# terms

id: PBO:0063175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenazine biosynthesis like protein domain containing","termid":"PBO:0063175"}


id: PBO:0046443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPN2 intronic transcript 1","termid":"PBO:0046443"}


id: PBO:0044771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 53","termid":"PBO:0044771"}


id: PBO:0044380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYP1B1 antisense RNA 1","termid":"PBO:0044380"}


id: PBO:0091139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein","termid":"PBO:0091139"}


id: MONDO:1012665
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any lysosomal storage disorder characterized by deficient iduronate-2-sulfatase (IDS) activity that occurs in dogs.","definition_xrefs":["PMID:9598589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis or mucopolysaccharidosis-like disorder, non-human animal","termid":"MONDO:1012581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucopolysaccharidosis II, dog","secondary_identifiers":["OMIA:001317-9615"],"synonyms":[{"name":"Hunter syndrome, dog","type":"related"},{"name":"MPS II","type":"exact"}],"termid":"MONDO:1012665","xrefs":{"Monarch":{"xref_id":"1012665"}}}


id: PBO:0092018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Leucine (uaa), mitochondrial","termid":"PBO:0092018"}


id: FYPO:0007596
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitophagy, i.e. autophagic degradation of the mitochondria, is decreased when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased mitophagy","termid":"FYPO:0000500"},{"relation_name":"is_a","term_name":"abnormal mitophagy during nitrogen starvation","termid":"FYPO:0007593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased mitophagy during nitrogen starvation","synonyms":[{"name":"decreased autophagy of mitochondrion during nitrogen depletion","type":"exact"},{"name":"decreased autophagy of mitochondrion during nitrogen deprivation","type":"exact"},{"name":"decreased autophagy of mitochondrion during nitrogen starvation","type":"exact"},{"name":"reduced autophagy of mitochondrion during nitrogen starvation","type":"exact"}],"termid":"FYPO:0007596"}


id: PBO:0068415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA guanylyltransferase and 5'-phosphatase pseudogene 1","termid":"PBO:0068415"}


id: MONDO:0004670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune, connective tissue chronic inflammatory disorder affecting the skin, joints, kidneys, lungs, heart, and the peripheral blood cells. It is more commonly seen in women than men. Variants include discoid and systemic lupus erythematosus.","definition_xrefs":["NCIT:C27153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"},{"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":"lupus erythematosus","secondary_identifiers":["ICD10CM:L93","icd11.foundation:1443317238","MEDGEN:98043","SCTID:200936003","UMLS:C0409974","ICD9:695.4","DOID:8857"],"synonyms":[{"name":"lupus","type":"exact"},{"name":"lupus erythematosus","type":"exact"}],"termid":"MONDO:0004670","xrefs":{"Monarch":{"xref_id":"0004670"}}}


id: PBO:0071448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 54","termid":"PBO:0071448"}


id: GO:0004090
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a secondary alcohol + NADP+ = a ketone + H+ + NADPH.","definition_xrefs":["RHEA:19257"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol dehydrogenase (NADP+) activity","termid":"GO:0008106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"carbonyl reductase (NADPH) activity","secondary_identifiers":["Reactome:R-HSA-8937419","MetaCyc:CARBONYL-REDUCTASE-NADPH-RXN","EC:1.1.1.184"],"synonyms":[{"name":"ALR3","type":"related"},{"name":"NADPH-dependent carbonyl reductase activity","type":"related"},{"name":"NADPH2-dependent carbonyl reductase activity","type":"related"},{"name":"aldehyde reductase 1","type":"related"},{"name":"aldehyde reductase I activity","type":"related"},{"name":"carbonyl reductase activity","type":"related"},{"name":"nonspecific NADPH-dependent carbonyl reductase activity","type":"related"},{"name":"prostaglandin 9-ketoreductase activity","type":"narrow"},{"name":"secondary-alcohol:NADP+ oxidoreductase activity","type":"related"},{"name":"xenobiotic ketone reductase activity","type":"narrow"}],"termid":"GO:0004090"}


id: MONDO:0010210
data:
  {"annotated_genes":["SJAG_02334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86612],"is_not":false,"summary":null,"term":"MONDO:0010210"}]},"cv_name":"mondo","definition":"Any xeroderma pigmentosum in which the cause of the disease is a mutation in the XPA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xeroderma pigmentosum","termid":"MONDO:0019600"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02334":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0021190","MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"xeroderma pigmentosum group A","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0268135","GARD:5624","NCIT:C3965","DOID:0110843","MEDGEN:82775","OMIM:278700","Orphanet:276249","SCTID:43477006"],"synonyms":[{"name":"XP group A","type":"exact"},{"name":"XP, group A","type":"related"},{"name":"XP-A","type":"exact"},{"name":"XP1","type":"exact"},{"name":"XPA","type":"exact"},{"name":"XPA xeroderma pigmentosum","type":"exact"},{"name":"xeroderma pigmentosum 1","type":"exact"},{"name":"xeroderma pigmentosum caused by mutation in XPA","type":"exact"},{"name":"xeroderma pigmentosum complementation group A","type":"exact"},{"name":"xeroderma pigmentosum group A","type":"exact"},{"name":"xeroderma pigmentosum group type A","type":"exact"},{"name":"xeroderma pigmentosum, complementation group A","type":"related"},{"name":"xeroderma pigmentosum, complementation group type a","type":"exact"},{"name":"xeroderma pigmentosum, group A","type":"exact"},{"name":"xeroderma pigmentosum, type 1","type":"related"}],"termid":"MONDO:0010210","terms_by_termid":{"MONDO:0010210":null},"xrefs":{"Monarch":{"xref_id":"0010210"}}}


id: FYPO:0000994
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 phosphatidylinositol-4-phosphate measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered cellular phosphatidylinositol-4-phosphate level","termid":"FYPO:0001015"},{"relation_name":"is_a","term_name":"increased cellular phosphoinositide level","termid":"FYPO:0001286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular phosphatidylinositol-4-phosphate level","synonyms":[{"name":"increased PI-4-P accumulation","type":"related"},{"name":"increased cellular PI(4)P level","type":"exact"},{"name":"increased cellular PI-4-P level","type":"exact"},{"name":"increased cellular phosphatidylinositol-4-phosphate level during mitotic cell cycle","type":"related"},{"name":"increased cellular phosphatidylinositol-4-phosphate level during vegetative growth","type":"exact"}],"termid":"FYPO:0000994"}


id: PBO:0065733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PWWP domain containing 4","termid":"PBO:0065733"}


id: PBO:0034666
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_microtubule_bundle","termid":"PBO:0034666"}


id: PBO:0079482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taxilin gamma pseudogene, Y-linked","termid":"PBO:0079482"}


id: GO:0005702
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A region of the polytene chromosome where the diameter is considerably decreased, probably resulting from local differences in chromosome organization.","definition_xrefs":["GOC:bf","ISBN:0120649012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"polytene chromosome","termid":"GO:0005700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005575","GO:0005694"],"is_obsolete":false,"name":"polytene chromosome weak point","synonyms":[{"name":"constriction","type":"broad"}],"termid":"GO:0005702"}


id: PBO:0010094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UTP-glucose-1-phosphate uridylyltransferase Fyu1","termid":"PBO:0010094"}


id: GO:0050209
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: polyvinyl alcohol + O2 = oxidized polyvinyl alcohol + H2O2.","definition_xrefs":["EC:1.1.3.30","MetaCyc:POLYVINYL-ALCOHOL-OXIDASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"polyvinyl-alcohol oxidase activity","secondary_identifiers":["RHEA:21688"],"synonyms":[{"name":"PVA oxidase activity","type":"related"},{"name":"dehydrogenase, polyvinyl alcohol","type":"related"},{"name":"polyvinyl-alcohol:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0050209"}


id: GO:1990032
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A parallel fiber results from the bifurcation of a cerebellar granule cell axon in the molecular layer into two diametrically opposed branches, that are oriented parallel to the long axis of the folium.","definition_xrefs":["ISBN:0195159551","NIF_Subcellular:nlx_330"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon","termid":"GO:0030424"}],"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":"parallel fiber","termid":"GO:1990032"}


id: PBO:0061423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAD(P)H quinone dehydrogenase 1","termid":"PBO:0061423"}


id: PBO:0114478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA (adenine) methyltransferase activity Bmt2/human SAMTOR (S-adenosylmethionine sensor for the MTOR) ortholog","termid":"PBO:0114478"}


id: GO:0015691
data:
  {"annotated_genes":["SJAG_03497","SJAG_01007"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036249"},{"annotations":[63827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070574"}]},"cv_name":"biological_process","definition":"The directed movement of cadmium (Cd) ions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transport","termid":"GO:0000041"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01007":null,"SJAG_03497":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"cadmium ion transport","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"cadmium transport","type":"exact"}],"termid":"GO:0015691","terms_by_termid":{"GO:0036249":null,"GO:0070574":null}}


id: MOD:00043
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-phospho-L-cysteine.","definition_xrefs":["RESID:AA0034","Unimod:21#C","PubMed:3142516","PubMed:8128219","PubMed:7961745"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorylated residue","termid":"MOD:00696"},{"relation_name":"is_a","term_name":"residues isobaric at 182.96-182.98 Da","termid":"MOD:00777"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00696"},{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905","MOD:00696"],"is_obsolete":false,"name":"S-phospho-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-(phosphonosulfanyl)propanoic acid","type":"exact"},{"name":"2-azanyl-3-(phosphonosulfanyl)propanoic acid","type":"exact"},{"name":"ACT_SITE Phosphocysteine intermediate","type":"exact"},{"name":"MOD_RES Phosphocysteine","type":"exact"},{"name":"PCys","type":"exact"},{"name":"Phospho","type":"related"},{"name":"Phosphorylation","type":"related"},{"name":"S-phospho-L-cysteine","type":"exact"},{"name":"S-phosphonocysteine","type":"exact"},{"name":"S-phosphorylated L-cysteine","type":"exact"},{"name":"S3-phosphocysteine","type":"exact"},{"name":"cysteine phosphate thioester","type":"exact"}],"termid":"MOD:00043"}


id: PR:O14170
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pop2 gene.","definition_xrefs":["UniProtKB:O14170","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":"WD repeat-containing protein pop2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.03","synonyms":[{"name":"Spom972h-pop2","type":"exact"},{"name":"proteolysis factor sud1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14170"}


id: MONDO:0012532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemorrhagic telangiectasia","termid":"MONDO:0019180"}],"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":"hereditary hemorrhagic telangiectasia type 4","secondary_identifiers":["OMIM:610655","GARD:10615","UMLS:C1857688","MESH:C565691","MEDGEN:341824"],"synonyms":[{"name":"HHT4","type":"related"},{"name":"telangiectasia, hereditary hemorrhagic, type 4","type":"related"}],"termid":"MONDO:0012532","xrefs":{"Monarch":{"xref_id":"0012532"}}}


id: PBO:0025501
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rrm-containing Cyclophilin regulating Transcription","termid":"PBO:0025501"}


id: GO:0048893
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an afferent axon in a lateral line nerve over time from its formation to the mature structure. This process includes axonogenesis and pathfinding of the afferent axons in any lateral line nerve.","definition_xrefs":["PMID:15832385"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon development","termid":"GO:0061564"},{"relation_name":"part_of","term_name":"lateral line nerve development","termid":"GO:0048892"}],"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":"afferent axon development in lateral line nerve","termid":"GO:0048893"}


id: GO:0043156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Structural changes to eukaryotic chromatin occurring as a result of cation stress, an increase or decrease in the concentration of positively charged ions in the environment.","definition_xrefs":["PMID:14762213","GOC:vw","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete chromatin remodeling in response to cation stress (obsolete GO:0043156)","termid":"GO:0043156"}


id: GO:0035457
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interferon-alpha stimulus. Interferon-alpha is a type I interferon.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to interferon-alpha","termid":"GO:0035455"},{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to interferon-alpha","synonyms":[{"name":"cellular response to interferon alfa-n1","type":"related"},{"name":"cellular response to interferon alfa-n3","type":"related"},{"name":"cellular response to leukocyte interferon","type":"exact"},{"name":"cellular response to lymphoblast interferon","type":"exact"},{"name":"cellular response to lymphoblastoid interferon","type":"exact"}],"termid":"GO:0035457"}


id: PBO:0001289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"damaged DNA binding protein Ddb1","termid":"PBO:0001289"}


id: PBO:0090776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology domain protein Meu6","termid":"PBO:0090776"}


id: PBO:0090074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding splicing factor Ntr1","termid":"PBO:0090074"}


id: GO:0016758
data:
  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of the transfer of a hexosyl group from one compound (donor) to another (acceptor).","definition_xrefs":["EC:2.4.1.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosyltransferase 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id: PR:000050542
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding protein gtr1 (Schizosaccharomyces pombe) that is non-covalently bound to GDP.","definition_xrefs":["PomBase:VW","PMID:33534698","PMID:27227887","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"},{"relation_name":"is_a","term_name":"GTP-binding protein gtr1 (Schizosaccharomyces pombe)","termid":"PR:000050541"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gtr1/GDP+","pombase_gene_id":"SPBC337.13c","synonyms":[{"name":"PomBase_original_PRO_term_name: GTP-binding protein gtr1, GDP-bound form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-gtr1/GDP+","type":"exact"},{"name":"gtr1/GDP+","type":"exact"},{"name":"Gtr1/GDP+","type":"exact"}],"termid":"PR:000050542"}


id: GO:0060640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that initiates the formation of a tooth bud by the secretion of a signal from a mesenchymal cell and its reception and subsequent change in the identity of an epithelial cell of the tooth bud.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of odontogenesis of dentin-containing tooth","termid":"GO:0042488"},{"relation_name":"is_a","term_name":"mesenchymal-epithelial cell signaling","termid":"GO:0060638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of dentin-containing tooth bud formation by mesenchymal-epithelial signaling","synonyms":[{"name":"positive regulation of dentine-containing tooth bud formation by mesenchymal-epithelial signaling","type":"related"},{"name":"positive regulation of dentine-containing tooth bud formation by mesenchymal-epithelial signalling","type":"exact"}],"termid":"GO:0060640"}


id: PBO:0062852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otoferlin","termid":"PBO:0062852"}


id: GO:0048529
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: magnesium protoporphyrin IX 13-monomethyl ester + 3 NADPH + 3 H+ + 3 O2 = divinylprotochlorophyllide + 3 NADP+ + 5 H2O.","definition_xrefs":["EC:1.14.13.81","RHEA:33235"],"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:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"magnesium-protoporphyrin IX monomethyl ester (oxidative) cyclase activity","synonyms":[{"name":"Mg-protoporphyrin IX monomethyl ester (oxidative) cyclase activity","type":"related"},{"name":"Mg-protoporphyrin IX monomethyl ester oxidative cyclase activity","type":"related"},{"name":"magnesium-protoporphyrin-IX 13-monomethyl ester,NADPH:oxygen oxidoreductase (hydroxylating)","type":"related"}],"termid":"GO:0048529"}


id: SO:0000908
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute to describe a feature that has been predicted using sequence similarity of a known domain.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supported_by_sequence_similarity","termid":"SO:0000907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"supported_by_domain_match","synonyms":[{"name":"supported by domain match","type":"exact"}],"termid":"SO:0000908"}


id: GO:0022400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of opsin-mediated signaling.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor signaling pathway","termid":"GO:0008277"},{"relation_name":"is_a","term_name":"regulation of response to external stimulus","termid":"GO:0032101"},{"relation_name":"regulates","term_name":"G protein-coupled opsin signaling pathway","termid":"GO:0016056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of opsin-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-2514859"],"synonyms":[{"name":"regulation of rhodopsin mediated signaling pathway","type":"exact"},{"name":"regulation of rhodopsin mediated signalling","type":"exact"},{"name":"regulation of rhodopsin-mediated signaling pathway","type":"narrow"}],"termid":"GO:0022400"}


id: PBO:0113109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUP240 Family Protein","termid":"PBO:0113109"}


id: FYPO:0002842
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the centromere outer repeat regions of a chromosome is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during vegetative growth","termid":"FYPO:0000449"},{"relation_name":"is_a","term_name":"decreased protein localization to chromosome during vegetative growth","termid":"FYPO:0002839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to centromere outer repeat","synonyms":[{"name":"decreased protein localisation to centromere outer repeat","type":"exact"},{"name":"decreased protein localisation to centromeric outer repeat region","type":"exact"},{"name":"decreased protein localization to centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased protein localization to chromosome, centric outer repeat region","type":"exact"},{"name":"decreased protein localization to chromosome, centromeric outer repeat region","type":"exact"},{"name":"decreased protein localization to pericentric region","type":"related"},{"name":"decreased protein localization to pericentromeric region","type":"related"},{"name":"reduced protein localization to centromere outer repeat","type":"exact"}],"termid":"FYPO:0002842"}


id: MONDO:0013821
data:
  {"annotated_genes":["SJAG_04755","SJAG_05313"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86248,86249],"is_not":false,"summary":null,"term":"MONDO:0013821"}]},"cv_name":"mondo","definition":"Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCA4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"Coffin-Siris syndrome","termid":"MONDO:0015452"},{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04755":null,"SJAG_05313":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual disability, autosomal dominant 16","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:766163","GARD:15822","OMIM:614609","UMLS:C3553249","DOID:0070046"],"synonyms":[{"name":"COFFIN-SIRIS syndrome 4","type":"exact"},{"name":"CSS4","type":"exact"},{"name":"Coffin-Siris syndrome caused by mutation in SMARCA4","type":"exact"},{"name":"MRD16","type":"exact"},{"name":"SMARCA4 Coffin-Siris syndrome","type":"exact"},{"name":"SMARCA4-related BAFopathy","type":"exact"},{"name":"autosomal dominant intellectual disability 16","type":"exact"},{"name":"autosomal dominant mental retardation 16","type":"exact"},{"name":"intellectual disability, autosomal dominant 16","type":"exact"},{"name":"intellectual disability, autosomal dominant type 16","type":"exact"},{"name":"mental retardation, autosomal dominant 16","type":"related"},{"name":"mental retardation, autosomal dominant type 16","type":"exact"}],"termid":"MONDO:0013821","terms_by_termid":{"MONDO:0013821":null},"xrefs":{"Monarch":{"xref_id":"0013821"}}}


id: GO:0140888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by type II interferon binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription. Type II interferon is also known as interferon-gamma.","definition_xrefs":["GOC:dph","PMID:32464097","GOC:add","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"interferon-mediated signaling pathway","synonyms":[{"name":"interferon signaling pathway","type":"exact"},{"name":"interferon-activated signaling pathway","type":"exact"}],"termid":"GO:0140888"}


id: PBO:0109607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A15","termid":"PBO:0109607"}


id: PBO:0081135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP28 divergent transcript","termid":"PBO:0081135"}


id: PBO:0049520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A.L variant histone 1Q","termid":"PBO:0049520"}


id: MONDO:0015076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of tumor of parathyroid gland that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare parathyroid tumor (obsolete MONDO:0015076)","secondary_identifiers":["ICD10CM:D35.1","Orphanet:100090"],"synonyms":[{"name":"rare tumor of parathyroid gland","type":"exact"}],"termid":"MONDO:0015076","xrefs":{"Monarch":{"xref_id":"0015076"}}}


id: PBO:0075623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SREBF pathway regulator in golgi 1","termid":"PBO:0075623"}


id: PBO:0062324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily C member 6","termid":"PBO:0062324"}


id: MONDO:0018585
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"arterial disorder","termid":"MONDO:0000473"},{"relation_name":"is_a","term_name":"stroke disorder","termid":"MONDO:0005098"},{"relation_name":"is_a","term_name":"brain ischemia","termid":"MONDO:0005299"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pediatric arterial ischemic stroke","secondary_identifiers":["GARD:21824","MEDGEN:1803840","Orphanet:439175","UMLS:C5680049"],"synonyms":[{"name":"childhood AIS","type":"exact"},{"name":"childhood arterial ischaemic stroke","type":"exact"},{"name":"childhood arterial ischemic stroke","type":"exact"},{"name":"paediatric AIS","type":"exact"},{"name":"pediatric AIS","type":"exact"}],"termid":"MONDO:0018585","xrefs":{"Monarch":{"xref_id":"0018585"}}}


id: PBO:0042251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper chaperone for superoxide dismutase","termid":"PBO:0042251"}


id: GO:0071328
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 maltose stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to maltose","termid":"GO:0034286"},{"relation_name":"is_a","term_name":"cellular response to disaccharide stimulus","termid":"GO:0071324"}],"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 maltose stimulus","termid":"GO:0071328"}


id: GO:1902995
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of phospholipid efflux.","definition_xrefs":["GOC:TermGenie","GOC:sjp","PMID:12042316","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phospholipid efflux","termid":"GO:1902994"},{"relation_name":"is_a","term_name":"positive regulation of phospholipid transport","termid":"GO:2001140"},{"relation_name":"positively_regulates","term_name":"phospholipid efflux","termid":"GO:0033700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of phospholipid efflux","synonyms":[{"name":"activation of phospholipid efflux","type":"narrow"},{"name":"activation of phospholipid export","type":"narrow"},{"name":"positive regulation of phospholipid export","type":"exact"},{"name":"up regulation of phospholipid efflux","type":"exact"},{"name":"up regulation of phospholipid export","type":"exact"},{"name":"up-regulation of phospholipid efflux","type":"exact"},{"name":"up-regulation of phospholipid export","type":"exact"},{"name":"upregulation of phospholipid efflux","type":"exact"},{"name":"upregulation of phospholipid export","type":"exact"}],"termid":"GO:1902995"}


id: PBO:0084224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hsp70 protein that interacts with Zuo1p (a DnaJ homolog); interacts with Zuo1p to form a ribosome-associated complex that binds the ribosome via the Zuo1p subunit; also involved in pleiotropic drug resistance via sequential activation of PDR1 and PDR5; binds ATP","termid":"PBO:0084224"}


id: PBO:0061157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NmrA like redox sensor 2, pseudogene","termid":"PBO:0061157"}


id: GO:0050428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 3'-phosphoadenosine 5'-phosphosulfate, a naturally occurring mixed anhydride. It is an intermediate in the formation of a variety of sulfo compounds in biological systems.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide biosynthetic process","termid":"GO:0009152"},{"relation_name":"is_a","term_name":"purine ribonucleoside bisphosphate biosynthetic process","termid":"GO:0034036"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"},{"relation_name":"is_a","term_name":"3'-phosphoadenosine 5'-phosphosulfate metabolic process","termid":"GO:0050427"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"3'-phosphoadenosine 5'-phosphosulfate biosynthetic process","secondary_identifiers":["MetaCyc:PWY-5340"],"synonyms":[{"name":"3'-phosphoadenosine 5'-phosphosulfate anabolism","type":"exact"},{"name":"3'-phosphoadenosine 5'-phosphosulfate biosynthesis","type":"exact"},{"name":"3'-phosphoadenosine 5'-phosphosulfate formation","type":"exact"},{"name":"3'-phosphoadenosine 5'-phosphosulfate synthesis","type":"exact"},{"name":"3'-phosphoadenosine 5'-phosphosulphate biosynthesis","type":"exact"},{"name":"3'-phosphoadenosine 5'-phosphosulphate biosynthetic process","type":"exact"},{"name":"3'-phosphoadenylyl-sulfate biosynthesis","type":"exact"},{"name":"3'-phosphoadenylyl-sulfate biosynthetic process","type":"exact"},{"name":"PAPS biosynthesis","type":"exact"},{"name":"PAPS biosynthetic process","type":"exact"},{"name":"adenosine 3'-phosphate 5'-phosphosulfate biosynthesis","type":"exact"},{"name":"adenosine 3'-phosphate 5'-phosphosulfate biosynthetic process","type":"exact"},{"name":"phosphoadenosine phosphosulfate biosynthesis","type":"exact"},{"name":"phosphoadenosine phosphosulfate biosynthetic process","type":"exact"}],"termid":"GO:0050428"}


id: PBO:0062571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily B member 1 pseudogene","termid":"PBO:0062571"}


id: GO:0006939
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within smooth muscle tissue, resulting in a change in muscle geometry. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. Smooth muscle differs from striated muscle in the much higher actin/myosin ratio, the absence of conspicuous sarcomeres and the ability to contract to a much smaller fraction of its resting length.","definition_xrefs":["GOC:ef","GOC:jl","GOC:mtg_muscle","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle contraction","termid":"GO:0006936"}],"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":"smooth muscle contraction","synonyms":[{"name":"visceral muscle contraction","type":"exact"}],"termid":"GO:0006939"}


id: GO:0120291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that inhibits or decreases the rate of mitotic recombination-dependent replication fork processing. Suppression of recombination at replication forks is necessary to prevent template switching.","definition_xrefs":["PMID:30667359","GOC:mah","PMID:31149897","GOC:krc","PMID:28586299"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"negative regulation of DNA metabolic process","termid":"GO:0051053"},{"relation_name":"is_a","term_name":"regulation of mitotic recombination-dependent replication fork processing","termid":"GO:1903221"},{"relation_name":"negatively_regulates","term_name":"mitotic recombination-dependent replication fork processing","termid":"GO:1990426"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mitotic recombination-dependent replication fork processing","synonyms":[{"name":"maintenance of template fidelity during replication fork processing","type":"exact"},{"name":"negative regulation of mitotic recombination involved in replication fork processing","type":"related"},{"name":"negative regulation of template switch recombination involved in replication fork processing","type":"exact"},{"name":"suppression of template switching during replication fork processing","type":"exact"}],"termid":"GO:0120291"}


id: PBO:0070120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 34 pseudogene","termid":"PBO:0070120"}


id: MONDO:0005132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A herpesvirus infection caused by Cytomegalovirus. Healthy individuals generally do not produce symptoms. However, the infection may be life-threatening in affected immunocompromised patients. The virus may cause retinitis, esophagitis, gastritis, and colitis. Morphologically, it is characterized by the presence of intranuclear inclusion bodies.","definition_xrefs":["NCIT:C53649"],"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":"cytomegalovirus infection","secondary_identifiers":["MEDGEN:8239","SCTID:28944009","MESH:D003586","EFO:0001062","UMLS:C0010823","ICD9:078.5"],"synonyms":[{"name":"CMV infection","type":"exact"},{"name":"Cytomegaloviral infection","type":"exact"},{"name":"HCMV infection","type":"exact"}],"termid":"MONDO:0005132","xrefs":{"Monarch":{"xref_id":"0005132"}}}


id: PBO:0081607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF529 antisense RNA 1","termid":"PBO:0081607"}


id: MONDO:1010046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Patent urachus that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary system disorder, non-human animal","termid":"MONDO:1011365"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patent urachus, non-human animal","secondary_identifiers":["OMIA:000781"],"termid":"MONDO:1010046","xrefs":{"Monarch":{"xref_id":"1010046"}}}


id: PBO:0086694
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; in many strains, YML002W is continuous with YML003W, and is predicted to encode a single protein of 1090 aa with a full-length VPS9 domain; in strains S288C, W303, and CEN.PK, a single thymine residue is deleted near the 3' end of YML003W at ChrXIII:264337, causing a frameshift and premature stop codon, truncating YML003W","termid":"PBO:0086694"}


id: GO:0051613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of serotonin into a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of neurotransmitter uptake","termid":"GO:0051582"},{"relation_name":"is_a","term_name":"regulation of serotonin uptake","termid":"GO:0051611"},{"relation_name":"positively_regulates","term_name":"serotonin uptake","termid":"GO:0051610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of serotonin uptake","synonyms":[{"name":"activation of serotonin uptake","type":"narrow"},{"name":"positive regulation of 5-HT uptake","type":"exact"},{"name":"positive regulation of 5-hydroxytryptamine uptake","type":"exact"},{"name":"positive regulation of 5HT uptake","type":"exact"},{"name":"positive regulation of serotonin import","type":"exact"},{"name":"stimulation of serotonin uptake","type":"narrow"},{"name":"up regulation of serotonin uptake","type":"exact"},{"name":"up-regulation of serotonin uptake","type":"exact"},{"name":"upregulation of serotonin uptake","type":"exact"}],"termid":"GO:0051613"}


id: MOD:01451
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that converts an L-serine residue to O-phosphopantetheine-L-serine with secondary neutral loss of pantetheine resulting in O-phospho-L-serine.","definition_xrefs":["PubMed:17042494","PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"O-phosphopantetheine-L-serine","termid":"MOD:00159"},{"relation_name":"is_a","term_name":"O-phospho-L-serine","termid":"MOD:00046"},{"relation_name":"is_a","term_name":"modified residue with a secondary neutral loss","termid":"MOD:00431"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00696"}],"interesting_parent_ids":["MOD:00696"],"is_obsolete":false,"name":"O-phospho-L-serine arising from O-phosphopantetheine-L-serine after neutral loss of pantetheine","termid":"MOD:01451"}


id: GO:0102477
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 6C-glucosyl-2,5,7-trihydroxyflavanone = H+ + 6C-hexosyl chrysin + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,5,7-trihydroxyflavanone 6C-glucoside dehydratase activity (obsolete GO:0102477)","termid":"GO:0102477"}


id: PBO:0001617
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.41","termid":"PBO:0001617"}


id: GO:0002657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of tolerance induction to nonself antigen.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tolerance induction dependent upon immune response","termid":"GO:0002654"},{"relation_name":"is_a","term_name":"regulation of tolerance induction to nonself antigen","termid":"GO:0002655"},{"relation_name":"positively_regulates","term_name":"tolerance induction to nonself antigen","termid":"GO:0002462"}],"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 tolerance induction to nonself antigen","synonyms":[{"name":"activation of tolerance induction to nonself antigen","type":"narrow"},{"name":"stimulation of tolerance induction to nonself antigen","type":"narrow"},{"name":"up regulation of tolerance induction to nonself antigen","type":"exact"},{"name":"up-regulation of tolerance induction to nonself antigen","type":"exact"},{"name":"upregulation of tolerance induction to nonself antigen","type":"exact"}],"termid":"GO:0002657"}


id: GO:0042939
data:
  {"annotated_genes":["SJAG_01344","SJAG_03497","SJAG_05213","SJAG_01983","SJAG_03577","SJAG_01660"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098709"},{"annotations":[113153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160007"},{"annotations":[118233,97037,96045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071996"},{"annotations":[103015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140207"}]},"cv_name":"biological_process","definition":"The directed movement of a tripeptide, a compound containing three amino acids linked together by peptide bonds, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligopeptide transport","termid":"GO:0006857"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01344":null,"SJAG_01660":null,"SJAG_01983":null,"SJAG_03497":null,"SJAG_03577":null,"SJAG_05213":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":"tripeptide transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0042939","terms_by_termid":{"GO:0071996":null,"GO:0098709":null,"GO:0140207":null,"GO:0160007":null}}


id: PBO:0065610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTP4A1 pseudogene 4","termid":"PBO:0065610"}


id: GO:1902523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein K63-linked ubiquitination.","definition_xrefs":["PMID:21931591","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein K63-linked ubiquitination","termid":"GO:1900044"},{"relation_name":"is_a","term_name":"positive regulation of protein polyubiquitination","termid":"GO:1902916"},{"relation_name":"positively_regulates","term_name":"protein K63-linked ubiquitination","termid":"GO:0070534"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0070647"},{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0070647"],"is_obsolete":false,"name":"positive regulation of protein K63-linked ubiquitination","synonyms":[{"name":"activation of protein K63-linked polyubiquitination","type":"narrow"},{"name":"activation of protein K63-linked ubiquitination","type":"narrow"},{"name":"positive regulation of protein K63-linked polyubiquitination","type":"exact"},{"name":"up regulation of protein K63-linked polyubiquitination","type":"exact"},{"name":"up regulation of protein K63-linked ubiquitination","type":"exact"},{"name":"up-regulation of protein K63-linked polyubiquitination","type":"exact"},{"name":"up-regulation of protein K63-linked ubiquitination","type":"exact"},{"name":"upregulation of protein K63-linked polyubiquitination","type":"exact"},{"name":"upregulation of protein K63-linked ubiquitination","type":"exact"}],"termid":"GO:1902523"}


id: MONDO:0042600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sammartino-Decreccio syndrome","secondary_identifiers":["MEDGEN:419806","UMLS:C2931447"],"synonyms":[{"name":"Sammartino Decreccio syndrome","type":"related"},{"name":"superficial annular corneal dystrophy, ichthyosis nigrans, microcephaly and mild mental subnormality","type":"related"}],"termid":"MONDO:0042600","xrefs":{"Monarch":{"xref_id":"0042600"}}}


id: GO:0055050
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The aggregation, arrangement and bonding together of a set of components to form the astral spindle in male meiotic cells.","definition_xrefs":["GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete astral spindle assembly involved in male meiosis (obsolete GO:0055050)","termid":"GO:0055050"}


id: PBO:0117021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KRT86 antisense RNA 2","termid":"PBO:0117021"}


id: MONDO:0800402
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited retinopathy caused by bi-allelic variants in the TRPM1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"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":"TRPM1-related retinopathy","termid":"MONDO:0800402","xrefs":{"Monarch":{"xref_id":"0800402"}}}


id: GO:0048139
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of a single follicular epithelium around the germ-line derived cells of a cyst formed in the female gonad.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"germ-line cyst encapsulation","termid":"GO:0048138"},{"relation_name":"part_of","term_name":"female gamete generation","termid":"GO:0007292"}],"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":"female germ-line cyst encapsulation","termid":"GO:0048139"}


id: PBO:0064866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 26","termid":"PBO:0064866"}


id: MONDO:0019081
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete alopecia universalis (obsolete MONDO:0019081)","termid":"MONDO:0019081","xrefs":{"Monarch":{"xref_id":"0019081"}}}


id: GO:1903797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of inorganic anion transmembrane transport.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:11336802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of transmembrane transport","termid":"GO:0034764"},{"relation_name":"is_a","term_name":"regulation of inorganic anion transmembrane transport","termid":"GO:1903795"},{"relation_name":"positively_regulates","term_name":"inorganic anion transmembrane transport","termid":"GO:0098661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of inorganic anion transmembrane transport","synonyms":[{"name":"activation of inorganic anion membrane transport","type":"narrow"},{"name":"activation of inorganic anion transmembrane transport","type":"narrow"},{"name":"activation of transmembrane inorganic anion transport","type":"narrow"},{"name":"positive regulation of inorganic anion membrane transport","type":"exact"},{"name":"positive regulation of transmembrane inorganic anion transport","type":"exact"},{"name":"up regulation of inorganic anion membrane transport","type":"exact"},{"name":"up regulation of inorganic anion transmembrane transport","type":"exact"},{"name":"up regulation of transmembrane inorganic anion transport","type":"exact"},{"name":"up-regulation of inorganic anion membrane transport","type":"exact"},{"name":"up-regulation of inorganic anion transmembrane transport","type":"exact"},{"name":"up-regulation of transmembrane inorganic anion transport","type":"exact"},{"name":"upregulation of inorganic anion membrane transport","type":"exact"},{"name":"upregulation of inorganic anion transmembrane transport","type":"exact"},{"name":"upregulation of transmembrane inorganic anion transport","type":"exact"}],"termid":"GO:1903797"}


id: GO:0035920
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 high voltage-gated calcium channel in another organism. A high voltage-gated channel is a channel whose open state is dependent on high voltage across the membrane in which it is embedded.","definition_xrefs":["GOC:bf","ISBN:0815340729","PMID:20920515","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of high voltage-gated calcium channel activity in another organism (obsolete GO:0035920)","synonyms":[{"name":"down-regulation of high voltage-gated calcium channel activity in other organism","type":"exact"},{"name":"downregulation of high voltage-gated calcium channel activity in other organism","type":"exact"},{"name":"inhibition of high voltage-gated calcium channel activity in other organism","type":"narrow"},{"name":"negative regulation of high voltage gated calcium channel activity in other organism","type":"exact"},{"name":"negative regulation of high voltage-dependent calcium channel activity in other organism","type":"exact"},{"name":"negative regulation of high voltage-gated calcium channel activity in other organism","type":"exact"}],"termid":"GO:0035920"}


id: PBO:0069111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 360, pseudogene","termid":"PBO:0069111"}


id: PBO:0029947
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_tyrosine_phosphorylation_during_cellular_response_to_osmotic_stress","termid":"PBO:0029947"}


id: FYPO:0001907
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell is unable to synthesize thiamine, and therefore requires thiamine in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxotrophy","termid":"FYPO:0000128"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype","termid":"FYPO:0004638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"growth auxotrophic for thiamine","synonyms":[{"name":"growth auxotrophic for thiamin","type":"exact"},{"name":"growth auxotrophic for thiamine during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for thiamine during vegetative growth","type":"exact"},{"name":"growth auxotrophic for vitamin B1","type":"exact"},{"name":"thiamine auxotrophy","type":"exact"}],"termid":"FYPO:0001907"}


id: GO:0098964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a messenger ribonucleoprotein complex along microtubules in nerve cell dendrites towards the postsynapse.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterograde dendritic transport","termid":"GO:0098937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"anterograde dendritic transport of messenger ribonucleoprotein complex","synonyms":[{"name":"anterograde dendritic transport of mRNA RNP complex","type":"exact"}],"termid":"GO:0098964"}


id: PATO:0000232
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000232 taste (obsolete PATO:0000232)","termid":"PATO:0000232"}


id: MONDO:1012605
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease that occurs in dogs due to a glycogen branching enzyme (GBE) deficiency.","definition_xrefs":["OMIA:000420-9615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease, non-human animal","termid":"MONDO:1011419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogen storage disease IV, dog","termid":"MONDO:1012605","xrefs":{"Monarch":{"xref_id":"1012605"}}}


id: FYPO:0004033
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at tRNA genes is increased.","definition_xrefs":["PomBase:mah","PMID:25392932"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to chromatin at ncRNA genes","termid":"FYPO:0007011"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased protein localization to chromatin at tRNA genes","synonyms":[{"name":"increased protein localisation to chromatin at tRNA genes","type":"exact"},{"name":"increased protein localization to chromatin at tRNA genes during mitotic cell cycle","type":"related"},{"name":"increased protein localization to chromatin at tRNA genes during vegetative growth","type":"exact"},{"name":"increased protein localization to chromatin at transfer RNA genes","type":"exact"}],"termid":"FYPO:0004033"}


id: GO:1904367
data:
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id: GO:0072571
data:
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id: PBO:0085794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; component of the SWR1 complex, which exchanges histone variant H2AZ (Htz1p) for chromatin-bound histone H2A; required for formation of nuclear-associated array of smooth endoplasmic reticulum known as karmellae","termid":"PBO:0085794"}


id: PBO:0054017
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 1347","termid":"PBO:0054017"}


id: PBO:0061932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 1 subfamily L member 3","termid":"PBO:0061932"}


id: PR:Q9URV6
data:
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id: GO:0051649
data:
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id: GO:0008456
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of terminal non-reducing N-acetyl-D-galactosamine residues in N-acetyl-alpha-D-galactosaminides.","definition_xrefs":["EC:3.2.1.49"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosaminidase activity","termid":"GO:0015929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016798","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"alpha-N-acetylgalactosaminidase activity","secondary_identifiers":["MetaCyc:3.2.1.49-RXN","RHEA:15085"],"synonyms":[{"name":"N-acetyl-alpha-D-galactosaminidase activity","type":"related"},{"name":"N-acetyl-alpha-galactosaminidase activity","type":"related"},{"name":"alpha-N-acetyl-D-galactosaminide N-acetylgalactosaminohydrolase activity","type":"related"},{"name":"alpha-NAGA activity","type":"related"},{"name":"alpha-acetylgalactosaminidase activity","type":"related"},{"name":"alpha-galactosidase B activity","type":"related"}],"termid":"GO:0008456"}


id: MONDO:0003748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An overwhelming, irrational, and persistent fear of traveling in an aircraft.","definition_xrefs":["NCIT:C35413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specific phobia","termid":"MONDO:0012000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flying phobia","secondary_identifiers":["UMLS:C0344318","DOID:605","EFO:1001889","MEDGEN:83369"],"termid":"MONDO:0003748","xrefs":{"Monarch":{"xref_id":"0003748"}}}


id: GO:1990667
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of the serine protease PCSK9 (proprotein convertase subtilisin/kexin-9) and annexin A2 (AnxA2).","definition_xrefs":["GOC:nc","GOC:BHF","PMID:22848640"],"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":"PCSK9-AnxA2 complex","synonyms":[{"name":"PCSK9-Annexin A2 complex","type":"exact"},{"name":"PCSK9.AnxA2 complex","type":"exact"},{"name":"PCSK9:ANXA2 complex","type":"exact"}],"termid":"GO:1990667"}


id: GO:0045633
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mechanoreceptor differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mechanoreceptor differentiation","termid":"GO:0045631"},{"relation_name":"is_a","term_name":"positive regulation of neuron differentiation","termid":"GO:0045666"},{"relation_name":"positively_regulates","term_name":"mechanoreceptor differentiation","termid":"GO:0042490"}],"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 mechanoreceptor differentiation","synonyms":[{"name":"activation of mechanoreceptor differentiation","type":"narrow"},{"name":"stimulation of mechanoreceptor differentiation","type":"narrow"},{"name":"up regulation of mechanoreceptor differentiation","type":"exact"},{"name":"up-regulation of mechanoreceptor differentiation","type":"exact"},{"name":"upregulation of mechanoreceptor differentiation","type":"exact"}],"termid":"GO:0045633"}


id: PBO:0045528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deltex E3 ubiquitin ligase 1","termid":"PBO:0045528"}


id: PATO:0002385
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being marked by narrow lines, usually parallel, with at least one salient angle on the margin","definition_xrefs":["FNA:FNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striated","termid":"PATO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"striate-angular","termid":"PATO:0002385"}


id: GO:0042730
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that solubilizes fibrin in the bloodstream of a multicellular organism, chiefly by the proteolytic action of plasmin.","definition_xrefs":["PMID:15842654","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of blood coagulation","termid":"GO:0030195"}],"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":"fibrinolysis","secondary_identifiers":["Reactome:R-HSA-75205","Wikipedia:Fibrinolysis"],"termid":"GO:0042730"}


id: MONDO:0018470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Renal agenesis (RA) is a form of renal tract malformation characterized by the complete absence of development of one or both kidneys (unilateral RA or bilateral RA respectively), accompanied by absent ureter(s).","definition_xrefs":["Orphanet:411709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"}],"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":"renal agenesis","secondary_identifiers":["SCTID:204942005","OMIMPS:191830","DOID:14766","GARD:9228","HP:0008678","MEDGEN:154237","HP:0000104","NCIT:C99041","NANDO:2200156","icd11.foundation:683319223","UMLS:C0542519"],"synonyms":[{"name":"absent/small kidney","type":"exact"},{"name":"absent/underdeveloped kidney","type":"exact"},{"name":"hereditary renal aplasia","type":"exact"},{"name":"hereditary urogenital adysplasia","type":"exact"},{"name":"renal adysplasia","type":"exact"},{"name":"renal agenesis","type":"exact"},{"name":"renal agenesis (disease)","type":"exact"},{"name":"renal agenesis/hypoplasia","type":"exact"},{"name":"renal aplasia","type":"exact"},{"name":"renal hypodysplasia/aplasia","type":"related"}],"termid":"MONDO:0018470","xrefs":{"Monarch":{"xref_id":"0018470"}}}


id: GO:0070905
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 2-amino-3-hydroxypropanoic acid.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid binding","termid":"GO:0016597"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"serine binding","synonyms":[{"name":"Ser binding","type":"exact"}],"termid":"GO:0070905"}


id: GO:0045862
data:
  {"annotated_genes":["SJAG_01210","SJAG_00712","SJAG_03048","SJAG_00766","SJAG_02723","SJAG_00077","SJAG_01131","SJAG_03699","SJAG_00642","SJAG_01544","SJAG_01489","SJAG_04477","SJAG_00071"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89916],"is_not":false,"summary":null,"term":"GO:0045862"},{"annotations":[88900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[67084,61472,65590,68118,66860,68463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901800"},{"annotations":[117098,106671,108910,111729,102386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the hydrolysis of a peptide bond or bonds within a protein.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proteolysis","termid":"GO:0030162"},{"relation_name":"is_a","term_name":"positive regulation of protein metabolic process","termid":"GO:0051247"},{"relation_name":"positively_regulates","term_name":"proteolysis","termid":"GO:0006508"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00077":null,"SJAG_00642":null,"SJAG_00712":null,"SJAG_00766":null,"SJAG_01131":null,"SJAG_01210":null,"SJAG_01489":null,"SJAG_01544":null,"SJAG_02723":null,"SJAG_03048":null,"SJAG_03699":null,"SJAG_04477":null},"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 proteolysis","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"activation of proteolysis","type":"narrow"},{"name":"positive regulation of peptidolysis","type":"exact"},{"name":"stimulation of proteolysis","type":"narrow"},{"name":"up regulation of proteolysis","type":"exact"},{"name":"up-regulation of proteolysis","type":"exact"},{"name":"upregulation of proteolysis","type":"exact"}],"termid":"GO:0045862","terms_by_termid":{"GO:0032436":null,"GO:0045862":null,"GO:1901800":null,"GO:1905786":null}}


id: MONDO:0005191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanoma that has spread from its primary site to another anatomic site. Melanomas frequently metastasize to lymph nodes, liver, lungs, and brain.","definition_xrefs":["NCIT:C8925"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanoma","termid":"MONDO:0005105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metastatic melanoma","secondary_identifiers":["MEDGEN:83002","EFO:0002617","UMLS:C0278883","SCTID:443493003"],"synonyms":[{"name":"metastatic malignant melanoma","type":"exact"},{"name":"metastatic melanoma","type":"exact"}],"termid":"MONDO:0005191","xrefs":{"Monarch":{"xref_id":"0005191"}}}


id: GO:0103078
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + quercetin 3-O-rhamnoside + UDP-L-rhamnose = quercetin-3-rhamnoside-7-rhamnoside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete quercetin 3-rhamnoside 7-O-rhamnosyltransferase activity (obsolete GO:0103078)","termid":"GO:0103078"}


id: PBO:0036398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribose diphosphatase, NudF subfamily Ysa1 (predicted)","termid":"PBO:0036398"}


id: MONDO:0009321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hallux varus-preaxial polysyndactyly syndrome is a rare, genetic, congenital limb malformation disorder characterized by bilateral medial displacement of the hallux and preaxial polysyndactyly of the first toes. Radiographs show broad, shortened, misshapen first metatarsals and may associate incomplete or complete duplication of proximal phalanges and duplication or triplication of distal phalanges. There have been no further descriptions in the literature since 1980.","definition_xrefs":["Orphanet:2110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hallux varus-preaxial polysyndactyly syndrome","secondary_identifiers":["MEDGEN:341088","OMIM:234280","GARD:3118","MESH:C536885","UMLS:C1856197"],"synonyms":[{"name":"Kleiner Holmes syndrome","type":"related"},{"name":"Kleiner-Holmes syndrome","type":"exact"},{"name":"hallux varus and preaxial polysyndactyly","type":"related"}],"termid":"MONDO:0009321","xrefs":{"Monarch":{"xref_id":"0009321"}}}


id: FYPO:0004761
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 histone exchange occurs to a greater extent than normal in regions of pericentric heterochromatin. Histone exchange is replacement, within chromatin, of resident histones or histone subunits with alternative, sometimes variant, histones or subunits.","definition_xrefs":["GO:0043486","PomBase:mah","GO:0005721","PMID:24095277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"},{"relation_name":"is_a","term_name":"increased protein exchange at pericentric heterochromatin","termid":"FYPO:0006360"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased histone exchange at pericentric heterochromatin","synonyms":[{"name":"increased histone exchange at dh repeat","type":"narrow"},{"name":"increased histone exchange at pericentric heterochromatin during mitotic cell cycle","type":"related"},{"name":"increased histone exchange at pericentric heterochromatin during vegetative growth","type":"exact"}],"termid":"FYPO:0004761"}


id: FYPO:0006338
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the divided nuclei are located near the cell tips (instead of at the midpoint of the long axis of each daughter cell) during telophase of the mitotic cell cycle.","definition_xrefs":["PMID:15937127","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized nucleus during mitotic telophase","termid":"FYPO:0009105"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"nucleus mislocalized towards cell tip during mitotic telophase","synonyms":[{"name":"nuclear displacement towards cell tip during mitotic telophase","type":"exact"},{"name":"nucleus displaced towards cell tip during mitotic telophase","type":"exact"},{"name":"nucleus mislocalised to cell tip during mitotic telophase","type":"exact"},{"name":"nucleus mislocalized towards cell end during mitotic telophase","type":"exact"},{"name":"nucleus mislocalized towards cell tip during mitotic telophase during mitotic cell cycle","type":"related"},{"name":"nucleus mislocalized towards cell tip during mitotic telophase during vegetative growth","type":"exact"},{"name":"telophase nucleus mislocalized to cell tip","type":"exact"}],"termid":"FYPO:0006338"}


id: PBO:0091674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tgp1 sense interfering RNA","termid":"PBO:0091674"}


id: PBO:0053981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1297","termid":"PBO:0053981"}


id: PBO:0116301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the TTT complex and the telomere cap complex; subunit of the TTT Hsp90 cochaperone complex that is involved in chromatin remodeling and telomeric chromatin regulation, and  involved in chromatin remodeling and the telomere cap complex; DNA-binding protein specific to single-stranded yeast telomeric DNA repeats; required for telomere length regulation and telomere position effect; involved in the stability or biogenesis of PIKKs such as TORC1","termid":"PBO:0116301"}


id: PBO:0059822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metadherin pseudogene 2","termid":"PBO:0059822"}


id: FYPO:0002663
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of alpha,alpha-trehalase activity does not increase as a result of a hydrogen peroxide stimulus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal alpha,alpha-trehalase activity","termid":"FYPO:0001479"},{"relation_name":"is_a","term_name":"abnormal cellular response to nutrient","termid":"FYPO:0001484"}],"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:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0001985","FYPO:0000298","FYPO:0000707","FYPO:0000002","FYPO:0000654","FYPO:0000661","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"alpha,alpha-trehalase activity increase abolished during cellular response to hydrogen peroxide","synonyms":[{"name":"absent increase in trehalase activity following hydrogen peroxide stimulus","type":"exact"},{"name":"alpha,alpha-trehalase activity increase abolished during cellular response to H2O2","type":"exact"},{"name":"neutral trehalase activity increase abolished during cellular response to hydrogen peroxide","type":"exact"},{"name":"trehalase activity increase abolished during cellular response to hydrogen peroxide","type":"broad"}],"termid":"FYPO:0002663"}


id: PBO:0073022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol carrier protein 2","termid":"PBO:0073022"}


id: PBO:0045439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPY19L3 divergent transcript","termid":"PBO:0045439"}


id: PBO:0030661
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_Man8GlcNAc_level","termid":"PBO:0030661"}


id: PBO:0053762
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 1004","termid":"PBO:0053762"}


id: PBO:0003732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR adaptor protein","termid":"PBO:0003732"}


id: MONDO:0030677
data:
  {"annotated_genes":["SJAG_00637"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87069],"is_not":false,"summary":null,"term":"MONDO:0030677"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"},{"relation_name":"is_a","term_name":"POLR3B-related disorder","termid":"MONDO:0700277"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00637":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, demyelinating, IIA 1I","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619742","UMLS:C5676914","MEDGEN:1811493"],"synonyms":[{"name":"CMT1I","type":"exact"},{"name":"Charcot-Marie-Tooth disease neuropathy, IIA 1I","type":"exact"},{"name":"Charcot-Marie-Tooth disease, demyelinating, IIA 1I","type":"exact"}],"termid":"MONDO:0030677","terms_by_termid":{"MONDO:0030677":null},"xrefs":{"Monarch":{"xref_id":"0030677"}}}


id: GO:1904300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of transcytosis.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:9664076"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of transcytosis","termid":"GO:1904298"},{"relation_name":"positively_regulates","term_name":"transcytosis","termid":"GO:0045056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"positive regulation of transcytosis","synonyms":[{"name":"activation of transcytosis","type":"narrow"},{"name":"up regulation of transcytosis","type":"exact"},{"name":"up-regulation of transcytosis","type":"exact"},{"name":"upregulation of transcytosis","type":"exact"}],"termid":"GO:1904300"}


id: GO:0000981
data:
  {"annotated_genes":["SJAG_00802","SJAG_00386","SJAG_02149","SJAG_05153","SJAG_03388","SJAG_04388","SJAG_00210","SJAG_04839","SJAG_03879","SJAG_00926","SJAG_04092","SJAG_00979","SJAG_02472","SJAG_04374","SJAG_05006","SJAG_03183","SJAG_03538","SJAG_03473","SJAG_02569","SJAG_02326","SJAG_02956","SJAG_00698","SJAG_04249","SJAG_02138","SJAG_05343","SJAG_02938","SJAG_02752","SJAG_03918","SJAG_03241","SJAG_02406","SJAG_03346","SJAG_03484","SJAG_00266","SJAG_01725","SJAG_03143","SJAG_04191","SJAG_00304","SJAG_03911","SJAG_02252","SJAG_02810","SJAG_01916","SJAG_02311","SJAG_03519","SJAG_01343","SJAG_02048","SJAG_04584","SJAG_04749","SJAG_01243","SJAG_01583","SJAG_04712","SJAG_01307","SJAG_01694","SJAG_05234","SJAG_00163","SJAG_02730","SJAG_05288","SJAG_06576","SJAG_06599","SJAG_02218","SJAG_04421","SJAG_00037","SJAG_02709","SJAG_01930","SJAG_04855","SJAG_00792","SJAG_00664","SJAG_04036","SJAG_04009","SJAG_01441","SJAG_02052","SJAG_00987","SJAG_00124","SJAG_00693","SJAG_05337","SJAG_05247","SJAG_04813","SJAG_01062","SJAG_03735","SJAG_01740"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57306,57934,58105,58339,58740,59016,59899,60317,60458,60834,61814,62723,62743,64790,66251,68348,68823,69106,69458,72498,72918,73342,74620,76915,97044,97361,102053,102703,108653,109370,113427,114856],"is_not":false,"summary":null,"term":"GO:0000981"},{"annotations":[96559,57396,105858,111898,116101,116497,117517,99504,61124,108825,100500,68437,89420,88411,75767,113704,107991,74802,96263,77422,110740,72345,97284,106127,87548,114604,75684,95666,102285,80036,91882,88995,87915,79515,77356,74833,87986,88747,98417,109062,107593,104450,92723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001228"},{"annotations":[80399,93271,94697,94032,104452,108826,106268,116102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001227"}]},"cv_name":"molecular_function","definition":"A DNA-binding transcription factor activity that modulates the transcription of specific gene sets transcribed by RNA polymerase II.","definition_xrefs":["GOC:txnOH-2018"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-binding transcription factor 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transcription factor activity, RNA polymerase II-specific","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0001203","GO:0003705","GO:0001200","GO:0001201","GO:0001202","GO:0001133","GO:0000982"],"synonyms":[{"name":"RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity","type":"narrow"},{"name":"RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, copper ion regulated core promoter proximal region sequence-specific binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, copper ion regulated proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, metal ion regulated core promoter proximal region sequence-specific binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, metal ion regulated proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, metal ion regulated sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, sequence-specific DNA binding","type":"exact"},{"name":"RNA polymerase II transcription factor activity, sequence-specific transcription regulatory region DNA binding","type":"exact"},{"name":"RNA polymerase II transcription factor activity, zinc ion regulated core promoter proximal region sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, zinc ion regulated proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"copper ion regulated core promoter proximal region sequence-specific DNA binding RNA polymerase II transcription factor activity","type":"narrow"},{"name":"metal ion regulated core promoter proximal region sequence-specific DNA binding RNA polymerase II transcription factor activity","type":"narrow"},{"name":"metal ion regulated sequence-specific DNA binding RNA polymerase II transcription factor activity","type":"narrow"},{"name":"sequence-specific DNA binding RNA polymerase II transcription factor activity","type":"exact"},{"name":"sequence-specific distal enhancer binding RNA polymerase II transcription factor activity","type":"narrow"},{"name":"sequence-specific transcription regulatory region DNA binding RNA polymerase II transcription factor recruiting transcription factor activity","type":"related"},{"name":"transcription factor","type":"broad"},{"name":"transcription factor activity, RNA polymerase II core promoter proximal region sequence-specific binding","type":"narrow"},{"name":"transcription factor activity, RNA polymerase II distal enhancer sequence-specific binding","type":"narrow"},{"name":"transcription factor activity, RNA polymerase II proximal promoter sequence-specific DNA binding","type":"narrow"},{"name":"zinc ion regulated core promoter proximal region sequence-specific DNA binding RNA polymerase II transcription factor activity","type":"narrow"}],"termid":"GO:0000981","terms_by_termid":{"GO:0000981":null,"GO:0001227":null,"GO:0001228":null}}


id: PBO:0069533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 803, pseudogene","termid":"PBO:0069533"}


id: PBO:0043639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COP9 signalosome subunit 2","termid":"PBO:0043639"}


id: GO:2000319
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of T-helper 17 cell differentiation.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T-helper cell differentiation","termid":"GO:0045622"},{"relation_name":"is_a","term_name":"regulation of T-helper 17 type immune response","termid":"GO:2000316"},{"relation_name":"regulates","term_name":"T-helper 17 cell differentiation","termid":"GO:0072539"}],"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 T-helper 17 cell differentiation","synonyms":[{"name":"regulation of T-helper 17 cell development","type":"related"}],"termid":"GO:2000319"}


id: PBO:0042390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD300 molecule like family member d","termid":"PBO:0042390"}


id: PBO:0088231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6-phosphofructo-2-kinase","termid":"PBO:0088231"}


id: PBO:0076188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO1 pseudogene 3","termid":"PBO:0076188"}


id: PBO:0049913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEXIM P-TEFb complex subunit 1","termid":"PBO:0049913"}


id: PR:Q9HDU1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBPB2B2.14c gene.","definition_xrefs":["UniProtKB:Q9HDU1","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":"UPF0494 membrane protein PB2B2.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBPB2B2.14c","synonyms":[{"name":"Spom972h-SPBPB2B2.14c","type":"exact"}],"termid":"PR:Q9HDU1"}


id: GO:0042822
data:
  {"annotated_genes":["SJAG_00691","SJAG_00252","SJAG_01383","SJAG_00283","SJAG_01881","SJAG_00707"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036001"},{"annotations":[78105,75117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009443"},{"annotations":[75434,64039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042823"},{"annotations":[111842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010144"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving pyridoxal phosphate, pyridoxal phosphorylated at the hydroxymethyl group of C-5, the active form of vitamin B6.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde metabolic process","termid":"GO:0006081"},{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"},{"relation_name":"is_a","term_name":"organophosphate metabolic process","termid":"GO:0019637"},{"relation_name":"is_a","term_name":"vitamin B6 metabolic process","termid":"GO:0042816"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00252":null,"SJAG_00283":null,"SJAG_00691":null,"SJAG_00707":null,"SJAG_01383":null,"SJAG_01881":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006766"],"is_obsolete":false,"name":"pyridoxal phosphate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"active vitamin B6 metabolic process","type":"exact"},{"name":"active vitamin B6 metabolism","type":"exact"},{"name":"pyridoxal phosphate metabolism","type":"exact"}],"termid":"GO:0042822","terms_by_termid":{"GO:0009443":null,"GO:0010144":null,"GO:0036001":null,"GO:0042823":null}}


id: PBO:0040081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arylsulfatase C, isozyme F","termid":"PBO:0040081"}


id: PBO:0015270
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homomeric(3)","termid":"PBO:0015270"}


id: MONDO:0850007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal apparatus disorder","termid":"MONDO:0001854"}],"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":"syndromic lacrimal system disorder","secondary_identifiers":["UMLS:C5681383","MEDGEN:1842875","GARD:22083","Orphanet:519274"],"termid":"MONDO:0850007","xrefs":{"Monarch":{"xref_id":"0850007"}}}


id: GO:1903851
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cristae formation.","definition_xrefs":["GO_REF:0000058","PMID:19279012","GOC:PARL","GOC:pad","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organelle organization","termid":"GO:0010639"},{"relation_name":"is_a","term_name":"regulation of cristae formation","termid":"GO:1903850"},{"relation_name":"negatively_regulates","term_name":"cristae formation","termid":"GO:0042407"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"negatively_regulates","termid":"GO:0061024"},{"rel_name":"negatively_regulates","termid":"GO:0007005"}],"interesting_parent_ids":["GO:0008150","GO:0007005","GO:0061024"],"is_obsolete":false,"name":"negative regulation of cristae formation","synonyms":[{"name":"down regulation of cristae formation","type":"exact"},{"name":"down-regulation of cristae formation","type":"exact"},{"name":"downregulation of cristae formation","type":"exact"},{"name":"inhibition of cristae formation","type":"narrow"}],"termid":"GO:1903851"}


id: SO:0001980
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A regulatory promoter element identified in mutation experiments, with consensus sequence: CACGTG. Present in promoters, intergenic regions, coding regions, and introns. They are involved in gene expression responses to light and interact with G-box binding factor and I-box binding factor 1a.","definition_xrefs":["PMID:19249238","SO:ml","PMID:8571452"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulatory_promoter_element","termid":"SO:0001678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G_box","synonyms":[{"name":"G-box","type":"exact"},{"name":"GBF binding sequence","type":"exact"}],"termid":"SO:0001980"}


id: PATO:0001432
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's decomposition into component parts.","definition_xrefs":["Medical-dictionary:Medical-dictionary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viability","termid":"PATO:0000169"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decayed","termid":"PATO:0001432"}


id: GO:1904443
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of thyroid gland epithelial cell proliferation.","definition_xrefs":["GO_REF:0000058","PMID:17646383","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell proliferation","termid":"GO:0050679"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of thyroid gland epithelial cell proliferation","termid":"GO:1904441"},{"relation_name":"positively_regulates","term_name":"thyroid gland epithelial cell proliferation","termid":"GO:1990789"}],"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 thyroid gland epithelial cell proliferation","synonyms":[{"name":"activation of Hurthle cell proliferation","type":"narrow"},{"name":"activation of thyroid follicular cell proliferation","type":"narrow"},{"name":"activation of thyroid gland epithelial cell proliferation","type":"narrow"},{"name":"positive regulation of Hurthle cell proliferation","type":"narrow"},{"name":"positive regulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"up regulation of Hurthle cell proliferation","type":"narrow"},{"name":"up regulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"up regulation of thyroid gland epithelial cell proliferation","type":"exact"},{"name":"up-regulation of Hurthle cell proliferation","type":"narrow"},{"name":"up-regulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"up-regulation of thyroid gland epithelial cell proliferation","type":"exact"},{"name":"upregulation of Hurthle cell proliferation","type":"narrow"},{"name":"upregulation of thyroid follicular cell proliferation","type":"narrow"},{"name":"upregulation of thyroid gland epithelial cell proliferation","type":"exact"}],"termid":"GO:1904443"}


id: PBO:0066606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ras homolog family member U","termid":"PBO:0066606"}


id: MONDO:1011881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tomaculous neuropathy, non-human animal","secondary_identifiers":["OMIA:001491"],"termid":"MONDO:1011881","xrefs":{"Monarch":{"xref_id":"1011881"}}}


id: PBO:0047087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 136 member F, pseudogene","termid":"PBO:0047087"}


id: GO:1904717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of AMPA glutamate receptor clustering.","definition_xrefs":["GO_REF:0000058","GOC:hjd","GOC:TermGenie","PMID:21558424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glutamate receptor clustering","termid":"GO:0106104"},{"relation_name":"regulates","term_name":"AMPA glutamate receptor clustering","termid":"GO:0097113"}],"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 AMPA glutamate receptor clustering","synonyms":[{"name":"regulation of AMPA receptor clustering","type":"exact"},{"name":"regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate selective glutamate receptor clustering","type":"exact"}],"termid":"GO:1904717"}


id: MONDO:0019161
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, primary form of mineralocorticoid resistance characterized by mild to profound salt wasting either restricted to the kidney (renal pseudohypoaldosteronism type 1), or generalized affecting many organs (generalized pseudohypoaldosteronism type 1). Clinical presentation is in the neonatal period with failure to thrive, vomiting and dehydration with biochemical findings of hyperkalaemia, metabolic acidosis and, elevated plasma aldosterone and renin concentration.","definition_xrefs":["Orphanet:756"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited renal tubular disease","termid":"MONDO:0015962"},{"relation_name":"is_a","term_name":"inherited pseudohypoaldosteronism","termid":"MONDO:0100323"}],"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":"pseudohypoaldosteronism type 1","secondary_identifiers":["MEDGEN:82805","SCTID:43941006","OMIMPS:177735","NANDO:2200368","GARD:16545","ICD9:275.8","UMLS:C0268436","NCIT:C123251","icd11.foundation:1576878036"],"synonyms":[{"name":"PHA type 1","type":"exact"},{"name":"PHA1B","type":"narrow"},{"name":"pseudohypoaldosteronism type I autosomal recessive","type":"narrow"},{"name":"pseudohypoaldosteronism, type I","type":"exact"}],"termid":"MONDO:0019161","xrefs":{"Monarch":{"xref_id":"0019161"}}}


id: MONDO:0003615
data:
  {"annotated_genes":["SJAG_04300"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020730"}]},"cv_name":"mondo","definition":"Any nerve disorder caused by the entrapment and compression of a nerve.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral neuropathy","termid":"MONDO:0005244"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04300":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"nerve compression syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:266933","NCIT:C27221","UMLS:C1510429","MESH:D009408","SCTID:45781009","DOID:573","EFO:0009487"],"synonyms":[{"name":"compression neuropathy","type":"exact"},{"name":"entrapment neuropathy","type":"exact"},{"name":"peripheral nerve entrapment syndrome","type":"exact"}],"termid":"MONDO:0003615","terms_by_termid":{"MONDO:0020730":null},"xrefs":{"Monarch":{"xref_id":"0003615"}}}


id: PBO:0079875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UPF3A pseudogene 2","termid":"PBO:0079875"}


id: GO:0004977
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with melanocortin to initiate a change in cell activity.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled peptide receptor activity","termid":"GO:0008528"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"melanocortin receptor activity","termid":"GO:0004977"}


id: PBO:0074815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 15B","termid":"PBO:0074815"}


id: GO:1990850
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane glycoprotein complex with aspartyl proteinase and metalloproteinase activity which is expressed in the gut. An example of this is found in the nematode Haemonchus contortus.","definition_xrefs":["PMID:11166393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"peptidase complex","termid":"GO:1905368"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"H-gal-GP complex","synonyms":[{"name":"Haemonchus galactose-containing glycoprotein complex","type":"exact"},{"name":"galactose-containing glycoprotein complex","type":"narrow"}],"termid":"GO:1990850"}


id: PR:Q9Y7Z3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An acyl-CoA-binding protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR23310:SF12","OMA:SCHPO04104","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":"acyl-CoA-binding protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1539.06","secondary_identifiers":["UniProtKB:Q9Y7Z3"],"synonyms":[{"name":"ACBP (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-DBI","type":"exact"}],"termid":"PR:Q9Y7Z3"}


id: PBO:0017504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium ion transmembrane transporter Trk2","termid":"PBO:0017504"}


id: PBO:0051069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 5-5","termid":"PBO:0051069"}


id: PR:O94695
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pet2 gene.","definition_xrefs":["UniProtKB:O94695","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":"transporter C83.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC83.11","synonyms":[{"name":"Spom972h-pet2","type":"exact"}],"termid":"PR:O94695"}


id: PBO:0049010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1","termid":"PBO:0049010"}


id: GO:0071736
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of two identical immunoglobulin heavy chains of an IgG isotype and two identical immunoglobulin light chains, held together by disulfide bonds, and present in the extracellular space, in mucosal areas or other tissues, or circulating in the blood or lymph.","definition_xrefs":["ISBN:0781765196","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin complex, circulating","termid":"GO:0042571"},{"relation_name":"is_a","term_name":"IgG immunoglobulin complex","termid":"GO:0071735"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005576","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"IgG immunoglobulin complex, circulating","synonyms":[{"name":"IgG antibody","type":"narrow"},{"name":"IgG1 antibody","type":"narrow"},{"name":"IgG2 antibody","type":"narrow"},{"name":"IgG2a antibody","type":"narrow"},{"name":"IgG2b antibody","type":"narrow"},{"name":"IgG2c antibody","type":"narrow"},{"name":"IgG3 antibody","type":"narrow"},{"name":"IgG4 antibody","type":"narrow"}],"termid":"GO:0071736"}


id: GO:0000147
data:
  {"annotated_genes":["SJAG_04886","SJAG_01964","SJAG_01732","SJAG_02075","SJAG_02228","SJAG_02511","SJAG_03044","SJAG_03119","SJAG_03146","SJAG_04100","SJAG_04052","SJAG_02245","SJAG_04465","SJAG_00521","SJAG_04001","SJAG_00649","SJAG_01384","SJAG_03086"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73216,73423,75147,77227,79397,88103,90636,94768,97907,99682,99862,103067,103258,103314,105174,110701,112181,112204],"is_not":false,"summary":null,"term":"GO:0000147"}]},"cv_name":"biological_process","definition":"Assembly of an actin cortical patch, a discrete actin-containing structure found at the plasma membrane of fungal cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"cortical actin cytoskeleton organization","termid":"GO:0030866"},{"relation_name":"is_a","term_name":"actin cortical patch organization","termid":"GO:0044396"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00521":null,"SJAG_00649":null,"SJAG_01384":null,"SJAG_01732":null,"SJAG_01964":null,"SJAG_02075":null,"SJAG_02228":null,"SJAG_02245":null,"SJAG_02511":null,"SJAG_03044":null,"SJAG_03086":null,"SJAG_03119":null,"SJAG_03146":null,"SJAG_04001":null,"SJAG_04052":null,"SJAG_04100":null,"SJAG_04465":null,"SJAG_04886":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0030036","GO:0007010","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"actin cortical patch assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0000147","terms_by_termid":{"GO:0000147":null}}


id: GO:0099699
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the synaptic membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of synaptic membrane (obsolete GO:0099699)","termid":"GO:0099699"}


id: _global:symbiotically_interacts_with
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"A biotic interaction in which the two organisms live together in more or less intimate association.","direct_ancestors":[{"relation_name":"is_a","term_name":"participates_in_a_biotic-biotic_interaction_with","termid":"_global:participates_in_a_biotic-biotic_interaction_with"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"symbiotically_interacts_with","secondary_identifiers":["RO:0002440"],"termid":"_global:symbiotically_interacts_with"}


id: PBO:0076368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trace amine associated receptor 5","termid":"PBO:0076368"}


id: FYPO:0006278
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the structure of an O-linked glycan moiety of a nascent or mature glycoprotein differs from wild type.","definition_xrefs":["PomBase:mah","PMID:22988247"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glycoprotein glycan structure","termid":"FYPO:0003290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0003290"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0003290","FYPO:0005447","FYPO:0001320","FYPO:0002494","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"abnormal O-linked glycoprotein glycan structure","synonyms":[{"name":"abnormal O-linked glycoprotein oligosaccharide structure","type":"related"}],"termid":"FYPO:0006278"}


id: MONDO:0002746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from glandular epithelial cells of the fallopian tube","direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"fallopian tube carcinoma","termid":"MONDO:0006206"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"fallopian tube adenocarcinoma","secondary_identifiers":["MEDGEN:232183","NCIT:C6265","DOID:3706","UMLS:C1333590"],"synonyms":[{"name":"adenocarcinoma of fallopian tube","type":"exact"},{"name":"adenocarcinoma of the fallopian tube","type":"exact"},{"name":"fallopian tube adenocarcinoma","type":"exact"}],"termid":"MONDO:0002746","xrefs":{"Monarch":{"xref_id":"0002746"}}}


id: GO:0046129
data:
  {"annotated_genes":["SJAG_00044","SJAG_03881","SJAG_03096","SJAG_06634","SJAG_01859","SJAG_01070","SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046086"},{"annotations":[116863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006169"},{"annotations":[69759],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006190"},{"annotations":[73410,66447,93726,61750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006166"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of any purine ribonucleoside, a nucleoside in which purine base is linked to a ribose (beta-D-ribofuranose) molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleoside biosynthetic process","termid":"GO:0042451"},{"relation_name":"is_a","term_name":"ribonucleoside biosynthetic process","termid":"GO:0042455"},{"relation_name":"is_a","term_name":"purine ribonucleoside metabolic process","termid":"GO:0046128"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00134":null,"SJAG_01070":null,"SJAG_01859":null,"SJAG_03096":null,"SJAG_03881":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"purine ribonucleoside biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"synonyms":[{"name":"purine ribonucleoside anabolism","type":"exact"},{"name":"purine ribonucleoside biosynthesis","type":"exact"},{"name":"purine ribonucleoside formation","type":"exact"},{"name":"purine ribonucleoside synthesis","type":"exact"}],"termid":"GO:0046129","terms_by_termid":{"GO:0006166":null,"GO:0006169":null,"GO:0006190":null,"GO:0046086":null}}


id: MONDO:0015168
data:
  {"annotated_genes":["SJAG_05194","SJAG_00773","SJAG_02096","SJAG_03106","SJAG_03847","SJAG_00875","SJAG_01065","SJAG_00853","SJAG_03379"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032903"},{"annotations":[86489],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030281"},{"annotations":[86496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008822"},{"annotations":[86091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100104"},{"annotations":[86980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010532"},{"annotations":[85940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012750"},{"annotations":[85388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014552"},{"annotations":[85772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014806"},{"annotations":[85771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014807"}]},"cv_name":"mondo","definition":"Arthrogryposis multiplex congenita (AMC) is a group of disorders characterized by congenital limb contractures. It manifests as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. AMC is always associated with decreased intrauterine fetal movement which leads secondarily to the contractures.","definition_xrefs":["Orphanet:1037"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"arthrogryposis syndrome","termid":"MONDO:0015225"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00773":null,"SJAG_00853":null,"SJAG_00875":null,"SJAG_01065":null,"SJAG_02096":null,"SJAG_03106":null,"SJAG_03379":null,"SJAG_03847":null,"SJAG_05194":null},"genotype_count":0,"is_obsolete":false,"name":"arthrogryposis multiplex congenita","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:617468","icd11.foundation:1930990330","NORD:810","UMLS:C5779613","DOID:0080954","MedDRA:10051643","GARD:777","MEDGEN:1830310"],"synonyms":[{"name":"AMC","type":"exact"},{"name":"Arthromyodysplasia congenita","type":"exact"},{"name":"Guerin-Stern syndrome","type":"related"},{"name":"Guérin-Stern syndrome","type":"related"},{"name":"Otto syndrome","type":"related"},{"name":"Rossi syndrome","type":"related"},{"name":"amyoplasia congenita","type":"related"},{"name":"arthrogryposis multiplex congenita","type":"exact"},{"name":"congenital amyoplasia","type":"related"},{"name":"congenital arthromyodysplasia","type":"exact"},{"name":"fibrous ankylosis of multiple joints","type":"related"},{"name":"multiple congenital arthrogryposis","type":"exact"},{"name":"myodysplasia","type":"exact"},{"name":"myodystrophia fetalis deformans","type":"related"},{"name":"rocher-Sheldon syndrome","type":"related"}],"termid":"MONDO:0015168","terms_by_termid":{"MONDO:0008822":null,"MONDO:0010532":null,"MONDO:0012750":null,"MONDO:0014552":null,"MONDO:0014806":null,"MONDO:0014807":null,"MONDO:0030281":null,"MONDO:0032903":null,"MONDO:0100104":null},"xrefs":{"Monarch":{"xref_id":"0015168"}}}


id: PBO:0076973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transglutaminase 4","termid":"PBO:0076973"}


id: PBO:0088653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome base subcomplex ATPase subunit Rpt4","termid":"PBO:0088653"}


id: PBO:0082455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-5 sterol desaturase; glycoprotein that catalyzes the introduction of a C-5(6) double bond into episterol, a precursor in ergosterol biosynthesis; transcriptionally down-regulated when ergosterol is in excess; mutants are viable, but cannot grow on non-fermentable carbon sources; substrate of HRD ubiquitin ligase; mutation is functionally complemented by human SC5D","termid":"PBO:0082455"}


id: GO:0061344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the extent of cell adhesion contributing to the shaping of the heart.","definition_xrefs":["PMID:16860783","GOC:dph","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell adhesion","termid":"GO:0030155"},{"relation_name":"regulates","term_name":"cell adhesion involved in heart morphogenesis","termid":"GO:0061343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"regulation of cell adhesion involved in heart morphogenesis","termid":"GO:0061344"}


id: GO:0034620
data:
  {"annotated_genes":["SJAG_04118","SJAG_04262","SJAG_01768","SJAG_02601","SJAG_00403","SJAG_03482","SJAG_00530","SJAG_04567","SJAG_00226","SJAG_03841","SJAG_00681","SJAG_03611","SJAG_04103","SJAG_03815","SJAG_04471","SJAG_04435","SJAG_00564","SJAG_01516","SJAG_04283","SJAG_00790"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102928,110023,110024],"is_not":false,"summary":null,"term":"GO:0034620"},{"annotations":[71104,114095,98713,116055,77157,70528,113824,114228,107190,116803,67971,76199,117253,101240],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030968"},{"annotations":[77833,93066],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036498"},{"annotations":[77554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034514"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an unfolded protein stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to unfolded protein","termid":"GO:0006986"},{"relation_name":"is_a","term_name":"cellular response to topologically incorrect protein","termid":"GO:0035967"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00226":null,"SJAG_00403":null,"SJAG_00530":null,"SJAG_00564":null,"SJAG_00681":null,"SJAG_00790":null,"SJAG_01516":null,"SJAG_01768":null,"SJAG_02601":null,"SJAG_03482":null,"SJAG_03611":null,"SJAG_03815":null,"SJAG_03841":null,"SJAG_04103":null,"SJAG_04118":null,"SJAG_04262":null,"SJAG_04283":null,"SJAG_04435":null,"SJAG_04471":null,"SJAG_04567":null},"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 unfolded protein","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"heat shock protein activity","type":"related"}],"termid":"GO:0034620","terms_by_termid":{"GO:0030968":null,"GO:0034514":null,"GO:0034620":null,"GO:0036498":null}}


id: PBO:0052021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Josephin domain containing 1","termid":"PBO:0052021"}


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


id: PBO:0055228
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 2654","termid":"PBO:0055228"}


id: MONDO:0002511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal apparatus disorder","termid":"MONDO:0001854"}],"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":"stenosis of lacrimal sac","secondary_identifiers":["SCTID:11772001","ICD9:375.54","MEDGEN:509871","DOID:3096","UMLS:C0155246"],"termid":"MONDO:0002511","xrefs":{"Monarch":{"xref_id":"0002511"}}}


id: MONDO:0010828
data:
  {"annotated_genes":["SJAG_04529"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86037],"is_not":false,"summary":null,"term":"MONDO:0010828"}]},"cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF31 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"PRPF31-related retinopathy","termid":"MONDO:0800395"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04529":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005328","MONDO:0004736"],"is_obsolete":false,"name":"retinitis pigmentosa 11","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C563991","UMLS:C1838601","GARD:10383","ICD10CM:H35.5","DOID:0110408","MEDGEN:325055","OMIM:600138"],"synonyms":[{"name":"PRPF31 retinitis pigmentosa","type":"exact"},{"name":"RP 11","type":"related"},{"name":"RP11","type":"exact"},{"name":"retinitis pigmentosa 11","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in PRPF31","type":"exact"},{"name":"retinitis pigmentosa type 11","type":"exact"}],"termid":"MONDO:0010828","terms_by_termid":{"MONDO:0010828":null},"xrefs":{"Monarch":{"xref_id":"0010828"}}}


id: PBO:0066913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 214","termid":"PBO:0066913"}


id: MONDO:0002402
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm characterized by then presence of atypical giant cells.","definition_xrefs":["NCIT:C4090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"giant cell tumor","termid":"MONDO:0002171"},{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant giant cell tumor","secondary_identifiers":["DOID:2705","MEDGEN:90745","UMLS:C0334229","ICDO:8003/3"],"synonyms":[{"name":"giant cell tumor, malignant","type":"exact"},{"name":"malignant giant cell neoplasm","type":"exact"},{"name":"malignant giant cell tumor","type":"exact"},{"name":"malignant tumor, giant cell type","type":"exact"},{"name":"malignant tumor, giant cell type (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0002402","xrefs":{"Monarch":{"xref_id":"0002402"}}}


id: MONDO:0014058
data:
  {"annotated_genes":["SJAG_02908"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85088],"is_not":false,"summary":null,"term":"MONDO:0014058"}]},"cv_name":"mondo","definition":"A rare genetic disease characterized by facial dysmorphism with malar hypoplasia and high forehead, immunodeficiency resulting in recurrent infections, impaired growth (with normal growth hormone production and response) resulting in short stature, and livedo affecting face and extremities. Immunological analyzes show low memory B-cell and naïve T cell counts, decreased T cell proliferation, and reduced IgM, IgG2 and IgG4 titers. Patients do not exhibit increased susceptibility to cancer.","definition_xrefs":["Orphanet:352712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02908":null},"genotype_count":0,"is_obsolete":false,"name":"facial dysmorphism-immunodeficiency-livedo-short stature syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:767490","UMLS:C3554576","GARD:17528","OMIM:615139"],"synonyms":[{"name":"facial dysmorphism, immunodeficiency, livedo, and short stature","type":"related"},{"name":"fils","type":"related"},{"name":"fils syndrome","type":"exact"}],"termid":"MONDO:0014058","terms_by_termid":{"MONDO:0014058":null},"xrefs":{"Monarch":{"xref_id":"0014058"}}}


id: GO:0033751
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: linoleate + O2 = (9Z,12Z)-(7S,8S)-dihydroxyoctadeca-9,12-dienoate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete linoleate 8R-lipoxygenase (obsolete GO:0033751)","synonyms":[{"name":"5,8-linoleate diol synthase (bifunctional enzyme)","type":"related"},{"name":"7,8-linoleate diol synthase (bifunctional enzyme)","type":"related"},{"name":"linoleate diol synthase activity","type":"related"}],"termid":"GO:0033751"}


id: MONDO:0032933
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 1","termid":"MONDO:0017012"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant","secondary_identifiers":["DOID:0070470","MEDGEN:1708515","OMIM:618815","UMLS:C5394150","Orphanet:656279"],"synonyms":[{"name":"CHROMOSOME 1p36.33 DUPLICATION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL DOMINANT","type":"related"}],"termid":"MONDO:0032933","xrefs":{"Monarch":{"xref_id":"0032933"}}}


id: GO:0080096
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a phosphatidate + a sterol = a sterol ester + a lysophosphatidate.","definition_xrefs":["PMID:16020547"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016746"],"is_obsolete":false,"name":"phosphatidate-sterol O-acyltransferase activity","termid":"GO:0080096"}


id: PBO:0054829
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 2242","termid":"PBO:0054829"}


id: GO:1903942
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of respiratory gaseous exchange.","definition_xrefs":["GOC:TermGenie","PMID:22819705","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of respiratory gaseous exchange","termid":"GO:0043576"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"respiratory gaseous exchange by respiratory system","termid":"GO:0007585"}],"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 respiratory gaseous exchange","synonyms":[{"name":"activation of respiratory gaseous exchange","type":"narrow"},{"name":"up regulation of respiratory gaseous exchange","type":"exact"},{"name":"up-regulation of respiratory gaseous exchange","type":"exact"},{"name":"upregulation of respiratory gaseous exchange","type":"exact"}],"termid":"GO:1903942"}


id: GO:0034083
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A polyketide synthase complex that consists of two identical ketosynthase polypeptides.","definition_xrefs":["PMID:12636085","GOC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide synthase complex","termid":"GO:0034081"}],"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":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"type III polyketide synthase complex","synonyms":[{"name":"type III PKS","type":"exact"},{"name":"type III PKS complex","type":"exact"},{"name":"type III polyketide synthase","type":"exact"}],"termid":"GO:0034083"}


id: GO:0097111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the endoplasmic reticulum (ER)-Golgi intermediate compartment.","definition_xrefs":["PMID:18287528","GOC:br"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle organization","termid":"GO:0006996"}],"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":"endoplasmic reticulum-Golgi intermediate compartment organization","synonyms":[{"name":"ER-Golgi intermediate compartment organization","type":"exact"},{"name":"ERGIC organization","type":"exact"},{"name":"endoplasmic reticulum-Golgi intermediate compartment organisation","type":"exact"},{"name":"endoplasmic reticulum-Golgi intermediate compartment organization and biogenesis","type":"related"}],"termid":"GO:0097111"}


id: MONDO:0017016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary interstitial lung disease specific to childhood due to alveolar structure disorder (obsolete MONDO:0017016)","secondary_identifiers":["Orphanet:264670"],"synonyms":[{"name":"primary ILD specific to childhood due to alveolar structure disorder","type":"exact"}],"termid":"MONDO:0017016","xrefs":{"Monarch":{"xref_id":"0017016"}}}


id: MONDO:0100017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of skin conditions that cause constant inflammation and scaling of the skin. People with PRP have reddish, scaly patches that may occur everywhere on the body, or only on certain areas. Some people with PRP also develop thickened skin on the underside of the hands and feet (palmoplantar keratoderma), various nail abnormalities, and/or thinning of the hair. There are several types of PRP classified by age when symptoms begin, body areas involved, and whether other conditions are present. This condition occurs in adults (adult onset PRP) as well as children (juvenile onset PRP).","definition_xrefs":["GARD:0007401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exanthem","termid":"MONDO:0006547"},{"relation_name":"is_a","term_name":"erythrokeratoderma","termid":"MONDO:0019270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"pityriasis rubra pilaris","secondary_identifiers":["MESH:D010916","NCIT:C85014","GARD:7401","ICD10CM:L44.0","icd11.foundation:2048594962","UMLS:C0032027","NORD:1582","ICD9:696.4","MEDGEN:45939","DOID:9212","SCTID:3755001"],"termid":"MONDO:0100017","xrefs":{"Monarch":{"xref_id":"0100017"}}}


id: MONDO:0001810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the hypoglossal nerve.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"glossopharyngeal nerve disorder","termid":"MONDO:0002639"},{"relation_name":"is_a","term_name":"cranial nerve neuropathy","termid":"MONDO:0003569"},{"relation_name":"is_a","term_name":"peripheral nervous system disorder","termid":"MONDO:0003620"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoglossal nerve disorder","secondary_identifiers":["MESH:D020437","NCIT:C26954","SCTID:24777009","UMLS:C0152181","DOID:13814","ICD9:352.5","MEDGEN:57513"],"synonyms":[{"name":"disease of hypoglossal nerve","type":"exact"},{"name":"disease or disorder of hypoglossal nerve","type":"exact"},{"name":"disorder of 12th nerve","type":"exact"},{"name":"disorder of XII nerve","type":"exact"},{"name":"disorder of hypoglossal [12th] nerve","type":"exact"},{"name":"disorder of hypoglossal nerve","type":"exact"},{"name":"disorder of the XII nerve","type":"exact"},{"name":"hypoglossal nerve disease","type":"exact"},{"name":"hypoglossal nerve disease or disorder","type":"exact"},{"name":"hypoglossal nerve disorder","type":"exact"},{"name":"twelfth nerve disorder","type":"exact"}],"termid":"MONDO:0001810","xrefs":{"Monarch":{"xref_id":"0001810"}}}


id: PBO:0003200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homocysteine synthase Met17","termid":"PBO:0003200"}


id: GO:0120063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within gastric smooth muscle tissue, resulting in a change in muscle geometry. This process occurs throughout the length of the stomach.","definition_xrefs":["PMID:15890336","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastro-intestinal system smooth muscle contraction","termid":"GO:0014831"}],"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":"stomach smooth muscle contraction","termid":"GO:0120063"}


id: MONDO:0010074
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive brachyolmia","termid":"MONDO:0018662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0006025"],"is_obsolete":false,"name":"brachyolmia type 1, toledo type","secondary_identifiers":["icd11.foundation:637954533","GARD:4977","MEDGEN:376504","MESH:C535787","OMIM:271630","Orphanet:93303","UMLS:C1849048"],"synonyms":[{"name":"BCYM1B","type":"exact"},{"name":"PAPS-chondroitin sulfate sulfotransferase deficiency","type":"related"},{"name":"PAPS-chondroitin sulphate sulfotransferase deficiency","type":"related"},{"name":"Sed, chondroitin sulfate type","type":"related"},{"name":"Sed, chondroitin sulphate type","type":"related"},{"name":"brachyolmia type 1, Toledo type","type":"related"},{"name":"spondyloepiphyseal dysplasia tarda, Toledo type","type":"related"}],"termid":"MONDO:0010074","xrefs":{"Monarch":{"xref_id":"0010074"}}}


id: PBO:0045469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dopamine receptor D5 pseudogene 1","termid":"PBO:0045469"}


id: PR:O74450
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pop23 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74450"],"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":"ribonucleases P/MRP protein subunit pop3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16C4.05","synonyms":[{"name":"RNA-processing protein pop3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-pop23","type":"exact"}],"termid":"PR:O74450"}


id: GO:1902604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of N-(4-aminobenzoyl)-L-glutamate across a membrane.","definition_xrefs":["GO_REF:0000069","GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"p-aminobenzoyl-glutamate transport","termid":"GO:0015814"},{"relation_name":"is_a","term_name":"dipeptide transmembrane transport","termid":"GO:0035442"},{"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:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"p-aminobenzoyl-glutamate transmembrane transport","synonyms":[{"name":"N-(4-aminobenzoyl)-L-glutamate transmembrane transport","type":"exact"}],"termid":"GO:1902604"}


id: GO:1903751
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of intrinsic apoptotic signaling pathway in response to hydrogen peroxide.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:18681888"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of hydrogen peroxide-mediated programmed cell death","termid":"GO:1901299"},{"relation_name":"is_a","term_name":"negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway","termid":"GO:1902176"},{"relation_name":"is_a","term_name":"regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","termid":"GO:1903750"},{"relation_name":"negatively_regulates","term_name":"intrinsic apoptotic signaling pathway in response to hydrogen peroxide","termid":"GO:0036481"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","synonyms":[{"name":"down regulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"down regulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"down regulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"},{"name":"down regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"exact"},{"name":"down-regulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"down-regulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"down-regulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"},{"name":"down-regulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"exact"},{"name":"downregulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"downregulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"downregulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"},{"name":"downregulation of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"exact"},{"name":"inhibition of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"inhibition of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"narrow"},{"name":"inhibition of intrinsic apoptotic signaling pathway in response to H2O2","type":"narrow"},{"name":"inhibition of intrinsic apoptotic signaling pathway in response to hydrogen peroxide","type":"narrow"},{"name":"negative regulation of H2O2-induced intrinsic apoptotic signaling pathway","type":"related"},{"name":"negative regulation of hydrogen peroxide-induced intrinsic apoptotic signaling pathway","type":"exact"},{"name":"negative regulation of intrinsic apoptotic signaling pathway in response to H2O2","type":"exact"}],"termid":"GO:1903751"}


id: PBO:0030023
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_asymmetric_protein_localization_to_old_or_new_mitotic_spindle_pole_body","termid":"PBO:0030023"}


id: PBO:0056896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial elongation factor 1","termid":"PBO:0056896"}


id: MONDO:0006178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solitary fibrous tumor characterized by the presence of areas of abrupt transition to high grade sarcoma.","definition_xrefs":["NCIT:C79948"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solitary fibrous tumor","termid":"MONDO:0016238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dedifferentiated solitary fibrous tumor","secondary_identifiers":["UMLS:C2699572","MEDGEN:396654","EFO:1000214"],"termid":"MONDO:0006178","xrefs":{"Monarch":{"xref_id":"0006178"}}}


id: GO:0007189
data:
  {"annotated_genes":["SJAG_02311","SJAG_04312","SJAG_01254","SJAG_03081","SJAG_00266","SJAG_00472","SJAG_00574","SJAG_01699","SJAG_02426","SJAG_02481","SJAG_01245","SJAG_01754","SJAG_02444","SJAG_04026"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116587,105919,101852,109027,106507,109534,106859,94198,115555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010619"},{"annotations":[92055,107983,92718,116406,100438],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0110034"}]},"cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway in which the signal is transmitted via the activation of adenylyl cyclase activity which results in an increase in the intracellular concentration of cyclic AMP (cAMP). This pathway is negatively regulated by phosphodiesterase, which cleaves cAMP and terminates the signaling.","definition_xrefs":["GOC:mah","ISBN:0815316194","GOC:dph","GOC:tb","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylate cyclase-modulating G protein-coupled receptor signaling pathway","termid":"GO:0007188"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_00472":null,"SJAG_00574":null,"SJAG_01245":null,"SJAG_01254":null,"SJAG_01699":null,"SJAG_01754":null,"SJAG_02311":null,"SJAG_02426":null,"SJAG_02444":null,"SJAG_02481":null,"SJAG_03081":null,"SJAG_04026":null,"SJAG_04312":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"adenylate cyclase-activating G protein-coupled receptor signaling pathway","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0010579","GO:0010580","Reactome:R-HSA-170660"],"synonyms":[{"name":"G protein signaling, adenylate cyclase activating pathway","type":"exact"},{"name":"G protein signaling, adenylyl cyclase activating pathway","type":"exact"},{"name":"G protein signalling, adenylate cyclase activating pathway","type":"exact"},{"name":"G protein signalling, adenylyl cyclase activating pathway","type":"exact"},{"name":"G-protein signaling, adenylate cyclase activating pathway","type":"exact"},{"name":"G-protein signaling, adenylyl cyclase activating pathway","type":"exact"},{"name":"G-protein signalling, adenylate cyclase activating pathway","type":"exact"},{"name":"G-protein signalling, adenylyl cyclase activating pathway","type":"exact"},{"name":"GPCR signaling pathway via activation of adenylate cyclase","type":"exact"},{"name":"GPCR signaling pathway via activation of adenylate cyclase activity","type":"exact"},{"name":"activation of adenylate cyclase activity by G-protein signaling pathway","type":"related"},{"name":"activation of adenylate cyclase activity involved in G-protein signaling","type":"related"},{"name":"adenylate cyclase-activating GPCR signaling pathway","type":"exact"},{"name":"positive regulation of adenylate cyclase activity by G-protein signaling pathway","type":"related"},{"name":"positive regulation of adenylate cyclase activity by G-protein signalling pathway","type":"related"},{"name":"positive regulation of adenylate cyclase activity involved in G-protein coupled receptor signaling pathway","type":"exact"}],"termid":"GO:0007189","terms_by_termid":{"GO:0010619":null,"GO:0110034":null}}


id: PBO:0082694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the INO80 chromatin remodeling complex; critical for INO80 function; involved in regulation of chromosome segregation and maintenance of normal centromeric chromatin structure; human ortholog INO80C is a member of the human INO80 complex; implicated in DNA repair based on genetic interactions with RAD52 epistasis genes","termid":"PBO:0082694"}


id: PBO:0054913
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 2327","termid":"PBO:0054913"}


id: GO:0060061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of the specialized region on the dorsalmost side of the embryo that acts as the main signaling center establishing the vertebrate body plan.","definition_xrefs":["GOC:bf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"developmental induction","termid":"GO:0031128"}],"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":"Spemann organizer formation","synonyms":[{"name":"Spemann's organizer formation","type":"exact"},{"name":"Spemann-Mangold organizer formation","type":"exact"}],"termid":"GO:0060061"}


id: PBO:0082519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of the SWI/SNF chromatin remodeling complex; involved in transcriptional regulation; contains DNA-stimulated ATPase activity; functions interdependently in transcriptional activation with Snf5p and Snf6p","termid":"PBO:0082519"}


id: FYPO:0009061
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in mitotic interphase in which the localization of a protein to the cell cortex is increased.","direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to cell cortex during vegetative growth","termid":"FYPO:0009059"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"increased protein localization to cell cortex during mitotic interphase","synonyms":[{"name":"increased protein localisation to cell cortex during mitotic interphase","type":"exact"}],"termid":"FYPO:0009061"}


id: PBO:0003643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin Act1","termid":"PBO:0003643"}


id: PBO:0088142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar RNase of the T(2) family; relocalizes to the cytosol where it cleaves tRNAs upon oxidative or stationary phase stress; required for tRNA-specific translational pausing during oxidative stress; promotes apoptosis under stress conditions and this function is independent of Rny1p catalytic activity","termid":"PBO:0088142"}


id: PBO:0074029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 17","termid":"PBO:0074029"}


id: PBO:0044697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDX3 interacting lncRNA 1","termid":"PBO:0044697"}


id: MONDO:0012944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tibial aplasia-ectrodactyly syndrome","termid":"MONDO:0018050"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"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":"chromosome 17P13.3, telomeric, duplication syndrome","secondary_identifiers":["MEDGEN:390813","OMIM:612576","UMLS:C2675492","MESH:C567245","GARD:15572"],"synonyms":[{"name":"chromosome 17P13.3, telomeric, duplication syndrome","type":"exact"},{"name":"split-hand/foot malformation with long bone deficiency 3","type":"related"}],"termid":"MONDO:0012944","xrefs":{"Monarch":{"xref_id":"0012944"}}}


id: MONDO:0014811
data:
  {"annotated_genes":["SJAG_02437"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85777],"is_not":false,"summary":null,"term":"MONDO:0014811"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"},{"relation_name":"is_a","term_name":"complex neurodevelopmental disorder with motor features","termid":"MONDO:0100516"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02437":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"cerebellar atrophy, visual impairment, and psychomotor retardation;","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:905041","UMLS:C4225172","DOID:0081276","OMIM:616875"],"synonyms":[{"name":"CAVIPMR","type":"related"},{"name":"cerebellar atrophy, visual impairment, and psychomotor retardation","type":"related"}],"termid":"MONDO:0014811","terms_by_termid":{"MONDO:0014811":null},"xrefs":{"Monarch":{"xref_id":"0014811"}}}


id: MONDO:0002165
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the rectum. Representative examples of benign neoplasms include lipoma and leiomyoma. Representative examples of malignant neoplasms include carcinoma, lymphoma, and sarcoma. Rectal adenomas always exhibit epithelial dysplasia and are considered premalignant neoplasms.","definition_xrefs":["NCIT:C3350"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rectal disorder","termid":"MONDO:0001593"},{"relation_name":"is_a","term_name":"colorectal neoplasm","termid":"MONDO:0005335"}],"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":"rectal neoplasm","secondary_identifiers":["UMLS:C0034885","SCTID:126847008","MEDGEN:11148","MESH:D012004","DOID:1984"],"synonyms":[{"name":"neoplasm of rectum","type":"exact"},{"name":"neoplasm of the rectum","type":"exact"},{"name":"rectal neoplasm","type":"exact"},{"name":"rectal tumor","type":"exact"},{"name":"rectal tumour","type":"exact"},{"name":"rectum neoplasm","type":"exact"},{"name":"rectum neoplasm (disease)","type":"exact"},{"name":"rectum tumor","type":"exact"},{"name":"rectum tumour","type":"exact"},{"name":"tumor of rectum","type":"exact"},{"name":"tumor of the rectum","type":"exact"},{"name":"tumour of rectum","type":"exact"},{"name":"tumour of the rectum","type":"exact"}],"termid":"MONDO:0002165","xrefs":{"Monarch":{"xref_id":"0002165"}}}


id: PBO:0052264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KDM3A pseudogene 1","termid":"PBO:0052264"}


id: MONDO:0003702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign neoplasm characterized by the presence of smooth muscle cells growing within the veins of the uterine corpus. The intravascular neoplasm growth occurs outside the confines of an adjacent leiomyoma.","definition_xrefs":["NCIT:C5356"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"uterine corpus diffuse leiomyomatosis","termid":"MONDO:0003704"},{"relation_name":"is_a","term_name":"uterine benign neoplasm","termid":"MONDO:0000632"},{"relation_name":"is_a","term_name":"intravenous leiomyomatosis","termid":"MONDO:0003614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterus intravascular leiomyomatosis","secondary_identifiers":["DOID:5915"],"synonyms":[{"name":"intravascular leiomyomatosis of the uterus","type":"exact"},{"name":"intravascular leiomyomatosis of uterus","type":"exact"},{"name":"intravenous leiomyomatosis of the uterus","type":"exact"},{"name":"intravenous leiomyomatosis of uterus","type":"exact"},{"name":"uterine corpus intravenous leiomyomatosis","type":"exact"},{"name":"uterus intravenous leiomyomatosis","type":"exact"}],"termid":"MONDO:0003702","xrefs":{"Monarch":{"xref_id":"0003702"}}}


id: PBO:0079335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 21","termid":"PBO:0079335"}


id: PBO:0005645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transthyretin (predicted)","termid":"PBO:0005645"}


id: PBO:0075748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRSF protein kinase 1","termid":"PBO:0075748"}


id: PR:Q9P7R9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pre-mRNA-splicing factor SYF1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03889","PRO:DNx","PANTHER:PTHR11246:SF5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA-splicing factor cwf3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC211.02c","secondary_identifiers":["UniProtKB:Q9P7R9"],"synonyms":[{"name":"Spom972h-XAB2","type":"exact"},{"name":"complexed with cdc5 protein 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7R9"}


id: MONDO:0010023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Combined immunodeficiency due to ZAP70 deficiency is a very rare, severe, genetic, combined immunodeficiency disorder characterized by lymphocytosis, decreased peripheral CD8+ T-cells, and presence of normal circulating CD4+ T-cells, leading to immune dysfunction.","definition_xrefs":["Orphanet:911"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"combined immunodeficiency","termid":"MONDO:0015131"}],"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":"combined immunodeficiency due to ZAP70 deficiency","secondary_identifiers":["GARD:387","UMLS:C5575025","icd11.foundation:1718367094","NANDO:1200327","MEDGEN:1809040","MESH:C536722","SCTID:716378008","DOID:0111943","NANDO:2200700","OMIM:269840"],"synonyms":[{"name":"IMD48","type":"related"},{"name":"STCD","type":"related"},{"name":"ZAP-70 deficiency","type":"related"},{"name":"immunodeficiency 48","type":"related"},{"name":"selective T-cell defect","type":"related"},{"name":"severe combined immunodeficiency due to ZAP70 deficiency","type":"related"},{"name":"zeta-associated-protein 70 deficiency","type":"exact"}],"termid":"MONDO:0010023","xrefs":{"Monarch":{"xref_id":"0010023"}}}


id: PBO:0076356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin like 3","termid":"PBO:0076356"}


id: PBO:0090796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER flavin-containing N,N-dimethylaniline monooxygenase activity Fmo1","termid":"PBO:0090796"}


id: MONDO:1012037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar Purkinje cell degeneration, non-human animal","termid":"MONDO:1011833"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar Purkinje cell degeneration, dog","secondary_identifiers":["OMIA:000174-9615"],"termid":"MONDO:1012037","xrefs":{"Monarch":{"xref_id":"1012037"}}}


id: GO:0032108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a response to nutrient levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"negatively_regulates","term_name":"response to nutrient levels","termid":"GO:0031667"}],"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 response to nutrient levels","synonyms":[{"name":"down regulation of response to nutrient levels","type":"exact"},{"name":"down-regulation of response to nutrient levels","type":"exact"},{"name":"downregulation of response to nutrient levels","type":"exact"},{"name":"inhibition of response to nutrient levels","type":"narrow"}],"termid":"GO:0032108"}


id: FYPO:0005735
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the kinetochore of a chromosome is increased during mitotic M-phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to kinetochore during vegetative growth","termid":"FYPO:0003003"},{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore during mitotic M phase","termid":"FYPO:0008164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased protein localization to kinetochore during mitotic M phase","synonyms":[{"name":"increased protein localisation to kinetochore during mitosis","type":"exact"},{"name":"increased protein localization to kinetochore during mitotic M phase","type":"related"},{"name":"increased protein localization to kinetochore during mitotic nuclear division","type":"exact"}],"termid":"FYPO:0005735"}


id: MONDO:0023214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gas bloat syndrome","secondary_identifiers":["UMLS:C2930966","MEDGEN:419298","MESH:C535647"],"synonyms":[{"name":"post-fundoplication syndrome","type":"related"}],"termid":"MONDO:0023214","xrefs":{"Monarch":{"xref_id":"0023214"}}}


id: PBO:0000345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE","termid":"PBO:0000345"}


id: GO:0035981
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a tongue muscle cell.","definition_xrefs":["GOC:yaf","CL:0002673","PMID:3393851"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal muscle fiber differentiation","termid":"GO:0098528"}],"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":"tongue muscle cell differentiation","termid":"GO:0035981"}


id: GO:0004098
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a cerebroside 3-sulfate + H2O = a cerebroside + sulfate.","definition_xrefs":["EC:3.1.6.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfuric ester hydrolase activity","termid":"GO:0008484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"cerebroside-sulfatase activity","secondary_identifiers":["Reactome:R-HSA-1606807","Reactome:R-HSA-9840949","MetaCyc:CEREBROSIDE-SULFATASE-RXN","RHEA:21300"],"synonyms":[{"name":"arylsulfatase A activity","type":"related"},{"name":"cerebroside sulfate sulfatase activity","type":"related"},{"name":"cerebroside-3-sulfate 3-sulfohydrolase activity","type":"related"},{"name":"cerebroside-sulphatase activity","type":"exact"}],"termid":"GO:0004098"}


id: MONDO:0009973
data:
  {"annotated_genes":["SJAG_02038"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85611],"is_not":false,"summary":null,"term":"MONDO:0009973"}]},"cv_name":"mondo","definition":"Reticular dysgenesis is the most severe form of severe combined immunodeficiency (SCID) and is characterized by bilateral sensorineural deafness and a lack of innate and adaptive immune functions leading to fatal septicemia within days after birth if not treated.","definition_xrefs":["Orphanet:33355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T-B- severe combined immunodeficiency","termid":"MONDO:0017855"},{"relation_name":"is_a","term_name":"familial severe combined immunodeficiency","termid":"MONDO:0031520"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02038":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"reticular dysgenesis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:267500","MEDGEN:124417","NCIT:C27070","DOID:0060020","NANDO:2200695","SCTID:111584000","MESH:C538361","GARD:8625","UMLS:C0272167","NANDO:1200322"],"synonyms":[{"name":"AK2 deficiency","type":"exact"},{"name":"De Vaal disease","type":"exact"},{"name":"DeVaal disease","type":"related"},{"name":"RD","type":"related"},{"name":"SCID with leukopenia","type":"exact"},{"name":"aleukocytosis","type":"related"},{"name":"congenital Aleukia","type":"related"},{"name":"congenital aleukocytosis","type":"exact"},{"name":"generalised haematopoietic hypoplasia","type":"exact"},{"name":"generalized hematopoietic hypoplasia","type":"exact"},{"name":"haematopoietic hypoplasia, generalised","type":"related"},{"name":"hematopoietic hypoplasia, generalized","type":"related"},{"name":"reticular Dysgenesia","type":"related"},{"name":"reticular dysgenesis","type":"exact"},{"name":"severe combined immunodeficiency with leukopenia","type":"exact"}],"termid":"MONDO:0009973","terms_by_termid":{"MONDO:0009973":null},"xrefs":{"Monarch":{"xref_id":"0009973"}}}


id: GO:0070183
data:
  {"annotated_genes":["SJAG_04840"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71205],"is_not":false,"summary":null,"term":"GO:0070183"}]},"cv_name":"biological_process","definition":"The process of coupling tryptophan to tryptophanyl-tRNA in a mitochondrion, catalyzed by tryptophanyl-tRNA synthetase. In tRNA aminoacylation, the amino acid is first activated by linkage to AMP and then transferred to either the 2'- or the 3'-hydroxyl group of the 3'-adenosine residue of the tRNA.","definition_xrefs":["GOC:mcc","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tryptophanyl-tRNA aminoacylation","termid":"GO:0006436"},{"relation_name":"is_a","term_name":"tRNA aminoacylation for mitochondrial protein translation","termid":"GO:0070127"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04840":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0140053"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0140053","GO:0006399","GO:0010467"],"is_obsolete":false,"name":"mitochondrial tryptophanyl-tRNA aminoacylation","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0070183","terms_by_termid":{"GO:0070183":null}}


id: GO:0071309
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 phylloquinone (vitamin K1) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to phylloquinone","termid":"GO:0032573"},{"relation_name":"is_a","term_name":"cellular response to vitamin K","termid":"GO:0071307"}],"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 phylloquinone","synonyms":[{"name":"cellular response to vitamin K1","type":"exact"}],"termid":"GO:0071309"}


id: MONDO:1010602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital hypothyroidism that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypothyroidism, non-human animal","termid":"MONDO:1010057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital hypothyroidism, dog","secondary_identifiers":["OMIA:000536-9615"],"termid":"MONDO:1010602","xrefs":{"Monarch":{"xref_id":"1010602"}}}


id: PBO:0002826
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates pss1","termid":"PBO:0002826"}


id: GO:0042887
data:
  {"annotated_genes":["SJAG_03503","SJAG_02029","SJAG_02779","SJAG_01344","SJAG_00922","SJAG_02125","SJAG_05182","SJAG_02139","SJAG_02602","SJAG_03497","SJAG_02780","SJAG_03577","SJAG_05175","SJAG_04325","SJAG_01660","SJAG_01983","SJAG_03452","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015421"},{"annotations":[118236,97039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044604"},{"annotations":[59596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008521"},{"annotations":[79241,71698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015225"},{"annotations":[70363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015228"},{"annotations":[71697,79240],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901604"},{"annotations":[71793,118376,118377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071916"},{"annotations":[73772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008517"},{"annotations":[113154,95499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034634"},{"annotations":[102805,110044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015182"},{"annotations":[72352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015233"},{"annotations":[107999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901584"},{"annotations":[71791],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042937"},{"annotations":[70481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015204"}]},"cv_name":"molecular_function","definition":"Enables the transfer of an amide, any compound containing one, two, or three acyl groups attached to a nitrogen atom, from one side of a membrane to the other.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00922":null,"SJAG_01344":null,"SJAG_01660":null,"SJAG_01983":null,"SJAG_02029":null,"SJAG_02125":null,"SJAG_02139":null,"SJAG_02602":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_03452":null,"SJAG_03497":null,"SJAG_03503":null,"SJAG_03577":null,"SJAG_04325":null,"SJAG_04725":null,"SJAG_05175":null,"SJAG_05182":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"amide transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"amine/amide/polyamine channel activity","type":"narrow"}],"termid":"GO:0042887","terms_by_termid":{"GO:0008517":null,"GO:0008521":null,"GO:0015182":null,"GO:0015204":null,"GO:0015225":null,"GO:0015228":null,"GO:0015233":null,"GO:0015421":null,"GO:0034634":null,"GO:0042937":null,"GO:0044604":null,"GO:0071916":null,"GO:1901584":null,"GO:1901604":null}}


id: PR:O94726
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ER degradation-enhancing alpha-mannosidase-like protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11742:SF11","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER degradation-enhancing alpha-mannosidase-like protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23A1.04c","secondary_identifiers":["UniProtKB:O94726"],"synonyms":[{"name":"SPAC23A1.04c","type":"related"},{"name":"Spom972h-EDEM1","type":"exact"}],"termid":"PR:O94726"}


id: PBO:0065984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid early transcript 1K pseudogene","termid":"PBO:0065984"}


id: GO:1901881
data:
  {"annotated_genes":["SJAG_04312"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031117"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein depolymerization.","definition_xrefs":["GOC:rl","GOC:BHF","PMID:12032137","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex disassembly","termid":"GO:0043243"},{"relation_name":"is_a","term_name":"regulation of protein depolymerization","termid":"GO:1901879"},{"relation_name":"positively_regulates","term_name":"protein depolymerization","termid":"GO:0051261"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04312":null},"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 protein depolymerization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of protein depolymerization","type":"narrow"},{"name":"activation of protein polymer breakdown","type":"exact"},{"name":"activation of protein polymer catabolic process","type":"exact"},{"name":"activation of protein polymer catabolism","type":"exact"},{"name":"activation of protein polymer degradation","type":"exact"},{"name":"positive regulation of protein polymer breakdown","type":"exact"},{"name":"positive regulation of protein polymer catabolic process","type":"exact"},{"name":"positive regulation of protein polymer catabolism","type":"exact"},{"name":"positive regulation of protein polymer degradation","type":"exact"},{"name":"up regulation of protein depolymerization","type":"exact"},{"name":"up regulation of protein polymer breakdown","type":"exact"},{"name":"up regulation of protein polymer catabolic process","type":"exact"},{"name":"up regulation of protein polymer catabolism","type":"exact"},{"name":"up regulation of protein polymer degradation","type":"exact"},{"name":"up-regulation of protein depolymerization","type":"exact"},{"name":"up-regulation of protein polymer breakdown","type":"exact"},{"name":"up-regulation of protein polymer catabolic process","type":"exact"},{"name":"up-regulation of protein polymer catabolism","type":"exact"},{"name":"up-regulation of protein polymer degradation","type":"exact"},{"name":"upregulation of protein depolymerization","type":"exact"},{"name":"upregulation of protein polymer breakdown","type":"exact"},{"name":"upregulation of protein polymer catabolic process","type":"exact"},{"name":"upregulation of protein polymer catabolism","type":"exact"},{"name":"upregulation of protein polymer degradation","type":"exact"}],"termid":"GO:1901881","terms_by_termid":{"GO:0031117":null}}


id: PBO:0076754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teratocarcinoma-derived growth factor 1 pseudogene 4","termid":"PBO:0076754"}


id: MONDO:0002044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectropion","termid":"MONDO:0002043"}],"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":"spastic ectropion","secondary_identifiers":["ICD9:374.13","SCTID:80846000","UMLS:C0155195","MEDGEN:509843","DOID:1571"],"termid":"MONDO:0002044","xrefs":{"Monarch":{"xref_id":"0002044"}}}


id: PBO:0089695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar CorA family magnesium ion transmembrane transporter Mnr2","termid":"PBO:0089695"}


id: PBO:0050146
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 2","termid":"PBO:0050146"}


id: GO:0050485
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which X-H and Y-H form X-Y and the acceptor is disulfide.","definition_xrefs":["EC:1.21.4.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on X-H and Y-H to form an X-Y bond","termid":"GO:0046992"}],"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on X-H and Y-H to form an X-Y bond, with a disulfide as acceptor","synonyms":[{"name":"oxidoreductase activity, acting on X-H and Y-H to form an X-Y bond, with a disulphide as acceptor","type":"exact"}],"termid":"GO:0050485"}


id: PBO:0050446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein U","termid":"PBO:0050446"}


id: PBO:0052954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KTN1 antisense RNA 1","termid":"PBO:0052954"}


id: MONDO:1010091
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microtia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental defect during embryogenesis, non-human animal","termid":"MONDO:1011310"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease, non-human animal","termid":"MONDO:1011342"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtia, non-human animal","secondary_identifiers":["OMIA:001952"],"termid":"MONDO:1010091","xrefs":{"Monarch":{"xref_id":"1010091"}}}


id: GO:0036094
data:
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id: GO:0033324
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of choline (2-hydroxyethyltrimethylammonium), via the intermediate N-monomethylethanolamine.","definition_xrefs":["GOC:mah","MetaCyc:PWY-3542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choline biosynthetic process","termid":"GO:0042425"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"choline biosynthetic process via N-monomethylethanolamine","synonyms":[{"name":"choline anabolism via N-monomethylethanolamine","type":"exact"},{"name":"choline biosynthesis via N-monomethylethanolamine","type":"exact"},{"name":"choline formation via N-monomethylethanolamine","type":"exact"},{"name":"choline synthesis via N-monomethylethanolamine","type":"exact"}],"termid":"GO:0033324"}


id: MONDO:0017676
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete marginal papular palmoplantar keratoderma (obsolete MONDO:0017676)","secondary_identifiers":["Orphanet:307995"],"synonyms":[{"name":"marginal papular palmoplantar hyperkeratosis","type":"exact"}],"termid":"MONDO:0017676","xrefs":{"Monarch":{"xref_id":"0017676"}}}


id: PBO:0079572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin B pseudogene 4","termid":"PBO:0079572"}


id: PBO:0060610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear cap binding subunit 3","termid":"PBO:0060610"}


id: PBO:0069460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 725, pseudogene","termid":"PBO:0069460"}


id: GO:0019532
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of oxalate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Oxalate, or ethanedioic acid, occurs in many plants and is highly toxic to animals.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transport","termid":"GO:0006835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"oxalate transport","synonyms":[{"name":"ethanedioate transport","type":"exact"},{"name":"ethanedioic acid transport","type":"exact"},{"name":"oxalic acid transport","type":"exact"}],"termid":"GO:0019532"}


id: GO:0006969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete melanotic tumor response (obsolete GO:0006969)","synonyms":[{"name":"melanotic mass response","type":"exact"},{"name":"melanotic tumor response","type":"exact"}],"termid":"GO:0006969"}


id: GO:0021875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of a fibroblast growth factor receptor binding to one of its physiological ligands that contributes to the self renewal of neuroblasts in the forebrain.","definition_xrefs":["GOC:dph","PMID:16226447","GO_REF:0000021","GOC:dgh","GOC:cls","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblast growth factor receptor signaling pathway","termid":"GO:0008543"},{"relation_name":"part_of","term_name":"forebrain neuroblast division","termid":"GO:0021873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"fibroblast growth factor receptor signaling pathway involved in forebrain neuroblast division","synonyms":[{"name":"fibroblast growth factor receptor signalling pathway in forebrain neuroblast division","type":"exact"}],"termid":"GO:0021875"}


id: SO:0002201
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A repeat at the ends of and within the sequence for which it has functional significance other than long terminal repeat.","direct_ancestors":[{"relation_name":"is_a","term_name":"repeat_region","termid":"SO:0000657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"terminal_repeat","synonyms":[{"name":"INSDC_feature:repeat_region","type":"broad"},{"name":"INSDC_qualifier:terminal","type":"exact"},{"name":"terminal repeat","type":"exact"}],"termid":"SO:0002201"}


id: MONDO:1011995
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gyrate atrophy of choroid and retina, non-human animal","secondary_identifiers":["OMIA:001774"],"termid":"MONDO:1011995","xrefs":{"Monarch":{"xref_id":"1011995"}}}


id: PBO:0024812
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-causal_relation_between_material_entities","termid":"PBO:0024812"}


id: PBO:0029012
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_chromosome_during_vegetative_growth","termid":"PBO:0029012"}


id: PR:O74545
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC777.06c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74545"],"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":"hydrolase C777.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC777.06c","synonyms":[{"name":"Spom972h-SPCC777.06c","type":"exact"}],"termid":"PR:O74545"}


id: MOD:01587
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-(2-aminoethylphosphoryl)-L-serine.","definition_xrefs":["PubMed:16825186","PubMed:16949362","PubMed:15249686","RESID:AA0497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-(2-aminoethylphosphoryl)-L-serine","synonyms":[{"name":"(2S)-2-amino-3-([(2-aminoethoxy)(hydroxy)phosphoryl]oxy)propanoic acid","type":"exact"},{"name":"MOD_RES O-(2-aminoethylphosphoryl)serine","type":"exact"},{"name":"O-(2-aminoethylphosphoryl)-L-serine","type":"exact"},{"name":"O3-(2-aminoethylphosphoryl)-L-serine","type":"exact"},{"name":"O3-(phosphoethanolamine)-L-serine","type":"exact"},{"name":"serine ethanolamine phosphate","type":"exact"},{"name":"serine ethanolamine phosphodiester","type":"exact"}],"termid":"MOD:01587"}


id: GO:0014011
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of Schwann cells by cell division, resulting in the expansion of their population in response to an axonal lesion. The newly generated Schwann cells support subsequent axon regeneration in the peripheral nervous system.","definition_xrefs":["ISBN:0878932585","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schwann cell proliferation","termid":"GO:0014010"},{"relation_name":"part_of","term_name":"peripheral nervous system axon regeneration","termid":"GO:0014012"}],"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":"Schwann cell proliferation involved in axon regeneration","termid":"GO:0014011"}


id: PR:Q9Y7P9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC191.05c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7P9"],"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 C191.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC191.05c","synonyms":[{"name":"Spom972h-SPCC191.05c","type":"exact"}],"termid":"PR:Q9Y7P9"}


id: PBO:0034712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiolipin synthase/ hydrolase fusion protein Crd1 (predicted)","termid":"PBO:0034712"}


id: PBO:0060173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule associated scaffold protein 2","termid":"PBO:0060173"}


id: MONDO:0021834
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by frontal bossing, cloudy corneae, low nasal ridge, and micrognathia, hypoplastic thorax, and rhizomelic micromelia.","definition_xrefs":["PMID:8989469"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"}],"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":"Akaba Hayasaka syndrome","secondary_identifiers":["MESH:C535609","UMLS:C2930948","MEDGEN:443940"],"synonyms":[{"name":"frontal bossing, cloudy corneae, low nasal ridge, and micrognathia, hypoplastic thorax, and rhizomelic micromelia","type":"related"}],"termid":"MONDO:0021834","xrefs":{"Monarch":{"xref_id":"0021834"}}}


id: GO:0097502
data:
  {"annotated_genes":["SJAG_04316","SJAG_04053","SJAG_01264"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93004,105978,101546],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035269"}]},"cv_name":"biological_process","definition":"The covalent attachment of a mannose residue to a substrate molecule.","definition_xrefs":["GOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylation","termid":"GO:0070085"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01264":null,"SJAG_04053":null,"SJAG_04316":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mannosylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0097502","terms_by_termid":{"GO:0035269":null}}


id: PBO:0004579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (guanine-N2-)-methyltransferase catalytic subunit Trm11 (predicted)","termid":"PBO:0004579"}


id: FYPO:0003897
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An abnormal intracellular mitochondrion distribution phenotype observed in the vegetative growth phase of the life cycle in which mitochondria cluster together more than normal during a cellular response to reactive oxygen species.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial aggregation","termid":"FYPO:0000895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"mitochondrial aggregation during cellular response to reactive oxygen species","synonyms":[{"name":"aggregated mitochondria during cellular response to reactive oxygen species","type":"narrow"},{"name":"mitochondrial aggregation at cell end during cellular response to reactive oxygen species","type":"related"},{"name":"mitochondrial aggregation at cell tip during cellular response to reactive oxygen species","type":"related"},{"name":"mitochondrial aggregation during cellular response to ROS","type":"exact"},{"name":"mitochondrial aggregation during cellular response to reactive oxygen species during mitotic cell cycle","type":"related"},{"name":"mitochondrial aggregation during cellular response to reactive oxygen species during vegetative growth","type":"exact"}],"termid":"FYPO:0003897"}


id: GO:0070548
data:
  {"annotated_genes":["SJAG_04728"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004360"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an amino group from L-glutamine to an acceptor, usually a 2-oxo acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04728":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016769","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"L-glutamine aminotransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0070548","terms_by_termid":{"GO:0004360":null}}


id: MONDO:0008639
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":"vascular helix of umbilical cord","secondary_identifiers":["UMLS:C1860520","MEDGEN:349836","OMIM:192300"],"synonyms":[{"name":"vascular helix of umbilical cord","type":"exact"}],"termid":"MONDO:0008639","xrefs":{"Monarch":{"xref_id":"0008639"}}}


id: PBO:0066151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBBP4 pseudogene 7","termid":"PBO:0066151"}


id: GO:0034365
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A newly formed high-density lipoprotein particle; consists of a phospholipid bilayer surrounded by two or more APOA1 molecules. The discoidal HDL particle is formed when lipid-free or lipid-poor APOA1 acquires phospholipids and unesterified cholesterol from either cell membranes or triglyceride-rich lipoproteins (undergoing lipolysis by lipoprotein lipase).","definition_xrefs":["GOC:rl","GOC:expert_pt","GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"high-density lipoprotein particle","termid":"GO:0034364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005576","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"discoidal high-density lipoprotein particle","synonyms":[{"name":"discoidal HDL","type":"exact"},{"name":"nascent HDL","type":"exact"},{"name":"nascent high-density lipoprotein particle","type":"exact"}],"termid":"GO:0034365"}


id: SO:0002242
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene which codes for 25S_rRNA, which functions as a component of the large subunit of the ribosome in some eukaryotes.","direct_ancestors":[{"relation_name":"is_a","term_name":"cytosolic_LSU_rRNA_gene","termid":"SO:0002361"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic_rRNA_25S_gene","synonyms":[{"name":"25S rRNA gene","type":"exact"},{"name":"25S_rRNA_gene","type":"exact"}],"termid":"SO:0002242"}


id: PBO:0074434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 34","termid":"PBO:0074434"}


id: PBO:0031620
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_transposition","termid":"PBO:0031620"}


id: MONDO:0033653
data:
  {"annotated_genes":["SJAG_01190"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85711],"is_not":false,"summary":null,"term":"MONDO:0033653"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex IV deficiency, nuclear-type","termid":"MONDO:0033885"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01190":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 4 deficiency, nuclear type 18","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1752734","OMIM:619062","UMLS:C5436720","DOID:0070503","GARD:16415"],"synonyms":[{"name":"MC4DN18","type":"exact"},{"name":"mitochondrial complex IV deficiency, nuclear type 18","type":"exact"}],"termid":"MONDO:0033653","terms_by_termid":{"MONDO:0033653":null},"xrefs":{"Monarch":{"xref_id":"0033653"}}}


id: GO:0016884
data:
  {"annotated_genes":["SJAG_03355","SJAG_04549","SJAG_05560","SJAG_02721","SJAG_00412","SJAG_04634","SJAG_02618","SJAG_02832","SJAG_00964","SJAG_01577","SJAG_00392"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57636,79214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004066"},{"annotations":[106535,71819,70223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004088"},{"annotations":[75021,118429,71656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050567"},{"annotations":[93395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003922"},{"annotations":[74673],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0003921"},{"annotations":[77425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003952"},{"annotations":[69738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004642"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of the amide nitrogen of glutamine to a substrate. Usually composed of two subunits or domains, one that first hydrolyzes glutamine, and then transfers the resulting ammonia to the second subunit (or domain), where it acts as a source of nitrogen.","definition_xrefs":["PMID:12360532"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00392":null,"SJAG_00412":null,"SJAG_00964":null,"SJAG_01577":null,"SJAG_02618":null,"SJAG_02721":null,"SJAG_02832":null,"SJAG_03355":null,"SJAG_04549":null,"SJAG_04634":null,"SJAG_05560":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"carbon-nitrogen ligase activity, with glutamine as amido-N-donor","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:6.3.5.-","GO:0016003"],"termid":"GO:0016884","terms_by_termid":{"GO:0003921":null,"GO:0003922":null,"GO:0003952":null,"GO:0004066":null,"GO:0004088":null,"GO:0004642":null,"GO:0050567":null}}


id: MONDO:0034937
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndromic ectopia lentis (obsolete MONDO:0034937)","secondary_identifiers":["Orphanet:519292"],"termid":"MONDO:0034937","xrefs":{"Monarch":{"xref_id":"0034937"}}}


id: PBO:0049667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyaluronan binding protein 2","termid":"PBO:0049667"}


id: GO:0090068
data:
  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id: PBO:0114733
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translational activator, PPR repeat Ppr10","termid":"PBO:0114733"}


id: PBO:0065336
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosyl transferase domain containing 1","termid":"PBO:0065336"}


id: GO:0032183
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to the small ubiquitin-like protein SUMO.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein binding","termid":"GO:0032182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"SUMO binding","synonyms":[{"name":"Smt3 binding","type":"related"},{"name":"Smt3 monomer binding","type":"narrow"}],"termid":"GO:0032183"}


id: PBO:0081123
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger homeobox 2","termid":"PBO:0081123"}


id: PBO:0047004
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A7","termid":"PBO:0047004"}


id: MONDO:0030517
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  {"annotated_genes":["SJAG_01797"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86063],"is_not":false,"summary":null,"term":"MONDO:0030517"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"trichothiodystrophy","termid":"MONDO:0018053"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01797":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"trichothiodystrophy 8, nonphotosensitive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619691","MEDGEN:1794267","UMLS:C5562057"],"synonyms":[{"name":"TTD8","type":"exact"}],"termid":"MONDO:0030517","terms_by_termid":{"MONDO:0030517":null},"xrefs":{"Monarch":{"xref_id":"0030517"}}}


id: MONDO:0013346
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  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete brain calcification, Rajab type (obsolete MONDO:0013346)","termid":"MONDO:0013346","xrefs":{"Monarch":{"xref_id":"0013346"}}}


id: GO:0005599
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  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(X) chains; type X collagen triple helices form hexagonal networks (sheets).","definition_xrefs":["PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"network-forming collagen trimer","termid":"GO:0098642"},{"relation_name":"part_of","term_name":"interstitial hexagonal collagen network","termid":"GO:0098646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"collagen type X trimer","termid":"GO:0005599"}


id: PBO:0052627
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 6A","termid":"PBO:0052627"}


id: FYPO:0000168
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  {"alleles_by_uniquename":{"SJAG_01330:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01330","name":"mad2delta","uniquename":"SJAG_01330:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119238,119216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004318"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the spindle assembly checkpoint of a mitotic cell cycle is abnormal. The mitotic spindle assembly checkpoint normally delays the metaphase/anaphase transition of a mitotic nuclear division until the spindle is correctly assembled and chromosomes are attached to the spindle. In a mutant, the checkpoint may fail to arrest or delay cell cycle progression under appropriate conditions, or the incidence or duration of arrest or delay may differ from wild type under any specified set of conditions.","definition_xrefs":["GO:0007094","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal regulation of mitotic metaphase/anaphase transition","termid":"FYPO:0000200"},{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle checkpoint","termid":"FYPO:0001704"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01330":null},"genotype_count":1,"genotypes_by_uniquename":{"mad2delta":{"display_name":"mad2delta","display_uniquename":"mad2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01330:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000298","FYPO:0000002"],"is_obsolete":false,"name":"abnormal mitotic spindle assembly checkpoint","references_by_uniquename":{"PMID:21802294":null,"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01330"],"single_locus_genotype_uniquenames":["mad2delta"],"synonyms":[{"name":"abnormal mitotic cell cycle spindle assembly checkpoint","type":"exact"},{"name":"abnormal mitotic spindle assembly checkpoint activation","type":"related"}],"termid":"FYPO:0000168","terms_by_termid":{"FYECO:0000162":null,"FYPO:0004318":null}}


id: GO:0102608
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: tetracenomycin B3 + S-adenosyl-L-methionine = tetracenomycin E + S-adenosyl-L-homocysteine + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete tetracenomycin B3 8-O-methyl transferase activity (obsolete GO:0102608)","termid":"GO:0102608"}


id: MONDO:0003495
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell tumor that arises from the ovary and is not associated with a germ cell tumor.","definition_xrefs":["NCIT:C40092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian epithelial tumor","termid":"MONDO:0002229"},{"relation_name":"is_a","term_name":"squamous cell neoplasm","termid":"MONDO:0002532"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian squamous cell neoplasm","secondary_identifiers":["DOID:5532"],"synonyms":[{"name":"ovarian squamous cell neoplasm","type":"exact"},{"name":"ovarian squamous cell tumor","type":"exact"},{"name":"ovarian squamous cell tumour","type":"exact"},{"name":"ovary squamous cell neoplasm","type":"exact"}],"termid":"MONDO:0003495","xrefs":{"Monarch":{"xref_id":"0003495"}}}


id: GO:0035905
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the ascending aorta over time, from its initial formation to the mature structure. The ascending aorta is the portion of the aorta in a two-pass circulatory system that lies between the heart and the arch of aorta. In a two-pass circulatory system blood passes twice through the heart to supply the body once.","definition_xrefs":["UBERON:0001496","MA:0002570","Wikipedia:Ascending_aorta","GOC:dgh","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"aorta development","termid":"GO:0035904"}],"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":"ascending aorta development","termid":"GO:0035905"}


id: MONDO:1010047
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spina bifida that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder, non-human animal","termid":"MONDO:1011308"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spina bifida, non-human animal","secondary_identifiers":["OMIA:000933"],"termid":"MONDO:1010047","xrefs":{"Monarch":{"xref_id":"1010047"}}}


id: GO:0007377
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Elongation of the germ band on the ventral side of the embryo, accompanied by a halving in width. The elongation process pushes the posterior midgut invagination closed and compresses the amnioserosa further.","definition_xrefs":["ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"gastrulation involving germ band extension","termid":"GO:0010004"}],"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":"germ-band extension","termid":"GO:0007377"}


id: FYPO:0007943
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which any process of chromatin organization is abnormal during the meiotic cell cycle. Chromatin organization results in the specification, formation or maintenance of the physical structure of eukaryotic chromatin.","definition_xrefs":["PomBase:val"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin organization","termid":"FYPO:0000642"},{"relation_name":"is_a","term_name":"abnormal meiotic chromosome organization","termid":"FYPO:0006759"},{"relation_name":"is_a","term_name":"abnormal cellular process during meiotic cell cycle","termid":"FYPO:0007260"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000641","FYPO:0000002","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"name":"abnormal chromatin organization during meiotic cell cycle","termid":"FYPO:0007943"}


id: PBO:0082164
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adenylosuccinate lyase; catalyzes two steps in the 'de novo' purine nucleotide biosynthetic pathway; expression is repressed by adenine and activated by Bas1p and Pho2p; mutations in human ortholog ADSL cause adenylosuccinase deficiency; human ADSL can complement yeast ADE13 null mutant","termid":"PBO:0082164"}


id: MONDO:0003653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"capillary hemangioma","termid":"MONDO:0002407"},{"relation_name":"is_a","term_name":"capillary malformation","termid":"MONDO:0016231"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stork bite","secondary_identifiers":["MEDGEN:870384","SCTID:254211001","UMLS:C4024829","DOID:5806"],"synonyms":[{"name":"Salmon patch nevus","type":"exact"},{"name":"Unna's nevus","type":"exact"}],"termid":"MONDO:0003653","xrefs":{"Monarch":{"xref_id":"0003653"}}}


id: PBO:0046685
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation termination factor 1 pseudogene 3","termid":"PBO:0046685"}


id: PBO:0031332
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  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_calcium","termid":"PBO:0031332"}


id: SO:0000869
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  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A frameshift caused by inserting two bases.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"frameshift","termid":"SO:0000865"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plus_2_framshift","synonyms":[{"name":"plus 2 framshift","type":"exact"}],"termid":"SO:0000869"}


id: GO:0014824
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within smooth muscle tissue, resulting in a change in muscle geometry. This process occurs in the artery. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. The artery is a vessel carrying blood away from the heart.","definition_xrefs":["MA:0000708","MSH:D001158","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tonic smooth muscle contraction","termid":"GO:0014820"},{"relation_name":"is_a","term_name":"vascular associated smooth muscle contraction","termid":"GO:0014829"}],"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":"artery smooth muscle contraction","termid":"GO:0014824"}


id: PBO:0113798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDP-Man:Man1GlcNAc2-PP-Dol alpha-1,3-mannosyltransferase/ GDP-Man:Man2GlcNAc2-PP-dolichol alpha-1,6-mannosyltransferase","termid":"PBO:0113798"}


id: GO:0044616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism induces paralysis, the loss of the ability to voluntarily control muscles, in another organism by blocking nerve signals or directly interfering with muscle contraction mechanisms.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in modulation of process in another organism","termid":"GO:0035738"}],"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":"envenomation resulting in paralysis in another organism","synonyms":[{"name":"modulation of relaxation of muscle in another organism","type":"related"},{"name":"modulation of relaxation of muscle in other organism","type":"exact"},{"name":"regulation of relaxation of muscle in other organism","type":"exact"}],"termid":"GO:0044616"}


id: GO:0102063
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate(3-) = diphosphoric acid + (-)-beta-curcumene.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete beta-curcumene synthase activity (obsolete GO:0102063)","termid":"GO:0102063"}


id: GO:0050463
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nitrite + NAD(P)+ + H2O = nitrate + NAD(P)H + H+.","definition_xrefs":["EC:1.7.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrate reductase activity","termid":"GO:0008940"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor","termid":"GO:0046857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"nitrate reductase [NAD(P)H] activity","synonyms":[{"name":"NAD(P)H bispecific nitrate reductase activity","type":"related"},{"name":"NAD(P)H-nitrate reductase activity","type":"related"},{"name":"NAD(P)H2:nitrate oxidoreductase activity","type":"related"},{"name":"NAD(P)H:nitrate oxidoreductase activity","type":"related"},{"name":"assimilatory NAD(P)H-nitrate reductase activity","type":"related"},{"name":"assimilatory nitrate reductase activity","type":"related"},{"name":"nitrate reductase (reduced nicotinamide adenine dinucleotide (phosphate)) activity","type":"related"},{"name":"nitrate reductase NAD(P)H activity","type":"related"},{"name":"nitrate reductase [NAD(P)H2]","type":"related"},{"name":"nitrite:NAD(P)+ oxidoreductase activity","type":"related"}],"termid":"GO:0050463"}


id: PBO:0001038
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter contains RLM1 element","termid":"PBO:0001038"}


id: GO:0042880
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of D-glucuronate, the D-enantiomer of glucuronate, from one side of a membrane to the other.","definition_xrefs":["GOC:mah","GOC:jl","GOC:jsg","GOC:mtg_transport","ISBN:0815340729","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucuronate transmembrane transporter activity","termid":"GO:0015135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"D-glucuronate transmembrane transporter activity","termid":"GO:0042880"}


id: FYPO:0004746
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 heterochromatin assembly involved in chromatin silencing at the centromere outer repeat region does not occur.","definition_xrefs":["GO:0031507","PomBase:mah","PMID:24240238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal heterochromatin assembly at centromere outer repeat during vegetative growth","termid":"FYPO:0003098"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"},{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000641"],"is_obsolete":false,"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat","synonyms":[{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere otr","type":"exact"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat during vegetative growth","type":"exact"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat region","type":"exact"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at pericentric region","type":"related"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at pericentromeric region","type":"related"},{"name":"heterochromatin assembly involved in chromatin silencing at centromere outer repeat abolished","type":"exact"}],"termid":"FYPO:0004746"}


id: SO:0000314
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A repeat where the same sequence is repeated in the same direction. Example: GCTGA-followed by-GCTGA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"repeat_region","termid":"SO:0000657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"direct_repeat","secondary_identifiers":["http://en.wikipedia.org/wiki/Direct_repeat"],"synonyms":[{"name":"INSDC_feature:repeat_region","type":"broad"},{"name":"INSDC_qualifier:direct","type":"exact"},{"name":"direct repeat","type":"exact"}],"termid":"SO:0000314"}


id: GO:0010174
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a nucleoside, from one side of a membrane to the other, up a concentration gradient.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside transmembrane transporter activity","termid":"GO:0005337"},{"relation_name":"is_a","term_name":"secondary active transmembrane transporter activity","termid":"GO:0015291"}],"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:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"nucleoside transmembrane transporter activity, against a concentration gradient","synonyms":[{"name":"concentrative nucleoside transporter activity","type":"exact"}],"termid":"GO:0010174"}


id: PBO:0065055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRELI domain containing 3B pseudogene 9","termid":"PBO:0065055"}


id: PBO:0063195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate cancer associated transcript 14","termid":"PBO:0063195"}


id: PBO:0041847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CASK interacting protein 1","termid":"PBO:0041847"}


id: FYPO:0000481
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic recombination is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA recombination during vegetative growth","termid":"FYPO:0001345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000293","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal mitotic recombination","synonyms":[{"name":"abnormal mitotic recombination during mitotic cell cycle","type":"related"},{"name":"abnormal mitotic recombination during vegetative growth","type":"exact"},{"name":"mitotic recombination: abnormal","type":"related"}],"termid":"FYPO:0000481"}


id: MONDO:1010433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrial septal defect that occurs in koala.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial septal defect, non-human animal","termid":"MONDO:1010009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrial septal defect, koala","secondary_identifiers":["OMIA:000089-38626"],"termid":"MONDO:1010433","xrefs":{"Monarch":{"xref_id":"1010433"}}}


id: PBO:0062405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 29 pseudogene","termid":"PBO:0062405"}


id: PBO:0034676
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_frequency_of_meiotic_crossover_associated_with_gene_conversion","termid":"PBO:0034676"}


id: PBO:0051088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy joining 1","termid":"PBO:0051088"}


id: MOD:01296
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to monosodium L-glutamate.","definition_xrefs":["Unimod:30#E","PubMed:12216740"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosodium salt","termid":"MOD:00423"},{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monosodium L-glutamate","synonyms":[{"name":"Cation:Na","type":"related"},{"name":"MSG","type":"exact"},{"name":"Na1Glu","type":"exact"},{"name":"Sodium adduct","type":"related"}],"termid":"MOD:01296"}


id: PBO:0041077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biogenesis of ribosomes BRX1","termid":"PBO:0041077"}


id: PBO:0059045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MMS22 like, DNA repair protein","termid":"PBO:0059045"}


id: FYPO:0004444
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the prospore membrane is decreased, and the protein is instead present in the plasma membrane, during the second meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:21832151"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"decreased protein localization to prospore membrane","termid":"FYPO:0004442"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein localization to prospore membrane during meiosis II with protein mislocalized to plasma membrane","synonyms":[{"name":"decreased protein localisation to prospore membrane during meiosis II with protein mislocalized to plasma membrane","type":"exact"},{"name":"decreased protein localization to forespore membrane during meiosis II with protein mislocalized to plasma membrane","type":"exact"},{"name":"decreased protein localization to prospore membrane during second meiotic nuclear division with protein mislocalized to plasma membrane","type":"exact"},{"name":"decreased protein localization to prospore membrane with protein mislocalized to plasma membrane during meiosis II","type":"related"},{"name":"reduced protein localization to prospore membrane during meiosis II with protein mislocalized to plasma membrane","type":"exact"}],"termid":"FYPO:0004444"}


id: GO:0045706
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of salivary gland determination.","definition_xrefs":["GOC:tb","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of salivary gland boundary specification","termid":"GO:0045704"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"salivary gland boundary specification","termid":"GO:0007432"}],"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 salivary gland boundary specification","synonyms":[{"name":"activation of salivary gland determination","type":"narrow"},{"name":"positive regulation of salivary gland determination","type":"exact"},{"name":"stimulation of salivary gland determination","type":"narrow"},{"name":"up regulation of salivary gland determination","type":"exact"},{"name":"up-regulation of salivary gland determination","type":"exact"},{"name":"upregulation of salivary gland determination","type":"exact"}],"termid":"GO:0045706"}


id: GO:0071539
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained at, the centrosome.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to microtubule organizing center","termid":"GO:1905508"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to centrosome","synonyms":[{"name":"protein localisation to centrosome","type":"exact"}],"termid":"GO:0071539"}


id: PATO:0001844
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An acidity which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"acidity","termid":"PATO:0001842"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased acidity","synonyms":[{"name":"high acidity","type":"exact"}],"termid":"PATO:0001844"}


id: GO:0060256
data:
  {"annotated_genes":["SJAG_00910","SJAG_00926","SJAG_04191","SJAG_03484","SJAG_02380","SJAG_01253","SJAG_03473","SJAG_03802"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103557,106266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060257"},{"annotations":[108651,105912,111390,116169,108774,114104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900735"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the non-sexual aggregation of single-celled organisms.","definition_xrefs":["PMID:10591965","PMID:15466424","PMID:16568252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-cell adhesion","termid":"GO:0022407"},{"relation_name":"regulates","term_name":"flocculation","termid":"GO:0000128"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00910":null,"SJAG_00926":null,"SJAG_01253":null,"SJAG_02380":null,"SJAG_03473":null,"SJAG_03484":null,"SJAG_03802":null,"SJAG_04191":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"regulation of flocculation","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:1900455"],"synonyms":[{"name":"regulation of flocculation via cell wall protein-carbohydrate interaction","type":"related"}],"termid":"GO:0060256","terms_by_termid":{"GO:0060257":null,"GO:1900735":null}}


id: PBO:0038877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate cyclase 4","termid":"PBO:0038877"}


id: PBO:0062542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily I member 1","termid":"PBO:0062542"}


id: GO:0101027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regrowth of axons of the optical nerve following their loss or damage.","definition_xrefs":["GOC:pga","PMID:16699509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon regeneration","termid":"GO:0031103"}],"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":"optical nerve axon regeneration","termid":"GO:0101027"}


id: PBO:0071347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 5","termid":"PBO:0071347"}


id: PBO:0110155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome-associated protein, implicated in ribosome assembly or ribosome quality control","termid":"PBO:0110155"}


id: GO:1903884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of chemokine (C-C motif) ligand 20 production.","definition_xrefs":["GOC:krc","GO_REF:0000058","PMID:20054338","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemokine production","termid":"GO:0032642"},{"relation_name":"regulates","term_name":"chemokine (C-C motif) ligand 20 production","termid":"GO:0036392"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of chemokine (C-C motif) ligand 20 production","synonyms":[{"name":"regulation of C-C motif chemokine 20 production","type":"exact"},{"name":"regulation of CCL-20 production","type":"exact"},{"name":"regulation of CCL20 production","type":"exact"}],"termid":"GO:1903884"}


id: PBO:0065668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase receptor type Q","termid":"PBO:0065668"}


id: PBO:0066893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 193","termid":"PBO:0066893"}


id: PBO:0043510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CNTNAP3 pseudogene 5","termid":"PBO:0043510"}


id: PBO:0057003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 96","termid":"PBO:0057003"}


id: MONDO:0022655
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"cardiomyopathy hypogonadism metabolic anomalies","secondary_identifiers":["GARD:1109"],"termid":"MONDO:0022655","xrefs":{"Monarch":{"xref_id":"0022655"}}}


id: PBO:0004801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexaprenyldihydroxybenzoate methyltransferase (predicted)","termid":"PBO:0004801"}


id: PBO:0090361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3, unknown specificity","termid":"PBO:0090361"}


id: PBO:0065128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase cGMP-dependent 1","termid":"PBO:0065128"}


id: SO:0001750
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL5 RNA leader sequence to the 5' end of an mRNA. SL5 acceptor sites occur in genes in internal segments of polycistronic transcripts.","definition_xrefs":["SO:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SL2_acceptor_site","termid":"SO:0000709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SL5_acceptor_site","synonyms":[{"name":"SL5 acceptor site","type":"exact"}],"termid":"SO:0001750"}


id: PBO:0001980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase alpha accessory factor Mcl1","termid":"PBO:0001980"}


id: PBO:0079575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin D","termid":"PBO:0079575"}


id: PBO:0071640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36 pseudogene 4","termid":"PBO:0071640"}


id: MONDO:0043468
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic eruption of fibrous papules that develop and fuse to form a thick sclerotic, hypertrophic band at a site of deep folliculitis, usually along the posterior hairline of the scalp. It is most commonly seen in men of African descent.","definition_xrefs":["NCIT:C34346"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keloid","termid":"MONDO:0005348"},{"relation_name":"is_a","term_name":"folliculitis","termid":"MONDO:0006552"}],"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":"acne keloid","secondary_identifiers":["MESH:D000153","MEDGEN:1720","SCTID:238746008","UMLS:C0001145"],"synonyms":[{"name":"Acnes, nuchal keloid","type":"related"},{"name":"Capillitii, dermatitis papillaris","type":"related"},{"name":"Capillitius, dermatitis papillaris","type":"related"},{"name":"Keloidalis nuchae, folliculitis","type":"related"},{"name":"Keloidalis nuchae, lichen","type":"related"},{"name":"acne Keloidalis","type":"related"},{"name":"acne keloid","type":"exact"},{"name":"acne keloids","type":"related"},{"name":"acne, keloidal","type":"related"},{"name":"acne, nuchal keloid","type":"related"},{"name":"dermatitis papillaris Capillitii","type":"related"},{"name":"dermatitis papillaris Capillitius","type":"related"},{"name":"folliculitis Keloidalis","type":"related"},{"name":"folliculitis Keloidalis nuchae","type":"related"},{"name":"keloid Acnes, nuchal","type":"related"},{"name":"keloid acne, nuchal","type":"related"},{"name":"keloid, acne","type":"related"},{"name":"keloidal Acnes","type":"related"},{"name":"keloidal acne","type":"related"},{"name":"keloidal folliculitis","type":"exact"},{"name":"keloids, acne","type":"related"},{"name":"lichen Keloidalis nuchae","type":"related"},{"name":"nuchae, folliculitis Keloidalis","type":"related"},{"name":"nuchae, lichen Keloidalis","type":"related"},{"name":"nuchal keloid Acnes","type":"related"},{"name":"nuchal keloid acne","type":"related"},{"name":"papillaris Capillitii, dermatitis","type":"related"},{"name":"papillaris Capillitius, dermatitis","type":"related"}],"termid":"MONDO:0043468","xrefs":{"Monarch":{"xref_id":"0043468"}}}


id: PBO:0017679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase with rhodanese domain (predicted)","termid":"PBO:0017679"}


id: PBO:0040913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 17","termid":"PBO:0040913"}


id: FYPO:0006046
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 in which chromosomes do not align at the midpoint of the long axis of the mitotic spindle during metaphase chromosome congression.","definition_xrefs":["PomBase:mah","PMID:27146110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic chromosome congression","termid":"FYPO:0000030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0000631","FYPO:0000337","FYPO:0000641"],"is_obsolete":false,"name":"uncentered mitotic chromosome congression","synonyms":[{"name":"abnormal mitotic chromosome congression with loss of chromosome centering","type":"exact"},{"name":"loss of mitotic chromosome centering","type":"exact"},{"name":"uncentered chromosome congression during mitosis","type":"exact"},{"name":"uncentered chromosome congression during mitotic metaphase","type":"exact"},{"name":"uncentered mitotic chromosome congression during vegetative growth","type":"exact"}],"termid":"FYPO:0006046"}


id: GO:0004058
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-amino acid + H+ = R-H + CO2.","definition_xrefs":["EC:4.1.1.28"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"aromatic-L-amino-acid decarboxylase activity","secondary_identifiers":["Reactome:R-HSA-209924","MetaCyc:AROMATIC-L-AMINO-ACID-DECARBOXYLASE-RXN","GO:0016400","Reactome:R-HSA-209859"],"synonyms":[{"name":"5-hydroxytryptophan decarboxylase activity","type":"narrow"},{"name":"DOPA decarboxylase activity","type":"narrow"},{"name":"L-DOPA decarboxylase activity","type":"narrow"},{"name":"aromatic amino acid decarboxylase activity","type":"related"},{"name":"aromatic-L-amino-acid carboxy-lyase (tryptamine-forming)","type":"narrow"},{"name":"aromatic-L-amino-acid carboxy-lyase activity","type":"related"},{"name":"hydroxytryptophan decarboxylase activity","type":"narrow"},{"name":"tryptophan decarboxylase activity","type":"narrow"}],"termid":"GO:0004058"}


id: PBO:0030743
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_phosphatidylinositol-4-phosphate_level","termid":"PBO:0030743"}


id: GO:0015214
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a pyrimidine nucleoside, a pyrimidine base covalently bonded to a ribose or deoxyribose sugar from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside transmembrane transporter activity","termid":"GO:0005337"}],"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":"pyrimidine nucleoside transmembrane transporter activity","termid":"GO:0015214"}


id: FYPO:0007457
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells contain more nuclear envelope than normal during interphase of the mitotic cell cycle. Excess nuclear envelopes may take the form of intranuclear membrane stacks or invaginations, or small cytoplasmic spheres that are attached to the nucleus, have double lipid bilayer membranes, and may contain structures resembling nuclear pores.","definition_xrefs":["PomBase:mah","PMID:32848252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"excess nuclear envelope present","termid":"FYPO:0001556"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0002403","FYPO:0000002"],"is_obsolete":false,"name":"excess nuclear envelope present during mitotic interphase","synonyms":[{"name":"excess nuclear envelope present during interphase of mitotic cell cycle","type":"exact"},{"name":"excess nuclear envelope present during mitotic interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0007457"}


id: MONDO:0017533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"postaxial polydactyly type B","termid":"MONDO:0019674"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly type B, unilateral","secondary_identifiers":["Orphanet:295167","icd11.foundation:154207037"],"termid":"MONDO:0017533","xrefs":{"Monarch":{"xref_id":"0017533"}}}


id: PBO:0083276
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; not conserved in closely related Saccharomyces species; deletion mutation blocks replication of Brome mosaic virus in S. cerevisiae, but this is likely due to effects on the overlapping gene SCS2","termid":"PBO:0083276"}


id: PBO:0078559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 47","termid":"PBO:0078559"}


id: GO:0043219
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Non-compact myelin located adjacent to the nodes of Ranvier in a myelin segment. These non-compact regions include cytoplasm from the cell responsible for synthesizing the myelin. Lateral loops are found in the paranodal region adjacent to the nodes of Ranvier, while Schmidt-Lantermann clefts are analogous structures found within the compact myelin internode.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"myelin sheath","termid":"GO:0043209"}],"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":"lateral loop","secondary_identifiers":["NIF_Subcellular:sao1354781919","NIF_Subcellular:sao1067215520"],"synonyms":[{"name":"Schwann cell paranodal termination","type":"related"},{"name":"oligodendrocyte paranodal termination","type":"related"},{"name":"paranodal loop","type":"related"}],"termid":"GO:0043219"}


id: GO:0044477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant stopping, prevention or reduction in the frequency, rate or extent of platelet aggregation in the bitten organism.","definition_xrefs":["GOC:fj","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in modulation of process in another organism","termid":"GO:0035738"}],"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":"envenomation resulting in negative regulation of platelet aggregation in another organism","synonyms":[{"name":"envenomation resulting in negative regulation of platelet aggregation in other organism","type":"exact"}],"termid":"GO:0044477"}


id: FYPO:0004025
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of the tubulin poison carbendazim (mecarzole; MBC) than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0002682","FYPO:0000139"],"is_obsolete":false,"name":"resistance to carbendazim","synonyms":[{"name":"resistance to MBC","type":"exact"},{"name":"resistance to carbendazim during mitotic cell cycle","type":"related"},{"name":"resistance to carbendazim during vegetative growth","type":"exact"},{"name":"resistance to methyl benzimidazole-2-yl-carbamate","type":"exact"},{"name":"resistance to methylbenzylcarbamylate","type":"exact"},{"name":"resistant to carbendazim","type":"exact"}],"termid":"FYPO:0004025"}


id: GO:0061004
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 kidney to which cells respond and eventually are instructed to differentiate.","definition_xrefs":["GOC:dph","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"},{"relation_name":"part_of","term_name":"kidney development","termid":"GO:0001822"},{"relation_name":"part_of","term_name":"renal system pattern specification","termid":"GO:0072048"}],"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":"pattern specification involved in kidney development","synonyms":[{"name":"kidney pattern formation","type":"related"},{"name":"kidney pattern specification","type":"exact"},{"name":"pattern formation involved in kidney development","type":"related"}],"termid":"GO:0061004"}


id: PBO:0001293
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mouse Glia Maturation Factor homolog","termid":"PBO:0001293"}


id: GO:0034372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The acquisition, loss or modification of a protein or lipid within a very-low-density lipoprotein particle, including the hydrolysis of triglyceride by hepatic lipase or lipoprotein lipase and the subsequent loss of free fatty acid.","definition_xrefs":["GOC:expert_pt","GOC:BHF","GOC:mah","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triglyceride-rich lipoprotein particle remodeling","termid":"GO:0034370"}],"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":"very-low-density lipoprotein particle remodeling","synonyms":[{"name":"VDL formation","type":"related"},{"name":"VDL remodeling","type":"exact"},{"name":"VDL remodelling","type":"exact"},{"name":"very-low-density lipoprotein particle remodelling","type":"exact"}],"termid":"GO:0034372"}


id: GO:0052211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An interaction with a second organism mediated by a substance secreted by the first organism by a type II secretion system, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete interaction with other organism via protein secreted by type II secretion system involved in symbiotic interaction (obsolete GO:0052211)","synonyms":[{"name":"interaction with other organism via protein secreted by type II secretion system during symbiotic interaction","type":"related"}],"termid":"GO:0052211"}


id: MONDO:0005842
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or chronic inflammatory process affecting the mucous membrane of the maxillary sinus.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sinusitis","termid":"MONDO:0005961"},{"relation_name":"is_a","term_name":"mouth disorder","termid":"MONDO:0006858"},{"relation_name":"is_a","term_name":"disorder of facial skeleton","termid":"MONDO:0023369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maxillary sinusitis","secondary_identifiers":["SCTID:88348008","EFO:0007361","DOID:2051","UMLS:C0024959","NCIT:C34809","MEDGEN:44313","MESH:D015523"],"termid":"MONDO:0005842","xrefs":{"Monarch":{"xref_id":"0005842"}}}


id: PBO:0054024
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 1355","termid":"PBO:0054024"}


id: MONDO:0018918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Carcinoma of the gallbladder (GBC) is the most common and aggressive form of biliary tract cancer (BTC) usually arising in the fundus of the gallbladder, rapidly metastasizing to lymph nodes and distant sites.","definition_xrefs":["Orphanet:56044"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrahepatic bile duct neoplasm","termid":"MONDO:0021385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"carcinoma of gallbladder and extrahepatic biliary tract","secondary_identifiers":["MedDRA:10007426","GARD:18850","MEDGEN:1797980","UMLS:C5566557"],"synonyms":[{"name":"carcinoma of gallbladder and EBT","type":"exact"}],"termid":"MONDO:0018918","xrefs":{"Monarch":{"xref_id":"0018918"}}}


id: MONDO:0001111
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete thrombotic thrombocytopenic purpura (obsolete MONDO:0001111)","termid":"MONDO:0001111","xrefs":{"Monarch":{"xref_id":"0001111"}}}


id: GO:0009706
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The inner, i.e. lumen-facing, lipid bilayer of the chloroplast envelope; also faces the chloroplast stroma.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid inner membrane","termid":"GO:0009528"},{"relation_name":"is_a","term_name":"chloroplast membrane","termid":"GO:0031969"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"chloroplast inner membrane","synonyms":[{"name":"chloroplast inner envelope","type":"exact"}],"termid":"GO:0009706"}


id: MONDO:0010623
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":"ichthyosis and male hypogonadism","secondary_identifiers":["ICD9:759.89","MESH:C537365","SCTID:2355008","OMIM:308200","Orphanet:431","UMLS:C1839989","MEDGEN:333456"],"synonyms":[{"name":"Ichthyosis-male hypogonadism syndrome","type":"exact"},{"name":"Ruds","type":"related"},{"name":"ichthyosis and male hypogonadism","type":"exact"},{"name":"rud syndrome","type":"related"}],"termid":"MONDO:0010623","xrefs":{"Monarch":{"xref_id":"0010623"}}}


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


id: PBO:0111065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"huamn GCFC2 ortholog","termid":"PBO:0111065"}


id: PBO:0030500
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_DNA_damage_checkpoint","termid":"PBO:0030500"}


id: MONDO:0002104
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Conversion disorder is a disorder in which a person experiences blindness, paralysis, or other symptoms affecting the nervous system that cannot be explained solely by a physical illness or injury. Symptoms usually begin suddenly after a period of emotional or physical distress or psychological conflict. Conversion disorder is thought to be caused by the bodys reaction to a stressful physical or emotional event. Some research has identified potential neurological changes that may be related to symptoms of the disorder. Diagnosis of conversion disorder is based on identifying particular signs that are common among people with the disorder, as well as performing tests to rule out other causes of the symptoms. Treatment may include psychotherapy, hypnosis, and stress management training to help reduce symptoms. Treatment of any underlying psychological disorder is also recommended. The affected body part may require physical or occupational therapy until symptoms resolve.","direct_ancestors":[{"relation_name":"is_a","term_name":"somatoform disorder","termid":"MONDO:0003117"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conversion disorder","secondary_identifiers":["ICD9:300.11","MEDGEN:3230","UMLS:C0009946","DOID:1768","MESH:D003291"],"synonyms":[{"name":"FND","type":"related"},{"name":"conversion hysteria or reaction","type":"exact"},{"name":"conversion hysterical neurosis","type":"exact"},{"name":"functional movement disorder","type":"related"},{"name":"functional neurological disorder","type":"related"},{"name":"hysterical neurosis, conversion type","type":"exact"}],"termid":"MONDO:0002104","xrefs":{"Monarch":{"xref_id":"0002104"}}}


id: PBO:0058737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6862-1","termid":"PBO:0058737"}


id: PBO:0055604
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 3042","termid":"PBO:0055604"}


id: PBO:0030137
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_GTPase_activity","termid":"PBO:0030137"}


id: PBO:0051989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"JAKMIP1 divergent transcript","termid":"PBO:0051989"}


id: PBO:0068482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 63, pseudogene","termid":"PBO:0068482"}


id: PR:Q8TFH5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPB17E12.09 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q8TFH5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated protein PB17E12.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB17E12.09","synonyms":[{"name":"Spom972h-SPAPB17E12.09","type":"exact"}],"termid":"PR:Q8TFH5"}


id: GO:0060399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of the growth hormone receptor signaling pathway. The growth hormone receptor signaling pathway is the series of molecular signals generated as a consequence of growth hormone receptor binding to its physiological ligand.","definition_xrefs":["GOC:dph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of growth hormone receptor signaling pathway","termid":"GO:0060398"},{"relation_name":"positively_regulates","term_name":"growth hormone receptor signaling pathway","termid":"GO:0060396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of growth hormone receptor signaling pathway","synonyms":[{"name":"positive regulation of growth hormone receptor signalling pathway","type":"exact"}],"termid":"GO:0060399"}


id: PBO:0002950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U1 snRNP-associated protein Usp104","termid":"PBO:0002950"}


id: FYECO:0000286
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in medium containing glucose (typically <2% w/v), salts, water and with no adenine.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucose MM, no adenine","termid":"FYECO:0000286"}


id: FYPO:0002054
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cut phenotype that is observed when a cell is exposed to hydroxyurea. In a cut phenotype, a cell undergoes septation despite abnormal chromosome segregation.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cut during cellular response to hydroxyurea (obsolete FYPO:0002054)","synonyms":[{"name":"cut during cellular response to HU","type":"exact"},{"name":"cut during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"cut during cellular response to hydroxyurea during vegetative growth","type":"exact"}],"termid":"FYPO:0002054"}


id: SO:0000050
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A part of a gene, that has no other route in the ontology back to region. This concept is necessary for logical inference as these parts must have the properties of region. It also allows us to associate all the parts of genes with a gene.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000050 gene_part (obsolete SO:0000050)","termid":"SO:0000050"}


id: PBO:0071247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 88","termid":"PBO:0071247"}


id: PBO:0056357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule associated protein 10","termid":"PBO:0056357"}


id: MONDO:0003618
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The presence of pus in the fallopian tube. It is usually caused by acute salpingitis. The fallopian tube is distended and filled with pus. Histologic examination reveals edema and acute and chronic inflammation. Symptoms include fever, vaginal discharge, and pelvic pain.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salpingitis","termid":"MONDO:0003619"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyosalpinx","secondary_identifiers":["UMLS:C0034220","DOID:5732","SCTID:397810006","MEDGEN:18785","NCIT:C34968"],"synonyms":[{"name":"pyosalpingitis","type":"exact"}],"termid":"MONDO:0003618","xrefs":{"Monarch":{"xref_id":"0003618"}}}


id: FYPO:0003021
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to ethyl N-phenylcarbamate (EPC). Cells stop growing (and may die) at a concentration of EPC that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000003","FYPO:0002683","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to EPC","synonyms":[{"name":"hypersensitive to EPC","type":"exact"},{"name":"sensitive to EPC during mitotic cell cycle","type":"related"},{"name":"sensitive to EPC during vegetative growth","type":"exact"},{"name":"sensitive to ethyl N-phenylcarbamate","type":"exact"}],"termid":"FYPO:0003021"}


id: PR:O13979
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug105 gene.","definition_xrefs":["UniProtKB:O13979","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 105 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25H1.04","synonyms":[{"name":"Spom972h-mug105","type":"exact"}],"termid":"PR:O13979"}


id: SO:0001889
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature amplification of a region containing a transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_amplification","termid":"SO:0001880"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcript_amplification","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences"],"synonyms":[{"name":"VEP:transcript_amplification","type":"exact"},{"name":"transcript amplification","type":"exact"}],"termid":"SO:0001889"}


id: PBO:0081911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 878","termid":"PBO:0081911"}


id: FYPO:0006743
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the nucleus is decreased during a cellular response to osmotic stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to nucleus during vegetative growth","termid":"FYPO:0001514"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to nucleus during cellular response to osmotic stress","synonyms":[{"name":"decreased protein localisation to nucleus during cellular response to osmotic stress","type":"exact"},{"name":"decreased protein localization to nucleus during cellular response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to nucleus during cellular response to osmotic stress during vegetative growth","type":"exact"},{"name":"decreased protein localization to nucleus during osmotic stress","type":"exact"},{"name":"reduced protein localization to nucleus during cellular response to osmotic stress","type":"exact"}],"termid":"FYPO:0006743"}


id: SOFP:aminoacid
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","definition":"amino acid coded for by a tRNA transcript feature","definition_xrefs":["so:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminoacid","termid":"SOFP:aminoacid"}


