# terms

id: PBO:0047153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 183 member D, pseudogene","termid":"PBO:0047153"}


id: GO:0002215
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A response to protect an organism from a directly detected or perceived external threat from a nematode or nematodes, which results in restriction of damage to the organism attacked or prevention/recovery from the infection caused by the attack.","definition_xrefs":["PMID:14506883","GOC:add","PMID:11516579"],"direct_ancestors":[{"relation_name":"is_a","term_name":"defense response","termid":"GO:0006952"},{"relation_name":"is_a","term_name":"response to other organism","termid":"GO:0051707"}],"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":"defense response to nematode","secondary_identifiers":["GO:0002216"],"synonyms":[{"name":"physiological defense response to nematode","type":"exact"}],"termid":"GO:0002215"}


id: SO:0002098
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A pseudogene derived from an immunoglobulin gene.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immune_system_pseudogene","termid":"SO:0002097"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin_pseudogene","synonyms":[{"name":"immunoglobulin pseudogene","type":"exact"}],"termid":"SO:0002098"}


id: FYPO:0003498
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the initiation of nuclear DNA replication begins earlier than normal.","definition_xrefs":["PMID:22970243","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic DNA replication initiation","termid":"FYPO:0001344"},{"relation_name":"output_of","term_name":"abnormal regulation of mitotic DNA replication initiation","termid":"FYPO:0001248"}],"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:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0000293"],"is_obsolete":false,"name":"premature mitotic DNA replication initiation","synonyms":[{"name":"advanced mitotic DNA replication initiation","type":"exact"},{"name":"premature DNA replication initiation during mitotic cell cycle","type":"exact"},{"name":"premature DNA replication initiation during vegetative growth","type":"exact"}],"termid":"FYPO:0003498"}


id: PBO:0028824
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cytoskeleton_morphology","termid":"PBO:0028824"}


id: GO:0000459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Exonucleolytic digestion of a pre-rRNA molecule in the process to generate a mature rRNA molecule.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete exonucleolytic trimming involved in rRNA processing (obsolete GO:0000459)","synonyms":[{"name":"exonucleolytic trimming during rRNA processing","type":"related"}],"termid":"GO:0000459"}


id: PBO:0012551
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is not functionally complemented by S. cerevisiae TEM1","termid":"PBO:0012551"}


id: PBO:0075982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal transducer and activator of transcription 6","termid":"PBO:0075982"}


id: MONDO:1010642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Factor XII deficiency that occurs in common bottlenose dolphin.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"factor XII deficiency, non-human animal","termid":"MONDO:1010074"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"factor XII deficiency, common bottlenose dolphin","secondary_identifiers":["OMIA:000364-9739"],"termid":"MONDO:1010642","xrefs":{"Monarch":{"xref_id":"1010642"}}}


id: PBO:0059249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L18","termid":"PBO:0059249"}


id: PR:Q9P7U4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC977.05c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7U4"],"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":"VEL1-related protein AC977.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC977.05c","synonyms":[{"name":"Spom972h-SPAC977.05c","type":"exact"}],"termid":"PR:Q9P7U4"}


id: FYPO:0007031
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 cell cortex of one or both cell tips  does not occur during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to cell tip during mitotic interphase","termid":"FYPO:0003329"},{"relation_name":"is_a","term_name":"abolished protein localization to cell cortex of cell tip during vegetative growth","termid":"FYPO:0006502"},{"relation_name":"is_a","term_name":"abnormal protein localization to cell cortex of cell tip during vegetative growth","termid":"FYPO:0006875"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to cell cortex of cell tip during mitotic interphase","synonyms":[{"name":"abolished protein localisation to cell cortex of cell tip during mitotic interphase","type":"exact"},{"name":"abolished protein localization to cell cortex of cell end during mitotic interphase during vegetative growth","type":"related"},{"name":"abolished protein localization to cell cortex of cell tip during interphase of mitotic cell cycle","type":"exact"},{"name":"abolished protein localization to cell tip cortex during mitotic interphase","type":"exact"},{"name":"protein localization to cell cortex of cell tip abolished during mitotic interphase","type":"exact"}],"termid":"FYPO:0007031"}


id: PBO:0083940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gamma-aminobutyrate (GABA) transaminase; also known as 4-aminobutyrate aminotransferase; involved in the 4-aminobutyrate and glutamate degradation pathways; required for normal oxidative stress tolerance and nitrogen utilization; protein abundance increases in response to DNA replication stress","termid":"PBO:0083940"}


id: PR:O43012
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dcd1 gene.","definition_xrefs":["UniProtKB:O43012","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":"deoxycytidylate deaminase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2G2.13c","synonyms":[{"name":"Spom972h-dcd1","type":"exact"},{"name":"dCMP deaminase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43012"}


id: GO:0019931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-lysine to form N6-3,4-didehydroretinylidene-L-lysine.","definition_xrefs":["RESID:AA0312"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-chromophore linkage via peptidyl-N6-3-dehydroretinal-L-lysine (obsolete GO:0019931)","termid":"GO:0019931"}


id: GO:0031332
data:
  {"annotated_genes":["SJAG_02594","SJAG_03042","SJAG_02621","SJAG_03706","SJAG_04061","SJAG_03916"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[65740],"is_not":false,"summary":null,"term":"GO:0031332"},{"annotations":[90543,119939,63626],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033167"},{"annotations":[114040,93040,119945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030958"}]},"cv_name":"cellular_component","definition":"Any protein complex that mediates the effects of small interfering RNAs on gene expression. Most known examples contain one or more members of the Argonaute family of proteins.","definition_xrefs":["GOC:mah","PMID:14704433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoprotein complex","termid":"GO:1990904"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02594":null,"SJAG_02621":null,"SJAG_03042":null,"SJAG_03706":null,"SJAG_03916":null,"SJAG_04061":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"RNAi effector complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"termid":"GO:0031332","terms_by_termid":{"GO:0030958":null,"GO:0031332":null,"GO:0033167":null}}


id: PATO:0000300
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A mobility quality inhering in a bearer by virtue of the bearer's being incapable to move freely.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mobility","termid":"PATO:0000004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immobile","synonyms":[{"name":"fixed","type":"related"}],"termid":"PATO:0000300"}


id: PBO:0068433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 3","termid":"PBO:0068433"}


id: GO:0031053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involved in the conversion of a primary microRNA transcript into a pre-microRNA molecule.","definition_xrefs":["PMID:15211354","GOC:sl","PMID:25799998"],"direct_ancestors":[{"relation_name":"is_a","term_name":"miRNA processing","termid":"GO:0035196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"primary miRNA processing","secondary_identifiers":["GO:1990744","GO:1990729"],"synonyms":[{"name":"pri-miRNA processing","type":"exact"},{"name":"primary miRNA methylation","type":"narrow"},{"name":"primary miRNA modification","type":"exact"},{"name":"primary microRNA processing","type":"exact"}],"termid":"GO:0031053"}


id: GO:0033616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a proton-transporting ATP synthase in the plasma membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton-transporting ATP synthase complex assembly","termid":"GO:0043461"},{"relation_name":"part_of","term_name":"plasma membrane organization","termid":"GO:0007009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"plasma membrane proton-transporting ATP synthase complex assembly","termid":"GO:0033616"}


id: GO:0005289
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of arginine from one side of a membrane to the other. In high-affinity transport the transporter is able to bind the solute even if it is only present at very low concentrations.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"high-affinity basic amino acid transmembrane transporter activity","termid":"GO:0005287"},{"relation_name":"is_a","term_name":"L-arginine transmembrane transporter activity","termid":"GO:0061459"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"high-affinity L-arginine transmembrane transporter activity","synonyms":[{"name":"high affinity arginine transmembrane transporter activity","type":"exact"},{"name":"high-affinity arginine transmembrane transporter activity","type":"exact"},{"name":"high-affinity arginine transporter activity","type":"broad"}],"termid":"GO:0005289"}


id: GO:0050194
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + phosphonoacetaldehyde = acetaldehyde + H+ + phosphate.","definition_xrefs":["RHEA:18905"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-phosphorus bonds","termid":"GO:0016827"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"phosphonoacetaldehyde hydrolase activity","secondary_identifiers":["EC:3.11.1.1","KEGG_REACTION:R00747","MetaCyc:PHOSPHONOACETALDEHYDE-HYDROLASE-RXN"],"synonyms":[{"name":"2-oxoethylphosphonate phosphonohydrolase activity","type":"related"},{"name":"2-phosphonoacetylaldehyde phosphonohydrolase activity","type":"related"},{"name":"phosphonatase activity","type":"related"},{"name":"phosphonoacetylaldehyde phosphonohydrolase activity","type":"related"}],"termid":"GO:0050194"}


id: PBO:0073086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SDHA pseudogene 2","termid":"PBO:0073086"}


id: MONDO:0022598
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":"brachydactyly absence of distal phalanges","termid":"MONDO:0022598","xrefs":{"Monarch":{"xref_id":"0022598"}}}


id: PBO:0048497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ganglioside induced differentiation associated protein 1","termid":"PBO:0048497"}


id: PBO:0042758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 20","termid":"PBO:0042758"}


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


id: PBO:0064240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol specific phospholipase C X domain containing 3","termid":"PBO:0064240"}


id: PBO:0034348
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-connected_to","termid":"PBO:0034348"}


id: MOD:00465
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to a dihydroxyphenylalanine.","definition_xrefs":["PubMed:1610822","PubMed:1903612","PubMed:3734192","PubMed:9252331","RESID:AA0146#var","Unimod:425#F","OMSSA:39"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dihydroxylated residue","termid":"MOD:00428"},{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydroxyphenylalanine (Phe)","synonyms":[{"name":"Dioxidation","type":"related"},{"name":"dihydroxy","type":"related"},{"name":"dihydroxyf","type":"exact"}],"termid":"MOD:00465"}


id: MONDO:0009157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any split hand-foot malformation in which the cause of the disease is a mutation in the WNT10B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"split hand-foot malformation","termid":"MONDO:0016576"}],"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":"split hand-foot malformation 6","secondary_identifiers":["GARD:15166","MEDGEN:440845","MESH:C567616","OMIM:225300","UMLS:C2749665","DOID:0090026"],"synonyms":[{"name":"SHFM6","type":"exact"},{"name":"WNT10B split hand-foot malformation","type":"exact"},{"name":"ectrodactyly, autosomal recessive","type":"related"},{"name":"split hand-foot malformation caused by mutation in WNT10B","type":"exact"},{"name":"split hand-foot malformation type 6","type":"exact"},{"name":"split-hand/foot malformation 6","type":"related"},{"name":"split-hand/foot malformation type 6","type":"exact"}],"termid":"MONDO:0009157","xrefs":{"Monarch":{"xref_id":"0009157"}}}


id: GO:0002621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of non-professional antigen presenting cell antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of antigen processing and presentation","termid":"GO:0002579"},{"relation_name":"is_a","term_name":"regulation of non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002619"},{"relation_name":"positively_regulates","term_name":"non-professional antigen presenting cell antigen processing and presentation","termid":"GO:0002473"}],"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 non-professional antigen presenting cell antigen processing and presentation","synonyms":[{"name":"activation of non-professional antigen presenting cell antigen processing and presentation","type":"narrow"},{"name":"stimulation of non-professional antigen presenting cell antigen processing and presentation","type":"narrow"},{"name":"up regulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"},{"name":"up-regulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"},{"name":"upregulation of non-professional antigen presenting cell antigen processing and presentation","type":"exact"}],"termid":"GO:0002621"}


id: GO:0072754
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 purvalanol A stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to purine-containing compound","termid":"GO:0071415"},{"relation_name":"is_a","term_name":"response to purvalanol A","termid":"GO:1901560"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"}],"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 purvalanol A","termid":"GO:0072754"}


id: PBO:0017423
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-located_in","termid":"PBO:0017423"}


id: GO:0050818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of coagulation, the process in which a fluid solution, or part of it, changes into a solid or semisolid mass.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"coagulation","termid":"GO:0050817"}],"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 coagulation","synonyms":[{"name":"regulation of clotting","type":"exact"}],"termid":"GO:0050818"}


id: GO:0106317
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: methane + NADH + H+ + O2 = methanol + NAD+ + H2O.","definition_xrefs":["RHEA:13637"],"gene_count":0,"genotype_count":0,"name":"obsolete methane monooxygenase NADH activity (obsolete GO:0106317)","termid":"GO:0106317"}


id: MONDO:0007839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aase-Smith syndrome type I is a very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures.","definition_xrefs":["Orphanet:916"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0020022","MONDO:0002320"],"is_obsolete":false,"name":"Aase-Smith syndrome","secondary_identifiers":["MESH:C535332","SCTID:718576001","UMLS:C0220686","GARD:5642","MEDGEN:66316","OMIM:147800","MedDRA:10063429"],"synonyms":[{"name":"Aase-Smith I syndrome","type":"exact"},{"name":"Aase-Smith syndrome","type":"exact"},{"name":"Aase-Smith syndrome 1","type":"related"},{"name":"Aase-Smith syndrome I","type":"related"},{"name":"Aase-Smith syndrome type 1","type":"exact"},{"name":"Joint contractures with Other abnormalities","type":"related"},{"name":"hydrocephalus-cleft palate-joint contractures syndrome","type":"exact"}],"termid":"MONDO:0007839","xrefs":{"Monarch":{"xref_id":"0007839"}}}


id: GO:0090669
data:
  {"annotated_genes":["SJAG_04586"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92406],"is_not":false,"summary":null,"term":"GO:0090669"}]},"cv_name":"biological_process","definition":"Prevention of degradation of telomerase RNA (TERC) molecules.","definition_xrefs":["GOC:BHF_telomere","GOC:nc","PMID:25467444","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA stabilization","termid":"GO:0043489"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04586":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"telomerase RNA stabilization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"TERC stabilization","type":"exact"}],"termid":"GO:0090669","terms_by_termid":{"GO:0090669":null}}


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


id: GO:0140049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocardial cushion to mesenchymal transition.","definition_xrefs":["GOC:BHF_miRNA","GOC:BHF","GOC:rph","PMID:21778427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac epithelial to mesenchymal transition","termid":"GO:0062042"},{"relation_name":"regulates","term_name":"endocardial cushion to mesenchymal transition","termid":"GO:0090500"}],"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 endocardial cushion to mesenchymal transition","termid":"GO:0140049"}


id: GO:0036434
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ethylnitronate + FMNH(2) + O2 = acetaldehyde + FMN + H2O + H+ + nitrite.","definition_xrefs":["RHEA:26458"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of one atom of oxygen (internal monooxygenases or internal mixed function oxidases)","termid":"GO:0016703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"nitronate monooxygenase (FMN-linked) activity","secondary_identifiers":["KEGG_REACTION:R00025"],"termid":"GO:0036434"}


id: SO:0001475
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a primary transcript, that is removed via trans splicing.","definition_xrefs":["SO:ke","PMID:16401417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary_transcript_region","termid":"SO:0000835"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outron","termid":"SO:0001475"}


id: PBO:0089421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARP2/3 actin-organizing complex WD repeat subunit Sop2","termid":"PBO:0089421"}


id: MONDO:0037254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transitional cell neoplasm","secondary_identifiers":["UMLS:C0334265","MEDGEN:90754","NCIT:C6783"],"synonyms":[{"name":"transitional cell neoplasm","type":"exact"},{"name":"transitional cell tumor","type":"exact"},{"name":"transitional cell tumour","type":"exact"}],"termid":"MONDO:0037254","xrefs":{"Monarch":{"xref_id":"0037254"}}}


id: PBO:0082367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR domain protein that localizes to early and late Golgi vesicles; required for adaptation to varying nutrient concentrations, fluid-phase endocytosis, polarization of the actin cytoskeleton, and vacuole biogenesis","termid":"PBO:0082367"}


id: PBO:0078343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (CTC) 9-1","termid":"PBO:0078343"}


id: PBO:0085168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-glycosylated plasma membrane protein; acts as a sensor for cell wall integrity signaling and activates the pathway; interacts with Rom2p, a guanine nucleotide exchange factor for Rho1p, and with cell integrity pathway protein Zeo1p; MID2 has a paralog, MTL1, that arose from the whole genome duplication","termid":"PBO:0085168"}


id: GO:0050923
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of a motile cell or organism towards a lower concentration in a concentration gradient of a specific chemical.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"regulates","term_name":"negative chemotaxis","termid":"GO:0050919"}],"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 negative chemotaxis","termid":"GO:0050923"}


id: PBO:0003776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial PPR repeat protein Ppr2","termid":"PBO:0003776"}


id: GO:0046626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of insulin receptor signaling.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"insulin receptor signaling pathway","termid":"GO:0008286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of insulin receptor signaling pathway","synonyms":[{"name":"regulation of insulin receptor signalling pathway","type":"exact"}],"termid":"GO:0046626"}


id: PBO:0081816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 736 pseudogene 9, Y-linked","termid":"PBO:0081816"}


id: PBO:0057169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 320e","termid":"PBO:0057169"}


id: PBO:0061472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor binding protein 1","termid":"PBO:0061472"}


id: PBO:0049574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B.W histone 2","termid":"PBO:0049574"}


id: PBO:0111887
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:0111887"}


id: MONDO:1012108
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrophic neuropathy, non-human animal","termid":"MONDO:1011844"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrophic neuropathy, dog","secondary_identifiers":["OMIA:000518-9615"],"termid":"MONDO:1012108","xrefs":{"Monarch":{"xref_id":"1012108"}}}


id: PBO:0005568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin family protein","termid":"PBO:0005568"}


id: GO:0050998
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to nitric-oxide synthase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"nitric-oxide synthase binding","synonyms":[{"name":"NOS binding","type":"exact"}],"termid":"GO:0050998"}


id: GO:0071494
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 UV-C radiation stimulus. UV-C radiation (UV-C light) spans the wavelengths 100 to 280 nm.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to UV-C","termid":"GO:0010225"},{"relation_name":"is_a","term_name":"cellular response to UV","termid":"GO:0034644"}],"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 UV-C","synonyms":[{"name":"cellular response to UV-C light stimulus","type":"exact"},{"name":"cellular response to UV-C radiation stimulus","type":"exact"},{"name":"cellular response to UVC light stimulus","type":"exact"},{"name":"cellular response to UVC radiation stimulus","type":"exact"},{"name":"cellular response to germicidal ultraviolet light stimulus","type":"exact"},{"name":"cellular response to germicidal ultraviolet radiation stimulus","type":"exact"},{"name":"cellular response to shortwave ultraviolet light stimulus","type":"exact"},{"name":"cellular response to shortwave ultraviolet radiation stimulus","type":"exact"}],"termid":"GO:0071494"}


id: MONDO:0020641
data:
  {"annotated_genes":["SJAG_03453","SJAG_00229","SJAG_04114","SJAG_03689"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88553,88554,89106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008903"},{"annotations":[88091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011014"}]},"cv_name":"mondo","definition":"A benign or malignant, primary or metastatic neoplasm involving the respiratory tract.","definition_xrefs":["NCIT:C3355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"},{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00229":null,"SJAG_03453":null,"SJAG_03689":null,"SJAG_04114":null},"genotype_count":0,"is_obsolete":false,"name":"respiratory tract neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:11200","SCTID:126667002","ICD10CM:C30-C39","EFO:0003853","UMLS:C0035244","MESH:D012142"],"synonyms":[{"name":"neoplasm of respiratory tract","type":"exact"},{"name":"neoplasm of the respiratory tract","type":"exact"},{"name":"neoplasm, respiratory tract","type":"exact"},{"name":"neoplasms, respiratory tract","type":"exact"},{"name":"respiratory system neoplasm","type":"exact"},{"name":"respiratory tract neoplasm","type":"exact"},{"name":"respiratory tract tumor","type":"exact"},{"name":"respiratory tract tumour","type":"exact"},{"name":"tract neoplasm, respiratory","type":"exact"},{"name":"tract neoplasms, respiratory","type":"exact"},{"name":"tumor of respiratory tract","type":"exact"},{"name":"tumor of the respiratory tract","type":"exact"},{"name":"tumour of respiratory tract","type":"exact"},{"name":"tumour of the respiratory tract","type":"exact"}],"termid":"MONDO:0020641","terms_by_termid":{"MONDO:0008903":null,"MONDO:0011014":null},"xrefs":{"Monarch":{"xref_id":"0020641"}}}


id: GO:1905763
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a MTREC complex.","definition_xrefs":["GOC:TermGenie","PMID:26942678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"MTREC complex binding","synonyms":[{"name":"Mtl1-Red1 core complex binding","type":"exact"},{"name":"NURS complex binding","type":"exact"},{"name":"PAXT complex binding","type":"exact"}],"termid":"GO:1905763"}


id: GO:0072470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of cell size control checkpoint signaling.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to mitotic cell cycle checkpoint signaling","termid":"GO:0072414"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cell size control checkpoint signaling","synonyms":[{"name":"cell size control checkpoint effector process","type":"exact"},{"name":"response to mitotic cell cycle cell size control checkpoint signaling","type":"exact"},{"name":"response to signal involved in cell size control checkpoint","type":"exact"}],"termid":"GO:0072470"}


id: GO:0031483
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A myosin complex containing one or more class XIII myosin heavy chains and associated light chains.","definition_xrefs":["PMID:10722873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unconventional myosin complex","termid":"GO:0016461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015629"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0015629","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"myosin XIII complex","termid":"GO:0031483"}


id: FYPO:0008106
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell size phenotype in which a cell has a volume that is larger than normal during stationary phase.","definition_xrefs":["PMID:37128864"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cell size","termid":"FYPO:0008096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cell size during stationary phase","termid":"FYPO:0008106"}


id: PBO:0049980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIKESHI pseudogene 1","termid":"PBO:0049980"}


id: FYPO:0001078
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 beta-D-glucan measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal polysaccharide level","termid":"FYPO:0001077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal beta-glucan level","synonyms":[{"name":"normal beta-D-glucan level","type":"exact"},{"name":"normal beta-glucan accumulation","type":"related"},{"name":"normal beta-glucan level during mitotic cell cycle","type":"related"},{"name":"normal beta-glucan level during vegetative growth","type":"exact"},{"name":"normal cellular beta-glucan level","type":"exact"}],"termid":"FYPO:0001078"}


id: PATO:0001436
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An attachment quality inhering in a flower by virtue of the bearer's lacking a stalk, as in flowers or leaves that grow directly from the stem.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Sessility_(botany)"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment quality","termid":"PATO:0001435"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sessile (sensu botany)","termid":"PATO:0001436"}


id: PBO:0029359
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_dATP_level","termid":"PBO:0029359"}


id: GO:0097449
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A prolongation or process extending from the soma of an astrocyte and wrapping around neurons.","definition_xrefs":["NIF_Subcellular:sao1630537580"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell projection","termid":"GO:0097386"}],"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":"astrocyte projection","synonyms":[{"name":"astrocyte process","type":"exact"},{"name":"peripheral astrocyte process","type":"related"},{"name":"vellous process","type":"related"}],"termid":"GO:0097449"}


id: GO:0036303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of lymph vessels are generated and organized. The lymph vessel is the vasculature carrying lymph.","definition_xrefs":["GOC:BHF","GOC:gr","PMID:18093989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"lymph vessel development","termid":"GO:0001945"}],"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":"lymph vessel morphogenesis","termid":"GO:0036303"}


id: PR:G2TRL0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC922.09 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRL0"],"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 C922.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC922.09","synonyms":[{"name":"Spom972h-SPAC922.09","type":"exact"}],"termid":"PR:G2TRL0"}


id: FYPO:0000180
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A stress response phenotype in which a cellular response to oxidative stress is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to stress","termid":"FYPO:0000162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"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:0000002","FYPO:0000298","FYPO:0001985"],"is_obsolete":false,"name":"abnormal cellular response to oxidative stress","synonyms":[{"name":"abnormal oxidative stress response","type":"exact"}],"termid":"FYPO:0000180"}


id: PBO:0113105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA repair methyltransferase (6-O-methylguanine-DNA methylase); involved in protection against DNA alkylation damage; localizes to the peroxisome in a Pex5p-dependent manner","termid":"PBO:0113105"}


id: PBO:0040165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetylserotonin O-methyltransferase","termid":"PBO:0040165"}


id: MONDO:1012717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinal dystrophy that occurs in the Bengal breed of domestic cats characterized as early-onset primary photoreceptor disorder that leads to blindness within the ﬁrst year of age.","definition_xrefs":["PMID:21923821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal dystrophy, domestic cat","termid":"MONDO:1012243"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early-onset retinal dystrophy, Bengal, domestic cat","secondary_identifiers":["OMIA:001613-9685"],"termid":"MONDO:1012717","xrefs":{"Monarch":{"xref_id":"1012717"}}}


id: MONDO:0016249
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorectal cancer (HNPCC) due to mutations in DNA mismatch-repair genes. Mutations in STK11 gene, causing Peutz-Jeghers syndrome, are also associated with a risk of ovarian cancer (typically sex cord stromal tumors). Mutations in other genes, including RAD51C, RAD51D, PALB2, confer an elevated ovarian cancer risk in a minority of patients.","definition_xrefs":["Orphanet:213524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial ovarian cancer","termid":"MONDO:0016248"}],"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":"hereditary site-specific ovarian cancer syndrome","secondary_identifiers":["MEDGEN:1650574","GARD:20468","icd11.foundation:123305976","UMLS:C4749652"],"termid":"MONDO:0016249","xrefs":{"Monarch":{"xref_id":"0016249"}}}


id: GO:0015537
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: xanthosine(out) + H+(out) = xanthosine(in) + H+(in).","definition_xrefs":["TC:2.A.1.10.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside:proton symporter activity","termid":"GO:0015506"},{"relation_name":"is_a","term_name":"xanthosine transmembrane transporter activity","termid":"GO:0015553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"xanthosine:proton symporter activity","synonyms":[{"name":"xanthosine permease activity","type":"related"},{"name":"xanthosine:hydrogen ion symporter activity","type":"exact"}],"termid":"GO:0015537"}


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:0088354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphosphoinositol pentakisphosphate kinase/IP8 pyrophosphatase","termid":"PBO:0088354"}


id: MONDO:0008579
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toes, relative length of first and second","secondary_identifiers":["MEDGEN:396051","OMIM:189200","UMLS:C1861059"],"synonyms":[{"name":"toes, relative length of first and second","type":"exact"}],"termid":"MONDO:0008579","xrefs":{"Monarch":{"xref_id":"0008579"}}}


id: FYPO:0005700
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 equatorial microtubule organizing center (eMTOC) does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000934"},{"relation_name":"is_a","term_name":"abolished protein localization to cell division site","termid":"FYPO:0001880"},{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule organizing center","termid":"FYPO:0005702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to eMTOC","synonyms":[{"name":"abolished protein localisation to eMTOC","type":"exact"},{"name":"abolished protein localization to eMTOC during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to eMTOC during vegetative growth","type":"exact"},{"name":"abolished protein localization to equatorial microtubule organizing center","type":"exact"},{"name":"protein absent from eMTOC","type":"related"},{"name":"protein localization to eMTOC abolished","type":"exact"}],"termid":"FYPO:0005700"}


id: PBO:0063765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PH domain containing endocytic trafficking adaptor 2","termid":"PBO:0063765"}


id: PBO:0069683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 960, pseudogene","termid":"PBO:0069683"}


id: PBO:0083762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential kinetochore protein; component of the CBF3 multisubunit complex that binds to the CDEIII region of the centromere; Cbf2p also binds to the CDEII region possibly forming a different multimeric complex, ubiquitinated in vivo; sumoylated in an Mms21p-dependent manner; relative distribution to the spindle pole body decreases upon DNA replication stress","termid":"PBO:0083762"}


id: PBO:0087719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; required for stable association of Srb10p-Srb11p kinase; essential for transcriptional regulation","termid":"PBO:0087719"}


id: PBO:0069063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 310, pseudogene","termid":"PBO:0069063"}


id: PBO:0075619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sepiapterin reductase","termid":"PBO:0075619"}


id: MONDO:0002073
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell tumor that arises in the pineal region. Representative examples include germinoma, immature teratoma, choriocarcinoma, embryonal carcinoma and yolk sac tumor.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system germ cell tumor","termid":"MONDO:0003000"},{"relation_name":"is_a","term_name":"extragonadal germ cell cancer","termid":"MONDO:0003113"},{"relation_name":"is_a","term_name":"pineal gland cancer","termid":"MONDO:0003249"}],"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 pineal area germ cell neoplasm","secondary_identifiers":["MEDGEN:233159","ICD9:239.7","UMLS:C1334612","NCIT:C6767","SCTID:277508009","DOID:1660"],"synonyms":[{"name":"malignant germ cell neoplasm of pineal gland","type":"exact"},{"name":"malignant germ cell neoplasm of pineal parenchyma","type":"exact"},{"name":"malignant germ cell neoplasm of the pineal gland","type":"exact"},{"name":"malignant germ cell neoplasm of the pineal parenchyma","type":"exact"},{"name":"malignant germ cell tumor of pineal gland","type":"exact"},{"name":"malignant germ cell tumor of pineal parenchyma","type":"exact"},{"name":"malignant germ cell tumor of the pineal gland","type":"exact"},{"name":"malignant germ cell tumor of the pineal parenchyma","type":"exact"},{"name":"malignant germ cell tumour of pineal gland","type":"exact"},{"name":"malignant germ cell tumour of pineal parenchyma","type":"exact"},{"name":"malignant germ cell tumour of the pineal gland","type":"exact"},{"name":"malignant germ cell tumour of the pineal parenchyma","type":"exact"},{"name":"malignant pineal area germ cell tumor","type":"exact"},{"name":"malignant pineal area germ cell tumour","type":"exact"},{"name":"malignant pineal gland germ cell neoplasm","type":"exact"},{"name":"malignant pineal gland germ cell tumor","type":"exact"},{"name":"malignant pineal gland germ cell tumour","type":"exact"},{"name":"malignant pineal parenchymal germ cell neoplasm","type":"exact"},{"name":"malignant pineal parenchymal germ cell tumor","type":"exact"},{"name":"malignant pineal parenchymal germ cell tumour","type":"exact"},{"name":"malignant pineal region germ cell neoplasm","type":"exact"},{"name":"malignant pineal region germ cell tumor","type":"exact"},{"name":"malignant pineal region germ cell tumour","type":"exact"},{"name":"pineal cell tumor","type":"related"},{"name":"pineal cell tumour","type":"related"},{"name":"pineal germ cell neoplasm, malignant","type":"exact"},{"name":"pineal germ cell tumor","type":"exact"},{"name":"pineal germ cell tumour","type":"exact"},{"name":"pineal region germ cell tumor","type":"exact"},{"name":"pineal region germ cell tumour","type":"exact"},{"name":"pineal region germinoma","type":"related"}],"termid":"MONDO:0002073","xrefs":{"Monarch":{"xref_id":"0002073"}}}


id: PBO:0071410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 16","termid":"PBO:0071410"}


id: GO:0072312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a metanephric glomerular epithelial cell. Metanephric glomerular epithelial cells are specialized epithelial cells that form part of the metanephric glomerulus; there are two types, metanephric glomerular parietal epithelial cells and metanephric glomerular visceral epithelial cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation involved in metanephros development","termid":"GO:0072202"},{"relation_name":"is_a","term_name":"glomerular epithelial cell differentiation","termid":"GO:0072311"},{"relation_name":"part_of","term_name":"metanephric glomerular epithelium development","termid":"GO:0072244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric glomerular epithelial cell differentiation","termid":"GO:0072312"}


id: GO:0110108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of imaginal disc-derived wing vein specification.","definition_xrefs":["PMID:11861482","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of imaginal disc-derived wing vein specification","termid":"GO:0110107"},{"relation_name":"positively_regulates","term_name":"imaginal disc-derived wing vein specification","termid":"GO:0007474"}],"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 imaginal disc-derived wing vein specification","termid":"GO:0110108"}


id: GO:0100053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that positively regulates sulfate assimilation.","definition_xrefs":["GOC:obol","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of sulfate assimilation by transcription from RNA polymerase II promoter (obsolete GO:0100053)","termid":"GO:0100053"}


id: PBO:0089999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protoheme IX farnesyltransferase","termid":"PBO:0089999"}


id: MONDO:0001132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by recurrent sexual urges, fantasies, or behaviors involving acts (real, not simulated) in which the psychological or physical suffering of a victim is sexually exciting to the individual.","definition_xrefs":["NCIT:C94358"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sexual disorder","termid":"MONDO:0000595"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sexual sadism disorder","secondary_identifiers":["ICD10CM:F65.52","MEDGEN:19957","ICD9:302.84","DOID:10817","MESH:D012448","SCTID:59394009","UMLS:C0036913"],"synonyms":[{"name":"sexual sadism","type":"exact"}],"termid":"MONDO:0001132","xrefs":{"Monarch":{"xref_id":"0001132"}}}


id: GO:0036475
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any biological process that results in permanent cessation of all vital functions of a neuron upon exposure to an oxidative stress stimulus.","definition_xrefs":["GOC:bf","GOC:PARL"],"gene_count":0,"genotype_count":0,"name":"obsolete neuron death in response to oxidative stress (obsolete GO:0036475)","synonyms":[{"name":"neuronal cell death in response to oxidative stress","type":"exact"},{"name":"oxidative stress-induced neuron death","type":"exact"}],"termid":"GO:0036475"}


id: GO:0180029
data:
  {"annotated_genes":["SJAG_00233"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117631],"is_not":false,"summary":null,"term":"GO:0180029"}]},"cv_name":"biological_process","definition":"The directed movement of phosphate ions (Pi) from inside of a cell, across the plasma membrane and into the extracellular region.","definition_xrefs":["PMID:37949217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate ion transmembrane transport","termid":"GO:0035435"},{"relation_name":"is_a","term_name":"export across plasma membrane","termid":"GO:0140115"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00233":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"phosphate ion export across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0180029","terms_by_termid":{"GO:0180029":null}}


id: PBO:0017652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-aminoadipate transaminase (predicted)","termid":"PBO:0017652"}


id: PBO:0028750
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_spindle_pole_body","termid":"PBO:0028750"}


id: MONDO:0008040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A myeloid proliferation occurring in newborns with Down syndrome. It is clinically and morphologically indistinguishable from acute myeloid leukemia and is associated with GATA1 mutations. The blasts display morphologic and immunophenotypic features of megakaryocytic lineage. In the majority of patients the myeloid proliferation undergoes spontaneous remission.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloproliferative neoplasm","termid":"MONDO:0020076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"transient myeloproliferative syndrome","secondary_identifiers":["UMLS:C1834582","SCTID:721307000","HP:0005534","MESH:C563551","GARD:12765","DOID:0060888","MEDGEN:331782","ICDO:9898/1","OMIM:159595","ONCOTREE:TAM","NCIT:C82339","Orphanet:420611"],"synonyms":[{"name":"MST","type":"exact"},{"name":"Mst","type":"related"},{"name":"TAM","type":"exact"},{"name":"TMD","type":"exact"},{"name":"Transient abnormal myelopoiesis associated with Down syndrome","type":"exact"},{"name":"leukemia, transient","type":"related"},{"name":"leukemia, transient, of Down syndrome","type":"exact"},{"name":"myeloproliferative syndrome, transient","type":"related"},{"name":"transient abnormal myelopoiesis","type":"exact"},{"name":"transient leukaemia","type":"exact"},{"name":"transient leukemia","type":"exact"},{"name":"transient leurkemia of Down syndrome","type":"exact"},{"name":"transient myeloproliferative disease","type":"exact"},{"name":"transient myeloproliferative disorder","type":"exact"},{"name":"transient myeloproliferative syndrome","type":"exact"},{"name":"transient myeloproliferative syndrome (disease)","type":"exact"}],"termid":"MONDO:0008040","xrefs":{"Monarch":{"xref_id":"0008040"}}}


id: MONDO:0003115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from the subglottic area.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"},{"relation_name":"is_a","term_name":"benign neoplasm of subglottis","termid":"MONDO:0021530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subglottic hemangioma","secondary_identifiers":["UMLS:C1336518","MEDGEN:234907","DOID:472","NCIT:C6026"],"synonyms":[{"name":"angioma of subglottis","type":"exact"},{"name":"angioma of the subglottis","type":"exact"},{"name":"hemangioma of subglottis","type":"exact"},{"name":"hemangioma of the subglottis","type":"exact"},{"name":"subglottic angioma","type":"exact"},{"name":"subglottic hemangioma","type":"exact"},{"name":"subglottis angioma","type":"exact"},{"name":"subglottis hemangioma","type":"exact"}],"termid":"MONDO:0003115","xrefs":{"Monarch":{"xref_id":"0003115"}}}


id: PBO:0077143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tight junction protein 3","termid":"PBO:0077143"}


id: MONDO:0859514
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"congenital myopathy 18","secondary_identifiers":["OMIM:620246","DOID:0081350","MEDGEN:1840919","UMLS:C5830283"],"termid":"MONDO:0859514","xrefs":{"Monarch":{"xref_id":"0859514"}}}


id: GO:0090481
data:
  {"annotated_genes":["SJAG_04697","SJAG_04162","SJAG_04406","SJAG_00434","SJAG_01177"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90136,76537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097624"},{"annotations":[77682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072334"},{"annotations":[76741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015786"},{"annotations":[114209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120112"},{"annotations":[79272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990569"},{"annotations":[67529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015790"}]},"cv_name":"biological_process","definition":"The process in which a pyrimidine nucleotide-sugar is transported across a membrane. Pyrimidine nucleotide-sugars are pyrimidine nucleotides in glycosidic linkage with a monosaccharide or monosaccharide derivative.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar transmembrane transport","termid":"GO:0015780"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00434":null,"SJAG_01177":null,"SJAG_04162":null,"SJAG_04406":null,"SJAG_04697":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"pyrimidine nucleotide-sugar transmembrane transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0015781"],"synonyms":[{"name":"pyrimidine nucleotide-sugar membrane transport","type":"exact"},{"name":"pyrimidine nucleotide-sugar transport","type":"related"}],"termid":"GO:0090481","terms_by_termid":{"GO:0015786":null,"GO:0015790":null,"GO:0072334":null,"GO:0097624":null,"GO:0120112":null,"GO:1990569":null}}


id: FYPO:0004696
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 one or more fatty acids (usually supplied as the corresponding anions). Cells stop growing (and may die) at a concentration of fatty acid that allows wild type cells to grow.","definition_xrefs":["PMID:12963726","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0002683","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to fatty acid","synonyms":[{"name":"hypersensitive to fatty acid","type":"exact"},{"name":"sensitive to fatty acid anion","type":"exact"},{"name":"sensitive to fatty acid during mitotic cell cycle","type":"related"},{"name":"sensitive to fatty acid during vegetative growth","type":"exact"},{"name":"sensitive to free fatty acids","type":"exact"}],"termid":"FYPO:0004696"}


id: GO:1990194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of proteins and RNA molecules to form a cytoplasmic U snRNP body.","definition_xrefs":["PMID:19464282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-RNA complex assembly","termid":"GO:0022618"},{"relation_name":"is_a","term_name":"membraneless organelle assembly","termid":"GO:0140694"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"cytoplasmic U snRNP body assembly","synonyms":[{"name":"U body assembly","type":"related"}],"termid":"GO:1990194"}


id: MONDO:0006918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the choroid as well as the retina and vitreous body. Some form of visual disturbance is usually present. The most important characteristics of posterior uveitis are vitreous opacities, choroiditis, and chorioretinitis.","definition_xrefs":["MESH:D015866"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uveitis","termid":"MONDO:0020283"}],"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":"posterior uveitis","secondary_identifiers":["DOID:12574","EFO:1001119","SCTID:43363007","MEDGEN:22597","MedDRA:10036370","NCIT:C35111","SCTID:46627006","UMLS:C0042167"],"synonyms":[{"name":"chorioretinal region inflammation","type":"exact"},{"name":"inflammation of chorioretinal region","type":"exact"},{"name":"uveitis, posterior","type":"exact"}],"termid":"MONDO:0006918","xrefs":{"Monarch":{"xref_id":"0006918"}}}


id: MONDO:0030454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 39","secondary_identifiers":["MEDGEN:1794210","OMIM:619562","UMLS:C5562000"],"synonyms":[{"name":"JBTS39","type":"exact"}],"termid":"MONDO:0030454","xrefs":{"Monarch":{"xref_id":"0030454"}}}


id: PBO:0081053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZCCHC10 pseudogene 1","termid":"PBO:0081053"}


id: PBO:0048827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 12","termid":"PBO:0048827"}


id: PBO:0084665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial acetyl-coenzyme A carboxylase; catalyzes production of malonyl-CoA in mitochondrial fatty acid biosynthesis; relocalizes from mitochondrion to cytoplasm upon DNA replication stress; genetic and comparative analysis suggests that translation begins at a non-canonical (Ile) start codon at -372 relative to the annotated start codon","termid":"PBO:0084665"}


id: GO:0061358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the controlled release of a Wnt protein from a cell.","definition_xrefs":["PMID:19223472","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell communication","termid":"GO:0010648"},{"relation_name":"is_a","term_name":"negative regulation of signaling","termid":"GO:0023057"},{"relation_name":"is_a","term_name":"negative regulation of protein secretion","termid":"GO:0050709"},{"relation_name":"is_a","term_name":"regulation of Wnt protein secretion","termid":"GO:0061356"},{"relation_name":"negatively_regulates","term_name":"Wnt protein secretion","termid":"GO:0061355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"negative regulation of Wnt protein secretion","termid":"GO:0061358"}


id: PBO:0067896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 198","termid":"PBO:0067896"}


id: MONDO:0012044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lattice corneal dystrophy type 3A is rare condition that affects the cornea. It is characterized primarily by protein clumps in the clear, outer covering of the eye which cloud the cornea and impair vision. Affected people also experience recurrent corneal erosion (separation of certain layers of the cornea), which is associated with severe pain and sensitivity to bright light. Lattice corneal dystrophy type 3A is caused by changes (mutations) in the TGFBI gene and is inherited in an autosomal dominant manner. The condition is usually treated surgically.","definition_xrefs":["GARD:0010320"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lattice corneal dystrophy type I","termid":"MONDO:0007380"},{"relation_name":"is_a","term_name":"epithelial-stromal TGFBI dystrophy","termid":"MONDO:0000764"},{"relation_name":"is_a","term_name":"lattice corneal dystrophy","termid":"MONDO:0004686"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"corneal dystrophy, lattice type 3A","secondary_identifiers":["MEDGEN:332989","MESH:C563923","UMLS:C1837974","GARD:10320","OMIM:608471"],"synonyms":[{"name":"CDL3A","type":"related"},{"name":"corneal dystrophy, lattice type IIIA","type":"related"},{"name":"lattice corneal dystrophy type 3A","type":"related"},{"name":"lattice corneal dystrophy type III A","type":"related"},{"name":"lattice corneal dystrophy, type 3A","type":"related"}],"termid":"MONDO:0012044","xrefs":{"Monarch":{"xref_id":"0012044"}}}


id: PBO:0061116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family pyrin domain containing 7","termid":"PBO:0061116"}


id: PBO:0060690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A1","termid":"PBO:0060690"}


id: GO:0016464
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O = ADP + phosphate; drives the transport of proteins into the chloroplast stroma.","definition_xrefs":["EC:7.4.2.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-transporting ATPase activity","termid":"GO:0015450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0140318"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140318","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"chloroplast protein-transporting ATPase activity","secondary_identifiers":["MetaCyc:3.6.3.52-RXN"],"synonyms":[{"name":"AAA chloroplast protein-transporting ATPase","type":"exact"},{"name":"ATPase-coupled chloroplast protein transporter activity","type":"exact"}],"termid":"GO:0016464"}


id: GO:0002307
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a CD8-positive, alpha-beta regulatory T cell.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CD8-positive, alpha-beta T cell differentiation","termid":"GO:0043374"},{"relation_name":"is_a","term_name":"regulatory T cell differentiation","termid":"GO:0045066"}],"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":"CD8-positive, alpha-beta regulatory T cell differentiation","synonyms":[{"name":"CD8-positive, alpha-beta regulatory T cell development","type":"related"},{"name":"CD8-positive, alpha-beta regulatory T lymphocyte differentiation","type":"exact"},{"name":"CD8-positive, alpha-beta regulatory T-cell differentiation","type":"exact"},{"name":"CD8-positive, alpha-beta regulatory T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002307"}


id: PBO:0046582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K member 24","termid":"PBO:0046582"}


id: PBO:0062845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoclastogenesis associated transmembrane protein 1","termid":"PBO:0062845"}


id: PBO:0062927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purinergic receptor P2Y14","termid":"PBO:0062927"}


id: MONDO:0001572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well-circumscribed benign smooth muscle neoplasm characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C3157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign smooth muscle neoplasm","termid":"MONDO:0006106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leiomyoma","secondary_identifiers":["SCTID:146801000119103","UMLS:C0023267","DOID:127","ICD9:215.9","ICDO:8890/0","MEDGEN:9710","MESH:D007889"],"synonyms":[{"name":"fibroid","type":"exact"},{"name":"fibroid neoplasm","type":"exact"},{"name":"fibroid tumor","type":"exact"},{"name":"fibroid tumour","type":"exact"},{"name":"leiomyoma","type":"exact"},{"name":"leiomyoma, benign","type":"exact"},{"name":"leiomyomatous neoplasm","type":"exact"},{"name":"leiomyomatous neoplasm (morphologic abnormality)","type":"exact"},{"name":"leiomyomatous tumor","type":"exact"},{"name":"leiomyomatous tumour","type":"exact"}],"termid":"MONDO:0001572","xrefs":{"Monarch":{"xref_id":"0001572"}}}


id: PBO:0071140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 3","termid":"PBO:0071140"}


id: PBO:0067067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 93, pseudogene","termid":"PBO:0067067"}


id: PBO:0111950
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-DBF type","termid":"PBO:0111950"}


id: PBO:0059218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maestro heat like repeat family member 1","termid":"PBO:0059218"}


id: PBO:0085036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-catalytic subunit of the NatB N-terminal acetyltransferase; NatB catalyzes N-acetylation of proteins with specific N-terminal sequences; involved in mitochondrial inheritance and actin assembly","termid":"PBO:0085036"}


id: PBO:0005258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin Nup61","termid":"PBO:0005258"}


id: GO:0003719
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor binding, cytoplasmic sequestering (obsolete GO:0003719)","synonyms":[{"name":"transcription factor binding, cytoplasmic sequestering","type":"exact"}],"termid":"GO:0003719"}


id: MONDO:0012091
data:
  {"annotated_genes":["SJAG_00082"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88363],"is_not":false,"summary":null,"term":"MONDO:0012091"}]},"cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3.","definition_xrefs":["DOID:0110491","PMID:12634867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00082":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 32","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:373370","UMLS:C1837608","MESH:C563884","OMIM:608653","DOID:0110466","GARD:22610"],"synonyms":[{"name":"CDC14A autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"DFNB105","type":"narrow"},{"name":"DFNB32","type":"narrow"},{"name":"autosomal recessive deafness 105","type":"narrow"},{"name":"autosomal recessive deafness 32","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 105","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 32","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in CDC14A","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 105","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 32","type":"narrow"},{"name":"deafness, autosomal recessive 105","type":"narrow"},{"name":"deafness, autosomal recessive 32","type":"narrow"},{"name":"deafness, autosomal recessive 32, with or without immotile sperm","type":"narrow"},{"name":"deafness, autosomal recessive type 105","type":"narrow"}],"termid":"MONDO:0012091","terms_by_termid":{"MONDO:0012091":null},"xrefs":{"Monarch":{"xref_id":"0012091"}}}


id: MONDO:1011563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuroaxonal dystrophy that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroaxonal dystrophy, non-human animal","termid":"MONDO:1011444"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroaxonal dystrophy, horse","secondary_identifiers":["OMIA:000715-9796"],"termid":"MONDO:1011563","xrefs":{"Monarch":{"xref_id":"1011563"}}}


id: PBO:0071740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 38","termid":"PBO:0071740"}


id: PBO:0069275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 531, pseudogene","termid":"PBO:0069275"}


id: MONDO:0016152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete qualitative or quantitative defects of calpain (obsolete MONDO:0016152)","secondary_identifiers":["Orphanet:207104"],"termid":"MONDO:0016152","xrefs":{"Monarch":{"xref_id":"0016152"}}}


id: PBO:0075269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 18 pseudogene 22","termid":"PBO:0075269"}


id: PBO:0036446
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"no evidence for translation from proteomics, synteny, or ribosome profiling","termid":"PBO:0036446"}


id: GO:0097545
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cellular anatomical entity that is part of an axoneme consisting of a doublet microtubule.","definition_xrefs":["GOC:pr","PMID:5664206","Wikipedia:Axoneme","GOC:krc","GOC:cilia","PMID:5044758"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"axoneme","termid":"GO:0005930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"axonemal doublet microtubule","synonyms":[{"name":"DMT","type":"related"},{"name":"axonemal outer doublet","type":"exact"},{"name":"axoneme outer doublet","type":"exact"},{"name":"outer doublet","type":"broad"},{"name":"outer-doublet microtubules","type":"related"}],"termid":"GO:0097545"}


id: PBO:0046360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endosulfine alpha pseudogene 2","termid":"PBO:0046360"}


id: MONDO:0011210
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":"mitochondrial intermembrane space protein Tim12, yeast, homolog of","secondary_identifiers":["UMLS:C1865698","OMIM:602252","MEDGEN:400824"],"synonyms":[{"name":"mitochondrial intermembrane space protein Tim12, yeast, homolog of","type":"exact"}],"termid":"MONDO:0011210","xrefs":{"Monarch":{"xref_id":"0011210"}}}


id: MONDO:0025003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diseases of the domestic or wild goat of the genus Capra.","definition_xrefs":["MESH:D015511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"goat disease","synonyms":[{"name":"caprine disease","type":"related"},{"name":"caprine diseases","type":"related"},{"name":"disease, caprine","type":"related"},{"name":"disease, goat","type":"related"},{"name":"diseases, caprine","type":"related"},{"name":"diseases, goat","type":"related"},{"name":"goat disease","type":"exact"}],"termid":"MONDO:0025003","xrefs":{"Monarch":{"xref_id":"0025003"}}}


id: PATO:0000494
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000494 period value (obsolete PATO:0000494)","termid":"PATO:0000494"}


id: FYECO:0000431
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which itraconazole was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ itraconazole","synonyms":[{"name":"+ itraconazole","type":"exact"}],"termid":"FYECO:0000431"}


id: GO:1904798
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of core promoter binding.","definition_xrefs":["GOC:BHF_telomere","GOC:nc","GOC:TermGenie","PMID:22723415","GO_REF:0000059","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of transcription regulatory region DNA binding","termid":"GO:2000679"}],"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 core promoter binding","synonyms":[{"name":"activation of core promoter binding","type":"narrow"},{"name":"up regulation of core promoter binding","type":"exact"},{"name":"up-regulation of core promoter binding","type":"exact"},{"name":"upregulation of core promoter binding","type":"exact"}],"termid":"GO:1904798"}


id: PBO:0041129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTBD9 antisense RNA 1","termid":"PBO:0041129"}


id: MONDO:0014732
data:
  {"annotated_genes":["SJAG_01772","SJAG_04966"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87678,87679],"is_not":false,"summary":null,"term":"MONDO:0014732"}]},"cv_name":"mondo","definition":"Any leukodystrophy in which the cause of the disease is a mutation in the VPS11 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"},{"relation_name":"is_a","term_name":"VPS11-related neurological disorder","termid":"MONDO:0100617"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01772":null,"SJAG_04966":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hypomyelinating leukodystrophy 12","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:905068","GARD:17837","DOID:0060796","OMIM:616683","Orphanet:466934","UMLS:C4225247"],"synonyms":[{"name":"HLD12","type":"exact"},{"name":"VPS11 leukodystrophy","type":"exact"},{"name":"VPS11-related autosomal recessive hypomyelinating leukodystrophy","type":"related"},{"name":"VPS11-related autosomal recessive hypomyelinating leukoencephalopathy","type":"exact"},{"name":"hypomyelinating leukodystrophy type 12","type":"exact"},{"name":"leukodystrophy caused by mutation in VPS11","type":"exact"},{"name":"leukodystrophy, hypomyelinating, 12","type":"exact"},{"name":"leukodystrophy, hypomyelinating, type 12","type":"exact"}],"termid":"MONDO:0014732","terms_by_termid":{"MONDO:0014732":null},"xrefs":{"Monarch":{"xref_id":"0014732"}}}


id: PR:O13637
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein transport protein Sec31A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02845"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein transport protein sec31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC8D2.20c","secondary_identifiers":["UniProtKB:O13637"],"synonyms":[{"name":"Spom972h-SEC31A","type":"exact"}],"termid":"PR:O13637"}


id: PBO:0088980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxyacyl-CoA dehydratase involved in very long-chain fatty acid elongation Phs1","termid":"PBO:0088980"}


id: MONDO:1010568
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes insipidus that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes insipidus, non-human animal","termid":"MONDO:1010051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes insipidus, domestic cat","secondary_identifiers":["OMIA:000278-9685"],"termid":"MONDO:1010568","xrefs":{"Monarch":{"xref_id":"1010568"}}}


id: GO:0044508
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with glucagon-like peptide 1 and transmitting the signal across the membrane by activating an associated G-protein.","definition_xrefs":["GOC:jl","PMID:12529935"],"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:0003674","GO:0038023"],"is_obsolete":false,"name":"glucagon-like peptide 1 receptor activity","termid":"GO:0044508"}


id: FYPO:0004922
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is inviable, contains one nucleus, has no septum, is elongated, and progression through the mitotic cell cycle is arrested at the mitotic G2/M phase transition.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated mononucleate aseptate cell","termid":"FYPO:0000839"},{"relation_name":"is_a","term_name":"inviable mononucleate aseptate cell with cell cycle arrest at mitotic G2/M phase transition","termid":"FYPO:0005367"},{"relation_name":"is_a","term_name":"inviable elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition","termid":"FYPO:0007701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000032","FYPO:0000631","FYPO:0001320","FYPO:0000004"],"is_obsolete":false,"name":"inviable elongated mononucleate aseptate cell with cell cycle arrest at mitotic G2/M phase transition","synonyms":[{"name":"elongated inviable mononucleate aseptate cell with mitotic cell cycle arrest at mitotic G2/M phase transition during vegetative growth","type":"exact"},{"name":"elongated inviable mononucleate aseptate vegetative cell with cell cycle arrest at mitotic G2/M phase transition","type":"exact"},{"name":"inviable elongated mononucleate aseptate vegetative cell arrested at G2/M","type":"exact"},{"name":"inviable elongated mononucleate aseptate vegetative cell with cell cycle arrest at mitotic G2/M phase transition","type":"exact"},{"name":"inviable elongated mononucleate aseptate vegetative cell with cell cycle arrest at mitotic G2/M phase transition during mitotic cell cycle","type":"exact"},{"name":"inviable elongated mononucleate aseptate vegetative cell with cell cycle arrest in mitotic G2 phase","type":"related"},{"name":"inviable elongated mononucleate aseptate vegetative cell with mitotic G2/M phase transition arrest","type":"exact"},{"name":"inviable elongated mononucleate aseptate vegetative cell with mitotic cell cycle arrest at mitotic G2/M phase transition","type":"exact"},{"name":"lethal; elongated mononucleate aseptate vegetative cell with cell cycle arrest at mitotic G2/M phase transition","type":"exact"},{"name":"mitotic G2-phase arrested elongated inviable mononucleate aseptate vegetative cell","type":"related"},{"name":"mitotic cell cycle arrest in G2-phase with elongated inviable mononucleate aseptate cell","type":"related"}],"termid":"FYPO:0004922"}


id: PBO:0066000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RALBP1 pseudogene 2","termid":"PBO:0066000"}


id: PBO:0027135
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_telomere-nuclear_envelope_distance","termid":"PBO:0027135"}


id: PBO:0112996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribosylation factor; GTPase of the Ras superfamily that regulates coated vesicle formation during intracellular trafficking within the Golgi; regulates mitochondrial fission, fusion and function, controlling the flow of fatty acids and metabolites from lipid droplets to peroxisomes and mitochondria; localizes to the Golgi apparatus and the active form to ER and lipid droplets; arf1 arf2 double null mutation is complemented by human ARF1, ARF4, ARF5, or ARF6","termid":"PBO:0112996"}


id: MONDO:0018976
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The combination of two or more of the following anomalies: neural tube defects (e.g. anencephaly, encephalocele, spina bifida cystica), cleft lip/palate, omphalocele and congenital diaphragmatic hernia. These anomalies are associated at a higher frequency than would be expected with random combination rates.","definition_xrefs":["Orphanet:63862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"schisis association","secondary_identifiers":["SCTID:718095000","UMLS:C2931271","MEDGEN:444017","MESH:C536633","GARD:246"],"synonyms":[{"name":"Midline development field defects","type":"related"}],"termid":"MONDO:0018976","xrefs":{"Monarch":{"xref_id":"0018976"}}}


id: PBO:0083292
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; open reading frame overlaps 5' end of the essential gene SPT6","termid":"PBO:0083292"}


id: PBO:0087905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor, activates transcription of stress response genes; nuclear localization is positively regulated by calcineurin-mediated dephosphorylation; rapidly localizes to the nucleus under blue light stress; can be activated in stochastic pulses of nuclear localization in response to calcium","termid":"PBO:0087905"}


id: PBO:0088206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zn(II)2Cys6 family transcription factor; positively regulates sterol uptake genes under anaerobic conditions; involved in hypoxic gene expression; represses filamentation-inducing genes during vegetative growth; positively regulates mating with SUT2 by repressing expression of genes that act as mating inhibitors; repressed by STE12; relocalizes from the nucleus to the cytoplasm upon DNA replication stress; SUT1 has a paralog, SUT2, that arose from the whole genome duplication","termid":"PBO:0088206"}


id: PBO:0045588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 3","termid":"PBO:0045588"}


id: GO:0102200
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H2O + an N-acylphosphatidylethanolamine = H+ + an N-acylethanolamine + a 1,2-diacyl-sn-glycerol 3-phosphate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete N-acetylphosphatidylethanolamine-hydrolysing phospholipase activity (obsolete GO:0102200)","termid":"GO:0102200"}


id: MONDO:0009292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases.","definition_xrefs":["Orphanet:367"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete muscular glycogenosis (obsolete MONDO:0016118)","termid":"MONDO:0016118"},{"relation_name":"excluded_subClassOf","term_name":"familial dilated cardiomyopathy","termid":"MONDO:0016333"},{"relation_name":"is_a","term_name":"disorder of glycogen metabolism","termid":"MONDO:0002412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"glycogen storage disease due to glycogen branching enzyme deficiency","secondary_identifiers":["OMIM:232500","SCTID:124267007","UMLS:C0017923","NANDO:1200827","GARD:2520","MEDGEN:6642","NANDO:1200850","NANDO:2200540","NORD:770","DOID:2750","ICD9:277.6","MedDRA:10053249","NCIT:C84737"],"synonyms":[{"name":"Andersen Disease (GSD IV)","type":"exact"},{"name":"Andersen disease","type":"exact"},{"name":"Andersen's disease","type":"exact"},{"name":"GBE1 glycogen storage disease","type":"exact"},{"name":"GSD 4","type":"related"},{"name":"GSD IV","type":"related"},{"name":"GSD IV, classic hepatic","type":"related"},{"name":"GSD IV, neuromuscular form, adult, with isolated myopathy","type":"related"},{"name":"GSD IV, neuromuscular form, childhood","type":"related"},{"name":"GSD IV, neuromuscular form, congenital","type":"related"},{"name":"GSD IV, neuromuscular form, fatal perinatal","type":"related"},{"name":"GSD IV, nonprogressive hepatic","type":"related"},{"name":"GSD due to glycogen branching enzyme deficiency","type":"exact"},{"name":"GSD type 4","type":"exact"},{"name":"GSD type IV","type":"exact"},{"name":"GSD4","type":"related"},{"name":"Gbe1 deficiency","type":"related"},{"name":"amylopectinosis","type":"exact"},{"name":"brancher deficiency","type":"related"},{"name":"brancher deficiency glycogenosis","type":"exact"},{"name":"branching-transferase deficiency glycogenosis","type":"exact"},{"name":"cirrhosis, familial, with deposition of abnormal glycogen","type":"related"},{"name":"deficiency of 1,4-alpha-glucan branching enzyme","type":"exact"},{"name":"glycogen branching enzyme deficiency","type":"related"},{"name":"glycogen storage disease 4","type":"related"},{"name":"glycogen storage disease IV","type":"related"},{"name":"glycogen storage disease caused by mutation in GBE1","type":"exact"},{"name":"glycogen storage disease due to glycogen branching enzyme deficiency","type":"exact"},{"name":"glycogen storage disease type 4","type":"exact"},{"name":"glycogen storage disease type IV","type":"exact"},{"name":"glycogen storage disease, type IV","type":"exact"},{"name":"glycogenosis 4","type":"related"},{"name":"glycogenosis due to glycogen branching enzyme deficiency","type":"exact"},{"name":"glycogenosis type 4","type":"exact"},{"name":"glycogenosis type IV","type":"exact"}],"termid":"MONDO:0009292","xrefs":{"Monarch":{"xref_id":"0009292"}}}


id: GO:0005804
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete secretory vesicle membrane (obsolete GO:0005804)","synonyms":[{"name":"secretory vesicle membrane","type":"exact"}],"termid":"GO:0005804"}


id: MOD:02069
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-glutamine residue coordinated to one or more metal atoms or metal clusters.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-glutamine residue","termid":"MOD:00907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metal or metal cluster coordinated L-glutamine residue","termid":"MOD:02069"}


id: PBO:0049751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxycarboxylic acid receptor 1","termid":"PBO:0049751"}


id: GO:0052014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the breakdown of protein macromolecules within the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by symbiont of host protein (obsolete GO:0052014)","synonyms":[{"name":"catabolism by organism of host protein","type":"exact"}],"termid":"GO:0052014"}


id: PBO:0079102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TSBP1 and BTNL2 antisense RNA 1","termid":"PBO:0079102"}


id: GO:0051450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of myoblasts, resulting in the expansion of a myoblast cell population. A myoblast is a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into skeletal muscle fibers.","definition_xrefs":["GOC:mtg_muscle","CL:0000056","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"myoblast proliferation","termid":"GO:0051450"}


id: MONDO:0000790
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A allergy involving a Salmo salar.","definition_xrefs":["MONDO:patterns/allergy"],"gene_count":0,"genotype_count":0,"name":"obsolete Atlantic salmon allergy (obsolete MONDO:0000790)","secondary_identifiers":["DOID:0060515"],"synonyms":[{"name":"Salmo salar allergic disease","type":"exact"},{"name":"Salmo salar caused allergic disease","type":"exact"},{"name":"Salmo salar fish allergy","type":"exact"},{"name":"allergy of Salmo salar","type":"exact"}],"termid":"MONDO:0000790","xrefs":{"Monarch":{"xref_id":"0000790"}}}


id: PR:Q8TFH4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPB17E12.10c gene.","definition_xrefs":["UniProtKB:Q8TFH4","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":"ribosomal RNA methyltransferase PB17E12.10c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB17E12.10c","synonyms":[{"name":"Spom972h-SPAPB17E12.10c","type":"exact"},{"name":"rRNA (uridine-2'-O-)-methyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q8TFH4"}


id: PBO:0090315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA 5' exonuclease","termid":"PBO:0090315"}


id: MOD:00002
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O3-glycosylserine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosylated residue","termid":"MOD:00396"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-glycosyl-L-serine","synonyms":[{"name":"OGlycoSer","type":"exact"}],"termid":"MOD:00002"}


id: PBO:0041354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement C4B (Chido blood group)","termid":"PBO:0041354"}


id: PBO:0073734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC1A2 antisense RNA 2","termid":"PBO:0073734"}


id: GO:0099065
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the spine apparatus 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 spine apparatus membrane (obsolete GO:0099065)","termid":"GO:0099065"}


id: PBO:0073050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small cysteine and glycine repeat containing 8","termid":"PBO:0073050"}


id: MONDO:0012657
data:
  {"annotated_genes":["SJAG_01067"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87224],"is_not":false,"summary":null,"term":"MONDO:0012657"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01067":null},"genotype_count":0,"is_obsolete":false,"name":"Mungan syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:611376","UMLS:C1969653","MESH:C548078","MEDGEN:369554"],"synonyms":[{"name":"MGS","type":"exact"},{"name":"MUNGAN syndrome","type":"exact"},{"name":"pseudoobstruction chronic idiopathic intestinal with Barrett esophagus and cardiac abnormalities","type":"related"},{"name":"pseudoobstruction chronic idiopathic intestinal with Barrett oesophagus and cardiac abnormalities","type":"related"},{"name":"pseudoobstruction, chronic idiopathic intestinal, with Barrett esophagus and Cardiac abnormalities","type":"related"},{"name":"pseudoobstruction, chronic idiopathic intestinal, with Barrett oesophagus and Cardiac abnormalities","type":"related"},{"name":"visceral Neuromyopathy, familial, with pseudoobstruction, Megaduodenum, Barrett esophagus, and Cardiac abnormalities","type":"related"},{"name":"visceral neuromyopathy familial with pseudoobstruction megaduodenum Barrett esophagus and cardiac abnormalities","type":"related"},{"name":"visceral neuromyopathy familial with pseudoobstruction megaduodenum Barrett oesophagus and cardiac abnormalities","type":"related"}],"termid":"MONDO:0012657","terms_by_termid":{"MONDO:0012657":null},"xrefs":{"Monarch":{"xref_id":"0012657"}}}


id: PBO:0063684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piggyBac transposable element derived 4 pseudogene 8","termid":"PBO:0063684"}


id: GO:0003109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the secretion of norepinephrine into the bloodstream modulates the force of heart muscle contraction.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of the force of heart contraction by norepinephrine","termid":"GO:0003061"}],"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 the force of heart contraction by circulating norepinephrine","synonyms":[{"name":"increased force of heart contraction by circulating noradrenaline","type":"related"},{"name":"increased force of heart contraction by circulating norepinephrine","type":"exact"}],"termid":"GO:0003109"}


id: GO:0034549
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-cyclopropylammelide + H2O = cyclopropylamine + cyanuric acid.","definition_xrefs":["UM-BBD_reactionID:r0827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","termid":"GO:0016814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"N-cyclopropylammelide alkylamino hydrolase activity","secondary_identifiers":["KEGG_REACTION:R06972","MetaCyc:RXN-8020"],"termid":"GO:0034549"}


id: FYPO:0005054
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the regulation of the mitotic cell cycle in response to latrunculin A is normal (i.e. indistinguishable from wild type). Normally, cell cycle progression is slowed or arrested transiently following exposure to latrunculin A.","definition_xrefs":["PomBase:mah","PMID:15537703"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal regulation of mitotic cell cycle","termid":"FYPO:0001928"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal cell cycle regulation during cellular response to latrunculin A","synonyms":[{"name":"normal cell cycle delay following latrunculin A exposure","type":"narrow"},{"name":"normal cell cycle regulation during cellular response to LatA","type":"exact"},{"name":"normal cell cycle regulation during cellular response to latrunculin A during mitotic cell cycle","type":"related"},{"name":"normal cell cycle regulation during cellular response to latrunculin A during vegetative growth","type":"exact"},{"name":"normal cell cycle regulation in response to latrunculin A","type":"exact"},{"name":"normal mitotic cell cycle regulation during cellular response to latrunculin A","type":"exact"}],"termid":"FYPO:0005054"}


id: PBO:0035893
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_protein_modification_during_vegetative_growth","termid":"PBO:0035893"}


id: GO:0048564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a photosystem I complex on the thylakoid membrane.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"photosynthesis, light reaction","termid":"GO:0019684"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0006091"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0006091","GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"photosystem I assembly","secondary_identifiers":["GO:0010251"],"termid":"GO:0048564"}


id: PBO:0117423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zDHHC palmitoyltransferase 18","termid":"PBO:0117423"}


id: PBO:0003759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA Z15","termid":"PBO:0003759"}


id: GO:0090035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate, or extent of chaperone-mediated protein complex assembly. Chaperone-mediated protein complex assembly is the aggregation, arrangement and bonding together of a set of components to form a protein complex, mediated by chaperone molecules that do not form part of the finished complex.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of chaperone-mediated protein complex assembly","termid":"GO:0090034"},{"relation_name":"positively_regulates","term_name":"chaperone-mediated protein complex assembly","termid":"GO:0051131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"positive regulation of chaperone-mediated protein complex assembly","termid":"GO:0090035"}


id: PBO:0005732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L22 (predicted)","termid":"PBO:0005732"}


id: GO:0072251
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the juxtaglomerulus cells of the metanephros as it progresses from its formation to the mature state.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"juxtaglomerulus cell differentiation","termid":"GO:0072052"},{"relation_name":"is_a","term_name":"cell differentiation involved in metanephros development","termid":"GO:0072202"},{"relation_name":"part_of","term_name":"metanephric juxtaglomerular apparatus development","termid":"GO:0072206"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric juxtaglomerulus cell differentiation","termid":"GO:0072251"}


id: PBO:0052066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine acetyltransferase 6B","termid":"PBO:0052066"}


id: PBO:0060091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 38","termid":"PBO:0060091"}


id: PBO:0057935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3661","termid":"PBO:0057935"}


id: PATO:0002101
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A cellular quality inhering in a bearer by virtue of having changed from one fully differentiated state into another.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular potency","termid":"PATO:0001397"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaplastic","synonyms":[{"name":"trans-differentiated","type":"related"}],"termid":"PATO:0002101"}


id: PBO:0075281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin family member 21","termid":"PBO:0075281"}


id: MONDO:1011505
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrocartilaginous embolic myelopathy that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrocartilaginous embolic myelopathy, non-human animal","termid":"MONDO:1011445"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrocartilaginous embolic myelopathy, horse","secondary_identifiers":["OMIA:001120-9796"],"termid":"MONDO:1011505","xrefs":{"Monarch":{"xref_id":"1011505"}}}


id: PBO:0085973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; predicted to encode a pyridoxal 5'-phosphate synthase based on sequence similarity but purified protein does not possess this activity, nor does it bind flavin mononucleotide (FMN); null mutant displays increased resistance to antifungal agents gliotoxin, cycloheximide and H2O2; YLR456W has a paralog, YPR172W, that arose from the whole genome duplication","termid":"PBO:0085973"}


id: PBO:0069044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 289, pseudogene","termid":"PBO:0069044"}


id: GO:0050763
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of depsipeptides, a linear or cyclic compound composed of both amino acids and hydroxy acids in peptide and ester bonds respectively.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"depsipeptide metabolic process","termid":"GO:0050761"}],"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":"depsipeptide biosynthetic process","synonyms":[{"name":"depsipeptide anabolism","type":"exact"},{"name":"depsipeptide biosynthesis","type":"exact"},{"name":"depsipeptide formation","type":"exact"},{"name":"depsipeptide synthesis","type":"exact"}],"termid":"GO:0050763"}


id: MONDO:0014831
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progeroid and marfanoid aspect-lipodystrophy syndrome","secondary_identifiers":["UMLS:C4310796","Orphanet:300382","MEDGEN:934763","OMIM:616914","GARD:17371"],"synonyms":[{"name":"MFLS","type":"related"},{"name":"Marfan lipodystrophy syndrome","type":"exact"},{"name":"Marfan-progeroid-lipodystrophy syndrome","type":"related"},{"name":"Marfanoid-progeroid syndrome","type":"related"}],"termid":"MONDO:0014831","xrefs":{"Monarch":{"xref_id":"0014831"}}}


id: PBO:0060682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NDRG family member 2","termid":"PBO:0060682"}


id: PBO:0077203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TM4SF19 antisense RNA 1","termid":"PBO:0077203"}


id: PBO:0043264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"claudin 23","termid":"PBO:0043264"}


id: PBO:0078674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon TTT) 7-1","termid":"PBO:0078674"}


id: PBO:0052086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch repeat and BTB domain containing 2","termid":"PBO:0052086"}


id: PBO:0054224
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 1606","termid":"PBO:0054224"}


id: GO:0072574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of hepatocytes, resulting in the expansion of a cell population. Hepatocytes form the main structural component of the liver. They are specialized epithelial cells that are organized into interconnected plates called lobules.","definition_xrefs":["GOC:mah","CL:0000182","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell proliferation involved in liver morphogenesis","termid":"GO:0072575"}],"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":"hepatocyte proliferation","termid":"GO:0072574"}


id: PBO:0026701
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cell_population_growth_on_glutamine_nitrogen_source","termid":"PBO:0026701"}


id: PBO:0056386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPK associated protein 1","termid":"PBO:0056386"}


id: PBO:0047902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(7)(q36)","termid":"PBO:0047902"}


id: PBO:0083843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Exomer-dependent cargo protein; induces appearance of [PIN+] prion when overproduced; prion-like domain serves as a retention signal in the trans-Golgi network; predicted to be palmitoylated","termid":"PBO:0083843"}


id: PBO:0036151
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H2A_phosphorylation_at_G4_motif_during_vegetative_growth","termid":"PBO:0036151"}


id: GO:0070175
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of enamel mineralization, the deposition of calcium salts in tooth enamel.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tooth mineralization","termid":"GO:0070172"},{"relation_name":"is_a","term_name":"regulation of enamel mineralization","termid":"GO:0070173"},{"relation_name":"positively_regulates","term_name":"enamel mineralization","termid":"GO:0070166"}],"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 enamel mineralization","termid":"GO:0070175"}


id: PBO:0031853
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_hydrogen_sulfide_biosynthesis","termid":"PBO:0031853"}


id: PBO:0059974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 19","termid":"PBO:0059974"}


id: GO:0012506
data:
  {"annotated_genes":["SJAG_04391","SJAG_01379","SJAG_04002","SJAG_02282","SJAG_04513","SJAG_04489","SJAG_01809","SJAG_02234","SJAG_05289","SJAG_04936","SJAG_04822","SJAG_00900","SJAG_00104","SJAG_00192","SJAG_03511","SJAG_04565","SJAG_04349","SJAG_03892","SJAG_04609","SJAG_03558","SJAG_01633","SJAG_01939","SJAG_02100","SJAG_00108","SJAG_04912","SJAG_00416","SJAG_00072","SJAG_02482","SJAG_03153","SJAG_02587","SJAG_00314","SJAG_00800","SJAG_05210","SJAG_04474","SJAG_00906","SJAG_01981","SJAG_04569","SJAG_01508","SJAG_03250","SJAG_00299","SJAG_02177","SJAG_03385","SJAG_01236","SJAG_04024","SJAG_04517","SJAG_05344","SJAG_01167","SJAG_02453","SJAG_02160","SJAG_05207","SJAG_00638","SJAG_05345","SJAG_07012","SJAG_04070","SJAG_04644","SJAG_02429","SJAG_01242","SJAG_01112","SJAG_02805","SJAG_02349","SJAG_00301","SJAG_00557","SJAG_03347","SJAG_00379","SJAG_03907","SJAG_03783","SJAG_02539","SJAG_00490","SJAG_00339","SJAG_04023","SJAG_01025","SJAG_00284"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[81371,110373],"is_not":false,"summary":null,"term":"GO:0012506"},{"annotations":[114832,114620,62726,79315],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030121"},{"annotations":[79959,58581,76140,110149],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030122"},{"annotations":[58991,66540],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030130"},{"annotations":[75509,81472],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030125"},{"annotations":[95957,68372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030665"},{"annotations":[100232,81588,108935,65234,80028,75320,72546,79712,95000],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030126"},{"annotations":[58162,64225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030663"},{"annotations":[80150,76876,73027,73149,74689,77321,78211,78786,97292,76522],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030127"},{"annotations":[92344],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010009"},{"annotations":[99170,59640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030659"},{"annotations":[82005,101496,97677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031901"},{"annotations":[61328,74321,103761,81805,103773,100467,79857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010008"},{"annotations":[72128,102868,75576,68706,77796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0012507"},{"annotations":[89885,73844],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000813"},{"annotations":[80167,73808,72605],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000814"},{"annotations":[71814,79415,72711,72385,77488,77913],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000815"},{"annotations":[77792,80165,93776,99443,101293,102870,89886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031902"},{"annotations":[60848,121377,63039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032585"},{"annotations":[100649,76991],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034424"}]},"cv_name":"cellular_component","definition":"The lipid bilayer surrounding any membrane-bounded vesicle in the cell.","definition_xrefs":["GOC:mah","GOC:vesicle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle membrane","termid":"GO:0031090"},{"relation_name":"part_of","term_name":"vesicle","termid":"GO:0031982"}],"gene_count":72,"genes_by_uniquename":{"SJAG_00072":null,"SJAG_00104":null,"SJAG_00108":null,"SJAG_00192":null,"SJAG_00284":null,"SJAG_00299":null,"SJAG_00301":null,"SJAG_00314":null,"SJAG_00339":null,"SJAG_00379":null,"SJAG_00416":null,"SJAG_00490":null,"SJAG_00557":null,"SJAG_00638":null,"SJAG_00800":null,"SJAG_00900":null,"SJAG_00906":null,"SJAG_01025":null,"SJAG_01112":null,"SJAG_01167":null,"SJAG_01236":null,"SJAG_01242":null,"SJAG_01379":null,"SJAG_01508":null,"SJAG_01633":null,"SJAG_01809":null,"SJAG_01939":null,"SJAG_01981":null,"SJAG_02100":null,"SJAG_02160":null,"SJAG_02177":null,"SJAG_02234":null,"SJAG_02282":null,"SJAG_02349":null,"SJAG_02429":null,"SJAG_02453":null,"SJAG_02482":null,"SJAG_02539":null,"SJAG_02587":null,"SJAG_02805":null,"SJAG_03153":null,"SJAG_03250":null,"SJAG_03347":null,"SJAG_03385":null,"SJAG_03511":null,"SJAG_03558":null,"SJAG_03783":null,"SJAG_03892":null,"SJAG_03907":null,"SJAG_04002":null,"SJAG_04023":null,"SJAG_04024":null,"SJAG_04070":null,"SJAG_04349":null,"SJAG_04391":null,"SJAG_04474":null,"SJAG_04489":null,"SJAG_04513":null,"SJAG_04517":null,"SJAG_04565":null,"SJAG_04569":null,"SJAG_04609":null,"SJAG_04644":null,"SJAG_04822":null,"SJAG_04912":null,"SJAG_04936":null,"SJAG_05207":null,"SJAG_05210":null,"SJAG_05289":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_07012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"vesicle membrane","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"PMID:32109380":null},"secondary_identifiers":["NIF_Subcellular:sao1153182838"],"termid":"GO:0012506","terms_by_termid":{"GO:0000813":null,"GO:0000814":null,"GO:0000815":null,"GO:0010008":null,"GO:0010009":null,"GO:0012506":null,"GO:0012507":null,"GO:0030121":null,"GO:0030122":null,"GO:0030125":null,"GO:0030126":null,"GO:0030127":null,"GO:0030130":null,"GO:0030659":null,"GO:0030663":null,"GO:0030665":null,"GO:0031901":null,"GO:0031902":null,"GO:0032585":null,"GO:0034424":null}}


id: FYPO:0003131
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins is normal (i.e. indistinguishable from wild type) during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during vegetative growth","termid":"FYPO:0000776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein phosphorylation during cellular response to ionizing radiation","synonyms":[{"name":"normal protein phosphorylation during cellular response to IR","type":"exact"},{"name":"normal protein phosphorylation during cellular response to ionizing radiation during mitotic cell cycle","type":"related"},{"name":"normal protein phosphorylation during cellular response to ionizing radiation during vegetative growth","type":"exact"}],"termid":"FYPO:0003131"}


id: PBO:0089905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoskeletal signaling protein Slm1","termid":"PBO:0089905"}


id: PBO:0082520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc42p-activated signal transducing kinase; involved in pheromone response, pseudohyphal/invasive growth, vacuole inheritance, down-regulation of sterol uptake; GBB motif binds Ste4p; member of the PAK (p21-activated kinase) family","termid":"PBO:0082520"}


id: MONDO:0014395
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An amyotrophic lateral sclerosis that has material basis in mutation in the CHCHD10 gene on chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis.","definition_xrefs":["DOID:0060214","OMIM:615911","PMID:24934289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"},{"relation_name":"is_a","term_name":"frontotemporal dementia with motor neuron disease","termid":"MONDO:0017161"},{"relation_name":"is_a","term_name":"frontotemporal dementia and/or amyotrophic lateral sclerosis","termid":"MONDO:0030923"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"frontotemporal dementia and/or amyotrophic lateral sclerosis 2","secondary_identifiers":["MEDGEN:863085","UMLS:C4014648","GARD:18397"],"synonyms":[{"name":"FTDALS2","type":"exact"},{"name":"frontotemporal dementia and/or amyotrophic lateral sclerosis 2","type":"exact"},{"name":"frontotemporal dementia and/or amyotrophic lateral sclerosis type 2","type":"exact"}],"termid":"MONDO:0014395","xrefs":{"Monarch":{"xref_id":"0014395"}}}


id: GO:0004517
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arginine + n NADPH + n H+ + m O2 = citrulline + nitric oxide + n NADP+.","definition_xrefs":["RHEA:19897","EC:1.14.13.39"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"nitric-oxide synthase activity","secondary_identifiers":["Reactome:R-HSA-418436","Reactome:R-HSA-202127","MetaCyc:NITRIC-OXIDE-SYNTHASE-RXN"],"synonyms":[{"name":"L-arginine,NADPH:oxygen oxidoreductase (nitric-oxide-forming) activity","type":"related"},{"name":"NADPH-diaphorase activity","type":"related"},{"name":"NO synthase activity","type":"related"},{"name":"endothelium-derived relaxation factor-forming enzyme activity","type":"related"},{"name":"endothelium-derived relaxing factor synthase activity","type":"related"},{"name":"nitric oxide synthase activity","type":"exact"},{"name":"nitric oxide synthetase activity","type":"related"},{"name":"nitric-oxide synthetase activity","type":"related"}],"termid":"GO:0004517"}


id: PBO:0013773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy protein Atg101","termid":"PBO:0013773"}


id: MONDO:0001998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An eye disorder characterized by an insidious reduction in vision in one eye, accompanied by clinically significant papilledema in the fellow eye. The unilateral loss of vision and optic atrophy is due to compressive optic atrophy, which causes elevated intracranial pressure that leads to swelling in the fellow eye.","definition_xrefs":["PMID:35892442"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete papilledema (obsolete MONDO:0002003)","termid":"MONDO:0002003"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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":"Foster-Kennedy syndrome","secondary_identifiers":["SCTID:87764000","MEDGEN:57505","icd11.foundation:288363660","UMLS:C0152112","EFO:1001330","DOID:14555","ICD9:377.04","ICD10CM:H47.14"],"termid":"MONDO:0001998","xrefs":{"Monarch":{"xref_id":"0001998"}}}


id: MONDO:1011278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macular corneal dystrophy that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macular corneal dystrophy, non-human animal","termid":"MONDO:1010350"},{"relation_name":"is_a","term_name":"corneal dystrophy, dog","termid":"MONDO:1011219"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macular corneal dystrophy, dog","secondary_identifiers":["OMIA:002071-9615"],"termid":"MONDO:1011278","xrefs":{"Monarch":{"xref_id":"1011278"}}}


id: SO:0000045
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"To remove a subsection of sequence.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000045 delete (obsolete SO:0000045)","termid":"SO:0000045"}


id: GO:0032251
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 adenosine into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of purine nucleoside transport","termid":"GO:0032248"},{"relation_name":"is_a","term_name":"regulation of adenosine transport","termid":"GO:0032249"},{"relation_name":"positively_regulates","term_name":"adenosine transport","termid":"GO:0032238"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of adenosine transport","synonyms":[{"name":"activation of adenosine transport","type":"narrow"},{"name":"stimulation of adenosine transport","type":"narrow"},{"name":"up regulation of adenosine transport","type":"exact"},{"name":"up-regulation of adenosine transport","type":"exact"},{"name":"upregulation of adenosine transport","type":"exact"}],"termid":"GO:0032251"}


id: MONDO:0700067
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any myopathy in which the cause of the disease is a variation in the FKTN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan","termid":"MONDO:0016155"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0002320","MONDO:0005066","MONDO:0005336"],"is_obsolete":false,"name":"myopathy caused by variation in FKTN","synonyms":[{"name":"FKTN myopathy","type":"exact"},{"name":"FKTN-related myopathy","type":"exact"},{"name":"myopathy caused by mutation in FKTN","type":"exact"}],"termid":"MONDO:0700067","xrefs":{"Monarch":{"xref_id":"0700067"}}}


id: PBO:0017884
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae FPR1","termid":"PBO:0017884"}


id: PBO:0051771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol-pentakisphosphate 2-kinase","termid":"PBO:0051771"}


id: PBO:0078624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 73","termid":"PBO:0078624"}


id: GO:0097343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a ripoptosome, a protein complex whose formation can induce an extrinsic apoptotic signaling pathway or a necroptotic signaling pathway. The composition of this protein complex may depend on several factors including nature of the signal, cell type and more.","definition_xrefs":["GOC:mtg_apoptosis","PMID:22274400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"ripoptosome assembly","termid":"GO:0097343"}


id: PBO:0058505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5695","termid":"PBO:0058505"}


id: MONDO:0056799
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder that involves the layer of synovial tissue.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synovium disorder","secondary_identifiers":["UMLS:C0263945","ICD9:727.89","SCTID:3519007","MEDGEN:538212","ICD9:727.9"],"synonyms":[{"name":"disease of layer of synovial tissue","type":"exact"},{"name":"disease or disorder of layer of synovial tissue","type":"exact"},{"name":"disorder of layer of synovial tissue","type":"exact"},{"name":"disorder of synovium","type":"exact"},{"name":"layer of synovial tissue disease","type":"exact"},{"name":"layer of synovial tissue disease or disorder","type":"exact"}],"termid":"MONDO:0056799","xrefs":{"Monarch":{"xref_id":"0056799"}}}


id: SO:0002345
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Mitochondrial LSU rRNA is an RNA component of the large subunit of mitochondrial ribosomes.","definition_xrefs":["PMID:3044395"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mt_rRNA","termid":"SO:0002128"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mt_LSU_rRNA","synonyms":[{"name":"MT LSU rRNA","type":"exact"},{"name":"mitochondrial LSU rRNA","type":"exact"},{"name":"mitochondrial large subunit rRNA","type":"exact"}],"termid":"SO:0002345"}


id: PBO:0075057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 116-20","termid":"PBO:0075057"}


id: MONDO:0019268
data:
  {"annotated_genes":["SJAG_03352","SJAG_02842","SJAG_02326","SJAG_05011","SJAG_01229","SJAG_02698","SJAG_01356","SJAG_00379","SJAG_04167","SJAG_02488","SJAG_03158","SJAG_01938","SJAG_03349","SJAG_02885","SJAG_16459","SJAG_04565","SJAG_01307","SJAG_01338","SJAG_04290","SJAG_00104","SJAG_01878","SJAG_03850","SJAG_04865","SJAG_01474","SJAG_00580","SJAG_02085","SJAG_01798"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88980,88982,88981],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007507"},{"annotations":[87013,87012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014010"},{"annotations":[87192,87193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008695"},{"annotations":[88437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007417"},{"annotations":[87260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033014"},{"annotations":[88275],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008218"},{"annotations":[87758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014131"},{"annotations":[87466,87465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009440"},{"annotations":[87597,87598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100221"},{"annotations":[87355],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859355"},{"annotations":[88515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011169"},{"annotations":[86924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012251"},{"annotations":[86749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007858"},{"annotations":[88478,88479,88480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008416"},{"annotations":[88532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011405"},{"annotations":[88865,88866],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008293"},{"annotations":[87888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013868"},{"annotations":[87744,87745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014713"},{"annotations":[87380,87379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007574"}]},"cv_name":"mondo","definition":"A skin disease that involves the epidermis.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":27,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00379":null,"SJAG_00580":null,"SJAG_01229":null,"SJAG_01307":null,"SJAG_01338":null,"SJAG_01356":null,"SJAG_01474":null,"SJAG_01798":null,"SJAG_01878":null,"SJAG_01938":null,"SJAG_02085":null,"SJAG_02326":null,"SJAG_02488":null,"SJAG_02698":null,"SJAG_02842":null,"SJAG_02885":null,"SJAG_03158":null,"SJAG_03349":null,"SJAG_03352":null,"SJAG_03850":null,"SJAG_04167":null,"SJAG_04290":null,"SJAG_04565":null,"SJAG_04865":null,"SJAG_05011":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"epidermal disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5681492","MEDGEN:1842776","Orphanet:79353"],"synonyms":[{"name":"epidermal disease","type":"exact"},{"name":"rare epidermal disease","type":"exact"}],"termid":"MONDO:0019268","terms_by_termid":{"MONDO:0007417":null,"MONDO:0007507":null,"MONDO:0007574":null,"MONDO:0007858":null,"MONDO:0008218":null,"MONDO:0008293":null,"MONDO:0008416":null,"MONDO:0008695":null,"MONDO:0009440":null,"MONDO:0011169":null,"MONDO:0011405":null,"MONDO:0012251":null,"MONDO:0013868":null,"MONDO:0014010":null,"MONDO:0014131":null,"MONDO:0014713":null,"MONDO:0033014":null,"MONDO:0100221":null,"MONDO:0859355":null},"xrefs":{"Monarch":{"xref_id":"0019268"}}}


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


id: PBO:0087743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the SWI/SNF chromatin remodeling complex; involved in transcriptional regulation; interacts with a highly conserved 40-residue sequence of Snf2p; relocates to the cytosol under hypoxic conditions","termid":"PBO:0087743"}


id: PBO:0032695
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_mitotic_spindle_midzone_assembly","termid":"PBO:0032695"}


id: MONDO:1010703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease that occurs in cattle due to a mutation in the PYGM gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"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, PYGM-related, cattle","secondary_identifiers":["OMIA:001139-9913"],"synonyms":[{"name":"glycogen storage disease V, cattle","type":"related"},{"name":"myophosphorylase deficiency, cattle","type":"exact"}],"termid":"MONDO:1010703","xrefs":{"Monarch":{"xref_id":"1010703"}}}


id: PBO:0031250
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_crossover","termid":"PBO:0031250"}


id: FYPO:0003039
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which RNA stability is decreased during a cellular response to ultraviolet light. RNA molecules are more likely to degrade over a given time period than in wild type. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah","PMID:10954610"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vegetative cell phenotype","termid":"FYPO:0001320"},{"relation_name":"is_a","term_name":"abnormal RNA stability","termid":"FYPO:0003038"}],"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"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased RNA stability during cellular response to UV","synonyms":[{"name":"decreased RNA stability during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"decreased RNA stability during cellular response to UV during vegetative growth","type":"exact"},{"name":"decreased RNA stability during cellular response to ultraviolet light","type":"exact"},{"name":"reduced RNA stability during cellular response to UV","type":"exact"}],"termid":"FYPO:0003039"}


id: GO:0035386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the Roundabout signaling pathway.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"Roundabout signaling pathway","termid":"GO:0035385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of Roundabout signaling pathway","synonyms":[{"name":"regulation of Roundabout signalling pathway","type":"exact"}],"termid":"GO:0035386"}


id: GO:0097289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving alpha-ribazole, the benzimidazole nucleoside in adenosyl cobalamin (vitamin B12).","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosyl compound metabolic process","termid":"GO:1901657"}],"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":"alpha-ribazole metabolic process","synonyms":[{"name":"alpha-ribazole metabolism","type":"exact"}],"termid":"GO:0097289"}


id: GO:0102618
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oryzalexin D + NAD(P) = oryzalexin B + H+ + NAD(P)H.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oryzalexin B synthase activity (obsolete GO:0102618)","termid":"GO:0102618"}


id: SO:0000426
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The long terminal repeat found at the three-prime end of the sequence to be inserted into the host genome.","direct_ancestors":[{"relation_name":"is_a","term_name":"long_terminal_repeat","termid":"SO:0000286"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_LTR","synonyms":[{"name":"3' LTR","type":"exact"},{"name":"3' long terminal repeat","type":"exact"},{"name":"three prime LTR","type":"exact"}],"termid":"SO:0000426"}


id: GO:0042195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of gallate, the anion of gallic acid, in the presence of oxygen.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gallate catabolic process","termid":"GO:0019396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"aerobic gallate catabolic process","synonyms":[{"name":"aerobic gallate breakdown","type":"exact"},{"name":"aerobic gallate catabolism","type":"exact"},{"name":"aerobic gallate degradation","type":"exact"},{"name":"aerobic gallic acid catabolic process","type":"exact"},{"name":"aerobic gallic acid catabolism","type":"exact"}],"termid":"GO:0042195"}


id: PBO:0038912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor F2","termid":"PBO:0038912"}


id: PBO:0050165
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 21","termid":"PBO:0050165"}


id: PBO:0064314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid phosphatase 3","termid":"PBO:0064314"}


id: PBO:0057595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR924 host gene","termid":"PBO:0057595"}


id: PATO:0002143
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"sloped","termid":"PATO:0001481"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sloped downward","termid":"PATO:0002143"}


id: GO:1905042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of epithelium regeneration.","definition_xrefs":["GOC:rph","GOC:BHF_miRNA","GO_REF:0000058","GOC:TermGenie","GOC:BHF","PMID:23221517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental growth","termid":"GO:0048640"},{"relation_name":"is_a","term_name":"regulation of epithelium regeneration","termid":"GO:1905041"},{"relation_name":"negatively_regulates","term_name":"epithelium regeneration","termid":"GO:1990399"}],"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 epithelium regeneration","synonyms":[{"name":"down regulation of epithelium regeneration","type":"exact"},{"name":"down regulation of regeneration of epithelium","type":"exact"},{"name":"down-regulation of epithelium regeneration","type":"exact"},{"name":"down-regulation of regeneration of epithelium","type":"exact"},{"name":"downregulation of epithelium regeneration","type":"exact"},{"name":"downregulation of regeneration of epithelium","type":"exact"},{"name":"inhibition of epithelium regeneration","type":"narrow"},{"name":"inhibition of regeneration of epithelium","type":"narrow"},{"name":"negative regulation of regeneration of epithelium","type":"exact"}],"termid":"GO:1905042"}


id: PBO:0045869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 2","termid":"PBO:0045869"}


id: FYPO:0007669
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 a cell is viable, has a larger volume than normal, and undergoes one or more rounds of rereplication of the entire genome. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PMID:8121488","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal negative regulation of mitotic DNA replication initiation","termid":"FYPO:0000216"},{"relation_name":"is_a","term_name":"viable swollen vegetative cell","termid":"FYPO:0002377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000005","FYPO:0005447","FYPO:0001320","FYPO:0000631","FYPO:0001985","FYPO:0000004"],"is_obsolete":false,"name":"viable swollen vegetative cell with complete DNA rereplication","synonyms":[{"name":"viable enlarged vegetative cell with complete DNA rereplication","type":"related"},{"name":"viable large vegetative cell with complete DNA rereplication","type":"related"},{"name":"viable swollen cell with complete DNA rereplication during vegetative growth","type":"exact"},{"name":"viable swollen vegetative cell with abnormal negative regulation of mitotic DNA replication initiation resulting in complete rereplication","type":"exact"},{"name":"viable swollen vegetative cell with complete DNA rereplication during mitotic cell cycle","type":"related"},{"name":"viable swollen vegetative cell with increased ploidy","type":"exact"},{"name":"viable vegetative cell with increased cell size and complete DNA rereplication","type":"related"},{"name":"viable vegetative cell with increased cell volume and complete DNA rereplication","type":"exact"}],"termid":"FYPO:0007669"}


id: GO:1902579
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A localization which involves another organism.","definition_xrefs":["GOC:jl","GO_REF:0000089","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete multi-organism localization (obsolete GO:1902579)","synonyms":[{"name":"multi organism localization","type":"exact"}],"termid":"GO:1902579"}


id: RO:0002214
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x has prototype y if and only if x is an instance of C and y is a prototypical instance of C. For example, every instance of heart, both normal and abnormal is related by the has prototype relation to some instance of a \\\"canonical\\\" heart, which participates in blood circulation.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_prototype","termid":"RO:0002214"}


id: GO:0097742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Centriole assembly in which a centriole arises de novo, rather than by replication from an existing centriole. This process may occur via different mechanisms. Examples include the deuterosome pathway in multicilated epithelial animal cells and formation of centrioles during parthenogenesis in some insects.","definition_xrefs":["GOC:cilia","PMID:25047614","PMID:25291643"],"direct_ancestors":[{"relation_name":"is_a","term_name":"centriole assembly","termid":"GO:0098534"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0000226"}],"interesting_parent_ids":["GO:0008150","GO:0000226","GO:0007010","GO:0044085"],"is_obsolete":false,"name":"de novo centriole assembly","synonyms":[{"name":"acentriolar basal body biogenesis","type":"related"},{"name":"de novo basal body amplification","type":"related"},{"name":"de novo basal body assembly","type":"related"},{"name":"de novo basal body biogenesis","type":"related"},{"name":"de novo basal body generation","type":"related"},{"name":"de novo centriole amplification","type":"related"},{"name":"de novo ciliary basal body assembly","type":"related"},{"name":"multiciliation","type":"related"},{"name":"multiciliogenesis","type":"related"}],"termid":"GO:0097742"}


id: PR:P0CF96
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mzt1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CF96"],"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":"mitotic-spindle organizing protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9G1.15c","synonyms":[{"name":"Spom972h-mzt1","type":"exact"},{"name":"mitotic-spindle organizing protein associated with a ring of gamma-tubulin 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"transcripts altered in meiosis protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P0CF96"}


id: PATO:0001643
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A size quality inhering in a bearer by virtue of the bearer's having a short, stocky build.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stubby","termid":"PATO:0001643"}


id: PBO:0059922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 8","termid":"PBO:0059922"}


id: GO:0052621
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 GTP = cyclic di-3',5'-guanylate + 2 diphosphate + 2 H+.","definition_xrefs":["RHEA:24898","EC:2.7.7.65"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotidyltransferase activity","termid":"GO:0016779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016779"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016779","GO:0003824"],"is_obsolete":false,"name":"diguanylate cyclase activity","secondary_identifiers":["GO:0043789","MetaCyc:RXN0-5359","KEGG_REACTION:R08057"],"synonyms":[{"name":"GTP:GTP guanylyltransferase activity","type":"broad"}],"termid":"GO:0052621"}


id: PR:Q9USQ1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A chromosome transmission fidelity protein 18 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR23389:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome transmission fidelity protein 18 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC902.02c","secondary_identifiers":["UniProtKB:Q9USQ1"],"synonyms":[{"name":"SPBC902.02c","type":"related"},{"name":"Spom972h-CHTF18","type":"exact"},{"name":"chl12","type":"related"}],"termid":"PR:Q9USQ1"}


id: GO:0051108
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-carnitine + CoA + ATP = AMP + diphosphate + D-carnitinyl-CoA.","definition_xrefs":["MetaCyc:DCARNCOALIG-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-ligase activity","termid":"GO:0016405"},{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"carnitine-CoA ligase activity","secondary_identifiers":["RHEA:30543"],"synonyms":[{"name":"carnitine synthetase activity","type":"exact"},{"name":"crotonobetaine/carnitine-CoA ligase activity","type":"broad"}],"termid":"GO:0051108"}


id: PBO:0053389
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 316","termid":"PBO:0053389"}


id: PBO:0073053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCY1 like pseudokinase 1","termid":"PBO:0073053"}


id: PBO:0077109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of inner mitochondrial membrane 17A","termid":"PBO:0077109"}


id: PATO:0000952
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of dark orange, red, of very low intensity.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Brown"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color","termid":"PATO:0000014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brown","termid":"PATO:0000952"}


id: SO:1000095
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000095 sequence_variant_causing_nonconservative_amino_acid_substitution (obsolete SO:1000095)","synonyms":[{"name":"mutation causing nonconservative amino acid substitution","type":"related"},{"name":"sequence variant causing nonconservative amino acid substitution","type":"exact"}],"termid":"SO:1000095"}


id: PBO:0076548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TatD DNase domain containing 2","termid":"PBO:0076548"}


id: SO:0000574
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Rearranged genomic DNA of immunoglobulin/T-cell receptor gene including L-part1, V-intron and V-D-J-exon, with the 5'UTR (SO:0000204) and 3'UTR (SO:0000205).","direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_segment","termid":"SO:0000936"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VDJ_gene_segment","synonyms":[{"name":"V-D-J-GENE","type":"exact"},{"name":"VDJ gene","type":"exact"}],"termid":"SO:0000574"}


id: FYPO:0006404
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the spindle pole body is broken into fragments.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body morphology","termid":"FYPO:0004607"}],"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":"fragmented spindle pole body","synonyms":[{"name":"fragmented SPB","type":"exact"},{"name":"spindle pole body fragmentation","type":"exact"}],"termid":"FYPO:0006404"}


id: MONDO:0011059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Holoprosencephaly-craniosynostosis syndrome is a rare developmental defect during embryogenesis syndrome characterized by the association of primary craniosynostosis (usually involving the coronal and metopic sutures) with holoprosencephaly (ranging from alobar to, most commonly, semilobar) and various skeletal anomalies (typically, hand and feet anomalies including fifth digit clinodactyly, hypoplastic phalanges and cone-shaped epiphyses, small vertebral bodies, scoliosis, coxa valga and/or flexion deformities of hips). Craniofacial asymmetry, microcephaly, brachy/plagiocephaly, short stature and psychomotor delay are additional common features.","definition_xrefs":["Orphanet:2163"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"holoprosencephaly-craniosynostosis syndrome","secondary_identifiers":["GARD:2454","UMLS:C1832424","MESH:C537684","MEDGEN:330464","SCTID:715434005","ICD10CM:Q04.2","OMIM:601370"],"synonyms":[{"name":"Camero-Lituania-Cohen syndrome","type":"exact"},{"name":"Genoa syndrome","type":"exact"},{"name":"Semilobar holoprosencephaly and primary craniosynostosis","type":"related"},{"name":"camera Lituania Cohen syndrome","type":"related"},{"name":"holoprosencephaly craniosynostosis","type":"related"},{"name":"holoprosencephaly, SEMILOBAR, with craniosynostosis","type":"related"}],"termid":"MONDO:0011059","xrefs":{"Monarch":{"xref_id":"0011059"}}}


id: MONDO:0001943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Malaria resulting from infection by Plasmodium malariae.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malaria","termid":"MONDO:0005136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"Plasmodium malariae malaria","secondary_identifiers":["ICD9:084.2","SCTID:27618009","NCIT:C34799","UMLS:C0024536","MEDGEN:44259","DOID:14324","ICD10CM:B52"],"synonyms":[{"name":"malaria by Plasmodium malariae","type":"exact"},{"name":"quartan malaria","type":"exact"}],"termid":"MONDO:0001943","xrefs":{"Monarch":{"xref_id":"0001943"}}}


id: PBO:0077495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 214","termid":"PBO:0077495"}


id: PBO:0084383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low affinity glucose transporter of the major facilitator superfamily; expression is induced in low or high glucose conditions; HXT3 has a paralog, HXT5, that arose from the whole genome duplication","termid":"PBO:0084383"}


id: PATO:0000108
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000108 salt sensitivity (obsolete PATO:0000108)","termid":"PATO:0000108"}


id: GO:0060602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The growth process in which a branch increases in length from its base to its tip.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axis elongation","termid":"GO:0003401"},{"relation_name":"part_of","term_name":"morphogenesis of a branching epithelium","termid":"GO:0061138"}],"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":"branch elongation of an epithelium","termid":"GO:0060602"}


id: PBO:0080070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP34 divergent transcript","termid":"PBO:0080070"}


id: PBO:0047250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 239 member A","termid":"PBO:0047250"}


id: GO:0002616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of macrophage antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation","termid":"GO:0002577"},{"relation_name":"regulates","term_name":"macrophage antigen processing and presentation","termid":"GO:0002472"}],"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 macrophage antigen processing and presentation","termid":"GO:0002616"}


id: MONDO:0015532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-Langerhans cell histiocytosis","termid":"MONDO:0015531"}],"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":"generalized eruptive histiocytosis","secondary_identifiers":["GARD:20018","Orphanet:157991","MEDGEN:578001","SCTID:110980006","UMLS:C0347404"],"synonyms":[{"name":"generalised eruptive histiocytoma","type":"exact"},{"name":"generalized eruptive histiocytoma","type":"exact"}],"termid":"MONDO:0015532","xrefs":{"Monarch":{"xref_id":"0015532"}}}


id: PBO:0002637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation release factor eRF1","termid":"PBO:0002637"}


id: FYPO:0005388
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the number of sites at which the protein Rad51 accumulates is lower than normal during a cellular response to ionizing radiation.","definition_xrefs":["PMID:12023299","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased number of Rad51 foci during cellular response to ionizing radiation","synonyms":[{"name":"decreased number of Rad51 foci during cellular response to IR","type":"exact"},{"name":"decreased number of Rad51 foci during cellular response to ionizing radiation during mitotic cell cycle","type":"related"},{"name":"decreased number of Rad51 foci during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"reduced number of Rad51 foci during cellular response to ionizing radiation","type":"exact"}],"termid":"FYPO:0005388"}


id: PBO:0090193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiosis specific cyclin Rem1","termid":"PBO:0090193"}


id: MONDO:0007433
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":"dementia/parkinsonism with non-Alzheimer amyloid plaques","secondary_identifiers":["OMIM:125320","UMLS:C1852223","MESH:C565115","MEDGEN:338883"],"synonyms":[{"name":"dementia/parkinsonism with non-Alzheimer amyloid plaques","type":"exact"}],"termid":"MONDO:0007433","xrefs":{"Monarch":{"xref_id":"0007433"}}}


id: PBO:0027678
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitochondrial_translation","termid":"PBO:0027678"}


id: MONDO:0971014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"MHC class II deficiency","termid":"MONDO:0008855"}],"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":"MHC class II deficiency 3","secondary_identifiers":["OMIM:620816","UMLS:C1859536","MEDGEN:347175"],"termid":"MONDO:0971014","xrefs":{"Monarch":{"xref_id":"0971014"}}}


id: MONDO:0957430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"schizophrenia","termid":"MONDO:0005090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039"],"is_obsolete":false,"name":"childhood-onset schizophrenia","secondary_identifiers":["GARD:4766","Orphanet:641496","MEDGEN:48576","UMLS:C0036346"],"termid":"MONDO:0957430","xrefs":{"Monarch":{"xref_id":"0957430"}}}


id: PBO:0113183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipid-binding ER tricalbin involved in ER-plasma membrane tethering; one of at least 7 proteins (Ice2p, Ist2p, Scs2/Scs22p, Tcb1-Tcb3p) that affect cER tethering and contact with the plasma membrane (PM); regulates PI4P levels by controlling access of Sac1p to its substrate PI4P in the PM; regulates PM phospholipid homeostasis; contains 3 calcium and lipid binding domains; localizes to the cortical ER, the cell periphery and is enriched in bud membranes; mRNA is targeted to the bud tip","termid":"PBO:0113183"}


id: MONDO:0003140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the glomeruli characterized by the accumulation of antibody-antigen immune complexes, resulting in glomerular damage and impaired kidney function.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulonephritis","termid":"MONDO:0002462"}],"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":"immune-complex glomerulonephritis","secondary_identifiers":["ICD9:583.89","MEDGEN:148168","SCTID:123752003","DOID:4784","NCIT:C35800","UMLS:C0744421"],"synonyms":[{"name":"immune Complex glomerulonephritis","type":"exact"}],"termid":"MONDO:0003140","xrefs":{"Monarch":{"xref_id":"0003140"}}}


id: PBO:0059519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3","termid":"PBO:0059519"}


id: MONDO:0001942
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anxiety disorder characterized by excessive and difficult-to-control worry about a number of life situations. The worry is accompanied by restlessness, fatigue, inability to concentrate, irritability, muscle tension, and/or sleep disturbance and lasts for at least 6 months.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anxiety disorder","termid":"MONDO:0005618"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"generalized anxiety disorder","secondary_identifiers":["NCIT:C92622","ICD10CM:F41.1","EFO:1001892","ICD9:300.02","MEDGEN:452363","DOID:14320","SCTID:21897009","UMLS:C0270549"],"synonyms":[{"name":"GAD","type":"exact"}],"termid":"MONDO:0001942","xrefs":{"Monarch":{"xref_id":"0001942"}}}


id: PBO:0082718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Paf1 complex; which associates with RNA polymerase II and is involved in histone methylation; plays a role in regulating Ty1 transposition; involved in transcription elongation as demonstrated by the G-less-based run-on (GLRO) assay","termid":"PBO:0082718"}


id: FYPO:0007956
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype observed in the vegetative growth phase of the life cycle in which the duration of microtubule growth events is abnormal.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule dynamics during vegetative growth","termid":"FYPO:0000901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"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:0000054","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal duration of microtubule growth event","termid":"FYPO:0007956"}


id: GO:0110082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to cell division site involved in mitotic actomyosin contractile ring assembly.","definition_xrefs":["GOC:vw","PMID:29343550"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell division site","termid":"GO:1901900"},{"relation_name":"regulates","term_name":"protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:1903476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:0110082"}


id: PBO:0074666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 52","termid":"PBO:0074666"}


id: PBO:0059247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L16","termid":"PBO:0059247"}


id: MONDO:0859365
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures","secondary_identifiers":["OMIM:620224","UMLS:C5830244","MEDGEN:1840880"],"termid":"MONDO:0859365","xrefs":{"Monarch":{"xref_id":"0859365"}}}


id: PBO:0035891
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_phosphatidylserine_externalization","termid":"PBO:0035891"}


id: PBO:0071931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 8","termid":"PBO:0071931"}


id: PBO:0054626
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 2031","termid":"PBO:0054626"}


id: FYPO:0004795
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the meiotic nuclear divisions are normal (i.e. indistinguishable from wild type) during a cycle of zygotic meiosis and sporulation. Zygotic meiosis and sporulation take place under conditions of continuous nitrogen starvation, in which haploid cells of the opposite mating types conjugate to form diploid zygotes that proceed immediately to undergo meiosis and sporulation.","definition_xrefs":["PMID:25891897","PomBase:mah","PMID:22558440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal meiosis","termid":"FYPO:0000478"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal zygotic meiosis","synonyms":[{"name":"normal meiosis during zygotic meiosis","type":"exact"},{"name":"normal zygotic meiotic nuclear division","type":"exact"}],"termid":"FYPO:0004795"}


id: GO:0033321
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving homomethionine, a non-protein amino acid synthesized from methionine via chain elongation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"homomethionine metabolic process","synonyms":[{"name":"homomethionine metabolism","type":"exact"}],"termid":"GO:0033321"}


id: PR:Q9UU81
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- apl4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UU81"],"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":"AP-1 complex subunit gamma-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCP1E11.06","synonyms":[{"name":"Spom972h-apl4","type":"exact"},{"name":"clathrin assembly protein complex 1 gamma-1 large chain (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"clathrin assembly protein large gamma-1 chain (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"gamma-adaptin (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UU81"}


id: PATO:0000141
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphology quality inhering in a bearer by virtue of the bearer's relative position, shape, arrangements and connectivity of an organism's various parts; the pattern underlying its form.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphology","termid":"PATO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structure","secondary_identifiers":["PATO:0001452"],"synonyms":[{"name":"relational structural quality","type":"exact"}],"termid":"PATO:0000141"}


id: PBO:0076207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO2 pseudogene 17","termid":"PBO:0076207"}


id: GO:0089707
data:
  {"annotated_genes":["SJAG_03400"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99135],"is_not":false,"summary":null,"term":"GO:0089707"}]},"cv_name":"biological_process","definition":"The directed movement of L-lysine out of the vacuole, across the vacuolar membrane.","definition_xrefs":["PMID:21307582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid transmembrane export from vacuole","termid":"GO:0032974"},{"relation_name":"is_a","term_name":"L-lysine transmembrane transport","termid":"GO:1903401"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03400":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"L-lysine transmembrane export from vacuole","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0089707","terms_by_termid":{"GO:0089707":null}}


id: PBO:0081126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFHX3 antisense RNA 1","termid":"PBO:0081126"}


id: PBO:0026858
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_anaphase-promoting_complex_assembly","termid":"PBO:0026858"}


id: FYPO:0001498
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 cytochalasin B. Cells stop growing (and may die) at a concentration of cytochalasin B 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:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000139","FYPO:0002683","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to cytochalasin B","synonyms":[{"name":"hypersensitive to cytochalasin B","type":"exact"},{"name":"sensitive to cytochalasin B during mitotic cell cycle","type":"related"},{"name":"sensitive to cytochalasin B during vegetative growth","type":"exact"}],"termid":"FYPO:0001498"}


id: PATO:0002323
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A temporal distribution pattern of process occurrences within a regulation/reference process.","definition_xrefs":["PATOC:LC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality of a process","termid":"PATO:0002062"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"temporal distribution quality","termid":"PATO:0002323"}


id: PBO:0064317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid phosphatase 6","termid":"PBO:0064317"}


id: MONDO:1012429
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal dysplasia and internal hydrocephalus, non-human animal","termid":"MONDO:1011887"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal dysplasia and internal hydrocephalus, cattle","secondary_identifiers":["OMIA:001663-9913"],"termid":"MONDO:1012429","xrefs":{"Monarch":{"xref_id":"1012429"}}}


id: PBO:0090294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [4Fe-4S] cluster assembly and transfer protein Isa1","termid":"PBO:0090294"}


id: GO:0046347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of mannosomine, 2-amino-2-deoxymannose; the D-isomer is a constituent of neuraminic acids as well as mucolipids and mucoproteins.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannosamine metabolic process","termid":"GO:0006050"},{"relation_name":"is_a","term_name":"amino sugar biosynthetic process","termid":"GO:0046349"}],"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":"mannosamine biosynthetic process","synonyms":[{"name":"mannosamine anabolism","type":"exact"},{"name":"mannosamine biosynthesis","type":"exact"},{"name":"mannosamine formation","type":"exact"},{"name":"mannosamine synthesis","type":"exact"}],"termid":"GO:0046347"}


id: PBO:0031500
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_response_to_pH","termid":"PBO:0031500"}


id: GO:0080180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 2-methylguanosine.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanosine-containing compound metabolic process","termid":"GO:1901068"}],"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:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"2-methylguanosine metabolic process","termid":"GO:0080180"}


id: PR:O60171
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcription initiation factor TFIID subunit 10 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR21242:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription initiation factor TFIID subunit 10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21H7.02","secondary_identifiers":["UniProtKB:O60171"],"synonyms":[{"name":"SPBC21H7.02","type":"related"},{"name":"Spom972h-TAF10","type":"exact"},{"name":"TBP-associated factor 10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60171"}


id: GO:0047775
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + citramalate = acetate + (3S)-citramalyl-CoA.","definition_xrefs":["EC:2.8.3.11","MetaCyc:CITRAMALATE-COA-TRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-transferase activity","termid":"GO:0008410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016782","GO:0003824"],"is_obsolete":false,"name":"citramalate CoA-transferase activity","secondary_identifiers":["RHEA:17621"],"synonyms":[{"name":"acetyl-CoA:citramalate CoA-transferase activity","type":"related"}],"termid":"GO:0047775"}


id: PBO:0085056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-essential protein of unknown function; null mutation results in a decrease in plasma membrane electron transport","termid":"PBO:0085056"}


id: GO:0050201
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-fucose + ATP = beta-L-fucose 1-phosphate + ADP + 2 H+.","definition_xrefs":["RHEA:13241","EC:2.7.1.52"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016301"],"is_obsolete":false,"name":"fucokinase activity","secondary_identifiers":["Reactome:R-HSA-6787540","KEGG_REACTION:R03161","MetaCyc:FUCOKINASE-RXN"],"synonyms":[{"name":"ATP:6-deoxy-L-galactose 1-phosphotransferase activity","type":"related"},{"name":"ATP:beta-L-fucose 1-phosphotransferase activity","type":"related"},{"name":"L-fucokinase activity","type":"related"},{"name":"L-fucose kinase activity","type":"related"},{"name":"fucokinase (phosphorylating) activity","type":"related"},{"name":"fucose kinase activity","type":"related"}],"termid":"GO:0050201"}


id: PR:O14111
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- psd3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14111"],"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":"phosphatidylserine decarboxylase proenzyme 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC31G5.15","synonyms":[{"name":"Spom972h-psd3","type":"exact"}],"termid":"PR:O14111"}


id: PBO:0001350
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"swi5delta rhp57delta double mutant produced each recombination class (gene conversion, crossover and long tract gene conversion) at frequencies similar to that of the rhp51delta single mutant","termid":"PBO:0001350"}


id: PBO:0051613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 36 gamma","termid":"PBO:0051613"}


id: PBO:0078132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 12-3","termid":"PBO:0078132"}


id: PR:O74772
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein BUD31 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03236","PANTHER:PTHR19411:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA-splicing factor cwf14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC24C6.11","secondary_identifiers":["UniProtKB:O74772"],"synonyms":[{"name":"Spom972h-BUD31","type":"exact"},{"name":"complexed with cdc5 protein 14 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74772"}


id: GO:0019712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The methyl esterification of peptidyl-glutamic acid.","definition_xrefs":["RESID:AA0072"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-L-glutamic acid 5-methyl ester biosynthetic process from glutamic acid (obsolete GO:0019712)","synonyms":[{"name":"peptidyl-L-glutamic acid 5-methyl ester anabolism from glutamic acid","type":"exact"},{"name":"peptidyl-L-glutamic acid 5-methyl ester formation from glutamic acid","type":"exact"},{"name":"peptidyl-L-glutamic acid 5-methyl ester synthesis from glutamic acid","type":"exact"}],"termid":"GO:0019712"}


id: GO:0009003
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of a signal peptide from a protein precursor.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete signal peptidase activity (obsolete GO:0009003)","synonyms":[{"name":"signal peptidase activity","type":"exact"}],"termid":"GO:0009003"}


id: GO:0060430
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a lung saccule from an initial condition to its mature state. The lung saccule is the primitive gas exchange portion of the lung composed of type I and type II cells.","definition_xrefs":["GOC:dph","GOC:mtg_lung"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"lung alveolus development","termid":"GO:0048286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lung saccule development","synonyms":[{"name":"lung saccular development","type":"broad"}],"termid":"GO:0060430"}


id: MONDO:0016686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low-grade (WHO grade II) astrocytic neoplasm. It is characterized by diffuse infiltration of neighboring central nervous system structures. These lesions typically affect young adults and have a tendency for progression to anaplastic astrocytoma and glioblastoma. Based on the IDH genes mutation status, diffuse astrocytomas are classified as IDH-mutant, IDH-wildtype, and not otherwise specified.","definition_xrefs":["NCIT:C7173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"low-grade astrocytoma","termid":"MONDO:0016685"},{"relation_name":"is_a","term_name":"grade II glioma","termid":"MONDO:0021639"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diffuse astrocytoma","secondary_identifiers":["GARD:5907","MEDGEN:83708","DOID:4857","NANDO:2200085","ONCOTREE:DASTR","Orphanet:251595","UMLS:C0280785"],"synonyms":[{"name":"WHO grade II astrocytoma","type":"exact"},{"name":"astrocytoma, diffuse","type":"exact"},{"name":"astrocytoma, diffuse, malignant","type":"exact"},{"name":"diffuse astrocytoma","type":"exact"},{"name":"fibrillary astrocytoma (histologic variant)","type":"related"},{"name":"gemistocytic astrocytoma (histologic variant)","type":"related"},{"name":"grade II astrocytic neoplasm","type":"exact"},{"name":"grade II astrocytic tumor","type":"exact"},{"name":"grade II astrocytic tumour","type":"exact"},{"name":"grade II astrocytoma","type":"exact"},{"name":"low-grade diffuse astrocytoma","type":"related"},{"name":"protoplasmic astrocytoma (histologic variant)","type":"related"}],"termid":"MONDO:0016686","xrefs":{"Monarch":{"xref_id":"0016686"}}}


id: GO:0008397
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a steroid + reduced [NADPH--hemoprotein reductase] + O2 = a 12-alpha-hydroxysteroid + oxidized [NADPH--hemoprotein reductase]- H2O +H+.","definition_xrefs":["EC:1.14.14.139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hydroxylase activity","termid":"GO:0008395"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"sterol 12-alpha-hydroxylase activity","secondary_identifiers":["Reactome:R-HSA-193845","Reactome:R-HSA-192157","RHEA:46752","Reactome:R-HSA-193709"],"synonyms":[{"name":"cytochrome P450 CYP8B1","type":"narrow"}],"termid":"GO:0008397"}


id: PBO:0090660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear cap-binding complex large subunit","termid":"PBO:0090660"}


id: PBO:0057725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR1302-9 host gene","termid":"PBO:0057725"}


id: PBO:0028922
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_transcription_during_glucose_starvation","termid":"PBO:0028922"}


id: MONDO:0859763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibromatosis/schwannomatosis","termid":"MONDO:0859008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mosaic neurofibromatosis type 1","secondary_identifiers":["Orphanet:634461","UMLS:C5782097","MEDGEN:1843428"],"termid":"MONDO:0859763","xrefs":{"Monarch":{"xref_id":"0859763"}}}


id: PBO:0091782
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing protein","termid":"PBO:0091782"}


id: PBO:0046497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERH mRNA splicing and mitosis factor","termid":"PBO:0046497"}


id: PBO:0035783
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_deubiquitination_following_cellular_response_to_methyl_methanesulfonate_during_vegetative_growth","termid":"PBO:0035783"}


id: MONDO:0025489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoid neoplastic disease in cattle caused by the bovine leukemia virus. Enzootic bovine leukosis may take the form of lymphosarcoma, malignant lymphoma, or leukemia but the presence of malignant cells in the blood is not a consistent finding.","definition_xrefs":["MESH:D016583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bovine leukemia","termid":"MONDO:0700135"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enzootic bovine leukosis","synonyms":[{"name":"bovine Leukoses","type":"related"},{"name":"bovine Leukoses, enzootic","type":"related"},{"name":"bovine Lymphomas","type":"related"},{"name":"bovine Lymphosarcomas","type":"related"},{"name":"bovine leukaemia","type":"related"},{"name":"bovine leukemia","type":"related"},{"name":"bovine leukemias","type":"related"},{"name":"bovine leukosis","type":"related"},{"name":"bovine leukosis, enzootic","type":"related"},{"name":"bovine lymphoma","type":"related"},{"name":"bovine lymphosarcoma","type":"related"},{"name":"enzootic bovine Leukoses","type":"related"},{"name":"leukemia, bovine","type":"related"},{"name":"leukemias, bovine","type":"related"},{"name":"leukoses, bovine","type":"related"},{"name":"leukoses, enzootic bovine","type":"related"},{"name":"leukosis, bovine","type":"related"},{"name":"leukosis, enzootic bovine","type":"related"},{"name":"lymphoma, bovine","type":"related"},{"name":"lymphomas, bovine","type":"related"},{"name":"lymphosarcoma, bovine","type":"related"},{"name":"lymphosarcomas, bovine","type":"related"}],"termid":"MONDO:0025489","xrefs":{"Monarch":{"xref_id":"0025489"}}}


id: GO:1904328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of myofibroblast contraction.","definition_xrefs":["PMID:19239477","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament-based movement","termid":"GO:1903115"},{"relation_name":"regulates","term_name":"myofibroblast contraction","termid":"GO:1990764"}],"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 myofibroblast contraction","synonyms":[{"name":"regulation of MF contraction","type":"exact"},{"name":"regulation of MFB contraction","type":"exact"}],"termid":"GO:1904328"}


id: PBO:0038960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenosine kinase","termid":"PBO:0038960"}


id: MONDO:0002020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Blount disease (obsolete MONDO:0002020)","synonyms":[{"name":"obsolete Blount's disease","type":"exact"}],"termid":"MONDO:0002020","xrefs":{"Monarch":{"xref_id":"0002020"}}}


id: MONDO:1012600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cystinuria that occurs in cats due to a mutation in the SLC3A1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cystinuria, non-human animal","termid":"MONDO:1012968"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystinuria, SLC3A1-related, domestic cat","secondary_identifiers":["OMIA:000256-9685"],"synonyms":[{"name":"cystinuria, type I - A, domestic cat","type":"related"}],"termid":"MONDO:1012600","xrefs":{"Monarch":{"xref_id":"1012600"}}}


id: GO:0019799
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + (alpha-tubulin) L-lysine = CoA + (alpha-tubulin) N6-acetyl-L-lysine. In most organisms it acetylates L-lysine at position 40 of alpha- tubulin.","definition_xrefs":["EC:2.3.1.108"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-lysine-acetyltransferase activity","termid":"GO:0061733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0016746","GO:0016740","GO:0034212","GO:0003674"],"is_obsolete":false,"name":"tubulin N-acetyltransferase activity","secondary_identifiers":["RHEA:15277","MetaCyc:TUBULIN-N-ACETYLTRANSFERASE-RXN"],"synonyms":[{"name":"TAT activity","type":"related"},{"name":"acetyl-CoA:alpha-tubulin-L-lysine 6-N-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:alpha-tubulin-L-lysine N6-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:alpha-tubulin-lysine N-acetyltransferase activity","type":"related"},{"name":"alpha-tubulin N-acetyltransferase activity","type":"related"},{"name":"alpha-tubulin acetylase activity","type":"related"},{"name":"alpha-tubulin acetyltransferase activity","type":"related"},{"name":"tubulin acetyltransferase activity","type":"related"}],"termid":"GO:0019799"}


id: PBO:0067984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 286","termid":"PBO:0067984"}


id: PR:P36595
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerases I, II, and III subunit RPABC2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10773:SF8","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":"DNA-directed RNA polymerases I, II, and III subunit RPABC2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1020.04c","secondary_identifiers":["UniProtKB:P36595"],"synonyms":[{"name":"DNA-directed RNA polymerases I, II, and III 15 kDa polypeptide (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerases I, II, and III subunit ABC2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RPC16 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPCC1020.04c","type":"related"},{"name":"Spom972h-POLR2F","type":"exact"},{"name":"rpo15","type":"related"}],"termid":"PR:P36595"}


id: MOD:00576
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other","definition_xrefs":["PubMed:11283024","Unimod:253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Unimod","termid":"MOD:00003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crotonaldehyde","synonyms":[{"name":"Crotonaldehyde","type":"related"}],"termid":"MOD:00576"}


id: GO:0010379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phaseic acid (PA), a catabolite of the plant hormone abscisic acid (ABA).","definition_xrefs":["MetaCyc:PWY-5271"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpenoid biosynthetic process","termid":"GO:0016106"},{"relation_name":"is_a","term_name":"apocarotenoid biosynthetic process","termid":"GO:0043289"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"phaseic acid biosynthetic process","termid":"GO:0010379"}


id: PBO:0090027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aromatic ring-opening dioxygenase","termid":"PBO:0090027"}


id: MONDO:0006687
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by a burning or tingling sensation on the lips, tongue, or entire mouth.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"headache disorder","termid":"MONDO:0021146"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"mouth disorder","termid":"MONDO:0006858"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"burning mouth syndrome","secondary_identifiers":["DOID:4331","GARD:5974","Orphanet:353253","MedDRA:10068065","EFO:1000850","MESH:D002054","UMLS:C0006430","NCIT:C62545","MEDGEN:14254","SCTID:399165002","icd11.foundation:618998878"],"synonyms":[{"name":"BMS","type":"exact"},{"name":"Orodynia","type":"exact"},{"name":"Stomatopyrosis","type":"exact"},{"name":"oral dysesthesia","type":"exact"},{"name":"stomatodynia","type":"exact"}],"termid":"MONDO:0006687","xrefs":{"Monarch":{"xref_id":"0006687"}}}


id: GO:0006312
data:
  {"annotated_genes":["SJAG_02339","SJAG_02556","SJAG_01076","SJAG_00995","SJAG_00757","SJAG_05105","SJAG_01677","SJAG_04530","SJAG_02828","SJAG_06597","SJAG_01419","SJAG_05173","SJAG_01832","SJAG_03221","SJAG_03097","SJAG_02079","SJAG_06642","SJAG_00640","SJAG_02460","SJAG_02226","SJAG_02724","SJAG_02267","SJAG_05353","SJAG_05239","SJAG_01601","SJAG_01410","SJAG_01495","SJAG_03898","SJAG_00247"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73995,76795,77469,78829,105662,109565],"is_not":false,"summary":null,"term":"GO:0006312"},{"annotations":[99202,120630,89698,118645,108444,97959,116863,102370,100902,107877,90937,112648,91065,112125,110329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007534"},{"annotations":[81067],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045951"},{"annotations":[97799],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071140"},{"annotations":[114784,114782,114785,113565,114781,114783,81917,97965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000722"}]},"cv_name":"biological_process","definition":"The exchange, reciprocal or nonreciprocal, of genetic material between one DNA molecule and a homologous DNA region that occurs during mitotic cell cycles.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA recombination","termid":"GO:0006310"}],"gene_count":29,"genes_by_uniquename":{"SJAG_00247":null,"SJAG_00640":null,"SJAG_00757":null,"SJAG_00995":null,"SJAG_01076":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01495":null,"SJAG_01601":null,"SJAG_01677":null,"SJAG_01832":null,"SJAG_02079":null,"SJAG_02226":null,"SJAG_02267":null,"SJAG_02339":null,"SJAG_02460":null,"SJAG_02556":null,"SJAG_02724":null,"SJAG_02828":null,"SJAG_03097":null,"SJAG_03221":null,"SJAG_03898":null,"SJAG_04530":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05239":null,"SJAG_05353":null,"SJAG_06597":null,"SJAG_06642":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0008150","GO:0006310","GO:0006259"],"is_obsolete":false,"name":"mitotic recombination","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Mitotic_crossover"],"termid":"GO:0006312","terms_by_termid":{"GO:0000722":null,"GO:0006312":null,"GO:0007534":null,"GO:0045951":null,"GO:0071140":null}}


id: GO:2001222
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of neuron migration.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"regulates","term_name":"neuron migration","termid":"GO:0001764"}],"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 neuron migration","synonyms":[{"name":"regulation of neuron chemotaxis","type":"exact"},{"name":"regulation of neuron guidance","type":"related"},{"name":"regulation of neuronal migration","type":"exact"}],"termid":"GO:2001222"}


id: GO:0009115
data:
  {"annotated_genes":["SJAG_04297"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73898],"is_not":false,"summary":null,"term":"GO:0009115"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of xanthine, 2,6-dihydroxypurine, a purine formed in the metabolic breakdown of guanine but not present in nucleic acids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleobase catabolic process","termid":"GO:0006145"},{"relation_name":"is_a","term_name":"xanthine metabolic process","termid":"GO:0046110"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04297":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"xanthine catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0006151"],"synonyms":[{"name":"xanthine breakdown","type":"exact"},{"name":"xanthine catabolism","type":"exact"},{"name":"xanthine degradation","type":"exact"},{"name":"xanthine oxidation","type":"narrow"}],"termid":"GO:0009115","terms_by_termid":{"GO:0009115":null}}


id: GO:0000493
data:
  {"annotated_genes":["SJAG_03125","SJAG_03551"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78345,82054],"is_not":false,"summary":null,"term":"GO:0000493"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of proteins and a box H/ACA snoRNA to form a box H/ACA small nucleolar ribonucleoprotein (snoRNP) complex.","definition_xrefs":["GOC:krc","PMID:12515383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small nucleolar ribonucleoprotein complex assembly","termid":"GO:0000491"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03125":null,"SJAG_03551":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"box H/ACA snoRNP assembly","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"box H/ACA small nucleolar ribonucleoprotein complex assembly","type":"exact"}],"termid":"GO:0000493","terms_by_termid":{"GO:0000493":null}}


id: MONDO:0001657
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm affecting the brain.","definition_xrefs":["NCIT:C3568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system cancer","termid":"MONDO:0002714"},{"relation_name":"is_a","term_name":"brain neoplasm","termid":"MONDO:0021211"}],"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":"brain cancer","secondary_identifiers":["MESH:D001932","SCTID:428061005","UMLS:C0153633","DOID:1319","ICD9:191","ICD9:191.9","ICD9:191.8","CSP:2006-2736","ICD10CM:C71","MEDGEN:57796","NCIT:C4952","ICD9:239.6"],"synonyms":[{"name":"BT - brain tumor","type":"related"},{"name":"BT - brain tumour","type":"related"},{"name":"adult brain tumor","type":"narrow"},{"name":"adult brain tumour","type":"narrow"},{"name":"adult malignant brain neoplasm","type":"narrow"},{"name":"brain cancer","type":"exact"},{"name":"brain neoplasm","type":"broad"},{"name":"brain neoplasm, adult","type":"related"},{"name":"brain neoplasms, malignant","type":"exact"},{"name":"brain tumor, adult","type":"related"},{"name":"cancer of brain","type":"exact"},{"name":"cancer of the brain","type":"exact"},{"name":"malignant brain neoplasm","type":"exact"},{"name":"malignant brain tumor","type":"exact"},{"name":"malignant brain tumour","type":"exact"},{"name":"malignant neoplasm of brain","type":"exact"},{"name":"malignant neoplasm of the brain","type":"exact"},{"name":"malignant primary brain neoplasm","type":"narrow"},{"name":"malignant primary brain tumor","type":"narrow"},{"name":"malignant primary brain tumour","type":"narrow"},{"name":"malignant tumor of adult brain","type":"narrow"},{"name":"malignant tumor of brain","type":"exact"},{"name":"malignant tumor of the brain","type":"exact"},{"name":"malignant tumour of adult brain","type":"narrow"},{"name":"malignant tumour of brain","type":"exact"},{"name":"malignant tumour of the brain","type":"exact"},{"name":"neoplasm of unspecified nature of brain","type":"related"},{"name":"primary brain neoplasm","type":"related"},{"name":"primary brain tumor","type":"related"},{"name":"primary brain tumour","type":"related"},{"name":"primary malignant neoplasm of brain","type":"exact"},{"name":"tumor of the brain","type":"broad"},{"name":"tumour of the brain","type":"broad"}],"termid":"MONDO:0001657","xrefs":{"Monarch":{"xref_id":"0001657"}}}


id: PBO:0030411
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_maltase_activity","termid":"PBO:0030411"}


id: GO:0022026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of a epidermal growth factor receptor binding to one of its physiological ligands that contributes to the commitment of a neuroblast to a neuronal fate. The neuron will reside in the forebrain.","definition_xrefs":["GOC:dph","GOC:dgh","GO_REF:0000021","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal growth factor receptor signaling pathway","termid":"GO:0007173"},{"relation_name":"part_of","term_name":"commitment of multipotent stem cells to neuronal lineage in forebrain","termid":"GO:0021898"}],"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":"epidermal growth factor signaling pathway involved in forebrain neuron fate commitment","synonyms":[{"name":"epidermal growth factor signalling pathway involved in forebrain neuron fate commitment","type":"exact"}],"termid":"GO:0022026"}


id: MONDO:0008406
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal recessive form of Emery-Dreifuss muscular dystrophy.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive Emery-Dreifuss muscular dystrophy (obsolete MONDO:0008406)","secondary_identifiers":["Orphanet:98855"],"synonyms":[{"name":"EDMD3","type":"exact"},{"name":"Emery-Dreifuss muscular dystrophy, autosomal recessive","type":"exact"}],"termid":"MONDO:0008406","xrefs":{"Monarch":{"xref_id":"0008406"}}}


id: PBO:0065240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 14","termid":"PBO:0065240"}


id: GO:0035392
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The maintenance of chromatin in a transcriptionally silent state such as heterochromatin at the telomere.","definition_xrefs":["GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete maintenance of chromatin silencing at telomere (obsolete GO:0035392)","termid":"GO:0035392"}


id: PBO:0057533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 649","termid":"PBO:0057533"}


id: PBO:0000438
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inhibits Cdr2 localization at non-growing cell end","termid":"PBO:0000438"}


id: PBO:0076470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transport and golgi organization 6 homolog","termid":"PBO:0076470"}


id: FYPO:0004652
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 size, shape, and structure of the actomyosin contractile ring is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal actomyosin contractile ring","termid":"FYPO:0004740"}],"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:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal actomyosin contractile ring morphology","synonyms":[{"name":"normal actomyosin contractile ring morphology during mitotic cell cycle","type":"related"},{"name":"normal actomyosin contractile ring morphology during vegetative growth","type":"exact"},{"name":"normal mitotic contractile ring morphology","type":"exact"}],"termid":"FYPO:0004652"}


id: PBO:0110814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, zf-GATA-type, amino acid sensing","termid":"PBO:0110814"}


id: MONDO:0010584
data:
  {"annotated_genes":["SJAG_04754"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88228],"is_not":false,"summary":null,"term":"MONDO:0010584"}]},"cv_name":"mondo","definition":"X-linked form of dyskeratosis congenita.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"DKC1-related disorder","termid":"MONDO:0100152"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"dyskeratosis congenita, X-linked","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C126352","DOID:0070025","OMIM:305000","SCTID:708536001","UMLS:C1148551","GARD:2007","MEDGEN:216941"],"synonyms":[{"name":"DKCX","type":"exact"},{"name":"Growth retardation, prenatal, with progressive pancytopenia and cerebellar hypoplasia","type":"related"},{"name":"Hoyeraal Hreidarsson syndrome","type":"exact"},{"name":"X-linked dyskeratosis congenita","type":"exact"},{"name":"Zinsser-Cole-Engman syndrome","type":"exact"},{"name":"cerebellar hypoplasia with pancytopenia","type":"related"},{"name":"dyskeratosis congenita X-linked","type":"related"},{"name":"dyskeratosis congenita, X-linked","type":"exact"},{"name":"dyskeratosis congenita, X-linked, X-linked recessive","type":"exact"}],"termid":"MONDO:0010584","terms_by_termid":{"MONDO:0010584":null},"xrefs":{"Monarch":{"xref_id":"0010584"}}}


id: PR:O42964
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- iws1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42964"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor iws1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19G7.16","synonyms":[{"name":"Spom972h-iws1","type":"exact"}],"termid":"PR:O42964"}


id: MONDO:0026730
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Basilicata-Akhtar syndrome","secondary_identifiers":["UMLS:C5231394","OMIM:301032","DOID:0111838","MEDGEN:1684820"],"synonyms":[{"name":"Basilicata-Akhtar syndrome","type":"exact"},{"name":"Basilicata-Akhtar syndrome, X-linked dominant","type":"exact"},{"name":"MRXSBA","type":"related"},{"name":"Mental Retardation, X-Linked, Syndromic 36","type":"related"},{"name":"Mental Retardation, X-Linked, Syndromic, Basilicata-Akhtar Type","type":"related"}],"termid":"MONDO:0026730","xrefs":{"Monarch":{"xref_id":"0026730"}}}


id: PR:Q09176
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- uaf2 gene.","definition_xrefs":["UniProtKB:Q09176","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":"splicing factor U2AF 23 kDa subunit (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP8A3.06","synonyms":[{"name":"Spom972h-uaf2","type":"exact"},{"name":"U2 auxiliary factor 23 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"U2 snRNP auxiliary factor small subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"U2AF23 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09176"}


id: PBO:0079694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin like 5 pseudogene 2","termid":"PBO:0079694"}


id: MONDO:0006908
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, potentially life-threatening disorder caused by acute ischemic infarction or hemorrhage in the pituitary gland. It is most often associated with the presence of a pituitary gland adenoma. Signs and symptoms include headache, vomiting, visual disturbances, and endocrine dysfunction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pituitary gland infarction","termid":"MONDO:0001259"},{"relation_name":"is_a","term_name":"acquired pituitary hormone deficiency","termid":"MONDO:0019832"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pituitary apoplexy","secondary_identifiers":["ICD9:253.8","DOID:1129","MedDRA:10056447","SCTID:237701005","MEDGEN:18489","MESH:D010899","NCIT:C26853","UMLS:C0032001","Orphanet:95613","EFO:1001108","GARD:19287","icd11.foundation:1938573221"],"synonyms":[{"name":"pituitary gland apoplexy","type":"exact"}],"termid":"MONDO:0006908","xrefs":{"Monarch":{"xref_id":"0006908"}}}


id: GO:0033486
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of delphinidin 3-O-glucoside, a basic, water-soluble anthocyanin responsible for blue coloration of flowers and fruits.","definition_xrefs":["GOC:mah","MetaCyc:PWY-5153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavonoid biosynthetic process","termid":"GO:0009813"},{"relation_name":"is_a","term_name":"beta-glucoside biosynthetic process","termid":"GO:1901806"}],"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":"delphinidin 3-O-glucoside biosynthetic process","synonyms":[{"name":"delphinidin 3-O-glucoside anabolism","type":"exact"},{"name":"delphinidin 3-O-glucoside biosynthesis","type":"exact"},{"name":"delphinidin 3-O-glucoside formation","type":"exact"},{"name":"delphinidin 3-O-glucoside synthesis","type":"exact"}],"termid":"GO:0033486"}


id: PBO:0087414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit (60 kDa) of TFIID and SAGA complexes; involved in transcription initiation of RNA polymerase II and in chromatin modification, similar to histone H4; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0087414"}


id: GO:0080094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a trehalose-6-phosphate stimulus.","definition_xrefs":["PMID:19193861"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to organophosphorus","termid":"GO:0046683"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to trehalose-6-phosphate","synonyms":[{"name":"response to trehalose-6-phosphate stimulus","type":"exact"}],"termid":"GO:0080094"}


id: PBO:0041518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 15 open reading frame 62","termid":"PBO:0041518"}


id: PBO:0080571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WDFY family member 4","termid":"PBO:0080571"}


id: GO:0034244
data:
  {"annotated_genes":["SJAG_01707"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119784],"is_not":false,"summary":null,"term":"GO:0034244"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of transcription elongation, the extension of an RNA molecule after transcription initiation and promoter clearance by the addition of ribonucleotides, catalyzed by RNA polymerase II.","definition_xrefs":["GOC:mah","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of DNA-templated transcription, elongation","termid":"GO:0032785"},{"relation_name":"is_a","term_name":"regulation of transcription elongation by RNA polymerase II","termid":"GO:0034243"},{"relation_name":"negatively_regulates","term_name":"transcription elongation by RNA polymerase II","termid":"GO:0006368"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01707":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0010467","GO:0006351","GO:0008150","GO:0006355"],"is_obsolete":false,"name":"negative regulation of transcription elongation by RNA polymerase II","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0090041"],"synonyms":[{"name":"negative regulation of RNA elongation from RNA polymerase II promoter","type":"exact"},{"name":"negative regulation of gene-specific transcription elongation from RNA polymerase II promoter","type":"related"},{"name":"negative regulation of transcription elongation from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0034244","terms_by_termid":{"GO:0034244":null}}


id: GO:0098890
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of the postsynaptic membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:autophagy","GOC:mf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of synaptic membrane","termid":"GO:0099243"},{"relation_name":"part_of","term_name":"postsynaptic membrane","termid":"GO:0045211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"extrinsic component of postsynaptic membrane","termid":"GO:0098890"}


id: PBO:0042723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENPB DNA-binding domain containing 1, pseudogene","termid":"PBO:0042723"}


id: MONDO:0005324
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Allergic rhinitis caused by outdoor allergens.","definition_xrefs":["NCIT:C92188"],"direct_ancestors":[{"relation_name":"is_a","term_name":"allergic rhinitis","termid":"MONDO:0011786"}],"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":"seasonal allergic rhinitis","secondary_identifiers":["EFO:0003956","MEDGEN:42335","UMLS:C0018621","SCTID:367498001","MESH:D006255"],"synonyms":[{"name":"hay fever","type":"exact"},{"name":"seasonal allergic rhinitis","type":"exact"}],"termid":"MONDO:0005324","xrefs":{"Monarch":{"xref_id":"0005324"}}}


id: PBO:0001015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein, involved in splicing (predicted)","termid":"PBO:0001015"}


id: GO:0004064
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a phenyl acetate + H2O = a phenol + acetate.","definition_xrefs":["EC:3.1.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0016788","GO:0003674"],"is_obsolete":false,"name":"arylesterase activity","secondary_identifiers":["MetaCyc:ARYLESTERASE-RXN","RHEA:17309","UM-BBD_reactionID:r0757"],"synonyms":[{"name":"A-esterase activity","type":"broad"},{"name":"aromatic esterase","type":"narrow"},{"name":"aryl-ester hydrolase","type":"narrow"},{"name":"paraoxonase activity","type":"broad"}],"termid":"GO:0004064"}


id: SO:0000005
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The many tandem repeats (identical or related) of a short basic repeating unit; many have a base composition or other property different from the genome average that allows them to be separated from the bulk (main band) genomic DNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"tandem_repeat","termid":"SO:0000705"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"satellite_DNA","secondary_identifiers":["http://en.wikipedia.org/wiki/Satellite_DNA"],"synonyms":[{"name":"INSDC_feature:repeat_region","type":"broad"},{"name":"INSDC_qualifier:satellite","type":"exact"},{"name":"satellite DNA","type":"exact"}],"termid":"SO:0000005"}


id: PBO:0081508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 415","termid":"PBO:0081508"}


id: PBO:0036029
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transcription_during_cellular_response_to_heat","termid":"PBO:0036029"}


id: PBO:0003666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L36, Rtc6 (predicted)","termid":"PBO:0003666"}


id: GO:0018198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of peptidyl-cysteine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptidyl-cysteine modification","termid":"GO:0018198"}


id: MONDO:0010230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 23","secondary_identifiers":["UMLS:C0796229","GARD:22666","MESH:C563144","MEDGEN:163234","DOID:0112049","OMIM:300046"],"synonyms":[{"name":"MRX23","type":"exact"},{"name":"intellectual disability, X-linked 23","type":"exact"},{"name":"mental retardation, X-linked 23","type":"related"}],"termid":"MONDO:0010230","xrefs":{"Monarch":{"xref_id":"0010230"}}}


id: MONDO:0000590
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hypersensitivity reaction type II disease that involves the peripheral nervous system.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of the nervous system","termid":"MONDO:0002977"},{"relation_name":"is_a","term_name":"peripheral nervous system disorder","termid":"MONDO:0003620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune disorder of peripheral nervous system","secondary_identifiers":["DOID:0060033"],"synonyms":[{"name":"peripheral nervous system autoimmune disease","type":"exact"},{"name":"peripheral nervous system hypersensitivity reaction type II disease","type":"exact"}],"termid":"MONDO:0000590","xrefs":{"Monarch":{"xref_id":"0000590"}}}


id: GO:0052536
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of systemic acquired resistance in the symbiont organism; systemic acquired resistance is a salicylic acid-mediated response that confers broad spectrum systemic resistance. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of systemic acquired resistance in symbiont (obsolete GO:0052536)","synonyms":[{"name":"positive regulation by organism of systemic acquired resistance in symbiont","type":"exact"}],"termid":"GO:0052536"}


id: PBO:0071562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 28","termid":"PBO:0071562"}


id: GO:0052515
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of the innate immune response of the symbiont organism; the innate immune response is the symbiont's first line of defense against infection. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of symbiont innate immunity (obsolete GO:0052515)","synonyms":[{"name":"positive regulation by organism of symbiont innate immunity","type":"exact"},{"name":"positive regulation of symbiont innate immune response","type":"exact"}],"termid":"GO:0052515"}


id: GO:0015439
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O + heme(in) = ADP + phosphate + heme(out).","definition_xrefs":["RHEA:19261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme transmembrane transporter activity","termid":"GO:0015232"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"ABC-type heme transporter activity","secondary_identifiers":["EC:7.6.2.5","GO:0103115","Reactome:R-HSA-382560","Reactome:R-HSA-1369065","Reactome:R-HSA-5683355","MetaCyc:3.6.3.41-RXN","Reactome:R-HSA-917979"],"synonyms":[{"name":"ATP-dependent heme transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled heme transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled heme transporter activity","type":"related"},{"name":"haem-transporting ATPase activity","type":"exact"},{"name":"heme ABC transporter","type":"narrow"},{"name":"heme-transporting ATPase activity","type":"exact"},{"name":"protoheme IX ABC transporter activity","type":"related"}],"termid":"GO:0015439"}


id: PBO:0069075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 322, pseudogene","termid":"PBO:0069075"}


id: MOD:01439
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-[2-(pyridin-4-yl)ethyl]-L-cysteine.","definition_xrefs":["PubMed:6528972","PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-pyridylethyl-L-cysteine","termid":"MOD:00424"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-[2-(pyridin-4-yl)ethyl]-L-cysteine","synonyms":[{"name":"4-PEC","type":"exact"},{"name":"Pyridylethyl","type":"related"},{"name":"Pyridylethyl Cystenyl","type":"exact"},{"name":"S-(pyridin-4-ylethyl)-L-cysteine","type":"exact"},{"name":"S-pyridylethylation","type":"related"}],"termid":"MOD:01439"}


id: PBO:0117015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1191 antisense RNA 1","termid":"PBO:0117015"}


id: FYPO:0000254
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular metabolism phenotype observed in the vegetative growth phase of the life cycle in which the observed occurrence of protein processing is increased.","definition_xrefs":["PomBase:mah","PMID:19520858"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein processing during vegetative growth","termid":"FYPO:0001421"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"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:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0001320","FYPO:0005447","FYPO:0006551","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased protein processing during vegetative growth","synonyms":[{"name":"increased Sre1 cleavage","type":"narrow"},{"name":"increased protein processing during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000254"}


id: MONDO:0043089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an acquired, inflammatory eye condition affecting the retina, retinal pigment epithelium (pigmented layer of the retina), and choroid. It usually affects both eyes and is characterized by multiple, yellow-white lesions in the back of the eye. The condition can significantly impair visual acuity if the macula is involved. APMPPE typically resolves on its own in weeks to months. While the cause is unknown, about a third of cases appear to develop after a flu-like illness. Non-ocular symptoms are uncommon, but cerebral vasculitis can be present and may cause permanent and/or severe neurological complications.","definition_xrefs":["GARD:0002183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"multifocal choroiditis","termid":"MONDO:0023833"}],"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":"acute posterior multifocal placoid pigment epitheliopathy","secondary_identifiers":["ICD10CM:H30.14","NORD:1101","GARD:2183","icd11.foundation:2036282532","MEDGEN:56348","SCTID:89188001","UMLS:C0154884"],"synonyms":[{"name":"AMPPE","type":"related"},{"name":"APMPPE","type":"related"},{"name":"Epitheliopathy, Acute Posterior Multifocal Placoid Pigment","type":"exact"},{"name":"acute multifocal placoid pigment epitheliopathy","type":"related"},{"name":"acute placoid pigment epitheliopathy","type":"related"},{"name":"acute posterior multifocal placoid pigment epitheliopathy","type":"exact"},{"name":"amppe - acute multifocal placoid pigment epitheliopathy","type":"related"},{"name":"apmppe","type":"related"},{"name":"epitheliopathy, acute posterior multifocal placoid pigment","type":"related"},{"name":"multifocal placoid pigment epitheliopathy","type":"related"},{"name":"pigment epitheliopathy, disseminated retinitis and retinochoroiditis","type":"related"}],"termid":"MONDO:0043089","xrefs":{"Monarch":{"xref_id":"0043089"}}}


id: PBO:0045283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 1 pseudogene 34","termid":"PBO:0045283"}


id: GO:0120226
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to succinyl-CoA, an omega-carboxyacyl-CoA having succinoyl as the S-acyl component.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA binding","termid":"GO:0120227"}],"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":"succinyl-CoA binding","synonyms":[{"name":"succinyl-coenzyme A binding","type":"exact"}],"termid":"GO:0120226"}


id: MONDO:0000721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A metabolic metabolic disorder characterized by excess urinary excretion of the purine base xanthine.","direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"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":"xanthinuria","secondary_identifiers":["ICD9:277.2","MEDGEN:450997","NANDO:2200588","icd11.foundation:1565213608","SCTID:190919008","UMLS:C0220988"],"termid":"MONDO:0000721","xrefs":{"Monarch":{"xref_id":"0000721"}}}


id: MONDO:0009746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary sensory and autonomic neuropathy, type 4 (HSAN4) is an inherited disorder characterized by anhidrosis, insensitivity to pain, self-mutilating behavior and episodes of fever.","definition_xrefs":["Orphanet:642"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy","termid":"MONDO:0015364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"hereditary sensory and autonomic neuropathy type 4","secondary_identifiers":["NCIT:C118633","NORD:1236","UMLS:C0020074","OMIM:256800","MEDGEN:6915","NANDO:2200854","SCTID:62985007","NANDO:1200553","icd11.foundation:1831234152","DOID:0070146","GARD:3006","PMID:14272277","PMID:8696348"],"synonyms":[{"name":"CIP-anhidrosis syndrome","type":"exact"},{"name":"CIPA","type":"related"},{"name":"HSAN 4","type":"related"},{"name":"HSAN IV","type":"related"},{"name":"HSAN4","type":"exact"},{"name":"HSNAN4","type":"related"},{"name":"Hereditary Sensory and Autonomic Neuropathy Type IV","type":"exact"},{"name":"NTRK1 hereditary sensory and autonomic neuropathy","type":"exact"},{"name":"congenital insensitivity to pain with anhidrosis","type":"exact"},{"name":"congenital insensitivity to pain-anhidrosis syndrome","type":"exact"},{"name":"familial dysautonomia, type 2","type":"related"},{"name":"hereditary sensory and autonomic neuropathy 4","type":"related"},{"name":"hereditary sensory and autonomic neuropathy caused by mutation in NTRK1","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type IV","type":"exact"},{"name":"hereditary sensory neuropathy type 4","type":"related"},{"name":"hereditary sensory neuropathy type IV","type":"exact"},{"name":"insensitivity to pain, congenital, with anhidrosis","type":"exact"},{"name":"neuropathy, congenital sensory, with anhidrosis","type":"related"}],"termid":"MONDO:0009746","xrefs":{"Monarch":{"xref_id":"0009746"}}}


id: PBO:0110986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cis-acting regulatory lncRNA prt2, pho84 repressing","termid":"PBO:0110986"}


id: GO:1904652
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any protein localization to cell division site that is involved in cell separation after cytokinesis.","definition_xrefs":["GOC:TermGenie","GO_REF:0000060","PMID:25411334"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to cell division site","termid":"GO:0072741"},{"relation_name":"part_of","term_name":"septum digestion after cytokinesis","termid":"GO:0000920"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to cell division site involved in cell separation after cytokinesis","termid":"GO:1904652"}


id: PBO:0111442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation inhibitor, IMPACT domain protein","termid":"PBO:0111442"}


id: PBO:0078190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 4-3","termid":"PBO:0078190"}


id: GO:0061982
data:
  {"annotated_genes":["SJAG_03525","SJAG_03942","SJAG_03217","SJAG_00727","SJAG_02465","SJAG_01620","SJAG_02561","SJAG_02104","SJAG_04280","SJAG_01677","SJAG_02460","SJAG_00908","SJAG_05333","SJAG_01419","SJAG_03567","SJAG_00364","SJAG_01371","SJAG_02045","SJAG_04332","SJAG_01224","SJAG_01156","SJAG_00794","SJAG_05226","SJAG_01278","SJAG_01873","SJAG_03437","SJAG_00368","SJAG_01777","SJAG_01863","SJAG_01775","SJAG_04076","SJAG_03073","SJAG_03926","SJAG_02490","SJAG_01370","SJAG_02311","SJAG_00397","SJAG_02295","SJAG_01330","SJAG_01837","SJAG_05196","SJAG_03219","SJAG_00113","SJAG_04271","SJAG_03854","SJAG_02616","SJAG_01515","SJAG_03698","SJAG_00756","SJAG_05323","SJAG_04748","SJAG_04287","SJAG_03683","SJAG_03327","SJAG_01538","SJAG_05319","SJAG_03751","SJAG_00600","SJAG_00229","SJAG_01044","SJAG_01708","SJAG_05260","SJAG_01601","SJAG_02267","SJAG_00757","SJAG_02771","SJAG_05373","SJAG_07002","SJAG_03287","SJAG_01832","SJAG_00418","SJAG_01082","SJAG_04001","SJAG_03989","SJAG_02814","SJAG_03220","SJAG_01067","SJAG_00172","SJAG_03221","SJAG_01662","SJAG_00666","SJAG_04143","SJAG_00918","SJAG_00935","SJAG_02731","SJAG_02187","SJAG_03720","SJAG_02346","SJAG_05295","SJAG_01805","SJAG_05019","SJAG_02652","SJAG_03685","SJAG_01410","SJAG_03048","SJAG_02181","SJAG_05266","SJAG_02822","SJAG_00377","SJAG_03092","SJAG_00980","SJAG_04457","SJAG_02737","SJAG_05185","SJAG_04950","SJAG_03681","SJAG_03673","SJAG_05220","SJAG_01211","SJAG_04303","SJAG_04259","SJAG_04623","SJAG_03680","SJAG_01076","SJAG_00100","SJAG_02556","SJAG_02606","SJAG_01263","SJAG_00623","SJAG_01138","SJAG_02339","SJAG_02708","SJAG_04126","SJAG_02286","SJAG_00140","SJAG_02294"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59158],"is_not":false,"summary":null,"term":"GO:0061982"},{"annotations":[109473,90310,90934,100838,118642],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990918"},{"annotations":[112883,89524,115785,93620,113234,92763,99360,118791,93156,96990,102516,104764,105055],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030989"},{"annotations":[92056,89579,118909,95569,100402,117380,109634,103130,115623],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031619"},{"annotations":[112379,80524,89525,113056,109635],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007129"},{"annotations":[62285,91133,118710,61461],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045143"},{"annotations":[108401,103230,113057],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032118"},{"annotations":[91367,118910],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030999"},{"annotations":[119091,109530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007127"},{"annotations":[116337,108125],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905318"},{"annotations":[65476,91537],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070197"},{"annotations":[101712,104617,89162,106910,91538],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032121"},{"annotations":[115064,116338,106297,109636,95573,103064,103591,115624,100905,117742],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990813"},{"annotations":[93242,108536,96528,81070,81087,90938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042138"},{"annotations":[106683,92108,110565,111469,112958],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0010780"},{"annotations":[80243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000707"},{"annotations":[112127,109475],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0010772"},{"annotations":[93201,108426,117898],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0033315"},{"annotations":[102336,91066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006311"},{"annotations":[80519,98698,103318,109476,112128,118951,90251,64137],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000709"},{"annotations":[58096,109563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000710"},{"annotations":[95656,112006],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051755"},{"annotations":[102434],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902346"},{"annotations":[109477,100841,112129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000708"},{"annotations":[90252,80522,102338],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0010774"},{"annotations":[119407,119545,98498,117784],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045141"},{"annotations":[115825],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044821"},{"annotations":[101928,100474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990949"},{"annotations":[80287,72367],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0110031"},{"annotations":[75161],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0110032"},{"annotations":[115627],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[110177,104175],"is_not":false,"rel_names":["positively_regulates","regulates","part_of"],"summary":null,"term":"GO:1905263"},{"annotations":[105663,102373,106126,70858,108537,92575,91370,93243,106647,79466,117381,102436,81071,94452,102935,94525,72723],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007131"},{"annotations":[103133],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"},{"annotations":[118525],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904967"},{"annotations":[119146,76019,109964,80999,78519,76613,110903,73430,112151,119294],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000712"},{"annotations":[118074],"is_not":false,"rel_names":["part_of","regulates"],"summary":null,"term":"GO:0062209"},{"annotations":[91522,97096,103134,117767,92752,99688,100410,109638,112185,115067,118763,115937,109321,111717,90915,104234,110964,97342,107281,102313,110707,95586,112141],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051455"}]},"cv_name":"biological_process","definition":"A process that contributes to the first meiotic division. The first meiotic division is the reductive division resulting in the separation of homologous chromosome pairs.","definition_xrefs":["PMID:29385397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"}],"gene_count":126,"genes_by_uniquename":{"SJAG_00100":null,"SJAG_00113":null,"SJAG_00140":null,"SJAG_00172":null,"SJAG_00229":null,"SJAG_00364":null,"SJAG_00368":null,"SJAG_00377":null,"SJAG_00397":null,"SJAG_00418":null,"SJAG_00600":null,"SJAG_00623":null,"SJAG_00666":null,"SJAG_00727":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00794":null,"SJAG_00908":null,"SJAG_00918":null,"SJAG_00935":null,"SJAG_00980":null,"SJAG_01044":null,"SJAG_01067":null,"SJAG_01076":null,"SJAG_01082":null,"SJAG_01138":null,"SJAG_01156":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01263":null,"SJAG_01278":null,"SJAG_01330":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01515":null,"SJAG_01538":null,"SJAG_01601":null,"SJAG_01620":null,"SJAG_01662":null,"SJAG_01677":null,"SJAG_01708":null,"SJAG_01775":null,"SJAG_01777":null,"SJAG_01805":null,"SJAG_01832":null,"SJAG_01837":null,"SJAG_01863":null,"SJAG_01873":null,"SJAG_02045":null,"SJAG_02104":null,"SJAG_02181":null,"SJAG_02187":null,"SJAG_02267":null,"SJAG_02286":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02311":null,"SJAG_02339":null,"SJAG_02346":null,"SJAG_02460":null,"SJAG_02465":null,"SJAG_02490":null,"SJAG_02556":null,"SJAG_02561":null,"SJAG_02606":null,"SJAG_02616":null,"SJAG_02652":null,"SJAG_02708":null,"SJAG_02731":null,"SJAG_02737":null,"SJAG_02771":null,"SJAG_02814":null,"SJAG_02822":null,"SJAG_03048":null,"SJAG_03073":null,"SJAG_03092":null,"SJAG_03217":null,"SJAG_03219":null,"SJAG_03220":null,"SJAG_03221":null,"SJAG_03287":null,"SJAG_03327":null,"SJAG_03437":null,"SJAG_03525":null,"SJAG_03567":null,"SJAG_03673":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03683":null,"SJAG_03685":null,"SJAG_03698":null,"SJAG_03720":null,"SJAG_03751":null,"SJAG_03854":null,"SJAG_03926":null,"SJAG_03942":null,"SJAG_03989":null,"SJAG_04001":null,"SJAG_04076":null,"SJAG_04126":null,"SJAG_04143":null,"SJAG_04259":null,"SJAG_04271":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04303":null,"SJAG_04332":null,"SJAG_04457":null,"SJAG_04623":null,"SJAG_04748":null,"SJAG_04950":null,"SJAG_05019":null,"SJAG_05185":null,"SJAG_05196":null,"SJAG_05220":null,"SJAG_05226":null,"SJAG_05260":null,"SJAG_05266":null,"SJAG_05295":null,"SJAG_05319":null,"SJAG_05323":null,"SJAG_05333":null,"SJAG_05373":null,"SJAG_07002":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"meiosis I cell cycle process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"first meiotic cell division","type":"exact"}],"termid":"GO:0061982","terms_by_termid":{"GO:0000707":null,"GO:0000708":null,"GO:0000709":null,"GO:0000710":null,"GO:0000712":null,"GO:0006311":null,"GO:0007127":null,"GO:0007129":null,"GO:0007131":null,"GO:0010772":null,"GO:0010774":null,"GO:0010780":null,"GO:0030989":null,"GO:0030999":null,"GO:0031619":null,"GO:0032118":null,"GO:0032121":null,"GO:0033315":null,"GO:0042138":null,"GO:0044821":null,"GO:0045141":null,"GO:0045143":null,"GO:0051455":null,"GO:0051755":null,"GO:0061982":null,"GO:0062209":null,"GO:0070197":null,"GO:0110031":null,"GO:0110032":null,"GO:1902346":null,"GO:1904967":null,"GO:1905263":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:1990813":null,"GO:1990918":null,"GO:1990949":null}}


id: PATO:0000107
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000107 alkali sensitivity (obsolete PATO:0000107)","termid":"PATO:0000107"}


id: GO:0110072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The actin-mediated process that results in contraction of the apical end of a polarized columnar epithelial cell, contributing to formation of a ventral indentation (furrow) from the blastoderm epithelium, which is internalized to form a tube in the interior of the embryo, marking the start of gastrulation.","definition_xrefs":["GOC:ha","PMID:28495958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apical constriction involved in gastrulation","termid":"GO:0003384"},{"relation_name":"part_of","term_name":"ventral furrow formation","termid":"GO:0007370"}],"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":"apical constriction involved in ventral furrow formation","termid":"GO:0110072"}


id: PBO:0109140
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 3110","termid":"PBO:0109140"}


id: GO:0045108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the assembly or disassembly of intermediate filaments by the addition or removal of monomers from a filament; this usually occurs through the opposing action of kinases and phosphatases.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"intermediate filament polymerization or depolymerization","termid":"GO:0045105"}],"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 intermediate filament polymerization or depolymerization","termid":"GO:0045108"}


id: GO:0018833
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane = 1,1-dichloro-2,2-bis(4-chlorophenyl)ethylene + chloride + H+.","definition_xrefs":["EC:4.5.1.1","RHEA:19217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-halide lyase activity","termid":"GO:0016848"}],"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":"DDT-dehydrochlorinase activity","secondary_identifiers":["KEGG_REACTION:R04522","MetaCyc:DDT-DEHYDROCHLORINASE-RXN","UM-BBD_reactionID:r0439"],"synonyms":[{"name":"1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane chloride-lyase [1,1-dichloro-2,2-bis(4-chlorophenyl)ethylene-forming]","type":"related"},{"name":"1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane chloride-lyase activity","type":"related"},{"name":"DDT dehydrochlorinase activity","type":"exact"},{"name":"DDT-as","type":"related"},{"name":"DDT-ase activity","type":"related"},{"name":"DDTase activity","type":"related"}],"termid":"GO:0018833"}


id: PBO:0081125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger homeobox 3","termid":"PBO:0081125"}


id: FYPO:0002875
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which transcription occurs to a greater extent than normal. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"increased RNA level","termid":"FYPO:0001890"},{"relation_name":"is_a","term_name":"abnormal transcription","termid":"FYPO:0005502"},{"relation_name":"is_a","term_name":"increased gene expression","termid":"FYPO:0006548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0000294","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased transcription","termid":"FYPO:0002875"}


id: PBO:0002507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein Nnf1","termid":"PBO:0002507"}


id: PBO:0074652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 40C","termid":"PBO:0074652"}


id: PBO:0114849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial and nucleatr DNA polymerase zeta subunit Rev7","termid":"PBO:0114849"}


id: RO:0002589
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"p results in catabolism of c if and only if p is a catabolic process, and the execution of p results in c being broken into smaller parts with energy being released.","direct_ancestors":[{"relation_name":"is_a","term_name":"results_in_breakdown_of","termid":"RO:0002586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_catabolism_of","termid":"RO:0002589"}


id: GO:0046290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of isoflavonoid phytoalexins, a group of water-soluble phenolic derivatives isomeric with flavonoids that possess antibiotic activity and are produced by plant tissues in response to infection.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoflavonoid catabolic process","termid":"GO:0046288"},{"relation_name":"is_a","term_name":"isoflavonoid phytoalexin metabolic process","termid":"GO:0046289"},{"relation_name":"is_a","term_name":"phytoalexin catabolic process","termid":"GO:0052316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0098754","GO:0019748"],"is_obsolete":false,"name":"isoflavonoid phytoalexin catabolic process","synonyms":[{"name":"isoflavonoid phytoalexin breakdown","type":"exact"},{"name":"isoflavonoid phytoalexin catabolism","type":"exact"},{"name":"isoflavonoid phytoalexin degradation","type":"exact"}],"termid":"GO:0046290"}


id: PBO:0034766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hrd1p ubiquitin ligase complex Npl4 (predicted)","termid":"PBO:0034766"}


id: PBO:0060708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 5","termid":"PBO:0060708"}


id: PBO:0043785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxypeptidase D","termid":"PBO:0043785"}


id: GO:0009476
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete class IV cytochrome c (obsolete GO:0009476)","synonyms":[{"name":"class IV cytochrome c","type":"exact"}],"termid":"GO:0009476"}


id: MONDO:0021660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A deep folliculitis due to a cutaneous dermatophyte infection, usually on the legs. It is most commonly caused by trichophyton rubrum and is characterized by the formation of spongy granulomas which persist for three to four months and leaves deep scars.","definition_xrefs":["NCIT:C35073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tinea infection","termid":"MONDO:0005982"}],"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":"deep seated dermatophytosis","secondary_identifiers":["GARD:21631","Orphanet:397587","MEDGEN:235599","UMLS:C1395264"],"synonyms":[{"name":"deep dermatophytosis","type":"exact"},{"name":"deep seated dermatophytosis","type":"exact"},{"name":"disseminated granulomatous dermatophytosis","type":"exact"}],"termid":"MONDO:0021660","xrefs":{"Monarch":{"xref_id":"0021660"}}}


id: MONDO:0021211
data:
  {"annotated_genes":["SJAG_03429","SJAG_00579"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88477],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"},{"annotations":[89108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007959"}]},"cv_name":"mondo","definition":"A neoplasm (disease) that involves the brain.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"central nervous system neoplasm","termid":"MONDO:0006130"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00579":null,"SJAG_03429":null},"genotype_count":0,"is_obsolete":false,"name":"brain neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C2907","EFO:0003833","UMLS:C0006118","MEDGEN:14216"],"synonyms":[{"name":"brain neoplasm (disease)","type":"exact"},{"name":"brain neoplasms","type":"exact"},{"name":"brain tumor","type":"exact"},{"name":"brain tumour","type":"exact"},{"name":"neoplasm of brain","type":"exact"},{"name":"neoplasm of the brain","type":"exact"},{"name":"tumor of brain","type":"exact"},{"name":"tumor of the Brain","type":"exact"},{"name":"tumour of brain","type":"exact"},{"name":"tumour of the Brain","type":"exact"}],"termid":"MONDO:0021211","terms_by_termid":{"MONDO:0007959":null,"MONDO:0009050":null},"xrefs":{"Monarch":{"xref_id":"0021211"}}}


id: PBO:0063025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase pseudogene 5","termid":"PBO:0063025"}


id: PBO:0012842
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Renal cell cancer","termid":"PBO:0012842"}


id: PBO:0031506
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_leptomycin_B","termid":"PBO:0031506"}


id: GO:0032305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the controlled release of an icosanoid from a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of icosanoid secretion","termid":"GO:0032303"},{"relation_name":"is_a","term_name":"positive regulation of secretion","termid":"GO:0051047"},{"relation_name":"is_a","term_name":"positive regulation of fatty acid transport","termid":"GO:2000193"},{"relation_name":"positively_regulates","term_name":"icosanoid secretion","termid":"GO:0032309"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of icosanoid secretion","synonyms":[{"name":"activation of icosanoid secretion","type":"narrow"},{"name":"positive regulation of eicosanoid secretion","type":"exact"},{"name":"stimulation of icosanoid secretion","type":"narrow"},{"name":"up regulation of icosanoid secretion","type":"exact"},{"name":"up-regulation of icosanoid secretion","type":"exact"},{"name":"upregulation of icosanoid secretion","type":"exact"}],"termid":"GO:0032305"}


id: PBO:0029857
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_spheroid_vegetative_cell","termid":"PBO:0029857"}


id: PBO:0052453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kruppel like factor 4 pseudogene 1","termid":"PBO:0052453"}


id: GO:1900051
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone exchange.","definition_xrefs":["GOC:TermGenie","PMID:20332092"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone exchange (obsolete GO:1900051)","synonyms":[{"name":"activation of histone chaperone","type":"related"},{"name":"activation of histone exchange","type":"related"},{"name":"activation of histone replacement","type":"exact"},{"name":"positive regulation of histone chaperone","type":"related"},{"name":"positive regulation of histone replacement","type":"exact"},{"name":"up regulation of histone chaperone","type":"related"},{"name":"up regulation of histone exchange","type":"related"},{"name":"up regulation of histone replacement","type":"exact"},{"name":"up-regulation of histone chaperone","type":"related"},{"name":"up-regulation of histone exchange","type":"related"},{"name":"up-regulation of histone replacement","type":"exact"},{"name":"upregulation of histone chaperone","type":"related"},{"name":"upregulation of histone exchange","type":"related"},{"name":"upregulation of histone replacement","type":"exact"}],"termid":"GO:1900051"}


id: MONDO:0005858
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive adenocarcinoma characterized by cystic changes and the presence of malignant glandular cells which contain intracytoplasmic mucin. It may arise from the ovary, pancreas, appendix, and lung.","definition_xrefs":["NCIT:C3776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"},{"relation_name":"is_a","term_name":"cystadenocarcinoma","termid":"MONDO:0005596"}],"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":"mucinous cystadenocarcinoma","secondary_identifiers":["DOID:3603","MEDGEN:60211","UMLS:C0206699","MESH:D018282","ICDO:8470/3","EFO:0007378"],"synonyms":[{"name":"Pseudomucinous adenocarcinoma","type":"exact"},{"name":"Pseudomucinous cystadenocarcinoma","type":"exact"},{"name":"mucinous cystadenocarcinoma","type":"exact"},{"name":"mucinous cystadenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"mucinous cystadenocarcinoma NOS (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0005858","xrefs":{"Monarch":{"xref_id":"0005858"}}}


id: MONDO:0030827
data:
  {"annotated_genes":["SJAG_04387","SJAG_02509"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88714,88715],"is_not":false,"summary":null,"term":"MONDO:0030827"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant macrothrombocytopenia","termid":"MONDO:0015372"},{"relation_name":"is_a","term_name":"macrothrombocytopenia, isolated","termid":"MONDO:0031447"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02509":null,"SJAG_04387":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"macrothrombocytopenia, isolated, 2, autosomal dominant","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1802965","OMIM:619840","UMLS:C5676968"],"synonyms":[{"name":"MACTHC2","type":"exact"},{"name":"macrothrombocytopenia, isolated, 2, autosomal dominant","type":"exact"}],"termid":"MONDO:0030827","terms_by_termid":{"MONDO:0030827":null},"xrefs":{"Monarch":{"xref_id":"0030827"}}}


id: PBO:0078191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 5-1","termid":"PBO:0078191"}


id: GO:0098582
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A vocalisation behavior that is innate, i.e. that does not need to be learned in order to occur.","definition_xrefs":["GOC:dos","GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vocalization behavior","termid":"GO:0071625"}],"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":"innate vocalization behavior","termid":"GO:0098582"}


id: GO:0061852
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Transporter complex that recognises, binds and returns endoplasmic reticulum (ER) resident proteins that have trafficked to Golgi compartments. Targets proteins lacking the HDEL motif recognised by COPI-coated vesicles.","definition_xrefs":["GOC:bhm","PMID:16093310"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transporter complex","termid":"GO:1990351"}],"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":"retrograde transporter complex, Golgi to ER","synonyms":[{"name":"ERV41-ERV46 retrograde receptor complex","type":"narrow"},{"name":"retrograde receptor complex, Golgi to ER","type":"exact"},{"name":"retrograde receptor complex, Golgi to endoplasmic reticulum","type":"exact"},{"name":"retrograde transporter complex, Golgi to endoplasmic reticulum","type":"exact"}],"termid":"GO:0061852"}


id: PBO:0085899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; may be involved in chitin biosynthesis by regulation of Chs3p export from the ER; relocalizes from bud neck to ER upon DNA replication stress","termid":"PBO:0085899"}


id: PBO:0048140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FXYD domain containing ion transport regulator 4","termid":"PBO:0048140"}


id: PBO:0004124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule-associated protein Mug164","termid":"PBO:0004124"}


id: PBO:0063523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDYN antisense RNA 1","termid":"PBO:0063523"}


id: MONDO:0100144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tubulinopathy with material basis in TUBB2B that is characterized by variations in R390Q, quadrupedal locomotion, cerebellar hypoplasia and does not have basal ganglia malformations.","definition_xrefs":["PMID:28013290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"tubulinopathy","termid":"MONDO:0100153"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Uner Tan Syndrome","synonyms":[{"name":"recessive quadrupedalism","type":"exact"}],"termid":"MONDO:0100144","xrefs":{"Monarch":{"xref_id":"0100144"}}}


id: PBO:0054328
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 1721","termid":"PBO:0054328"}


id: MONDO:0018147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, acquired, eye disease characterized by progressive visual loss, due to bilateral juxtafoveolar capillary occlusions, capillary telangiectasia, and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease.","definition_xrefs":["Orphanet:353351"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"idiopathic macular telangiectasia type 3","secondary_identifiers":["MEDGEN:1658435","GARD:21532","ICD10CM:H35.5","UMLS:C4751436"],"synonyms":[{"name":"occlusive idiopathic juxtafoveolar retinal telangiectasis","type":"exact"}],"termid":"MONDO:0018147","xrefs":{"Monarch":{"xref_id":"0018147"}}}


id: MOD:01222
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-formyl-L-serine.","definition_xrefs":["Unimod:122#S","PubMed:15627961","PubMed:15799070"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-formylated residue","termid":"MOD:01483"},{"relation_name":"is_a","term_name":"O3-acylated L-serine","termid":"MOD:02003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-formyl-L-serine","synonyms":[{"name":"Formyl","type":"related"},{"name":"Formylation","type":"related"}],"termid":"MOD:01222"}


id: MONDO:0002069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the UBERON:0035289.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female breast carcinoma","termid":"MONDO:0004379"}],"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":"female breast axillary tail cancer","secondary_identifiers":["SCTID:188156001","UMLS:C0153554","ICD10CM:C50.6","DOID:1650","ICD9:174.6","MEDGEN:509328"],"synonyms":[{"name":"axillary tail of breast cancer","type":"exact"},{"name":"cancer of axillary tail of breast","type":"exact"},{"name":"malignant axillary tail of breast neoplasm","type":"exact"},{"name":"malignant neoplasm of axillary tail of breast","type":"exact"},{"name":"malignant neoplasm of axillary tail of female breast","type":"exact"}],"termid":"MONDO:0002069","xrefs":{"Monarch":{"xref_id":"0002069"}}}


id: PBO:0040476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxin 1","termid":"PBO:0040476"}


id: GO:0007311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Polarization of the oocyte along the dorsal-ventral axis, by a gene product encoded by cells of the germ line. An example of this is found in Drosophila melanogaster.","definition_xrefs":["ISBN:0879694238","GOC:mtg_sensu","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oocyte dorsal/ventral axis specification","termid":"GO:0007310"}],"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":"maternal specification of dorsal/ventral axis, oocyte, germ-line encoded","secondary_identifiers":["GO:0048124"],"synonyms":[{"name":"maternal determination of dorsal/ventral axis, oocyte, germ-line encoded","type":"exact"},{"name":"maternal specification of dorsal-ventral axis, oocyte, germ-line encoded","type":"exact"},{"name":"maternal specification of dorsoventral axis, oocyte, germ-line encoded","type":"exact"}],"termid":"GO:0007311"}


id: GO:0006110
data:
  {"annotated_genes":["SJAG_02785","SJAG_05314","SJAG_00685"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71694],"is_not":false,"summary":null,"term":"GO:0006110"},{"annotations":[74768,77826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glycolysis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of purine nucleotide catabolic process","termid":"GO:0033121"},{"relation_name":"is_a","term_name":"regulation of generation of precursor metabolites and energy","termid":"GO:0043467"},{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"is_a","term_name":"regulation of ATP metabolic process","termid":"GO:1903578"},{"relation_name":"regulates","term_name":"glycolytic process","termid":"GO:0006096"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_02785":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281","GO:0055086","GO:0006091"],"is_obsolete":false,"name":"regulation of glycolytic process","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0090525","Reactome:R-HSA-170822"],"synonyms":[{"name":"regulation of glycolysis involved in cellular glucose homeostasis","type":"exact"}],"termid":"GO:0006110","terms_by_termid":{"GO:0006110":null,"GO:0045820":null}}


id: GO:0004978
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with corticotropin to initiate a change in cell activity.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanocortin receptor activity","termid":"GO:0004977"},{"relation_name":"is_a","term_name":"neuropeptide receptor activity","termid":"GO:0008188"}],"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":"corticotropin receptor activity","synonyms":[{"name":"ACTH receptor activity","type":"exact"},{"name":"adrenocorticotropic hormone receptor activity","type":"exact"},{"name":"adrenocorticotropin receptor activity","type":"exact"}],"termid":"GO:0004978"}


id: GO:0033475
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an indole-3-acetic acid amide conjugate, a form of indoleacetic acid covalently bound to an amino acid or polypeptide through an amide bond.","definition_xrefs":["GOC:mah","MetaCyc:PWY-1782"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indoleacetic acid conjugate biosynthetic process","termid":"GO:0033474"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"indoleacetic acid amide conjugate biosynthetic process","synonyms":[{"name":"IAA amide conjugate biosynthetic process","type":"exact"},{"name":"indole acetic acid amide conjugate biosynthesis","type":"exact"},{"name":"indole acetic acid amide conjugate biosynthetic process","type":"exact"},{"name":"indoleacetic acid amide conjugate anabolism","type":"exact"},{"name":"indoleacetic acid amide conjugate biosynthesis","type":"exact"},{"name":"indoleacetic acid amide conjugate formation","type":"exact"},{"name":"indoleacetic acid amide conjugate synthesis","type":"exact"}],"termid":"GO:0033475"}


id: GO:0048076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment of a pattern of pigment in the compound eye.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of eye pigmentation","termid":"GO:0048073"},{"relation_name":"regulates","term_name":"compound eye pigmentation","termid":"GO:0048072"}],"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 compound eye pigmentation","termid":"GO:0048076"}


id: PBO:0077259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 9","termid":"PBO:0077259"}


id: PBO:0071613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 31","termid":"PBO:0071613"}


id: GO:0045616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of keratinocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epidermal cell differentiation","termid":"GO:0045604"},{"relation_name":"regulates","term_name":"keratinocyte differentiation","termid":"GO:0030216"}],"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 keratinocyte differentiation","secondary_identifiers":["Reactome:R-HSA-8939242"],"termid":"GO:0045616"}


id: FYPO:0007236
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 early replication origins (i.e. origins that normally fire early in S phase) begins later than normal.","definition_xrefs":["PMID:22279046","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"delayed onset of protein localization to chromatin at replication origin","termid":"FYPO:0006734"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"delayed onset of protein localization to chromatin at early replication origin","synonyms":[{"name":"delayed onset of protein localisation to chromatin at early replication origin","type":"exact"},{"name":"delayed onset of protein localization to chromatin at early origin","type":"exact"},{"name":"delayed onset of protein localization to chromatin at early replication origins during mitotic cell cycle","type":"related"},{"name":"delayed onset of protein localization to chromatin at early replication origins during vegetative growth","type":"exact"},{"name":"delayed protein localization to chromatin at early replication origin","type":"exact"}],"termid":"FYPO:0007236"}


id: PBO:0109278
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 3113","termid":"PBO:0109278"}


id: GO:0042188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane (DDT), a chlorinated broad spectrum contact insecticide.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane metabolic process","termid":"GO:0018977"},{"relation_name":"is_a","term_name":"chlorinated hydrocarbon catabolic process","termid":"GO:0042205"},{"relation_name":"is_a","term_name":"insecticide catabolic process","termid":"GO:0046701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098754","GO:0019748"],"is_obsolete":false,"name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane catabolic process","synonyms":[{"name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane breakdown","type":"exact"},{"name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane catabolism","type":"exact"},{"name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane degradation","type":"exact"},{"name":"DDT catabolic process","type":"exact"},{"name":"DDT catabolism","type":"exact"}],"termid":"GO:0042188"}


id: PBO:0071676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37 pseudogene 8","termid":"PBO:0071676"}


id: PBO:0038537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 12B","termid":"PBO:0038537"}


id: GO:0031578
data:
  {"annotated_genes":["SJAG_04943"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80623],"is_not":false,"summary":null,"term":"GO:0031578"}]},"cv_name":"biological_process","definition":"A signaling process that monitors and signals errors in the placement or orientation of the spindle in the cell. This delays the completion of anaphase until errors are corrected.","definition_xrefs":["PMID:14616062","GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of exit from mitosis","termid":"GO:0001100"},{"relation_name":"is_a","term_name":"mitotic spindle checkpoint signaling","termid":"GO:0071174"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04943":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0044772"},{"rel_name":"regulates","termid":"GO:0044772"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0007049","GO:0044772"],"is_obsolete":false,"name":"mitotic spindle orientation checkpoint signaling","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0072483"],"synonyms":[{"name":"SOC","type":"exact"},{"name":"SPOC","type":"exact"},{"name":"mitotic cell cycle spindle orientation checkpoint","type":"exact"},{"name":"mitotic spindle orientation checkpoint","type":"exact"},{"name":"signal transduction involved in mitotic cell cycle spindle orientation checkpoint","type":"exact"},{"name":"spindle position checkpoint","type":"exact"}],"termid":"GO:0031578","terms_by_termid":{"GO:0031578":null}}


id: PR:Q9USQ9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proteasome subunit beta type-4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11599:SF5","PRO:DNx","OMA:SCHPO02584"],"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":"proteasome subunit beta type-7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC577.10","secondary_identifiers":["UniProtKB:Q9USQ9"],"synonyms":[{"name":"Spom972h-PSMB4","type":"exact"}],"termid":"PR:Q9USQ9"}


id: MONDO:0021605
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87619],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008097"}]},"cv_name":"mondo","definition":"A non-metastasizing neoplasm that arises from the upper or lower eyelid.","definition_xrefs":["NCIT:C4354"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eyelid neoplasm","termid":"MONDO:0002235"},{"relation_name":"is_a","term_name":"benign neoplasm of skin","termid":"MONDO:0021440"},{"relation_name":"is_a","term_name":"benign neoplasm of eye","termid":"MONDO:0021454"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"benign eyelid neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0339107","MEDGEN:137911","SCTID:231824001"],"synonyms":[{"name":"benign eyelid neoplasm","type":"exact"},{"name":"benign eyelid tumor","type":"exact"},{"name":"benign eyelid tumour","type":"exact"},{"name":"benign neoplasm of eyelid","type":"exact"},{"name":"benign neoplasm of the eyelid","type":"exact"},{"name":"benign tumor of eyelid","type":"exact"},{"name":"benign tumor of the eyelid","type":"exact"},{"name":"benign tumour of eyelid","type":"exact"},{"name":"benign tumour of the eyelid","type":"exact"},{"name":"eyelid benign neoplasm","type":"exact"}],"termid":"MONDO:0021605","terms_by_termid":{"MONDO:0008097":null},"xrefs":{"Monarch":{"xref_id":"0021605"}}}


id: GO:0070290
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N-acyl-1,2-diacyl-sn-glycero-3-phosphoethanolamine (NAPE) = a 1,2-diacyl-sn-glycero-3-phosphate + an N-acylethanolamine (NAE) + H+.","definition_xrefs":["PMID:15878693","RHEA:33159","PMID:14634025"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase activity","termid":"GO:0004620"},{"relation_name":"is_a","term_name":"phosphoric diester hydrolase activity","termid":"GO:0008081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016788"],"is_obsolete":false,"name":"N-acylphosphatidylethanolamine-specific phospholipase D activity","secondary_identifiers":["Reactome:R-HSA-2466831","EC:3.1.4.54","MetaCyc:RXN-12116"],"synonyms":[{"name":"N-acyl-phosphatidylethanolamine-specific phospholipase D activity","type":"exact"},{"name":"NAPE-specific phospholipase D activity","type":"exact"}],"termid":"GO:0070290"}


id: PBO:0043537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"component of oligomeric golgi complex 5","termid":"PBO:0043537"}


id: PBO:0076071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stimulated by retinoic acid 8","termid":"PBO:0076071"}


id: GO:0042268
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the rupture of cell membranes and the loss of cytoplasm.","definition_xrefs":["GOC:mtg_apoptosis","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"cytolysis","termid":"GO:0019835"}],"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 cytolysis","termid":"GO:0042268"}


id: GO:0035574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H4 by the removal of a methyl group from lysine at position 20 of the histone.","definition_xrefs":["GOC:sp","PMID:20622853"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H4-K20 demethylation (obsolete GO:0035574)","termid":"GO:0035574"}


id: FYPO:0006495
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA-DNA hybrid molecules is greater than normal at tRNA genes.","definition_xrefs":["PomBase:mah","PMID:29622660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased number of R-loops","termid":"FYPO:0007901"}],"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"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased number of R-loops at tRNA genes","synonyms":[{"name":"increased RNA-DNA hybrid level at tRNA genes","type":"exact"},{"name":"increased level of DNA:RNA hybrids at tRNA genes","type":"exact"},{"name":"increased level of RNA-DNA hybrids at tDNA","type":"exact"},{"name":"increased level of RNA-DNA hybrids at tRNA genes","type":"exact"},{"name":"increased level of RNA-DNA hybrids at tRNA genes during mitotic cell cycle","type":"related"},{"name":"increased level of RNA-DNA hybrids at tRNA genes during vegetative growth","type":"exact"}],"termid":"FYPO:0006495"}


id: GO:0047919
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-alpha-D-mannose + H2O + 2 NAD+ = GDP-D-mannuronate + 3 H+ + 2 NADH.","definition_xrefs":["EC:1.1.1.132","RHEA:21728"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"GDP-mannose 6-dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R00880","MetaCyc:GDP-MANNOSE-6-DEHYDROGENASE-RXN"],"synonyms":[{"name":"GDP mannose dehydrogenase activity","type":"related"},{"name":"GDP-D-mannose:NAD+ 6-oxidoreductase activity","type":"related"},{"name":"GDPmannose 6-dehydrogenase activity","type":"related"},{"name":"guanosine diphospho-D-mannose dehydrogenase activity","type":"related"},{"name":"guanosine diphosphomannose dehydrogenase activity","type":"related"}],"termid":"GO:0047919"}


id: GO:0048092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of establishment of a pattern of pigment in males.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental pigmentation","termid":"GO:0048086"},{"relation_name":"is_a","term_name":"regulation of male pigmentation","termid":"GO:0048088"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_regulates","term_name":"male pigmentation","termid":"GO:0048094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of male pigmentation","synonyms":[{"name":"down regulation of male pigmentation","type":"exact"},{"name":"down-regulation of male pigmentation","type":"exact"},{"name":"downregulation of male pigmentation","type":"exact"},{"name":"inhibition of male pigmentation","type":"narrow"}],"termid":"GO:0048092"}


id: MONDO:1010563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acromegaly that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acromegaly, non-human animal","termid":"MONDO:1010049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acromegaly, domestic cat","secondary_identifiers":["OMIA:000008-9685"],"termid":"MONDO:1010563","xrefs":{"Monarch":{"xref_id":"1010563"}}}


id: PBO:0091733
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"previously thought to be a ribosomal protein","termid":"PBO:0091733"}


id: GO:1904161
data:
  {"annotated_genes":["SJAG_05197","SJAG_04877","SJAG_02818","SJAG_00814"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78566,97019,104625,110927],"is_not":false,"summary":null,"term":"GO:1904161"}]},"cv_name":"biological_process","definition":"Any DNA synthesis that is involved in UV-damage excision repair.","definition_xrefs":["PMID:10704216","GO_REF:0000060","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA synthesis involved in DNA repair","termid":"GO:0000731"},{"relation_name":"part_of","term_name":"UV-damage excision repair","termid":"GO:0070914"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00814":null,"SJAG_02818":null,"SJAG_04877":null,"SJAG_05197":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006281"],"is_obsolete":false,"name":"DNA synthesis involved in UV-damage excision repair","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"DNA synthesis during UV-damage excision repair","type":"related"},{"name":"DNA synthesis during UV-damaged DNA endonuclease-dependent excision repair","type":"related"},{"name":"DNA synthesis during UVDE-dependent excision repair","type":"related"},{"name":"DNA synthesis during UVER","type":"related"},{"name":"DNA synthesis involved in AER","type":"related"},{"name":"DNA synthesis involved in UV-damaged DNA endonuclease-dependent excision repair","type":"exact"},{"name":"DNA synthesis involved in UVDE-dependent excision repair","type":"exact"},{"name":"DNA synthesis involved in UVER","type":"exact"},{"name":"DNA synthesis involved in alternative excision repair","type":"related"},{"name":"mitotic DNA repair synthesis involved in UV-damage excision repair","type":"narrow"},{"name":"mitotic DNA repair synthesis involved in UV-damaged DNA endonuclease-dependent excision repair","type":"narrow"},{"name":"mitotic DNA repair synthesis involved in UVDE-dependent excision repair","type":"narrow"},{"name":"mitotic DNA repair synthesis involved in UVER","type":"narrow"}],"termid":"GO:1904161","terms_by_termid":{"GO:1904161":null}}


id: MONDO:0005098
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sudden loss of neurological function secondary to hemorrhage or ischemia in the brain parenchyma due to a vascular event.","definition_xrefs":["NCIT:C3390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebrovascular disorder","termid":"MONDO:0011057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stroke disorder","secondary_identifiers":["EFO:0000712","SCTID:230690007","HP:0001297","MESH:D020521","UMLS:C0038454","MEDGEN:52522","birnlex:12783"],"synonyms":[{"name":"CVA","type":"exact"},{"name":"CVA, cerebrovascular accident","type":"exact"},{"name":"cerebral infarction","type":"related"},{"name":"cerebrovascular accident","type":"exact"},{"name":"cerebrovascular accident, (CVA)","type":"exact"},{"name":"stroke","type":"exact"},{"name":"stroke syndrome","type":"exact"},{"name":"syndrome, stroke","type":"exact"},{"name":"undetermined stroke","type":"exact"}],"termid":"MONDO:0005098","xrefs":{"Monarch":{"xref_id":"0005098"}}}


id: PBO:0005426
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functional septation initiation network required","termid":"PBO:0005426"}


id: PBO:0060524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asparaginyl-tRNA synthetase 1 pseudogene 2","termid":"PBO:0060524"}


id: MONDO:0033672
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Duane anomaly-myopathy-scoliosis syndrome is characterized by the association of bilateral Duane anomaly type 3, severe scoliosis of early onset, congenital myopathy with hypotonia without muscular weakness, delayed motor development, and short stature. It has been described in one pair of sibs. The Duane type 3 anomaly consists of eye abduction and adduction palsy, globe retraction and narrowing of the palpebral fissure. Muscular biopsy shows aspecific myopathy. Intellectual development is normal. The syndrome is most likely inherited in an autosomal recessive manner. It differs from the Crisfield-Dretakis-Sharpe syndrome, in which short stature and muscular features are absent. Surgery of the scoliosis is necessary. Functional prognosis depends on the severity of the visual handicap.","definition_xrefs":["Orphanet:50817"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Duane anomaly-myopathy-scoliosis syndrome","secondary_identifiers":["GARD:18842","UMLS:C4302550","MEDGEN:928219"],"termid":"MONDO:0033672","xrefs":{"Monarch":{"xref_id":"0033672"}}}


id: MONDO:0002918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A WHO grade II morphologic variant of meningioma characterized by the presence of clear glycogen-rich polygonal cells.","definition_xrefs":["NCIT:C4722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clear cell meningioma","secondary_identifiers":["ONCOTREE:CCM","MEDGEN:98459","ICDO:9538/1","UMLS:C0431121","DOID:4210"],"synonyms":[{"name":"CCM","type":"related"},{"name":"clear cell meningioma","type":"exact"},{"name":"clear cell meningioma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0002918","xrefs":{"Monarch":{"xref_id":"0002918"}}}


id: PBO:0036065
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_transport_during_vegetative_growth","termid":"PBO:0036065"}


id: PBO:0047149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 181 member B","termid":"PBO:0047149"}


id: GO:0048366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the leaf over time, from its formation to the mature structure.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phyllome development","termid":"GO:0048827"}],"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":"leaf development","termid":"GO:0048366"}


id: PBO:0040409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V1 subunit G3","termid":"PBO:0040409"}


id: GO:0106147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of fraxetin.","definition_xrefs":["GOC:lr","PMID:29581584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coumarin biosynthetic process","termid":"GO:0009805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"fraxetin biosynthesis","termid":"GO:0106147"}


id: FYPO:0001279
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to oxidative stress is higher than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased RNA level during cellular response to oxidative stress","synonyms":[{"name":"increased RNA accumulation during cellular response to oxidative stress","type":"related"},{"name":"increased RNA level during cellular response to oxidative stress during mitotic cell cycle","type":"related"},{"name":"increased RNA level during cellular response to oxidative stress during vegetative growth","type":"exact"},{"name":"increased RNA level during oxidative stress response","type":"exact"},{"name":"increased mRNA level during cellular response to oxidative stress","type":"narrow"},{"name":"increased transcript level during cellular response to oxidative stress","type":"exact"}],"termid":"FYPO:0001279"}


id: PBO:0087001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho-family GTPase interacting protein and Cdc42p effector; required with Gic2p for polarity establishment and initiation of budding; involved in recruitment of septins to the presumptive bud site; interacts with Cdc42p via the Cdc42/Rac-interactive binding (CRIB) domain; gic1 gic2 double mutants are defective for polarizing Cdc42p at elevated temperature, so may function both up- and downstream of Cdc42p; regulates mitotic exit; relocalizes from bud neck to nucleus upon DNA replication stress","termid":"PBO:0087001"}


id: GO:0045572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of imaginal disc growth.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of imaginal disc growth","termid":"GO:0045570"},{"relation_name":"is_a","term_name":"positive regulation of developmental growth","termid":"GO:0048639"},{"relation_name":"positively_regulates","term_name":"imaginal disc growth","termid":"GO:0007446"}],"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 imaginal disc growth","synonyms":[{"name":"activation of imaginal disc growth","type":"narrow"},{"name":"stimulation of imaginal disc growth","type":"narrow"},{"name":"up regulation of imaginal disc growth","type":"exact"},{"name":"up-regulation of imaginal disc growth","type":"exact"},{"name":"upregulation of imaginal disc growth","type":"exact"}],"termid":"GO:0045572"}


id: GO:0046165
data:
  {"annotated_genes":["SJAG_03538","SJAG_04270","SJAG_04018","SJAG_02719","SJAG_00413","SJAG_00244","SJAG_04866","SJAG_03018","SJAG_02104","SJAG_02044","SJAG_03275","SJAG_03098","SJAG_03750","SJAG_00381","SJAG_03598","SJAG_00453","SJAG_02305","SJAG_03743","SJAG_00370","SJAG_00880","SJAG_00827","SJAG_04810","SJAG_03235","SJAG_00409","SJAG_01474","SJAG_00624","SJAG_02420","SJAG_01970","SJAG_04178","SJAG_04067","SJAG_02321","SJAG_01012","SJAG_03024","SJAG_04499","SJAG_02421","SJAG_00717","SJAG_04842","SJAG_02734","SJAG_03362","SJAG_02406","SJAG_01057","SJAG_03715","SJAG_00321","SJAG_03409","SJAG_02855","SJAG_02982","SJAG_04217","SJAG_02429","SJAG_03509","SJAG_04282","SJAG_02706","SJAG_01307","SJAG_03929","SJAG_03739","SJAG_00770","SJAG_03249","SJAG_03531","SJAG_01148"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73178,72855,75562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000949"},{"annotations":[75645,73221,111909,67058,78179,90243,118387,91433,75990,81817,96410,109657,71530,117072,109344,72602,78187,73425,82029,74840,111067,78915,82003,77822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006696"},{"annotations":[63798,70760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006114"},{"annotations":[67119],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006021"},{"annotations":[58639,76464,77197,72906,95153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032958"},{"annotations":[95657],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0010895"},{"annotations":[111675],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0070452"},{"annotations":[115522,90809],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090180"},{"annotations":[77177],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0045540"},{"annotations":[90332,107644],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032443"},{"annotations":[107797,78540,75381,80611,98682,111539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046512"},{"annotations":[71563,110339],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006729"},{"annotations":[80146,62136,71744,78698,75673,75615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009228"},{"annotations":[112274,101311,112273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036172"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of alcohols, any of a class of compounds containing one or more hydroxyl groups attached to a saturated carbon atom.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol metabolic process","termid":"GO:0006066"},{"relation_name":"is_a","term_name":"small molecule biosynthetic process","termid":"GO:0044283"}],"gene_count":58,"genes_by_uniquename":{"SJAG_00244":null,"SJAG_00321":null,"SJAG_00370":null,"SJAG_00381":null,"SJAG_00409":null,"SJAG_00413":null,"SJAG_00453":null,"SJAG_00624":null,"SJAG_00717":null,"SJAG_00770":null,"SJAG_00827":null,"SJAG_00880":null,"SJAG_01012":null,"SJAG_01057":null,"SJAG_01148":null,"SJAG_01307":null,"SJAG_01474":null,"SJAG_01970":null,"SJAG_02044":null,"SJAG_02104":null,"SJAG_02305":null,"SJAG_02321":null,"SJAG_02406":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02429":null,"SJAG_02706":null,"SJAG_02719":null,"SJAG_02734":null,"SJAG_02855":null,"SJAG_02982":null,"SJAG_03018":null,"SJAG_03024":null,"SJAG_03098":null,"SJAG_03235":null,"SJAG_03249":null,"SJAG_03275":null,"SJAG_03362":null,"SJAG_03409":null,"SJAG_03509":null,"SJAG_03531":null,"SJAG_03538":null,"SJAG_03598":null,"SJAG_03715":null,"SJAG_03739":null,"SJAG_03743":null,"SJAG_03750":null,"SJAG_03929":null,"SJAG_04018":null,"SJAG_04067":null,"SJAG_04178":null,"SJAG_04217":null,"SJAG_04270":null,"SJAG_04282":null,"SJAG_04499":null,"SJAG_04810":null,"SJAG_04842":null,"SJAG_04866":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"alcohol biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"alcohol anabolism","type":"exact"},{"name":"alcohol biosynthesis","type":"exact"},{"name":"alcohol formation","type":"exact"},{"name":"alcohol synthesis","type":"exact"}],"termid":"GO:0046165","terms_by_termid":{"GO:0000949":null,"GO:0006021":null,"GO:0006114":null,"GO:0006696":null,"GO:0006729":null,"GO:0009228":null,"GO:0010895":null,"GO:0032443":null,"GO:0032958":null,"GO:0036172":null,"GO:0045540":null,"GO:0046512":null,"GO:0070452":null,"GO:0090180":null}}


id: PBO:0042317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD36 molecule","termid":"PBO:0042317"}


id: MONDO:0019278
data:
  {"annotated_genes":["SJAG_03126","SJAG_02536","SJAG_00155","SJAG_03469","SJAG_01202"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014027"},{"annotations":[88183,88182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014384"},{"annotations":[87248,87247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054588"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of pilosebaceous unit","termid":"MONDO:0002917"},{"relation_name":"is_a","term_name":"skin appendage disorder","termid":"MONDO:0024481"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00155":null,"SJAG_01202":null,"SJAG_02536":null,"SJAG_03126":null,"SJAG_03469":null},"genotype_count":0,"is_obsolete":false,"name":"hair anomaly","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:79363","UMLS:C0265991","MEDGEN:539624"],"termid":"MONDO:0019278","terms_by_termid":{"MONDO:0014027":null,"MONDO:0014384":null,"MONDO:0054588":null},"xrefs":{"Monarch":{"xref_id":"0019278"}}}


id: GO:1990698
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a palmitoleoyl group, a 16-carbon monounsaturated fatty acid (C16:1), to an acceptor molecule.","definition_xrefs":["PMID:17141155","PMID:25731175"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016746","GO:0003824"],"is_obsolete":false,"name":"palmitoleoyltransferase activity","termid":"GO:1990698"}


id: FYPO:0006875
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 cell cortex of one or both cell tips is abnormal.","definition_xrefs":["PMID:17895368","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cell cortex during vegetative growth","termid":"FYPO:0000928"},{"relation_name":"is_a","term_name":"abnormal protein localization to cell tip during vegetative growth","termid":"FYPO:0001584"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal protein localization to cell cortex of cell tip during vegetative growth","synonyms":[{"name":"abnormal protein localisation to cell cortex of cell tip during vegetative growth","type":"exact"},{"name":"abnormal protein localization to cell cortex of cell end during vegetative growth","type":"exact"},{"name":"abnormal protein localization to cell cortex of cell tip during mitotic cell cycle","type":"related"},{"name":"abnormal protein localization to cell tip cortex during vegetative growth","type":"exact"}],"termid":"FYPO:0006875"}


id: FYECO:0000250
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which silver nitrate was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ AgNO3","synonyms":[{"name":"+ silver nitrate","type":"exact"}],"termid":"FYECO:0000250"}


id: GO:0003161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cardiac conduction system over time, from its formation to the mature structure. The cardiac conduction system consists of specialized cardiomyocytes that regulate the frequency of heart beat.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle tissue development","termid":"GO:0048738"}],"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":"cardiac conduction system development","synonyms":[{"name":"cardiac impulse conducting system development","type":"exact"},{"name":"heart conduction system development","type":"exact"}],"termid":"GO:0003161"}


id: FYPO:0003580
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the number of sites at which the protein Sad1 accumulates is greater than normal during a cellular response to DNA damage.","definition_xrefs":["PMID:24943839","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased number of Sad1 foci during response to DNA damage","synonyms":[{"name":"increased number of Sad1 foci during DNA damage response","type":"exact"},{"name":"increased number of Sad1 foci during response to DNA damage during mitotic cell cycle","type":"related"},{"name":"increased number of Sad1 foci during response to DNA damage during vegetative growth","type":"exact"}],"termid":"FYPO:0003580"}


id: GO:0050608
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + NAD+ + vanillin = 2 H+ + NADH + vanillate.","definition_xrefs":["RHEA:13309","EC:1.2.1.67"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"vanillin dehydrogenase activity","secondary_identifiers":["MetaCyc:1.2.1.67-RXN","KEGG_REACTION:R05699"],"synonyms":[{"name":"vanillin:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0050608"}


id: PR:C6Y4C1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pet117 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4C1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein pet117, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.25","synonyms":[{"name":"Spom972h-pet117","type":"exact"}],"termid":"PR:C6Y4C1"}


id: GO:0010090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the structures of a hair cell (trichome) cell are generated and organized. This process occurs while the initially relatively unspecialized epidermal cell is acquiring the specialized features of a hair cell. An example of this process is found in Arabidopsis thaliana.","definition_xrefs":["GOC:tair_curators","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"part_of","term_name":"trichome differentiation","termid":"GO:0010026"},{"relation_name":"part_of","term_name":"plant epidermis morphogenesis","termid":"GO:0090626"}],"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":"trichome morphogenesis","secondary_identifiers":["GO:0048272"],"synonyms":[{"name":"trichome cell morphogenesis during differentiation","type":"exact"}],"termid":"GO:0010090"}


id: PR:G2TRQ5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC3E7.17 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRQ5"],"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 C3E7.17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3E7.17","synonyms":[{"name":"Spom972h-SPBC3E7.17","type":"exact"}],"termid":"PR:G2TRQ5"}


id: GO:1905115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lateral attachment of mitotic spindle microtubules to kinetochore.","definition_xrefs":["PMID:22375062","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of attachment of mitotic spindle microtubules to kinetochore","termid":"GO:1902423"},{"relation_name":"regulates","term_name":"lateral attachment of mitotic spindle microtubules to kinetochore","termid":"GO:0099607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0000070"}],"interesting_parent_ids":["GO:0008150","GO:0000070","GO:0007049"],"is_obsolete":false,"name":"regulation of lateral attachment of mitotic spindle microtubules to kinetochore","termid":"GO:1905115"}


id: MONDO:0000967
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign well-circumscribed tumor, composed of lobules of mature adipocytes, that arises within subcutaneous tissue, deep soft tissues or on the surface of bones.","definition_xrefs":["NCIT:C27530"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conventional lipoma","secondary_identifiers":["DOID:10193","MEDGEN:272486","UMLS:C1333059"],"synonyms":[{"name":"classic type lipoma","type":"exact"},{"name":"conventional lipoma","type":"exact"}],"termid":"MONDO:0000967","xrefs":{"Monarch":{"xref_id":"0000967"}}}


id: MONDO:0005829
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute tick-borne arbovirus infection causing meningoencephalomyelitis of sheep.","definition_xrefs":["MESH:D008146"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sheep disease","termid":"MONDO:0024985"},{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"louping ill","secondary_identifiers":["DOID:10250","ICD9:063.1"],"synonyms":[{"name":"Louping ill","type":"exact"}],"termid":"MONDO:0005829","xrefs":{"Monarch":{"xref_id":"0005829"}}}


id: PBO:0078089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trafficking protein particle complex 2 pseudogene 6","termid":"PBO:0078089"}


id: PBO:0081375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF213 antisense RNA 1 (head to head)","termid":"PBO:0081375"}


id: MONDO:0003556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare endometrial carcinoma characterized by the presence of both malignant glandular and malignant squamous cellular components.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenosquamous carcinoma","termid":"MONDO:0006074"},{"relation_name":"is_a","term_name":"endometrial squamous cell carcinoma","termid":"MONDO:0006198"}],"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":"endometrial adenosquamous carcinoma","secondary_identifiers":["EFO:1001952","UMLS:C3896969","DOID:5631","NCIT:C114656","MEDGEN:856563"],"synonyms":[{"name":"adenosquamous carcinoma of endometrium","type":"exact"},{"name":"adenosquamous carcinoma of the endometrium","type":"related"},{"name":"endometrial adenosquamous cancer","type":"related"},{"name":"endometrial adenosquamous carcinoma","type":"exact"},{"name":"endometrium adenosquamous carcinoma","type":"exact"}],"termid":"MONDO:0003556","xrefs":{"Monarch":{"xref_id":"0003556"}}}


id: MONDO:0034668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete terminal transverse limb defect (obsolete MONDO:0034668)","secondary_identifiers":["Orphanet:498461"],"termid":"MONDO:0034668","xrefs":{"Monarch":{"xref_id":"0034668"}}}


id: PBO:0038989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenoceptor beta 3","termid":"PBO:0038989"}


id: GO:1904699
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of acinar cell proliferation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:9788538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of epithelial cell proliferation","termid":"GO:0050679"},{"relation_name":"is_a","term_name":"regulation of acinar cell proliferation","termid":"GO:1904697"},{"relation_name":"positively_regulates","term_name":"acinar cell proliferation","termid":"GO:1990863"}],"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 acinar cell proliferation","synonyms":[{"name":"activation of acinar cell proliferation","type":"narrow"},{"name":"activation of acinic cell proliferation","type":"narrow"},{"name":"activation of acinous cell proliferation","type":"narrow"},{"name":"positive regulation of acinic cell proliferation","type":"exact"},{"name":"positive regulation of acinous cell proliferation","type":"exact"},{"name":"up regulation of acinar cell proliferation","type":"exact"},{"name":"up regulation of acinic cell proliferation","type":"exact"},{"name":"up regulation of acinous cell proliferation","type":"exact"},{"name":"up-regulation of acinar cell proliferation","type":"exact"},{"name":"up-regulation of acinic cell proliferation","type":"exact"},{"name":"up-regulation of acinous cell proliferation","type":"exact"},{"name":"upregulation of acinar cell proliferation","type":"exact"},{"name":"upregulation of acinic cell proliferation","type":"exact"},{"name":"upregulation of acinous cell proliferation","type":"exact"}],"termid":"GO:1904699"}


id: MOD:00810
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O3-mannosylserine.","definition_xrefs":["RESID:AA0402","PubMed:391559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosyl-L-serine","termid":"MOD:00002"},{"relation_name":"is_a","term_name":"mannosylated residue","termid":"MOD:00595"},{"relation_name":"is_a","term_name":"monohexosylated (Hex1)","termid":"MOD:00761"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-mannosyl-L-serine","synonyms":[{"name":"(2S)-2-amino-3-(alpha-D-mannopyranosyloxy)propanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (Hex)","type":"exact"},{"name":"CARBOHYD O-linked (Man) serine","type":"exact"},{"name":"O-glycosylserine","type":"exact"},{"name":"O-mannopyranosylserine","type":"exact"},{"name":"O-mannosyl-L-serine","type":"exact"},{"name":"O3-mannosylserine","type":"exact"},{"name":"OManSer","type":"exact"}],"termid":"MOD:00810"}


id: PBO:0091851
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Defective In Sister chromatid joining","termid":"PBO:0091851"}


id: FYPO:0004686
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 streptothricin. Cells stop growing (and may die) at a concentration of streptothricin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000139","FYPO:0002683","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to streptothricin","synonyms":[{"name":"hypersensitive to streptothricin","type":"exact"},{"name":"sensitive to streptothricin during mitotic cell cycle","type":"related"},{"name":"sensitive to streptothricin during vegetative growth","type":"exact"}],"termid":"FYPO:0004686"}


id: GO:1901704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-glutamine.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamine biosynthetic process","termid":"GO:0006542"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"L-glutamine biosynthetic process","synonyms":[{"name":"L-glutamine anabolism","type":"exact"},{"name":"L-glutamine biosynthesis","type":"exact"},{"name":"L-glutamine formation","type":"exact"},{"name":"L-glutamine synthesis","type":"exact"}],"termid":"GO:1901704"}


id: RO:0000092
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of has disposition","direct_ancestors":[{"relation_name":"is_a","term_name":"inheres_in","termid":"RO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disposition_of","termid":"RO:0000092"}


id: GO:0052191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of phagocytosis, the engulfing by phagocytes of external particulate material, in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by symbiont of host phagocytosis (obsolete GO:0052191)","synonyms":[{"name":"activation by symbiont of host phagocytosis","type":"narrow"},{"name":"stimulation by symbiont of host phagocytosis","type":"narrow"},{"name":"up regulation by symbiont of host phagocytosis","type":"exact"},{"name":"up-regulation by symbiont of host phagocytosis","type":"exact"},{"name":"upregulation by symbiont of host phagocytosis","type":"exact"}],"termid":"GO:0052191"}


id: MONDO:0003045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tumors or cancer of the anal gland.","definition_xrefs":["MESH:D000694"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anus neoplasm","termid":"MONDO:0003046"}],"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":"anal gland neoplasm","secondary_identifiers":["UMLS:C0002757","DOID:4550","MEDGEN:1897"],"synonyms":[{"name":"gland of anal canal neoplasm","type":"exact"},{"name":"gland of anal canal neoplasm (disease)","type":"exact"},{"name":"gland of anal canal tumor","type":"exact"},{"name":"gland of anal canal tumour","type":"exact"},{"name":"neoplasm of gland of anal canal","type":"exact"},{"name":"tumor of gland of anal canal","type":"exact"},{"name":"tumour of gland of anal canal","type":"exact"}],"termid":"MONDO:0003045","xrefs":{"Monarch":{"xref_id":"0003045"}}}


id: MONDO:0044210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The inheritance of only one mutated beta-globin allele (beta+ or beta0).","definition_xrefs":["SCDO:0000114"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-thalassemia HBB/LCRB","termid":"MONDO:0013517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"thalassemia minor","secondary_identifiers":["MEDGEN:450549","MedDRA:10054662","UMLS:C0869532","ICD10CM:D56.3","DOID:0080774","SCTID:19442009"],"synonyms":[{"name":"beta thalassemia trait","type":"exact"}],"termid":"MONDO:0044210","xrefs":{"Monarch":{"xref_id":"0044210"}}}


id: MONDO:0002293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A ganglioneuroma arising from the skin.","definition_xrefs":["NCIT:C4481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin cancer","termid":"MONDO:0002898"},{"relation_name":"is_a","term_name":"ganglioneuroma","termid":"MONDO:0005033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"cutaneous ganglioneuroma","secondary_identifiers":["SCTID:254766004","MEDGEN:91077","DOID:2425","UMLS:C0346063"],"synonyms":[{"name":"cutaneous ganglioneuroma","type":"exact"},{"name":"ganglioneuroma of skin","type":"exact"},{"name":"ganglioneuroma of the skin","type":"exact"},{"name":"skin ganglioneuroma","type":"exact"}],"termid":"MONDO:0002293","xrefs":{"Monarch":{"xref_id":"0002293"}}}


id: PBO:0053993
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 1312","termid":"PBO:0053993"}


id: MONDO:0012999
data:
  {"annotated_genes":["SJAG_02271"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87194],"is_not":false,"summary":null,"term":"MONDO:0012999"}]},"cv_name":"mondo","definition":"A creatine deficiency syndrome characterized by global developmental delay/intellectual disability (DD/ID), prominent speech delay, autistic/hyperactive behavioral disorders, seizures, and various types of pyramidal and/or extra-pyramidal manifestations.","definition_xrefs":["Orphanet:382"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral creatine deficiency syndrome","termid":"MONDO:0000456"},{"relation_name":"is_a","term_name":"creatine biosynthetic process disease","termid":"MONDO:0045018"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02271":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"guanidinoacetate methyltransferase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:1201034","OMIM:612736","GARD:2578","MEDGEN:154356","SCTID:124239003","ICD9:277.6","NORD:1967","MESH:C537622","NANDO:2201300","DOID:0050799","UMLS:C0574080","icd11.foundation:1811642217"],"synonyms":[{"name":"CCDS2","type":"related"},{"name":"GAMT deficiency","type":"exact"},{"name":"cerebral creatine deficiency syndrome 2","type":"exact"},{"name":"cerebral creatine deficiency syndrome type 2","type":"exact"},{"name":"creatine deficiency syndrome due to GAMT deficiency","type":"related"},{"name":"disorder of guanidinoacetate N-methyltransferase activity","type":"exact"},{"name":"guanidinoacetate N-methyltransferase activity disease","type":"exact"},{"name":"guanidinoacetate methyltransferase deficiency","type":"exact"}],"termid":"MONDO:0012999","terms_by_termid":{"MONDO:0012999":null},"xrefs":{"Monarch":{"xref_id":"0012999"}}}


id: PBO:0088500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-amino-6-(5-phosphoribosylamino) uracil reductase Rib7","termid":"PBO:0088500"}


id: PBO:0069910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1201, pseudogene","termid":"PBO:0069910"}


id: PBO:0073642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sialic acid binding Ig like lectin 29, pseudogene","termid":"PBO:0073642"}


id: PBO:0066410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RELT like 2","termid":"PBO:0066410"}


id: GO:0055014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an atrial cardiac muscle cell over time, from its formation to the mature state. Cardiac muscle cells are striated muscle cells that are responsible for heart contraction. The atrium is the part of the heart that receives blood into the organ.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell development","termid":"GO:0055013"},{"relation_name":"part_of","term_name":"atrial cardiac muscle cell differentiation","termid":"GO:0055011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"atrial cardiac muscle cell development","synonyms":[{"name":"atrial cardiomyocyte development","type":"exact"},{"name":"atrial heart muscle development","type":"exact"}],"termid":"GO:0055014"}


id: GO:0102833
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1D-5-O-methyl-myo-inositol + alpha-D-galactosyl-(1->3)-1D-myo-inositol = D-galactosylononitol + myo-inositol.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete sequoyitol galactinol:D-galactosylononitol galactosyltransferase activity (obsolete GO:0102833)","termid":"GO:0102833"}


id: PBO:0089203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GID complex subunit, Ran GTPase binding protein Gid1","termid":"PBO:0089203"}


id: PBO:0054465
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 1864","termid":"PBO:0054465"}


id: MONDO:0007399
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any craniosynostosis in which the cause of the disease is a mutation in the TWIST1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene","PMID:17343269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated oxycephaly","termid":"MONDO:0018971"}],"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":"TWIST1-related craniosynostosis","secondary_identifiers":["UMLS:C4551902","MEDGEN:1646646","GARD:18045","NORD:1606","OMIM:123100","SCTID:57219006"],"synonyms":[{"name":"CRS","type":"related"},{"name":"CRS1","type":"related"},{"name":"Primary Craniosynostosis","type":"exact"},{"name":"TWIST1-related craniosynostosis","type":"exact"},{"name":"craniostenosis","type":"related"},{"name":"craniosynostosis 1","type":"exact"},{"name":"craniosynostosis type 1","type":"exact"}],"termid":"MONDO:0007399","xrefs":{"Monarch":{"xref_id":"0007399"}}}


id: MONDO:0018678
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder","termid":"MONDO:0005570"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"polyclonal hyperviscosity syndrome","secondary_identifiers":["Orphanet:450322","UMLS:C5681102","ICD10CM:D89.0","GARD:21887","MEDGEN:1814466"],"termid":"MONDO:0018678","xrefs":{"Monarch":{"xref_id":"0018678"}}}


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":["GOC:TermGenie","PMID:17646383","GO_REF:0000058"],"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:0088934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intermembrane lipid transfer protein, chorein family Vps13a","termid":"PBO:0088934"}


id: SO:0001723
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 36th residue (a lysine), from the start of the H3 histone protein is dimethylated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"H3K36_methylation_site","termid":"SO:0001733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H3K36_dimethylation_site","synonyms":[{"name":"H3K36 di-methylation site","type":"exact"},{"name":"H3K36Me2","type":"related"}],"termid":"SO:0001723"}


id: MONDO:0009698
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Unverricht-Lundborg disease (ULD) is a rare progressive myoclonic epilepsy disorder characterized by action- and stimulus-sensitive myoclonus, and tonic-clonic seizures with ataxia, but with only a mild cognitive decline over time.","definition_xrefs":["Orphanet:308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"Unverricht-Lundborg syndrome","secondary_identifiers":["DOID:3535","MEDGEN:155923","DOID:0111452","GARD:3876","UMLS:C0751785","MedDRA:10054895","NANDO:1200954","OMIM:254800","SCTID:230423006","NANDO:2200880","MESH:D020194"],"synonyms":[{"name":"Baltic myoclonic epilepsy","type":"related"},{"name":"EPM1","type":"related"},{"name":"PME type 1","type":"exact"},{"name":"ULD","type":"exact"},{"name":"Uld","type":"related"},{"name":"Unverricht - Lundborg disease","type":"exact"},{"name":"Unverricht's disease","type":"exact"},{"name":"Unverricht-Lundborg disease","type":"exact"},{"name":"Unverricht-Lundborg syndrome","type":"exact"},{"name":"epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)","type":"exact"},{"name":"epilepsy, progressive myoclonic type 1","type":"related"},{"name":"epilepsy, progressive myoclonic, 1","type":"related"},{"name":"epilepsy, progressive myoclonic, 1A","type":"related"},{"name":"epilepsy, progressive myoclonus 1","type":"related"},{"name":"myoclonic epilepsy of Unverricht and Lundborg","type":"related"},{"name":"myoclonus progressive epilepsy of Unverricht and Lundborg","type":"related"},{"name":"progressive myoclonic epilepsy","type":"related"},{"name":"progressive myoclonic epilepsy type 1","type":"exact"},{"name":"progressive myoclonus epilepsy Baltic myoclonic epilepsy","type":"related"},{"name":"progressive myoclonus epilepsy type 1","type":"exact"}],"termid":"MONDO:0009698","xrefs":{"Monarch":{"xref_id":"0009698"}}}


id: GO:0034045
data:
  {"annotated_genes":["SJAG_01382","SJAG_04963","SJAG_04219","SJAG_00115","SJAG_00645","SJAG_00763","SJAG_01251","SJAG_02441","SJAG_02699","SJAG_03136","SJAG_01876","SJAG_03100","SJAG_00004","SJAG_04655","SJAG_06309","SJAG_05017","SJAG_00059","SJAG_04232","SJAG_02640","SJAG_04502","SJAG_04860","SJAG_03851","SJAG_01783"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[60292,61166,61336,63165,66630,73503,73760,74372,75075,81300,81381,81410,81556,94398,94682,96594,101483,112099,113349,113521,117000,117061],"is_not":false,"summary":null,"term":"GO:0034045"},{"annotations":[96397],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097632"}]},"cv_name":"cellular_component","definition":"A cellular membrane associated with the phagophore assembly site.","definition_xrefs":["PMID:17382324","GOC:rph","GOC:mah","PMID:16874040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane","termid":"GO:0016020"},{"relation_name":"part_of","term_name":"phagophore assembly site","termid":"GO:0000407"}],"gene_count":23,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00059":null,"SJAG_00115":null,"SJAG_00645":null,"SJAG_00763":null,"SJAG_01251":null,"SJAG_01382":null,"SJAG_01783":null,"SJAG_01876":null,"SJAG_02441":null,"SJAG_02640":null,"SJAG_02699":null,"SJAG_03100":null,"SJAG_03136":null,"SJAG_03851":null,"SJAG_04219":null,"SJAG_04232":null,"SJAG_04502":null,"SJAG_04655":null,"SJAG_04860":null,"SJAG_04963":null,"SJAG_05017":null,"SJAG_06309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000407"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0000407","GO:0005575"],"is_obsolete":false,"name":"phagophore assembly site membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"PAS membrane","type":"exact"},{"name":"isolation membrane","type":"related"},{"name":"phagophore","type":"related"},{"name":"pre-autophagosomal structure membrane","type":"narrow"}],"termid":"GO:0034045","terms_by_termid":{"GO:0034045":null,"GO:0097632":null}}


id: PBO:0067078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 110, pseudogene","termid":"PBO:0067078"}


id: GO:0004342
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucosamine 6-phosphate + H2O = beta-D-fructose 6-phosphate + NH4.","definition_xrefs":["EC:3.5.99.6","RHEA:12172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016810","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"glucosamine-6-phosphate deaminase activity","secondary_identifiers":["KEGG_REACTION:R00765","MetaCyc:GLUCOSAMINE-6-P-DEAMIN-RXN","Reactome:R-HSA-6799604"],"synonyms":[{"name":"2-amino-2-deoxy-D-glucose-6-phosphate aminohydrolase (ketol isomerizing)","type":"related"},{"name":"GlcN6P deaminase activity","type":"related"},{"name":"aminodeoxyglucosephosphate isomerase activity","type":"related"},{"name":"glucosamine phosphate deaminase activity","type":"related"},{"name":"glucosamine-6-phosphate isomerase activity","type":"related"},{"name":"glucosaminephosphate isomerase","type":"broad"},{"name":"phosphoglucosamine isomerase activity","type":"related"},{"name":"phosphoglucosaminisomerase activity","type":"related"}],"termid":"GO:0004342"}


id: GO:0018996
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The periodic shedding of part or all of a collagen and cuticulin-based cuticle, which is then replaced by a new collagen and cuticulin-based cuticle. An example of this is found in the Nematode worm, Caenorhabditis elegans.","definition_xrefs":["GOC:mtg_sensu","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molting cycle","termid":"GO:0042303"}],"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":"molting cycle, collagen and cuticulin-based cuticle","synonyms":[{"name":"collagen and cuticulin-based cuticle molting cycle","type":"exact"}],"termid":"GO:0018996"}


id: MONDO:0045046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of thyroid hormone metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland disorder","termid":"MONDO:0003240"},{"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":"inherited thyroid metabolism disease","secondary_identifiers":["MEDGEN:543589","SCTID:36985004","ICD9:246.8","UMLS:C0271824"],"synonyms":[{"name":"inborn error of thyroid hormone metabolic process","type":"exact"},{"name":"inborn thyroid hormone metabolic process disorder","type":"exact"},{"name":"inherited disorder of thyroid metabolism","type":"exact"},{"name":"rare inborn error of thyroid hormone metabolic process","type":"exact"}],"termid":"MONDO:0045046","xrefs":{"Monarch":{"xref_id":"0045046"}}}


id: GO:0047220
data:
  {"annotated_genes":["SJAG_00183"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107570],"is_not":false,"summary":null,"term":"GO:0047220"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-beta-D-galactosyl-O-beta-D-xylosylprotein + UDP-galactose = 3-beta-D-galactosyl-4-beta-D-galactosyl-O-beta-D-xylosylprotein + UDP.","definition_xrefs":["EC:2.4.1.134","MetaCyc:2.4.1.134-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a glycoprotein","termid":"GO:0140103"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00183":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0140096","GO:0016740","GO:0016757","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"galactosylxylosylprotein 3-beta-galactosyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-4420365","Reactome:R-HSA-1889978","RHEA:11780"],"synonyms":[{"name":"UDP-galactose:4-beta-D-galactosyl-O-beta-D-xylosylprotein 3-beta-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:4-beta-D-galactosyl-O-beta-D-xylosylprotein 3-beta-D-galactosyltransferase activity","type":"related"},{"name":"galactosyltransferase II activity","type":"related"},{"name":"uridine diphosphogalactose-galactosylxylose galactosyltransferase activity","type":"related"}],"termid":"GO:0047220","terms_by_termid":{"GO:0047220":null}}


id: PBO:0031069
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_small_spore","termid":"PBO:0031069"}


id: PBO:0090393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 histone deacetylase associated PHD finger protein Cph1","termid":"PBO:0090393"}


id: MONDO:0018140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete burning mouth syndrome (obsolete MONDO:0018140)","termid":"MONDO:0018140","xrefs":{"Monarch":{"xref_id":"0018140"}}}


id: MONDO:1010772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pemphigus that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pemphigus, non-human animal","termid":"MONDO:1010138"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pemphigus, dog","secondary_identifiers":["OMIA:001188-9615"],"termid":"MONDO:1010772","xrefs":{"Monarch":{"xref_id":"1010772"}}}


id: MONDO:0015742
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Periventricular leukomalacia (PVL) is a brain injury disorder characterized by the death of the white matter of the brain due to softening of the brain tissue. It can affect fetuses or newborns, and premature babies are at the greatest risk of the disorder. PVL is caused by a lack of oxygen or blood flow to thearea around the ventricles of the brain, which results in the death of brain tissue. Although babies with PVL generally have no apparent signs or symptoms of the disorder at delivery, they are at risk for motor disorders, cerebral palsy, delayed mental development, coordination problems, and vision and hearing impairments. There is no cure for PVL. Treatment is generally supportive. Prognosis is dependent on the extent of damage to the ventricles.","direct_ancestors":[{"relation_name":"is_a","term_name":"encephalomalacia","termid":"MONDO:0006741"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"periventricular leukomalacia","secondary_identifiers":["ICD9:742.8","Orphanet:171676","MESH:D007969","EFO:1001101","SCTID:230769007","ICD9:779.7","MedDRA:10052594","MEDGEN:6072","DOID:13088","NCIT:C99013","UMLS:C0023529"],"synonyms":[{"name":"PVL","type":"related"}],"termid":"MONDO:0015742","xrefs":{"Monarch":{"xref_id":"0015742"}}}


id: PBO:0045540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual oxidase maturation factor 2","termid":"PBO:0045540"}


id: GO:0051872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sphingosine (sphing-4-enine), trans-D-erytho-2-amino-octadec-4-ene-1,3-diol, a long chain amino diol sphingoid base that occurs in most sphingolipids in animal tissues.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphingosine metabolic process","termid":"GO:0006670"},{"relation_name":"is_a","term_name":"diol catabolic process","termid":"GO:0034313"},{"relation_name":"is_a","term_name":"sphingoid catabolic process","termid":"GO:0046521"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"sphingosine catabolic process","synonyms":[{"name":"(4E)-sphing-4-enine catabolic process","type":"exact"},{"name":"(4E)-sphing-4-enine catabolism","type":"exact"},{"name":"sphing-4-enine catabolic process","type":"exact"},{"name":"sphing-4-enine catabolism","type":"exact"}],"termid":"GO:0051872"}


id: PBO:0027694
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_latrunculin_A","termid":"PBO:0027694"}


id: PBO:0071258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23 pseudogene 3","termid":"PBO:0071258"}


id: MONDO:0015945
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Polymalformative genetic syndrome with increased risk of developing cancer (PGSIRC) comprises a wide range of syndromes characterized by congenital malformations with a high risk of developing tumors including up to 50 different rare diseases.","definition_xrefs":["Orphanet:183422"],"gene_count":0,"genotype_count":0,"name":"obsolete polymalformative genetic syndrome with increased risk of developing cancer (obsolete MONDO:0015945)","synonyms":[{"name":"PGSIRC","type":"exact"}],"termid":"MONDO:0015945","xrefs":{"Monarch":{"xref_id":"0015945"}}}


id: PBO:0109121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycoside hydrolase family protein Ghs2","termid":"PBO:0109121"}


id: FYPO:0002123
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 4,6-pyruvylated D-galactose (4,6-O-[(1R)-1-carboxyethylidene]-D-galactose) measured in a cell is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance absent from cell during vegetative growth","termid":"FYPO:0001208"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"pyruvylated galactose absent from cell","synonyms":[{"name":"4,6-O-[(1R)-1-carboxyethylidene]-D-galactose absent from cell","type":"exact"},{"name":"4,6-pyruvylated D-galactose absent from cell","type":"exact"},{"name":"PvGal absent from cell","type":"exact"},{"name":"pyruvylated galactose absent from cell during mitotic cell cycle","type":"related"},{"name":"pyruvylated galactose absent from cell during vegetative growth","type":"exact"}],"termid":"FYPO:0002123"}


id: RO:0002242
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A broad relationship between an exposure event or process and a process by which the exposure stressor comes into contact with the exposure receptor","direct_ancestors":[{"relation_name":"is_a","term_name":"related_via_exposure_to","termid":"RO:0002244"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_exposure_route","termid":"RO:0002242"}


id: PBO:0077856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPM1 antisense RNA","termid":"PBO:0077856"}


id: PBO:0091592
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Elongated at Low PH","termid":"PBO:0091592"}


id: MONDO:1010471
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent truncus arteriosus that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"persistent truncus arteriosus, non-human animal","termid":"MONDO:1010018"},{"relation_name":"is_a","term_name":"conotruncal heart malformations, dog","termid":"MONDO:1010453"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent truncus arteriosus, dog","secondary_identifiers":["OMIA:000795-9615"],"termid":"MONDO:1010471","xrefs":{"Monarch":{"xref_id":"1010471"}}}


id: MONDO:0017130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic urogenital tumor (obsolete MONDO:0017130)","secondary_identifiers":["Orphanet:271844"],"termid":"MONDO:0017130","xrefs":{"Monarch":{"xref_id":"0017130"}}}


id: PBO:0073419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"seizure related 6 homolog","termid":"PBO:0073419"}


id: PBO:0045192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJB6 pseudogene 5","termid":"PBO:0045192"}


id: GO:0070213
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The ADP-ribosylation by a protein of one or more of its own amino acid residues, or residues on an identical protein.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-translational protein modification","termid":"GO:0043687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein auto-ADP-ribosylation","synonyms":[{"name":"protein amino acid auto-ADP-ribosylation","type":"exact"}],"termid":"GO:0070213"}


id: GO:0030258
data:
  {"annotated_genes":["SJAG_04792","SJAG_00706"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78514],"is_not":false,"summary":null,"term":"GO:0030258"},{"annotations":[74919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001561"}]},"cv_name":"biological_process","definition":"The covalent alteration of one or more fatty acids in a lipid, resulting in a change in the properties of the lipid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid metabolic process","termid":"GO:0006629"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00706":null,"SJAG_04792":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"lipid modification","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0030258","terms_by_termid":{"GO:0001561":null,"GO:0030258":null}}


id: MONDO:0007598
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":"factors VIII, IX and XI, combined deficiency of","secondary_identifiers":["OMIM:134520","UMLS:C1851375","MEDGEN:341993","MESH:C565023"],"synonyms":[{"name":"factors VIII, 9 and Xi, combined deficiency of","type":"related"},{"name":"factors VIII, IX and XI, combined deficiency of","type":"exact"},{"name":"familial multiple coagulation Factor deficiency 5","type":"related"},{"name":"multiple coagulation Factor deficiency 5","type":"related"}],"termid":"MONDO:0007598","xrefs":{"Monarch":{"xref_id":"0007598"}}}


id: FYPO:0007619
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 is normal (i.e. indistinguishable from wild type) when the cell is subject to oxidative stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin during vegetative growth","termid":"FYPO:0001509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to chromatin during cellular response to oxidative stress","synonyms":[{"name":"normal protein localisation to chromatin during cellular response to oxidative stress","type":"exact"},{"name":"normal protein localization to chromatin during cellular response to oxidative stress during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin during cellular response to oxidative stress during vegetative growth","type":"exact"},{"name":"normal protein localization to chromatin during oxidative stress response","type":"exact"}],"termid":"FYPO:0007619"}


id: MONDO:0010339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features characterized by epilepsy, learning difficulties, macrocephaly, and aggressive behavior. It has been described in males from a four-generation kindred. It is transmitted as an X-linked recessive trait and is likely to be caused by mutations in the gene encoding synapsin I (Xp11.3-q12).","definition_xrefs":["Orphanet:85294"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features","termid":"MONDO:0859390"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"epilepsy, X-linked 1, with variable learning disabilities and behavior disorders","secondary_identifiers":["DOID:0112122","MEDGEN:1823951","MESH:C564505","OMIM:300491","UMLS:C5774177","GARD:16748"],"synonyms":[{"name":"X-linked epilepsy-learning disabilities-behavior disorders syndrome","type":"exact"},{"name":"epilepsy, X-linked, with variable learning disabilities and behavior disorders","type":"related"},{"name":"epilepsy, X-linked, with variable learning disabilities and behavior disorders, X-linked recessive, X-linked dominant","type":"exact"},{"name":"epilepsy, X-linked, with variable learning disabilities and behaviour disorders","type":"related"},{"name":"epilepsy, X-linked, with variable learning disabilities and behaviour disorders, X-linked recessive, X-linked dominant","type":"exact"}],"termid":"MONDO:0010339","xrefs":{"Monarch":{"xref_id":"0010339"}}}


id: PBO:0034183
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-directly_inhibits","termid":"PBO:0034183"}


id: PBO:0048688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GLIPR1 antisense RNA 1","termid":"PBO:0048688"}


id: GO:0008611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ether lipids, lipids that contain (normally) one lipid alcohol in ether linkage to one of the carbon atoms (normally C-1) of glycerol.","definition_xrefs":["PMID:15337120","GOC:ma","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid biosynthetic process","termid":"GO:0008610"},{"relation_name":"is_a","term_name":"ether lipid metabolic process","termid":"GO:0046485"},{"relation_name":"is_a","term_name":"glycerol ether biosynthetic process","termid":"GO:0046504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"ether lipid biosynthetic process","secondary_identifiers":["Reactome:R-HSA-75896"],"synonyms":[{"name":"ether lipid anabolism","type":"exact"},{"name":"ether lipid biosynthesis","type":"exact"},{"name":"ether lipid formation","type":"exact"},{"name":"ether lipid synthesis","type":"exact"},{"name":"plasmalogen biosynthetic process","type":"narrow"}],"termid":"GO:0008611"}


