}


id: MONDO:0044636
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare hyperkinetic movement disorder (obsolete MONDO:0044636)","secondary_identifiers":["Orphanet:494457"],"termid":"MONDO:0044636","xrefs":{"Monarch":{"xref_id":"0044636"}}}


id: GO:0036002
data:
  {"annotated_genes":["SJAG_04497","SJAG_04898","SJAG_03448","SJAG_00249","SJAG_02622","SJAG_00058","SJAG_03983","SJAG_01200","SJAG_03383","SJAG_03995","SJAG_04117","SJAG_00225"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79177,79615,90856],"is_not":false,"summary":null,"term":"GO:0036002"},{"annotations":[57750,78316,73886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030628"},{"annotations":[81096,115117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030627"},{"annotations":[66527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045131"},{"annotations":[77728,102700,119983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097157"}]},"cv_name":"molecular_function","definition":"Binding to a pre-messenger RNA (pre-mRNA), an intermediate molecule between DNA and protein that may contain introns and, at least in part, encodes one or more proteins. Introns are removed from pre-mRNA to form a mRNA molecule.","definition_xrefs":["GOC:kmv","GOC:bf","PMID:21901112","SO:0000120"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00058":null,"SJAG_00225":null,"SJAG_00249":null,"SJAG_01200":null,"SJAG_02622":null,"SJAG_03383":null,"SJAG_03448":null,"SJAG_03983":null,"SJAG_03995":null,"SJAG_04117":null,"SJAG_04497":null,"SJAG_04898":null},"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:0003674"}],"interesting_parent_ids":["GO:0003723","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"pre-mRNA binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"protein-coding primary transcript binding","type":"related"}],"termid":"GO:0036002","terms_by_termid":{"GO:0030627":null,"GO:0030628":null,"GO:0036002":null,"GO:0045131":null,"GO:0097157":null}}


id: MONDO:0003549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenosquamous carcinoma that arises from the bile ducts.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell bile duct carcinoma","termid":"MONDO:0003500"},{"relation_name":"is_a","term_name":"liver adenosquamous carcinoma","termid":"MONDO:0056815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"adenosquamous bile duct carcinoma","secondary_identifiers":["UMLS:C0861854","DOID:5624","MEDGEN:163666"],"synonyms":[{"name":"adenosquamous bile duct carcinoma","type":"exact"},{"name":"adenosquamous carcinoma of bile duct","type":"exact"},{"name":"adenosquamous carcinoma of the bile duct","type":"exact"},{"name":"bile duct adenosquamous carcinoma","type":"exact"}],"termid":"MONDO:0003549","xrefs":{"Monarch":{"xref_id":"0003549"}}}


id: GO:0035072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process induced by ecdysone that directly activates salivary gland programmed cell death during salivary gland histolysis.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete ecdysone-mediated induction of salivary gland cell autophagic cell death (obsolete GO:0035072)","termid":"GO:0035072"}


id: PBO:0030237
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_immediate_intracellular_calcium_spike_following_extracellular_calcium_stimulus","termid":"PBO:0030237"}


id: PR:O13784
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps2401 gene.","definition_xrefs":["UniProtKB:O13784","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":"40S ribosomal protein S24-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.06","synonyms":[{"name":"Spom972h-rps2401","type":"exact"}],"termid":"PR:O13784"}


id: GO:0060268
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate frequency or extent of a phase of elevated metabolic activity, during which oxygen consumption increases; this leads to the production, by an NADH dependent system, of hydrogen peroxide (H2O2), superoxide anions and hydroxyl radicals.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of metabolic process","termid":"GO:0009892"},{"relation_name":"is_a","term_name":"regulation of respiratory burst","termid":"GO:0060263"},{"relation_name":"negatively_regulates","term_name":"respiratory burst","termid":"GO:0045730"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of respiratory burst","termid":"GO:0060268"}


id: PBO:0057748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1843","termid":"PBO:0057748"}


id: GO:0045745
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of G protein-coupled receptor signaling pathway activity.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor signaling pathway","termid":"GO:0008277"},{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"positively_regulates","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":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of G protein-coupled receptor signaling pathway","synonyms":[{"name":"activation of G-protein coupled receptor protein signaling pathway","type":"narrow"},{"name":"positive regulation of G protein coupled receptor protein signaling pathway","type":"exact"},{"name":"positive regulation of G protein coupled receptor protein signalling pathway","type":"exact"},{"name":"positive regulation of G-protein coupled receptor protein signaling pathway","type":"exact"},{"name":"positive regulation of G-protein coupled receptor protein signalling pathway","type":"exact"},{"name":"positive regulation of G-protein-coupled receptor protein signaling pathway","type":"exact"},{"name":"positive regulation of G-protein-coupled receptor protein signalling pathway","type":"exact"},{"name":"positive regulation of GPCR protein signaling pathway","type":"exact"},{"name":"positive regulation of GPCR protein signalling pathway","type":"exact"},{"name":"stimulation of G-protein coupled receptor protein signaling pathway","type":"narrow"},{"name":"up regulation of G-protein coupled receptor protein signaling pathway","type":"exact"},{"name":"up-regulation of G-protein coupled receptor protein signaling pathway","type":"exact"},{"name":"upregulation of G-protein coupled receptor protein signaling pathway","type":"exact"}],"termid":"GO:0045745"}


id: MONDO:0004839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neurofibroma (obsolete MONDO:0004839)","termid":"MONDO:0004839","xrefs":{"Monarch":{"xref_id":"0004839"}}}


id: PBO:0072188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17 pseudogene 5","termid":"PBO:0072188"}


id: MONDO:0020769
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Menke-Hennekam syndrome","termid":"MONDO:0020774"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Menke-Hennekam syndrome 2","secondary_identifiers":["UMLS:C5193035","OMIM:618333","MEDGEN:1676668"],"synonyms":[{"name":"MKHK2","type":"related"},{"name":"Menke-Hennekam syndrome 2","type":"exact"}],"termid":"MONDO:0020769","xrefs":{"Monarch":{"xref_id":"0020769"}}}


id: PR:O74844
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fta7 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74844"],"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":"kinetochore protein fta7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.07","synonyms":[{"name":"Spom972h-fta7","type":"exact"},{"name":"sim4 complex subunit fta7 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sim4-mal2-associated protein 7 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74844"}


id: GO:0008061
data:
  {"annotated_genes":["SJAG_00620","SJAG_03013"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[68379,93547],"is_not":false,"summary":null,"term":"GO:0008061"}]},"cv_name":"molecular_function","definition":"Binding to chitin, a linear polysaccharide consisting of beta-(1->4)-linked N-acetyl-D-glucosamine residues.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative binding","termid":"GO:0097367"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00620":null,"SJAG_03013":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"chitin binding","references_by_uniquename":{"GO_REF:0000043":null,"GO_REF:0000107":null},"termid":"GO:0008061","terms_by_termid":{"GO:0008061":null}}


id: GO:0035240
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to dopamine, a catecholamine neurotransmitter formed by aromatic-L-amino-acid decarboxylase from 3,4-dihydroxy-L-phenylalanine.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"},{"relation_name":"is_a","term_name":"catecholamine binding","termid":"GO:1901338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"dopamine binding","termid":"GO:0035240"}


id: PBO:0066717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 14","termid":"PBO:0066717"}


id: PBO:0031320
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_pravastatin","termid":"PBO:0031320"}


id: MONDO:0010843
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"dyslexia","termid":"MONDO:0005489"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dyslexia, susceptibility to, 2","secondary_identifiers":["MEDGEN:325025","OMIM:600202","UMLS:C1838436"],"synonyms":[{"name":"DYX2","type":"exact"},{"name":"dyslexia, susceptibility to, 2","type":"exact"},{"name":"reading disability, specific, 2","type":"related"}],"termid":"MONDO:0010843","xrefs":{"Monarch":{"xref_id":"0010843"}}}


id: MONDO:0015123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare lipid metabolism disorder.","gene_count":0,"genotype_count":0,"name":"obsolete rare inherited dyslipidemia (obsolete MONDO:0015123)","secondary_identifiers":["Orphanet:101953","ICD10CM:E78.5"],"synonyms":[{"name":"rare dyslipidemia","type":"related"},{"name":"rare lipid metabolism disorder","type":"exact"}],"termid":"MONDO:0015123","xrefs":{"Monarch":{"xref_id":"0015123"}}}


id: SO:0002229
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant extending the CDS at the 3' end, that causes elongation of the resulting polypeptide sequence at the C terminus.","definition_xrefs":["PMID:32020195","PMID:14732127","PMID:15864293","PMID:27984720","PMID:31216041"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CDS_extension","termid":"SO:0002227"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDS_three_prime_extension","synonyms":[{"name":"CDS Extension 3 prime","type":"exact"},{"name":"CDS Extension three prime","type":"exact"},{"name":"elongated CDS three prime","type":"exact"},{"name":"elongated_CDS_three_prime","type":"exact"}],"termid":"SO:0002229"}


id: GO:0000256
data:
  {"annotated_genes":["SJAG_05287","SJAG_00035"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63070,76960],"is_not":false,"summary":null,"term":"GO:0000256"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of allantoin, (2,5-dioxo-4-imidazolidinyl)urea.","definition_xrefs":["GOC:mah","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"allantoin metabolic process","termid":"GO:0000255"},{"relation_name":"is_a","term_name":"amide catabolic process","termid":"GO:0043605"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00035":null,"SJAG_05287":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"allantoin catabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"allantoin breakdown","type":"exact"},{"name":"allantoin catabolism","type":"exact"},{"name":"allantoin degradation","type":"exact"}],"termid":"GO:0000256","terms_by_termid":{"GO:0000256":null}}


id: PBO:0113352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for nuclear retention of unspliced pre-mRNAs; required along with Mlp1p and Pml1p; anchored to the nuclear pore complex through an interaction between its bimodular nuclear basket-interaction domain (NuBaID) and Mlp1p and Mlp2p; localizes to the nuclear basket enables linkage between subpopulations of Mlp1p; associates with the subset of nuclear pores farthest from the nucleolus; homologous to human ZC3HC1, a NuBaID containing protein","termid":"PBO:0113352"}


id: PBO:0113289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Positive regulator of the Gcn2p kinase activity; important for disaggregation of ordered and disordered protein aggregates; forms a complex with Gcn1p; proposed to stimulate Gcn2p activation by an uncharged tRNA; suppresses frameshifting at stalled ribosomes","termid":"PBO:0113289"}


id: MONDO:0006621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Seborrheic keratosis that arises from follicular structures in the vulva. It is characterized by the presence of prominent squamous eddies.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inverted follicular keratosis","termid":"MONDO:0006563"},{"relation_name":"is_a","term_name":"vulvar seborrheic keratosis","termid":"MONDO:0006622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"vulvar inverted follicular keratosis","secondary_identifiers":["DOID:6943","MEDGEN:274414","NCIT:C40291","UMLS:C1520084"],"synonyms":[{"name":"inverted follicular keratosis of mammalian vulva","type":"exact"},{"name":"mammalian vulva inverted follicular keratosis","type":"exact"}],"termid":"MONDO:0006621","xrefs":{"Monarch":{"xref_id":"0006621"}}}


id: PBO:0016965
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CORnichon","termid":"PBO:0016965"}


id: PR:Q9P7S7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nucleolar protein 58 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10894:SF0","OMA:SCHPO00338","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":"nucleolar protein 58 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23G3.06","secondary_identifiers":["UniProtKB:Q9P7S7"],"synonyms":[{"name":"Spom972h-NOP58","type":"exact"}],"termid":"PR:Q9P7S7"}


id: PBO:0035885
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-asymmetric_mitochondrial_aggregation","termid":"PBO:0035885"}


id: FYPO:0001550
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein measured in a cell differs from normal during a cellular response to zinc ions. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered protein level during vegetative growth","termid":"FYPO:0001325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0006551","FYPO:0005447"],"is_obsolete":false,"name":"altered protein level during cellular response to zinc ion","synonyms":[{"name":"abnormal protein level during cellular response to zinc ion","type":"exact"},{"name":"altered cellular protein level during cellular response to zinc ion during vegetative growth","type":"exact"},{"name":"altered protein level during cellular response to zinc","type":"exact"},{"name":"altered protein level during cellular response to zinc ion during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001550"}


id: MONDO:0009789
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nonarteritic anterior ischemic optic neuropathy, susceptibility to","secondary_identifiers":["MEDGEN:338294","OMIM:258660","UMLS:C1847711"],"synonyms":[{"name":"Naion, susceptibility to","type":"related"},{"name":"nonarteritic anterior ischemic optic neuropathy, susceptibility to","type":"exact"},{"name":"optic neuropathy, anterior ischemic, susceptibility to","type":"related"},{"name":"susceptibility to nonarteritic anterior ischaemic optic neuropathy","type":"related"},{"name":"susceptibility to nonarteritic anterior ischemic optic neuropathy","type":"related"}],"termid":"MONDO:0009789","xrefs":{"Monarch":{"xref_id":"0009789"}}}


id: MONDO:0033644
data:
  {"annotated_genes":["SJAG_00983"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87509],"is_not":false,"summary":null,"term":"MONDO:0033644"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00983":null},"genotype_count":0,"is_obsolete":false,"name":"microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5436769","MEDGEN:1755099","GARD:18383","OMIM:619082"],"synonyms":[{"name":"MRCS1","type":"exact"}],"termid":"MONDO:0033644","terms_by_termid":{"MONDO:0033644":null},"xrefs":{"Monarch":{"xref_id":"0033644"}}}


id: GO:0032043
data:
  {"annotated_genes":["SJAG_01948"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92150],"is_not":false,"summary":null,"term":"GO:0032043"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of mitochondrial DNA.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA catabolic process","termid":"GO:0006308"},{"relation_name":"is_a","term_name":"mitochondrial DNA metabolic process","termid":"GO:0032042"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01948":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007005"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0007005"],"is_obsolete":false,"name":"mitochondrial DNA catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial DNA breakdown","type":"exact"},{"name":"mitochondrial DNA catabolism","type":"exact"},{"name":"mitochondrial DNA degradation","type":"exact"},{"name":"mtDNA breakdown","type":"exact"},{"name":"mtDNA catabolic process","type":"exact"},{"name":"mtDNA catabolism","type":"exact"},{"name":"mtDNA degradation","type":"exact"}],"termid":"GO:0032043","terms_by_termid":{"GO:0032043":null}}


id: MONDO:0002793
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete medullomyoblastoma (obsolete MONDO:0002793)","termid":"MONDO:0002793","xrefs":{"Monarch":{"xref_id":"0002793"}}}


id: PBO:0034780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lid2 complex PHD finger and jmjC subunit Lid2","termid":"PBO:0034780"}


id: SO:0002323
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A frameshift_variant (SO:0001589) that is degraded by nonsense-mediated decay (NMD).","definition_xrefs":["GenCC:AR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"frameshift_variant","termid":"SO:0001589"},{"relation_name":"is_a","term_name":"NMD_triggering_variant","termid":"SO:0002319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frameshift_variant_NMD_triggering","synonyms":[{"name":"frameshift variant-NMD triggering","type":"exact"},{"name":"frameshift variant-nonsense-mediated decay triggering","type":"exact"}],"termid":"SO:0002323"}


id: PR:O74859
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hnt3 gene.","definition_xrefs":["UniProtKB:O74859","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":"aprataxin-like protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18.09c","synonyms":[{"name":"Hit family protein 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-hnt3","type":"exact"}],"termid":"PR:O74859"}


id: MONDO:1010774
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pemphigus that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pemphigus, non-human animal","termid":"MONDO:1010138"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pemphigus, horse","secondary_identifiers":["OMIA:001188-9796"],"termid":"MONDO:1010774","xrefs":{"Monarch":{"xref_id":"1010774"}}}


id: SO:0002270
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"RTE retrotransposons are LINE elements (SO:0000194) that contain a domain with homology to the apurinic-apyrimidic (AP) endonucleases in addition to the previously identified reverse transcriptase domain.","definition_xrefs":["PMID:9729877"],"direct_ancestors":[{"relation_name":"is_a","term_name":"LINE_element","termid":"SO:0000194"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RTE_LINE_retrotransposon","synonyms":[{"name":"RIT retrotransposon","type":"exact"},{"name":"RTE LINE retrotransposon","type":"exact"},{"name":"RTE retrotransposon","type":"exact"}],"termid":"SO:0002270"}


id: PBO:0059487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methionine sulfoxide reductase B2","termid":"PBO:0059487"}


id: PBO:0072633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arginine and serine rich protein 1","termid":"PBO:0072633"}


id: MONDO:0009631
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A microphthalmia that has material basis in variation in the chromosomal region 14q32.","definition_xrefs":["DOID:0060840","PMID:9545413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated microphthalmia","termid":"MONDO:0000062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"isolated microphthalmia 1","secondary_identifiers":["OMIM:251600","UMLS:C1855052","MEDGEN:381546","MESH:C565377"],"synonyms":[{"name":"MCOP1","type":"exact"},{"name":"Mcop","type":"related"},{"name":"anophthalmia, clinical, isolated","type":"related"},{"name":"isolated microphthalmia type 1","type":"exact"},{"name":"microphthalmia, isolated 1","type":"related"},{"name":"microphthalmos, autosomal recessive","type":"related"}],"termid":"MONDO:0009631","xrefs":{"Monarch":{"xref_id":"0009631"}}}


id: PATO:0001973
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being tapering gradually into a rigid point.","definition_xrefs":["ISBN:0881923214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tapered","termid":"PATO:0001500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cuspidate","termid":"PATO:0001973"}


id: PBO:0082633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of Dsc E3 ligase complex in Golgi and endosomes; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum; diploid deletion strain has high budding index","termid":"PBO:0082633"}


id: SO:0001000
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Cytosolic 16S rRNA is an RNA component of the small subunit of cytosolic ribosomes in prokaryotes.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"cytosolic_rRNA_16S_gene","termid":"SO:0002237"},{"relation_name":"is_a","term_name":"cytosolic_SSU_rRNA","termid":"SO:0000650"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic_16S_rRNA","secondary_identifiers":["http://en.wikipedia.org/wiki/16S_ribosomal_RNA"],"synonyms":[{"name":"cytosolic 16S SSU RNA","type":"exact"},{"name":"cytosolic 16S rRNA","type":"related"},{"name":"cytosolic 16S ribosomal RNA","type":"exact"},{"name":"cytosolic rRNA 16S","type":"exact"}],"termid":"SO:0001000"}


id: PR:O14018
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A serine--tRNA ligase, cytoplasmic that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11778:SF0","PRO:DNx","OMA:SCHPO02129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine--tRNA ligase, cytoplasmic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.15","secondary_identifiers":["UniProtKB:O14018"],"synonyms":[{"name":"SerRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SARS","type":"exact"},{"name":"seryl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"seryl-tRNA(Ser/Sec) synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14018"}


id: PBO:0062901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxidoreductase NAD binding domain containing 1","termid":"PBO:0062901"}


id: PBO:0061012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicolin 2, pseudogene","termid":"PBO:0061012"}


id: GO:0005190
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete seminal fluid protein (obsolete GO:0005190)","synonyms":[{"name":"seminal fluid protein","type":"exact"}],"termid":"GO:0005190"}


id: PBO:0054593
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 1996","termid":"PBO:0054593"}


id: PBO:0045215
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 C8","termid":"PBO:0045215"}


id: PBO:0049367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTF2I repeat domain containing 2","termid":"PBO:0049367"}


id: PBO:0049782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 17","termid":"PBO:0049782"}


id: PBO:0110408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 59","termid":"PBO:0110408"}


id: SO:0001548
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that increases transcript stability with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_stability_variant","termid":"SO:0001546"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased_transcript_stability_variant","synonyms":[{"name":"increased transcript stability variant","type":"exact"}],"termid":"SO:0001548"}


id: GO:0047813
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabinitol + NAD+ = D-xylulose + NADH.","definition_xrefs":["EC:1.1.1.11","MetaCyc:D-ARABINITOL-4-DEHYDROGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"D-arabinitol 4-dehydrogenase activity","secondary_identifiers":["RHEA:17921"],"termid":"GO:0047813"}


id: MONDO:0020148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A aniridia that is part of a larger syndrome.","definition_xrefs":["MONDO:patterns/syndromic"],"gene_count":0,"genotype_count":0,"name":"obsolete syndromic aniridia (obsolete MONDO:0020148)","secondary_identifiers":["Orphanet:98557"],"synonyms":[{"name":"syndrome associated with aniridia","type":"exact"},{"name":"syndromic aniridia","type":"exact"}],"termid":"MONDO:0020148","xrefs":{"Monarch":{"xref_id":"0020148"}}}


id: MONDO:0014099
data:
  {"annotated_genes":["SJAG_03361"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86732],"is_not":false,"summary":null,"term":"MONDO:0014099"}]},"cv_name":"mondo","definition":"Any nephrotic syndrome in which the cause of the disease is a mutation in the ARHGDIA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial idiopathic steroid-resistant nephrotic syndrome","termid":"MONDO:0019006"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03361":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"nephrotic syndrome, type 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:815283","OMIM:615244","DOID:0080389","GARD:15925","UMLS:C3808953"],"synonyms":[{"name":"ARHGDIA nephrotic syndrome","type":"exact"},{"name":"NPHS8","type":"related"},{"name":"nephrotic syndrome caused by mutation in ARHGDIA","type":"exact"},{"name":"nephrotic syndrome, type 8","type":"exact"}],"termid":"MONDO:0014099","terms_by_termid":{"MONDO:0014099":null},"xrefs":{"Monarch":{"xref_id":"0014099"}}}


id: PBO:0064895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 regulatory subunit B'alpha","termid":"PBO:0064895"}


id: MONDO:0005899
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the parotid gland.","direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland disorder","termid":"MONDO:0001142"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parotid disorder","secondary_identifiers":["DOID:10302","MEDGEN:10593","MESH:D010305","UMLS:C0030579","EFO:0007422"],"synonyms":[{"name":"disease of parotid gland","type":"exact"},{"name":"disease or disorder of parotid gland","type":"exact"},{"name":"disorder of parotid gland","type":"exact"},{"name":"parotid gland disease","type":"exact"},{"name":"parotid gland disease or disorder","type":"exact"}],"termid":"MONDO:0005899","xrefs":{"Monarch":{"xref_id":"0005899"}}}


id: GO:0032890
data:
  {"annotated_genes":["SJAG_02605","SJAG_00991","SJAG_05346","SJAG_03970","SJAG_04920","SJAG_03591"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905533"},{"annotations":[91700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035432"},{"annotations":[95102,100662,93518,112367],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905589"},{"annotations":[93519,100663,95103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905534"},{"annotations":[95104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905626"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of organic acids into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"organic acid transport","termid":"GO:0015849"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00991":null,"SJAG_02605":null,"SJAG_03591":null,"SJAG_03970":null,"SJAG_04920":null,"SJAG_05346":null},"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 organic acid transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0032890","terms_by_termid":{"GO:0035432":null,"GO:1905533":null,"GO:1905534":null,"GO:1905589":null,"GO:1905626":null}}


id: PATO:0000272
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000272 relative neurobehavioral function (obsolete PATO:0000272)","termid":"PATO:0000272"}


id: PBO:0078335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon CTC) 1-7","termid":"PBO:0078335"}


id: PATO:0001755
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A peramorphic growth quality which is due to a delayed offset.","definition_xrefs":["PATOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peramorphic growth","termid":"PATO:0001752"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypermorphic growth","termid":"PATO:0001755"}


id: GO:0030265
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A phospholipase C-activating receptor G protein-coupled receptor signaling pathway that starts with an opsin being activated by a photon, and transmitting the signal through the Gq-mediated activation of phospholipase C (PLC). PLC hydrolyses phosphatidylinositol 4,5-bisphosphate (PIP2) into the second messengers inositol-1,4,5,-triphosphate (IP3) and diacylglycerol (DAG). The second messengers, including cGMP, activate channels that result in transmission of the light signal  through the synapses. Typical examples are rhabdomeric photoreceptors in the eyes of protostomes.","definition_xrefs":["PMID:22498302","PMID:8823931","PMID:19720651"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase C-activating G protein-coupled receptor signaling pathway","termid":"GO:0007200"},{"relation_name":"is_a","term_name":"G protein-coupled opsin signaling pathway","termid":"GO:0016056"}],"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":"phospholipase C-activating opsin-mediated signaling pathway","synonyms":[{"name":"PLC-activating rhodopsin mediated signaling pathway","type":"narrow"},{"name":"phospholipase C-activating rhodopsin mediated G-protein coupled receptor signaling pathway","type":"narrow"},{"name":"phospholipase C-activating rhodopsin mediated signaling pathway","type":"narrow"},{"name":"rhodopsin mediated G protein signaling, coupled to IP3 second messenger","type":"narrow"},{"name":"rhodopsin mediated G protein signalling, coupled to IP3 second messenger","type":"narrow"},{"name":"rhodopsin mediated G-protein signaling, coupled to IP3 second messenger","type":"narrow"},{"name":"rhodopsin mediated G-protein signalling, coupled to IP3 second messenger","type":"narrow"}],"termid":"GO:0030265"}


id: GO:0015636
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of short-chain fatty acids from one side of a membrane to the other. A short-chain fatty acid has an aliphatic tail containing fewer than 6 carbons.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid transmembrane transporter activity","termid":"GO:0015245"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"short-chain fatty acid transmembrane transporter activity","secondary_identifiers":["GO:0015635"],"synonyms":[{"name":"short-chain fatty acid transporter activity","type":"related"},{"name":"short-chain fatty acid uptake transporter activity","type":"related"}],"termid":"GO:0015636"}


id: FYPO:0004398
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of phenylarsine oxide than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0000003","FYPO:0005447","FYPO:0002682"],"is_obsolete":false,"name":"resistance to phenylarsine oxide","synonyms":[{"name":"resistance to phenylarsine oxide during mitotic cell cycle","type":"related"},{"name":"resistance to phenylarsine oxide during vegetative growth","type":"exact"},{"name":"resistant to phenylarsine oxide","type":"exact"}],"termid":"FYPO:0004398"}


id: MONDO:0043519
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A traumatic injury involving interruption of tissue cohesiveness that results from exposure to caustic chemicals, extreme heat, extreme cold or excessive radiation.","definition_xrefs":["NCIT:C34441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"injury","termid":"MONDO:0021178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"burn","secondary_identifiers":["MESH:D002056","ICD10CM:T20-T25","SCTID:125666000"],"synonyms":[{"name":"Burn","type":"exact"},{"name":"Burn(s)","type":"exact"},{"name":"burn","type":"exact"}],"termid":"MONDO:0043519","xrefs":{"Monarch":{"xref_id":"0043519"}}}


id: PBO:0045781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectodysplasin A2 receptor","termid":"PBO:0045781"}


id: PBO:0054425
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 1821","termid":"PBO:0054425"}


id: GO:0120319
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an (omega-1)-ethyl long-chain fatty acid + O2 + reduced [NADPH-hemoprotein reductase] = an (omega-1)-hydroxy-long-chain fatty acid + H+ + H2O + oxidized [NADPH-hemoprotein reductase. A long-chain fatty acid has an aliphatic tail containing 13 to 22 carbons.","definition_xrefs":["RHEA:60936","PMID:18577768","PMID:24242247","GOC:nhn","PMID:22772592"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid omega-1 hydroxylase activity","termid":"GO:0120502"}],"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":"long-chain fatty acid omega-1 hydroxylase activity","synonyms":[{"name":"cytochrome P450 fatty acid omega-1 hydroxylase activity","type":"related"}],"termid":"GO:0120319"}


id: GO:0005155
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mah","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete epidermal growth factor receptor activating ligand activity (obsolete GO:0005155)","synonyms":[{"name":"EGF receptor activating ligand activity","type":"exact"},{"name":"EGFR activating ligand activity","type":"exact"},{"name":"epidermal growth factor receptor activating ligand activity","type":"exact"}],"termid":"GO:0005155"}


id: GO:0031928
data:
  {"annotated_genes":["SJAG_02152","SJAG_03808","SJAG_02962","SJAG_03652"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91921,91922,119322,120623],"is_not":false,"summary":null,"term":"GO:0031928"}]},"cv_name":"molecular_function","definition":"Enables the transfer of pyridoxine from one side of a membrane to the other. Pyridoxine, 2-methyl-3-hydroxy-4,5-bis(hydroxymethyl)pyridine, is one of the vitamin B6 compounds. Pyridoxal, pyridoxamine and pyridoxine are collectively known as vitamin B6, and are efficiently converted to the biologically active form of vitamin B6, pyridoxal phosphate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02152":null,"SJAG_02962":null,"SJAG_03652":null,"SJAG_03808":null},"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:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"pyridoxine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pyridoxine transporter activity","type":"broad"}],"termid":"GO:0031928","terms_by_termid":{"GO:0031928":null}}


id: PBO:0070804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 34","termid":"PBO:0070804"}


id: PBO:0081094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger DHHC-type containing 20 pseudogene 3","termid":"PBO:0081094"}


id: GO:0141003
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a phosphate group to a histone variant H2AX.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone kinase activity","termid":"GO:0035173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0004672","GO:0016740","GO:0140096","GO:0016301"],"is_obsolete":false,"name":"histone H2AX kinase activity","termid":"GO:0141003"}


id: MONDO:0017646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neurodegenerative disease with chorea (obsolete MONDO:0017646)","secondary_identifiers":["Orphanet:306719"],"termid":"MONDO:0017646","xrefs":{"Monarch":{"xref_id":"0017646"}}}


id: PBO:0004520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial and cytoplasmic histidine-tRNA ligase Hrs1 (predicted)","termid":"PBO:0004520"}


id: PBO:0070479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 14","termid":"PBO:0070479"}


id: GO:0009973
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: A + AMP + 2 H+ + sulfite = adenosine 5'-phosphosulfate + AH2.","definition_xrefs":["RHEA:24240","PMID:5421934"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors","termid":"GO:0016667"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"adenylyl-sulfate reductase activity","secondary_identifiers":["MetaCyc:ADENYLYLSULFATE-REDUCTASE-RXN","EC:1.8.99.2"],"synonyms":[{"name":"APS reductase activity","type":"related"},{"name":"adenosine phosphosulfate reductase activity","type":"related"},{"name":"adenylyl-sulphate reductase activity","type":"related"}],"termid":"GO:0009973"}


id: PBO:0062057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily W member 4 pseudogene","termid":"PBO:0062057"}


id: GO:0043655
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The space within a host but external to the plasma membrane of host cells, e.g. within host bloodstream.","definition_xrefs":["GOC:cc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cellular component","termid":"GO:0018995"}],"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 extracellular space","synonyms":[{"name":"extracellular space of host","type":"exact"}],"termid":"GO:0043655"}


id: PBO:0045481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"desmocollin 3","termid":"PBO:0045481"}


id: PBO:0066201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 17 pseudogene 2","termid":"PBO:0066201"}


id: GO:0010626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency or extent of the multiplication or reproduction of Schwann cells, resulting in the expansion of their population. Schwann cells are a type of glial cell in the peripheral nervous system.","definition_xrefs":["GOC:dph","GOC:sl","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Schwann cell proliferation","termid":"GO:0010624"},{"relation_name":"is_a","term_name":"negative regulation of glial cell proliferation","termid":"GO:0060253"},{"relation_name":"negatively_regulates","term_name":"Schwann cell proliferation","termid":"GO:0014010"}],"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 Schwann cell proliferation","termid":"GO:0010626"}


id: PBO:0087973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Trimeric heat shock transcription factor; activates multiple genes in response to highly diverse stresses and transient intracellular acidification; recognizes variable heat shock elements (HSEs) consisting of inverted NGAAN repeats; monitors translational status of cell through an RQC (Ribosomal Quality Control)-mediated translation-stress signal; involved in diauxic shift; posttranslationally regulated; human homolog HSF1 with linker region mutations can complement yeast hsf1 mutant","termid":"PBO:0087973"}


id: PBO:0110235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER and nuclear envelope ubiquitin-protein ligase E3 Doa10","termid":"PBO:0110235"}


id: GO:0003954
data:
  {"annotated_genes":["SJAG_01539","SJAG_04152"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98502,114695],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050136"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: NADH + H+ + acceptor = NAD+ + reduced acceptor.","definition_xrefs":["RHEA:11356"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H","termid":"GO:0016651"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01539":null,"SJAG_04152":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"NADH dehydrogenase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DPNH diaphorase activity","type":"related"},{"name":"NADH diaphorase activity","type":"related"},{"name":"NADH hydrogenase activity","type":"related"},{"name":"NADH oxidoreductase activity","type":"related"},{"name":"NADH-menadione oxidoreductase activity","type":"narrow"},{"name":"NADH2 dehydrogenase activity","type":"related"},{"name":"NADH:(acceptor) oxidoreductase activity","type":"related"},{"name":"NADH:acceptor oxidoreductase activity","type":"related"},{"name":"NADH:cytochrome c oxidoreductase activity","type":"narrow"},{"name":"beta-NADH dehydrogenase dinucleotide activity","type":"related"},{"name":"cytochrome c reductase activity","type":"related"},{"name":"diaphorase activity","type":"broad"},{"name":"dihydrocodehydrogenase I dehydrogenase activity","type":"related"},{"name":"dihydronicotinamide adenine dinucleotide dehydrogenase activity","type":"related"},{"name":"diphosphopyridine diaphorase activity","type":"related"},{"name":"diphosphopyrinase activity","type":"related"},{"name":"reduced diphosphopyridine nucleotide diaphorase activity","type":"related"},{"name":"type 1 dehydrogenase activity","type":"related"},{"name":"type I dehydrogenase activity","type":"related"}],"termid":"GO:0003954","terms_by_termid":{"GO:0050136":null}}


id: MONDO:0016955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 4q duplication is a chromosome abnormality characterized by an extra copy (duplication) of genetic material on the long arm (q) of chromosome 4. The severity and specific symptoms depend on the size and location of the duplication, and which genes are involved. Features that have been described in some people with chromosome 4q duplication include developmental delay, intellectual disability, behavioral problems, birth defects, and distinctive facial features. Most cases are inherited from an unaffected parent with a chromosomal rearrangement called a balanced translocation. Some cases are not inherited and occur sporadically. Treatment is based on the signs and symptoms present in each person.","definition_xrefs":["GARD:0005347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of chromosome 4","termid":"MONDO:0016924"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial duplication of the long arm of chromosome 4","secondary_identifiers":["MEDGEN:162874","MESH:C537644","Orphanet:262860","UMLS:C0795812","GARD:5347","DOID:0111159","icd11.foundation:959729903"],"synonyms":[{"name":"4q duplication","type":"related"},{"name":"4q trisomy","type":"related"},{"name":"Duplication 4q","type":"related"},{"name":"Duplication 4q syndrome, partial","type":"exact"},{"name":"chromosome 4, partial trisomy 4q","type":"exact"},{"name":"chromosome 4q duplication","type":"related"},{"name":"distal 4q trisomy","type":"exact"},{"name":"dup(4q) syndrome, partial","type":"exact"},{"name":"partial duplication of chromosome 4q","type":"exact"},{"name":"partial duplication of the long arm of chromosome type 4","type":"exact"},{"name":"partial trisomy 4q","type":"related"},{"name":"partial trisomy 4q syndrome","type":"exact"},{"name":"partial trisomy distal 4q","type":"related"},{"name":"partial trisomy of chromosome 4q","type":"exact"},{"name":"partial trisomy of the long arm of chromosome 4","type":"exact"},{"name":"trisomy 4q","type":"related"}],"termid":"MONDO:0016955","xrefs":{"Monarch":{"xref_id":"0016955"}}}


id: MONDO:0100513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Mendelian disease in which the cause of the disease is a mutation in the TRAF3 gene. TRAF3 haploinsufficiency caused by heterozygous loss of function (null) variants presents as an immune dysregulation syndrome of recurrent bacterial infections, autoimmunity, systemic inflammation, B cell lymphoproliferation, and hypergammaglobulinemia.","definition_xrefs":["PMID:35960817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAF3 haploinsufficiency","termid":"MONDO:0100513","xrefs":{"Monarch":{"xref_id":"0100513"}}}


id: PBO:0057838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3154","termid":"PBO:0057838"}


id: MONDO:1010111
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare and debilitating renal pain disorder characterized by chronic, severe loin pain with or without micro- or macroscopic hematuria.","definition_xrefs":["PMID:30984919","PMID:33532147","PMID:38106595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"chronic pain syndrome","termid":"MONDO:0024317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"loin pain hematuria syndrome","synonyms":[{"name":"LPHS","type":"exact"}],"termid":"MONDO:1010111","xrefs":{"Monarch":{"xref_id":"1010111"}}}


id: PBO:0005776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase complex subunit, SAP128 family (predicted)","termid":"PBO:0005776"}


id: PBO:0053100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late cornified envelope 6A","termid":"PBO:0053100"}


id: FYPO:0000679
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype that affects a developmental process.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process phenotype","termid":"FYPO:0000300"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmental process phenotype","synonyms":[{"name":"fission yeast developmental process phenotype","type":"exact"}],"termid":"FYPO:0000679"}


id: GO:0062142
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-beta-ethynylserine. L-beta-ethynylserine is an antibiotic produced by Streptomyces bacteria.","definition_xrefs":["PMID:3082841","PMID:30867596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal acetylenic compound biosynthetic process","termid":"GO:0120237"},{"relation_name":"is_a","term_name":"L-amino acid biosynthetic process","termid":"GO:0170034"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid biosynthetic process","termid":"GO:0170043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"L-beta-ethynylserine biosynthetic process","termid":"GO:0062142"}


id: MONDO:0001707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sarcoidosis affecting the tissues of the heart.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-familial restrictive cardiomyopathy","termid":"MONDO:0016345"},{"relation_name":"is_a","term_name":"sarcoidosis","termid":"MONDO:0019338"}],"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":"cardiac sarcoidosis","secondary_identifiers":["SCTID:75403004","UMLS:C0392077","DOID:13405","MEDGEN:140260","NCIT:C35589"],"synonyms":[{"name":"heart sarcoidosis","type":"exact"},{"name":"sarcoidosis of heart","type":"exact"}],"termid":"MONDO:0001707","xrefs":{"Monarch":{"xref_id":"0001707"}}}


id: PATO:0001089
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001089 elasticity value (obsolete PATO:0001089)","termid":"PATO:0001089"}


id: PBO:0069235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 490, pseudogene","termid":"PBO:0069235"}


id: GO:1903958
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of nitric-oxide synthase activity.","definition_xrefs":["PMID:25417112","GOC:bhm","GOC:TermGenie","GO_REF:0000088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"nitric-oxide synthase complex","synonyms":[{"name":"iNOS-S100A8/A9 complex","type":"narrow"}],"termid":"GO:1903958"}


id: FYPO:0006618
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the number of sites at which the protein Rad52 (also called Rad22) accumulates is greater than normal during a cellular response to bleomycin.","definition_xrefs":["PMID:22064477","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased number of Rad52 foci during vegetative growth","termid":"FYPO:0000972"}],"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:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased number of Rad52 foci during cellular response to bleomycin","synonyms":[{"name":"increased number of Rad22 foci during cellular response to bleomycin","type":"exact"},{"name":"increased number of Rad52 foci during cellular response to DNA damage","type":"related"},{"name":"increased number of Rad52 foci during cellular response to bleomycin during mitotic cell cycle","type":"related"},{"name":"increased number of Rad52 foci during cellular response to bleomycin during vegetative growth","type":"exact"}],"termid":"FYPO:0006618"}


id: PBO:0044087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis antigen family 45 member A7","termid":"PBO:0044087"}


id: PBO:0087077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L38; homologous to mammalian ribosomal protein L38, no bacterial homolog","termid":"PBO:0087077"}


id: PBO:0051791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQ motif containing H","termid":"PBO:0051791"}


id: PR:Q9P779
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1711.11 gene.","definition_xrefs":["UniProtKB:Q9P779","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":"sorting nexin C1711.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1711.11","synonyms":[{"name":"Spom972h-SPBC1711.11","type":"exact"}],"termid":"PR:Q9P779"}


id: PBO:0027189
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_actomyosin_contractile_ring","termid":"PBO:0027189"}


id: PBO:0055076
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 2493","termid":"PBO:0055076"}


id: MONDO:0006186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from glandular epithelial cells of the duodenum.","direct_ancestors":[{"relation_name":"is_a","term_name":"small intestine adenocarcinoma","termid":"MONDO:0003198"},{"relation_name":"is_a","term_name":"carcinoma of duodenum","termid":"MONDO:0021335"}],"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:0004335","MONDO:0004992"],"is_obsolete":false,"name":"duodenal adenocarcinoma","secondary_identifiers":["SCTID:408644002","ONCOTREE:DA","DOID:10816","UMLS:C0278804","EFO:1000223","MEDGEN:82985","NCIT:C7889"],"synonyms":[{"name":"adenocarcinoma of duodenum","type":"exact"},{"name":"adenocarcinoma of the duodenum","type":"exact"},{"name":"duodenal adenocarcinoma","type":"exact"},{"name":"duodenum adenocarcinoma","type":"exact"}],"termid":"MONDO:0006186","xrefs":{"Monarch":{"xref_id":"0006186"}}}


id: PBO:0084941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Multicopy suppressor of HER2 involved in mitochondrial translation; mutant is defective in directing meiotic recombination events to homologous chromatids","termid":"PBO:0084941"}


id: PBO:0048003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FRMD4A antisense RNA 1","termid":"PBO:0048003"}


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


id: PBO:0111650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone chaperone/ATP-dependent chromatin remodeller SMARCAD1 family Fft2","termid":"PBO:0111650"}


id: MOD:01862
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the hydrogen atom of a cysteine sulfanyl group with a substituted sulfanyl group, forming a disulfide bond that does not cross-link two encoded peptide chains.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiolated residue","termid":"MOD:01886"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disulfide conjugated residue","synonyms":[{"name":"S-thiolation","type":"exact"}],"termid":"MOD:01862"}


id: PBO:0053981
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 1297","termid":"PBO:0053981"}


id: GO:0052118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism on, within or near its host organism towards a higher level of a physical stimulus involved in energy generation, such as light, oxygen, and oxidizable substrates. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive energy taxis in host environment (obsolete GO:0052118)","synonyms":[{"name":"positive energy taxis in response to host environment","type":"exact"}],"termid":"GO:0052118"}


id: GO:0008261
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with allatostatin to initiate a change in cell activity.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled peptide receptor activity","termid":"GO:0008528"}],"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":"allatostatin receptor activity","termid":"GO:0008261"}


id: MONDO:0005845
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the meninges and brain, generally secondary to an infectious cause. Pathogens may be bacterial, viral, fungal, or protozoan.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"encephalitis","termid":"MONDO:0019956"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meningoencephalitis","secondary_identifiers":["MEDGEN:6301","MESH:D008590","SCTID:7125002","DOID:10554","EFO:0007364","NCIT:C34813","UMLS:C0025309"],"termid":"MONDO:0005845","xrefs":{"Monarch":{"xref_id":"0005845"}}}


id: GO:0050681
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nuclear androgen receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear receptor binding","termid":"GO:0016922"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"nuclear androgen receptor binding","synonyms":[{"name":"AR binding","type":"exact"},{"name":"androgen receptor binding","type":"broad"}],"termid":"GO:0050681"}


id: PBO:0113069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of U1 snRNP required for mRNA splicing via spliceosome; substrate of arginine methyltransferase Hmt1p; may interact with poly(A) polymerase to regulate polyadenylation; homolog of human U1-70K, which has been linked to several types of autoimmune and neurodegenerative diseases","termid":"PBO:0113069"}


id: PBO:0073257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 7 pseudogene 1","termid":"PBO:0073257"}


id: GO:0007117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the bud portion of a cell that reproduces by budding irreversibly increases in size over time by accretion and biosynthetic production of matter similar to that already present.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth","termid":"GO:0040007"},{"relation_name":"part_of","term_name":"cell budding","termid":"GO:0007114"}],"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":"budding cell bud growth","synonyms":[{"name":"bud growth","type":"broad"}],"termid":"GO:0007117"}


id: PBO:0059645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 11","termid":"PBO:0059645"}


id: PR:Q9P7A0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sgo1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7A0"],"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":"shugoshin-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP35G2.03c","synonyms":[{"name":"Spom972h-sgo1","type":"exact"}],"termid":"PR:Q9P7A0"}


id: PBO:0080999
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 37","termid":"PBO:0080999"}


id: GO:0021637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the oculomotor nerve. This process pertains to the physical shaping of a rudimentary structure. The trigeminal nerve is composed of three large branches. They are the ophthalmic (V1, sensory), maxillary (V2, sensory) and mandibular (V3, motor and sensory) branches. The sensory ophthalmic branch travels through the superior orbital fissure and passes through the orbit to reach the skin of the forehead and top of the head. The maxillary nerve contains sensory branches that reach the pterygopalatine fossa via the inferior orbital fissure (face, cheek and upper teeth) and pterygopalatine canal (soft and hard palate, nasal cavity and pharynx). The motor part of the mandibular branch is distributed to the muscles of mastication, the mylohyoid muscle and the anterior belly of the digastric. The mandibular nerve also innervates the tensor veli palatini and tensor tympani muscles. The sensory part of the mandibular nerve is composed of branches that carry general sensory information from the mucous membranes of the mouth and cheek, anterior two-thirds of the tongue, lower teeth, skin of the lower jaw, side of the head and scalp and meninges of the anterior and middle cranial fossae.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:cls","ISBN:0838580343","GOC:jid","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve structural organization","termid":"GO:0021604"},{"relation_name":"part_of","term_name":"trigeminal nerve morphogenesis","termid":"GO:0021636"}],"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":"trigeminal nerve structural organization","synonyms":[{"name":"CN V structural organization","type":"related"},{"name":"trigeminal nerve structural organisation","type":"exact"}],"termid":"GO:0021637"}


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


id: FYPO:0004909
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein that is normally localized to discrete regions in the nucleus, visible as foci or dots by microscopy, is abnormally localized such that dots cannot be observed, and the protein is instead distributed throughout the nucleus.","definition_xrefs":["PomBase:mah","PMID:8937982"],"direct_ancestors":[{"relation_name":"is_a","term_name":"loss of punctate nuclear protein localization","termid":"FYPO:0005863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"loss of punctate nuclear protein localization, with protein distributed in nucleus","synonyms":[{"name":"abolished punctate nuclear protein localization, with protein distributed in nucleus","type":"exact"},{"name":"loss of punctate nuclear protein localisation, with protein distributed in nucleus","type":"exact"},{"name":"loss of punctate nuclear protein localization, with protein dispersed through nucleus","type":"exact"},{"name":"loss of punctate nuclear protein localization, with protein distributed in nucleus, during mitotic cell cycle","type":"related"},{"name":"loss of punctate nuclear protein localization, with protein distributed in nucleus, during vegetative growth","type":"exact"},{"name":"loss of punctate nuclear protein localization, with protein distributed throughout nucleus","type":"exact"}],"termid":"FYPO:0004909"}


id: RO:0002237
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A sub-relation of parasite-of in which the parasite is a plant, and the parasite is parasitic under natural conditions and is also photosynthetic to some degree. Hemiparasites may just obtain water and mineral nutrients from the host plant. Many obtain at least part of their organic nutrients from the host as well.","direct_ancestors":[{"relation_name":"is_a","term_name":"parasite_of","termid":"RO:0002444"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemiparasite_of","termid":"RO:0002237"}


id: GO:1904158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form an axonemal central apparatus.","definition_xrefs":["GOC:TermGenie","GOC:krc","PMID:9295136","GO_REF:0000079","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"part_of","term_name":"axoneme assembly","termid":"GO:0035082"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0000226","GO:0007010"],"is_obsolete":false,"name":"axonemal central apparatus assembly","synonyms":[{"name":"axonemal central apparatus formation","type":"exact"}],"termid":"GO:1904158"}


id: PBO:0042874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 126","termid":"PBO:0042874"}


id: GO:1990917
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The cytoplasm of an ovum.","definition_xrefs":["PMID:19022436"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"ooplasm","termid":"GO:1990917"}


id: PR:O14048
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A UBX domain-containing protein 7 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01778","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":"UBX domain-containing protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2C4.15c","secondary_identifiers":["UniProtKB:O14048"],"synonyms":[{"name":"Spom972h-UBXN7","type":"exact"}],"termid":"PR:O14048"}


id: PBO:0028863
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mRNA_level_during_vegetative_growth","termid":"PBO:0028863"}


id: PBO:0056748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase 4, N6-adenosine","termid":"PBO:0056748"}


id: PBO:0062181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily N member 2","termid":"PBO:0062181"}


id: RO:0002574
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"biotically_interacts_with","termid":"RO:0002437"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"participates_in_a_biotic-biotic_interaction_with","termid":"RO:0002574"}


id: PBO:0071243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 84","termid":"PBO:0071243"}


id: MONDO:0004236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A somatostatin-producing neuroendocrine tumor that arises from the duodenum. It is characterized by the presence of tubulo-glandular structures.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"duodenum cancer","termid":"MONDO:0000920"},{"relation_name":"is_a","term_name":"duodenal neuroendocrine tumor, well differentiated, low or intermediate grade","termid":"MONDO:0015063"}],"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":"duodenal somatostatinoma","secondary_identifiers":["UMLS:C1333320","DOID:7479","MEDGEN:234205","NCIT:C27407"],"synonyms":[{"name":"duodenal delta cell somatostatin producing tumor","type":"exact"},{"name":"duodenal delta cell somatostatin producing tumour","type":"exact"},{"name":"duodenal somatostatin producing tumor","type":"exact"},{"name":"duodenal somatostatin producing tumour","type":"exact"},{"name":"duodenal somatostatin-producing NET","type":"exact"},{"name":"duodenal somatostatin-producing neuroendocrine tumor","type":"exact"},{"name":"duodenal somatostatin-producing neuroendocrine tumour","type":"exact"},{"name":"duodenal somatostatinoma","type":"exact"}],"termid":"MONDO:0004236","xrefs":{"Monarch":{"xref_id":"0004236"}}}


id: PR:Q9USP4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug1 gene.","definition_xrefs":["UniProtKB:Q9USP4","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":"meiotically up-regulated gene 1 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC11E10.03","synonyms":[{"name":"Spom972h-mug1","type":"exact"}],"termid":"PR:Q9USP4"}


id: GO:0046632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of an alpha-beta T cell. An alpha-beta T cell is a T cell that expresses an alpha-beta T cell receptor complex.","definition_xrefs":["CL:0000789","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell differentiation","termid":"GO:0030217"},{"relation_name":"is_a","term_name":"alpha-beta T cell activation","termid":"GO:0046631"}],"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":"alpha-beta T cell differentiation","synonyms":[{"name":"alpha-beta T cell development","type":"related"},{"name":"alpha-beta T lymphocyte differentiation","type":"exact"},{"name":"alpha-beta T-cell differentiation","type":"exact"},{"name":"alpha-beta T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0046632"}


id: GO:0043934
data:
  {"annotated_genes":["SJAG_03587","SJAG_04184","SJAG_03013","SJAG_04238","SJAG_04922","SJAG_04080","SJAG_03915","SJAG_04275","SJAG_02718","SJAG_02241","SJAG_01017","SJAG_03250","SJAG_02248","SJAG_01483","SJAG_04140","SJAG_02712","SJAG_00974","SJAG_00114","SJAG_02169","SJAG_01769","SJAG_00663","SJAG_04271","SJAG_00993","SJAG_04859","SJAG_03746","SJAG_04010","SJAG_03057","SJAG_03557","SJAG_04236","SJAG_01662","SJAG_03688","SJAG_03483","SJAG_03090","SJAG_01321","SJAG_05309","SJAG_00486","SJAG_00821","SJAG_04868","SJAG_04483","SJAG_02320","SJAG_00971","SJAG_00826","SJAG_02529","SJAG_03536","SJAG_04781","SJAG_04901","SJAG_04615","SJAG_00405","SJAG_01531","SJAG_04853","SJAG_04470"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106928,102515,113342,98301,98717,114548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030437"},{"annotations":[113147,95791],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071998"},{"annotations":[96240],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034413"},{"annotations":[93546,89978,92018,90472],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030476"},{"annotations":[74681],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034412"},{"annotations":[119638,105966,119630,115920,110891],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070591"},{"annotations":[106782,74683,93273],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031321"},{"annotations":[109199,120401,120702,120885,100612,99372,111939,115768,107092,101692,99335,103505,93062,97154],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032120"},{"annotations":[104717,108644,109529,101622,94063,115769,101621,98651,99336,105924],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031322"},{"annotations":[113030],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0075297"},{"annotations":[104085],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0075296"},{"annotations":[92497],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903024"},{"annotations":[93959],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0034307"},{"annotations":[107821,96281,117811,101623,101624,101909],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070583"}]},"cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a spore over time, from its initiation to the mature structure. A spore is a structure that can be used for dissemination, for survival of adverse conditions because of its heat and desiccation resistance, and/or for reproduction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process","termid":"GO:0032502"}],"gene_count":51,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00405":null,"SJAG_00486":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00971":null,"SJAG_00974":null,"SJAG_00993":null,"SJAG_01017":null,"SJAG_01321":null,"SJAG_01483":null,"SJAG_01531":null,"SJAG_01662":null,"SJAG_01769":null,"SJAG_02169":null,"SJAG_02241":null,"SJAG_02248":null,"SJAG_02320":null,"SJAG_02529":null,"SJAG_02712":null,"SJAG_02718":null,"SJAG_03013":null,"SJAG_03057":null,"SJAG_03090":null,"SJAG_03250":null,"SJAG_03483":null,"SJAG_03536":null,"SJAG_03557":null,"SJAG_03587":null,"SJAG_03688":null,"SJAG_03746":null,"SJAG_03915":null,"SJAG_04010":null,"SJAG_04080":null,"SJAG_04140":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04271":null,"SJAG_04275":null,"SJAG_04470":null,"SJAG_04483":null,"SJAG_04615":null,"SJAG_04781":null,"SJAG_04853":null,"SJAG_04859":null,"SJAG_04868":null,"SJAG_04901":null,"SJAG_04922":null,"SJAG_05309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"sporulation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Spore"],"termid":"GO:0043934","terms_by_termid":{"GO:0030437":null,"GO:0030476":null,"GO:0031321":null,"GO:0031322":null,"GO:0032120":null,"GO:0034307":null,"GO:0034412":null,"GO:0034413":null,"GO:0070583":null,"GO:0070591":null,"GO:0071998":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


id: PBO:0042948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 2","termid":"PBO:0042948"}


id: PBO:0066042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAP1A, member of RAS oncogene family pseudogene","termid":"PBO:0066042"}


id: PBO:0040799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic helix-loop-helix family member e22","termid":"PBO:0040799"}


id: PBO:0049718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAUS augmin like complex subunit 4","termid":"PBO:0049718"}


id: MONDO:0023255
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":"glossopalatine ankylosis micrognathia ear anomalies","termid":"MONDO:0023255","xrefs":{"Monarch":{"xref_id":"0023255"}}}


id: GO:0020039
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The structure enclosing certain parasite cells such as certain apicomplexa and Euglenozoa; consists of the cell membrane with its associated infrastructure of microtubules, microfilaments and other organelles.","definition_xrefs":["GOC:mb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"pellicle","termid":"GO:0020039"}


id: GO:0052569
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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 nitric oxide produced as part of the defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete response to defense-related symbiont nitric oxide production (obsolete GO:0052569)","synonyms":[{"name":"response to defense-related symbiont nitric oxide production","type":"exact"}],"termid":"GO:0052569"}


id: PBO:0051059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 3-16","termid":"PBO:0051059"}


id: PBO:0026873
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_meiotic_DNA_double-strand_break_resectioning","termid":"PBO:0026873"}


id: GO:0005655
data:
  {"annotated_genes":["SJAG_04582","SJAG_01369","SJAG_01623","SJAG_02547","SJAG_03796","SJAG_06613","SJAG_00306","SJAG_03234","SJAG_00955","SJAG_02553","SJAG_04916"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[60948,64471,72859,73092,73428,92855,101271,106355,117143,117231,120458],"is_not":false,"summary":null,"term":"GO:0005655"}]},"cv_name":"cellular_component","definition":"A ribonuclease P complex located in the nucleolus of a eukaryotic cell, where it catalyzes the 5' endonucleolytic cleavage of precursor tRNAs to yield mature tRNAs. Eukaryotic nucleolar ribonuclease P complexes generally contain a single RNA molecule that is necessary but not sufficient for catalysis, and several protein molecules.","definition_xrefs":["GOC:mah","PMID:12045094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multimeric ribonuclease P complex","termid":"GO:0030681"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nucleolus","termid":"GO:0005730"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00306":null,"SJAG_00955":null,"SJAG_01369":null,"SJAG_01623":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_03234":null,"SJAG_03796":null,"SJAG_04582":null,"SJAG_04916":null,"SJAG_06613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005730"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991","GO:0005730"],"is_obsolete":false,"name":"nucleolar ribonuclease P complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"nucleolar RNase P complex","type":"exact"}],"termid":"GO:0005655","terms_by_termid":{"GO:0005655":null}}


id: GO:0034699
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 luteinizing hormone stimulus.","definition_xrefs":["GOC:BHF","GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to gonadotropin","termid":"GO:0034698"},{"relation_name":"is_a","term_name":"response to peptide hormone","termid":"GO:0043434"}],"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 luteinizing hormone","synonyms":[{"name":"response to luteinizing hormone stimulus","type":"exact"}],"termid":"GO:0034699"}


id: PATO:0000226
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000226 tactile response (obsolete PATO:0000226)","termid":"PATO:0000226"}


id: PR:000027505
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitogen-activated protein kinase HOG1 unmodified form in Schizosaccharomyces pombe.","definition_xrefs":["PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitogen-activated protein kinase HOG1","termid":"PR:000027499"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sty1/UnMod","pombase_gene_id":"SPAC24B11.06c","synonyms":[{"name":"PomBase_original_PRO_term_name: mitogen-activated protein kinase sty1 unmodified form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-HOG1/UnMod","type":"exact"},{"name":"sty1/UnMod","type":"exact"}],"termid":"PR:000027505"}


id: PBO:0113240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear-enriched ubiquitin-like polyubiquitin-binding protein; K48-Ub chain binding protein that also binds K63-linked chains in vitro; required for spindle pole body (SPB) duplication and for transit through the G2/M phase of the cell cycle; involved in proteolysis; interacts with the proteasome; contains an N-terminal Ub-like (UBL) and a C-terminal Ub-associated (UBA) domain; protein abundance increases in response to DNA replication stress","termid":"PBO:0113240"}


id: GO:0031234
data:
  {"annotated_genes":["SJAG_02444","SJAG_03081","SJAG_02605","SJAG_02233","SJAG_04026"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[112365],"is_not":false,"summary":null,"term":"GO:0031234"},{"annotations":[76982,82093,75892,108306],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005834"}]},"cv_name":"cellular_component","definition":"The component of a plasma membrane consisting of gene products and protein complexes that are loosely bound to its cytoplasmic surface, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of plasma membrane","termid":"GO:0019897"},{"relation_name":"part_of","term_name":"cytoplasmic side of plasma membrane","termid":"GO:0009898"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02233":null,"SJAG_02444":null,"SJAG_02605":null,"SJAG_03081":null,"SJAG_04026":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"extrinsic component of cytoplasmic side of plasma membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"extrinsic to cytoplasmic side of plasma membrane","type":"narrow"},{"name":"extrinsic to internal leaflet of plasma membrane","type":"exact"},{"name":"extrinsic to internal side of plasma membrane","type":"exact"}],"termid":"GO:0031234","terms_by_termid":{"GO:0005834":null,"GO:0031234":null}}


id: MONDO:1011207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypophosphatasia that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypophosphatasia, non-human animal","termid":"MONDO:1010316"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypophosphatasia, dog","secondary_identifiers":["OMIA:002162-9615"],"termid":"MONDO:1011207","xrefs":{"Monarch":{"xref_id":"1011207"}}}


id: PR:000035574
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A MAD2:MAD3 complex whose components are encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:KER","PMID:12676091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAD2:MAD3 complex (Schizosaccharomyces pombe 972h-)","synonyms":[{"name":"Spom972h-(MAD2:MAD3)","type":"exact"}],"termid":"PR:000035574"}


id: GO:0009106
data:
  {"annotated_genes":["SJAG_03553","SJAG_01271","SJAG_03198"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98944,99646,76704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009107"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving lipoate, 1,2-dithiolane-3-pentanoate, the anion derived from lipoic acid.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid metabolic process","termid":"GO:0006631"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01271":null,"SJAG_03198":null,"SJAG_03553":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"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006790","GO:0006629"],"is_obsolete":false,"name":"lipoate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0000273"],"synonyms":[{"name":"lipoate metabolism","type":"exact"},{"name":"lipoic acid metabolic process","type":"exact"},{"name":"lipoic acid metabolism","type":"exact"}],"termid":"GO:0009106","terms_by_termid":{"GO:0009107":null}}


id: PBO:0030221
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_guanosine-diphosphatase_activity","termid":"PBO:0030221"}


id: PBO:0053423
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 365","termid":"PBO:0053423"}


id: GO:1902440
data:
  {"annotated_genes":["SJAG_05319","SJAG_05266","SJAG_01371","SJAG_03437","SJAG_01224","SJAG_00918","SJAG_02731","SJAG_05220","SJAG_01211","SJAG_01546","SJAG_01775"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118762,111716,92751,100408,109320,110706,115936,90914,102312,98556,91521],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990976"}]},"cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a mitotic spindle pole body.","definition_xrefs":["GOC:TermGenie","PMID:22438582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to spindle pole body","termid":"GO:0071988"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01371":null,"SJAG_01546":null,"SJAG_01775":null,"SJAG_02731":null,"SJAG_03437":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05319":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":"protein localization to mitotic spindle pole body","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1990975"],"synonyms":[{"name":"establishment of protein localization to mitotic spindle pole body","type":"narrow"},{"name":"protein localisation in mitotic spindle pole body","type":"exact"},{"name":"protein localisation to mitotic spindle pole body","type":"exact"},{"name":"protein localization in mitotic spindle pole body","type":"exact"}],"termid":"GO:1902440","terms_by_termid":{"GO:1990976":null}}


id: MONDO:0100544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A precancerous condition characterized by the gradual, clonal expansion of hematopoietic stem and progenitor cells carrying specific, disruptive, and recurrent genetic variants, in individuals without clear diagnosis of hematological malignancies. It is associated with an increased risk of developing hematologic cancers.","definition_xrefs":["NCIT:C155821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clonal hematopoiesis","termid":"MONDO:0100542"}],"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":"age-related clonal hematopoiesis","secondary_identifiers":["UMLS:C4722404","MEDGEN:1670618"],"synonyms":[{"name":"ARCH","type":"exact"}],"termid":"MONDO:0100544","xrefs":{"Monarch":{"xref_id":"0100544"}}}


id: GO:0047446
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (1-hydroxycyclohexan-1-yl)acetyl-CoA = acetyl-CoA + cyclohexanone.","definition_xrefs":["EC:4.1.3.35","RHEA:23868"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxo-acid-lyase activity","termid":"GO:0016833"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"(1-hydroxycyclohexan-1-yl)acetyl-CoA lyase activity","secondary_identifiers":["MetaCyc:4.1.3.35-RXN","KEGG_REACTION:R02232"],"synonyms":[{"name":"(1-hydroxycyclohexan-1-yl)acetyl-CoA cyclohexanone-lyase (acetyl-CoA-forming)","type":"related"},{"name":"(1-hydroxycyclohexan-1-yl)acetyl-CoA cyclohexanone-lyase activity","type":"related"}],"termid":"GO:0047446"}


id: PBO:0030602
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_alpha-glucosidase_activity","termid":"PBO:0030602"}


id: GO:0102797
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: geranial + O2 + H2O = H+ + geranate + hydrogen peroxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete geranial:oxygen oxidoreductase activity (obsolete GO:0102797)","termid":"GO:0102797"}


id: GO:0102180
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4alpha-hydroxymethyl-stigmasta-7,24(241)-dien-3beta-ol + NADH + O2 + H+ = 4alpha-formyl-stigmasta-7,24(241)-dien-3beta-ol + NAD + 2 H2O.","definition_xrefs":["GOC:pz","RHEA:59036"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"4alpha-hydroxymethyl-stigmasta-7,24(241)-dien-3beta-ol-methyl oxidase activity","secondary_identifiers":["MetaCyc:RXN-11936"],"termid":"GO:0102180"}


id: PBO:0078421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon GCC) 2-2","termid":"PBO:0078421"}


id: PBO:0053299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lin-7 homolog A, crumbs cell polarity complex component","termid":"PBO:0053299"}


id: MONDO:0030487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylometaphyseal dysplasia, pagnamenta type","secondary_identifiers":["OMIM:619638","MEDGEN:1794240","UMLS:C5562030"],"synonyms":[{"name":"SMDP","type":"exact"}],"termid":"MONDO:0030487","xrefs":{"Monarch":{"xref_id":"0030487"}}}


id: PBO:0091306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-citrate synthase subunit 2","termid":"PBO:0091306"}


id: PBO:0091784
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kcat/KM 4.3x10^7 M-1 min-1","termid":"PBO:0091784"}


id: GO:0044226
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Portion of a neuron cell soma closest to the point where the basilar dendrite emerges.","definition_xrefs":["NIF_Subcellular:sao1186862860"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell pole","termid":"GO:0060187"},{"relation_name":"part_of","term_name":"neuronal cell body","termid":"GO:0043025"}],"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":"basal pole of neuron","termid":"GO:0044226"}


id: PBO:0108914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STAG3 cohesin complex component","termid":"PBO:0108914"}


id: PBO:0013804
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae HUT1","termid":"PBO:0013804"}


id: PR:Q9HGQ2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trm401 gene.","definition_xrefs":["UniProtKB:Q9HGQ2","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":"multisite-specific tRNA:(cytosine-C(5))-methyltransferase trm4a (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17D4.04","synonyms":[{"name":"Spom972h-trm401","type":"exact"},{"name":"tRNA (cytosine-5-)-methyltransferase trm4a (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9HGQ2"}


id: GO:0072398
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A signal transduction process that contributes to a cytokinesis checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic cell cycle checkpoint signaling","termid":"GO:0007093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"signal transduction involved in cytokinesis checkpoint","secondary_identifiers":["GO:0072419"],"termid":"GO:0072398"}


id: PBO:0043212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC28 protein kinase regulatory subunit 1B pseudogene 5","termid":"PBO:0043212"}


id: PBO:0081359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 185 with LIM domain","termid":"PBO:0081359"}


id: MONDO:0016369
data:
  {"annotated_genes":["SJAG_04995","SJAG_02200"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86783,86784],"is_not":false,"summary":null,"term":"MONDO:0016369"}]},"cv_name":"mondo","definition":"Rothmund-Thomson syndrome type 2 is a subform of Rothmund-Thomson syndrome (RTS) presenting with a characteristic facial rash (poikiloderma) and frequently associated with short stature, sparse scalp hair, sparse or absent eyelashes and/or eyebrows, congenital bone defects and an increased risk of osteosarcoma in childhood and squamous cell carcinoma later in life.","definition_xrefs":["Orphanet:221016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"Rothmund-Thomson syndrome","termid":"MONDO:0010002"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02200":null,"SJAG_04995":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"Rothmund-Thomson syndrome type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17135","OMIM:268400","MEDGEN:1684753","NCIT:C178827","icd11.foundation:2111040755","UMLS:C5203410"],"synonyms":[{"name":"RTS2","type":"exact"},{"name":"Rothmund-Thomson syndrome, type 2","type":"exact"},{"name":"poikiloderma of Rothmund-Thomson type 2","type":"exact"}],"termid":"MONDO:0016369","terms_by_termid":{"MONDO:0016369":null},"xrefs":{"Monarch":{"xref_id":"0016369"}}}


id: MONDO:0011079
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rhizomelic dysplasia, Patterson-Lowry type is a rare primary bone dysplasia characterized by short stature, severe rhizomelic shortening of the upper limbs associated with specific malformations of humeri (including marked widening and flattening of proximal metaphyses, medial flattening of the proximal epiphyses, and lateral bowing with medial cortical thickening of the proximal diaphyses), marked coxa vara with dysplastic femoral heads and brachimetacarpalia.","definition_xrefs":["Orphanet:2831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhizomelic dysplasia, Patterson-Lowry type","secondary_identifiers":["SCTID:715505002","GARD:4703","UMLS:C1832359","icd11.foundation:1681747199","MEDGEN:321940","MESH:C537609","OMIM:601438"],"synonyms":[{"name":"Patterson Lowry syndrome","type":"related"},{"name":"Patterson-Lowry rhizomelic dysplasia","type":"related"},{"name":"rhizomelic dysplasia Patterson Lowry type","type":"related"},{"name":"rhizomelic dysplasia, Patterson-Lowry type","type":"exact"}],"termid":"MONDO:0011079","xrefs":{"Monarch":{"xref_id":"0011079"}}}


id: PR:P41893
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A low molecular weight phosphotyrosine protein phosphatase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01610"],"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":"low molecular weight phosphotyrosine protein phosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1071.12c","secondary_identifiers":["UniProtKB:P41893"],"synonyms":[{"name":"PTPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ACP1","type":"exact"},{"name":"low molecular weight cytosolic acid phosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"small tyrosine phosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P41893"}


id: GO:0035370
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A heterodimeric ubiquitin conjugating enzyme complex that catalyzes assembly of K63-linked polyubiquitin chains and is involved in NF-kappaB activation. In humans at least, the complex comprises the ubiquitin-conjugating enzyme UBC13 and ubiquitin-conjugating enzyme variant 1A (UEV1A).","definition_xrefs":["GOC:amm","PMID:16129784"],"gene_count":0,"genotype_count":0,"name":"obsolete UBC13-UEV1A complex (obsolete GO:0035370)","termid":"GO:0035370"}


id: GO:0086061
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a sodium ion by a voltage-gated channel through the plasma membrane of a bundle of His cardiac muscle cell contributing to the depolarization phase of an action potential. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated sodium channel activity involved in cardiac muscle cell action potential","termid":"GO:0086006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"voltage-gated sodium channel activity involved in bundle of His cell action potential","synonyms":[{"name":"voltage-gated sodium channel activity involved in bundle of His cardiac muscle cell action potential","type":"exact"}],"termid":"GO:0086061"}


id: MONDO:0016360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macrothrombocytopenia with mitral valve insufficiency is a rare hemorrhagic disorder due to a platelet anomaly characterized by dysfunctional platelets of abnormally large size, moderate thrombocytopenia, prolonged bleeding time and mild bleeding diathesis (ecchymoses and epistaxis), associated with mitral valve insufficiency.","definition_xrefs":["Orphanet:220448"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic constitutional thrombocytopenia","termid":"MONDO:0018795"}],"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":"marcothrombocytopenia with mitral valve insufficiency","secondary_identifiers":["UMLS:C4749648","MEDGEN:1649052","GARD:20538"],"termid":"MONDO:0016360","xrefs":{"Monarch":{"xref_id":"0016360"}}}


id: GO:0046639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of alpha-beta T cell differentiation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell differentiation","termid":"GO:0045581"},{"relation_name":"is_a","term_name":"negative regulation of alpha-beta T cell activation","termid":"GO:0046636"},{"relation_name":"is_a","term_name":"regulation of alpha-beta T cell differentiation","termid":"GO:0046637"},{"relation_name":"negatively_regulates","term_name":"alpha-beta T cell differentiation","termid":"GO:0046632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of alpha-beta T cell differentiation","synonyms":[{"name":"down regulation of alpha-beta T cell differentiation","type":"exact"},{"name":"down-regulation of alpha-beta T cell differentiation","type":"exact"},{"name":"downregulation of alpha-beta T cell differentiation","type":"exact"},{"name":"inhibition of alpha-beta T cell differentiation","type":"narrow"},{"name":"negative regulation of alpha-beta T cell development","type":"related"},{"name":"negative regulation of alpha-beta T lymphocyte differentiation","type":"exact"},{"name":"negative regulation of alpha-beta T-cell differentiation","type":"exact"},{"name":"negative regulation of alpha-beta T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0046639"}


id: GO:1903727
data:
  {"annotated_genes":["SJAG_02613"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902648"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of phospholipid metabolic process.","definition_xrefs":["PMID:10657240","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid metabolic process","termid":"GO:0045834"},{"relation_name":"is_a","term_name":"positive regulation of phosphate metabolic process","termid":"GO:0045937"},{"relation_name":"is_a","term_name":"regulation of phospholipid metabolic process","termid":"GO:1903725"},{"relation_name":"positively_regulates","term_name":"phospholipid metabolic process","termid":"GO:0006644"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"positive regulation of phospholipid metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of phospholipid metabolic process","type":"narrow"},{"name":"activation of phospholipid metabolism","type":"narrow"},{"name":"positive regulation of phospholipid metabolism","type":"exact"},{"name":"up regulation of phospholipid metabolic process","type":"exact"},{"name":"up regulation of phospholipid metabolism","type":"exact"},{"name":"up-regulation of phospholipid metabolic process","type":"exact"},{"name":"up-regulation of phospholipid metabolism","type":"exact"},{"name":"upregulation of phospholipid metabolic process","type":"exact"},{"name":"upregulation of phospholipid metabolism","type":"exact"}],"termid":"GO:1903727","terms_by_termid":{"GO:1902648":null}}


id: PBO:0060436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NACA pseudogene 5","termid":"PBO:0060436"}


id: GO:0106437
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalytic reaction: ATP + L-glutamate + L-glutamyl-[protein] = ADP + H+ + L-gamma-glutamyl-L-glutamyl-[protein] + phosphate.","definition_xrefs":["RHEA:60144","PMID:32747782"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-glutamic acid ligase activity","termid":"GO:0070739"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"protein-glutamic acid ligase activity, initiating","termid":"GO:0106437"}


id: GO:0045471
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ethanol stimulus.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to ethanol","secondary_identifiers":["GO:0017036"],"termid":"GO:0045471"}


id: GO:0030192
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Modulates the activity of chaperones of the Hsp70/Hsc70 class.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete Hsp70/Hsc70 protein regulator activity (obsolete GO:0030192)","synonyms":[{"name":"Hsp70/Hsc70 protein regulator activity","type":"exact"}],"termid":"GO:0030192"}


id: MONDO:1010611
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Thyroiditis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroiditis, non-human animal","termid":"MONDO:1010059"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroiditis, dog","secondary_identifiers":["OMIA:001005-9615"],"termid":"MONDO:1010611","xrefs":{"Monarch":{"xref_id":"1010611"}}}


id: PBO:0084069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase involved in G-protein signaling in adenylate cyclase activation; plays a role in regulation of cell proliferation; localized to the plasma membrane; activated by increased levels of glycolysis intermediate fructose-1,6-bisphosphate; homolog of mammalian RAS proto-oncogenes; relative distribution to the nucleus increases upon DNA replication stress; RAS1 has a paralog, RAS2, that arose from the whole genome duplication","termid":"PBO:0084069"}


id: PBO:0040177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartate dehydrogenase domain containing","termid":"PBO:0040177"}


id: SO:0000071
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute to describe a gene when it is located within the intron of another gene and on the same strand.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inside_intron","termid":"SO:0000069"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inside_intron_parallel","synonyms":[{"name":"inside intron parallel","type":"exact"}],"termid":"SO:0000071"}


id: PBO:0067055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 76, pseudogene","termid":"PBO:0067055"}


id: GO:0043686
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of covalently altering one or more amino acids in a protein after translation has begun but before the protein has been released from the ribosome.","definition_xrefs":["GOC:jsg"],"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":"co-translational protein modification","synonyms":[{"name":"co-translational amino acid modification","type":"exact"},{"name":"co-translational modification","type":"exact"},{"name":"cotranslational amino acid modification","type":"exact"},{"name":"cotranslational modification","type":"exact"},{"name":"cotranslational protein modification","type":"exact"}],"termid":"GO:0043686"}


id: PBO:0034329
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_prototype","termid":"PBO:0034329"}


id: PBO:0030745
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_phosphatidylinositol-3-phosphate_level","termid":"PBO:0030745"}


id: PR:Q9Y7T7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-dependent RNA helicase DDX23 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04476"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA-splicing ATP-dependent RNA helicase prp28 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC63.11","secondary_identifiers":["UniProtKB:Q9Y7T7"],"synonyms":[{"name":"Spom972h-DDX23","type":"exact"}],"termid":"PR:Q9Y7T7"}


id: FYECO:0000055
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Both M-factor and P-factor, endogenously produced by cells, were present in the experiment.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000055 M and P factor produced (obsolete FYECO:0000055)","synonyms":[{"name":"presence of M-factor and P-factor","type":"exact"},{"name":"presence of mating pheromones","type":"exact"}],"termid":"FYECO:0000055"}


id: MONDO:0024482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hamartoma characterized by localized eccrine sweat gland malformation.","definition_xrefs":["NCIT:C5564"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eccrine sweat gland neoplasm","termid":"MONDO:0002090"},{"relation_name":"is_a","term_name":"hamartoma of skin appendage","termid":"MONDO:0021539"}],"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":"eccrine sweat gland hamartoma","secondary_identifiers":["MEDGEN:232145","UMLS:C1333372"],"synonyms":[{"name":"eccrine sweat gland hamartoma","type":"exact"},{"name":"eccrine sweat gland hamartoma (disease)","type":"exact"},{"name":"hamartoma of eccrine sweat gland","type":"exact"},{"name":"hamartoma of the eccrine sweat gland","type":"exact"}],"termid":"MONDO:0024482","xrefs":{"Monarch":{"xref_id":"0024482"}}}


id: GO:0016209
data:
  {"annotated_genes":["SJAG_00668","SJAG_01292","SJAG_04823","SJAG_04953","SJAG_03623","SJAG_00141","SJAG_04125","SJAG_01199","SJAG_01162","SJAG_02630","SJAG_03653","SJAG_01734","SJAG_05181","SJAG_01216","SJAG_04632","SJAG_04788","SJAG_03166","SJAG_00489","SJAG_04399","SJAG_03303","SJAG_02515"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[101794],"is_not":false,"summary":null,"term":"GO:0016209"},{"annotations":[72685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004096"},{"annotations":[99734,68993,91178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004602"},{"annotations":[80787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004362"},{"annotations":[108609,81229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004601"},{"annotations":[64684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051920"},{"annotations":[78506],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032542"},{"annotations":[75895,78923,58389,66172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004784"},{"annotations":[110656,71924,81119,96981,77529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008379"},{"annotations":[74932,81322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004791"}]},"cv_name":"molecular_function","definition":"Inhibition of the reactions brought about by dioxygen (O2) or peroxides. Usually the antioxidant is effective because it can itself be more easily oxidized than the substance protected. The term is often applied to components that can trap free radicals, thereby breaking the chain reaction that normally leads to extensive biological damage.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00141":null,"SJAG_00489":null,"SJAG_00668":null,"SJAG_01162":null,"SJAG_01199":null,"SJAG_01216":null,"SJAG_01292":null,"SJAG_01734":null,"SJAG_02515":null,"SJAG_02630":null,"SJAG_03166":null,"SJAG_03303":null,"SJAG_03623":null,"SJAG_03653":null,"SJAG_04125":null,"SJAG_04399":null,"SJAG_04632":null,"SJAG_04788":null,"SJAG_04823":null,"SJAG_04953":null,"SJAG_05181":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"antioxidant activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0016209","terms_by_termid":{"GO:0004096":null,"GO:0004362":null,"GO:0004601":null,"GO:0004602":null,"GO:0004784":null,"GO:0004791":null,"GO:0008379":null,"GO:0016209":null,"GO:0032542":null,"GO:0051920":null}}


id: PBO:0049511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 18","termid":"PBO:0049511"}


id: PBO:0049514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 21","termid":"PBO:0049514"}


id: PBO:0061957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily A member 13 pseudogene","termid":"PBO:0061957"}


id: MOD:01790
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an an N-terminal L-tyrosine residue to tyrosine immonium ion.","definition_xrefs":["PubMed:18688235","PubMed:17074506"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"},{"relation_name":"is_a","term_name":"residue reporter fragment","termid":"MOD:01527"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine immonium ion","synonyms":[{"name":"2-(4-hydroxyphenyl)ethaniminium","type":"exact"}],"termid":"MOD:01790"}


id: PBO:0065791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"R3H domain and coiled-coil containing 1 like","termid":"PBO:0065791"}


id: FYPO:0004310
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle phenotype in which the duration of M phase of the mitotic cell cycle is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic cell cycle phase","termid":"FYPO:0002740"}],"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:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal duration of mitotic M phase","secondary_identifiers":["FYPO:0005632"],"synonyms":[{"name":"normal duration of M phase of mitotic cell cycle","type":"exact"},{"name":"normal duration of mitosis","type":"related"},{"name":"normal duration of mitosis during vegetative growth","type":"related"},{"name":"normal duration of mitotic division","type":"related"},{"name":"normal duration of mitotic nuclear division","type":"related"}],"termid":"FYPO:0004310"}


id: PBO:0050223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 1","termid":"PBO:0050223"}


id: PBO:0048760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"germ cell-less 1, spermatogenesis associated","termid":"PBO:0048760"}


id: PBO:0038670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA synthetase long chain family member 4","termid":"PBO:0038670"}


id: PATO:0000682
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000682 rate value (obsolete PATO:0000682)","termid":"PATO:0000682"}


id: GO:0033468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of CMP-keto-3-deoxy-D-manno-octulosonic acid, a substance composed of the acidic sugar 3-deoxy-D-manno-octulosonic acid in glycosidic linkage with cytidine monophosphate.","definition_xrefs":["MetaCyc:PWY-1269","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"CMP-keto-3-deoxy-D-manno-octulosonic acid metabolic process","termid":"GO:0033467"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid biosynthetic process","synonyms":[{"name":"CMP-KDO biosynthesis","type":"exact"},{"name":"CMP-KDO biosynthetic process","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid anabolism","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid biosynthesis","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid formation","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid synthesis","type":"exact"},{"name":"CMP-ketodeoxyoctanoate biosynthetic process","type":"related"}],"termid":"GO:0033468"}


id: MONDO:0001669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lung cancer (obsolete MONDO:0001669)","termid":"MONDO:0001669","xrefs":{"Monarch":{"xref_id":"0001669"}}}


id: MONDO:0011832
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the CCDC50 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 44","secondary_identifiers":["UMLS:C1843895","GARD:18118","MESH:C564399","DOID:0110569","MEDGEN:334525","OMIM:607453"],"synonyms":[{"name":"CCDC50 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"DFNA44","type":"narrow"},{"name":"autosomal dominant deafness 44","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 44","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in CCDC50","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 44","type":"narrow"},{"name":"deafness, autosomal dominant 44","type":"narrow"},{"name":"deafness, autosomal dominant type 44","type":"narrow"}],"termid":"MONDO:0011832","xrefs":{"Monarch":{"xref_id":"0011832"}}}


id: MONDO:0020245
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disease predisposing to age-related macular degeneration (obsolete MONDO:0020245)","secondary_identifiers":["Orphanet:98667"],"termid":"MONDO:0020245","xrefs":{"Monarch":{"xref_id":"0020245"}}}


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:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"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: PBO:0040044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin related protein 2/3 complex subunit 1A","termid":"PBO:0040044"}


id: GO:1900117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of execution phase of apoptosis.","definition_xrefs":["GOC:TermGenie","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"execution phase of apoptosis","termid":"GO:0097194"}],"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 execution phase of apoptosis","termid":"GO:1900117"}


id: GO:0070093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of glucagon.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucagon secretion","termid":"GO:0070092"},{"relation_name":"is_a","term_name":"negative regulation of peptide hormone secretion","termid":"GO:0090278"},{"relation_name":"negatively_regulates","term_name":"glucagon secretion","termid":"GO:0070091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"negative regulation of glucagon secretion","synonyms":[{"name":"down regulation of glucagon secretion","type":"exact"},{"name":"down-regulation of glucagon secretion","type":"exact"},{"name":"downregulation of glucagon secretion","type":"exact"},{"name":"inhibition of glucagon secretion","type":"narrow"}],"termid":"GO:0070093"}


id: PBO:0050751
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 13","termid":"PBO:0050751"}


id: GO:0043517
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the rate of the cascade of processes induced by the cell cycle regulator phosphoprotein p53, or an equivalent protein, in response to the detection of DNA damage.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA damage response, signal transduction by p53 class mediator","termid":"GO:0043516"},{"relation_name":"is_a","term_name":"positive regulation of signal transduction by p53 class mediator","termid":"GO:1901798"},{"relation_name":"positively_regulates","term_name":"DNA damage response, signal transduction by p53 class mediator","termid":"GO:0030330"}],"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 DNA damage response, signal transduction by p53 class mediator","synonyms":[{"name":"activation of DNA damage response, signal transduction by p53 class mediator","type":"narrow"},{"name":"positive regulation of p53 induced by DNA damage response","type":"exact"},{"name":"stimulation of DNA damage response, signal transduction by p53 class mediator","type":"narrow"},{"name":"up regulation of DNA damage response, signal transduction by p53 class mediator","type":"exact"},{"name":"up-regulation of DNA damage response, signal transduction by p53 class mediator","type":"exact"},{"name":"upregulation of DNA damage response, signal transduction by p53 class mediator","type":"exact"}],"termid":"GO:0043517"}


id: PATO:0001301
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An optical quality that is the mixture, purity or pattern of wavelengths of light perceived by the observer.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"optical quality","termid":"PATO:0001300"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromatic property","termid":"PATO:0001301"}


id: MONDO:0011363
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"type 2 diabetes mellitus","termid":"MONDO:0005148"},{"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:0004335"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005015","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"diabetes mellitus, noninsulin-dependent, 3","secondary_identifiers":["UMLS:C1863594","MESH:C566342","OMIM:603694","MEDGEN:400332"],"synonyms":[{"name":"NIDDM3","type":"related"},{"name":"diabetes mellitus, noninsulin-dependent, 3","type":"exact"},{"name":"diabetes mellitus, noninsulin-dependent, type 3","type":"exact"},{"name":"noninsulin-dependent diabetes mellitus 3","type":"related"},{"name":"type 2 diabetes mellitus 3","type":"exact"}],"termid":"MONDO:0011363","xrefs":{"Monarch":{"xref_id":"0011363"}}}


id: PBO:0070689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 60","termid":"PBO:0070689"}


id: MOD:00316
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to N4,N4-dimethyl-L-asparagine.","definition_xrefs":["Unimod:36#N","RESID:AA0311","PubMed:12964758","PubMed:14570711","PubMed:8783012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dimethylated residue","termid":"MOD:00429"},{"relation_name":"is_a","term_name":"N-methylated residue","termid":"MOD:00602"},{"relation_name":"is_a","term_name":"methylated asparagine","termid":"MOD:00673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"N4,N4-dimethyl-L-asparagine","synonyms":[{"name":"(2S)-2-amino-4-(dimethylamino)-4-oxobutanoic acid","type":"exact"},{"name":"2-amino-N4,N4-dimethylbutanediamic acid","type":"exact"},{"name":"Dimethyl","type":"related"},{"name":"MOD_RES N4,N4-dimethylasparagine","type":"exact"},{"name":"N(gamma),N(gamma)-dimethylasparagine","type":"exact"},{"name":"N4,N4-dimethyl-L-asparagine","type":"exact"},{"name":"N4,N4-dimethylated L-asparagine","type":"exact"},{"name":"N4Me2Asn","type":"exact"},{"name":"beta-dimethylasparagine","type":"related"},{"name":"di-Methylation","type":"related"}],"termid":"MOD:00316"}


id: PBO:0049616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 19","termid":"PBO:0049616"}


id: GO:0086019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from one cell to another and contributes to the heart process that regulates cardiac muscle contraction; beginning with the generation of an action potential in the sinoatrial node and ending with regulation of contraction of the myocardium.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling","termid":"GO:0007267"},{"relation_name":"is_a","term_name":"cell communication involved in cardiac conduction","termid":"GO:0086065"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"cell-cell signaling involved in cardiac conduction","synonyms":[{"name":"cell-cell signalling involved in cardiac conduction","type":"exact"}],"termid":"GO:0086019"}


id: PBO:0072490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 19","termid":"PBO:0072490"}


id: MONDO:0008853
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Barber Say syndrome (BSS) is a rare ectodermal dysplasia with neonatal onset characterized by congenital generalized hypertrichosis, atrophic skin, ectropion and microstomia.","definition_xrefs":["Orphanet:1231"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis of eyelid","termid":"MONDO:0001334"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"congenital entropion","termid":"MONDO:0020159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005093"],"is_obsolete":false,"name":"Barber-Say syndrome","secondary_identifiers":["OMIM:209885","NORD:875","icd11.foundation:37248895","SCTID:408537003","UMLS:C1319466","DOID:0060549","MESH:C537908","MEDGEN:230818","GARD:819"],"synonyms":[{"name":"BARBER-SAY syndrome","type":"related"},{"name":"BBRSAY","type":"related"},{"name":"Barber Say syndrome","type":"related"},{"name":"Barber-Say syndrome","type":"exact"},{"name":"Brown Séquard Syndrome","type":"exact"},{"name":"Bss","type":"related"},{"name":"hypertrichosis atrophic skin ectropion macrostomia","type":"related"},{"name":"hypertrichosis, atrophic skin, ectropion, and macrostomia","type":"related"},{"name":"hypertrichosis-atrophic skin-ectropion-macrostomia syndrome","type":"exact"}],"termid":"MONDO:0008853","xrefs":{"Monarch":{"xref_id":"0008853"}}}


id: PBO:0088103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Uridine/cytidine kinase; component of the pyrimidine ribonucleotide salvage pathway that converts uridine into UMP and cytidine into CMP; involved in the pyrimidine deoxyribonucleotide salvage pathway, converting deoxycytidine into dCMP","termid":"PBO:0088103"}


id: MOD:00443
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Covalent modification of a peptide or protein L-arginine residue to protonated omega-N,omega-N-dimethlyated L-arginine with secondary neutral loss of an N,N-dimethylamine molecular fragment.","definition_xrefs":["PubMed:15835918","PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue with a secondary neutral loss","termid":"MOD:00431"},{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protonated omega-N,omega-N-dimethlyated L-arginine with secondary neutral loss of N,N-dimethylamine","synonyms":[{"name":"dDMA-NoMe2+Arg","type":"exact"}],"termid":"MOD:00443"}


id: GO:0018308
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transient modification of lysine by pyruvate to form N6-pyruvic acid 2-iminyl-L-lysine, found in the active site of dihydrodipicolinate synthase.","definition_xrefs":["RESID:AA0287","PMID:1463470"],"gene_count":0,"genotype_count":0,"name":"obsolete enzyme active site formation via N6-pyruvic acid 2-iminyl-L-lysine (obsolete GO:0018308)","synonyms":[{"name":"enzyme active site formation via N6-pyruvic acid 2-iminyl-L-lysine","type":"exact"}],"termid":"GO:0018308"}


id: PBO:0065875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB28, member RAS oncogene family pseudogene 3","termid":"PBO:0065875"}


id: GO:0050910
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events involved in the perception of sound vibration in which the vibration is received and converted into a molecular signal.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system process","termid":"GO:0050877"},{"relation_name":"is_a","term_name":"detection of mechanical stimulus involved in sensory perception","termid":"GO:0050974"},{"relation_name":"part_of","term_name":"sensory perception of sound","termid":"GO:0007605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of mechanical stimulus involved in sensory perception of sound","secondary_identifiers":["GO:0009592","GO:0055128"],"synonyms":[{"name":"detection of sound","type":"exact"},{"name":"hearing, sensory transduction of sound","type":"exact"},{"name":"perception of sound, detection of mechanical stimulus","type":"exact"},{"name":"perception of sound, sensory detection of mechanical stimulus","type":"exact"},{"name":"perception of sound, sensory transduction of mechanical stimulus","type":"exact"},{"name":"sensory detection of mechanical stimulus during perception of sound","type":"exact"},{"name":"sensory transduction of mechanical stimulus during perception of sound","type":"exact"},{"name":"sensory transduction of sound","type":"exact"}],"termid":"GO:0050910"}


id: PR:Q9UU96
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- grc3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UU96"],"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":"polynucleotide 5'-hydroxyl-kinase grc3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC830.03","synonyms":[{"name":"Spom972h-grc3","type":"exact"}],"termid":"PR:Q9UU96"}


id: PBO:0082516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of the NatC type N-terminal acetyltransferase (NAT); involved in subcellular targeting of select N-terminally acetylated substrates to the Golgi apparatus (Arl3p and Grh1p) and the inner nuclear membrane (Trm1p); required for replication of dsRNA virus; human NatC ortholog, NAA30, functionally complements the null, requiring either auxiliary subunit Mak10p or co-expression of human ortholog, NAA35; NAA60, the human NatF gene, also complements the null allele","termid":"PBO:0082516"}


id: GO:0061394
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Modulation of the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of an arsenic stimulus from compounds containing arsenic, including arsenates, arsenites, and arsenides.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter in response to arsenic-containing substance (obsolete GO:0061394)","termid":"GO:0061394"}


id: MONDO:1012168
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lower motor neuron disease, non-human animal","termid":"MONDO:1011848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lower motor neuron disease, horse","secondary_identifiers":["OMIA:000662-9796"],"termid":"MONDO:1012168","xrefs":{"Monarch":{"xref_id":"1012168"}}}


id: PBO:0005685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol binding protein (predicted)","termid":"PBO:0005685"}


id: GO:0102796
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3,4-dihydroxybenzaldehyde + O2 + H2O = H+ + 3,4-dihydroxybenzoate + hydrogen peroxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete protocatechualdehyde:oxygen oxidoreductase activity (obsolete GO:0102796)","termid":"GO:0102796"}


id: MONDO:0001527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"strabismus","termid":"MONDO:0003432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conjugate gaze palsy","secondary_identifiers":["DOID:12445","MEDGEN:675273","ICD9:378.81","SCTID:1534008","UMLS:C0702143"],"synonyms":[{"name":"palsy of conjugate gaze","type":"exact"}],"termid":"MONDO:0001527","xrefs":{"Monarch":{"xref_id":"0001527"}}}


id: GO:0018195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of peptidyl-arginine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptidyl-arginine modification","termid":"GO:0018195"}


id: PBO:0074045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 27","termid":"PBO:0074045"}


id: FYPO:0000975
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the cellular response to mercury ions is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to chemical stimulus during vegetative growth","termid":"FYPO:0001318"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0000298"],"is_obsolete":false,"name":"normal cellular response to mercury ion","synonyms":[{"name":"normal cellular response to mercury","type":"exact"},{"name":"normal cellular response to mercury ion during mitotic cell cycle","type":"related"},{"name":"normal cellular response to mercury ion during vegetative growth","type":"exact"}],"termid":"FYPO:0000975"}


id: FYECO:0000138
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in rich medium containing glycerol as the sole carbon source, yeast extract and other components. The concentration of glycerol is typically around 2-3% and supplemented with trace amounts of another carbon source (e.g. glucose).","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping rich medium","termid":"FYECO:0000080"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol YE","secondary_identifiers":["FYECO:0000083"],"synonyms":[{"name":"glycerol rich medium","type":"broad"},{"name":"glycerol sole carbon source YE","type":"related"},{"name":"glycerol sole carbon source rich medium","type":"exact"},{"name":"non-fermentable glycerol sole carbon source rich medium","type":"exact"},{"name":"nonfermentable glycerol sole carbon source rich medium","type":"related"}],"termid":"FYECO:0000138"}


id: MONDO:0003745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spindle cell melanoma that involves the optic choroid.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle cell intraocular melanoma","termid":"MONDO:0003744"},{"relation_name":"is_a","term_name":"malignant choroid melanoma","termid":"MONDO:0003878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"choroid spindle cell melanoma","secondary_identifiers":["UMLS:C1333027","MEDGEN:272477","DOID:6041","NCIT:C6099"],"synonyms":[{"name":"optic choroid spindle cell melanoma","type":"exact"},{"name":"spindle cell melanoma of choroid","type":"exact"},{"name":"spindle cell melanoma of optic choroid","type":"exact"},{"name":"spindle cell melanoma of the choroid","type":"exact"}],"termid":"MONDO:0003745","xrefs":{"Monarch":{"xref_id":"0003745"}}}


id: GO:0042860
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving achromobactin, a citrate siderophore.","definition_xrefs":["GOC:jl","PMID:10928541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"siderophore metabolic process","termid":"GO:0009237"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"achromobactin metabolic process","synonyms":[{"name":"achromobactin metabolism","type":"exact"}],"termid":"GO:0042860"}


id: GO:0018776
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: trans-3-chloroacrylic acid + H2O = H+ + malonate semialdehyde.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete trans-chloroacrylic acid dehalogenase activity (obsolete GO:0018776)","termid":"GO:0018776"}


id: PBO:0017406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene characterisation status","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein, uncharacterized","termid":"PBO:0017406"}


id: PBO:0069388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 648, pseudogene","termid":"PBO:0069388"}


id: GO:0046311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of prenylcysteine, 3-methyl-2-buten-1-yl-cysteine, a derivative of the amino acid cysteine formed by the covalent addition of a prenyl residue.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenylcysteine metabolic process","termid":"GO:0030329"},{"relation_name":"is_a","term_name":"modified amino acid biosynthetic process","termid":"GO:0042398"}],"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":"prenylcysteine biosynthetic process","synonyms":[{"name":"prenylcysteine anabolism","type":"exact"},{"name":"prenylcysteine biosynthesis","type":"exact"},{"name":"prenylcysteine formation","type":"exact"},{"name":"prenylcysteine synthesis","type":"exact"}],"termid":"GO:0046311"}


id: PATO:0002265
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A behavioral quality of a process inhering in a bearer by virtue of the bearer's disposition to exhibit marked activity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavioral quality","termid":"PATO:0000186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"behavioural activity","termid":"PATO:0002265"}


id: PBO:0003057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenine deaminase Dea2","termid":"PBO:0003057"}


id: PBO:0043572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type VIII alpha 2 chain","termid":"PBO:0043572"}


id: PBO:0004820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-C","termid":"PBO:0004820"}


id: PBO:0069819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1105, pseudogene","termid":"PBO:0069819"}


id: MONDO:0004560
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hair follicle neoplasm","termid":"MONDO:0003413"}],"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":"follicular infundibulum tumor","secondary_identifiers":["MEDGEN:138031","DOID:8426","SCTID:254694002","NCIT:C4469","UMLS:C0346006","ICD9:239.2"],"synonyms":[{"name":"basal cell hamartoma with follicular differentiation","type":"exact"},{"name":"follicular infundibulum neoplasm","type":"exact"},{"name":"neoplasm of the follicular infundibulum","type":"exact"},{"name":"tumor of follicular infundibulum","type":"exact"},{"name":"tumor of the follicular infundibulum","type":"exact"},{"name":"tumour of follicular infundibulum","type":"exact"},{"name":"tumour of the follicular infundibulum","type":"exact"}],"termid":"MONDO:0004560","xrefs":{"Monarch":{"xref_id":"0004560"}}}


id: PBO:0074381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMG1 pseudogene 7","termid":"PBO:0074381"}


id: GO:0043211
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O = ADP + phosphate, to directly drive the transport of carbohydrates and their derivatives across a membrane.","definition_xrefs":["EC:7.5.2.-","GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transmembrane transporter activity","termid":"GO:0015144"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"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:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"ABC-type carbohydrate transporter activity","synonyms":[{"name":"ATP-dependent carbohydrate transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled carbohydrate transmembrane transporter activity","type":"broad"},{"name":"carbohydrate ABC transporter","type":"narrow"},{"name":"carbohydrate-transporting ATPase activity","type":"exact"}],"termid":"GO:0043211"}


id: GO:1903636
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein insertion into mitochondrial outer membrane.","definition_xrefs":["PMID:16374546","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitochondrion organization","termid":"GO:0010821"},{"relation_name":"is_a","term_name":"regulation of intracellular protein transport","termid":"GO:0033157"},{"relation_name":"is_a","term_name":"regulation of protein targeting to mitochondrion","termid":"GO:1903214"},{"relation_name":"is_a","term_name":"regulation of protein localization to membrane","termid":"GO:1905475"},{"relation_name":"regulates","term_name":"protein insertion into mitochondrial outer membrane","termid":"GO:0045040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007005"},{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006605"}],"interesting_parent_ids":["GO:0008150","GO:0006605","GO:0061024","GO:0007005","GO:0006810"],"is_obsolete":false,"name":"regulation of protein insertion into mitochondrial outer membrane","synonyms":[{"name":"regulation of mitochondrial outer membrane protein import","type":"exact"},{"name":"regulation of protein import into mitochondrial outer membrane","type":"exact"},{"name":"regulation of protein transport into mitochondrial outer membrane","type":"exact"}],"termid":"GO:1903636"}


id: PBO:0090869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (m5U54) methyltransferase Trm2","termid":"PBO:0090869"}


id: PBO:0005333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triosephosphate isomerase","termid":"PBO:0005333"}


id: GO:0065008
data:
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