# terms

id: MONDO:0018404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare genetic male infertility.","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic male infertility (obsolete MONDO:0018404)","secondary_identifiers":["Orphanet:399980"],"synonyms":[{"name":"rare genetic male infertility","type":"exact"}],"termid":"MONDO:0018404","xrefs":{"Monarch":{"xref_id":"0018404"}}}


id: PBO:0059052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAX network transcriptional repressor","termid":"PBO:0059052"}


id: PBO:0014599
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Orc4 determines sequence specificity of ORC binding to DNA replication origins","termid":"PBO:0014599"}


id: GO:0005297
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: proline(out) + H+(out) = proline(in) + H+(in).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid:proton symporter activity","termid":"GO:0005280"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"proline:proton symporter activity","synonyms":[{"name":"hydrogen/proline transporter","type":"broad"}],"termid":"GO:0005297"}


id: PBO:0060952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear factor I X","termid":"PBO:0060952"}


id: PBO:0084831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein required for translation of the COB mRNA; forms a complex with Cbp3p that binds to mt ribosomes near the polypeptide tunnel exit and promotes efficient translation of the COB mRNA; Cbp3p-Cbp6p complex also interacts with newly synthesized cytochrome b (Cobp) and Cbp4p to promote assembly of Cobp into the cytochrome bc1 complex; Cbp3p-Cbp6p complex is sequestered if assembly of Complex III is blocked, downregulating COB mRNA translation","termid":"PBO:0084831"}


id: FYPO:0004057
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of intragenic meiotic recombination is increased. Intragenic meiotic recombination can result in gene conversion events.","definition_xrefs":["PMID:19436749","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased meiotic recombination","termid":"FYPO:0000487"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000293","FYPO:0000631","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased intragenic meiotic recombination","synonyms":[{"name":"increased meiotic intragenic recombination","type":"exact"}],"termid":"FYPO:0004057"}


id: PBO:0110050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoinositide PI4,5P(2) binding protein Slm1","termid":"PBO:0110050"}


id: PBO:0067159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 211, pseudogene","termid":"PBO:0067159"}


id: MONDO:0014601
data:
  {"annotated_genes":["SJAG_04822"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87014],"is_not":false,"summary":null,"term":"MONDO:0014601"}]},"cv_name":"mondo","definition":"Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the SNX14 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04822":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559","MONDO:0020022","MONDO:0002320"],"is_obsolete":false,"name":"autosomal recessive spinocerebellar ataxia 20","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5190595","DOID:0080066","OMIM:616354","MEDGEN:1684324","GARD:17636","Orphanet:397709"],"synonyms":[{"name":"SCAR20","type":"exact"},{"name":"SNX14 autosomal recessive cerebellar ataxia","type":"exact"},{"name":"autosomal recessive cerebellar ataxia caused by mutation in SNX14","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia type 20","type":"exact"},{"name":"intellectual disability-coarse face-macrocephaly-cerebellar hypoplasia syndrome","type":"exact"},{"name":"intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive 20","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 20","type":"exact"}],"termid":"MONDO:0014601","terms_by_termid":{"MONDO:0014601":null},"xrefs":{"Monarch":{"xref_id":"0014601"}}}


id: PBO:0069232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 487, pseudogene","termid":"PBO:0069232"}


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


id: PBO:0087053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L25; primary rRNA-binding ribosomal protein component of large ribosomal subunit; binds to 25S rRNA via a conserved C-terminal motif; homologous to mammalian ribosomal protein L23A and bacterial L23","termid":"PBO:0087053"}


id: GO:0043172
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of ferredoxin, any simple, nonenzymatic iron-sulfur protein that is characterized by having equal numbers of atoms of iron and labile sulfur. Iron and sulfur atoms are present in one or two clusters of two or four atoms of each.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete ferredoxin biosynthetic process (obsolete GO:0043172)","synonyms":[{"name":"ferredoxin anabolism","type":"exact"},{"name":"ferredoxin biosynthesis","type":"exact"},{"name":"ferredoxin formation","type":"exact"},{"name":"ferredoxin synthesis","type":"exact"}],"termid":"GO:0043172"}


id: GO:0062036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive a hot temperature stimulus, convert it to a molecular signal, and recognize and characterize the signal.","definition_xrefs":["PMID:21335241"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thermoception","termid":"GO:0050955"}],"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 perception of hot stimulus","termid":"GO:0062036"}


id: GO:0007504
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the larval fat body over time, from its formation to the mature structure. The larval fat body consists of a bilaterally symmetrical monolayer of cells lying between the gut and the muscles of the body wall. As in other tissues of the larva, the cells of the fat body complete their divisions in the embryo and increase in size and ploidy during larval life.","definition_xrefs":["ISBN:0879694238","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fat body development","termid":"GO:0007503"},{"relation_name":"part_of","term_name":"instar larval development","termid":"GO:0002168"}],"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 fat body development","termid":"GO:0007504"}


id: GO:2000080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of canonical Wnt signaling pathway modulating the rate or frequency of pancreatic B cell proliferation.","definition_xrefs":["GOC:yaf","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of canonical Wnt signaling pathway involved in controlling type B pancreatic cell proliferation (obsolete GO:2000080)","synonyms":[{"name":"negative regulation of canonical Wnt receptor signaling pathway involved in controlling pancreatic B cell proliferation","type":"exact"},{"name":"negative regulation of canonical Wnt receptor signaling pathway involved in controlling type B pancreatic cell proliferation","type":"exact"},{"name":"negative regulation of canonical Wnt receptor signaling pathway involved in pancreatic beta cell proliferation","type":"exact"},{"name":"negative regulation of canonical Wnt receptor signalling pathway involved in controlling pancreatic B cell proliferation","type":"exact"},{"name":"negative regulation of canonical Wnt receptor signalling pathway involved in controlling type B pancreatic cell proliferation","type":"exact"},{"name":"negative regulation of canonical Wnt-activated signaling pathway involved in controlling type B pancreatic cell proliferation","type":"exact"}],"termid":"GO:2000080"}


id: PBO:0068239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 18S ribosomal N5","termid":"PBO:0068239"}


id: PBO:0028531
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-explosive_cytokinetic_cell_separation_resulting_in_vegetative_cell_lysis","termid":"PBO:0028531"}


id: GO:0015791
data:
  {"annotated_genes":["SJAG_04506","SJAG_03595"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73711,74708],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904679"}]},"cv_name":"biological_process","definition":"The directed movement of polyols, any polyhydric alcohol, across a membrane.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03595":null,"SJAG_04506":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"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:0055085","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"polyol transmembrane transport","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0015791","terms_by_termid":{"GO:1904679":null}}


id: GO:0019722
data:
  {"annotated_genes":["SJAG_02858","SJAG_03501","SJAG_03631","SJAG_03486","SJAG_03793","SJAG_04551","SJAG_00296","SJAG_04668","SJAG_01181","SJAG_02429","SJAG_04471","SJAG_04871","SJAG_03802","SJAG_03799","SJAG_03879"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66549,92987,99444,119230],"is_not":false,"summary":null,"term":"GO:0019722"},{"annotations":[74738,94171,81256,99888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097720"},{"annotations":[117981,118322,120083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061762"},{"annotations":[102786,117968],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0106057"},{"annotations":[103940,112808],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0050850"}]},"cv_name":"biological_process","definition":"Any intracellular signal transduction in which the signal is passed on within the cell via calcium ions.","definition_xrefs":["GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signaling cassette","termid":"GO:0141124"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00296":null,"SJAG_01181":null,"SJAG_02429":null,"SJAG_02858":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03631":null,"SJAG_03793":null,"SJAG_03799":null,"SJAG_03802":null,"SJAG_03879":null,"SJAG_04471":null,"SJAG_04551":null,"SJAG_04668":null,"SJAG_04871":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"calcium-mediated signaling","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Calcium_signaling"],"synonyms":[{"name":"calcium ion signaling","type":"exact"},{"name":"calcium signaling","type":"exact"},{"name":"calcium signalling","type":"exact"},{"name":"calcium-mediated signalling","type":"exact"}],"termid":"GO:0019722","terms_by_termid":{"GO:0019722":null,"GO:0050850":null,"GO:0061762":null,"GO:0097720":null,"GO:0106057":null}}


id: MONDO:0008662
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant vitreoretinochoroidopathy (ADVIRC) is a genetic vitreous-retinal disease characterized by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. Abnormal chorioretinal pigmentation is present, usually lying between the vortex veins and the ora serrata for 360 degrees.","definition_xrefs":["Orphanet:3086"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BEST1-related vitreoretinochoroidopathy","termid":"MONDO:0700240"}],"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":"autosomal dominant vitreoretinochoroidopathy","secondary_identifiers":["DOID:0111569","MESH:C536352","SCTID:711162004","GARD:5507","ICD10CM:H35.5","MEDGEN:854768","OMIM:193220","icd11.foundation:96951767","UMLS:C3888099"],"synonyms":[{"name":"ADVIRC","type":"exact"},{"name":"VRCP","type":"related"},{"name":"VRCP autosomal dominant","type":"related"},{"name":"microcornea, Rod-cone dystrophy, cataract, and posterior staphyloma","type":"related"},{"name":"vitreoretinochoroidopathy","type":"related"},{"name":"vitreoretinochoroidopathy dominant","type":"related"},{"name":"vitreoretinochoroidopathy with microcornea, glaucoma, and cataract","type":"related"},{"name":"vitreoretinochoroidopathy, autosomal dominant","type":"related"},{"name":"vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos","type":"related"}],"termid":"MONDO:0008662","xrefs":{"Monarch":{"xref_id":"0008662"}}}


id: PBO:0064594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 1 homeobox 1","termid":"PBO:0064594"}


id: MONDO:0010458
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypospadias","termid":"MONDO:0005345"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypospadias 4, X-linked","secondary_identifiers":["GARD:18187","UMLS:C3275458","MEDGEN:477089","OMIM:300856"],"synonyms":[{"name":"HYSP4","type":"related"},{"name":"hypospadias 4, X-linked, susceptibility to","type":"related"}],"termid":"MONDO:0010458","xrefs":{"Monarch":{"xref_id":"0010458"}}}


id: GO:0034219
data:
  {"annotated_genes":["SJAG_03820","SJAG_03960","SJAG_02719","SJAG_04905","SJAG_02958","SJAG_03608","SJAG_00057","SJAG_04068","SJAG_03606"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58433,61433,61449,65738],"is_not":false,"summary":null,"term":"GO:0034219"},{"annotations":[112472,116014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046323"},{"annotations":[119059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098708"},{"annotations":[112473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140425"},{"annotations":[66010,104782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008645"},{"annotations":[97547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106081"},{"annotations":[97548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106082"}]},"cv_name":"biological_process","definition":"The process in which a carbohydrate is transported across a membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transport","termid":"GO:0008643"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00057":null,"SJAG_02719":null,"SJAG_02958":null,"SJAG_03606":null,"SJAG_03608":null,"SJAG_03820":null,"SJAG_03960":null,"SJAG_04068":null,"SJAG_04905":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"carbohydrate transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"carbohydrate membrane transport","type":"exact"},{"name":"transmembrane carbohydrate transport","type":"exact"}],"termid":"GO:0034219","terms_by_termid":{"GO:0008645":null,"GO:0034219":null,"GO:0046323":null,"GO:0098708":null,"GO:0106081":null,"GO:0106082":null,"GO:0140425":null}}


id: PBO:0120085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EWSR1 pseudogene 1","termid":"PBO:0120085"}


id: PBO:0072376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS27A pseudogene 2","termid":"PBO:0072376"}


id: PBO:0016991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell surface glycoprotein, flocculin, related to Gsf2","termid":"PBO:0016991"}


id: MONDO:0014045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Cowden disease in which the cause of the disease is a mutation in the SDHD gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Cowden disease","termid":"MONDO:0016063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0000426"],"is_obsolete":false,"name":"Cowden syndrome 3","secondary_identifiers":["OMIM:615106"],"synonyms":[{"name":"CWS3","type":"related"},{"name":"Cowden disease caused by mutation in SDHD","type":"exact"},{"name":"Cowden syndrome 3","type":"exact"},{"name":"Cowden syndrome type 3","type":"exact"},{"name":"SDHD Cowden disease","type":"exact"}],"termid":"MONDO:0014045","xrefs":{"Monarch":{"xref_id":"0014045"}}}


id: GO:0072367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of lipid transport by modulating the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:BHF","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of lipid transport by regulation of transcription from RNA polymerase II promoter (obsolete GO:0072367)","synonyms":[{"name":"regulation of lipid transport by regulation of transcription from an RNA polymerase II promoter","type":"exact"}],"termid":"GO:0072367"}


id: PBO:0052417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell immunoglobulin like receptor, three Ig domains X1 (pseudogene)","termid":"PBO:0052417"}


id: GO:0052008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or function of a host cellular anatomical structure. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated disruption of host anatomical structure","termid":"GO:0052111"}],"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 disruption of host cellular anatomical structure","synonyms":[{"name":"catabolism of host cellular component by organism","type":"exact"},{"name":"catabolism of host structural constituent by organism","type":"exact"},{"name":"cytopathogenic effect","type":"related"},{"name":"degradation of host cellular component by organism","type":"exact"},{"name":"disassembly by organism of host cellular component","type":"exact"},{"name":"disassembly by symbiont of host cellular component","type":"related"},{"name":"disruption by symbiont of host cellular component","type":"exact"},{"name":"symbiont-mediated disruption of host cellular anatomical entity","type":"exact"},{"name":"symbiont-mediated disruption of host cellular component","type":"broad"}],"termid":"GO:0052008"}


id: PBO:0090678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase S6K family Sck2","termid":"PBO:0090678"}


id: PBO:0058918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA let-7a-1","termid":"PBO:0058918"}


id: PBO:0039319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arachidonate 5-lipoxygenase","termid":"PBO:0039319"}


id: PBO:0011082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"para-hydroxybenzoate--polyprenyltransferase Ppt1","termid":"PBO:0011082"}


id: FYPO:0003285
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of alpha,alpha-trehalase activity is lower than normal during a cellular response to nutrient.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal alpha,alpha-trehalase activity","termid":"FYPO:0001479"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000654","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"decreased alpha,alpha-trehalase activity during cellular response to nutrient","synonyms":[{"name":"decreased neutral trehalase activity during cellular response to nutrient","type":"exact"},{"name":"decreased trehalase activity during cellular response to nutrient","type":"broad"},{"name":"reduced alpha,alpha-trehalase activity during cellular response to nutrient","type":"exact"}],"termid":"FYPO:0003285"}


id: MONDO:0008192
data:
  {"annotated_genes":["SJAG_02398"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87580],"is_not":false,"summary":null,"term":"MONDO:0008192"}]},"cv_name":"mondo","definition":"Any paraganglioma in which the cause of the disease is a mutation in the SDHD gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraganglioma","termid":"MONDO:0000448"},{"relation_name":"is_a","term_name":"hereditary pheochromocytoma-paraganglioma","termid":"MONDO:0017366"},{"relation_name":"is_a","term_name":"adrenal gland neoplasm","termid":"MONDO:0021227"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02398":null},"genotype_count":0,"is_obsolete":false,"name":"paragangliomas 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:168000","UMLS:C3494181","GARD:7324","MEDGEN:488134"],"synonyms":[{"name":"PGL1","type":"related"},{"name":"Paragangliomata","type":"related"},{"name":"SDHD paraganglioma","type":"exact"},{"name":"carotid body tumors","type":"related"},{"name":"carotid body tumours","type":"related"},{"name":"chemodectomas","type":"related"},{"name":"glomus jugulare tumors","type":"related"},{"name":"glomus jugulare tumours","type":"related"},{"name":"glomus tumors, familial, 1","type":"related"},{"name":"paraganglioma caused by mutation in SDHD","type":"exact"},{"name":"paraganglioma, carotid body","type":"related"},{"name":"paragangliomas 1","type":"exact"},{"name":"paragangliomas 1, with or without deafness","type":"exact"},{"name":"paragangliomas type 1","type":"exact"},{"name":"paragangliomas with sensorineural hearing loss","type":"related"},{"name":"paragangliomas, familial nonchromaffin, 1","type":"related"},{"name":"paragangliomas, familial, 1","type":"related"}],"termid":"MONDO:0008192","terms_by_termid":{"MONDO:0008192":null},"xrefs":{"Monarch":{"xref_id":"0008192"}}}


id: GO:0075259
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a spore-bearing structure over time, from its formation to the mature structure. A spore-bearing structure is an anatomical structure that produces new spores.","definition_xrefs":["GOC:di","GOC:mcc","GOC:pamgo_curators","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"}],"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":"spore-bearing structure development","synonyms":[{"name":"fruiting structure development","type":"exact"},{"name":"sporangium development","type":"broad"},{"name":"spore-bearing organ development","type":"related"},{"name":"sporophore development","type":"exact"}],"termid":"GO:0075259"}


id: PBO:0029917
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_squalene_level","termid":"PBO:0029917"}


id: PBO:0028869
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_snoRNA_level","termid":"PBO:0028869"}


id: MONDO:0020579
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the mucous membranes.","definition_xrefs":["NCIT:C115965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucositis","secondary_identifiers":["MEDGEN:87165","MESH:D052016","UMLS:C0333355"],"synonyms":[{"name":"inflammation of mucosa","type":"exact"},{"name":"mucosa inflammation","type":"exact"},{"name":"mucositis","type":"exact"}],"termid":"MONDO:0020579","xrefs":{"Monarch":{"xref_id":"0020579"}}}


id: PBO:0113512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Type V myosin motor involved in actin-based transport of cargos; required for the polarized delivery of secretory vesicles, the vacuole, late Golgi elements, peroxisomes, lipid droplets, and the mitotic spindle; effector of Ypt11p, a rab-type small GTPase; MYO2 has a paralog, MYO4, that arose from the whole genome duplication","termid":"PBO:0113512"}


id: MONDO:0000914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.","definition_xrefs":["PMID:10476042","PMID:8878478","DOID:0111035"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy","termid":"MONDO:0007432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1","secondary_identifiers":["OMIM:125310","UMLS:C4551768","SCTID:390936003","NCIT:C84606","NORD:883","Orphanet:136","MedDRA:10065551","icd11.foundation:1621899838","MEDGEN:1634330","MESH:D046589","GARD:1049"],"synonyms":[{"name":"CADASIL","type":"exact"},{"name":"CADASIL 1","type":"exact"},{"name":"CADASIL syndrome","type":"exact"},{"name":"CADASIL type 1","type":"exact"},{"name":"CADASIL1","type":"exact"},{"name":"CASIL","type":"exact"},{"name":"autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1","type":"exact"},{"name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy","type":"related"},{"name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1","type":"exact"},{"name":"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1","type":"exact"},{"name":"cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy","type":"broad"},{"name":"dementia, hereditary multi-infarct type","type":"exact"},{"name":"familial vascular leukoencephalopathy","type":"related"},{"name":"hereditary multi-infarct dementia","type":"exact"}],"termid":"MONDO:0000914","xrefs":{"Monarch":{"xref_id":"0000914"}}}


id: PBO:0068054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 359","termid":"PBO:0068054"}


id: GO:0031747
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 2 cysteinyl leukotriene receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteinyl leukotriene receptor binding","termid":"GO:0031745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"type 2 cysteinyl leukotriene receptor binding","synonyms":[{"name":"type 2 cysteinyl leukotriene receptor ligand","type":"narrow"}],"termid":"GO:0031747"}


id: GO:1900581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (17Z)-protosta-17(20),24-dien-3beta-ol.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid biosynthetic process","termid":"GO:0006694"},{"relation_name":"is_a","term_name":"tetracyclic triterpenoid biosynthetic process","termid":"GO:0010686"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"(17Z)-protosta-17(20),24-dien-3beta-ol metabolic process","termid":"GO:1900579"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"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:0019748"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281","GO:0006629"],"is_obsolete":false,"name":"(17Z)-protosta-17(20),24-dien-3beta-ol biosynthetic process","synonyms":[{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol anabolism","type":"exact"},{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol biosynthesis","type":"exact"},{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol formation","type":"exact"},{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol synthesis","type":"exact"}],"termid":"GO:1900581"}


id: PBO:0064910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 4 regulatory subunit 1 like (pseudogene)","termid":"PBO:0064910"}


id: GO:0030700
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Complex that possesses glycine reductase activity; usually comprises three subunits, of which two are selenoproteins; the subunits are typically designated selenoprotein A, selenoprotein B and protein C.","definition_xrefs":["GOC:mah","PMID:2018775"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"glycine reductase complex","termid":"GO:0030700"}


id: MONDO:0012791
data:
  {"annotated_genes":["SJAG_03813"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88061],"is_not":false,"summary":null,"term":"MONDO:0012791"}]},"cv_name":"mondo","definition":"Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria is characterized by the association of a mitochondrial encephalomyopathy and an aminoacidopathy. It has been described in two brothers presenting with developmental delay, neurological signs, deafness, exercise intolerance, lactic acidosis and elevation of several plasmatic amino acids. Mitochondria morphology was found to be abnormal on muscle biopsy. Transmission is likely to be linked to maternal mitochondrial DNA.","definition_xrefs":["Orphanet:1933"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"mitochondrial DNA depletion syndrome, encephalomyopathic form","termid":"MONDO:0016796"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03813":null},"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":"mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C2749864","GARD:3681","MEDGEN:413170","DOID:0080124","MESH:C567624","OMIM:612073"],"synonyms":[{"name":"MTDPS5","type":"related"},{"name":"booth-Haworth-Dilling syndrome","type":"exact"},{"name":"encephalomyopathy","type":"related"},{"name":"mitochondrial DNA depletion syndrome 5","type":"exact"},{"name":"mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)","type":"related"},{"name":"mitochondrial DNA depletion syndrome type 5","type":"exact"},{"name":"mitochondrial DNA depletion syndrome, encephalomyopathic form, with or without methylmalonic aciduria, autosomal recessive, Sucla2-related","type":"related"},{"name":"mitochondrial dna depletion syndrome, encephalomyopathic form with methylmalonic aciduria, autosomal recessive","type":"related"},{"name":"mitochondrial encephalomyopathy aminoacidopathy","type":"related"},{"name":"mitochondrial encephalomyopathy-aminoacidopathy syndrome","type":"exact"},{"name":"mtDNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria","type":"exact"}],"termid":"MONDO:0012791","terms_by_termid":{"MONDO:0012791":null},"xrefs":{"Monarch":{"xref_id":"0012791"}}}


id: GO:0046051
data:
  {"annotated_genes":["SJAG_02887"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[65570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006228"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving UTP, uridine (5'-)triphosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleoside triphosphate metabolic process","termid":"GO:0009208"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide metabolic process","termid":"GO:0009218"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"UTP metabolic process","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"UTP metabolism","type":"exact"}],"termid":"GO:0046051","terms_by_termid":{"GO:0006228":null}}


id: MONDO:0016583
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"volvulus of midgut","termid":"MONDO:0008666"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial intestinal malrotation-facial anomalies syndrome","secondary_identifiers":["Orphanet:2454"],"synonyms":[{"name":"Stalker Chitayat syndrome","type":"related"},{"name":"Stalker-Chitayat syndrome","type":"exact"},{"name":"intestinal malrotation facial anomalies familial type","type":"related"}],"termid":"MONDO:0016583","xrefs":{"Monarch":{"xref_id":"0016583"}}}


id: GO:0043315
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neutrophil degranulation.","definition_xrefs":["ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of myeloid leukocyte mediated immunity","termid":"GO:0002888"},{"relation_name":"is_a","term_name":"positive regulation of leukocyte degranulation","termid":"GO:0043302"},{"relation_name":"is_a","term_name":"regulation of neutrophil degranulation","termid":"GO:0043313"},{"relation_name":"is_a","term_name":"positive regulation of immune response","termid":"GO:0050778"},{"relation_name":"positively_regulates","term_name":"neutrophil degranulation","termid":"GO:0043312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"positive regulation of neutrophil degranulation","synonyms":[{"name":"activation of neutrophil degranulation","type":"narrow"},{"name":"positive regulation of neutrophil granule exocytosis","type":"exact"},{"name":"stimulation of neutrophil degranulation","type":"narrow"},{"name":"up regulation of neutrophil degranulation","type":"exact"},{"name":"up-regulation of neutrophil degranulation","type":"exact"},{"name":"upregulation of neutrophil degranulation","type":"exact"}],"termid":"GO:0043315"}


id: PBO:0049765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 4 pseudogene 2","termid":"PBO:0049765"}


id: PR:Q11120
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ofd1 gene.","definition_xrefs":["UniProtKB:Q11120","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":"prolyl 3,4-dihydroxylase ofd1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC6B1.08c","synonyms":[{"name":"2-oxoglutarate and Fe(II) dioxygenase domain-containing protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PKHD-type hydroxylase ofd1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ofd1","type":"exact"}],"termid":"PR:Q11120"}


id: PR:Q9USJ8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lsg1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USJ8"],"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":"CTD kinase subunit gamma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4B3.08","synonyms":[{"name":"CTD kinase subunit 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"CTDK-I gamma subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-lsg1","type":"exact"}],"termid":"PR:Q9USJ8"}


id: MONDO:0004259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the endocervix.","direct_ancestors":[{"relation_name":"is_a","term_name":"cervical carcinoma","termid":"MONDO:0005131"},{"relation_name":"is_a","term_name":"malignant neoplasm of endocervix","termid":"MONDO:0021309"}],"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":"endocervical carcinoma","secondary_identifiers":["NCIT:C28327","DOID:7519","MEDGEN:226966","UMLS:C1299237","SCTID:372098004"],"synonyms":[{"name":"carcinoma of endocervix","type":"exact"},{"name":"carcinoma of the endocervix","type":"exact"},{"name":"endocervical adenocarcinoma","type":"narrow"},{"name":"endocervical cancer","type":"exact"},{"name":"endocervical carcinoma","type":"exact"},{"name":"endocervix carcinoma","type":"exact"}],"termid":"MONDO:0004259","xrefs":{"Monarch":{"xref_id":"0004259"}}}


id: MONDO:0015904
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare hypolipidemia (obsolete MONDO:0015904)","secondary_identifiers":["Orphanet:181431"],"termid":"MONDO:0015904","xrefs":{"Monarch":{"xref_id":"0015904"}}}


id: MONDO:0020164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epicanthal fold (obsolete MONDO:0020164)","secondary_identifiers":["Orphanet:98573"],"termid":"MONDO:0020164","xrefs":{"Monarch":{"xref_id":"0020164"}}}


id: GO:0015968
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A specific global change in the metabolism of a bacterial cell (the downregulation of nucleic acid and protein synthesis, and the simultaneous upregulation of protein degradation and amino acid synthesis) as a result of starvation.","definition_xrefs":["GOC:jl","ISBN:0124325653","PMID:11282471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to starvation","termid":"GO:0009267"}],"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":"stringent response","secondary_identifiers":["Wikipedia:Stringent_response"],"termid":"GO:0015968"}


id: MONDO:0033537
data:
  {"annotated_genes":["SJAG_02201"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87103],"is_not":false,"summary":null,"term":"MONDO:0033537"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02201":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"combined oxidative phosphorylation deficiency 47","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5436476","OMIM:618958","MEDGEN:1775535","DOID:0112114"],"synonyms":[{"name":"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 47","type":"related"},{"name":"COXPD47","type":"related"}],"termid":"MONDO:0033537","terms_by_termid":{"MONDO:0033537":null},"xrefs":{"Monarch":{"xref_id":"0033537"}}}


id: MONDO:0018890
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lyell syndrome is an extended form of toxic epidermal necrolysis characterized by destruction and detachment of the skin epithelium and mucous membranes involving more than 30% of the body surface area.","definition_xrefs":["Orphanet:537"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxic epidermal necrolysis","termid":"MONDO:0019810"}],"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":"Lyell syndrome","secondary_identifiers":["GARD:18696"],"termid":"MONDO:0018890","xrefs":{"Monarch":{"xref_id":"0018890"}}}


id: PR:Q9USV7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A high affinity copper uptake protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper transport protein ctr6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC23G7.16","secondary_identifiers":["UniProtKB:Q9USV7"],"synonyms":[{"name":"SPBC23G7.16","type":"related"},{"name":"Spom972h-SLC31A1","type":"exact"},{"name":"copper transporter 6 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USV7"}


id: PBO:0055491
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 2925","termid":"PBO:0055491"}


id: GO:1903003
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein deubiquitination.","definition_xrefs":["GO_REF:0000058","GOC:bf","PMID:22970133","GOC:TermGenie","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein deubiquitination","termid":"GO:0090085"},{"relation_name":"is_a","term_name":"positive regulation of protein modification by small protein conjugation or removal","termid":"GO:1903322"},{"relation_name":"positively_regulates","term_name":"protein deubiquitination","termid":"GO:0016579"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0070647"},{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein deubiquitination","synonyms":[{"name":"activation of deubiquitination","type":"narrow"},{"name":"activation of protein deubiquitination","type":"narrow"},{"name":"activation of protein deubiquitinylation","type":"narrow"},{"name":"activation of protein deubiquitylation","type":"narrow"},{"name":"positive regulation of deubiquitination","type":"exact"},{"name":"positive regulation of protein deubiquitinylation","type":"exact"},{"name":"positive regulation of protein deubiquitylation","type":"exact"},{"name":"up regulation of deubiquitination","type":"exact"},{"name":"up regulation of protein deubiquitination","type":"exact"},{"name":"up regulation of protein deubiquitinylation","type":"exact"},{"name":"up regulation of protein deubiquitylation","type":"exact"},{"name":"up-regulation of deubiquitination","type":"exact"},{"name":"up-regulation of protein deubiquitination","type":"exact"},{"name":"up-regulation of protein deubiquitinylation","type":"exact"},{"name":"up-regulation of protein deubiquitylation","type":"exact"},{"name":"upregulation of deubiquitination","type":"exact"},{"name":"upregulation of protein deubiquitination","type":"exact"},{"name":"upregulation of protein deubiquitinylation","type":"exact"},{"name":"upregulation of protein deubiquitylation","type":"exact"}],"termid":"GO:1903003"}


id: PBO:0052744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 36","termid":"PBO:0052744"}


id: GO:1902404
data:
  {"annotated_genes":["SJAG_02700","SJAG_04776","SJAG_03631","SJAG_03936","SJAG_04498","SJAG_03703","SJAG_04077","SJAG_00268","SJAG_01665","SJAG_01894","SJAG_04887","SJAG_00845","SJAG_03581","SJAG_02431","SJAG_04597","SJAG_03379"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58757,90028,97072,99433,99813,100684,102489,102721,104219,114141],"is_not":false,"summary":null,"term":"GO:1902404"},{"annotations":[105492],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903472"},{"annotations":[96187,115200,96357,89295,112351],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903473"}]},"cv_name":"biological_process","definition":"Any actomyosin contractile ring contraction that is involved in mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actomyosin contractile ring contraction","termid":"GO:0000916"},{"relation_name":"is_a","term_name":"mitotic cytokinetic process","termid":"GO:1902410"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00268":null,"SJAG_00845":null,"SJAG_01665":null,"SJAG_01894":null,"SJAG_02431":null,"SJAG_02700":null,"SJAG_03379":null,"SJAG_03581":null,"SJAG_03631":null,"SJAG_03703":null,"SJAG_03936":null,"SJAG_04077":null,"SJAG_04498":null,"SJAG_04597":null,"SJAG_04776":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0008150","GO:0030036","GO:0000281","GO:0007049","GO:0007010"],"is_obsolete":false,"name":"mitotic actomyosin contractile ring contraction","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"contractile ring contraction involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"exact"},{"name":"cytokinesis, actomyosin ring contraction involved in mitotic cell cycle","type":"exact"},{"name":"mitotic actomyosin contractile ring constriction","type":"exact"}],"termid":"GO:1902404","terms_by_termid":{"GO:1902404":null,"GO:1903472":null,"GO:1903473":null}}


id: MONDO:0020782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic painless inflammation of the gums. It is characterized by erythema and edema of the gums and bleeding while brushing the teeth.","definition_xrefs":["NCIT:C34474"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gingivitis","termid":"MONDO:0002508"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic gingivitis","secondary_identifiers":["ICD9:523.10","ICD10CM:K05.1","MEDGEN:965","SCTID:72621003","ICD9:523.1","UMLS:C0008684","icd11.foundation:1542018172"],"synonyms":[{"name":"Chronic Gingivitis","type":"related"},{"name":"Chronic gingivitis","type":"related"},{"name":"chronic gingivitis","type":"exact"}],"termid":"MONDO:0020782","xrefs":{"Monarch":{"xref_id":"0020782"}}}


id: PBO:0062580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily G member 4","termid":"PBO:0062580"}


id: PBO:0061479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear respiratory factor 1","termid":"PBO:0061479"}


id: MONDO:0002308
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Conjunctivitis that is associated with contact lens wear, and which is characterized by giant papillae in the tarsal conjunctiva.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blepharoconjunctivitis","termid":"MONDO:0002307"},{"relation_name":"is_a","term_name":"papillary conjunctivitis","termid":"MONDO:0002309"}],"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":"giant papillary conjunctivitis","secondary_identifiers":["MEDGEN:3210","SCTID:231857004","UMLS:C0009769","DOID:2457","NCIT:C34507","icd11.foundation:8559059","ICD9:372.39"],"synonyms":[{"name":"GPC","type":"related"}],"termid":"MONDO:0002308","xrefs":{"Monarch":{"xref_id":"0002308"}}}


id: GO:0002648
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of central tolerance induction.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tolerance induction","termid":"GO:0002645"},{"relation_name":"is_a","term_name":"regulation of central tolerance induction","termid":"GO:0002646"},{"relation_name":"positively_regulates","term_name":"central tolerance induction","termid":"GO:0002508"}],"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 central tolerance induction","synonyms":[{"name":"activation of central tolerance induction","type":"narrow"},{"name":"stimulation of central tolerance induction","type":"narrow"},{"name":"up regulation of central tolerance induction","type":"exact"},{"name":"up-regulation of central tolerance induction","type":"exact"},{"name":"upregulation of central tolerance induction","type":"exact"}],"termid":"GO:0002648"}


id: PBO:0066183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 7","termid":"PBO:0066183"}


id: PBO:0041850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 1","termid":"PBO:0041850"}


id: PBO:0088447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase (CK1 family) Cki1","termid":"PBO:0088447"}


id: PBO:0085727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in the nonsense-mediated mRNA decay (NMD) pathway; interacts with Nam7p and Upf3p; involved in telomere maintenance","termid":"PBO:0085727"}


id: MONDO:0002181
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Non-neoplastic overgrowth of bone.","definition_xrefs":["NCIT:C3029"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperostosis","termid":"MONDO:0002185"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exostosis","secondary_identifiers":["DOID:203","UMLS:C1442903","SCTID:235231000119100","MEDGEN:257035","SCTID:416189003","ICD9:726.91"],"synonyms":[{"name":"bone osteophyte","type":"exact"},{"name":"bone spur","type":"exact"},{"name":"bony outgrowth","type":"exact"},{"name":"exostosis","type":"exact"},{"name":"orbital exostosis","type":"narrow"},{"name":"osteophyte","type":"exact"},{"name":"swimmer's exostosis","type":"narrow"}],"termid":"MONDO:0002181","xrefs":{"Monarch":{"xref_id":"0002181"}}}


id: GO:0019969
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-10.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"},{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"interleukin-10 binding","synonyms":[{"name":"IL-10 binding","type":"exact"}],"termid":"GO:0019969"}


id: MONDO:0009021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Toriello Carey syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysmorphic features, cerebral anomalies, swallowing difficulties, cardiac defects and hypotonia.","definition_xrefs":["Orphanet:3338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Toriello-Carey syndrome","secondary_identifiers":["MESH:C563127","MEDGEN:163225","OMIM:217980","SCTID:722477003","UMLS:C0796184","GARD:5225","icd11.foundation:147297969"],"synonyms":[{"name":"Toriello-Carey syndrome","type":"exact"},{"name":"agenesis of corpus callosum with facial anomalies and Robin sequence","type":"related"},{"name":"corpus callosum agenesis facial anomalies Robin sequence","type":"related"},{"name":"corpus callosum agenesis-blepharophimosis-Robin sequence syndrome","type":"exact"},{"name":"corpus callosum, agenesis of, with facial anomalies and ROBIN sequence","type":"related"}],"termid":"MONDO:0009021","xrefs":{"Monarch":{"xref_id":"0009021"}}}


id: PR:O13733
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An N-terminal kinase-like protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01548","PANTHER:PTHR12984:SF3","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":"protein kinase domain-containing protein ppk3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC15A10.13","secondary_identifiers":["UniProtKB:O13733"],"synonyms":[{"name":"Spom972h-SCYL1","type":"exact"}],"termid":"PR:O13733"}


id: GO:0046759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A form of viral release in which the nucleocapsid evaginates from the host nuclear membrane system, resulting in envelopment of the virus and cell lysis.","definition_xrefs":["ISBN:0072370319"],"gene_count":0,"genotype_count":0,"name":"obsolete lytic virus budding from plasma membrane (obsolete GO:0046759)","synonyms":[{"name":"lytic plasma membrane viral budding","type":"exact"},{"name":"lytic viral budding from plasma membrane","type":"exact"},{"name":"lytic virus budding from plasma membrane","type":"exact"}],"termid":"GO:0046759"}


id: SO:0000226
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding seryl tRNA (SO:000269).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine_tRNA_primary_transcript","synonyms":[{"name":"serine tRNA primary transcript","type":"exact"}],"termid":"SO:0000226"}


id: GO:0036408
data:
  {"annotated_genes":["SJAG_02165","SJAG_02773"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[92527,93185],"is_not":false,"summary":null,"term":"GO:0036408"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H3 L-lysine (position 14) = CoA + histone H3 N6-acetyl-L-lysine (position 14).","definition_xrefs":["PMID:19056256","PMID:21289066","GOC:vw","PMID:18552846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 acetyltransferase activity","termid":"GO:0010484"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02165":null,"SJAG_02773":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0034212","GO:0016740","GO:0003824","GO:0016746","GO:0140096","GO:0003674"],"is_obsolete":false,"name":"histone H3K14 acetyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"histone H3-K14 acetyltransferase activity","type":"exact"},{"name":"histone acetylase activity (H3-K14 specific)","type":"exact"},{"name":"histone acetyltransferase activity (H3-K14 specific)","type":"exact"},{"name":"histone lysine N-acetyltransferase activity (H3-K14 specific)","type":"exact"}],"termid":"GO:0036408","terms_by_termid":{"GO:0036408":null}}


id: GO:0015772
data:
  {"annotated_genes":["SJAG_03960"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106081"},{"annotations":[97548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106082"}]},"cv_name":"biological_process","definition":"The directed movement of oligosaccharides into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Oligosaccharides are molecules with between two and (about) 20 monosaccharide residues connected by glycosidic linkages.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transport","termid":"GO:0008643"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03960":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"oligosaccharide transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0015772","terms_by_termid":{"GO:0106081":null,"GO:0106082":null}}


id: PBO:0061587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"netrin G2","termid":"PBO:0061587"}


id: PBO:0000381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospho-2-dehydro-3-deoxyheptonate aldolase (predicted)","termid":"PBO:0000381"}


id: GO:1901149
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to salicylic acid.","definition_xrefs":["PMID:22699612","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid binding","termid":"GO:0033293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"salicylic acid binding","synonyms":[{"name":"salicylic acid receptor","type":"narrow"}],"termid":"GO:1901149"}


id: MONDO:1012589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculocutaneous albinism that occurs in Japanese medaka due to a mutation in the TYR gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, TYR-related, Japanese medaka","secondary_identifiers":["OMIA:000202-8090"],"synonyms":[{"name":"coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related in Oryzias latipes (Japanese medaka)","type":"exact"}],"termid":"MONDO:1012589","xrefs":{"Monarch":{"xref_id":"1012589"}}}


id: PBO:0073137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC22 homolog A, vesicle trafficking protein","termid":"PBO:0073137"}


id: MONDO:0003308
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm that arises from the mesothelial cells of the pleura. The primary cause is exposure to asbestos. The major histologic variants are the epithelioid malignant mesothelioma, desmoplastic malignant mesothelioma, and sarcomatoid malignant mesothelioma. Patients present with persistent cough and shortness of breath.","definition_xrefs":["NCIT:C9351"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesothelioma","termid":"MONDO:0005065"},{"relation_name":"is_a","term_name":"pleural neoplasm","termid":"MONDO:0021065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleural mesothelioma","secondary_identifiers":["MEDGEN:237179","HP:0100002","ONCOTREE:PLMESO","ICD10CM:C45.0","DOID:5157","EFO:1000485","SCTID:109372009","UMLS:C1377913"],"synonyms":[{"name":"benign pleural mesothelioma","type":"narrow"},{"name":"mesothelioma of pleura","type":"exact"},{"name":"mesothelioma of the pleura","type":"exact"},{"name":"pleura mesothelioma","type":"exact"},{"name":"pleural mesothelioma","type":"exact"},{"name":"pleural mesothelioma (disease)","type":"exact"},{"name":"pleural mesothelioma (disease), benign","type":"narrow"}],"termid":"MONDO:0003308","xrefs":{"Monarch":{"xref_id":"0003308"}}}


id: PR:Q9Y7S4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC569.05c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7S4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized transporter C569.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC569.05c","synonyms":[{"name":"Spom972h-SPCC569.05c","type":"exact"}],"termid":"PR:Q9Y7S4"}


id: PBO:0072948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small Cajal body-specific RNA 28","termid":"PBO:0072948"}


id: GO:0004791
data:
  {"annotated_genes":["SJAG_04399","SJAG_03653"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74932,81322],"is_not":false,"summary":null,"term":"GO:0004791"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: thioredoxin-dithiol + NADP+ = thioredoxin-disulfide + H+ + NADPH.","definition_xrefs":["RHEA:20345"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antioxidant activity","termid":"GO:0016209"},{"relation_name":"is_a","term_name":"protein-disulfide reductase [NAD(P)H] activity","termid":"GO:0047134"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03653":null,"SJAG_04399":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0015036"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003824","GO:0140096","GO:0003674","GO:0015036","GO:0016491"],"is_obsolete":false,"name":"thioredoxin-disulfide reductase (NADPH) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:1.8.1.9","KEGG_REACTION:R02016","Reactome:R-HSA-1222485","Reactome:R-HSA-3323050","Reactome:R-HSA-73646","MetaCyc:THIOREDOXIN-REDUCT-NADPH-RXN","Reactome:R-HSA-9617735"],"synonyms":[{"name":"NADPH:oxidized thioredoxin oxidoreductase activity","type":"exact"},{"name":"thioredoxin disulfide reductase activity","type":"broad"},{"name":"thioredoxin reductase (NADPH) activity","type":"exact"},{"name":"thioredoxin-disulfide reductase (NADP) activity","type":"exact"},{"name":"thioredoxin-disulfide reductase activity","type":"broad"},{"name":"thioredoxin-disulphide reductase activity","type":"broad"}],"termid":"GO:0004791","terms_by_termid":{"GO:0004791":null}}


id: PBO:0003128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ran GTPase binding protein Sbp1","termid":"PBO:0003128"}


id: PR:O94270
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ER lumen protein-retaining receptor 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER lumen protein-retaining receptor (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP8B7.22","secondary_identifiers":["UniProtKB:O94270"],"synonyms":[{"name":"SPBP8B7.22","type":"related"},{"name":"Spom972h-KDELR1","type":"exact"}],"termid":"PR:O94270"}


id: GO:0071683
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A dendrite that is found on a sensory neuron, and directly transduces a sensory signal from the sensory neuron to another neuron.","definition_xrefs":["GOC:kmv","GOC:dos","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite","termid":"GO:0030425"}],"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":"sensory dendrite","termid":"GO:0071683"}


id: PBO:0000122
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiotic Expression Upregulated","termid":"PBO:0000122"}


id: PBO:0034486
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_lipid_metabolism_gene_mRNA_during_cellular_response_to_hypoxia","termid":"PBO:0034486"}


id: PBO:0003981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR7 ortholog","termid":"PBO:0003981"}


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


id: PBO:0056579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple C2 and transmembrane domain containing 2","termid":"PBO:0056579"}


id: MONDO:0019098
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune form of thrombocytopenia.","definition_xrefs":["MONDO:patterns/autoimmune"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thrombocytopenia","termid":"MONDO:0002049"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"autoimmune thrombocytopenia","secondary_identifiers":["MedDRA:10050245","GARD:18906","SCTID:128091003","UMLS:C0242584","Orphanet:71203","MEDGEN:116621"],"termid":"MONDO:0019098","xrefs":{"Monarch":{"xref_id":"0019098"}}}


id: GO:0047893
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + a flavonol = UDP + a flavonol 3-O-D-glucoside.","definition_xrefs":["EC:2.4.1.91","MetaCyc:FLAVONOL-3-O-GLUCOSYLTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"flavonol 3-O-glucosyltransferase activity","secondary_identifiers":["RHEA:22300"],"synonyms":[{"name":"GTI","type":"related"},{"name":"UDP-glucose flavonol 3-O-glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:flavonol 3-O-D-glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:flavonol 3-O-glucosyltransferase activity","type":"related"},{"name":"UDPG:flavonoid-3-O-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:flavonol 3-O-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-flavonol 3-O-glucosyltransferase activity","type":"related"}],"termid":"GO:0047893"}


id: MONDO:0003291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the arrector pili muscle, tunica media of blood vessels, and dartos muscle of the genitalia. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"dermis tumor","termid":"MONDO:0002300"},{"relation_name":"is_a","term_name":"benign neoplasm of skin","termid":"MONDO:0021440"}],"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":"leiomyoma cutis","secondary_identifiers":["MEDGEN:87533","NCIT:C4482","SCTID:254767008","DOID:5132","UMLS:C0346064"],"synonyms":[{"name":"cutaneous (skin) leiomyoma","type":"exact"},{"name":"cutaneous leiomyoma","type":"exact"},{"name":"leiomyoma cutis","type":"exact"},{"name":"leiomyoma of skin","type":"exact"},{"name":"leiomyoma of the skin","type":"exact"},{"name":"leiomyoma of zone of skin","type":"exact"},{"name":"skin leiomyoma","type":"exact"},{"name":"zone of skin leiomyoma","type":"exact"}],"termid":"MONDO:0003291","xrefs":{"Monarch":{"xref_id":"0003291"}}}


id: MONDO:0023243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The Glass-Chapman-Hockley syndrome is a very rare disease. To date, the syndrome has only been reported in one family with five members affected in three generations. The first patients were two brothers that had an abnormally-shaped head due to coronal craniosynostosis. Their mother, maternal aunt, and maternal grandmother were also found to have the syndrome. The signs and symptoms varied from person to person; however, the signs and symptoms included coronal craniosynostosis, small middle part of the face (midfacial hypoplasia), and short fingers (brachydactyly).The inheritance is thought to be autosomal dominant. No genes have been identified for this syndrome. Treatment included surgery to correct the craniosynostosis. No issues with development and normal intelligence were reported. This is an n-of-1 use case where only one patient or family has been described with this disorder.","definition_xrefs":["GARD:0002479"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"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:0000426"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0000426"],"is_obsolete":false,"name":"glass-chapman-hockley syndrome","secondary_identifiers":["Orphanet:1535","SCTID:720814001"],"synonyms":[{"name":"craniosynostosis - dysmorphism - brachydactyly","type":"related"},{"name":"craniosynostosis brachydactyly","type":"related"},{"name":"craniosynostosis with facial dysmorphism and brachydactyly syndrome","type":"exact"},{"name":"craniosynostosis-dysmorphism-brachydactyly syndrome","type":"related"},{"name":"glass chapman hockley syndrome","type":"related"}],"termid":"MONDO:0023243","xrefs":{"Monarch":{"xref_id":"0023243"}}}


id: GO:0030614
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a phosphorus- or arsenic-containing group acts as a hydrogen or electron donor and reduces a disulfide.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on phosphorus or arsenic in donors","termid":"GO:0030613"}],"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":"oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor","secondary_identifiers":["EC:1.20.4.-"],"synonyms":[{"name":"oxidoreductase activity, acting on phosphorus or arsenic in donors, with disulphide as acceptor","type":"exact"}],"termid":"GO:0030614"}


id: PR:O94259
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- utp16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94259"],"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":"U3 small nucleolar RNA-associated protein 16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP8B7.10c","synonyms":[{"name":"Spom972h-utp16","type":"exact"},{"name":"U3 snoRNA-associated protein 16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94259"}


id: GO:0031676
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The pigmented membrane of a plasma membrane-derived thylakoid.","definition_xrefs":["GOC:mah","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thylakoid membrane","termid":"GO:0042651"},{"relation_name":"is_a","term_name":"plasma membrane-derived chromatophore membrane","termid":"GO:0042717"},{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"},{"relation_name":"part_of","term_name":"bacterial thylakoid","termid":"GO:0030075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"plasma membrane-derived thylakoid membrane","synonyms":[{"name":"plasma membrane thylakoid membrane","type":"exact"}],"termid":"GO:0031676"}


id: PBO:0054313
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 1705","termid":"PBO:0054313"}


id: GO:0050153
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 10-hydroxydecanoate + NAD+ = 10-oxodecanoate + H+ + NADH.","definition_xrefs":["EC:1.1.1.66","RHEA:20880"],"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"omega-hydroxydecanoate dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R03886","MetaCyc:OMEGA-HYDROXYDECANOATE-DEHYDROGENASE-RXN"],"synonyms":[{"name":"10-hydroxydecanoate:NAD+ 10-oxidoreductase activity","type":"related"},{"name":"w-hydroxydecanoate dehydrogenase activity","type":"exact"}],"termid":"GO:0050153"}


id: MONDO:0019483
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Methotrexate-associated lymphoproliferative disorders are rare immunodeficiency-associated lymphoproliferative diseases characterized by lymphoid proliferation or lymphomas (large B-cell lymphoma, T-cell lymphoma, Hodgkin lymphoma, reactive lymphadenitis and a polymorphic post-transplant lymphoproliferative disorder) that develop in patients with different autoimmune diseases treated with methotrexate. Swelling is the predominant manifestation of the disease and regression after methotrexate withdrawal is observed in a significant proportion of patients.","definition_xrefs":["Orphanet:86904"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"},{"relation_name":"is_a","term_name":"immunodeficiency-associated lymphoproliferative disease","termid":"MONDO:0020083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"methotrexate-associated lymphoproliferative disorders","secondary_identifiers":["UMLS:C1334749","DOID:5821","MEDGEN:233702","NCIT:C7184","GARD:19083","icd11.foundation:1520483526"],"synonyms":[{"name":"MTX-LPD","type":"exact"},{"name":"MTX-associated lymphoproliferative disorders","type":"exact"},{"name":"methotrexate-associated lymphoproliferation","type":"exact"},{"name":"methotrexate-associated lymphoproliferative disorder","type":"exact"}],"termid":"MONDO:0019483","xrefs":{"Monarch":{"xref_id":"0019483"}}}


id: PBO:0053304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIN28A pseudogene 1","termid":"PBO:0053304"}


id: FYPO:0007575
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 one or more proteins is localized to the medial cortical nodes for a shorter time than normal.","definition_xrefs":["PomBase:mah","PMID:25501814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased duration of protein localization to cell division site","termid":"FYPO:0002528"},{"relation_name":"is_a","term_name":"abnormal protein localization to medial cortical node","termid":"FYPO:0003289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased duration of protein localization to medial cortical node","synonyms":[{"name":"decreased duration of protein localisation to cytokinetic nodes","type":"exact"},{"name":"decreased duration of protein localisation to medial cortical dot","type":"exact"},{"name":"decreased duration of protein localisation to medial cortical node","type":"exact"},{"name":"decreased duration of protein localization to medial cortical node during mitotic cell cycle","type":"related"},{"name":"decreased duration of protein localization to medial cortical node during vegetative growth","type":"exact"},{"name":"decreased duration of protein localization to medial cortical nodes","type":"exact"},{"name":"decreased duration of protein recruitment to medial cortical node","type":"related"},{"name":"reduced duration protein localization to medial cortical node","type":"exact"}],"termid":"FYPO:0007575"}


id: PBO:0078042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 32","termid":"PBO:0078042"}


id: PBO:0061599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative regulator of ubiquitin like proteins 1","termid":"PBO:0061599"}


id: SO:0000134
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Imprinted genes are epigenetically modified genes that are expressed monoallelically according to their parent of origin.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulated","termid":"SO:0000119"},{"relation_name":"is_a","term_name":"epigenetically_modified","termid":"SO:0000133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genomically_imprinted","secondary_identifiers":["http:http\\://en.wikipedia.org/wiki/Genomic_imprinting"],"synonyms":[{"name":"genomically imprinted","type":"exact"},{"name":"imprinted","type":"broad"}],"termid":"SO:0000134"}


id: GO:0047635
data:
  {"annotated_genes":["SJAG_04145"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[113067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004021"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-alanine + a 2-oxo acid = pyruvate + an L-amino acid.","definition_xrefs":["EC:2.6.1.12","MetaCyc:ALANINE--OXO-ACID-AMINOTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04145":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016769"],"is_obsolete":false,"name":"alanine-oxo-acid transaminase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:19953"],"synonyms":[{"name":"L-alanine-alpha-keto acid aminotransferase activity","type":"related"},{"name":"L-alanine:2-oxo-acid aminotransferase activity","type":"related"},{"name":"alanine--oxo-acid aminotransferase activity","type":"related"},{"name":"alanine-keto acid aminotransferase activity","type":"related"},{"name":"alanine-oxo acid aminotransferase activity","type":"related"},{"name":"alanine-oxo-acid aminotransferase activity","type":"exact"},{"name":"leucine-alanine transaminase activity","type":"related"}],"termid":"GO:0047635","terms_by_termid":{"GO:0004021":null}}


id: GO:0031022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the nucleus along microfilaments within the cell, mediated by motor proteins.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear migration","termid":"GO:0007097"},{"relation_name":"is_a","term_name":"actin filament-based movement","termid":"GO:0030048"},{"relation_name":"is_a","term_name":"actin filament-based transport","termid":"GO:0099515"}],"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":"nuclear migration along microfilament","synonyms":[{"name":"nuclear migration, microfilament-mediated","type":"exact"}],"termid":"GO:0031022"}


id: MOD:00400
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a carboxamido group with a carboxyl group, with both a gain of oxygen and loss of a nitrogen and a hydrogen.","definition_xrefs":["Unimod:7","DeltaMass:32","OMSSA:4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deamidated residue","synonyms":[{"name":"Deamidated","type":"related"},{"name":"Deamidation","type":"related"},{"name":"Deamidation of Asparagine and Glutamine to Aspartate and Glutamate","type":"exact"},{"name":"dNRes","type":"exact"},{"name":"deamidationkq","type":"exact"}],"termid":"MOD:00400"}


id: GO:0047500
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+)-borneol + NAD+ = (1R, 4R)-camphor + H+ + NADH.","definition_xrefs":["RHEA:17329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"(+)-borneol dehydrogenase activity","secondary_identifiers":["EC:1.1.1.198","KEGG_REACTION:R02944","MetaCyc:+-BORNEOL-DEHYDROGENASE-RXN"],"synonyms":[{"name":"(+)-borneol:NAD+ oxidoreductase activity","type":"related"},{"name":"bicyclic monoterpenol dehydrogenase activity","type":"related"}],"termid":"GO:0047500"}


id: PBO:0004893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial PPR repeat protein Ppr7","termid":"PBO:0004893"}


id: MONDO:0021508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the epicardium.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm of epicardium","termid":"MONDO:0021379"},{"relation_name":"is_a","term_name":"benign neoplasm of heart","termid":"MONDO:0021450"},{"relation_name":"is_a","term_name":"benign neoplasm of pericardium","termid":"MONDO:0021514"}],"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":"benign neoplasm of epicardium","secondary_identifiers":["icd11.foundation:1295571347","SCTID:92087008","MEDGEN:146342","UMLS:C0685115","NCIT:C8535"],"synonyms":[{"name":"benign epicardial neoplasm","type":"exact"},{"name":"benign epicardial tumor","type":"exact"},{"name":"benign epicardial tumour","type":"exact"},{"name":"benign neoplasm of the epicardium","type":"exact"},{"name":"benign tumor of epicardium","type":"exact"},{"name":"benign tumor of the epicardium","type":"exact"},{"name":"benign tumour of epicardium","type":"exact"},{"name":"benign tumour of the epicardium","type":"exact"},{"name":"epicardium benign neoplasm","type":"exact"}],"termid":"MONDO:0021508","xrefs":{"Monarch":{"xref_id":"0021508"}}}


id: GO:0032233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the assembly of actin filament bundles.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament bundle assembly","termid":"GO:0032231"},{"relation_name":"is_a","term_name":"positive regulation of cellular component biogenesis","termid":"GO:0044089"},{"relation_name":"is_a","term_name":"positive regulation of cytoskeleton organization","termid":"GO:0051495"},{"relation_name":"is_a","term_name":"positive regulation of supramolecular fiber organization","termid":"GO:1902905"},{"relation_name":"positively_regulates","term_name":"actin filament bundle assembly","termid":"GO:0051017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0007010"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0044085","GO:0030036"],"is_obsolete":false,"name":"positive regulation of actin filament bundle assembly","synonyms":[{"name":"activation of actin filament bundle formation","type":"narrow"},{"name":"stimulation of actin filament bundle formation","type":"narrow"},{"name":"up regulation of actin filament bundle formation","type":"exact"},{"name":"up-regulation of actin filament bundle formation","type":"exact"},{"name":"upregulation of actin filament bundle formation","type":"exact"}],"termid":"GO:0032233"}


id: PBO:0044346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 30","termid":"PBO:0044346"}


id: PBO:0077673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor superfamily member 19","termid":"PBO:0077673"}


id: GO:0052451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of the inflammatory response of a symbiont organism; the inflammatory response is the immediate defensive reaction (by vertebrate tissue) to infection or injury caused by chemical or physical agents. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of symbiont inflammatory response (obsolete GO:0052451)","synonyms":[{"name":"modulation by organism of symbiont inflammatory response","type":"exact"}],"termid":"GO:0052451"}


id: PBO:0055229
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 2655","termid":"PBO:0055229"}


id: MONDO:0044335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm that arises from the soft tissue.","definition_xrefs":["NCIT:C4242"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign connective and soft tissue neoplasm","termid":"MONDO:0000654"},{"relation_name":"is_a","term_name":"soft tissue neoplasm","termid":"MONDO:0006424"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign soft tissue neoplasm","secondary_identifiers":["UMLS:C0334450","SCTID:92069005","MEDGEN:83151","ICDO:8800/0"],"synonyms":[{"name":"benign neoplasm of soft tissue","type":"exact"},{"name":"benign neoplasm of the soft tissue","type":"exact"},{"name":"benign soft tissue neoplasm","type":"exact"},{"name":"benign soft tissue tumor","type":"exact"},{"name":"benign soft tissue tumour","type":"exact"},{"name":"benign tumor of soft tissue","type":"exact"},{"name":"benign tumor of the soft tissue","type":"exact"},{"name":"benign tumour of soft tissue","type":"exact"},{"name":"benign tumour of the soft tissue","type":"exact"},{"name":"soft tissue neoplasm, benign","type":"exact"}],"termid":"MONDO:0044335","xrefs":{"Monarch":{"xref_id":"0044335"}}}


id: MONDO:0006781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with organisms of the genus HELICOBACTER, particularly, in humans, HELICOBACTER PYLORI. The clinical manifestations are focused in the stomach, usually the gastric mucosa and antrum, and the upper duodenum. This infection plays a major role in the pathogenesis of type B gastritis and peptic ulcer disease.","definition_xrefs":["MESH:D016481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gram-negative bacterial infections","termid":"MONDO:0021678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Helicobacter pylori infectious disease","secondary_identifiers":["EFO:1000961"],"synonyms":[{"name":"Helicobacter infection","type":"related"},{"name":"Helicobacter pylori caused disease or disorder","type":"exact"},{"name":"Helicobacter pylori disease or disorder","type":"exact"},{"name":"Helicobacter pylori infection, susceptibility to","type":"related"},{"name":"infection, Helicobacter","type":"related"},{"name":"infections, Helicobacter","type":"related"}],"termid":"MONDO:0006781","xrefs":{"Monarch":{"xref_id":"0006781"}}}


id: PBO:0075909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST13, Hsp70 interacting protein pseudogene 1","termid":"PBO:0075909"}


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


id: FYPO:0005279
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 glucose-repressed mRNAs measured in a cell is higher than normal (i.e. higher than observed in wild-type cells). Glucose-repressed mRNAs are transcribed from genes whose transcription is negatively regulated when glucose is present.","definition_xrefs":["PMID:18430926","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":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"increased level of glucose-repressed gene mRNA during vegetative growth","secondary_identifiers":["FYPO:0005287"],"synonyms":[{"name":"increased glucose starvation gene mRNA accumulation during vegetative growth","type":"related"},{"name":"increased glucose-repressed gene mRNA accumulation during vegetative growth","type":"related"},{"name":"increased level of cellular response to glucose starvation gene mRNA during vegetative growth","type":"exact"},{"name":"increased level of glucose depletion gene mRNA during vegetative growth","type":"exact"},{"name":"increased level of glucose deprivation gene mRNA during vegetative growth","type":"exact"},{"name":"increased level of glucose starvation gene RNA during vegetative growth","type":"exact"},{"name":"increased level of glucose starvation gene mRNA during mitotic cell cycle","type":"related"},{"name":"increased level of glucose starvation gene mRNA during vegetative growth","type":"exact"},{"name":"increased level of glucose starvation gene transcripts during vegetative growth","type":"exact"},{"name":"increased level of glucose-repressed gene RNA during vegetative growth","type":"exact"},{"name":"increased level of glucose-repressed gene mRNA during mitotic cell cycle","type":"related"},{"name":"increased level of glucose-repressed gene transcripts during vegetative growth","type":"exact"}],"termid":"FYPO:0005279"}


id: PBO:0058291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4666a","termid":"PBO:0058291"}


id: MONDO:0015751
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Capra-DeMarco syndrome is characterized by sagittal craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis. Other clinical findings include blepharophimosis, small low-set ears, hypoplastic philtrum, kidney malformation, and hypogenitalism.","definition_xrefs":["Orphanet:171839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome","secondary_identifiers":["GARD:20127","UMLS:C3267187","SCTID:720815000","MEDGEN:923699"],"synonyms":[{"name":"Berant syndrome","type":"exact"},{"name":"Capra-DeMarco syndrome","type":"exact"},{"name":"familial scaphocephaly-radioulnar synostosis syndrome","type":"exact"}],"termid":"MONDO:0015751","xrefs":{"Monarch":{"xref_id":"0015751"}}}


id: SO:0001253
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A DNA fragment generated by sonication. Sonication is a technique used to sheer DNA into smaller fragments.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"assembly_component","termid":"SO:0000143"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sonicate_fragment","synonyms":[{"name":"sonicate fragment","type":"exact"}],"termid":"SO:0001253"}


id: PBO:0066016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAMP2 antisense RNA 1","termid":"PBO:0066016"}


id: MONDO:0000502
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epithelial neoplasm morphologically characterized by the presence of a villous architectural pattern. Most often it occurs in the large intestine, small intestine, and the stomach in which the neoplastic epithelial cells show dysplastic features. It may also arise in the urinary bladder, urethra, and vagina.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenoma","termid":"MONDO:0004972"},{"relation_name":"is_a","term_name":"glandular cell neoplasm","termid":"MONDO:0024276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"villous adenoma","secondary_identifiers":["ICDO:8261/0","DOID:0050869","MEDGEN:60206","UMLS:C0206674","MESH:D018253","NCIT:C7399"],"synonyms":[{"name":"villous adenoma","type":"exact"}],"termid":"MONDO:0000502","xrefs":{"Monarch":{"xref_id":"0000502"}}}


id: PBO:0065312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 35","termid":"PBO:0065312"}


id: GO:0048354
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mucilage that occur as part of seed coat development; mucilage is normally synthesized during seed coat development.","definition_xrefs":["GOC:dph","GOC:jid","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucilage biosynthetic process","termid":"GO:0010192"},{"relation_name":"is_a","term_name":"mucilage metabolic process involved in seed coat development","termid":"GO:0048359"}],"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":"mucilage biosynthetic process involved in seed coat development","synonyms":[{"name":"mucilage anabolism during seed coat development","type":"exact"},{"name":"mucilage biosynthetic process during seed coat development","type":"related"},{"name":"mucilage formation during seed coat development","type":"exact"},{"name":"mucilage synthesis during seed coat development","type":"exact"}],"termid":"GO:0048354"}


id: PR:000060258
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A eukaryotic translation initiation factor 2 subunit alpha (Schizosaccharomyces pombe) that lacks phosphorylation on the residue at the position equivalent to Ser-52 of the amino acid sequence represented by UniProtKB:P56286. UniProtKB:P56286, Ser-52, PR:000026291.","definition_xrefs":["PMID:28771613","PRO:DAN","PomBase:VW","PMID:31048492"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tif211/UnPhos(S52)","pombase_gene_id":"SPAC3G9.09c","synonyms":[{"name":"PomBase_original_PRO_term_name: eukaryotic translation initiation factor 2 subunit alpha unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-EIF2S1/UnPhos:1","type":"exact"},{"name":"Tif211/UnPhos(S52)","type":"exact"},{"name":"UniProtKB:P56286, Ser-52, PR:000026291","type":"narrow"},{"name":"UniProtKB:P56286-1, Ser-52, PR:000026291","type":"narrow"}],"termid":"PR:000060258"}


id: PBO:0001838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit Rpn11","termid":"PBO:0001838"}


id: PBO:0086068
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 localizes to mitochondria; overexpression affects endocytic protein trafficking; YDR514C has a paralog, GFD2, that arose from the whole genome duplication","termid":"PBO:0086068"}


id: GO:0061983
data:
  {"annotated_genes":["SJAG_00486","SJAG_00646","SJAG_04271","SJAG_00666","SJAG_00678","SJAG_04853","SJAG_00207","SJAG_03090","SJAG_03989","SJAG_04508","SJAG_00145"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95605,89635],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051456"},{"annotations":[106929,109531,108645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007135"},{"annotations":[89770,113516,115065],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045144"},{"annotations":[104084,101929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990950"},{"annotations":[96943],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905191"}]},"cv_name":"biological_process","definition":"A process that coontributes to the second meiotic division. The second meiotic division separates chromatids resulting in a haploid number of chromosomes.","definition_xrefs":["PMID:29385397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00145":null,"SJAG_00207":null,"SJAG_00486":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00678":null,"SJAG_03090":null,"SJAG_03989":null,"SJAG_04271":null,"SJAG_04508":null,"SJAG_04853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"meiosis II cell cycle process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"second meiotic division","type":"exact"}],"termid":"GO:0061983","terms_by_termid":{"GO:0007135":null,"GO:0045144":null,"GO:0051456":null,"GO:1905191":null,"GO:1990950":null}}


id: GO:0002549
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of the plasma kallikrein-kinin cascade.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of kinin cascade","termid":"GO:0002257"},{"relation_name":"is_a","term_name":"regulation of plasma kallikrein-kinin cascade","termid":"GO:0002529"},{"relation_name":"negatively_regulates","term_name":"plasma kallikrein-kinin cascade","termid":"GO:0002353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0051604"},{"rel_name":"negatively_regulates","termid":"GO:0051604"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051604","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of plasma kallikrein-kinin cascade","synonyms":[{"name":"down regulation of plasma kallikrein-kinin cascade","type":"exact"},{"name":"down-regulation of plasma kallikrein-kinin cascade","type":"exact"},{"name":"downregulation of plasma kallikrein-kinin cascade","type":"exact"},{"name":"inhibition of plasma kallikrein-kinin cascade","type":"narrow"}],"termid":"GO:0002549"}


id: PBO:0013835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferrochelatase Hem15 (predicted)","termid":"PBO:0013835"}


id: GO:0072702
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 methyl methanesulfonate (MMS) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"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 methyl methanesulfonate","synonyms":[{"name":"response to MMS","type":"exact"}],"termid":"GO:0072702"}


id: GO:0061989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chromosome organization process in which meiotic chromosomes in the spem nucleus cluster together to form a compact spherical structure called the karyosome.","definition_xrefs":["PMID:19696886"],"direct_ancestors":[{"relation_name":"is_a","term_name":"karyosome formation","termid":"GO:0061988"},{"relation_name":"part_of","term_name":"spermatogenesis","termid":"GO:0007283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"sperm karyosome formation","termid":"GO:0061989"}


id: PBO:0024830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage and polyadenylation specificity factor (predicted)","termid":"PBO:0024830"}


id: MONDO:0958013
data:
  {"annotated_genes":["SJAG_02208","SJAG_02330"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87839,87840],"is_not":false,"summary":null,"term":"MONDO:0958013"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"common variable immunodeficiency","termid":"MONDO:0015517"},{"relation_name":"is_a","term_name":"SEC61A1 deficiency","termid":"MONDO:0100337"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02208":null,"SJAG_02330":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"immunodeficiency, common variable, 15","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620670","UMLS:C5882741","MEDGEN:1847802"],"termid":"MONDO:0958013","terms_by_termid":{"MONDO:0958013":null},"xrefs":{"Monarch":{"xref_id":"0958013"}}}


id: PBO:0061332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore complex interacting protein family, member B10, pseudogene","termid":"PBO:0061332"}


id: MONDO:0024538
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral striopallidodentate calcinosis","termid":"MONDO:0008947"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basal ganglia calcification, idiopathic, 1","secondary_identifiers":["MESH:C537657","OMIM:213600","MEDGEN:1637664","NCIT:C129973","OMIM:606656","UMLS:C4551624","NANDO:1200208"],"synonyms":[{"name":"Fahr disease, familial","type":"related"},{"name":"Fahr disease, familial, formerly","type":"related"},{"name":"IBGC1","type":"exact"},{"name":"IBGC2","type":"exact"},{"name":"basal ganglia calcification, idiopathic, 1","type":"exact"},{"name":"basal ganglia calcification, idiopathic, 2","type":"exact"},{"name":"basal ganglia calcification, idiopathic, 3","type":"related"},{"name":"basal ganglia calcification, idiopathic, 3, formerly","type":"related"},{"name":"basal ganglia calcification, idiopathic, type 1","type":"exact"},{"name":"cerebral calcification, nonarteriosclerotic, idiopathic, adult-onset","type":"related"},{"name":"ferrocalcinosis, cerebrovascular","type":"related"},{"name":"idiopathic basal ganglia calcification 1","type":"exact"},{"name":"striopallidodentate calcinosis, autosomal dominant, adult-onset","type":"related"},{"name":"striopallidodentate calcinosis, bilateral","type":"related"}],"termid":"MONDO:0024538","xrefs":{"Monarch":{"xref_id":"0024538"}}}


id: PBO:0074605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 11F","termid":"PBO:0074605"}


id: PBO:0028239
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_localization_to_nucleus_during_meiotic_anaphase_II","termid":"PBO:0028239"}


id: MONDO:0011180
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":"broad terminal phalanges, familial","secondary_identifiers":["MESH:C566588","MEDGEN:400879","UMLS:C1865923","OMIM:602071"],"synonyms":[{"name":"broad terminal phalanges, familial","type":"exact"}],"termid":"MONDO:0011180","xrefs":{"Monarch":{"xref_id":"0011180"}}}


id: MONDO:0007478
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant form of Kenny-Caffey Syndrome due to mutation(s) in the FAM111A gene, encoding protein FAM111A. This condition is characterized by transient hypocalcemia, delayed closure of the anterior fontanel, eye anomalies, including microphthalmia, proportionate short stature, and cortical thickening and medullary stenosis of the tubular bones.","definition_xrefs":["NCIT:C130993"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"Kenny-Caffey syndrome","termid":"MONDO:0016516"}],"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":"autosomal dominant Kenny-Caffey syndrome","secondary_identifiers":["DOID:0080723","GARD:83","UMLS:C4316787","MEDGEN:1373312","OMIM:127000","Orphanet:93325"],"synonyms":[{"name":"KCS2","type":"related"},{"name":"Kenny syndrome","type":"broad"},{"name":"Kenny-Caffey syndrome type 2","type":"exact"},{"name":"Kenny-Caffey syndrome, autosomal dominant","type":"exact"},{"name":"Kenny-Caffey syndrome, type 2","type":"related"},{"name":"dwarfism, cortical thickening of tubular bones and transient hypocalcemia","type":"related"},{"name":"dwarfism, cortical thickening of tubular bones, and transient hypocalcemia","type":"related"}],"termid":"MONDO:0007478","xrefs":{"Monarch":{"xref_id":"0007478"}}}


id: GO:0043467
data:
  {"annotated_genes":["SJAG_01376","SJAG_01062","SJAG_05314","SJAG_02433","SJAG_02785","SJAG_00963","SJAG_05006","SJAG_00685","SJAG_00698","SJAG_02592"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80716,78783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045719"},{"annotations":[74768,77826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[98357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001172"},{"annotations":[91466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905857"},{"annotations":[111514,113711,96150,99408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903715"},{"annotations":[71694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006110"},{"annotations":[77825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043456"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of precursor metabolites, substances from which energy is derived, and the processes involved in the liberation of energy from these substances.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"generation of precursor metabolites and energy","termid":"GO:0006091"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_00698":null,"SJAG_00963":null,"SJAG_01062":null,"SJAG_01376":null,"SJAG_02433":null,"SJAG_02592":null,"SJAG_02785":null,"SJAG_05006":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"regulation of generation of precursor metabolites and energy","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-163685"],"termid":"GO:0043467","terms_by_termid":{"GO:0006110":null,"GO:0043456":null,"GO:0045719":null,"GO:0045820":null,"GO:1903715":null,"GO:1905857":null,"GO:2001172":null}}


id: GO:0110103
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A conserved protein complex capable of 5'-3' exoribonuclease activity. It is able to promote RNA polymerase II (RNAPII) transcription termination by degrading pre-mRNA from the newly formed 5' phosphorylated end.","definition_xrefs":["PMID:23200120","PMID:25722373","GOC:lnp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"is_a","term_name":"exoribonuclease complex","termid":"GO:1905354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"RNA polymerase II termination complex","synonyms":[{"name":"TXT complex","type":"exact"}],"termid":"GO:0110103"}


id: PBO:0052883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 9-6","termid":"PBO:0052883"}


id: PBO:0031668
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_protein_transport","termid":"PBO:0031668"}


id: PBO:0081836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 771","termid":"PBO:0081836"}


id: PBO:0030551
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_arginine_import","termid":"PBO:0030551"}


id: MONDO:0003236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenomyoma characterized by the presence of marked glandular architectural complexity.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenomyoma","termid":"MONDO:0005635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atypical polypoid adenomyoma","secondary_identifiers":["MEDGEN:266248","DOID:4993","UMLS:C1300347","NCIT:C6895"],"synonyms":[{"name":"atypical polypoid adenomyoma","type":"exact"},{"name":"atypical polypoid adenomyoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003236","xrefs":{"Monarch":{"xref_id":"0003236"}}}


id: MONDO:0018212
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of cervical artery dissection 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":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"cervical artery dissection","termid":"MONDO:0006061"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial cervical artery dissection","secondary_identifiers":["MEDGEN:1659372","Orphanet:36382","GARD:18823","UMLS:C4755308"],"synonyms":[{"name":"familial CAD","type":"exact"},{"name":"hereditary CAD","type":"exact"},{"name":"hereditary cervical artery dissection","type":"exact"}],"termid":"MONDO:0018212","xrefs":{"Monarch":{"xref_id":"0018212"}}}


id: PBO:0080612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 46","termid":"PBO:0080612"}


id: GO:0140060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the terminal anatomical structures of an axon are generated and organized into branches of specialised projections, or boutons. An axon is the long process of a neuron that conducts nerve impulses, usually away from the cell body to the terminal branches.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:23764288"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axonogenesis","termid":"GO:0007409"},{"relation_name":"is_a","term_name":"neuron projection arborization","termid":"GO:0140058"}],"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":"axon arborization","termid":"GO:0140060"}


id: PBO:0110288
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"named after human ortholog CAPRIN-1","termid":"PBO:0110288"}


id: PBO:0061010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"niban apoptosis regulator 3","termid":"PBO:0061010"}


id: GO:0060337
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by type I interferon binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription. Type I interferons include the interferon-alpha, beta, delta, episilon, zeta, kappa, tau, and omega gene families.","definition_xrefs":["GOC:add","PMID:32464097","GOC:signaling","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interferon-mediated signaling pathway","termid":"GO:0140888"},{"relation_name":"part_of","term_name":"cellular response to type I interferon","termid":"GO:0071357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"type I interferon-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-909733"],"synonyms":[{"name":"type I interferon signaling pathway","type":"exact"},{"name":"type I interferon-activated signaling pathway","type":"exact"}],"termid":"GO:0060337"}


id: PBO:0011170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PXA domain protein","termid":"PBO:0011170"}


id: MOD:00274
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the hydrogen atom of a cysteine sulfanyl group with a sulfanyl group, forming a disulfanyl group, and converting an L-cysteine residue to L-cysteine persulfide.","definition_xrefs":["RESID:AA0269","ChEBI:28839","PubMed:15096637","PubMed:4276457","Unimod:421","PubMed:8161529"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"thiolated residue","termid":"MOD:01886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-cysteine persulfide","synonyms":[{"name":"(R)-2-amino-3-disulfanylpropanoic acid","type":"exact"},{"name":"2-amino-3-disulfanylpropanoic acid","type":"exact"},{"name":"2-amino-3-hydrodisulfidopropanoic acid","type":"exact"},{"name":"2-amino-3-hydropersulfidopropanoic acid","type":"exact"},{"name":"2-amino-3-persulfhydrylpropanoic acid","type":"exact"},{"name":"3-(thiosulfeno)-alanine","type":"exact"},{"name":"3-disulfanylalanine","type":"exact"},{"name":"ACT_SITE Cysteine persulfide intermediate","type":"exact"},{"name":"L-cysteine persulfide","type":"exact"},{"name":"MOD_RES Cysteine persulfide","type":"exact"},{"name":"S-mercaptocysteine","type":"exact"},{"name":"S-sulfanylcysteine","type":"exact"},{"name":"Sulfide","type":"related"},{"name":"persulfide","type":"related"},{"name":"thiocysteine","type":"exact"}],"termid":"MOD:00274"}


id: GO:0048813
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a dendrite are generated and organized.","definition_xrefs":["GOC:jl","ISBN:0198506732","PMID:22683681","GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection morphogenesis","termid":"GO:0048812"},{"relation_name":"part_of","term_name":"dendrite development","termid":"GO:0016358"},{"relation_name":"part_of","term_name":"cell morphogenesis involved in neuron differentiation","termid":"GO:0048667"}],"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":"dendrite morphogenesis","termid":"GO:0048813"}


id: MONDO:0033618
data:
  {"annotated_genes":["SJAG_03597"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87457],"is_not":false,"summary":null,"term":"MONDO:0033618"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03597":null},"genotype_count":0,"is_obsolete":false,"name":"Vissers-Bodmer syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1776566","OMIM:619033","DOID:0081397","UMLS:C5436647"],"synonyms":[{"name":"VIBOS","type":"exact"}],"termid":"MONDO:0033618","terms_by_termid":{"MONDO:0033618":null},"xrefs":{"Monarch":{"xref_id":"0033618"}}}


id: PBO:0047136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 172 member B, pseudogene","termid":"PBO:0047136"}


id: GO:1905429
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 glycine stimulus.","definition_xrefs":["PMID:18984164","GO_REF:0000071","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to amino acid","termid":"GO:0043200"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"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 glycine","synonyms":[{"name":"response to Gly","type":"exact"},{"name":"response to aminoacetic acid","type":"exact"},{"name":"response to aminoethanoic acid","type":"exact"},{"name":"response to glycin","type":"exact"}],"termid":"GO:1905429"}


id: PATO:0002450
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A hardness quality of giving significant resistance to pressure.","definition_xrefs":["PATOC:CM"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hardness","termid":"PATO:0000048"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"firm","termid":"PATO:0002450"}


id: PR:Q9Y808
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- med15 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y808"],"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 C146.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC146.01","synonyms":[{"name":"Spom972h-med15","type":"exact"}],"termid":"PR:Q9Y808"}


id: PBO:0089815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome passenger complex subunit, INCENP ortholog Pic1","termid":"PBO:0089815"}


id: PBO:0042636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromodomain protein Y-linked 11 pseudogene","termid":"PBO:0042636"}


id: FYPO:0006008
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 site of cell division begins at the normal (i.e. indistinguishable from wild type) time relative to other cell cycle events.","definition_xrefs":["PMID:26941334","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to cell division site","termid":"FYPO:0002442"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"normal onset of protein localization to cell division site","synonyms":[{"name":"normal onset of protein localisation to cell division site","type":"exact"},{"name":"normal onset of protein localization to cell division site during mitotic cell cycle","type":"related"},{"name":"normal onset of protein localization to cell division site during vegetative growth","type":"exact"},{"name":"normal onset of protein recruitment to cell division site","type":"related"},{"name":"normal timing of protein localization to cell division site","type":"related"}],"termid":"FYPO:0006008"}


id: PBO:0065395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome subunit alpha 2 pseudogene 1","termid":"PBO:0065395"}


id: PBO:0048302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 1","termid":"PBO:0048302"}


id: GO:0008766
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-meso-2,6-diaminoheptanedioate + D-alanyl-D-alanine = ADP + phosphate + UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-6-carboxy-L-lysyl-D-alanyl-D-alanine.","definition_xrefs":["RHEA:28374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0003824"],"is_obsolete":false,"name":"UDP-N-acetylmuramoylalanyl-D-glutamyl-2,6-diaminopimelate-D-alanyl-D-alanine ligase activity","secondary_identifiers":["MetaCyc:UDP-NACMURALGLDAPAALIG-RXN"],"termid":"GO:0008766"}


id: GO:0006490
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of an oligosaccharide-lipid intermediate, such as a molecule of dolichol-P-man or dolicol-P-Glc used in N-linked glycosylation.","definition_xrefs":["GOC:rb","GOC:dph","GOC:pr","GOC:isa_complete","GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete oligosaccharide-lipid intermediate biosynthetic process (obsolete GO:0006490)","synonyms":[{"name":"oligosaccharide-lipid intermediate assembly","type":"narrow"}],"termid":"GO:0006490"}


id: MONDO:0859301
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 craniofacial dysmorphism and skeletal defects","secondary_identifiers":["OMIM:620083","UMLS:C5774235","MEDGEN:1824008","Orphanet:662207"],"termid":"MONDO:0859301","xrefs":{"Monarch":{"xref_id":"0859301"}}}


id: PBO:0065870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB27A, member RAS oncogene family","termid":"PBO:0065870"}


id: PBO:0069089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 336, pseudogene","termid":"PBO:0069089"}


id: PBO:0054945
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 2359","termid":"PBO:0054945"}


id: PBO:0034640
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_chromosome_condensation_during_telophase","termid":"PBO:0034640"}


id: FYPO:0005140
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the repair of double-strand breaks formed as part of meiotic recombination does not occur.","definition_xrefs":["PMID:15238514","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic recombination double-strand break repair","termid":"FYPO:0005139"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000631","FYPO:0000298","FYPO:0005447","FYPO:0000293"],"is_obsolete":false,"name":"abolished meiotic recombination double-strand break repair","synonyms":[{"name":"abolished DSB repair involved in reciprocal meiotic recombination","type":"exact"},{"name":"abolished double-strand break repair during meiotic recombination","type":"exact"},{"name":"abolished double-strand break repair involved in reciprocal meiotic recombination","type":"exact"},{"name":"meiotic recombination double-strand break repair abolished","type":"exact"}],"termid":"FYPO:0005140"}


id: MONDO:0019995
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Peripheral resistance to thyroid hormones may be a cause of permanent congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth.","definition_xrefs":["Orphanet:97927"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral hypothyroidism","termid":"MONDO:0016412"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peripheral resistance to thyroid hormones","secondary_identifiers":["GARD:12734","MEDGEN:902322","UMLS:C4273673","SCTID:718193005"],"termid":"MONDO:0019995","xrefs":{"Monarch":{"xref_id":"0019995"}}}


id: MONDO:0031230
data:
  {"annotated_genes":["SJAG_01671","SJAG_00260","SJAG_07005","SJAG_02398"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030935"},{"annotations":[87321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030937"},{"annotations":[87293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030974"},{"annotations":[87942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100294"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial myopathy","termid":"MONDO:0009637"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01671":null,"SJAG_02398":null,"SJAG_07005":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005336","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex II deficiency, nuclear type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:252011"],"termid":"MONDO:0031230","terms_by_termid":{"MONDO:0030935":null,"MONDO:0030937":null,"MONDO:0030974":null,"MONDO:0100294":null},"xrefs":{"Monarch":{"xref_id":"0031230"}}}


id: GO:0070020
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that consists of a dimeric transforming growth factor beta (TGF-beta) type II receptor bound to a TGF-beta1 dimer.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta1-type II receptor complex (obsolete GO:0070020)","synonyms":[{"name":"TGF-beta receptor II-TGF-beta1 complex","type":"exact"},{"name":"TGF-beta1-type II receptor complex","type":"exact"}],"termid":"GO:0070020"}


id: GO:1901943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (+)-epi-alpha-bisabolol.","definition_xrefs":["PMID:22867794","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpenoid biosynthetic process","termid":"GO:0016106"},{"relation_name":"is_a","term_name":"(+)-epi-alpha-bisabolol metabolic process","termid":"GO:1901941"}],"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":"(+)-epi-alpha-bisabolol biosynthetic process","synonyms":[{"name":"(+)-epi-alpha-bisabolol anabolism","type":"exact"},{"name":"(+)-epi-alpha-bisabolol biosynthesis","type":"exact"},{"name":"(+)-epi-alpha-bisabolol formation","type":"exact"},{"name":"(+)-epi-alpha-bisabolol synthesis","type":"exact"}],"termid":"GO:1901943"}


id: PBO:0070907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 15","termid":"PBO:0070907"}


id: GO:0106375
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dNTP + H2O = 2'-deoxynucleoside + H+ + triphosphate.","definition_xrefs":["RHEA:46148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triphosphoric monoester hydrolase activity","termid":"GO:0016793"}],"gene_count":0,"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:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"deoxynucleoside triphosphate hydrolase activity","termid":"GO:0106375"}


id: PBO:0085464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Predicted tail-anchored plasma membrane protein; contains conserved CYSTM module; related proteins in other organisms may be involved in response to stress; N- and C-terminal fusion proteins localize to the cell periphery; YDR034W-B has a paralog, YBR056W-A, that arose from the whole genome duplication","termid":"PBO:0085464"}


id: GO:0032616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-13 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:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-13 production","secondary_identifiers":["GO:0042231","GO:0072611"],"synonyms":[{"name":"IL-13 production","type":"exact"},{"name":"interleukin-13 biosynthetic process","type":"narrow"},{"name":"interleukin-13 secretion","type":"narrow"}],"termid":"GO:0032616"}


id: MONDO:0004168
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of testicular seminoma characterized by the presence of seminoma cells arranged in cribriform patterns and few lymphocytes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular seminoma","termid":"MONDO:0003669"}],"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":"cribriform variant testicular seminoma","secondary_identifiers":["UMLS:C1515292","DOID:7269","NCIT:C40957","MEDGEN:308258"],"synonyms":[{"name":"testicular seminoma, cribriform variant","type":"exact"}],"termid":"MONDO:0004168","xrefs":{"Monarch":{"xref_id":"0004168"}}}


id: GO:1903180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dopamine biosynthetic process.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:bf","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of dopamine metabolic process","termid":"GO:0045963"},{"relation_name":"is_a","term_name":"regulation of dopamine biosynthetic process","termid":"GO:1903179"},{"relation_name":"negatively_regulates","term_name":"dopamine biosynthetic process","termid":"GO:0042416"}],"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 dopamine biosynthetic process","synonyms":[{"name":"down regulation of dopamine anabolism","type":"exact"},{"name":"down regulation of dopamine biosynthesis","type":"exact"},{"name":"down regulation of dopamine biosynthetic process","type":"exact"},{"name":"down regulation of dopamine formation","type":"exact"},{"name":"down regulation of dopamine synthesis","type":"exact"},{"name":"down-regulation of dopamine anabolism","type":"exact"},{"name":"down-regulation of dopamine biosynthesis","type":"exact"},{"name":"down-regulation of dopamine biosynthetic process","type":"exact"},{"name":"down-regulation of dopamine formation","type":"exact"},{"name":"down-regulation of dopamine synthesis","type":"exact"},{"name":"downregulation of dopamine anabolism","type":"exact"},{"name":"downregulation of dopamine biosynthesis","type":"exact"},{"name":"downregulation of dopamine biosynthetic process","type":"exact"},{"name":"downregulation of dopamine formation","type":"exact"},{"name":"downregulation of dopamine synthesis","type":"exact"},{"name":"inhibition of dopamine anabolism","type":"narrow"},{"name":"inhibition of dopamine biosynthesis","type":"narrow"},{"name":"inhibition of dopamine biosynthetic process","type":"narrow"},{"name":"inhibition of dopamine formation","type":"narrow"},{"name":"inhibition of dopamine synthesis","type":"narrow"},{"name":"negative regulation of dopamine anabolism","type":"exact"},{"name":"negative regulation of dopamine biosynthesis","type":"exact"},{"name":"negative regulation of dopamine formation","type":"exact"},{"name":"negative regulation of dopamine synthesis","type":"exact"}],"termid":"GO:1903180"}


id: FYPO:0002349
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 stress granule assembly begins later than normal.","definition_xrefs":["PMID:21098141","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal stress granule assembly during vegetative growth","termid":"FYPO:0002347"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"delayed onset of stress granule assembly during vegetative growth","synonyms":[{"name":"delayed onset of cytoplasmic stress granule assembly during vegetative growth","type":"exact"},{"name":"delayed onset of stress granule assembly during mitotic cell cycle","type":"related"},{"name":"delayed onset of stress granule formation during vegetative growth","type":"exact"},{"name":"delayed stress granule assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0002349"}


id: PBO:0048121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fucosyltransferase 2","termid":"PBO:0048121"}


id: PBO:0065737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PX domain containing serine/threonine kinase like","termid":"PBO:0065737"}


id: PR:O42645
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A secretion-regulating guanine nucleotide exchange factor that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RCC1 repeat-containing protein C10F6.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC10F6.04","secondary_identifiers":["UniProtKB:O42645"],"synonyms":[{"name":"Spom972h-SERGEF","type":"exact"}],"termid":"PR:O42645"}


id: PBO:0057545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 661","termid":"PBO:0057545"}


id: GO:0061718
data:
  {"annotated_genes":["SJAG_03373","SJAG_04192","SJAG_00027","SJAG_06622","SJAG_02009","SJAG_02135","SJAG_02945","SJAG_06621","SJAG_03903","SJAG_03828","SJAG_04495","SJAG_00605","SJAG_03660","SJAG_02796","SJAG_00461","SJAG_04334","SJAG_00839","SJAG_01310","SJAG_02369","SJAG_02107"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111218,111213,118191,79530,107259,107260,107628,96301,107629,111216,105179,100047,74116,111214,111219,107258,111215,105436,99776,111217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glucose, with the production of pyruvate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucose catabolic process","termid":"GO:0006007"},{"relation_name":"is_a","term_name":"pyruvate metabolic process","termid":"GO:0006090"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00839":null,"SJAG_01310":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02369":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":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:0005975"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"glucose catabolic process to pyruvate","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"glucose catabolism to pyruvate","type":"exact"}],"termid":"GO:0061718","terms_by_termid":{"GO:0061621":null}}


id: PR:O59801
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ski2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59801"],"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":"ATP-dependent RNA helicase C550.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC550.03c","synonyms":[{"name":"Spom972h-ski2","type":"exact"}],"termid":"PR:O59801"}


id: PBO:0089459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2 snRNP-associated protein, WD repeat protein Sap130","termid":"PBO:0089459"}


id: PBO:0070527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L6 pseudogene 26","termid":"PBO:0070527"}


id: MONDO:0012014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive intermediate Charcot-Marie-Tooth disease type A is a subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by severe, early childhood-onset CMT neuropathy with prominent pes equinovarus deformity and impairment of hand muscles. Nerve conduction velocities usually range between 25-35 m/s and both axonal and demyelinating changes are observed on peripheral nerve pathology.","definition_xrefs":["Orphanet:217055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive intermediate Charcot-Marie-Tooth disease","termid":"MONDO:0017058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease recessive intermediate A","secondary_identifiers":["UMLS:C1842197","MEDGEN:334012","GARD:12453","OMIM:608340","DOID:0110201","MESH:C564256"],"synonyms":[{"name":"CMTRIA","type":"exact"},{"name":"Charcot-Marie-Tooth disease caused by mutation in GDAP1","type":"exact"},{"name":"Charcot-Marie-Tooth disease recessive intermediate type A","type":"exact"},{"name":"Charcot-Marie-Tooth disease, recessive Intermediate type a","type":"exact"},{"name":"Charcot-Marie-Tooth disease, recessive intermediate A","type":"related"},{"name":"Charcot-Marie-Tooth disease, recessive intermediate, A","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy recessive intermediate A","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, recessive Intermediate a","type":"related"},{"name":"GDAP1 Charcot-Marie-Tooth disease","type":"exact"},{"name":"RI-CMT type A","type":"exact"},{"name":"RI-CMTA","type":"exact"},{"name":"Ri-Cmta","type":"related"},{"name":"autosomal recessive intermediate Charcot-Marie-Tooth disease type A","type":"exact"}],"termid":"MONDO:0012014","xrefs":{"Monarch":{"xref_id":"0012014"}}}


id: PBO:0039816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor 6","termid":"PBO:0039816"}


id: PBO:0078218
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 8-2 (pseudogene)","termid":"PBO:0078218"}


id: PBO:0069097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 344, pseudogene","termid":"PBO:0069097"}


id: GO:0007522
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the visceral muscle over time, from its formation to the mature structure.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle organ development","termid":"GO:0007517"}],"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":"visceral muscle development","termid":"GO:0007522"}


id: PR:O43040
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ctf1 gene.","definition_xrefs":["UniProtKB:O43040","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":"cleavage and termination factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B9.11c","synonyms":[{"name":"Spom972h-ctf1","type":"exact"},{"name":"transcription termination factor ctf1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43040"}


id: GO:0035512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The hydrolytic removal of the methyl group from one or more nucleotides within a DNA molecule.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrolytic DNA demethylation (obsolete GO:0035512)","termid":"GO:0035512"}


id: PBO:0008804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial Membrane Bound O-Acyl Transferase (MBOAT) family","termid":"PBO:0008804"}


id: PBO:0035880
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_methylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0035880"}


id: PBO:0039064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AGK pseudogene 1","termid":"PBO:0039064"}


id: GO:0033457
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a GAU 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:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0060090","GO:0003674","GO:0003723"],"is_obsolete":false,"name":"GAU codon-amino acid adaptor activity","synonyms":[{"name":"GAT codon-amino acid adaptor activity","type":"exact"},{"name":"aspartic acid tRNA","type":"related"}],"termid":"GO:0033457"}


id: FYPO:0005262
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is increased relative to normal in a medium containing maltose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002057","FYPO:0005447","FYPO:0001985","FYPO:0000139","FYPO:0002058"],"is_obsolete":false,"name":"increased cell population growth on maltose carbon source","synonyms":[{"name":"increased growth on maltose carbon source","type":"broad"},{"name":"increased vegetative cell growth on maltose carbon source","type":"exact"}],"termid":"FYPO:0005262"}


id: PBO:0051642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol monophosphatase 1 pseudogene 1","termid":"PBO:0051642"}


id: PR:O13821
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sst4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13821"],"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 protein sorting-associated protein 27 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19A8.05c","synonyms":[{"name":"Spom972h-sst4","type":"exact"},{"name":"suppressor of ste12 deletion protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13821"}


id: PBO:0081432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 285B, pseudogene","termid":"PBO:0081432"}


id: PATO:0000782
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000782 defensive function value (obsolete PATO:0000782)","termid":"PATO:0000782"}


id: GO:0008802
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: betaine aldehyde + NAD+ + H2O = betaine + NADH + H+.","definition_xrefs":["EC:1.2.1.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase (NAD+) activity","termid":"GO:0004029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"betaine-aldehyde dehydrogenase (NAD+) activity","secondary_identifiers":["Reactome:R-HSA-6797955","RHEA:15305","MetaCyc:BADH-RXN"],"synonyms":[{"name":"BADH activity","type":"related"},{"name":"BetB","type":"related"},{"name":"betaine aldehyde dehydrogenase activity","type":"related"},{"name":"betaine aldehyde oxidase activity","type":"related"},{"name":"betaine-aldehyde:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0008802"}


id: PBO:0044797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin alpha 10, pseudogene","termid":"PBO:0044797"}


id: PBO:0084019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycosylated integral membrane protein localized to plasma membrane; plays a role in fructose-1,6-bisphosphatase (FBPase) degradation; involved in FBPase transport from the cytosol to Vid (vacuole import and degradation) vesicles; VID22 has a paralog, ENV11, that arose from the whole genome duplication","termid":"PBO:0084019"}


id: PBO:0070217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 149 pseudogene","termid":"PBO:0070217"}


id: FYPO:0003755
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype that shows detectable differences from normal at the level of an individual cell, when the cell is in the vegetative growth phase of the cell cycle. In fission yeast, the characteristics of wild type cells of the sequenced strain (972 h-) or the isogenic h+ or h90 strains are regarded as normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"inheres_in","term_name":"vegetative cell phenotype","termid":"FYPO:0001320"},{"relation_name":"is_a","term_name":"vegetative cell phenotype","termid":"FYPO:0001320"},{"relation_name":"is_a","term_name":"abnormal cell phenotype","termid":"FYPO:0003037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal vegetative cell phenotype","synonyms":[{"name":"abnormal cell phenotype during vegetative growth","type":"exact"},{"name":"abnormal vegetative cell phenotype during mitotic cell cycle","type":"related"},{"name":"abnormal vegetative fission yeast cell phenotype","type":"exact"}],"termid":"FYPO:0003755"}


id: FYPO:0002573
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the number of sites at which the protein Ssb1 accumulates is greater than normal.","definition_xrefs":["PMID:22927644","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased number of Ssb1 foci","synonyms":[{"name":"increased number of RPA foci","type":"exact"},{"name":"increased number of Rad11 foci","type":"exact"},{"name":"increased number of Rpa1 foci","type":"exact"},{"name":"increased number of Ssb1 foci during mitotic cell cycle","type":"related"},{"name":"increased number of Ssb1 foci during vegetative growth","type":"exact"}],"termid":"FYPO:0002573"}


id: PBO:0058791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7160","termid":"PBO:0058791"}


id: GO:0055124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of the neural plate before the appropriate time.","definition_xrefs":["GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete premature neural plate formation (obsolete GO:0055124)","synonyms":[{"name":"premature neural plate formation","type":"exact"}],"termid":"GO:0055124"}


id: GO:0140474
data:
  {"annotated_genes":["SJAG_01305","SJAG_03710","SJAG_04370","SJAG_03416"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[92675,107657,109339,109463],"is_not":false,"summary":null,"term":"GO:0140474"}]},"cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together a mitochondrion and an ER membrane either via membrane lipid binding or by interacting with a mitochondrial outer membrane protein, to establish or maintain the localization of the mitochondrion.","definition_xrefs":["PMID:27875684","PMID:19556461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum-organelle membrane tether activity","termid":"GO:0170009"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01305":null,"SJAG_03416":null,"SJAG_03710":null,"SJAG_04370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030674","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"mitochondrion-endoplasmic reticulum membrane tether activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ER-mitochondrion membrane adaptor activity","type":"exact"},{"name":"ER-mitochondrion membrane tether activity","type":"exact"},{"name":"endoplasmic reticulum-mitochondrion membrane adaptor activity","type":"exact"},{"name":"endoplasmic reticulum-mitochondrion membrane tether activity","type":"exact"},{"name":"mitochondrion-ER membrane adaptor activity","type":"exact"},{"name":"mitochondrion-ER membrane tether activity","type":"exact"},{"name":"mitochondrion-endoplasmic reticulum membrane adaptor activity","type":"exact"}],"termid":"GO:0140474","terms_by_termid":{"GO:0140474":null}}


id: FYPO:0005833
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein transport along microtubules to the cell tip is decreased. Transport of all proteins or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to cell tip during vegetative growth","termid":"FYPO:0001586"},{"relation_name":"is_a","term_name":"decreased protein transport along microtubule during vegetative growth","termid":"FYPO:0005494"},{"relation_name":"is_a","term_name":"abnormal protein transport along microtubule to cell tip during vegetative growth","termid":"FYPO:0005831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein transport along microtubule to cell tip during vegetative growth","synonyms":[{"name":"decreased protein movement along microtubule to cell tip during vegetative growth","type":"exact"},{"name":"decreased protein transport during mitotic cell cycle","type":"related"},{"name":"reduced protein transport along microtubule to cell tip during vegetative growth","type":"exact"}],"termid":"FYPO:0005833"}


id: MONDO:0001510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disease of orbital part of eye adnexa","termid":"MONDO:0004751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lateral displacement of eye","secondary_identifiers":["MEDGEN:509888","SCTID:48747004","UMLS:C0155272","DOID:12360","ICD9:376.36"],"synonyms":[{"name":"lateral displacement of globe","type":"exact"}],"termid":"MONDO:0001510","xrefs":{"Monarch":{"xref_id":"0001510"}}}


id: PBO:0088786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial matrix Lon protease","termid":"PBO:0088786"}


id: PBO:0042972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CHD1 helical C-terminal domain containing 1","termid":"PBO:0042972"}


id: GO:1902413
data:
  {"annotated_genes":["SJAG_01386","SJAG_02838","SJAG_02392","SJAG_03048","SJAG_01787","SJAG_02592","SJAG_00845","SJAG_01464","SJAG_04943","SJAG_04551"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94615,101453,103938,108910],"is_not":false,"summary":null,"term":"GO:1902413"},{"annotations":[112592,104164,92537,97634,96144,105491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903500"},{"annotations":[105492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903472"},{"annotations":[104169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905757"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mitotic cytokinesis.","definition_xrefs":["GOC:TermGenie","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokinesis","termid":"GO:0032466"},{"relation_name":"is_a","term_name":"regulation of mitotic cytokinesis","termid":"GO:1902412"},{"relation_name":"negatively_regulates","term_name":"mitotic cytokinesis","termid":"GO:0000281"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00845":null,"SJAG_01386":null,"SJAG_01464":null,"SJAG_01787":null,"SJAG_02392":null,"SJAG_02592":null,"SJAG_02838":null,"SJAG_03048":null,"SJAG_04551":null,"SJAG_04943":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0000281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0000281"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0000281","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mitotic cytokinesis","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of cytokinesis after mitosis","type":"exact"},{"name":"down regulation of mitotic cytokinesis","type":"exact"},{"name":"down-regulation of cytokinesis after mitosis","type":"exact"},{"name":"down-regulation of mitotic cytokinesis","type":"exact"},{"name":"downregulation of cytokinesis after mitosis","type":"exact"},{"name":"downregulation of mitotic cytokinesis","type":"exact"},{"name":"inhibition of cytokinesis after mitosis","type":"narrow"},{"name":"inhibition of mitotic cytokinesis","type":"narrow"},{"name":"negative regulation of cytokinesis after mitosis","type":"exact"}],"termid":"GO:1902413","terms_by_termid":{"GO:1902413":null,"GO:1903472":null,"GO:1903500":null,"GO:1905757":null}}


id: FYPO:0000634
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 centromere of a chromosome does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during vegetative growth","termid":"FYPO:0000449"},{"relation_name":"is_a","term_name":"abolished protein localization to chromosome during vegetative growth","termid":"FYPO:0002841"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to centromere during vegetative growth","synonyms":[{"name":"abolished protein localisation to centromere during vegetative growth","type":"exact"},{"name":"abolished protein localisation to chromosome, centromeric region during vegetative growth","type":"exact"},{"name":"abolished protein localization to centromere during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to chromosome, centric region during vegetative growth","type":"exact"},{"name":"abolished protein localization to chromosome, centromeric region during vegetative growth","type":"exact"},{"name":"protein absent from centromere during vegetative growth","type":"related"},{"name":"protein localization to centromere abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0000634"}


id: GO:0016816
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of any non-peptide carbon-nitrogen bond in substances other than amides, amidines and nitriles.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in other compounds (obsolete GO:0016816)","synonyms":[{"name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in other compounds","type":"exact"}],"termid":"GO:0016816"}


id: MONDO:0002663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete systemic mastocytosis (obsolete MONDO:0002663)","termid":"MONDO:0002663","xrefs":{"Monarch":{"xref_id":"0002663"}}}


id: FYPO:0005480
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 one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal during a cellular response to arsenite ions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein phosphorylation during cellular hyperosmotic response","termid":"FYPO:0001265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0002274","FYPO:0002494","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased protein phosphorylation during cellular response to arsenite ion","synonyms":[{"name":"increased protein phosphorylation during cellular response to arsenite","type":"exact"},{"name":"increased protein phosphorylation during cellular response to arsenite ion during mitotic cell cycle","type":"related"},{"name":"increased protein phosphorylation during cellular response to arsenite ion during vegetative growth","type":"exact"}],"termid":"FYPO:0005480"}


id: GO:0009519
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Layer of intercellular material, chiefly pectic substances, cementing together the primary walls of contiguous cells.","definition_xrefs":["ISBN:0471245208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specialized extracellular matrix","termid":"GO:0140047"}],"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":"middle lamella","secondary_identifiers":["Wikipedia:Middle_lamella"],"termid":"GO:0009519"}


id: GO:0005540
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to hyaluronic acid, a polymer composed of repeating dimeric units of glucuronic acid and N-acetyl glucosamine.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosaminoglycan binding","termid":"GO:0005539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"hyaluronic acid binding","synonyms":[{"name":"hyaluronan binding","type":"exact"}],"termid":"GO:0005540"}


id: MONDO:0007076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ocular albinism with sensorineural deafness (obsolete MONDO:0007076)","termid":"MONDO:0007076","xrefs":{"Monarch":{"xref_id":"0007076"}}}


id: GO:1990079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A tissue homeostatic process involved in the maintenance of an internal equilibrium within cartilage, including control of cellular proliferation and death and control of metabolic function.","definition_xrefs":["GOC:hjd","PMID:21652695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue homeostasis","termid":"GO:0001894"}],"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":"cartilage homeostasis","secondary_identifiers":["GO:1902096","GO:1902094","GO:1902095"],"synonyms":[{"name":"negative regulation of cartilage homeostasis","type":"related"},{"name":"positive regulation of cartilage homeostasis","type":"related"},{"name":"regulation of cartilage homeostasis","type":"related"}],"termid":"GO:1990079"}


id: PBO:0087363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sporulation-specific enzyme required for spore wall maturation; involved in the production of a soluble LL-dityrosine-containing precursor of the spore wall; transcripts accumulate at the time of prospore enclosure","termid":"PBO:0087363"}


id: GO:0019266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of asparagine from other compounds, including oxaloacetate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxaloacetate metabolic process","termid":"GO:0006107"},{"relation_name":"is_a","term_name":"asparagine biosynthetic process","termid":"GO:0006529"},{"relation_name":"is_a","term_name":"dicarboxylic acid catabolic process","termid":"GO:0043649"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"asparagine biosynthetic process from oxaloacetate","secondary_identifiers":["MetaCyc:ASPARAGINE-BIOSYNTHESIS"],"synonyms":[{"name":"asparagine anabolism from oxaloacetate","type":"exact"},{"name":"asparagine formation from oxaloacetate","type":"exact"},{"name":"asparagine synthesis from oxaloacetate","type":"exact"}],"termid":"GO:0019266"}


id: PR:P07334
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cdr1 gene.","definition_xrefs":["UniProtKB:P07334","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":"mitosis inducer protein kinase cdr1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC644.06c","synonyms":[{"name":"Spom972h-cdr1","type":"exact"},{"name":"protein kinase nim1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P07334"}


id: PBO:0002677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome-c reductase complex subunit 7","termid":"PBO:0002677"}


id: MONDO:0009554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any 3MC syndrome in which the cause of the disease is a mutation in the COLEC10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3MC syndrome","termid":"MONDO:0017398"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3MC syndrome 3","secondary_identifiers":["GARD:8531","MEDGEN:208657","DOID:0060577","MESH:C535704","UMLS:C0796032","OMIM:248340","Orphanet:2453"],"synonyms":[{"name":"3MC syndrome 3","type":"exact"},{"name":"3MC syndrome caused by mutation in COLEC10","type":"exact"},{"name":"3MC syndrome type 3","type":"exact"},{"name":"3MC3","type":"related"},{"name":"3Mc syndrome type 3","type":"exact"},{"name":"COLEC10 3MC syndrome","type":"exact"},{"name":"Malpuech Facial clefting syndrome","type":"related"},{"name":"Malpuech Facial clefting syndrome, formerly","type":"related"},{"name":"facial clefting syndrome, Gypsy type","type":"related"}],"termid":"MONDO:0009554","xrefs":{"Monarch":{"xref_id":"0009554"}}}


id: GO:0043329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of directing proteins towards a membrane using signals contained within the protein, occurring that contributes to ubiquitin-dependent protein catabolism via the MVB pathway; the destruction of a protein or peptide covalently tagged with a ubiquitin, via the multivesicular body (MVB) sorting pathway.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete protein targeting to membrane involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway (obsolete GO:0043329)","synonyms":[{"name":"protein membrane targeting during ubiquitin-dependent protein catabolic process via the MVB pathway","type":"exact"},{"name":"protein membrane targeting during ubiquitin-dependent protein catabolism via the MVB pathway","type":"exact"},{"name":"protein targeting to membrane during ubiquitin-dependent protein breakdown via the MVB pathway","type":"exact"},{"name":"protein targeting to membrane during ubiquitin-dependent protein catabolic process via the MVB pathway","type":"related"},{"name":"protein targeting to membrane during ubiquitin-dependent protein degradation via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein breakdown via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein catabolic process via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein catabolism via the MVB pathway","type":"exact"},{"name":"protein-membrane targeting during ubiquitin-dependent protein degradation via the MVB pathway","type":"exact"}],"termid":"GO:0043329"}


id: GO:2000038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of stomatal complex development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of post-embryonic development","termid":"GO:0048580"},{"relation_name":"regulates","term_name":"stomatal complex development","termid":"GO:0010374"}],"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 stomatal complex development","termid":"GO:2000038"}


id: PBO:0053049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"La ribonucleoprotein 7, transcriptional regulator","termid":"PBO:0053049"}


id: PR:O13777
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- saf5 gene.","definition_xrefs":["UniProtKB:O13777","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 C1610.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1610.01","synonyms":[{"name":"Spom972h-saf5","type":"exact"}],"termid":"PR:O13777"}


id: GO:0090452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of lithium ions (Li+) across a membrane.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lithium ion transport","termid":"GO:0010351"},{"relation_name":"is_a","term_name":"monoatomic cation transmembrane transport","termid":"GO:0098655"},{"relation_name":"is_a","term_name":"inorganic cation transmembrane transport","termid":"GO:0098662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"lithium ion transmembrane transport","synonyms":[{"name":"lithium ion import","type":"narrow"},{"name":"lithium ion uptake","type":"exact"}],"termid":"GO:0090452"}


id: PBO:0073140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC22 homolog B3, pseudogene","termid":"PBO:0073140"}


id: PBO:0087838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Third-largest subunit of DNA polymerase II (DNA polymerase epsilon); required to maintain fidelity of chromosomal replication and also for inheritance of telomeric silencing; stabilizes the interaction of Pol epsilon with primer-template DNA, positively affecting the processivity of the polymerase and exonuclease activities of Pol epsilon; mRNA abundance peaks at the G1/S boundary of the cell cycle; DPB3 has a paralog, DLS1, that arose from the whole genome duplication","termid":"PBO:0087838"}


id: MONDO:0006680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intradermal nevus characterized by the presence of benign pigmented dendritic spindle-shaped melanocytes. It most frequently occurs in the skin of the distal upper extremities, followed by the lower extremities, scalp, face, and buttocks. It usually presents as a single blue or blue-black papular lesion less than 1cm in diameter. Simple excision is usually curative.","definition_xrefs":["NCIT:C3803"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"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":"blue nevus","secondary_identifiers":["MESH:D018329","ICDO:8780/0","MedDRA:10062788","MEDGEN:104930","SCTID:254806009","UMLS:C0206736","EFO:1000841"],"synonyms":[{"name":"Jadassohn-TiC(che nevus","type":"related"},{"name":"Jadassohn-TiC(che syndrome","type":"related"},{"name":"Jadassohn-Tièche nevus","type":"related"},{"name":"Jadassohn-Tièche syndrome","type":"related"},{"name":"Tièche-Jadassohn nevus","type":"related"},{"name":"benign mesenchymal melanoma","type":"related"},{"name":"blue Nevus of skin","type":"exact"},{"name":"blue Nevus of the skin","type":"exact"},{"name":"blue neuronevus","type":"related"},{"name":"blue nevus","type":"exact"},{"name":"blue skin Nevus","type":"exact"}],"termid":"MONDO:0006680","xrefs":{"Monarch":{"xref_id":"0006680"}}}


id: MONDO:0023206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low or intermediate grade well differentiated tumor with neuroendocrine differentiation that arises from the pancreas. It is characterized by the presence of a clinical syndrome that results from hormone hypersecretion.","definition_xrefs":["NCIT:C45840"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic neuroendocrine tumor","termid":"MONDO:0019954"},{"relation_name":"is_a","term_name":"functioning endocrine neoplasm","termid":"MONDO:0021120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"functional pancreatic neuroendocrine tumor","secondary_identifiers":["GARD:22053","UMLS:C1708107","MEDGEN:310778","Orphanet:506060"],"synonyms":[{"name":"functional pancreatic NET","type":"exact"},{"name":"functional pancreatic neuroendocrine tumor","type":"exact"},{"name":"functioning PNET","type":"exact"},{"name":"functioning neuroendocrine tumor of pancreas","type":"related"},{"name":"functioning neuroendocrine tumour of pancreas","type":"related"},{"name":"functioning pancreatic NET","type":"exact"},{"name":"functioning pancreatic endocrine tumor","type":"exact"},{"name":"functioning pancreatic endocrine tumour","type":"exact"},{"name":"functioning pancreatic neuroendocrine tumor","type":"exact"},{"name":"functioning pancreatic neuroendocrine tumour","type":"exact"},{"name":"functioning well differentiated pancreatic endocrine neoplasm","type":"exact"},{"name":"functioning well differentiated pancreatic endocrine tumor","type":"exact"},{"name":"functioning well differentiated pancreatic endocrine tumour","type":"exact"},{"name":"functioning well-differentiated NEN of pancreas","type":"exact"},{"name":"functioning well-differentiated neuroendocrine neoplasm of pancreas","type":"exact"},{"name":"functioning well-differentiated pancreatic NEN","type":"exact"},{"name":"functioning well-differentiated pancreatic neuroendocrine neoplasm","type":"exact"},{"name":"syndromic pancreatic NET","type":"exact"},{"name":"syndromic pancreatic neuroendocrine tumor","type":"exact"},{"name":"syndromic pancreatic neuroendocrine tumour","type":"exact"}],"termid":"MONDO:0023206","xrefs":{"Monarch":{"xref_id":"0023206"}}}


id: GO:0033470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of gibberellin 12, (1R,2S,3S,4R,8S,9S,12R)-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid 1meta,4a-dimethyl-8-methylidene-4aalpha,4bbeta-gibbane-1alpha,10beta-dicarboxylic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gibberellin biosynthetic process","termid":"GO:0009686"},{"relation_name":"is_a","term_name":"gibberellin 12 metabolic process","termid":"GO:0033469"},{"relation_name":"is_a","term_name":"dicarboxylic acid biosynthetic process","termid":"GO:0043650"}],"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:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"gibberellin 12 biosynthetic process","secondary_identifiers":["MetaCyc:PWY-5034"],"synonyms":[{"name":"GA12 biosynthetic process","type":"exact"},{"name":"gibberellin 12 anabolism","type":"exact"},{"name":"gibberellin 12 biosynthesis","type":"exact"},{"name":"gibberellin 12 formation","type":"exact"},{"name":"gibberellin 12 synthesis","type":"exact"},{"name":"gibberellin A12 biosynthetic process","type":"exact"}],"termid":"GO:0033470"}


id: PBO:0040333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit c locus 1 pseudogene 8","termid":"PBO:0040333"}


id: GO:0047002
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arabinitol + NAD+ = L-ribulose + H+ + NADH.","definition_xrefs":["RHEA:21356","EC:1.1.1.13"],"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:0016491","GO:0003824"],"is_obsolete":false,"name":"L-arabinitol 2-dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R02441","MetaCyc:1.1.1.13-RXN"],"synonyms":[{"name":"L-arabinitol 2-dehydrogenase (ribulose forming) activity","type":"exact"}],"termid":"GO:0047002"}


id: PR:O74815
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk27 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74815"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein kinase ppk27 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC337.04","synonyms":[{"name":"Spom972h-ppk27","type":"exact"}],"termid":"PR:O74815"}


id: PR:Q9USQ0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC902.03 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USQ0"],"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":"sporulation-specific protein spo7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC902.03","synonyms":[{"name":"Spom972h-SPBC902.03","type":"exact"}],"termid":"PR:Q9USQ0"}


id: PBO:0059091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MORC family CW-type zinc finger 3","termid":"PBO:0059091"}


id: MONDO:0016943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 6p duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the short arm (p) of chromosome 6. The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. Features that often occur in people with chromosome 6p duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. This condition can occur sporadically or be inherited from a parent who is either mildy affected (has the deletion) or carries a balanced translocation. Treatment is based on the signs and symptoms present in each person.","definition_xrefs":["GARD:0005352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of chromosome 6","termid":"MONDO:0016927"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial duplication of the short arm of chromosome 6","secondary_identifiers":["icd11.foundation:657610285","UMLS:C5679721","GARD:5352","MEDGEN:1826043","MESH:C537811","Orphanet:262740"],"synonyms":[{"name":"6p duplication","type":"related"},{"name":"6p trisomy","type":"related"},{"name":"Duplication 6p","type":"related"},{"name":"chromosome 6p duplication","type":"related"},{"name":"partial duplication of chromosome 6p","type":"exact"},{"name":"partial duplication of the short arm of chromosome type 6","type":"exact"},{"name":"partial trisomy 6p","type":"related"},{"name":"partial trisomy of chromosome 6p","type":"exact"},{"name":"partial trisomy of the short arm of chromosome 6","type":"exact"},{"name":"trisomy 6p","type":"related"}],"termid":"MONDO:0016943","xrefs":{"Monarch":{"xref_id":"0016943"}}}


id: MOD:01916
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tyrosine residue to O4'-(N-acetylamino)galactosyl-L-tyrosine.","definition_xrefs":["PubMed:21712440","PubMed:21983924","RESID:AA0577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetylaminogalactosylated residue","termid":"MOD:00563"},{"relation_name":"is_a","term_name":"O-glycosyl-L-tyrosine","termid":"MOD:01927"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O4'-(N-acetylamino)galactosyl-L-tyrosine","synonyms":[{"name":"(2S)-2-amino-3-(D-2-acetamido-2-deoxygalactopyranosyloxy)phenylpropanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (GalNAc) tyrosine","type":"exact"},{"name":"O4'-(N-acetylamino)galactosyl-L-tyrosine","type":"exact"},{"name":"O4'-(N-acetylgalactosaminyl)tyrosine","type":"exact"},{"name":"O4'-glycosyl-L-tyrosine","type":"exact"},{"name":"mucin type O-glycosyltyrosine","type":"exact"}],"termid":"MOD:01916"}


id: PBO:0004232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ClC chloride channel (predicted)","termid":"PBO:0004232"}


id: GO:1904057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of sensory perception of pain.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:17167094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nervous system process","termid":"GO:0031645"},{"relation_name":"is_a","term_name":"regulation of sensory perception of pain","termid":"GO:0051930"},{"relation_name":"negatively_regulates","term_name":"sensory perception of pain","termid":"GO:0019233"}],"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 sensory perception of pain","synonyms":[{"name":"down regulation of nociception","type":"exact"},{"name":"down regulation of perception of physiological pain","type":"narrow"},{"name":"down regulation of sensory perception of pain","type":"exact"},{"name":"down-regulation of nociception","type":"exact"},{"name":"down-regulation of perception of physiological pain","type":"narrow"},{"name":"down-regulation of sensory perception of pain","type":"exact"},{"name":"downregulation of nociception","type":"exact"},{"name":"downregulation of perception of physiological pain","type":"narrow"},{"name":"downregulation of sensory perception of pain","type":"exact"},{"name":"inhibition of nociception","type":"narrow"},{"name":"inhibition of perception of physiological pain","type":"narrow"},{"name":"inhibition of sensory perception of pain","type":"narrow"},{"name":"negative regulation of nociception","type":"exact"},{"name":"negative regulation of perception of physiological pain","type":"narrow"}],"termid":"GO:1904057"}


id: PBO:0113539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar protein; involved in oxidative stress response and modulation of replicative lifespan; targeted to vacuole via AP-3 pathway; undergoes autophosphorylation, which is abolished by mutation of Asp781 in catalytic motif (D781N); P5 ATPase subfamily member with similarity to yeast Spf1p and homology to human ATP13A2 (PARK9), mutations in which are associated with Parkinson disease and Kufor-Rakeb syndrome","termid":"PBO:0113539"}


id: GO:0098934
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of organelles or molecules along microtubules in a dendrite from the postsynapse towards the cell body.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendritic transport","termid":"GO:0098935"}],"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":"retrograde dendritic transport","termid":"GO:0098934"}


id: MOD:00930
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"tyrosine adduct with substrate analog inhibitor 1,2-dideoxy-2'-methyl-alpha-D-glucopyranoso-[2,1-d]-Delta2'-thiazoline.","definition_xrefs":["Unimod:514","PubMed:15795231"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"propyl-NAG tyrosine adduct","termid":"MOD:00930"}


id: MONDO:0003153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brain stem glioma that occurs in an adult.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain stem glioma","termid":"MONDO:0002911"},{"relation_name":"is_a","term_name":"adult brain stem neoplasm","termid":"MONDO:0024797"}],"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":"adult brainstem glioma","secondary_identifiers":["NCIT:C9091","MEDGEN:124526","UMLS:C0278873","DOID:4813"],"synonyms":[{"name":"adult brain stem glioma","type":"exact"},{"name":"adult brainstem glioma","type":"exact"},{"name":"adult brainstem neuroglial neoplasm","type":"exact"},{"name":"adult brainstem neuroglial tumor","type":"exact"},{"name":"adult brainstem neuroglial tumour","type":"exact"},{"name":"brain stem glioma","type":"broad"},{"name":"brain stem glioma of adults","type":"exact"},{"name":"glioma of adult brain stem","type":"exact"},{"name":"glioma of the adult brain stem","type":"exact"}],"termid":"MONDO:0003153","xrefs":{"Monarch":{"xref_id":"0003153"}}}


id: MONDO:0013544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial atrial fibrillation in which the cause of the disease is a mutation in the GJA5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"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, 11","secondary_identifiers":["MEDGEN:481323","OMIM:614049","GARD:15747","UMLS:C3279693"],"synonyms":[{"name":"ATFB11","type":"related"},{"name":"GJA5 familial atrial fibrillation","type":"exact"},{"name":"atrial fibrillation, familial, 11","type":"exact"},{"name":"atrial fibrillation, familial, type 11","type":"exact"},{"name":"familial atrial fibrillation caused by mutation in GJA5","type":"exact"}],"termid":"MONDO:0013544","xrefs":{"Monarch":{"xref_id":"0013544"}}}


id: PBO:0001875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho family GTPase Rho4","termid":"PBO:0001875"}


id: GO:0034367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The acquisition, loss, or modification of macromolecules within a complex, resulting in the alteration of an existing complex.","definition_xrefs":["GOC:rl","GOC:BHF","GOC:mah","GOC:mtg_mpo"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex organization","termid":"GO:0043933"}],"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":"protein-containing complex remodeling","synonyms":[{"name":"macromolecular complex remodeling","type":"related"},{"name":"macromolecular complex remodelling","type":"related"},{"name":"protein-containing complex remodelling","type":"exact"}],"termid":"GO:0034367"}


id: GO:0033769
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: 2-dimethylallyl-(6aS,11aS)-3,6a,9-trihydroxypterocarpan + NADPH + H+ + O2 = glyceollin II or glyceollin III + NADP+ + 2 H2O, and 4-dimethylallyl-(6aS,11aS)-3,6a,9-trihydroxypterocarpan + NADPH + H+ + O2 = glyceollin I + NADP+ + 2 H2O.","definition_xrefs":["EC:1.14.14.135"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"glyceollin synthase activity","synonyms":[{"name":"dimethylallyl-3,6a,9-trihydroxypterocarpan cyclase activity","type":"exact"}],"termid":"GO:0033769"}


id: PBO:0002719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannosyltransferase complex subunit, Anp family Mnn9 (predicted)","termid":"PBO:0002719"}


id: PATO:0000041
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000041 absolutedistance (obsolete PATO:0000041)","termid":"PATO:0000041"}


id: PBO:0079346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 30, pseudogene","termid":"PBO:0079346"}


id: FYPO:0003377
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to nitrosative stress is lower than normal. Total RNA or a specific RNA may be affected. Nitrosative stress often results from exposure to high levels of nitric oxide (NO) or the highly reactive oxidant peroxynitrite, which is produced following interaction of NO with superoxide anions.","definition_xrefs":["PMID:20204527","PomBase:mah","GO:0071500"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"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:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0006551","FYPO:0005447"],"is_obsolete":false,"name":"decreased RNA level during cellular response to nitrosative stress","synonyms":[{"name":"decreased RNA accumulation during cellular response to nitrosative stress","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to nitrosative stress","type":"narrow"},{"name":"decreased transcript level during cellular response to nitrosative stress","type":"exact"},{"name":"reduced RNA level during cellular response to nitrosative stress","type":"exact"}],"termid":"FYPO:0003377"}


id: GO:1905239
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of canonical Wnt signaling pathway involved in osteoblast differentiation.","definition_xrefs":["GOC:rph","GOC:BHF_miRNA","GOC:TermGenie","GO_REF:0000058","GOC:BHF","PMID:19342382"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of canonical Wnt signaling pathway involved in osteoblast differentiation (obsolete GO:1905239)","synonyms":[{"name":"regulation of canonical Wnt receptor signaling pathway involved in osteoblast differentiation","type":"exact"},{"name":"regulation of canonical Wnt receptor signalling pathway involved in osteoblast differentiation","type":"exact"},{"name":"regulation of canonical Wnt-activated signaling pathway involved in osteoblast differentiation","type":"exact"}],"termid":"GO:1905239"}


id: PBO:0000206
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deletion mutant expression profiling","termid":"PBO:0000206"}


id: PBO:0033779
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_attachment_of_mitotic_spindle_microtubules_to_kinetochore","termid":"PBO:0033779"}


id: GO:0047262
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-D-galacturonate + 1,4-alpha-D-galacturonosyl(n) = 1,4-alpha-D-galacturonosyl(n+1) + UDP.","definition_xrefs":["EC:2.4.1.43","MetaCyc:2.4.1.43-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"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:0016757","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"polygalacturonate 4-alpha-galacturonosyltransferase activity","secondary_identifiers":["RHEA:13573","GO:0050375"],"synonyms":[{"name":"UDP galacturonate-polygalacturonate alpha-galacturonosyltransferase activity","type":"related"},{"name":"UDP-D-galacturonate:1,4-alpha-poly-D-galacturonate 4-alpha-D-galacturonosyltransferase activity","type":"related"},{"name":"uridine diphosphogalacturonate-polygalacturonate alpha-galacturonosyltransferase activity","type":"related"}],"termid":"GO:0047262"}


id: PBO:0053359
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 265-2, pseudogene","termid":"PBO:0053359"}


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


id: GO:0035355
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex containing Toll-like receptor 2 (TLR2) and Toll-like receptor 6 (TLR6).","definition_xrefs":["GOC:signaling","GOC:add","PMID:19931471","PMID:21481769"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane signaling receptor complex","termid":"GO:0098802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"Toll-like receptor 2-Toll-like receptor 6 protein complex","secondary_identifiers":["GO:0038126"],"synonyms":[{"name":"TLR2-TLR6 protein complex","type":"exact"},{"name":"TLR2:TLR6 heterodimer","type":"exact"},{"name":"TLR6:TLR2 complex","type":"exact"},{"name":"toll-like receptor TLR6:TLR2 heterodimeric complex","type":"exact"}],"termid":"GO:0035355"}


id: MONDO:0013117
data:
  {"annotated_genes":["SJAG_00885"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87268],"is_not":false,"summary":null,"term":"MONDO:0013117"}]},"cv_name":"mondo","definition":"Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RRM2B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant progressive external ophthalmoplegia","termid":"MONDO:0008003"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320","MONDO:0000426","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111518","OMIM:613077","GARD:16501","MEDGEN:413981","MESH:C567768","UMLS:C2751319"],"synonyms":[{"name":"PEOA5","type":"related"},{"name":"RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5","type":"exact"},{"name":"progressive external ophthalmoplegia, autosomal dominant 5","type":"related"}],"termid":"MONDO:0013117","terms_by_termid":{"MONDO:0013117":null},"xrefs":{"Monarch":{"xref_id":"0013117"}}}


id: FYPO:0001038
data:
  {"alleles_by_uniquename":{"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121213],"is_not":false,"summary":null,"term":"FYPO:0001038"}]},"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 one or more specific proteins occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein modification during vegetative growth","termid":"FYPO:0000547"},{"relation_name":"is_a","term_name":"abnormal protein phosphorylation during vegetative growth","termid":"FYPO:0000775"},{"relation_name":"is_a","term_name":"increased protein phosphorylation","termid":"FYPO:0002680"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01787":null,"SJAG_04551":null},"genotype_count":1,"genotypes_by_uniquename":{"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002494","FYPO:0001320","FYPO:0002274","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased protein phosphorylation during vegetative growth","references_by_uniquename":{"PMID:34198697":null},"single_locus_annotated_genes":["SJAG_01787"],"single_locus_genotype_uniquenames":["pck1delta"],"synonyms":[{"name":"increased protein phosphorylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001038","terms_by_termid":{"FYPO:0001038":null}}


id: GO:1903962
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of arachidonate from one side of a membrane to the other.","definition_xrefs":["PMID:15642721","GOC:TermGenie","GO_REF:0000066","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid transmembrane transporter activity","termid":"GO:0005324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"arachidonate transmembrane transporter activity","synonyms":[{"name":"arachidonate transporter activity","type":"related"},{"name":"arachidonic acid transporter activity","type":"related"}],"termid":"GO:1903962"}


id: PBO:0113198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiotic regulator; involved in maintaining sister chromatid cohesion during meiosis I as well as promoting proper attachment of kinetochores to the spindle during meiosis I and meiosis II; promotes phosphorylation of Cdc5p substrates in MI and impacts Hrr25p function in MII; substrate of the anaphase-promoting complex (APC) that is degraded during anaphase I; expressed solely in meiotic cells","termid":"PBO:0113198"}


id: MONDO:0006759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuropathy of the femoral nerve.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mononeuropathy","termid":"MONDO:0001397"},{"relation_name":"is_a","term_name":"peripheral nerve lesion","termid":"MONDO:0024334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"femoral neuropathy","secondary_identifiers":["MEDGEN:148421","ICD9:355.2","MESH:D020428","NCIT:C27595","DOID:4196","SCTID:25690000","UMLS:C0751931"],"synonyms":[{"name":"femoral nerve dysfunction","type":"exact"},{"name":"femoral nerve lesions","type":"exact"},{"name":"femoral nerve peripheral nerve lesion","type":"exact"},{"name":"peripheral nerve lesion of femoral nerve","type":"exact"}],"termid":"MONDO:0006759","xrefs":{"Monarch":{"xref_id":"0006759"}}}


id: PBO:0117417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zDHHC palmitoyltransferase 12","termid":"PBO:0117417"}


id: MONDO:0016332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-familial hypertrophic cardiomyopathy","termid":"MONDO:0016330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"hypertrophic cardiomyopathy due to intensive athletic training","secondary_identifiers":["Orphanet:217601","icd11.foundation:183927358"],"termid":"MONDO:0016332","xrefs":{"Monarch":{"xref_id":"0016332"}}}


id: PBO:0035900
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_re-entry_into_mitotic_cell_cycle_after_arrest_in_response_to_heat_shock","termid":"PBO:0035900"}


id: PR:Q09673
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pantothenate synthetase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00056"],"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":"pantoate--beta-alanine ligase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5H10.08c","secondary_identifiers":["UniProtKB:Q09673"],"synonyms":[{"name":"Spom972h-panC","type":"exact"},{"name":"pantoate-activating enzyme (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"pantothenate synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09673"}


id: GO:0047806
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 H2 + ferricytochrome c3 = 4 H+ + ferrocytochrome c3.","definition_xrefs":["EC:1.12.2.1","MetaCyc:CYTOCHROME-C3-HYDROGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on hydrogen as donor, cytochrome as acceptor","termid":"GO:0016697"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"cytochrome-c3 hydrogenase activity","secondary_identifiers":["RHEA:20625"],"synonyms":[{"name":"H(2):ferricytochrome c3 oxidoreductase activity","type":"related"},{"name":"H2:ferricytochrome c3 oxidoreductase activity","type":"related"},{"name":"cytochrome c3 reductase activity","type":"related"},{"name":"cytochrome hydrogenase activity","type":"broad"},{"name":"hydrogen:ferricytochrome-c3 oxidoreductase activity","type":"related"}],"termid":"GO:0047806"}


id: PBO:0047589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrinogen gamma chain","termid":"PBO:0047589"}


id: GO:0023042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which information is sent from one location to another, within a living organism or between living organisms, via a protein/peptide mediator.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signaling via protein/peptide mediator (obsolete GO:0023042)","synonyms":[{"name":"signaling via protein/peptide mediator","type":"exact"},{"name":"signalling via protein/peptide mediator","type":"exact"}],"termid":"GO:0023042"}


id: PBO:0085305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatase and transcription/RNA-processing factor; associates with TFIIB and cleavage/polyadenylation factor Pta1p; exhibits phosphatase activity on serine-5 and serine-7 of the RNA polymerase II C-terminal domain; affects start site selection and transcriptional read through in vivo","termid":"PBO:0085305"}


id: PBO:0002947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA U24","termid":"PBO:0002947"}


id: GO:0047440
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-dehydro-3-deoxy-D-arabinonate = glycolaldehyde + pyruvate.","definition_xrefs":["EC:4.1.2.28","RHEA:20609"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-dehydro-3-deoxy-D-pentonate aldolase activity","secondary_identifiers":["KEGG_REACTION:R01782","MetaCyc:4.1.2.28-RXN"],"synonyms":[{"name":"2-dehydro-3-deoxy-D-pentonate glycolaldehyde-lyase activity","type":"related"},{"name":"2-keto-3-deoxy-D-pentonate aldolase activity","type":"related"},{"name":"3-deoxy-D-pentulosonic acid aldolase","type":"broad"}],"termid":"GO:0047440"}


id: MONDO:0010581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"nephrogenic diabetes insipidus","termid":"MONDO:0016383"}],"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":"diabetes insipidus, nephrogenic, X-linked","secondary_identifiers":["MEDGEN:288785","GARD:15289","UMLS:C1563705","DOID:0081060","OMIM:304800"],"synonyms":[{"name":"Ndi","type":"related"},{"name":"diabetes insipidus, nephrogenic, 1, X-linked recessive","type":"exact"},{"name":"diabetes insipidus, nephrogenic, X-linked","type":"exact"},{"name":"diabetes insipidus, nephrogenic, type 1","type":"related"}],"termid":"MONDO:0010581","xrefs":{"Monarch":{"xref_id":"0010581"}}}


id: MONDO:0017257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic posterior uveitis is a rare, potentially sight-threatening, ocular disease, not attributed to any specific ocular or systemic cause, characterized by focal, multifocal or diffuse non-infectious inflammation in the posterior uvea (i.e. choroiditis, chorioretinitis, retinitis and neuroretinitis). Visual morbidity due to complications (including cystoid macular edema and choroidal neovascularization) has been reported.","definition_xrefs":["Orphanet:280917"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"choroiditis","termid":"MONDO:0001280"},{"relation_name":"is_a","term_name":"uveitis","termid":"MONDO:0020283"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"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":"idiopathic posterior uveitis","secondary_identifiers":["GARD:21099","MEDGEN:1657160","UMLS:C4751435"],"termid":"MONDO:0017257","xrefs":{"Monarch":{"xref_id":"0017257"}}}


id: PBO:0048788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit alpha i1","termid":"PBO:0048788"}


id: PBO:0085396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane permease; mediates uptake of glycerophosphoinositol and glycerophosphocholine as sources of the nutrients inositol and phosphate; expression and transport rate are regulated by phosphate and inositol availability","termid":"PBO:0085396"}


id: PBO:0071535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a","termid":"PBO:0071535"}


id: GO:0097164
data:
  {"annotated_genes":["SJAG_02901","SJAG_03861","SJAG_03641"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75859,79742,98192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019464"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving the ammonium ion.","definition_xrefs":["GOC:tb","GOC:dhl","PMID:14671018"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02901":null,"SJAG_03641":null,"SJAG_03861":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"ammonium ion metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"ammonium ion metabolism","type":"exact"},{"name":"ammonium metabolic process","type":"related"}],"termid":"GO:0097164","terms_by_termid":{"GO:0019464":null}}


id: PBO:0042306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD24 molecule","termid":"PBO:0042306"}


id: GO:1990794
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of a cell situated by the cell sides which interface adjacent cells and near the base. Often used in reference to animal polarized epithelial cells.","definition_xrefs":["PMID:18495799"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"basal part of cell","termid":"GO:0045178"},{"relation_name":"part_of","term_name":"lateral part of cell","termid":"GO:0097574"}],"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":"basolateral part of cell","termid":"GO:1990794"}


id: PR:Q10182
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- erf4 gene.","definition_xrefs":["UniProtKB:Q10182","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":"ras modification protein erf4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3F10.07c","synonyms":[{"name":"Spom972h-erf4","type":"exact"},{"name":"meiotically up-regulated gene 91 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10182"}


id: PR:O74462
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcription initiation factor TFIID subunit 6 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10221:SF7","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":"transcription initiation factor TFIID subunit 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16C4.18c","secondary_identifiers":["UniProtKB:O74462"],"synonyms":[{"name":"SPCC16C4.18c","type":"related"},{"name":"Spom972h-TAF6","type":"exact"},{"name":"TAFII-50 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TAFII50 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TBP-associated factor 50 kDa (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TBP-associated factor 6 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"taf50","type":"related"}],"termid":"PR:O74462"}


id: MONDO:0100077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital alveolar dysplasia characterized anatomically by a defective and hypoplastic development of pulmonary alveoli that is commonly associated with atelectasis and can be responsible for atelectasis.","definition_xrefs":["PMID:18874463"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital pulmonary veins anomaly","termid":"MONDO:0020295"}],"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":"congenital alveolar dysplasia","secondary_identifiers":["UMLS:C0035220","MEDGEN:20539"],"synonyms":[{"name":"CAD","type":"exact"}],"termid":"MONDO:0100077","xrefs":{"Monarch":{"xref_id":"0100077"}}}


id: MONDO:0017853
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypersensitivity pneumonitis (HP) is a pulmonary disease with symptoms of dyspnea and cough resulting from the inhalation of an antigen to which the subject has been previously sensitized.","definition_xrefs":["Orphanet:31740"],"direct_ancestors":[{"relation_name":"is_a","term_name":"allergic respiratory disease","termid":"MONDO:0000771"},{"relation_name":"is_a","term_name":"interstitial lung disease","termid":"MONDO:0015925"},{"relation_name":"is_a","term_name":"pneumonitis","termid":"MONDO:0043905"}],"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":"hypersensitivity pneumonitis","secondary_identifiers":["MESH:D000542","ICD9:495.9","ICD10CM:J67.2","NCIT:C34369","ICD10CM:J67.1","NORD:761","SCTID:37471005","GARD:12","UMLS:C0002390","MedDRA:10001890","ICD9:495","DOID:841","ICD9:495.8","MEDGEN:1446"],"synonyms":[{"name":"HP","type":"exact"},{"name":"allergic form of pneumonitis","type":"exact"},{"name":"allergic interstitial pneumonitis","type":"related"},{"name":"allergic pneumonitis","type":"exact"},{"name":"alveolitis","type":"exact"},{"name":"alveolitis, extrinsic allergic","type":"related"},{"name":"exogen allergic alveolitis","type":"exact"},{"name":"extrinsic allergic alveolitis","type":"exact"},{"name":"extrinsic allergic pneumonia hypersensitivity pneumonitis","type":"related"},{"name":"hypersensitivity pneumonitis","type":"exact"}],"termid":"MONDO:0017853","xrefs":{"Monarch":{"xref_id":"0017853"}}}


id: PBO:0084955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Multi-transmembrane subunit of the DSC ubiquitin ligase complex; similar in sequence to rhomboid pseudoproteases Der1p and UBAC2 that function in ERAD; ortholog of fission yeast dsc2","termid":"PBO:0084955"}


id: MONDO:0017226
data:
  {"annotated_genes":["SJAG_00564","SJAG_02263"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009843"},{"annotations":[89013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012824"}]},"cv_name":"mondo","definition":"Pelizaeus-Merzbacher like disease (PMLD) is an autosomal recessive leukodystrophy sharing identical clinical and radiological features as X-linked Pelizaeus-Merzbacher disease (PMD).","definition_xrefs":["Orphanet:280270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00564":null,"SJAG_02263":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"Pelizaeus-Merzbacher-like disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:1200577","SCTID:717042001","icd11.foundation:1101042369","GARD:12300","MEDGEN:894734","NANDO:2201289","UMLS:C4274084"],"synonyms":[{"name":"PMLD","type":"exact"}],"termid":"MONDO:0017226","terms_by_termid":{"MONDO:0009843":null,"MONDO:0012824":null},"xrefs":{"Monarch":{"xref_id":"0017226"}}}


id: PBO:0075419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPAG5 antisense RNA 1","termid":"PBO:0075419"}


id: PATO:0001256
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of orange color and low brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orange","termid":"PATO:0000953"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dark orange","termid":"PATO:0001256"}


id: MONDO:0012362
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the PLN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"dilated cardiomyopathy 1P","secondary_identifiers":["MEDGEN:322782","GARD:15469","MESH:C563690","UMLS:C1835928","DOID:0110439","OMIM:609909"],"synonyms":[{"name":"CMD1P","type":"exact"},{"name":"PLN familial isolated dilated cardiomyopathy","type":"exact"},{"name":"cardiomyopathy, dilated, 1P","type":"exact"},{"name":"cardiomyopathy, dilated, type 1P","type":"exact"},{"name":"dilated cardiomyopathy type 1P","type":"exact"},{"name":"familial isolated dilated cardiomyopathy caused by mutation in PLN","type":"exact"}],"termid":"MONDO:0012362","xrefs":{"Monarch":{"xref_id":"0012362"}}}


id: PBO:0039222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AKR7A2 pseudogene 1","termid":"PBO:0039222"}


id: MONDO:0008326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pseudocholinesterase, increase in plasma level of (obsolete MONDO:0008326)","secondary_identifiers":["OMIM:177600"],"synonyms":[{"name":"pseudocholinesterase, increase in plasma level OF","type":"related"}],"termid":"MONDO:0008326","xrefs":{"Monarch":{"xref_id":"0008326"}}}


id: PATO:0002186
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A molecular quality that inheres in a molecular entity by virtue of whether or not the molecular entity has a separation of electric charge which leads to the molecule having an electric dipole.","definition_xrefs":["PATOC:JH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular quality","termid":"PATO:0002182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polarity","termid":"PATO:0002186"}


id: PBO:0001633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOPs complex subunit Pep5/Vps11 (predicted)","termid":"PBO:0001633"}


id: GO:0017084
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H+ + L-glutamate + NADPH = ADP + L-glutamate 5-semialdehyde + NADP+ + phosphate.","definition_xrefs":["RHEA:33207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"delta1-pyrroline-5-carboxylate synthetase activity","secondary_identifiers":["Reactome:R-HSA-508040"],"synonyms":[{"name":"D1-pyrroline-5-carboxylate synthetase activity","type":"exact"}],"termid":"GO:0017084"}


id: GO:0046528
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process following disc eversion whereby imaginal discs fuse with adjacent disc derivatives to form a continuous adult epidermis.","definition_xrefs":["PMID:11494317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"imaginal disc morphogenesis","termid":"GO:0007560"}],"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":"imaginal disc fusion","termid":"GO:0046528"}


id: FYPO:0004647
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to copper ions 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:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0005447","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased RNA level during cellular response to copper ion","synonyms":[{"name":"increased RNA accumulation during cellular response to copper ion","type":"related"},{"name":"increased RNA level during cellular response to copper","type":"exact"},{"name":"increased RNA level during cellular response to copper ion during mitotic cell cycle","type":"related"},{"name":"increased RNA level during cellular response to copper ion during vegetative growth","type":"exact"},{"name":"increased transcript level during cellular response to copper ion","type":"exact"}],"termid":"FYPO:0004647"}


id: MONDO:0030054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"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, 86","secondary_identifiers":["UMLS:C5394462","DOID:0112220","GARD:16391","MEDGEN:1711964","OMIM:618910"],"synonyms":[{"name":"DEE86","type":"exact"},{"name":"EIEE86","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 86","type":"exact"},{"name":"developmental and epileptic encephalopathy 86","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 86","type":"exact"}],"termid":"MONDO:0030054","xrefs":{"Monarch":{"xref_id":"0030054"}}}


id: MONDO:0004401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Malignant testicular germ cell tumor that is resistant to treatment.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant testicular germ cell tumor","termid":"MONDO:0003510"},{"relation_name":"is_a","term_name":"refractory malignant neoplasm","termid":"MONDO:0036501"}],"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":"testis refractory cancer","secondary_identifiers":["UMLS:C1377904","NCIT:C9077","DOID:7928","MEDGEN:235122"],"synonyms":[{"name":"refractory cancer of testis","type":"exact"},{"name":"refractory cancer of the testis","type":"exact"},{"name":"refractory malignant testicular germ cell tumor","type":"exact"},{"name":"refractory malignant testicular germ cell tumour","type":"exact"},{"name":"refractory testicular cancer","type":"exact"},{"name":"refractory testicular carcinoma","type":"exact"}],"termid":"MONDO:0004401","xrefs":{"Monarch":{"xref_id":"0004401"}}}


id: PR:000044698
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.1, initiator methionine removed K9-methylated form (Schizosaccharomyces pombe) whose methylation type is dimethylation. Example: UniProtKB:P09988-1, 2-136, Lys-10, MOD:00084.","definition_xrefs":["PMID:23849629","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hht1/Me(K9)","termid":"PR:000027578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.1, initiator methionine removed K9-dimethylated form (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC1834.04","synonyms":[{"name":"Spom-hht1/InitMet-/K9me2","type":"exact"}],"termid":"PR:000044698"}


id: MOD:01274
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that is produced by formation of an adduct with 4-(2-aminoethyl)benzenesulfonyl fluoride, AEBS, and an L-histidine residue.","definition_xrefs":["Unimod:276#H","PubMed:8597590"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-(2-aminoethyl)benzenesulfonyl fluoride derivatized residue","termid":"MOD:00596"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N'-[4-(2-aminoethyl)benzenesulfonyl] derivatized histidine","synonyms":[{"name":"AEBS","type":"related"},{"name":"Aminoethylbenzenesulfonylation","type":"related"}],"termid":"MOD:01274"}


id: PBO:0066437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"resistin","termid":"PBO:0066437"}


id: MONDO:0020332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Systemic mastocytosis with an associated clonal hematological non-mast cell lineage disease is a form of systemic mastocytosis (SM) associated with malignancy (other than mast cell leukemia).","definition_xrefs":["Orphanet:98849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"systemic mastocytosis","termid":"MONDO:0016586"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease","secondary_identifiers":["DOID:4797","ICDO:9741/3","MEDGEN:226985","UMLS:C1301365","GARD:19596","NCIT:C9284","EFO:1000559","ONCOTREE:SMAHN","SCTID:397015000"],"synonyms":[{"name":"SM-AHN","type":"exact"},{"name":"SM-AHNMD","type":"exact"},{"name":"SMAHN","type":"exact"},{"name":"systemic mastocytosis with an associated haematological neoplasm","type":"exact"},{"name":"systemic mastocytosis with an associated haematological neoplasm (SM-AHN)","type":"exact"},{"name":"systemic mastocytosis with an associated hematological neoplasm","type":"exact"},{"name":"systemic mastocytosis with an associated hematological neoplasm (SM-AHN)","type":"exact"},{"name":"systemic mastocytosis with associated clonal haematological non-mast cell lineage disease","type":"exact"},{"name":"systemic mastocytosis with associated clonal haematological non-mast-cell lineage disease","type":"exact"},{"name":"systemic mastocytosis with associated clonal hematological non-mast cell lineage disease","type":"exact"},{"name":"systemic mastocytosis with associated clonal hematological non-mast-cell lineage disease","type":"exact"},{"name":"systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease","type":"exact"},{"name":"systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease (morphologic abnormality)","type":"exact"},{"name":"systemic mastocytosis with associated hematologic neoplasm","type":"exact"}],"termid":"MONDO:0020332","xrefs":{"Monarch":{"xref_id":"0020332"}}}


id: PBO:0041384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 5 open reading frame 24","termid":"PBO:0041384"}


id: MONDO:0017531
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, unilateral","secondary_identifiers":["Orphanet:295163","icd11.foundation:471986216"],"termid":"MONDO:0017531","xrefs":{"Monarch":{"xref_id":"0017531"}}}


id: MONDO:0021475
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the nasal cavity.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system benign neoplasm","termid":"MONDO:0000382"},{"relation_name":"is_a","term_name":"sensory organ benign neoplasm","termid":"MONDO:0000633"},{"relation_name":"is_a","term_name":"nasal cavity neoplasm","termid":"MONDO:0004756"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of nasal cavity","secondary_identifiers":["ICD9:212.0","icd11.foundation:44101401","MEDGEN:83859","NCIT:C4603","SCTID:92241005","UMLS:C0347215"],"synonyms":[{"name":"benign nasal cavity neoplasm","type":"exact"},{"name":"benign nasal cavity tumor","type":"exact"},{"name":"benign nasal cavity tumour","type":"exact"},{"name":"benign neoplasm of the nasal cavity","type":"exact"},{"name":"benign tumor of nasal cavity","type":"exact"},{"name":"benign tumor of the nasal cavity","type":"exact"},{"name":"benign tumour of nasal cavity","type":"exact"},{"name":"benign tumour of the nasal cavity","type":"exact"},{"name":"nasal cavity benign neoplasm","type":"exact"}],"termid":"MONDO:0021475","xrefs":{"Monarch":{"xref_id":"0021475"}}}


id: PBO:0066009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RALY heterogeneous nuclear ribonucleoprotein","termid":"PBO:0066009"}


id: RO:0002529
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x is downstream of the sequence of y iff either (1) x and y have sequence units, and all units of x are downstream of all units of y, or (2) x and y are sequence units, and x is either immediately downstream of y, or transitively downstream of y.","direct_ancestors":[{"relation_name":"is_a","term_name":"does_not_overlap_sequence_of","termid":"RO:0002527"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_downstream_of_sequence_of","termid":"RO:0002529"}


id: PBO:0030851
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_DNA_content","termid":"PBO:0030851"}


id: GO:1905360
data:
  {"annotated_genes":["SJAG_01794","SJAG_00457","SJAG_04509","SJAG_03081","SJAG_04026","SJAG_03453","SJAG_03371","SJAG_02233","SJAG_02444","SJAG_00514","SJAG_00845","SJAG_00596"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[105482,89640,92602,91624,95240,106322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071521"},{"annotations":[74215,78128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990131"},{"annotations":[75892,76982,82093,108306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005834"}]},"cv_name":"cellular_component","definition":"A protein complex which is capable of GTPase activity.","definition_xrefs":["PMID:9178006","GOC:TermGenie","GO_REF:0000088","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00457":null,"SJAG_00514":null,"SJAG_00596":null,"SJAG_00845":null,"SJAG_01794":null,"SJAG_02233":null,"SJAG_02444":null,"SJAG_03081":null,"SJAG_03371":null,"SJAG_03453":null,"SJAG_04026":null,"SJAG_04509":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"GTPase complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"HRAS-SOS1 complex","type":"narrow"},{"name":"RASH-SOS1 complex","type":"narrow"}],"termid":"GO:1905360","terms_by_termid":{"GO:0005834":null,"GO:0071521":null,"GO:1990131":null}}


id: GO:0098951
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic recycling endosome 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:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of postsynaptic recycling endosome membrane (obsolete GO:0098951)","synonyms":[{"name":"intrinsic to postsynaptic recycling endosome membrane","type":"exact"}],"termid":"GO:0098951"}


id: PBO:0059006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MMADHC pseudogene 2","termid":"PBO:0059006"}


id: MONDO:0000919
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the ampulla of Vater.","definition_xrefs":["NCIT:C3536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"duodenum cancer","termid":"MONDO:0000920"},{"relation_name":"is_a","term_name":"ampulla of vater neoplasm","termid":"MONDO:0000921"},{"relation_name":"is_a","term_name":"malignant tumor of extrahepatic bile duct","termid":"MONDO:0021321"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"ampulla of vater cancer","secondary_identifiers":["DOID:10020","ICD9:156.2","MEDGEN:57785","SCTID:363417006","ICD10CM:C24.1","UMLS:C0153454"],"synonyms":[{"name":"cancer of hepatopancreatic ampulla","type":"exact"},{"name":"hepatopancreatic ampulla cancer","type":"exact"},{"name":"malignant ampulla of Vater neoplasm","type":"exact"},{"name":"malignant ampulla of Vater tumor","type":"exact"},{"name":"malignant ampulla of Vater tumour","type":"exact"},{"name":"malignant hepatopancreatic ampulla neoplasm","type":"exact"},{"name":"malignant neoplasm of ampulla of Vater","type":"exact"},{"name":"malignant neoplasm of hepatopancreatic ampulla","type":"exact"},{"name":"malignant neoplasm of the ampulla of Vater","type":"exact"},{"name":"malignant tumor of ampulla of Vater","type":"exact"},{"name":"malignant tumor of ampulla of vater","type":"exact"},{"name":"malignant tumor of the ampulla of Vater","type":"exact"},{"name":"malignant tumour of ampulla of Vater","type":"exact"},{"name":"malignant tumour of ampulla of vater","type":"exact"},{"name":"malignant tumour of the ampulla of Vater","type":"exact"}],"termid":"MONDO:0000919","xrefs":{"Monarch":{"xref_id":"0000919"}}}


id: GO:0051011
data:
  {"annotated_genes":["SJAG_03835","SJAG_02609"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72835,73265],"is_not":false,"summary":null,"term":"GO:0051011"}]},"cv_name":"molecular_function","definition":"Binding to the minus end of a microtubule.","definition_xrefs":["PMID:14614826","GOC:ai","PMID:14557818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule binding","termid":"GO:0008017"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02609":null,"SJAG_03835":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0008092"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008017"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0008017","GO:0005488","GO:0005515","GO:0003674","GO:0008092"],"is_obsolete":false,"name":"microtubule minus-end binding","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0051011","terms_by_termid":{"GO:0051011":null}}


id: MONDO:0015074
data:
  {"annotated_genes":["SJAG_01970","SJAG_04067","SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87591,89068,89069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008566"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm affecting the thyroid gland.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine gland neoplasm","termid":"MONDO:0002082"},{"relation_name":"is_a","term_name":"thyroid gland disorder","termid":"MONDO:0003240"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01970":null,"SJAG_03453":null,"SJAG_04067":null},"genotype_count":0,"is_obsolete":false,"name":"thyroid tumor","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C3414","EFO:0003841","MEDGEN:21546","SCTID:127018007","Orphanet:100087","UMLS:C0040136","MONDO:0021217","GARD:19762","ICD9:239.7","ONCOTREE:THYROID"],"synonyms":[{"name":"THYROID","type":"related"},{"name":"neoplasm of the thyroid","type":"exact"},{"name":"neoplasm of the thyroid gland","type":"exact"},{"name":"neoplasm of thyroid","type":"exact"},{"name":"neoplasm of thyroid gland","type":"exact"},{"name":"thyroid gland neoplasm","type":"exact"},{"name":"thyroid gland neoplasm (disease)","type":"exact"},{"name":"thyroid gland tumor","type":"exact"},{"name":"thyroid gland tumour","type":"exact"},{"name":"thyroid neoplasm","type":"exact"},{"name":"thyroid neoplasms","type":"exact"},{"name":"thyroid tumor","type":"exact"},{"name":"tumor of the thyroid","type":"exact"},{"name":"tumor of the thyroid gland","type":"exact"},{"name":"tumor of thyroid","type":"exact"},{"name":"tumor of thyroid gland","type":"exact"},{"name":"tumour of the thyroid","type":"exact"},{"name":"tumour of the thyroid gland","type":"exact"},{"name":"tumour of thyroid","type":"exact"},{"name":"tumour of thyroid gland","type":"exact"}],"termid":"MONDO:0015074","terms_by_termid":{"MONDO:0008566":null},"xrefs":{"Monarch":{"xref_id":"0015074"}}}


id: MONDO:0017308
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Hypothesized form of Marfan; dubious","gene_count":0,"genotype_count":0,"name":"obsolete Marfan syndrome type 2 (obsolete MONDO:0017308)","secondary_identifiers":["MESH:C535911","NCIT:C75007","Orphanet:284973"],"synonyms":[{"name":"MFS2","type":"exact"},{"name":"Marfan syndrome type II","type":"exact"}],"termid":"MONDO:0017308","xrefs":{"Monarch":{"xref_id":"0017308"}}}


id: SO:0001178
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding pyrrolysyl tRNA (SO:0000766).","definition_xrefs":["RSC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyrrolysine_tRNA_primary_transcript","synonyms":[{"name":"pyrrolysine tRNA primary transcript","type":"exact"}],"termid":"SO:0001178"}


id: GO:1901101
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving gramicidin S.","definition_xrefs":["GOC:TermGenie","GOC:yaf","UniPathway:UPA00102"],"gene_count":0,"genotype_count":0,"name":"obsolete gramicidin S metabolic process (obsolete GO:1901101)","synonyms":[{"name":"gramicidin S metabolism","type":"exact"}],"termid":"GO:1901101"}


id: PBO:0119670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein regulatory complex subunit 9","termid":"PBO:0119670"}


id: MONDO:0021637
data:
  {"annotated_genes":["SJAG_01111","SJAG_04213"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89080,89079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024517"}]},"cv_name":"mondo","definition":"A grade I or grade II glioma arising from the central nervous system. This category includes pilocytic astrocytoma, diffuse astrocytoma, subependymal giant cell astrocytoma, ependymoma, oligodendroglioma, oligoastrocytoma, and angiocentric glioma.","definition_xrefs":["NCIT:C132067"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glioma","termid":"MONDO:0021042"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01111":null,"SJAG_04213":null},"genotype_count":0,"is_obsolete":false,"name":"low grade glioma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1997217","DOID:0080829","MEDGEN:744283"],"synonyms":[{"name":"low grade glioma","type":"exact"},{"name":"low-grade glioma","type":"exact"}],"termid":"MONDO:0021637","terms_by_termid":{"MONDO:0024517":null},"xrefs":{"Monarch":{"xref_id":"0021637"}}}


id: FYPO:0001360
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the import of one or more amino acids into the cell occurs to a lower extent than normal in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased amino acid import","termid":"FYPO:0001058"},{"relation_name":"is_a","term_name":"abnormal amino acid import during vegetative growth","termid":"FYPO:0001361"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"decreased amino acid import during vegetative growth","synonyms":[{"name":"decreased amino acid import across plasma membrane during vegetative growth","type":"exact"},{"name":"decreased amino acid import during mitotic cell cycle","type":"related"},{"name":"decreased amino acid import into cell during vegetative growth","type":"exact"},{"name":"decreased amino acid uptake during vegetative growth","type":"exact"},{"name":"reduced amino acid import during vegetative growth","type":"exact"}],"termid":"FYPO:0001360"}


id: PBO:0054850
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 2264","termid":"PBO:0054850"}


id: PBO:0080132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VANGL planar cell polarity protein 2","termid":"PBO:0080132"}


id: PBO:0005511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoside diphosphatase Ynd1","termid":"PBO:0005511"}


id: PBO:0051935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inter-alpha-trypsin inhibitor heavy chain family member 6","termid":"PBO:0051935"}


id: FYPO:0004189
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 a cellular response to hydroxyurea 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":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"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:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0006551","FYPO:0005447"],"is_obsolete":false,"name":"increased protein level during cellular response to hydroxyurea","synonyms":[{"name":"increased protein accumulation during cellular response to hydroxyurea","type":"related"},{"name":"increased protein level during cellular response to HU","type":"exact"},{"name":"increased protein level during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"increased protein level during cellular response to hydroxyurea during vegetative growth","type":"exact"}],"termid":"FYPO:0004189"}


id: PBO:0005412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smc5-6 complex non-SMC subunit 1","termid":"PBO:0005412"}


id: MONDO:0021096
data:
  {"annotated_genes":["SJAG_01144"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0003789"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01144":null},"genotype_count":0,"is_obsolete":false,"name":"papillary epithelial neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:235456","NCIT:C8429","UMLS:C1335324"],"synonyms":[{"name":"papillary epithelial neoplasm","type":"exact"}],"termid":"MONDO:0021096","terms_by_termid":{"MONDO:0003789":null},"xrefs":{"Monarch":{"xref_id":"0021096"}}}


id: PATO:0001649
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature quality inhering in a bearer by virtue of the bearer's being curved towards the side.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curved","termid":"PATO:0000406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curved lateral","termid":"PATO:0001649"}


id: PBO:0045018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"divergent protein kinase domain 1C","termid":"PBO:0045018"}


id: PBO:0027770
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_recombination_frequency","termid":"PBO:0027770"}


id: MONDO:0008379
data:
  {"annotated_genes":["SJAG_01298"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88066],"is_not":false,"summary":null,"term":"MONDO:0008379"}]},"cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the IMPDH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"IMPDH1-related retinopathy","termid":"MONDO:1040051"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01298":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005328","MONDO:0004736"],"is_obsolete":false,"name":"retinitis pigmentosa 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0110388","ICD10CM:H35.5","UMLS:C1867299","GARD:15110","MEDGEN:357247","OMIM:180105","MESH:C566715"],"synonyms":[{"name":"IMPDH1 retinitis pigmentosa","type":"exact"},{"name":"RP10","type":"exact"},{"name":"retinitis pigmentosa 10","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in IMPDH1","type":"exact"},{"name":"retinitis pigmentosa type 10","type":"exact"}],"termid":"MONDO:0008379","terms_by_termid":{"MONDO:0008379":null},"xrefs":{"Monarch":{"xref_id":"0008379"}}}


id: MONDO:0004169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A combination of distressing physical, psychologic, or behavioral changes that occur during the luteal phase of the menstrual cycle. Symptoms of pms are diverse (such as pain, water-retention, anxiety, cravings, and depression) and they diminish markedly 2 or 3 days after the initiation of menses.","definition_xrefs":["MESH:D011293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"premenstrual tension","secondary_identifiers":["ICD9:625.4","SCTID:82639001","DOID:727","MEDGEN:87683","UMLS:C0376356"],"termid":"MONDO:0004169","xrefs":{"Monarch":{"xref_id":"0004169"}}}


id: GO:0031901
data:
  {"annotated_genes":["SJAG_01112","SJAG_01379","SJAG_00314"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[82005,97677,101496],"is_not":false,"summary":null,"term":"GO:0031901"}]},"cv_name":"cellular_component","definition":"The lipid bilayer surrounding an early endosome.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endosome membrane","termid":"GO:0010008"},{"relation_name":"part_of","term_name":"early endosome","termid":"GO:0005769"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00314":null,"SJAG_01112":null,"SJAG_01379":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0031410","GO:0005768","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"early endosome membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0031901","terms_by_termid":{"GO:0031901":null}}


id: MONDO:0004076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign tumor, composed of mature adipocytes, that arises within the tendon sheath.","definition_xrefs":["NCIT:C6499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"},{"relation_name":"is_a","term_name":"benign synovial neoplasm","termid":"MONDO:0024715"},{"relation_name":"is_a","term_name":"tendon sheath disorder","termid":"MONDO:0024876"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tendon sheath lipoma","secondary_identifiers":["UMLS:C1336703","MEDGEN:277806","DOID:7016"],"synonyms":[{"name":"lipoma of tendon sheath","type":"exact"},{"name":"lipoma of the tendon sheath","type":"exact"},{"name":"tendon sheath lipoma","type":"exact"}],"termid":"MONDO:0004076","xrefs":{"Monarch":{"xref_id":"0004076"}}}


id: PBO:0036484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase involved in endocytosis Cki1","termid":"PBO:0036484"}


id: PBO:0034409
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-requires_modification_(obsolete_requires_modification)","termid":"PBO:0034409"}


id: PBO:0058077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4295","termid":"PBO:0058077"}


id: GO:0052482
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A type of cell wall modification, in which the cell wall is reinforced and made thicker, that occurs as part of the defense response of an organism.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"defense response","termid":"GO:0006952"},{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"},{"relation_name":"is_a","term_name":"cell wall thickening","termid":"GO:0052386"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0071554","GO:0008150"],"is_obsolete":false,"name":"defense response by cell wall thickening","synonyms":[{"name":"cell wall thickening during defense response","type":"related"}],"termid":"GO:0052482"}


id: GO:0051393
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to alpha-actinin, one of a family of proteins that cross-link F-actin as antiparallel homodimers. Alpha-actinin has a molecular mass of 93-103 KDa; at the N-terminus there are two calponin homology domains, at the C-terminus there are two EF-hands. These two domains are connected by the rod domain. This domain is formed by triple-helical spectrin repeats.","definition_xrefs":["PMID:11699871","PMID:10984498","PMID:15014165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actinin binding","termid":"GO:0042805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0008092"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0008092","GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"alpha-actinin binding","secondary_identifiers":["GO:0051372"],"synonyms":[{"name":"alpha-actinin 1 binding","type":"narrow"},{"name":"alpha-actinin 4 binding","type":"narrow"},{"name":"nonmuscle alpha-actinin binding","type":"narrow"}],"termid":"GO:0051393"}


id: MONDO:0011362
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive muscular dystrophy","termid":"MONDO:0016106"},{"relation_name":"is_a","term_name":"autosomal dominant distal myopathy","termid":"MONDO:0016108"},{"relation_name":"is_a","term_name":"hereditary inclusion-body myopathy","termid":"MONDO:0016112"},{"relation_name":"is_a","term_name":"autosomal dominant titinopathy","termid":"MONDO:0100494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320","MONDO:0000426"],"is_obsolete":false,"name":"myopathy, myofibrillar, 9, with early respiratory failure","secondary_identifiers":["OMIM:607569","MESH:C564377","OMIM:603689","Orphanet:34521","SCTID:702373006","Orphanet:178464","SCTID:733490006","UMLS:C1863599","MEDGEN:350930","GARD:12591","MESH:C566343","DOID:0111188"],"synonyms":[{"name":"ADMERF","type":"exact"},{"name":"Edstrom myopathy","type":"exact"},{"name":"Edström myopathy","type":"exact"},{"name":"HIBM-ERF","type":"exact"},{"name":"HMERF","type":"exact"},{"name":"HMERF-ERF","type":"exact"},{"name":"distal myopathy with early respiratory muscle involvement","type":"exact"},{"name":"hereditary inclusion body myopathy with early respiratory failure","type":"exact"},{"name":"hereditary proximal myopathy with early respiratory failure","type":"exact"},{"name":"myofibrillar myopathy with early respiratory failure","type":"exact"},{"name":"myopathy, distal, with early respiratory failure, autosomal dominant","type":"exact"},{"name":"myopathy, proximal, with early respiratory muscle involvement","type":"exact"}],"termid":"MONDO:0011362","xrefs":{"Monarch":{"xref_id":"0011362"}}}


id: MONDO:0009430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive hypophosphatemic rickets in which the cause of the disease is a mutation in the DMP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive hypophosphatemic rickets","termid":"MONDO:0017324"},{"relation_name":"is_a","term_name":"abnormal mineralization disorder","termid":"MONDO:0800096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"hypophosphatemic rickets, autosomal recessive, 1","secondary_identifiers":["MEDGEN:1632314","GARD:18416","MESH:C562792","UMLS:C4551495","OMIM:241520"],"synonyms":[{"name":"ARHR1","type":"related"},{"name":"Arhr","type":"related"},{"name":"DMP1 autosomal recessive hypophosphatemic rickets","type":"exact"},{"name":"autosomal recessive hypophosphatemic rickets caused by mutation in DMP1","type":"exact"},{"name":"hypophosphatemia, autosomal recessive","type":"related"},{"name":"hypophosphatemic rickets, AR","type":"exact"},{"name":"hypophosphatemic rickets, autosomal recessive, 1","type":"exact"},{"name":"hypophosphatemic rickets, autosomal recessive, type 1","type":"exact"}],"termid":"MONDO:0009430","xrefs":{"Monarch":{"xref_id":"0009430"}}}


id: PBO:0045296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 1 pseudogene 48","termid":"PBO:0045296"}


id: GO:0004181
data:
  {"annotated_genes":["SJAG_00451","SJAG_03586"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58368,76080],"is_not":false,"summary":null,"term":"GO:0004181"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a single C-terminal amino acid residue from a polypeptide chain by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.","direct_ancestors":[{"relation_name":"is_a","term_name":"carboxypeptidase activity","termid":"GO:0004180"},{"relation_name":"is_a","term_name":"metalloexopeptidase activity","termid":"GO:0008235"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00451":null,"SJAG_03586":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0008233","GO:0016787","GO:0140096","GO:0003674"],"is_obsolete":false,"name":"metallocarboxypeptidase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-9023163","EC:3.4.17.-","Reactome:R-HSA-8852809","Reactome:R-HSA-8955712","Reactome:R-HSA-2022379","Reactome:R-HSA-2022378","Reactome:R-HSA-8866105","Reactome:R-HSA-2028294","Reactome:R-HSA-9023159"],"termid":"GO:0004181","terms_by_termid":{"GO:0004181":null}}


id: PBO:0027327
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_surface_pyruvylated_galactose_level","termid":"PBO:0027327"}


id: PBO:0035704
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_Zeocin","termid":"PBO:0035704"}


id: PBO:0000328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEAT repeat","termid":"PBO:0000328"}


id: MONDO:0010709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal ganglia disorder characterized by Parkinsonian-type symptoms (postural changes, tremor, rigidity), megalencephaly and variable intellectual deficit. Other signs are frontal bossing, persistent frontal lobe reflexes, strabismus and seizures. It has been described in three generations of one family. Transmission is X-linked, and the gene is located on chromosomal region Xq27.3-qter.","definition_xrefs":["Orphanet:2379"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"parkinsonian disorder","termid":"MONDO:0021095"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early-onset parkinsonism-intellectual disability syndrome","secondary_identifiers":["MEDGEN:208674","UMLS:C0796195","OMIM:311510","SCTID:716107009","icd11.foundation:937544163","GARD:3203","MESH:C537179","DOID:0111781"],"synonyms":[{"name":"BGMR","type":"related"},{"name":"Laxova Brown hogan syndrome","type":"related"},{"name":"Laxova-Opitz syndrome","type":"exact"},{"name":"Parkinsonism, early onset with intellectual disability","type":"related"},{"name":"Parkinsonism, early onset with mental retardation","type":"related"},{"name":"Parkinsonism, early-onset, with intellectual disability","type":"related"},{"name":"Parkinsonism, early-onset, with mental retardation","type":"related"},{"name":"WAISMAN syndrome","type":"related"},{"name":"WSMN","type":"related"},{"name":"Waisman syndrome","type":"exact"},{"name":"Waisman syndrome, X-linked recessive","type":"exact"},{"name":"Wsn","type":"related"},{"name":"X-linked recessive basal ganglia disorder with intellectual disability","type":"related"},{"name":"X-linked recessive basal ganglia disorder with mental retardation","type":"related"},{"name":"basal ganglia disorder with intellectual disability","type":"related"},{"name":"basal ganglia disorder with mental retardation","type":"related"},{"name":"basal ganglion disorder with intellectual disability","type":"related"},{"name":"basal ganglion disorder with mental retardation","type":"related"},{"name":"early-onset parkinsonism-intellectual disability syndrome","type":"exact"}],"termid":"MONDO:0010709","xrefs":{"Monarch":{"xref_id":"0010709"}}}


id: PR:Q9P7M7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAP27G11.11c gene.","definition_xrefs":["UniProtKB:Q9P7M7","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 P27G11.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.11c","synonyms":[{"name":"Spom972h-SPAP27G11.11c","type":"exact"}],"termid":"PR:Q9P7M7"}


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


id: PBO:0003729
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoregulation","termid":"PBO:0003729"}


id: PBO:0057783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3059","termid":"PBO:0057783"}


id: PBO:0080409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS37C subunit of ESCRT-I","termid":"PBO:0080409"}


id: MONDO:0004394
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the mucosal epithelial surface of the maxillary sinus. Patients may present with nasal fullness, obstruction, and/or epistaxis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maxillary sinus carcinoma","termid":"MONDO:0001748"},{"relation_name":"is_a","term_name":"oral cavity squamous cell carcinoma","termid":"MONDO:0004958"},{"relation_name":"is_a","term_name":"paranasal sinus squamous cell carcinoma","termid":"MONDO:0044705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"maxillary sinus squamous cell carcinoma","secondary_identifiers":["MEDGEN:277348","NCIT:C6064","UMLS:C1334647","SCTID:707354003","DOID:7910"],"synonyms":[{"name":"epidermoid carcinoma of maxillary antrum","type":"exact"},{"name":"epidermoid carcinoma of maxillary sinus","type":"exact"},{"name":"epidermoid carcinoma of maxillofacial sinus","type":"exact"},{"name":"epidermoid carcinoma of the maxillary antrum","type":"exact"},{"name":"epidermoid carcinoma of the maxillary sinus","type":"exact"},{"name":"epidermoid carcinoma of the maxillofacial sinus","type":"exact"},{"name":"maxillary antrum epidermoid carcinoma","type":"exact"},{"name":"maxillary antrum squamous cell carcinoma","type":"exact"},{"name":"maxillary sinus epidermoid carcinoma","type":"exact"},{"name":"maxillary sinus squamous cell carcinoma","type":"exact"},{"name":"maxillofacial sinus epidermoid carcinoma","type":"exact"},{"name":"maxillofacial sinus squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of maxillary antrum","type":"exact"},{"name":"squamous cell carcinoma of maxillary sinus","type":"exact"},{"name":"squamous cell carcinoma of maxillofacial sinus","type":"exact"},{"name":"squamous cell carcinoma of the maxillary antrum","type":"exact"},{"name":"squamous cell carcinoma of the maxillary sinus","type":"exact"},{"name":"squamous cell carcinoma of the maxillofacial sinus","type":"exact"}],"termid":"MONDO:0004394","xrefs":{"Monarch":{"xref_id":"0004394"}}}


id: PBO:0089772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane TRP-like ion channel","termid":"PBO:0089772"}


id: GO:0097159
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to an organic cyclic compound, any molecular entity that contains carbon arranged in a cyclic molecular structure.","definition_xrefs":["GOC:sjw","PMID:7583672"],"gene_count":0,"genotype_count":0,"name":"obsolete organic cyclic compound binding (obsolete GO:0097159)","termid":"GO:0097159"}


id: MONDO:0017269
data:
  {"annotated_genes":["SJAG_02855"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"}]},"cv_name":"mondo","definition":"X-linked form of inherited ichthyosis syndromic form.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02855":null},"genotype_count":0,"is_obsolete":false,"name":"X-linked ichthyosis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10048063","Orphanet:281210","GARD:21109"],"synonyms":[{"name":"X-linked inherited ichthyosis syndromic form","type":"exact"},{"name":"inherited ichthyosis syndromic form, X-linked","type":"exact"}],"termid":"MONDO:0017269","terms_by_termid":{"MONDO:0010621":null},"xrefs":{"Monarch":{"xref_id":"0017269"}}}


id: PBO:0062439
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 103 pseudogene","termid":"PBO:0062439"}


id: MONDO:0004152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A recently recognized variant of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) expressing somatic hypermutations of the Immunoglobulin heavy chain (IGH) genes. The recognition of this variant alters the belief that CLL/SLL is always derived from a naive, pregerminal center B-cell. The presence of somatic hypermutations of IGH genes occurs in approximately 50% of CLL/SLL cases and implies a postgerminal center, memory origin. Patients with this variant of CLL/SLL have a favorable prognosis, with a reported median survival of more than 24 years.","definition_xrefs":["NCIT:C37201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic lymphocytic leukemia/small lymphocytic lymphoma","termid":"MONDO:0003864"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation","secondary_identifiers":["MEDGEN:232076","UMLS:C1333037","DOID:7230"],"synonyms":[{"name":"CLL/SLL with IGVH SHM","type":"exact"},{"name":"chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation","type":"exact"},{"name":"postgerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma","type":"exact"},{"name":"postgerminal centre chronic lymphocytic leukemia/small lymphocytic lymphoma","type":"exact"}],"termid":"MONDO:0004152","xrefs":{"Monarch":{"xref_id":"0004152"}}}


id: PBO:0064881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPP2CA divergent transcript","termid":"PBO:0064881"}


id: PBO:0057528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 645","termid":"PBO:0057528"}


id: GO:0072104
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a glomerular capillary. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiogenesis","termid":"GO:0001525"},{"relation_name":"part_of","term_name":"glomerulus vasculature morphogenesis","termid":"GO:0072103"}],"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":"glomerular capillary formation","termid":"GO:0072104"}


id: PBO:0001626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Rrp36, DUF947 family (predicted)","termid":"PBO:0001626"}


id: PBO:0035752
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_trimethylation_at_centromere_inner_repeat_during_vegetative_growth","termid":"PBO:0035752"}


id: GO:0070267
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cellular process that results in swelling of the cell body, and that is morphologically characteristic of necrotic cell death.","definition_xrefs":["PMID:17873035","PMID:18846107"],"gene_count":0,"genotype_count":0,"name":"obsolete oncosis (obsolete GO:0070267)","termid":"GO:0070267"}


id: MONDO:0017832
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Mycobacterium xenopi.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mycobacterial infectious disease","termid":"MONDO:0020590"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mycobacterium xenopi infection","secondary_identifiers":["MEDGEN:546776","UMLS:C0275715","Orphanet:314946"],"synonyms":[{"name":"M. xenopi","type":"related"},{"name":"Mycobacterium xenopi","type":"related"},{"name":"Mycobacterium xenopi caused disease or disorder","type":"exact"},{"name":"Mycobacterium xenopi disease or disorder","type":"exact"},{"name":"Mycobacterium xenopi infectious disease","type":"exact"}],"termid":"MONDO:0017832","xrefs":{"Monarch":{"xref_id":"0017832"}}}


id: PBO:0027359
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_1,3-beta-D-glucan_synthase_activity_during_sporulation","termid":"PBO:0027359"}


id: GO:0016712
data:
  {"annotated_genes":["SJAG_04000"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[61180],"is_not":false,"summary":null,"term":"GO:0016712"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which hydrogen or electrons are transferred from reduced flavin or flavoprotein and one other donor, and one atom of oxygen is incorporated into one donor.","definition_xrefs":["EC:1.14.14.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","references_by_uniquename":{"GO_REF:0000104":null},"secondary_identifiers":["Reactome:R-HSA-211966","GO:0008402","Reactome:R-HSA-194678","GO:0050381"],"synonyms":[{"name":"aryl hydrocarbon hydroxylase activity","type":"narrow"},{"name":"aryl-4-monooxygenase activity","type":"narrow"},{"name":"cytochrome P450 CYP19","type":"narrow"},{"name":"cytochrome p450 activity","type":"narrow"},{"name":"flavoprotein monooxygenase activity","type":"narrow"},{"name":"flavoprotein-linked monooxygenase activity","type":"narrow"},{"name":"microsomal P-450","type":"narrow"},{"name":"microsomal monooxygenase activity","type":"narrow"},{"name":"microsomal p450 activity","type":"narrow"},{"name":"substrate,reduced-flavoprotein:oxygen oxidoreductase (RH-hydroxylating or -epoxidizing)","type":"related"},{"name":"unspecific monooxygenase activity","type":"narrow"},{"name":"xenobiotic monooxygenase activity","type":"narrow"}],"termid":"GO:0016712","terms_by_termid":{"GO:0016712":null}}


id: PBO:0040407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V1 subunit G2","termid":"PBO:0040407"}


id: PBO:0046280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elastin microfibril interfacer 2","termid":"PBO:0046280"}


id: FYPO:0002577
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of chromatin binding by a gene product (usually a protein) in a mutant is decreased. The affected gene product may be encoded by the mutated gene, or by a different gene, and may normally bind DNA, protein, or both in chromatin.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin binding","termid":"FYPO:0002576"}],"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:0000652","FYPO:0001985"],"is_obsolete":false,"name":"decreased chromatin binding","synonyms":[{"name":"reduced chromatin binding","type":"exact"}],"termid":"FYPO:0002577"}


id: PBO:0041942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBX3 pseudogene 10","termid":"PBO:0041942"}


id: PBO:0000680
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcripts Altered in Meiosis","termid":"PBO:0000680"}


id: PBO:0004999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDK regulator, involved in ribosome export (predicted)","termid":"PBO:0004999"}


id: GO:0007318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a protein is transported to, or maintained in, the oocyte pole plasm. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein localization","termid":"GO:0008104"},{"relation_name":"part_of","term_name":"pole plasm assembly","termid":"GO:0007315"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0044085"],"is_obsolete":false,"name":"pole plasm protein localization","secondary_identifiers":["GO:0048115"],"synonyms":[{"name":"establishment and maintenance of pole plasm protein localization","type":"exact"},{"name":"oocyte pole plasm protein localization","type":"exact"},{"name":"pole plasm protein localisation","type":"exact"}],"termid":"GO:0007318"}


id: FYPO:0000890
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 trimethylation of lysine at position 9 of histone H3 in centromere outer repeat regions occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone H3-K9 trimethylation at centromere during vegetative growth","termid":"FYPO:0000883"},{"relation_name":"is_a","term_name":"abnormal histone H3-K9 trimethylation at centromere outer repeat during vegetative growth","termid":"FYPO:0000885"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0002494","FYPO:0002274"],"is_obsolete":false,"name":"decreased histone H3-K9 trimethylation at centromere outer repeat during vegetative growth","synonyms":[{"name":"decreased histone H3 K9 trimethylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 trimethylation at centromere otr during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 trimethylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"decreased histone H3-K9 trimethylation at centromeric outer repeat region during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 trimethylation at pericentric region during vegetative growth","type":"related"},{"name":"decreased histone H3-K9 trimethylation at pericentromeric region during vegetative growth","type":"related"},{"name":"decreased histone H3K9 trimethylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone H3K9me3 at centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K9 trimethylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"reduced histone H3-K9 trimethylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0000890"}


id: MONDO:0018650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hemochromatosis type 5 (obsolete MONDO:0018650)","termid":"MONDO:0018650","xrefs":{"Monarch":{"xref_id":"0018650"}}}


id: PBO:0034272
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-attached_to_part_of","termid":"PBO:0034272"}


id: PBO:0005348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NuA4 histone acetyltransferase complex subunit Vid21","termid":"PBO:0005348"}


id: PBO:0088203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zn2Cys6 family transcription factor; positively regulates sterol uptake under anaerobic conditions with SUT1; represses filamentation-inducing genes during non-starvation conditions; positively regulates mating along with SUT1 by repressing the expression of genes (PRR2, NCE102 and RHO5) which function as mating inhibitors; multicopy suppressor of mutations that cause low activity of the cAMP/PKA pathway; SUT2 has a paralog, SUT1, that arose from the whole genome duplication","termid":"PBO:0088203"}


id: PBO:0058094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4310","termid":"PBO:0058094"}


id: RO:0000302
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relation that holds between a neuron that is synapsed_to another neuron or a neuron that is connected indirectly to another by a chain of neurons, each synapsed_to the next.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_neural_circuit_with","termid":"RO:0000300"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"downstream_in_neural_circuit_with","termid":"RO:0000302"}


id: PBO:0088596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor Moc3","termid":"PBO:0088596"}


id: PBO:0071791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease P/MRP subunit p30","termid":"PBO:0071791"}


id: FYPO:0001067
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 tyrosine into the cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal amino acid import during vegetative growth","termid":"FYPO:0001361"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"abnormal tyrosine import","synonyms":[{"name":"abnormal L-tyrosine import","type":"exact"},{"name":"abnormal L-tyrosine import across plasma membrane","type":"exact"},{"name":"abnormal tyrosine import during mitotic cell cycle","type":"related"},{"name":"abnormal tyrosine import during vegetative growth","type":"exact"},{"name":"abnormal tyrosine import into cell","type":"exact"},{"name":"abnormal tyrosine uptake","type":"exact"}],"termid":"FYPO:0001067"}


id: MONDO:0054780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary elliptocytosis","termid":"MONDO:0017319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"elliptocytosis 3","secondary_identifiers":["MEDGEN:357139","MESH:C566678","OMIM:617948","UMLS:C1866810","GARD:16273"],"synonyms":[{"name":"EL3","type":"related"},{"name":"anemia, neonatal hemolytic, fatal or near-fatal","type":"exact"},{"name":"anemia, perinatal hemolytic, fatal or near-fatal","type":"related"},{"name":"elliptocytosis 3","type":"exact"},{"name":"elliptocytosis-3","type":"exact"}],"termid":"MONDO:0054780","xrefs":{"Monarch":{"xref_id":"0054780"}}}


id: PBO:0017523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab GTPase binding Yip5 (predicted)","termid":"PBO:0017523"}


id: PBO:0091452
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human QNG1","termid":"PBO:0091452"}


id: PBO:0003046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexose transporter Ght4","termid":"PBO:0003046"}


id: GO:0000400
data:
  {"annotated_genes":["SJAG_02262","SJAG_02226","SJAG_04752","SJAG_02708","SJAG_02690","SJAG_02294"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79747,80248,81148,96657,107884],"is_not":false,"summary":null,"term":"GO:0000400"},{"annotations":[76971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000402"}]},"cv_name":"molecular_function","definition":"Binding to a DNA segment containing four-way junctions, also known as Holliday junctions, a structure where two DNA double strands are held together by reciprocal exchange of two of the four strands, one strand each from the two original helices.","definition_xrefs":["PMID:15563464","GOC:krc","ISBN:0815332181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA secondary structure binding","termid":"GO:0000217"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02226":null,"SJAG_02262":null,"SJAG_02294":null,"SJAG_02690":null,"SJAG_02708":null,"SJAG_04752":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003677"],"is_obsolete":false,"name":"four-way junction DNA binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"Holliday junction binding","type":"exact"},{"name":"forked DNA binding","type":"broad"}],"termid":"GO:0000400","terms_by_termid":{"GO:0000400":null,"GO:0000402":null}}


id: PBO:0050823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HYDIN axonemal central pair apparatus protein","termid":"PBO:0050823"}


id: PBO:0064376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PMS1 homolog 1, mismatch repair system component","termid":"PBO:0064376"}


id: PBO:0050852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ICAM4 antisense RNA 1","termid":"PBO:0050852"}


id: PBO:0057163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 320b-1","termid":"PBO:0057163"}


id: GO:0015447
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete type II protein secretor activity (obsolete GO:0015447)","synonyms":[{"name":"type II protein secretor activity","type":"exact"}],"termid":"GO:0015447"}


id: PBO:0031750
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_methylation","termid":"PBO:0031750"}


id: PBO:0042475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 2","termid":"PBO:0042475"}


id: PBO:0049954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIG1 hypoxia inducible domain family member 1A","termid":"PBO:0049954"}


id: FYPO:0007542
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of double-stranded DNA binding by a gene product is normal (i.e. indistinguishable from wild type). The relevant 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":"normal DNA binding","termid":"FYPO:0000655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000653"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000653","FYPO:0000257"],"is_obsolete":false,"name":"normal double-stranded DNA binding","synonyms":[{"name":"normal dsDNA binding","type":"exact"}],"termid":"FYPO:0007542"}


id: GO:0006451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The continuation of translation beyond a stop codon by the use of a special tRNA that recognizes the UAG and UGA codons as modified amino acids, rather than as termination codons.","definition_xrefs":["GOC:jsg","PMID:11179232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational elongation","termid":"GO:0006414"},{"relation_name":"is_a","term_name":"regulation of translation","termid":"GO:0006417"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"translational readthrough","synonyms":[{"name":"natural nonsense suppression","type":"related"}],"termid":"GO:0006451"}


id: MONDO:0014822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"15q14 microdeletion syndrome is a recently described syndrome characterized by developmental delay, short stature and facial dysmorphism.","definition_xrefs":["Orphanet:261190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 15","termid":"MONDO:0016913"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"15q14 microdeletion syndrome","secondary_identifiers":["UMLS:C4305230","OMIM:616898","MEDGEN:930899","SCTID:719575008","GARD:17242"],"synonyms":[{"name":"Del(15)(q14)","type":"exact"},{"name":"chromosome 15q14 deletion syndrome","type":"related"},{"name":"monosomy 15q14","type":"exact"}],"termid":"MONDO:0014822","xrefs":{"Monarch":{"xref_id":"0014822"}}}


id: PATO:0000067
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000067 relative pilosity (obsolete PATO:0000067)","termid":"PATO:0000067"}


id: PBO:0005587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NatA N-acetyltransferase subunit Naa50 (predicted)","termid":"PBO:0005587"}


id: GO:0047347
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: aldose 1-phosphate + NDP = phosphate + NDP-aldose.","definition_xrefs":["MetaCyc:2.7.7.37-RXN","EC:2.7.7.37"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotidyltransferase activity","termid":"GO:0016779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016779","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"aldose-1-phosphate nucleotidyltransferase activity","synonyms":[{"name":"NDP sugar phosphorylase activity","type":"related"},{"name":"NDP-aldose phosphorylase activity","type":"related"},{"name":"NDP-sugar phosphorylase activity","type":"broad"},{"name":"NDP:aldose-1-phosphate nucleotidyltransferase activity","type":"related"},{"name":"NDP:alpha-D-aldose-1-phosphate nucleotidyltransferase activity","type":"related"},{"name":"NDPaldose phosphorylase activity","type":"related"},{"name":"glucose 1-phosphate inosityltransferase activity","type":"related"},{"name":"nucleoside diphosphate sugar:orthophosphate nucleotidyltransferase activity","type":"related"},{"name":"nucleoside diphosphosugar phosphorylase activity","type":"related"},{"name":"sugar nucleotide phosphorylase activity","type":"related"},{"name":"sugar phosphate nucleotidyltransferase activity","type":"related"},{"name":"sugar-1-phosphate nucleotidyltransferase activity","type":"broad"}],"termid":"GO:0047347"}


id: SO:0001969
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript variant occurring within an intron of a coding transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intron_variant","termid":"SO:0001627"},{"relation_name":"is_a","term_name":"coding_transcript_variant","termid":"SO:0001968"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coding_transcript_intron_variant","synonyms":[{"name":"Jannovar:coding_transcript_intron_variant","type":"exact"},{"name":"coding sequence intron variant","type":"exact"}],"termid":"SO:0001969"}


id: FYPO:0007483
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which meiotic spindle pole body duplication is abnormal during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:27889481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle pole body duplication","termid":"FYPO:0007258"}],"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:0000054"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000054","FYPO:0000002","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"name":"abnormal meiotic spindle pole body duplication during meiosis I","synonyms":[{"name":"abnormal meiotic SPB duplication during meiosis I","type":"exact"},{"name":"abnormal meiotic spindle pole body duplication during first meiotic nuclear division","type":"exact"},{"name":"abnormal spindle pole body duplication during meiosis I","type":"exact"}],"termid":"FYPO:0007483"}


id: GO:0048307
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 H2O + NH4+ + 6 oxidized [2Fe-2S]-[ferredoxin] = 8 H+ + nitrite + 6 reduced [2Fe-2S]-[ferredoxin].","definition_xrefs":["RHEA:18041"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, iron-sulfur protein as acceptor","termid":"GO:0016664"},{"relation_name":"is_a","term_name":"nitrite reductase activity","termid":"GO:0098809"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"ferredoxin-nitrite reductase activity","secondary_identifiers":["MetaCyc:FERREDOXIN--NITRITE-REDUCTASE-RXN","EC:1.7.7.1"],"synonyms":[{"name":"ammonia:ferredoxin oxidoreductase activity","type":"related"}],"termid":"GO:0048307"}


id: GO:0016846
data:
  {"annotated_genes":["SJAG_03199","SJAG_03671","SJAG_04726","SJAG_04008","SJAG_02205","SJAG_03856","SJAG_05256"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72206],"is_not":false,"summary":null,"term":"GO:0016846"},{"annotations":[69864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047804"},{"annotations":[72613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990411"},{"annotations":[78895,74528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004408"},{"annotations":[69718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004462"},{"annotations":[97317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051907"}]},"cv_name":"molecular_function","definition":"Catalysis of the elimination of hydrogen sulfide or substituted H2S.","definition_xrefs":["EC:4.4.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lyase activity","termid":"GO:0016829"}],"gene_count":7,"genes_by_uniquename":{"SJAG_02205":null,"SJAG_03199":null,"SJAG_03671":null,"SJAG_03856":null,"SJAG_04008":null,"SJAG_04726":null,"SJAG_05256":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"carbon-sulfur lyase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1614591","Reactome:R-HSA-1614567","Reactome:R-HSA-1614614"],"synonyms":[{"name":"carbon-sulphur lyase activity","type":"exact"}],"termid":"GO:0016846","terms_by_termid":{"GO:0004408":null,"GO:0004462":null,"GO:0016846":null,"GO:0047804":null,"GO:0051907":null,"GO:1990411":null}}


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:0091366
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rad57 facilitates Rad51 assembly at damage sites independently of Swi5","termid":"PBO:0091366"}


id: PBO:0076529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 42","termid":"PBO:0076529"}


id: MONDO:0014086
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteogenesis imperfecta in which the cause of the disease is a mutation in the WNT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"osteogenesis imperfecta type 15","secondary_identifiers":["OMIM:615220","UMLS:C3808844","DOID:0110347","GARD:15919","MEDGEN:815174"],"synonyms":[{"name":"OI, type 15","type":"related"},{"name":"OI15","type":"exact"},{"name":"WNT1 osteogenesis imperfecta","type":"exact"},{"name":"osteogenesis imperfecta caused by mutation in WNT1","type":"exact"},{"name":"osteogenesis imperfecta type XV","type":"exact"},{"name":"osteogenesis imperfecta, type 15","type":"related"},{"name":"osteogenesis imperfecta, type XV","type":"related"}],"termid":"MONDO:0014086","xrefs":{"Monarch":{"xref_id":"0014086"}}}


id: MONDO:0006998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm that affects the tonsil.","definition_xrefs":["NCIT:C7404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Waldeyer's ring cancer","termid":"MONDO:0004685"},{"relation_name":"is_a","term_name":"tonsil neoplasm","termid":"MONDO:0021250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"tonsil cancer","secondary_identifiers":["ICD9:146.0","UMLS:C0751560","DOID:8858","ICD10CM:C09","MESH:D014067","MEDGEN:148341","SCTID:363393007","EFO:1001214","MedDRA:10044002"],"synonyms":[{"name":"cancer of tonsil","type":"broad"},{"name":"malignant neoplasm of faucial tonsil","type":"exact"},{"name":"malignant neoplasm of palatine tonsil","type":"exact"},{"name":"malignant neoplasm of the tonsil","type":"exact"},{"name":"malignant neoplasm of tonsil","type":"exact"},{"name":"malignant neoplasm of tonsil, faucial","type":"exact"},{"name":"malignant tonsil neoplasm","type":"exact"},{"name":"malignant tonsil tumor","type":"exact"},{"name":"malignant tonsil tumour","type":"exact"},{"name":"malignant tonsillar neoplasm","type":"exact"},{"name":"malignant tonsillar tumor","type":"exact"},{"name":"malignant tonsillar tumour","type":"exact"},{"name":"malignant tumor of the tonsil","type":"exact"},{"name":"malignant tumor of tonsil","type":"exact"},{"name":"malignant tumour of the tonsil","type":"exact"},{"name":"malignant tumour of tonsil","type":"exact"},{"name":"tonsil cancer","type":"exact"}],"termid":"MONDO:0006998","xrefs":{"Monarch":{"xref_id":"0006998"}}}


id: GO:1990209
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents, or reduces the frequency, rate or extent of the RNA levels in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:18703740","GOC:ml"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by symbiont of RNA levels in host (obsolete GO:1990209)","termid":"GO:1990209"}


id: GO:0098947
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic endocytic zone membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of postsynaptic endocytic zone membrane (obsolete GO:0098947)","synonyms":[{"name":"intrinsic to postsynaptic active zone membrane","type":"narrow"}],"termid":"GO:0098947"}


id: PBO:0031183
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_mating_efficiency","termid":"PBO:0031183"}


id: GO:0010352
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of lithium ion out of a cell or organelle.","definition_xrefs":["PMID:17270011"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lithium ion transmembrane transport","termid":"GO:0090452"},{"relation_name":"is_a","term_name":"export across plasma membrane","termid":"GO:0140115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"lithium ion export across the plasma membrane","synonyms":[{"name":"lithium export","type":"exact"},{"name":"lithium ion efflux","type":"related"},{"name":"lithium ion export","type":"related"}],"termid":"GO:0010352"}


id: PBO:0073431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor 3b subunit 1","termid":"PBO:0073431"}


id: PATO:0000792
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000792 repair function value (obsolete PATO:0000792)","termid":"PATO:0000792"}


id: PBO:0044088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis antigen family 45 member A8","termid":"PBO:0044088"}


id: PR:Q9P7U5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC977.03 gene.","definition_xrefs":["UniProtKB:Q9P7U5","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 methyltransferase C977.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC977.03","synonyms":[{"name":"Spom972h-SPAC977.03","type":"exact"}],"termid":"PR:Q9P7U5"}


id: GO:0150052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of postsynapse assembly, the aggregation, arrangement and bonding together of a set of components to form a postsynapse.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:28185854","PMID:16672654","PMID:16394100"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synapse assembly","termid":"GO:0051963"},{"relation_name":"is_a","term_name":"regulation of postsynapse organization","termid":"GO:0099175"},{"relation_name":"regulates","term_name":"postsynapse assembly","termid":"GO:0099068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of postsynapse assembly","termid":"GO:0150052"}


id: FYPO:0000300
data:
  {"alleles_by_uniquename":{"SJAG_00028:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00028","name":"rga6delta","uniquename":"SJAG_00028:allele-1"},"SJAG_00118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00118","name":"mid2delta","uniquename":"SJAG_00118:allele-1"},"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_00364:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00364","name":"rad3delta","uniquename":"SJAG_00364:allele-1"},"SJAG_00370:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00370","name":"erg1delta","uniquename":"SJAG_00370:allele-1"},"SJAG_00409:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00409","name":"gpd1delta","uniquename":"SJAG_00409:allele-1"},"SJAG_00426:allele-1":{"allele_type":"amino_acid_mutation","description":"P363S","gene_uniquename":"SJAG_00426","name":"bbl1-P363S","uniquename":"SJAG_00426:allele-1"},"SJAG_00429:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00429","name":"rad26delta","uniquename":"SJAG_00429:allele-1"},"SJAG_00514:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00514","name":"scd1delta","uniquename":"SJAG_00514:allele-1"},"SJAG_00601:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00601","name":"rip1delta","uniquename":"SJAG_00601:allele-1"},"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_00871:allele-1":{"allele_type":"amino_acid_mutation","description":"cut3-T19E","gene_uniquename":"SJAG_00871","name":"cut3-T19E","uniquename":"SJAG_00871:allele-1"},"SJAG_00993:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00993","name":"byr1delta","uniquename":"SJAG_00993:allele-1"},"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_01143:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"711-723","gene_uniquename":"SJAG_01143","name":"mid1-delta(711-723 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hyperactive (chk1-hyp)","reference":"PMID:23090706","type":"exact"},{"name":"chk1-hyperactive 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ts","gene_uniquename":"SJAG_01956","name":"nuc2-1051","uniquename":"SJAG_01956:allele-1"},"SJAG_02252:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02252","name":"ace2delta","uniquename":"SJAG_02252:allele-1"},"SJAG_02266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02266","name":"rad24delta","uniquename":"SJAG_02266:allele-1"},"SJAG_02379:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02379","name":"gap1delta","uniquename":"SJAG_02379:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_02486:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02486","name":"ste6delta","uniquename":"SJAG_02486:allele-1"},"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of 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phosphorylation","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-6"},"SJAG_02796:allele-1":{"allele_type":"amino_acid_mutation","description":"A343T","gene_uniquename":"SJAG_02796","name":"pyk1-A343T","uniquename":"SJAG_02796:allele-1"},"SJAG_02819:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02819","name":"efc25delta","uniquename":"SJAG_02819:allele-1"},"SJAG_02860:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02860","name":"wcs1delta","uniquename":"SJAG_02860:allele-1"},"SJAG_02923:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02923","name":"spk1delta","uniquename":"SJAG_02923:allele-1"},"SJAG_03118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03118","name":"leo1delta","uniquename":"SJAG_03118:allele-1"},"SJAG_03143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03143","name":"sep1delta","uniquename":"SJAG_03143:allele-1"},"SJAG_03198:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03198","name":"oar2delta","uniquename":"SJAG_03198:allele-1"},"SJAG_03198:allele-2":{"allele_type":"amino_acid_mutation","description":"Y189D 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