# terms

id: PBO:0079848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unc-50 inner nuclear membrane RNA binding protein","termid":"PBO:0079848"}


id: PBO:0048728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycolipid transfer protein domain containing 2","termid":"PBO:0048728"}


id: PBO:0011122
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chromsome Segregation in Meiosis","termid":"PBO:0011122"}


id: GO:0042579
data:
  {"annotated_genes":["SJAG_03781","SJAG_03324","SJAG_03715","SJAG_00891","SJAG_05950","SJAG_02693","SJAG_03091","SJAG_01685","SJAG_00702","SJAG_03493","SJAG_04467","SJAG_02848","SJAG_02384","SJAG_04823","SJAG_02997","SJAG_04428","SJAG_03440","SJAG_02619","SJAG_03671","SJAG_04146","SJAG_01165","SJAG_03166","SJAG_02630","SJAG_01474","SJAG_00706","SJAG_04315","SJAG_02247","SJAG_00326","SJAG_00114","SJAG_02496","SJAG_00947","SJAG_04763","SJAG_04299"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104774,89947,111298,111281,114189,115203,117724],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005782"},{"annotations":[89939,98077,116698,116748,110690,102575,115204,89736,114343,114744,111299,104710,110842,94928,117609,100797,106155,96458],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0005778"},{"annotations":[99339,104582,97084,99452,102250,109077,113509,111300,96091,113375,116167,102576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005777"}]},"cv_name":"cellular_component","definition":"Cytoplasmic organelles, spherical or oval in shape, that are bounded by a single membrane and contain oxidative enzymes, especially those utilizing hydrogen peroxide (H2O2).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":33,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00326":null,"SJAG_00702":null,"SJAG_00706":null,"SJAG_00891":null,"SJAG_00947":null,"SJAG_01165":null,"SJAG_01474":null,"SJAG_01685":null,"SJAG_02247":null,"SJAG_02384":null,"SJAG_02496":null,"SJAG_02619":null,"SJAG_02630":null,"SJAG_02693":null,"SJAG_02848":null,"SJAG_02997":null,"SJAG_03091":null,"SJAG_03166":null,"SJAG_03324":null,"SJAG_03440":null,"SJAG_03493":null,"SJAG_03671":null,"SJAG_03715":null,"SJAG_03781":null,"SJAG_04146":null,"SJAG_04299":null,"SJAG_04315":null,"SJAG_04428":null,"SJAG_04467":null,"SJAG_04763":null,"SJAG_04823":null,"SJAG_05950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"microbody","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Microbody"],"termid":"GO:0042579","terms_by_termid":{"GO:0005777":null,"GO:0005778":null,"GO:0005782":null}}


id: GO:0097478
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any of the two layers of lipid molecules that constitute a membrane.","definition_xrefs":["GOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"membrane","termid":"GO:0016020"}],"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":"leaflet of membrane bilayer","synonyms":[{"name":"membrane leaflet","type":"exact"}],"termid":"GO:0097478"}


id: FYECO:0000224
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which histidine was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ his","synonyms":[{"name":"histidine added","type":"exact"}],"termid":"FYECO:0000224"}


id: GO:0036107
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate, a precursor of 4-amino-4-deoxy-L-arabinose (L-Ara4N).","definition_xrefs":["PMID:15695810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid metabolic process","termid":"GO:0006644"},{"relation_name":"is_a","term_name":"glycolipid metabolic process","termid":"GO:0006664"},{"relation_name":"is_a","term_name":"terpenoid metabolic process","termid":"GO:0006721"}],"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":"4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate metabolic process","synonyms":[{"name":"4-amino-4-deoxy-alpha-L-arabinose undecaprenyl phosphate metabolic process","type":"exact"},{"name":"undecaprenyl phosphate alpha-L-Ara4N metabolism","type":"exact"}],"termid":"GO:0036107"}


id: GO:0051715
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The killing by an organism of a cell in another organism by means of the rupture of cell membranes and the loss of cytoplasm.","definition_xrefs":["GOC:ai","PMID:22484288"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytolysis","termid":"GO:0019835"},{"relation_name":"is_a","term_name":"killing of cells of another organism","termid":"GO:0031640"}],"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":"cytolysis in another organism","secondary_identifiers":["GO:0001901","GO:0044649"],"synonyms":[{"name":"cytolysis in other organism","type":"exact"},{"name":"cytolysis of cells of another organism","type":"exact"},{"name":"envenomation resulting in cytolysis in another organism","type":"narrow"},{"name":"envenomation resulting in cytolysis in other organism","type":"narrow"}],"termid":"GO:0051715"}


id: GO:2000776
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any histone H4 acetylation that is involved in a response to DNA damage stimulus.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H4 acetylation involved in response to DNA damage stimulus (obsolete GO:2000776)","synonyms":[{"name":"histone H4 acetylation of DNA damage response","type":"exact"},{"name":"histone H4 acetylation of cellular DNA damage response","type":"exact"},{"name":"histone H4 acetylation of cellular response to DNA damage stimulus","type":"exact"},{"name":"histone H4 acetylation of response to DNA damage stimulus","type":"exact"},{"name":"histone H4 acetylation of response to genotoxic stress","type":"exact"}],"termid":"GO:2000776"}


id: PBO:0042573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDKN2A interacting protein N-terminal like pseudogene 2","termid":"PBO:0042573"}


id: GO:0070122
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of an isopeptide bond. An isopeptide bond is an amide linkage between a carboxyl group of one amino acid and an amino group of another amino acid in which at least one of these groups is not on the a-carbon of one of the amino acids (for example, the link between an epsilon-amino group of a lysine molecule to a carboxyl group on a second amino acid is an isopeptide bond).","definition_xrefs":["Wikipedia:Isopeptidase","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete isopeptidase activity (obsolete GO:0070122)","termid":"GO:0070122"}


id: PBO:0054332
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 1725","termid":"PBO:0054332"}


id: GO:1904459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of substance P secretion.","definition_xrefs":["PMID:11278900","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of peptide hormone secretion","termid":"GO:0090278"},{"relation_name":"is_a","term_name":"regulation of substance P secretion","termid":"GO:1904458"},{"relation_name":"negatively_regulates","term_name":"substance P secretion","termid":"GO:1990772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of substance P secretion","synonyms":[{"name":"down regulation of substance P secretion","type":"exact"},{"name":"down-regulation of substance P secretion","type":"exact"},{"name":"downregulation of substance P secretion","type":"exact"},{"name":"inhibition of substance P secretion","type":"narrow"}],"termid":"GO:1904459"}


id: GO:0003675
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete protein (obsolete GO:0003675)","synonyms":[{"name":"protein","type":"exact"}],"termid":"GO:0003675"}


id: PBO:0047918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, BrdU type, common, fra(10)(q21)","termid":"PBO:0047918"}


id: PBO:0030013
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_Calcofluor_White","termid":"PBO:0030013"}


id: PBO:0043161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell death inducing DFFA like effector a","termid":"PBO:0043161"}


id: PR:O42914
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- oga1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42914"],"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 C16A3.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16A3.08c","synonyms":[{"name":"Spom972h-oga1","type":"exact"}],"termid":"PR:O42914"}


id: PBO:0000803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COP9/signalosome complex subunit Csn4","termid":"PBO:0000803"}


id: PR:P50999
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A T-complex protein 1 subunit delta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02432","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-complex protein 1 subunit delta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC106.06","secondary_identifiers":["UniProtKB:P50999"],"synonyms":[{"name":"CCT-delta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CCT4","type":"exact"},{"name":"TCP-1-delta (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P50999"}


id: PBO:0011439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate-semialdehyde dehydrogenase [NAD(P)+] (predicted)","termid":"PBO:0011439"}


id: PBO:0060232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloid associated differentiation marker like 2","termid":"PBO:0060232"}


id: PBO:0085098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear pore-associated protein; component of TREX-2 complex (Sac3p-Thp1p-Sus1p-Cdc31p) involved in transcription elongation and mRNA export from the nucleus; involved in post-transcriptional tethering of active genes to the nuclear periphery and to non-nascent mRNP; contains a PAM domain implicated in protein-protein binding","termid":"PBO:0085098"}


id: PBO:0030880
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_component_organization_during_vegetative_growth","termid":"PBO:0030880"}


id: GO:0071201
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A voltage-gated potassium channel complex that contains the peptidase-related protein DPP6 associated with the channel via interaction with the Kv alpha subunit 4.3.","definition_xrefs":["PMID:15911355","PMID:12575952"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel complex","termid":"GO:0008076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"Kv4.3-DPP6 channel complex","secondary_identifiers":["CORUM:599"],"synonyms":[{"name":"Kv4.3-DPPX channel complex","type":"exact"}],"termid":"GO:0071201"}


id: PBO:0068592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 43, pseudogene","termid":"PBO:0068592"}


id: MONDO:0020054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete partial autosomal monosomy (obsolete MONDO:0020054)","secondary_identifiers":["icd11.foundation:343448541","ICD10CM:Q93.3","Orphanet:98142"],"synonyms":[{"name":"partial autosomal deletion","type":"exact"}],"termid":"MONDO:0020054","xrefs":{"Monarch":{"xref_id":"0020054"}}}


id: PBO:0003886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S9 (predicted)","termid":"PBO:0003886"}


id: PBO:0060747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B2","termid":"PBO:0060747"}


id: MONDO:0014867
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 43 is a rare autosomal dominant cerebellar ataxia type I disorder characterized by late adult-onset of slowly progressive cerebellar ataxia, typically presenting with balance and gait disturbances, in association with axonal peripheral neuropathy resulting in reduced/absent deep tendon reflexes and sensory impairment. Lower limb pain and amyotrophy may be present, as well as various cerebellar signs, including dysarthria, nystagmus, hypometric saccades and tremor.","definition_xrefs":["Orphanet:497764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia","termid":"MONDO:0020380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039","MONDO:0000426"],"is_obsolete":false,"name":"spinocerebellar ataxia 43","secondary_identifiers":["UMLS:C4310763","DOID:0111745","MEDGEN:934730","GARD:17917","OMIM:617018"],"synonyms":[{"name":"MME autosomal dominant cerebellar ataxia","type":"exact"},{"name":"SCA43","type":"exact"},{"name":"autosomal dominant cerebellar ataxia caused by mutation in MME","type":"exact"},{"name":"spinocerebellar ataxia 43","type":"exact"},{"name":"spinocerebellar ataxia 43; SCA43","type":"exact"},{"name":"spinocerebellar ataxia type 43","type":"exact"}],"termid":"MONDO:0014867","xrefs":{"Monarch":{"xref_id":"0014867"}}}


id: FYPO:0003287
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the meiotic cell cycle is arrested during the first meiotic interphase, before premeiotic DNA replication has taken place.","definition_xrefs":["GO:0051328","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormally arrested meiotic cell cycle","termid":"FYPO:0002224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal cell cycle arrest in meiotic interphase before premeiotic DNA replication","synonyms":[{"name":"abnormal cell cycle arrest in meiotic interphase preceding premeiotic DNA replication","type":"exact"},{"name":"abnormal meiotic cell cycle arrest in interphase before premeiotic DNA replication","type":"exact"}],"termid":"FYPO:0003287"}


id: GO:1901201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of extracellular matrix assembly.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"is_a","term_name":"regulation of extracellular matrix organization","termid":"GO:1903053"},{"relation_name":"regulates","term_name":"extracellular matrix assembly","termid":"GO:0085029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of extracellular matrix assembly","termid":"GO:1901201"}


id: PBO:0002688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sim4 and Mal2 associated (4 and 2 associated) protein 6","termid":"PBO:0002688"}


id: GO:0071243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arsenic stimulus from compounds containing arsenic, including arsenates, arsenites, and arsenides.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to arsenic-containing substance","termid":"GO:0046685"},{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to arsenic-containing substance","synonyms":[{"name":"cellular response to arsenic","type":"exact"}],"termid":"GO:0071243"}


id: MONDO:0009900
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polysyndactyly-cardiac malformation syndrome is characterized by polysyndactyly, hexadactyly (duplication of the first toe) and complex cardiac malformation (including atrial and ventricular septal defect, single ventricle, aortic dextroposition, or dilation of the right heart). It has been described in six patients from three unrelated families. Other manifestations were present in some patients (i.e. facial dysmorphism, hepatic cysts).","definition_xrefs":["Orphanet:2934"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polysyndactyly-cardiac malformation syndrome","secondary_identifiers":["SCTID:724066002","MEDGEN:337895","GARD:4428","MESH:C564875","OMIM:263630","UMLS:C1849719"],"synonyms":[{"name":"Bonneau syndrome","type":"exact"},{"name":"polysyndactyly cardiac malformation","type":"related"},{"name":"polysyndactyly with CARDIAC malformation","type":"related"}],"termid":"MONDO:0009900","xrefs":{"Monarch":{"xref_id":"0009900"}}}


id: MOD:00908
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that modifies a glycine residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by amino acid modified","termid":"MOD:01157"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified glycine residue","synonyms":[{"name":"ModGly","type":"exact"}],"termid":"MOD:00908"}


id: GO:1900701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of orcinol biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"orcinol biosynthetic process","termid":"GO:0046197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"regulation of orcinol biosynthetic process","synonyms":[{"name":"regulation of orcinol anabolism","type":"exact"},{"name":"regulation of orcinol biosynthesis","type":"exact"},{"name":"regulation of orcinol formation","type":"exact"},{"name":"regulation of orcinol synthesis","type":"exact"}],"termid":"GO:1900701"}


id: PR:O74341
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A T-complex protein 1 subunit gamma that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03080"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-complex protein 1 subunit gamma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1A4.08c","secondary_identifiers":["UniProtKB:O74341"],"synonyms":[{"name":"CCT-gamma (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CCT3","type":"exact"},{"name":"TCP-1-gamma (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74341"}


id: PBO:0056525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanocortin 2 receptor","termid":"PBO:0056525"}


id: GO:0048768
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Localized growth of a plant root hair tip by extension of the cell wall.","definition_xrefs":["GOC:ki","PMID:12468740","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell tip growth","termid":"GO:0009932"},{"relation_name":"part_of","term_name":"root hair elongation","termid":"GO:0048767"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"root hair cell tip growth","synonyms":[{"name":"root hair tip growth","type":"exact"}],"termid":"GO:0048768"}


id: PBO:0085095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear import receptor; mediates the nuclear localization of proteins involved in mRNA-nucleus export; promotes dissociation of mRNAs from the nucleus-cytoplasm mRNA shuttling protein Npl3p; required for retrograde import of mature tRNAs; relocalizes from cytoplasm to the nuclear periphery upon DNA replication stress","termid":"PBO:0085095"}


id: GO:0031145
data:
  {"annotated_genes":["SJAG_03037","SJAG_02186","SJAG_03809","SJAG_01956","SJAG_04853","SJAG_03858","SJAG_04520","SJAG_03561","SJAG_04661","SJAG_03350","SJAG_03048","SJAG_02651","SJAG_00146","SJAG_05236","SJAG_01679","SJAG_00666","SJAG_00071","SJAG_03351","SJAG_05329"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88201,88457,89855,91262,94667,96102,99102,99107,99628,100287,101326,101777,104340,105649,107064,111663,113710,114387],"is_not":false,"summary":null,"term":"GO:0031145"},{"annotations":[101850],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905785"},{"annotations":[88460],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905786"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a protein or peptide by hydrolysis of its peptide bonds, initiated by the covalent attachment of ubiquitin, with ubiquitin-protein ligation catalyzed by the anaphase-promoting complex, and mediated by the proteasome.","definition_xrefs":["GOC:mah","PMID:15380083","PMID:15840442"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome-mediated ubiquitin-dependent protein catabolic process","termid":"GO:0043161"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00146":null,"SJAG_00666":null,"SJAG_01679":null,"SJAG_01956":null,"SJAG_02186":null,"SJAG_02651":null,"SJAG_03037":null,"SJAG_03048":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03561":null,"SJAG_03809":null,"SJAG_03858":null,"SJAG_04520":null,"SJAG_04661":null,"SJAG_04853":null,"SJAG_05236":null,"SJAG_05329":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030163"},{"rel_name":"part_of","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030163","GO:0008150"],"is_obsolete":false,"name":"anaphase-promoting complex-dependent catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-174154","Reactome:R-HSA-174048","Reactome:R-HSA-174143","Reactome:R-HSA-174184","GO:0008054"],"synonyms":[{"name":"APC-dependent proteasomal ubiquitin-dependent protein catabolic process","type":"exact"},{"name":"APC-dependent proteasomal ubiquitin-dependent protein catabolism","type":"exact"},{"name":"anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein breakdown","type":"exact"},{"name":"anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process","type":"exact"},{"name":"anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolism","type":"exact"},{"name":"anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein degradation","type":"exact"},{"name":"cyclin breakdown","type":"narrow"},{"name":"cyclin catabolic process","type":"narrow"},{"name":"cyclin catabolism","type":"narrow"},{"name":"cyclin degradation","type":"narrow"},{"name":"degradation of cyclin","type":"narrow"},{"name":"negative regulation of cyclin-dependent protein serine/threonine kinase by cyclin degradation","type":"narrow"}],"termid":"GO:0031145","terms_by_termid":{"GO:0031145":null,"GO:1905785":null,"GO:1905786":null}}


id: PBO:0085630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in fluoride export; nearly identical to FEX1, and deletion of both proteins results in a large increase in fluoride sensitivity compared with the single mutant; contains two FEX domains connected by a linker; part of a widespread family of conserved fluoride export proteins","termid":"PBO:0085630"}


id: PBO:0108557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Esf1","termid":"PBO:0108557"}


id: PBO:0084492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiosis-specific protein essential for chromosome synapsis; involved in completion of nuclear divisions during meiosis; induced early in meiosis","termid":"PBO:0084492"}


id: MONDO:0022895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniosynostosis cleft lip palate arthrogryposis","secondary_identifiers":["GARD:1590"],"termid":"MONDO:0022895","xrefs":{"Monarch":{"xref_id":"0022895"}}}


id: PBO:0040671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B cell receptor associated protein 29","termid":"PBO:0040671"}


id: GO:0008479
data:
  {"annotated_genes":["SJAG_06284","SJAG_00683"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89192,95299],"is_not":false,"summary":null,"term":"GO:0008479"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: guanosine34 in tRNA + queuine = guanine + queuosine34 in tRNA.","definition_xrefs":["RHEA:16633"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00683":null,"SJAG_06284":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0140101"}],"interesting_parent_ids":["GO:0140101","GO:0140098","GO:0016740","GO:0003674","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"tRNA-guanosine(34) queuine transglycosylase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:2.4.2.64","Reactome:R-HSA-6782443","MetaCyc:QUEUOSINE-TRNA-RIBOSYLTRANSFERASE-RXN"],"synonyms":[{"name":"Q-insertase","type":"broad"},{"name":"TGT","type":"broad"},{"name":"eTGT","type":"exact"},{"name":"guanine insertion enzyme","type":"related"},{"name":"queuine tRNA-ribosyltransferase","type":"exact"},{"name":"queuine tRNA-ribosyltransferase activity","type":"broad"},{"name":"queuine(34) transfer ribonucleate ribosyltransferase","type":"exact"},{"name":"tRNA guanine transglycosylase","type":"broad"},{"name":"tRNA transglycosylase","type":"broad"},{"name":"tRNA-guanosine(34) queuine transglycosylase","type":"exact"}],"termid":"GO:0008479","terms_by_termid":{"GO:0008479":null}}


id: PBO:0030999
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_degradation_during_vegetative_growth","termid":"PBO:0030999"}


id: MONDO:0017595
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"B-cell non-Hodgkin lymphoma","termid":"MONDO:0015759"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"aggressive B-cell non-Hodgkin lymphoma","secondary_identifiers":["MEDGEN:1791561","NCIT:C178541","Orphanet:300846","UMLS:C5555120","GARD:21245"],"synonyms":[{"name":"aggressive B-cell NHL","type":"exact"}],"termid":"MONDO:0017595","xrefs":{"Monarch":{"xref_id":"0017595"}}}


id: MONDO:0003309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pleural cancer (obsolete MONDO:0003309)","termid":"MONDO:0003309","xrefs":{"Monarch":{"xref_id":"0003309"}}}


id: MONDO:1010327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Strabismus that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"strabismus, non-human animal","secondary_identifiers":["OMIA:000949"],"termid":"MONDO:1010327","xrefs":{"Monarch":{"xref_id":"1010327"}}}


id: GO:0071013
data:
  {"annotated_genes":["SJAG_05240","SJAG_00322","SJAG_03711","SJAG_01301","SJAG_02722","SJAG_00859","SJAG_03460","SJAG_02687","SJAG_05235","SJAG_01214","SJAG_00446","SJAG_02469","SJAG_02317","SJAG_00571","SJAG_04230","SJAG_00414","SJAG_04117","SJAG_00147","SJAG_02843","SJAG_04497","SJAG_02879","SJAG_00639","SJAG_01870","SJAG_04898","SJAG_05224","SJAG_02396","SJAG_16453","SJAG_02304","SJAG_00911","SJAG_00602","SJAG_02308","SJAG_03601","SJAG_04318","SJAG_04694","SJAG_01629","SJAG_02844","SJAG_02279","SJAG_00498","SJAG_00643","SJAG_01008"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[91868,92191,92268,92552,92872,94419,94669,94834,95094,97508,97943,102191,102500,103966,105333,106224,107105,107697,108317,108684,109510,109516,110068,110731,111155,111188,111230,112318,112539,112608,112898,114369,115841,116320,117266],"is_not":false,"summary":null,"term":"GO:0071013"},{"annotations":[105872,106012,96341,108223,116661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071007"}]},"cv_name":"cellular_component","definition":"A spliceosomal complex that contains three snRNPs, including U5, bound to a splicing intermediate in which the first catalytic cleavage of the 5' splice site has occurred. The precise subunit composition differs significantly from that of the catalytic step 1, or activated, spliceosome, and includes many proteins in addition to those found in the associated snRNPs.","definition_xrefs":["GOC:mah","ISBN:0879695897","ISBN:0879697393","GOC:ab","PMID:18322460","GOC:krc","PMID:19239890"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal complex","termid":"GO:0005681"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":40,"genes_by_uniquename":{"SJAG_00147":null,"SJAG_00322":null,"SJAG_00414":null,"SJAG_00446":null,"SJAG_00498":null,"SJAG_00571":null,"SJAG_00602":null,"SJAG_00639":null,"SJAG_00643":null,"SJAG_00859":null,"SJAG_00911":null,"SJAG_01008":null,"SJAG_01214":null,"SJAG_01301":null,"SJAG_01629":null,"SJAG_01870":null,"SJAG_02279":null,"SJAG_02304":null,"SJAG_02308":null,"SJAG_02317":null,"SJAG_02396":null,"SJAG_02469":null,"SJAG_02687":null,"SJAG_02722":null,"SJAG_02843":null,"SJAG_02844":null,"SJAG_02879":null,"SJAG_03460":null,"SJAG_03601":null,"SJAG_03711":null,"SJAG_04117":null,"SJAG_04230":null,"SJAG_04318":null,"SJAG_04497":null,"SJAG_04694":null,"SJAG_04898":null,"SJAG_05224":null,"SJAG_05235":null,"SJAG_05240":null,"SJAG_16453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"catalytic step 2 spliceosome","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mammalian spliceosomal complex C","type":"narrow"},{"name":"mammalian spliceosomal complex C1","type":"narrow"},{"name":"yeast spliceosomal complex A2-2","type":"narrow"}],"termid":"GO:0071013","terms_by_termid":{"GO:0071007":null,"GO:0071013":null}}


id: PBO:0028521
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K9_acetylation","termid":"PBO:0028521"}


id: GO:0032678
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-9 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-9 production","termid":"GO:0032638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-9 production","secondary_identifiers":["GO:0045417"],"synonyms":[{"name":"regulation of IL-9 production","type":"exact"},{"name":"regulation of interleukin-9 biosynthetic process","type":"narrow"}],"termid":"GO:0032678"}


id: PBO:0003088
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed during S phase","termid":"PBO:0003088"}


id: MONDO:0023258
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease due to glucose-6-phosphatase deficiency in which the cause of the disease is a mutation in the SLC37A4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease I","termid":"MONDO:0002413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"glycogen storage disease type 1 due to SLC37A4 mutation","secondary_identifiers":["NANDO:1200841","UMLS:C2931345","MESH:C536831","HGNC:4061","GARD:2501","MEDGEN:419390"],"synonyms":[{"name":"G6P translocase deficiency","type":"broad"},{"name":"SLC37A4 glycogen storage disease I","type":"exact"},{"name":"glucose-6-phosphate translocase deficiency","type":"exact"},{"name":"glycogen storage disease I caused by mutation in SLC37A4","type":"exact"}],"termid":"MONDO:0023258","xrefs":{"Monarch":{"xref_id":"0023258"}}}


id: PBO:0082034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory particle lid subcomplex component; role in Ub-dependent proteolysis and proteasome stability; involved in TREX-2 mediated mRNA export, and in the prevention of transcription-associated genome instability; ubiquitinated by Nedd4-like E3-ligase, Rsp5p; human ortholog DSS1, a BRCA1 binding protein implicated in cancer, complements the yeast null; drives trinucleotide repeat expansion; protein abundance increases in response to DNA replication stress","termid":"PBO:0082034"}


id: GO:0034417
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2R)-2,3-bisphosphoglycerate + H2O = (2R)-2-phosphoglycerate + phosphate.","definition_xrefs":["PMID:18413611","RHEA:27381","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016788","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"bisphosphoglycerate 3-phosphatase activity","secondary_identifiers":["KEGG_REACTION:R09532","EC:3.1.3.80","MetaCyc:RXN-11102"],"synonyms":[{"name":"2,3-bisphospho-D-glycerate 3-phosphohydrolase activity","type":"related"}],"termid":"GO:0034417"}


id: PBO:0003197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3 methyltransferase Clr4","termid":"PBO:0003197"}


id: PBO:0058440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5004","termid":"PBO:0058440"}


id: MONDO:0044346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An disease or disorder caused by infection with Echinococcus granulosus.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"echinococcosis","termid":"MONDO:0005738"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"echinococcus granulosus infectious disease","secondary_identifiers":["UMLS:C0152068","ICD9:122.4","SCTID:75006000","ICD9:122.3","MEDGEN:508866"],"synonyms":[{"name":"Echinococcus granulosus caused disease or disorder","type":"exact"},{"name":"Echinococcus granulosus disease or disorder","type":"exact"},{"name":"Echinococcus granulosus infectious disease","type":"exact"},{"name":"echinococcus granulosus infection","type":"exact"},{"name":"echinococcus granulosus infectious disease","type":"exact"},{"name":"unilocular hydatid disease","type":"related"}],"termid":"MONDO:0044346","xrefs":{"Monarch":{"xref_id":"0044346"}}}


id: MONDO:0014720
data:
  {"annotated_genes":["SJAG_02656"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007429"}]},"cv_name":"mondo","definition":"Autosomal dominant optic atrophy plus syndrome (ADOA plus) is a variant of autosomal dominant optic atrophy (ADOA) associating the typical optic atrophy with other extra-ocular manifestations such as sensorineural deafness, myopathy, chronic progressive external ophthalmoplegia, ataxia and peripheral neuropathy. More rarely, other manifestations have been associated with this condition, such as spastic paraplegia, multiple-sclerosis like illness.","definition_xrefs":["Orphanet:1215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant optic atrophy","termid":"MONDO:0020250"},{"relation_name":"is_a","term_name":"mitochondrial disease","termid":"MONDO:0044970"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02656":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005328","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant optic atrophy plus syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1149710475","GARD:5243","SCTID:715374003","DOID:0111340"],"synonyms":[{"name":"DOA+","type":"exact"},{"name":"Treft-Sanborn-Carey syndrome","type":"related"},{"name":"dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy","type":"related"},{"name":"optic atrophy - deafness- polyneuropathy - myopathy","type":"related"},{"name":"optic atrophy type 8","type":"exact"},{"name":"optic atrophy-deafness-polyneuropathy-myopathy syndrome","type":"exact"}],"termid":"MONDO:0014720","terms_by_termid":{"MONDO:0007429":null},"xrefs":{"Monarch":{"xref_id":"0014720"}}}


id: PBO:0003360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"farnesyl pyrophosphate synthetase","termid":"PBO:0003360"}


id: SO:0001283
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"2'-O-methylcytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"two_prime_O_methylcytidine","secondary_identifiers":["RNAMOD:022"],"synonyms":[{"name":"2'-O-methylcytidine","type":"exact"},{"name":"Cm","type":"exact"},{"name":"two prime O methylcytidine","type":"exact"}],"termid":"SO:0001283"}


id: PBO:0066426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arginine-glutamic acid dipeptide repeats pseudogene 1 Y-linked","termid":"PBO:0066426"}


id: GO:0034473
data:
  {"annotated_genes":["SJAG_04818","SJAG_04084","SJAG_04824"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103891,104736,117742],"is_not":false,"summary":null,"term":"GO:0034473"}]},"cv_name":"biological_process","definition":"Any process involved in forming the mature 3' end of a U1 snRNA molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA 3'-end processing","termid":"GO:0034472"}],"gene_count":3,"genes_by_uniquename":{"SJAG_04084":null,"SJAG_04818":null,"SJAG_04824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016073"}],"interesting_parent_ids":["GO:0010467","GO:0016073","GO:0008150"],"is_obsolete":false,"name":"U1 snRNA 3'-end processing","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"U1 snRNA 3' end processing","type":"exact"}],"termid":"GO:0034473","terms_by_termid":{"GO:0034473":null}}


id: GO:0038029
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An epidermal growth factor receptor signaling pathway in which the signal is transmitted via the MAPKKK cascade.","definition_xrefs":["GOC:bf","PMID:21167805","GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete epidermal growth factor receptor signaling pathway via MAPK cascade (obsolete GO:0038029)","synonyms":[{"name":"EGFR signaling pathway via MAPKKK cascade","type":"exact"},{"name":"EGFR signaling via MAPKKK cascade","type":"exact"},{"name":"EGFR/MAPK signaling","type":"exact"},{"name":"epidermal growth factor receptor signaling pathway via MAPKKK cascade","type":"exact"},{"name":"epidermal growth factor receptor signalling pathway via MAPKKK cascade","type":"exact"}],"termid":"GO:0038029"}


id: PBO:0077270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 11","termid":"PBO:0077270"}


id: PR:Q9USY0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug131 gene.","definition_xrefs":["UniProtKB:Q9USY0","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 131 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1861.06c","synonyms":[{"name":"Spom972h-mug131","type":"exact"}],"termid":"PR:Q9USY0"}


id: PBO:0091442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial conserved fungal protein Rrg8","termid":"PBO:0091442"}


id: GO:1903924
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to estradiol.","definition_xrefs":["GO_REF:0000067","GOC:TermGenie","PMID:9048584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid binding","termid":"GO:0005496"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"estradiol binding","termid":"GO:1903924"}


id: PBO:0053596
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 623","termid":"PBO:0053596"}


id: PBO:0034181
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-results_in_developmental_regression_of","termid":"PBO:0034181"}


id: MONDO:0021077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that contains a single or multiple cystic spaces. Examples include cystadenoma, mucinous cystadenocarcinoma, and serous cystadenocarcinoma.","definition_xrefs":["NCIT:C6784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystic neoplasm","secondary_identifiers":["UMLS:C1333190","MEDGEN:232404"],"synonyms":[{"name":"cystic neoplasm","type":"exact"},{"name":"cystic tumor","type":"exact"},{"name":"cystic tumour","type":"exact"}],"termid":"MONDO:0021077","xrefs":{"Monarch":{"xref_id":"0021077"}}}


id: MONDO:0008004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of mitral valve prolapse (disease) that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitral valve prolapse","termid":"MONDO:0004910"},{"relation_name":"is_a","term_name":"congenital mitral valve insufficiency and/or stenosis","termid":"MONDO:0019817"},{"relation_name":"is_a","term_name":"inherited mitral valve disease","termid":"MONDO:0042966"}],"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":"familial mitral valve prolapse","secondary_identifiers":["GARD:3687","UMLS:C0340364","OMIMPS:157700","Orphanet:741","MEDGEN:573696","SCTID:233858000"],"synonyms":[{"name":"MVP","type":"related"},{"name":"hereditary mitral valve prolapse (disease)","type":"exact"},{"name":"mitral valve prolapse, familial","type":"related"},{"name":"mitral valve prolapse, familial, autosomal dominant","type":"related"}],"termid":"MONDO:0008004","xrefs":{"Monarch":{"xref_id":"0008004"}}}


id: GO:0004483
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + m7G(5')pppR-RNA = S-adenosyl-L-homocysteine + m7G(5')pppRm-RNA. R may be guanosine or adenosine.","definition_xrefs":["EC:2.1.1.57"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"},{"relation_name":"is_a","term_name":"mRNA methyltransferase activity","termid":"GO:0008174"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0003674","GO:0016741","GO:0003824","GO:0016740","GO:0140098"],"is_obsolete":false,"name":"mRNA (nucleoside-2'-O-)-methyltransferase activity","secondary_identifiers":["Reactome:R-HSA-9684030","Reactome:R-HSA-9684032","MetaCyc:2.1.1.57-RXN","Reactome:R-HSA-9694499","Reactome:R-HSA-9694721","Reactome:R-HSA-9834003","Reactome:R-HSA-9684033","Reactome:R-HSA-9694521"],"synonyms":[{"name":"S-adenosyl-L-methionine:mRNA (nucleoside-2'-O-)-methyltransferase activity","type":"related"},{"name":"mRNA (adenosine-2'-O-)-methyltransferase activity","type":"related"},{"name":"messenger RNA (nucleoside-2'-)-methyltransferase activity","type":"related"},{"name":"messenger ribonucleate nucleoside 2'-methyltransferase activity","type":"related"}],"termid":"GO:0004483"}


id: GO:0015735
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which uronic acid is transported across a lipid bilayer, from one side of a membrane to the other.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transport","termid":"GO:0015718"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"uronic acid transmembrane transport","synonyms":[{"name":"uronic acid transport","type":"related"}],"termid":"GO:0015735"}


id: GO:0075174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism modulates the frequency, rate or extent of its cAMP-mediated signal transduction as a result of detecting molecules of its host organism. 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 regulation of cAMP-mediated signaling in response to host (obsolete GO:0075174)","synonyms":[{"name":"regulation of cAMP-mediated signal transduction in response to host","type":"exact"},{"name":"regulation of cAMP-mediated signalling in response to host","type":"exact"},{"name":"regulation of symbiont cAMP-mediated signal transduction in response to host","type":"exact"}],"termid":"GO:0075174"}


id: PBO:0066901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 202","termid":"PBO:0066901"}


id: PBO:0074090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC26A5 antisense RNA 1","termid":"PBO:0074090"}


id: GO:2000026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of multicellular organismal development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"multicellular organism development","termid":"GO:0007275"}],"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 multicellular organismal development","termid":"GO:2000026"}


id: PBO:0078256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 30","termid":"PBO:0078256"}


id: PBO:0084716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane m-AAA protease component; mediates degradation of misfolded or unassembled proteins; also required for correct assembly of mitochondrial enzyme complexes; overexpression of human AFG3L2 complements respiratory defect of yeast afg3 yta12 double null mutation, but overexpression of disease-associated AFG3L2 variants does not; expression of both human SPG7 (paraplegin) and AFG3L2 complements yeast yta12 afg3 double mutation","termid":"PBO:0084716"}


id: MONDO:0012164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Meacham syndrome is a multiple malformation syndrome characterized by congenital diaphragmatic abnormalities, genital defects and cardiac malformations.","definition_xrefs":["Orphanet:3097"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meacham syndrome","secondary_identifiers":["MEDGEN:373234","MESH:C538162","OMIM:608978","GARD:3432","icd11.foundation:1307620543","UMLS:C1837026","SCTID:722461004"],"synonyms":[{"name":"Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype","type":"related"},{"name":"Meacham Winn Culler syndrome","type":"related"},{"name":"Meacham syndrome","type":"exact"},{"name":"Meacham-Winn-Culler syndrome","type":"exact"},{"name":"Rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome","type":"exact"}],"termid":"MONDO:0012164","xrefs":{"Monarch":{"xref_id":"0012164"}}}


id: PR:O59768
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A calcium/proton antiporter that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04535","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":"vacuolar calcium ion transporter (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1795.02c","secondary_identifiers":["UniProtKB:O59768"],"synonyms":[{"name":"Spom972h-chaA","type":"exact"},{"name":"vacuolar Ca(2+)/H(+) exchanger (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O59768"}


id: PATO:0001801
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A composition quality inhering in an bearer by virtue of the reduction in amount of water the bearer contains.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Dehydrated"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"water composition","termid":"PATO:0001800"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased water composition","synonyms":[{"name":"dehydrated","type":"exact"},{"name":"dry","type":"related"}],"termid":"PATO:0001801"}


id: GO:0097019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of neurotransmitter receptors.","definition_xrefs":["GOC:kmv"],"gene_count":0,"genotype_count":0,"name":"obsolete neurotransmitter receptor catabolic process (obsolete GO:0097019)","synonyms":[{"name":"neurotransmitter receptor breakdown","type":"exact"},{"name":"neurotransmitter receptor catabolism","type":"exact"},{"name":"neurotransmitter receptor degradation","type":"exact"}],"termid":"GO:0097019"}


id: GO:0035216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Progression of the haltere imaginal disc over time, from its initial formation through to its metamorphosis to form the adult capitellum, pedicel, haltere sclerite, metathoracic spiracle and metanotum.","definition_xrefs":["GOC:bf","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc development","termid":"GO:0007444"}],"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":"haltere disc development","termid":"GO:0035216"}


id: GO:0052791
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2-keto-3-deoxynononic acid)n + H2O = (2-keto-3-deoxynononic acid)n-1 + 2-keto-3-deoxynononic acid. This reaction is the hydrolysis of a 2-keto-3-deoxynononic acid residue from a poly-2-keto-3-deoxynononic acid chain.","definition_xrefs":["GOC:mengo_curators","PMID:21247893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-sialidase activity","termid":"GO:0016997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"3-deoxy-D-glycero-D-galacto-2-nonulosonic acid hydrolase activity","synonyms":[{"name":"2-keto-3-deoxynononic acid sialidase activity","type":"exact"}],"termid":"GO:0052791"}


id: PBO:0069576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 849, pseudogene","termid":"PBO:0069576"}


id: GO:0034264
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the cytokinin 6-isopentenyladenine.","definition_xrefs":["GOC:mah","PMID:18216168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokinin metabolic process","termid":"GO:0009690"},{"relation_name":"is_a","term_name":"purine-containing compound metabolic process","termid":"GO:0072521"}],"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":"isopentenyl adenine metabolic process","synonyms":[{"name":"isopentenyl adenine metabolism","type":"exact"},{"name":"isopentenyladenine metabolic process","type":"exact"}],"termid":"GO:0034264"}


id: PBO:0059151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGUK p55 scaffold protein 3","termid":"PBO:0059151"}


id: PBO:0044890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEP domain containing 1 pseudogene 1","termid":"PBO:0044890"}


id: FYPO:0008010
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of RNA-dependent RNA polymerase activity is decreased.","definition_xrefs":["PMID:15615848","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000707"],"is_obsolete":false,"name":"decreased RNA-dependent RNA polymerase","termid":"FYPO:0008010"}


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


id: PATO:0001800
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A composition quality inhering in an bearer by virtue of the quantities or relative ratios of water of the inhering entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"composition","termid":"PATO:0000025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"water composition","termid":"PATO:0001800"}


id: PBO:0074961
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 114-3","termid":"PBO:0074961"}


id: PBO:0045802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EDNRB antisense RNA 1","termid":"PBO:0045802"}


id: PBO:0109813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane protein Mdm31, mitochondrion inheritance factor, interacts with ERMES","termid":"PBO:0109813"}


id: MONDO:0015192
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete unclassified intestinal pseudoobstruction (obsolete MONDO:0015192)","secondary_identifiers":["Orphanet:104078"],"termid":"MONDO:0015192","xrefs":{"Monarch":{"xref_id":"0015192"}}}


id: MONDO:0020188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital absence of the eyebrow/eyelashes (obsolete MONDO:0020188)","secondary_identifiers":["Orphanet:98598"],"termid":"MONDO:0020188","xrefs":{"Monarch":{"xref_id":"0020188"}}}


id: MONDO:0100170
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing restless legs syndrome.","definition_xrefs":["MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restless legs syndrome, susceptibility to","secondary_identifiers":["OMIMPS:102300"],"termid":"MONDO:0100170","xrefs":{"Monarch":{"xref_id":"0100170"}}}


id: PBO:0065176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prominin 2","termid":"PBO:0065176"}


id: GO:0045692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of embryo sac central cell differentiation.","definition_xrefs":["GOC:go_curators","GOC:mtg_plant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"regulation of embryo sac central cell differentiation","termid":"GO:0045691"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"embryo sac central cell differentiation","termid":"GO:0009559"}],"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 embryo sac central cell differentiation","synonyms":[{"name":"down regulation of female gametophyte central cell differentiation","type":"exact"},{"name":"down-regulation of female gametophyte central cell differentiation","type":"exact"},{"name":"downregulation of female gametophyte central cell differentiation","type":"exact"},{"name":"inhibition of female gametophyte central cell differentiation","type":"narrow"},{"name":"negative regulation of female gametophyte central cell differentiation","type":"exact"}],"termid":"GO:0045692"}


id: PBO:0059752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 26","termid":"PBO:0059752"}


id: PBO:0062009
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 J member 3","termid":"PBO:0062009"}


id: PBO:0083157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; almost completely overlaps ORF YNL227C/JJJ1","termid":"PBO:0083157"}


id: FYPO:0002908
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription occurs to a greater extent than normal in telomeric regions. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"},{"relation_name":"is_a","term_name":"abnormal transcription at telomere","termid":"FYPO:0007420"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000294","FYPO:0005447","FYPO:0000002","FYPO:0006551","FYPO:0001320"],"is_obsolete":false,"name":"increased transcription at telomere during vegetative growth","synonyms":[{"name":"increased telomeric transcription during vegetative growth","type":"exact"},{"name":"increased transcription at telomere during mitotic cell cycle","type":"related"},{"name":"increased transcription from telomere during vegetative growth","type":"exact"}],"termid":"FYPO:0002908"}


id: GO:0033673
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of kinase activity, the catalysis of the transfer of a phosphate group, usually from ATP, to a substrate molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of phosphorylation","termid":"GO:0042326"},{"relation_name":"is_a","term_name":"regulation of kinase activity","termid":"GO:0043549"},{"relation_name":"is_a","term_name":"negative regulation of transferase activity","termid":"GO:0051348"}],"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 kinase activity","synonyms":[{"name":"down regulation of kinase activity","type":"exact"},{"name":"down-regulation of kinase activity","type":"exact"},{"name":"downregulation of kinase activity","type":"exact"},{"name":"inhibition of kinase activity","type":"narrow"},{"name":"kinase inhibitor","type":"narrow"}],"termid":"GO:0033673"}


id: PBO:0038347
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-creates_habitat_for","termid":"PBO:0038347"}


id: PATO:0000571
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000571 absolute length value (obsolete PATO:0000571)","termid":"PATO:0000571"}


id: MONDO:0014718
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC12A5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant migrating partial seizures of infancy","termid":"MONDO:0017385"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 34","secondary_identifiers":["MEDGEN:899149","DOID:0080460","OMIM:616645","UMLS:C4225257","GARD:16147"],"synonyms":[{"name":"DEE34","type":"exact"},{"name":"EIEE34","type":"exact"},{"name":"SLC12A5 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 34","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in SLC12A5","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 34","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 34; EIEE34","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 34","type":"exact"}],"termid":"MONDO:0014718","xrefs":{"Monarch":{"xref_id":"0014718"}}}


id: GO:0032635
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-6 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"interleukin-6 production","secondary_identifiers":["GO:0042226","GO:0072604"],"synonyms":[{"name":"IL-6 production","type":"exact"},{"name":"interleukin-6 biosynthetic process","type":"narrow"},{"name":"interleukin-6 secretion","type":"narrow"}],"termid":"GO:0032635"}


id: GO:0060714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of the labyrinthine layer of the placenta.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"labyrinthine layer morphogenesis","termid":"GO:0060713"}],"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":"labyrinthine layer formation","termid":"GO:0060714"}


id: PBO:0057141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 219b","termid":"PBO:0057141"}


id: MONDO:0008307
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":"presenile dementia, Kraepelin type","secondary_identifiers":["UMLS:C1867772","MEDGEN:356847","MESH:C535273","OMIM:176600"],"synonyms":[{"name":"Kraepelin disease","type":"related"},{"name":"catatonia of Kraepelin","type":"related"},{"name":"presenile dementia, Kraepelin type","type":"exact"}],"termid":"MONDO:0008307","xrefs":{"Monarch":{"xref_id":"0008307"}}}


id: PBO:0057117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR202 host gene","termid":"PBO:0057117"}


id: PBO:0060792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase core subunit S3","termid":"PBO:0060792"}


id: MONDO:1010979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hydranencephaly that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydranencephaly, non-human animal","termid":"MONDO:1010232"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydranencephaly, dog","secondary_identifiers":["OMIA:000486-9615"],"termid":"MONDO:1010979","xrefs":{"Monarch":{"xref_id":"1010979"}}}


id: MONDO:0021187
data:
  {"annotated_genes":["SJAG_01072","SJAG_04785","SJAG_02432"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86034,86033,86035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011369"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01072":null,"SJAG_02432":null,"SJAG_04785":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hyperlipidemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D006949","ICD10CM:E78.5","HP:0003077","ICD9:272.4","SCTID:55822004","UMLS:C0020473","MEDGEN:5692"],"synonyms":[{"name":"hyperlipemia","type":"related"},{"name":"hyperlipemias","type":"related"},{"name":"hyperlipidemia","type":"exact"},{"name":"hyperlipidemia (disease)","type":"exact"},{"name":"lipemia","type":"related"},{"name":"lipemias","type":"related"},{"name":"lipidemia","type":"related"},{"name":"lipidemias","type":"related"}],"termid":"MONDO:0021187","terms_by_termid":{"MONDO:0011369":null},"xrefs":{"Monarch":{"xref_id":"0021187"}}}


id: PBO:0080279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 42 pseudogene","termid":"PBO:0080279"}


id: PBO:0058883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10399","termid":"PBO:0058883"}


id: GO:0039699
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An innate immune response evasion mechanism in which a symbiont methylates the 2'-O-ribose of the first or second transcribed nucleotide of its mRNAs. Methylation allows evasion of the host innate immune response, which degrades cap0 (non-methylated) mRNAs. This mechanism of immune evasion is used by viruses.","definition_xrefs":["PMID:35215972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated evasion of recognition by host innate immune effector","termid":"GO:0141177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated evasion of mRNA degradation by host via mRNA cap methylation","synonyms":[{"name":"IFIT mRNA restriction evasion by virus","type":"exact"},{"name":"evasion of mRNA degradation by host via mRNA cap methylation","type":"exact"},{"name":"viral mRNA cap methylation","type":"related"}],"termid":"GO:0039699"}


id: PBO:0057090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 186","termid":"PBO:0057090"}


id: MOD:00277
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to 5-methyl-L-arginine.","definition_xrefs":["PubMed:9367957","RESID:AA0272","PubMed:11875433","PubMed:10660523"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monomethylated L-arginine","termid":"MOD:00414"},{"relation_name":"is_a","term_name":"C-methylated residue","termid":"MOD:00656"}],"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":"5-methyl-L-arginine","synonyms":[{"name":"(2S,5S)-2-amino-5-carbamimidamidohexanoic acid","type":"exact"},{"name":"2-amino-5-guanidinohexanoic acid","type":"exact"},{"name":"4-methylarginine","type":"related"},{"name":"5-methyl-L-arginine","type":"exact"},{"name":"5-methylated L-arginine","type":"exact"},{"name":"C5Me1Arg","type":"exact"},{"name":"MOD_RES 5-methylarginine","type":"exact"},{"name":"Methyl","type":"related"},{"name":"Methylation","type":"related"},{"name":"delta-methylarginine","type":"exact"}],"termid":"MOD:00277"}


id: MONDO:0013855
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":"influenza, severe, susceptibility to","secondary_identifiers":["MEDGEN:766376","UMLS:C3553462","OMIM:614680"],"synonyms":[{"name":"influenza, severe, susceptibility to","type":"exact"},{"name":"susceptibility to severe influenza","type":"related"}],"termid":"MONDO:0013855","xrefs":{"Monarch":{"xref_id":"0013855"}}}


id: FYPO:0004732
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 cells contain fewer astral microtubules than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubules present in decreased numbers","termid":"FYPO:0003430"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0002399","FYPO:0005447","FYPO:0000054","FYPO:0001320"],"is_obsolete":false,"name":"astral microtubules present in decreased numbers","synonyms":[{"name":"astral microtubules present in decreased numbers during mitotic cell cycle","type":"related"},{"name":"astral microtubules present in decreased numbers during vegetative growth","type":"exact"},{"name":"astral microtubules present in reduced numbers","type":"exact"},{"name":"decreased level of astral microtubules","type":"exact"},{"name":"reduced number of astral microtubules","type":"exact"}],"termid":"FYPO:0004732"}


id: PBO:0087776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit Va of cytochrome c oxidase; cytochrome c oxidase is the terminal member of the mitochondrial inner membrane electron transport chain; Cox5Ap is predominantly expressed during aerobic growth while its isoform Vb (Cox5Bp) is expressed during anaerobic growth; COX5A has a paralog, COX5B, that arose from the whole genome duplication","termid":"PBO:0087776"}


id: GO:0006711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of estrogens, C18 steroid hormones that can stimulate the development of female sexual characteristics. Also found in plants.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid catabolic process","termid":"GO:0006706"},{"relation_name":"is_a","term_name":"estrogen metabolic process","termid":"GO:0008210"},{"relation_name":"is_a","term_name":"hormone catabolic process","termid":"GO:0042447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"estrogen catabolic process","synonyms":[{"name":"estrogen breakdown","type":"exact"},{"name":"estrogen catabolism","type":"exact"},{"name":"estrogen degradation","type":"exact"},{"name":"oestrogen catabolic process","type":"exact"},{"name":"oestrogen catabolism","type":"exact"}],"termid":"GO:0006711"}


id: GO:0006805
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a xenobiotic compound, a compound foreign to the organism exposed to it. It may be synthesized by another organism (like ampicilin) or it can be a synthetic chemical.","definition_xrefs":["GOC:krc","GOC:cab2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"},{"relation_name":"part_of","term_name":"cellular response to xenobiotic stimulus","termid":"GO:0071466"}],"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":"xenobiotic metabolic process","secondary_identifiers":["Reactome:R-HSA-9748784","GO:0017144","Reactome:R-HSA-2161541","Reactome:R-HSA-211859","Wikipedia:Drug_metabolism","Wikipedia:Xenobiotic_metabolism","Reactome:R-HSA-211981"],"synonyms":[{"name":"drug metabolic process","type":"related"},{"name":"drug metabolism","type":"related"},{"name":"xenobiotic metabolism","type":"exact"}],"termid":"GO:0006805"}


id: FYPO:0002768
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of ubiquitination of one or more specific proteins, or of specific protein sites, is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein ubiquitination during vegetative growth","termid":"FYPO:0000905"},{"relation_name":"is_a","term_name":"decreased protein ubiquitination","termid":"FYPO:0007946"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002494","FYPO:0002274","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein ubiquitination during vegetative growth","synonyms":[{"name":"decreased protein ubiquitination during mitotic cell cycle","type":"related"},{"name":"decreased protein ubiquitinylation during vegetative growth","type":"exact"},{"name":"decreased protein ubiquitylation during vegetative growth","type":"exact"},{"name":"reduced protein ubiquitination during vegetative growth","type":"exact"}],"termid":"FYPO:0002768"}


id: GO:0016935
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that forms a transmembrane channel through which chloride ions may pass in response to glycine binding to the channel complex or one of its constituent parts.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chloride channel complex","termid":"GO:0034707"},{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"glycine-gated chloride channel complex","termid":"GO:0016935"}


id: FYPO:0004512
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to EGTA. Cells stop growing (and may die) at a concentration of EGTA that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0002683","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to EGTA","synonyms":[{"name":"hypersensitive to EGTA","type":"exact"},{"name":"sensitive to EGTA during mitotic cell cycle","type":"related"},{"name":"sensitive to EGTA during vegetative growth","type":"exact"},{"name":"sensitive to ethylene glycol bis(2-aminoethyl)tetraacetic acid","type":"exact"}],"termid":"FYPO:0004512"}


id: PR:P0CH06
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubi1 gene.","definition_xrefs":["PRO:DAN","UniProtKB:P0CH06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-60S ribosomal protein L40-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11G7.04","synonyms":[{"name":"SPAC11G7.04","type":"related"},{"name":"Spom972h-ubi1","type":"exact"}],"termid":"PR:P0CH06"}


id: PBO:0044262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X-C motif chemokine ligand 1","termid":"PBO:0044262"}


id: PBO:0071338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L28 pseudogene 2","termid":"PBO:0071338"}


id: MONDO:1010343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetic cataract that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cataract, non-human animal","termid":"MONDO:1012962"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetic cataract, non-human animal","secondary_identifiers":["OMIA:001865"],"termid":"MONDO:1010343","xrefs":{"Monarch":{"xref_id":"1010343"}}}


id: GO:0044748
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the sequential cleavage of mononucleotides from a free 3' terminus of an RNA molecule that contributes to forming distinct miRNA isoforms from a mature miRNA.","definition_xrefs":["GOC:sart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3'-5'-RNA exonuclease activity","termid":"GO:0000175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0004527"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0140098","GO:0016787","GO:0004527","GO:0003674","GO:0003824","GO:0016788"],"is_obsolete":false,"name":"3'-5'-exoribonuclease activity involved in mature miRNA 3'-end processing","synonyms":[{"name":"exonucleolytic trimming to generate 3' end of miRNA","type":"broad"}],"termid":"GO:0044748"}


id: PBO:0002317
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"previusly annotated as dubious","termid":"PBO:0002317"}


id: MONDO:0044230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epiblepharon of upper 51d (obsolete MONDO:0044230)","secondary_identifiers":["OMIM:131460"],"synonyms":[{"name":"epiblepharon of upper lid","type":"related"}],"termid":"MONDO:0044230","xrefs":{"Monarch":{"xref_id":"0044230"}}}


id: GO:0002875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of a chronic inflammatory response to an antigenic stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of chronic inflammatory response","termid":"GO:0002677"},{"relation_name":"is_a","term_name":"negative regulation of inflammatory response to antigenic stimulus","termid":"GO:0002862"},{"relation_name":"is_a","term_name":"regulation of chronic inflammatory response to antigenic stimulus","termid":"GO:0002874"},{"relation_name":"negatively_regulates","term_name":"chronic inflammatory response to antigenic stimulus","termid":"GO:0002439"}],"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 chronic inflammatory response to antigenic stimulus","synonyms":[{"name":"down regulation of chronic inflammatory response to antigenic stimulus","type":"exact"},{"name":"down-regulation of chronic inflammatory response to antigenic stimulus","type":"exact"},{"name":"downregulation of chronic inflammatory response to antigenic stimulus","type":"exact"},{"name":"inhibition of chronic inflammatory response to antigenic stimulus","type":"narrow"}],"termid":"GO:0002875"}


id: MONDO:0009664
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A prenatal onset growth disorder with multiorgan manifestations.","definition_xrefs":["Orphanet:2576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"disorder of defective peroxisome oxidative status","termid":"MONDO:0100306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0019053","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"mulibrey nanism","secondary_identifiers":["DOID:0050436","MEDGEN:99347","ICD9:759.89","NCIT:C84906","OMIM:253250","SCTID:81604003","GARD:95","UMLS:C0524582","NORD:1465","icd11.foundation:1167260635","MESH:D050336"],"synonyms":[{"name":"MUL","type":"exact"},{"name":"Perheentupa syndrome","type":"exact"},{"name":"mulibrey dwarfism","type":"exact"},{"name":"mulibrey nanism","type":"exact"},{"name":"muscle-liver-brain-eye nanism","type":"exact"},{"name":"pericardial constriction and Growth failure","type":"related"},{"name":"pericardial constriction and growth failure","type":"exact"},{"name":"pericardial constriction-growth failure syndrome","type":"exact"}],"termid":"MONDO:0009664","xrefs":{"Monarch":{"xref_id":"0009664"}}}


id: PBO:0041663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel auxiliary subunit gamma 8","termid":"PBO:0041663"}


id: GO:0044053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of peptides or proteins produced by a symbiont organism to a location within the host cell cytoplasm.","definition_xrefs":["MITRE:tk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translocation of peptides or proteins into host","termid":"GO:0042000"}],"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":"translocation of peptides or proteins into host cell cytoplasm","synonyms":[{"name":"translocation of symbiont peptides or proteins into host cell cytoplasm","type":"exact"},{"name":"transport of peptides or proteins into host cell cytoplasm","type":"exact"}],"termid":"GO:0044053"}


id: GO:0052407
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism involving carbohydrates within a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete metabolism by organism of carbohydrate in other organism involved in symbiotic interaction (obsolete GO:0052407)","synonyms":[{"name":"metabolism by organism of carbohydrate in other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052407"}


id: FYPO:0007253
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which binding to a lipid in a membrane by a gene product does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished lipid binding","termid":"FYPO:0006937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000652"],"is_obsolete":false,"name":"abolished membrane lipid binding","synonyms":[{"name":"abolished binding to lipid in membrane","type":"exact"},{"name":"membrane lipid binding abolished","type":"exact"}],"termid":"FYPO:0007253"}


id: GO:0009559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the two uncellularized polar nuclei cellularize, fuse and acquire the specialized features of a mononucleate diploid central cell.","definition_xrefs":["GOC:mtg_plant","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"megagametogenesis","termid":"GO:0009561"}],"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":"embryo sac central cell differentiation","synonyms":[{"name":"embryo sac endosperm mother cell differentiation","type":"exact"},{"name":"female gametophyte central cell differentiation","type":"exact"}],"termid":"GO:0009559"}


id: MONDO:0004813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pneumothorax in which air enters into the pleural cavity.","definition_xrefs":["DOID:9534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumothorax","termid":"MONDO:0002076"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tuberculous pneumothorax","secondary_identifiers":["ICD9:011.7","MEDGEN:509067","ICD9:011.73","ICD9:011.70","ICD9:011.76","UMLS:C0152600","ICD9:011.71","ICD9:011.72","SCTID:29731002"],"termid":"MONDO:0004813","xrefs":{"Monarch":{"xref_id":"0004813"}}}


id: MONDO:0957210
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":"neurooculorenal syndrome","secondary_identifiers":["MEDGEN:1841013","OMIM:620305","UMLS:C5830377"],"termid":"MONDO:0957210","xrefs":{"Monarch":{"xref_id":"0957210"}}}


id: GO:0048478
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that prevents the collapse of stalled replication forks.","definition_xrefs":["GOC:vw","PMID:14560029"],"gene_count":0,"genotype_count":0,"name":"obsolete replication fork protection (obsolete GO:0048478)","synonyms":[{"name":"replication fork maintenance","type":"broad"},{"name":"replication fork stabilization","type":"broad"}],"termid":"GO:0048478"}


id: PBO:0049927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatocyte growth factor-regulated tyrosine kinase substrate","termid":"PBO:0049927"}


id: PR:O74520
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trp663 gene.","definition_xrefs":["UniProtKB:O74520","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized membrane protein C663.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC663.14c","synonyms":[{"name":"Spom972h-trp663","type":"exact"}],"termid":"PR:O74520"}


id: PBO:0081121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFAT antisense RNA 1","termid":"PBO:0081121"}


id: GO:0097307
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 farnesol stimulus.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"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 farnesol","termid":"GO:0097307"}


id: PR:Q92377
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mdm12 gene.","definition_xrefs":["UniProtKB:Q92377","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":"mitochondrial distribution and morphology protein 12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC28F2.06c","synonyms":[{"name":"Spom972h-mdm12","type":"exact"},{"name":"mitochondrial inheritance component mdm12 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q92377"}


id: PBO:0017821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LEM domain protein Man1, Sad1 interacting factor","termid":"PBO:0017821"}


id: FYPO:0000094
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to benomyl. Cells stop growing (and may die) at a concentration of benomyl that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000003","FYPO:0002683","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to benomyl","synonyms":[{"name":"hypersensitive to benomyl","type":"exact"},{"name":"sensitive to benomyl during mitotic cell cycle","type":"related"},{"name":"sensitive to benomyl during vegetative growth","type":"exact"},{"name":"sensitive to methyl [1-(butylcarbamoyl)-1H-benzimidazol-2-yl]carbamate","type":"exact"}],"termid":"FYPO:0000094"}


id: PBO:0038528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 2, acylglycerol lipase","termid":"PBO:0038528"}


id: MONDO:0018489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune encephalopathy with parasomnia and obstructive sleep apnea is a rare neurologic disorder characterized by a unique non-REM and REM parasomnia with sleep breathing dysfunction, gait instability and repetitive episodes of respiratory insufficiency, as well as autoantibodies against IgLON5. Patients may present stridor, chorea, limb ataxia, abnormal ocular movements, and bulbar symptoms (i.e. dysphagia, dysarthria, episodic central hypoventilation) with normal brain MRI. Excessive day sleepiness and cognitive deterioration have also been reported.","definition_xrefs":["Orphanet:420789"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of central nervous system","termid":"MONDO:0000568"},{"relation_name":"is_a","term_name":"sleep-wake disorder","termid":"MONDO:0003406"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune encephalopathy with parasomnia and obstructive sleep apnea","secondary_identifiers":["MEDGEN:1644256","SCTID:765751002","UMLS:C4707562","GARD:21749"],"synonyms":[{"name":"anti-IgLON5 disease","type":"exact"},{"name":"anti-IgLON5 syndrome","type":"exact"}],"termid":"MONDO:0018489","xrefs":{"Monarch":{"xref_id":"0018489"}}}


id: MOD:01238
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by formation of an adduct of an L-lysine residue with 4-hydroxynonenal.","definition_xrefs":["PubMed:11327326","Unimod:53#K","PubMed:9629898","PubMed:15133838"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-hydroxynonenal adduct","termid":"MOD:00446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"lysine 4-hydroxynonenal adduct","synonyms":[{"name":"4-hydroxynonenal (HNE)","type":"related"},{"name":"HNE","type":"related"}],"termid":"MOD:01238"}


id: PATO:0002518
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer being level or even with another surface.","definition_xrefs":["WordReference:flush"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flush","termid":"PATO:0002518"}


id: MONDO:0017345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Epstein-Barr virus-related tumor","termid":"MONDO:0017342"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Epstein-Barr virus-associated mesenchymal tumor","secondary_identifiers":["GARD:21149","MEDGEN:1843096","UMLS:C5679941","Orphanet:289656"],"synonyms":[{"name":"EBV-associated mesenchymal tumor","type":"exact"},{"name":"EBV-associated mesenchymal tumour","type":"exact"}],"termid":"MONDO:0017345","xrefs":{"Monarch":{"xref_id":"0017345"}}}


id: MONDO:1010822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Split hand that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"split hand, non-human animal","termid":"MONDO:1010159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"split hand, domestic cat","secondary_identifiers":["OMIA:000942-9685"],"termid":"MONDO:1010822","xrefs":{"Monarch":{"xref_id":"1010822"}}}


id: FYPO:0006679
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing chromium ions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002057","FYPO:0000257","FYPO:0000003","FYPO:0002058","FYPO:0002060"],"is_obsolete":false,"name":"normal growth on chromium","synonyms":[{"name":"normal cell population growth in presence of chromium","type":"exact"},{"name":"normal cell population growth on chromium","type":"exact"},{"name":"normal cell population growth on chromium ion","type":"exact"},{"name":"normal cellular response to chromium","type":"related"},{"name":"normal growth on chromium ions","type":"exact"},{"name":"normal vegetative cell population growth on chromium","type":"exact"}],"termid":"FYPO:0006679"}


id: MONDO:0009624
data:
  {"annotated_genes":["SJAG_01756"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86783],"is_not":false,"summary":null,"term":"MONDO:0009624"}]},"cv_name":"mondo","definition":"An autosomal recessive disorder caused by mutation(s) in the TUBGCP6 gene, encoding gamma-tubulin complex component 6. It is characterized by microcephaly and chorioretinopathy.","definition_xrefs":["NCIT:C129306"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"microcephaly and chorioretinopathy","termid":"MONDO:0000181"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01756":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005328"],"is_obsolete":false,"name":"microcephaly and chorioretinopathy 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16603","DOID:0080105","MEDGEN:480111","UMLS:C3278481","Orphanet:2518","OMIM:251270"],"synonyms":[{"name":"MCCRP1","type":"related"},{"name":"Pseudotoxoplasmosis syndrome","type":"exact"},{"name":"TUBGCP6 microcephaly and chorioretinopathy","type":"exact"},{"name":"autosomal recessive chorioretinopathy-microcephaly syndrome","type":"related"},{"name":"autosomal recessive chorioretinopathy-microcephaly-intellectual disability syndrome","type":"exact"},{"name":"microcephaly and chorioretinopathy 1","type":"exact"},{"name":"microcephaly and chorioretinopathy caused by mutation in TUBGCP6","type":"exact"},{"name":"microcephaly and chorioretinopathy type 1","type":"exact"},{"name":"microcephaly and chorioretinopathy, autosomal recessive, 1","type":"related"},{"name":"microcephaly and chorioretinopathy, autosomal recessive, type 1","type":"exact"}],"termid":"MONDO:0009624","terms_by_termid":{"MONDO:0009624":null},"xrefs":{"Monarch":{"xref_id":"0009624"}}}


id: PBO:0075399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SP140 nuclear body protein","termid":"PBO:0075399"}


id: PBO:0067305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 391, pseudogene","termid":"PBO:0067305"}


id: PBO:0044264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-X-C motif chemokine ligand 2","termid":"PBO:0044264"}


id: PBO:0088175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xylulokinase; converts D-xylulose and ATP to xylulose 5-phosphate and ADP; rate limiting step in fermentation of xylulose; required for xylose fermentation by recombinant S. cerevisiae strains","termid":"PBO:0088175"}


id: FYPO:0003289
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the medial cortical nodes is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortex during vegetative growth","termid":"FYPO:0000731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to medial cortical node","synonyms":[{"name":"abnormal protein localisation to medial cortical node","type":"exact"},{"name":"abnormal protein localization to cortical medial dot","type":"exact"},{"name":"abnormal protein localization to cytokinetic nodes","type":"related"},{"name":"abnormal protein localization to medial cortical node during mitotic cell cycle","type":"related"},{"name":"abnormal protein localization to medial cortical node during vegetative growth","type":"exact"},{"name":"abnormal protein localization to medial cortical nodes","type":"exact"},{"name":"abnormal protein recruitment to medial cortical node","type":"related"}],"termid":"FYPO:0003289"}


id: PR:Q9UT20
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 3-oxo-5-alpha-steroid 4-dehydrogenase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00594","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 C9.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9.08c","secondary_identifiers":["UniProtKB:Q9UT20"],"synonyms":[{"name":"Spom972h-SRD5A1","type":"exact"}],"termid":"PR:Q9UT20"}


id: GO:0061706
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sucrose into pyruvate through both glucose and fructose intermediates, with the concomitant production of a small amount of ATP and the reduction of NAD(P) to NAD(P)H. Glycolysis begins with the metabolism of a carbohydrate to generate products that can enter the pathway and ends with the production of pyruvate. Pyruvate may be converted to acetyl-coenzyme A, ethanol, lactate, or other small molecules.","definition_xrefs":["GOC:dph","MetaCyc:PWY-1042","GOC:glycolysis","PMID:15012287"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolytic process through fructose-6-phosphate","termid":"GO:0061615"},{"relation_name":"is_a","term_name":"glycolytic process from sucrose","termid":"GO:0061704"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150","GO:0006091","GO:0005975"],"is_obsolete":false,"name":"glycolytic process from sucrose through glucose and fructose","termid":"GO:0061706"}


id: PBO:0042198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin E2","termid":"PBO:0042198"}


id: PBO:0074369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smith-Magenis syndrome chromosome region, candidate 2","termid":"PBO:0074369"}


id: GO:0003265
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardioblast proliferation in the primary heart field. A cardioblast is a cardiac precursor cell. It is a cell that has been committed to a cardiac fate, but will undergo more cell division rather than terminally differentiating. In mammals the primary heart field gives rise to the left ventricle.","definition_xrefs":["GOC:rl","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardioblast proliferation","termid":"GO:0003264"}],"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 primary heart field cardioblast proliferation","synonyms":[{"name":"regulation of FHF cardioblast proliferation","type":"exact"},{"name":"regulation of first heart field cardiac proliferation","type":"related"},{"name":"regulation of first heart field cardioblast proliferation","type":"exact"}],"termid":"GO:0003265"}


id: PBO:0080111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urotensin 2B","termid":"PBO:0080111"}


id: FYPO:0004672
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is inviable, is elongated, and contains a nucleus that is broken into small fragments.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"is_a","term_name":"fragmented nucleus during vegetative growth","termid":"FYPO:0001919"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002403","FYPO:0001985","FYPO:0000004","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000005"],"is_obsolete":false,"name":"inviable elongated vegetative cell with fragmented nucleus","synonyms":[{"name":"elongated inviable cell with fragmented nucleus","type":"exact"},{"name":"inviable elongated cell with fragmented nucleus during vegetative growth","type":"exact"},{"name":"inviable elongated vegetative cell with fragmented DNA","type":"related"},{"name":"inviable elongated vegetative cell with fragmented nucleus during mitotic cell cycle","type":"related"},{"name":"lethal; elongated vegetative cell with fragmented nucleus","type":"exact"}],"termid":"FYPO:0004672"}


id: PBO:0074104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 28 member 1","termid":"PBO:0074104"}


id: MONDO:0007080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial hyperaldosteronism type I (FH-I) is a rare heritable, glucocorticoid remediable form of primary aldosteronism (PA) characterized by early-onset hypertension, hyperaldosteronism, variable hypokalemia, low plasma renin activity (PRA), and abnormal production of 18-oxocortisol and 18-hydroxycortisol.","definition_xrefs":["Orphanet:403"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperaldosteronism","termid":"MONDO:0016525"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucocorticoid-remediable aldosteronism","secondary_identifiers":["ICD10CM:E26.02","MEDGEN:824577","GARD:2790","DOID:14080","UMLS:C3838731","ICD9:255.11","MESH:C563177","OMIM:103900"],"synonyms":[{"name":"ACTH-dependent hyperaldosteronism syndrome","type":"related"},{"name":"FH 1","type":"related"},{"name":"FH-I","type":"exact"},{"name":"FH1","type":"exact"},{"name":"GRA","type":"exact"},{"name":"HALD1","type":"related"},{"name":"aldosteronism, glucocorticoid-remediable","type":"exact"},{"name":"aldosteronism, sensitive to dexamethasone","type":"related"},{"name":"dexamethasone sensitive hypertension","type":"related"},{"name":"dexamethasone-sensitive hypertension","type":"exact"},{"name":"familial hyperaldosteronism type 1","type":"exact"},{"name":"familial hyperaldosteronism type I","type":"related"},{"name":"glucocorticoid sensitive hypertension","type":"related"},{"name":"glucocorticoid-remediable aldosteronism","type":"exact"},{"name":"glucocorticoid-sensitive hypertension","type":"exact"},{"name":"glucocorticoid-suppressible hyperaldosteronism","type":"related"},{"name":"hyperaldosteronism, familial type 1","type":"related"},{"name":"hyperaldosteronism, familial, type 1","type":"related"},{"name":"hyperaldosteronism, familial, type I","type":"related"}],"termid":"MONDO:0007080","xrefs":{"Monarch":{"xref_id":"0007080"}}}


id: PBO:0053272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukocyte immunoglobulin like receptor A5","termid":"PBO:0053272"}


id: FYPO:0007539
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 phosphorylation of the threonine residue at position 4 within one or more copies of the heptapeptide repeat (YSPTSPS) of the C-terminal domain of RNA polymerase II normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:30282034","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during vegetative growth","termid":"FYPO:0000776"}],"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:0001312","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal phosphorylation of RNA polymerase II C-terminal domain threonine 4 residues during vegetative growth","synonyms":[{"name":"normal phosphorylation of RNA polymerase II C-terminal domain threonine 4 residues during mitotic cell cycle","type":"related"},{"name":"normal phosphorylation of RNA polymerase II CTD threonine 4 residues during vegetative growth","type":"exact"}],"termid":"FYPO:0007539"}


id: GO:0033414
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UGC codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0060090","GO:0005488","GO:0003723"],"is_obsolete":false,"name":"UGC codon-amino acid adaptor activity","synonyms":[{"name":"TGC codon-amino acid adaptor activity","type":"exact"},{"name":"cysteine tRNA","type":"related"}],"termid":"GO:0033414"}


id: PBO:0087595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the ASTRA complex, involved in chromatin remodeling; telomere length regulator involved in the stability or biogenesis of PIKKs such as TORC1; similar to S. pombe Tti1p; detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0087595"}


id: PBO:0062411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 38 pseudogene","termid":"PBO:0062411"}


id: MONDO:0010464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic syndrome with a cerebellar malformation as major feature characterized by cerebellar vermis hypo- or aplasia, ventriculomegaly, agenesis of corpus callosum and abnormalities of the brainstem and cerebral cortex in association with ocular coloboma. Clinically, patients show hydrocephalus at birth, neonatal hypotonia with abnormal breathing pattern, ocular abnormalities with impaired vision, severe psychomotor delay, and seizures.","definition_xrefs":["Orphanet:163961"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"X-linked cerebral-cerebellar-coloboma syndrome syndrome","secondary_identifiers":["OMIM:300864","GARD:17006","MEDGEN:477118","UMLS:C3275487"],"synonyms":[{"name":"X-linked cerebral-cerebellar-coloboma syndrome","type":"related"},{"name":"X-linked intellectual disability, Kroes type","type":"exact"},{"name":"cerebral-cerebellar-coloboma syndrome, X-linked","type":"related"},{"name":"cerebral-cerebellar-coloboma syndrome, X-linked, X-linked recessive","type":"exact"}],"termid":"MONDO:0010464","xrefs":{"Monarch":{"xref_id":"0010464"}}}


id: PBO:0025498
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Suppressor of Cdc Eleven","termid":"PBO:0025498"}


id: GO:0014071
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 cycloalkane stimulus. A cycloalkane is a cyclic saturated hydrocarbon having the general formula CnH2n.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to organic cyclic compound","termid":"GO:0014070"}],"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 cycloalkane","termid":"GO:0014071"}


id: PBO:0065603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTOV1 antisense RNA 1","termid":"PBO:0065603"}


id: MONDO:0013158
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive muscular dystrophy caused by mutations in the LARGE gene. It is associated with characteristic brain and eye malformations, profound mental retardation, and death usually in the first years of life.","definition_xrefs":["NCIT:C126743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type A","termid":"MONDO:0000171"},{"relation_name":"is_a","term_name":"muscle-eye-brain disease","termid":"MONDO:0018939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6","secondary_identifiers":["OMIM:613154","DOID:0111242","GARD:15626","MEDGEN:461764","UMLS:C3150414"],"synonyms":[{"name":"MDDGA6","type":"related"},{"name":"Walker-Warburg syndrome or muscle-eye-brain disease, large-related","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 6","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6","type":"related"}],"termid":"MONDO:0013158","xrefs":{"Monarch":{"xref_id":"0013158"}}}


id: PBO:0051169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-53","termid":"PBO:0051169"}


id: PBO:0034525
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_cellular_process","termid":"PBO:0034525"}


id: FYPO:0001228
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in vegetative growth phase of the life cycle, in which the amount of protein measured in the cell nucleus is higher than normal during a cellular response to hydrogen peroxide. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased nuclear protein level during vegetative growth","termid":"FYPO:0000255"},{"relation_name":"is_a","term_name":"increased protein level during cellular response to hydrogen peroxide","termid":"FYPO:0001102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002403","FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased nuclear protein level during cellular response to hydrogen peroxide","synonyms":[{"name":"increased nuclear protein level during cellular response to H2O2","type":"exact"},{"name":"increased nuclear protein level during cellular response to hydrogen peroxide during mitotic cell cycle","type":"related"},{"name":"increased nuclear protein level during cellular response to hydrogen peroxide during vegetative growth","type":"exact"},{"name":"increased protein level in nucleus during cellular response to hydrogen peroxide","type":"related"},{"name":"nuclear accumulation of protein during cellular response to hydrogen peroxide","type":"exact"},{"name":"nuclear protein accumulation during cellular response to hydrogen peroxide","type":"related"},{"name":"nuclear protein accumulation during cellular response to hydrogen peroxide during vegetative growth","type":"related"},{"name":"nuclear protein accumulation in response to hydrogen peroxide","type":"related"}],"termid":"FYPO:0001228"}


id: _global:results_in_morphogenesis_of
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","definition":"The relationship that links an entity with the process that results in the formation and shaping of that entity over time from an immature to a mature state.","direct_ancestors":[{"relation_name":"is_a","term_name":"has_participant","termid":"RO:0000057"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"},{"relation_name":"is_a","term_name":"results_in_changes_to_anatomical_or_cellular_structure","termid":"_global:results_in_changes_to_anatomical_or_cellular_structure"},{"relation_name":"is_a","term_name":"results_in_developmental_progression_of","termid":"_global:results_in_developmental_progression_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_morphogenesis_of","secondary_identifiers":["RO:0002298","GOREL:0001015"],"termid":"_global:results_in_morphogenesis_of"}


id: GO:0003900
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: nucleoside triphosphate + RNA(n) = diphosphate + RNA(n+1).","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA-directed RNA polymerase I activity (obsolete GO:0003900)","synonyms":[{"name":"DNA-directed RNA polymerase I activity","type":"exact"}],"termid":"GO:0003900"}


id: GO:0047237
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucuronyl-1,3-beta-D-galactosylproteoglycan + UDP-N-acetylgalactosamine = N-acetyl-D-galactosaminyl-1,4-beta-D-glucuronyl-1,3-beta-D-galactosylproteoglycan + UDP.","definition_xrefs":["EC:2.4.1.174","MetaCyc:2.4.1.174-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylgalactosaminyltransferase activity","termid":"GO:0008376"}],"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:0016757"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase activity","secondary_identifiers":["RHEA:23464"],"synonyms":[{"name":"N-acetylgalactosaminyltransferase I activity","type":"exact"},{"name":"UDP-N-acetyl-D-galactosamine:D-glucuronyl-1,3-beta-D-galactosyl-proteoglycan beta-1,4-N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"glucuronylgalactosylproteoglycan beta-1,4-N-acetylgalactosaminyltransferase activity","type":"exact"},{"name":"uridine diphosphoacetylgalactosamine-chondroitin acetylgalactosaminyltransferase I","type":"related"},{"name":"uridine diphosphoacetylgalactosamine-chondroitinacetylgalactosaminyltransferase I activity","type":"related"}],"termid":"GO:0047237"}


id: PBO:0059791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 17","termid":"PBO:0059791"}


id: MONDO:0011066
data:
  {"annotated_genes":["SJAG_03248"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85749],"is_not":false,"summary":null,"term":"MONDO:0011066"}]},"cv_name":"mondo","definition":"Charcot-Marie-Tooth disease type 4B1 (CMT4B1) is a subtype of Charcot-Marie-Tooth disease type 4 characterized by an early childhood-onset of severe, demyelinating sensorimotor neuropathy, various degrees of complex myelin outfoldings seen on peripheral nerve biopsy, very slow, and often undetectable, nerve conduction velocities, and the typical CMT phenotype (i.e. distal muscle weakness and atrophy, sensory loss, and frequent pes cavus). Other reported features include facial weakness, vocal cord paresis, respiratory difficulties, and skeletal deformities (e.g. chest deformities, claw hands, pes equinovarus).","definition_xrefs":["Orphanet:99955"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 4","termid":"MONDO:0018995"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03248":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 4B1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C535420","GARD:1253","SCTID:715803003","icd11.foundation:776238355","UMLS:C1832399","DOID:0110191","MEDGEN:321947","OMIM:601382"],"synonyms":[{"name":"CMT 4B","type":"related"},{"name":"CMT 4B1","type":"related"},{"name":"CMT4B1","type":"exact"},{"name":"Charcot Marie Tooth disease type 4B1","type":"related"},{"name":"Charcot-Marie-Tooth disease type 4 caused by mutation in MTMR2","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 4B1","type":"exact"},{"name":"Charcot-Marie-Tooth disease, autosomal recessive, with focally folded myelin sheaths, autosomal recessive, type 4B1","type":"related"},{"name":"Charcot-Marie-Tooth disease, type 4B","type":"related"},{"name":"Charcot-Marie-Tooth disease, type 4B1","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy type 4B1","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 4B1","type":"related"},{"name":"MTMR2 Charcot-Marie-Tooth disease type 4","type":"exact"},{"name":"autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1","type":"exact"}],"termid":"MONDO:0011066","terms_by_termid":{"MONDO:0011066":null},"xrefs":{"Monarch":{"xref_id":"0011066"}}}


id: GO:1990513
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Transcription factor complex which interacts with E-box regulatory elements in target genes, including Period (Per1, Per2, Per3) and Cryptochrome (Cry1, Cry2), to activate their transcription during the daytime. The CRY-PER complexes inhibit CLOCK-BMAL1-driven transcription in a negative feedback loop to generate circadian rhythms.","definition_xrefs":["PMID:23229515","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"CLOCK-BMAL transcription complex","synonyms":[{"name":"CLOCK/BMAL complex","type":"exact"}],"termid":"GO:1990513"}


id: MONDO:0010821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial developmental dysphasia is a severe form of developmental verbal apraxia characterized by a deficit in spontaneous speech, writing, grammatical judgment and repetition, defective articulation, moderate to severe degree of dyspraxia, a reduced use of consonant clusters, and comprehension delay. Hearing and intelligence are normal.","definition_xrefs":["Orphanet:1799"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"specific language disorder","termid":"MONDO:0016226"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial developmental dysphasia","secondary_identifiers":["SCTID:721220004","UMLS:C1838630","GARD:1823","MESH:C563997","ICD10CM:F80.1","OMIM:600117","MEDGEN:374015"],"synonyms":[{"name":"Billard-Toutain-Maheut syndrome","type":"exact"},{"name":"FOXP2-associated dysphasia","type":"exact"},{"name":"developmental dysphasia familial","type":"related"},{"name":"developmental language disorder","type":"related"},{"name":"dysphasia, familial developmental","type":"related"},{"name":"specific language impairment","type":"related"}],"termid":"MONDO:0010821","xrefs":{"Monarch":{"xref_id":"0010821"}}}


id: MONDO:0100468
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital myopathy in which a family of 6 siblings presented in infancy the picture of 'amyotonia congenita' and later in life a nonprogressive myopathy.","definition_xrefs":["OMIM:255300"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"Batten-Turner congenital myopathy","secondary_identifiers":["UMLS:C0027127","DOID:0081335","MEDGEN:10158"],"termid":"MONDO:0100468","xrefs":{"Monarch":{"xref_id":"0100468"}}}


id: PBO:0067513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 654, pseudogene","termid":"PBO:0067513"}


id: MONDO:1011691
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"platelet function defect, non-human animal","secondary_identifiers":["OMIA:000803"],"termid":"MONDO:1011691","xrefs":{"Monarch":{"xref_id":"1011691"}}}


id: FYPO:0006749
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 one or more transfer RNA precursor(s) (pre-tRNA) measured in a cell is higher than normal. Total pre-tRNA or a specific pre-tRNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered tRNA level during vegetative growth","termid":"FYPO:0008101"},{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased pre-tRNA level during vegetative growth","synonyms":[{"name":"increased pre-tRNA accumulation during vegetative growth","type":"related"},{"name":"increased pre-tRNA level during mitotic cell cycle","type":"related"},{"name":"increased pre-tRNA transcript level during vegetative growth","type":"exact"},{"name":"increased tRNA level during vegetative growth","type":"broad"},{"name":"increased tRNA primary transcript level during vegetative growth","type":"exact"},{"name":"increased transfer RNA precursor level during vegetative growth","type":"exact"}],"termid":"FYPO:0006749"}


id: PBO:0049428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GUSB pseudogene 5","termid":"PBO:0049428"}


id: PBO:0063392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 6 interacting protein","termid":"PBO:0063392"}


id: GO:0034910
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 6-hydroxy-3-succinoylpyridine + H2O = succinic semialdehyde + 2,5-dihydroxypyridine.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 6-hydroxy-3-succinoylpyridine hydrolase activity (obsolete GO:0034910)","termid":"GO:0034910"}


id: FYPO:0006542
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during mitosis is higher than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"}],"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":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased RNA level during mitosis","synonyms":[{"name":"increased RNA accumulation during mitosis","type":"related"},{"name":"increased RNA level during M phase of mitotic cell cycle","type":"related"},{"name":"increased RNA level during mitosis during vegetative growth","type":"exact"},{"name":"increased RNA level during mitotic M phase","type":"related"},{"name":"increased mRNA level during mitosis","type":"narrow"},{"name":"increased transcript level during mitosis","type":"exact"}],"termid":"FYPO:0006542"}


id: GO:0010505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency or rate of cell cycle arrest in response to nitrogen starvation.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cell cycle arrest in response to nitrogen starvation (obsolete GO:0010505)","termid":"GO:0010505"}


id: PATO:0001787
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature quality inhering in a bearer by virtue of the bearer's being curved around an axis.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curvature","termid":"PATO:0001591"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rotational curvature","termid":"PATO:0001787"}


id: PBO:0078414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon CCC) 8-1","termid":"PBO:0078414"}


id: GO:0001039
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a sequence of DNA that is a part of a hybrid type promoter that controls transcription by RNA polymerase III (Pol III). A hybrid Pol III promoter contains both regulatory elements both upstream and downstream of the transcription initiation site. An example gene with such a promoter is the S. cerevisiae U6 gene.","definition_xrefs":["GOC:txnOH","PMID:12381659"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase III cis-regulatory region sequence-specific DNA binding","termid":"GO:0000992"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0000976"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003677","GO:0000976","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"RNA polymerase III hybrid type promoter sequence-specific DNA binding","secondary_identifiers":["GO:0001037"],"synonyms":[{"name":"RNA polymerase III hybrid type promoter DNA binding","type":"related"}],"termid":"GO:0001039"}


id: GO:0006836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a neurotransmitter into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Neurotransmitters are any chemical substance that is capable of transmitting (or inhibiting the transmission of) a nerve impulse from a neuron to another cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"neurotransmitter transport","secondary_identifiers":["Reactome:R-HSA-264642","Reactome:R-HSA-181430","Reactome:R-HSA-181429","Reactome:R-HSA-212676","Reactome:R-HSA-210500"],"synonyms":[{"name":"sodium:neurotransmitter transport","type":"narrow"}],"termid":"GO:0006836"}


id: MONDO:0030910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual disability, autosomal dominant 45","secondary_identifiers":["MEDGEN:1616472","OMIM:617600","DOID:0080236","UMLS:C4539848"],"synonyms":[{"name":"MRD45","type":"related"},{"name":"autosomal dominant intellectual disability 45","type":"related"},{"name":"autosomal dominant mental retardation 45","type":"related"},{"name":"intellectual disability, autosomal dominant 45","type":"exact"},{"name":"mental retardation, autosomal dominant 45","type":"related"}],"termid":"MONDO:0030910","xrefs":{"Monarch":{"xref_id":"0030910"}}}


id: GO:0004965
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the amino acid gamma-aminobutyric acid (GABA, 4-aminobutyrate) and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["Wikipedia:GABAB_receptor","IUPHAR_RECEPTOR:1276","GOC:ai","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"},{"relation_name":"is_a","term_name":"GABA receptor activity","termid":"GO:0016917"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"G protein-coupled GABA receptor activity","secondary_identifiers":["Reactome:R-HSA-1013012","Reactome:R-HSA-1013013"],"synonyms":[{"name":"G-protein coupled GABA receptor activity","type":"exact"},{"name":"GABA-B receptor activity","type":"related"},{"name":"metabotropic GABA receptor","type":"related"}],"termid":"GO:0004965"}


id: PBO:0071572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35 pseudogene 1","termid":"PBO:0071572"}


id: MONDO:0010142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypothyroidism due to thyroid-stimulating hormone (TSH) receptor mutations is a type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth due to thyroid resistance to TSH.","definition_xrefs":["Orphanet:90673"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypothyroidism, congenital, nongoitrous","termid":"MONDO:0000045"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypothyroidism due to TSH receptor mutations","secondary_identifiers":["OMIM:275200","MEDGEN:487729","DOID:0070126","UMLS:C3493776","GARD:16793"],"synonyms":[{"name":"CHNG1","type":"exact"},{"name":"TSH resistance","type":"exact"},{"name":"congenital nongoitrous hypothyroidism 1","type":"related"},{"name":"hypothyroidism due to unresponsiveness to thyrotropin","type":"related"},{"name":"hypothyroidism, Nonautoimmune","type":"related"},{"name":"hypothyroidism, congenital, due to TSH resistance","type":"related"},{"name":"hypothyroidism, congenital, nongoitrous, 1","type":"related"},{"name":"hypothyroidism, congenital, nongoitrous, type 1","type":"exact"},{"name":"thyroid-stimulating hormone, resistance to","type":"related"},{"name":"thyrotropin resistance","type":"related"}],"termid":"MONDO:0010142","xrefs":{"Monarch":{"xref_id":"0010142"}}}


id: PBO:0065051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRELI domain containing 3B pseudogene 5","termid":"PBO:0065051"}


id: GO:0016519
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with gastric inhibitory peptide (GIP) and transmitting the signal across the membrane to activate an associated G-protein.","definition_xrefs":["GOC:mah","PMID:8243312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"gastric inhibitory peptide receptor activity","synonyms":[{"name":"GIP receptor activity","type":"exact"},{"name":"glucose-dependent insulinotropic polypeptide receptor activity","type":"exact"}],"termid":"GO:0016519"}


id: FYPO:0006323
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable after stalled replication forks accumulate.","definition_xrefs":["PomBase:mah","PMID:29215009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"},{"relation_name":"is_a","term_name":"cell population viability","termid":"FYPO:0002057"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0002057"],"is_obsolete":false,"name":"loss of viability following replication fork stalling","synonyms":[{"name":"decreased viability following replication fork stalling","type":"exact"},{"name":"loss of cell population viability following replication fork stalling","type":"exact"},{"name":"reduced viability following replication fork stalling","type":"related"}],"termid":"FYPO:0006323"}


id: PBO:0054660
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 2066","termid":"PBO:0054660"}


id: PBO:0053750
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 987","termid":"PBO:0053750"}


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


id: MONDO:0000891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A fibrolamellar carcinoma that is characterized by the presence of both pure fibrolamellar hepatocellular carcinoma and and conventional hepatocellular carcinoma components.","definition_xrefs":["DOID:0080182"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrolamellar hepatocellular carcinoma","termid":"MONDO:0006210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992","MONDO:0002515"],"is_obsolete":false,"name":"mixed fibrolamellar hepatocellular carcinoma","termid":"MONDO:0000891","xrefs":{"Monarch":{"xref_id":"0000891"}}}


id: PATO:0002140
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the bearer not being suitable for use as food.","definition_xrefs":["PATOC:VO"],"direct_ancestors":[{"relation_name":"is_a","term_name":"edibility","termid":"PATO:0002138"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inedible","termid":"PATO:0002140"}


id: GO:1902549
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a Mei2 nuclear dot.","definition_xrefs":["GOC:TermGenie","PMID:23980030"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to nucleus","termid":"GO:0034504"}],"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":"protein localization to Mei2 nuclear dot","synonyms":[{"name":"protein localisation in Mei2 nuclear dot","type":"exact"},{"name":"protein localisation to Mei2 nuclear dot","type":"exact"},{"name":"protein localization in Mei2 nuclear dot","type":"exact"},{"name":"protein localization to Mei2 dot","type":"exact"}],"termid":"GO:1902549"}


id: MONDO:0700061
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease characteristic in which the cause of the disease is present in some of the cells of the organism, or in all the cells of the organism.","direct_ancestors":[{"relation_name":"is_a","term_name":"disease characteristic","termid":"MONDO:0021125"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mosaic vs complete","termid":"MONDO:0700061","xrefs":{"Monarch":{"xref_id":"0700061"}}}


id: SO:1001188
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is alternately spliced, but encodes only one polypeptide.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"encodes_alternately_spliced_transcripts","termid":"SO:0000463"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encodes_1_polypeptide","synonyms":[{"name":"encodes 1 polypeptide","type":"exact"}],"termid":"SO:1001188"}


id: GO:0050897
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a cobalt ion (Co2+).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion binding","termid":"GO:0046914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0046872"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0046872","GO:0005488"],"is_obsolete":false,"name":"cobalt ion binding","synonyms":[{"name":"Co ion binding","type":"exact"},{"name":"cobalt binding","type":"exact"}],"termid":"GO:0050897"}


id: PBO:0051240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (II)-51-2 (pseudogene)","termid":"PBO:0051240"}


id: MONDO:0022553
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":"BD syndrome","termid":"MONDO:0022553","xrefs":{"Monarch":{"xref_id":"0022553"}}}


id: GO:0006205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete pyrimidine metabolic process (obsolete GO:0006205)","synonyms":[{"name":"pyrimidine metabolic process","type":"exact"}],"termid":"GO:0006205"}


id: PBO:0038351
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_positive_regulatory_component_activity","termid":"PBO:0038351"}


id: MONDO:0054838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiomyopathy, familial hypertrophic 27","secondary_identifiers":["OMIM:618052","UMLS:C4748014","MEDGEN:1648325"],"synonyms":[{"name":"CMH27","type":"related"},{"name":"cardiomyopathy, FAMILIAL hypertrophic 27","type":"related"}],"termid":"MONDO:0054838","xrefs":{"Monarch":{"xref_id":"0054838"}}}


id: GO:0043098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process which produces a purine deoxyribonucleoside from derivatives of it, without de novo synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine-containing compound salvage","termid":"GO:0043101"},{"relation_name":"is_a","term_name":"nucleoside salvage","termid":"GO:0043174"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside biosynthetic process","termid":"GO:0046123"}],"gene_count":0,"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:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"purine deoxyribonucleoside salvage","termid":"GO:0043098"}


id: GO:0007007
data:
  {"annotated_genes":["SJAG_02002","SJAG_03282","SJAG_03515","SJAG_01949","SJAG_05241","SJAG_00404","SJAG_01405","SJAG_05302","SJAG_02656","SJAG_02398","SJAG_02524","SJAG_02028","SJAG_01640","SJAG_04237","SJAG_02501","SJAG_03633","SJAG_04996","SJAG_04965","SJAG_03502","SJAG_01120","SJAG_01917","SJAG_00687","SJAG_05300","SJAG_04208"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99753],"is_not":false,"summary":null,"term":"GO:0007007"},{"annotations":[89006,109480,114082,101193,117226,106785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042407"},{"annotations":[104374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990627"},{"annotations":[107033,107055,92292,89904,112639,88173,115713,106976,98927,102409,106761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[98510,112790,114140,88315,100407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032979"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the mitochondrial inner membrane.","definition_xrefs":["GOC:dph","GOC:mah","GOC:ai","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial membrane organization","termid":"GO:0007006"}],"gene_count":24,"genes_by_uniquename":{"SJAG_00404":null,"SJAG_00687":null,"SJAG_01120":null,"SJAG_01405":null,"SJAG_01640":null,"SJAG_01917":null,"SJAG_01949":null,"SJAG_02002":null,"SJAG_02028":null,"SJAG_02398":null,"SJAG_02501":null,"SJAG_02524":null,"SJAG_02656":null,"SJAG_03282":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03633":null,"SJAG_04208":null,"SJAG_04237":null,"SJAG_04965":null,"SJAG_04996":null,"SJAG_05241":null,"SJAG_05300":null,"SJAG_05302":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024","GO:0007005"],"is_obsolete":false,"name":"inner mitochondrial membrane organization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"inner mitochondrial membrane organisation","type":"exact"},{"name":"inner mitochondrial membrane organization and biogenesis","type":"related"},{"name":"mitochondrial inner membrane organization","type":"exact"}],"termid":"GO:0007007","terms_by_termid":{"GO:0007007":null,"GO:0032979":null,"GO:0042407":null,"GO:0045039":null,"GO:1990627":null}}


id: GO:0005957
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete debranching enzyme (obsolete GO:0005957)","synonyms":[{"name":"debranching enzyme","type":"exact"}],"termid":"GO:0005957"}


id: PBO:0056697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiosis initiator","termid":"PBO:0056697"}


id: MONDO:0015340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterized by a generalized skin rash, fever, eosinophilia, lymphocytosis and visceral involvement (hepatitis, nephritis, pneumonitis, pericarditis and myocarditis) and, in some patients, reactivation of human herpes virus 6.","definition_xrefs":["Orphanet:139402"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"urticaria","termid":"MONDO:0005492"},{"relation_name":"is_a","term_name":"severe cutaneous adverse reaction","termid":"MONDO:0005594"},{"relation_name":"is_a","term_name":"toxic dermatosis","termid":"MONDO:0017396"}],"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":"drug rash with eosinophilia and systemic symptoms","secondary_identifiers":["MEDGEN:762193","NCIT:C112208","icd11.foundation:516577496","SCTID:702809001","GARD:13629","MESH:D063926","MedDRA:10058919","UMLS:C3541994"],"synonyms":[{"name":"DHS","type":"exact"},{"name":"DRESS","type":"exact"},{"name":"DRESS syndrome","type":"exact"},{"name":"Drug hypersensitivity syndrome","type":"exact"},{"name":"Drug reaction with eosinophilia and Systemic symptoms","type":"exact"},{"name":"dress","type":"exact"},{"name":"drug reaction eosinophilic systemic syndrome","type":"exact"}],"termid":"MONDO:0015340","xrefs":{"Monarch":{"xref_id":"0015340"}}}


id: MONDO:0002738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of non-suppurative otitis media.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-suppurative otitis media","termid":"MONDO:0001212"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute transudative otitis media","secondary_identifiers":["ICD9:381.0","ICD9:381.00","SCTID:359609001","UMLS:C0271432","MEDGEN:543339","DOID:3697"],"synonyms":[{"name":"acute non-suppurative otitis media","type":"exact"},{"name":"acute nonsuppurative otitis media","type":"exact"},{"name":"acute otitis media with effusion","type":"exact"},{"name":"acute secretory otitis media","type":"exact"},{"name":"acute transudative otitis media","type":"exact"},{"name":"non-suppurative otitis media, acute","type":"exact"}],"termid":"MONDO:0002738","xrefs":{"Monarch":{"xref_id":"0002738"}}}


id: PBO:0079366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin alpha like 3","termid":"PBO:0079366"}


id: PBO:0028867
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_mRNA_level_during_vegetative_growth","termid":"PBO:0028867"}


id: PATO:0001362
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's disposition to being easily damaged or destroyed.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fragility","termid":"PATO:0001662"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile","termid":"PATO:0001362"}


id: PBO:0048733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate dehydrogenase 1 pseudogene 4","termid":"PBO:0048733"}


id: PBO:0024801
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-involved_in","termid":"PBO:0024801"}


id: PBO:0111967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dsl1/NZR complex secretory pathway protein RINT1 family","termid":"PBO:0111967"}


id: PBO:0077276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 14D, pseudogene","termid":"PBO:0077276"}


id: GO:0086098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An angiotensin receptor signaling pathway which contributes to a circulatory system process carried out by the heart.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11","PMID:17376402"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiotensin-activated signaling pathway","termid":"GO:0038166"},{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway involved in heart process","termid":"GO:0086103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"angiotensin-activated signaling pathway involved in heart process","synonyms":[{"name":"angiotensin receptor signaling pathway involved in heart process","type":"exact"},{"name":"angiotensin receptor signalling pathway involved in heart process","type":"exact"},{"name":"angiotensin-mediated signaling pathway involved in heart process","type":"related"}],"termid":"GO:0086098"}


id: MONDO:0019447
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atypical lichen myxedematosus is an intermediate form of lichen myxedematosus (LM) (a form of mucin dermal deposit) which does not meet the criteria for either scleromyxedema or the localized form. Three clinical subtypes have been described and include scleromyxedema without monoclonal gammopathy; localized forms with monoclonal gammopathy and/or systemic symptoms; localized forms with mixed features of the 5 subtypes of localized LM (discrete form, acral persistent papular mucinosis, self-healing papular mucinosis, papular mucinosis of infancy, and a pure nodular form). The course of atypical LM is unpredictable because only a few cases have been reported.","definition_xrefs":["Orphanet:86797"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lichen myxedematosus","termid":"MONDO:0018432"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"atypical lichen myxedematosus","secondary_identifiers":["MEDGEN:1383234","UMLS:C4510874","SCTID:725148000","GARD:19066"],"synonyms":[{"name":"Intermediate lichen myxedematosus","type":"exact"}],"termid":"MONDO:0019447","xrefs":{"Monarch":{"xref_id":"0019447"}}}


id: PATO:0000336
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color quality inhering in a bearer by virtue of the bearer's having color.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color","termid":"PATO:0000014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colored","secondary_identifiers":["PATO:0000332"],"synonyms":[{"name":"pigmented","type":"related"}],"termid":"PATO:0000336"}


id: GO:0047681
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an aromatic alcohol + NADP+ = an aromatic aldehyde + NADPH.","definition_xrefs":["MetaCyc:ARYL-ALCOHOL-DEHYDROGENASE-NADP+-RXN","EC:1.1.1.91"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"aryl-alcohol dehydrogenase (NADP+) activity","secondary_identifiers":["RHEA:17761"],"synonyms":[{"name":"NADPH-linked benzaldehyde reductase activity","type":"related"},{"name":"aryl alcohol dehydrogenase (nicotinamide adenine dinucleotide phosphate)","type":"related"},{"name":"aryl-alcohol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047681"}


id: GO:0140348
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the movement of lysophosphatidylcholine from the exoplasmic to the cytosolic leaflet of a membrane, using energy from the hydrolysis of ATP.","definition_xrefs":["PMID:26945070"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerophospholipid flippase activity","termid":"GO:0140333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140303"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0140303"],"is_obsolete":false,"name":"lysophosphatidylcholine flippase activity","synonyms":[{"name":"lysophosphatidylcholine flippase activity (exoplasmic to cytosolic leaflet)","type":"exact"}],"termid":"GO:0140348"}


id: MONDO:0004611
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm that affects the soft palate.","definition_xrefs":["NCIT:C3529"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oropharynx cancer","termid":"MONDO:0004608"},{"relation_name":"is_a","term_name":"palatal neoplasm","termid":"MONDO:0005286"},{"relation_name":"is_a","term_name":"oral cavity cancer","termid":"MONDO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"soft palate cancer","secondary_identifiers":["ICD9:145.3","MEDGEN:57552","SCTID:363388009","UMLS:C0153376","DOID:8578","ICD10CM:C05.1"],"synonyms":[{"name":"cancer of soft palate","type":"exact"},{"name":"malignant neoplasm of soft palate","type":"exact"},{"name":"malignant neoplasm of the soft palate","type":"exact"},{"name":"malignant soft palate neoplasm","type":"exact"},{"name":"malignant soft palate tumor","type":"exact"},{"name":"malignant soft palate tumour","type":"exact"},{"name":"malignant tumor of soft palate","type":"exact"},{"name":"malignant tumor of the soft palate","type":"exact"},{"name":"malignant tumour of soft palate","type":"exact"},{"name":"malignant tumour of the soft palate","type":"exact"},{"name":"soft palate cancer","type":"exact"}],"termid":"MONDO:0004611","xrefs":{"Monarch":{"xref_id":"0004611"}}}


id: GO:0090339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of formin-nucleated actin cable assembly. Formin-nucleated actin cable assembly is the aggregation, arrangement and bonding together of a set of components to form a formin-nucleated actin cable. A formin-nucleated actin cable is an actin filament bundle that consists of short filaments organized into bundles of uniform polarity, and is nucleated by formins.","definition_xrefs":["GOC:tb","PMID:15923184","GOC:jh","PMID:12810699"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of actin filament bundle assembly","termid":"GO:0032232"},{"relation_name":"is_a","term_name":"regulation of formin-nucleated actin cable assembly","termid":"GO:0090337"},{"relation_name":"negatively_regulates","term_name":"formin-nucleated actin cable assembly","termid":"GO:0070649"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0044085","GO:0030036","GO:0008150"],"is_obsolete":false,"name":"negative regulation of formin-nucleated actin cable assembly","termid":"GO:0090339"}


id: PBO:0027093
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_rDNA_copy_number","termid":"PBO:0027093"}


id: GO:0001509
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of proteins and small-molecule substrates at Asn-Xaa bonds.","definition_xrefs":["EC:3.4.22.34"],"gene_count":0,"genotype_count":0,"name":"obsolete legumain activity (obsolete GO:0001509)","synonyms":[{"name":"PRSC1 gene product (Homo sapiens)","type":"related"},{"name":"asparaginyl endopeptidase activity","type":"related"},{"name":"bean endopeptidase activity","type":"related"},{"name":"citvac","type":"related"},{"name":"hemoglobinase activity","type":"related"},{"name":"legumain activity","type":"exact"},{"name":"phaseolin activity","type":"related"},{"name":"proteinase B","type":"related"},{"name":"vicilin peptidohydrolase activity","type":"related"}],"termid":"GO:0001509"}


id: FYPO:0001592
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 import of arginine into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased amino acid import during vegetative growth","termid":"FYPO:0001360"},{"relation_name":"is_a","term_name":"abnormal arginine import","termid":"FYPO:0001654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased arginine import","synonyms":[{"name":"decreased L-arginine import","type":"exact"},{"name":"decreased L-arginine import across plasma membrane","type":"exact"},{"name":"decreased arginine import during mitotic cell cycle","type":"related"},{"name":"decreased arginine import during vegetative growth","type":"exact"},{"name":"decreased arginine import into cell","type":"exact"},{"name":"decreased arginine uptake","type":"exact"},{"name":"reduced arginine import","type":"exact"}],"termid":"FYPO:0001592"}


id: GO:1900795
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of terrequinone A.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete terrequinone A catabolic process (obsolete GO:1900795)","synonyms":[{"name":"terrequinone A breakdown","type":"exact"},{"name":"terrequinone A catabolism","type":"exact"},{"name":"terrequinone A degradation","type":"exact"}],"termid":"GO:1900795"}


id: GO:1905097
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of guanyl-nucleotide exchange factor activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:20484009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of GTPase activity","termid":"GO:0043087"},{"relation_name":"is_a","term_name":"regulation of binding","termid":"GO:0051098"}],"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 guanyl-nucleotide exchange factor activity","synonyms":[{"name":"regulation of GDP-dissociation stimulator activity","type":"exact"},{"name":"regulation of GDS","type":"exact"},{"name":"regulation of GEF","type":"exact"},{"name":"regulation of GNRP","type":"narrow"},{"name":"regulation of guanyl-nucleotide release factor activity","type":"exact"},{"name":"regulation of guanyl-nucleotide releasing factor","type":"exact"}],"termid":"GO:1905097"}


id: GO:0032444
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transcriptionally active complex that binds to an activin response element (ARE) in the promoter of target genes, and is composed of two SMAD2 proteins, one SMAD4 protein and a Forkhead activin signal transducer (FAST) transcription factor.","definition_xrefs":["PMID:12374795","PMID:9288972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"activin responsive factor complex","synonyms":[{"name":"ARF complex","type":"exact"}],"termid":"GO:0032444"}


id: GO:0004102
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + choline = acetylcholine + CoA.","definition_xrefs":["EC:2.3.1.6","RHEA:18821"],"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:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016746","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"choline O-acetyltransferase activity","secondary_identifiers":["KEGG_REACTION:R01023","MetaCyc:CHOLINE-O-ACETYLTRANSFERASE-RXN","Reactome:R-HSA-264622"],"synonyms":[{"name":"CHOACTase activity","type":"related"},{"name":"acetyl-CoA:choline O-acetyltransferase activity","type":"related"},{"name":"choline acetylase activity","type":"related"},{"name":"choline acetyltransferase activity","type":"related"}],"termid":"GO:0004102"}


id: GO:0047062
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+-)-trans-acenaphthene-1,2-diol + 2 NADP+ = acenaphthene-1,2-dione + 2 H+ + 2 NADPH.","definition_xrefs":["EC:1.10.1.1","RHEA:22184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors, NAD or NADP as acceptor","termid":"GO:0016680"}],"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:0016491","GO:0003674"],"is_obsolete":false,"name":"trans-acenaphthene-1,2-diol dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R04059","MetaCyc:1.10.1.1-RXN"],"synonyms":[{"name":"(+-)-trans-acenaphthene-1,2-diol:NADP+ oxidoreductase activity","type":"related"},{"name":"trans-1,2-acenaphthenediol dehydrogenase activity","type":"related"}],"termid":"GO:0047062"}


id: FYPO:0006729
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 regions of chromatin distal to replication origins is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to chromatin during vegetative growth","termid":"FYPO:0002909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein localization to chromatin distal to replication origin","synonyms":[{"name":"decreased protein localisation to chromatin distal to replication origin","type":"exact"},{"name":"decreased protein localization to chromatin distal to replication origin during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to chromatin distal to replication origin during vegetative growth","type":"exact"},{"name":"reduced protein localization to chromatin distal to replication origin","type":"exact"}],"termid":"FYPO:0006729"}


id: MONDO:0009018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Central cloudy dystrophy of François is a very rare form of stromal corneal dystrophy characterized by polygonal or rounded stromal opacities surrounded by clear tissue, and generally no effect on vision.","definition_xrefs":["Orphanet:98972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stromal corneal dystrophy","termid":"MONDO:0020213"},{"relation_name":"is_a","term_name":"posterior corneal dystrophy","termid":"MONDO:0020214"}],"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":"central cloudy dystrophy of François","secondary_identifiers":["MESH:C563262","SCTID:419074008","UMLS:C1622427","GARD:16881","OMIM:217600","MEDGEN:302006"],"synonyms":[{"name":"CCDF","type":"exact"},{"name":"central cloudy corneal dystrophy of François","type":"exact"},{"name":"central cloudy dystrophy of Francois","type":"exact"},{"name":"central cloudy dystrophy of François","type":"exact"},{"name":"corneal dystrophy, central type","type":"related"}],"termid":"MONDO:0009018","xrefs":{"Monarch":{"xref_id":"0009018"}}}


id: MONDO:0013589
data:
  {"annotated_genes":["SJAG_04001"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85467],"is_not":false,"summary":null,"term":"MONDO:0013589"}]},"cv_name":"mondo","definition":"Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the MYO1E gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited focal segmental glomerulosclerosis","termid":"MONDO:0005363"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04001":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"focal segmental glomerulosclerosis 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:614131","DOID:0111131","UMLS:C3279905","GARD:15761","MEDGEN:481535"],"synonyms":[{"name":"FSGS6","type":"exact"},{"name":"MYO1E focal segmental glomerulosclerosis","type":"exact"},{"name":"focal segmental glomerulosclerosis 6","type":"exact"},{"name":"focal segmental glomerulosclerosis caused by mutation in MYO1E","type":"exact"},{"name":"focal segmental glomerulosclerosis type 6","type":"exact"},{"name":"glomerulosclerosis, focal segmental, 6","type":"related"}],"termid":"MONDO:0013589","terms_by_termid":{"MONDO:0013589":null},"xrefs":{"Monarch":{"xref_id":"0013589"}}}


id: MONDO:0035592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lipomatosis","termid":"MONDO:0006574"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital infiltrating lipomatosis of the face","secondary_identifiers":["Orphanet:583097","UMLS:C5680341","GARD:22333","ICD10CM:Q87.3","icd11.foundation:1669603167","MEDGEN:1814459"],"synonyms":[{"name":"CIL-F","type":"exact"},{"name":"facial infused lipomatosis","type":"exact"},{"name":"fibroadipose infiltrating lipomatosis","type":"exact"}],"termid":"MONDO:0035592","xrefs":{"Monarch":{"xref_id":"0035592"}}}


id: PATO:0002287
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An elasticity which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"elastic","termid":"PATO:0001171"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased elasticity","termid":"PATO:0002287"}


id: PATO:0001092
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001092 flux value (obsolete PATO:0001092)","termid":"PATO:0001092"}


id: FYPO:0006114
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 during S phase of the mitotic cell cycle is higher than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0006551","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased protein level during mitotic S phase","synonyms":[{"name":"increased protein accumulation during mitotic S phase","type":"related"},{"name":"increased protein level during S phase of mitotic cell cycle","type":"related"},{"name":"increased protein level during mitotic S phase during vegetative growth","type":"exact"}],"termid":"FYPO:0006114"}


id: FYPO:0001544
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 sulfur measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal cellular sulfur level","synonyms":[{"name":"normal cellular sulfur accumulation","type":"related"},{"name":"normal cellular sulfur level during mitotic cell cycle","type":"related"},{"name":"normal cellular sulfur level during vegetative growth","type":"exact"},{"name":"normal cellular sulphur level","type":"exact"}],"termid":"FYPO:0001544"}


id: PBO:0000283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein Pfs2","termid":"PBO:0000283"}


id: PBO:0080191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular endothelial growth factor D","termid":"PBO:0080191"}


id: PBO:0086580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; deletion mutant has no detectable phenotype","termid":"PBO:0086580"}


id: GO:0048406
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to nerve growth factor (NGF).","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotrophin binding","termid":"GO:0043121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"nerve growth factor binding","synonyms":[{"name":"NGF binding","type":"exact"},{"name":"beta-nerve growth factor binding","type":"exact"},{"name":"neurotrophin TRKA receptor activity","type":"related"}],"termid":"GO:0048406"}


id: PBO:0031149
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_polysaccharide_level","termid":"PBO:0031149"}


id: MONDO:0019676
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by incomplete development (hypoplasia) or absence of the outermost bones of the fingers and toes (distal phalanges) and nails. Additional features may include hypoplasia of the middle phalanges, fusion of the joints (symphalangism), broad thumbs, and webbed fingers (syndactyly). The feet are often less severely affected than the hands. There are 2 types of this condition, designated as type 1 and 2. BDB type 1 is caused by mutations in the ROR2 gene. BDB type 2 is caused by mutations in the NOG gene. Inheritance of both types is autosomal dominant. Treatment may include surgery if the condition affects hand function, or for cosmetic reasons.","definition_xrefs":["GARD:0000985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly","termid":"MONDO:0021004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly type B","secondary_identifiers":["UMLS:C1300267","GARD:985","MEDGEN:722046","Orphanet:93383","SCTID:389168002","icd11.foundation:1534264812"],"termid":"MONDO:0019676","xrefs":{"Monarch":{"xref_id":"0019676"}}}


id: PBO:0044206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cathepsin L pseudogene 4","termid":"PBO:0044206"}


id: GO:0060579
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a ventral spinal cord interneuron. Ventral spinal cord interneurons are cells located in the ventral portion of the spinal cord that transmit signals between sensory and motor neurons and are required for reflexive responses.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron fate commitment","termid":"GO:0048663"},{"relation_name":"is_a","term_name":"cell fate commitment involved in pattern specification","termid":"GO:0060581"},{"relation_name":"part_of","term_name":"spinal cord dorsal/ventral patterning","termid":"GO:0021513"},{"relation_name":"part_of","term_name":"ventral spinal cord interneuron differentiation","termid":"GO:0021514"}],"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":"ventral spinal cord interneuron fate commitment","termid":"GO:0060579"}


id: PBO:0005879
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein in cox1 intron-1","termid":"PBO:0005879"}


id: PBO:0041647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel auxiliary subunit alpha2delta 2","termid":"PBO:0041647"}


id: GO:0008993
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + L-rhamnulose = ADP + L-rhamnulose 1-phosphate.","definition_xrefs":["EC:2.7.1.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"carbohydrate kinase activity","termid":"GO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"rhamnulokinase activity","secondary_identifiers":["MetaCyc:RHAMNULOKIN-RXN","RHEA:20117"],"synonyms":[{"name":"ATP:L-rhamnulose 1-phosphotransferase activity","type":"related"},{"name":"L-rhamnulokinase activity","type":"related"},{"name":"L-rhamnulose kinase activity","type":"related"},{"name":"RhuK","type":"related"},{"name":"rhamnulokinase (phosphorylating)","type":"related"},{"name":"rhamnulose kinase activity","type":"related"}],"termid":"GO:0008993"}


id: MONDO:0010743
data:
  {"annotated_genes":["SJAG_01732"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86717],"is_not":false,"summary":null,"term":"MONDO:0010743"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited thrombocytopenia","termid":"MONDO:0100241"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01732":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombocytopenia 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:313900","GARD:5176","Orphanet:852","MESH:C564052","MEDGEN:326416","UMLS:C1839163","NCIT:C176617"],"synonyms":[{"name":"THC","type":"related"},{"name":"THC1","type":"related"},{"name":"X-linked thrombocytopenia","type":"related"},{"name":"X-linked thrombocytopenia with normal platelets","type":"exact"},{"name":"XLT","type":"related"},{"name":"thrombocytopenia 1","type":"exact"},{"name":"thrombocytopenia type 1","type":"exact"},{"name":"thrombocytopenia, X-linked","type":"related"},{"name":"thrombocytopenia, X-linked, 1","type":"related"},{"name":"thrombocytopenia, X-linked, X-linked recessive","type":"exact"},{"name":"thrombocytopenia, X-linked, intermittent","type":"related"},{"name":"thrombocytopenia, X-linked, intermittent, X-linked recessive","type":"exact"}],"termid":"MONDO:0010743","terms_by_termid":{"MONDO:0010743":null},"xrefs":{"Monarch":{"xref_id":"0010743"}}}


id: PBO:0034331
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-before","termid":"PBO:0034331"}


id: PBO:0063893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class Q pseudogene 1","termid":"PBO:0063893"}


id: MONDO:0033200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"hearing loss, autosomal recessive 108","secondary_identifiers":["MEDGEN:1627841","OMIM:617654","UMLS:C4539997","DOID:0080263","GARD:22658"],"synonyms":[{"name":"DFNB108","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 108","type":"narrow"},{"name":"deafness, autosomal recessive 108","type":"narrow"}],"termid":"MONDO:0033200","xrefs":{"Monarch":{"xref_id":"0033200"}}}


id: GO:0032086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of a type III restriction endodeoxyribonuclease activity.","definition_xrefs":["GOC:dph","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of type III site-specific deoxyribonuclease activity (obsolete GO:0032086)","synonyms":[{"name":"regulation of type III restriction endoribonuclease activity","type":"exact"},{"name":"type III restriction endodeoxyribonuclease regulator","type":"related"},{"name":"type III restriction enzyme regulator","type":"related"}],"termid":"GO:0032086"}


id: PBO:0082978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic trifunctional enzyme; catalyzes sequential reactions 10-formyl-THF synthetase (EC 6.3.4.3), 5,10-methenyl-THF cyclohydrolase (EC 3.5.4.9), and 5,10-methylene-THF dehydrogenase (EC 1.5.1.5), to supply forms of activated one-carbon units required for biosynthesis of purines, histidine, methionine, pantothenic acid, the formyl group of mitochondrial fMet-tRNAfMet, and the methyl group of thymidylate; null mutation causes auxotrophy for adenine and histidine in rich medium","termid":"PBO:0082978"}


id: MONDO:0014210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability-hypotonia-spasticity-sleep disorder syndrome","secondary_identifiers":["Orphanet:356996","UMLS:C3809672","DOID:0081202","MEDGEN:816002","GARD:17541","OMIM:615493"],"synonyms":[{"name":"MRT37","type":"related"},{"name":"intellectual disability, autosomal recessive 37","type":"related"},{"name":"intellectual disability, autosomal recessive type 37","type":"exact"},{"name":"mental retardation, autosomal recessive 37","type":"related"},{"name":"mental retardation, autosomal recessive type 37","type":"exact"},{"name":"mental retardation, autosomal recessive, 37","type":"exact"}],"termid":"MONDO:0014210","xrefs":{"Monarch":{"xref_id":"0014210"}}}


id: PBO:0065096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase AMP-activated non-catalytic subunit gamma 3","termid":"PBO:0065096"}


id: PBO:0028318
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_mitochondrial_fission_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0028318"}


id: PBO:0001864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S2 (predicted)","termid":"PBO:0001864"}


id: PBO:0083414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the essential gene RPP0","termid":"PBO:0083414"}


id: PBO:0054481
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 1881","termid":"PBO:0054481"}


id: PBO:0075039
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 116-2","termid":"PBO:0075039"}


id: PBO:0089155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterochromatin (HP1) family chromodomain protein Swi6","termid":"PBO:0089155"}


id: GO:0044092
data:
  {"annotated_genes":["SJAG_03088","SJAG_04887"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104620,94792],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904530"}]},"cv_name":"biological_process","definition":"Any process that stops or reduces the rate or extent of a molecular function, an elemental biological activity occurring at the molecular level, such as catalysis or binding.","definition_xrefs":["GO:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of molecular function","termid":"GO:0065009"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03088":null,"SJAG_04887":null},"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 molecular function","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0044092","terms_by_termid":{"GO:1904530":null}}


id: GO:1901533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of hematopoietic progenitor cell differentiation.","definition_xrefs":["GOC:BHF","GOC:rl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"regulation of hematopoietic progenitor cell differentiation","termid":"GO:1901532"},{"relation_name":"negatively_regulates","term_name":"hematopoietic progenitor cell differentiation","termid":"GO:0002244"}],"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 hematopoietic progenitor cell differentiation","synonyms":[{"name":"down regulation of haematopoietic progenitor cell differentiation","type":"exact"},{"name":"down regulation of haemopoietic progenitor cell differentiation","type":"exact"},{"name":"down regulation of hematopoietic progenitor cell differentiation","type":"related"},{"name":"down regulation of hemopoietic progenitor cell differentiation","type":"exact"},{"name":"down-regulation of haematopoietic progenitor cell differentiation","type":"exact"},{"name":"down-regulation of haemopoietic progenitor cell differentiation","type":"exact"},{"name":"down-regulation of hematopoietic progenitor cell differentiation","type":"related"},{"name":"down-regulation of hemopoietic progenitor cell differentiation","type":"exact"},{"name":"downregulation of haematopoietic progenitor cell differentiation","type":"exact"},{"name":"downregulation of haemopoietic progenitor cell differentiation","type":"exact"},{"name":"downregulation of hematopoietic progenitor cell differentiation","type":"related"},{"name":"downregulation of hemopoietic progenitor cell differentiation","type":"exact"},{"name":"inhibition of haematopoietic progenitor cell differentiation","type":"exact"},{"name":"inhibition of haemopoietic progenitor cell differentiation","type":"exact"},{"name":"inhibition of hematopoietic progenitor cell differentiation","type":"related"},{"name":"inhibition of hemopoietic progenitor cell differentiation","type":"narrow"},{"name":"negative regulation of haematopoietic progenitor cell differentiation","type":"exact"},{"name":"negative regulation of haemopoietic progenitor cell differentiation","type":"exact"},{"name":"negative regulation of hemopoietic progenitor cell differentiation","type":"exact"}],"termid":"GO:1901533"}


id: PBO:0003751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EST1 family protein (predicted)","termid":"PBO:0003751"}


id: PBO:0042733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein K","termid":"PBO:0042733"}


id: FYPO:0004995
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the first meiotic nuclear division begins at the normal (i.e. indistinguishable from wild type) time relative to other cell cycle events.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal meiosis I","termid":"FYPO:0003563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal onset of meiosis I","synonyms":[{"name":"normal meiosis I progression","type":"related"},{"name":"normal onset of first meiotic nuclear division","type":"exact"},{"name":"normal timing of meiosis I","type":"related"}],"termid":"FYPO:0004995"}


id: PBO:0027786
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_serine_phosphorylation_during_nitrogen_starvation","termid":"PBO:0027786"}


id: GO:0102438
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: laricitrin(1-) + S-adenosyl-L-methionine = H+ + 3',4'-dimethylmyricetin + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete laricitrin 4'-O-methyltransferase activity (obsolete GO:0102438)","termid":"GO:0102438"}


id: GO:0048286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the alveolus over time, from its formation to the mature structure. The alveolus is a sac for holding air in the lungs; formed by the terminal dilation of air passageways.","definition_xrefs":["PMID:9751757","GOC:mtg_lung"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"lung development","termid":"GO:0030324"}],"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":"lung alveolus development","synonyms":[{"name":"alveolarization","type":"exact"},{"name":"alveologenesis","type":"exact"}],"termid":"GO:0048286"}


id: PBO:0004441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"snoRNP pseudouridylase box H/ACA snoRNP complex protein Gar1","termid":"PBO:0004441"}


id: PBO:0111536
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSF-Responsive amino acid Gene","termid":"PBO:0111536"}


id: GO:0016410
data:
  {"annotated_genes":["SJAG_00469","SJAG_01826","SJAG_04131","SJAG_04535","SJAG_01638","SJAG_01619","SJAG_01877","SJAG_02309","SJAG_04791","SJAG_03961","SJAG_00097","SJAG_02773","SJAG_00695","SJAG_04631","SJAG_01592","SJAG_02842","SJAG_00102","SJAG_00676","SJAG_02296","SJAG_01899","SJAG_01204","SJAG_03112","SJAG_02165","SJAG_00246","SJAG_03288","SJAG_00519","SJAG_03162","SJAG_02990","SJAG_02726","SJAG_03537","SJAG_02085"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104866],"is_not":false,"summary":null,"term":"GO:0016410"},{"annotations":[95280,77986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003870"},{"annotations":[100116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004059"},{"annotations":[92267],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046941"},{"annotations":[87748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047198"},{"annotations":[100117,86928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004145"},{"annotations":[70472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004343"},{"annotations":[102113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004358"},{"annotations":[107827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004379"},{"annotations":[90923,98469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140068"},{"annotations":[117981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043998"},{"annotations":[90924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010484"},{"annotations":[90272,90925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036408"},{"annotations":[90926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043993"},{"annotations":[98470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044016"},{"annotations":[108784,108783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032931"},{"annotations":[90927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043992"},{"annotations":[117982,98471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010485"},{"annotations":[87945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043997"},{"annotations":[87946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043995"},{"annotations":[87947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043996"},{"annotations":[102114,111358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004042"},{"annotations":[116696,110567,102075,102510],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008080"},{"annotations":[98472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106226"},{"annotations":[117427,114792,103067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004596"},{"annotations":[98473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140065"},{"annotations":[98474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034212"},{"annotations":[88909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008999"},{"annotations":[88910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990190"},{"annotations":[103478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061733"},{"annotations":[103068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120518"},{"annotations":[88911,117983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990189"},{"annotations":[111515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046027"},{"annotations":[92124],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990883"},{"annotations":[91413,109532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050291"},{"annotations":[92126,106790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051392"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an acyl group to a nitrogen atom on the acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":31,"genes_by_uniquename":{"SJAG_00097":null,"SJAG_00102":null,"SJAG_00246":null,"SJAG_00469":null,"SJAG_00519":null,"SJAG_00676":null,"SJAG_00695":null,"SJAG_01204":null,"SJAG_01592":null,"SJAG_01619":null,"SJAG_01638":null,"SJAG_01826":null,"SJAG_01877":null,"SJAG_01899":null,"SJAG_02085":null,"SJAG_02165":null,"SJAG_02296":null,"SJAG_02309":null,"SJAG_02726":null,"SJAG_02773":null,"SJAG_02842":null,"SJAG_02990":null,"SJAG_03112":null,"SJAG_03162":null,"SJAG_03288":null,"SJAG_03537":null,"SJAG_03961":null,"SJAG_04131":null,"SJAG_04535":null,"SJAG_04631":null,"SJAG_04791":null},"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:0016740","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"N-acyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9858752","Reactome:R-HSA-177160","Reactome:R-HSA-6792572"],"termid":"GO:0016410","terms_by_termid":{"GO:0003870":null,"GO:0004042":null,"GO:0004059":null,"GO:0004145":null,"GO:0004343":null,"GO:0004358":null,"GO:0004379":null,"GO:0004596":null,"GO:0008080":null,"GO:0008999":null,"GO:0010484":null,"GO:0010485":null,"GO:0016410":null,"GO:0032931":null,"GO:0034212":null,"GO:0036408":null,"GO:0043992":null,"GO:0043993":null,"GO:0043995":null,"GO:0043996":null,"GO:0043997":null,"GO:0043998":null,"GO:0044016":null,"GO:0046027":null,"GO:0046941":null,"GO:0047198":null,"GO:0050291":null,"GO:0051392":null,"GO:0061733":null,"GO:0106226":null,"GO:0120518":null,"GO:0140065":null,"GO:0140068":null,"GO:1990189":null,"GO:1990190":null,"GO:1990883":null}}


id: GO:0090637
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The desmosomal part containing the C-termini of desmoplakins which interact with the keratin intermediate filaments, serving to tether the intermediate filaments to the plasma membrane.","definition_xrefs":["PMID:20066089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"desmosome","termid":"GO:0030057"}],"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":"inner dense plaque of desmosome","termid":"GO:0090637"}


id: MONDO:0010635
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3.","definition_xrefs":["NCIT:C75480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kallmann syndrome","termid":"MONDO:0018800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 1 with or without anosmia","secondary_identifiers":["MEDGEN:295872","UMLS:C1563719","DOID:0090094","GARD:3071","OMIM:308700","ICD10CM:E23.0"],"synonyms":[{"name":"ANOS1 hypogonadotropic hypogonadism","type":"exact"},{"name":"HH1","type":"related"},{"name":"KAL1","type":"related"},{"name":"KMS","type":"related"},{"name":"Kallmann syndrome 1","type":"related"},{"name":"Kallmann syndrome, X-linked","type":"related"},{"name":"Kallmann syndrome, type 1, X-linked","type":"related"},{"name":"anosmic hypogonadism","type":"related"},{"name":"dysplasia Olfactogenitalis of De Morsier","type":"related"},{"name":"dysplasia olfactogenitalis of de Morsier","type":"exact"},{"name":"hypogonadotropic hypogonadism 1 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive","type":"exact"},{"name":"hypogonadotropic hypogonadism and anosmia","type":"related"},{"name":"hypogonadotropic hypogonadism caused by mutation in ANOS1","type":"exact"}],"termid":"MONDO:0010635","xrefs":{"Monarch":{"xref_id":"0010635"}}}


id: MONDO:1010209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lymphosarcoma that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-hodgkin lymphoma, non-human animal","termid":"MONDO:1010214"},{"relation_name":"is_a","term_name":"lymphoid system disorder, non-human animal","termid":"MONDO:1011330"},{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lymphosarcoma, non-human animal","secondary_identifiers":["OMIA:000615"],"termid":"MONDO:1010209","xrefs":{"Monarch":{"xref_id":"1010209"}}}


id: PR:O43026
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gpd3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43026"],"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":"glyceraldehyde-3-phosphate dehydrogenase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.12","synonyms":[{"name":"GAPDH 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gpd3","type":"exact"}],"termid":"PR:O43026"}


id: PBO:0075706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLIT-ROBO Rho GTPase activating protein 2","termid":"PBO:0075706"}


id: PBO:0083052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Diacylglycerol kinase; localized to the endoplasmic reticulum (ER); overproduction induces enlargement of ER-like membrane structures and suppresses a temperature-sensitive sly1 mutation; contains a CTP transferase domain","termid":"PBO:0083052"}


id: MONDO:0020492
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemimegalencephaly is a rare cerebral malformation characterized by overgrowth of all or part of a cerebral hemisphere, often with ipsilateral severe cortical dysplasia or dysgenesis, white matter hypertrophy and dilated lateral ventricle, presenting in early infancy with progressive hemiparesis, severe psychomotor retardation and intractable seizures. Hemimegalencephaly may be an isolated finding or associated with other syndromes such as angioosteohypertrophic syndrome, epidermal nevus syndrome and Ito hypomelanosis. Management includes seizure control by antiepileptic medications and early hemispherectomy.","definition_xrefs":["Orphanet:99802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes","termid":"MONDO:0100283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"hemimegalencephaly","secondary_identifiers":["NCIT:C177779","NANDO:1200563","icd11.foundation:961229160","GARD:2637","ICD9:742.4","MEDGEN:140910","NORD:1220","MESH:D065705","SCTID:253170008","UMLS:C0431391"],"synonyms":[{"name":"macrencephaly","type":"related"},{"name":"unilateral megalencephaly","type":"exact"}],"termid":"MONDO:0020492","xrefs":{"Monarch":{"xref_id":"0020492"}}}


id: PR:O74968
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- usp102 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74968"],"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":"U1 small nuclear ribonucleoprotein usp102 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4B4.07c","synonyms":[{"name":"Spom972h-usp102","type":"exact"},{"name":"U1 snRNP protein usp102 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74968"}


id: PBO:0041936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBX3 pseudogene 4","termid":"PBO:0041936"}


id: FYPO:0003488
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is elongated during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete elongated cell during cellular response to ionizing radiation (obsolete FYPO:0003488)","synonyms":[{"name":"elongated cell during cellular response to IR","type":"exact"},{"name":"elongated cell during cellular response to ionizing radiation during mitotic cell cycle","type":"related"},{"name":"elongated cell during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"elongated in response to ionizing radiation","type":"exact"}],"termid":"FYPO:0003488"}


id: GO:0033223
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of 2-aminoethylphosphonate, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"2-aminoethylphosphonate transport","synonyms":[{"name":"2-phosphonoethylamine transport","type":"exact"},{"name":"ciliatine transport","type":"exact"}],"termid":"GO:0033223"}


id: PBO:0076852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymocyte expressed, positive selection associated 1","termid":"PBO:0076852"}


id: FYPO:0007132
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of a protein to one or more microtubules occurs to a greater extent than normal. The affected protein may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein-protein interaction","termid":"FYPO:0001571"},{"relation_name":"is_a","term_name":"abnormal microtubule binding","termid":"FYPO:0001943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000702","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"increased microtubule binding","termid":"FYPO:0007132"}


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:0030596
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_substance_in_cytosol","termid":"PBO:0030596"}


id: PBO:0066258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMX like 1","termid":"PBO:0066258"}


id: PBO:0090965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase III complex large subunit Rpc1","termid":"PBO:0090965"}


id: MONDO:0032591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hyperparathyroidism","termid":"MONDO:0016166"},{"relation_name":"is_a","term_name":"abnormal mineralization disorder","termid":"MONDO:0800096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperparathyroidism, transient neonatal","secondary_identifiers":["MEDGEN:722059","OMIM:618188","UMLS:C1300287","GARD:16304"],"synonyms":[{"name":"HRPTTN","type":"exact"},{"name":"hyperparathyroidism, transient neonatal","type":"exact"}],"termid":"MONDO:0032591","xrefs":{"Monarch":{"xref_id":"0032591"}}}


id: PBO:0082217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha 6 subunit of the 20S proteasome; protein abundance increases in response to DNA replication stress","termid":"PBO:0082217"}


id: GO:0060311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of elastin catabolism, the chemical reactions and pathways resulting in the breakdown of elastin.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein catabolic process","termid":"GO:0042177"},{"relation_name":"is_a","term_name":"regulation of elastin catabolic process","termid":"GO:0060310"},{"relation_name":"is_a","term_name":"negative regulation of glycoprotein metabolic process","termid":"GO:1903019"},{"relation_name":"negatively_regulates","term_name":"elastin catabolic process","termid":"GO:0060309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0030163"},{"rel_name":"negatively_regulates","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030163","GO:0008150"],"is_obsolete":false,"name":"negative regulation of elastin catabolic process","synonyms":[{"name":"down-regulation of elastin catabolic process","type":"exact"},{"name":"negative regulation of elastin breakdown","type":"exact"},{"name":"negative regulation of elastin catabolism","type":"exact"},{"name":"negative regulation of elastin degradation","type":"exact"}],"termid":"GO:0060311"}


id: PBO:0003040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adducin","termid":"PBO:0003040"}


id: PBO:0109085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosylceramidase beta 1 like, pseudogene","termid":"PBO:0109085"}


id: GO:0045462
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the 3-O-acetylation of a trichothecene. Trichothecenes are sesquiterpene epoxide mycotoxins that act as potent inhibitors of eukaryotic protein synthesis.","definition_xrefs":["PMID:10583973"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"trichothecene 3-O-acetyltransferase activity","termid":"GO:0045462"}


id: GO:0047710
data:
  {"annotated_genes":["SJAG_04939"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110901],"is_not":false,"summary":null,"term":"GO:0047710"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: P(1),P(3)-bis(5'-adenosyl) triphosphate + H2O = ADP + AMP + 2 H+.","definition_xrefs":["EC:3.6.1.29","RHEA:13893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04939":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"bis(5'-adenosyl)-triphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:BIS5-ADENOSYL-TRIPHOSPHATASE-RXN","KEGG_REACTION:R00187"],"synonyms":[{"name":"1-P,3-P-bis(5'-adenosyl)-triphosphate adenylohydrolase activity","type":"related"},{"name":"AP(3)A hydrolase activity","type":"related"},{"name":"AP(3)Aase activity","type":"related"},{"name":"AP3A hydrolase activity","type":"related"},{"name":"AP3Aase activity","type":"related"},{"name":"P1,P3-bis(5'-adenosyl)-triphosphate adenylohydrolase activity","type":"related"},{"name":"diadenosine 5',5'''-P(1),P(3)-triphosphate hydrolase activity","type":"related"},{"name":"diadenosine 5',5'''-P1,P3-triphosphate hydrolase activity","type":"related"},{"name":"diadenosine 5,5-P1,P3-triphosphatase activity","type":"related"},{"name":"dinucleosidetriphosphatase activity","type":"related"}],"termid":"GO:0047710","terms_by_termid":{"GO:0047710":null}}


id: PBO:0085181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"One of three alternate beta subunits of the Snf1 kinase complex; involved in the response to glucose starvation; null mutants exhibit accelerated aging; N-myristoylprotein localized to the cytoplasm and the plasma membrane; SIP2 has a paralog, GAL83, that arose from the whole genome duplication","termid":"PBO:0085181"}


id: MONDO:0001668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth resorption","termid":"MONDO:0001670"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internal pathological resorption of tooth","secondary_identifiers":["MEDGEN:540237","DOID:13239","SCTID:52994003","ICD9:521.41","UMLS:C0266880"],"synonyms":[{"name":"internal granuloma of pulp","type":"related"},{"name":"internal pathologic resorption","type":"exact"},{"name":"internal pathological resorption","type":"related"},{"name":"internal resorption of crown of tooth","type":"related"},{"name":"internal resorption of tooth","type":"exact"},{"name":"pathological tooth resorption - internal","type":"related"},{"name":"pink spot lesion of tooth","type":"related"},{"name":"pink tooth of mummery","type":"related"}],"termid":"MONDO:0001668","xrefs":{"Monarch":{"xref_id":"0001668"}}}


id: GO:1904494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of substance P secretion, neurotransmission.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:15292051"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neurotransmitter secretion","termid":"GO:0046928"},{"relation_name":"is_a","term_name":"regulation of substance P secretion","termid":"GO:1904458"},{"relation_name":"regulates","term_name":"substance P secretion, neurotransmission","termid":"GO:1990793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"regulation of substance P secretion, neurotransmission","termid":"GO:1904494"}


id: PBO:0061900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opioid receptor delta 1","termid":"PBO:0061900"}


id: MONDO:0859286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures","secondary_identifiers":["DOID:0070536","MEDGEN:1823986","OMIM:620029","UMLS:C5774213"],"termid":"MONDO:0859286","xrefs":{"Monarch":{"xref_id":"0859286"}}}


id: MONDO:0100386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly t(v;11q23.3). (A chromosomal abnormality consisting of the translocation of genetic material from any one of several chromosomes to the 11q23.3 region, resulting in an MLL gene rearrangement.)","definition_xrefs":["NCIT:C36517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"acute myeloid leukemia, t(v;11q23.3)","synonyms":[{"name":"AML, 11q23.3 Translocation","type":"exact"},{"name":"AML, t(11;v)(q23.3;v)","type":"exact"},{"name":"AML, t(11;v)(q23;v)","type":"exact"},{"name":"AML, t(V;11)(v;q23)","type":"exact"},{"name":"AML, t(V;11)(v;q23.3)","type":"exact"},{"name":"AML, t(v;11q23.3)","type":"exact"}],"termid":"MONDO:0100386","xrefs":{"Monarch":{"xref_id":"0100386"}}}


id: GO:0009626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The rapid, localized death of plant cells in response to invasion by a pathogen.","definition_xrefs":["ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"},{"relation_name":"is_a","term_name":"symbiont-induced defense-related programmed cell death","termid":"GO:0034050"},{"relation_name":"is_a","term_name":"innate immune response","termid":"GO:0045087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"plant-type hypersensitive response","synonyms":[{"name":"HR","type":"broad"},{"name":"HR-PCD","type":"exact"},{"name":"plant hypersensitive response","type":"exact"}],"termid":"GO:0009626"}


id: FYPO:0003688
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 nucleolus is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus during vegetative growth","termid":"FYPO:0001424"},{"relation_name":"is_a","term_name":"abnormal protein localization to nucleolus","termid":"FYPO:0003687"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to nucleolus","synonyms":[{"name":"abolished protein localisation to nucleolus","type":"exact"},{"name":"abolished protein localization in nucleolus","type":"exact"},{"name":"abolished protein localization to nucleolus during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to nucleolus during vegetative growth","type":"exact"},{"name":"protein localization to nucleolus abolished","type":"exact"}],"termid":"FYPO:0003688"}


id: FYPO:0001410
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 sulfide (S2-, also called acid labile sulfide) measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal cellular sulfide level","synonyms":[{"name":"normal cellular acid labile sulfide level","type":"exact"},{"name":"normal cellular sulfide accumulation","type":"related"},{"name":"normal cellular sulfide ion level","type":"exact"},{"name":"normal cellular sulfide level during mitotic cell cycle","type":"related"},{"name":"normal cellular sulfide level during vegetative growth","type":"exact"},{"name":"normal cellular sulphide level","type":"exact"}],"termid":"FYPO:0001410"}


id: PBO:0016072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial S-adenosylmethionine transporter (predicted)","termid":"PBO:0016072"}


id: GO:0018179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The desulfurization of peptidyl-L-cysteine to yield L-alanine and elemental sulfur; peptidyl-L-cysteine persulfide is an intermediate.","definition_xrefs":["RESID:AA0269"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-cysteine desulfurization (obsolete GO:0018179)","synonyms":[{"name":"peptidyl-cysteine desulfurization","type":"exact"},{"name":"peptidyl-cysteine desulphurization","type":"exact"}],"termid":"GO:0018179"}


id: PBO:0064608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 4 homeobox 2","termid":"PBO:0064608"}


id: PBO:0076226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPT7 like, STAGA complex subunit gamma","termid":"PBO:0076226"}


id: PATO:0002435
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer touching another entity along a border or with a projecting part.","definition_xrefs":["merriam-webster:merriam-webster"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abut","termid":"PATO:0002435"}


id: PBO:0060957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFKB inhibitor delta","termid":"PBO:0060957"}


id: FYPO:0006077
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 methylation of lysine at position 9 of histone H3 occurs to a greater extent than normal at ribosomal DNA.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000871"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002274","FYPO:0000002","FYPO:0002494","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased histone H3-K9 methylation at rDNA during vegetative growth","synonyms":[{"name":"increased histone H3 K9 methylation at rDNA during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 methylation at rDNA during mitotic cell cycle","type":"related"},{"name":"increased histone H3-K9 methylation at ribosomal DNA during vegetative growth","type":"exact"},{"name":"increased histone H3K9 methylation at rDNA during vegetative growth","type":"exact"},{"name":"increased histone H3K9me at rDNA during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 methylation at rDNA during vegetative growth","type":"exact"}],"termid":"FYPO:0006077"}


id: PBO:0083345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the verified gene DAD4/YDR320C-A","termid":"PBO:0083345"}


id: PBO:0043128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIBAR1 divergent transcript","termid":"PBO:0043128"}


id: PBO:0075839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSU72 homolog, RNA polymerase II CTD phosphatase","termid":"PBO:0075839"}


id: GO:1903412
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 bile acid stimulus.","definition_xrefs":["GOC:BHF","GO_REF:0000071","PMID:21757002","GOC:rl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to organic cyclic compound","termid":"GO:0014070"},{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to bile acid","termid":"GO:1903412"}


id: PBO:0083020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Deleted ORF; does not encode a protein; included in the original annotation of Chromosome I but later withdrawn","termid":"PBO:0083020"}


id: FYPO:0005747
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which protein transport is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport phenotype","termid":"FYPO:0000149"},{"relation_name":"is_a","term_name":"normal protein localization","termid":"FYPO:0003627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0000257"],"is_obsolete":false,"name":"normal protein transport","termid":"FYPO:0005747"}


id: PBO:0055379
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 2809","termid":"PBO:0055379"}


id: MONDO:0007282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in variation in the region 2pter-p24.","definition_xrefs":["PMID:15933805","DOID:0110232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cataract","termid":"MONDO:0005129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 29","secondary_identifiers":["UMLS:C3805409","GARD:18233","MEDGEN:811739","OMIM:115800"],"synonyms":[{"name":"CTRCT29","type":"related"},{"name":"cataract 29","type":"exact"},{"name":"cataract 29 coralliform","type":"exact"},{"name":"cataract 29, coralliform","type":"related"},{"name":"cataract type 29","type":"exact"}],"termid":"MONDO:0007282","xrefs":{"Monarch":{"xref_id":"0007282"}}}


id: PBO:0039324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arachidonate 12-lipoxygenase pseudogene 1","termid":"PBO:0039324"}


id: PBO:0080891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YTH domain family member 1 pseudogene 1","termid":"PBO:0080891"}


id: GO:0039655
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transport of a virus between adjacent cells in a multicellular organism using plasmodesmata. Plasmodesma is a fine cytoplasmic channel found in all higher plants, which connects the cytoplasm of one cell to that of an adjacent cell.","definition_xrefs":["VZ:1018","UniProtKB-KW:KW-0916"],"gene_count":0,"genotype_count":0,"name":"obsolete transport of virus in host, cell to cell via plasmodesmata (obsolete GO:0039655)","synonyms":[{"name":"spread of virus in host, cell to cell via plasmodesmata","type":"related"},{"name":"viral movement protein","type":"related"}],"termid":"GO:0039655"}


id: MONDO:0002788
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A craniopharyngioma composed of sheets of squamous epithelium which separate to form pseudopapillae. This variant typically lacks nuclear palisading, wet keratin, calcification, and cholesterol deposits. Clinically, endocrine deficiencies are more often associated with papillary craniopharyngioma than with the adamantinomatous type. (Adapted from WHO)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"craniopharyngioma","termid":"MONDO:0018907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillary craniopharyngioma","secondary_identifiers":["ICDO:9352/1","UMLS:C0431128","MEDGEN:98125","DOID:3847","NCIT:C4725"],"synonyms":[{"name":"craniopharyngioma, papillary","type":"exact"},{"name":"craniopharyngioma, papillary (morphologic abnormality)","type":"exact"},{"name":"papillary Rathke pouch neoplasm","type":"exact"},{"name":"papillary Rathke's pouch neoplasm","type":"exact"},{"name":"papillary Rathke's pouch tumor","type":"exact"},{"name":"papillary Rathke's pouch tumour","type":"exact"},{"name":"papillary craniopharyngioma (morphologic abnormality)","type":"exact"},{"name":"papillary neoplasm of Rathke's pouch","type":"exact"},{"name":"papillary tumor of Rathke's pouch","type":"exact"},{"name":"papillary tumour of Rathke's pouch","type":"exact"}],"termid":"MONDO:0002788","xrefs":{"Monarch":{"xref_id":"0002788"}}}


id: GO:0004575
data:
  {"annotated_genes":["SJAG_04301"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115569],"is_not":false,"summary":null,"term":"GO:0004575"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: sucrose + H2O = alpha-D-glucose + beta-D-fructose.","definition_xrefs":["RHEA:33795"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-fructofuranosidase activity","termid":"GO:0004564"},{"relation_name":"is_a","term_name":"alpha-glucosidase activity","termid":"GO:0090599"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04301":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"sucrose alpha-glucosidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-189069","MetaCyc:3.2.1.48-RXN","KEGG_REACTION:R00802","Reactome:R-HSA-5659926","EC:3.2.1.48"],"synonyms":[{"name":"alpha-D-glucopyranosyl beta-D-fructofuranoside hydrolysis","type":"broad"},{"name":"beta-D-fructofuranosyl alpha-D-glucopyranoside hydrolysis","type":"broad"},{"name":"intestinal sucrase activity","type":"related"},{"name":"sucrase activity","type":"related"},{"name":"sucrase(invertase)","type":"related"},{"name":"sucrase-isomaltase activity","type":"related"},{"name":"sucrose alpha-D-glucohydrolase activity","type":"exact"},{"name":"sucrose alpha-glucohydrolase activity","type":"related"},{"name":"sucrose hydrolysis","type":"broad"},{"name":"sucrose-alpha-D-glucohydrolase activity","type":"related"}],"termid":"GO:0004575","terms_by_termid":{"GO:0004575":null}}


id: GO:2001075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of metanephric ureteric bud development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of metanephric ureteric bud development","termid":"GO:2001074"},{"relation_name":"negatively_regulates","term_name":"metanephric part of ureteric bud development","termid":"GO:0035502"}],"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 metanephric ureteric bud development","termid":"GO:2001075"}


id: FYECO:0000001
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Any aspect of an experiment that the experimenter controls and that does not depend on which strain/organism/cells are used.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fission yeast phenotype condition","synonyms":[{"name":"phenotype condition","type":"related"}],"termid":"FYECO:0000001"}


id: PBO:0069317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 575, pseudogene","termid":"PBO:0069317"}


id: PBO:0109283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NRXN1 divergent transcript","termid":"PBO:0109283"}


id: PBO:0000183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP complex subunit Trs33 (predicted)","termid":"PBO:0000183"}


id: GO:1990694
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the Golgi medial cisterna membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:bhm","PMID:16038056","PMID:24119662"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of Golgi medial cisterna membrane (obsolete GO:1990694)","synonyms":[{"name":"intrinsic component of medial-Golgi cisterna membrane","type":"exact"}],"termid":"GO:1990694"}


id: GO:0030139
data:
  {"annotated_genes":["SJAG_00104","SJAG_03146","SJAG_00677","SJAG_01167","SJAG_03504","SJAG_00800","SJAG_02805","SJAG_02833","SJAG_01189"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[93321,107019,110136,110238,114907],"is_not":false,"summary":null,"term":"GO:0030139"},{"annotations":[95767,111041,111100,107790],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030122"}]},"cv_name":"cellular_component","definition":"A membrane-bounded intracellular vesicle formed by invagination of the plasma membrane around an extracellular substance. Endocytic vesicles fuse with early endosomes to deliver the cargo for further sorting.","definition_xrefs":["GOC:go_curators","PMID:19696797"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle","termid":"GO:0031410"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00677":null,"SJAG_00800":null,"SJAG_01167":null,"SJAG_01189":null,"SJAG_02805":null,"SJAG_02833":null,"SJAG_03146":null,"SJAG_03504":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"endocytic vesicle","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["NIF_Subcellular:sao1362520468"],"synonyms":[{"name":"endocytotic transport vesicle","type":"exact"},{"name":"endocytotic vesicle","type":"exact"}],"termid":"GO:0030139","terms_by_termid":{"GO:0030122":null,"GO:0030139":null}}


id: FYPO:0006140
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 1-eicosenoylglycerophosphocholine (20:1n9) measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah","PMID:28667014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased phospholipid level","termid":"FYPO:0001288"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular 1-eicosenoylglycerophosphocholine (20:1n9) level","synonyms":[{"name":"increased 1-eicosenoylglycerophosphocholine (20:1n9) accumulation","type":"related"},{"name":"increased cellular 1-(11Z)-icosenoyl-sn-glycero-3-phosphocholine level","type":"exact"},{"name":"increased cellular 1-eicosenoylglycerophosphocholine (20:1n9) level during mitotic cell cycle","type":"related"},{"name":"increased cellular 1-eicosenoylglycerophosphocholine (20:1n9) level during vegetative growth","type":"exact"}],"termid":"FYPO:0006140"}


id: PBO:0040672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B cell receptor associated protein 31","termid":"PBO:0040672"}


id: GO:0033787
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cob(I)alamin + hydrogen cyanide + NADP+ = cyanocob(III)alamin + H+ + NADPH.","definition_xrefs":["RHEA:16113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on metal ions, NAD or NADP as acceptor","termid":"GO:0016723"}],"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":"cyanocobalamin reductase (cyanide-eliminating) (NADP+) activity","secondary_identifiers":["MetaCyc:1.6.99.12-RXN","Reactome:R-HSA-3149519","EC:1.16.1.6","KEGG_REACTION:R02999"],"synonyms":[{"name":"NADPH2:cyanocob(III)alamin oxidoreductase (cyanide-eliminating) activity","type":"related"},{"name":"NADPH:cyanocob(III)alamin oxidoreductase (cyanide-eliminating) activity","type":"related"},{"name":"cob(I)alamin, cyanide:NADP+ oxidoreductase activity","type":"related"},{"name":"cyanocobalamin reductase (NADPH, cyanide-eliminating) activity","type":"related"},{"name":"cyanocobalamin reductase (NADPH; CN-eliminating) activity","type":"related"},{"name":"cyanocobalamin reductase activity","type":"related"}],"termid":"GO:0033787"}


id: GO:0098778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The secretion of soluble curli subunits through the outer membrane, coupled to nucleation of curli fiber formation at the membrane surface.","definition_xrefs":["PMID:24080089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein secretion by the type VIII secretion system","termid":"GO:0098777"},{"relation_name":"part_of","term_name":"curli assembly","termid":"GO:0098775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085","GO:0051179","GO:0044085"],"is_obsolete":false,"name":"curli subunit secretion coupled to curli assembly","synonyms":[{"name":"extracellular nucleation-precipitation pathway","type":"exact"}],"termid":"GO:0098778"}


id: GO:0050374
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + UDP-alpha-D-galacturonate = CO2 + UDP-L-arabinose.","definition_xrefs":["EC:4.1.1.67","RHEA:19725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"UDP-galacturonate decarboxylase activity","secondary_identifiers":["MetaCyc:UDP-GALACTURONATE-DECARBOXYLASE-RXN","KEGG_REACTION:R02636"],"synonyms":[{"name":"UDP-D-galacturonate carboxy-lyase (UDP-L-arabinose-forming)","type":"related"},{"name":"UDP-D-galacturonate carboxy-lyase activity","type":"related"},{"name":"UDP-galacturonic acid decarboxylase activity","type":"related"},{"name":"UDPGalUA carboxy lyase activity","type":"related"},{"name":"UDPgalacturonate decarboxylase activity","type":"related"}],"termid":"GO:0050374"}


id: GO:1904823
data:
  {"annotated_genes":["SJAG_00760","SJAG_03777"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098702"},{"annotations":[111990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098710"},{"annotations":[114593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140140"}]},"cv_name":"biological_process","definition":"The process in which a purine nucleobase is transported across a membrane.","definition_xrefs":["GO_REF:0000069","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleobase transport","termid":"GO:0006863"},{"relation_name":"is_a","term_name":"purine-containing compound transmembrane transport","termid":"GO:0072530"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00760":null,"SJAG_03777":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"purine nucleobase transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1904823","terms_by_termid":{"GO:0098702":null,"GO:0098710":null,"GO:0140140":null}}


id: GO:0043555
data:
  {"annotated_genes":["SJAG_04873","SJAG_03869","SJAG_02072","SJAG_04383","SJAG_02592","SJAG_00786","SJAG_00690","SJAG_00169","SJAG_01942"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109134,92318,92022,98834,93873,115059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"},{"annotations":[94725,102813,103447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990611"}]},"cv_name":"biological_process","definition":"Modulation of the frequency, rate or extent of translation as a result of a stimulus indicating the organism is under stress. The stress is usually, but not necessarily, exogenous (e.g. temperature, humidity, ionizing radiation).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation","termid":"GO:0006417"},{"relation_name":"part_of","term_name":"cellular response to stress","termid":"GO:0033554"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00690":null,"SJAG_00786":null,"SJAG_01942":null,"SJAG_02072":null,"SJAG_02592":null,"SJAG_03869":null,"SJAG_04383":null,"SJAG_04873":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of translation in response to stress","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"translational stress response","type":"exact"}],"termid":"GO:0043555","terms_by_termid":{"GO:1990611":null,"GO:1990625":null}}


id: PBO:0072829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SANT and BTB domain regulator of CSR","termid":"PBO:0072829"}


id: MONDO:0010737
data:
  {"annotated_genes":["SJAG_03467"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85949],"is_not":false,"summary":null,"term":"MONDO:0010737"}]},"cv_name":"mondo","definition":"X-linked spondyloepiphyseal dysplasia tarda is an inherited skeletal disorder that affects males only. Physical characteristics include moderate short-stature (dwarfism); moderate to severe spinal deformities; barrel-chest; disproportionately short trunk and neck;disproportionatelylong arms,and premature osteoarthritis, especially in the hip joints. Final male adult height ranges from 4 feet 10 inches to 5 feet 6 inches. Other skeletal features of this condition include decreased mobility of the elbow and hip joints, arthritis, and abnormalities of the hip joint which causes the upper leg bones to turn inward. This condition is caused by mutations in the TRAPPC2 gene and is inherited in an X-linked recessive pattern.","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia tarda","termid":"MONDO:0019667"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03467":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"spondyloepiphyseal dysplasia tarda, X-linked","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080362","GARD:4985","icd11.foundation:219612045","UMLS:C3541456","MEDGEN:762085","OMIM:313400"],"synonyms":[{"name":"SED","type":"related"},{"name":"SEDT","type":"related"},{"name":"Sed tarda, X-linked","type":"related"},{"name":"X linked spondyloepiphyseal dysplasia tarda","type":"related"},{"name":"X-linked spondyloepiphyseal dysplasia","type":"related"},{"name":"spondyloepiphyseal dysplasia tarda X-linked","type":"related"},{"name":"spondyloepiphyseal dysplasia tarda, X-linked","type":"exact"},{"name":"spondyloepiphyseal dysplasia tarda, X-linked recessive","type":"exact"},{"name":"spondyloepiphyseal dysplasia, late","type":"related"}],"termid":"MONDO:0010737","terms_by_termid":{"MONDO:0010737":null},"xrefs":{"Monarch":{"xref_id":"0010737"}}}


id: PBO:0027749
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_DNA_replication_gene_mRNA_during_nitrogen_starvation","termid":"PBO:0027749"}


id: MONDO:0001480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"testicular cancer","termid":"MONDO:0005447"}],"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 tumor of undescended testis","secondary_identifiers":["DOID:12276","ICD9:186.0","MEDGEN:509335","SCTID:188219004","UMLS:C0153595"],"synonyms":[{"name":"malignant neoplasm of retained testis","type":"exact"},{"name":"malignant neoplasm of undescended testis","type":"exact"},{"name":"malignant tumor of retained testis","type":"exact"},{"name":"malignant tumour of retained testis","type":"exact"}],"termid":"MONDO:0001480","xrefs":{"Monarch":{"xref_id":"0001480"}}}


id: FYPO:0001477
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of guanosine-diphosphatase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal guanosine-diphosphatase activity","termid":"FYPO:0001476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000661","FYPO:0000652","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"decreased guanosine-diphosphatase activity","synonyms":[{"name":"decreased GDPase activity","type":"exact"},{"name":"reduced guanosine-diphosphatase activity","type":"exact"}],"termid":"FYPO:0001477"}


id: PBO:0027130
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_nitrogen_starvation_gene_mRNA_during_meiotic_cell_cycle","termid":"PBO:0027130"}


id: PBO:0089661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid-translocating ATPase complex Lem3 family subunit","termid":"PBO:0089661"}


id: PBO:0004514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiosis specific cyclin Crs1","termid":"PBO:0004514"}


id: GO:0051885
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of timing of anagen, the growth phase of the hair cycle.","definition_xrefs":["GOC:pr","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of hair follicle maturation","termid":"GO:0048818"},{"relation_name":"is_a","term_name":"regulation of timing of anagen","termid":"GO:0051884"},{"relation_name":"positively_regulates","term_name":"anagen","termid":"GO:0042640"}],"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 timing of anagen","synonyms":[{"name":"activation of anagen","type":"narrow"},{"name":"positive regulation of anagen","type":"related"},{"name":"stimulation of anagen","type":"narrow"},{"name":"up regulation of anagen","type":"related"},{"name":"up-regulation of anagen","type":"related"},{"name":"upregulation of anagen","type":"related"}],"termid":"GO:0051885"}


id: PBO:0043281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 4 member E","termid":"PBO:0043281"}


id: PBO:0049706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan synthase 1","termid":"PBO:0049706"}


id: MONDO:1010856
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Krabbe disease that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Krabbe disease, non-human animal","termid":"MONDO:1010170"},{"relation_name":"is_a","term_name":"lysosomal storage disease, domestic cat","termid":"MONDO:1010861"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Krabbe disease, domestic cat","secondary_identifiers":["OMIA:000578-9685"],"termid":"MONDO:1010856","xrefs":{"Monarch":{"xref_id":"1010856"}}}


id: PBO:0029991
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-growth_auxotrophic_for_thiamine","termid":"PBO:0029991"}


id: GO:0008623
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An ISWI complex that contains an ATPase subunit of the ISWI family (SNF2H in mammals, Isw2 in S. cerevisiae), an ACF1 homolog, and additional small histone fold subunits (generally two of these, but Xenopus has only one and some additional non-conserved subunits). CHRAC plays roles in the regulation of RNA polymerase II transcription and in DNA replication and repair.","definition_xrefs":["PMID:15284901","GOC:bf","GOC:krc","PMID:16568949","PMID:21810179","PMID:9252192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ISWI-type complex","termid":"GO:0031010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"CHRAC","secondary_identifiers":["GO:0016588"],"synonyms":[{"name":"ISW2 complex","type":"narrow"},{"name":"chromatin accessibility complex","type":"exact"}],"termid":"GO:0008623"}


id: GO:0042428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving serotonin (5-hydroxytryptamine), a monoamine neurotransmitter occurring in the peripheral and central nervous systems, also having hormonal properties.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"indole-containing compound metabolic process","termid":"GO:0042430"},{"relation_name":"is_a","term_name":"ammonium ion metabolic process","termid":"GO:0097164"},{"relation_name":"is_a","term_name":"primary amino compound metabolic process","termid":"GO:1901160"}],"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":"serotonin metabolic process","synonyms":[{"name":"serotonin metabolism","type":"exact"}],"termid":"GO:0042428"}


id: PBO:0026838
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_protein_localization_to_mitotic_spindle_pole_body_during_anaphase","termid":"PBO:0026838"}


id: GO:0033152
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which immunoglobulin gene segments are recombined within a single locus utilizing the conserved heptamer and nonomer recombination signal sequences (RSS). For immunoglobulin heavy chains V, D, and J gene segments are joined, and for immunoglobulin light chains V and J gene segments are joined.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic recombination of immunoglobulin gene segments","termid":"GO:0016447"},{"relation_name":"is_a","term_name":"V(D)J recombination","termid":"GO:0033151"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0006310","GO:0010467","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"immunoglobulin V(D)J recombination","synonyms":[{"name":"immunoglobulin V(D)J joining","type":"exact"},{"name":"immunoglobulin V-D-J joining","type":"narrow"},{"name":"immunoglobulin V-D-J recombination","type":"narrow"},{"name":"immunoglobulin V-J joining","type":"narrow"},{"name":"immunoglobulin V-J recombination","type":"narrow"}],"termid":"GO:0033152"}


id: PBO:0088172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xylitol dehydrogenase; converts xylitol to D-xylulose; expression induced by xylose, even though this pentose sugar is not well utilized by S. cerevisiae; null mutant has cell wall defect","termid":"PBO:0088172"}


id: MONDO:0005363
data:
  {"annotated_genes":["SJAG_01143","SJAG_04001","SJAG_00118","SJAG_04621"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011303"},{"annotations":[85467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013589"},{"annotations":[86401,86402],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014462"}]},"cv_name":"mondo","definition":"An instance of focal segmental glomerulosclerosis that is caused by an inherited genomic modification in an individual.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"},{"relation_name":"is_a","term_name":"focal segmental glomerulosclerosis","termid":"MONDO:0100313"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_01143":null,"SJAG_04001":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":"inherited focal segmental glomerulosclerosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2200113","NANDO:1200722","OMIMPS:603278"],"termid":"MONDO:0005363","terms_by_termid":{"MONDO:0011303":null,"MONDO:0013589":null,"MONDO:0014462":null},"xrefs":{"Monarch":{"xref_id":"0005363"}}}


id: PBO:0014580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"electron transfer flavoprotein beta subunit EtfB (predicted)","termid":"PBO:0014580"}


id: PBO:0039739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein L1","termid":"PBO:0039739"}


id: MONDO:0800349
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"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":"atrial fibrillation, familial, 16","secondary_identifiers":["MEDGEN:862136","UMLS:C4013699"],"synonyms":[{"name":"ATFB16","type":"exact"}],"termid":"MONDO:0800349","xrefs":{"Monarch":{"xref_id":"0800349"}}}


id: PBO:0044986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAH-box helicase 37","termid":"PBO:0044986"}


id: GO:0048880
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a sensory system over time from its formation to the mature structure.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"system development","termid":"GO:0048731"}],"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":"sensory system development","termid":"GO:0048880"}


id: MONDO:0014271
data:
  {"annotated_genes":["SJAG_04127"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85189],"is_not":false,"summary":null,"term":"MONDO:0014271"}]},"cv_name":"mondo","definition":"STT3B-CDG is a form of congenital disorders of N-linked glycosylation characterized by intrauterine growth retardation, microcephaly, failure to thrive, developmental delay, intellectual disability, hypotonia, seizures, optic nerve atrophy and respiratory difficulties. Genital abnormalities (micropenis, hypoplastic scrotum, undescended testes) have also been reported. STT3B-CDG is caused by mutations in the gene STT3B (3p24.1).","definition_xrefs":["Orphanet:370924"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type I","termid":"MONDO:0005500"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04127":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"STT3B-congenital disorder of glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:419309","UMLS:C2931007","OMIM:615597","GARD:17603","SCTID:733112007","MESH:C535751","DOID:0080573"],"synonyms":[{"name":"CDG IX","type":"related"},{"name":"CDG syndrome type IX","type":"exact"},{"name":"CDG-Ix","type":"exact"},{"name":"CDG1X","type":"exact"},{"name":"STT3B-CDG","type":"exact"},{"name":"STT3B-congenital disorder of glycosylation","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IX","type":"exact"},{"name":"congenital disorder of glycosylation type 1x","type":"exact"},{"name":"congenital disorder of glycosylation type IX","type":"exact"},{"name":"congenital disorder of glycosylation, type IX","type":"related"}],"termid":"MONDO:0014271","terms_by_termid":{"MONDO:0014271":null},"xrefs":{"Monarch":{"xref_id":"0014271"}}}


id: PBO:0079818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin interaction motif containing 1","termid":"PBO:0079818"}


id: PBO:0051055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 2/OR15-2B (non-functional)","termid":"PBO:0051055"}


id: SO:0001571
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant whereby a new splice site is created due to the activation of a new donor.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cryptic_splice_site_variant","termid":"SO:0001569"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryptic_splice_donor","synonyms":[{"name":"cryptic splice donor","type":"exact"}],"termid":"SO:0001571"}


id: PBO:0113519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-like protein conjugated to phosphatidylethanolamine (PE); role in membrane fusion and phagophore expansion during autophagosome formation; deconjugation is also required for biogenesis; targets Atg1p to autophagosomes; binds to the Atg1p-Atg13p complex, triggers its vacuolar degradation; role in vacuolar membrane protein turnover during early stationary phase; component of autophagosomes and Cvt vesicles; targeted to vacuole via AP-3 pathway","termid":"PBO:0113519"}


id: PBO:0116269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Highly-conserved N-terminally anchored AAA-ATPase; distributed in the mitochondrial outer membrane and peroxisomes; involved in mitochondrial protein sorting; ATP-driven extractase that pulls mislocalized tail-anchored proteins into the cytosol, passing them to the GET pathway for transfer to the ER membrane for degradation, ensuring fidelity of organelle-specific localization of tail-anchored proteins; contains an N-terminal transmembrane domain and C-terminal cytoplasmic ATPase domain","termid":"PBO:0116269"}


id: GO:0150151
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of interleukin-17A production.","definition_xrefs":["PMID:27901018","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of interleukin-17 production","termid":"GO:0032660"},{"relation_name":"regulates","term_name":"interleukin-17A production","termid":"GO:0097087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-17A production","synonyms":[{"name":"regulation of interleukin-17A biosynthetic process","type":"narrow"}],"termid":"GO:0150151"}


id: MONDO:0859177
data:
  {"annotated_genes":["SJAG_03693"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85893],"is_not":false,"summary":null,"term":"MONDO:0859177"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03693":null},"genotype_count":0,"is_obsolete":false,"name":"VISS syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5561955","OMIM:619472","MEDGEN:1794165"],"termid":"MONDO:0859177","terms_by_termid":{"MONDO:0859177":null},"xrefs":{"Monarch":{"xref_id":"0859177"}}}


id: PBO:0086063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function that contains 2 PY motifs; ubiquinated by Rsp5p; overexpression confers resistance to arsenite; green fluorescent protein (GFP)-fusion protein localizes it to the cytoplasm; non-essential gene","termid":"PBO:0086063"}


id: MONDO:0010859
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any atrioventricular septal defect in which the cause of the disease is a mutation in the GJA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"gene_count":0,"genotype_count":0,"name":"obsolete atrioventricular septal defect 3 (obsolete MONDO:0010859)","secondary_identifiers":["OMIM:600309"],"synonyms":[{"name":"AVSD3","type":"related"},{"name":"GJA1 atrioventricular septal defect","type":"exact"},{"name":"atrioventricular septal defect 3","type":"exact"},{"name":"atrioventricular septal defect caused by mutation in GJA1","type":"exact"},{"name":"atrioventricular septal defect type 3","type":"exact"}],"termid":"MONDO:0010859","xrefs":{"Monarch":{"xref_id":"0010859"}}}


id: PBO:0059775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 1","termid":"PBO:0059775"}


id: GO:0099175
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the physical form of a postsynapse.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synapse organization","termid":"GO:0050807"},{"relation_name":"regulates","term_name":"postsynapse organization","termid":"GO:0099173"}],"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 postsynapse organization","synonyms":[{"name":"regulation of postsynapse organisation","type":"exact"},{"name":"regulation of postsynapse organization and biogenesis","type":"related"},{"name":"regulation of postsynapse structure","type":"exact"}],"termid":"GO:0099175"}


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:0019424
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A sulfide oxidation process that proceeds via the reaction catalyzed by siroheme sulfite reductase.","definition_xrefs":["MetaCyc:P223-PWY"],"gene_count":0,"genotype_count":0,"name":"obsolete sulfide oxidation, using siroheme sulfite reductase (obsolete GO:0019424)","synonyms":[{"name":"sulfide oxidation, using sirohaem sulfite reductase","type":"exact"},{"name":"sulfur oxidation, using sirohaem sulfite reductase","type":"related"},{"name":"sulfur oxidation, using siroheme sulfite reductase","type":"related"},{"name":"sulphide oxidation, using siroheme sulphite reductase","type":"exact"},{"name":"sulphur oxidation, using siroheme sulphite reductase","type":"related"}],"termid":"GO:0019424"}


id: MONDO:1012367
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"protein-losing nephropathy, non-human animal","termid":"MONDO:1011914"},{"relation_name":"is_a","term_name":"renal disease, dog","termid":"MONDO:1012235"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-losing nephropathy, dog","secondary_identifiers":["OMIA:001326-9615"],"termid":"MONDO:1012367","xrefs":{"Monarch":{"xref_id":"1012367"}}}


id: MONDO:0019916
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 16 disorder","termid":"MONDO:0700023"},{"relation_name":"is_a","term_name":"uniparental disomy","termid":"MONDO:0700086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternal uniparental disomy of chromosome 16","secondary_identifiers":["GARD:19336","Orphanet:96185","UMLS:C4750769","MEDGEN:1650997","icd11.foundation:635736420"],"synonyms":[{"name":"UPD(16)mat","type":"exact"},{"name":"maternal uniparental disomy of chromosome type 16","type":"exact"}],"termid":"MONDO:0019916","xrefs":{"Monarch":{"xref_id":"0019916"}}}


id: PBO:0058162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4456","termid":"PBO:0058162"}


id: GO:0051709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the killing by an organism of cells in another organism.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell killing","termid":"GO:0031341"},{"relation_name":"is_a","term_name":"modulation of process of another organism","termid":"GO:0035821"},{"relation_name":"regulates","term_name":"killing of cells of another organism","termid":"GO:0031640"}],"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 killing of cells of another organism","secondary_identifiers":["GO:0052248","GO:0044531","GO:0052433","GO:0052459"],"synonyms":[{"name":"modulation by organism of apoptotic process in other organism involved in symbiotic interaction","type":"narrow"},{"name":"modulation of programmed cell death in other organism","type":"narrow"},{"name":"modulation of programmed cell death in other organism involved in symbiotic interaction","type":"narrow"},{"name":"regulation of killing of cells of other organism","type":"exact"}],"termid":"GO:0051709"}


id: GO:1902788
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 isooctane stimulus.","definition_xrefs":["PMID:22328008","GO_REF:0000071","GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alkane","termid":"GO:1902778"}],"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 isooctane","termid":"GO:1902788"}


id: PBO:0086436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative integral membrane protein of unknown function; interacts with Ulp1p at the nuclear periphery; member of DUP240 gene family","termid":"PBO:0086436"}


id: GO:0052354
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the breakdown of carbohydrate molecules within a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by organism of carbohydrate in other organism involved in symbiotic interaction (obsolete GO:0052354)","synonyms":[{"name":"catabolism by organism of carbohydrate in other organism during symbiotic interaction","type":"related"}],"termid":"GO:0052354"}


id: GO:0071533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process of protein complex assembly in which the arrangement and bonding together of the set of components that form the protein complex is mediated by an ankyrin repeat interaction.","definition_xrefs":["GOC:amm","InterPro:IPR002110"],"gene_count":0,"genotype_count":0,"name":"obsolete ankyrin repeat-mediated complex assembly (obsolete GO:0071533)","synonyms":[{"name":"ANK repeat-mediated complex assembly","type":"exact"}],"termid":"GO:0071533"}


id: PBO:0071901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 39","termid":"PBO:0071901"}


id: PBO:0027841
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_phosphorylation_during_mitotic_G2_phase_during_cellular_response_to_ionizing_radiation","termid":"PBO:0027841"}


id: PR:O59732
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cfh4 gene.","definition_xrefs":["UniProtKB:O59732","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":"chitin synthase regulatory factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3E7.12c","synonyms":[{"name":"Chs four homolog 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-cfh4","type":"exact"}],"termid":"PR:O59732"}


id: FYPO:0004823
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the number of ribosomal DNA (rDNA) repeats present in the rDNA arrays on chromosome III is abnormal (significantly greater or less than the range in wild type cells).","definition_xrefs":["PMID:25417108","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal rDNA copy number","synonyms":[{"name":"abnormal ribosomal DNA copy number","type":"exact"}],"termid":"FYPO:0004823"}


id: PR:G2TRS6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBP35G2.17 gene.","definition_xrefs":["UniProtKB:G2TRS6","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 P35G2.17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP35G2.17","synonyms":[{"name":"Spom972h-SPBP35G2.17","type":"exact"}],"termid":"PR:G2TRS6"}


id: PBO:0063401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosducin like 2","termid":"PBO:0063401"}


id: SO:0002122
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A germline immunoglobulin gene.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immune_system_gene","termid":"SO:0002121"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin_gene","synonyms":[{"name":"All_IG_genes","type":"exact"},{"name":"IG_genes","type":"exact"}],"termid":"SO:0002122"}


id: GO:0071541
data:
  {"annotated_genes":["SJAG_02164","SJAG_02995","SJAG_04981","SJAG_03147","SJAG_04744","SJAG_04900","SJAG_03472","SJAG_02628","SJAG_04891"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89451,94292,96354,97229,97288,98430,104789,105075,110148],"is_not":false,"summary":null,"term":"GO:0071541"}]},"cv_name":"cellular_component","definition":"An eukaryotic translation initiation factor 3 complex that contains the PCI-domain protein eIF3m.","definition_xrefs":["PMID:19061185","PMID:15904532"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eukaryotic translation initiation factor 3 complex","termid":"GO:0005852"}],"gene_count":9,"genes_by_uniquename":{"SJAG_02164":null,"SJAG_02628":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03472":null,"SJAG_04744":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04981":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 complex, eIF3m","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"eIF3m-containing eukaryotic translation initiation factor 3 complex","type":"exact"}],"termid":"GO:0071541","terms_by_termid":{"GO:0071541":null}}


id: MONDO:0017532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"postaxial polydactyly type A","termid":"MONDO:0019673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly type A, bilateral","secondary_identifiers":["Orphanet:295165","icd11.foundation:1050812995"],"termid":"MONDO:0017532","xrefs":{"Monarch":{"xref_id":"0017532"}}}


id: PBO:0074561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA host gene 15","termid":"PBO:0074561"}


id: GO:0062162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of a pyocyanine biosynthetic process.","definition_xrefs":["PMID:28715477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of biosynthetic process","termid":"GO:0009891"},{"relation_name":"is_a","term_name":"regulation of pyocyanine biosynthetic process","termid":"GO:0062161"},{"relation_name":"positively_regulates","term_name":"pyocyanine biosynthetic process","termid":"GO:0106220"}],"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 pyocyanine biosynthetic process","synonyms":[{"name":"positive regulation of pyocyanin biosynthetic process","type":"exact"}],"termid":"GO:0062162"}


id: PBO:0057401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548h-3","termid":"PBO:0057401"}


id: GO:0044282
data:
  {"annotated_genes":["SJAG_02988","SJAG_04660","SJAG_02235","SJAG_01903","SJAG_02496","SJAG_04299","SJAG_01596","SJAG_03434","SJAG_01271","SJAG_04192","SJAG_02901","SJAG_03293","SJAG_00493","SJAG_02107","SJAG_00944","SJAG_04679","SJAG_01543","SJAG_03903","SJAG_00714","SJAG_01673","SJAG_05256","SJAG_04570","SJAG_00957","SJAG_00674","SJAG_04320","SJAG_03828","SJAG_04048","SJAG_02796","SJAG_00706","SJAG_04870","SJAG_04954","SJAG_04276","SJAG_03312","SJAG_00633","SJAG_02945","SJAG_01209","SJAG_03771","SJAG_03174","SJAG_04404","SJAG_00461","SJAG_06622","SJAG_01310","SJAG_03786","SJAG_02009","SJAG_02763","SJAG_00244","SJAG_02010","SJAG_00027","SJAG_03398","SJAG_02450","SJAG_00937","SJAG_03804","SJAG_03958","SJAG_03743","SJAG_04842","SJAG_00605","SJAG_02135","SJAG_02369","SJAG_04495","SJAG_04334","SJAG_04145","SJAG_02960","SJAG_04726","SJAG_01432","SJAG_02106","SJAG_02734","SJAG_03290","SJAG_00237","SJAG_02959","SJAG_03660","SJAG_02766","SJAG_01359","SJAG_04927","SJAG_03852","SJAG_00281","SJAG_02580","SJAG_00839","SJAG_03861","SJAG_01457","SJAG_06621","SJAG_04674","SJAG_00495","SJAG_03373","SJAG_03641","SJAG_04827"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87102,87103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006154"},{"annotations":[88122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019564"},{"annotations":[94521,95255,100672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019568"},{"annotations":[106238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019544"},{"annotations":[96850,112646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019547"},{"annotations":[96851,112647,106239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010121"},{"annotations":[97851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009074"},{"annotations":[96763,96764,88020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000949"},{"annotations":[111262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019266"},{"annotations":[111264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006533"},{"annotations":[103949,104925,97494,108849,103126,108384,104924,104926,105294,105295,108387,108385,97772,108848,108851,108390,108853,108854,102870,108389,108388,94030,108852,115796,108850,108386,94517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[88707,107838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009972"},{"annotations":[114191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019478"},{"annotations":[79884,79525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046177"},{"annotations":[103837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019303"},{"annotations":[87118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036088"},{"annotations":[100673,94523,95256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042843"},{"annotations":[100356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006068"},{"annotations":[111282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001561"},{"annotations":[90969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009062"},{"annotations":[95037,102963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046294"},{"annotations":[108356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019388"},{"annotations":[86960,87937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009450"},{"annotations":[79212,91215],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006538"},{"annotations":[115798,92568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019563"},{"annotations":[97363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006546"},{"annotations":[88187,112472,86946,95907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019464"},{"annotations":[88123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[100521,104558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009436"},{"annotations":[114488,88229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071545"},{"annotations":[110685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042853"},{"annotations":[111218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903457"},{"annotations":[113201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042758"},{"annotations":[87489,102282,112255,99817,91953],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019243"},{"annotations":[58887,104515,60655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061727"},{"annotations":[61212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016095"},{"annotations":[106587,117443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010133"},{"annotations":[90585,90167,111620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006152"},{"annotations":[90168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046135"},{"annotations":[104518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006062"},{"annotations":[93711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006567"},{"annotations":[106245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006572"},{"annotations":[113511],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019628"},{"annotations":[118428,90959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043419"},{"annotations":[107548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006574"},{"annotations":[100363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042820"},{"annotations":[118457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005998"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of small molecules, any low molecular weight, monomeric, non-encoded molecule.","definition_xrefs":["GOC:curators","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"small molecule metabolic process","termid":"GO:0044281"}],"gene_count":85,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00237":null,"SJAG_00244":null,"SJAG_00281":null,"SJAG_00461":null,"SJAG_00493":null,"SJAG_00495":null,"SJAG_00605":null,"SJAG_00633":null,"SJAG_00674":null,"SJAG_00706":null,"SJAG_00714":null,"SJAG_00839":null,"SJAG_00937":null,"SJAG_00944":null,"SJAG_00957":null,"SJAG_01209":null,"SJAG_01271":null,"SJAG_01310":null,"SJAG_01359":null,"SJAG_01432":null,"SJAG_01457":null,"SJAG_01543":null,"SJAG_01596":null,"SJAG_01673":null,"SJAG_01903":null,"SJAG_02009":null,"SJAG_02010":null,"SJAG_02106":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02235":null,"SJAG_02369":null,"SJAG_02450":null,"SJAG_02496":null,"SJAG_02580":null,"SJAG_02734":null,"SJAG_02763":null,"SJAG_02766":null,"SJAG_02796":null,"SJAG_02901":null,"SJAG_02945":null,"SJAG_02959":null,"SJAG_02960":null,"SJAG_02988":null,"SJAG_03174":null,"SJAG_03290":null,"SJAG_03293":null,"SJAG_03312":null,"SJAG_03373":null,"SJAG_03398":null,"SJAG_03434":null,"SJAG_03641":null,"SJAG_03660":null,"SJAG_03743":null,"SJAG_03771":null,"SJAG_03786":null,"SJAG_03804":null,"SJAG_03828":null,"SJAG_03852":null,"SJAG_03861":null,"SJAG_03903":null,"SJAG_03958":null,"SJAG_04048":null,"SJAG_04145":null,"SJAG_04192":null,"SJAG_04276":null,"SJAG_04299":null,"SJAG_04320":null,"SJAG_04334":null,"SJAG_04404":null,"SJAG_04495":null,"SJAG_04570":null,"SJAG_04660":null,"SJAG_04674":null,"SJAG_04679":null,"SJAG_04726":null,"SJAG_04827":null,"SJAG_04842":null,"SJAG_04870":null,"SJAG_04927":null,"SJAG_04954":null,"SJAG_05256":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"small molecule catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"small molecule catabolism","type":"exact"}],"termid":"GO:0044282","terms_by_termid":{"GO:0000949":null,"GO:0001561":null,"GO:0005998":null,"GO:0006062":null,"GO:0006068":null,"GO:0006152":null,"GO:0006154":null,"GO:0006533":null,"GO:0006538":null,"GO:0006546":null,"GO:0006567":null,"GO:0006572":null,"GO:0006574":null,"GO:0009062":null,"GO:0009074":null,"GO:0009436":null,"GO:0009450":null,"GO:0009972":null,"GO:0010121":null,"GO:0010133":null,"GO:0016095":null,"GO:0019243":null,"GO:0019266":null,"GO:0019303":null,"GO:0019388":null,"GO:0019464":null,"GO:0019478":null,"GO:0019544":null,"GO:0019547":null,"GO:0019563":null,"GO:0019564":null,"GO:0019568":null,"GO:0019628":null,"GO:0036088":null,"GO:0042758":null,"GO:0042820":null,"GO:0042843":null,"GO:0042853":null,"GO:0043419":null,"GO:0046135":null,"GO:0046177":null,"GO:0046294":null,"GO:0061613":null,"GO:0061621":null,"GO:0061727":null,"GO:0071545":null,"GO:1903457":null}}


id: PBO:0058719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6847","termid":"PBO:0058719"}


id: PBO:0029418
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_palmitoylation_during_meiosis","termid":"PBO:0029418"}


id: PBO:0056343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase kinase kinase 2","termid":"PBO:0056343"}


id: GO:0072219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metanephric cortical collecting duct over time, from its formation to the mature structure. The metanephric cortical collecting duct is the portion of the metanephric collecting duct that resides in the renal cortex.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cortical collecting duct development","termid":"GO:0072059"}],"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":"metanephric cortical collecting duct development","termid":"GO:0072219"}


id: PBO:0034651
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_glycerol_level_during_cellular_response_to_osmotic_stress","termid":"PBO:0034651"}


id: PBO:0090630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin binding vezatin family protein involved in peroxisome inheritance Inp2","termid":"PBO:0090630"}


id: GO:0033432
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CGG codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"}],"interesting_parent_ids":["GO:0003723","GO:0005488","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"CGG codon-amino acid adaptor activity","synonyms":[{"name":"arginine tRNA","type":"related"}],"termid":"GO:0033432"}


id: GO:0070475
data:
  {"annotated_genes":["SJAG_01958","SJAG_03877","SJAG_02281","SJAG_02024","SJAG_02417","SJAG_03008"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90830,94690,95121,113056,115646],"is_not":false,"summary":null,"term":"GO:0070475"},{"annotations":[94405],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070476"}]},"cv_name":"biological_process","definition":"The addition of a methyl group to an atom in the nucleoside base portion of a nucleotide residue in an rRNA molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA methylation","termid":"GO:0031167"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01958":null,"SJAG_02024":null,"SJAG_02281":null,"SJAG_02417":null,"SJAG_03008":null,"SJAG_03877":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0042254","GO:0044085"],"is_obsolete":false,"name":"rRNA base methylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0070475","terms_by_termid":{"GO:0070475":null,"GO:0070476":null}}


id: PBO:0088553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Utp1","termid":"PBO:0088553"}


id: PBO:0066694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enriched in melanoma 3","termid":"PBO:0066694"}


id: MONDO:0030875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"},{"relation_name":"is_a","term_name":"frontotemporal dementia and/or amyotrophic lateral sclerosis","termid":"MONDO:0030923"}],"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":"frontotemporal dementia and/or amyotrophic lateral sclerosis 5","secondary_identifiers":["UMLS:C5436884","OMIM:619141","MEDGEN:1756201","GARD:16427"],"synonyms":[{"name":"FTDALS5","type":"exact"},{"name":"frontotemporal dementia and/or amyotrophic lateral sclerosis 5","type":"exact"}],"termid":"MONDO:0030875","xrefs":{"Monarch":{"xref_id":"0030875"}}}


id: PBO:0069066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 313, pseudogene","termid":"PBO:0069066"}


id: PBO:0070565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 31","termid":"PBO:0070565"}


id: PBO:0083311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps ORF ARN2/YHL047C","termid":"PBO:0083311"}


id: GO:0047355
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycerophosphate(n) + CDP-glycerol = glycerophosphate(n+1) + CMP.","definition_xrefs":["EC:2.7.8.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016780"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016780","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"CDP-glycerol glycerophosphotransferase activity","secondary_identifiers":["MetaCyc:TEICHOICSYN4-RXN","RHEA:13565"],"synonyms":[{"name":"CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase activity","type":"related"},{"name":"CDPglycerol glycerophosphotransferase activity","type":"related"},{"name":"CGPTase activity","type":"related"},{"name":"cytidine diphosphoglycerol glycerophosphotransferase activity","type":"related"},{"name":"glycerophosphate synthetase activity","type":"related"},{"name":"poly(glycerol phosphate) polymerase activity","type":"related"},{"name":"teichoic acid glycerol transferase activity","type":"related"},{"name":"teichoic-acid synthase activity","type":"broad"}],"termid":"GO:0047355"}


id: PBO:0083178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the characterized snoRNA gene snR73","termid":"PBO:0083178"}


id: GO:0051980
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of the iron chelate iron-nicotianamine (Fe-NA) from one side of a membrane to the other.","definition_xrefs":["GOC:ai","PMID:20625001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron chelate transmembrane transporter activity","termid":"GO:0015603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"iron-nicotianamine transmembrane transporter activity","synonyms":[{"name":"Fe-NA chelate transporter activity","type":"exact"}],"termid":"GO:0051980"}


id: PBO:0067291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 376, pseudogene","termid":"PBO:0067291"}


id: SO:0000738
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"DNA belonging to the nuclear genome of cell.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_location","termid":"SO:0000735"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear_sequence","synonyms":[{"name":"nuclear sequence","type":"exact"}],"termid":"SO:0000738"}


id: GO:0022610
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The attachment of a cell or organism to a substrate, another cell, or other organism. Biological adhesion includes intracellular attachment between membrane regions.","definition_xrefs":["GOC:isa_complete"],"gene_count":0,"genotype_count":0,"name":"obsolete biological adhesion (obsolete GO:0022610)","termid":"GO:0022610"}


id: GO:0060796
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that results in cells adopting an endoderm, ectoderm or mesoderm cell fate.","definition_xrefs":["GOC:dph","GOC:tb","GOC:sdb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription involved in primary germ layer cell fate commitment (obsolete GO:0060796)","termid":"GO:0060796"}


id: MONDO:0015374
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system vasculitis","termid":"MONDO:0003346"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary central nervous system vasculitis","secondary_identifiers":["MEDGEN:419271","Orphanet:140989","MESH:C537295","GARD:8703","UMLS:C2930862","MESH:D020293"],"synonyms":[{"name":"PACNS","type":"exact"},{"name":"PCNSV","type":"exact"},{"name":"granulomatous angiitis of the central nervous system","type":"related"},{"name":"isolated angiitis of the central nervous system","type":"exact"},{"name":"primary CNS vasculitis","type":"related"},{"name":"primary angiitis of the central nervous system","type":"exact"},{"name":"primary central nervous system vasculitis","type":"exact"},{"name":"primary vasculitis of the central nervous system","type":"exact"}],"termid":"MONDO:0015374","xrefs":{"Monarch":{"xref_id":"0015374"}}}


id: PBO:0046769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosome component 9","termid":"PBO:0046769"}


id: PBO:0004622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP protein Utp4 (predicted)","termid":"PBO:0004622"}


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


id: MONDO:0003450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm arising from the sweat glands. It is characterized by the presence of eccrine ducts in the dermis containing intraluminal papillary projections.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eccrine sweat gland neoplasm","termid":"MONDO:0002090"},{"relation_name":"is_a","term_name":"papillary adenoma","termid":"MONDO:0002533"},{"relation_name":"is_a","term_name":"sweat gland adenoma","termid":"MONDO:0021110"}],"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 papillary adenoma","secondary_identifiers":["UMLS:C0334350","DOID:5446","ICDO:8408/0","MEDGEN:137747","NCIT:C4173","SCTID:253021007"],"synonyms":[{"name":"Papillary eccrine adenoma","type":"exact"},{"name":"eccrine papillary adenoma of skin","type":"exact"}],"termid":"MONDO:0003450","xrefs":{"Monarch":{"xref_id":"0003450"}}}


id: GO:0071722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces or removes the toxicity of compounds containing arsenic, including arsenates, arsenites, and arsenides. These include transport of such compounds away from sensitive areas and to compartments or complexes whose purpose is sequestration of arsenic or arsenic-containing compounds.","definition_xrefs":["PMID:20221439","GOC:kmv","PMID:11313333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification","termid":"GO:0098754"},{"relation_name":"part_of","term_name":"response to arsenic-containing substance","termid":"GO:0046685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0098754","GO:0008150"],"is_obsolete":false,"name":"detoxification of arsenic-containing substance","synonyms":[{"name":"detoxification of arsenic","type":"exact"}],"termid":"GO:0071722"}


id: GO:0061010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the gallbladder over time, from its initial formation to the mature structure. The gallbladder is a cavitated organ that stores bile.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ development","termid":"GO:0048513"},{"relation_name":"part_of","term_name":"hepaticobiliary system development","termid":"GO:0061008"}],"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":"gallbladder development","termid":"GO:0061010"}


id: GO:0002164
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the larva over time, from its formation to the mature structure. The larva is the early, immature form of an that at birth or hatching is fundamentally unlike its parent and must metamorphose before assuming the adult characters.","definition_xrefs":["ISBN:0877795088","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organism development","termid":"GO:0007275"},{"relation_name":"is_a","term_name":"post-embryonic development","termid":"GO:0009791"}],"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":"larval development","termid":"GO:0002164"}


id: PBO:0003793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho-type GTPase activating protein Rga4","termid":"PBO:0003793"}


id: GO:0048777
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of leucophore differentiation.","definition_xrefs":["GOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leucophore differentiation","termid":"GO:0048775"},{"relation_name":"is_a","term_name":"positive regulation of pigment cell differentiation","termid":"GO:0050942"},{"relation_name":"positively_regulates","term_name":"leucophore differentiation","termid":"GO:0048772"}],"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 leucophore differentiation","synonyms":[{"name":"activation of leucophore differentiation","type":"narrow"},{"name":"stimulation of leucophore differentiation","type":"narrow"},{"name":"up regulation of leucophore differentiation","type":"exact"},{"name":"up-regulation of leucophore differentiation","type":"exact"},{"name":"upregulation of leucophore differentiation","type":"exact"}],"termid":"GO:0048777"}


id: GO:1905906
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of amyloid fibril formation.","definition_xrefs":["PMID:23106396","GOC:TermGenie","GOC:aruk","GO_REF:0000058","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein metabolic process","termid":"GO:0051246"},{"relation_name":"is_a","term_name":"regulation of supramolecular fiber organization","termid":"GO:1902903"},{"relation_name":"regulates","term_name":"amyloid fibril formation","termid":"GO:1990000"}],"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 amyloid fibril formation","synonyms":[{"name":"regulation of amyloid fibril assembly","type":"related"},{"name":"regulation of amyloid structure assembly","type":"related"},{"name":"regulation of amyloid structure formation","type":"related"}],"termid":"GO:1905906"}


id: PBO:0061954
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 7","termid":"PBO:0061954"}


id: GO:0032743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interleukin-2 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 interleukin-2 production","termid":"GO:0032663"},{"relation_name":"positively_regulates","term_name":"interleukin-2 production","termid":"GO:0032623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of interleukin-2 production","secondary_identifiers":["GO:1900042","GO:0045086"],"synonyms":[{"name":"activation of interleukin-2 production","type":"narrow"},{"name":"positive regulation of IL-2 production","type":"exact"},{"name":"positive regulation of interleukin-2 biosynthetic process","type":"narrow"},{"name":"positive regulation of interleukin-2 secretion","type":"narrow"},{"name":"stimulation of interleukin-2 production","type":"narrow"},{"name":"up regulation of interleukin-2 production","type":"exact"},{"name":"up-regulation of interleukin-2 production","type":"exact"},{"name":"upregulation of interleukin-2 production","type":"exact"}],"termid":"GO:0032743"}


id: MONDO:0957316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epidermolytic hyperkeratosis (obsolete MONDO:0957316)","termid":"MONDO:0957316","xrefs":{"Monarch":{"xref_id":"0957316"}}}


id: PBO:0003434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell surface glycoprotein (predicted), DUF1773 family protein 6","termid":"PBO:0003434"}


id: GO:0052748
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: baicalin + H2O = baicalein + D-glucuronate.","definition_xrefs":["RHEA:28130","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"baicalin beta-D-glucuronidase activity","secondary_identifiers":["EC:3.2.1.167","KEGG_REACTION:R09533","MetaCyc:RXN-11760"],"synonyms":[{"name":"5,6,7-trihydroxyflavone-7-O-beta-D-glucupyranosiduronate glucuronosylhydrolase activity","type":"related"},{"name":"baicalinase activity","type":"broad"}],"termid":"GO:0052748"}


id: GO:0050480
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-(4-oxo-4,5-dihydro-1H-imidazol-5-yl)propanoic acid + H2O = N-formimidoyl-L-glutamate + H+.","definition_xrefs":["RHEA:23660","EC:3.5.2.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides","termid":"GO:0016812"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016810","GO:0016787"],"is_obsolete":false,"name":"imidazolonepropionase activity","secondary_identifiers":["KEGG_REACTION:R02288","MetaCyc:IMIDAZOLONEPROPIONASE-RXN"],"synonyms":[{"name":"3-(5-oxo-4,5-dihydro-3H-imidazol-4-yl)propanoate amidohydrolase activity","type":"related"},{"name":"4(5)-imidazolone-5(4)-propionic acid hydrolase activity","type":"related"},{"name":"imidazolone propionic acid hydrolase activity","type":"related"},{"name":"imidazolone-5-propionate hydrolase activity","type":"related"}],"termid":"GO:0050480"}


id: PBO:0071617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 35","termid":"PBO:0071617"}


id: PATO:0001535
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color pattern inhering in a bearer by virtue of bearer's being marked with small spots, patches, or specks of hue or degree of saturation differing from that of the background.","definition_xrefs":["merriam-webster.:merriam-webster."],"direct_ancestors":[{"relation_name":"is_a","term_name":"multi-colored","termid":"PATO:0001533"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dappled","synonyms":[{"name":"speckled","type":"related"}],"termid":"PATO:0001535"}


id: MONDO:0009898
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":"polysaccharide, storage of unusual","secondary_identifiers":["OMIM:263600","MESH:C564877","MEDGEN:376645","UMLS:C1849721"],"synonyms":[{"name":"polysaccharide, storage of unusual","type":"exact"}],"termid":"MONDO:0009898","xrefs":{"Monarch":{"xref_id":"0009898"}}}


id: MONDO:0024884
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that has spread to the bone from another, primary anatomic site. Bone is one of the most frequent sites of metastatic carcinoma. Common sites of origin include lung, breast, and prostate.","definition_xrefs":["NCIT:C36082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone carcinoma","termid":"MONDO:0002415"},{"relation_name":"is_a","term_name":"metastatic carcinoma","termid":"MONDO:0024879"}],"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":"metastatic carcinoma in the bone","secondary_identifiers":["UMLS:C0700110","MEDGEN:195970"],"synonyms":[{"name":"metastatic carcinoma in the bone","type":"exact"},{"name":"metastatic carcinoma to the bone","type":"exact"}],"termid":"MONDO:0024884","xrefs":{"Monarch":{"xref_id":"0024884"}}}


id: MONDO:0032646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital anomaly of kidney and urinary tract","termid":"MONDO:0019719"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"congenital anomalies of kidney and urinary tract 3","secondary_identifiers":["MEDGEN:1648427","UMLS:C4748921","OMIM:618270"],"synonyms":[{"name":"CAKUT3","type":"related"},{"name":"CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3","type":"related"}],"termid":"MONDO:0032646","xrefs":{"Monarch":{"xref_id":"0032646"}}}


id: PBO:0005865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S. pombe specific UPF0321 family protein 2","termid":"PBO:0005865"}


id: GO:0006372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete lariat formation, 5'-splice site cleavage (obsolete GO:0006372)","synonyms":[{"name":"lariat formation, 5'-splice site cleavage","type":"exact"}],"termid":"GO:0006372"}


id: PBO:0070406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication protein A2","termid":"PBO:0070406"}


id: PBO:0052594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin subunit alpha 2 pseudogene 3","termid":"PBO:0052594"}


id: MONDO:0007416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic tubulointerstitial nephropathy that affects people in certain rural areas along the Danube river in the Balkans. It leads to end-stage renal disease.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interstitial nephritis","termid":"MONDO:0001085"},{"relation_name":"is_a","term_name":"hereditary nephritis","termid":"MONDO:0005334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"Balkan nephropathy","secondary_identifiers":["MESH:D001449","NCIT:C123025","UMLS:C0004698","ICD9:583.89","OMIM:124100","SCTID:26121002","EFO:0007164","ICD10CM:N15.0","MEDGEN:495","DOID:3052","icd11.foundation:18497836"],"synonyms":[{"name":"AAN","type":"related"},{"name":"BEN","type":"related"},{"name":"Balkan endemic nephropathy","type":"exact"},{"name":"Chinese herb endemic nephropathy","type":"exact"},{"name":"DEFN","type":"related"},{"name":"Danubian endemic familial nephropathy","type":"exact"},{"name":"aristolochic acid nephropathy","type":"exact"},{"name":"endemic nephropathy","type":"exact"},{"name":"nephropathia epidemica","type":"related"}],"termid":"MONDO:0007416","xrefs":{"Monarch":{"xref_id":"0007416"}}}


id: GO:0033145
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the activity of any intracellular steroid hormone receptor signaling pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular steroid hormone receptor signaling pathway","termid":"GO:0033143"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"nuclear receptor-mediated steroid hormone signaling pathway","termid":"GO:0030518"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of intracellular steroid hormone receptor signaling pathway","synonyms":[{"name":"positive regulation of steroid hormone receptor signaling pathway","type":"broad"},{"name":"positive regulation of steroid hormone receptor signalling pathway","type":"broad"}],"termid":"GO:0033145"}


id: MONDO:0013727
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any pregnancy loss, recurrent, susceptibility in which the cause of the disease is a mutation in the F5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pregnancy loss, recurrent, susceptibility","termid":"MONDO:0000144"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pregnancy loss, recurrent, susceptibility to, 1","secondary_identifiers":["MEDGEN:482300","OMIM:614389","UMLS:C3280670"],"synonyms":[{"name":"F5 pregnancy loss, recurrent, susceptibility","type":"exact"},{"name":"RPRGL1","type":"related"},{"name":"Rpl","type":"related"},{"name":"Rprgl","type":"related"},{"name":"abortion, spontaneous, recurrent","type":"related"},{"name":"embryonic loss, recurrent","type":"related"},{"name":"fetal loss, recurrent, susceptibility to","type":"related"},{"name":"foetal loss, recurrent, susceptibility to","type":"related"},{"name":"miscarriage, recurrent","type":"related"},{"name":"pregnancy loss, recurrent, susceptibility caused by mutation in F5","type":"exact"},{"name":"pregnancy loss, recurrent, susceptibility to, 1","type":"exact"},{"name":"pregnancy loss, recurrent, susceptibility to, type 1","type":"exact"},{"name":"stillbirth, recurrent","type":"related"}],"termid":"MONDO:0013727","xrefs":{"Monarch":{"xref_id":"0013727"}}}


id: MONDO:0000575
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0000575 (obsolete MONDO:0000575)","termid":"MONDO:0000575","xrefs":{"Monarch":{"xref_id":"0000575"}}}


id: PATO:0000045
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000045 absolute frequency (obsolete PATO:0000045)","termid":"PATO:0000045"}


id: PBO:0056656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 23","termid":"PBO:0056656"}


id: PBO:0002057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridoxal reductase (predicted)","termid":"PBO:0002057"}


id: PBO:0028705
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_DNA_damage","termid":"PBO:0028705"}


id: MONDO:0018861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare mitochondrial disorder characterized by facial dysmorphism similar to that seen in Zellweger syndrome, such as frontal bossing, high forehead, upslanting palpebral fissures, hypoplastic supraorbital ridges, and epicanthal folds, and in addition, pale skin, profound hypotonia, developmental delay, and minor metabolic anomalies. No peroxysomal defects, however, have been reported. Transmission is thought to be autosomal recessive.","definition_xrefs":["Orphanet:50812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"Zellweger-like syndrome without peroxisomal anomalies","secondary_identifiers":["icd11.foundation:697302760","UMLS:C4305104","MEDGEN:930773","SCTID:718880003","GARD:18841"],"synonyms":[{"name":"AHN-Lerman-Sagie syndrome","type":"exact"}],"termid":"MONDO:0018861","xrefs":{"Monarch":{"xref_id":"0018861"}}}


id: MONDO:0024637
data:
  {"annotated_genes":["SJAG_05313","SJAG_00490","SJAG_01111","SJAG_04755","SJAG_04213","SJAG_03689"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011655"},{"annotations":[84715,84714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012252"},{"annotations":[86854,86853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013224"},{"annotations":[86467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859046"}]},"cv_name":"mondo","definition":"A malignant neoplasm arising exclusively from the soft tissues.","definition_xrefs":["NCIT:C4867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"soft tissue neoplasm","termid":"MONDO:0006424"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00490":null,"SJAG_01111":null,"SJAG_03689":null,"SJAG_04213":null,"SJAG_04755":null,"SJAG_05313":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant soft tissue neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:269469005","UMLS:C4551686","MEDGEN:1632429"],"synonyms":[{"name":"malignant neoplasm of soft tissue","type":"exact"},{"name":"malignant neoplasm of the soft tissue","type":"exact"},{"name":"malignant soft tissue neoplasm","type":"exact"},{"name":"malignant soft tissue tumor","type":"exact"},{"name":"malignant soft tissue tumour","type":"exact"},{"name":"malignant tumor of soft tissue","type":"exact"},{"name":"malignant tumor of the soft tissue","type":"exact"},{"name":"malignant tumour of soft tissue","type":"exact"},{"name":"malignant tumour of the soft tissue","type":"exact"}],"termid":"MONDO:0024637","terms_by_termid":{"MONDO:0011655":null,"MONDO:0012252":null,"MONDO:0013224":null,"MONDO:0859046":null},"xrefs":{"Monarch":{"xref_id":"0024637"}}}


id: PBO:0050932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon alpha 1","termid":"PBO:0050932"}


id: MONDO:0011465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"},{"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:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"infundibulocystic basal cell carcinoma","secondary_identifiers":["OMIM:604451","UMLS:C1304297","GARD:9788","MEDGEN:220984","NCIT:C27540","DOID:4279","MESH:C537655"],"synonyms":[{"name":"basal cell carcinoma with follicular differentiation","type":"related"},{"name":"basal cell carcinoma, infundibulocystic","type":"related"},{"name":"skin infundibulocystic basal cell carcinoma","type":"exact"}],"termid":"MONDO:0011465","xrefs":{"Monarch":{"xref_id":"0011465"}}}


id: MONDO:0010770
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":"ubiquitin-activating enzyme, Y-linked","secondary_identifiers":["OMIM:489000","MEDGEN:326389","UMLS:C1839046"],"synonyms":[{"name":"Ube1Y","type":"related"},{"name":"ubiquitin-activating enzyme, Y-linked","type":"exact"}],"termid":"MONDO:0010770","xrefs":{"Monarch":{"xref_id":"0010770"}}}


id: GO:0071479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a ionizing radiation stimulus. Ionizing radiation is radiation with sufficient energy to remove electrons from atoms and may arise from spontaneous decay of unstable isotopes, resulting in alpha and beta particles and gamma rays. Ionizing radiation also includes X-rays.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to ionizing radiation","termid":"GO:0010212"},{"relation_name":"is_a","term_name":"cellular response to radiation","termid":"GO:0071478"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to ionizing radiation","synonyms":[{"name":"cellular response to ionising radiation","type":"exact"},{"name":"cellular response to ionizing radiation stimulus","type":"exact"}],"termid":"GO:0071479"}


id: PBO:0090001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3/SUMO transferase, Topors, possibly associated with DNA damage","termid":"PBO:0090001"}


id: GO:0007454
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures derived from the labial disc are generated and organized. This includes the transformation of a labial imaginal disc from a monolayered epithelium in the larvae of holometabolous insects into recognizable adult structures including parts of the proboscis.","definition_xrefs":["GOC:bf","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc morphogenesis","termid":"GO:0007560"},{"relation_name":"part_of","term_name":"labial disc development","termid":"GO:0035217"}],"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":"labial disc morphogenesis","synonyms":[{"name":"labial disc metamorphosis","type":"exact"}],"termid":"GO:0007454"}


id: PBO:0053442
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 388","termid":"PBO:0053442"}


id: GO:0032625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-21 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-21 production","secondary_identifiers":["GO:0042238","GO:0072619"],"synonyms":[{"name":"IL-21 production","type":"exact"},{"name":"interleukin-21 biosynthetic process","type":"narrow"},{"name":"interleukin-21 secretion","type":"narrow"}],"termid":"GO:0032625"}


id: PBO:0086469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative mitochondrial porin (voltage-dependent anion channel); not required for mitochondrial membrane permeability or mitochondrial osmotic stability; POR2 has a paralog, POR1, that arose from the whole genome duplication","termid":"PBO:0086469"}


id: MONDO:0012747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glycogen storage disease due to aldolase A deficiency is an extremely rare glycogen storage disease characterized by hemolytic anemia with or without myopathy or intellectual deficit. Myopathy can be severe enough to result in fatal rhabdomyolysis in some patients. A family with episodic rhabdomyolysis (triggered by fever) without hemolytic anemia has recently been reported.","definition_xrefs":["Orphanet:57"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"disorder of glycogen metabolism","termid":"MONDO:0002412"},{"relation_name":"is_a","term_name":"familial hemolytic anemia","termid":"MONDO:0003689"},{"relation_name":"is_a","term_name":"disorder of glycolysis","termid":"MONDO:0017688"},{"relation_name":"is_a","term_name":"anemia due to erythrocyte enzyme disorder","termid":"MONDO:0020585"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0037792","MONDO:0019254","MONDO:0005066","MONDO:0002280"],"is_obsolete":false,"name":"glycogen storage disease due to aldolase A deficiency","secondary_identifiers":["UMLS:C0272066","ICD9:282.3","MESH:C562718","NANDO:1200834","GARD:600","SCTID:111578003","MEDGEN:82895","icd11.foundation:1020924235","OMIM:611881"],"synonyms":[{"name":"Aldoa deficiency","type":"related"},{"name":"GSD 12","type":"related"},{"name":"GSD due to aldolase A deficiency","type":"exact"},{"name":"GSD type 12","type":"exact"},{"name":"GSD type XII","type":"exact"},{"name":"GSD12","type":"related"},{"name":"Red cell aldolase deficiency","type":"related"},{"name":"aldolase a deficiency","type":"related"},{"name":"aldolase deficiency red cell","type":"related"},{"name":"aldolase deficiency, Red cell","type":"related"},{"name":"glycogen storage disease 12","type":"related"},{"name":"glycogen storage disease XII","type":"related"},{"name":"glycogen storage disease due to aldolase A deficiency","type":"exact"},{"name":"glycogen storage disease type 12","type":"exact"},{"name":"glycogen storage disease type XII","type":"exact"},{"name":"glycogenosis due to aldolase A deficiency","type":"exact"},{"name":"glycogenosis type 12","type":"exact"},{"name":"glycogenosis type XII","type":"exact"}],"termid":"MONDO:0012747","xrefs":{"Monarch":{"xref_id":"0012747"}}}


id: GO:0050211
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-galactose + procollagen 5-hydroxy-L-lysine = UDP + procollagen 5-(D-galactosyloxy)-L-lysine.","definition_xrefs":["MetaCyc:PROCOLLAGEN-GALACTOSYLTRANSFERASE-RXN","EC:2.4.1.50"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0140096","GO:0016757","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"procollagen galactosyltransferase activity","secondary_identifiers":["Reactome:R-HSA-1981128","RHEA:12637","Reactome:R-HSA-1981120"],"synonyms":[{"name":"UDP galactose-collagen galactosyltransferase activity","type":"related"},{"name":"UDP-galactose:procollagen-5-hydroxy-L-lysine D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:5-hydroxylysine-collagen galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:procollagen-5-hydroxy-L-lysine D-galactosyltransferase activity","type":"related"},{"name":"collagen galactosyltransferase activity","type":"related"},{"name":"collagen hydroxylysyl galactosyltransferase activity","type":"related"},{"name":"hydroxylysine galactosyltransferase activity","type":"related"},{"name":"uridine diphosphogalactose-collagen galactosyltransferase activity","type":"related"}],"termid":"GO:0050211"}


id: PBO:0003208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication licensing factor Cdt1","termid":"PBO:0003208"}


id: PBO:0061062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NKAIN1 pseudogene 2","termid":"PBO:0061062"}


id: GO:0000338
data:
  {"annotated_genes":["SJAG_05977","SJAG_00776","SJAG_03733","SJAG_00795","SJAG_00720","SJAG_04011","SJAG_04948","SJAG_03325","SJAG_02341","SJAG_02764"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89150,90965,92392,92513,94798,100805,104762,105960,108453,109789],"is_not":false,"summary":null,"term":"GO:0000338"}]},"cv_name":"biological_process","definition":"The removal of a ubiquitin-like protein of the NEDD8 type from a protein.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification by small protein removal","termid":"GO:0070646"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00720":null,"SJAG_00776":null,"SJAG_00795":null,"SJAG_02341":null,"SJAG_02764":null,"SJAG_03325":null,"SJAG_03733":null,"SJAG_04011":null,"SJAG_04948":null,"SJAG_05977":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"protein deneddylation","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0010388"],"synonyms":[{"name":"cullin deneddylation","type":"narrow"}],"termid":"GO:0000338","terms_by_termid":{"GO:0000338":null}}


id: MONDO:0054794
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hydrocephalus","termid":"MONDO:0016349"}],"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":"hydrocephalus, congenital, 3, with brain anomalies","secondary_identifiers":["MEDGEN:1648319","OMIM:617967","UMLS:C4747885"],"synonyms":[{"name":"HYC3","type":"related"},{"name":"hydrocephalus, CONGENITAL, 3, with brain anomalies","type":"related"},{"name":"hydrocephalus, nonsyndromic, autosomal recessive 3","type":"related"},{"name":"hydrocephalus, nonsyndromic, autosomal recessive 3, formerly","type":"related"}],"termid":"MONDO:0054794","xrefs":{"Monarch":{"xref_id":"0054794"}}}


id: MONDO:0000524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mixed germ cell cancer that is located in areas of the body other than the ovary or testicle.","definition_xrefs":["DOID:0050907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extragonadal germ cell cancer","termid":"MONDO:0003113"},{"relation_name":"is_a","term_name":"mixed germ cell tumor","termid":"MONDO:0015864"}],"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":"mixed extragonadal germ cell cancer","termid":"MONDO:0000524","xrefs":{"Monarch":{"xref_id":"0000524"}}}


id: PBO:0000255
data:
  {"annotation_feature_type":"gene","cv_name":"m_f_g","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chaperone","termid":"PBO:0000255"}


id: MONDO:0016537
data:
  {"annotated_genes":["SJAG_03453","SJAG_01787","SJAG_00610"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013767"},{"annotations":[85349,85350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000024"}]},"cv_name":"mondo","definition":"A disorder characterized by proliferation of lymphocytes at various stages of differentiation. Lymphoproliferative disorders can be neoplastic (clonal, as in lymphomas and leukemias) or reactive (polyclonal, as in infectious mononucleosis).","definition_xrefs":["NCIT:C9308"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"lymphoproliferative syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:20633","SCTID:277466009","UMLS:C0024314","Orphanet:238510","MEDGEN:6162","DOID:0060704","MESH:D008232","OMIMPS:308240"],"synonyms":[{"name":"lymphoproliferative disorder","type":"exact"},{"name":"lymphoproliferative syndrome","type":"exact"}],"termid":"MONDO:0016537","terms_by_termid":{"MONDO:0013767":null,"MONDO:8000024":null},"xrefs":{"Monarch":{"xref_id":"0016537"}}}


id: GO:0015971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of guanine tetraphosphate (5'-ppGpp-3'), a derivative of guanine riboside with four phosphates.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide catabolic process","termid":"GO:0009154"},{"relation_name":"is_a","term_name":"guanosine tetraphosphate metabolic process","termid":"GO:0015969"},{"relation_name":"is_a","term_name":"purine ribonucleoside bisphosphate catabolic process","termid":"GO:0034037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"guanosine tetraphosphate catabolic process","synonyms":[{"name":"guanosine tetraphosphate (5'-ppGpp-3') catabolic process","type":"exact"},{"name":"guanosine tetraphosphate (5'-ppGpp-3') catabolism","type":"exact"},{"name":"guanosine tetraphosphate breakdown","type":"exact"},{"name":"guanosine tetraphosphate catabolism","type":"exact"},{"name":"guanosine tetraphosphate degradation","type":"exact"}],"termid":"GO:0015971"}


id: MONDO:1011321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary disease, non-human animal","termid":"MONDO:1011321","xrefs":{"Monarch":{"xref_id":"1011321"}}}


id: PR:Q09195
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A delta(14)-sterol reductase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04051","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":"delta(14)-sterol reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16G5.18","secondary_identifiers":["UniProtKB:Q09195"],"synonyms":[{"name":"C-14 sterol reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-TM7SF2","type":"exact"},{"name":"sterol C14-reductase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09195"}


id: MONDO:0015598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acrodermatitis continua suppurativa of Hallopeau (obsolete MONDO:0015598)","termid":"MONDO:0015598","xrefs":{"Monarch":{"xref_id":"0015598"}}}


id: MONDO:0000226
data:
  {"annotated_genes":["SJAG_03316","SJAG_01351","SJAG_02805","SJAG_03553","SJAG_04459","SJAG_02007","SJAG_04425","SJAG_04016","SJAG_03701","SJAG_01417","SJAG_03556","SJAG_01995","SJAG_01941","SJAG_03866","SJAG_02397","SJAG_03641","SJAG_02463","SJAG_03069","SJAG_01612","SJAG_01162","SJAG_05277","SJAG_03475","SJAG_03659","SJAG_00988","SJAG_01070","SJAG_00582","SJAG_03712","SJAG_01164","SJAG_03222","SJAG_00115","SJAG_03290","SJAG_01466","SJAG_01199","SJAG_00084","SJAG_01216","SJAG_01147","SJAG_04042","SJAG_03671","SJAG_02117","SJAG_02306","SJAG_01880","SJAG_04757"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009825"},{"annotations":[84729,84730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010966"},{"annotations":[85163],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100255"},{"annotations":[86268,86269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009727"},{"annotations":[84855,84856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009352"},{"annotations":[84568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009058"},{"annotations":[86322,86323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009107"},{"annotations":[86541],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015003"},{"annotations":[85006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010926"},{"annotations":[85756,85757],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009285"},{"annotations":[85437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009259"},{"annotations":[85311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009947"},{"annotations":[85741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009284"},{"annotations":[85038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011417"},{"annotations":[86389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019531"},{"annotations":[85808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009666"},{"annotations":[84799,84800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009353"},{"annotations":[86441],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013404"},{"annotations":[86464,86463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"},{"annotations":[86174],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013762"},{"annotations":[84973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014576"},{"annotations":[85501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009607"},{"annotations":[84777,84776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009354"},{"annotations":[85388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009609"},{"annotations":[86208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"},{"annotations":[85282,85281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009189"},{"annotations":[84674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011582"},{"annotations":[85201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013675"},{"annotations":[85552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014132"},{"annotations":[84820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014611"},{"annotations":[84887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033282"},{"annotations":[85530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054785"},{"annotations":[85875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957382"},{"annotations":[86449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010476"},{"annotations":[85165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014290"},{"annotations":[84741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009529"},{"annotations":[85330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014803"},{"annotations":[84839,84840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019666"},{"annotations":[84681],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009593"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":42,"genes_by_uniquename":{"SJAG_00084":null,"SJAG_00115":null,"SJAG_00582":null,"SJAG_00988":null,"SJAG_01070":null,"SJAG_01147":null,"SJAG_01162":null,"SJAG_01164":null,"SJAG_01199":null,"SJAG_01216":null,"SJAG_01351":null,"SJAG_01417":null,"SJAG_01466":null,"SJAG_01612":null,"SJAG_01880":null,"SJAG_01941":null,"SJAG_01995":null,"SJAG_02007":null,"SJAG_02117":null,"SJAG_02306":null,"SJAG_02397":null,"SJAG_02463":null,"SJAG_02805":null,"SJAG_03069":null,"SJAG_03222":null,"SJAG_03290":null,"SJAG_03316":null,"SJAG_03475":null,"SJAG_03553":null,"SJAG_03556":null,"SJAG_03641":null,"SJAG_03659":null,"SJAG_03671":null,"SJAG_03701":null,"SJAG_03712":null,"SJAG_03866":null,"SJAG_04016":null,"SJAG_04042":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04757":null,"SJAG_05277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"mineral metabolism disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:45744005","ICD9:275.8","UMLS:C0154260","EFO:0009556","ICD9:275.9","MEDGEN:509562","ICD10CM:E83"],"synonyms":[{"name":"disease of mineral metabolism","type":"exact"},{"name":"disorder of mineral metabolism","type":"exact"}],"termid":"MONDO:0000226","terms_by_termid":{"MONDO:0009058":null,"MONDO:0009107":null,"MONDO:0009189":null,"MONDO:0009259":null,"MONDO:0009284":null,"MONDO:0009285":null,"MONDO:0009352":null,"MONDO:0009353":null,"MONDO:0009354":null,"MONDO:0009529":null,"MONDO:0009593":null,"MONDO:0009607":null,"MONDO:0009609":null,"MONDO:0009666":null,"MONDO:0009727":null,"MONDO:0009825":null,"MONDO:0009947":null,"MONDO:0010184":null,"MONDO:0010476":null,"MONDO:0010926":null,"MONDO:0010966":null,"MONDO:0011417":null,"MONDO:0011582":null,"MONDO:0011706":null,"MONDO:0013404":null,"MONDO:0013675":null,"MONDO:0013762":null,"MONDO:0014132":null,"MONDO:0014290":null,"MONDO:0014576":null,"MONDO:0014611":null,"MONDO:0014803":null,"MONDO:0015003":null,"MONDO:0019531":null,"MONDO:0019666":null,"MONDO:0033282":null,"MONDO:0054785":null,"MONDO:0100255":null,"MONDO:0957382":null},"xrefs":{"Monarch":{"xref_id":"0000226"}}}


id: FYPO:0000177
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which assembly of the mitotic spindle is abnormal. Spindle assembly is the aggregation, arrangement and bonding together of a set of components to form the spindle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"abnormal mitotic spindle","termid":"FYPO:0000338"},{"relation_name":"is_a","term_name":"abnormal spindle assembly","termid":"FYPO:0000119"},{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton organization during vegetative growth","termid":"FYPO:0001350"},{"relation_name":"is_a","term_name":"abnormal cellular component assembly during vegetative growth","termid":"FYPO:0001354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000054","FYPO:0000337","FYPO:0001985","FYPO:0000631","FYPO:0000002","FYPO:0005447","FYPO:0000641"],"is_obsolete":false,"name":"abnormal mitotic spindle assembly","secondary_identifiers":["FYPO:0001349"],"synonyms":[{"name":"abnormal bipolar spindle formation","type":"exact"},{"name":"abnormal mitotic spindle assembly during vegetative growth","type":"exact"},{"name":"abnormal spindle assembly during mitotic cell cycle","type":"related"},{"name":"abnormal spindle assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0000177"}


id: GO:0005205
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete chondroitin sulfate/dermatan sulfate proteoglycan (obsolete GO:0005205)","synonyms":[{"name":"chondroitin sulfate/dermatan sulfate proteoglycan","type":"exact"},{"name":"chondroitin sulphate/dermatan sulphate proteoglycan","type":"exact"}],"termid":"GO:0005205"}


id: PBO:0059138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MPHOSPH10 pseudogene 5","termid":"PBO:0059138"}


id: GO:0070538
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to oleic acid, the 18-carbon monounsaturated fatty acid (9Z)-octadec-9-enoic acid.","definition_xrefs":["GOC:mah","GOC:lp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid binding","termid":"GO:0036041"}],"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:0008289"}],"interesting_parent_ids":["GO:0003674","GO:0008289","GO:0005488"],"is_obsolete":false,"name":"oleic acid binding","termid":"GO:0070538"}


id: PBO:0051228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (II)-22-1 (pseudogene)","termid":"PBO:0051228"}


id: GO:0038146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of the chemokine CXCL12 to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","GOC:nhn","Wikipedia:Stromal_cell-derived_factor-1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine-mediated signaling pathway","termid":"GO:0070098"}],"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":"chemokine (C-X-C motif) ligand 12 signaling pathway","synonyms":[{"name":"CXCL12 signaling pathway","type":"exact"},{"name":"CXCL12-activated CXCR7 signaling pathway","type":"narrow"},{"name":"SDF1 signaling pathway","type":"exact"},{"name":"stromal cell-derived factor-1 signaling pathway","type":"exact"}],"termid":"GO:0038146"}


id: PBO:0082218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha 7 subunit of the 20S proteasome; protein abundance increases in response to DNA replication stress","termid":"PBO:0082218"}


id: MONDO:0034976
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acquired Creutzfeldt-Jakob disease","termid":"MONDO:0018686"},{"relation_name":"is_a","term_name":"nosocomial infection","termid":"MONDO:0043544"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iatrogenic Creutzfeldt-Jakob disease","secondary_identifiers":["UMLS:C2349757","MEDGEN:908476","Orphanet:576379","NANDO:1200193","GARD:22329","icd11.foundation:437591130"],"termid":"MONDO:0034976","xrefs":{"Monarch":{"xref_id":"0034976"}}}


id: FYPO:0007752
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a short spindle assembles during the first meiotic nuclear division, and may begin elongation, but then become shorter instead of continuing or resuming elongation.","definition_xrefs":["PomBase:mah","PMID:32723864"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiosis I","termid":"FYPO:0003603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"spindle regression during meiosis I","synonyms":[{"name":"meiosis I spindle regression","type":"exact"},{"name":"meiosis I spindle shrinkage","type":"exact"},{"name":"meiotic spindle regression during meiosis I","type":"exact"},{"name":"spindle regression during first meiotic nuclear division","type":"exact"},{"name":"spindle shrinkage during meiosis I","type":"exact"}],"termid":"FYPO:0007752"}


id: GO:0047369
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-hydroxy-3-methylglutarate + succinyl-CoA = 3-hydroxy-3-methyl-glutaryl-CoA + succinate.","definition_xrefs":["EC:2.8.3.13","MetaCyc:2.8.3.13-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-transferase activity","termid":"GO:0008410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016782","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"succinate-hydroxymethylglutarate CoA-transferase activity","secondary_identifiers":["RHEA:12284"],"synonyms":[{"name":"dicarboxyl-CoA:dicarboxylic acid coenzyme A transferase activity","type":"related"},{"name":"hydroxymethylglutarate coenzyme A-transferase activity","type":"related"},{"name":"succinate:(S)-3-hydroxy-3-methylglutarate CoA-transferase activity","type":"related"}],"termid":"GO:0047369"}


id: PBO:0025424
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA repair-deficiency disorders","termid":"PBO:0025424"}


id: PBO:0045312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartyl aminopeptidase","termid":"PBO:0045312"}


id: FYPO:0005336
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 histone H3 measured in the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular histone level","termid":"FYPO:0004981"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal level of histone H3 in cell","synonyms":[{"name":"normal accumulation of histone H3 in cell","type":"related"},{"name":"normal cellular histone H3 level","type":"exact"},{"name":"normal histone H3 level during vegetative growth","type":"exact"},{"name":"normal level of histone H3 in cell during mitotic cell cycle","type":"related"},{"name":"normal level of histone H3 in cell during vegetative growth","type":"exact"}],"termid":"FYPO:0005336"}


id: PBO:0084357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lectin-like protein with similarity to Flo1p; thought to be expressed and involved in flocculation","termid":"PBO:0084357"}


id: FYPO:0002805
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 sodium ion import into the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transport","termid":"FYPO:0001071"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0000257"],"is_obsolete":false,"name":"normal sodium import","synonyms":[{"name":"normal sodium import across plasma membrane","type":"exact"},{"name":"normal sodium import during mitotic cell cycle","type":"related"},{"name":"normal sodium import during vegetative growth","type":"exact"},{"name":"normal sodium import into cell","type":"exact"},{"name":"normal sodium ion import into cell","type":"exact"},{"name":"normal sodium uptake","type":"exact"}],"termid":"FYPO:0002805"}


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


id: MONDO:0005834
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection with the organism Mycobacterium.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlamydia trachomatis infectious disease","termid":"MONDO:0005701"},{"relation_name":"is_a","term_name":"granuloma inguinale","termid":"MONDO:0005777"},{"relation_name":"is_a","term_name":"lymphatic system disorder","termid":"MONDO:0005833"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"lymphogranuloma venereum","secondary_identifiers":["MESH:D008219","UMLS:C0024286","DOID:13819","ICD9:099.1","SCTID:186946009","EFO:0007353","MEDGEN:44221","NCIT:C26822"],"synonyms":[{"name":"Durand-Nicolas-Favre disease","type":"exact"},{"name":"LGV","type":"related"},{"name":"Poradenitis inguinale","type":"exact"},{"name":"climatic or tropical bubo","type":"exact"},{"name":"lymph granuloma inguinale","type":"exact"},{"name":"lymphogranuloma inguinale","type":"exact"},{"name":"strumous bubo","type":"exact"}],"termid":"MONDO:0005834","xrefs":{"Monarch":{"xref_id":"0005834"}}}


id: MONDO:0009906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital bowing of long bones","termid":"MONDO:0008882"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prenatal bowing","secondary_identifiers":["UMLS:C1849701","MEDGEN:337891","MESH:C564873","GARD:15225","OMIM:264050"],"synonyms":[{"name":"prenatal bowing","type":"exact"}],"termid":"MONDO:0009906","xrefs":{"Monarch":{"xref_id":"0009906"}}}


id: PBO:0057059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 143","termid":"PBO:0057059"}


id: GO:0071522
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ureidoglycine + H2O = S-ureidoglycolate + NH3.","definition_xrefs":["MetaCyc:URUR-RXN","PMID:19935661","PMID:20038185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines","termid":"GO:0016813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"ureidoglycine aminohydrolase activity","secondary_identifiers":["RHEA:25241","EC:3.5.3.26"],"termid":"GO:0071522"}


id: MONDO:0022535
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"carotid artery disorder","termid":"MONDO:0005269"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autonomic facial cephalgia","secondary_identifiers":["UMLS:C0238902","SCTID:230482003","ICD9:337.09","MEDGEN:536866"],"synonyms":[{"name":"Autonomic facial cephalgia","type":"related"},{"name":"Carotidynia","type":"related"},{"name":"Carotodynia","type":"related"},{"name":"carotidynia","type":"exact"}],"termid":"MONDO:0022535","xrefs":{"Monarch":{"xref_id":"0022535"}}}


id: GO:0033077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a T cell via a differentiation pathway dependent upon transit through the thymus.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell differentiation","termid":"GO:0030217"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"T cell differentiation in thymus","synonyms":[{"name":"T cell development in thymus","type":"related"},{"name":"thymic T cell differentiation","type":"exact"},{"name":"thymocyte cell differentiation","type":"exact"},{"name":"thymocyte differentiation","type":"exact"}],"termid":"GO:0033077"}


id: GO:0098676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a virus improves the virulence of its host for that host's respective host. Common in but not limited to bacteriophages; also occurs in phage-bearing bacteria infecting plants or animals for example. Mechanisms include the expression of factors that modulate a bacterial adhesion to a host cell, spread through host tissues, production of exotoxins or provide protection against host immune defenses.","definition_xrefs":["PMID:11553559","PMID:8658163","VZ:3965","PMID:10913072","PMID:22919604"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host process","termid":"GO:0044003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated modulation of host virulence","synonyms":[{"name":"modulation of host virulence by virus","type":"narrow"}],"termid":"GO:0098676"}


id: PBO:0002466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin","termid":"PBO:0002466"}


id: GO:0008166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete viral replication (obsolete GO:0008166)","synonyms":[{"name":"viral replication","type":"exact"}],"termid":"GO:0008166"}


id: MONDO:0017908
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hyperekplexia (obsolete MONDO:0017908)","termid":"MONDO:0017908","xrefs":{"Monarch":{"xref_id":"0017908"}}}


id: MONDO:0011017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterized by peculiar wooly hair and palmoplantar keratoderma.","definition_xrefs":["Orphanet:34217"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diffuse palmoplantar keratoderma","termid":"MONDO:0017666"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic hair shaft abnormality (obsolete MONDO:0019282)","termid":"MONDO:0019282"},{"relation_name":"is_a","term_name":"familial cardiomyopathy","termid":"MONDO:0005217"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"arrhythmogenic right ventricular cardiomyopathy","termid":"MONDO:0016587"},{"relation_name":"is_a","term_name":"cardioectodermal syndrome","termid":"MONDO:0100080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0006025"],"is_obsolete":false,"name":"Naxos disease","secondary_identifiers":["DOID:0080551","GARD:9795","OMIM:601214","UMLS:C1832600","MESH:C538346","icd11.foundation:633516876","MEDGEN:321991","SCTID:715535009"],"synonyms":[{"name":"KWWH type I","type":"exact"},{"name":"Mal De Naxos","type":"related"},{"name":"NAXOS disease","type":"exact"},{"name":"NXD","type":"exact"},{"name":"Naxos disease","type":"exact"},{"name":"cardiomyopathy, arrhythmogenic right ventricular, with skin, hair, and nail abnormalities","type":"related"},{"name":"keratoderma with woolly hair type I","type":"exact"},{"name":"keratoderma with wooly hair type I","type":"exact"},{"name":"keratosis palmoplantaris arrythmogenic cardiomyopathy woolly hair","type":"related"},{"name":"keratosis palmoplantaris arrythmogenic cardiomyopathy wooly hair","type":"related"},{"name":"keratosis palmoplantaris with arrhythmogenic cardiomyopathy","type":"related"},{"name":"keratosis palmoplantaris with arrythmogenic cardiomyopathy","type":"exact"},{"name":"palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy","type":"exact"},{"name":"palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and woolly hair","type":"related"},{"name":"palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and wooly hair","type":"related"},{"name":"palmoplantar keratoderma with arrythmogenic cardiomyopathy","type":"exact"},{"name":"woolly hair palmoplantar keratoderma cardiac abnormalities","type":"related"},{"name":"woolly hair, palmoplantar keratoderma, and Cardiac abnormalities","type":"related"},{"name":"wooly hair palmoplantar keratoderma cardiac abnormalities","type":"related"},{"name":"wooly hair, palmoplantar keratoderma, and Cardiac abnormalities","type":"related"}],"termid":"MONDO:0011017","xrefs":{"Monarch":{"xref_id":"0011017"}}}


id: FYPO:0004613
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 spindle pole body is not attached to any interphase cytoplasmic microtubules; as a result, the microtubules are not connected to the nucleus. Normally, the spindle pole body is attached to at least one cytoplasmic microtubule bundle.","definition_xrefs":["PomBase:mah","PomBase:vw","PMID:15772152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle pole body morphology","termid":"FYPO:0001474"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abolished microtubule attachment to spindle pole body","synonyms":[{"name":"SPB detached from cytoplasmic microtubules","type":"exact"},{"name":"abolished microtubule attachment to nucleus","type":"broad"},{"name":"abolished microtubule attachment to spindle pole body during mitotic cell cycle","type":"related"},{"name":"abolished microtubule attachment to spindle pole body during vegetative growth","type":"exact"},{"name":"cytoplasmic microtubules absent from mitotic spindle pole body","type":"exact"},{"name":"cytoplasmic microtubules detached from spindle pole body","type":"exact"},{"name":"interphase microtubules detached from nucleus","type":"exact"},{"name":"interphase microtubules detached from spindle pole body","type":"exact"},{"name":"spindle pole body detached from cytoplasmic microtubules","type":"exact"}],"termid":"FYPO:0004613"}


