# terms

id: PBO:0087466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of a palmitoyltransferase; this complex adds a palmitoyl lipid moiety to heterolipidated substrates such as Ras1p and Ras2p through a thioester linkage; mutants partially mislocalize Ras2p to the vacuole; palmitoyltransferase is composed of Erf2p and Shr5p","termid":"PBO:0087466"}


id: GO:0047071
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3,4-dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione + O2 = 3-hydroxy-5,9,17-trioxo-4,5:9,10-disecoandrosta-1(10),2-dien-4-oate + H+.","definition_xrefs":["RHEA:21352","EC:1.13.11.25"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"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:0003674","GO:0016491"],"is_obsolete":false,"name":"3,4-dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione 4,5-dioxygenase activity","secondary_identifiers":["KEGG_REACTION:R04597","UM-BBD_reactionID:r1151","MetaCyc:1.13.11.25-RXN"],"synonyms":[{"name":"3,4-dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione:oxygen 4,5-oxidoreductase (decyclizing)","type":"related"},{"name":"3-alkylcatechol 2,3-dioxygenase activity","type":"related"},{"name":"steroid 4,5-dioxygenase activity","type":"broad"}],"termid":"GO:0047071"}


id: GO:0050635
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-methylanthranilyl-CoA + 3 H+ + 3 malonyl-CoA = 1,3-dihydroxy-N-methylacridone + 3 CO2 + 4 CoA + H2O.","definition_xrefs":["EC:2.3.1.159","RHEA:22224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"acridone synthase activity","secondary_identifiers":["KEGG_REACTION:R07250","MetaCyc:2.3.1.159-RXN"],"synonyms":[{"name":"malonyl-CoA:N-methylanthraniloyl-CoA malonyltransferase (cyclizing)","type":"related"}],"termid":"GO:0050635"}


id: PR:Q9P7C1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- erj5 gene.","definition_xrefs":["UniProtKB:Q9P7C1","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 J domain-containing protein C2E1P5.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2E1P5.03","synonyms":[{"name":"Spom972h-erj5","type":"exact"}],"termid":"PR:Q9P7C1"}


id: PBO:0046959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 81 member A","termid":"PBO:0046959"}


id: GO:0102947
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + (+)-delta-cadinene + NADPH + O2 = 8-hydroxy-(+)-delta-cadinene + NADP + H2O.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"(+)-delta-cadinene-8-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-9045"],"termid":"GO:0102947"}


id: PBO:0034290
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_target_end_location","termid":"PBO:0034290"}


id: GO:0032713
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of interleukin-4 production.","definition_xrefs":["PMID:29778524","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of interleukin-4 production","termid":"GO:0032673"},{"relation_name":"negatively_regulates","term_name":"interleukin-4 production","termid":"GO:0032633"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of interleukin-4 production","secondary_identifiers":["GO:0150134","GO:0045403"],"synonyms":[{"name":"down regulation of interleukin-4 production","type":"exact"},{"name":"down-regulation of interleukin-4 production","type":"exact"},{"name":"downregulation of interleukin-4 production","type":"exact"},{"name":"inhibition of interleukin-4 production","type":"narrow"},{"name":"negative regulation of IL-4 production","type":"exact"},{"name":"negative regulation of interleukin-4 biosynthetic process","type":"narrow"},{"name":"negative regulation of interleukin-4 secretion","type":"narrow"}],"termid":"GO:0032713"}


id: PBO:0030581
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vacuolar_asparagine_level","termid":"PBO:0030581"}


id: GO:0047695
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: benzoin = 2 benzaldehyde.","definition_xrefs":["EC:4.1.2.38","RHEA:21460"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"benzoin aldolase activity","secondary_identifiers":["KEGG_REACTION:R00027","MetaCyc:BENZOIN-ALDOLASE-RXN"],"synonyms":[{"name":"2-hydroxy-1,2-diphenylethanone benzaldehyde-lyase 2-hydroxy-1,2- activity","type":"related"},{"name":"2-hydroxy-1,2-diphenylethanone benzaldehyde-lyase 2-hydroxy-1,2-diphenylethanone benzaldehyde-lyase (benzaldehyde-forming)","type":"related"},{"name":"2-hydroxy-1,2-diphenylethanone benzaldehyde-lyase 2-hydroxy-1,2-diphenylethanone benzaldehyde-lyase activity","type":"related"},{"name":"benzaldehyde lyase activity","type":"related"},{"name":"diphenylethanone benzaldehyde-lyase activity","type":"related"}],"termid":"GO:0047695"}


id: GO:0015775
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of beta-glucans into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Beta-glucans are compounds composed of glucose residues linked by beta-glucosidic bonds.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide transport","termid":"GO:0015774"}],"gene_count":0,"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:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"beta-glucan transport","termid":"GO:0015775"}


id: PBO:0041633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CACNA1C antisense RNA 3","termid":"PBO:0041633"}


id: PBO:0012837
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mature peptide sequence is YTPKVPYM","termid":"PBO:0012837"}


id: PBO:0086080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function with similarity to Tfs1p; transcription is activated by paralogous proteins Yrm1p and Yrr1p along with proteins involved in multidrug resistance; GFP-tagged protein localizes to the cytoplasm and nucleus","termid":"PBO:0086080"}


id: PBO:0063428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDE4DIP pseudogene 2","termid":"PBO:0063428"}


id: PBO:0042355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD99 molecule (Xg blood group)","termid":"PBO:0042355"}


id: GO:0090010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by an extracellular ligand binding to a transforming growth factor beta receptor on the surface of a target cell, which contributes to the formation of the primitive streak.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sdb_2009"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor signaling pathway involved in primitive streak formation (obsolete GO:0090010)","synonyms":[{"name":"TGFbeta signaling pathway involved in primitive streak formation","type":"related"},{"name":"transforming growth factor beta receptor signalling pathway involved in primitive streak formation","type":"exact"}],"termid":"GO:0090010"}


id: PBO:0116599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IL12B antisense RNA 1","termid":"PBO:0116599"}


id: MONDO:0014524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the FMN2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 47","secondary_identifiers":["DOID:0081211","GARD:22569","MEDGEN:863881","OMIM:616193","UMLS:C4015444"],"synonyms":[{"name":"FMN2 autosomal recessive non-syndromic intellectual disability","type":"exact"},{"name":"MRT47","type":"related"},{"name":"autosomal recessive non-syndromic intellectual disability caused by mutation in FMN2","type":"exact"},{"name":"intellectual developmental disorder, autosomal recessive 47","type":"exact"},{"name":"intellectual disability, autosomal recessive 47","type":"exact"},{"name":"intellectual disability, autosomal recessive type 47","type":"exact"},{"name":"mental retardation, autosomal recessive 47","type":"related"},{"name":"mental retardation, autosomal recessive type 47","type":"exact"}],"termid":"MONDO:0014524","xrefs":{"Monarch":{"xref_id":"0014524"}}}


id: MONDO:0013043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atypical hemolytic uremic syndrome with complement gene abnormality","termid":"MONDO:0035290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"atypical hemolytic-uremic syndrome with C3 anomaly","secondary_identifiers":["GARD:18555","MEDGEN:442875","UMLS:C2752037","OMIM:612925","Orphanet:93575"],"synonyms":[{"name":"AHUS5","type":"related"},{"name":"Ahus, susceptibility to, 5","type":"related"},{"name":"D-HUS with C3 anomaly","type":"exact"},{"name":"aHUS with C3 anomaly","type":"exact"},{"name":"atypical HUS with C3 anomaly","type":"exact"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, 5","type":"related"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, type 5","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhea with C3 anomaly","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhoea with C3 anomaly","type":"exact"},{"name":"susceptibility to atypical hemolytic uremic syndrome 5","type":"related"}],"termid":"MONDO:0013043","xrefs":{"Monarch":{"xref_id":"0013043"}}}


id: GO:0003185
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structure of the sinoatrial valve is generated and organized.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart valve morphogenesis","termid":"GO:0003179"},{"relation_name":"part_of","term_name":"sinoatrial valve development","termid":"GO:0003172"}],"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":"sinoatrial valve morphogenesis","synonyms":[{"name":"SA valve morphogenesis","type":"exact"}],"termid":"GO:0003185"}


id: PBO:0085494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protease that specifically cleaves Smt3p protein conjugates; required for cell cycle progression; associates with nucleoporins and may interact with septin rings during telophase; contributes to regulation of telomeric silencing; sequestered to the nucleolus under stress conditions","termid":"PBO:0085494"}


id: MONDO:0003432
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Strabismus is the intermittent or constant misalignment of an eye so that its line of vision is not pointed at the same object as the other eye. Strabismus is caused by an imbalance in the extraocular muscles which control the positioning of the eyes. Strabismus is normal in newborns but should resolve by the time the baby is 6 months old. In older children with strabismus, the brain may learn to ignore the input from one eye, and this may lead to amblyopia, a potentially permanent decrease in vision in that eye if not corrected.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hyperopia","termid":"MONDO:0004891"},{"relation_name":"is_a","term_name":"ocular motility disease","termid":"MONDO:0001584"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"strabismus","secondary_identifiers":["MESH:D013285","DOID:540","MEDGEN:21337","UMLS:C0038379","ICD9:378.7","ICD9:378.40","SCTID:22066006","NCIT:C35040"],"synonyms":[{"name":"squint","type":"exact"},{"name":"strabismus","type":"exact"}],"termid":"MONDO:0003432","xrefs":{"Monarch":{"xref_id":"0003432"}}}


id: FYPO:0007019
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 posttranscriptional methylation of a guanosine residue in a tRNA molecule to form 7-methylguanosine is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:25404562","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal tRNA methylation","termid":"FYPO:0001763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal tRNA guanosine 7-methylation","synonyms":[{"name":"normal 7-methylguanosine level in tRNA","type":"related"},{"name":"normal tRNA 7-methylguanosine formation","type":"exact"},{"name":"normal tRNA guanosine 7-methylation during mitotic cell cycle","type":"related"},{"name":"normal tRNA guanosine 7-methylation during vegetative growth","type":"exact"},{"name":"normal tRNA m7G formation","type":"exact"}],"termid":"FYPO:0007019"}


id: MONDO:0021653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous mucinosis","termid":"MONDO:0002523"}],"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":"cutaneous focal mucinosis","secondary_identifiers":["MEDGEN:590585","SCTID:110981005","UMLS:C0406659","ICD9:701.8"],"synonyms":[{"name":"focal mucinoses","type":"related"},{"name":"focal mucinosis","type":"related"}],"termid":"MONDO:0021653","xrefs":{"Monarch":{"xref_id":"0021653"}}}


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


id: PBO:0079830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"upstream master lncRNA of the inflammatory chemokine locus","termid":"PBO:0079830"}


id: PBO:0067323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 414, pseudogene","termid":"PBO:0067323"}


id: PBO:0075593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine peptidase inhibitor, Kunitz type 5, pseudogene","termid":"PBO:0075593"}


id: PBO:0078292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 25-1","termid":"PBO:0078292"}


id: PBO:0042891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement factor B","termid":"PBO:0042891"}


id: PBO:0074958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 113-9","termid":"PBO:0074958"}


id: PBO:0067418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 535, pseudogene","termid":"PBO:0067418"}


id: PBO:0059640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 6","termid":"PBO:0059640"}


id: GO:1904423
data:
  {"annotated_genes":["SJAG_00554","SJAG_02163"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[71857,74364],"is_not":false,"summary":null,"term":"GO:1904423"}]},"cv_name":"cellular_component","definition":"A protein complex which is capable of dehydrodolichyl diphosphate synthase activity.","definition_xrefs":["GO_REF:0000088","GOC:TermGenie","PMID:25066056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyprenyl diphosphate synthase complex","termid":"GO:0032476"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00554":null,"SJAG_02163":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"dehydrodolichyl diphosphate synthase complex","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:1904423","terms_by_termid":{"GO:1904423":null}}


id: PBO:0076877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TEX28 pseudogene 1","termid":"PBO:0076877"}


id: GO:0051733
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: NTP + 5'-dephospho-DNA = NDP + 5'-phospho-DNA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete polydeoxyribonucleotide kinase activity (obsolete GO:0051733)","synonyms":[{"name":"DNA 5'-hydroxyl kinase activity","type":"exact"},{"name":"DNA kinase activity","type":"exact"}],"termid":"GO:0051733"}


id: MONDO:0013454
data:
  {"annotated_genes":["SJAG_01298"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86870],"is_not":false,"summary":null,"term":"MONDO:0013454"}]},"cv_name":"mondo","definition":"Any Leber congenital amaurosis 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":"Leber congenital amaurosis","termid":"MONDO:0018998"},{"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:0005328"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005328"],"is_obsolete":false,"name":"Leber congenital amaurosis 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:326698","OMIM:613837","GARD:10488","DOID:0110216","MESH:C564140","HGNC:6052","UMLS:C1840284","ICD10CM:H35.5"],"synonyms":[{"name":"IMPDH1 Leber congenital amaurosis","type":"exact"},{"name":"LCA11","type":"exact"},{"name":"Leber congenital amaurosis 11","type":"exact"},{"name":"Leber congenital amaurosis caused by mutation in IMPDH1","type":"exact"},{"name":"Leber congenital amaurosis type 11","type":"exact"},{"name":"amaurosis congenita of Leber, type 11","type":"related"}],"termid":"MONDO:0013454","terms_by_termid":{"MONDO:0013454":null},"xrefs":{"Monarch":{"xref_id":"0013454"}}}


id: MONDO:0014476
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary episodic ataxia","termid":"MONDO:0016227"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"episodic ataxia type 8","secondary_identifiers":["DOID:0050996","OMIM:616055","MEDGEN:863545","Orphanet:401953","GARD:17665","UMLS:C4015108"],"synonyms":[{"name":"EA8","type":"related"},{"name":"episodic ataxia type 8","type":"exact"},{"name":"episodic ataxia with slurred speech","type":"related"},{"name":"episodic ataxia, type 8","type":"related"}],"termid":"MONDO:0014476","xrefs":{"Monarch":{"xref_id":"0014476"}}}


id: MONDO:0013319
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 4","termid":"MONDO:0016955"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 4Q32.1-q32.2 triplication syndrome","secondary_identifiers":["UMLS:C3150857","MEDGEN:462207","OMIM:613603"],"synonyms":[{"name":"chromosome 4Q32.1-q32.2 triplication syndrome","type":"exact"}],"termid":"MONDO:0013319","xrefs":{"Monarch":{"xref_id":"0013319"}}}


id: PBO:0025458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase with bromodomain protein","termid":"PBO:0025458"}


id: MONDO:0009938
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"congenital pulmonary valve stenosis","termid":"MONDO:0017865"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonic stenosis","secondary_identifiers":["GARD:10071","MEDGEN:408291","OMIM:265500","UMLS:C1956257","HP:0001642"],"synonyms":[{"name":"pulmonary stenosis","type":"exact"},{"name":"pulmonic stenosis","type":"exact"},{"name":"pulmonic stenosis (disease)","type":"exact"},{"name":"valvular pulmonic stenosis","type":"related"}],"termid":"MONDO:0009938","xrefs":{"Monarch":{"xref_id":"0009938"}}}


id: PBO:0066862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 162","termid":"PBO:0066862"}


id: PATO:0005017
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's being compressed from the side facing the lips to the side facing the tongue.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flattened","termid":"PATO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"labiolingually compressed","termid":"PATO:0005017"}


id: SO:0001498
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of sequence from the end of a YAC clone that may provide a highly specific marker.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"read","termid":"SO:0000150"},{"relation_name":"part_of","term_name":"YAC","termid":"SO:0000152"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YAC_end","synonyms":[{"name":"YAC end","type":"exact"}],"termid":"SO:0001498"}


id: PBO:0078289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 22-1","termid":"PBO:0078289"}


id: PBO:0036467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial DNA branch migration helicase Irc3 (predicted)","termid":"PBO:0036467"}


id: GO:0017054
data:
  {"annotated_genes":["SJAG_03095","SJAG_00958"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70355,71130],"is_not":false,"summary":null,"term":"GO:0017054"}]},"cv_name":"cellular_component","definition":"A heterodimeric protein complex that can stably associate with TATA-binding protein on promoters, thereby preventing the assembly of transcription factors TFIIA and TFIIB and leading to repression of RNA polymerase II transcription. The two subunits, NC2alpha (Drap1) and NC2beta (Dr1), dimerize through histone fold domains of the H2A/H2B type present in the amino termini.","definition_xrefs":["PMID:15574413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription repressor complex","termid":"GO:0090571"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00958":null,"SJAG_03095":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"negative cofactor 2 complex","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0017054","terms_by_termid":{"GO:0017054":null}}


id: GO:1990377
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An extracellular matrix consisting of a densely packed organomineral assembly in which the mineral phase represents the majority of the material by weight.","definition_xrefs":["GOC:jh2","PMID:15994301"],"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":"organomineral extracellular matrix","termid":"GO:1990377"}


id: GO:0033625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of integrin activation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of integrin activation","termid":"GO:0033623"},{"relation_name":"positively_regulates","term_name":"integrin activation","termid":"GO:0033622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of integrin activation","synonyms":[{"name":"positive regulation of integrin complex activation","type":"exact"}],"termid":"GO:0033625"}


id: PR:P36583
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pck2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P36583"],"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 C-like 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12D12.04c","synonyms":[{"name":"Spom972h-pck2","type":"exact"}],"termid":"PR:P36583"}


id: PBO:0003599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIIIC complex subunit Sfc9 (predicted)","termid":"PBO:0003599"}


id: PBO:0063383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 2 like","termid":"PBO:0063383"}


id: GO:0048858
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a cell projection are generated and organized.","definition_xrefs":["GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"is_a","term_name":"cell projection organization","termid":"GO:0030030"},{"relation_name":"part_of","term_name":"cell morphogenesis","termid":"GO:0000902"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell projection morphogenesis","termid":"GO:0048858"}


id: GO:0000414
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the covalent addition of a methyl group to the lysine at position 36 of histone H3.","definition_xrefs":["GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H3-K36 methylation (obsolete GO:0000414)","termid":"GO:0000414"}


id: GO:0015607
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction ATP + H2O + fatty acyl CoA(Side 1) = ADP + phosphate + fatty acyl CoA(Side 2). A fatty acyl CoA group is any acyl group derived from a fatty acid with a coenzyme A group attached to it.","definition_xrefs":["RHEA:15181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"organophosphate ester transmembrane transporter activity","termid":"GO:0015605"},{"relation_name":"is_a","term_name":"nucleobase-containing compound transmembrane transporter activity","termid":"GO:0015932"},{"relation_name":"is_a","term_name":"ATPase-coupled lipid transmembrane transporter activity","termid":"GO:0034040"},{"relation_name":"is_a","term_name":"amide transmembrane transporter activity","termid":"GO:0042887"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"},{"relation_name":"is_a","term_name":"sulfur compound transmembrane transporter activity","termid":"GO:1901682"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"ABC-type fatty-acyl-CoA transporter activity","secondary_identifiers":["MetaCyc:3.6.3.47-RXN","EC:7.6.2.4"],"synonyms":[{"name":"ABC-type fatty-acyl-CoA transporter","type":"exact"},{"name":"ATPase-coupled fatty-acyl-CoA transmembrane transporter activity","type":"related"},{"name":"fatty acyl CoA transporter activity","type":"related"},{"name":"fatty-acyl-CoA transmembrane transporter activity","type":"broad"},{"name":"fatty-acyl-CoA-transporting ATPase","type":"related"}],"termid":"GO:0015607"}


id: GO:1901478
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of amitrole from one side of a membrane to the other.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"azole transmembrane transporter activity","termid":"GO:1901474"}],"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:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"aminotriazole transmembrane transporter activity","secondary_identifiers":["GO:0015241"],"synonyms":[{"name":"aminotriazole transporter activity","type":"broad"}],"termid":"GO:1901478"}


id: PBO:0049916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hes related family bHLH transcription factor with YRPW motif 1","termid":"PBO:0049916"}


id: PBO:0072082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 12","termid":"PBO:0072082"}


id: PBO:0056813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major facilitator superfamily domain containing 6","termid":"PBO:0056813"}


id: PBO:0061861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligodendrocyte transcription factor 2","termid":"PBO:0061861"}


id: PBO:0001403
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell cycle regulated","termid":"PBO:0001403"}


id: GO:1900260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of RNA-directed 5'-3' RNA polymerase activity.","definition_xrefs":["GOC:pf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transferase activity","termid":"GO:0051348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of RNA-dependent RNA polymerase activity","synonyms":[{"name":"down regulation of PB1 proteins","type":"related"},{"name":"down regulation of PB2 proteins","type":"related"},{"name":"down regulation of RDRP","type":"related"},{"name":"down regulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"down regulation of RNA replicase activity","type":"exact"},{"name":"down regulation of RNA synthetase activity","type":"related"},{"name":"down regulation of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"down regulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"down regulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"down regulation of RNA-directed RNA polymerase activity","type":"exact"},{"name":"down regulation of phage f2 replicase","type":"narrow"},{"name":"down regulation of polymerase L","type":"related"},{"name":"down regulation of ribonucleic acid replicase activity","type":"exact"},{"name":"down regulation of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"down regulation of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"down regulation of ribonucleic replicase activity","type":"exact"},{"name":"down regulation of ribonucleic synthetase activity","type":"related"},{"name":"down regulation of transcriptase","type":"broad"},{"name":"down-regulation of PB1 proteins","type":"related"},{"name":"down-regulation of PB2 proteins","type":"related"},{"name":"down-regulation of RDRP","type":"related"},{"name":"down-regulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"down-regulation of RNA replicase activity","type":"exact"},{"name":"down-regulation of RNA synthetase activity","type":"related"},{"name":"down-regulation of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"down-regulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"down-regulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"down-regulation of RNA-directed RNA polymerase activity","type":"exact"},{"name":"down-regulation of phage f2 replicase","type":"narrow"},{"name":"down-regulation of polymerase L","type":"related"},{"name":"down-regulation of ribonucleic acid replicase activity","type":"exact"},{"name":"down-regulation of ribonucleic synthetase activity","type":"related"},{"name":"down-regulation of transcriptase","type":"broad"},{"name":"downregulation of PB1 proteins","type":"related"},{"name":"downregulation of PB2 proteins","type":"related"},{"name":"downregulation of RDRP","type":"related"},{"name":"downregulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"downregulation of RNA replicase activity","type":"exact"},{"name":"downregulation of RNA synthetase activity","type":"related"},{"name":"downregulation of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"downregulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"downregulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"downregulation of RNA-directed RNA polymerase activity","type":"exact"},{"name":"downregulation of nucleoside-triphosphate:RNA nucleotidyltransferase (RNA-directed)","type":"exact"},{"name":"downregulation of phage f2 replicase","type":"narrow"},{"name":"downregulation of polymerase L","type":"related"},{"name":"downregulation of ribonucleic acid replicase activity","type":"exact"},{"name":"downregulation of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"downregulation of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"downregulation of ribonucleic replicase activity","type":"exact"},{"name":"downregulation of ribonucleic synthetase activity","type":"related"},{"name":"downregulation of transcriptase","type":"broad"},{"name":"inhibition of PB1 proteins","type":"related"},{"name":"inhibition of PB2 proteins","type":"related"},{"name":"inhibition of RDRP","type":"related"},{"name":"inhibition of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"inhibition of RNA replicase activity","type":"exact"},{"name":"inhibition of RNA synthetase activity","type":"related"},{"name":"inhibition of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"inhibition of RNA-dependent RNA replicase activity","type":"exact"},{"name":"inhibition of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"inhibition of RNA-directed RNA polymerase activity","type":"narrow"},{"name":"inhibition of nucleoside-triphosphate:RNA nucleotidyltransferase (RNA-directed)","type":"exact"},{"name":"inhibition of phage f2 replicase","type":"narrow"},{"name":"inhibition of polymerase L","type":"related"},{"name":"inhibition of ribonucleic acid replicase activity","type":"exact"},{"name":"inhibition of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"inhibition of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"inhibition of ribonucleic replicase activity","type":"exact"},{"name":"inhibition of ribonucleic synthetase activity","type":"related"},{"name":"inhibition of transcriptase","type":"broad"},{"name":"negative regulation of 3D polymerase activity","type":"exact"},{"name":"negative regulation of PB1 proteins","type":"related"},{"name":"negative regulation of PB2 proteins","type":"related"},{"name":"negative regulation of RDRP","type":"related"},{"name":"negative regulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"negative regulation of RNA replicase activity","type":"exact"},{"name":"negative regulation of RNA synthetase activity","type":"related"},{"name":"negative regulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"negative regulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"negative regulation of RNA-directed 5'-3' RNA polymerase activity","type":"exact"},{"name":"negative regulation of RNA-directed RNA polymerase activity","type":"broad"},{"name":"negative regulation of nucleoside-triphosphate:RNA nucleotidyltransferase (RNA-directed)","type":"exact"},{"name":"negative regulation of phage f2 replicase","type":"narrow"},{"name":"negative regulation of polymerase L","type":"related"},{"name":"negative regulation of ribonucleic acid replicase activity","type":"exact"},{"name":"negative regulation of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"negative regulation of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"negative regulation of ribonucleic replicase activity","type":"exact"},{"name":"negative regulation of ribonucleic synthetase activity","type":"related"},{"name":"negative regulation of transcriptase","type":"broad"}],"termid":"GO:1900260"}


id: PR:Q9USL1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A THO complex subunit 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04432","PRO:DNx","PANTHER:PTHR22839:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized WD repeat-containing protein C18B5.10c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18B5.10c","secondary_identifiers":["UniProtKB:Q9USL1"],"synonyms":[{"name":"Spom972h-THOC3","type":"exact"}],"termid":"PR:Q9USL1"}


id: PBO:0053661
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 838","termid":"PBO:0053661"}


id: PBO:0075157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide C pseudogene 13","termid":"PBO:0075157"}


id: PBO:0000873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chaperonin-containing T-complex epsilon subunit Cct5","termid":"PBO:0000873"}


id: PBO:0076225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPT6 homolog, histone chaperone and transcription elongation factor","termid":"PBO:0076225"}


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: PBO:0071067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 69","termid":"PBO:0071067"}


id: GO:0047729
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: carnitine + H+ = 2-methylcholine + CO2.","definition_xrefs":["RHEA:21576","EC:4.1.1.42"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"carnitine decarboxylase activity","secondary_identifiers":["MetaCyc:CARNITINE-DECARBOXYLASE-RXN","KEGG_REACTION:R02398"],"synonyms":[{"name":"carnitine carboxy-lyase (2-methylcholine-forming)","type":"related"},{"name":"carnitine carboxy-lyase activity","type":"related"}],"termid":"GO:0047729"}


id: PBO:0017678
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alzheimer's disease","termid":"PBO:0017678"}


id: PBO:0108970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciliary microtubule inner protein 2B","termid":"PBO:0108970"}


id: GO:1901988
data:
  {"annotated_genes":["SJAG_04280","SJAG_04999","SJAG_01118","SJAG_03854","SJAG_04943","SJAG_02451","SJAG_00486","SJAG_00526","SJAG_02771","SJAG_02332","SJAG_01044","SJAG_02098","SJAG_04699","SJAG_00318","SJAG_01082","SJAG_00883","SJAG_03927","SJAG_01146","SJAG_01330","SJAG_03942","SJAG_01076","SJAG_03720","SJAG_01401","SJAG_00600","SJAG_03026","SJAG_01429","SJAG_03126","SJAG_01679","SJAG_02336","SJAG_03353","SJAG_03073","SJAG_03681","SJAG_02169","SJAG_04287","SJAG_03898","SJAG_02723","SJAG_04140","SJAG_00623","SJAG_01708","SJAG_00991","SJAG_00071","SJAG_04332","SJAG_00429","SJAG_03327","SJAG_04259","SJAG_02592","SJAG_04597","SJAG_01677","SJAG_00327","SJAG_03067","SJAG_02858","SJAG_03438","SJAG_02563","SJAG_03695","SJAG_01515","SJAG_01837","SJAG_04394","SJAG_02266","SJAG_00082","SJAG_01210","SJAG_05346","SJAG_04884","SJAG_01297","SJAG_00364","SJAG_03529","SJAG_03160","SJAG_01084","SJAG_04126","SJAG_02074","SJAG_04671","SJAG_01205","SJAG_01010","SJAG_00640","SJAG_05373","SJAG_01855","SJAG_01605","SJAG_03048","SJAG_01873","SJAG_00996","SJAG_03602","SJAG_02576","SJAG_03591","SJAG_00169","SJAG_06592","SJAG_02392","SJAG_01680","SJAG_02026"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113799,107246,108268,115926,103895,99589,111975,90686,114288],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[106330,114518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[78797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044778"},{"annotations":[116085,91396,106628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[106629,114278,116086,89014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051598"},{"annotations":[75209,116694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[94378,116030,89952,100537,101440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044878"},{"annotations":[111213,114489,116258,116031,77944,93534,79981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044773"},{"annotations":[109331,74703,99358,112050,116087,78803,100538,117129,72122,79383,116828,93931,99191,70971,91397,117302,106631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033314"},{"annotations":[108905,102362,115928,88898,101625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031568"},{"annotations":[91273,109684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031571"},{"annotations":[95824,94510,116032,98425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031569"},{"annotations":[100539,72120,101053,117043,106632,111745,79246,109332,117741,75153,89075,91761,99360,91398,90171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007095"},{"annotations":[74252,107680,99361,116089,78802,73783,95986,100860,106633,94511,89121,79251,91399,102363,79137,111746,112051,90408,89076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031573"},{"annotations":[99433,106332,109921,114521,115580,101802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[102369,67721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001100"},{"annotations":[93299,92127,91707,98873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000134"},{"annotations":[78435,93535,94338,92893,104502,93185,106663,111451,108589,111836,112494,107027,114490,100998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010972"},{"annotations":[70452,78439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110031"},{"annotations":[98691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902103"},{"annotations":[94170],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[113804],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[116701],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[101341],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell cycle phase transition.","definition_xrefs":["GOC:TermGenie","GOC:mtg_cell_cycle","PMID:22841721"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"regulation of cell cycle phase transition","termid":"GO:1901987"},{"relation_name":"negatively_regulates","term_name":"cell cycle phase transition","termid":"GO:0044770"}],"gene_count":87,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00082":null,"SJAG_00169":null,"SJAG_00318":null,"SJAG_00327":null,"SJAG_00364":null,"SJAG_00429":null,"SJAG_00486":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_00623":null,"SJAG_00640":null,"SJAG_00883":null,"SJAG_00991":null,"SJAG_00996":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01118":null,"SJAG_01146":null,"SJAG_01205":null,"SJAG_01210":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01401":null,"SJAG_01429":null,"SJAG_01515":null,"SJAG_01605":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01708":null,"SJAG_01837":null,"SJAG_01855":null,"SJAG_01873":null,"SJAG_02026":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02169":null,"SJAG_02266":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02392":null,"SJAG_02451":null,"SJAG_02563":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02723":null,"SJAG_02771":null,"SJAG_02858":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03067":null,"SJAG_03073":null,"SJAG_03126":null,"SJAG_03160":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03438":null,"SJAG_03529":null,"SJAG_03591":null,"SJAG_03602":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03720":null,"SJAG_03854":null,"SJAG_03898":null,"SJAG_03927":null,"SJAG_03942":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04394":null,"SJAG_04597":null,"SJAG_04671":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04943":null,"SJAG_04999":null,"SJAG_05346":null,"SJAG_05373":null,"SJAG_06592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cell cycle phase transition","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of cell cycle phase transition","type":"exact"},{"name":"down regulation of cell cycle transition","type":"exact"},{"name":"down-regulation of cell cycle phase transition","type":"exact"},{"name":"down-regulation of cell cycle transition","type":"exact"},{"name":"downregulation of cell cycle phase transition","type":"exact"},{"name":"downregulation of cell cycle transition","type":"exact"},{"name":"inhibition of cell cycle phase transition","type":"narrow"},{"name":"inhibition of cell cycle transition","type":"exact"},{"name":"negative regulation of cell cycle transition","type":"exact"}],"termid":"GO:1901988","terms_by_termid":{"GO:0001100":null,"GO:0007094":null,"GO:0007095":null,"GO:0010972":null,"GO:0031568":null,"GO:0031569":null,"GO:0031571":null,"GO:0031573":null,"GO:0033314":null,"GO:0033315":null,"GO:0033316":null,"GO:0044773":null,"GO:0044778":null,"GO:0044878":null,"GO:0051598":null,"GO:0090267":null,"GO:0110031":null,"GO:0140499":null,"GO:1902103":null,"GO:1902426":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:2000134":null}}


id: PBO:0061289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal PAS domain protein 1","termid":"PBO:0061289"}


id: MONDO:0002708
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the retina.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"},{"relation_name":"is_a","term_name":"posterior uveitis","termid":"MONDO:0006918"}],"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":"retinitis","secondary_identifiers":["DOID:3612","UMLS:C0035333","MEDGEN:19765","MESH:D012173","NCIT:C115993","SCTID:399463004"],"synonyms":[{"name":"inflammation of retina","type":"exact"},{"name":"retina inflammation","type":"exact"}],"termid":"MONDO:0002708","xrefs":{"Monarch":{"xref_id":"0002708"}}}


id: PBO:0051448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 4-60","termid":"PBO:0051448"}


id: PBO:0002753
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed in M-type mating cells","termid":"PBO:0002753"}


id: MONDO:0000711
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete amyotrophic lateral sclerosis type 13 (obsolete MONDO:0000711)","termid":"MONDO:0000711","xrefs":{"Monarch":{"xref_id":"0000711"}}}


id: GO:0097655
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a member of the serpin protein family (serine protease inhibitors or classified inhibitor family I4). Serpins are a broadly distributed family of protease inhibitors that use a conformational change to inhibit target enzymes. They are central in controlling many important proteolytic cascades. The majority of serpins inhibit serine proteases, but serpins that inhibit caspases and papain-like cysteine proteases have also been identified. Rarely, serpins perform a non-inhibitory function; for example, several human serpins function as hormone transporters and certain serpins function as molecular chaperones or tumor suppressors.","definition_xrefs":["InterPro:IPR000215","GOC:mr","PMID:16737556"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"serpin family protein binding","termid":"GO:0097655"}


id: SO:0002282
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Terminal inverted repeat (TIR) transposons of the superfamily Transib contain the DDE motif, which is related to the RAG1 protein involved in V(D)J recombination.","definition_xrefs":["PMID:17984973"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transib_TIR_transposon","synonyms":[{"name":"DTR transposon","type":"exact"},{"name":"Transib TIR transposon","type":"exact"},{"name":"transib transposon","type":"exact"}],"termid":"SO:0002282"}


id: PBO:0003944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Centaurin 5","termid":"PBO:0003944"}


id: MONDO:0016402
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial disease with epilepsy (obsolete MONDO:0016402)","secondary_identifiers":["Orphanet:225700"],"termid":"MONDO:0016402","xrefs":{"Monarch":{"xref_id":"0016402"}}}


id: GO:1990784
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 double-stranded DNA stimulus.","definition_xrefs":["PMID:10051633"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"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 dsDNA","synonyms":[{"name":"response to double-stranded DNA","type":"exact"}],"termid":"GO:1990784"}


id: MONDO:0006164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyp that arises from the colon or rectum. It is characterized by the presence of serrated glands and the absence of generalized dysplasia. Some authors have suggested that it is a precursor lesion for some colorectal adenocarcinomas with microsatellite instability.","definition_xrefs":["NCIT:C83176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal adenoma","termid":"MONDO:0005484"}],"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":"colorectal sessile serrated adenoma/polyp","secondary_identifiers":["MEDGEN:415420","UMLS:C2826783","EFO:1000197"],"synonyms":[{"name":"colorectal SSA","type":"exact"},{"name":"colorectal SSA/P","type":"exact"},{"name":"colorectal SSP","type":"exact"},{"name":"colorectal mixed hyperplastic adenomatous polyp","type":"exact"},{"name":"colorectal mixed hyperplastic adenomatous polyp/serrated adenoma","type":"exact"},{"name":"colorectal sessile serrated adenoma","type":"exact"},{"name":"colorectal sessile serrated adenoma/polyp","type":"exact"},{"name":"colorectal sessile serrated polyp","type":"exact"}],"termid":"MONDO:0006164","xrefs":{"Monarch":{"xref_id":"0006164"}}}


id: PBO:0038882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate cyclase 8","termid":"PBO:0038882"}


id: MONDO:0013825
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital diarrhea in which the cause of the disease is a mutation in the GUCY2C gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital diarrhea","termid":"MONDO:0000824"},{"relation_name":"is_a","term_name":"intestinal motility disease","termid":"MONDO:0021189"}],"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":"congenital diarrhea 6","secondary_identifiers":["MEDGEN:766184","DOID:0060780","GARD:17417","Orphanet:314373","UMLS:C3553270","OMIM:614616"],"synonyms":[{"name":"DIAR6","type":"related"},{"name":"GUCY2C congenital diarrhea","type":"exact"},{"name":"GUCY2C congenital diarrhoea","type":"exact"},{"name":"chronic diarrhea due to guanylate cyclase 2C overactivity","type":"exact"},{"name":"chronic diarrhoea due to guanylate cyclase 2C overactivity","type":"exact"},{"name":"congenital diarrhea caused by mutation in GUCY2C","type":"exact"},{"name":"congenital diarrhea type 6","type":"exact"},{"name":"congenital diarrhoea caused by mutation in GUCY2C","type":"exact"},{"name":"congenital diarrhoea type 6","type":"exact"},{"name":"diarrhea 6","type":"related"},{"name":"diarrhea type 6","type":"exact"},{"name":"diarrhoea 6","type":"related"},{"name":"diarrhoea type 6","type":"exact"}],"termid":"MONDO:0013825","xrefs":{"Monarch":{"xref_id":"0013825"}}}


id: GO:0061993
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: Ca2+(in) + H+(out) = Ca2+(out) + H+(in).","definition_xrefs":["PMID:19098009","PMID:28645169","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter complex","termid":"GO:1902495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"calcium:proton antiporter complex","synonyms":[{"name":"CAX1 homodimer","type":"narrow"},{"name":"CAX1-CAX3 complex","type":"narrow"},{"name":"CAX3 homodimer","type":"narrow"}],"termid":"GO:0061993"}


id: GO:0004454
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + D-fructose = ADP + D-fructose 1-phosphate.","definition_xrefs":["EC:2.7.1.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"carbohydrate kinase activity","termid":"GO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"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:0003824","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"ketohexokinase activity","secondary_identifiers":["RHEA:18145","Reactome:R-HSA-70333","Reactome:R-HSA-5656459","MetaCyc:KETOHEXOKINASE-RXN"],"synonyms":[{"name":"ATP:D-fructose 1-phosphotransferase activity","type":"related"},{"name":"hepatic fructokinase activity","type":"narrow"},{"name":"ketohexokinase (phosphorylating)","type":"related"}],"termid":"GO:0004454"}


id: MONDO:0006750
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Erdheim-Chester disease (obsolete MONDO:0006750)","termid":"MONDO:0006750","xrefs":{"Monarch":{"xref_id":"0006750"}}}


id: PBO:0050890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immediate early response 3","termid":"PBO:0050890"}


id: GO:1900321
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of maltotetraose transport.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"maltotetraose transport","termid":"GO:2001099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of maltotetraose transport","termid":"GO:1900321"}


id: PBO:0085367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphorylated protein of the mitochondrial outer membrane; localizes only to mitochondria of the bud; interacts with Myo2p to mediate mitochondrial distribution to buds; mRNA is targeted to the bud via the transport system involving She2p","termid":"PBO:0085367"}


id: GO:0160179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which iron is taken up from the contents of the intestine.","definition_xrefs":["PMID:17729393","PMID:16054062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal absorption","termid":"GO:0050892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"intestinal iron absorption","termid":"GO:0160179"}


id: PBO:0000042
data:
  {"annotation_feature_type":"gene","cv_name":"feature_relationshipprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"source_database","termid":"PBO:0000042"}


id: GO:0051625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of epinephrine into a cell, typically presynaptic neurons or glial cells. Epinephrine is a hormone produced by the medulla of the adrenal glands that increases heart activity, improves the power and prolongs the action of muscles, and increases the rate and depth of breathing. It is synthesized by the methylation of norepinephrine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"epinephrine uptake","synonyms":[{"name":"adrenaline reuptake","type":"exact"},{"name":"adrenaline uptake","type":"exact"},{"name":"epinephrine import","type":"exact"},{"name":"epinephrine reuptake","type":"exact"}],"termid":"GO:0051625"}


id: MONDO:1010625
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune thrombocytopenia that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune thrombocytopenia, non-human animal","termid":"MONDO:1010069"},{"relation_name":"is_a","term_name":"thrombocytopenia, dog","termid":"MONDO:1010659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune thrombocytopenia, dog","secondary_identifiers":["OMIA:000095-9615"],"termid":"MONDO:1010625","xrefs":{"Monarch":{"xref_id":"1010625"}}}


id: PBO:0113040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone for eEF1A; ribosome-associated chaperone dedicated to facilitating high-level expression of eEF1A; transiently binds nascent GTPase domain of eEF1A as soon as it emerges from ribosome tunnel; forms complex with NAC by binding UBA domain of Egd2p; inactivation results in disturbed proteostasis and Hsf1p activation due to abberant eEF1A biogenesis; overlapping phenotypes support notion that Chp1p functions in same eEF1A biogenesis pathway as chaperone Zpr1p-Aim29p","termid":"PBO:0113040"}


id: PBO:0117081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLXNA4 antisense RNA 1","termid":"PBO:0117081"}


id: MONDO:0017267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Self-healing collodion baby (SHCB) is a minor variant of autosomal recessive congenital ichthyosis (ARCI) characterized by the presence of a collodion membrane at birth that heals within the first weeks of life.","definition_xrefs":["Orphanet:281122"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive congenital ichthyosis","termid":"MONDO:0017265"}],"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":"self-healing collodion baby","secondary_identifiers":["MESH:C565473","UMLS:C1855789","MEDGEN:383772","GARD:17303","icd11.foundation:34721911","SCTID:718632004"],"synonyms":[{"name":"SHCB","type":"exact"},{"name":"SICI","type":"exact"},{"name":"self-improving collodion baby","type":"related"},{"name":"self-improving congenital ichthyosis","type":"exact"}],"termid":"MONDO:0017267","xrefs":{"Monarch":{"xref_id":"0017267"}}}


id: FYPO:0008164
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 kinetochore of a chromosome is abnormal during mitotic M-phase.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore during vegetative growth","termid":"FYPO:0001268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"abnormal protein localization to kinetochore during mitotic M phase","termid":"FYPO:0008164"}


id: PBO:0111819
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PQ loop","termid":"PBO:0111819"}


id: GO:0021820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that leads to the deposition of extracellular matrix signals in the marginal zone of the developing cerebral cortex. This extracellular matrix controls the movement of migrating cells. In mammals, the matrix is modified by Cajal-Retzius cells.","definition_xrefs":["PMID:12626695","GO_REF:0000021","GOC:dgh","GOC:jid","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix organization","termid":"GO:0030198"},{"relation_name":"part_of","term_name":"layer formation in cerebral cortex","termid":"GO:0021819"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"extracellular matrix organization in marginal zone involved in cerebral cortex radial glia guided migration","synonyms":[{"name":"extracellular matrix organisation in marginal zone involved in cerebral cortex radial glia guided migration","type":"exact"},{"name":"organization of extracellular matrix in the marginal zone involved in cerebral cortex glial-mediated radial migration","type":"exact"}],"termid":"GO:0021820"}


id: PBO:0048393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth arrest specific 2 like 1","termid":"PBO:0048393"}


id: PBO:0046874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAM3 metabolism regulating signaling molecule D","termid":"PBO:0046874"}


id: GO:0055093
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 stimulus indicating increased oxygen tension.","definition_xrefs":["GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to increased oxygen levels","termid":"GO:0036296"}],"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 hyperoxia","synonyms":[{"name":"response to hyperoxic stress","type":"exact"},{"name":"response to increased oxygen tension","type":"exact"}],"termid":"GO:0055093"}


id: GO:0009899
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ent-copalyl diphosphate = ent-kaur-16-ene + diphosphate.","definition_xrefs":["EC:4.2.3.19","RHEA:22220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpene synthase activity","termid":"GO:0010333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"ent-kaurene synthase activity","secondary_identifiers":["MetaCyc:4.2.3.19-RXN","KEGG_REACTION:R05092"],"synonyms":[{"name":"ent-copalyl-diphosphate diphosphate-lyase (cyclizing)","type":"related"},{"name":"ent-copalyl-diphosphate diphosphate-lyase (cyclizing, ent-kaurene-forming)","type":"related"},{"name":"ent-kaurene synthase B activity","type":"narrow"},{"name":"ent-kaurene synthetase B activity","type":"narrow"}],"termid":"GO:0009899"}


id: GO:0050766
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of phagocytosis.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endocytosis","termid":"GO:0045807"},{"relation_name":"is_a","term_name":"regulation of phagocytosis","termid":"GO:0050764"},{"relation_name":"positively_regulates","term_name":"phagocytosis","termid":"GO:0006909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of phagocytosis","synonyms":[{"name":"activation of phagocytosis","type":"narrow"},{"name":"stimulation of phagocytosis","type":"narrow"},{"name":"up regulation of phagocytosis","type":"exact"},{"name":"up-regulation of phagocytosis","type":"exact"},{"name":"upregulation of phagocytosis","type":"exact"}],"termid":"GO:0050766"}


id: PR:O59702
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- clr6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59702"],"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":"histone deacetylase clr6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC36.05c","synonyms":[{"name":"Spom972h-clr6","type":"exact"},{"name":"cryptic loci regulator 6 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O59702"}


id: PBO:0080737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WW domain containing E3 ubiquitin protein ligase 1 pseudogene 1","termid":"PBO:0080737"}


id: PBO:0061665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 43","termid":"PBO:0061665"}


id: MONDO:0011776
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic Infantile Neurological, Cutaneous, and Articular (CINCA) syndrome is characterized by skin rash, joint involvement, chronic meningitis with granulocytes and, in some cases, sensorineural hearing loss and ocular signs.","definition_xrefs":["Orphanet:1451"],"direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"},{"relation_name":"is_a","term_name":"cryopyrin-associated periodic syndrome","termid":"MONDO:0016168"}],"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":"CINCA syndrome","secondary_identifiers":["SCTID:239826001","ICD9:759.89","DOID:0090029","NANDO:2201066","NCIT:C116380","NORD:1496","GARD:1356","OMIM:607115","MEDGEN:98370","UMLS:C0409818","NANDO:1200468"],"synonyms":[{"name":"CINCA","type":"related"},{"name":"CINCA syndrome","type":"exact"},{"name":"CINCA/NOMID","type":"exact"},{"name":"Cryopyrin-associated periodic syndrome 3","type":"related"},{"name":"IOMID","type":"related"},{"name":"IOMID syndrome","type":"exact"},{"name":"NOMID","type":"exact"},{"name":"NOMID syndrome","type":"exact"},{"name":"Neonatal-Onset Multisystem Inflammatory Disease","type":"exact"},{"name":"Prieur Griscelli syndrome","type":"related"},{"name":"Prieur-Griscelli syndrome","type":"exact"},{"name":"chronic infantile neurological cutaneous and articular syndrome","type":"exact"},{"name":"chronic infantile neurological cutaneous articular syndrome","type":"exact"},{"name":"chronic neurologic cutaneous and articular syndrome","type":"exact"},{"name":"cryopyrin-associated periodic syndrome 3","type":"exact"},{"name":"infantile onset multisystem inflammatory disease","type":"related"},{"name":"infantile-onset multisystem inflammatory disease","type":"exact"},{"name":"multisystem inflammatory disease, neonatal-onset","type":"related"},{"name":"neonatal onset multisystem inflammatory disease","type":"related"},{"name":"neonatal-onset multisystem inflammatory disease","type":"exact"}],"termid":"MONDO:0011776","xrefs":{"Monarch":{"xref_id":"0011776"}}}


id: GO:0060503
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a bud in the lung increases radially.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axis elongation","termid":"GO:0003401"},{"relation_name":"part_of","term_name":"epithelial tube branching involved in lung morphogenesis","termid":"GO:0060441"}],"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":"bud dilation involved in lung branching","synonyms":[{"name":"bud expansion","type":"exact"}],"termid":"GO:0060503"}


id: GO:0001113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the melting of the DNA hybrid of the core promoter region within the transcriptional closed complex of an RNA polymerase II preinitiation complex (PIC) to produce an open complex where the DNA duplex around the transcription initiation site is unwound to form the transcription bubble.","definition_xrefs":["GOC:txnOH","PMID:15020047","PMID:18280161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription open complex formation","termid":"GO:0001112"},{"relation_name":"part_of","term_name":"transcription initiation at RNA polymerase II promoter","termid":"GO:0006367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006351","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"transcription open complex formation at RNA polymerase II promoter","synonyms":[{"name":"RNA polymerase II promoter melting","type":"exact"},{"name":"transcriptional open complex formation at RNA polymerase II promoter","type":"exact"}],"termid":"GO:0001113"}


id: MONDO:0017892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive myogenic arthrogryposis multiplex congenita is a rare inherited neuromuscular disease characterized by prenatal presentation (usually in the second trimester) of reduced fetal movements and abnormal positioning resulting in joint abnormalities that may involve both lower and upper extremities and is usually symmetric, severe hypotonia at birth with bilateral club foot, motor development delay, mild facial weakness without opthalmoplegia, absent deep tendon reflexes, normal motor and sensory nerve conduction velocities, no cerebellar or pyramidal involvement, and progressive disease course with loss of ambulation after the first decade of life.","definition_xrefs":["Orphanet:319332"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"},{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"autosomal recessive myogenic arthrogryposis multiplex congenita","secondary_identifiers":["SCTID:764812008","MEDGEN:1647450","GARD:17447","UMLS:C4707155"],"synonyms":[{"name":"SYNE1-related AMC","type":"exact"},{"name":"SYNE1-related arthrogryposis multiplex congenita","type":"exact"},{"name":"autosomal recessive myogenic AMC","type":"exact"}],"termid":"MONDO:0017892","xrefs":{"Monarch":{"xref_id":"0017892"}}}


id: PBO:0047228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 229 member B","termid":"PBO:0047228"}


id: PBO:0058039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4260","termid":"PBO:0058039"}


id: GO:0075317
data:
  {"annotated_genes":["SJAG_03501"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118260],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0075319"}]},"cv_name":"biological_process","definition":"The process that leads to the development of ascus, a sac-like structure produced by fungi of the phylum Ascomycota (sac fungi) in which sexually produced spores (ascospores), usually four or eight in number, are formed.","definition_xrefs":["GOC:di","GOC:mcc","GOC:mah","GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spore-bearing structure development","termid":"GO:0075259"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03501":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"ascus development","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0075317","terms_by_termid":{"GO:0075319":null}}


id: PBO:0038953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adiponectin receptor 1","termid":"PBO:0038953"}


id: GO:0120202
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Stack of disc membranes located inside a rod photoreceptor outer segment, and containing densely packed molecules of rhodopsin photoreceptor proteins that traverse the lipid bilayer. It is thought that rod disc membranes arise as evaginations of the ciliary membrane near the base of the outer segment, which then become completely separated from the ciliary membrane, during the development of the rod outer segment.","definition_xrefs":["PMID:6771304","GOC:krc","GOC:pde","PMID:19501669","PMID:26574505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle membrane","termid":"GO:0030659"},{"relation_name":"is_a","term_name":"photoreceptor disc membrane","termid":"GO:0097381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005575"],"is_obsolete":false,"name":"rod photoreceptor disc membrane","termid":"GO:0120202"}


id: PBO:0039359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APC membrane recruitment protein 1","termid":"PBO:0039359"}


id: PBO:0059618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ATP6 pseudogene 30","termid":"PBO:0059618"}


id: MONDO:0014042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any left ventricular noncompaction in which the cause of the disease is a mutation in the MIB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"left ventricular noncompaction","termid":"MONDO:0018901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"left ventricular noncompaction 7","secondary_identifiers":["OMIM:615092","UMLS:C3554496","GARD:15906","NCIT:C157266","MEDGEN:767410"],"synonyms":[{"name":"LVNC7","type":"related"},{"name":"MIB1 left ventricular noncompaction","type":"exact"},{"name":"left ventricular noncompaction 7","type":"exact"},{"name":"left ventricular noncompaction caused by mutation in MIB1","type":"exact"},{"name":"left ventricular noncompaction type 7","type":"exact"}],"termid":"MONDO:0014042","xrefs":{"Monarch":{"xref_id":"0014042"}}}


id: PBO:0004164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L39 (predicted)","termid":"PBO:0004164"}


id: GO:0006125
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_electron_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete thioredoxin pathway (obsolete GO:0006125)","synonyms":[{"name":"thioredoxin pathway","type":"exact"},{"name":"thioredoxin reduction","type":"narrow"}],"termid":"GO:0006125"}


id: GO:0002435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of immune complex clearance by erythrocytes. The process often starts with binding of complement receptor 1 (CR1) on the surface of erythrocytes to a complement coated immune complex. The complex bound to erythrocyte CR1 is then transported to the liver or spleen where it is presented to phagocytes. The process ends when the complex is removed from CR1, allowing the erythrocyte to return to general circulation.","definition_xrefs":["GOC:add","PMID:11414352","PMID:24022490"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune complex clearance","termid":"GO:0002434"}],"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":"immune complex clearance by erythrocytes","secondary_identifiers":["Wikipedia:Immune_complex"],"synonyms":[{"name":"immune complex clearance by RBCs","type":"exact"},{"name":"immune complex clearance by red blood cells","type":"exact"}],"termid":"GO:0002435"}


id: GO:0072591
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + citrate + L-glutamate = ADP + phosphate + beta-citryl-L-glutamate.","definition_xrefs":["PMID:20657015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"citrate-L-glutamate ligase activity","termid":"GO:0072591"}


id: PBO:0003101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA export factor, cytoplasmic nucleoporin Gle1","termid":"PBO:0003101"}


id: PBO:0004377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosylamine-glycine ligase","termid":"PBO:0004377"}


id: MONDO:0004888
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary choroidal atrophy","termid":"MONDO:0004883"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005328"],"is_obsolete":false,"name":"partial circumpapillary choroid dystrophy","secondary_identifiers":["ICD9:363.51","MEDGEN:509704","DOID:9811","SCTID:193466003","UMLS:C0154895"],"termid":"MONDO:0004888","xrefs":{"Monarch":{"xref_id":"0004888"}}}


id: PBO:0079826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ULK4 pseudogene 1","termid":"PBO:0079826"}


id: _global:has_relative_magnitude
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_relative_magnitude","termid":"_global:has_relative_magnitude"}


id: FYPO:0008025
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed during mitotic M-phase in which the localization of a protein to the CENP-A containing chromatin is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:35970865","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to CENP-A containing chromatin","termid":"FYPO:0004314"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to CENP-A containing chromatin during mitosis","synonyms":[{"name":"normal protein localization to CENP-A containing chromatin during mitotic M-phase","type":"exact"},{"name":"normal protein localization to centromeric core region chromatin during mitosis","type":"exact"}],"termid":"FYPO:0008025"}


id: GO:0035444
data:
  {"annotated_genes":["SJAG_04830"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098716"}]},"cv_name":"biological_process","definition":"The directed movement of nickel (Ni) cations across a membrane by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nickel cation transport","termid":"GO:0015675"},{"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":1,"genes_by_uniquename":{"SJAG_04830":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:0051179","GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"nickel cation transmembrane transport","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"nickel cation membrane transport","type":"exact"}],"termid":"GO:0035444","terms_by_termid":{"GO:0098716":null}}


id: SO:0001052
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0001052 nested_repeat (obsolete SO:0001052)","termid":"SO:0001052"}


id: GO:0051802
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism modulates the frequency, rate or extent of the cytolysis by that organism of cells in a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cytolysis in other organism involved in symbiotic interaction (obsolete GO:0051802)","synonyms":[{"name":"regulation of cytolysis of cells in other organism during symbiotic interaction","type":"related"},{"name":"regulation of cytolysis of cells in other organism involved in symbiotic interaction","type":"exact"}],"termid":"GO:0051802"}


id: GO:0043845
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A subcomplex of DNA polymerase III composed of the epsilon subunit which has proofreading activity, and the theta subunit which enhances the epsilon subunit's proofreading activity.","definition_xrefs":["PMID:16973612","Wikipedia:Pol_III"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"DNA polymerase III, core complex","termid":"GO:0044776"}],"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:0005634"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"DNA polymerase III, proofreading complex","synonyms":[{"name":"DNA polymerase III, proof-reading complex","type":"exact"},{"name":"DNA polymerase III, proof-reading subcomplex","type":"exact"},{"name":"DNA polymerase III, proofreading subcomplex","type":"exact"}],"termid":"GO:0043845"}


id: MONDO:0005274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0005274 (obsolete MONDO:0005274)","termid":"MONDO:0005274","xrefs":{"Monarch":{"xref_id":"0005274"}}}


id: MONDO:0005313
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Necrotizing enterocolitis (NEC) is a devastating disease that affects mostly the intestine of premature infants. The wall of the intestine is invaded by bacteria, which cause local infection and inflammation that can ultimately destroy the wall of the bowel (intestine). Such bowel wall destruction can lead to perforation of the intestine and spillage of stool into the infant's abdomen, which can result in an overwhelming infection and death.","direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"},{"relation_name":"is_a","term_name":"enterocolitis","termid":"MONDO:0009172"}],"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":"necrotizing enterocolitis","secondary_identifiers":["icd11.foundation:141267925","UMLS:C0520459","NCIT:C84915","MESH:D020345","SCTID:2707005","EFO:0003928","GARD:9767","Orphanet:391673","ICD9:777.5","MEDGEN:105440"],"synonyms":[{"name":"NEC","type":"exact"},{"name":"necrotizing enterocolitis","type":"exact"},{"name":"necrotizing enterocolitis in fetus or newborn","type":"narrow"},{"name":"necrotizing enterocolitis in foetus or newborn","type":"narrow"}],"termid":"MONDO:0005313","xrefs":{"Monarch":{"xref_id":"0005313"}}}


id: PBO:0003823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol 24-C-methyltransferase Erg6","termid":"PBO:0003823"}


id: MONDO:0042602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Samson-Viljoen syndrome","secondary_identifiers":["MESH:C537231","UMLS:C2931449","MEDGEN:419808"],"synonyms":[{"name":"Samson Viljoen syndrome","type":"related"},{"name":"lateral facial cleft, cleft lip and palate, anophthalmia, microtia, clavicular agenesis and asternia","type":"related"}],"termid":"MONDO:0042602","xrefs":{"Monarch":{"xref_id":"0042602"}}}


id: PBO:0073411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET pseudogene 15","termid":"PBO:0073411"}


id: GO:0044620
data:
  {"annotated_genes":["SJAG_01238"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000036"}]},"cv_name":"molecular_function","definition":"Binding to the attachment site of the phosphopantetheine prosthetic group of an acyl carrier protein (ACP).","definition_xrefs":["GOC:jl","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prosthetic group binding","termid":"GO:0051192"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01238":null},"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":"ACP phosphopantetheine attachment site binding","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0044620","terms_by_termid":{"GO:0000036":null}}


id: PATO:0002480
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in an bearer by virtue of the bearer's possessing only minor levels of ossification.","definition_xrefs":["PATOC:AD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ossified","termid":"PATO:0001448"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poorly ossified","termid":"PATO:0002480"}


id: MONDO:0100553
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any open angle glaucoma in which the cause of the disease is a mutation in the OPTN gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"open-angle glaucoma","termid":"MONDO:0005338"},{"relation_name":"is_a","term_name":"hereditary glaucoma","termid":"MONDO:0018174"}],"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":"OPTN-related open angle glaucoma","secondary_identifiers":["MEDGEN:87389","UMLS:C0339573","OMIM:137760"],"synonyms":[{"name":"OPTN-related open angle glaucoma","type":"exact"},{"name":"glaucoma 1, open angle, E","type":"exact"}],"termid":"MONDO:0100553","xrefs":{"Monarch":{"xref_id":"0100553"}}}


id: PBO:0091203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asp","termid":"PBO:0091203"}


id: PBO:0051560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 11 receptor subunit alpha","termid":"PBO:0051560"}


id: GO:0047572
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-phospho-D-glycerate + H2O = D-glycerate + phosphate.","definition_xrefs":["EC:3.1.3.38","RHEA:12412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016788"],"is_obsolete":false,"name":"3-phosphoglycerate phosphatase activity","secondary_identifiers":["MetaCyc:3-PHOSPHOGLYCERATE-PHOSPHATASE-RXN","KEGG_REACTION:R01511"],"synonyms":[{"name":"3-PGA phosphatase activity","type":"related"},{"name":"D-3-phosphoglycerate phosphatase activity","type":"related"},{"name":"D-glycerate-3-phosphate phosphohydrolase activity","type":"related"}],"termid":"GO:0047572"}


id: GO:0097659
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The synthesis of an RNA transcript from a nucleic acid template (DNA or RNA).","definition_xrefs":["GOC:txnOH","GOC:vw","GOC:pr"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleic acid-templated transcription (obsolete GO:0097659)","termid":"GO:0097659"}


id: MONDO:0030927
data:
  {"annotated_genes":["SJAG_00750"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85559],"is_not":false,"summary":null,"term":"MONDO:0030927"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00750":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myofibrillar myopathy 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1782465","DOID:0081338","UMLS:C5543038","OMIM:619178"],"synonyms":[{"name":"MFM11","type":"exact"},{"name":"myofibrillar myopathy 11","type":"exact"},{"name":"myopathy, congenital, with eccentric cores","type":"exact"}],"termid":"MONDO:0030927","terms_by_termid":{"MONDO:0030927":null},"xrefs":{"Monarch":{"xref_id":"0030927"}}}


id: GO:0019435
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sophorosyloxydocosanoate, 13-sophorosyloxydocosanoate 6',6''-diacetate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"},{"relation_name":"is_a","term_name":"sophorosyloxydocosanoate metabolic process","termid":"GO:0019434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"sophorosyloxydocosanoate biosynthetic process","secondary_identifiers":["MetaCyc:SOPHOROSYLOXYDOCOSANOATE-SYN-PWY"],"synonyms":[{"name":"sophorosyloxydocosanoate anabolism","type":"exact"},{"name":"sophorosyloxydocosanoate biosynthesis","type":"exact"},{"name":"sophorosyloxydocosanoate formation","type":"exact"},{"name":"sophorosyloxydocosanoate synthesis","type":"exact"}],"termid":"GO:0019435"}


id: PBO:0057979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3714","termid":"PBO:0057979"}


id: PBO:0064892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 regulatory subunit B''alpha","termid":"PBO:0064892"}


id: BFO:0000050
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"a core relation that holds between a part and its whole","direct_ancestors":[{"relation_name":"is_a","term_name":"overlaps","termid":"RO:0002131"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"},{"relation_name":"is_a","term_name":"overlaps","termid":"_global:overlaps"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"part_of","secondary_identifiers":["BFO:0000050","OBO_REL:part_of"],"synonyms":[{"name":"part of","type":"exact"}],"termid":"BFO:0000050"}


id: PBO:0011144
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondria microtubule binder","termid":"PBO:0011144"}


id: PBO:0067592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 753, pseudogene","termid":"PBO:0067592"}


id: GO:1901866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of capsorubin.","definition_xrefs":["UniPathway:UPA00807","MetaCyc:PWY-5174","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll biosynthetic process","termid":"GO:0016123"},{"relation_name":"is_a","term_name":"capsorubin metabolic process","termid":"GO:1901864"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"capsorubin biosynthetic process","synonyms":[{"name":"capsorubin anabolism","type":"exact"},{"name":"capsorubin biosynthesis","type":"exact"},{"name":"capsorubin formation","type":"exact"},{"name":"capsorubin synthesis","type":"exact"}],"termid":"GO:1901866"}


id: PBO:0054370
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 1764","termid":"PBO:0054370"}


id: PBO:0113299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in aromatic amino acid biosynthesis; up-regulated following GCN4 induction, amino acid starvation, rapamycin treatment in GCN4-dependent manner; promoter contains Gcn4 control response element, which is bound by Gcn4p in vivo","termid":"PBO:0113299"}


id: FYPO:0001255
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 the level of oxygen is higher than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"increased protein level during cellular response to oxygen","synonyms":[{"name":"increased protein accumulation during cellular response to oxygen","type":"related"},{"name":"increased protein level during cellular response to oxygen during mitotic cell cycle","type":"related"},{"name":"increased protein level during cellular response to oxygen during vegetative growth","type":"exact"},{"name":"increased protein level during cellular response to oxygen levels","type":"exact"}],"termid":"FYPO:0001255"}


id: PBO:0052316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1143","termid":"PBO:0052316"}


id: MONDO:1011442
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Enteropathy-associated T cell lymphoma that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-hodgkin lymphoma, non-human animal","termid":"MONDO:1010214"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enteropathy-associated T cell lymphoma, non-human animal","secondary_identifiers":["OMIA:002526"],"termid":"MONDO:1011442","xrefs":{"Monarch":{"xref_id":"1011442"}}}


id: MONDO:0014047
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Cowden disease in which the cause of the disease is a mutation in the PIK3CA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Cowden disease","termid":"MONDO:0016063"},{"relation_name":"is_a","term_name":"PIK3CA-related overgrowth spectrum","termid":"MONDO:1040002"}],"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 5","secondary_identifiers":["DOID:0081001","OMIM:615108","UMLS:C3554518","GARD:16464","MEDGEN:767432"],"synonyms":[{"name":"CWS5","type":"related"},{"name":"Cowden disease caused by mutation in PIK3CA","type":"exact"},{"name":"Cowden syndrome 5","type":"exact"},{"name":"Cowden syndrome type 5","type":"exact"},{"name":"PIK3CA Cowden disease","type":"exact"}],"termid":"MONDO:0014047","xrefs":{"Monarch":{"xref_id":"0014047"}}}


id: MONDO:1010546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microvillus inclusion disease that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microvillus inclusion disease, non-human animal","termid":"MONDO:1010044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microvillus inclusion disease, pig","secondary_identifiers":["OMIA:002247-9823"],"termid":"MONDO:1010546","xrefs":{"Monarch":{"xref_id":"1010546"}}}


id: GO:0032730
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interleukin-1 alpha production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of interleukin-1 alpha production","termid":"GO:0032650"},{"relation_name":"is_a","term_name":"positive regulation of interleukin-1 production","termid":"GO:0032732"},{"relation_name":"positively_regulates","term_name":"interleukin-1 alpha production","termid":"GO:0032610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of interleukin-1 alpha production","secondary_identifiers":["GO:0050717","GO:0050726"],"synonyms":[{"name":"activation of interleukin-1 alpha production","type":"narrow"},{"name":"positive regulation of IL-1 alpha production","type":"exact"},{"name":"positive regulation of interleukin-1 alpha biosynthetic process","type":"narrow"},{"name":"positive regulation of interleukin-1 alpha secretion","type":"narrow"},{"name":"stimulation of interleukin-1 alpha production","type":"narrow"},{"name":"up regulation of interleukin-1 alpha production","type":"exact"},{"name":"up-regulation of interleukin-1 alpha production","type":"exact"},{"name":"upregulation of interleukin-1 alpha production","type":"exact"}],"termid":"GO:0032730"}


id: PBO:0056128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysosomal trafficking regulator","termid":"PBO:0056128"}


id: PBO:0001524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scaffold protein Scd2","termid":"PBO:0001524"}


id: PBO:0049300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase mu 3","termid":"PBO:0049300"}


id: PBO:0043237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride voltage-gated channel Ka","termid":"PBO:0043237"}


id: PBO:0026739
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_ethionine","termid":"PBO:0026739"}


id: GO:0071640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of macrophage inflammatory protein 1 alpha.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemokine production","termid":"GO:0032642"},{"relation_name":"regulates","term_name":"macrophage inflammatory protein-1 alpha production","termid":"GO:0071608"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of macrophage inflammatory protein 1 alpha production","synonyms":[{"name":"regulation of CCL3 production","type":"exact"},{"name":"regulation of MIP-1a production","type":"exact"},{"name":"regulation of chemokine (C-C motif) ligand 3 production","type":"exact"},{"name":"regulation of macrophage inflammatory protein production","type":"broad"}],"termid":"GO:0071640"}


id: MONDO:0009004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete combined inflammatory and immunologic defect (obsolete MONDO:0009004)","termid":"MONDO:0009004","xrefs":{"Monarch":{"xref_id":"0009004"}}}


id: PR:O74483
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U6 snRNA-associated Sm-like protein LSm8 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR15588:SF5","OMA:SCHPO05010","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":"U6 snRNA-associated Sm-like protein LSm8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1840.10","secondary_identifiers":["UniProtKB:O74483"],"synonyms":[{"name":"Spom972h-LSM8","type":"exact"}],"termid":"PR:O74483"}


id: PBO:0073614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SID1 transmembrane family member 1","termid":"PBO:0073614"}


id: GO:1902314
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to hydroquinone.","definition_xrefs":["GOC:TermGenie","GOC:bhm","PMID:15667223"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"hydroquinone binding","synonyms":[{"name":"quinol binding","type":"exact"}],"termid":"GO:1902314"}


id: GO:2000798
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of amniotic stem cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mesenchymal stem cell differentiation","termid":"GO:2000740"},{"relation_name":"is_a","term_name":"regulation of amniotic stem cell differentiation","termid":"GO:2000797"},{"relation_name":"negatively_regulates","term_name":"amniotic stem cell differentiation","termid":"GO:0097086"}],"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 amniotic stem cell differentiation","termid":"GO:2000798"}


id: PBO:0078704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon CAA) 6-1","termid":"PBO:0078704"}


id: RO:HOM0000048
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Orthology that involves two genes that experienced duplications more recent than the species split that created them.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_orthology_relationship_with","termid":"RO:HOM0000017"},{"relation_name":"is_a","term_name":"in_many_to_many_homology_relationship_with","termid":"RO:HOM0000036"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_many_to_many_orthology_relationship_with","synonyms":[{"name":"co-orthology","type":"related"},{"name":"many to many orthologous to","type":"exact"},{"name":"many-to-many orthology","type":"exact"},{"name":"many:many orthology","type":"exact"},{"name":"trans-homology","type":"related"},{"name":"trans-orthology","type":"exact"}],"termid":"RO:HOM0000048"}


id: MONDO:0007651
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"}],"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":"gastrocutaneous syndrome","secondary_identifiers":["MEDGEN:338154","icd11.foundation:1431211717","GARD:2438","MESH:C535651","OMIM:137270","Orphanet:2069","UMLS:C1850899"],"synonyms":[{"name":"gastrocutaneous syndrome","type":"exact"},{"name":"peptic Ulcer/hiatal hernia, multiple lentigines/cafe-Au-lait Spots, hypertelorism, myopia","type":"related"}],"termid":"MONDO:0007651","xrefs":{"Monarch":{"xref_id":"0007651"}}}


id: MONDO:0015174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune enteropathy","termid":"MONDO:0019787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"autoimmune enteropathy type 3","secondary_identifiers":["Orphanet:103917","icd11.foundation:1137579941"],"termid":"MONDO:0015174","xrefs":{"Monarch":{"xref_id":"0015174"}}}


id: GO:0098017
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The part of the viral capsid that comprises the most common capsomere type. For example, in a T=3 icosahedral capsid, which is composed of 12 pentameric and 20 hexameric capsomeres, the hexameric capsomeres are major subunits.","definition_xrefs":["GOC:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"capsomere","termid":"GO:0046727"}],"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":"viral capsid, major subunit","synonyms":[{"name":"major capsomere","type":"exact"},{"name":"major head protein","type":"related"}],"termid":"GO:0098017"}


id: PBO:0058384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4756","termid":"PBO:0058384"}


id: GO:1901122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving bacitracin A.","definition_xrefs":["GOC:TermGenie","GOC:yaf","UniPathway:UPA00179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"bacitracin A metabolic process","synonyms":[{"name":"bacitracin A metabolism","type":"exact"}],"termid":"GO:1901122"}


id: PBO:0004242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium-dependent serine/threonine protein phosphatase calcineurin, catalytic subunit Ppb1","termid":"PBO:0004242"}


id: GO:0043169
data:
  {"annotated_genes":["SJAG_04859","SJAG_03855","SJAG_03985","SJAG_01648","SJAG_01584","SJAG_00964","SJAG_03227","SJAG_05010","SJAG_05118","SJAG_00946","SJAG_01734","SJAG_03883","SJAG_01137","SJAG_03370","SJAG_00719","SJAG_02253","SJAG_04679","SJAG_04579","SJAG_01212","SJAG_03945","SJAG_05223","SJAG_01075","SJAG_00406","SJAG_01575","SJAG_01707","SJAG_04584","SJAG_02464","SJAG_05337","SJAG_03771","SJAG_00552","SJAG_00188","SJAG_00032","SJAG_04516","SJAG_02689","SJAG_04410","SJAG_00701","SJAG_02340","SJAG_01325","SJAG_04024","SJAG_02203","SJAG_02741","SJAG_02897","SJAG_00119","SJAG_01150","SJAG_04641","SJAG_04791","SJAG_01626","SJAG_00399","SJAG_00181","SJAG_04213","SJAG_03388","SJAG_04788","SJAG_03430","SJAG_00865","SJAG_00464","SJAG_00485","SJAG_03578","SJAG_02730","SJAG_01858","SJAG_02247","SJAG_00988","SJAG_03588","SJAG_00249","SJAG_03599","SJAG_04621","SJAG_00439","SJAG_01400","SJAG_01046","SJAG_02954","SJAG_03225","SJAG_00309","SJAG_01731","SJAG_04249","SJAG_04768","SJAG_02080","SJAG_00173","SJAG_01765","SJAG_04080","SJAG_00500","SJAG_02261","SJAG_00204","SJAG_01694","SJAG_00934","SJAG_01372","SJAG_03822","SJAG_01044","SJAG_02582","SJAG_04724","SJAG_00403","SJAG_04407","SJAG_01523","SJAG_03893","SJAG_04043","SJAG_03496","SJAG_04051","SJAG_02763","SJAG_03051","SJAG_03153","SJAG_03286","SJAG_03983","SJAG_MIT04","SJAG_02786","SJAG_03665","SJAG_03398","SJAG_01948","SJAG_03142","SJAG_02369","SJAG_03548","SJAG_02206","SJAG_04242","SJAG_00561","SJAG_03850","SJAG_00096","SJAG_04913","SJAG_00337","SJAG_03241","SJAG_04487","SJAG_04743","SJAG_02668","SJAG_02149","SJAG_03362","SJAG_01004","SJAG_04842","SJAG_01715","SJAG_00063","SJAG_04189","SJAG_02348","SJAG_03112","SJAG_02746","SJAG_02349","SJAG_00832","SJAG_00577","SJAG_04553","SJAG_03695","SJAG_02461","SJAG_03911","SJAG_00610","SJAG_01194","SJAG_00509","SJAG_02007","SJAG_02347","SJAG_00664","SJAG_01684","SJAG_04373","SJAG_06599","SJAG_03191","SJAG_03761","SJAG_03831","SJAG_04765","SJAG_03939","SJAG_03005","SJAG_03268","SJAG_05264","SJAG_00081","SJAG_00456","SJAG_03032","SJAG_04048","SJAG_04865","SJAG_00321","SJAG_04183","SJAG_00402","SJAG_02399","SJAG_02796","SJAG_06576","SJAG_01498","SJAG_01572","SJAG_00013","SJAG_00116","SJAG_04619","SJAG_00527","SJAG_01281","SJAG_03613","SJAG_02138","SJAG_03135","SJAG_02903","SJAG_02794","SJAG_03943","SJAG_03249","SJAG_01740","SJAG_01776","SJAG_05345","SJAG_03519","SJAG_04990","SJAG_03465","SJAG_03862","SJAG_01088","SJAG_02694","SJAG_03723","SJAG_03755","SJAG_05274","SJAG_02447","SJAG_06636","SJAG_01404","SJAG_02459","SJAG_04574","SJAG_04309","SJAG_00304","SJAG_04238","SJAG_03884","SJAG_01574","SJAG_02043","SJAG_04429","SJAG_02990","SJAG_04915","SJAG_03562","SJAG_01129","SJAG_02252","SJAG_06639","SJAG_02808","SJAG_04425","SJAG_02290","SJAG_01929","SJAG_06642","SJAG_03103","SJAG_01600","SJAG_05173","SJAG_05343","SJAG_01254","SJAG_01560","SJAG_02299","SJAG_01507","SJAG_00044","SJAG_05105","SJAG_03029","SJAG_01992","SJAG_00502","SJAG_00067","SJAG_03840","SJAG_MIT20","SJAG_04970","SJAG_02938","SJAG_00498","SJAG_00166","SJAG_02627","SJAG_00532","SJAG_03689","SJAG_03254","SJAG_01450","SJAG_03643","SJAG_02370","SJAG_02521","SJAG_02539","SJAG_02199","SJAG_03811","SJAG_01859","SJAG_00449","SJAG_03018","SJAG_03538","SJAG_00827","SJAG_04151","SJAG_01533","SJAG_03482","SJAG_03974","SJAG_02583","SJAG_05353","SJAG_04972","SJAG_00755","SJAG_00926","SJAG_01996","SJAG_04089","SJAG_05237","SJAG_02691","SJAG_01673","SJAG_02511","SJAG_04368","SJAG_03175","SJAG_03879","SJAG_03396","SJAG_03539","SJAG_01511","SJAG_03976","SJAG_03918","SJAG_01351","SJAG_03473","SJAG_01269","SJAG_01787","SJAG_00644","SJAG_04789","SJAG_03626","SJAG_00724","SJAG_00296","SJAG_01179","SJAG_02851","SJAG_00751","SJAG_01200","SJAG_01457","SJAG_04781","SJAG_03185","SJAG_00074","SJAG_03120","SJAG_01226","SJAG_04571","SJAG_01414","SJAG_03071","SJAG_02575","SJAG_00163","SJAG_01665","SJAG_03743","SJAG_01945","SJAG_03647","SJAG_04496","SJAG_04898","SJAG_05239","SJAG_04882","SJAG_01854","SJAG_05373","SJAG_03303","SJAG_03628","SJAG_04434","SJAG_04396","SJAG_03984","SJAG_04991","SJAG_01875","SJAG_00510","SJAG_01896","SJAG_02503","SJAG_01535","SJAG_02813","SJAG_01910","SJAG_02215","SJAG_03313","SJAG_04448","SJAG_04336","SJAG_05245","SJAG_01583","SJAG_04682","SJAG_00792","SJAG_05003","SJAG_00134","SJAG_03428","SJAG_00410","SJAG_03387","SJAG_02397","SJAG_00228","SJAG_04106","SJAG_02629","SJAG_02766","SJAG_02652","SJAG_02532","SJAG_01772","SJAG_03276","SJAG_00668","SJAG_04449","SJAG_00475","SJAG_03744","SJAG_02709","SJAG_02734","SJAG_00052","SJAG_02277","SJAG_04414","SJAG_01284","SJAG_00989","SJAG_03861","SJAG_02659","SJAG_00451","SJAG_01768","SJAG_01298","SJAG_02381","SJAG_01669","SJAG_05344","SJAG_06022","SJAG_02908","SJAG_04233","SJAG_01637","SJAG_01930","SJAG_01593","SJAG_01630","SJAG_00819","SJAG_04391","SJAG_03090","SJAG_01997","SJAG_04030","SJAG_01253","SJAG_03734","SJAG_03750","SJAG_00386","SJAG_03697","SJAG_05311","SJAG_03096","SJAG_01280","SJAG_03405","SJAG_02569","SJAG_04896","SJAG_03088","SJAG_04901","SJAG_01321","SJAG_04845","SJAG_02048","SJAG_02165","SJAG_01702","SJAG_03275","SJAG_01418","SJAG_05323","SJAG_01209","SJAG_01149","SJAG_02415","SJAG_04757","SJAG_04217","SJAG_01029","SJAG_04205","SJAG_04403","SJAG_00467","SJAG_01832","SJAG_05679","SJAG_05398","SJAG_03140","SJAG_02510","SJAG_00341","SJAG_03324","SJAG_04016","SJAG_03043","SJAG_02406","SJAG_01310","SJAG_02096","SJAG_02785","SJAG_03346","SJAG_04538","SJAG_02003","SJAG_03044","SJAG_02847","SJAG_01355","SJAG_02319","SJAG_00221","SJAG_04747","SJAG_03322","SJAG_01430","SJAG_01140","SJAG_00037","SJAG_03752","SJAG_05242","SJAG_03255","SJAG_02052","SJAG_02589","SJAG_02033","SJAG_00501","SJAG_00642","SJAG_00853","SJAG_03813","SJAG_05338","SJAG_00555","SJAG_00727","SJAG_00483","SJAG_00199","SJAG_00237","SJAG_02956","SJAG_01672","SJAG_02648","SJAG_05273","SJAG_01110","SJAG_04886","SJAG_05209","SJAG_04292","SJAG_03326","SJAG_01375","SJAG_04726","SJAG_02752","SJAG_02679","SJAG_02433","SJAG_00637","SJAG_05012","SJAG_04712","SJAG_00717","SJAG_03886","SJAG_04063","SJAG_02019","SJAG_03615","SJAG_03635","SJAG_00209","SJAG_03222","SJAG_04374","SJAG_00669","SJAG_00225","SJAG_01797","SJAG_04479","SJAG_03006","SJAG_03793","SJAG_03658","SJAG_04297","SJAG_03657","SJAG_03183","SJAG_01542","SJAG_03022","SJAG_03448","SJAG_06597","SJAG_03812","SJAG_05354","SJAG_03240","SJAG_05236","SJAG_00240","SJAG_05192","SJAG_04466","SJAG_03250","SJAG_01728","SJAG_00396","SJAG_03373","SJAG_01465","SJAG_00381","SJAG_02169","SJAG_00612","SJAG_06611","SJAG_04054","SJAG_01081","SJAG_00752","SJAG_04362","SJAG_03930","SJAG_02298","SJAG_01052","SJAG_03393","SJAG_04966","SJAG_00803","SJAG_03968","SJAG_03180","SJAG_01686","SJAG_04013","SJAG_01165","SJAG_04353","SJAG_00758","SJAG_05234","SJAG_03509","SJAG_00153","SJAG_04677","SJAG_01266","SJAG_02334","SJAG_00896","SJAG_04998","SJAG_00638","SJAG_04533","SJAG_03982","SJAG_01955","SJAG_04129","SJAG_03866","SJAG_00742","SJAG_00251","SJAG_02435","SJAG_02963","SJAG_03196","SJAG_00802","SJAG_01677","SJAG_03230","SJAG_02818","SJAG_02107","SJAG_00353","SJAG_00072","SJAG_00923","SJAG_01313","SJAG_01760","SJAG_00412","SJAG_05243","SJAG_00910","SJAG_00124","SJAG_03618","SJAG_03231","SJAG_00436","SJAG_00111","SJAG_00461","SJAG_05200","SJAG_00045","SJAG_00706","SJAG_02587","SJAG_00231"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58893,61789,63452,64877,117014],"is_not":false,"summary":null,"term":"GO:0043169"},{"annotations":[69935,68441,88840,73820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016208"},{"annotations":[97356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046870"},{"annotations":[60220,67921,117556,59653,68927,78861,59957,101637,106138,59209,66596,112328,117022,118228,67706,58873,96269,59271,60096,66479,72081,118897,65721,61076,78116,103628,108074,59828,67270,60589,108310,58832,113783,73942,117666,111041,78471,79305,63659,105303,106490,68928,68979,61209,60100,89569,108688,59586,74908,102860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005509"},{"annotations":[68630,78003,106877,115059,117081,119107,119058,102128,74230,77669,66100,61284,74892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005507"},{"annotations":[71418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008199"},{"annotations":[66791,71417,77947,100576,101227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008198"},{"annotations":[74148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016594"},{"annotations":[94034,112815,117389,57071,59919,60065,61764,75080,58703,63478,73623,79801,57134,68014,77496,59032,67466,59577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005506"},{"annotations":[59990,65320,68502,58138,64244,67291,64419,97195,105925,90275,58869,91640,79879,91428,103761,61519,68227,60593,56949,102939,62688,62454,58578,67763,79424,60863,60490,61662,57659,59126,61099,61690,67497,68476,57744,70909,77489,58360,62672,88655,99848,56983,63251,67757,91522,62507,57128,64974,61252,58019,65525,63361,65983,65779,101108,110157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000287"},{"annotations":[65994,60101,77071,99849,105775,70339,68259,115687,105926,57779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030145"},{"annotations":[93284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046911"},{"annotations":[62404,59880,60716,59322,67943,69143,60524,69369,73684,63938,62704,92246,66676,103292,104744,60819,63136,57720,69409,102775,60286,57972,64148,61494,57674,67235,66798,69355,60501,63278,62244,64048,64260,59272,66375,66766,79138,58649,65389,65885,57044,66731,58077,59408,65867,64976,62837,65264,96166,96403,60238,63349,59834,62987,61434],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046872"},{"annotations":[58971,65294,65509,58702,59312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016151"},{"annotations":[69718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031210"},{"annotations":[68478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030955"},{"annotations":[87659,87658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901691"},{"annotations":[97840,57345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904047"},{"annotations":[67005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030975"},{"annotations":[61691,64420,58579,58870,57597,73075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030976"},{"annotations":[64113,65520,112981,60319,61082,61682,64239,64565,91507,95694,109586,61604,64550,59277,58883,67547,90363,66661,66702,61741,60091,60419,60833,64083,66623,68739,69280,65065,66252,87980,60740,109565,67100,60049,64443,57360,66195,67541,68177,63628,98148,56974,62707,67955,64243,62899,65101,66725,68646,76456,57420,62298,64564,67607,115692,101704,91609,63045,65416,70989,60230,62744,65110,63687,65295,67207,69479,97422,105752,69612,92971,114264,63359,98972,65433,64913,60278,66877,61941,112217,97939,78953,71557,62785,99506,65783,63954,107897,64583,63974,66077,57676,61318,67355,67621,68797,113685,59964,114640,62261,62073,66033,61241,63034,66935,68675,67584,59213,63287,102748,89487,112978,59900,66415,72537,61757,67245,64386,60017,57137,66648,94468,58642,66255,66430,65838,69086,90723,59055,118068,106840,57935,111876,113160,65827,60460,63236,102799,87454,66185,62928,60838,61166,64780,71299,113657,60371,62655,65900,65642,57718,72598,59012,62628,59377,62079,78344,64024,90166,61660,90554,57644,61583,96568,62135,67087,99804,65464,66913,103578,58815,115719,90140,61554,57069,112979,64909,57058,58867,60782,62198,76941,75057,63770,62168,59388,64079,63848,103605,65115,65442,65895,66174,68838,65757,69131,95388,96654,60500,61815,64817,68929,68862,62009,68273,59018,69423,61961,67580,66465,69459,66154,89938,60150,62151,68825,67059,57610,61352,67417,61064,65795,59313,72861,58218,98307,112218,58738,62956,110690,68114,60991,78100,59624,60264,60345,60788,64791,104891,117352,60692,62767,64885,58602,67434,77085,89505,102335,105032,62724,94982,59587,57158,59709,97605,107644,59836,67180,69108,58107,68350,61632,88563,62594,56913,58741,60801,58223,64950,66994,99805,58162,57500,62137,66671,108251,58428,59636,65187,66792,58323,90209,58341,118882,64347,64311,69002,91903,65012,64703,69000,63296,94070,67474,68167,60835,65061,67284,63429,75070,67461,57363,59281,60375,60399,67967,60848,62872,69744,105751,64334,115759,57307,63742,112977,66131,114675,88266,57649,88990,63015,63190,66677,65972,87348,65907,62702,58572,61391,64074,61529,66043,66355,57580,58472,63885,64478,67725,116022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008270"}]},"cv_name":"molecular_function","definition":"Binding to a cation, a charged atom or group of atoms with a net positive charge.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ion binding","termid":"GO:0043167"}],"gene_count":560,"genes_by_uniquename":{"SJAG_00013":null,"SJAG_00032":null,"SJAG_00037":null,"SJAG_00044":null,"SJAG_00045":null,"SJAG_00052":null,"SJAG_00063":null,"SJAG_00067":null,"SJAG_00072":null,"SJAG_00074":null,"SJAG_00081":null,"SJAG_00096":null,"SJAG_00111":null,"SJAG_00116":null,"SJAG_00119":null,"SJAG_00124":null,"SJAG_00134":null,"SJAG_00153":null,"SJAG_00163":null,"SJAG_00166":null,"SJAG_00173":null,"SJAG_00181":null,"SJAG_00188":null,"SJAG_00199":null,"SJAG_00204":null,"SJAG_00209":null,"SJAG_00221":null,"SJAG_00225":null,"SJAG_00228":null,"SJAG_00231":null,"SJAG_00237":null,"SJAG_00240":null,"SJAG_00249":null,"SJAG_00251":null,"SJAG_00296":null,"SJAG_00304":null,"SJAG_00309":null,"SJAG_00321":null,"SJAG_00337":null,"SJAG_00341":null,"SJAG_00353":null,"SJAG_00381":null,"SJAG_00386":null,"SJAG_00396":null,"SJAG_00399":null,"SJAG_00402":null,"SJAG_00403":null,"SJAG_00406":null,"SJAG_00410":null,"SJAG_00412":null,"SJAG_00436":null,"SJAG_00439":null,"SJAG_00449":null,"SJAG_00451":null,"SJAG_00456":null,"SJAG_00461":null,"SJAG_00464":null,"SJAG_00467":null,"SJAG_00475":null,"SJAG_00483":null,"SJAG_00485":null,"SJAG_00498":null,"SJAG_00500":null,"SJAG_00501":null,"SJAG_00502":null,"SJAG_00509":null,"SJAG_00510":null,"SJAG_00527":null,"SJAG_00532":null,"SJAG_00552":null,"SJAG_00555":null,"SJAG_00561":null,"SJAG_00577":null,"SJAG_00610":null,"SJAG_00612":null,"SJAG_00637":null,"SJAG_00638":null,"SJAG_00642":null,"SJAG_00644":null,"SJAG_00664":null,"SJAG_00668":null,"SJAG_00669":null,"SJAG_00701":null,"SJAG_00706":null,"SJAG_00717":null,"SJAG_00719":null,"SJAG_00724":null,"SJAG_00727":null,"SJAG_00742":null,"SJAG_00751":null,"SJAG_00752":null,"SJAG_00755":null,"SJAG_00758":null,"SJAG_00792":null,"SJAG_00802":null,"SJAG_00803":null,"SJAG_00819":null,"SJAG_00827":null,"SJAG_00832":null,"SJAG_00853":null,"SJAG_00865":null,"SJAG_00896":null,"SJAG_00910":null,"SJAG_00923":null,"SJAG_00926":null,"SJAG_00934":null,"SJAG_00946":null,"SJAG_00964":null,"SJAG_00988":null,"SJAG_00989":null,"SJAG_01004":null,"SJAG_01029":null,"SJAG_01044":null,"SJAG_01046":null,"SJAG_01052":null,"SJAG_01075":null,"SJAG_01081":null,"SJAG_01088":null,"SJAG_01110":null,"SJAG_01129":null,"SJAG_01137":null,"SJAG_01140":null,"SJAG_01149":null,"SJAG_01150":null,"SJAG_01165":null,"SJAG_01179":null,"SJAG_01194":null,"SJAG_01200":null,"SJAG_01209":null,"SJAG_01212":null,"SJAG_01226":null,"SJAG_01253":null,"SJAG_01254":null,"SJAG_01266":null,"SJAG_01269":null,"SJAG_01280":null,"SJAG_01281":null,"SJAG_01284":null,"SJAG_01298":null,"SJAG_01310":null,"SJAG_01313":null,"SJAG_01321":null,"SJAG_01325":null,"SJAG_01351":null,"SJAG_01355":null,"SJAG_01372":null,"SJAG_01375":null,"SJAG_01400":null,"SJAG_01404":null,"SJAG_01414":null,"SJAG_01418":null,"SJAG_01430":null,"SJAG_01450":null,"SJAG_01457":null,"SJAG_01465":null,"SJAG_01498":null,"SJAG_01507":null,"SJAG_01511":null,"SJAG_01523":null,"SJAG_01533":null,"SJAG_01535":null,"SJAG_01542":null,"SJAG_01560":null,"SJAG_01572":null,"SJAG_01574":null,"SJAG_01575":null,"SJAG_01583":null,"SJAG_01584":null,"SJAG_01593":null,"SJAG_01600":null,"SJAG_01626":null,"SJAG_01630":null,"SJAG_01637":null,"SJAG_01648":null,"SJAG_01665":null,"SJAG_01669":null,"SJAG_01672":null,"SJAG_01673":null,"SJAG_01677":null,"SJAG_01684":null,"SJAG_01686":null,"SJAG_01694":null,"SJAG_01702":null,"SJAG_01707":null,"SJAG_01715":null,"SJAG_01728":null,"SJAG_01731":null,"SJAG_01734":null,"SJAG_01740":null,"SJAG_01760":null,"SJAG_01765":null,"SJAG_01768":null,"SJAG_01772":null,"SJAG_01776":null,"SJAG_01787":null,"SJAG_01797":null,"SJAG_01832":null,"SJAG_01854":null,"SJAG_01858":null,"SJAG_01859":null,"SJAG_01875":null,"SJAG_01896":null,"SJAG_01910":null,"SJAG_01929":null,"SJAG_01930":null,"SJAG_01945":null,"SJAG_01948":null,"SJAG_01955":null,"SJAG_01992":null,"SJAG_01996":null,"SJAG_01997":null,"SJAG_02003":null,"SJAG_02007":null,"SJAG_02019":null,"SJAG_02033":null,"SJAG_02043":null,"SJAG_02048":null,"SJAG_02052":null,"SJAG_02080":null,"SJAG_02096":null,"SJAG_02107":null,"SJAG_02138":null,"SJAG_02149":null,"SJAG_02165":null,"SJAG_02169":null,"SJAG_02199":null,"SJAG_02203":null,"SJAG_02206":null,"SJAG_02215":null,"SJAG_02247":null,"SJAG_02252":null,"SJAG_02253":null,"SJAG_02261":null,"SJAG_02277":null,"SJAG_02290":null,"SJAG_02298":null,"SJAG_02299":null,"SJAG_02319":null,"SJAG_02334":null,"SJAG_02340":null,"SJAG_02347":null,"SJAG_02348":null,"SJAG_02349":null,"SJAG_02369":null,"SJAG_02370":null,"SJAG_02381":null,"SJAG_02397":null,"SJAG_02399":null,"SJAG_02406":null,"SJAG_02415":null,"SJAG_02433":null,"SJAG_02435":null,"SJAG_02447":null,"SJAG_02459":null,"SJAG_02461":null,"SJAG_02464":null,"SJAG_02503":null,"SJAG_02510":null,"SJAG_02511":null,"SJAG_02521":null,"SJAG_02532":null,"SJAG_02539":null,"SJAG_02569":null,"SJAG_02575":null,"SJAG_02582":null,"SJAG_02583":null,"SJAG_02587":null,"SJAG_02589":null,"SJAG_02627":null,"SJAG_02629":null,"SJAG_02648":null,"SJAG_02652":null,"SJAG_02659":null,"SJAG_02668":null,"SJAG_02679":null,"SJAG_02689":null,"SJAG_02691":null,"SJAG_02694":null,"SJAG_02709":null,"SJAG_02730":null,"SJAG_02734":null,"SJAG_02741":null,"SJAG_02746":null,"SJAG_02752":null,"SJAG_02763":null,"SJAG_02766":null,"SJAG_02785":null,"SJAG_02786":null,"SJAG_02794":null,"SJAG_02796":null,"SJAG_02808":null,"SJAG_02813":null,"SJAG_02818":null,"SJAG_02847":null,"SJAG_02851":null,"SJAG_02897":null,"SJAG_02903":null,"SJAG_02908":null,"SJAG_02938":null,"SJAG_02954":null,"SJAG_02956":null,"SJAG_02963":null,"SJAG_02990":null,"SJAG_03005":null,"SJAG_03006":null,"SJAG_03018":null,"SJAG_03022":null,"SJAG_03029":null,"SJAG_03032":null,"SJAG_03043":null,"SJAG_03044":null,"SJAG_03051":null,"SJAG_03071":null,"SJAG_03088":null,"SJAG_03090":null,"SJAG_03096":null,"SJAG_03103":null,"SJAG_03112":null,"SJAG_03120":null,"SJAG_03135":null,"SJAG_03140":null,"SJAG_03142":null,"SJAG_03153":null,"SJAG_03175":null,"SJAG_03180":null,"SJAG_03183":null,"SJAG_03185":null,"SJAG_03191":null,"SJAG_03196":null,"SJAG_03222":null,"SJAG_03225":null,"SJAG_03227":null,"SJAG_03230":null,"SJAG_03231":null,"SJAG_03240":null,"SJAG_03241":null,"SJAG_03249":null,"SJAG_03250":null,"SJAG_03254":null,"SJAG_03255":null,"SJAG_03268":null,"SJAG_03275":null,"SJAG_03276":null,"SJAG_03286":null,"SJAG_03303":null,"SJAG_03313":null,"SJAG_03322":null,"SJAG_03324":null,"SJAG_03326":null,"SJAG_03346":null,"SJAG_03362":null,"SJAG_03370":null,"SJAG_03373":null,"SJAG_03387":null,"SJAG_03388":null,"SJAG_03393":null,"SJAG_03396":null,"SJAG_03398":null,"SJAG_03405":null,"SJAG_03428":null,"SJAG_03430":null,"SJAG_03448":null,"SJAG_03465":null,"SJAG_03473":null,"SJAG_03482":null,"SJAG_03496":null,"SJAG_03509":null,"SJAG_03519":null,"SJAG_03538":null,"SJAG_03539":null,"SJAG_03548":null,"SJAG_03562":null,"SJAG_03578":null,"SJAG_03588":null,"SJAG_03599":null,"SJAG_03613":null,"SJAG_03615":null,"SJAG_03618":null,"SJAG_03626":null,"SJAG_03628":null,"SJAG_03635":null,"SJAG_03643":null,"SJAG_03647":null,"SJAG_03657":null,"SJAG_03658":null,"SJAG_03665":null,"SJAG_03689":null,"SJAG_03695":null,"SJAG_03697":null,"SJAG_03723":null,"SJAG_03734":null,"SJAG_03743":null,"SJAG_03744":null,"SJAG_03750":null,"SJAG_03752":null,"SJAG_03755":null,"SJAG_03761":null,"SJAG_03771":null,"SJAG_03793":null,"SJAG_03811":null,"SJAG_03812":null,"SJAG_03813":null,"SJAG_03822":null,"SJAG_03831":null,"SJAG_03840":null,"SJAG_03850":null,"SJAG_03855":null,"SJAG_03861":null,"SJAG_03862":null,"SJAG_03866":null,"SJAG_03879":null,"SJAG_03883":null,"SJAG_03884":null,"SJAG_03886":null,"SJAG_03893":null,"SJAG_03911":null,"SJAG_03918":null,"SJAG_03930":null,"SJAG_03939":null,"SJAG_03943":null,"SJAG_03945":null,"SJAG_03968":null,"SJAG_03974":null,"SJAG_03976":null,"SJAG_03982":null,"SJAG_03983":null,"SJAG_03984":null,"SJAG_03985":null,"SJAG_04013":null,"SJAG_04016":null,"SJAG_04024":null,"SJAG_04030":null,"SJAG_04043":null,"SJAG_04048":null,"SJAG_04051":null,"SJAG_04054":null,"SJAG_04063":null,"SJAG_04080":null,"SJAG_04089":null,"SJAG_04106":null,"SJAG_04129":null,"SJAG_04151":null,"SJAG_04183":null,"SJAG_04189":null,"SJAG_04205":null,"SJAG_04213":null,"SJAG_04217":null,"SJAG_04233":null,"SJAG_04238":null,"SJAG_04242":null,"SJAG_04249":null,"SJAG_04292":null,"SJAG_04297":null,"SJAG_04309":null,"SJAG_04336":null,"SJAG_04353":null,"SJAG_04362":null,"SJAG_04368":null,"SJAG_04373":null,"SJAG_04374":null,"SJAG_04391":null,"SJAG_04396":null,"SJAG_04403":null,"SJAG_04407":null,"SJAG_04410":null,"SJAG_04414":null,"SJAG_04425":null,"SJAG_04429":null,"SJAG_04434":null,"SJAG_04448":null,"SJAG_04449":null,"SJAG_04466":null,"SJAG_04479":null,"SJAG_04487":null,"SJAG_04496":null,"SJAG_04516":null,"SJAG_04533":null,"SJAG_04538":null,"SJAG_04553":null,"SJAG_04571":null,"SJAG_04574":null,"SJAG_04579":null,"SJAG_04584":null,"SJAG_04619":null,"SJAG_04621":null,"SJAG_04641":null,"SJAG_04677":null,"SJAG_04679":null,"SJAG_04682":null,"SJAG_04712":null,"SJAG_04724":null,"SJAG_04726":null,"SJAG_04743":null,"SJAG_04747":null,"SJAG_04757":null,"SJAG_04765":null,"SJAG_04768":null,"SJAG_04781":null,"SJAG_04788":null,"SJAG_04789":null,"SJAG_04791":null,"SJAG_04842":null,"SJAG_04845":null,"SJAG_04859":null,"SJAG_04865":null,"SJAG_04882":null,"SJAG_04886":null,"SJAG_04896":null,"SJAG_04898":null,"SJAG_04901":null,"SJAG_04913":null,"SJAG_04915":null,"SJAG_04966":null,"SJAG_04970":null,"SJAG_04972":null,"SJAG_04990":null,"SJAG_04991":null,"SJAG_04998":null,"SJAG_05003":null,"SJAG_05010":null,"SJAG_05012":null,"SJAG_05105":null,"SJAG_05118":null,"SJAG_05173":null,"SJAG_05192":null,"SJAG_05200":null,"SJAG_05209":null,"SJAG_05223":null,"SJAG_05234":null,"SJAG_05236":null,"SJAG_05237":null,"SJAG_05239":null,"SJAG_05242":null,"SJAG_05243":null,"SJAG_05245":null,"SJAG_05264":null,"SJAG_05273":null,"SJAG_05274":null,"SJAG_05311":null,"SJAG_05323":null,"SJAG_05337":null,"SJAG_05338":null,"SJAG_05343":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_05353":null,"SJAG_05354":null,"SJAG_05373":null,"SJAG_05398":null,"SJAG_05679":null,"SJAG_06022":null,"SJAG_06576":null,"SJAG_06597":null,"SJAG_06599":null,"SJAG_06611":null,"SJAG_06636":null,"SJAG_06639":null,"SJAG_06642":null,"SJAG_MIT04":null,"SJAG_MIT20":null},"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":"cation binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0043169","terms_by_termid":{"GO:0000287":null,"GO:0005506":null,"GO:0005507":null,"GO:0005509":null,"GO:0008198":null,"GO:0008199":null,"GO:0008270":null,"GO:0016151":null,"GO:0016208":null,"GO:0016594":null,"GO:0030145":null,"GO:0030955":null,"GO:0030975":null,"GO:0030976":null,"GO:0031210":null,"GO:0043169":null,"GO:0046870":null,"GO:0046872":null,"GO:0046911":null,"GO:1901691":null,"GO:1904047":null}}


id: PBO:0080518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WASP family member 4, pseudogene","termid":"PBO:0080518"}


id: MONDO:0009542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"malabsorption syndrome","termid":"MONDO:0020598"}],"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":"lysine malabsorption syndrome","secondary_identifiers":["MEDGEN:167097","MESH:C563080","UMLS:C0796023","OMIM:247950"],"synonyms":[{"name":"lysine malabsorption syndrome","type":"exact"}],"termid":"MONDO:0009542","xrefs":{"Monarch":{"xref_id":"0009542"}}}


id: PBO:0068451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 27, pseudogene","termid":"PBO:0068451"}


id: MONDO:0016039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"superficial Fibromatosis","termid":"MONDO:0016037"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infantile digital fibromatosis","secondary_identifiers":["ICD9:238.8","GARD:8487","MEDGEN:232929","SCTID:399903008","HP:0025197","NCIT:C3456","Orphanet:199267","UMLS:C1318562"],"synonyms":[{"name":"IDF","type":"related"},{"name":"Reye tumor","type":"exact"},{"name":"Reye tumour","type":"exact"},{"name":"Reye's tumor","type":"exact"},{"name":"Reye's tumour","type":"exact"},{"name":"asymptomatic nodular proliferation of fibrous tissue on the dorsal and lateral aspects of the fingers or toes","type":"related"},{"name":"digital fibrous tumor of Reye","type":"exact"},{"name":"digital fibrous tumour of Reye","type":"exact"},{"name":"inclusion body fibromatosis","type":"exact"},{"name":"inclusion body fibromatosis (disease)","type":"exact"},{"name":"infantile digital fibroma/fibromatosis","type":"exact"},{"name":"infantile digital fibromatosis","type":"exact"},{"name":"recurring digital fibrous tumor of childhood","type":"exact"},{"name":"recurring digital fibrous tumour of childhood","type":"exact"}],"termid":"MONDO:0016039","xrefs":{"Monarch":{"xref_id":"0016039"}}}


id: PBO:0058534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6079","termid":"PBO:0058534"}


id: MONDO:1012449
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma of the digit, non-human animal","termid":"MONDO:1011822"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"squamous cell carcinoma of the digit, dog","secondary_identifiers":["OMIA:001787-9615"],"termid":"MONDO:1012449","xrefs":{"Monarch":{"xref_id":"1012449"}}}


id: GO:0140736
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of the chemical reactions and pathways resulting in the formation of lovastin.","definition_xrefs":["PMID:10334994","PMID:19781329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid biosynthetic process","termid":"GO:0046889"},{"relation_name":"is_a","term_name":"positive regulation of polyketide biosynthetic process","termid":"GO:1900734"},{"relation_name":"positively_regulates","term_name":"lovastatin biosynthetic process","termid":"GO:0140735"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"positively_regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748","GO:0006629"],"is_obsolete":false,"name":"positive regulation of lovastatin biosynthetic process","synonyms":[{"name":"positive regulation of mevacor biosynthetic process","type":"exact"},{"name":"positive regulation of mevinolin biosynthetic process","type":"exact"},{"name":"positive regulation of monacolin K biosynthetic process","type":"exact"}],"termid":"GO:0140736"}


id: GO:0001812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of type I hypersensitivity, a type of inflammatory response.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of type I hypersensitivity","termid":"GO:0001810"},{"relation_name":"is_a","term_name":"positive regulation of hypersensitivity","termid":"GO:0002885"},{"relation_name":"is_a","term_name":"positive regulation of immunoglobulin mediated immune response","termid":"GO:0002891"},{"relation_name":"positively_regulates","term_name":"type I hypersensitivity","termid":"GO:0016068"}],"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 type I hypersensitivity","synonyms":[{"name":"activation of type I hypersensitivity","type":"narrow"},{"name":"stimulation of type I hypersensitivity","type":"narrow"},{"name":"up regulation of type I hypersensitivity","type":"exact"},{"name":"up-regulation of type I hypersensitivity","type":"exact"},{"name":"upregulation of type I hypersensitivity","type":"exact"}],"termid":"GO:0001812"}


id: PBO:0028404
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ubiquinone_binding","termid":"PBO:0028404"}


id: PBO:0083815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential splicing factor; associated with Prp19p and the spliceosome, contains an N-terminal c-Myb DNA binding motif necessary for cell viability but not for Prp19p association, evolutionarily conserved and homologous to S. pombe Cdc5p","termid":"PBO:0083815"}


id: PBO:0069796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1082, pseudogene","termid":"PBO:0069796"}


id: GO:0102198
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-idonate + NAD+ = 5-dehydro-D-gluconate + NADH + H+.","definition_xrefs":["RHEA:21172","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"L-idonate 5-dehydrogenase (NAD+) activity","secondary_identifiers":["EC:1.1.1.366","MetaCyc:RXN-12107"],"synonyms":[{"name":"L-idonate 5-dehydrogenase activity (NAD-dependent)","type":"exact"}],"termid":"GO:0102198"}


id: MONDO:0017304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity.","definition_xrefs":["MESH:D016117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of melanin metabolism","termid":"MONDO:0018134"},{"relation_name":"is_a","term_name":"disorder of visual system","termid":"MONDO:0024458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"ocular albinism","secondary_identifiers":["SCTID:26399002","icd11.foundation:1147926040","UMLS:C0078917","DOID:0050633","GARD:21124","HP:0001107","Orphanet:284804","MedDRA:10065276","NORD:1516","ICD9:270.2","MEDGEN:38147"],"synonyms":[{"name":"XLOA","type":"narrow"},{"name":"ocular albinism","type":"exact"},{"name":"ocular albinism (disease)","type":"exact"}],"termid":"MONDO:0017304","xrefs":{"Monarch":{"xref_id":"0017304"}}}


id: PBO:0042540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 7 pseudogene 1","termid":"PBO:0042540"}


id: PBO:0000598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4-Not complex subunit Mot2 (predicted)","termid":"PBO:0000598"}


id: MONDO:0007744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperlipidemia","termid":"MONDO:0001336"},{"relation_name":"is_a","term_name":"hyperalphalipoproteinemia","termid":"MONDO:0015903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"cholesterol-ester transfer protein deficiency","secondary_identifiers":["SCTID:15771000119109","GARD:16724","UMLS:C3875011","MEDGEN:840020","Orphanet:79506","OMIM:143470","DOID:0111369"],"synonyms":[{"name":"CEPT deficiency","type":"exact"},{"name":"CETP deficiency","type":"related"},{"name":"HALP1","type":"related"},{"name":"Hdlcq10","type":"related"},{"name":"cholesterol ester transfer Protein deficiency","type":"related"},{"name":"familial hyperalphalipoproteinemia","type":"exact"},{"name":"high density lipoprotein cholesterol level QTL 10","type":"exact"},{"name":"high density lipoprotein cholesterol level quantitative trait locus 10","type":"related"},{"name":"hyperalphalipoproteinemia","type":"broad"},{"name":"hyperalphalipoproteinemia 1","type":"exact"},{"name":"hyperalphalipoproteinemia type 1","type":"exact"}],"termid":"MONDO:0007744","xrefs":{"Monarch":{"xref_id":"0007744"}}}


id: PBO:0053529
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 526","termid":"PBO:0053529"}


id: PBO:0047132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 171 member A1","termid":"PBO:0047132"}


id: PBO:0076657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-box transcription factor 19","termid":"PBO:0076657"}


id: PBO:0090582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome complex subunit beta 3, Pup3","termid":"PBO:0090582"}


id: GO:0061202
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a clathrin-sculpted gamma-aminobutyric acid transport vesicle.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-coated vesicle membrane","termid":"GO:0030665"},{"relation_name":"part_of","term_name":"clathrin-sculpted gamma-aminobutyric acid transport vesicle","termid":"GO:0061200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"clathrin-sculpted gamma-aminobutyric acid transport vesicle membrane","synonyms":[{"name":"clathrin sculpted GABA transport vesicle membrane","type":"exact"},{"name":"clathrin sculpted gamma-aminobutyric acid transport vesicle membrane","type":"exact"}],"termid":"GO:0061202"}


id: FYPO:0005940
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which the replicative lifespan of a cell population, i.e. the number of divisions cells in the population undergo before death, is higher than normal.","definition_xrefs":["PomBase:mah","PMID:28139976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"increased replicative lifespan","synonyms":[{"name":"increased cell population replicative lifespan","type":"exact"},{"name":"increased population replicative lifespan","type":"exact"}],"termid":"FYPO:0005940"}


id: PBO:0078190
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 4-3","termid":"PBO:0078190"}


id: PBO:0042233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin Y like 5 (pseudogene)","termid":"PBO:0042233"}


id: FYPO:0006817
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 acetylation of lysine at position 14 of histone H3 in centromere inner repeat regions is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:30652128","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H3-K14 acetylation during vegetative growth","termid":"FYPO:0003224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal histone H3-K14 acetylation at centromere inner repeat during vegetative growth","synonyms":[{"name":"normal histone H3-K14 acetylation at centromere imr during vegetative growth","type":"exact"},{"name":"normal histone H3-K14 acetylation at centromere inner repeat during mitotic cell cycle","type":"related"},{"name":"normal histone H3-K14 acetylation at centromere inner repeat region during vegetative growth","type":"exact"},{"name":"normal histone H3K14 acetylation at centromere inner repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0006817"}


id: GO:0034697
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 prostagladin I stimulus.","definition_xrefs":["GOC:BHF","GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to prostaglandin","termid":"GO:0034694"},{"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 prostaglandin I","synonyms":[{"name":"response to prostaglandin I stimulus","type":"exact"}],"termid":"GO:0034697"}


id: PBO:0004275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sir antagonist ortholog (predicted)","termid":"PBO:0004275"}


id: PBO:0075771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRSF2 pseudogene 1","termid":"PBO:0075771"}


id: PBO:0078680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon TTT) 13-1","termid":"PBO:0078680"}


id: GO:0042547
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events resulting in chemical or structural changes to existing cell walls and contribute to multidimensional cell growth.","definition_xrefs":["GOC:dph","GOC:tb","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall modification","termid":"GO:0042545"},{"relation_name":"part_of","term_name":"multidimensional cell growth","termid":"GO:0009825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0071554"],"is_obsolete":false,"name":"cell wall modification involved in multidimensional cell growth","synonyms":[{"name":"cell wall modification during cell expansion","type":"exact"},{"name":"cell wall modification during multidimensional cell growth","type":"related"}],"termid":"GO:0042547"}


id: GO:1900014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell in response to the presence of 3',5'-cAMP that results in a change in state or activity (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a calcium ion stimulus.","definition_xrefs":["PMID:21239624","GOC:TermGenie","GOC:pf","PMID:8937985","PMID:19363786"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular response to calcium ion involved in chemotaxis to cAMP (obsolete GO:1900014)","synonyms":[{"name":"cellular response to Ca2+ ion of chemotaxis to 3',5' cAMP","type":"exact"},{"name":"cellular response to Ca2+ ion of chemotaxis to 3',5'-cAMP","type":"exact"},{"name":"cellular response to Ca2+ ion of chemotaxis to adenosine 3',5'-cyclophosphate","type":"exact"},{"name":"cellular response to Ca2+ ion of chemotaxis to cAMP","type":"related"},{"name":"cellular response to Ca2+ ion of chemotaxis to cyclic AMP","type":"exact"},{"name":"cellular response to calcium ion involved in chemotaxis to cAMP","type":"exact"},{"name":"cellular response to calcium ion of chemotaxis to 3',5' cAMP","type":"related"},{"name":"cellular response to calcium ion of chemotaxis to 3',5'-cAMP","type":"related"},{"name":"cellular response to calcium ion of chemotaxis to adenosine 3',5'-cyclophosphate","type":"related"},{"name":"cellular response to calcium ion of chemotaxis to cAMP","type":"related"},{"name":"cellular response to calcium ion of chemotaxis to cyclic AMP","type":"related"}],"termid":"GO:1900014"}


id: PR:Q9P6R0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcription factor IIIB 90 kDa subunit that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03542","PRO:DNx","PANTHER:PTHR11618:SF4"],"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 factor IIIB 60 kDa subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC13E7.10c","secondary_identifiers":["UniProtKB:Q9P6R0"],"synonyms":[{"name":"B-related factor 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"BRF-1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-BRF1","type":"exact"},{"name":"TFIIB-related factor (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TFIIIB (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P6R0"}


id: GO:0032413
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the activity of an ion transporter.","definition_xrefs":["GOC:mah","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transporter activity","termid":"GO:0032410"},{"relation_name":"is_a","term_name":"regulation of monoatomic ion transmembrane transporter activity","termid":"GO:0032412"},{"relation_name":"is_a","term_name":"negative regulation of monoatomic ion transmembrane transport","termid":"GO:0034766"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of ion transmembrane transporter activity","synonyms":[{"name":"down regulation of ion transporter activity","type":"exact"},{"name":"down-regulation of ion transporter activity","type":"exact"},{"name":"downregulation of ion transporter activity","type":"exact"},{"name":"inhibition of ion transporter activity","type":"narrow"},{"name":"negative regulation of ion transporter activity","type":"exact"}],"termid":"GO:0032413"}


id: PBO:0030964
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_trimethylation_at_centromere_inner_repeat","termid":"PBO:0030964"}


id: MONDO:0003990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive malignant tumor that arises from the breast. It is characterized by the presence of spindle-shaped myoepithelial cells. Mitoses are present. Rarely, local recurrences and distant metastases have been reported.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast myoepithelial tumor","termid":"MONDO:0002483"},{"relation_name":"is_a","term_name":"malignant myoepithelioma","termid":"MONDO:0003158"},{"relation_name":"is_a","term_name":"invasive breast carcinoma","termid":"MONDO:0006256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant breast myoepithelioma","secondary_identifiers":["UMLS:C1518167","MEDGEN:309375","DOID:6776","NCIT:C40395"],"synonyms":[{"name":"breast malignant myoepithelioma","type":"exact"},{"name":"breast myoepithelial carcinoma","type":"exact"},{"name":"malignant breast myoepithelioma","type":"exact"}],"termid":"MONDO:0003990","xrefs":{"Monarch":{"xref_id":"0003990"}}}


id: GO:0005151
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a Type II interleukin-1 receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-1 receptor binding","termid":"GO:0005149"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"interleukin-1, type II receptor binding","synonyms":[{"name":"IL-1 type II","type":"narrow"},{"name":"interleukin-1, type II receptor ligand","type":"narrow"}],"termid":"GO:0005151"}


id: GO:0031625
data:
  {"annotated_genes":["SJAG_00615","SJAG_03643","SJAG_01134","SJAG_02253","SJAG_00452","SJAG_01686","SJAG_00803","SJAG_03575","SJAG_04335","SJAG_01540","SJAG_01226","SJAG_01365","SJAG_02591","SJAG_00032"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67035,70242,71742,72668,72840,74727,75630,76820,78463,79010,79123,79176,79639,80356],"is_not":false,"summary":null,"term":"GO:0031625"}]},"cv_name":"molecular_function","definition":"Binding to a ubiquitin protein ligase enzyme, any of the E3 proteins.","definition_xrefs":["GOC:vp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein ligase binding","termid":"GO:0044389"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00032":null,"SJAG_00452":null,"SJAG_00615":null,"SJAG_00803":null,"SJAG_01134":null,"SJAG_01226":null,"SJAG_01365":null,"SJAG_01540":null,"SJAG_01686":null,"SJAG_02253":null,"SJAG_02591":null,"SJAG_03575":null,"SJAG_03643":null,"SJAG_04335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"ubiquitin protein ligase binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"ubiquitin ligase binding","type":"exact"}],"termid":"GO:0031625","terms_by_termid":{"GO:0031625":null}}


id: PBO:0065541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTENP1 antisense RNA","termid":"PBO:0065541"}


id: PBO:0074757
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 116","termid":"PBO:0074757"}


id: GO:0010463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of cells, resulting in the expansion of a mesenchymal cell population. A mesenchymal cell is a cell that normally gives rise to other cells that are organized as three-dimensional masses, rather than sheets.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"}],"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":"mesenchymal cell proliferation","termid":"GO:0010463"}


id: PBO:0071567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 33","termid":"PBO:0071567"}


id: PBO:0081812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 736 pseudogene 5, Y-linked","termid":"PBO:0081812"}


id: GO:0033425
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CAU 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:0005488"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0005488","GO:0003723","GO:0003674","GO:0060090"],"is_obsolete":false,"name":"CAU codon-amino acid adaptor activity","synonyms":[{"name":"CAT codon-amino acid adaptor activity","type":"exact"},{"name":"histidine tRNA","type":"related"}],"termid":"GO:0033425"}


id: GO:2000875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glyoxylate cycle.","definition_xrefs":["GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of glyoxylate cycle","termid":"GO:2000874"},{"relation_name":"negatively_regulates","term_name":"glyoxylate cycle","termid":"GO:0006097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of glyoxylate cycle","synonyms":[{"name":"negative regulation of glyoxylate bypass","type":"exact"}],"termid":"GO:2000875"}


id: GO:1990343
data:
  {"annotated_genes":["SJAG_01601"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[119264],"is_not":false,"summary":null,"term":"GO:1990343"}]},"cv_name":"cellular_component","definition":"A region of heterochromatin that is formed dynamically under specific growth conditions by a process that requires RNAi, and is enriched in histone H3 methylated on lysine 9 (H3K9me).","definition_xrefs":["PMID:24210919","PMID:23151475"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heterochromatin","termid":"GO:0000792"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01601":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005575","GO:0005694"],"is_obsolete":false,"name":"heterochromatin domain","references_by_uniquename":{"PMID:32109380":null},"synonyms":[{"name":"HOOD","type":"exact"}],"termid":"GO:1990343","terms_by_termid":{"GO:1990343":null}}


id: SO:0001429
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A binding site that, in the molecule, interacts selectively and non-covalently with DNA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide_binding_site","termid":"SO:0001655"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA_binding_site","synonyms":[{"name":"DNA binding site","type":"exact"}],"termid":"SO:0001429"}


id: PBO:0001793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin family C2 domain protein, Syn1","termid":"PBO:0001793"}


id: GO:1901574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of chemical substance.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete chemical substance biosynthetic process (obsolete GO:1901574)","synonyms":[{"name":"chemical substance anabolism","type":"exact"},{"name":"chemical substance biosynthesis","type":"exact"},{"name":"chemical substance biosynthetic process","type":"exact"},{"name":"chemical substance formation","type":"exact"},{"name":"chemical substance synthesis","type":"exact"}],"termid":"GO:1901574"}


id: PBO:0047638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 1A pseudogene 1","termid":"PBO:0047638"}


id: MONDO:0002833
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare transitional cell carcinoma that arises from the fallopian tube.","definition_xrefs":["NCIT:C40104"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube carcinoma","termid":"MONDO:0006206"},{"relation_name":"is_a","term_name":"transitional cell carcinoma","termid":"MONDO:0006474"}],"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":"fallopian tube transitional cell carcinoma","secondary_identifiers":["MEDGEN:274492","UMLS:C1517128","DOID:4008"],"synonyms":[{"name":"fallopian tube transitional cell cancer","type":"exact"},{"name":"fallopian tube transitional cell carcinoma","type":"exact"}],"termid":"MONDO:0002833","xrefs":{"Monarch":{"xref_id":"0002833"}}}


id: MONDO:1011616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Von Willebrand disease that occurs in rabbit.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Von Willebrand disease, non-human animal","termid":"MONDO:1011411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Von Willebrand disease, rabbit","secondary_identifiers":["OMIA:001056-9986"],"termid":"MONDO:1011616","xrefs":{"Monarch":{"xref_id":"1011616"}}}


id: GO:0015959
data:
  {"annotated_genes":["SJAG_04870","SJAG_01352","SJAG_04939","SJAG_04169"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901909"},{"annotations":[79155],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901907"},{"annotations":[96990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015966"},{"annotations":[111465,117114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015964"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving diadenosine polyphosphate, a derivative of the nucleoside adenosine with phosphate groups attached.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide metabolic process","termid":"GO:0009117"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01352":null,"SJAG_04169":null,"SJAG_04870":null,"SJAG_04939":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:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"diadenosine polyphosphate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"diadenosine polyphosphate metabolism","type":"exact"}],"termid":"GO:0015959","terms_by_termid":{"GO:0015964":null,"GO:0015966":null,"GO:1901907":null,"GO:1901909":null}}


id: PBO:0045905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EF-hand calcium binding domain 3","termid":"PBO:0045905"}


id: PBO:0110333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP5PF pseudogene 3","termid":"PBO:0110333"}


id: MONDO:0008630
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":"urinary bladder, atony of","secondary_identifiers":["OMIM:191800","UMLS:C5231389","MEDGEN:1684829"],"synonyms":[{"name":"atony of urinary bladder","type":"exact"},{"name":"bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT","type":"exact"},{"name":"urinary bladder, atony of","type":"exact"}],"termid":"MONDO:0008630","xrefs":{"Monarch":{"xref_id":"0008630"}}}


id: GO:0071889
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a 14-3-3 protein. A 14-3-3 protein is any of a large family of approximately 30kDa acidic proteins which exist primarily as homo- and heterodimers within all eukaryotic cells, and have been implicated in the modulation of distinct biological processes by binding to specific phosphorylated sites on diverse target proteins, thereby forcing conformational changes or influencing interactions between their targets and other molecules. Each 14-3-3 protein sequence can be roughly divided into three sections: a divergent amino terminus, the conserved core region and a divergent carboxy-terminus. The conserved middle core region of the 14-3-3s encodes an amphipathic groove that forms the main functional domain, a cradle for interacting with client proteins.","definition_xrefs":["GOC:mah","PMID:19575580","GOC:cna","PMID:15167810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"14-3-3 protein binding","termid":"GO:0071889"}


id: PBO:0066409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RELT like 1","termid":"PBO:0066409"}


id: PBO:0113011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Atypical protein kinase; along with its paralog, ALK1, required for proper spindle positioning and nuclear segregation following mitotic arrest, proper organization of formins and polarisome components in mitosis, and survival after spindle assembly checkpoint delay; negatively regulates the morphogenesis checkpoint in response to polarity insults in opposition to ALK1; phosphorylated in response to DNA damage; similar to mammalian haspins","termid":"PBO:0113011"}


id: MONDO:0043185
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pointer syndrome","secondary_identifiers":["MESH:C536323","MEDGEN:208668","UMLS:C0796118"],"synonyms":[{"name":"skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties","type":"related"}],"termid":"MONDO:0043185","xrefs":{"Monarch":{"xref_id":"0043185"}}}


id: PBO:0072826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"survival associated mitochondrial melanoma specific oncogenic non-coding RNA","termid":"PBO:0072826"}


id: MONDO:0007998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microspherophakia - metaphyseal dysplasia is a very rare syndrome associating bone dysplasia with micromelic dwarfism and eye defects.","definition_xrefs":["Orphanet:2551"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete lens size anomaly (obsolete MONDO:0020235)","termid":"MONDO:0020235"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microspherophakia-metaphyseal dysplasia syndrome","secondary_identifiers":["UMLS:C1834880","GARD:5481","MEDGEN:322520","MESH:C536540","OMIM:157151"],"synonyms":[{"name":"Verloes Van Maldergem Marneffe syndrome","type":"related"},{"name":"Verloes-Van Maldergem-de Marneffe syndrome","type":"exact"},{"name":"dominantly inherited bone dysplasia with severe eye involvement","type":"related"},{"name":"microspherophakia-metaphyseal dysplasia","type":"related"}],"termid":"MONDO:0007998","xrefs":{"Monarch":{"xref_id":"0007998"}}}


id: SO:0000956
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Structural unit composed of a self-replicating, single-stranded DNA molecule.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"single","termid":"SO:0000984"},{"relation_name":"is_a","term_name":"DNA_chromosome","termid":"SO:0000954"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"single_stranded_DNA_chromosome","synonyms":[{"name":"single stranded DNA chromosome","type":"exact"}],"termid":"SO:0000956"}


id: PBO:0056678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myocyte enhancer factor 2C","termid":"PBO:0056678"}


id: PBO:0060125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 26","termid":"PBO:0060125"}


id: PBO:0007182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingosine-1-phosphate phosphatase","termid":"PBO:0007182"}


id: PBO:0086349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-type ATPase, ion transporter of the ER membrane; required to maintain normal lipid and sterol composition of intracellular compartments and proper targeting of mitochondrial outer membrane tail-anchored proteins; involved in ER function and Ca2+ homeostasis; required for regulating Hmg2p degradation; confers sensitivity to a killer toxin (SMKT) produced by Pichia farinosa KK1; null mutation is complemented by human Parkinson disease-related ATP13A1","termid":"PBO:0086349"}


id: GO:0150020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a dendritic tree are generated on the basal neuron side and organized into dendritic branches.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:22683681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite arborization","termid":"GO:0140059"},{"relation_name":"is_a","term_name":"basal dendrite morphogenesis","termid":"GO:0150019"}],"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":"basal dendrite arborization","termid":"GO:0150020"}


id: GO:1902537
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A pinocytosis which involves another organism.","definition_xrefs":["GOC:TermGenie","GOC:bf","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete multi-organism pinocytosis (obsolete GO:1902537)","termid":"GO:1902537"}


id: GO:0140367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An defense response against a bacteria mediated through an innate immune response. An innate immune response is mediated by germline encoded components that directly recognize components of potential pathogens.","definition_xrefs":["PMID:23006328","PMID:16177355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"defense response to bacterium","termid":"GO:0042742"},{"relation_name":"is_a","term_name":"innate immune response","termid":"GO:0045087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"antibacterial innate immune response","termid":"GO:0140367"}


id: GO:0072144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a glomerular mesangial cell in the kidney over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell development","termid":"GO:0002064"},{"relation_name":"is_a","term_name":"mesangial cell development","termid":"GO:0072143"},{"relation_name":"part_of","term_name":"glomerular mesangial cell differentiation","termid":"GO:0072008"}],"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 mesangial cell development","termid":"GO:0072144"}


id: MONDO:0012495
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare primary bone dysplasia characterized by severe developmental delay and skeletal dysplasia (including short stature, premature carpal ossification, platyspondyly, longitudinal metaphyseal striations, and small epiphyses), as well as moderate to severe intellectual disability and facial dysmorphism, including prominent forehead, mild synophrys, depressed nasal bridge, prominent bulbous nasal tip and full lips.","definition_xrefs":["Orphanet:168454"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia","termid":"MONDO:0100510"}],"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":"spondyloepimetaphyseal dysplasia, Genevieve type","secondary_identifiers":["MESH:C535785","DOID:0080576","OMIM:610442","UMLS:C1864872","icd11.foundation:1383217537","GARD:10057","MEDGEN:355314"],"synonyms":[{"name":"Nans deficiency","type":"related"},{"name":"SEMD Genevieve type","type":"related"},{"name":"SEMD, Genevieve type","type":"related"},{"name":"SEMD, Geneviève type","type":"exact"},{"name":"SEMDG","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia Genevieve type","type":"related"},{"name":"spondyloepimetaphyseal dysplasia, Camera-Genevieve type","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia, Genevieve type","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia, Geneviève type","type":"related"}],"termid":"MONDO:0012495","xrefs":{"Monarch":{"xref_id":"0012495"}}}


id: PBO:0086236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that interacts with Ulp1p; a Ubl (ubiquitin-like protein)-specific protease for Smt3p protein conjugates; detected in a phosphorylated state in the mitochondrial outer membrane; also detected in ER and nuclear envelope","termid":"PBO:0086236"}


id: PBO:0073440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scm like with four mbt domains 2","termid":"PBO:0073440"}


id: PR:000050528
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the hhf3 gene in Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H4, hhf3 gene translation product (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC1105.12","termid":"PR:000050528"}


id: PBO:0039822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor guanine nucleotide exchange factor 2","termid":"PBO:0039822"}


id: MONDO:1012682
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinal disorder characterized by multiple areas of retinal degeneration that occurs in dogs due to a C(73)T stop mutation in the BEST1 gene.","definition_xrefs":["PMID:17460247"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal degeneration, non-human animal","termid":"MONDO:1010326"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multifocal retinopathy 1, BEST1-related, dog","secondary_identifiers":["OMIA:001444-9615"],"synonyms":[{"name":"CMR1","type":"exact"},{"name":"multifocal retinopathy 1, dog","type":"related"}],"termid":"MONDO:1012682","xrefs":{"Monarch":{"xref_id":"1012682"}}}


id: PBO:0111299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial outer membrane protein, TspO/MBR-related, tspO","termid":"PBO:0111299"}


id: MONDO:0024490
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"general tumor grading characteristic","termid":"MONDO:0024489"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor grade X, general grading system","synonyms":[{"name":"undetermined grade","type":"exact"}],"termid":"MONDO:0024490","xrefs":{"Monarch":{"xref_id":"0024490"}}}


id: PBO:0062766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily T member 1 pseudogene","termid":"PBO:0062766"}


id: GO:1900019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein kinase C activity.","definition_xrefs":["GOC:TermGenie","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein serine/threonine kinase activity","termid":"GO:0071900"}],"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 protein kinase C activity","synonyms":[{"name":"regulation of PKC","type":"related"},{"name":"regulation of PKC activity","type":"exact"}],"termid":"GO:1900019"}


id: GO:0106017
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-phosphatidyl-1D-myo-inositol 3,4-bisphosphate + H2O = 1-phosphatidyl-1D-myo-inositol phosphate + phosphate.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol bisphosphate phosphatase activity","termid":"GO:0034593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"phosphatidylinositol-3,4-bisphosphate phosphatase activity","termid":"GO:0106017"}


id: GO:0010449
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The increase in size or mass of a root meristem, a population of undifferentiated cells in a plant root which maintains a continuous balance between the production of stem cells and the incorporation of their derivatives into the growth of the root.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meristem growth","termid":"GO:0035266"},{"relation_name":"part_of","term_name":"root development","termid":"GO:0048364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"root meristem growth","termid":"GO:0010449"}


id: PBO:0090647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER protein, Erd1 homolog, required for glycosylation and ER retention Erd1/Gmn2","termid":"PBO:0090647"}


id: GO:1905962
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a glutamatergic neuron.","definition_xrefs":["GO_REF:0000086","GOC:TermGenie","PMID:24030726"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron differentiation","termid":"GO:0030182"}],"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":"glutamatergic neuron differentiation","termid":"GO:1905962"}


id: PBO:0091422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dipeptidyl peptidase","termid":"PBO:0091422"}


id: GO:0140114
data:
  {"annotated_genes":["SJAG_01973"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113759],"is_not":false,"summary":null,"term":"GO:0140114"}]},"cv_name":"biological_process","definition":"Any process carried out at the cellular level that reduces or removes the toxicity of a fluoride. These may include chemical modification or transport of fluoride away from sensitive areas and to compartments or complexes whose purpose is sequestration of the toxic substance.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification of inorganic compound","termid":"GO:0061687"},{"relation_name":"is_a","term_name":"cellular detoxification","termid":"GO:1990748"},{"relation_name":"part_of","term_name":"cellular response to fluoride","termid":"GO:1902618"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01973":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"cellular detoxification of fluoride","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140114","terms_by_termid":{"GO:0140114":null}}


id: GO:0050107
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + a monoterpenol = CoA + a monoterpenol acetate ester.","definition_xrefs":["EC:2.3.1.69","MetaCyc:MONOTERPENOL-O-ACETYLTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"monoterpenol O-acetyltransferase activity","synonyms":[{"name":"acetyl-CoA:monoterpenol O-acetyltransferase activity","type":"related"},{"name":"menthol transacetylase activity","type":"narrow"}],"termid":"GO:0050107"}


id: MONDO:0006533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic lesion characterized by the proliferation of keratinizing squamous epithelium in the middle ear that results in the accumulation of keratin and cells. It is usually caused by repeated infections. If left untreated, it may increase in size and destroy the adjacent delicate bones of the middle ear.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"middle ear disorder","termid":"MONDO:0003276"},{"relation_name":"is_a","term_name":"cholesteatoma","termid":"MONDO:0006530"}],"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":"cholesteatoma of middle ear","secondary_identifiers":["EFO:1000678","ICD9:385.33","MEDGEN:57836","icd11.foundation:2134365487","ICD9:385.32","NCIT:C3654","ICD10CM:H71","DOID:10964","ICD9:385.3","MESH:D018424","UMLS:C0155490","SCTID:194339007"],"synonyms":[{"name":"Epidermosis of ear","type":"exact"},{"name":"Epidermosis of middle ear","type":"exact"},{"name":"cholesteatoma (disease) of middle ear","type":"exact"},{"name":"cholesteatoma of middle ear","type":"exact"},{"name":"cholesteatoma of middle ear and mastoid","type":"exact"},{"name":"cholesteatoma of middle ear and/or mastoid","type":"exact"},{"name":"cholesteatoma of the middle ear","type":"exact"},{"name":"middle ear cholesteatoma","type":"exact"},{"name":"middle ear cholesteatoma (disease)","type":"exact"},{"name":"unspecified cholesteatoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0006533","xrefs":{"Monarch":{"xref_id":"0006533"}}}


id: PBO:0047274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FA complementation group A","termid":"PBO:0047274"}


id: GO:1900167
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glial cell-derived neurotrophic factor production.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of glial cell-derived neurotrophic factor production","termid":"GO:1900166"},{"relation_name":"negatively_regulates","term_name":"glial cell-derived neurotrophic factor production","termid":"GO:0044467"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of glial cell-derived neurotrophic factor production","synonyms":[{"name":"inhibition of GDNF secretion","type":"narrow"},{"name":"inhibition of glial cell line-derived neurotrophic factor secretion","type":"narrow"},{"name":"negative regulation of GDNF secretion","type":"exact"},{"name":"negative regulation of glial cell line-derived neurotrophic factor secretion","type":"related"},{"name":"negative regulation of glial cell-derived neurotrophic factor secretion","type":"narrow"}],"termid":"GO:1900167"}


id: MOD:00096
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to L-glutamic acid 1-amide.","definition_xrefs":["RESID:AA0087","PubMed:1093875","PubMed:14550575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-glutamic acid 1-amide","synonyms":[{"name":"(2S)-2-amino-1-pentanediamic acid","type":"exact"},{"name":"1-amidated L-glutamic acid","type":"exact"},{"name":"4,5-diamino-5-oxopentanoic acid","type":"exact"},{"name":"GluN","type":"exact"},{"name":"L-glutamic acid 1-amide","type":"exact"},{"name":"MOD_RES Glutamic acid 1-amide","type":"exact"},{"name":"isoglutamine","type":"exact"}],"termid":"MOD:00096"}


id: GO:0097498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any endothelial tube morphogenesis process by which the tube is increased in length.","definition_xrefs":["PMID:23698350","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial tube morphogenesis","termid":"GO:0061154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"endothelial tube lumen extension","termid":"GO:0097498"}


id: MONDO:0021474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the ear.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory organ benign neoplasm","termid":"MONDO:0000633"},{"relation_name":"is_a","term_name":"ear neoplasm","termid":"MONDO:0021233"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of ear","secondary_identifiers":["UMLS:C0347354","MEDGEN:138081","SCTID:255181009","NCIT:C8417"],"synonyms":[{"name":"aural neoplasms, benign","type":"exact"},{"name":"benign Ear neoplasm","type":"exact"},{"name":"benign Ear tumor","type":"exact"},{"name":"benign Ear tumour","type":"exact"},{"name":"benign neoplasm of the Ear","type":"exact"},{"name":"benign tumor of Ear","type":"exact"},{"name":"benign tumor of the Ear","type":"exact"},{"name":"benign tumour of Ear","type":"exact"},{"name":"benign tumour of the Ear","type":"exact"},{"name":"ear benign neoplasm","type":"exact"}],"termid":"MONDO:0021474","xrefs":{"Monarch":{"xref_id":"0021474"}}}


id: MOD:00337
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-carbamoyl-L-cysteine.","definition_xrefs":["RESID:AA0332","Unimod:5#C","PubMed:12586941","PubMed:240389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbamoylated residue","termid":"MOD:00398"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-carbamoyl-L-cysteine","synonyms":[{"name":"(R)-2-amino-3-(carbamoylsulfanyl)propanoic acid","type":"exact"},{"name":"2-amino-3-(aminocarbonyl)sulfanylpropanoic acid","type":"exact"},{"name":"2-amino-3-(aminocarbonyl)thiopropanoic acid","type":"exact"},{"name":"MOD_RES S-carbamoylcysteine","type":"exact"},{"name":"S-(aminocarbonyl)cysteine","type":"exact"},{"name":"S-carbamoyl-L-cysteine","type":"exact"},{"name":"S-carbamoylcysteine","type":"exact"},{"name":"S-carbamylcysteine","type":"exact"},{"name":"S-cysteinyl carbamate ester","type":"exact"},{"name":"SCbmCys","type":"exact"},{"name":"alpha-amino-beta-carbamylthiopropionic acid","type":"exact"},{"name":"beta-carbamylthioalanine","type":"exact"}],"termid":"MOD:00337"}


id: PBO:0056479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MATN1 antisense RNA 1","termid":"PBO:0056479"}


id: MONDO:0005018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete diffuse large B-cell lymphoma (obsolete MONDO:0005018)","termid":"MONDO:0005018","xrefs":{"Monarch":{"xref_id":"0005018"}}}


id: PBO:0004691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3,4-dihydroxy-2-butanone 4-phosphate synthase (predicted)","termid":"PBO:0004691"}


id: GO:1903472
data:
  {"annotated_genes":["SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103699],"is_not":false,"summary":null,"term":"GO:1903472"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mitotic actomyosin contractile ring contraction.","definition_xrefs":["GOC:TermGenie","PMID:1234","GOC:mtg_cell_cycle","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of mitotic cytokinetic process","termid":"GO:1903437"},{"relation_name":"is_a","term_name":"regulation of mitotic actomyosin contractile ring contraction","termid":"GO:1903471"},{"relation_name":"negatively_regulates","term_name":"mitotic actomyosin contractile ring contraction","termid":"GO:1902404"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00845":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0000281"},{"rel_name":"regulates","termid":"GO:0000281"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0000281"],"is_obsolete":false,"name":"negative regulation of mitotic actomyosin contractile ring contraction","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of contractile ring contraction involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"exact"},{"name":"down regulation of cytokinesis, actomyosin ring contraction involved in mitotic cell cycle","type":"exact"},{"name":"down regulation of mitotic actomyosin contractile ring contraction","type":"exact"},{"name":"down-regulation of contractile ring contraction involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"exact"},{"name":"down-regulation of cytokinesis, actomyosin ring contraction involved in mitotic cell cycle","type":"exact"},{"name":"down-regulation of mitotic actomyosin contractile ring contraction","type":"exact"},{"name":"downregulation of contractile ring contraction involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"exact"},{"name":"downregulation of cytokinesis, actomyosin ring contraction involved in mitotic cell cycle","type":"exact"},{"name":"downregulation of mitotic actomyosin contractile ring contraction","type":"exact"},{"name":"inhibition of contractile ring contraction involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"narrow"},{"name":"inhibition of cytokinesis, actomyosin ring contraction involved in mitotic cell cycle","type":"narrow"},{"name":"inhibition of mitotic actomyosin contractile ring contraction","type":"narrow"},{"name":"negative regulation of contractile ring contraction involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"exact"},{"name":"negative regulation of cytokinesis, actomyosin ring contraction involved in mitotic cell cycle","type":"exact"},{"name":"negative regulation of mitotic actomyosin contractile ring constriction","type":"exact"}],"termid":"GO:1903472","terms_by_termid":{"GO:1903472":null}}


id: FYPO:0007970
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype observed in the vegetative growth phase of the life cycle in which microtubule polymerization, i.e. the addition of tubulin dimers to the plus end of a microtubule occurs at a higher rate, or speed, than normal.","definition_xrefs":["PMID:35293864","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal rate of microtubule polymerization during vegetative growth","termid":"FYPO:0007955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased rate of microtuble polymerization during vegetative growth","termid":"FYPO:0007970"}


id: PATO:0002205
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's ability to hold an electrical charge.","definition_xrefs":["Wikipedia:Wikipedia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular quality","termid":"PATO:0002182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capacitance","termid":"PATO:0002205"}


id: GO:0061697
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N(6)-glutaryl-L-lysyl-[protein] + NAD+ = 2''-O-glutaryl-ADP-D-ribose + L-lysyl-[protein] + nicotinamide.","definition_xrefs":["GOC:dph","PMID:24703693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016810","GO:0016787","GO:0140096"],"is_obsolete":false,"name":"protein-glutaryllysine deglutarylase activity","secondary_identifiers":["RHEA:47664"],"termid":"GO:0061697"}


id: MONDO:0001027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A gonorrhea that involves the seminal vesicle.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gonorrhea","termid":"MONDO:0004277"},{"relation_name":"is_a","term_name":"vesiculitis","termid":"MONDO:0004767"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gonococcal seminal vesiculitis","secondary_identifiers":["DOID:10400","UMLS:C0578661","icd11.foundation:1226540022","MEDGEN:662073","SCTID:301990003"],"synonyms":[{"name":"gonococcal seminal vesiculitis (acute)","type":"exact"},{"name":"gonorrhea of seminal vesicle","type":"exact"},{"name":"gonorrhoea of seminal vesicle","type":"exact"},{"name":"seminal vesicle gonorrhea","type":"exact"},{"name":"seminal vesicle gonorrhoea","type":"exact"}],"termid":"MONDO:0001027","xrefs":{"Monarch":{"xref_id":"0001027"}}}


id: PBO:0052210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNQ5 antisense RNA 1","termid":"PBO:0052210"}


id: GO:1903432
data:
  {"annotated_genes":["SJAG_01142","SJAG_01187","SJAG_03089","SJAG_04496","SJAG_01983","SJAG_02231","SJAG_00875","SJAG_02424","SJAG_05346","SJAG_04910","SJAG_02605","SJAG_00209","SJAG_05184","SJAG_03928","SJAG_03072","SJAG_00457","SJAG_01032","SJAG_03501","SJAG_00824","SJAG_02765","SJAG_03371","SJAG_03405","SJAG_03486","SJAG_00169","SJAG_00991","SJAG_01184","SJAG_04249","SJAG_03355","SJAG_03799","SJAG_00688","SJAG_04235","SJAG_03678","SJAG_00561"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92862,94024,107863,115505,117826],"is_not":false,"summary":null,"term":"GO:1903432"},{"annotations":[116155,116509,117068,93300,79915,109282,113995,118259,103014,96073,73482,98874,105144,73511,109687,114600,113178,101455,107164,99573,87976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904262"},{"annotations":[94290,112879,73968,76364,75811,110555,96074,76742,72391,75224,88264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904263"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of TORC1 signaling.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of TOR signaling","termid":"GO:0032006"},{"relation_name":"regulates","term_name":"TORC1 signaling","termid":"GO:0038202"}],"gene_count":33,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00209":null,"SJAG_00457":null,"SJAG_00561":null,"SJAG_00688":null,"SJAG_00824":null,"SJAG_00875":null,"SJAG_00991":null,"SJAG_01032":null,"SJAG_01142":null,"SJAG_01184":null,"SJAG_01187":null,"SJAG_01983":null,"SJAG_02231":null,"SJAG_02424":null,"SJAG_02605":null,"SJAG_02765":null,"SJAG_03072":null,"SJAG_03089":null,"SJAG_03355":null,"SJAG_03371":null,"SJAG_03405":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03678":null,"SJAG_03799":null,"SJAG_03928":null,"SJAG_04235":null,"SJAG_04249":null,"SJAG_04496":null,"SJAG_04910":null,"SJAG_05184":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of TORC1 signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"regulation of TORC1 signal transduction","type":"exact"}],"termid":"GO:1903432","terms_by_termid":{"GO:1903432":null,"GO:1904262":null,"GO:1904263":null}}


id: GO:0009853
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A light-dependent catabolic process occurring concomitantly with photosynthesis in plants (especially C3 plants) whereby dioxygen (O2) is consumed and carbon dioxide (CO2) is evolved. The substrate is glycolate formed in large quantities in chloroplasts from 2-phosphoglycolate generated from ribulose 1,5-bisphosphate by the action of ribulose-bisphosphate carboxylase; the glycolate enters the peroxisomes where it is converted by glycolate oxidase to glyoxylate which undergoes transamination to glycine. This then passes into the mitochondria where it is decarboxylated forming one molecule of serine for every two molecules of glycine. This pathway also exists in photosynthetic bacteria.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic compound salvage","termid":"GO:0043094"}],"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":"photorespiration","secondary_identifiers":["MetaCyc:PWY-181","Wikipedia:Photorespiration"],"synonyms":[{"name":"photorespiratory pathway","type":"exact"}],"termid":"GO:0009853"}


id: PBO:0011137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor Pho7","termid":"PBO:0011137"}


id: PBO:0041115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bone marrow stromal cell antigen 2","termid":"PBO:0041115"}


id: PBO:0035814
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H4-K16_acetylation_at_centromere_central_core_during_vegetative_growth","termid":"PBO:0035814"}


id: PBO:0052178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium two pore domain channel subfamily K member 9","termid":"PBO:0052178"}


id: PBO:0046297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EMSY divergent transcript","termid":"PBO:0046297"}


id: GO:0060642
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a preadipocyte acquires specialized features of a white adipocyte of the mammary gland. White adipocytes have cytoplasmic lipids arranged in a unique vacuole.","definition_xrefs":["PMID:12558599","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"white fat cell differentiation","termid":"GO:0050872"},{"relation_name":"part_of","term_name":"mammary gland fat development","termid":"GO:0060611"}],"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":"white fat cell differentiation involved in mammary gland fat development","termid":"GO:0060642"}


id: GO:1902710
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of GABA receptor activity. Upon binding of gamma-aminobutyric acid (GABA) it transmits the signal from one side of the membrane to the other to initiate a change in cell activity. Major inhibitory receptor in vertebrate brain. Also found in other vertebrate tissues, invertebrates and possibly in plants. Effective benzodiazepine receptor.","definition_xrefs":["GOC:bhm","PMID:18790874","GO_REF:0000088","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor complex","termid":"GO:0043235"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"GABA receptor complex","synonyms":[{"name":"gamma-aminobutyric acid receptor complex","type":"exact"}],"termid":"GO:1902710"}


id: GO:0086059
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a calcium ion by a voltage-gated channel across the plasma membrane of an SA node cardiac muscle cell that contributes to the depolarization phase of an action potential. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated calcium channel activity involved in cardiac muscle cell action potential","termid":"GO:0086007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"voltage-gated calcium channel activity involved SA node cell action potential","synonyms":[{"name":"voltage-gated calcium channel activity involved in SA node cardiac muscle cell action potential","type":"exact"},{"name":"voltage-gated calcium channel activity involved in SAN cardiac muscle cell action potential","type":"exact"},{"name":"voltage-gated calcium channel activity involved in sinoatrial node cardiac muscle cell action potential","type":"exact"},{"name":"voltage-gated calcium channel activity involved in sinus node cardiac muscle cell action potential","type":"narrow"}],"termid":"GO:0086059"}


id: PBO:0041233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 56","termid":"PBO:0041233"}


id: MONDO:0011023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary mixed polyposis syndrome (HMPS) describes an autosomal dominantly inherited large-bowel disease characterized by the presence of a mixture of hyperplastic, atypical juvenile and adenomatous polyps that are associated with an increased risk of developing colorectal cancer if left untreated.","definition_xrefs":["Orphanet:157794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder","termid":"MONDO:0004335"},{"relation_name":"is_a","term_name":"intestinal polyposis syndrome","termid":"MONDO:0015185"}],"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":"hereditary mixed polyposis syndrome","secondary_identifiers":["MESH:C563365","UMLS:C5192681","OMIMPS:601228","DOID:0111684","GARD:16981","MEDGEN:1672870","icd11.foundation:219068911"],"synonyms":[{"name":"HMPS","type":"exact"},{"name":"hereditary mixed polyposis syndrome","type":"exact"}],"termid":"MONDO:0011023","xrefs":{"Monarch":{"xref_id":"0011023"}}}


id: PBO:0052284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinase insert domain receptor","termid":"PBO:0052284"}


id: PBO:0039558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain containing 50","termid":"PBO:0039558"}


id: MONDO:0018508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of small intestine carcinoma that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare carcinoma of small intestine (obsolete MONDO:0018508)","secondary_identifiers":["Orphanet:423957"],"synonyms":[{"name":"rare carcinoma of small bowel","type":"exact"},{"name":"rare small intestine carcinoma","type":"exact"}],"termid":"MONDO:0018508","xrefs":{"Monarch":{"xref_id":"0018508"}}}


id: PBO:0004011
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Birt-Hogg-Dube syndrome","termid":"PBO:0004011"}


id: GO:0007438
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the oenocyte over time, from its formation to the mature structure. The oenocytes are large secretory cells found in clusters underlying the epidermis of larval abdominal segments.","definition_xrefs":["PMID:11171397","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"oenocyte differentiation","termid":"GO:0001742"}],"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":"oenocyte development","termid":"GO:0007438"}


id: PBO:0051056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 3-3","termid":"PBO:0051056"}


id: PBO:0002295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-glucoside transporter Sut1","termid":"PBO:0002295"}


id: GO:0014020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of the neural tube from an epithelial cell sheet (the neuroepithelium or neural plate). In primary neurulation, the cells surrounding the neural plate direct the neural plate cells to proliferate, invaginate, and pinch off from the surface to form a hollow epithelial tube. Primary neurulation is the typical mechanism of formation of the anterior neural tube.","definition_xrefs":["ISBN:0878932585","PMID:15327780","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic epithelial tube formation","termid":"GO:0001838"},{"relation_name":"part_of","term_name":"neural tube formation","termid":"GO:0001841"}],"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":"primary neural tube formation","secondary_identifiers":["GO:0014024"],"synonyms":[{"name":"neural rod cavitation","type":"related"},{"name":"primary neural tube morphogenesis","type":"exact"},{"name":"primary neurulation","type":"exact"}],"termid":"GO:0014020"}


id: MONDO:0013955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the IL12RB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited susceptibility to mycobacterial diseases","termid":"MONDO:0019146"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency","secondary_identifiers":["Orphanet:319552","MEDGEN:862386","OMIM:614891","UMLS:C4013949","DOID:0111990"],"synonyms":[{"name":"IL-12Râ1 deficiency","type":"related"},{"name":"IL12RB1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency","type":"exact"},{"name":"IL12RB1 deficiency","type":"related"},{"name":"IMD30","type":"related"},{"name":"MSMD due to complete IL12RB1 deficiency","type":"exact"},{"name":"MSMD due to complete interleukin 12 receptor beta 1 deficiency","type":"exact"},{"name":"Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency","type":"exact"},{"name":"Mendelian susceptibility to mycobacterial infections due to IL12 deficiency","type":"related"},{"name":"autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IL12RB1","type":"exact"},{"name":"immunodeficiency 30","type":"related"},{"name":"immunodeficiency type 30","type":"exact"}],"termid":"MONDO:0013955","xrefs":{"Monarch":{"xref_id":"0013955"}}}


id: MONDO:0011808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in mutation in the region 2p12.","definition_xrefs":["PMID:12091400","DOID:0110233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset nuclear cataract","termid":"MONDO:0020376"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 27","secondary_identifiers":["MEDGEN:335448","MESH:C564596","GARD:18235","OMIM:607304","UMLS:C1846520"],"synonyms":[{"name":"CTRCT27","type":"exact"},{"name":"Ccnp","type":"related"},{"name":"cataract 27","type":"exact"},{"name":"cataract 27 nuclear progressive","type":"exact"},{"name":"cataract 27, nuclear progressive","type":"related"},{"name":"cataract type 27","type":"exact"}],"termid":"MONDO:0011808","xrefs":{"Monarch":{"xref_id":"0011808"}}}


id: PBO:0031624
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_sporulation","termid":"PBO:0031624"}


id: PBO:0086621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus","termid":"PBO:0086621"}


id: MONDO:0000847
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pycnodysostosis (obsolete MONDO:0000847)","termid":"MONDO:0000847","xrefs":{"Monarch":{"xref_id":"0000847"}}}


id: PATO:0002113
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Perforated like a sieve.","definition_xrefs":["merriam-webster:merriam-webster"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perforate","termid":"PATO:0002112"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cribriform","termid":"PATO:0002113"}


id: PBO:0070929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 37","termid":"PBO:0070929"}


id: PBO:0070243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 183 pseudogene","termid":"PBO:0070243"}


id: GO:1990176
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Protein complex involved in maltose transport through the plasma membrane. In E. coli, the complex is a tetramer and consists of a cytoplasmic ATPase MalK homodimer together with a heterodimeric transmembrane subunit MalF-MalG.","definition_xrefs":["PMID:19250913","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"},{"relation_name":"part_of","term_name":"maltose transport complex","termid":"GO:1990060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"MalFGK2 complex","synonyms":[{"name":"MalF-MalG-MalK(2) complex","type":"exact"},{"name":"MalF-MalG-MalK-MalK complex","type":"exact"},{"name":"MalFGK(2) complex","type":"exact"},{"name":"maltose transport MalFGK2 complex","type":"exact"},{"name":"maltose transport complex, core subunit","type":"exact"}],"termid":"GO:1990176"}


id: GO:0070959
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the directed killing of a fungal cell by a neutrophil.","definition_xrefs":["GOC:mah","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neutrophil mediated killing of fungus","termid":"GO:0070953"},{"relation_name":"is_a","term_name":"negative regulation of neutrophil mediated killing of symbiont cell","termid":"GO:0070955"},{"relation_name":"negatively_regulates","term_name":"neutrophil-mediated killing of fungus","termid":"GO:0070947"}],"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 neutrophil mediated killing of fungus","synonyms":[{"name":"down regulation of neutrophil mediated killing of fungus","type":"exact"},{"name":"down-regulation of neutrophil mediated killing of fungus","type":"exact"},{"name":"downregulation of neutrophil mediated killing of fungus","type":"exact"},{"name":"inhibition of neutrophil mediated killing of fungus","type":"narrow"}],"termid":"GO:0070959"}


id: PBO:0031856
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-haploinsufficient","termid":"PBO:0031856"}


id: FYPO:0008134
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 polyphosphate measured in the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:37783794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell","termid":"FYPO:0001076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal cellular polyphosphate level","termid":"FYPO:0008134"}


id: PBO:0067194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 258, pseudogene","termid":"PBO:0067194"}


id: GO:0061931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of erythrocyte enucleation.","definition_xrefs":["PMID:25241935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of erythrocyte enucleation","termid":"GO:0061930"},{"relation_name":"positively_regulates","term_name":"erythrocyte enucleation","termid":"GO:0043131"}],"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 erythrocyte enucleation","termid":"GO:0061931"}


id: PBO:0042017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 74A","termid":"PBO:0042017"}


id: GO:2000898
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glucomannan catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide metabolic process","termid":"GO:0032881"},{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"regulates","term_name":"glucomannan catabolic process","termid":"GO:2000884"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of glucomannan catabolic process","synonyms":[{"name":"regulation of glucomannan catabolism","type":"exact"}],"termid":"GO:2000898"}


id: GO:0052033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that involves recognition of a pathogen-associated molecular pattern, and by which an organism activates, maintains or increases the frequency, rate or extent of the innate immune response of the host organism; the innate immune response is the host's first line of defense against infection. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete pathogen-associated molecular pattern dependent induction by symbiont of host innate immune response (obsolete GO:0052033)","synonyms":[{"name":"MAMP dependent activation of host innate immunity","type":"exact"},{"name":"MAMP dependent induction of host innate immunity","type":"exact"},{"name":"PAMP dependent activation of host innate immunity","type":"exact"},{"name":"PAMP dependent induction of host innate immunity","type":"exact"},{"name":"PTI","type":"related"},{"name":"general elicitor-dependent activation of host innate immunity","type":"exact"},{"name":"general elicitor-dependent induction of host innate immunity","type":"exact"},{"name":"pathogen-associated molecular pattern dependent activation by organism of host innate immunity","type":"exact"},{"name":"pathogen-associated molecular pattern dependent induction by symbiont of host innate immunity","type":"exact"},{"name":"pattern-triggered immunity","type":"related"}],"termid":"GO:0052033"}


id: PBO:0083484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene UIP4/YPL186C","termid":"PBO:0083484"}


id: PBO:0048518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerophosphodiester phosphodiesterase domain containing 1","termid":"PBO:0048518"}


id: GO:0036006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a macrophage colony-stimulating factor stimulus.","definition_xrefs":["PMID:14687666","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to macrophage colony-stimulating factor","termid":"GO:0036005"},{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to macrophage colony-stimulating factor stimulus","synonyms":[{"name":"cellular response to M-CSF stimulus","type":"exact"},{"name":"cellular response to macrophage colony-stimulating factor","type":"exact"}],"termid":"GO:0036006"}


id: MONDO:0010837
data:
  {"annotated_genes":["SJAG_01151"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007767"},{"annotations":[85631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007768"}]},"cv_name":"mondo","definition":"Hyperfunction of the parathyroid glands resulting in the overproduction of parathyroid hormone. It is caused by parathyroid adenoma, parathyroid hyperplasia, parathyroid carcinoma, and multiple endocrine neoplasia. It is associated with hypercalcemia and hypophosphatemia. Signs and symptoms include weakness, fatigue, nausea, vomiting, constipation, depression, bone pain, osteoporosis, cystic bone lesions, and kidney stones.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperparathyroidism","termid":"MONDO:0001741"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01151":null},"genotype_count":0,"is_obsolete":false,"name":"primary hyperparathyroidism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D049950","icd11.foundation:817194045","MEDGEN:66354","EFO:0008519","NCIT:C48280","SCTID:36348003","DOID:11202","ICD9:252.01","HP:0008200","UMLS:C0221002"],"synonyms":[{"name":"primary hyperparathyroidism","type":"exact"},{"name":"primary hyperparathyroidism (disease)","type":"exact"}],"termid":"MONDO:0010837","terms_by_termid":{"MONDO:0007767":null,"MONDO:0007768":null},"xrefs":{"Monarch":{"xref_id":"0010837"}}}


id: GO:0031253
data:
  {"annotated_genes":["SJAG_02989","SJAG_01978"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88091,98976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070250"}]},"cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding a plasma membrane bounded cell surface projection.","definition_xrefs":["GOC:mah","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"},{"relation_name":"part_of","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01978":null,"SJAG_02989":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"cell projection membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"membrane extension","type":"related"},{"name":"membrane projection","type":"related"}],"termid":"GO:0031253","terms_by_termid":{"GO:0070250":null}}


id: MONDO:0011570
data:
  {"annotated_genes":["SJAG_02680"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85464],"is_not":false,"summary":null,"term":"MONDO:0011570"}]},"cv_name":"mondo","definition":"Charcot-Marie-Tooth disease, type 2B2 (CMT2B2, also referred to as CMT4C3) is an axonal CMT peripheral sensorimotor polyneuropathy that has been described in a large consanguineous Costa Rican family of Spanish ancestry.","definition_xrefs":["Orphanet:101101"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02680":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 2B2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:1249","MESH:C537991","icd11.foundation:2009111705","DOID:0110179","OMIM:605589","SCTID:719981005","MEDGEN:381352","UMLS:C1854150"],"synonyms":[{"name":"AR-CMT2B2","type":"exact"},{"name":"ARCMT2B","type":"exact"},{"name":"Arcmt2B","type":"related"},{"name":"CMT 2B2","type":"related"},{"name":"CMT2B2","type":"exact"},{"name":"Charcot Marie Tooth disease type 2B2","type":"related"},{"name":"Charcot-Marie-Tooth disease neuronal type 2B2","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 2 caused by mutation in MED25","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 2B2","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, B2","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2B2","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2B2","type":"related"},{"name":"Charcot-Marie-Tooth disease, neuronal, type 2B2","type":"related"},{"name":"Charcot-Marie-Tooth disease, type 2B2","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy type 2B2","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 2B2","type":"related"},{"name":"MED25 Charcot-Marie-Tooth disease type 2","type":"exact"},{"name":"autosomal recessive axonal CMT4C3","type":"exact"},{"name":"autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2","type":"exact"}],"termid":"MONDO:0011570","terms_by_termid":{"MONDO:0011570":null},"xrefs":{"Monarch":{"xref_id":"0011570"}}}


id: GO:0008704
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-carboxymethyl-2-hydroxymuconate = 5-carboxy-2-oxohept-3-enedioate.","definition_xrefs":["EC:5.3.3.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, transposing C=C bonds","termid":"GO:0016863"}],"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:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"5-carboxymethyl-2-hydroxymuconate delta-isomerase activity","secondary_identifiers":["RHEA:18813","UM-BBD_reactionID:r0366","MetaCyc:5.3.3.10-RXN","GO:0018843"],"synonyms":[{"name":"2-hydroxyhepta-2,4-diene-1,7-dioate isomerase","type":"related"},{"name":"5-carboxymethyl-2-hydroxymuconate D-isomerase activity","type":"exact"},{"name":"5-carboxymethyl-2-hydroxymuconate delta2,Delta4-2-oxo,Delta3-isomerase activity","type":"related"},{"name":"5-carboxymethyl-2-hydroxymuconic acid isomerase activity","type":"related"},{"name":"CHM isomerase activity","type":"related"},{"name":"HHDD isomerase activity","type":"exact"},{"name":"hpaG-1","type":"related"},{"name":"hpaG1","type":"related"}],"termid":"GO:0008704"}


id: PBO:0060727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A13","termid":"PBO:0060727"}


id: PBO:0075449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated 2 pseudogene 1","termid":"PBO:0075449"}


id: GO:0014848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within smooth muscle tissue, resulting in a change in muscle geometry. This process occurs in the urinary tract. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. The urinary tract consists of organs of the body that produce and discharge urine. These include the kidneys, ureters, bladder, and urethra.","definition_xrefs":["MSH:D014551","GOC:ef","GOC:mtg_muscle","MA:0000325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smooth muscle contraction","termid":"GO:0006939"}],"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":"urinary tract smooth muscle contraction","termid":"GO:0014848"}


id: GO:0015742
data:
  {"annotated_genes":["SJAG_00275","SJAG_00522"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71538],"is_not":false,"summary":null,"term":"GO:0015742"},{"annotations":[96542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990550"}]},"cv_name":"biological_process","definition":"The directed movement of alpha-ketoglutarate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transport","termid":"GO:0006835"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00275":null,"SJAG_00522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"alpha-ketoglutarate transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"2-oxoglutarate transport","type":"exact"},{"name":"mitochondrial alpha-ketoglutarate/malate transport","type":"related"}],"termid":"GO:0015742","terms_by_termid":{"GO:0015742":null,"GO:1990550":null}}


id: GO:0061870
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of hepatic stellate cell migration.","definition_xrefs":["PMID:24204762"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of fibroblast migration","termid":"GO:0010763"},{"relation_name":"is_a","term_name":"regulation of hepatic stellate cell migration","termid":"GO:0061869"},{"relation_name":"positively_regulates","term_name":"hepatic stellate cell migration","termid":"GO:0061868"}],"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 hepatic stellate cell migration","termid":"GO:0061870"}


id: PBO:0050520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox D8","termid":"PBO:0050520"}


id: PBO:0071377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL30 antisense RNA 1","termid":"PBO:0071377"}


id: MONDO:0001039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the tonsillar tissue.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"upper respiratory tract disorder","termid":"MONDO:0004867"},{"relation_name":"is_a","term_name":"disorder of pharynx","termid":"MONDO:0020592"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"},{"relation_name":"is_a","term_name":"lymphoid system disorder","termid":"MONDO:0044986"}],"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":"tonsillitis","secondary_identifiers":["ICD9:474.00","MEDGEN:1781351","NCIT:C116006","ICD10CM:J35.01","UMLS:C0740402","MESH:D014069","DOID:10456","SCTID:90979004"],"synonyms":[{"name":"chronic tonsillitis","type":"exact"},{"name":"inflammation of tonsil","type":"exact"},{"name":"throat infection - tonsillitis","type":"exact"},{"name":"tonsil inflammation","type":"exact"},{"name":"tonsilitis","type":"exact"}],"termid":"MONDO:0001039","xrefs":{"Monarch":{"xref_id":"0001039"}}}


id: SO:0000111
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene encoded within a transposable element. For example gag, int, env and pol are the transposable element genes of the TY element in yeast.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"},{"relation_name":"part_of","term_name":"transposable_element","termid":"SO:0000101"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transposable_element_gene","synonyms":[{"name":"transposable element gene","type":"exact"}],"termid":"SO:0000111"}


id: MONDO:0001769
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nasolacrimal duct disorder","termid":"MONDO:0044984"}],"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":"acquired tear duct stenosis","secondary_identifiers":["DOID:13655","MEDGEN:509872","SCTID:193995004","UMLS:C0155248","ICD9:375.56"],"synonyms":[{"name":"acquired nasolacrimal duct stenosis","type":"exact"},{"name":"acquired stenosis of nasolacrimal duct","type":"exact"},{"name":"stenosis of nasolacrimal duct, acquired","type":"exact"},{"name":"tear duct - acquired stenosis","type":"exact"}],"termid":"MONDO:0001769","xrefs":{"Monarch":{"xref_id":"0001769"}}}


id: MONDO:0010393
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the BRWD3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 93","secondary_identifiers":["OMIM:300659","UMLS:C1970841","DOID:0112045","MEDGEN:410164","MESH:C567066"],"synonyms":[{"name":"BRWD3 non-syndromic X-linked intellectual disability","type":"exact"},{"name":"MRX93","type":"related"},{"name":"intellectual developmental disorder, X-linked 93, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked 93","type":"exact"},{"name":"intellectual disability, X-linked type 93","type":"exact"},{"name":"intellectual disability, X-linked, with macrocephaly","type":"related"},{"name":"mental retardation, X-linked 93","type":"related"},{"name":"mental retardation, X-linked type 93","type":"exact"},{"name":"mental retardation, X-linked, with macrocephaly","type":"related"},{"name":"non-syndromic X-linked intellectual disability caused by mutation in BRWD3","type":"exact"}],"termid":"MONDO:0010393","xrefs":{"Monarch":{"xref_id":"0010393"}}}


id: GO:0071877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of an adenylate cyclase-inhibiting adrenergic receptor signaling pathway activity. An adrenergic receptor signaling pathway is the series of molecular signals generated as a consequence of an adrenergic receptor binding to one of its physiological ligands.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor signaling pathway","termid":"GO:0008277"},{"relation_name":"regulates","term_name":"adenylate cyclase-inhibiting adrenergic receptor signaling pathway","termid":"GO:0071881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of adenylate cyclase-inhibiting adrenergic receptor signaling pathway","synonyms":[{"name":"regulation of adrenergic receptor signaling pathway","type":"exact"},{"name":"regulation of adrenergic receptor signalling pathway","type":"exact"}],"termid":"GO:0071877"}


id: FYPO:0004269
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 dissolution of the cell septum edging material is abnormal; may result in the formation of chains of attached cells.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell separation after cytokinesis","termid":"FYPO:0000164"},{"relation_name":"is_a","term_name":"abnormal cellular component organization during vegetative growth","termid":"FYPO:0001353"},{"relation_name":"is_a","term_name":"abnormal metabolic process during vegetative growth","termid":"FYPO:0001363"}],"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:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal cell septum edging catabolic process","synonyms":[{"name":"abnormal cell septum edging catabolic process during mitotic cell cycle","type":"related"},{"name":"abnormal cell septum edging catabolic process during vegetative growth","type":"exact"},{"name":"abnormal cell septum edging catabolism","type":"exact"},{"name":"abnormal cell septum edging hydrolysis","type":"exact"},{"name":"chained cells","type":"related"}],"termid":"FYPO:0004269"}


id: GO:0022889
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of serine from one side of a membrane to the other. Serine is 2-amino-3-hydroxypropanoic acid.","definition_xrefs":["GOC:mtg_transport","RHEA:35031","ISBN:0815340729"],"gene_count":0,"genotype_count":0,"name":"obsolete serine transmembrane transporter activity (obsolete GO:0022889)","termid":"GO:0022889"}


id: PBO:0044066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin 9-like pseudogene 2","termid":"PBO:0044066"}


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


id: PBO:0068240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 18S ribosomal pseudogene 2","termid":"PBO:0068240"}


id: GO:0000753
data:
  {"annotated_genes":["SJAG_02700","SJAG_02864","SJAG_01943","SJAG_01993","SJAG_02989","SJAG_01894"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88212,98284,92480,98896,114340,98978],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904600"}]},"cv_name":"biological_process","definition":"The change in form (cell shape and size) that occurs during sexual reproduction in order to facilitate direct contact between the compatible mating types in organisms that undergo conjugation cellular fusion.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"part_of","term_name":"conjugation with cellular fusion","termid":"GO:0000747"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01894":null,"SJAG_01943":null,"SJAG_01993":null,"SJAG_02700":null,"SJAG_02864":null,"SJAG_02989":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000747","GO:0008150"],"is_obsolete":false,"name":"cell morphogenesis involved in conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0007332"],"synonyms":[{"name":"shmoo orientation","type":"narrow"},{"name":"shmooing","type":"narrow"}],"termid":"GO:0000753","terms_by_termid":{"GO:1904600":null}}


id: MONDO:0015086
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"cloverleaf skull-asphyxiating thoracic dysplasia syndrome","secondary_identifiers":["UMLS:C5190852","GARD:853","Orphanet:100978","MEDGEN:1674171"],"synonyms":[{"name":"Benallegue Lacete syndrome","type":"related"},{"name":"Benallegue-Lacete syndrome","type":"exact"},{"name":"cloverleaf skull and asphyxiating thoracic dysplasia","type":"related"}],"termid":"MONDO:0015086","xrefs":{"Monarch":{"xref_id":"0015086"}}}


id: GO:1903412
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a bile acid stimulus.","definition_xrefs":["GOC:BHF","GOC:TermGenie","PMID:21757002","GO_REF:0000071","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to bile acid","termid":"GO:1903412"}


id: GO:0046559
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an alpha-D-glucuronoside + H2O = an alcohol + D-glucuronate.","definition_xrefs":["EC:3.2.1.139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"alpha-glucuronidase activity","secondary_identifiers":["MetaCyc:3.2.1.139-RXN","RHEA:20005"],"synonyms":[{"name":"alpha-D-glucosiduronate glucuronohydrolase activity","type":"related"},{"name":"alpha-glucosiduronase activity","type":"related"}],"termid":"GO:0046559"}


id: PBO:0113818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocon beta subunit, GEF Sbh1","termid":"PBO:0113818"}


id: GO:0030538
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring in the embryo, by which the anatomical structures of the genitalia are generated and organized.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genitalia morphogenesis","termid":"GO:0035112"},{"relation_name":"is_a","term_name":"embryonic organ morphogenesis","termid":"GO:0048562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"embryonic genitalia morphogenesis","synonyms":[{"name":"embryonic genital morphogenesis","type":"related"}],"termid":"GO:0030538"}


id: FYPO:0000477
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which one or both meiotic nuclear division(s) begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiosis","termid":"FYPO:0000051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"name":"delayed onset of meiosis","synonyms":[{"name":"delayed meiosis","type":"exact"},{"name":"delayed onset of meiotic nuclear division","type":"exact"},{"name":"meiosis: delayed","type":"related"}],"termid":"FYPO:0000477"}


id: PBO:0068997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 241, pseudogene","termid":"PBO:0068997"}


id: PBO:0036153
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_methyltransferase_activity","termid":"PBO:0036153"}


id: PBO:0060049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 37","termid":"PBO:0060049"}


id: GO:0008196
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Receiving vitellogenin, and delivering vitellogenin into the cell via endocytosis.","definition_xrefs":["PMID:12429745","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cargo receptor activity","termid":"GO:0038024"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038024"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038024"],"is_obsolete":false,"name":"vitellogenin receptor activity","termid":"GO:0008196"}


id: GO:0030990
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A nonmembrane-bound oligomeric protein complex that participates in bidirectional transport of molecules (cargo) along axonemal microtubules.","definition_xrefs":["PMID:22118932","PMID:23945166","GOC:kmv","GOC:cilia","PMID:14570576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"intraciliary transport particle","synonyms":[{"name":"IFT complex","type":"related"},{"name":"intraflagellar transport complex","type":"exact"},{"name":"intraflagellar transport particle","type":"exact"}],"termid":"GO:0030990"}


id: PBO:0071436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 42","termid":"PBO:0071436"}


id: PBO:0039780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aquaporin 7 pseudogene 5","termid":"PBO:0039780"}


id: RO:0002618
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"participates_in_a_biotic-biotic_interaction_with","termid":"RO:0002574"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"visits","termid":"RO:0002618"}


id: GO:0001920
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of receptor recycling.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of receptor recycling","termid":"GO:0001919"},{"relation_name":"is_a","term_name":"negative regulation of macromolecule metabolic process","termid":"GO:0010605"},{"relation_name":"is_a","term_name":"negative regulation of signaling","termid":"GO:0023057"},{"relation_name":"negatively_regulates","term_name":"receptor recycling","termid":"GO:0001881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of receptor recycling","synonyms":[{"name":"down regulation of receptor recycling","type":"exact"},{"name":"down-regulation of receptor recycling","type":"exact"},{"name":"downregulation of receptor recycling","type":"exact"},{"name":"inhibition of receptor recycling","type":"narrow"}],"termid":"GO:0001920"}


id: PBO:0030244
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_during_cellular_response_to_freezing","termid":"PBO:0030244"}


id: PBO:0074861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 47","termid":"PBO:0074861"}


id: MONDO:0009148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare congenital ectodermal dysplasia syndrome with a range of signs and symptoms including cleft lip or palate, mental retardation and various forms of ectodermal dysplasia. Additional symptoms may include fused eyelids, absent nails, delayed bone growth and dry skin. It is believed that this syndrome follows an autosomal dominant pattern of inheritance with incomplete penetrance, and caused by a mutation affecting the TP63 gene","definition_xrefs":["Wikipedia:Rosselli%E2%80%93Gulienetti_syndrome"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","termid":"MONDO:0007124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0005093"],"is_obsolete":false,"name":"Rosselli-Gulienetti syndrome","secondary_identifiers":["icd11.foundation:1430451924","UMLS:C0796139","MESH:C563117","OMIM:225000","MEDGEN:163221","Orphanet:90339"],"synonyms":[{"name":"Rosselli-Gulienetti syndrome","type":"exact"}],"termid":"MONDO:0009148","xrefs":{"Monarch":{"xref_id":"0009148"}}}


id: GO:0018472
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-hydroxy-2-naphthaldehyde + NAD+ + H2O = NADH + H+ + 1-hydroxy-2-naphthoate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-hydroxy-2-naphthaldehyde dehydrogenase activity (obsolete GO:0018472)","termid":"GO:0018472"}


id: GO:0046815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the viral genome is retained within the capsid during genome cleavage and packaging.","definition_xrefs":["PMID:9696839"],"gene_count":0,"genotype_count":0,"name":"obsolete genome retention in viral capsid (obsolete GO:0046815)","termid":"GO:0046815"}


id: PBO:0042129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical carcinoma expressed PCNA regulatory lncRNA","termid":"PBO:0042129"}


id: GO:0140366
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A non-stoichiometric protein complex formed by several galectins crosslinking glycosylated ligands to form a dynamic lattice. The galectin lattice modulates receptor kinase signaling and the functionality of membrane receptors, by regulating the diffusion, compartmentalization and endocytosis of plasma membrane glycoproteins and glycolipids.","definition_xrefs":["PMID:28893908","PMID:30951647","PMID:26092931","PMID:19021578"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein complex involved in cell-cell adhesion","termid":"GO:0098635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"galectin lattice","termid":"GO:0140366"}


id: PBO:0061237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NOP53 ribosome biogenesis factor","termid":"PBO:0061237"}


id: MONDO:0008749
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pseudohypoparathyroidism type 2 (PHP2) is a type of pseudohypoparathyroidism (PHP) characterized by resistance to parathyroid hormone (PTH), which manifests with hypocalcemia, hyperphosphatemia and elevated PTH levels, absence of Albright's hereditary osteodystrophy (AHO), and normal expression of the Gs protein with a normal urinary cAMP response.","definition_xrefs":["Orphanet:94090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohypoparathyroidism","termid":"MONDO:0019992"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0005066"],"is_obsolete":false,"name":"pseudohypoparathyroidism type 2","secondary_identifiers":["ICD9:275.49","NANDO:1201078","SCTID:42183005","OMIM:203330","UMLS:C2932717","icd11.foundation:1650158822","MEDGEN:444371","MESH:C548077","GARD:10682"],"synonyms":[{"name":"PHP II","type":"related"},{"name":"PHP2","type":"related"},{"name":"Php 2","type":"related"},{"name":"pseudohypoparathyroidism, type II","type":"related"}],"termid":"MONDO:0008749","xrefs":{"Monarch":{"xref_id":"0008749"}}}


id: PBO:0011116
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dynein LIc","termid":"PBO:0011116"}


id: PBO:0065089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase cAMP-activated catalytic subunit beta","termid":"PBO:0065089"}


id: GO:0060669
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the embryonic placenta is generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"embryonic placenta development","termid":"GO:0001892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"embryonic placenta morphogenesis","termid":"GO:0060669"}


id: GO:0102333
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: malonyl-CoA + 3 H+ + a stearoyl-[acp] = nonadec-1-ene + 2 carbon dioxide + coenzyme A + a holo-[acyl-carrier protein].","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete stearoyl-[acp] elongase/decarboxylase activity (obsolete GO:0102333)","termid":"GO:0102333"}


id: MONDO:0100393
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly t(8;16). (A cytogenetic abnormality that involves a translocation between chromosomes 8 and 16.)","definition_xrefs":["NCIT:C175583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"acute myeloid leukemia, t(8;16)","synonyms":[{"name":"AML, t(8;16)","type":"exact"}],"termid":"MONDO:0100393","xrefs":{"Monarch":{"xref_id":"0100393"}}}


id: MONDO:0003342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign mesenchymal neoplasm arising from the perivascular cells of the connective and soft tissues. It is characterized by the presence of pericytes that grow in a circumferential pattern around vessels.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"cardiovascular organ benign neoplasm","termid":"MONDO:0000629"},{"relation_name":"is_a","term_name":"pericytic neoplasm","termid":"MONDO:0002604"},{"relation_name":"is_a","term_name":"benign neoplasm","termid":"MONDO:0005165"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign perivascular tumor","secondary_identifiers":["NCIT:C6529","DOID:5238","UMLS:C1332532","MEDGEN:231437"],"synonyms":[{"name":"benign Pericytic neoplasm","type":"exact"},{"name":"benign Pericytic tumor","type":"exact"},{"name":"benign Pericytic tumour","type":"exact"},{"name":"benign pericytic neoplasm","type":"exact"},{"name":"benign perivascular neoplasm","type":"exact"},{"name":"benign perivascular tumor","type":"exact"},{"name":"pericytic neoplasm, benign","type":"exact"}],"termid":"MONDO:0003342","xrefs":{"Monarch":{"xref_id":"0003342"}}}


id: GO:0042133
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving neurotransmitters, any of a group of substances that are released on excitation from the axon terminal of a presynaptic neuron of the central or peripheral nervous system and travel across the synaptic cleft to either excite or inhibit the target cell.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete neurotransmitter metabolic process (obsolete GO:0042133)","synonyms":[{"name":"neurotransmitter metabolism","type":"exact"}],"termid":"GO:0042133"}


id: PBO:0060473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamide phosphoribosyltransferase pseudogene 3","termid":"PBO:0060473"}


id: PBO:0077910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPT1 pseudogene 1","termid":"PBO:0077910"}


id: PBO:0084849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; involved together with Mrp7p in assembly of cytochrome c oxidase","termid":"PBO:0084849"}


id: PBO:0071715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 13","termid":"PBO:0071715"}


id: MONDO:0012524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"familial hypoaldosteronism","termid":"MONDO:0018541"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corticosterone methyloxidase type 2 deficiency","secondary_identifiers":["OMIM:610600","UMLS:C3463917","MEDGEN:483046"],"synonyms":[{"name":"18-oxidase deficiency","type":"related"},{"name":"Cmo 2 deficiency","type":"related"},{"name":"aldosterone deficiency 2","type":"related"},{"name":"aldosterone deficiency due to deficiency of steroid 18-oxidase","type":"related"},{"name":"corticosterone methyloxidase type II deficiency","type":"related"},{"name":"hyperreninemic hypoaldosteronism, familial, 1","type":"related"},{"name":"hypoaldosteronism, congenital, due to CMO II deficiency","type":"exact"},{"name":"steroid 18-oxidase deficiency","type":"related"}],"termid":"MONDO:0012524","xrefs":{"Monarch":{"xref_id":"0012524"}}}


id: MONDO:0015224
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of poisoning that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare intoxication (obsolete MONDO:0015224)","secondary_identifiers":["Orphanet:108999"],"synonyms":[{"name":"rare poisoning","type":"exact"}],"termid":"MONDO:0015224","xrefs":{"Monarch":{"xref_id":"0015224"}}}


id: FYPO:0006212
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates but dies before forming a germ tube or dividing, when spore germination takes place under conditions of copper ion starvation. Such spores exit dormancy and undergo isotropic swelling but the spore wall does not rupture and no germ tube emerges.","definition_xrefs":["PomBase:mah","PMID:28572514"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, before germ tube formation","termid":"FYPO:0006211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000004"],"is_obsolete":false,"name":"inviable after spore germination, before germ tube formation, during copper ion starvation","synonyms":[{"name":"inviable after spore germination, before germ tube formation, during cellular response to copper ion starvation","type":"exact"},{"name":"inviable after spore germination, before germ tube formation, during copper starvation","type":"exact"},{"name":"inviable following spore germination, before germ tube formation, during copper ion starvation","type":"exact"},{"name":"inviable germinated spore, without germ tube formation, during copper ion starvation","type":"exact"},{"name":"lethal after spore germination, before germ tube formation, during copper ion starvation","type":"exact"}],"termid":"FYPO:0006212"}


id: GO:1904640
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 methionine stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:17716000"],"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 methionine","termid":"GO:1904640"}


id: GO:0048938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structure of a glial cell in a lateral line nerve is generated and organized. This process occurs while the initially relatively unspecialized cell is acquiring the specialized features of a glial cell in a lateral line nerve.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"part_of","term_name":"lateral line nerve glial cell development","termid":"GO:0048937"}],"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":"lateral line nerve glial cell morphogenesis involved in differentiation","termid":"GO:0048938"}


id: FYPO:0007872
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 bulk plasma membrane flow from the cell poles to lateral regions does not occur.","definition_xrefs":["PMID:34533984","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal plasma membrane organization","termid":"FYPO:0000813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abolished plasma membrane flow from cell pole to lateral region","synonyms":[{"name":"abolished bulk plasma membrane flow from cell pole to lateral region","type":"exact"},{"name":"abolished plasma membrane flow from cell pole to lateral region during mitotic cell cycle","type":"related"},{"name":"abolished plasma membrane flow from cell pole to lateral region during vegetative growth","type":"exact"},{"name":"plasma membrane flow from cell pole to lateral region abolished","type":"exact"}],"termid":"FYPO:0007872"}


id: GO:1903369
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of foraging behavior.","definition_xrefs":["GO_REF:0000058","GOC:mr","GOC:TermGenie","PMID:8677262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of behavior","termid":"GO:0048521"},{"relation_name":"is_a","term_name":"regulation of foraging behavior","termid":"GO:1903368"},{"relation_name":"negatively_regulates","term_name":"foraging behavior","termid":"GO:0060756"}],"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 foraging behavior","synonyms":[{"name":"down regulation of foraging behavior","type":"exact"},{"name":"down-regulation of foraging behavior","type":"exact"},{"name":"downregulation of foraging behavior","type":"exact"},{"name":"inhibition of foraging behavior","type":"narrow"}],"termid":"GO:1903369"}


id: FYPO:0001708
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of iron-sulfur cluster binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal molecular function","termid":"FYPO:0000706"},{"relation_name":"is_a","term_name":"binding phenotype","termid":"FYPO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal iron-sulfur cluster binding","synonyms":[{"name":"normal iron-sulphur cluster binding","type":"exact"}],"termid":"FYPO:0001708"}


id: PBO:0017910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMS complex subunit Mis13","termid":"PBO:0017910"}


id: GO:0019261
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 1,4-dichlorobenzene (p-dichlorobenzene or paramoth), a derivative of benzene with two chlorine atoms attached at opposite positions on the ring.","definition_xrefs":["GOC:ai","PMID:9148781"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"organohalogen metabolic process","termid":"GO:0090345"}],"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":"1,4-dichlorobenzene catabolic process","secondary_identifiers":["MetaCyc:14DICHLORBENZDEG-PWY","UM-BBD_pathwayID:dcz"],"synonyms":[{"name":"1,4-dichlorobenzene breakdown","type":"exact"},{"name":"1,4-dichlorobenzene catabolism","type":"exact"},{"name":"1,4-dichlorobenzene degradation","type":"exact"}],"termid":"GO:0019261"}


id: PBO:0027528
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_binucleate_aseptate_cell_with_mitotic_cell_cycle_arrest_in_G2_before_cell_separation","termid":"PBO:0027528"}


id: GO:0045211
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A specialized area of membrane facing the presynaptic membrane on the tip of the nerve ending and separated from it by a minute cleft (the synaptic cleft). Neurotransmitters cross the synaptic cleft and transmit the signal to the postsynaptic membrane.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synaptic membrane","termid":"GO:0097060"},{"relation_name":"part_of","term_name":"postsynapse","termid":"GO:0098794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"postsynaptic membrane","synonyms":[{"name":"post-synaptic membrane","type":"exact"}],"termid":"GO:0045211"}


id: PBO:0069631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 908, pseudogene","termid":"PBO:0069631"}


id: FYPO:0007595
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitophagy, i.e. autophagic degradation of the mitochondria, is increased when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased mitophagy","termid":"FYPO:0000501"},{"relation_name":"is_a","term_name":"abnormal mitophagy during nitrogen starvation","termid":"FYPO:0007593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased mitophagy during nitrogen starvation","synonyms":[{"name":"increased autophagy of mitochondrion during nitrogen depletion","type":"exact"},{"name":"increased autophagy of mitochondrion during nitrogen deprivation","type":"exact"},{"name":"increased autophagy of mitochondrion during nitrogen starvation","type":"exact"}],"termid":"FYPO:0007595"}


id: PBO:0048941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgi reassembly stacking protein 1","termid":"PBO:0048941"}


id: PBO:0081197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZIM2 antisense RNA 1","termid":"PBO:0081197"}


id: GO:0015531
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: citrate(out) + H+(out) = citrate(in) + H+(in).","definition_xrefs":["TC:2.A.1.6.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"},{"relation_name":"is_a","term_name":"citrate secondary active transmembrane transporter activity","termid":"GO:0071913"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"citrate:proton symporter activity","secondary_identifiers":["RHEA:32123"],"synonyms":[{"name":"citrate:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015531"}


id: PBO:0018000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA repair endonuclease non-catalytic subunit Swi10","termid":"PBO:0018000"}


id: PBO:0078116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 5","termid":"PBO:0078116"}


id: FYPO:0001166
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cells grow normally (i.e. indistinguishably from wild type) in a medium containing fructose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0002058","FYPO:0002057","FYPO:0000257","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on fructose carbon source","synonyms":[{"name":"normal cell population growth on fructose carbon source","type":"exact"},{"name":"normal vegetative cell population growth on fructose carbon source","type":"exact"}],"termid":"FYPO:0001166"}


id: MONDO:0019489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diffuse palmoplantar keratoderma-acrocyanosis syndrome is characterized by the association of diffuse palmoplantar keratoderma and acrocyanosis. It has been described in eight members of one family and in two sporadic cases. The mode of inheritance in the familial cases was autosomal dominant.","definition_xrefs":["Orphanet:86918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse palmoplantar keratoderma","termid":"MONDO:0017666"}],"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":"diffuse palmoplantar keratoderma - acrocyanosis syndrome","secondary_identifiers":["MEDGEN:929257","UMLS:C4303588","GARD:19089"],"synonyms":[{"name":"diffuse palmoplantar hyperkeratosis-acrocyanosis syndrome","type":"exact"}],"termid":"MONDO:0019489","xrefs":{"Monarch":{"xref_id":"0019489"}}}


id: MONDO:0956975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic asthma that is characterized by the pathophysiology phenotype combination (endotype) of early-onset allergic asthma, late-onset eosinophilic asthma, and aspirin-exacerbated respiratory disease.","definition_xrefs":["DOID:0080817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic asthma","termid":"MONDO:0850282"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T2-high asthma","termid":"MONDO:0956975","xrefs":{"Monarch":{"xref_id":"0956975"}}}


id: GO:0016584
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Ordering of successions of nucleosomes into regular arrays so that nucleosomes are positioned at defined distances from one another.","definition_xrefs":["GOC:bf","PMID:11447119","PMID:8676389"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleosome positioning (obsolete GO:0016584)","synonyms":[{"name":"nucleosome spacing","type":"exact"}],"termid":"GO:0016584"}


id: PBO:0088068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-specific protease; removes ubiquitin from ubiquitinated proteins; cleaves at the C terminus of ubiquitin fusions irrespective of their size; capable of cleaving polyubiquitin chains","termid":"PBO:0088068"}


id: GO:1901265
data:
  {"annotated_genes":["SJAG_01851","SJAG_03684","SJAG_02200","SJAG_04410","SJAG_02353","SJAG_01816","SJAG_00616","SJAG_03534","SJAG_04435","SJAG_03728","SJAG_04355","SJAG_04154","SJAG_00947","SJAG_04755","SJAG_03903","SJAG_00235","SJAG_04495","SJAG_03804","SJAG_02605","SJAG_00707","SJAG_02994","SJAG_02288","SJAG_03237","SJAG_04114","SJAG_03811","SJAG_03567","SJAG_04612","SJAG_03732","SJAG_05105","SJAG_04511","SJAG_02429","SJAG_03798","SJAG_00244","SJAG_03011","SJAG_02887","SJAG_03313","SJAG_02725","SJAG_03892","SJAG_02713","SJAG_00198","SJAG_01909","SJAG_00114","SJAG_00500","SJAG_01254","SJAG_04150","SJAG_01929","SJAG_02835","SJAG_00863","SJAG_01315","SJAG_03363","SJAG_01534","SJAG_00409","SJAG_04747","SJAG_02233","SJAG_03501","SJAG_02428","SJAG_03780","SJAG_04055","SJAG_00956","SJAG_02061","SJAG_01311","SJAG_02468","SJAG_01797","SJAG_03061","SJAG_04375","SJAG_01047","SJAG_02364","SJAG_03174","SJAG_02875","SJAG_01373","SJAG_00168","SJAG_00845","SJAG_01002","SJAG_00972","SJAG_02444","SJAG_02564","SJAG_03887","SJAG_03496","SJAG_02838","SJAG_05295","SJAG_02926","SJAG_01859","SJAG_04700","SJAG_04258","SJAG_03799","SJAG_02236","SJAG_04203","SJAG_04042","SJAG_03436","SJAG_02421","SJAG_02399","SJAG_04081","SJAG_04409","SJAG_05010","SJAG_04230","SJAG_01040","SJAG_01268","SJAG_02077","SJAG_01351","SJAG_01731","SJAG_02599","SJAG_04157","SJAG_04233","SJAG_04566","SJAG_00430","SJAG_01352","SJAG_04862","SJAG_01410","SJAG_00898","SJAG_02604","SJAG_05213","SJAG_01805","SJAG_00226","SJAG_02302","SJAG_02827","SJAG_02374","SJAG_03213","SJAG_02226","SJAG_00150","SJAG_00169","SJAG_00475","SJAG_01245","SJAG_02015","SJAG_04210","SJAG_03709","SJAG_02142","SJAG_01148","SJAG_01613","SJAG_01546","SJAG_00968","SJAG_00234","SJAG_03486","SJAG_01577","SJAG_00597","SJAG_02696","SJAG_01400","SJAG_00678","SJAG_01825","SJAG_00031","SJAG_00963","SJAG_01215","SJAG_03529","SJAG_00381","SJAG_00412","SJAG_04507","SJAG_02431","SJAG_00329","SJAG_03592","SJAG_00208","SJAG_00986","SJAG_04772","SJAG_02945","SJAG_00486","SJAG_06597","SJAG_01070","SJAG_00690","SJAG_04156","SJAG_02527","SJAG_05173","SJAG_01500","SJAG_04285","SJAG_02897","SJAG_02592","SJAG_02400","SJAG_01129","SJAG_02292","SJAG_02712","SJAG_05372","SJAG_03982","SJAG_00875","SJAG_01402","SJAG_02824","SJAG_03950","SJAG_00331","SJAG_03036","SJAG_00042","SJAG_04038","SJAG_03479","SJAG_01297","SJAG_03438","SJAG_03336","SJAG_01680","SJAG_03240","SJAG_00203","SJAG_03679","SJAG_00906","SJAG_03374","SJAG_02378","SJAG_04465","SJAG_01664","SJAG_03659","SJAG_00938","SJAG_00356","SJAG_01339","SJAG_00757","SJAG_04537","SJAG_01938","SJAG_03140","SJAG_00881","SJAG_00988","SJAG_01774","SJAG_01695","SJAG_02619","SJAG_04265","SJAG_01466","SJAG_01379","SJAG_02610","SJAG_00084","SJAG_00443","SJAG_04482","SJAG_01724","SJAG_05340","SJAG_00980","SJAG_04761","SJAG_05194","SJAG_02545","SJAG_02686","SJAG_04394","SJAG_04692","SJAG_03785","SJAG_01489","SJAG_00609","SJAG_04277","SJAG_05313","SJAG_16455","SJAG_00466","SJAG_01152","SJAG_00330","SJAG_02721","SJAG_02656","SJAG_03959","SJAG_04760","SJAG_02171","SJAG_02074","SJAG_03421","SJAG_01677","SJAG_05249","SJAG_04367","SJAG_00027","SJAG_03828","SJAG_00424","SJAG_02176","SJAG_03909","SJAG_01344","SJAG_04669","SJAG_01558","SJAG_05276","SJAG_04189","SJAG_02084","SJAG_00370","SJAG_00103","SJAG_01831","SJAG_05018","SJAG_01881","SJAG_02384","SJAG_04003","SJAG_04351","SJAG_01791","SJAG_02394","SJAG_02460","SJAG_04589","SJAG_02822","SJAG_01964","SJAG_01181","SJAG_03626","SJAG_01885","SJAG_00414","SJAG_00878","SJAG_01696","SJAG_02104","SJAG_00851","SJAG_03585","SJAG_01159","SJAG_04004","SJAG_03730","SJAG_02736","SJAG_02825","SJAG_03371","SJAG_03206","SJAG_02148","SJAG_02488","SJAG_01944","SJAG_04573","SJAG_04551","SJAG_03345","SJAG_02521","SJAG_02489","SJAG_06622","SJAG_02723","SJAG_01179","SJAG_05290","SJAG_01354","SJAG_01018","SJAG_03409","SJAG_04187","SJAG_02738","SJAG_01376","SJAG_04001","SJAG_04743","SJAG_00457","SJAG_01391","SJAG_03602","SJAG_04054","SJAG_02297","SJAG_03676","SJAG_00964","SJAG_00488","SJAG_01419","SJAG_02640","SJAG_04974","SJAG_06621","SJAG_04147","SJAG_00378","SJAG_01438","SJAG_05209","SJAG_00392","SJAG_03485","SJAG_04849","SJAG_02058","SJAG_01863","SJAG_04125","SJAG_03152","SJAG_00857","SJAG_02598","SJAG_01162","SJAG_02785","SJAG_00364","SJAG_02698","SJAG_02708","SJAG_02690","SJAG_04000","SJAG_00661","SJAG_03854","SJAG_01176","SJAG_03362","SJAG_02382","SJAG_03886","SJAG_04468","SJAG_01024","SJAG_04270","SJAG_01235","SJAG_01449","SJAG_04366","SJAG_04666","SJAG_00402","SJAG_03789","SJAG_03471","SJAG_03449","SJAG_03193","SJAG_04657","SJAG_02392","SJAG_03987","SJAG_02596","SJAG_00447","SJAG_00529","SJAG_00855","SJAG_02563","SJAG_04946","SJAG_03526","SJAG_03897","SJAG_03846","SJAG_03832","SJAG_05015","SJAG_00118","SJAG_01587","SJAG_01789","SJAG_02760","SJAG_00048","SJAG_01432","SJAG_03376","SJAG_00729","SJAG_02294","SJAG_03017","SJAG_03533","SJAG_01186","SJAG_04655","SJAG_03290","SJAG_00604","SJAG_01595","SJAG_01704","SJAG_02848","SJAG_01510","SJAG_00502","SJAG_02558","SJAG_03071","SJAG_02879","SJAG_03157","SJAG_03669","SJAG_03141","SJAG_02878","SJAG_02520","SJAG_02313","SJAG_01197","SJAG_00533","SJAG_03708","SJAG_00871","SJAG_02808","SJAG_01456","SJAG_05027","SJAG_02295","SJAG_00564","SJAG_03898","SJAG_01522","SJAG_03545","SJAG_04320","SJAG_01903","SJAG_00541","SJAG_00044","SJAG_04334","SJAG_04882","SJAG_03753","SJAG_02684","SJAG_04312","SJAG_02370","SJAG_01052","SJAG_16456","SJAG_02182","SJAG_02741","SJAG_03451","SJAG_01684","SJAG_02022","SJAG_02601","SJAG_02858","SJAG_04856","SJAG_03384","SJAG_02895","SJAG_00344","SJAG_04480","SJAG_01877","SJAG_00931","SJAG_04874","SJAG_04738","SJAG_04845","SJAG_01718","SJAG_03096","SJAG_04477","SJAG_00996","SJAG_00427","SJAG_02906","SJAG_04032","SJAG_02595","SJAG_00136","SJAG_04121","SJAG_03660","SJAG_03932","SJAG_05353","SJAG_01080","SJAG_02199","SJAG_04343","SJAG_03923","SJAG_00718","SJAG_03927","SJAG_04268","SJAG_01358","SJAG_03915","SJAG_02680","SJAG_04118","SJAG_01769","SJAG_02366","SJAG_02457","SJAG_00420","SJAG_01693","SJAG_03570","SJAG_04734","SJAG_04362","SJAG_04810","SJAG_00663","SJAG_02856","SJAG_02420","SJAG_00342","SJAG_01942","SJAG_02704","SJAG_00801","SJAG_01937","SJAG_04665","SJAG_00798","SJAG_01182","SJAG_01855","SJAG_01041","SJAG_04599","SJAG_00653","SJAG_00790","SJAG_01669","SJAG_01000","SJAG_00300","SJAG_02267","SJAG_00353","SJAG_05304","SJAG_00993","SJAG_00111","SJAG_00633","SJAG_03069","SJAG_02287","SJAG_04457","SJAG_00516","SJAG_02796","SJAG_04980","SJAG_03067","SJAG_01084","SJAG_02082","SJAG_04693","SJAG_03209","SJAG_04064","SJAG_00636","SJAG_04186","SJAG_04597","SJAG_05030","SJAG_01277","SJAG_03224","SJAG_01544","SJAG_00605","SJAG_01383","SJAG_00773","SJAG_04094","SJAG_03866","SJAG_03689","SJAG_03495","SJAG_00252","SJAG_01807","SJAG_04840","SJAG_04183","SJAG_01878","SJAG_01131","SJAG_02517","SJAG_03813","SJAG_03342","SJAG_00360","SJAG_02426","SJAG_04461","SJAG_04745","SJAG_01837","SJAG_04469","SJAG_01799","SJAG_00390","SJAG_01918","SJAG_00984","SJAG_04232","SJAG_02977","SJAG_04777","SJAG_00887","SJAG_02187","SJAG_04762","SJAG_03658","SJAG_00358","SJAG_03115","SJAG_04282","SJAG_01945","SJAG_01082","SJAG_00840","SJAG_04372","SJAG_01075","SJAG_04634","SJAG_01874","SJAG_04757","SJAG_00930","SJAG_00464","SJAG_01618","SJAG_04470","SJAG_02038","SJAG_03072","SJAG_00659","SJAG_01471","SJAG_05024","SJAG_04126","SJAG_02286","SJAG_01615","SJAG_01010","SJAG_04509","SJAG_04940","SJAG_03852","SJAG_00995","SJAG_04039","SJAG_02342","SJAG_03497","SJAG_01620","SJAG_00712","SJAG_00779","SJAG_00265","SJAG_04549","SJAG_03475","SJAG_03613","SJAG_01499","SJAG_02509","SJAG_02872","SJAG_03948","SJAG_01198","SJAG_00983","SJAG_00638","SJAG_03077","SJAG_00403","SJAG_03703","SJAG_03355","SJAG_01644","SJAG_03967","SJAG_05022","SJAG_03129","SJAG_03137","SJAG_03688","SJAG_04288","SJAG_01671","SJAG_01530","SJAG_01571","SJAG_03275","SJAG_03453","SJAG_00650","SJAG_01259","SJAG_04865","SJAG_02498","SJAG_04280","SJAG_04577","SJAG_02575","SJAG_04652","SJAG_04857","SJAG_04276","SJAG_01458","SJAG_00704","SJAG_01953","SJAG_01787","SJAG_00256","SJAG_00999","SJAG_01653","SJAG_04627","SJAG_04622","SJAG_02748","SJAG_02643","SJAG_02720","SJAG_00583","SJAG_03720","SJAG_02618","SJAG_02183","SJAG_03712","SJAG_05019","SJAG_00332","SJAG_02496","SJAG_04052","SJAG_04473","SJAG_00106","SJAG_05332","SJAG_01405","SJAG_00815","SJAG_00039","SJAG_02180","SJAG_02331","SJAG_03386","SJAG_02661","SJAG_03557","SJAG_04608","SJAG_04167","SJAG_04486","SJAG_03145","SJAG_03188","SJAG_00884","SJAG_01668","SJAG_01762","SJAG_04459","SJAG_01240","SJAG_04387","SJAG_01474","SJAG_03320","SJAG_01063","SJAG_00660","SJAG_04206","SJAG_00649","SJAG_04650","SJAG_00004","SJAG_01081","SJAG_04544","SJAG_03457","SJAG_02348","SJAG_03048","SJAG_02889","SJAG_02991","SJAG_04287","SJAG_03160","SJAG_02206","SJAG_03236","SJAG_00174","SJAG_03461","SJAG_02135","SJAG_04552","SJAG_00281","SJAG_02602","SJAG_01616","SJAG_01435","SJAG_02950","SJAG_03985","SJAG_02242","SJAG_00337","SJAG_03257","SJAG_01221","SJAG_01611","SJAG_05231","SJAG_05025","SJAG_00359","SJAG_03476","SJAG_03850","SJAG_03896","SJAG_00293","SJAG_02249","SJAG_04970","SJAG_03349","SJAG_02615","SJAG_00231","SJAG_01447","SJAG_03277","SJAG_00786","SJAG_00243","SJAG_00853","SJAG_02923","SJAG_03562","SJAG_01137","SJAG_00669","SJAG_01575","SJAG_06642","SJAG_02997","SJAG_00610","SJAG_01679","SJAG_00436","SJAG_02571","SJAG_02336","SJAG_02697","SJAG_03946","SJAG_00766","SJAG_01012","SJAG_01164","SJAG_00599"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69847,92823,72528,89171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043531"},{"annotations":[88840,68441,73820,69935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016208"},{"annotations":[59060,58858,66492,58727,61778,68433,61645,64491,73932,94723,65735,57110,63293,68563,111403,61735,61739,61375,71575,57327,58514,57896,58198,58993,60446,62637,65035,65242,102676,65886,76404,67786,57061,58420,66406,58952,69070,99690,113198,87749,57310,58926,59409,61553,68503,67407,67581,63211,62768,65207,65527,66170,69257,60077,62287,63399,68214,59495,58839,114538,92117,68636,61033,65849,61257,114133,67061,62715,64630,101106,60056,98795,64199,61762,65157,57260,91875,77497,62764,59395,59643,60742,59798,57612,64812,66426,66567,58551,67411,67616,58671,69338,106009,64262,59817,68654,58099,67817,62220,66663,56922,59550,61759,58281,60412,89008,61832,57191,62910,62967,66740,65038,58486,64821,66531,89031,61149,62416,58023,69084,102268,61267,107958,58352,64096,68568,98838,57146,57601,58171,65306,65730,69321,105512,58401,66103,68456,58451,58217,68810,58965,63373,60051,62252,64887,60976,62616,67233,69211,69333,105610,61992,61028,65949,60282,64540,59857,60491,57299,67949,110548,57386,59604,62304,60594,104648,100094,60148,65574,69342,63283,69230,60763,113109,103828,88760,57790,58980,59723,59903,67081,59588,67678,57408,57034,64193,67396,59246,57455,68066,69150,97489,58721,61870,57374,60545,63837,67225,57700,64077,63354,58418,59786,61128,61189,63680,58753,60012,57199,64933,67999,68131,69849,77720,113442,115723,62727,66971,67178,96434,61824,64902,65986,57996,60615,59677,92663,67341,66734,61523,57451,68323,66638,67776,68406,61650,59013,58732,66294,64709,66330,65767,66580,62533,64679,57421,66507,60437,68291,57568,64891,72714,88334,103328,105250,56940,61056,66149,69182,65759,60624,58848,61214,68546,58053,60769,59266,61727,62873,80107,89803,67809,62053,69368,69556,65743,62975,68184,67004,67712,63800,64514,57583,60168,63145,64641,67453,72339,111177,58650,69447,67691,68250,64849,58251,63336,58034,63728,67905,61569,66683,63310,68115,63756,112972,68445,112974,57549,62588,58598,64307,61096,99344,57103,68778,59094,59051,69573,67524,59740,67487,68063,69381,63423,91639,62822,58786,68197,103286,66857,60271,61469,60923,68448,66159,65145,104325,59697,116048,59994,58931,65386,69489,89173,59254,88107,63417,65278,63940,59911,59192,57938,67622,63494,61135,68460,67046,111094,57161,65490,59233,65751,58685,61791,63365,63611,64635,63893,69113,61336,59547,60989,65045,63459,63240,107809,69092,69302,68626,68848,58623,67856,58044,60470,74288,64440,91129,59939,66137,60888,57431,63129,64988,65022,58854,59535,66345,67845,71904,108523,68997,69560,65709,65314,57888,68209,58203,65586,57629,66848,91521,64104,64579,59502,99888,60157,98854,57443,63995,65927,66311,58565,66041,67603,64410,61558,66212,67362,61278,69136,67427,59121,57316,61588,58768,60118,62559,61355,62396,58300,65249,65456,65587,114079,64991,64209,60374,63445,57820,57737,58830,61234,64451,65423,66898,67381,67386,66053,57248,57697,66651,57975,68606,113609,117956,63046,89455,60324,60711,109082,58797,58058,57874,63966,58411,64360,65869,65923,99143,58575,67984,68584,58372,63839,61883,66273,60418,68924,59046,68707,72745,62673,60718,108722,61237,69588,118012,63174,65393,59008,62633,62748,66400,66177,60187,62279,65507,65181,61016,63273,67772,115789,67740,68621,59883,57273,63675,62555,65958,72530,68087,96463,111148,69138,60123,93672,58040,112973,67187,67935,63233,57852,108565,59159,68025,64510,66315,60044,62133,59459,65682,58665,58661,67657,64432,64064,62093,64657,113615,68852,63545,66200,58384,68480,62455,66915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005524"},{"annotations":[70936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030552"},{"annotations":[87692,90817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002135"},{"annotations":[76134,69504,64391,69486,113030,68873,70676,59301,109696,60648,70087,71746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071949"},{"annotations":[74451,112814,78277,60586,59581,79023,76044,71567,118808,65630,76266,62437,65794,79018,94083,76322,75953,77138,64776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050660"},{"annotations":[60703,65537,64037,68913,67305,57428,74450,63122,64740,78276,76321,77137,59580,89333,79022,59431,72525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010181"},{"annotations":[75094,72146,91667,92397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019003"},{"annotations":[88841,115714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019002"},{"annotations":[103669,77203,62741,58884,67021,101244,57920,61779,76357,67873,69741,59982,60352,70035,72202,73380,75091,64206,96253,65839,96485,105074,108488,118508,75783,70924,80023,66292,64140,58690,62204,72384,93424,62521,57474,80290,66611,113552,117521,118987,69154,65873,71400,68860,67753,58167,65162,65420,62849,74000,77672,67358,74286,77859,58001,77874,91895,57122,60842,61320,73126,95735,60074,62610,61743,77505,63010,69571,60349,73110,78476,61104,58112,68764,59565,58822,63586,63645,68191,74301,79942,93371,94202,64725,91048,68829,72143,66307,64633,57988,64402,72720,80002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005525"},{"annotations":[75817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036042"},{"annotations":[62691,63415,69545,60004,68898,109420,109421,61665,62736,109423,62756,58780,118809,69358,64358,63247,60971,64753,58021,109419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051287"},{"annotations":[111988,72181,78602,70699,77283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070403"},{"annotations":[109427,109428,109430,65701,114830,94084,64697,64369,64741,62735,67994,57657,62496,60003,68019,58505,80322,104464,69544,64357,109426,59663,70923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050661"},{"annotations":[58781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070401"},{"annotations":[103046,114813,74242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070402"},{"annotations":[90823,91644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002134"}]},"cv_name":"molecular_function","definition":"Binding to nucleoside phosphate.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":726,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00031":null,"SJAG_00039":null,"SJAG_00042":null,"SJAG_00044":null,"SJAG_00048":null,"SJAG_00084":null,"SJAG_00103":null,"SJAG_00106":null,"SJAG_00111":null,"SJAG_00114":null,"SJAG_00118":null,"SJAG_00136":null,"SJAG_00150":null,"SJAG_00168":null,"SJAG_00169":null,"SJAG_00174":null,"SJAG_00198":null,"SJAG_00203":null,"SJAG_00208":null,"SJAG_00226":null,"SJAG_00231":null,"SJAG_00234":null,"SJAG_00235":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00252":null,"SJAG_00256":null,"SJAG_00265":null,"SJAG_00281":null,"SJAG_00293":null,"SJAG_00300":null,"SJAG_00329":null,"SJAG_00330":null,"SJAG_00331":null,"SJAG_00332":null,"SJAG_00337":null,"SJAG_00342":null,"SJAG_00344":null,"SJAG_00353":null,"SJAG_00356":null,"SJAG_00358":null,"SJAG_00359":null,"SJAG_00360":null,"SJAG_00364":null,"SJAG_00370":null,"SJAG_00378":null,"SJAG_00381":null,"SJAG_00390":null,"SJAG_00392":null,"SJAG_00402":null,"SJAG_00403":null,"SJAG_00409":null,"SJAG_00412":null,"SJAG_00414":null,"SJAG_00420":null,"SJAG_00424":null,"SJAG_00427":null,"SJAG_00430":null,"SJAG_00436":null,"SJAG_00443":null,"SJAG_00447":null,"SJAG_00457":null,"SJAG_00464":null,"SJAG_00466":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00488":null,"SJAG_00500":null,"SJAG_00502":null,"SJAG_00516":null,"SJAG_00529":null,"SJAG_00533":null,"SJAG_00541":null,"SJAG_00564":null,"SJAG_00583":null,"SJAG_00597":null,"SJAG_00599":null,"SJAG_00604":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00610":null,"SJAG_00616":null,"SJAG_00633":null,"SJAG_00636":null,"SJAG_00638":null,"SJAG_00649":null,"SJAG_00650":null,"SJAG_00653":null,"SJAG_00659":null,"SJAG_00660":null,"SJAG_00661":null,"SJAG_00663":null,"SJAG_00669":null,"SJAG_00678":null,"SJAG_00690":null,"SJAG_00704":null,"SJAG_00707":null,"SJAG_00712":null,"SJAG_00718":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00773":null,"SJAG_00779":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00798":null,"SJAG_00801":null,"SJAG_00815":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00855":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00875":null,"SJAG_00878":null,"SJAG_00881":null,"SJAG_00884":null,"SJAG_00887":null,"SJAG_00898":null,"SJAG_00906":null,"SJAG_00930":null,"SJAG_00931":null,"SJAG_00938":null,"SJAG_00947":null,"SJAG_00956":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00968":null,"SJAG_00972":null,"SJAG_00980":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_00986":null,"SJAG_00988":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_00999":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01010":null,"SJAG_01012":null,"SJAG_01018":null,"SJAG_01024":null,"SJAG_01040":null,"SJAG_01041":null,"SJAG_01047":null,"SJAG_01052":null,"SJAG_01063":null,"SJAG_01070":null,"SJAG_01075":null,"SJAG_01080":null,"SJAG_01081":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01137":null,"SJAG_01148":null,"SJAG_01152":null,"SJAG_01159":null,"SJAG_01162":null,"SJAG_01164":null,"SJAG_01176":null,"SJAG_01179":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01186":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01215":null,"SJAG_01221":null,"SJAG_01235":null,"SJAG_01240":null,"SJAG_01245":null,"SJAG_01254":null,"SJAG_01259":null,"SJAG_01268":null,"SJAG_01277":null,"SJAG_01297":null,"SJAG_01311":null,"SJAG_01315":null,"SJAG_01339":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01379":null,"SJAG_01383":null,"SJAG_01391":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01432":null,"SJAG_01435":null,"SJAG_01438":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01458":null,"SJAG_01466":null,"SJAG_01471":null,"SJAG_01474":null,"SJAG_01489":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01510":null,"SJAG_01522":null,"SJAG_01530":null,"SJAG_01534":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01571":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01587":null,"SJAG_01595":null,"SJAG_01611":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01616":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01644":null,"SJAG_01653":null,"SJAG_01664":null,"SJAG_01668":null,"SJAG_01669":null,"SJAG_01671":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01684":null,"SJAG_01693":null,"SJAG_01695":null,"SJAG_01696":null,"SJAG_01704":null,"SJAG_01718":null,"SJAG_01724":null,"SJAG_01731":null,"SJAG_01762":null,"SJAG_01769":null,"SJAG_01774":null,"SJAG_01787":null,"SJAG_01789":null,"SJAG_01791":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01816":null,"SJAG_01825":null,"SJAG_01831":null,"SJAG_01837":null,"SJAG_01851":null,"SJAG_01855":null,"SJAG_01859":null,"SJAG_01863":null,"SJAG_01874":null,"SJAG_01877":null,"SJAG_01878":null,"SJAG_01881":null,"SJAG_01885":null,"SJAG_01903":null,"SJAG_01909":null,"SJAG_01918":null,"SJAG_01929":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_01953":null,"SJAG_01964":null,"SJAG_02015":null,"SJAG_02022":null,"SJAG_02038":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02104":null,"SJAG_02135":null,"SJAG_02142":null,"SJAG_02148":null,"SJAG_02171":null,"SJAG_02176":null,"SJAG_02180":null,"SJAG_02182":null,"SJAG_02183":null,"SJAG_02187":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02206":null,"SJAG_02226":null,"SJAG_02233":null,"SJAG_02236":null,"SJAG_02242":null,"SJAG_02249":null,"SJAG_02267":null,"SJAG_02286":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02292":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02302":null,"SJAG_02313":null,"SJAG_02331":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02348":null,"SJAG_02353":null,"SJAG_02364":null,"SJAG_02366":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02378":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02399":null,"SJAG_02400":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02429":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02457":null,"SJAG_02460":null,"SJAG_02468":null,"SJAG_02488":null,"SJAG_02489":null,"SJAG_02496":null,"SJAG_02498":null,"SJAG_02509":null,"SJAG_02517":null,"SJAG_02520":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02545":null,"SJAG_02558":null,"SJAG_02563":null,"SJAG_02564":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02592":null,"SJAG_02595":null,"SJAG_02596":null,"SJAG_02598":null,"SJAG_02599":null,"SJAG_02601":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02610":null,"SJAG_02615":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02640":null,"SJAG_02643":null,"SJAG_02656":null,"SJAG_02661":null,"SJAG_02680":null,"SJAG_02684":null,"SJAG_02686":null,"SJAG_02690":null,"SJAG_02696":null,"SJAG_02697":null,"SJAG_02698":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02720":null,"SJAG_02721":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02741":null,"SJAG_02748":null,"SJAG_02760":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02808":null,"SJAG_02822":null,"SJAG_02824":null,"SJAG_02825":null,"SJAG_02827":null,"SJAG_02835":null,"SJAG_02838":null,"SJAG_02848":null,"SJAG_02856":null,"SJAG_02858":null,"SJAG_02872":null,"SJAG_02875":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02906":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02945":null,"SJAG_02950":null,"SJAG_02977":null,"SJAG_02991":null,"SJAG_02994":null,"SJAG_02997":null,"SJAG_03011":null,"SJAG_03017":null,"SJAG_03036":null,"SJAG_03048":null,"SJAG_03061":null,"SJAG_03067":null,"SJAG_03069":null,"SJAG_03071":null,"SJAG_03072":null,"SJAG_03077":null,"SJAG_03096":null,"SJAG_03115":null,"SJAG_03129":null,"SJAG_03137":null,"SJAG_03140":null,"SJAG_03141":null,"SJAG_03145":null,"SJAG_03152":null,"SJAG_03157":null,"SJAG_03160":null,"SJAG_03174":null,"SJAG_03188":null,"SJAG_03193":null,"SJAG_03206":null,"SJAG_03209":null,"SJAG_03213":null,"SJAG_03224":null,"SJAG_03236":null,"SJAG_03237":null,"SJAG_03240":null,"SJAG_03257":null,"SJAG_03275":null,"SJAG_03277":null,"SJAG_03290":null,"SJAG_03313":null,"SJAG_03320":null,"SJAG_03336":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03349":null,"SJAG_03355":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03374":null,"SJAG_03376":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03409":null,"SJAG_03421":null,"SJAG_03436":null,"SJAG_03438":null,"SJAG_03449":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03457":null,"SJAG_03461":null,"SJAG_03471":null,"SJAG_03475":null,"SJAG_03476":null,"SJAG_03479":null,"SJAG_03485":null,"SJAG_03486":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03501":null,"SJAG_03526":null,"SJAG_03529":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03545":null,"SJAG_03557":null,"SJAG_03562":null,"SJAG_03567":null,"SJAG_03570":null,"SJAG_03585":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03613":null,"SJAG_03626":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03669":null,"SJAG_03676":null,"SJAG_03679":null,"SJAG_03684":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03703":null,"SJAG_03708":null,"SJAG_03709":null,"SJAG_03712":null,"SJAG_03720":null,"SJAG_03728":null,"SJAG_03730":null,"SJAG_03732":null,"SJAG_03753":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03789":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03804":null,"SJAG_03811":null,"SJAG_03813":null,"SJAG_03828":null,"SJAG_03832":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03852":null,"SJAG_03854":null,"SJAG_03866":null,"SJAG_03886":null,"SJAG_03887":null,"SJAG_03892":null,"SJAG_03896":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03909":null,"SJAG_03915":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03932":null,"SJAG_03946":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03959":null,"SJAG_03967":null,"SJAG_03982":null,"SJAG_03985":null,"SJAG_03987":null,"SJAG_04000":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04032":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04042":null,"SJAG_04052":null,"SJAG_04054":null,"SJAG_04055":null,"SJAG_04064":null,"SJAG_04081":null,"SJAG_04094":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04154":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04167":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04187":null,"SJAG_04189":null,"SJAG_04203":null,"SJAG_04206":null,"SJAG_04210":null,"SJAG_04230":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04258":null,"SJAG_04265":null,"SJAG_04268":null,"SJAG_04270":null,"SJAG_04276":null,"SJAG_04277":null,"SJAG_04280":null,"SJAG_04282":null,"SJAG_04285":null,"SJAG_04287":null,"SJAG_04288":null,"SJAG_04312":null,"SJAG_04320":null,"SJAG_04334":null,"SJAG_04343":null,"SJAG_04351":null,"SJAG_04355":null,"SJAG_04362":null,"SJAG_04366":null,"SJAG_04367":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04387":null,"SJAG_04394":null,"SJAG_04409":null,"SJAG_04410":null,"SJAG_04435":null,"SJAG_04457":null,"SJAG_04459":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04470":null,"SJAG_04473":null,"SJAG_04477":null,"SJAG_04480":null,"SJAG_04482":null,"SJAG_04486":null,"SJAG_04495":null,"SJAG_04507":null,"SJAG_04509":null,"SJAG_04511":null,"SJAG_04537":null,"SJAG_04544":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04566":null,"SJAG_04573":null,"SJAG_04577":null,"SJAG_04589":null,"SJAG_04597":null,"SJAG_04599":null,"SJAG_04608":null,"SJAG_04612":null,"SJAG_04622":null,"SJAG_04627":null,"SJAG_04634":null,"SJAG_04650":null,"SJAG_04652":null,"SJAG_04655":null,"SJAG_04657":null,"SJAG_04665":null,"SJAG_04666":null,"SJAG_04669":null,"SJAG_04692":null,"SJAG_04693":null,"SJAG_04700":null,"SJAG_04734":null,"SJAG_04738":null,"SJAG_04743":null,"SJAG_04745":null,"SJAG_04747":null,"SJAG_04755":null,"SJAG_04757":null,"SJAG_04760":null,"SJAG_04761":null,"SJAG_04762":null,"SJAG_04772":null,"SJAG_04777":null,"SJAG_04810":null,"SJAG_04840":null,"SJAG_04845":null,"SJAG_04849":null,"SJAG_04856":null,"SJAG_04857":null,"SJAG_04862":null,"SJAG_04865":null,"SJAG_04874":null,"SJAG_04882":null,"SJAG_04940":null,"SJAG_04946":null,"SJAG_04970":null,"SJAG_04974":null,"SJAG_04980":null,"SJAG_05010":null,"SJAG_05015":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05022":null,"SJAG_05024":null,"SJAG_05025":null,"SJAG_05027":null,"SJAG_05030":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05194":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05231":null,"SJAG_05249":null,"SJAG_05276":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05304":null,"SJAG_05313":null,"SJAG_05332":null,"SJAG_05340":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_06597":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06642":null,"SJAG_16455":null,"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"nucleoside phosphate binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:1901265","terms_by_termid":{"GO:0002134":null,"GO:0002135":null,"GO:0005524":null,"GO:0005525":null,"GO:0010181":null,"GO:0016208":null,"GO:0019002":null,"GO:0019003":null,"GO:0030552":null,"GO:0036042":null,"GO:0043531":null,"GO:0050660":null,"GO:0050661":null,"GO:0051287":null,"GO:0070401":null,"GO:0070402":null,"GO:0070403":null,"GO:0071949":null}}


id: PBO:0056061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine zipper protein 1","termid":"PBO:0056061"}


id: MONDO:1010042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Protein-losing enteropathy that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-losing enteropathy, non-human animal","secondary_identifiers":["OMIA:001325"],"termid":"MONDO:1010042","xrefs":{"Monarch":{"xref_id":"1010042"}}}


id: FYPO:0001807
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 adenine into the cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"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"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"abnormal adenine import","synonyms":[{"name":"abnormal adenine import across plasma membrane","type":"exact"},{"name":"abnormal adenine import during mitotic cell cycle","type":"related"},{"name":"abnormal adenine import during vegetative growth","type":"exact"},{"name":"abnormal adenine import into cell","type":"exact"},{"name":"abnormal adenine uptake","type":"exact"}],"termid":"FYPO:0001807"}


id: FYPO:0001497
data:
  {"alleles_by_uniquename":{"SJAG_04332:allele-1":{"allele_type":"amino_acid_mutation","description":"I30T,T572P","gene_uniquename":"SJAG_04332","name":"cdc25-D9","uniquename":"SJAG_04332:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007701"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is inviable and elongated, and progression through the mitotic cell cycle is arrested in interphase. The cell contains one nucleus and no septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"cell cycle arrest in mitotic interphase","termid":"FYPO:0000837"},{"relation_name":"is_a","term_name":"cell cycle arrest in mitotic interphase","termid":"FYPO:0000837"},{"relation_name":"is_a","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04332":null},"genotype_count":1,"genotypes_by_uniquename":{"cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cdc25-D9(I30T,T572P aa)","display_uniquename":"cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04332:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000005","FYPO:0001985","FYPO:0000631","FYPO:0000002","FYPO:0000004"],"is_obsolete":false,"name":"inviable elongated cell with mitotic cell cycle arrest in interphase","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_04332"],"single_locus_genotype_uniquenames":["cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"elongated inviable cell with mitotic cell cycle arrest in interphase during vegetative growth","type":"exact"},{"name":"elongated inviable vegetative cell with mitotic cell cycle arrest in interphase","type":"exact"},{"name":"inviable elongated mononucleate aseptate vegetative cell with cell cycle arrest in mitotic interphase","type":"exact"},{"name":"inviable elongated vegetative cell with cell cycle arrest in interphase during mitotic cell cycle","type":"exact"},{"name":"inviable elongated vegetative cell with mitotic cell cycle arrest in interphase","type":"exact"},{"name":"inviable elongated vegetative cell with mitotic interphase arrest","type":"exact"},{"name":"lethal; elongated vegetative cell with mitotic cell cycle arrest in interphase","type":"exact"},{"name":"mitotic cell cycle arrest in interphase with elongated inviable cell","type":"exact"},{"name":"mitotic interphase arrested elongated inviable vegetative cell","type":"exact"}],"termid":"FYPO:0001497","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000137":null,"FYPO:0007701":null,"FYPO_EXT:0000001":null}}


id: GO:0048037
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to a cofactor, a substance that is required for the activity of an enzyme or other protein. Cofactors may be inorganic, such as the metal atoms zinc, iron, and copper in certain forms, or organic, in which case they are referred to as coenzymes. Cofactors may either be bound tightly to active sites or bind loosely with the substrate.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete cofactor binding (obsolete GO:0048037)","termid":"GO:0048037"}


id: GO:0035294
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Allocation of embryonic cells to the wing disc founder populations, groups of cells that are committed to contribute to the formation of a wing imaginal disc.","definition_xrefs":["ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"determination of imaginal disc primordium","termid":"GO:0007445"},{"relation_name":"is_a","term_name":"wing disc development","termid":"GO:0035220"}],"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":"determination of wing disc primordium","termid":"GO:0035294"}


id: MONDO:0003620
data:
  {"annotated_genes":["SJAG_00252","SJAG_02464","SJAG_03072","SJAG_01383","SJAG_03320","SJAG_03064","SJAG_03345","SJAG_00243","SJAG_01229","SJAG_16459","SJAG_01402","SJAG_04765","SJAG_00237","SJAG_01111","SJAG_04334","SJAG_02398","SJAG_01522","SJAG_03163","SJAG_04285","SJAG_00570","SJAG_02242","SJAG_04843","SJAG_04213","SJAG_06603","SJAG_04300","SJAG_01671","SJAG_05950","SJAG_00459","SJAG_04882","SJAG_01466","SJAG_04763","SJAG_04409","SJAG_04495","SJAG_03781","SJAG_00326","SJAG_03310","SJAG_03290","SJAG_02693","SJAG_01165","SJAG_01159","SJAG_03081","SJAG_03324","SJAG_04522","SJAG_03495","SJAG_03553","SJAG_04567","SJAG_00495","SJAG_00031","SJAG_02997","SJAG_01190","SJAG_02658","SJAG_03815","SJAG_02119","SJAG_01199","SJAG_01352","SJAG_00702","SJAG_00835","SJAG_02158","SJAG_01043","SJAG_04146","SJAG_00933","SJAG_03248","SJAG_00866","SJAG_04418","SJAG_02399","SJAG_03598","SJAG_03137","SJAG_04178","SJAG_02006","SJAG_00637","SJAG_03894","SJAG_01895","SJAG_02286","SJAG_02619","SJAG_04568","SJAG_04000","SJAG_03712","SJAG_00891","SJAG_MIT15","SJAG_05289","SJAG_02788","SJAG_03440","SJAG_01537","SJAG_01649","SJAG_00488","SJAG_02289","SJAG_00858","SJAG_02016","SJAG_01114","SJAG_00103","SJAG_01865","SJAG_01797","SJAG_02695","SJAG_02919","SJAG_02305","SJAG_03811","SJAG_02680","SJAG_00663","SJAG_03046","SJAG_00773","SJAG_00260","SJAG_02278","SJAG_01866","SJAG_03920","SJAG_03923","SJAG_00721"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971004"},{"annotations":[86123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008076"},{"annotations":[85393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014557"},{"annotations":[85967],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014711"},{"annotations":[85812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008026"},{"annotations":[86271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012784"},{"annotations":[85221],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011436"},{"annotations":[85107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011585"},{"annotations":[85958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020730"},{"annotations":[86824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014455"},{"annotations":[87028,87027,87029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011687"},{"annotations":[86570,86569,86568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012096"},{"annotations":[86440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013212"},{"annotations":[85785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013644"},{"annotations":[86680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014511"},{"annotations":[85401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014566"},{"annotations":[85851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012012"},{"annotations":[85113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014074"},{"annotations":[87002,87001],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013338"},{"annotations":[86839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014467"},{"annotations":[85133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012231"},{"annotations":[85292,85293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010949"},{"annotations":[85464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011570"},{"annotations":[86035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011091"},{"annotations":[85912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014735"},{"annotations":[86183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011066"},{"annotations":[87024,87025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011534"},{"annotations":[86730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012640"},{"annotations":[85904],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014733"},{"annotations":[85209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010479"},{"annotations":[85441],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010689"},{"annotations":[86148,86149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010699"},{"annotations":[86103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014906"},{"annotations":[87065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032728"},{"annotations":[87207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011675"},{"annotations":[87069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030677"},{"annotations":[85422,85421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008695"},{"annotations":[86413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011829"},{"annotations":[86263],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013838"},{"annotations":[85834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033615"},{"annotations":[86262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013837"},{"annotations":[85335,85336,85337,85334],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011444"},{"annotations":[86260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013840"},{"annotations":[86259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[85389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011730"},{"annotations":[85615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009748"},{"annotations":[85895],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013584"},{"annotations":[85141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010043"},{"annotations":[85234,85235],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009353"},{"annotations":[86608],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013762"},{"annotations":[86642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"},{"annotations":[87012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008758"},{"annotations":[84983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010794"},{"annotations":[85398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014562"},{"annotations":[85310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030055"},{"annotations":[86293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957874"},{"annotations":[85983,85984,85982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008025"},{"annotations":[86593,86594,86592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012080"},{"annotations":[86276,86278,86277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013243"},{"annotations":[85284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015353"},{"annotations":[86132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013884"},{"annotations":[85661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030860"},{"annotations":[86157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011879"},{"annotations":[85187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060585"},{"annotations":[86460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011002"},{"annotations":[86919,86920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032792"},{"annotations":[86906],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008086"},{"annotations":[86999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013337"},{"annotations":[85042],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024309"},{"annotations":[85776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013634"},{"annotations":[86165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011871"},{"annotations":[87023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009796"},{"annotations":[86970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008759"},{"annotations":[85808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008192"},{"annotations":[86983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[86893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011544"},{"annotations":[85596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[85805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"},{"annotations":[87129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032771"},{"annotations":[87198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013948"},{"annotations":[86842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054549"},{"annotations":[87199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013949"},{"annotations":[87197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013950"},{"annotations":[87200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013951"},{"annotations":[87201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013952"},{"annotations":[87159,87158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013967"},{"annotations":[86805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008953"},{"annotations":[87149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011101"},{"annotations":[86794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008954"},{"annotations":[87063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008736"},{"annotations":[87181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013927"},{"annotations":[87183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013930"},{"annotations":[87184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013931"},{"annotations":[87186],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013936"},{"annotations":[87188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013937"},{"annotations":[87189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013938"},{"annotations":[87187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013939"},{"annotations":[87192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013942"},{"annotations":[87190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013943"},{"annotations":[87195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013945"},{"annotations":[86266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009959"},{"annotations":[85862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014754"},{"annotations":[86985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013382"},{"annotations":[86403],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010717"},{"annotations":[85889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013580"},{"annotations":[86737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009502"},{"annotations":[85176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009529"},{"annotations":[86738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009503"},{"annotations":[86401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012120"},{"annotations":[86004],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008972"},{"annotations":[85853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014743"},{"annotations":[86395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011835"},{"annotations":[87273,87272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024517"},{"annotations":[85841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859279"},{"annotations":[86150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009669"},{"annotations":[86406],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009673"},{"annotations":[86012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009672"},{"annotations":[86172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010056"},{"annotations":[85566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011801"},{"annotations":[86577,86578],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018996"},{"annotations":[86239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010338"},{"annotations":[87138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010378"}]},"cv_name":"mondo","definition":"A disease involving the peripheral nervous system.","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":106,"genes_by_uniquename":{"SJAG_00031":null,"SJAG_00103":null,"SJAG_00237":null,"SJAG_00243":null,"SJAG_00252":null,"SJAG_00260":null,"SJAG_00326":null,"SJAG_00459":null,"SJAG_00488":null,"SJAG_00495":null,"SJAG_00570":null,"SJAG_00637":null,"SJAG_00663":null,"SJAG_00702":null,"SJAG_00721":null,"SJAG_00773":null,"SJAG_00835":null,"SJAG_00858":null,"SJAG_00866":null,"SJAG_00891":null,"SJAG_00933":null,"SJAG_01043":null,"SJAG_01111":null,"SJAG_01114":null,"SJAG_01159":null,"SJAG_01165":null,"SJAG_01190":null,"SJAG_01199":null,"SJAG_01229":null,"SJAG_01352":null,"SJAG_01383":null,"SJAG_01402":null,"SJAG_01466":null,"SJAG_01522":null,"SJAG_01537":null,"SJAG_01649":null,"SJAG_01671":null,"SJAG_01797":null,"SJAG_01865":null,"SJAG_01866":null,"SJAG_01895":null,"SJAG_02006":null,"SJAG_02016":null,"SJAG_02119":null,"SJAG_02158":null,"SJAG_02242":null,"SJAG_02278":null,"SJAG_02286":null,"SJAG_02289":null,"SJAG_02305":null,"SJAG_02398":null,"SJAG_02399":null,"SJAG_02464":null,"SJAG_02619":null,"SJAG_02658":null,"SJAG_02680":null,"SJAG_02693":null,"SJAG_02695":null,"SJAG_02788":null,"SJAG_02919":null,"SJAG_02997":null,"SJAG_03046":null,"SJAG_03064":null,"SJAG_03072":null,"SJAG_03081":null,"SJAG_03137":null,"SJAG_03163":null,"SJAG_03248":null,"SJAG_03290":null,"SJAG_03310":null,"SJAG_03320":null,"SJAG_03324":null,"SJAG_03345":null,"SJAG_03440":null,"SJAG_03495":null,"SJAG_03553":null,"SJAG_03598":null,"SJAG_03712":null,"SJAG_03781":null,"SJAG_03811":null,"SJAG_03815":null,"SJAG_03894":null,"SJAG_03920":null,"SJAG_03923":null,"SJAG_04000":null,"SJAG_04146":null,"SJAG_04178":null,"SJAG_04213":null,"SJAG_04285":null,"SJAG_04300":null,"SJAG_04334":null,"SJAG_04409":null,"SJAG_04418":null,"SJAG_04495":null,"SJAG_04522":null,"SJAG_04567":null,"SJAG_04568":null,"SJAG_04763":null,"SJAG_04765":null,"SJAG_04843":null,"SJAG_04882":null,"SJAG_05289":null,"SJAG_05950":null,"SJAG_06603":null,"SJAG_16459":null,"SJAG_MIT15":null},"genotype_count":0,"is_obsolete":false,"name":"peripheral nervous system disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:892389","ICD9:350-359.99","EFO:0009387","ICD9:356.9","SCTID:42658009","UMLS:C4025831","DOID:574","NCIT:C27580","MESH:D010523"],"synonyms":[{"name":"PNS (peripheral nervous system) diseases","type":"exact"},{"name":"PNS disease","type":"exact"},{"name":"PNS diseases","type":"exact"},{"name":"disease of peripheral nervous system","type":"exact"},{"name":"disease or disorder of peripheral nervous system","type":"exact"},{"name":"disorder of peripheral nervous system","type":"exact"},{"name":"disorder of the peripheral nervous system","type":"exact"},{"name":"nerve disease, peripheral","type":"narrow"},{"name":"nerve diseases, peripheral","type":"narrow"},{"name":"neuropathy, peripheral","type":"narrow"},{"name":"peripheral Neuropathies","type":"narrow"},{"name":"peripheral nerve disease","type":"narrow"},{"name":"peripheral nerve diseases","type":"narrow"},{"name":"peripheral nervous system disease","type":"exact"},{"name":"peripheral nervous system disease or disorder","type":"exact"},{"name":"peripheral nervous system disorder","type":"exact"},{"name":"peripheral nervous system disorders","type":"exact"},{"name":"peripheral neuropathy","type":"narrow"}],"termid":"MONDO:0003620","terms_by_termid":{"MONDO:0007273":null,"MONDO:0008025":null,"MONDO:0008026":null,"MONDO:0008076":null,"MONDO:0008086":null,"MONDO:0008192":null,"MONDO:0008695":null,"MONDO:0008736":null,"MONDO:0008758":null,"MONDO:0008759":null,"MONDO:0008953":null,"MONDO:0008954":null,"MONDO:0008972":null,"MONDO:0009353":null,"MONDO:0009502":null,"MONDO:0009503":null,"MONDO:0009529":null,"MONDO:0009669":null,"MONDO:0009672":null,"MONDO:0009673":null,"MONDO:0009748":null,"MONDO:0009796":null,"MONDO:0009959":null,"MONDO:0010043":null,"MONDO:0010056":null,"MONDO:0010184":null,"MONDO:0010338":null,"MONDO:0010378":null,"MONDO:0010479":null,"MONDO:0010689":null,"MONDO:0010699":null,"MONDO:0010717":null,"MONDO:0010794":null,"MONDO:0010949":null,"MONDO:0011002":null,"MONDO:0011066":null,"MONDO:0011091":null,"MONDO:0011101":null,"MONDO:0011121":null,"MONDO:0011436":null,"MONDO:0011444":null,"MONDO:0011534":null,"MONDO:0011544":null,"MONDO:0011570":null,"MONDO:0011585":null,"MONDO:0011675":null,"MONDO:0011687":null,"MONDO:0011730":null,"MONDO:0011801":null,"MONDO:0011829":null,"MONDO:0011835":null,"MONDO:0011871":null,"MONDO:0011879":null,"MONDO:0012012":null,"MONDO:0012080":null,"MONDO:0012096":null,"MONDO:0012120":null,"MONDO:0012231":null,"MONDO:0012640":null,"MONDO:0012784":null,"MONDO:0013212":null,"MONDO:0013243":null,"MONDO:0013337":null,"MONDO:0013338":null,"MONDO:0013382":null,"MONDO:0013580":null,"MONDO:0013584":null,"MONDO:0013602":null,"MONDO:0013634":null,"MONDO:0013644":null,"MONDO:0013762":null,"MONDO:0013836":null,"MONDO:0013837":null,"MONDO:0013838":null,"MONDO:0013840":null,"MONDO:0013884":null,"MONDO:0013927":null,"MONDO:0013930":null,"MONDO:0013931":null,"MONDO:0013936":null,"MONDO:0013937":null,"MONDO:0013938":null,"MONDO:0013939":null,"MONDO:0013942":null,"MONDO:0013943":null,"MONDO:0013945":null,"MONDO:0013948":null,"MONDO:0013949":null,"MONDO:0013950":null,"MONDO:0013951":null,"MONDO:0013952":null,"MONDO:0013967":null,"MONDO:0014074":null,"MONDO:0014455":null,"MONDO:0014467":null,"MONDO:0014511":null,"MONDO:0014557":null,"MONDO:0014562":null,"MONDO:0014566":null,"MONDO:0014711":null,"MONDO:0014733":null,"MONDO:0014735":null,"MONDO:0014743":null,"MONDO:0014754":null,"MONDO:0014906":null,"MONDO:0015353":null,"MONDO:0018996":null,"MONDO:0020730":null,"MONDO:0024309":null,"MONDO:0024517":null,"MONDO:0030055":null,"MONDO:0030677":null,"MONDO:0030860":null,"MONDO:0032728":null,"MONDO:0032771":null,"MONDO:0032792":null,"MONDO:0033615":null,"MONDO:0054549":null,"MONDO:0060585":null,"MONDO:0859279":null,"MONDO:0957874":null,"MONDO:0971004":null},"xrefs":{"Monarch":{"xref_id":"0003620"}}}


id: PBO:0064013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 47","termid":"PBO:0064013"}


id: PBO:0109042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane palmitoyltransferase Pfa5","termid":"PBO:0109042"}


id: GO:0097723
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the controlled movement of an amoeboid sperm cell.","definition_xrefs":["GOC:krc","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sperm motility","termid":"GO:0097722"}],"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":"amoeboid sperm motility","synonyms":[{"name":"ameboid sperm motility","type":"exact"},{"name":"ameboid sperm movement","type":"exact"},{"name":"amoeboid sperm movement","type":"exact"}],"termid":"GO:0097723"}


id: PBO:0056182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAFG antisense RNA 1","termid":"PBO:0056182"}


id: PBO:0031551
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_peptidase_activity","termid":"PBO:0031551"}


id: MONDO:0020799
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplastic proliferation of basal cells in the epidermis (part of the skin) or other anatomic sites (most frequently the salivary glands). The basal cell neoplastic proliferation in the epidermis results in basal cell carcinomas. The basal cell neoplastic proliferation in the salivary glands can be benign, resulting in basal cell adenomas or malignant, resulting in basal cell adenocarcinomas.","definition_xrefs":["NCIT:C3784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basal cell neoplasm","secondary_identifiers":["MESH:D018295","MEDGEN:104921","EFO:1001763","ICDO:8090/1","SCTID:127570002","UMLS:C0206710"],"synonyms":[{"name":"basal cell tumor","type":"exact"},{"name":"basal cell tumour","type":"exact"},{"name":"neoplasm, basal cell","type":"related"}],"termid":"MONDO:0020799","xrefs":{"Monarch":{"xref_id":"0020799"}}}


id: PBO:0090246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EVE domain (PUA-related) protein, implicated in tRNA metabolism (possible RNA binding domain associated with tRNA methyltransferases)","termid":"PBO:0090246"}


id: PBO:0001532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin Seh1","termid":"PBO:0001532"}


id: GO:0010295
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+)-abscisate + H+ + NADPH + O2 = (+)-8'-hydroxyabscisate + H2O + NADP+.","definition_xrefs":["RHEA:12897","EC:1.14.14.137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"(+)-abscisic acid 8'-hydroxylase activity","secondary_identifiers":["MetaCyc:1.14.13.93-RXN","KEGG_REACTION:R07202"],"synonyms":[{"name":"(+)-ABA 8'-hydroxylase activity","type":"related"},{"name":"ABA 8'-Hydroxylase activity, Abscisate 8'-hydroxylase activity","type":"related"},{"name":"ABA 8'-hydroxylase activity","type":"related"},{"name":"abscisate,NADPH:oxygen oxidoreductase (8'-hydroxylating)","type":"related"},{"name":"abscisic acid 8'-hydroxylase activity","type":"exact"}],"termid":"GO:0010295"}


id: GO:1990509
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Protein complex involved in the disassembly of Mago-Y14 from the spliced mRNA during first round of translation, independently of the translational machinery. Conserved from fission yeast to humans.","definition_xrefs":["GOC:bhm","PMID:14968132"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"PYM-mago-Y14 complex","synonyms":[{"name":"PYM-mago-RNA-binding protein 8A complex","type":"exact"},{"name":"wibg-mago-tsu complex","type":"exact"}],"termid":"GO:1990509"}


id: MONDO:1012819
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital hypotrichosis that occurs in pigs due to a mutation in the HR gene created by genetic engineering or gene editing.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypotrichosis, non-human animal","termid":"MONDO:1012977"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis, HR-related, pig","secondary_identifiers":["OMIA:002229-9823"],"termid":"MONDO:1012819","xrefs":{"Monarch":{"xref_id":"1012819"}}}


id: PBO:0049186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRHL2 divergent transcript","termid":"PBO:0049186"}


id: PR:Q09783
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tim8 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial import inner membrane translocase subunit tim8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G6.04","synonyms":[{"name":"Spom972h-tim8","type":"exact"}],"termid":"PR:Q09783"}


id: GO:0060955
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of neural crest cells to cardiac glial cell fates and their capacity to differentiate into cardiac glial cells.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac glial cell fate commitment","termid":"GO:0060953"},{"relation_name":"part_of","term_name":"neural crest-derived cardiac glial cell differentiation","termid":"GO:0060951"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural crest-derived cardiac glial cell fate commitment","termid":"GO:0060955"}


id: GO:0018914
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of chlorobenzene, a derivative of benzene with a chlorine atoms attached to the ring. It is a colorless liquid that is manufactured for use as a solvent. It quickly evaporates in the air and is degraded by hydroxyl radicals that are produced photochemically. The gas acts as a source of ClOx, which helps in the breakdown of stratospheric ozone.","definition_xrefs":["PMID:8626733","PMID:10808489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"organohalogen metabolic process","termid":"GO:0090345"}],"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":"chlorobenzene catabolic process","secondary_identifiers":["UM-BBD_pathwayID:cb"],"synonyms":[{"name":"chlorobenzene metabolic process","type":"broad"},{"name":"chlorobenzene metabolism","type":"broad"}],"termid":"GO:0018914"}


id: GO:0021592
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the fourth ventricle over time, from its formation to the mature structure. The fourth ventricle is an irregularly shaped cavity in the rhombencephalon, between the medulla oblongata, the pons, and the isthmus in front, and the cerebellum behind. It is continuous with the central canal of the cord below and with the cerebral aqueduct above, and through its lateral and median apertures it communicates with the subarachnoid space.","definition_xrefs":["GOC:dgh","GO_REF:0000021","ISBN:0838580343","GOC:cls","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"ventricular system development","termid":"GO:0021591"},{"relation_name":"part_of","term_name":"hindbrain development","termid":"GO:0030902"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"fourth ventricle development","termid":"GO:0021592"}


id: SO:0001599
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that changes the resulting polypeptide structure.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational_product_function_variant","termid":"SO:0001539"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3D_polypeptide_structure_variant","synonyms":[{"name":"3D polypeptide structure variant","type":"exact"}],"termid":"SO:0001599"}


id: PBO:0072477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 6","termid":"PBO:0072477"}


id: PR:O94325
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A peroxisomal targeting signal 1 receptor that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10130:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal targeting signal receptor (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC725.07","secondary_identifiers":["UniProtKB:O94325"],"synonyms":[{"name":"PTS1 receptor (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PTS1R (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBC725.07","type":"related"},{"name":"Spom972h-PEX5","type":"exact"},{"name":"peroxin-5 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94325"}


id: PBO:0036368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4-NOT complex RNA-binding protein subunit Rcd1","termid":"PBO:0036368"}


id: PBO:0057185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 340","termid":"PBO:0057185"}


id: PBO:0076880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 29","termid":"PBO:0076880"}


id: PBO:0050452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-hydroxy-2-oxoglutarate aldolase 1","termid":"PBO:0050452"}


id: PBO:0072303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S25","termid":"PBO:0072303"}


id: PBO:0069904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1195, pseudogene","termid":"PBO:0069904"}


id: PBO:0051901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit alpha 9","termid":"PBO:0051901"}


id: PBO:0001315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-type ATPase V0 proteolipid subunit (predicted)","termid":"PBO:0001315"}


id: GO:0044205
data:
  {"annotated_genes":["SJAG_00964","SJAG_00197","SJAG_00694","SJAG_03164","SJAG_00444"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[57242,59106,59421,61093,61808],"is_not":false,"summary":null,"term":"GO:0044205"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of UMP, uridine monophosphate, starting with the synthesis of (S)-dihydroorotate from bicarbonate; UMP biosynthesis may either occur via reduction by quinone, NAD+ or oxygen.","definition_xrefs":["GOC:ecd","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UMP biosynthetic process","termid":"GO:0006222"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00444":null,"SJAG_00694":null,"SJAG_00964":null,"SJAG_03164":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"'de novo' UMP biosynthetic process","references_by_uniquename":{"GO_REF:0000041":null},"synonyms":[{"name":"'de novo' UMP biosynthesis","type":"exact"}],"termid":"GO:0044205","terms_by_termid":{"GO:0044205":null}}


id: PBO:0001043
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pop-Interacting Protein","termid":"PBO:0001043"}


id: GO:0090064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that starts the inactive process of microtubule nucleation. Microtubule nucleation is the 'de novo' formation of a microtubule, in which tubulin heterodimers form metastable oligomeric aggregates, some of which go on to support formation of a complete microtubule. Microtubule nucleation usually occurs from a specific site within a cell.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of microtubule nucleation","termid":"GO:0090063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0000226"},{"rel_name":"positively_regulates","termid":"GO:0000226"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000226","GO:0007010","GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"activation of microtubule nucleation","termid":"GO:0090064"}


id: MONDO:0005194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection with any of the rotaviruses. Specific infections include human infantile diarrhea, neonatal calf diarrhea, and epidemic diarrhea of infant mice.","definition_xrefs":["MESH:D012400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rotavirus infection","secondary_identifiers":["EFO:0002622","SCTID:18624000","UMLS:C0035869","ICD9:078.89","MEDGEN:19835"],"synonyms":[{"name":"Rotavirus caused disease or disorder","type":"exact"},{"name":"Rotavirus disease or disorder","type":"exact"},{"name":"Rotavirus infectious disease","type":"exact"}],"termid":"MONDO:0005194","xrefs":{"Monarch":{"xref_id":"0005194"}}}


id: PBO:0003170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTLH domain","termid":"PBO:0003170"}


id: GO:0005704
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A stretch of densely packed chromatin along the polytene chromosome, visible as a morphologically distinct band.","definition_xrefs":["PMID:11361342","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal region","termid":"GO:0098687"},{"relation_name":"part_of","term_name":"polytene chromosome","termid":"GO:0005700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575"],"is_obsolete":false,"name":"polytene chromosome band","termid":"GO:0005704"}


id: FYPO:0007386
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 ubiquitination of lysine at position 119 of histone H2B occurs to a lower extent than normal. Lysine 119 corresponds to the conserved C-terminal lysine of H2B.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H2B-K119 ubiquitination during vegetative growth","termid":"FYPO:0005607"},{"relation_name":"is_a","term_name":"decreased protein ubiquitination","termid":"FYPO:0007946"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0002494","FYPO:0001985","FYPO:0002274","FYPO:0005447"],"is_obsolete":false,"name":"decreased histone H2B-K119 ubiquitination during vegetative growth","synonyms":[{"name":"decreased histone H2B conserved C-terminal lysine ubiquitination during vegetative growth","type":"exact"},{"name":"decreased histone H2B-K119 ubiquitination during mitotic cell cycle","type":"related"},{"name":"reduced histone H2B-K119 ubiquitination during vegetative growth","type":"exact"}],"termid":"FYPO:0007386"}


id: PR:O94453
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ubiquinone biosynthesis protein COQ4, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00361","PANTHER:PTHR12922:SF5"],"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":"ubiquinone biosynthesis protein coq4, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.12c","secondary_identifiers":["UniProtKB:O94453"],"synonyms":[{"name":"Spom972h-COQ4","type":"exact"},{"name":"coenzyme Q biosynthesis protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94453"}


id: MONDO:0044981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity reaction disease","termid":"MONDO:0000605"}],"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":"pseudoallergy","secondary_identifiers":["MEDGEN:783416","UMLS:C3662262","SCTID:609397002","ICD9:V15.09"],"synonyms":[{"name":"non-allergic hypersensitivity to substance","type":"exact"},{"name":"pseudoallergy to substance","type":"exact"}],"termid":"MONDO:0044981","xrefs":{"Monarch":{"xref_id":"0044981"}}}


id: PBO:0086595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; expression induced during heat stress; YNL019C has a paralog, YNL033W, that arose from a segmental duplication","termid":"PBO:0086595"}


id: GO:0010152
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The final stages of microgametogenesis after the trinucleate stage has been reached resulting in viable pollen grains.","definition_xrefs":["PMID:11595796"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental maturation","termid":"GO:0021700"},{"relation_name":"part_of","term_name":"pollen development","termid":"GO:0009555"}],"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":"pollen maturation","termid":"GO:0010152"}


id: PBO:0001828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspan protein Dni1","termid":"PBO:0001828"}


id: MONDO:0001846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of uterine corpus leiomyoma characterized by significant cytologic atypia. The atypical cells are large with pleomophic hyperchromatic nuclei.","definition_xrefs":["NCIT:C40167"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bizarre leiomyoma","termid":"MONDO:0003288"},{"relation_name":"is_a","term_name":"uterine corpus leiomyoma","termid":"MONDO:0007886"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterine corpus bizarre leiomyoma","secondary_identifiers":["DOID:13958","MEDGEN:275555","UMLS:C1519853"],"synonyms":[{"name":"bizarre leiomyoma of body of uterus","type":"exact"},{"name":"body of uterus bizarre leiomyoma","type":"exact"},{"name":"uterine corpus Symplastic leiomyoma","type":"exact"},{"name":"uterine corpus bizarre leiomyoma","type":"exact"},{"name":"uterine corpus leiomyoma with bizarre nuclei","type":"exact"},{"name":"uterine corpus leiomyoma, atypical variant","type":"exact"}],"termid":"MONDO:0001846","xrefs":{"Monarch":{"xref_id":"0001846"}}}


id: PBO:0065424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit beta 9","termid":"PBO:0065424"}


id: GO:0002660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of peripheral tolerance induction.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tolerance induction dependent upon immune response","termid":"GO:0002654"},{"relation_name":"is_a","term_name":"regulation of peripheral tolerance induction","termid":"GO:0002658"},{"relation_name":"positively_regulates","term_name":"peripheral tolerance induction","termid":"GO:0002465"}],"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 peripheral tolerance induction","synonyms":[{"name":"activation of peripheral tolerance induction","type":"narrow"},{"name":"stimulation of peripheral tolerance induction","type":"narrow"},{"name":"up regulation of peripheral tolerance induction","type":"exact"},{"name":"up-regulation of peripheral tolerance induction","type":"exact"},{"name":"upregulation of peripheral tolerance induction","type":"exact"}],"termid":"GO:0002660"}


id: FYPO:0000516
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 nuclear import is normal (i.e. indistinguishable from wild type). Nuclear import is the directed movement of any substance into the nucleus; import of all substances or a specific substance may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal nucleocytoplasmic transport","termid":"FYPO:0008138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"normal nuclear import","synonyms":[{"name":"normal nuclear import during mitotic cell cycle","type":"related"},{"name":"normal nuclear import during vegetative growth","type":"exact"},{"name":"nuclear import: normal","type":"related"}],"termid":"FYPO:0000516"}


id: PBO:0029167
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-dTTP_absent_from_cell","termid":"PBO:0029167"}


id: GO:0015789
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of UDP-N-acetylgalactosamine into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. UDP-N-acetylgalactosamine is a substance composed of N-acetylgalactosamine, a common structural unit of oligosaccharides, in glycosidic linkage with uridine diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"},{"relation_name":"is_a","term_name":"pyrimidine nucleotide-sugar transmembrane transport","termid":"GO:0090481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"UDP-N-acetylgalactosamine transmembrane transport","synonyms":[{"name":"UDP-N-acetylgalactosamine transport","type":"related"}],"termid":"GO:0015789"}


id: GO:0032984
data:
  {"annotated_genes":["SJAG_03380","SJAG_02314","SJAG_00330","SJAG_03301","SJAG_02560","SJAG_02414","SJAG_05296","SJAG_01252","SJAG_00642","SJAG_01224","SJAG_03345","SJAG_05221","SJAG_01894","SJAG_00840","SJAG_02699","SJAG_04909","SJAG_01993","SJAG_02189","SJAG_00723","SJAG_04312","SJAG_03658","SJAG_02700","SJAG_00279","SJAG_01696","SJAG_02601","SJAG_01297","SJAG_01518","SJAG_02336","SJAG_04841","SJAG_02812","SJAG_02433","SJAG_00206","SJAG_03232","SJAG_00597","SJAG_00338","SJAG_06309","SJAG_00286","SJAG_01653","SJAG_03126","SJAG_04038","SJAG_05025","SJAG_04862","SJAG_02704","SJAG_05265","SJAG_03025","SJAG_04283","SJAG_03949","SJAG_00308","SJAG_02624"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73399,69837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030042"},{"annotations":[76246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060172"},{"annotations":[75448,70297,71975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097352"},{"annotations":[94597],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016240"},{"annotations":[80016,79113,92293,75582],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0051016"},{"annotations":[79626],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072318"},{"annotations":[107189,117525,94776,73740,109177,109176,116054,96457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002184"},{"annotations":[61926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903259"},{"annotations":[98618,89575,118178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007019"},{"annotations":[102075,104713,95912,111538,95472,98648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070126"},{"annotations":[103665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140516"},{"annotations":[90026,97070,116929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006337"},{"annotations":[103904,108280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070462"},{"annotations":[97612],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1901098"},{"annotations":[101855],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0031117"},{"annotations":[111979],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904595"},{"annotations":[68420,76381,66029],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045905"},{"annotations":[73843],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006449"},{"annotations":[76370,57311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035494"},{"annotations":[57338,87731,78494,104522,74732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000390"},{"annotations":[61847,77500],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006415"}]},"cv_name":"biological_process","definition":"The disaggregation of a protein-containing macromolecular complex into its constituent components.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component disassembly","termid":"GO:0022411"},{"relation_name":"is_a","term_name":"protein-containing complex organization","termid":"GO:0043933"}],"gene_count":49,"genes_by_uniquename":{"SJAG_00206":null,"SJAG_00279":null,"SJAG_00286":null,"SJAG_00308":null,"SJAG_00330":null,"SJAG_00338":null,"SJAG_00597":null,"SJAG_00642":null,"SJAG_00723":null,"SJAG_00840":null,"SJAG_01224":null,"SJAG_01252":null,"SJAG_01297":null,"SJAG_01518":null,"SJAG_01653":null,"SJAG_01696":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02189":null,"SJAG_02314":null,"SJAG_02336":null,"SJAG_02414":null,"SJAG_02433":null,"SJAG_02560":null,"SJAG_02601":null,"SJAG_02624":null,"SJAG_02699":null,"SJAG_02700":null,"SJAG_02704":null,"SJAG_02812":null,"SJAG_03025":null,"SJAG_03126":null,"SJAG_03232":null,"SJAG_03301":null,"SJAG_03345":null,"SJAG_03380":null,"SJAG_03658":null,"SJAG_03949":null,"SJAG_04038":null,"SJAG_04283":null,"SJAG_04312":null,"SJAG_04841":null,"SJAG_04862":null,"SJAG_04909":null,"SJAG_05025":null,"SJAG_05221":null,"SJAG_05265":null,"SJAG_05296":null,"SJAG_06309":null},"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 disassembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0034623","GO:0043624","GO:0043241"],"synonyms":[{"name":"cellular macromolecule complex disassembly","type":"related"},{"name":"cellular protein complex disassembly","type":"related"},{"name":"macromolecule complex disassembly","type":"related"},{"name":"protein complex disassembly","type":"exact"}],"termid":"GO:0032984","terms_by_termid":{"GO:0000390":null,"GO:0002184":null,"GO:0006337":null,"GO:0006415":null,"GO:0006449":null,"GO:0007019":null,"GO:0016240":null,"GO:0030042":null,"GO:0031117":null,"GO:0035494":null,"GO:0045905":null,"GO:0051016":null,"GO:0060172":null,"GO:0070126":null,"GO:0070462":null,"GO:0072318":null,"GO:0097352":null,"GO:0140516":null,"GO:1901098":null,"GO:1903259":null,"GO:1904595":null}}


id: PBO:0062643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 11 subfamily M member 1 pseudogene","termid":"PBO:0062643"}


id: GO:0048093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of establishment of a pattern of pigment in males.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental pigmentation","termid":"GO:0048087"},{"relation_name":"is_a","term_name":"regulation of male pigmentation","termid":"GO:0048088"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"male pigmentation","termid":"GO:0048094"}],"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 male pigmentation","synonyms":[{"name":"activation of male pigmentation","type":"narrow"},{"name":"stimulation of male pigmentation","type":"narrow"},{"name":"up regulation of male pigmentation","type":"exact"},{"name":"up-regulation of male pigmentation","type":"exact"},{"name":"upregulation of male pigmentation","type":"exact"}],"termid":"GO:0048093"}


id: PBO:0088838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichyl-di-phosphooligosaccharide-protein glycotransferase subunit Wbp1","termid":"PBO:0088838"}


id: PBO:0031839
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_shmoo_morphology","termid":"PBO:0031839"}


id: PBO:0047434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCF1 pseudogene 5","termid":"PBO:0047434"}


id: PBO:0088324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spliceosome complex disassembly protein Ntr2","termid":"PBO:0088324"}


id: PATO:0001385
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A ploidy quality inhering in a bearer by virtue of the bearer's containing a non-integral multiple of the monoploid number, due to extra or missing chromosomes.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Aneuploid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ploidy","termid":"PATO:0001374"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aneuploid","termid":"PATO:0001385"}


id: GO:1901051
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of atropine. Atropine is the racemic mixture of hyoscyamine.","definition_xrefs":["GOC:yaf","PMID:2879005","PMID:33572199","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tropane alkaloid biosynthetic process","termid":"GO:0009710"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"atropine biosynthetic process","secondary_identifiers":["GO:1901049"],"synonyms":[{"name":"atropine anabolism","type":"exact"},{"name":"atropine biosynthesis","type":"exact"},{"name":"atropine formation","type":"exact"},{"name":"atropine metabolic process","type":"broad"},{"name":"atropine metabolism","type":"broad"},{"name":"atropine synthesis","type":"exact"},{"name":"hyoscyamine biosynthetic process","type":"exact"}],"termid":"GO:1901051"}


id: SO:1000023
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Change of a purine nucleotide, A or G , into a pyrimidine nucleotide C or T.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transversion","termid":"SO:1000017"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purine_to_pyrimidine_transversion","synonyms":[{"name":"purine to pyrimidine transversion","type":"exact"}],"termid":"SO:1000023"}


id: MONDO:0010339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features characterized by epilepsy, learning difficulties, macrocephaly, and aggressive behavior. It has been described in males from a four-generation kindred. It is transmitted as an X-linked recessive trait and is likely to be caused by mutations in the gene encoding synapsin I (Xp11.3-q12).","definition_xrefs":["Orphanet:85294"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"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":"epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features","termid":"MONDO:0859390"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"epilepsy, X-linked 1, with variable learning disabilities and behavior disorders","secondary_identifiers":["UMLS:C5774177","DOID:0112122","MEDGEN:1823951","GARD:16748","MESH:C564505","OMIM:300491"],"synonyms":[{"name":"X-linked epilepsy-learning disabilities-behavior disorders syndrome","type":"exact"},{"name":"epilepsy, X-linked, with variable learning disabilities and behavior disorders","type":"related"},{"name":"epilepsy, X-linked, with variable learning disabilities and behavior disorders, X-linked recessive, X-linked dominant","type":"exact"},{"name":"epilepsy, X-linked, with variable learning disabilities and behaviour disorders","type":"related"},{"name":"epilepsy, X-linked, with variable learning disabilities and behaviour disorders, X-linked recessive, X-linked dominant","type":"exact"}],"termid":"MONDO:0010339","xrefs":{"Monarch":{"xref_id":"0010339"}}}


id: GO:1990895
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to cell cortex of cell tip.","definition_xrefs":["PMID:26150232","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell tip","termid":"GO:1903066"},{"relation_name":"is_a","term_name":"regulation of protein localization to cell cortex","termid":"GO:1904776"},{"relation_name":"regulates","term_name":"protein localization to cell cortex of cell tip","termid":"GO:1990896"}],"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 protein localization to cell cortex of cell tip","termid":"GO:1990895"}


id: MONDO:0011651
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":"intellectual disability, short stature, facial anomalies, and joint dislocations","secondary_identifiers":["MEDGEN:342897","OMIM:606220","MESH:C565248","UMLS:C1853507"],"synonyms":[{"name":"intellectual developmental disorder with short stature, facial anomalies, and speech defects","type":"exact"},{"name":"intellectual disability, short stature, facial anomalies, and JOINT dislocations","type":"related"},{"name":"mental retardation, short stature, facial anomalies, and JOINT dislocations","type":"related"}],"termid":"MONDO:0011651","xrefs":{"Monarch":{"xref_id":"0011651"}}}


