# terms

id: PBO:0029613
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_stubby_vegetative_cell","termid":"PBO:0029613"}


id: GO:0018252
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of the green fluorescent protein chromophore cross-link from the alpha-carboxyl carbon of residue n, a serine, to the alpha-amino nitrogen of residue n+2, a glycine, and a dehydration to form a double bond to the alpha-amino nitrogen of residue n+1. This cross-linking is coupled with a dehydrogenation of residue n+1 to form a double bond between the alpha and beta carbons.","definition_xrefs":["RESID:AA0184"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via L-seryl-5-imidazolinone glycine (obsolete GO:0018252)","synonyms":[{"name":"biosynthesis of protein-protein cross-link via L-seryl-5-imidazolinone glycine","type":"exact"},{"name":"biosynthetic process of protein-protein cross-link via L-seryl-5-imidazolinone glycine","type":"exact"}],"termid":"GO:0018252"}


id: GO:0060693
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of branching morphogenesis in the salivary gland epithelium.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of morphogenesis of a branching structure","termid":"GO:0060688"},{"relation_name":"is_a","term_name":"regulation of morphogenesis of an epithelium","termid":"GO:1905330"},{"relation_name":"is_a","term_name":"regulation of animal organ morphogenesis","termid":"GO:2000027"},{"relation_name":"regulates","term_name":"branching involved in salivary gland morphogenesis","termid":"GO:0060445"}],"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 branching involved in salivary gland morphogenesis","termid":"GO:0060693"}


id: MONDO:0002115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pancreatic cancer (obsolete MONDO:0002115)","termid":"MONDO:0002115","xrefs":{"Monarch":{"xref_id":"0002115"}}}


id: MONDO:0007722
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":"heterochromia iridis","secondary_identifiers":["HP:0001100","MEDGEN:98395","MESH:C538115","OMIM:142500","UMLS:C0423318"],"synonyms":[{"name":"heterochromia iridis","type":"exact"},{"name":"heterochromia iridis (disease)","type":"exact"}],"termid":"MONDO:0007722","xrefs":{"Monarch":{"xref_id":"0007722"}}}


id: PBO:0113386
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; conserved among S. cerevisiae strains; YDR278C is not an essential gene; overlaps tRNA-Glu/YNCD0021C","termid":"PBO:0113386"}


id: PBO:0044471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 11 subfamily A member 1","termid":"PBO:0044471"}


id: MONDO:0005884
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection with flukes of the genus Opisthorchis.","definition_xrefs":["MESH:D009889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"helminthiasis","termid":"MONDO:0004664"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opisthorchiasis","secondary_identifiers":["ICD10CM:B66.0","ICD9:121.0","UMLS:C0029106","MEDGEN:10453","SCTID:1059007","icd11.foundation:1401769984","EFO:0007404","DOID:13768"],"synonyms":[{"name":"infection by Opisthorchis","type":"exact"},{"name":"infection due to Opisthorchis (felineus)(viverrini)","type":"related"},{"name":"infection due to cat liver fluke","type":"related"}],"termid":"MONDO:0005884","xrefs":{"Monarch":{"xref_id":"0005884"}}}


id: PBO:0041914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellin 2 precursor","termid":"PBO:0041914"}


id: PBO:0054323
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 1716","termid":"PBO:0054323"}


id: PBO:0047402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 40","termid":"PBO:0047402"}


id: GO:0014704
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex cell-cell junction at which myofibrils terminate in cardiomyocytes; mediates mechanical and electrochemical integration between individual cardiomyocytes. The intercalated disc contains regions of tight mechanical attachment (fasciae adherentes and desmosomes) and electrical coupling (gap junctions) between adjacent cells.","definition_xrefs":["GOC:mtg_muscle","PMID:11732910"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell contact zone","termid":"GO:0044291"}],"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":"intercalated disc","secondary_identifiers":["Wikipedia:Intercalated_disc"],"synonyms":[{"name":"intercalated disk","type":"exact"}],"termid":"GO:0014704"}


id: PBO:0060008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 28","termid":"PBO:0060008"}


id: PBO:0038738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin like 10","termid":"PBO:0038738"}


id: PBO:0064830
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPP1R9A antisense RNA 1","termid":"PBO:0064830"}


id: GO:0016306
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A phosphoinositide 3-kinase which can only phosphorylate phosphatidylinositol.","definition_xrefs":["PMID:9759495"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphatidylinositol 3-kinase activity, class III (obsolete GO:0016306)","synonyms":[{"name":"phosphatidylinositol 3-kinase activity, class III","type":"exact"}],"termid":"GO:0016306"}


id: GO:0010724
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of definitive erythrocyte differentiation. Definitive erythrocyte differentiation occurs as part of the process of definitive hemopoiesis.","definition_xrefs":["GOC:tb","GOC:dph","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of erythrocyte differentiation","termid":"GO:0045646"},{"relation_name":"regulates","term_name":"definitive erythrocyte differentiation","termid":"GO:0060318"}],"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 definitive erythrocyte differentiation","synonyms":[{"name":"regulation of definitive RBC differentiation","type":"exact"},{"name":"regulation of definitive erythropoiesis","type":"exact"},{"name":"regulation of definitive red blood cell differentiation","type":"exact"}],"termid":"GO:0010724"}


id: MONDO:0004138
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete maxillary sinus adenoid cystic carcinoma (obsolete MONDO:0004138)","termid":"MONDO:0004138","xrefs":{"Monarch":{"xref_id":"0004138"}}}


id: GO:0051433
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a BH2 protein domain, present in Bcl-2 family members. Proteins that act as inhibitors of apoptosis harbour at least three BH domains: BH1, BH2 and BH3; the BH1 and BH2 domains are found in all death antagonists of the Bcl-2 family but only in one class of death agonists.","definition_xrefs":["PMID:11048732","PMID:12133724","PMID:9020082","PMID:9704409","Prosite:PS01258"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BH domain binding","termid":"GO:0051400"}],"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":"BH2 domain binding","termid":"GO:0051433"}


id: GO:0120112
data:
  {"annotated_genes":["SJAG_04162"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112389],"is_not":false,"summary":null,"term":"GO:0120112"}]},"cv_name":"biological_process","definition":"The directed movement of UDP-glucose from cytosol to endoplasmic reticulum.","definition_xrefs":["PMID:27587357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucose transmembrane transport","termid":"GO:0015786"},{"relation_name":"is_a","term_name":"cytosol to endoplasmic reticulum transport","termid":"GO:0046967"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04162":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"UDP-glucose transmembrane transport into endoplasmic reticulum","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0120112","terms_by_termid":{"GO:0120112":null}}


id: GO:0015289
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the transport of electrolytes and other small molecules across a cell membrane. They are synthesized by one cell and secreted for insertion into the membrane of another cell where they form transmembrane pores. They may exert their toxic effects by allowing the free flow of electrolytes and other small molecules across the membrane, or they may allow entry into the target cell cytoplasm of a toxin protein that ultimately kills the cell.","definition_xrefs":["PMID:10839820"],"gene_count":0,"genotype_count":0,"name":"obsolete pore-forming toxin activity (obsolete GO:0015289)","synonyms":[{"name":"pore-forming toxin activity","type":"exact"}],"termid":"GO:0015289"}


id: PBO:0046964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 83 member B","termid":"PBO:0046964"}


id: PBO:0050164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 20","termid":"PBO:0050164"}


id: GO:1990243
data:
  {"annotated_genes":["SJAG_02311","SJAG_00266"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[92715,107978],"is_not":false,"summary":null,"term":"GO:1990243"}]},"cv_name":"cellular_component","definition":"A heterodimeric transcription factor complex composed of the bZIP proteins atf1 and pcr1. The heterodimer binds m26 sites (homologous to CRE).","definition_xrefs":["PMID:24224056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription factor AP-1 complex","termid":"GO:0035976"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_02311":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"atf1-pcr1 complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990243","terms_by_termid":{"GO:1990243":null}}


id: MONDO:1012732
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any difference of sexual development that occurs in Japanese medaka due to a mutation in the DMRT1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"difference of sexual differentiation, non-human animal","termid":"MONDO:0700105"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"difference of sexual development, DMRT1-related, Japanese medaka","secondary_identifiers":["OMIA:001709-8090"],"termid":"MONDO:1012732","xrefs":{"Monarch":{"xref_id":"1012732"}}}


id: MONDO:0019182
data:
  {"annotated_genes":["SJAG_04398"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010961"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare genetic developmental defect during embryogenesis (obsolete MONDO:0015960)","termid":"MONDO:0015960"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"obesity disorder","termid":"MONDO:0011122"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04398":null},"genotype_count":0,"is_obsolete":false,"name":"inherited obesity","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:885912","Orphanet:77828","GARD:18935","UMLS:C4054476","OMIM:601665"],"synonyms":[{"name":"genetic obesity","type":"exact"},{"name":"genetic obesity (disease)","type":"exact"},{"name":"leanness, inherited, autosomal recessive","type":"exact"},{"name":"monogenic obesity","type":"exact"},{"name":"obesity, association with, Autosomal recessive","type":"exact"},{"name":"obesity, early-onset, susceptibility to, Autosomal recessive","type":"exact"},{"name":"obesity, late-onset, Autosomal recessive","type":"exact"},{"name":"obesity, mild, early-onset, Autosomal recessive","type":"exact"},{"name":"obesity, severe, Autosomal recessive","type":"exact"},{"name":"obesity, severe, and type II diabetes, Autosomal recessive","type":"exact"},{"name":"obesity, susceptibility to, Autosomal recessive","type":"exact"}],"termid":"MONDO:0019182","terms_by_termid":{"MONDO:0010961":null},"xrefs":{"Monarch":{"xref_id":"0019182"}}}


id: MONDO:0002009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An episode of depression lasting two or more weeks without an intervening episode of mania.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"depressive disorder","termid":"MONDO:0002050"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major depressive disorder","secondary_identifiers":["ICD9:296.20","ICD9:296.30","NCIT:C35094","OMIM:608516","SCTID:300706003","DOID:1470","ICD9:296.3","MEDGEN:266123","MESH:D003865","EFO:0003761","SCTID:370143000","UMLS:C1269683","MFOMD:0000143","ICD9:296.2"],"synonyms":[{"name":"major depression","type":"exact"},{"name":"major depressive disorder","type":"exact"},{"name":"major depressive disorder 1","type":"broad"},{"name":"major depressive disorder 2","type":"broad"},{"name":"major depressive disorder and accelerated response to antidepressant drug treatment","type":"exact"},{"name":"major depressive disorder, response to citalopram therapy in","type":"exact"},{"name":"recurrent major depression","type":"exact"},{"name":"single major depressive episode","type":"exact"},{"name":"unipolar depression","type":"exact"},{"name":"unipolar depression, susceptibility to","type":"exact"}],"termid":"MONDO:0002009","xrefs":{"Monarch":{"xref_id":"0002009"}}}


id: PBO:0075357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SOWAHC pseudogene 5","termid":"PBO:0075357"}


id: FYPO:0006244
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which mitotic chromosome condensation does not occur over short (less than 90 kb) ranges within a chromosome arm.","definition_xrefs":["PomBase:mah","PMID:28825727"],"gene_count":0,"genotype_count":0,"name":"obsolete abolished short range intra-arm mitotic chromosome condensation during interphase (obsolete FYPO:0006244)","termid":"FYPO:0006244"}


id: GO:0060432
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any developmental process that results in the creation of defined areas or spaces within the lung, to which cells respond and eventually are instructed to differentiate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"},{"relation_name":"part_of","term_name":"lung development","termid":"GO:0030324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lung pattern specification process","termid":"GO:0060432"}


id: MONDO:0023865
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A viral or bacterial infectious process affecting the cornea. Symptoms include pain and redness in the eye, photophobia and eye watering.","definition_xrefs":["NCIT:C83813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keratitis","termid":"MONDO:0003085"},{"relation_name":"is_a","term_name":"endophthalmitis","termid":"MONDO:0016047"}],"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":"corneal infection","secondary_identifiers":["UMLS:C0729777","SCTID:312428002","Orphanet:519278","MEDGEN:152673"],"synonyms":[{"name":"corneal infection","type":"exact"},{"name":"infection of cornea","type":"exact"},{"name":"infective keratitis","type":"exact"},{"name":"keratitis caused by infection","type":"exact"}],"termid":"MONDO:0023865","xrefs":{"Monarch":{"xref_id":"0023865"}}}


id: PBO:0031732
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_meiosis","termid":"PBO:0031732"}


id: PBO:0050540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoxanthine phosphoribosyltransferase 1 pseudogene 1","termid":"PBO:0050540"}


id: GO:0015744
data:
  {"annotated_genes":["SJAG_01406"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098720"}]},"cv_name":"biological_process","definition":"The directed movement of succinate, the dianion of ethane dicarboxylic acid, 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":"C4-dicarboxylate transport","termid":"GO:0015740"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01406":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:0051179","GO:0008150"],"is_obsolete":false,"name":"succinate transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0015744","terms_by_termid":{"GO:0098720":null}}


id: MONDO:0043303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder in which an individual has an abnormally low noise tolerance, and increased sensitivity to sounds.","definition_xrefs":["NCIT:C116366"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of ear","termid":"MONDO:0021205"},{"relation_name":"is_a","term_name":"auditory perceptual disorders","termid":"MONDO:0024422"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperacusis","secondary_identifiers":["UMLS:C0034880","icd11.foundation:652034206","SCTID:25289003","MESH:D012001","MEDGEN:20497"],"synonyms":[{"name":"Phonophobias","type":"related"},{"name":"auditory Hyperesthesias","type":"related"},{"name":"auditory hyperesthesia","type":"related"},{"name":"disturbance, loudness perception","type":"related"},{"name":"disturbances, loudness perception","type":"related"},{"name":"hyperacuses","type":"related"},{"name":"hyperacusia","type":"related"},{"name":"hyperacusias","type":"related"},{"name":"hyperacusis","type":"exact"},{"name":"hyperesthesia, auditory","type":"related"},{"name":"hyperesthesias, auditory","type":"related"},{"name":"loudness Recruitments","type":"related"},{"name":"loudness perception disturbance","type":"related"},{"name":"loudness perception disturbances","type":"related"},{"name":"loudness recruitment","type":"related"},{"name":"low tolerance to sound","type":"related"},{"name":"oversensitive hearing","type":"related"},{"name":"perception disturbance, loudness","type":"related"},{"name":"perception disturbances, loudness","type":"related"},{"name":"phonophobia","type":"related"},{"name":"recruitment, loudness","type":"related"},{"name":"sounds seem unnaturally loud","type":"related"}],"termid":"MONDO:0043303","xrefs":{"Monarch":{"xref_id":"0043303"}}}


id: PBO:0001672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIM1 family serine/threonine protein kinase Cdr1/Nim1","termid":"PBO:0001672"}


id: FYPO:0006670
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a haploid cell undergoes meiotic cell cycle.","definition_xrefs":["PomBase:mah","PMID:31278118","PMID:9755190","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic cell cycle entry","termid":"FYPO:0009006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"name":"meiotic cell cycle entry in haploid cell","synonyms":[{"name":"haploid meiosis","type":"narrow"},{"name":"meiosis in haploid cell","type":"related"}],"termid":"FYPO:0006670"}


id: PBO:0043087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic gamma subunit","termid":"PBO:0043087"}


id: MOD:01947
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-threonine residue and an L-aspartic acid residue with an ester bond to form  O-(L-isoaspartyl)-L-threonine.","definition_xrefs":["RESID:AA0525#TDX","PubMed:17157318","PubMed:8706862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ester crosslinked residues","termid":"MOD:00885"},{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"O-(L-isoaspartyl)-L-threonine","termid":"MOD:01978"},{"relation_name":"is_a","term_name":"crosslinked L-aspartic acid residue","termid":"MOD:02043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-(L-isoaspartyl)-L-threonine (cross-link)","synonyms":[{"name":"(2S)-2-amino-4-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-4-oxobutanoic acid","type":"exact"},{"name":"(2S,3R)-2-amino-3-([(4S)-3-amino-3-carboxypropanoyl]oxy)propanoic acid","type":"exact"},{"name":"CROSSLNK isoaspartyl threonine ester (Thr-Asp)","type":"exact"},{"name":"O(beta)-(beta-aspartyl)threonine","type":"exact"},{"name":"O-(L-isoaspartyl)-L-threonine","type":"exact"},{"name":"O3-(isoaspartyl)-threonine","type":"exact"}],"termid":"MOD:01947"}


id: GO:0075304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of basidiospore formation, a process in which a sexually produced fungal spore is formed on a basidium in the fungi basidiomycetes.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of sexual sporulation resulting in formation of a cellular spore","termid":"GO:0043942"},{"relation_name":"is_a","term_name":"regulation of basidiospore formation","termid":"GO:0075302"},{"relation_name":"negatively_regulates","term_name":"basidiospore formation","termid":"GO:0034295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of basidiospore formation","termid":"GO:0075304"}


id: PBO:0080879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yippee like 4","termid":"PBO:0080879"}


id: PBO:0091421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial NTPase Obg family, human OLA1 ortholog, implicated in mitochondrial translation, ribosome assembly, or tRNA metabolism","termid":"PBO:0091421"}


id: GO:0045444
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an adipocyte, an animal connective tissue cell specialized for the synthesis and storage of fat.","definition_xrefs":["CL:0000136","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"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":"fat cell differentiation","synonyms":[{"name":"adipocyte cell differentiation","type":"exact"},{"name":"adipocyte differentiation","type":"exact"},{"name":"adipogenesis","type":"related"},{"name":"adipose cell differentiation","type":"exact"}],"termid":"GO:0045444"}


id: MONDO:0003591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant adipose tissue neoplasm of the fat cells surrounding the kidney, usually of the well-differentiated or myxoid type. It may be associated with tuberous sclerosis.","definition_xrefs":["NCIT:C6185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney sarcoma","termid":"MONDO:0002930"},{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"kidney liposarcoma","secondary_identifiers":["DOID:5699","MEDGEN:235546","UMLS:C1335745"],"synonyms":[{"name":"kidney liposarcoma","type":"exact"},{"name":"liposarcoma of kidney","type":"exact"},{"name":"liposarcoma of the kidney","type":"exact"},{"name":"renal liposarcoma","type":"exact"}],"termid":"MONDO:0003591","xrefs":{"Monarch":{"xref_id":"0003591"}}}


id: PR:P78871
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rst2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P78871"],"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":"zinc finger protein rst2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F12.02","synonyms":[{"name":"Spom972h-rst2","type":"exact"}],"termid":"PR:P78871"}


id: PBO:0064723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 59","termid":"PBO:0064723"}


id: GO:0007006
data:
  {"annotated_genes":["SJAG_03502","SJAG_05268","SJAG_00404","SJAG_04208","SJAG_02028","SJAG_03282","SJAG_01305","SJAG_03563","SJAG_05300","SJAG_04370","SJAG_00576","SJAG_01949","SJAG_02501","SJAG_04996","SJAG_03168","SJAG_01120","SJAG_02361","SJAG_00168","SJAG_01951","SJAG_01780","SJAG_03700","SJAG_01470","SJAG_03416","SJAG_02355","SJAG_02002","SJAG_04317","SJAG_03710","SJAG_03515","SJAG_05241","SJAG_02656","SJAG_02398","SJAG_04965","SJAG_01640","SJAG_00687","SJAG_01917","SJAG_01405","SJAG_05302","SJAG_00569","SJAG_02524","SJAG_02797","SJAG_00230","SJAG_06440","SJAG_04237","SJAG_02034","SJAG_03633"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93010,96602,101287,102219,104390,105863,106223,107536,107662,109525,113037,117880],"is_not":false,"summary":null,"term":"GO:0007006"},{"annotations":[78466,89450,101707,107333,78656,74923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042407"},{"annotations":[75308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007007"},{"annotations":[104916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990627"},{"annotations":[58897,69821],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070096"},{"annotations":[58947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007008"},{"annotations":[107582,113216,73891,75545,73401,77767,88611,102926,90352,107604,116293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[58175,74357,78212,78562,78637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032979"},{"annotations":[107583,58896,110414,76498,98226,98579,110063,111808,69816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045040"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a mitochondrial membrane, either of the lipid bilayer surrounding a mitochondrion.","definition_xrefs":["GOC:ai","GOC:dph","GOC:mah","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrion organization","termid":"GO:0007005"},{"relation_name":"is_a","term_name":"membrane organization","termid":"GO:0061024"}],"gene_count":45,"genes_by_uniquename":{"SJAG_00168":null,"SJAG_00230":null,"SJAG_00404":null,"SJAG_00569":null,"SJAG_00576":null,"SJAG_00687":null,"SJAG_01120":null,"SJAG_01305":null,"SJAG_01405":null,"SJAG_01470":null,"SJAG_01640":null,"SJAG_01780":null,"SJAG_01917":null,"SJAG_01949":null,"SJAG_01951":null,"SJAG_02002":null,"SJAG_02028":null,"SJAG_02034":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02398":null,"SJAG_02501":null,"SJAG_02524":null,"SJAG_02656":null,"SJAG_02797":null,"SJAG_03168":null,"SJAG_03282":null,"SJAG_03416":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03563":null,"SJAG_03633":null,"SJAG_03700":null,"SJAG_03710":null,"SJAG_04208":null,"SJAG_04237":null,"SJAG_04317":null,"SJAG_04370":null,"SJAG_04965":null,"SJAG_04996":null,"SJAG_05241":null,"SJAG_05268":null,"SJAG_05300":null,"SJAG_05302":null,"SJAG_06440":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0007005","GO:0008150"],"is_obsolete":false,"name":"mitochondrial membrane organization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial membrane organisation","type":"exact"},{"name":"mitochondrial membrane organization and biogenesis","type":"related"}],"termid":"GO:0007006","terms_by_termid":{"GO:0007006":null,"GO:0007007":null,"GO:0007008":null,"GO:0032979":null,"GO:0042407":null,"GO:0045039":null,"GO:0045040":null,"GO:0070096":null,"GO:1990627":null}}


id: PBO:0043430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cornichon family AMPA receptor auxiliary protein 2","termid":"PBO:0043430"}


id: GO:0106263
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction:a 1-acyl-sn-glycero-3-phospho-L-serine + an acyl-CoA = a 1,2-diacyl-sn-glycero-3-phospho-L-serine + CoA.","definition_xrefs":["RHEA:33191","PMID:18287005"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"1-acylglycerophosphoserine O-acyltransferase activity","secondary_identifiers":["EC:2.3.1.n6"],"termid":"GO:0106263"}


id: PBO:0069182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 436, pseudogene","termid":"PBO:0069182"}


id: GO:0009474
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nonaheme cytochrome c (obsolete GO:0009474)","synonyms":[{"name":"nonaheme cytochrome c","type":"exact"}],"termid":"GO:0009474"}


id: PBO:0083250
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; identified by gene-trapping, microarray-based expression analysis, and genome-wide homology searching","termid":"PBO:0083250"}


id: MONDO:1012620
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inherited disorder of neuromuscular transmission resulting in muscle weakness and fatigability exacerbated by exercise that occurs in dogs due to a mutation in the CHRNE gene.","definition_xrefs":["PMID:38853290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"myasthenia, dog","termid":"MONDO:1012175"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital myasthenic syndrome, CHRNE-related, dog","secondary_identifiers":["OMIA:000685-9615"],"termid":"MONDO:1012620","xrefs":{"Monarch":{"xref_id":"1012620"}}}


id: MONDO:1011675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoadrenocorticism, non-human animal","secondary_identifiers":["OMIA:000519"],"termid":"MONDO:1011675","xrefs":{"Monarch":{"xref_id":"1011675"}}}


id: GO:0032935
data:
  {"annotated_genes":["SJAG_03715"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[114928],"is_not":false,"summary":null,"term":"GO:0032935"}]},"cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of a sterol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid sensor activity","termid":"GO:0106254"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03715":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0098772","GO:0140299","GO:0003674"],"is_obsolete":false,"name":"sterol sensor activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"sterol sensing activity","type":"exact"},{"name":"sterol-sensing domain","type":"narrow"}],"termid":"GO:0032935","terms_by_termid":{"GO:0032935":null}}


id: PBO:0084705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial hsp70-type molecular chaperone; required for assembly of iron/sulfur clusters into proteins at a step after cluster synthesis; involved in maturation of Grx5p and Yfh1p, which is a homolog of human frataxin implicated in Friedreich's ataxia","termid":"PBO:0084705"}


id: FYPO:0002583
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 mature transfer RNA (tRNA) measured in a cell is lower than normal. Total tRNA or a specific tRNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered mature tRNA level during vegetative growth","termid":"FYPO:0002579"},{"relation_name":"is_a","term_name":"decreased mature ncRNA level","termid":"FYPO:0006466"},{"relation_name":"is_a","term_name":"decreased pre-tRNA or mature level during vegetative growth","termid":"FYPO:0008342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased mature tRNA level during vegetative growth","synonyms":[{"name":"decreased mature tRNA accumulation during vegetative growth","type":"related"},{"name":"decreased mature tRNA level during mitotic cell cycle","type":"related"},{"name":"decreased mature tRNA transcript level during vegetative growth","type":"exact"},{"name":"decreased mature transfer RNA level during vegetative growth","type":"exact"},{"name":"decreased tRNA level during vegetative growth","type":"broad"},{"name":"reduced mature tRNA level during vegetative growth","type":"exact"}],"termid":"FYPO:0002583"}


id: MONDO:1011341
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Omphalitis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory disease, non-human animal","termid":"MONDO:1011327"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"omphalitis, non-human animal","termid":"MONDO:1011341","xrefs":{"Monarch":{"xref_id":"1011341"}}}


id: PBO:0043472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4-NOT transcription complex subunit 9","termid":"PBO:0043472"}


id: GO:0045815
data:
  {"annotated_genes":["SJAG_02589","SJAG_02447","SJAG_02170","SJAG_00735","SJAG_03694","SJAG_01016","SJAG_04576","SJAG_03839","SJAG_03431","SJAG_05192","SJAG_04194","SJAG_03884","SJAG_00441","SJAG_02303","SJAG_02541","SJAG_00739","SJAG_02768","SJAG_03599","SJAG_02329","SJAG_04613","SJAG_00746","SJAG_03366","SJAG_02314","SJAG_01465","SJAG_02385","SJAG_01611","SJAG_02773","SJAG_05020","SJAG_00440","SJAG_00045","SJAG_01475","SJAG_01513","SJAG_04989","SJAG_00584","SJAG_00873","SJAG_05313","SJAG_03579","SJAG_02549","SJAG_04755","SJAG_01111","SJAG_04097","SJAG_01230","SJAG_03145","SJAG_02869","SJAG_04205","SJAG_03441","SJAG_01658","SJAG_04005","SJAG_03668","SJAG_02500","SJAG_03255","SJAG_02798","SJAG_04213","SJAG_00896","SJAG_02466","SJAG_04596","SJAG_01622","SJAG_03776","SJAG_01653","SJAG_00184","SJAG_02458","SJAG_04758","SJAG_03033","SJAG_03752","SJAG_02254","SJAG_00349","SJAG_02571","SJAG_02981","SJAG_02927","SJAG_02846","SJAG_03787","SJAG_02906","SJAG_01804","SJAG_04274","SJAG_00743","SJAG_07011","SJAG_04038","SJAG_00868","SJAG_00769","SJAG_02066","SJAG_03576","SJAG_01110","SJAG_03758","SJAG_03944","SJAG_01325","SJAG_00087","SJAG_02872","SJAG_00581","SJAG_01711","SJAG_00641"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87610,87757,87936,88113,88296,88446,88829,89065,89238,89751,90028,90552,90659,90673,91378,92264,92762,93483,93749,93980,94091,94105,94125,94153,94181,94278,94613,95421,95446,95860,95867,96424,96633,97072,97811,98231,98499,98666,99142,99392,100978,101566,102783,103122,103369,103851,104572,105036,105044,105639,105788,106763,106915,107344,107457,107696,107895,108481,109081,109360,109484,109592,110490,110625,111768,112567,112994,113150,113169,113339,114242,114253,114326,114415,114740,115032,115280,115412,115426,115730,116313,116374,116563,116931,117297,117481,117574,117596,117644,117994],"is_not":false,"summary":null,"term":"GO:0045815"}]},"cv_name":"biological_process","definition":"An epigenetic mechanism of regulation of gene expression that involves chromatin remodeling to capacitate gene expression by either modifying the chromatin fiber, the nucleosomal histones, or the DNA.","definition_xrefs":["PMID:34414474"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of gene expression, epigenetic","termid":"GO:0141137"},{"relation_name":"part_of","term_name":"transcription initiation at RNA polymerase II 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remodeling","type":"exact"},{"name":"transcription initiation coupled chromatin remodelling","type":"exact"},{"name":"transcriptional initiation-coupled chromatin remodeling","type":"exact"},{"name":"transcriptional initiation-coupled chromatin remodelling","type":"exact"}],"termid":"GO:0045815","terms_by_termid":{"GO:0045815":null}}


id: GO:0051901
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of the change in the membrane potential of the mitochondria from negative to positive.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitochondrial depolarization","termid":"GO:0051900"},{"relation_name":"is_a","term_name":"positive regulation of membrane depolarization","termid":"GO:1904181"},{"relation_name":"positively_regulates","term_name":"mitochondrial depolarization","termid":"GO:0051882"}],"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 mitochondrial depolarization","synonyms":[{"name":"activation of mitochondrial depolarization","type":"narrow"},{"name":"stimulation of mitochondrial depolarization","type":"narrow"},{"name":"up regulation of mitochondrial depolarization","type":"exact"},{"name":"up-regulation of mitochondrial depolarization","type":"exact"},{"name":"upregulation of mitochondrial depolarization","type":"exact"}],"termid":"GO:0051901"}


id: PBO:0028762
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cytoplasmic_translational_initiation","termid":"PBO:0028762"}


id: PBO:0080854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YEATS2 antisense RNA 1","termid":"PBO:0080854"}


id: MONDO:0011537
data:
  {"annotated_genes":["SJAG_03131"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86791],"is_not":false,"summary":null,"term":"MONDO:0011537"}]},"cv_name":"mondo","definition":"An autosomal dominant disease characterized by macrocephaly, facial phenotypes including square outline with frontal bossing, 'dished-out' midface, biparietal narrowing, and long philtrum, developmental delay and autism that has material basis in heterozygous mutation in the PTEN gene on chromosome 10q23.","definition_xrefs":["DOID:0060867","PMID:1719811","PMID:15805158"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03131":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"macrocephaly-autism syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:210548","GARD:17112","OMIM:605309","MESH:C565342","UMLS:C1854416","MEDGEN:381416"],"synonyms":[{"name":"macrocephaly-intellectual disability-autism syndrome","type":"exact"},{"name":"macrocephaly/autism syndrome","type":"related"}],"termid":"MONDO:0011537","terms_by_termid":{"MONDO:0011537":null},"xrefs":{"Monarch":{"xref_id":"0011537"}}}


id: PBO:0084642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Microtubule-associated protein; component of the interface between microtubules and kinetochore, involved in sister chromatid separation; essential in polyploid cells but not in haploid or diploid cells; promotes plus-end directed movement of Dyn1p; ortholog of mammalian CLIP-170","termid":"PBO:0084642"}


id: GO:0046503
data:
  {"annotated_genes":["SJAG_02089","SJAG_02093","SJAG_03604","SJAG_01036","SJAG_02091","SJAG_02161","SJAG_04110","SJAG_02100","SJAG_00622","SJAG_03204","SJAG_02543"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77242,76441,71439,78503,97757],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046475"},{"annotations":[117002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034638"},{"annotations":[74311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006660"},{"annotations":[98464,71264,91861,117614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019433"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycerolipids, any lipid with a glycerol backbone.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid catabolic process","termid":"GO:0016042"},{"relation_name":"is_a","term_name":"glycerolipid metabolic process","termid":"GO:0046486"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00622":null,"SJAG_01036":null,"SJAG_02089":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02100":null,"SJAG_02161":null,"SJAG_02543":null,"SJAG_03204":null,"SJAG_03604":null,"SJAG_04110":null},"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":"glycerolipid catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"glycerolipid breakdown","type":"exact"},{"name":"glycerolipid catabolism","type":"exact"},{"name":"glycerolipid degradation","type":"exact"}],"termid":"GO:0046503","terms_by_termid":{"GO:0006660":null,"GO:0019433":null,"GO:0034638":null,"GO:0046475":null}}


id: GO:0019447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of D-cysteine, (S)-2-amino-3-mercaptopropanoic acid, which occurs naturally in firefly luciferin.","definition_xrefs":["PMID:11527960"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteine catabolic process","termid":"GO:0009093"},{"relation_name":"is_a","term_name":"D-amino acid catabolic process","termid":"GO:0019478"},{"relation_name":"is_a","term_name":"D-cysteine metabolic process","termid":"GO:0046438"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0044248","GO:0006790","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"D-cysteine catabolic process","synonyms":[{"name":"D-cysteine breakdown","type":"exact"},{"name":"D-cysteine catabolism","type":"exact"},{"name":"D-cysteine degradation","type":"exact"}],"termid":"GO:0019447"}


id: GO:0071669
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that results in the biosynthesis of constituent macromolecules, assembly, arrangement of constituent parts, or disassembly of a cellulose- and pectin-containing cell wall.","definition_xrefs":["GOC:mah","GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall organization or biogenesis","termid":"GO:0071554"}],"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:0071554","GO:0008150"],"is_obsolete":false,"name":"plant-type cell wall organization or biogenesis","synonyms":[{"name":"plant-type cell wall organisation or biogenesis","type":"exact"},{"name":"plant-type cell wall organization and biogenesis","type":"related"}],"termid":"GO:0071669"}


id: PBO:0047304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FARSA antisense RNA 1","termid":"PBO:0047304"}


id: MONDO:0015987
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scimitar syndrome is characterized by a combination of cardiopulmonary anomalies including partial anomalous pulmonary venous return connection of the right lung to the inferior caval vein leading to the creation of a left-to-right shunt.","definition_xrefs":["Orphanet:185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital pulmonary venous return anomaly","termid":"MONDO:0017705"},{"relation_name":"is_a","term_name":"congenital anomaly of the great arteries","termid":"MONDO:0020292"}],"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":"scimitar syndrome","secondary_identifiers":["ICD9:747.49","MedDRA:10051951","MESH:D012587","EFO:1001167","GARD:18680","icd11.foundation:1321054364","MEDGEN:20675","NCIT:C85056","UMLS:C0036400","SCTID:39905002"],"synonyms":[{"name":"Epibronchial right pulmonary vein syndrome","type":"exact"},{"name":"Halasz syndrome","type":"exact"},{"name":"congenital pulmonary venolobar syndrome","type":"exact"},{"name":"hypogenetic lung syndrome","type":"exact"}],"termid":"MONDO:0015987","xrefs":{"Monarch":{"xref_id":"0015987"}}}


id: PBO:0078646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon CTT) 2-2","termid":"PBO:0078646"}


id: GO:0005698
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The region of a eukaryotic chromosome that is attached to the spindle during nuclear division. It is defined genetically as the region of the chromosome that always segregates at the first division of meiosis; the region of the chromosome in which no crossing over occurs. At the start of M phase, each chromosome consists of two sister chromatids with a constriction at a point which forms the centromere. During late prophase two kinetochores assemble on each centromere, one kinetochore on each sister chromatid.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete centromere (obsolete GO:0005698)","synonyms":[{"name":"centromere","type":"exact"}],"termid":"GO:0005698"}


id: GO:1901129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of gentamycin.","definition_xrefs":["GOC:TermGenie","GOC:yaf","UniPathway:UPA00967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside antibiotic catabolic process","termid":"GO:0030649"},{"relation_name":"is_a","term_name":"polyol catabolic process","termid":"GO:0046174"},{"relation_name":"is_a","term_name":"gentamycin metabolic process","termid":"GO:1901128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"gentamycin catabolic process","synonyms":[{"name":"gentamycin breakdown","type":"exact"},{"name":"gentamycin catabolism","type":"exact"},{"name":"gentamycin degradation","type":"exact"}],"termid":"GO:1901129"}


id: PBO:0057236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 423","termid":"PBO:0057236"}


id: PBO:0081711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 630","termid":"PBO:0081711"}


id: GO:1902064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any regulation of transcription from RNA polymerase II promoter that is involved in spermatogenesis.","definition_xrefs":["GOC:kmv","GOC:TermGenie","PMID:22570621"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in spermatogenesis (obsolete GO:1902064)","synonyms":[{"name":"global transcription regulation from Pol II promoter involved in generation of spermatozoa","type":"related"},{"name":"global transcription regulation from Pol II promoter involved in spermatogenesis","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in generation of spermatozoa","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in spermatogenesis","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in generation of spermatozoa","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in spermatogenesis","type":"related"},{"name":"regulation of transcription from Pol II promoter involved in generation of spermatozoa","type":"exact"},{"name":"regulation of transcription from Pol II promoter involved in spermatogenesis","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter involved in generation of spermatozoa","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in generation of spermatozoa","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in spermatogenesis","type":"related"}],"termid":"GO:1902064"}


id: PBO:0110407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 35","termid":"PBO:0110407"}


id: PBO:0076293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin binding cytoplasmic RNA interacting protein","termid":"PBO:0076293"}


id: PBO:0080693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wnt family member 1","termid":"PBO:0080693"}


id: PBO:0033780
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_replication_fork_arrest_at_mating-type_locus","termid":"PBO:0033780"}


id: GO:0004512
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucose 6-phosphate = 1D-myo-inositol 3-phosphate. This reaction requires NAD, which dehydrogenates the CHOH group to CO at C-5 of the glucose 6-phosphate, making C-6 into an active methylene, able to condense with the aldehyde at C-1. Finally, the enzyme-bound NADH reconverts C-5 into the CHOH form.","definition_xrefs":["RHEA:10716","EC:5.5.1.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular lyase activity","termid":"GO:0016872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"inositol-3-phosphate synthase activity","secondary_identifiers":["Reactome:R-HSA-1855178","KEGG_REACTION:R07324","MetaCyc:MYO-INOSITOL-1-PHOSPHATE-SYNTHASE-RXN"],"synonyms":[{"name":"1L-myo-inositol-1-phosphate lyase (isomerizing)","type":"related"},{"name":"D-glucose 6-phosphate cycloaldolase activity","type":"related"},{"name":"glucocycloaldolase activity","type":"related"},{"name":"glucose 6-phosphate cyclase activity","type":"related"},{"name":"glucose-6-phosphate inositol monophosphate cycloaldolase activity","type":"related"},{"name":"inositol 1-phosphate synthatase activity","type":"related"},{"name":"inositol 1-phosphate synthetase activity","type":"related"}],"termid":"GO:0004512"}


id: GO:0052131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell or organism towards a higher concentration of environmental oxygen.","definition_xrefs":["GOC:mtg_pamgo_17jul06","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aerotaxis","termid":"GO:0009454"},{"relation_name":"is_a","term_name":"positive chemotaxis","termid":"GO:0050918"},{"relation_name":"is_a","term_name":"positive energy taxis","termid":"GO:0052128"}],"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 aerotaxis","termid":"GO:0052131"}


id: PBO:0051334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2-30","termid":"PBO:0051334"}


id: GO:0030383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any interaction between a pathogen and its host organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete host-pathogen interaction (obsolete GO:0030383)","synonyms":[{"name":"host-pathogen interaction","type":"exact"}],"termid":"GO:0030383"}


id: MONDO:0008593
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":"trichomegaly","secondary_identifiers":["MEDGEN:163139","OMIM:190330","UMLS:C0854699"],"synonyms":[{"name":"TCMGLY","type":"related"},{"name":"eyelashes, long","type":"related"},{"name":"trichomegaly","type":"exact"}],"termid":"MONDO:0008593","xrefs":{"Monarch":{"xref_id":"0008593"}}}


id: PBO:0084610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged open reading frame; does not encode a protein; YGL210W-A was originally annotated as an independent ORF, but as a result of a sequence change, it was merged with an adjacent ORF into a single reading frame, designated YGL211W","termid":"PBO:0084610"}


id: GO:0010772
data:
  {"annotated_genes":["SJAG_01708","SJAG_03221"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107677,110318],"is_not":false,"summary":null,"term":"GO:0010772"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of strand exchange proteins (recombinases) to form higher order oligomers on single-stranded DNA resulting in meiotic recombination. Meiotic recombination is the cell cycle process in which double strand breaks are formed and repaired through a double Holliday junction intermediate.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic DNA recombinase assembly","termid":"GO:0000707"},{"relation_name":"part_of","term_name":"reciprocal meiotic recombination","termid":"GO:0007131"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01708":null,"SJAG_03221":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0006281"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006310","GO:0044085","GO:0140013","GO:0065003","GO:0006281","GO:0007049"],"is_obsolete":false,"name":"meiotic DNA recombinase assembly involved in reciprocal meiotic recombination","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010772","terms_by_termid":{"GO:0010772":null}}


id: MONDO:0015245
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare intestinal disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare intestinal disease (obsolete MONDO:0015245)","secondary_identifiers":["Orphanet:117569"],"synonyms":[{"name":"rare intestinal disease","type":"exact"}],"termid":"MONDO:0015245","xrefs":{"Monarch":{"xref_id":"0015245"}}}


id: GO:1990346
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex consisting of BID and BCL-xl, members of the Bcl-2 family of anti- and proapoptotic regulators.","definition_xrefs":["GOC:bhm","PMID:14634621"],"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":"BID-BCL-xl complex","termid":"GO:1990346"}


id: GO:0071726
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 diacylated bacterial lipopeptide stimulus.","definition_xrefs":["PMID:12077222","GOC:add","PMID:12524386","PMID:2757794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to bacterial lipopeptide","termid":"GO:0071221"},{"relation_name":"is_a","term_name":"response to diacyl bacterial lipopeptide","termid":"GO:0071724"}],"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 diacyl bacterial lipopeptide","synonyms":[{"name":"cellular response to diacylated bacterial lipoprotein","type":"exact"}],"termid":"GO:0071726"}


id: GO:0045544
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 2-oxoglutarate + gibberellin A12 (GA12) + H+ + 3 O2 = 3 CO2 + gibberellin A9 (GA9) + 2 H2O + 2 succinate. This reaction results in the oxidation of C-20 gibberellins to form the corresponding C-19 lactones, via a three-step oxidation at C-20 of the GA skeleton. Also converts GA53 to GA20. GA25 is also formed as a minor product.","definition_xrefs":["PMID:32652020","PMID:7604047"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"gibberellin 20-oxidase activity","termid":"GO:0045544"}


id: GO:0044862
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a protein out of a plasma membrane raft.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport out of membrane raft","termid":"GO:0032599"},{"relation_name":"is_a","term_name":"establishment of protein localization to membrane","termid":"GO:0090150"},{"relation_name":"is_a","term_name":"protein transport within plasma membrane","termid":"GO:0099632"},{"relation_name":"is_a","term_name":"protein localization to cell periphery","termid":"GO:1990778"}],"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"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179","GO:0061024"],"is_obsolete":false,"name":"protein transport out of plasma membrane raft","termid":"GO:0044862"}


id: FYPO:0004872
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a 2-oxoglutarate-dependent dioxygenase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished dioxygenase activity","termid":"FYPO:0004365"},{"relation_name":"is_a","term_name":"abnormal 2-oxoglutarate dioxygenase activity","termid":"FYPO:0004871"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0000661","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abolished 2-oxoglutarate dioxygenase activity","synonyms":[{"name":"2-oxoglutarate dioxygenase activity abolished","type":"exact"},{"name":"abolished 2-oxoglutarate-dependent dioxygenase activity","type":"exact"},{"name":"abolished oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors","type":"exact"}],"termid":"FYPO:0004872"}


id: SO:0001997
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A heterochromatic region of the chromosome, adjacent to the telomere (on the centromeric side) that contains repetitive DNA and sometimes genes and it is transcribed.","definition_xrefs":["POMBE:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal_structural_element","termid":"SO:0000628"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subtelomere","termid":"SO:0001997"}


id: PR:O13743
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pos1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C16E8.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.08","synonyms":[{"name":"Spom972h-pos1","type":"exact"}],"termid":"PR:O13743"}


id: MONDO:0006091
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low grade tumor with neuroendocrine differentiation that arises from the appendix. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"appendix cancer","termid":"MONDO:0001235"},{"relation_name":"is_a","term_name":"cecum neuroendocrine tumor G1","termid":"MONDO:0006126"},{"relation_name":"is_a","term_name":"neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade","termid":"MONDO:0015066"}],"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":"appendix neuroendocrine tumor G1","secondary_identifiers":["SCTID:253002004","ICDO:8240/1","DOID:0050911","NCIT:C4138","MEDGEN:90758","UMLS:C0334298","EFO:1000092","ICD9:209.11"],"synonyms":[{"name":"appendiceal carcinoid tumor","type":"exact"},{"name":"appendiceal carcinoid tumour","type":"exact"},{"name":"appendix NET G1","type":"exact"},{"name":"appendix NET G1 (carcinoid)","type":"exact"},{"name":"appendix carcinoid endocrine tumor","type":"related"},{"name":"appendix carcinoid endocrine tumour","type":"related"},{"name":"appendix carcinoid tumor","type":"exact"},{"name":"appendix carcinoid tumour","type":"exact"},{"name":"appendix neuroendocrine tumor G1 (carcinoid)","type":"exact"},{"name":"appendix neuroendocrine tumour G1 (carcinoid)","type":"exact"},{"name":"carcinoid tumor of appendix","type":"exact"},{"name":"carcinoid tumor of the appendix","type":"exact"},{"name":"carcinoid tumour of appendix","type":"exact"},{"name":"carcinoid tumour of the appendix","type":"exact"},{"name":"grade 1 neuroendocrine neoplasm of vermiform appendix","type":"exact"},{"name":"vermiform appendix NET G1","type":"exact"},{"name":"vermiform appendix carcinoid tumor","type":"exact"},{"name":"vermiform appendix carcinoid tumor (disease)","type":"exact"},{"name":"vermiform appendix carcinoid tumour","type":"exact"},{"name":"vermiform appendix carcinoid tumour (disease)","type":"exact"},{"name":"vermiform appendix neuroendocrine neoplasm G1","type":"exact"},{"name":"vermiform appendix neuroendocrine tumor, well differentiated, low grade","type":"exact"}],"termid":"MONDO:0006091","xrefs":{"Monarch":{"xref_id":"0006091"}}}


id: PBO:0053117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipocalin 6","termid":"PBO:0053117"}


id: PBO:0042164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine ligand 25","termid":"PBO:0042164"}


id: PBO:0028187
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vegetative_cell_length","termid":"PBO:0028187"}


id: GO:0006593
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ornithine, an amino acid only rarely found in proteins, but which is important in living organisms as an intermediate in the reactions of the urea cycle and in arginine biosynthesis.","definition_xrefs":["ISBN:0192801023","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ornithine metabolic process","termid":"GO:0006591"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid catabolic process","termid":"GO:0170044"},{"relation_name":"is_a","term_name":"alpha-amino acid catabolic process","termid":"GO:1901606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044248","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"ornithine catabolic process","synonyms":[{"name":"ornithine breakdown","type":"exact"},{"name":"ornithine catabolism","type":"exact"},{"name":"ornithine degradation","type":"exact"}],"termid":"GO:0006593"}


id: FYPO:0006065
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 septin ring disassembly begins later than normal.","definition_xrefs":["PMID:15385632","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal septin ring disassembly during vegetative growth","termid":"FYPO:0006064"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of septin ring disassembly during vegetative growth","synonyms":[{"name":"delayed onset of septin ring disassembly during mitotic cell cycle","type":"related"},{"name":"delayed septin ring disassembly during vegetative growth","type":"exact"}],"termid":"FYPO:0006065"}


id: MONDO:0030973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 77","secondary_identifiers":["MEDGEN:1788976","OMIM:619223","UMLS:C5543173"],"synonyms":[{"name":"IMD77","type":"exact"},{"name":"immunodeficiency 77","type":"exact"}],"termid":"MONDO:0030973","xrefs":{"Monarch":{"xref_id":"0030973"}}}


id: PBO:0087402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Stretch-activated Ca2+-permeable cation channel; required for Ca2+ influx stimulated by mating pheromones and some abiotic stresses; sensor of compressive mechanical stress; N-glycosylated membrane protein of the ER and plasma membrane; interacts with Cch1p; oligomerizes; is an alpha2/delta-like protein and participates in the generation of stretch-activated Ca2+-permeable cation channel activity when expressed in mammalian cells","termid":"PBO:0087402"}


id: PBO:0042611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDRT15 pseudogene 11","termid":"PBO:0042611"}


id: MONDO:0018437
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute myeloid leukemia with NPM1 somatic mutations is a subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by clonal proliferation of myeloid blasts harboring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. Patients usually present with leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy.","definition_xrefs":["Orphanet:402026"],"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:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia with NPM1 somatic mutations","secondary_identifiers":["GARD:21713","MEDGEN:1633725","UMLS:C4706386","SCTID:763309005"],"synonyms":[{"name":"AML with NPM1 somatic mutations","type":"exact"}],"termid":"MONDO:0018437","xrefs":{"Monarch":{"xref_id":"0018437"}}}


id: MONDO:0017601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diffuse large B-cell lymphoma with chronic inflammation is an Epstein-Barr virus-associated malignant lymphoproliferative disorder, developing in a context of long-standing or slow-growing, chronically inflamed lesions, such as chronic pyothorax, metallic implants in bones and joints, chronic osteomyelitis, chronic venous ulcer, or, rarely granulomatous inflammation. The tumor is usually primarily localized, with no involvement of other organs.","definition_xrefs":["Orphanet:300888"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Epstein-Barr virus-associated malignant lymphoproliferative disorder","termid":"MONDO:0017343"},{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"diffuse large B-cell lymphoma with chronic inflammation","secondary_identifiers":["MEDGEN:1374328","UMLS:C4511460","GARD:21250","NCIT:C80289"],"synonyms":[{"name":"DLBCL with chronic inflammation","type":"exact"}],"termid":"MONDO:0017601","xrefs":{"Monarch":{"xref_id":"0017601"}}}


id: PBO:0072344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 30","termid":"PBO:0072344"}


id: GO:0034071
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + aminoglycoside = ADP + phosphoaminoglycoside.","definition_xrefs":["GOC:cb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"aminoglycoside phosphotransferase activity","secondary_identifiers":["EC:2.7.1.190"],"synonyms":[{"name":"aminoglycoside kinase activity","type":"exact"}],"termid":"GO:0034071"}


id: PATO:0001750
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A paedomorphic growth quality which is due to a delayed onset.","definition_xrefs":["PATOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paedomorphic growth","termid":"PATO:0001749"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postdisplaced growth","termid":"PATO:0001750"}


id: PBO:0073974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 22 member 25","termid":"PBO:0073974"}


id: GO:0052613
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: canthaxanthin + a reduced electron acceptor + oxygen = adonirubin + an oxidized electron acceptor + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete canthaxanthin 3-hydroxylase activity (obsolete GO:0052613)","synonyms":[{"name":"beta-carotene hydroxylase activity","type":"broad"},{"name":"carotene beta-ring hydroxylase activity","type":"broad"}],"termid":"GO:0052613"}


id: GO:0046761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A viral budding that starts with formation of a curvature in the host plasma membrane around which the virion particle assembles.","definition_xrefs":["GOC:bf","PMID:9394621","ISBN:0072370319","VZ:1947"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-lytic viral release","termid":"GO:0046753"},{"relation_name":"is_a","term_name":"viral budding","termid":"GO:0046755"}],"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":"viral budding from plasma membrane","secondary_identifiers":["GO:0046767","GO:0046766"],"synonyms":[{"name":"plasma membrane viral budding","type":"exact"},{"name":"plasma membrane viral budding during viral capsid envelopment","type":"related"},{"name":"viral budding from plasma membrane by viral capsid envelopment","type":"related"},{"name":"viral budding from plasma membrane during viral capsid envelopment","type":"related"},{"name":"virus budding from plasma membrane","type":"exact"},{"name":"virus budding from plasma membrane by viral capsid envelopment","type":"exact"},{"name":"virus budding from plasma membrane during viral capsid envelopment","type":"related"}],"termid":"GO:0046761"}


id: PBO:0061016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein interacting with the FHA domain of MKI67","termid":"PBO:0061016"}


id: MONDO:0009951
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":"radiculoneuropathy, fatal neonatal","secondary_identifiers":["MEDGEN:376592","MESH:C564857","OMIM:266250","UMLS:C1849471"],"synonyms":[{"name":"Radiculoneuropathy, fatal neonatal","type":"exact"}],"termid":"MONDO:0009951","xrefs":{"Monarch":{"xref_id":"0009951"}}}


id: MONDO:1011039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any oculocutaneous albinism that occurs in dogs due to a mutation in the SLC45A2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, SLC45A2-related, dog","secondary_identifiers":["OMIA:001821-9615"],"synonyms":[{"name":"coat color albinism, oculocutaneous type IV, dog","type":"related"}],"termid":"MONDO:1011039","xrefs":{"Monarch":{"xref_id":"1011039"}}}


id: MONDO:0003923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papilloma that arises from the ciliated respiratory mucosa that lines the ethmoid sinus. It is classified as inverted papilloma and oncocytic papilloma.","definition_xrefs":["NCIT:C6836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paranasal sinus Schneiderian papilloma","termid":"MONDO:0006353"},{"relation_name":"is_a","term_name":"benign neoplasm of ethmoidal sinus","termid":"MONDO:0021515"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ethmoid sinus Schneiderian papilloma","secondary_identifiers":["UMLS:C1333476","MEDGEN:232474","DOID:6559"],"synonyms":[{"name":"Schneiderian papilloma of ethmoid sinus","type":"related"},{"name":"Schneiderian papilloma of the ethmoid sinus","type":"exact"},{"name":"ethmoid sinus Schneiderian papilloma","type":"exact"}],"termid":"MONDO:0003923","xrefs":{"Monarch":{"xref_id":"0003923"}}}


id: GO:0060579
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a ventral spinal cord interneuron. Ventral spinal cord interneurons are cells located in the ventral portion of the spinal cord that transmit signals between sensory and motor neurons and are required for reflexive responses.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron fate commitment","termid":"GO:0048663"},{"relation_name":"is_a","term_name":"cell fate commitment involved in pattern specification","termid":"GO:0060581"},{"relation_name":"part_of","term_name":"spinal cord dorsal/ventral patterning","termid":"GO:0021513"},{"relation_name":"part_of","term_name":"ventral spinal cord interneuron differentiation","termid":"GO:0021514"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"ventral spinal cord interneuron fate commitment","termid":"GO:0060579"}


id: MONDO:0017487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"radial hemimelia","termid":"MONDO:0019671"}],"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":"radial hemimelia, bilateral","secondary_identifiers":["icd11.foundation:1701238542","Orphanet:295071"],"synonyms":[{"name":"radial longitidinal meromelia, bilateral","type":"exact"}],"termid":"MONDO:0017487","xrefs":{"Monarch":{"xref_id":"0017487"}}}


id: PBO:0052088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch repeat and BTB domain containing 4","termid":"PBO:0052088"}


id: PBO:0086973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulatory subunit of protein phosphatase 1 (Glc7p); involved in glycogen metabolism and chromosome segregation; proposed to regulate Glc7p activity via conformational alteration; ortholog of the mammalian protein phosphatase inhibitor 2; protein abundance increases in response to DNA replication stress","termid":"PBO:0086973"}


id: MONDO:0006892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by recurrent focal onset seizures which have sensory (i.e., olfactory, visual, tactile, gustatory, or auditory) manifestations. Partial seizures that feature alterations of consciousness are referred to as complex partial seizures (epilepsy, complex partial).","definition_xrefs":["MESH:D020937"],"direct_ancestors":[{"relation_name":"is_a","term_name":"focal epilepsy","termid":"MONDO:0005384"}],"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":"partial sensory epilepsy","secondary_identifiers":["DOID:3330","UMLS:C0544645","MEDGEN:107460"],"termid":"MONDO:0006892","xrefs":{"Monarch":{"xref_id":"0006892"}}}


id: PBO:0062076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 7 pseudogene","termid":"PBO:0062076"}


id: GO:0031130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which one cell or group of cells sends a signal over a short range to another cell or group of cells of different ancestry and developmental potential, thereby effecting a developmental change in the latter.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete creation of an inductive signal (obsolete GO:0031130)","termid":"GO:0031130"}


id: PBO:0040910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 14","termid":"PBO:0040910"}


id: PBO:0017542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial F1-F0 ATPase assembly protein (predicted)","termid":"PBO:0017542"}


id: MONDO:0008579
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":"toes, relative length of first and second","secondary_identifiers":["OMIM:189200","UMLS:C1861059","MEDGEN:396051"],"synonyms":[{"name":"toes, relative length of first and second","type":"exact"}],"termid":"MONDO:0008579","xrefs":{"Monarch":{"xref_id":"0008579"}}}


id: GO:2000218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of invasive growth in response to glucose limitation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of growth of unicellular organism as a thread of attached cells","termid":"GO:0070785"},{"relation_name":"is_a","term_name":"regulation of invasive growth in response to glucose limitation","termid":"GO:2000217"},{"relation_name":"negatively_regulates","term_name":"invasive growth in response to glucose limitation","termid":"GO:0001403"}],"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 invasive growth in response to glucose limitation","synonyms":[{"name":"negative regulation of colony morphology","type":"related"}],"termid":"GO:2000218"}


id: MONDO:0018348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete polyglucosan body myopathy type 1 (obsolete MONDO:0018348)","secondary_identifiers":["NANDO:2200456"],"termid":"MONDO:0018348","xrefs":{"Monarch":{"xref_id":"0018348"}}}


id: PBO:0039871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 29","termid":"PBO:0039871"}


id: GO:1900731
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of adenylate cyclase-inhibiting opioid receptor signaling pathway.","definition_xrefs":["GOC:sjw","GOC:TermGenie","PMID:17157995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of adenylate cyclase-inhibiting opioid receptor signaling pathway","termid":"GO:1900729"},{"relation_name":"is_a","term_name":"positive regulation of opioid receptor signaling pathway","termid":"GO:2000476"},{"relation_name":"positively_regulates","term_name":"adenylate cyclase-inhibiting opioid receptor signaling pathway","termid":"GO:0031635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of adenylate cyclase-inhibiting opioid receptor signaling pathway","synonyms":[{"name":"activation of adenylate cyclase-inhibiting opioid receptor signaling pathway","type":"narrow"},{"name":"activation of opioid receptor-mediated adenylate cyclase inhibition","type":"related"},{"name":"up regulation of adenylate cyclase-inhibiting opioid receptor signaling pathway","type":"exact"},{"name":"upregulation of adenylate cyclase-inhibiting opioid receptor signaling pathway","type":"exact"}],"termid":"GO:1900731"}


id: GO:0009728
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a gibberellic acid stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of hormone stimulus","termid":"GO:0009720"},{"relation_name":"is_a","term_name":"response to gibberellin","termid":"GO:0009739"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of gibberellic acid stimulus","synonyms":[{"name":"perception of gibberellic acid stimulus","type":"related"}],"termid":"GO:0009728"}


id: FYPO:0006610
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 a protein that is normally localized intermittently to the Cdr2 medial cortical node complex is associated with the complex for periods of longer duration than normal.","definition_xrefs":["PMID:29514920","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal intermittent protein localization to Cdr2 medial cortical node complex","termid":"FYPO:0006607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased protein dwell time during intermittent localization to Cdr2 medial cortical node complex","synonyms":[{"name":"increased duration of bursts of intermittent protein localization to Cdr2 medial cortical node complex","type":"related"},{"name":"increased duration of protein localization bursts to Cdr2 medial cortical node complex","type":"related"},{"name":"increased duration of protein visits to Cdr2 medial cortical node complex","type":"related"},{"name":"increased protein dwell time during intermittent localization to Cdr2 medial cortical node complex during mitotic cell cycle","type":"related"},{"name":"increased protein dwell time during intermittent localization to Cdr2 medial cortical node complex during vegetative growth","type":"exact"},{"name":"increased protein dwell time during transient localization to Cdr2 medial cortical node complex","type":"exact"}],"termid":"FYPO:0006610"}


id: MONDO:1010788
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Ehlers-Danlos syndrome in horses in which the cause of the disease is a mutation in the PLOD1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, horse","termid":"MONDO:1011495"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ehlers-Danlos syndrome, kyphoscoliotic type, PLOD1-related, horse","secondary_identifiers":["OMIA:001982-9796"],"synonyms":[{"name":"Fragile Foal Syndrome","type":"exact"},{"name":"kEDS","type":"exact"}],"termid":"MONDO:1010788","xrefs":{"Monarch":{"xref_id":"1010788"}}}


id: GO:0019911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of the myelin sheath of a nerve.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural molecule activity","termid":"GO:0005198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005198"}],"interesting_parent_ids":["GO:0003674","GO:0005198"],"is_obsolete":false,"name":"structural constituent of myelin sheath","termid":"GO:0019911"}


id: MONDO:0000257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of diarrhea.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diarrheal disease","termid":"MONDO:0001673"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"acute diarrhea","secondary_identifiers":["DOID:0050140","MEDGEN:677005","UMLS:C0740441","SCTID:409966000"],"synonyms":[{"name":"acute diarrheal disease","type":"exact"},{"name":"diarrhea (disease), acute","type":"exact"},{"name":"diarrhea, acute","type":"exact"},{"name":"diarrheal disease, acute","type":"exact"},{"name":"diarrhoea (disease), acute","type":"exact"}],"termid":"MONDO:0000257","xrefs":{"Monarch":{"xref_id":"0000257"}}}


id: MONDO:0040653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive form of ocular albinism (disease).","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"ocular albinism","termid":"MONDO:0017304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"autosomal recessive ocular albinism","secondary_identifiers":["MEDGEN:541337","SCTID:78921008","UMLS:C0268503"],"synonyms":[{"name":"AROA","type":"related"},{"name":"autosomal recessive ocular albinism","type":"exact"},{"name":"autosomal recessive ocular albinism (disease)","type":"exact"},{"name":"ocular albinism (disease), autosomal recessive","type":"exact"}],"termid":"MONDO:0040653","xrefs":{"Monarch":{"xref_id":"0040653"}}}


id: PBO:0047415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and WD repeat domain containing 7","termid":"PBO:0047415"}


id: MONDO:1012602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lysosomal storage disease that occurs in dogs in which there is a buildup of GM2 gangliosides in tissues due to the lack of the enzyme hexosaminidase. It is characterised by progressive neuromuscular dysfunction and impaired growth from an early age.","definition_xrefs":["OMIA:000403-9615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gangliosidosis, dog","termid":"MONDO:1010840"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GM2 gangliosidosis, dog","synonyms":[{"name":"gangliosidosis, GM2, generic, dog","type":"related"}],"termid":"MONDO:1012602","xrefs":{"Monarch":{"xref_id":"1012602"}}}


id: PBO:0052171
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 2","termid":"PBO:0052171"}


id: GO:0035917
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents or reduces the frequency, rate or extent of the activity of a calcium channel in another organism.","definition_xrefs":["GOC:bf","PMID:20920515","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of calcium channel activity in another organism (obsolete GO:0035917)","synonyms":[{"name":"down-regulation of calcium channel activity in other organism","type":"exact"},{"name":"downregulation of calcium channel activity in other organism","type":"exact"},{"name":"inhibition of calcium channel activity in other organism","type":"narrow"},{"name":"negative regulation of calcium channel activity in other organism","type":"exact"}],"termid":"GO:0035917"}


id: SO:0001409
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region which is intended for use in an experiment.","definition_xrefs":["SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"region","termid":"SO:0000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biomaterial_region","synonyms":[{"name":"biomaterial region","type":"exact"}],"termid":"SO:0001409"}


id: PBO:0074443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 44","termid":"PBO:0074443"}


id: PR:Q9P6K7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- asc1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6K7"],"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":"tRNA-aminoacylation cofactor arc1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC30C2.04","synonyms":[{"name":"Spom972h-asc1","type":"exact"}],"termid":"PR:Q9P6K7"}


id: GO:0098583
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A vocalization behavior that is the result of learning.","definition_xrefs":["GOC:dos","PMID:16418265","GOC:rl","PMID:17035521","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vocalization behavior","termid":"GO:0071625"},{"relation_name":"is_a","term_name":"learned vocalization behavior or vocal learning","termid":"GO:0098598"}],"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":"learned vocalization behavior","termid":"GO:0098583"}


id: PBO:0068940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 183, pseudogene","termid":"PBO:0068940"}


id: GO:0045007
data:
  {"annotated_genes":["SJAG_02261"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94835],"is_not":false,"summary":null,"term":"GO:0045007"}]},"cv_name":"biological_process","definition":"The disruption of the bond between the sugar in the backbone and the A or G base, causing the base to be removed and leaving a depurinated sugar.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"base-excision repair, AP site formation","termid":"GO:0006285"},{"relation_name":"is_a","term_name":"DNA modification","termid":"GO:0006304"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006281","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"depurination","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-73927","Wikipedia:Depurination"],"termid":"GO:0045007","terms_by_termid":{"GO:0045007":null}}


id: MONDO:0003130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solid, unencapsulated tumor of the kidney composed of spindle mesenchymal cells that resemble fibroblasts or muscle cells. The homogeneous mass typically extends into the renal parenchyma and replaces most of the kidney. In most cases, mesoblastic nephroma is benign and occurs in the fetus or newborn, and rarely in the older child or the adult.","definition_xrefs":["MESH:D018201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney cancer","termid":"MONDO:0002367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005240"],"is_obsolete":false,"name":"mesoblastic nephroma","secondary_identifiers":["UMLS:C0206628","ICD9:236.99","EFO:0007365","DOID:4772","SCTID:307604008","MEDGEN:64620"],"synonyms":[{"name":"mesoblastic nephroma","type":"exact"},{"name":"mesoblastic nephroma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003130","xrefs":{"Monarch":{"xref_id":"0003130"}}}


id: MONDO:0005720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mild, eruptive skin disease of milk cows caused by cowpox virus, with lesions occurring principally on the udder and teats. Human infection may occur while milking an infected animal.","definition_xrefs":["MESH:D015605"],"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":"cowpox","secondary_identifiers":["EFO:0007225","UMLS:C0010232","ICD9:051.01","SCTID:70090004","DOID:8956","ICD10CM:B08.010","icd11.foundation:1205745537","MEDGEN:3261"],"synonyms":[{"name":"yaba","type":"exact"}],"termid":"MONDO:0005720","xrefs":{"Monarch":{"xref_id":"0005720"}}}


id: GO:0034995
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consist of complement components C5b6 and C7 stably inserted in a cell membrane. Formation of the SC5b-7 complex is the first phase of membrane attack complex assembly.","definition_xrefs":["PMID:10090939"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"SC5b-7 complex","termid":"GO:0034995"}


id: GO:0106378
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-hydroxy-dATP + H2O = 2-hydroxy-dAMP + H+ + diphosphate.","definition_xrefs":["RHEA:31583","PMID:11139615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate diphosphatase activity","termid":"GO:0047429"}],"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:0047429"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0047429","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"2-hydroxy-dATP hydrolase activity","secondary_identifiers":["Reactome:R-HSA-2395818"],"termid":"GO:0106378"}


id: PBO:0064304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLLP pseudogene 1","termid":"PBO:0064304"}


id: MONDO:0009303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune disease that affects the lungs and kidneys and is characterized by pulmonary alveolar hemorrhage (bleeding in the lungs) and a kidney disease known as glomerulonephritis. Some use the term 'Goodpasture syndrome' for the findings of glomerulonephritis and pulmonary hemorrhage and the term 'Goodpasture disease' for those patients with glomerulonephritis, pulmonary hemorrhage, and anti-GBM antibodies. Currently, the preferred term for both conditions is “ anti-GBM antibody disease ”. Circulating antibodies are directed against the collagen of the part of the kidney known as the glomerular basement membrane (GBM), resulting in acute or rapidly progressive glomerulonephritis. Antibodies also attack the collagen of the air sacs of the lung (alveoli) resulting in bleeding of the lung (pulmonary hemorrhage). Symptoms may include general body discomfort or pain, bleeding from the nose and/or blood in the urine, respiratory problems, anemia, chest pain, and kidney failure. Anti-GBM disease is thought to result from an environmental insult (smoking, infections, exposure to certain drugs) in a person with genetic susceptibility, such as a specific human leukocyte antigen (HLA) type. Diagnosis is confirmed with the presence of anti-GBM antibody in the blood or in the kidney. The treatment of choice is plasmapheresis in conjunction with prednisone and cyclophosphamide.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete predominantly small-vessel vasculitis (obsolete MONDO:0015490)","termid":"MONDO:0015490"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary interstitial lung disease in childhood and adulthood associated with a systemic disease (obsolete MONDO:0017035)","termid":"MONDO:0017035"},{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"anti-glomerular basement membrane disease","secondary_identifiers":["MEDGEN:140788","ICD9:446.21","EFO:0007290","ICD10EXP:N08.5*","ICD10EXP:M31.0+","NORD:1198","NANDO:1200717","GARD:2551","MESH:D019867","UMLS:C0403529","icd11.foundation:591736785","NANDO:2200125","Orphanet:375","MedDRA:10018620","NCIT:C84566","DOID:9808","SCTID:236432001","OMIM:233450","NANDO:1200718"],"synonyms":[{"name":"Goodpasture Syndrome","type":"exact"},{"name":"Goodpasture syndrome","type":"exact"},{"name":"anti-GBM syndrome","type":"exact"},{"name":"anti-glomerular basement membrane antibody disease","type":"related"},{"name":"anti-glomerular basement membrane disease","type":"exact"},{"name":"glomerulonephritis - pulmonary haemorrhage","type":"related"},{"name":"glomerulonephritis - pulmonary hemorrhage","type":"related"},{"name":"pulmonary renal syndrome","type":"related"},{"name":"rapidly progressive glomerulonephritis with pulmonary haemorrhage","type":"related"},{"name":"rapidly progressive glomerulonephritis with pulmonary hemorrhage","type":"related"}],"termid":"MONDO:0009303","xrefs":{"Monarch":{"xref_id":"0009303"}}}


id: PBO:0078191
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 5-1","termid":"PBO:0078191"}


id: MONDO:0019124
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microscopic polyangiitis (MPA) is an inflammatory, necrotizing, systemic vasculitis that affects predominantly small vessels (i.e. small arteries, arterioles, capillaries, venules) in multiple organs.","definition_xrefs":["Orphanet:727"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"anti-neutrophil cytoplasmic antibody-associated vasculitis","termid":"MONDO:0015492"},{"relation_name":"is_a","term_name":"arteritis","termid":"MONDO:0043494"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microscopic polyangiitis","secondary_identifiers":["MESH:D055953","icd11.foundation:999231798","GARD:3652","NANDO:1200262","EFO:1000784","ICD10CM:M31.7","NCIT:C70549","SCTID:239928004","NANDO:2200426","UMLS:C2347126","MEDGEN:389393","MedDRA:10063344"],"synonyms":[{"name":"MPA","type":"exact"},{"name":"Micropolyangiitis","type":"exact"},{"name":"microscopic polyarteritis","type":"exact"}],"termid":"MONDO:0019124","xrefs":{"Monarch":{"xref_id":"0019124"}}}


id: PBO:0064481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase eta pseudogene 1","termid":"PBO:0064481"}


id: PBO:0001168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO deconjugating cysteine peptidase Ulp2 (predicted)","termid":"PBO:0001168"}


id: GO:1990516
data:
  {"annotated_genes":["SJAG_02039"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98112],"is_not":false,"summary":null,"term":"GO:1990516"}]},"cv_name":"biological_process","definition":"The pathway by which a ribonucleotide is removed from DNA and replaced by a deoxyribonucleotide. The ribonucleotide is incised by RNase H2, and further excised by an endonuclease. The resulting 1 nt gap is then repaired by DNA polymerase and DNA ligase.","definition_xrefs":["PMID:22864116","PMID:12475934"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mismatch repair involved in maintenance of fidelity involved in DNA-dependent DNA replication","termid":"GO:0070716"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02039":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006260","GO:0008150","GO:0006281","GO:0006259"],"is_obsolete":false,"name":"ribonucleotide excision repair","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990516","terms_by_termid":{"GO:1990516":null}}


id: MONDO:0004070
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete gemistocytic astrocytoma (obsolete MONDO:0004070)","termid":"MONDO:0004070","xrefs":{"Monarch":{"xref_id":"0004070"}}}


id: MONDO:0009017
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":"corneal degeneration, band-shaped spheroid","secondary_identifiers":["OMIM:217520","UMLS:C1857571","MEDGEN:347489"],"synonyms":[{"name":"corneal degeneration, band-shaped spheroid","type":"exact"}],"termid":"MONDO:0009017","xrefs":{"Monarch":{"xref_id":"0009017"}}}


id: PBO:0057613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1179","termid":"PBO:0057613"}


id: GO:1900576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving gerfelin.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catechol-containing compound metabolic process","termid":"GO:0009712"},{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"},{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"gerfelin metabolic process","synonyms":[{"name":"gerfelin metabolism","type":"exact"}],"termid":"GO:1900576"}


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


id: PBO:0087126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein; has similarity to mammalian heterogeneous nuclear RNP K protein, involved in the regulation of telomere position effect and telomere length; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0087126"}


id: PBO:0090250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone lysine methyltransferase Set5","termid":"PBO:0090250"}


id: GO:0039554
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts a cytoplasmic pattern recognition receptor signaling pathway by inhibiting the activity of MDA-5 (also known as IFIH1). The cytoplasmic pattern recognition receptor MDA-5 detects dsRNA synthesized during active viral replication and triggers a signaling pathway to protect the host against viral infection, for example by inducing the expression of antiviral cytokines.","definition_xrefs":["PMID:33727702","PMID:19019954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of MDA-5 activity","secondary_identifiers":["GO:0039539","VZ:603"],"synonyms":[{"name":"Inhibition of host MDA5 by virus","type":"related"},{"name":"inhibition by virus of host MDA-5 signaling","type":"related"},{"name":"inhibition of host IFIH1/MDA5 by virus","type":"related"},{"name":"suppression by virus of host IFIH1 signaling pathway","type":"related"},{"name":"suppression by virus of host MDA-5 activity","type":"related"},{"name":"suppression by virus of host MDA-5 signaling pathway","type":"related"},{"name":"suppression by virus of host MDA-5 signalling pathway","type":"related"},{"name":"suppression by virus of host viral-induced cytoplasmic pattern recognition receptor signaling pathway via inhibition of host MDA-5 activity","type":"narrow"}],"termid":"GO:0039554"}


id: MONDO:0100199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diffuse gastric and lobular breast cancer syndrome with or without cleft lip and/or palate","termid":"MONDO:0100199","xrefs":{"Monarch":{"xref_id":"0100199"}}}


id: GO:0045866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of genetic recombination within the DNA of the genes coding for ribosomal RNA.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of recombination within rDNA repeats (obsolete GO:0045866)","synonyms":[{"name":"positive regulation of recombination within rDNA repeats","type":"exact"}],"termid":"GO:0045866"}


id: GO:0005469
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: succinate(out) + fumarate(in) = succinate(in) + fumarate(out).","definition_xrefs":["TC:2.A.29.13.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fumarate transmembrane transporter activity","termid":"GO:0015138"},{"relation_name":"is_a","term_name":"succinate transmembrane transporter activity","termid":"GO:0015141"},{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"succinate:fumarate antiporter activity","secondary_identifiers":["RHEA:29323"],"termid":"GO:0005469"}


id: PBO:0061005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NHS like 1","termid":"PBO:0061005"}


id: GO:0086073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a bundle of His cell to a Purkinje myocyte via adhesion molecules that results in the cells being juxtaposed so that they can communicate.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heterotypic cell-cell adhesion","termid":"GO:0034113"},{"relation_name":"is_a","term_name":"cardiac muscle cell-cardiac muscle cell adhesion","termid":"GO:0086042"},{"relation_name":"part_of","term_name":"bundle of His cell to Purkinje myocyte communication","termid":"GO:0086069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"bundle of His cell-Purkinje myocyte adhesion involved in cell communication","termid":"GO:0086073"}


id: PBO:0056212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member B6B","termid":"PBO:0056212"}


id: PBO:0040330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit c locus 1 pseudogene 5","termid":"PBO:0040330"}


id: MONDO:0000669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An agnosia that is a loss of the ability to recognize a color, while being able to perceive or distinguish it.","definition_xrefs":["DOID:0060139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"visual agnosia","termid":"MONDO:0000685"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"color agnosia","termid":"MONDO:0000669","xrefs":{"Monarch":{"xref_id":"0000669"}}}


id: GO:0061120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of directed movement of a motile cell or organism up a concentration gradient of 3',5'-cAMP by the action of DIF-1. DIF-1 is a chlorinated alkylphenone.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of positive chemotaxis to cAMP by chlorinated alkylphenone","termid":"GO:0061119"}],"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 positive chemotaxis to cAMP by DIF-1","termid":"GO:0061120"}


id: MONDO:0000708
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Crohn ileitis","termid":"MONDO:0000709"},{"relation_name":"is_a","term_name":"Crohn jejunitis","termid":"MONDO:0021207"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"Crohn jejunoileitis","secondary_identifiers":["DOID:0060188","MEDGEN:1807919","UMLS:C5686428"],"synonyms":[{"name":"jejunoileitis","type":"related"}],"termid":"MONDO:0000708","xrefs":{"Monarch":{"xref_id":"0000708"}}}


id: PR:Q9P7M9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rib1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7M9"],"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":"GTP cyclohydrolase-2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.09c","synonyms":[{"name":"GTP cyclohydrolase II (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rib1","type":"exact"}],"termid":"PR:Q9P7M9"}


id: MONDO:0007637
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Fuchs' endothelial dystrophy in which the cause of the disease is a mutation in the COL8A2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fuchs' endothelial dystrophy","termid":"MONDO:0005321"}],"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":"corneal dystrophy, Fuchs endothelial, 1","secondary_identifiers":["OMIM:136800","MESH:C535478","GARD:18216","MEDGEN:338172","UMLS:C1850959"],"synonyms":[{"name":"COL8A2 Fuchs' endothelial dystrophy","type":"exact"},{"name":"FECD1","type":"related"},{"name":"Fuchs' endothelial dystrophy caused by mutation in COL8A2","type":"exact"},{"name":"corneal dystrophy, Fuchs endothelial, 1","type":"exact"},{"name":"corneal dystrophy, Fuchs endothelial, early-onset","type":"related"},{"name":"corneal dystrophy, Fuchs endothelial, type 1","type":"exact"}],"termid":"MONDO:0007637","xrefs":{"Monarch":{"xref_id":"0007637"}}}


id: GO:0046869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The incorporation of iron into a 2Fe-2S iron-sulfur cluster via tris-L-cysteinyl-L-aspartato diiron disulfide.","definition_xrefs":["RESID:AA0331"],"gene_count":0,"genotype_count":0,"name":"obsolete iron incorporation into iron-sulfur cluster via tris-L-cysteinyl-L-aspartato diiron disulfide (obsolete GO:0046869)","synonyms":[{"name":"iron incorporation into iron-sulphur cluster via tris-L-cysteinyl-L-aspartato diiron disulphide","type":"exact"}],"termid":"GO:0046869"}


id: PBO:0042672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule pseudogene 6","termid":"PBO:0042672"}


id: GO:0048775
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of leucophore differentiation.","definition_xrefs":["GOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pigment cell differentiation","termid":"GO:0050932"},{"relation_name":"regulates","term_name":"leucophore differentiation","termid":"GO:0048772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of leucophore differentiation","termid":"GO:0048775"}


id: GO:0034811
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: benzo(a)pyrene + O2 = benzo(a)pyrene-cis-9,10-dihydrodiol.","definition_xrefs":["UM-BBD_reactionID:r1132"],"gene_count":0,"genotype_count":0,"name":"obsolete benzo(a)pyrene 9,10-dioxygenase activity (obsolete GO:0034811)","termid":"GO:0034811"}


id: FYECO:0000202
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells were chilled by placing them on ice.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping experimental environment","termid":"FYECO:0000132"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chilled cells","synonyms":[{"name":"cold","type":"related"},{"name":"ice","type":"related"}],"termid":"FYECO:0000202"}


id: PBO:0065478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PSMD14 divergent transcript","termid":"PBO:0065478"}


id: PBO:0049930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hedgehog acyltransferase like","termid":"PBO:0049930"}


id: PBO:0081512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 418","termid":"PBO:0081512"}


id: PBO:0086447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative mannosidase involved in ER-associated protein degradation; localizes to the endoplasmic reticulum; sequence similarity with seven-hairpin glycosidase (GH47) family members, such as Mns1p and Mnl1p, that hydrolyze 1,2-linked alpha-D-mannose residues; non-essential gene","termid":"PBO:0086447"}


id: PR:Q9HDV3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBP19A11.07c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HDV3"],"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":"Hid-1 family protein P19A11.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP19A11.07c","synonyms":[{"name":"Down-regulated in multiple cancers 1 homolog 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPBP19A11.07c","type":"exact"}],"termid":"PR:Q9HDV3"}


id: GO:0031710
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a neuromedin B receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bombesin receptor binding","termid":"GO:0031705"}],"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":"neuromedin B receptor binding","synonyms":[{"name":"neuromedin B receptor ligand","type":"narrow"}],"termid":"GO:0031710"}


id: MONDO:0007315
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cherubism is a rare, self-limiting, fibro-osseous, genetic disease of childhood and adolescence characterized by varying degrees of progressive bilateral enlargement of the mandible and/or maxilla, with clinical repercussions in severe cases.","definition_xrefs":["Orphanet:184"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"cherubism","secondary_identifiers":["DOID:1856","MEDGEN:40219","NANDO:2200444","GARD:6036","MedDRA:10070535","NCIT:C84630","icd11.foundation:1729261719","ICD9:526.89","OMIM:118400","UMLS:C0008029","MESH:D002636","SCTID:76098004"],"synonyms":[{"name":"CRBM","type":"exact"},{"name":"Crbm","type":"related"},{"name":"cherubism","type":"exact"},{"name":"familial fibrous dysplasia of the jaws","type":"exact"},{"name":"familial multilocular cystic disease of the jaws","type":"exact"}],"termid":"MONDO:0007315","xrefs":{"Monarch":{"xref_id":"0007315"}}}


id: PBO:0052679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 47","termid":"PBO:0052679"}


id: PBO:0075831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structure specific recognition protein 1","termid":"PBO:0075831"}


id: GO:0030996
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which the mitotic cell cycle is halted during one of the normal phases (G1, S, G2, M) as a result of deprivation of nitrogen.","definition_xrefs":["GOC:mah","GOC:dph","GOC:vw","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete mitotic cell cycle arrest in response to nitrogen starvation (obsolete GO:0030996)","synonyms":[{"name":"cell cycle arrest in response to nitrogen starvation","type":"broad"}],"termid":"GO:0030996"}


id: PBO:0064097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paired like homeodomain 2","termid":"PBO:0064097"}


id: GO:0106163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of exonucleolytic nuclear-transcribed mRNA catabolic process involved in deadenylation-dependent decay.","definition_xrefs":["PMID:30601114","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of exonucleolytic catabolism of deadenylated mRNA (obsolete GO:0106163)","termid":"GO:0106163"}


id: PBO:0000277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyltransferase (predicted)","termid":"PBO:0000277"}


id: PBO:0054832
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 2245","termid":"PBO:0054832"}


id: GO:1900375
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A positive regulation of transcription from RNA polymerase II promoter that results in positive regulation of inositol biosynthetic process.","definition_xrefs":["GOC:TermGenie","PMID:2004420","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:1900375)","synonyms":[{"name":"activation of inositol anabolism by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"activation of inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"activation of inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"activation of inositol formation by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"activation of inositol synthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"activation of myo-inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"activation of myo-inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"activation of vitamin Bh biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"activation of vitamin Bh biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of inositol anabolism by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of inositol formation by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of inositol synthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of myo-inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"positive regulation of myo-inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"positive regulation of vitamin Bh biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of vitamin Bh biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up regulation of inositol anabolism by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up regulation of inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up regulation of inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up regulation of inositol formation by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up regulation of inositol synthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up regulation of myo-inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"up regulation of myo-inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"up regulation of vitamin Bh biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up regulation of vitamin Bh biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of inositol anabolism by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of inositol formation by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of inositol synthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of myo-inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"up-regulation of myo-inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"up-regulation of vitamin Bh biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"up-regulation of vitamin Bh biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of inositol anabolism by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of inositol formation by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of inositol synthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of myo-inositol biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"upregulation of myo-inositol biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"upregulation of vitamin Bh biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"upregulation of vitamin Bh biosynthetic process by positive regulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:1900375"}


id: PBO:0051650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine monophosphate dehydrogenase 1 pseudogene 5","termid":"PBO:0051650"}


id: PBO:0053905
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 1195","termid":"PBO:0053905"}


id: PBO:0028921
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transcription_during_glucose_starvation_and_oxidative_stress","termid":"PBO:0028921"}


id: MONDO:0035863
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability (obsolete MONDO:0035863)","secondary_identifiers":["Orphanet:611327"],"termid":"MONDO:0035863","xrefs":{"Monarch":{"xref_id":"0035863"}}}


id: GO:0051323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle phase, following prophase or prometaphase in higher eukaryotes, during which chromosomes become aligned on the equatorial plate of the cell.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic cell cycle phase","termid":"GO:0098762"},{"relation_name":"part_of","term_name":"M phase","termid":"GO:0000279"}],"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":"metaphase","secondary_identifiers":["Wikipedia:Metaphase"],"termid":"GO:0051323"}


id: MONDO:0012709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any microphthalmia, isolated, with coloboma in which the cause of the disease is a mutation in the SHH gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, isolated, with coloboma","termid":"MONDO:0000170"}],"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":"microphthalmia, isolated, with coloboma 5","secondary_identifiers":["MEDGEN:369356","MESH:C566899","GARD:15524","OMIM:611638","UMLS:C1968843"],"synonyms":[{"name":"MCOPCB5","type":"related"},{"name":"SHH microphthalmia, isolated, with coloboma","type":"exact"},{"name":"Shh microphthalmia, isolated, with coloboma","type":"exact"},{"name":"microphthalmia with coloboma 5","type":"exact"},{"name":"microphthalmia, isolated, with coloboma 5","type":"exact"},{"name":"microphthalmia, isolated, with coloboma caused by mutation in SHH","type":"exact"},{"name":"microphthalmia, isolated, with coloboma caused by mutation in Shh","type":"exact"},{"name":"microphthalmia, isolated, with coloboma type 5","type":"exact"}],"termid":"MONDO:0012709","xrefs":{"Monarch":{"xref_id":"0012709"}}}


id: PBO:0087055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L26B; binds to 5.8S rRNA; non-essential even when paralog is also deleted; deletion has minimal affections on ribosome biosynthesis; homologous to mammalian ribosomal protein L26 and bacterial L24; RPL26B has a paralog, RPL26A, that arose from the whole genome duplication","termid":"PBO:0087055"}


id: PBO:0034538
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_phosphorylation_during_cellular_response_to_bleomycin","termid":"PBO:0034538"}


id: MONDO:1010801
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brachydactyly that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly, non-human animal","termid":"MONDO:1010156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly, dog","secondary_identifiers":["OMIA:000146-9615"],"termid":"MONDO:1010801","xrefs":{"Monarch":{"xref_id":"1010801"}}}


id: PR:Q9Y7Z5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transmembrane protein 33 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04102"],"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":"tetra-spanning protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1539.04","secondary_identifiers":["UniProtKB:Q9Y7Z5"],"synonyms":[{"name":"Spom972h-TMEM33","type":"exact"}],"termid":"PR:Q9Y7Z5"}


id: GO:0060079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that leads to a temporary increase in postsynaptic potential due to the flow of positively charged ions into the postsynaptic cell. The flow of ions that causes an EPSP is an excitatory postsynaptic current (EPSC) and makes it easier for the neuron to fire an action potential.","definition_xrefs":["GOC:dph","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of postsynaptic membrane potential","termid":"GO:0060078"},{"relation_name":"part_of","term_name":"chemical synaptic transmission, postsynaptic","termid":"GO:0099565"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"excitatory postsynaptic potential","synonyms":[{"name":"regulation of EPSP","type":"related"},{"name":"regulation of excitatory post-synaptic membrane potential","type":"exact"}],"termid":"GO:0060079"}


id: PBO:0028189
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_aseptate_mononucleate_vegetative_cell,_normal_cell_length","termid":"PBO:0028189"}


id: PBO:0079261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TTC32 divergent transcript","termid":"PBO:0079261"}


id: GO:0061831
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Testis-specific junction between mature spermatids and Sertoli cells at the luminal end of the Sertoli cell.","definition_xrefs":["GOC:aruk","GOC:dph","GOC:bc","PMID:22332112","PMID:23546604"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell junction","termid":"GO:0005911"}],"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":"apical ectoplasmic specialization","synonyms":[{"name":"apical ES","type":"exact"}],"termid":"GO:0061831"}


id: GO:0018026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The methylation of peptidyl-lysine to form peptidyl-N6-methyl-L-lysine.","definition_xrefs":["RESID:AA0076"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-lysine methylation","termid":"GO:0018022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptidyl-lysine monomethylation","termid":"GO:0018026"}


id: PBO:0082238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-isopropylmalate synthase II (2-isopropylmalate synthase); catalyzes the first step in the leucine biosynthesis pathway; the minor isozyme, responsible for the residual alpha-IPMS activity detected in a leu4 null mutant; LEU9 has a paralog, LEU4, that arose from the whole genome duplication","termid":"PBO:0082238"}


id: FYPO:0004931
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA measured in a cell during sporulation is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level","termid":"FYPO:0000840"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal RNA level during sporulation","synonyms":[{"name":"normal RNA accumulation during sporulation","type":"related"},{"name":"normal cellular RNA level during sporulation","type":"exact"},{"name":"normal mRNA level during sporulation","type":"narrow"},{"name":"normal transcript level during sporulation","type":"exact"}],"termid":"FYPO:0004931"}


id: PBO:0064985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich protein BstNI subfamily 2","termid":"PBO:0064985"}


id: PBO:0052609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KRAB-A domain containing 2","termid":"PBO:0052609"}


id: PBO:0028171
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_RNA_pyrophosphohydrolase_activity","termid":"PBO:0028171"}


id: GO:0106024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate of onset of pupariation.","definition_xrefs":["PMID:26510564"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of post-embryonic development","termid":"GO:0048581"},{"relation_name":"is_a","term_name":"regulation of pupariation","termid":"GO:0106023"},{"relation_name":"negatively_regulates","term_name":"pupariation","termid":"GO:0035073"}],"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 pupariation","termid":"GO:0106024"}


id: PBO:0061287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore associated protein 1 pseudogene 8","termid":"PBO:0061287"}


id: GO:1905004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of picolinic acid.","definition_xrefs":["PMID:19843166","GOC:PARL","GOC:bf","GO_REF:0000068","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"},{"relation_name":"is_a","term_name":"pyridine-containing compound biosynthetic process","termid":"GO:0072525"},{"relation_name":"is_a","term_name":"picolinic acid metabolic process","termid":"GO:1905003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"picolinic acid biosynthetic process","synonyms":[{"name":"picolinate biosynthesis","type":"exact"},{"name":"picolinate biosynthetic process","type":"exact"},{"name":"picolinic acid anabolism","type":"exact"},{"name":"picolinic acid biosynthesis","type":"exact"},{"name":"picolinic acid formation","type":"exact"},{"name":"picolinic acid synthesis","type":"exact"}],"termid":"GO:1905004"}


id: MOD:01670
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-methyl-L-lysine.","definition_xrefs":["PubMed:17260957","RESID:AA0524","PubMed:16091367","PubMed:16195462"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"halogenated lysine","termid":"MOD:01672"},{"relation_name":"is_a","term_name":"monochlorinated residue","termid":"MOD:01911"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6-chloro-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-(chloroamino)hexanoic acid","type":"exact"},{"name":"N(zeta)-chlorolysine","type":"exact"},{"name":"N6-chloro-L-lysine","type":"exact"},{"name":"N6ClLys","type":"exact"},{"name":"epsilon-chlorolysine","type":"exact"},{"name":"lysine chloramine","type":"exact"}],"termid":"MOD:01670"}


id: PBO:0048237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G antigen 6","termid":"PBO:0048237"}


id: GO:0000936
data:
  {"annotated_genes":["SJAG_00667","SJAG_05285"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[100145,115842],"is_not":false,"summary":null,"term":"GO:0000936"}]},"cv_name":"cellular_component","definition":"A cell septum that forms following nuclear division.","definition_xrefs":["GOC:clt","ISBN:0471940526"],"direct_ancestors":[{"relation_name":"is_a","term_name":"division septum","termid":"GO:0000935"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00667":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0000935"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0000935","GO:0005575"],"is_obsolete":false,"name":"primary cell septum","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"primary septum","type":"broad"}],"termid":"GO:0000936","terms_by_termid":{"GO:0000936":null}}


id: PBO:0048427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine amidotransferase class 1 domain containing 3","termid":"PBO:0048427"}


id: MONDO:0002207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon intraepithelial malignant neoplasm of eccrine or apocrine origin, arising from the vulva. It usually affects post-menopausal women. In approximately 10-20% of the cases there is an associated anorectal, or urothelial carcinoma or a skin appendage adenocarcinoma identified. It presents as a red, eczematous lesion. Microscopically, it is characterized by the presence of the typical Paget cells which are large, round cells with abundant cytoplasm and prominent nuclei.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extramammary Paget disease","termid":"MONDO:0008177"},{"relation_name":"is_a","term_name":"vulvar adenocarcinoma","termid":"MONDO:0024336"}],"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":"vulval Paget disease","secondary_identifiers":["MEDGEN:266154","NCIT:C4027","UMLS:C1275217","SCTID:254898001","DOID:2097","ICD9:233.39"],"synonyms":[{"name":"Paget disease of the vulva","type":"exact"},{"name":"Paget's disease of the vulva","type":"exact"},{"name":"Paget's disease of vulva","type":"exact"},{"name":"mammalian vulva Paget disease","type":"exact"},{"name":"vulva Paget's disease","type":"exact"},{"name":"vulval Paget disease","type":"exact"},{"name":"vulval Paget's disease","type":"exact"},{"name":"vulvar Paget's disease","type":"exact"}],"termid":"MONDO:0002207","xrefs":{"Monarch":{"xref_id":"0002207"}}}


id: GO:0052001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Attachment of bacterial clusters to the surface of the host in a type IV pili dependent manner. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:ml"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adhesion of symbiont to host cell","termid":"GO:0044650"}],"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":"adhesion to host cell via type IV pili","synonyms":[{"name":"type IV pili-dependent localized adherence to host","type":"exact"}],"termid":"GO:0052001"}


id: PBO:0088313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [2Fe-2S] cluster assembly and tRNA modification cysteine desulfurase Nfs1","termid":"PBO:0088313"}


id: PBO:0030699
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_catalase_activity","termid":"PBO:0030699"}


id: PBO:0004596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S acidic ribosomal protein P2A subunit (predicted)","termid":"PBO:0004596"}


id: PBO:0077055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombospondin type 1 domain containing 1","termid":"PBO:0077055"}


id: PBO:0000397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cullin 3","termid":"PBO:0000397"}


id: PBO:0085815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; expressed at both mRNA and protein levels; partially overlaps HMS2","termid":"PBO:0085815"}


id: GO:0072469
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about cell size is received and converted into a molecular signal, contributing to a cell size control checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in cell size control checkpoint (obsolete GO:0072469)","synonyms":[{"name":"cell size control checkpoint sensor mechanism","type":"related"},{"name":"cell size control checkpoint sensor process","type":"related"},{"name":"detection of stimulus involved in mitotic cell cycle cell size control checkpoint","type":"exact"},{"name":"sensing involved in cell size control checkpoint","type":"related"}],"termid":"GO:0072469"}


id: GO:0035899
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism stops, prevents or reduces the frequency, rate or extent of blood coagulation in another organism. Blood coagulation is the sequential process in which the multiple coagulation factors of the blood interact, ultimately resulting in the formation of an insoluble fibrin clot.","definition_xrefs":["PMID:30563903","GOC:fj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"induction of blood coagulation in another organism","termid":"GO:0035807"}],"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":"suppression of blood coagulation in another organism","synonyms":[{"name":"disruption of blood coagulation in other organism","type":"exact"},{"name":"down-regulation of blood coagulation in other organism","type":"exact"},{"name":"downregulation of blood coagulation in other organism","type":"exact"},{"name":"inhibition of blood coagulation in other organism","type":"narrow"},{"name":"negative regulation of blood clotting in other organism","type":"exact"},{"name":"negative regulation of blood coagulation in another organism","type":"related"},{"name":"negative regulation of blood coagulation in other organism","type":"exact"},{"name":"suppression of blood clotting in another organism","type":"exact"}],"termid":"GO:0035899"}


id: MONDO:0011348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital anomaly of the hand or foot, marked by the presence of supernumerary digits.","definition_xrefs":["MESH:D017689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polydactyly","termid":"MONDO:0021003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-syndromic polydactyly","secondary_identifiers":["icd11.foundation:1534380955","MedDRA:10036063","Orphanet:2913"],"synonyms":[{"name":"Extra digits","type":"related"},{"name":"isolated polydactyly","type":"related"},{"name":"isolated polydactyly (disease)","type":"exact"},{"name":"nonsyndromic polydactyly","type":"exact"},{"name":"nonsyndromic polydactyly (disease)","type":"exact"},{"name":"polydactylia","type":"related"},{"name":"supernumerary digits","type":"related"}],"termid":"MONDO:0011348","xrefs":{"Monarch":{"xref_id":"0011348"}}}


id: MONDO:0002935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal cell carcinoma of the penis with an indolent clinical course. It is usually superficial and arises from the shaft and rarely the glans.","definition_xrefs":["NCIT:C39961"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"},{"relation_name":"is_a","term_name":"squamous cell carcinoma of penis","termid":"MONDO:0018352"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"penis basal cell carcinoma","secondary_identifiers":["UMLS:C1518949","MEDGEN:275349","DOID:4277"],"synonyms":[{"name":"basal cell carcinoma of the penis","type":"exact"},{"name":"penile basal cell cancer","type":"exact"},{"name":"penile basal cell carcinoma","type":"exact"},{"name":"penis skin basal cell carcinoma","type":"exact"},{"name":"skin basal cell carcinoma of penis","type":"exact"},{"name":"skin of penis skin basal cell carcinoma","type":"exact"}],"termid":"MONDO:0002935","xrefs":{"Monarch":{"xref_id":"0002935"}}}


id: MOD:00481
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label","definition_xrefs":["OMSSA:130","Unimod:106#C","URL:http://www.appliedbiosystems.com/products/productdetail.cfm?prod_id=153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(13)C isotope tagged reagent","termid":"MOD:01428"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Applied Biosystems cleavable ICAT(TM) heavy","synonyms":[{"name":"Applied Biosystems cleavable ICAT(TM) heavy","type":"related"},{"name":"ICAT-C:13C(9)","type":"related"},{"name":"icatheavy","type":"exact"}],"termid":"MOD:00481"}


id: PBO:0034793
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"this gene product was previously annotated to the NADH dehydrogenase of the mitochondrial respiratory chain complex I. This mapping was removed because fission yeast lacks the remaining 40 subunits found in mammals (PMID:1518044).","termid":"PBO:0034793"}


id: PBO:0085634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in histone H2B ubiquitination; acts as cofactor for Bre1p; null mutant forms abnormally large cells, and homozygous diploid null mutant displays delayed premeiotic DNA synthesis and reduced efficiency of meiotic nuclear division","termid":"PBO:0085634"}


id: MONDO:1012362
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"photoreceptor dysplasia, non-human animal","termid":"MONDO:1011987"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"photoreceptor dysplasia, dog","secondary_identifiers":["OMIA:001311-9615"],"termid":"MONDO:1012362","xrefs":{"Monarch":{"xref_id":"1012362"}}}


id: PBO:0047118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 166 member A","termid":"PBO:0047118"}


id: PBO:0039807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor 3","termid":"PBO:0039807"}


id: GO:0000094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete septin assembly and septum formation (obsolete GO:0000094)","synonyms":[{"name":"septin assembly and septum formation","type":"exact"}],"termid":"GO:0000094"}


id: PBO:0087549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of RNA polymerase III transcription initiation factor complex; one of six subunits of the RNA polymerase III transcription initiation factor complex (TFIIIC); part of the TauA globular domain of TFIIIC that binds DNA at the BoxA promoter sites of tRNA and similar genes; human homolog is TFIIIC-63","termid":"PBO:0087549"}


id: GO:0005298
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: proline(out) + Na+(out) = proline(in) + Na+(in).","definition_xrefs":["TC:2.A.22.2.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid:sodium symporter activity","termid":"GO:0005283"},{"relation_name":"is_a","term_name":"organic acid:sodium symporter activity","termid":"GO:0005343"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"proline:sodium symporter activity","secondary_identifiers":["RHEA:28967","MetaCyc:TRANS-RXN-118","Reactome:R-HSA-444100"],"synonyms":[{"name":"sodium/proline symporter activity","type":"exact"}],"termid":"GO:0005298"}


id: PBO:0113025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calcium release channel involved in ER calcium homeostasis; integrates ER calcium release with the regulation of sphingolipid metabolism and autophagy; required for mannosylation of inositolphosphorylceramide and for growth at high calcium concentrations; endoplasmic reticulum membrane protein; contains 10 transmembrane domains and a potential Ca2+ EF-hand motif; protein abundance increases in response to DNA replication stress","termid":"PBO:0113025"}


id: GO:0075072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which symbiont cells digest parts of their own cytoplasm during interaction with its host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete autophagy of symbiont cells involved in interaction with host (obsolete GO:0075072)","synonyms":[{"name":"autophagy of symbiont cells during interaction with host","type":"related"}],"termid":"GO:0075072"}


id: PBO:0072109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S13 pseudogene 7","termid":"PBO:0072109"}


id: PBO:0076173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 1C member 4","termid":"PBO:0076173"}


id: GO:0018813
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxo-3-enoate-4-benzenoid + H2O = pyruvate + benzaldehyde derivative. Substrates are (3E)-4-(5-amino-2-hydroxy-phenyl)-2-oxo-but-3-ene-1-oic-acid (forms 5-aminosalicylaldehyde) and trans-o-hydroxybenzylidenepyruvate (forms salicylaldehyde).","definition_xrefs":["UM-BBD_enzymeID:r0338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"trans-o-hydroxybenzylidenepyruvate hydratase-aldolase activity","secondary_identifiers":["EC:4.1.2.45","RHEA:27389"],"termid":"GO:0018813"}


id: PBO:0027936
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cell_population_growth_on_glycerol_carbon_source","termid":"PBO:0027936"}


id: GO:0007123
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete bud scar accumulation (obsolete GO:0007123)","synonyms":[{"name":"bud scar accumulation","type":"exact"}],"termid":"GO:0007123"}


id: GO:0045039
data:
  {"annotated_genes":["SJAG_02398","SJAG_02524","SJAG_01640","SJAG_04996","SJAG_00404","SJAG_01120","SJAG_04208","SJAG_00687","SJAG_03515","SJAG_03502","SJAG_01949"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73401,73891,75545,77767,88611,90352,102926,107582,107604,113216,116293],"is_not":false,"summary":null,"term":"GO:0045039"}]},"cv_name":"biological_process","definition":"The processes mediating the insertion of proteins into the mitochondrial inner membrane. Mitochondrial inner membrane proteins can get inserted from the cytosol, by crossing the outer membrane and being guided by an inner membrane translocase complex into their final destination in the inner membrane. Some proteins present in the intermembrane space can get inserted into the inner mitochondrial membrane. Finally, some proteins are inserted into the inner membrane from the matrix side of the membrane.","definition_xrefs":["GOC:mcc","PMID:18672008","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial transport","termid":"GO:0006839"},{"relation_name":"is_a","term_name":"intracellular protein transport","termid":"GO:0006886"},{"relation_name":"is_a","term_name":"inner mitochondrial membrane organization","termid":"GO:0007007"},{"relation_name":"is_a","term_name":"establishment of protein localization to mitochondrial membrane","termid":"GO:0090151"},{"relation_name":"part_of","term_name":"protein targeting to mitochondrion","termid":"GO:0006626"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00404":null,"SJAG_00687":null,"SJAG_01120":null,"SJAG_01640":null,"SJAG_01949":null,"SJAG_02398":null,"SJAG_02524":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_04208":null,"SJAG_04996":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007005","GO:0008150","GO:0006605","GO:0061024","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"protein insertion into mitochondrial inner membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrial inner membrane protein import","type":"exact"},{"name":"protein import into mitochondrial inner membrane","type":"exact"},{"name":"protein transport into mitochondrial inner membrane","type":"exact"}],"termid":"GO:0045039","terms_by_termid":{"GO:0045039":null}}


id: GO:1900573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving emodin.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"emodin metabolic process","synonyms":[{"name":"emodin metabolism","type":"exact"}],"termid":"GO:1900573"}


id: GO:2000632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of pre-microRNA processing.","definition_xrefs":["GOC:dph","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of miRNA processing","termid":"GO:1903799"},{"relation_name":"is_a","term_name":"regulation of pre-miRNA processing","termid":"GO:2000631"},{"relation_name":"negatively_regulates","term_name":"pre-miRNA processing","termid":"GO:0031054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of pre-miRNA processing","synonyms":[{"name":"negative regulation of miRNA maturation","type":"exact"},{"name":"negative regulation of pre-microRNA processing","type":"exact"}],"termid":"GO:2000632"}


id: MONDO:0022518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by rapidly progressive sensorineural hearing loss (SNHL), that is often bilateral, and is potentially reversible.","definition_xrefs":["PMID:26485595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disease of ear, nose and throat","termid":"MONDO:0000587"},{"relation_name":"is_a","term_name":"inner ear disorder","termid":"MONDO:0002467"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune inner ear disease","secondary_identifiers":["UMLS:C0395947","icd11.foundation:1392879169","MEDGEN:583162"],"synonyms":[{"name":"AIED","type":"related"}],"termid":"MONDO:0022518","xrefs":{"Monarch":{"xref_id":"0022518"}}}


id: PBO:0001149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ammonium transporter Amt2","termid":"PBO:0001149"}


id: PBO:0045508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"destrin, actin depolymerizing factor","termid":"PBO:0045508"}


id: PBO:0048234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G antigen 2E","termid":"PBO:0048234"}


id: GO:2000314
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of fibroblast growth factor receptor signaling pathway","termid":"GO:0040037"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation","termid":"GO:2000313"},{"relation_name":"negatively_regulates","term_name":"fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation","termid":"GO:0060825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation","synonyms":[{"name":"negative regulation of fibroblast growth factor receptor signalling pathway involved in neural plate anterior/posterior pattern formation","type":"exact"}],"termid":"GO:2000314"}


id: PBO:0004628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonucleotide reductase small subunit Suc22","termid":"PBO:0004628"}


id: GO:0004836
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydroxylation of tyramine to form octopamine.","definition_xrefs":["PMID:10745161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"tyramine-beta hydroxylase activity","termid":"GO:0004836"}


id: GO:0046601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of centriole replication.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of centriole replication","termid":"GO:0046599"},{"relation_name":"is_a","term_name":"positive regulation of cytoskeleton organization","termid":"GO:0051495"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"is_a","term_name":"positive regulation of organelle assembly","termid":"GO:1902117"},{"relation_name":"positively_regulates","term_name":"centriole replication","termid":"GO:0007099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007049","GO:0007010","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of centriole replication","synonyms":[{"name":"activation of centriole replication","type":"narrow"},{"name":"stimulation of centriole replication","type":"narrow"},{"name":"up regulation of centriole replication","type":"exact"},{"name":"up-regulation of centriole replication","type":"exact"},{"name":"upregulation of centriole replication","type":"exact"}],"termid":"GO:0046601"}


id: PBO:0069457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 722, pseudogene","termid":"PBO:0069457"}


id: PBO:0088081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ub-like protein; Ub-like protein conjugated to phosphatidylethanolamine (PE); role in membrane fusion during autophagosome formation; membrane anchored Atg8p-PE is involved in phagophore expansion during autophagosome formation; deconjugation is also required for biogenesis; targets Atg1p to autophagosomes; binds to the Atg1p-Atg13p complex, triggers its vacuolar degradation; role in vacuolar membrane protein turnover during early stationary phase; component of autophagosomes and Cvt vesicles","termid":"PBO:0088081"}


id: MONDO:0001780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by persistent or recurrent ejaculation before or after penetration and before the person wishes it.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sexual and gender identity disorders","termid":"MONDO:0000595"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"premature ejaculation","secondary_identifiers":["ICD10CM:F52.4","UMLS:C0033038","ICD9:302.75","MEDGEN:452112","DOID:13709","HP:0012876","MESH:D061686","NCIT:C94349"],"synonyms":[{"name":"premature ejaculation","type":"exact"},{"name":"premature ejaculation (disease)","type":"exact"}],"termid":"MONDO:0001780","xrefs":{"Monarch":{"xref_id":"0001780"}}}


id: PBO:0090882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudouridine synthase Cbf5","termid":"PBO:0090882"}


id: GO:0031421
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex formed by a recombinase, a regulatory protein, and the DNA sequences bound by each protein; catalyzes a reversible site-specific recombination reaction that results in the alternate expression of one or more genes in various contexts.","definition_xrefs":["PMID:11114897","PMID:9732277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"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":"invertasome","termid":"GO:0031421"}


id: PBO:0001806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fungal cellulose binding domain protein","termid":"PBO:0001806"}


id: GO:1904558
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 dextromethorphan stimulus.","definition_xrefs":["GOC:mr","PMID:25796330","GO_REF:0000071","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to isoquinoline alkaloid","termid":"GO:0014072"},{"relation_name":"is_a","term_name":"response to ether","termid":"GO:0045472"}],"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 dextromethorphan","termid":"GO:1904558"}


id: FYPO:0003610
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is elongated and a branch forms adjacent to an existing septum.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable branched, elongated vegetative cell","termid":"FYPO:0002459"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000002","FYPO:0000005","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"branched, elongated cell with branch forming adjacent to septum","synonyms":[{"name":"branched, elongated cell with branch forming adjacent to septum during mitotic cell cycle","type":"related"},{"name":"branched, elongated cell with branch forming adjacent to septum during vegetative growth","type":"exact"},{"name":"branched, elongated vegetative cell with branch forming adjacent to septum","type":"exact"}],"termid":"FYPO:0003610"}


id: GO:0099626
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Regulation of presynaptic cytosolic calcium ion concentrations via the action of voltage-gated calcium ion channels.","definition_xrefs":["GOC:dos","PMID:15548655"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated calcium channel activity involved in regulation of cytosolic calcium levels","termid":"GO:0099511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"voltage-gated calcium channel activity involved in regulation of presynaptic cytosolic calcium levels","synonyms":[{"name":"voltage-gated calcium channel activity involved in regulation of presynaptic cytosolic calcium levels","type":"exact"}],"termid":"GO:0099626"}


id: MONDO:0000170
data:
  {"annotated_genes":["SJAG_03497"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013783"}]},"cv_name":"mondo","definition":"A developmental disorder of the eye characterized by unilateral or bilateral microphthalmia associated with ocular coloboma.","definition_xrefs":["Orphanet:98938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated microphthalmia","termid":"MONDO:0000062"},{"relation_name":"is_a","term_name":"coloboma","termid":"MONDO:0001476"},{"relation_name":"is_a","term_name":"isolated anophthalmia-microphthalmia syndrome","termid":"MONDO:0016764"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03497":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"microphthalmia, isolated, with coloboma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:3644","UMLS:C2931500","MEDGEN:444071","OMIMPS:300345","MESH:C537463"],"synonyms":[{"name":"MAC","type":"exact"},{"name":"MCOPCB1","type":"related"},{"name":"colobomatous microphthalmia","type":"exact"},{"name":"microphthalmia associated with colobomatous cyst","type":"related"},{"name":"microphthalmia with colobomatous cyst","type":"exact"},{"name":"microphthalmia-anophthalmia-coloboma syndrome","type":"exact"},{"name":"microphthalmos bilateral, colobomatous orbital cyst","type":"related"}],"termid":"MONDO:0000170","terms_by_termid":{"MONDO:0013783":null},"xrefs":{"Monarch":{"xref_id":"0000170"}}}


id: MONDO:0004564
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anatomic abnormality of the thyroid gland.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland disorder","termid":"MONDO:0003240"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid malformation","secondary_identifiers":["UMLS:C0877367","MEDGEN:209098","DOID:8433","NCIT:C27331"],"synonyms":[{"name":"thyroid gland malformation","type":"exact"}],"termid":"MONDO:0004564","xrefs":{"Monarch":{"xref_id":"0004564"}}}


id: PBO:0053896
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 1181","termid":"PBO:0053896"}


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


id: MONDO:0018846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare congenital abnormality characterized by the complete absence of the penis. It may be associated with other genitourinary abnormalities.","definition_xrefs":["NCIT:C99009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"penile agenesis","secondary_identifiers":["MESH:C536649","SCTID:59981001","UMLS:C1387005","Orphanet:49","MEDGEN:278031","GARD:4272"],"synonyms":[{"name":"Aphallia","type":"exact"},{"name":"Aphallus","type":"exact"},{"name":"agenesis of the penis","type":"related"},{"name":"congenital absence of penis","type":"exact"},{"name":"micropenis","type":"related"},{"name":"penis agenesia","type":"related"},{"name":"penis agenesis","type":"exact"}],"termid":"MONDO:0018846","xrefs":{"Monarch":{"xref_id":"0018846"}}}


id: PBO:0049209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor NMDA type subunit 2C","termid":"PBO:0049209"}


id: PBO:0064896
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'beta","termid":"PBO:0064896"}


id: PBO:0065910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB GTPase activating protein 1 like","termid":"PBO:0065910"}


id: GO:0061499
data:
  {"annotated_genes":["SJAG_01188","SJAG_01215","SJAG_01464","SJAG_02737"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[74140,107110,108866,116964],"is_not":false,"summary":null,"term":"GO:0061499"}]},"cv_name":"cellular_component","definition":"One of three laminate structures that form the mitotic spindle pole body; the outer plaque is in the cytoplasm.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"outer plaque of spindle pole body","termid":"GO:0005824"},{"relation_name":"part_of","term_name":"mitotic spindle pole body","termid":"GO:0044732"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01188":null,"SJAG_01215":null,"SJAG_01464":null,"SJAG_02737":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005816"}],"interesting_parent_ids":["GO:0005575","GO:0015630","GO:0005816"],"is_obsolete":false,"name":"outer plaque of mitotic spindle pole body","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0061499","terms_by_termid":{"GO:0061499":null}}


id: PBO:0055211
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 2636","termid":"PBO:0055211"}


id: PBO:0028773
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_nitric_oxide_level","termid":"PBO:0028773"}


id: GO:0036384
data:
  {"annotated_genes":["SJAG_03676"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[113981],"is_not":false,"summary":null,"term":"GO:0036384"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: CDP + H2O = CMP + phosphate.","definition_xrefs":["GOC:al","RHEA:64880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside diphosphate phosphatase activity","termid":"GO:0017110"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03676":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"CDP phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"CDP diphosphatase activity","type":"broad"},{"name":"CDPase activity","type":"exact"},{"name":"cytidine diphosphatase activity","type":"exact"},{"name":"cytidine-diphosphatase activity","type":"exact"}],"termid":"GO:0036384","terms_by_termid":{"GO:0036384":null}}


id: GO:0070720
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the receptor adaptor proteins Grb2 and SHP-2, and is involved signaling via the PDGFR signaling pathway.","definition_xrefs":["PMID:8943348","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Grb2-SHP-2 complex","synonyms":[{"name":"GRB2-SHP-2 complex, PDGF stimulated","type":"narrow"}],"termid":"GO:0070720"}


id: PR:O14343
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- klp5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14343"],"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":"kinesin-like protein 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2F12.13","synonyms":[{"name":"Spom972h-klp5","type":"exact"}],"termid":"PR:O14343"}


id: PR:Q9P6J2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pcl1 gene.","definition_xrefs":["UniProtKB:Q9P6J2","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":"Fe(2+)/Mn(2+) transporter pcl1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1683.10c","synonyms":[{"name":"Spom972h-pcl1","type":"exact"},{"name":"pombe ccc1-like protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P6J2"}


id: FYPO:0001397
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which actin cortical patches are localized to only the old end of a cell following cell division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monopolar actin cortical patch localization during vegetative growth","termid":"FYPO:0001019"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0004803","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"monopolar actin cortical patch localization to old end","synonyms":[{"name":"decreased actin cortical patch localization at non-growing end","type":"related"},{"name":"monopolar F-actin patch localization to old end","type":"exact"},{"name":"monopolar actin cortical patch localisation to old end","type":"exact"},{"name":"monopolar actin cortical patch localization to old end during mitotic cell cycle","type":"related"},{"name":"monopolar actin cortical patch localization to old end during vegetative growth","type":"exact"},{"name":"monopolar actin cortical patch location at old end","type":"related"},{"name":"monopolar actin patch localization to old end","type":"exact"},{"name":"reduced actin patch localization to non-growing cell end","type":"related"}],"termid":"FYPO:0001397"}


id: FYPO:0007781
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the transition from yeast-form to hyphal growth begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal hyphal growth","termid":"FYPO:0007773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0007773"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0007773","FYPO:0000002"],"is_obsolete":false,"name":"delayed onset of hyphal transition","synonyms":[{"name":"delayed hyphal transition","type":"exact"},{"name":"delayed onset of transition to hyphal growth","type":"exact"}],"termid":"FYPO:0007781"}


id: PATO:0000083
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality that exists by virtue of being a particular point in the time of a cycle.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"temporal distribution quality","termid":"PATO:0002323"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phase","termid":"PATO:0000083"}


id: PBO:0046385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endothelium and lymphocyte associated ASCH domain 2","termid":"PBO:0046385"}


id: PBO:0084992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADPH-dependent medium chain alcohol dehydrogenase; has broad substrate specificity; member of the cinnamyl family of alcohol dehydrogenases; may be involved in fusel alcohol synthesis or in aldehyde tolerance","termid":"PBO:0084992"}


id: PBO:0041775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calpain 14","termid":"PBO:0041775"}


id: PBO:0040295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3","termid":"PBO:0040295"}


id: GO:0051462
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of cortisol from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucocorticoid secretion","termid":"GO:2000849"},{"relation_name":"regulates","term_name":"cortisol secretion","termid":"GO:0043400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"regulation of cortisol secretion","termid":"GO:0051462"}


id: PBO:0046559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K member 1","termid":"PBO:0046559"}


id: MONDO:0004958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status.","definition_xrefs":["NCIT:C4833"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lip and oral cavity squamous cell carcinoma","termid":"MONDO:0044710"},{"relation_name":"is_a","term_name":"oral cavity carcinoma","termid":"MONDO:0044925"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"oral cavity squamous cell carcinoma","secondary_identifiers":["EFO:0000199","MEDGEN:108436","ONCOTREE:OCSC","GARD:17932","DOID:0050866","Orphanet:502363","SCTID:307502000","UMLS:C0585362"],"synonyms":[{"name":"OCSC","type":"related"},{"name":"mouth scc","type":"exact"},{"name":"mouth squamous cell carcinoma","type":"exact"},{"name":"oral cavity scc","type":"exact"},{"name":"oral cavity squamous cell cancer","type":"exact"},{"name":"oral cavity squamous cell carcinoma","type":"exact"},{"name":"oral squamous cell carcinoma","type":"related"},{"name":"scc of mouth","type":"exact"},{"name":"scc of oral cavity","type":"exact"},{"name":"scc of the mouth","type":"exact"},{"name":"scc of the oral cavity","type":"exact"},{"name":"squamous cell carcinoma of mouth","type":"exact"},{"name":"squamous cell carcinoma of oral cavity","type":"exact"},{"name":"squamous cell carcinoma of the mouth","type":"exact"},{"name":"squamous cell carcinoma of the oral cavity","type":"exact"}],"termid":"MONDO:0004958","xrefs":{"Monarch":{"xref_id":"0004958"}}}


id: PBO:0089142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBX domain Sre1 cleavage protein","termid":"PBO:0089142"}


id: PBO:0045673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein cytoplasmic 1 light intermediate chain 1","termid":"PBO:0045673"}


id: GO:0007197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway initiated by acetylcholine binding to its receptor, and ending with the regulation of a downstream cellular process.","definition_xrefs":["GOC:tb","GOC:mah","GOC:dph","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway","termid":"GO:0007193"},{"relation_name":"is_a","term_name":"G protein-coupled acetylcholine receptor signaling pathway","termid":"GO:0007213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway","synonyms":[{"name":"inhibition of adenylate cyclase activity by G-protein coupled acetylcholine receptor signaling pathway","type":"related"},{"name":"inhibition of adenylate cyclase activity by muscarinic acetylcholine receptor signaling pathway","type":"related"},{"name":"inhibition of adenylate cyclase activity by muscarinic acetylcholine receptor signalling pathway","type":"related"},{"name":"muscarinic acetylcholine receptor, adenylate cyclase inhibiting pathway","type":"exact"},{"name":"muscarinic acetylcholine receptor, adenylyl cyclase inhibiting pathway","type":"exact"}],"termid":"GO:0007197"}


id: MONDO:0100355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A classic (severe) or non-classic (mild or intermediate) form of a genetic disease.","direct_ancestors":[{"relation_name":"is_a","term_name":"disease characteristic","termid":"MONDO:0021125"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"classic or non-classic genetic disease presentation","termid":"MONDO:0100355","xrefs":{"Monarch":{"xref_id":"0100355"}}}


id: MONDO:0021507
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the brainstem.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brainstem neoplasm","termid":"MONDO:0021228"},{"relation_name":"is_a","term_name":"benign neoplasm of brain","termid":"MONDO:0021451"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of brain stem","secondary_identifiers":["SCTID:92029009","MEDGEN:146353","UMLS:C0686400","NCIT:C8549"],"synonyms":[{"name":"benign brain stem neoplasm","type":"exact"},{"name":"benign brain stem neoplasms","type":"exact"},{"name":"benign brain stem tumor","type":"exact"},{"name":"benign brain stem tumour","type":"exact"},{"name":"benign brainstem neoplasm","type":"exact"},{"name":"benign brainstem neoplasms","type":"exact"},{"name":"benign brainstem tumor","type":"exact"},{"name":"benign brainstem tumors","type":"exact"},{"name":"benign brainstem tumour","type":"exact"},{"name":"benign brainstem tumours","type":"exact"},{"name":"benign neoplasm of brainstem","type":"exact"},{"name":"benign neoplasm of the brain stem","type":"exact"},{"name":"benign neoplasm of the brainstem","type":"exact"},{"name":"benign neoplasms of brainstem","type":"exact"},{"name":"benign neoplasms of the brainstem","type":"exact"},{"name":"benign tumor of brain stem","type":"exact"},{"name":"benign tumor of brainstem","type":"exact"},{"name":"benign tumor of the brain stem","type":"exact"},{"name":"benign tumor of the brainstem","type":"exact"},{"name":"benign tumors of brainstem","type":"exact"},{"name":"benign tumors of the brainstem","type":"exact"},{"name":"benign tumour of brain stem","type":"exact"},{"name":"benign tumour of brainstem","type":"exact"},{"name":"benign tumour of the brain stem","type":"exact"},{"name":"benign tumour of the brainstem","type":"exact"},{"name":"benign tumours of brainstem","type":"exact"},{"name":"benign tumours of the brainstem","type":"exact"},{"name":"brainstem benign neoplasm","type":"exact"}],"termid":"MONDO:0021507","xrefs":{"Monarch":{"xref_id":"0021507"}}}


id: PBO:0003463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ domain protein Mas5 (predicted)","termid":"PBO:0003463"}


id: PBO:0046971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 83 member H","termid":"PBO:0046971"}


id: PBO:0051522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 receptor accessory protein","termid":"PBO:0051522"}


id: MONDO:0018362
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent idiopathic facial pain","secondary_identifiers":["GARD:21649","MEDGEN:1673850","icd11.foundation:1799118131","Orphanet:398147","UMLS:C5191641"],"synonyms":[{"name":"AFP","type":"exact"},{"name":"PIFP","type":"exact"},{"name":"atypical facial pain","type":"exact"}],"termid":"MONDO:0018362","xrefs":{"Monarch":{"xref_id":"0018362"}}}


id: GO:0031521
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Structure within the hyphal tip of filamentous fungi that acts as an organizing center for hyphal tip growth; may function to supply vesicles to the elongating tip and/or to organize cytoskeletal microfilaments.","definition_xrefs":["PMID:15976451","PMID:15701784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"hyphal tip","termid":"GO:0001411"},{"relation_name":"part_of","term_name":"endomembrane system","termid":"GO:0012505"}],"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":"spitzenkorper","termid":"GO:0031521"}


id: PBO:0108678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoplasmic poly(A) polymerase Cid13","termid":"PBO:0108678"}


id: FYPO:0007490
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a mannosyltransferase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"normal mannosyltransferase activity","termid":"FYPO:0007490"}


id: MONDO:0019765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete celosomia (obsolete MONDO:0019765)","secondary_identifiers":["SCTID:44518003","ICD9:759.89","Orphanet:93942"],"termid":"MONDO:0019765","xrefs":{"Monarch":{"xref_id":"0019765"}}}


id: GO:0003289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which anatomical structure of an atrial septum primum is generated and organized.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial septum morphogenesis","termid":"GO:0060413"},{"relation_name":"part_of","term_name":"septum primum development","termid":"GO:0003284"}],"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":"atrial septum primum morphogenesis","termid":"GO:0003289"}


id: GO:0050932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of pigmented cell differentiation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"regulates","term_name":"pigment cell differentiation","termid":"GO:0050931"}],"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 pigment cell differentiation","termid":"GO:0050932"}


id: PBO:0084555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the seripauperin multigene family; encoded mainly in subtelomeric regions; SWAT-GFP fusion protein localizes to the endoplasmic reticulum and vacuole, while mCherry fusion localizes to just the vacuole; active during alcoholic fermentation; regulated by anaerobiosis; negatively regulated by oxygen; repressed by heme; identical to Pau18p","termid":"PBO:0084555"}


id: MONDO:0009988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinoschisis","termid":"MONDO:0004579"},{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"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":"retinoschisis of fovea","secondary_identifiers":["MESH:C538369","UMLS:C1849397","GARD:9143","MEDGEN:340313","OMIM:268080"],"synonyms":[{"name":"familial foveal retinoschisis","type":"related"},{"name":"foveal retinoschisis","type":"related"},{"name":"retinoschisis of fovea","type":"exact"}],"termid":"MONDO:0009988","xrefs":{"Monarch":{"xref_id":"0009988"}}}


id: GO:0070114
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outer, i.e. cytoplasm-facing, of the two lipid bilayers surrounding an organellar chromatophore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peribacteroid membrane","termid":"GO:0043661"},{"relation_name":"is_a","term_name":"organellar chromatophore membrane","termid":"GO:0070112"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"organellar chromatophore outer membrane","synonyms":[{"name":"Paulinella-type chromatophore outer membrane","type":"exact"}],"termid":"GO:0070114"}


id: PBO:0073962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 22 member 11","termid":"PBO:0073962"}


id: FYPO:0002096
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal during a cellular response to hydroxyurea.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein phosphorylation during vegetative growth","termid":"FYPO:0001038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002274","FYPO:0005447","FYPO:0000002","FYPO:0002494","FYPO:0001320"],"is_obsolete":false,"name":"increased protein phosphorylation during cellular response to hydroxyurea","synonyms":[{"name":"increased protein phosphorylation during cellular response to HU","type":"exact"},{"name":"increased protein phosphorylation during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"increased protein phosphorylation during cellular response to hydroxyurea during vegetative growth","type":"exact"}],"termid":"FYPO:0002096"}


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


id: PBO:0047187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 204 member C, pseudogene","termid":"PBO:0047187"}


id: GO:0044095
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"That part of a host cell's nuclear content other than the chromosomes or the nucleolus. The host is the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell nuclear part","termid":"GO:0044094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell nucleoplasm","termid":"GO:0044095"}


id: PBO:0055468
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 2901","termid":"PBO:0055468"}


id: PBO:0015678
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High Copy Sterile","termid":"PBO:0015678"}


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


id: PBO:0030029
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_adenylyl_cyclase_activity","termid":"PBO:0030029"}


id: GO:0009334
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Enzyme complex consisting of four proteins: the two subunits of the hydroxylase component (hcaE and hcaF), a ferredoxin (hcaC) and a ferredoxin reductase (hcaD). Converts 3-phenylpropionic acid (PP) into cis-3-(3-carboxyethyl)-3,5-cyclohexadiene-1,2-diol (PP-dihydrodiol).","definition_xrefs":["MetaCyc:HCAMULTI-CPLX","PMID:9603882","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"3-phenylpropionate dioxygenase complex","termid":"GO:0009334"}


id: PBO:0091282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short chain dehydrogenase, human DHRS7 family","termid":"PBO:0091282"}


id: MONDO:0043510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute and chronic (see also brain INJURIES, CHRONIC) injuries to the brain, including the cerebral hemispheres, CEREBELLUM, and brain STEM. Clinical manifestations depend on the nature of injury. Diffuse trauma to the brain is frequently associated with DIFFUSE AXONAL INJURY or COMA, POST-TRAUMATIC. Localized injuries may be associated with NEUROBEHAVIORAL MANIFESTATIONS; HEMIPARESIS, or other focal neurologic deficits.","definition_xrefs":["MESH:D001930"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"nervous system injury","termid":"MONDO:0044745"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain injury","synonyms":[{"name":"brain Traumas","type":"related"},{"name":"brain injury","type":"exact"},{"name":"brain trauma","type":"related"},{"name":"injury of brain","type":"exact"}],"termid":"MONDO:0043510","xrefs":{"Monarch":{"xref_id":"0043510"}}}


id: GO:0035950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of oligopeptide transport, by regulation of transcription from an RNA polymerase II promoter.","definition_xrefs":["PMID:17005992","GOC:dgf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of oligopeptide transport by regulation of transcription from RNA polymerase II promoter (obsolete GO:0035950)","synonyms":[{"name":"regulation of oligopeptide transport by regulation of transcription from Pol II promoter","type":"exact"}],"termid":"GO:0035950"}


id: SO:0000310
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000310 predicted_ab_initio_computation (obsolete SO:0000310)","termid":"SO:0000310"}


id: SO:0001390
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified cysteine amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_amino_acid_feature","termid":"SO:0001385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_L_cysteine","secondary_identifiers":["MOD:00905"],"synonyms":[{"name":"ModCys","type":"exact"},{"name":"modified L cysteine","type":"exact"},{"name":"modified L-cysteine","type":"exact"}],"termid":"SO:0001390"}


id: GO:0002676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of a chronic inflammatory response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inflammatory response","termid":"GO:0050727"},{"relation_name":"regulates","term_name":"chronic inflammatory response","termid":"GO:0002544"}],"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 chronic inflammatory response","termid":"GO:0002676"}


id: PBO:0065197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA processing factor 18","termid":"PBO:0065197"}


id: PBO:0043230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride voltage-gated channel 2","termid":"PBO:0043230"}


id: PR:O74421
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 3-demethylubiquinone-9 3-methyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04732","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":"ubiquinone biosynthesis O-methyltransferase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC162.05","secondary_identifiers":["UniProtKB:O74421"],"synonyms":[{"name":"3-demethylubiquinol 3-O-methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ubiG","type":"exact"},{"name":"polyprenyldihydroxybenzoate methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74421"}


id: PBO:0044057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin C","termid":"PBO:0044057"}


id: PBO:0063072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papilin, proteoglycan like sulfated glycoprotein","termid":"PBO:0063072"}


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


id: PBO:0034277
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_end_location","termid":"PBO:0034277"}


id: GO:0061218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of mesonephros development. Mesonephros development is the process whose specific outcome is the progression of the mesonephros over time, from its formation to the mature structure. The mesonephros is an organ that filters the blood and excretes the end products of body metabolism in the form of urine.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesonephros development","termid":"GO:0061217"},{"relation_name":"is_a","term_name":"negative regulation of kidney development","termid":"GO:0090185"},{"relation_name":"negatively_regulates","term_name":"mesonephros development","termid":"GO:0001823"}],"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 mesonephros development","termid":"GO:0061218"}


id: GO:0140698
data:
  {"annotated_genes":["SJAG_02698","SJAG_03449","SJAG_01745"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89029,91306,94574],"is_not":false,"summary":null,"term":"GO:0140698"}]},"cv_name":"biological_process","definition":"The process in which physical connections are formed between sub-telomeric heterochromatin and the nuclear envelope facilitating bouquet formation.","definition_xrefs":["PMID:31635174"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome attachment to the nuclear envelope","termid":"GO:0097240"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01745":null,"SJAG_02698":null,"SJAG_03449":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"attachment of telomeric heterochromatin to nuclear envelope","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"attachment of telomeres to nuclear envelope","type":"broad"},{"name":"attachment of telomeric chromatin to nuclear envelope","type":"broad"},{"name":"heterochromatin organization","type":"broad"}],"termid":"GO:0140698","terms_by_termid":{"GO:0140698":null}}


id: PBO:0034728
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds with high affinity to mammalian-type 5'-TTAGGG-3' telomeric repeats, and with very low affinity to less stringently conserved S. pombe telomeric repeats","termid":"PBO:0034728"}


id: GO:0090385
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation of a phagolysosome from a phagosome and a lysosome.","definition_xrefs":["GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle fusion","termid":"GO:0006906"},{"relation_name":"part_of","term_name":"phagolysosome assembly","termid":"GO:0001845"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810","GO:0044085","GO:0061024"],"is_obsolete":false,"name":"phagosome-lysosome fusion","termid":"GO:0090385"}


id: PBO:0003143
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.1","termid":"PBO:0003143"}


id: GO:0006583
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of melanin from other compounds, including tyrosine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tyrosine metabolic process","termid":"GO:0006570"},{"relation_name":"is_a","term_name":"melanin biosynthetic process","termid":"GO:0042438"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520","GO:0019748"],"is_obsolete":false,"name":"melanin biosynthetic process from tyrosine","synonyms":[{"name":"melanin anabolism from tyrosine","type":"exact"},{"name":"melanin formation from tyrosine","type":"exact"},{"name":"melanin synthesis from tyrosine","type":"exact"}],"termid":"GO:0006583"}


id: GO:0016146
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: GTP + H2O = GDP + phosphate.","definition_xrefs":["EC:3.6.1.48"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-synthesizing GTPase activity, initiation (obsolete GO:0016146)","synonyms":[{"name":"protein-synthesizing GTPase activity, initiation","type":"exact"}],"termid":"GO:0016146"}


id: PBO:0058237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4525","termid":"PBO:0058237"}


id: PBO:0042492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 13","termid":"PBO:0042492"}


id: PBO:0080833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosyl-tRNA synthetase 1","termid":"PBO:0080833"}


id: MONDO:1012116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypomyelinogenesis, non-human animal","termid":"MONDO:1011845"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hypomyelinogenesis, cattle","secondary_identifiers":["OMIA:000527-9913"],"termid":"MONDO:1012116","xrefs":{"Monarch":{"xref_id":"1012116"}}}


id: GO:0044251
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of a protein by pepsin in the stomach. Pepsin is generated from its precursor pepsinogen, which is activated by hydrolchloric acid (gastric acid).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete protein catabolic process by pepsin (obsolete GO:0044251)","synonyms":[{"name":"protein breakdown by pepsin","type":"exact"},{"name":"protein degradation by pepsin","type":"exact"}],"termid":"GO:0044251"}


id: MONDO:1012438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"sebaceous gland dysplasia, non-human animal","termid":"MONDO:1011757"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sebaceous gland dysplasia, domestic cat","secondary_identifiers":["OMIA:001710-9685"],"termid":"MONDO:1012438","xrefs":{"Monarch":{"xref_id":"1012438"}}}


id: GO:0061180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mammary gland epithelium over time, from its formation to the mature structure. The mammary gland is a large compound sebaceous gland that in female mammals is modified to secrete milk.","definition_xrefs":["GOC:yaf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelium development","termid":"GO:0060429"},{"relation_name":"part_of","term_name":"mammary gland development","termid":"GO:0030879"}],"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":"mammary gland epithelium development","synonyms":[{"name":"breast epithelium development","type":"exact"}],"termid":"GO:0061180"}


id: PR:Q9P7Q0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC186.05c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7Q0"],"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":"GDT1-like protein C186.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC186.05c","synonyms":[{"name":"Spom972h-SPAC186.05c","type":"exact"}],"termid":"PR:Q9P7Q0"}


id: PBO:0059732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 6","termid":"PBO:0059732"}


id: MONDO:1011739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hypotrichosis with thymic aplasia, non-human animal","secondary_identifiers":["OMIA:000544"],"termid":"MONDO:1011739","xrefs":{"Monarch":{"xref_id":"1011739"}}}


id: GO:1990877
data:
  {"annotated_genes":["SJAG_02231","SJAG_04910"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[96071,107161],"is_not":false,"summary":null,"term":"GO:1990877"}]},"cv_name":"cellular_component","definition":"A heterodimeric complex that functions as a GTPase-Activating Protein (GAP) Complex for members of the Rag family of GTPases. In the budding yeast, this complex contains Lst4 and Lst7, while the orthologous mammalian complex contains follicular (FLCN) and either follicular interacting protein 1 (FNIP1) or FNIP2.","definition_xrefs":["PMID:34805795","PMID:24095279","PMID:26387955","GOC:rn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GTPase activator complex","termid":"GO:1902773"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02231":null,"SJAG_04910":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:0032991","GO:0005575"],"is_obsolete":false,"name":"FNIP-folliculin RagC/D GAP","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"BFC complex","type":"exact"},{"name":"FLCN-FNIP1 complex","type":"exact"},{"name":"FLCN-FNIP2 complex","type":"exact"},{"name":"FNIP-Folliculin RagC/D GAP complex","type":"exact"},{"name":"Lst4-Lst7 complex","type":"exact"}],"termid":"GO:1990877","terms_by_termid":{"GO:1990877":null}}


id: MONDO:0021098
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glandular or squamous cell neoplastic proliferations characterized by the formation of multiple papillary structures diffusely involving a specific anatomic site.","definition_xrefs":["NCIT:C3713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary epithelial neoplasm","termid":"MONDO:0021096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillomatosis","secondary_identifiers":["MEDGEN:64459","UMLS:C0205875"],"synonyms":[{"name":"papillomatosis","type":"exact"}],"termid":"MONDO:0021098","xrefs":{"Monarch":{"xref_id":"0021098"}}}


id: PBO:0001860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar carboxypeptidase (predicted)","termid":"PBO:0001860"}


id: PBO:0088393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxyacyl-ACP dehydratase Htd2","termid":"PBO:0088393"}


id: PBO:0039872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP29 antisense RNA 1","termid":"PBO:0039872"}


id: PBO:0061890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligophrenin 1","termid":"PBO:0061890"}


id: GO:0018470
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-hydroxybutyraldehyde + H2O = 2 H+ + 2 e- + 4-hydroxybutanoate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-hydroxybutaraldehyde dehydrogenase activity (obsolete GO:0018470)","termid":"GO:0018470"}


id: GO:0052502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of symbiont MAP kinase-mediated signal transduction pathways during the symbiont defense response. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by host of defense-related symbiont MAP kinase-mediated signal transduction pathway (obsolete GO:0052502)","synonyms":[{"name":"activation by host of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"narrow"},{"name":"activation by organism of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"narrow"},{"name":"induction by organism of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"narrow"},{"name":"positive regulation by organism of defense-related symbiont MAPK-mediated signal transduction pathway","type":"exact"},{"name":"positive regulation by organism of defense-related symbiont mitogen-activated protein kinase-mediated signal transduction pathway","type":"exact"},{"name":"stimulation by host of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"narrow"},{"name":"up regulation by host of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"exact"},{"name":"up-regulation by host of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"exact"},{"name":"upregulation by host of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"exact"},{"name":"upregulation by organism of defense-related symbiont MAP kinase-mediated signal transduction pathway","type":"narrow"}],"termid":"GO:0052502"}


id: MONDO:0023670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Bardet-Biedl syndrome","termid":"MONDO:0015229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Bardet-Biedl syndrome 20","secondary_identifiers":["MEDGEN:934674","OMIM:619471","DOID:0081009","UMLS:C4310707"],"synonyms":[{"name":"BBS20","type":"exact"}],"termid":"MONDO:0023670","xrefs":{"Monarch":{"xref_id":"0023670"}}}


id: GO:0106145
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalyzes of the reaction: scopoletin + 2-oxoglutarate+O2=fraxetin +succinate+ CO2).","definition_xrefs":["RHEA:57848","GOC:lr","PMID:29361149","PMID:29581584"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"scopoletin 8-hydroxylase activity","secondary_identifiers":["EC:1.14.11.60"],"termid":"GO:0106145"}


id: PBO:0078567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif-containing 51","termid":"PBO:0078567"}


id: GO:0032110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein histidine kinase activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein kinase activity","termid":"GO:0045859"}],"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 histidine kinase activity","termid":"GO:0032110"}


id: PBO:0069918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1210, pseudogene","termid":"PBO:0069918"}


id: PBO:0049078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 119","termid":"PBO:0049078"}


id: PBO:0067052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 73, pseudogene","termid":"PBO:0067052"}


id: GO:0031337
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving sulfur amino acids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sulfur amino acid metabolic process","termid":"GO:0031335"},{"relation_name":"is_a","term_name":"positive regulation of sulfur metabolic process","termid":"GO:0051176"},{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"positively_regulates","term_name":"sulfur amino acid metabolic process","termid":"GO:0000096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0006790","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"positive regulation of sulfur amino acid metabolic process","synonyms":[{"name":"activation of sulfur amino acid metabolic process","type":"narrow"},{"name":"positive regulation of sulfur amino acid metabolism","type":"exact"},{"name":"stimulation of sulfur amino acid metabolic process","type":"narrow"},{"name":"up regulation of sulfur amino acid metabolic process","type":"exact"},{"name":"up-regulation of sulfur amino acid metabolic process","type":"exact"},{"name":"upregulation of sulfur amino acid metabolic process","type":"exact"}],"termid":"GO:0031337"}


id: GO:0018153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of an isopeptide cross-link between peptidyl-lysine and peptidyl-glutamine to produce N6-(L-isoglutamyl)-L-lysine.","definition_xrefs":["RESID:AA0124"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-glutamine modification","termid":"GO:0018199"},{"relation_name":"is_a","term_name":"peptidyl-lysine modification","termid":"GO:0018205"},{"relation_name":"is_a","term_name":"isopeptide cross-linking","termid":"GO:0018262"}],"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":"isopeptide cross-linking via N6-(L-isoglutamyl)-L-lysine","termid":"GO:0018153"}


id: PBO:0091799
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KM of ATP for ATPase activity 110 uM","termid":"PBO:0091799"}


id: MOD:01603
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 2x(15)N labeled L-lysine.","definition_xrefs":["PubMed:18688235","URL:http://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=609021|ALDRICH&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC&lang=en_US0.000000E+000"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(15)N labeled residue","termid":"MOD:00843"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2x(15)N labeled L-lysine","termid":"MOD:01603"}


id: PBO:0116580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane and mitochondrial outer membrane, implicated in cell integrity signaling, conserved fungal protein","termid":"PBO:0116580"}


id: PBO:0061063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium/potassium transporting ATPase interacting 2","termid":"PBO:0061063"}


id: PBO:0005160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3 Brl2","termid":"PBO:0005160"}


id: MONDO:0005125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of leprosy in which there are clinical manifestations of both principal types (lepromatous and tuberculoid). The disease may shift toward one of these two polar or principal forms.","definition_xrefs":["MESH:D015439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leprosy","termid":"MONDO:0005124"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"borderline leprosy","secondary_identifiers":["ICD10CM:A30.3","DOID:1023","ICD9:030.3","MEDGEN:7305","SCTID:400154003","UMLS:C0023346","EFO:0001055","icd11.foundation:56771163"],"synonyms":[{"name":"Midborderline leprosy","type":"exact"},{"name":"borderline leprosy [group B]","type":"exact"},{"name":"borderline or dimorphous leprosy","type":"exact"}],"termid":"MONDO:0005125","xrefs":{"Monarch":{"xref_id":"0005125"}}}


id: PBO:0003175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homoserine O-acetyltransferase (predicted)","termid":"PBO:0003175"}


id: MONDO:1012939
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any syndromic disease characterized by perinatal mortality that occurs in cattle due to a mutation in the GCK gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"syndromic disease, non-human animal","termid":"MONDO:1011360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"perinatal mortality syndrome, GCK-related, cattle","secondary_identifiers":["OMIA:002579-9913"],"termid":"MONDO:1012939","xrefs":{"Monarch":{"xref_id":"1012939"}}}


id: PR:O59802
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phosphatidylinositol N-acetylglucosaminyltransferase subunit C that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04589","PRO:DNx","PANTHER:PTHR12982: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":"phosphatidylinositol N-acetylglucosaminyltransferase GPI2 subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC550.04c","secondary_identifiers":["UniProtKB:O59802"],"synonyms":[{"name":"Spom972h-PIGC","type":"exact"}],"termid":"PR:O59802"}


id: GO:1902433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of water channel activity that is involved in maintenance of lens transparency.","definition_xrefs":["GOC:TermGenie","PMID:22095752","GOC:nhn"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of water channel activity involved in maintenance of lens transparency (obsolete GO:1902433)","synonyms":[{"name":"activation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"activation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"activation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"activation of water channel activity involved in maintenance of lens transparency","type":"narrow"},{"name":"activation of water channel activity involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"activation of water channel activity involved in preservation of lens transparency","type":"narrow"},{"name":"aquaporin activation involved in maintenance of lens transparency","type":"narrow"},{"name":"aquaporin activation involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"aquaporin activation involved in preservation of lens transparency","type":"narrow"},{"name":"positive regulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"positive regulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"positive regulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"positive regulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"positive regulation of water channel activity involved in preservation of lens transparency","type":"exact"},{"name":"up regulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"up regulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"up regulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"up regulation of water channel activity involved in maintenance of lens transparency","type":"exact"},{"name":"up regulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"up regulation of water channel activity involved in preservation of lens transparency","type":"exact"},{"name":"up-regulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"up-regulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"up-regulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"up-regulation of water channel activity involved in maintenance of lens transparency","type":"exact"},{"name":"up-regulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"up-regulation of water channel activity involved in preservation of lens transparency","type":"exact"},{"name":"upregulation of aquaporin involved in maintenance of lens transparency","type":"narrow"},{"name":"upregulation of aquaporin involved in maintenance of ocular lens transparency","type":"narrow"},{"name":"upregulation of aquaporin involved in preservation of lens transparency","type":"narrow"},{"name":"upregulation of water channel activity involved in maintenance of lens transparency","type":"exact"},{"name":"upregulation of water channel activity involved in maintenance of ocular lens transparency","type":"exact"},{"name":"upregulation of water channel activity involved in preservation of lens transparency","type":"exact"}],"termid":"GO:1902433"}


id: GO:0018204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of peptidyl-leucine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptidyl-leucine modification","termid":"GO:0018204"}


id: PBO:0056873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MHC class I polypeptide-related sequence C (pseudogene)","termid":"PBO:0056873"}


id: PBO:0060713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 10","termid":"PBO:0060713"}


id: PBO:0000685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HRI subfamily","termid":"PBO:0000685"}


id: MONDO:0007760
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":"hyperlipoproteinemia, type II, and deafness","secondary_identifiers":["OMIM:144300","UMLS:C1840425","MESH:C564170","MEDGEN:326732"],"synonyms":[{"name":"hyperlipoproteinemia, type II, and deafness","type":"exact"}],"termid":"MONDO:0007760","xrefs":{"Monarch":{"xref_id":"0007760"}}}


id: PBO:0085319
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatidylinositol 3-phosphate (PI3P) phosphatase; involved in various protein sorting pathways, including CVT targeting and endosome to vacuole transport; has similarity to the conserved myotubularin dual specificity phosphatase family","termid":"PBO:0085319"}


id: PBO:0079672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 V2 pseudogene 2","termid":"PBO:0079672"}


id: PBO:0016109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b5 reductase Cbr1 (predicted)","termid":"PBO:0016109"}


id: GO:0018126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of a hydroxy group to a protein amino acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein hydroxylation","secondary_identifiers":["Reactome:R-HSA-9629569"],"synonyms":[{"name":"protein amino acid hydroxylation","type":"exact"}],"termid":"GO:0018126"}


id: PBO:0034794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent helicase Slh1, human ASCC3 ortholog (predicted)","termid":"PBO:0034794"}


id: PBO:0043781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C3 and PZP like alpha-2-macroglobulin domain containing 8","termid":"PBO:0043781"}


id: FYPO:0000886
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the dimethylation of lysine at position 9 of histone H3 in centromere outer repeat regions is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 dimethylation at centromere during vegetative growth","termid":"FYPO:0000867"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0002494","FYPO:0001320","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"abnormal histone H3-K9 dimethylation at centromere outer repeat during vegetative growth","synonyms":[{"name":"abnormal histone H3 K9 dimethylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 dimethylation at centromere otr during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 dimethylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"abnormal histone H3-K9 dimethylation at centromeric outer repeat region during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 dimethylation at pericentric region during vegetative growth","type":"related"},{"name":"abnormal histone H3-K9 dimethylation at pericentromeric region during vegetative growth","type":"related"},{"name":"abnormal histone H3K9 dimethylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"abnormal histone H3K9me2 at centromere outer repeat during vegetative growth","type":"exact"},{"name":"abnormal histone lysine H3 K9 dimethylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0000886"}


id: PBO:0000574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FG repeat","termid":"PBO:0000574"}


id: MONDO:1012612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A liver disorder characterized by chronic conjugated hyperbilirubinemia and abundant intrahepatic pigment in a centrilobular and midzonal distribution that occurs in golden lion tamarins.","definition_xrefs":["PMID:8116141"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver disorder, non-human animal","termid":"MONDO:1012967"},{"relation_name":"is_a","term_name":"hyperbilirubinemia, non-human animal","termid":"MONDO:1012974"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conjugated hyperbilirubinemia, golden lion tamarin","secondary_identifiers":["OMIA:000498-30588"],"synonyms":[{"name":"Dubin-Johnson syndrome, golden lion tamarin","type":"related"},{"name":"hyperbilirubinaemia II-like, golden lion tamarin","type":"related"}],"termid":"MONDO:1012612","xrefs":{"Monarch":{"xref_id":"1012612"}}}


id: GO:0080026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an indolebutyric acid stimulus.","definition_xrefs":["PMID:18725356"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to auxin","termid":"GO:0009733"},{"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 indolebutyric acid","synonyms":[{"name":"response to IBA stimulus","type":"exact"},{"name":"response to indole-3-butyric acid stimulus","type":"narrow"},{"name":"response to indolebutyric acid stimulus","type":"exact"}],"termid":"GO:0080026"}


id: PBO:0089865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamide mononucleotide (NMN) adenylyltransferase","termid":"PBO:0089865"}


id: GO:0097295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of morphine, 17-methyl-7,8-didehydro-4,5alpha-epoxymorphinan-3,6alpha-diol. Morphine is a highly potent opiate analgesic psychoactive drug obtained form the opium poppy, Papaver somniferum.","definition_xrefs":["GOC:yaf","PMID:19567876"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoquinoline alkaloid biosynthetic process","termid":"GO:0033075"},{"relation_name":"is_a","term_name":"morphine metabolic process","termid":"GO:0071272"}],"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:0008150","GO:0019748"],"is_obsolete":false,"name":"morphine biosynthetic process","synonyms":[{"name":"morphine anabolism","type":"exact"},{"name":"morphine biosynthesis","type":"exact"},{"name":"morphine formation","type":"exact"},{"name":"morphine synthesis","type":"exact"}],"termid":"GO:0097295"}


id: MONDO:0009626
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Mendelian disease characterized by the presence of microcephaly and intracranial calcifications at birth accompanied by neurological delay, seizures and a clinical course similar to that seen in patients after intrauterine infection with Toxoplasma gondii, Rubella, Cytomegalovirus, Herpes simplex (so-called TORCH syndrome), or other agents, despite repeated tests revealing the absence of any known infectious agent.","definition_xrefs":["Orphanet:1229"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"pseudo-TORCH syndrome","secondary_identifiers":["MEDGEN:483678","DOID:0050656","SCTID:722390006","UMLS:C3489725","OMIMPS:251290","GARD:12426"],"synonyms":[{"name":"BLC-PMG","type":"exact"},{"name":"BLCPMG","type":"related"},{"name":"Baraitser Brett Piesowicz syndrome","type":"related"},{"name":"Baraitser-Brett-Piesowicz syndrome","type":"exact"},{"name":"Baraitser-Reardon syndrome","type":"exact"},{"name":"band-like calcification with simplified gyration and polymicrogyria","type":"exact"},{"name":"bilateral band-like calcification with polymicrogyria","type":"exact"},{"name":"congenital intrauterine infection-like syndrome","type":"related"},{"name":"microcephaly - intracranial calcification - intellectual disability","type":"related"},{"name":"microcephaly intracranial calcification","type":"related"},{"name":"microcephaly-intracranial calcification-intellectual disability syndrome","type":"exact"},{"name":"pseudo-TORCH syndrome","type":"exact"}],"termid":"MONDO:0009626","xrefs":{"Monarch":{"xref_id":"0009626"}}}


id: FYPO:0000872
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 methylation of lysine at position 9 of histone H3 occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000458"},{"relation_name":"is_a","term_name":"decreased histone methylation during vegetative growth","termid":"FYPO:0000870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0002274","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H3-K9 methylation during vegetative growth","synonyms":[{"name":"decreased histone H3 K9 methylation during vegetative growth","type":"exact"},{"name":"decreased histone H3-K9 methylation during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K9me during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K9 methylation during vegetative growth","type":"exact"},{"name":"reduced histone H3-K9 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000872"}


id: PBO:0085543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) ribosomal subunit; least basic of non-acidic ribosomal proteins; phosphorylated in vivo; essential for viability; homologous to mammalian ribosomal protein S5 and bacterial S7","termid":"PBO:0085543"}


id: MONDO:1011606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Vestibular disease that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibular disease, non-human animal","termid":"MONDO:1011414"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vestibular disease, dog","secondary_identifiers":["OMIA:002263-9615"],"termid":"MONDO:1011606","xrefs":{"Monarch":{"xref_id":"1011606"}}}


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


id: SO:0000127
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that is silenced.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"silenced","termid":"SO:0000893"},{"relation_name":"is_a","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silenced_gene","synonyms":[{"name":"silenced gene","type":"exact"}],"termid":"SO:0000127"}


id: MONDO:0008511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Proximal symphalangism is a very rare, genetic bone disorder characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients.","definition_xrefs":["Orphanet:3250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symphalangism","termid":"MONDO:0000151"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"proximal symphalangism","secondary_identifiers":["MESH:C536223","OMIMPS:185800","UMLS:C1861385","GARD:8182","MEDGEN:348856","icd11.foundation:49802338","HP:0100264","DOID:0050788"],"synonyms":[{"name":"Cushing's symphalangism","type":"exact"},{"name":"Strasburger-Hawkins-Eldridge syndrome","type":"related"},{"name":"Strasburger-Hawkins-Eldridge-Hargrave-McKusick syndrome","type":"related"},{"name":"hereditary absence of proximal interphalangeal joints","type":"related"},{"name":"hereditary absence of the proximal interphalangeal joints","type":"related"},{"name":"proximal symphalangism","type":"exact"},{"name":"proximal symphalangism (disease)","type":"exact"},{"name":"symphalangism, Cushing type","type":"exact"},{"name":"vessel’s syndrome","type":"related"}],"termid":"MONDO:0008511","xrefs":{"Monarch":{"xref_id":"0008511"}}}


id: PBO:0069658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 935, pseudogene","termid":"PBO:0069658"}


id: MONDO:0000845
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic, non-inheritable disorder caused by osteoblastic differentiation defects that result in the replacement of bone marrow and trabecular bone by fibrous stroma and immature bone. It usually affects a single bone and less frequently multiple bones. Skull, femur, tibia, and humerus are the most frequently affected bones. It manifests with pain, deformities, and fractures.","definition_xrefs":["NCIT:C34609"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","termid":"MONDO:0019708"},{"relation_name":"is_a","term_name":"bone remodeling disease","termid":"MONDO:0000833"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrous dysplasia","secondary_identifiers":["GARD:6444","MEDGEN:120444","DOID:0080031","Orphanet:249","SCTID:254145001","icd11.foundation:1704766818","SCTID:10623005","ICD9:733.29","MedDRA:10016664","NORD:1147","MESH:D005357","UMLS:C0259779"],"synonyms":[{"name":"fibrous dysplasia of bone","type":"exact"}],"termid":"MONDO:0000845","xrefs":{"Monarch":{"xref_id":"0000845"}}}


id: GO:0051304
data:
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Chromosome separation begins with the release of cohesin complexes from chromosomes; in budding yeast, this includes the cleavage of cohesin complexes along the chromosome arms, followed by the separation of the centromeric regions. Chromosome separation also includes formation of chromatid axes mediated by condensins, and ends with the disentangling of inter-sister catenation catalyzed by topoisomerase II (topo II).","definition_xrefs":["PMID:20352243","GOC:mtg_cell_cycle","GOC:lb","GOC:mah","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"chromosome segregation","termid":"GO:0007059"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00145":null,"SJAG_00146":null,"SJAG_00460":null,"SJAG_00666":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01515":null,"SJAG_01679":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01956":null,"SJAG_02104":null,"SJAG_02169":null,"SJAG_02186":null,"SJAG_02336":null,"SJAG_02380":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_02542":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03327":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04457":null,"SJAG_04573":null,"SJAG_04661":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04968":null,"SJAG_04999":null,"SJAG_05236":null,"SJAG_05329":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"chromosome separation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0034500"],"synonyms":[{"name":"chromatid release","type":"related"},{"name":"rDNA separation","type":"narrow"}],"termid":"GO:0051304","terms_by_termid":{"GO:0007094":null,"GO:0033316":null,"GO:0045842":null,"GO:0051306":null,"GO:0051307":null,"GO:0051755":null,"GO:0090267":null,"GO:0140499":null,"GO:1901970":null,"GO:1902103":null,"GO:1902426":null,"GO:1905191":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:1905824":null,"GO:2000816":null}}


id: GO:0005085
data:
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id: GO:0102900
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: dehydroabietadienal + NADPH + O2 = dehydroabietic acid + NADP + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete dehydroabietadienal hydroxylase activity (obsolete GO:0102900)","termid":"GO:0102900"}


id: PBO:0036526
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Jalili syndrome","termid":"PBO:0036526"}


id: GO:0022613
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id: FYPO:0002521
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id: PBO:0087590
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id: MONDO:0018862
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id: GO:0052323
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id: PBO:0065119
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id: PBO:0054518
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id: PBO:0028290
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id: GO:0045722
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id: GO:0006906
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id: GO:0102173
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id: PBO:0030770
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id: PR:O59744
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id: FYPO:0006552
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id: PBO:0082900
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id: PBO:0044195
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id: PBO:0071841
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id: MONDO:0021720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fetal alcohol spectrum disorders (obsolete MONDO:0021720)","termid":"MONDO:0021720","xrefs":{"Monarch":{"xref_id":"0021720"}}}


id: GO:1904644
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 curcumin stimulus.","definition_xrefs":["GOC:TermGenie","PMID:24755072","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to ether","termid":"GO:0071362"},{"relation_name":"is_a","term_name":"cellular response to ketone","termid":"GO:1901655"},{"relation_name":"is_a","term_name":"response to curcumin","termid":"GO:1904643"}],"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 curcumin","termid":"GO:1904644"}


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


id: FYPO:0007177
data:
  {"alleles_by_uniquename":{"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119282],"is_not":false,"summary":null,"term":"FYPO:0007177"}],"single_locus_phenotype":[{"annotations":[119271,119272,119279,119283],"is_not":false,"summary":null,"term":"FYPO:0007177"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the medial cortex of a cell is abolished during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to medial cortex during vegetative growth","termid":"FYPO:0002555"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01143":null,"SJAG_01665":null,"SJAG_02392":null,"SJAG_03596":null,"SJAG_03703":null,"SJAG_04498":null},"genotype_count":2,"genotypes_by_uniquename":{"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01143","SJAG_02392"],"name":"abolished protein localization to medial cortex during mitotic interphase","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_01143"],"single_locus_genotype_uniquenames":["mid1delta"],"synonyms":[{"name":"abolished protein localisation to medial cortex during mitotic interphase","type":"exact"},{"name":"abolished protein localization to medial cortex during interphase during vegetative growth","type":"exact"},{"name":"abolished protein localization to medial cortex during interphase of mitotic cell cycle","type":"exact"},{"name":"abolished protein localization to medial ring during mitotic interphase","type":"exact"},{"name":"protein localization to medial cortex abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007177","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0007177":null}}


id: PBO:0029189
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-enlarged_exocytic_vesicles","termid":"PBO:0029189"}


id: FYPO:0001625
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 L-glutamine measured in the vacuole is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in vacuole","termid":"FYPO:0001603"},{"relation_name":"is_a","term_name":"normal cellular glutamine level","termid":"FYPO:0001636"}],"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:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal vacuolar glutamine level","synonyms":[{"name":"normal level of glutamine in vacuole","type":"exact"},{"name":"normal vacuolar L-glutamine level","type":"exact"},{"name":"normal vacuolar glutamine level during mitotic cell cycle","type":"related"},{"name":"normal vacuolar glutamine level during vegetative growth","type":"exact"}],"termid":"FYPO:0001625"}


id: MONDO:0010763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"},{"relation_name":"is_a","term_name":"partial chromosome Y deletion","termid":"MONDO:0015607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure, Y-linked, 1","secondary_identifiers":["OMIM:400042","DOID:0070186","GARD:18503","MEDGEN:1634798","UMLS:C4551960"],"synonyms":[{"name":"SPGFY1","type":"related"},{"name":"Sertoli cell-only syndrome, Y-linked","type":"related"},{"name":"Sertoli cell-only syndrome, type 1","type":"related"},{"name":"Sertoli cell-only syndrome, type 2","type":"related"},{"name":"hypospermatogenesis","type":"related"},{"name":"incomplete Sertoli cell-only syndrome","type":"related"},{"name":"spermatogenic failure, Y-linked, 1","type":"exact"},{"name":"spermatogenic failure, Y-linked, 1, Y-linked","type":"exact"},{"name":"spermatogenic failure, Y-linked, type 1","type":"exact"}],"termid":"MONDO:0010763","xrefs":{"Monarch":{"xref_id":"0010763"}}}


id: MONDO:0030860
data:
  {"annotated_genes":["SJAG_01537"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85661],"is_not":false,"summary":null,"term":"MONDO:0030860"}]},"cv_name":"mondo","definition":"Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the BSCL2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, type 5","termid":"MONDO:0100350"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01537":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0000426","MONDO:0005244"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, type 5C","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18268","MEDGEN:1760720","DOID:0081401","UMLS:C5436838","OMIM:619112"],"synonyms":[{"name":"DHMN5C","type":"exact"},{"name":"HMN5C","type":"exact"},{"name":"neuropathy, distal hereditary motor, type VC","type":"exact"},{"name":"spinal muscular atrophy, distal, type 5C","type":"exact"}],"termid":"MONDO:0030860","terms_by_termid":{"MONDO:0030860":null},"xrefs":{"Monarch":{"xref_id":"0030860"}}}


id: PBO:0059567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1J, pseudogene","termid":"PBO:0059567"}


id: PR:Q9P7R5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gfh1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7R5"],"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":"gamma-tubulin complex component gfh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC211.06","synonyms":[{"name":"Spom972h-gfh1","type":"exact"},{"name":"gcp4 homolog 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7R5"}


id: MONDO:1012715
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any difference of sexual development that occurs in domestic cats with a XY karyotype.","definition_xrefs":["OMIA:001601-9685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"difference of sexual differentiation, non-human animal","termid":"MONDO:0700105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XY difference of sexual development, domestic cat","termid":"MONDO:1012715","xrefs":{"Monarch":{"xref_id":"1012715"}}}


id: MONDO:0003635
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare breast adenocarcinoma with sebaceous differentiation.","definition_xrefs":["NCIT:C40369"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast adenocarcinoma","termid":"MONDO:0004988"},{"relation_name":"is_a","term_name":"invasive breast carcinoma","termid":"MONDO:0006256"},{"relation_name":"is_a","term_name":"sebaceous adenocarcinoma","termid":"MONDO:0006962"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"sebaceous breast carcinoma","secondary_identifiers":["DOID:5760","MEDGEN:276789","UMLS:C1519207"],"synonyms":[{"name":"breast sebaceous adenocarcinoma","type":"exact"},{"name":"sebaceous adenocarcinoma of breast","type":"exact"},{"name":"sebaceous breast carcinoma","type":"exact"}],"termid":"MONDO:0003635","xrefs":{"Monarch":{"xref_id":"0003635"}}}


id: PBO:0034730
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heteromeric(12)","termid":"PBO:0034730"}


id: PBO:0049221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor kinase 4","termid":"PBO:0049221"}


id: GO:0090567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a reproductive shoot system over time, from its formation to the mature structure.","definition_xrefs":["GOC:pj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic development","termid":"GO:0009791"},{"relation_name":"is_a","term_name":"shoot system development","termid":"GO:0048367"},{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"reproductive shoot system development","termid":"GO:0090567"}


id: MONDO:0044718
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"alkaline ceramidase 3 deficiency","secondary_identifiers":["OMIM:617762","UMLS:C4540358","MEDGEN:1622324","Orphanet:502444","GARD:17936"],"synonyms":[{"name":"ACER3-related early childhood-onset progressive leukodystrophy","type":"exact"},{"name":"PLDECO","type":"related"},{"name":"leukodystrophy due to alkaline ceramidase 3 deficiency","type":"exact"},{"name":"leukodystrophy, progressive, early childhood-onset","type":"related"}],"termid":"MONDO:0044718","xrefs":{"Monarch":{"xref_id":"0044718"}}}


id: GO:2000460
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of eukaryotic cell surface binding.","definition_xrefs":["GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of eukaryotic cell surface binding (obsolete GO:2000460)","synonyms":[{"name":"regulation of eukaryotic cell surface binding","type":"exact"}],"termid":"GO:2000460"}


id: GO:0042356
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-6-deoxy-D-mannose + NAD(P)+ = GDP-4-dehydro-6-deoxy-D-mannose + NAD(P)H + H+. In the reverse reaction, a mixture of GDP-D-rhamnose and its C-4 epimer is formed.","definition_xrefs":["EC:1.1.1.187"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"GDP-4-dehydro-D-rhamnose reductase activity","synonyms":[{"name":"GDP-4-keto-6-deoxy-D-mannose reductase activity","type":"related"},{"name":"GDP-4-keto-D-rhamnose reductase activity","type":"related"},{"name":"GDP-6-deoxy-D-mannose:NAD(P)+ 4-oxidoreductase activity","type":"related"},{"name":"guanosine diphosphate-4-keto-D-rhamnose reductase activity","type":"related"}],"termid":"GO:0042356"}


id: GO:0004828
data:
  {"annotated_genes":["SJAG_02977","SJAG_04762"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72880,76749],"is_not":false,"summary":null,"term":"GO:0004828"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + L-serine + tRNA(Ser) = AMP + diphosphate + L-seryl-tRNA(Ser). Also catalyzes the formation of L-seryl-tRNA(Sec) from tRNA(Sec), the special tRNA for selenocysteine.","definition_xrefs":["EC:6.1.1.11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyl-tRNA ligase activity","termid":"GO:0004812"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02977":null,"SJAG_04762":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0016874","GO:0140101","GO:0003674","GO:0140098","GO:0003824"],"is_obsolete":false,"name":"serine-tRNA ligase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:SERINE--TRNA-LIGASE-RXN","Reactome:R-HSA-380239","Reactome:R-HSA-379992"],"synonyms":[{"name":"L-serine:tRNASer ligase (AMP-forming)","type":"related"},{"name":"SerRS activity","type":"related"},{"name":"serine translase activity","type":"related"},{"name":"seryl-tRNA synthetase activity","type":"exact"},{"name":"seryl-transfer RNA synthetase activity","type":"related"},{"name":"seryl-transfer ribonucleate synthetase activity","type":"related"},{"name":"seryl-transfer ribonucleic acid synthetase activity","type":"related"}],"termid":"GO:0004828","terms_by_termid":{"GO:0004828":null}}


id: GO:0002737
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of plasmacytoid dendritic cell cytokine production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of dendritic cell cytokine production","termid":"GO:0002731"},{"relation_name":"is_a","term_name":"regulation of plasmacytoid dendritic cell cytokine production","termid":"GO:0002736"},{"relation_name":"negatively_regulates","term_name":"plasmacytoid dendritic cell cytokine production","termid":"GO:0002373"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of plasmacytoid dendritic cell cytokine production","synonyms":[{"name":"down regulation of plasmacytoid dendritic cell cytokine production","type":"exact"},{"name":"down-regulation of plasmacytoid dendritic cell cytokine production","type":"exact"},{"name":"downregulation of plasmacytoid dendritic cell cytokine production","type":"exact"},{"name":"inhibition of plasmacytoid dendritic cell cytokine production","type":"narrow"}],"termid":"GO:0002737"}


id: PBO:0079196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific protein Y-linked 25, pseudogene","termid":"PBO:0079196"}


id: GO:0051026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which a connection between chromatids assembles, indicating where an exchange of homologous segments has taken place by the crossing-over of non-sister chromatids.","definition_xrefs":["PMID:23396135"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"homologous chromosome pairing at meiosis","termid":"GO:0007129"},{"relation_name":"part_of","term_name":"reciprocal meiotic recombination","termid":"GO:0007131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0007049","GO:0006310","GO:0008150","GO:0006259","GO:0140013","GO:0044085"],"is_obsolete":false,"name":"chiasma assembly","termid":"GO:0051026"}


id: MONDO:0024888
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epithelial neoplasm of the female reproductive system arising from mesonephric remnants.","definition_xrefs":["NCIT:C4295"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"},{"relation_name":"is_a","term_name":"kidney neoplasm","termid":"MONDO:0021163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"mesonephric neoplasm","secondary_identifiers":["MEDGEN:137779","UMLS:C0334531","ICDO:9110/1"],"synonyms":[{"name":"Wolffian duct neoplasm","type":"exact"},{"name":"Wolffian duct tumor","type":"exact"},{"name":"Wolffian duct tumour","type":"exact"},{"name":"mesonephric duct neoplasm","type":"exact"},{"name":"mesonephric duct tumor","type":"exact"},{"name":"mesonephric duct tumour","type":"exact"},{"name":"mesonephric neoplasm","type":"exact"},{"name":"mesonephric tumor","type":"exact"},{"name":"mesonephric tumour","type":"exact"},{"name":"mesonephroma","type":"exact"},{"name":"neoplasm of mesonephric duct","type":"exact"},{"name":"tumor of mesonephric duct","type":"exact"},{"name":"tumour of mesonephric duct","type":"exact"}],"termid":"MONDO:0024888","xrefs":{"Monarch":{"xref_id":"0024888"}}}


id: MONDO:0700166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sexually transmitted tumor arising from histiocytes and occurring in dogs.","definition_xrefs":["NCIT:C162473"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venereal tumors, veterinary","termid":"MONDO:0025478"},{"relation_name":"is_a","term_name":"canine neoplasm","termid":"MONDO:0700139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine transmissible venereal tumor","termid":"MONDO:0700166","xrefs":{"Monarch":{"xref_id":"0700166"}}}


id: PomGeneEx:0000007
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneEx","definition":"A gene expression qualifier that indicates that an RNA or protein is present at the same level or produced at a the same rate under two or more sets of conditions or over a time course.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression qualifier","termid":"PomGeneEx:0000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"constant","synonyms":[{"name":"gene expression constant","type":"exact"},{"name":"gene product level constant","type":"exact"}],"termid":"PomGeneEx:0000007"}


id: PBO:0070708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 13","termid":"PBO:0070708"}


id: GO:0016577
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histones by removal of methyl groups.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histone demethylation (obsolete GO:0016577)","termid":"GO:0016577"}


id: GO:0004229
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of gelatin types I and V and collagen types IV and V.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete gelatinase B activity (obsolete GO:0004229)","synonyms":[{"name":"92-kDa gelatinase activity","type":"narrow"},{"name":"92-kDa type IV collagenase activity","type":"narrow"},{"name":"95 kDa type IV collagenase/gelatinase activity","type":"related"},{"name":"MMP 9","type":"related"},{"name":"MMP-9","type":"exact"},{"name":"collagenase IV","type":"related"},{"name":"collagenase type IV","type":"related"},{"name":"gelatinase B activity","type":"exact"},{"name":"gelatinase MMP 9","type":"related"},{"name":"macrophage gelatinase activity","type":"narrow"},{"name":"matrix metalloproteinase 9 activity","type":"related"},{"name":"type IV collagen metalloproteinase","type":"broad"},{"name":"type V collagenase activity","type":"related"}],"termid":"GO:0004229"}


id: MONDO:0002574
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm of the prostate. It is characterized by the presence of skeletal muscle exhibiting embryonic features.","definition_xrefs":["NCIT:C5525"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostate rhabdomyosarcoma","termid":"MONDO:0006389"},{"relation_name":"is_a","term_name":"embryonal rhabdomyosarcoma","termid":"MONDO:0009993"},{"relation_name":"is_a","term_name":"prostate cancer, hereditary","termid":"MONDO:0700275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"prostate embryonal rhabdomyosarcoma","secondary_identifiers":["MEDGEN:233873","DOID:3251","UMLS:C1335508"],"synonyms":[{"name":"embryonal rhabdomyosarcoma (disease) of prostate gland","type":"exact"},{"name":"embryonal rhabdomyosarcoma of prostate","type":"exact"},{"name":"embryonal rhabdomyosarcoma of the prostate","type":"exact"},{"name":"prostate embryonal rhabdomyosarcoma","type":"exact"},{"name":"prostate gland embryonal rhabdomyosarcoma (disease)","type":"exact"}],"termid":"MONDO:0002574","xrefs":{"Monarch":{"xref_id":"0002574"}}}


id: GO:0180024
data:
  {"annotated_genes":["SJAG_05207"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103735],"is_not":false,"summary":null,"term":"GO:0180024"}]},"cv_name":"molecular_function","definition":"An activity in which a protein, or group of proteins, acts to restrict the size of a fenestration in a membrane or membrane system (i.e. restrict the diameter of a hole in a membrane). An example of this is the molecular function is performed by ESCRT-III proteins at the nuclear envelope of fission yeast during anaphase B.","definition_xrefs":["PMID:37783794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05207":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"membrane grommet activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0180024","terms_by_termid":{"GO:0180024":null}}


id: PBO:0088174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xylose and arabinose reductase; member of the aldo-keto reductase (AKR) family; GFP-fusion protein is induced in response to the DNA-damaging agent MMS","termid":"PBO:0088174"}


id: GO:0018649
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: tetrahydrofuran + O2 + 2 H+ + 2 e- = H2O + 2-hydroxytetrahydrofuran.","definition_xrefs":["UM-BBD_reactionID:r0017"],"gene_count":0,"genotype_count":0,"name":"obsolete tetrahydrofuran hydroxylase activity (obsolete GO:0018649)","termid":"GO:0018649"}


id: PBO:0049415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanylate cyclase 2E, pseudogene","termid":"PBO:0049415"}


id: PBO:0029134
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-spindle_pole_body_absent_from_cell","termid":"PBO:0029134"}


id: PBO:0065398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit alpha 3","termid":"PBO:0065398"}


id: PBO:0026644
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_G2_DNA_damage_checkpoint_during_cellular_response_to_UV","termid":"PBO:0026644"}


id: GO:0071915
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of lysine group to a lysine residue in a protein, producing N6-(lysyl)-L-lysine. This modification is observed in, and is probably unique to, translation elongation factor P (EF-P).","definition_xrefs":["GOC:imk","GOC:jsg","PMID:20729861"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-lysine lysylation (obsolete GO:0071915)","synonyms":[{"name":"protein amino acid lysylation","type":"exact"}],"termid":"GO:0071915"}


id: MONDO:0002496
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma of the colon that has invaded into the submucosa.","definition_xrefs":["NCIT:C38760"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon adenocarcinoma","termid":"MONDO:0002271"},{"relation_name":"is_a","term_name":"invasive carcinoma","termid":"MONDO:0040677"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"submucosal invasive colon adenocarcinoma","secondary_identifiers":["MEDGEN:271523","UMLS:C1515024","DOID:3038"],"synonyms":[{"name":"submucosal invasive colon adenocarcinoma","type":"exact"}],"termid":"MONDO:0002496","xrefs":{"Monarch":{"xref_id":"0002496"}}}


id: PBO:0049225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor kinase 6 pseudogene 1","termid":"PBO:0049225"}


id: MONDO:0020500
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Marburg hemorrhagic fever (MHF), caused by Marburg virus, is a severe viral hemorrhagic disease characterized by initial fever and malaise followed by gastrointestinal symptoms, bleeding, shock, and multi-organ system failure.","definition_xrefs":["Orphanet:99826"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Filoviridae infectious disease","termid":"MONDO:0005762"},{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Marburg hemorrhagic fever","secondary_identifiers":["MEDGEN:9888","DOID:4327","EFO:0007358","icd11.foundation:696598707","NCIT:C84883","SCTID:77503002","MESH:D008379","GARD:9444","MedDRA:10026822","ICD9:078.89","UMLS:C0024788"],"synonyms":[{"name":"Green monkey disease","type":"exact"},{"name":"MHF","type":"exact"},{"name":"Marburg disease","type":"exact"},{"name":"Marburg virus disease","type":"exact"}],"termid":"MONDO:0020500","xrefs":{"Monarch":{"xref_id":"0020500"}}}


id: PBO:0082758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the septin ring that is required for cytokinesis; septins are GTP-binding proteins that assemble with other septins into rod-like complexes that can associate with other rods to form filament polymers; septin rings at the mother-bud neck act as scaffolds for recruiting factors needed for cell division and as barriers to prevent diffusion of specific proteins between mother and daughter cells","termid":"PBO:0082758"}


id: PBO:0050521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox D9","termid":"PBO:0050521"}


id: GO:0061800
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A supramolecular fiber formed from fibronectin molecules. The fibrils are 5 to 25nm in diameter and can form branched meshworks.","definition_xrefs":["GOC:dph","PMID:20690820"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supramolecular fiber","termid":"GO:0099512"},{"relation_name":"part_of","term_name":"extracellular matrix","termid":"GO:0031012"}],"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":"fibronectin fibril","termid":"GO:0061800"}


id: GO:0003785
data:
  {"annotated_genes":["SJAG_04982","SJAG_01993"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71764,75579],"is_not":false,"summary":null,"term":"GO:0003785"}]},"cv_name":"molecular_function","definition":"Binding to monomeric actin, also known as G-actin.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin binding","termid":"GO:0003779"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01993":null,"SJAG_04982":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0008092"},{"rel_name":"is_a","termid":"GO:0003779"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003779","GO:0008092","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"actin monomer binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"G actin binding","type":"exact"}],"termid":"GO:0003785","terms_by_termid":{"GO:0003785":null}}


id: MONDO:0044406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"distal arthrogryposis","termid":"MONDO:0019942"}],"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":"arthrogryposis-ectodermal dysplasia-other anomalies syndrome","secondary_identifiers":["GARD:5029","MEDGEN:1674099","Orphanet:3200","UMLS:C5191837"],"synonyms":[{"name":"Stoll-Alembik-Finck syndrome","type":"exact"}],"termid":"MONDO:0044406","xrefs":{"Monarch":{"xref_id":"0044406"}}}


id: GO:0010675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, extent or frequency of the chemical reactions and pathways involving carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y, as carried out by individual cells.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular carbohydrate metabolic process (obsolete GO:0010675)","termid":"GO:0010675"}


id: PBO:0045233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 1","termid":"PBO:0045233"}


id: MONDO:0017867
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal 17p13.1 microdeletion syndrome is a rare chromosomal anomaly syndrome characterized by mild global developmental delay/intellectual disability with poor to absent speech, dysmorphic features (long midface, retrognathia with overbite, protruding ears), microcephaly, failure to thrive, wide-based gait and a body posture with knee and elbow flexion and hands held in a midline.","definition_xrefs":["Orphanet:319171"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"chromosome 17p13.1 deletion syndrome","termid":"MONDO:0013415"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal 17p13.1 microdeletion syndrome","secondary_identifiers":["MEDGEN:1657963","GARD:10996","UMLS:C4749349"],"synonyms":[{"name":"distal del(17)(p13.1)","type":"exact"}],"termid":"MONDO:0017867","xrefs":{"Monarch":{"xref_id":"0017867"}}}


id: PR:O14155
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A UPF0047 protein YjbQ that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01063","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":"UPF0047 protein C4A8.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.02c","secondary_identifiers":["UniProtKB:O14155"],"synonyms":[{"name":"Spom972h-yjbQ","type":"exact"}],"termid":"PR:O14155"}


id: GO:2000526
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any positive regulation of glycoprotein biosynthetic process that is involved in immunological synapse formation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of glycoprotein biosynthetic process","termid":"GO:0010560"},{"relation_name":"part_of","term_name":"immunological synapse formation","termid":"GO:0001771"}],"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 glycoprotein biosynthetic process involved in immunological synapse formation","synonyms":[{"name":"positive regulation of glycoprotein biosynthetic process of formation of immunological synapse","type":"exact"},{"name":"positive regulation of glycoprotein biosynthetic process of immunological synapse formation","type":"exact"}],"termid":"GO:2000526"}


id: GO:0046216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of indole phytoalexins, any indole compound produced by plants as part of their defense response.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indole-containing compound catabolic process","termid":"GO:0042436"},{"relation_name":"is_a","term_name":"indole phytoalexin metabolic process","termid":"GO:0046217"},{"relation_name":"is_a","term_name":"detoxification of nitrogen compound","termid":"GO:0051410"},{"relation_name":"is_a","term_name":"phytoalexin catabolic process","termid":"GO:0052316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0098754","GO:0008150","GO:0019748","GO:0044248"],"is_obsolete":false,"name":"indole phytoalexin catabolic process","synonyms":[{"name":"indole phytoalexin breakdown","type":"exact"},{"name":"indole phytoalexin catabolism","type":"exact"},{"name":"indole phytoalexin degradation","type":"exact"}],"termid":"GO:0046216"}


id: PBO:0058641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6770-3","termid":"PBO:0058641"}


id: PBO:0087757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the tRNA splicing endonuclease; tRNA splicing endonuclease (Sen complex) is composed of Sen2p, Sen15p, Sen34p, and Sen54p; Sen complex also cleaves the CBP1 mRNA at the mitochondrial surface; Sen2p contains the active site for tRNA 5' splice site cleavage and has similarity to Sen34p and to Archaeal tRNA splicing endonuclease;","termid":"PBO:0087757"}


id: PBO:0027898
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_siRNA_level","termid":"PBO:0027898"}


id: MONDO:0011385
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any disease of a degenerative nature that affects the intervertebral disk.","definition_xrefs":["NCIT:C26983"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete bone deterioration disease (obsolete MONDO:0000834)","termid":"MONDO:0000834"},{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intervertebral disk degenerative disorder","secondary_identifiers":["EFO:0004994","UMLS:C0158266","MEDGEN:102357","MESH:D055959","SCTID:77547008","OMIM:603932","ICD9:722.6","DOID:90"],"synonyms":[{"name":"IDD","type":"exact"},{"name":"cervical disc degenerative disease","type":"narrow"},{"name":"cervical disk degenerative disease","type":"narrow"},{"name":"degenerative disc disease","type":"exact"},{"name":"degenerative disk disease","type":"exact"},{"name":"degenerative disorder of intervertebral disc","type":"exact"},{"name":"degenerative disorder of intervertebral disk","type":"exact"},{"name":"intervertebral Disc Degeneration","type":"exact"},{"name":"intervertebral Disc degenerative disease","type":"exact"},{"name":"intervertebral Disc degenerative disorder","type":"exact"},{"name":"intervertebral disc degeneration","type":"exact"},{"name":"intervertebral disc disease","type":"exact"},{"name":"intervertebral disk degeneration","type":"exact"},{"name":"intervertebral disk degenerative disorder","type":"exact"},{"name":"intervertebral disk disease","type":"exact"},{"name":"lumbar disc degeneration","type":"narrow"},{"name":"lumbar disk degeneration","type":"narrow"},{"name":"vertebral Disc degenerative disease","type":"exact"},{"name":"vertebral Disc degenerative disorder","type":"exact"},{"name":"vertebral disc disease","type":"exact"},{"name":"vertebral disk disease","type":"exact"}],"termid":"MONDO:0011385","xrefs":{"Monarch":{"xref_id":"0011385"}}}


id: GO:0052574
data:
  {"annotated_genes":["SJAG_03818","SJAG_02951","SJAG_01784","SJAG_02954"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109605,113732,113739,113740],"is_not":false,"summary":null,"term":"GO:0052574"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of UDP-D-galactose, a substance composed of D-galactose in glycosidic linkage with guanosine diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"UDP-D-galactose metabolic process","termid":"GO:0052573"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01784":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_03818":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:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"UDP-galactose biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:PWY-7344"],"synonyms":[{"name":"UDP-D-galactopyranose biosynthesis","type":"exact"},{"name":"UDP-D-galactopyranose biosynthetic process","type":"exact"},{"name":"UDP-D-galactose biosynthesis","type":"exact"},{"name":"UDP-D-galactose biosynthetic process","type":"exact"},{"name":"UDP-alpha-D-galactose biosynthesis","type":"exact"},{"name":"UDP-galactose biosynthesis","type":"exact"},{"name":"uridine diphosphate galactose biosynthesis","type":"exact"},{"name":"uridine diphosphate galactose biosynthetic process","type":"exact"}],"termid":"GO:0052574","terms_by_termid":{"GO:0052574":null}}


id: PBO:0116607
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 3131","termid":"PBO:0116607"}


id: PBO:0089655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Brx1","termid":"PBO:0089655"}


id: PBO:0040529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-2-microglobulin regulator","termid":"PBO:0040529"}


id: MONDO:0014083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the PIK3R1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal agammaglobulinemia","termid":"MONDO:0011096"}],"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:0005046","MONDO:0005570"],"is_obsolete":false,"name":"agammaglobulinemia 7, autosomal recessive","secondary_identifiers":["MEDGEN:767603","OMIM:615214","DOID:0081139","GARD:15918","UMLS:C3554689"],"synonyms":[{"name":"AGM7","type":"related"},{"name":"PIK3R1 autosomal agammaglobulinemia","type":"exact"},{"name":"agammaglobulinemia 7, autosomal recessive","type":"exact"},{"name":"agammaglobulinemia, autosomal recessive, due to PIK3R1 defect","type":"related"},{"name":"autosomal agammaglobulinemia caused by mutation in PIK3R1","type":"exact"}],"termid":"MONDO:0014083","xrefs":{"Monarch":{"xref_id":"0014083"}}}


id: GO:0021881
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of Wnt protein to a receptor on the surface of the target cell that contributes to the commitment of a neuroblast to aneuronal fate. The neuron will reside in the forebrain.","definition_xrefs":["GO_REF:0000021","PMID:16226447","GOC:dgh","GOC:dph","GOC:cls","GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete Wnt-activated signaling pathway involved in forebrain neuron fate commitment (obsolete GO:0021881)","synonyms":[{"name":"Wnt receptor signaling pathway involved in forebrain neuron fate commitment","type":"exact"},{"name":"Wnt receptor signalling pathway involved in forebrain neuron fate commitment","type":"exact"}],"termid":"GO:0021881"}


id: PBO:0090028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage and polyadenylation specificity factor complex, metallo-beta-lactamase/beta-CASP protein Cft2","termid":"PBO:0090028"}


id: PBO:0056664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 28 pseudogene 2","termid":"PBO:0056664"}


id: PBO:0090768
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial complex III assembly protein Cbp6","termid":"PBO:0090768"}


id: PBO:0028216
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-fragmented_nucleus_during_cellular_response_to_salt_stress","termid":"PBO:0028216"}


id: PBO:0069497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 764, pseudogene","termid":"PBO:0069497"}


id: GO:1902839
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nuclear migration along microtubule.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:23087209"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of intracellular transport","termid":"GO:0032387"},{"relation_name":"is_a","term_name":"regulation of nuclear migration along microtubule","termid":"GO:1902838"},{"relation_name":"negatively_regulates","term_name":"nuclear migration along microtubule","termid":"GO:0030473"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of nuclear migration along microtubule","synonyms":[{"name":"down regulation of microtubule cytoskeleton-dependent nuclear positioning","type":"exact"},{"name":"down regulation of microtubule cytoskeleton-dependent nucleus positioning","type":"exact"},{"name":"down regulation of microtubule-dependent nuclear positioning","type":"exact"},{"name":"down regulation of microtubule-dependent nucleus positioning","type":"exact"},{"name":"down regulation of microtubule-mediated nuclear migration","type":"exact"},{"name":"down regulation of nuclear migration along microtubule","type":"exact"},{"name":"down regulation of nuclear migration, microtubule-mediated","type":"exact"},{"name":"down regulation of transport of nucleus by microtubules","type":"exact"},{"name":"down regulation of transport of nucleus, microtubule-mediated","type":"exact"},{"name":"down-regulation of microtubule cytoskeleton-dependent nuclear positioning","type":"exact"},{"name":"down-regulation of microtubule cytoskeleton-dependent nucleus positioning","type":"exact"},{"name":"down-regulation of microtubule-dependent nuclear positioning","type":"exact"},{"name":"down-regulation of microtubule-dependent nucleus positioning","type":"exact"},{"name":"down-regulation of microtubule-mediated nuclear migration","type":"exact"},{"name":"down-regulation of nuclear migration along microtubule","type":"exact"},{"name":"down-regulation of nuclear migration, microtubule-mediated","type":"exact"},{"name":"down-regulation of transport of nucleus by microtubules","type":"exact"},{"name":"down-regulation of transport of nucleus, microtubule-mediated","type":"exact"},{"name":"downregulation of microtubule cytoskeleton-dependent nuclear positioning","type":"exact"},{"name":"downregulation of microtubule cytoskeleton-dependent nucleus positioning","type":"exact"},{"name":"downregulation of microtubule-dependent nuclear positioning","type":"exact"},{"name":"downregulation of microtubule-dependent nucleus positioning","type":"exact"},{"name":"downregulation of microtubule-mediated nuclear migration","type":"exact"},{"name":"downregulation of nuclear migration along microtubule","type":"exact"},{"name":"downregulation of nuclear migration, microtubule-mediated","type":"exact"},{"name":"downregulation of transport of nucleus by microtubules","type":"exact"},{"name":"downregulation of transport of nucleus, microtubule-mediated","type":"exact"},{"name":"inhibition of microtubule cytoskeleton-dependent nuclear positioning","type":"narrow"},{"name":"inhibition of microtubule cytoskeleton-dependent nucleus positioning","type":"narrow"},{"name":"inhibition of microtubule-dependent nuclear positioning","type":"narrow"},{"name":"inhibition of microtubule-dependent nucleus positioning","type":"narrow"},{"name":"inhibition of microtubule-mediated nuclear migration","type":"narrow"},{"name":"inhibition of nuclear migration along microtubule","type":"narrow"},{"name":"inhibition of nuclear migration, microtubule-mediated","type":"narrow"},{"name":"inhibition of transport of nucleus by microtubules","type":"narrow"},{"name":"inhibition of transport of nucleus, microtubule-mediated","type":"narrow"},{"name":"negative regulation of microtubule cytoskeleton-dependent nuclear positioning","type":"exact"},{"name":"negative regulation of microtubule cytoskeleton-dependent nucleus positioning","type":"exact"},{"name":"negative regulation of microtubule-dependent nuclear positioning","type":"exact"},{"name":"negative regulation of microtubule-dependent nucleus positioning","type":"exact"},{"name":"negative regulation of microtubule-mediated nuclear migration","type":"exact"},{"name":"negative regulation of nuclear migration, microtubule-mediated","type":"exact"},{"name":"negative regulation of transport of nucleus by microtubules","type":"exact"},{"name":"negative regulation of transport of nucleus, microtubule-mediated","type":"exact"}],"termid":"GO:1902839"}


id: PBO:0067243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 316, pseudogene","termid":"PBO:0067243"}


id: PBO:0038928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor L2","termid":"PBO:0038928"}


id: PBO:0060628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NCKAP5 antisense RNA 2","termid":"PBO:0060628"}


id: GO:1901252
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of egress of virus within host cell.","definition_xrefs":["GOC:jl","GOC:TermGenie","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process involved in symbiotic interaction","termid":"GO:0043903"},{"relation_name":"is_a","term_name":"regulation of viral life cycle","termid":"GO:1903900"},{"relation_name":"regulates","term_name":"intracellular transport of virus","termid":"GO:0075733"}],"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 intracellular transport of viral material","synonyms":[{"name":"regulation of egress of virus within host cell","type":"related"},{"name":"regulation of movement of virus within host cell","type":"exact"},{"name":"regulation of viral egress","type":"exact"}],"termid":"GO:1901252"}


id: GO:0047436
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-aryl-2-methylmalonate + H+ = 2-arylpropionate + CO2.","definition_xrefs":["RHEA:20513","EC:4.1.1.76"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"arylmalonate decarboxylase activity","secondary_identifiers":["KEGG_REACTION:R05173","MetaCyc:4.1.1.76-RXN"],"synonyms":[{"name":"2-aryl-2-methylmalonate carboxy-lyase (2-arylpropanoate-forming)","type":"related"},{"name":"2-aryl-2-methylmalonate carboxy-lyase activity","type":"related"},{"name":"AMDASE","type":"related"},{"name":"AMDase activity","type":"related"}],"termid":"GO:0047436"}


id: FYPO:0000212
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the cellular response to heat is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to stress during vegetative growth","termid":"FYPO:0001341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000298","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal cellular response to heat","synonyms":[{"name":"abnormal cellular response to heat during mitotic cell cycle","type":"related"},{"name":"abnormal cellular response to heat during vegetative growth","type":"exact"}],"termid":"FYPO:0000212"}


id: PBO:0056396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPRE1 pseudogene 3","termid":"PBO:0056396"}


id: PBO:0062027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily P member 1 pseudogene","termid":"PBO:0062027"}


id: PBO:0064953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAME family member 5","termid":"PBO:0064953"}


id: PBO:0085774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein localized to COPII vesicles; proposed to be involved in ER to Golgi transport; interacts with members of the Rab GTPase family and Yip1p; also interacts with Rtn1p","termid":"PBO:0085774"}


id: GO:0097732
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A non-motile cilium where the axoneme has a ring of nine outer microtubule doublets plus two central microtubules (and is therefore called a 9+2 axoneme).","definition_xrefs":["PMID:21307074","PMID:22118931","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-motile cilium","termid":"GO:0097730"}],"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":"9+2 non-motile cilium","synonyms":[{"name":"9+2 immotile cilium","type":"related"},{"name":"non-motile 9+2 cilium","type":"exact"}],"termid":"GO:0097732"}


id: PBO:0069230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 485, pseudogene","termid":"PBO:0069230"}


id: GO:0060045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiac muscle cell proliferation.","definition_xrefs":["GOC:rph","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell population proliferation","termid":"GO:0008284"},{"relation_name":"is_a","term_name":"positive regulation of cardiac muscle tissue growth","termid":"GO:0055023"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle cell proliferation","termid":"GO:0060043"},{"relation_name":"positively_regulates","term_name":"cardiac muscle cell proliferation","termid":"GO:0060038"}],"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 cardiac muscle cell proliferation","synonyms":[{"name":"positive regulation of heart muscle cell proliferation","type":"related"}],"termid":"GO:0060045"}


id: PBO:0071853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 48","termid":"PBO:0071853"}


id: GO:0042333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell or organism in response to the presence of an oxidizable substrate, for example, fructose.","definition_xrefs":["PMID:11029423","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemotaxis","termid":"GO:0006935"},{"relation_name":"is_a","term_name":"energy taxis","termid":"GO:0009453"}],"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":"chemotaxis to oxidizable substrate","synonyms":[{"name":"taxis in response to oxidizable substrate","type":"exact"}],"termid":"GO:0042333"}


id: PBO:0025429
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trichothiodystrophy","termid":"PBO:0025429"}


id: PBO:0053077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LBX2 antisense RNA 1","termid":"PBO:0053077"}


id: PBO:0074724
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 80D","termid":"PBO:0074724"}


id: GO:0010578
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of adenylate cyclase (AC) activity that is an integral part of a G protein-coupled receptor signaling pathway.","definition_xrefs":["GOC:dph","GOC:signaling","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of adenylate cyclase activity involved in G protein-coupled receptor signaling pathway (obsolete GO:0010578)","synonyms":[{"name":"regulation of adenylate cyclase activity involved in G-protein coupled receptor signaling pathway","type":"exact"},{"name":"regulation of adenylate cyclase activity involved in G-protein signaling pathway","type":"exact"},{"name":"regulation of adenylate cyclase activity involved in G-protein signalling","type":"exact"}],"termid":"GO:0010578"}


id: MONDO:0012573
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any vesicoureteral reflux in which the cause of the disease is a mutation in the ROBO2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial vesicoureteral reflux","termid":"MONDO:0017329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicoureteral reflux 2","secondary_identifiers":["UMLS:C1970483","MEDGEN:370270","MESH:C567053","OMIM:610878","GARD:18419"],"synonyms":[{"name":"ROBO2 vesicoureteral reflux (disease)","type":"exact"},{"name":"VUR2","type":"related"},{"name":"vesicoureteral reflux (disease) caused by mutation in ROBO2","type":"exact"},{"name":"vesicoureteral reflux 2","type":"exact"},{"name":"vesicoureteral reflux type 2","type":"exact"}],"termid":"MONDO:0012573","xrefs":{"Monarch":{"xref_id":"0012573"}}}


id: MONDO:0013400
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, developmental defect during embryogenesis disorder characterized by severe, early-onset, salt-wasting adrenal insufficiency and ambiguous/female external genitalia (irrespective of chromosomal sex) due to mutations in the <i>CYP11A1</i> gene. Milder cases may present delayed onset of adrenal gland dysfunction and genitalia phenotype may range from normal male to female in individuals with 46,XY karyotype. Imaging studies reveal hypoplastic/absent adrenal glands and biochemical findings include low serum cortisol, mineralocorticoids, androgens, and sodium, with elevated potassium levels.","definition_xrefs":["Orphanet:168558"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"chronic primary adrenal insufficiency","termid":"MONDO:0015129"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"adrenal gland disorder","termid":"MONDO:0005495"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency","secondary_identifiers":["MEDGEN:462405","DOID:0050546","GARD:17033","MESH:C566130","NCIT:C131422","UMLS:C3151055","OMIM:613743"],"synonyms":[{"name":"46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency","type":"related"},{"name":"46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency syndrome","type":"related"},{"name":"XY sex reversal-adrenal failure","type":"exact"},{"name":"XY sex reversal-adrenal failure syndrome","type":"exact"},{"name":"adrenal insufficiency, congenital, with 46,XY SEX reversal, partial or complete","type":"exact"},{"name":"adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete","type":"exact"},{"name":"cholesterol side-chain cleavage deficiency","type":"exact"},{"name":"p450scc deficiency","type":"exact"}],"termid":"MONDO:0013400","xrefs":{"Monarch":{"xref_id":"0013400"}}}


id: GO:1904546
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any negative regulation of cAMP-dependent protein kinase activity that is involved in negative regulation of glucose mediated signaling pathway.","definition_xrefs":["GOC:TermGenie","GO_REF:0000060","PMID:21118717"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cAMP-dependent protein kinase activity involved in negative regulation of glucose mediated signaling pathway (obsolete GO:1904546)","synonyms":[{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in down regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in down regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in down-regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in down-regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in downregulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in downregulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in inhibition of glucose mediated signaling pathway","type":"narrow"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in inhibition of glucose mediated signalling","type":"narrow"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in negative regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5' cAMP-dependent protein kinase activity involved in negative regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in down regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in down regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in down-regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in down-regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in downregulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in downregulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in inhibition of glucose mediated signaling pathway","type":"narrow"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in inhibition of glucose mediated signalling","type":"narrow"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in negative regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of 3',5'-cAMP-dependent protein kinase activity involved in negative regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of AMPK involved in down regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of AMPK involved in down regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of AMPK involved in down-regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of AMPK involved in down-regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of AMPK involved in downregulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of AMPK involved in downregulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of AMPK involved in inhibition of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of AMPK involved in inhibition of glucose mediated signalling","type":"related"},{"name":"negative regulation of AMPK involved in negative regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of AMPK involved in negative regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in down regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in down regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in down-regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in down-regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in downregulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in downregulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in inhibition of glucose mediated signaling pathway","type":"narrow"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in inhibition of glucose mediated signalling","type":"narrow"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in negative regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of ATP:protein phosphotransferase (cAMP-dependent) activity involved in negative regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of PKA C involved in down regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA C involved in down regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA C involved in down-regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA C involved in down-regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA C involved in downregulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA C involved in downregulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA C involved in inhibition of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA C involved in inhibition of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA C involved in negative regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA C involved in negative regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA involved in down regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA involved in down regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA involved in down-regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA involved in down-regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA involved in downregulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA involved in downregulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA involved in inhibition of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA involved in inhibition of glucose mediated signalling","type":"related"},{"name":"negative regulation of PKA involved in negative regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of PKA involved in negative regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of STK22 involved in down regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of STK22 involved in down regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of STK22 involved in down-regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of STK22 involved in down-regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of STK22 involved in downregulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of STK22 involved in downregulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of STK22 involved in inhibition of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of STK22 involved in inhibition of glucose mediated signalling","type":"related"},{"name":"negative regulation of STK22 involved in negative regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of STK22 involved in negative regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in down regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in down regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in down-regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in down-regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in downregulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in downregulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in inhibition of glucose mediated signaling pathway","type":"narrow"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in inhibition of glucose mediated signalling","type":"narrow"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in negative regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of adenosine 3',5'-cyclophosphate-dependent protein kinase activity involved in negative regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in down regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in down regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in down-regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in down-regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in downregulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in downregulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in inhibition of glucose mediated signaling pathway","type":"narrow"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in inhibition of glucose mediated signalling","type":"narrow"},{"name":"negative regulation of cAMP-dependent protein kinase activity involved in negative regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in down regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in down regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in down-regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in down-regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in downregulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in downregulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in inhibition of glucose mediated signaling pathway","type":"narrow"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in inhibition of glucose mediated signalling","type":"narrow"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in negative regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cAMP-dependent protein kinase, intrinsic catalyst activity involved in negative regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in down regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in down regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in down-regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in down-regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in downregulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in downregulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in inhibition of glucose mediated signaling pathway","type":"narrow"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in inhibition of glucose mediated signalling","type":"narrow"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in negative regulation of glucose mediated signaling pathway","type":"exact"},{"name":"negative regulation of cyclic AMP-dependent protein kinase activity involved in negative regulation of glucose mediated signalling","type":"exact"},{"name":"negative regulation of protein kinase A activity involved in down regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of protein kinase A activity involved in down regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of protein kinase A activity involved in down-regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of protein kinase A activity involved in down-regulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of protein kinase A activity involved in downregulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of protein kinase A activity involved in downregulation of glucose mediated signalling","type":"related"},{"name":"negative regulation of protein kinase A activity involved in inhibition of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of protein kinase A activity involved in inhibition of glucose mediated signalling","type":"related"},{"name":"negative regulation of protein kinase A activity involved in negative regulation of glucose mediated signaling pathway","type":"related"},{"name":"negative regulation of protein kinase A activity involved in negative regulation of glucose mediated signalling","type":"related"}],"termid":"GO:1904546"}


