# terms

id: MONDO:0000119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart disease","termid":"MONDO:0005453"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"congenital heart defects, multiple types","synonyms":[{"name":"CHTD","type":"related"}],"termid":"MONDO:0000119","xrefs":{"Monarch":{"xref_id":"0000119"}}}


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


id: SO:0002082
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that intersects the coding sequence near a splice region of an incompletely annotated transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"incomplete_transcript_splice_region_variant","termid":"SO:0002079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"incomplete_transcript_coding_splice_variant","secondary_identifiers":["http://snp.gs.washington.edu/SeattleSeqAnnotation137/HelpHowToUse.jsp"],"synonyms":[{"name":"Seattleseq:coding-notMod3-near-splice","type":"exact"},{"name":"Seattleseq:coding-unknown-near-splice","type":"exact"},{"name":"incomplete transcript coding splice variant","type":"exact"}],"termid":"SO:0002082"}


id: GO:0002321
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a natural killer cell progenitor.","definition_xrefs":["GOC:add","PMID:16551251","PMID:16551264"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoid progenitor cell differentiation","termid":"GO:0002320"}],"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":"natural killer cell progenitor differentiation","termid":"GO:0002321"}


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


id: GO:1900245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of MDA-5 signaling pathway.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune effector process","termid":"GO:0002699"},{"relation_name":"is_a","term_name":"regulation of MDA-5 signaling pathway","termid":"GO:0039533"},{"relation_name":"is_a","term_name":"positive regulation of pattern recognition receptor signaling pathway","termid":"GO:0062208"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"MDA-5 signaling pathway","termid":"GO:0039530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of MDA-5 signaling pathway","synonyms":[{"name":"activation of IFIH1 signaling pathway","type":"narrow"},{"name":"activation of MDA-5 signaling pathway","type":"narrow"},{"name":"activation of MDA5 signaling pathway","type":"narrow"},{"name":"activation of melanoma differentiation-associated gene 5 signaling pathway","type":"narrow"},{"name":"positive regulation of IFIH1 signaling pathway","type":"exact"},{"name":"positive regulation of MDA-5 signalling pathway","type":"exact"},{"name":"positive regulation of MDA5 signaling pathway","type":"narrow"},{"name":"positive regulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"},{"name":"up regulation of IFIH1 signaling pathway","type":"exact"},{"name":"up regulation of MDA-5 signaling pathway","type":"exact"},{"name":"up regulation of MDA5 signaling pathway","type":"narrow"},{"name":"up regulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"},{"name":"up-regulation of IFIH1 signaling pathway","type":"exact"},{"name":"up-regulation of MDA-5 signaling pathway","type":"exact"},{"name":"up-regulation of MDA5 signaling pathway","type":"narrow"},{"name":"up-regulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"},{"name":"upregulation of IFIH1 signaling pathway","type":"exact"},{"name":"upregulation of MDA-5 signaling pathway","type":"exact"},{"name":"upregulation of MDA5 signaling pathway","type":"narrow"},{"name":"upregulation of melanoma differentiation-associated gene 5 signaling pathway","type":"exact"}],"termid":"GO:1900245"}


id: PBO:0060342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin VIIB","termid":"PBO:0060342"}


id: PBO:0088397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannan endo-1,6-alpha-mannosidase, Dfg502-like","termid":"PBO:0088397"}


id: PBO:0116800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DCAF12 antisense RNA 1","termid":"PBO:0116800"}


id: PBO:0058144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4440","termid":"PBO:0058144"}


id: SO:0000204
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region at the 5' end of a mature transcript (preceding the initiation codon) that is not translated into a protein.","direct_ancestors":[{"relation_name":"is_a","term_name":"UTR","termid":"SO:0000203"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_UTR","secondary_identifiers":["http://en.wikipedia.org/wiki/5'_UTR"],"synonyms":[{"name":"5' UTR","type":"exact"},{"name":"INSDC_feature:5'UTR","type":"exact"},{"name":"five prime UTR","type":"exact"},{"name":"five_prime_untranslated_region","type":"exact"}],"termid":"SO:0000204"}


id: GO:1901319
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of trehalose catabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"is_a","term_name":"positive regulation of carbohydrate metabolic process","termid":"GO:0045913"},{"relation_name":"is_a","term_name":"regulation of trehalose metabolic process","termid":"GO:0090062"},{"relation_name":"positively_regulates","term_name":"trehalose catabolic process","termid":"GO:0005993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"positive regulation of trehalose catabolic process","synonyms":[{"name":"activation of mycose catabolic process","type":"exact"},{"name":"activation of mycose catabolism","type":"exact"},{"name":"activation of mykose catabolic process","type":"exact"},{"name":"activation of mykose catabolism","type":"exact"},{"name":"activation of trehalose breakdown","type":"exact"},{"name":"activation of trehalose catabolic process","type":"narrow"},{"name":"activation of trehalose catabolism","type":"exact"},{"name":"activation of trehalose degradation","type":"exact"},{"name":"positive regulation of mycose catabolic process","type":"exact"},{"name":"positive regulation of mycose catabolism","type":"exact"},{"name":"positive regulation of mykose catabolic process","type":"exact"},{"name":"positive regulation of mykose catabolism","type":"exact"},{"name":"positive regulation of trehalose breakdown","type":"exact"},{"name":"positive regulation of trehalose catabolism","type":"exact"},{"name":"positive regulation of trehalose degradation","type":"exact"},{"name":"up regulation of mycose catabolic process","type":"exact"},{"name":"up regulation of mycose catabolism","type":"exact"},{"name":"up regulation of mykose catabolic process","type":"exact"},{"name":"up regulation of mykose catabolism","type":"exact"},{"name":"up regulation of trehalose breakdown","type":"exact"},{"name":"up regulation of trehalose catabolic process","type":"exact"},{"name":"up regulation of trehalose catabolism","type":"exact"},{"name":"up regulation of trehalose degradation","type":"exact"},{"name":"up-regulation of mycose catabolic process","type":"exact"},{"name":"up-regulation of mycose catabolism","type":"exact"},{"name":"up-regulation of mykose catabolic process","type":"exact"},{"name":"up-regulation of mykose catabolism","type":"exact"},{"name":"up-regulation of trehalose breakdown","type":"exact"},{"name":"up-regulation of trehalose catabolic process","type":"exact"},{"name":"up-regulation of trehalose catabolism","type":"exact"},{"name":"up-regulation of trehalose degradation","type":"exact"},{"name":"upregulation of mycose catabolic process","type":"exact"},{"name":"upregulation of mycose catabolism","type":"exact"},{"name":"upregulation of mykose catabolic process","type":"exact"},{"name":"upregulation of mykose catabolism","type":"exact"},{"name":"upregulation of trehalose breakdown","type":"exact"},{"name":"upregulation of trehalose catabolic process","type":"exact"},{"name":"upregulation of trehalose catabolism","type":"exact"},{"name":"upregulation of trehalose degradation","type":"exact"}],"termid":"GO:1901319"}


id: MOD:00881
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because Unimod entry 465 megerd with 199. Remap to MOD:00552 DiMethyl-CH2D.","definition_xrefs":["Unimod:465","PubMed:9252331"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:00881 N-reductive amination-D (obsolete MOD:00881)","termid":"MOD:00881"}


id: FYPO:0002321
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 ergosterol measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular sterol level","termid":"FYPO:0002326"}],"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 cellular ergosterol level","synonyms":[{"name":"decreased cellular ergosterol level during mitotic cell cycle","type":"related"},{"name":"decreased cellular ergosterol level during vegetative growth","type":"exact"},{"name":"decreased ergosterol accumulation","type":"related"},{"name":"reduced cellular ergosterol level","type":"exact"}],"termid":"FYPO:0002321"}


id: GO:0032453
data:
  {"annotated_genes":["SJAG_03635","SJAG_03286"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76719,71878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034647"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of a methyl group from a modified lysine residue at position 4 of the histone H3 protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 demethylase activity","termid":"GO:0141052"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03286":null,"SJAG_03635":null},"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:0140096"},{"rel_name":"is_a","termid":"GO:0032452"}],"interesting_parent_ids":["GO:0032452","GO:0003674","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"histone H3K4 demethylase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-9822461","Reactome:R-HSA-9822467"],"synonyms":[{"name":"histone H3-K4 demethylase activity","type":"exact"},{"name":"histone H3-methyl-lysine-4 demethylase activity","type":"exact"},{"name":"histone demethylase activity (H3-K4 specific)","type":"exact"},{"name":"histone demethylase activity (H3K4-specific)","type":"exact"}],"termid":"GO:0032453","terms_by_termid":{"GO:0034647":null}}


id: FYPO:0004002
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 duration of protein phosphorylation is longer than normal during a cellular response to hydroxyurea. All phosphorylation may be affected, or only phosphorylation of specific proteins, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of protein modification during vegetative growth","termid":"FYPO:0000548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased duration of protein phosphorylation during cellular response to hydroxyurea","synonyms":[{"name":"increased duration of protein phosphorylation during cellular response to HU","type":"exact"},{"name":"increased duration of protein phosphorylation during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"increased duration of protein phosphorylation during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"prolonged protein phosphorylation during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0004002"}


id: MONDO:0014838
data:
  {"annotated_genes":["SJAG_03576"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87453],"is_not":false,"summary":null,"term":"MONDO:0014838"}]},"cv_name":"mondo","definition":"Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the SMARCE1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Coffin-Siris syndrome","termid":"MONDO:0015452"},{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03576":null},"genotype_count":0,"is_obsolete":false,"name":"Coffin-Siris syndrome 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112368","OMIM:616938","GARD:16170","UMLS:C4310788","MEDGEN:934755"],"synonyms":[{"name":"COFFIN-SIRIS syndrome 5","type":"related"},{"name":"CSS5","type":"related"},{"name":"Coffin-Siris syndrome 5","type":"exact"},{"name":"Coffin-Siris syndrome caused by mutation in SMARCE1","type":"exact"},{"name":"Coffin-Siris syndrome type 5","type":"exact"},{"name":"SMARCE1 Coffin-Siris syndrome","type":"exact"}],"termid":"MONDO:0014838","terms_by_termid":{"MONDO:0014838":null},"xrefs":{"Monarch":{"xref_id":"0014838"}}}


id: FYPO:0003876
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the cytokinesis after mitosis checkpoint of a mitotic cell cycle is normal (i.e. indistinguishable from wild type). The cytokinesis after mitosis checkpoint normally delays the G2/M transition of a mitotic cell cycle if cytokinesis was not completed correctly in the previous cell cycle.","definition_xrefs":["GO:0044878","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic cell cycle checkpoint","termid":"FYPO:0001703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"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:0001320","FYPO:0000257","FYPO:0000002","FYPO:0000298","FYPO:0000631","FYPO:0001312"],"is_obsolete":false,"name":"normal cytokinesis checkpoint","synonyms":[{"name":"normal cytokinesis after mitosis checkpoint","type":"exact"},{"name":"normal cytokinesis checkpoint activation","type":"related"},{"name":"normal mitotic cell cycle cytokinesis checkpoint","type":"exact"},{"name":"normally activated cytokinesis checkpoint","type":"related"}],"termid":"FYPO:0003876"}


id: GO:0051803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents, or reduces the frequency, rate or extent of cytolysis by that organism of cells in a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cytolysis in other organism involved in symbiotic interaction (obsolete GO:0051803)","synonyms":[{"name":"down regulation of cytolysis of cells in other organism during symbiotic interaction","type":"related"},{"name":"down-regulation of cytolysis of cells in other organism during symbiotic interaction","type":"related"},{"name":"downregulation of cytolysis of cells in other organism during symbiotic interaction","type":"related"},{"name":"inhibition of cytolysis of cells in other organism during symbiotic interaction","type":"narrow"},{"name":"negative regulation of cytolysis of cells in other organism during symbiotic interaction","type":"related"},{"name":"negative regulation of cytolysis of cells in other organism involved in symbiotic interaction","type":"exact"}],"termid":"GO:0051803"}


id: GO:0021978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process that creates areas within the forebrain that will direct the behavior of cell migration in differentiation as the telencephalon develops.","definition_xrefs":["GOC:mgi_curators","GOC:dgh","GOC:cls","GOC:dph","GO_REF:0000021","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"part_of","term_name":"telencephalon development","termid":"GO:0021537"},{"relation_name":"part_of","term_name":"forebrain regionalization","termid":"GO:0021871"}],"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":"telencephalon regionalization","termid":"GO:0021978"}


id: GO:0016199
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The recognition of molecules at the central nervous system midline choice point by an axon growth cone; this choice point determines whether the growth cone will cross the midline.","definition_xrefs":["PMID:11376484"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon choice point recognition","termid":"GO:0016198"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"axon midline choice point recognition","termid":"GO:0016199"}


id: PBO:0066722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 19","termid":"PBO:0066722"}


id: PBO:0050961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon lambda 3 pseudogene 1","termid":"PBO:0050961"}


id: PBO:0047162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 187 member B","termid":"PBO:0047162"}


id: FYPO:0006934
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of one or more triglycerides 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 level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal cellular triglyceride level","synonyms":[{"name":"normal cellular TAG level","type":"exact"},{"name":"normal cellular triacylglycerol level","type":"exact"},{"name":"normal cellular triglyceride accumulation","type":"related"},{"name":"normal cellular triglyceride level during mitotic cell cycle","type":"related"},{"name":"normal cellular triglyceride level during vegetative growth","type":"exact"}],"termid":"FYPO:0006934"}


id: MONDO:0002216
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sarcoma arising from the brain.","definition_xrefs":["NCIT:C5154"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain cancer","termid":"MONDO:0001657"},{"relation_name":"is_a","term_name":"central nervous system sarcoma","termid":"MONDO:0002217"}],"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 sarcoma","secondary_identifiers":["DOID:2132","MEDGEN:272381","UMLS:C1332607"],"synonyms":[{"name":"brain sarcoma","type":"exact"},{"name":"primary brain sarcoma","type":"exact"},{"name":"sarcoma of brain","type":"exact"},{"name":"sarcoma of the brain","type":"exact"}],"termid":"MONDO:0002216","xrefs":{"Monarch":{"xref_id":"0002216"}}}


id: PBO:0111851
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"helix-hairpin-helix","termid":"PBO:0111851"}


id: GO:0120065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within gastric smooth muscle tissue, resulting in a change in muscle geometry. This process occurs in the widest part of the pylorus that is continuous with the body of the stomach.","definition_xrefs":["PMID:15890336","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stomach pylorus smooth muscle contraction","termid":"GO:0120064"}],"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":"pyloric antrum smooth muscle contraction","synonyms":[{"name":"antrum smooth muscle contraction","type":"exact"}],"termid":"GO:0120065"}


id: GO:0097242
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which amyloid-beta is removed from extracellular brain regions by mechanisms involving cell surface receptors.","definition_xrefs":["GOC:BHF","PMID:26005850","GOC:bc","PMID:18289866","PMID:19098903","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"}],"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":"amyloid-beta clearance","synonyms":[{"name":"beta-amyloid clearance","type":"exact"}],"termid":"GO:0097242"}


id: SOFP:encoded_symbol
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","definition":"dicistronic CDS/proteins are attached to a single gene feature representing the whole cassette - in which case the symbol refers to the cassette. encoded_symbol refers to a gene in the sense of non-overlapping CDS set. cf Adh and Adhr in dmel","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encoded_symbol","termid":"SOFP:encoded_symbol"}


id: GO:1902077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of lateral motor column neuron migration.","definition_xrefs":["PMID:20711475","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lateral motor column neuron migration","termid":"GO:1902076"},{"relation_name":"is_a","term_name":"negative regulation of motor neuron migration","termid":"GO:1905484"},{"relation_name":"negatively_regulates","term_name":"lateral motor column neuron migration","termid":"GO:0097477"}],"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 lateral motor column neuron migration","synonyms":[{"name":"down regulation of lateral motor column neuron migration","type":"exact"},{"name":"down-regulation of lateral motor column neuron migration","type":"exact"},{"name":"downregulation of lateral motor column neuron migration","type":"exact"},{"name":"inhibition of lateral motor column neuron migration","type":"narrow"}],"termid":"GO:1902077"}


id: MONDO:0009898
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":"polysaccharide, storage of unusual","secondary_identifiers":["MEDGEN:376645","UMLS:C1849721","MESH:C564877","OMIM:263600"],"synonyms":[{"name":"polysaccharide, storage of unusual","type":"exact"}],"termid":"MONDO:0009898","xrefs":{"Monarch":{"xref_id":"0009898"}}}


id: GO:1902012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly(ribitol phosphate) teichoic acid.","definition_xrefs":["UniPathway:UPA00790","PMID:11882717","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teichoic acid biosynthetic process","termid":"GO:0019350"},{"relation_name":"is_a","term_name":"poly(ribitol phosphate) teichoic acid metabolic process","termid":"GO:1902011"}],"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":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044085","GO:0044281","GO:0008150","GO:0071554"],"is_obsolete":false,"name":"poly(ribitol phosphate) teichoic acid biosynthetic process","synonyms":[{"name":"poly(ribitol phosphate) teichoic acid anabolism","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid biosynthesis","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid formation","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid synthesis","type":"exact"}],"termid":"GO:1902012"}


id: PBO:0062463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 154 pseudogene","termid":"PBO:0062463"}


id: PBO:0081992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and SCAN domain containing 22","termid":"PBO:0081992"}


id: FYPO:0000381
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of macroautophagy is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal macroautophagy","termid":"FYPO:0000163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased macroautophagy","synonyms":[{"name":"autophagy: decreased","type":"broad"},{"name":"decreased autophagy","type":"broad"},{"name":"reduced macroautophagy","type":"exact"}],"termid":"FYPO:0000381"}


id: GO:0001958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Replacement ossification wherein bone tissue replaces cartilage.","definition_xrefs":["GO_REF:0000034","ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"replacement ossification","termid":"GO:0036075"},{"relation_name":"part_of","term_name":"endochondral bone morphogenesis","termid":"GO:0060350"}],"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":"endochondral ossification","secondary_identifiers":["Wikipedia:Endochondral_ossification"],"termid":"GO:0001958"}


id: PR:P87110
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- itr2 gene.","definition_xrefs":["UniProtKB:P87110","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":"myo-inositol transporter 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20G8.03","synonyms":[{"name":"Spom972h-itr2","type":"exact"}],"termid":"PR:P87110"}


id: PBO:0064120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polycystin 2, transient receptor potential cation channel","termid":"PBO:0064120"}


id: GO:0008678
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-deoxy-D-gluconate + NAD+ = 3-dehydro-2-deoxy-D-gluconate + NADH + H+.","definition_xrefs":["EC:1.1.1.125"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"2-deoxy-D-gluconate 3-dehydrogenase activity","secondary_identifiers":["RHEA:12160","MetaCyc:KDUD-RXN"],"synonyms":[{"name":"2-deoxy-D-gluconate:NAD+ 3-oxidoreductase activity","type":"related"},{"name":"2-deoxygluconate dehydrogenase activity","type":"related"},{"name":"2-keto-3-deoxygluconate oxidoreductase activity","type":"related"}],"termid":"GO:0008678"}


id: GO:0050606
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-carboxy-2-hydroxymuconate semialdehyde hemiacetal + NADP+ = 2-oxo-2H-pyran-4,6-dicarboxylate + H+ + NADPH.","definition_xrefs":["RHEA:29587"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"4-carboxy-2-hydroxymuconate semialdehyde hemiacetal dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R04279","EC:1.1.1.312","MetaCyc:1.2.1.45-RXN"],"synonyms":[{"name":"2-hydroxy-4-carboxymuconate 6-semialdehyde dehydrogenase activity","type":"related"},{"name":"4-carboxy-2-hydroxy-cis,cis-muconate-6-semialdehyde:NADP(+) oxidoreductase activity","type":"related"},{"name":"4-carboxy-2-hydroxymuconate-6-semialdehyde dehydrogenase activity","type":"related"},{"name":"alpha-hydroxy-gamma-carboxymuconic epsilon-semialdehyde dehydrogenase activity","type":"related"}],"termid":"GO:0050606"}


id: GO:0047985
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2 + NAD+ = H+ + NADH.","definition_xrefs":["MetaCyc:HYDROGEN-DEHYDROGENASE-RXN","EC:1.12.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on hydrogen as donor, NAD or NADP as acceptor","termid":"GO:0016696"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"hydrogen dehydrogenase activity","secondary_identifiers":["RHEA:24636"],"synonyms":[{"name":"H(2):NAD(+) oxidoreductase activity","type":"related"},{"name":"H2:NAD+ oxidoreductase activity","type":"related"},{"name":"NAD-linked hydrogenase activity","type":"related"},{"name":"bidirectional hydrogenase activity","type":"broad"},{"name":"hydrogen:NAD+ oxidoreductase activity","type":"related"},{"name":"hydrogenase activity","type":"broad"}],"termid":"GO:0047985"}


id: MONDO:0044138
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammatory intraocular reaction with clouding and cells in vitreous; often accompanies inflammation of ciliary body, iris, choroid, or retina.","definition_xrefs":["NCIT:C50587"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate uveitis","termid":"MONDO:0006806"},{"relation_name":"is_a","term_name":"vitreous body disorder","termid":"MONDO:0044137"}],"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":"hyalitis","secondary_identifiers":["SCTID:95802009","MEDGEN:68620","UMLS:C0235812"],"synonyms":[{"name":"Vitreitis","type":"exact"},{"name":"Vitritis","type":"exact"},{"name":"hyalitis","type":"exact"},{"name":"hyaloiditis","type":"exact"},{"name":"vitritis","type":"exact"}],"termid":"MONDO:0044138","xrefs":{"Monarch":{"xref_id":"0044138"}}}


id: PBO:0072892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suprabasin","termid":"PBO:0072892"}


id: PR:O42652
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An aspartate aminotransferase, cytoplasmic that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11879: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":"aspartate aminotransferase, cytoplasmic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC10F6.13c","secondary_identifiers":["UniProtKB:O42652"],"synonyms":[{"name":"SPAC10F6.13c","type":"related"},{"name":"Spom972h-GOT1","type":"exact"},{"name":"transaminase A (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42652"}


id: PBO:0040144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anti-silencing function 1A histone chaperone","termid":"PBO:0040144"}


id: PBO:0068964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 208, pseudogene","termid":"PBO:0068964"}


id: PBO:0038426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"A2ML1 antisense RNA 2","termid":"PBO:0038426"}


id: PBO:0080199
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VENT homeobox pseudogene 7","termid":"PBO:0080199"}


id: PBO:0027209
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_telomeric_heterochromatin_during_horsetail_movement","termid":"PBO:0027209"}


id: PBO:0029662
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_endodeoxyribonuclease_activity","termid":"PBO:0029662"}


id: GO:0030105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Extreme immunological sensitivity of the body or tissues to the reintroduction of an antigen. It is a form of anamnestic reaction and is accompanied by pathological changes in tissues or organs due to the release of pharmacologically active substances.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete anaphylaxis (obsolete GO:0030105)","synonyms":[{"name":"anaphylaxis","type":"exact"}],"termid":"GO:0030105"}


id: PBO:0063378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosducin","termid":"PBO:0063378"}


id: MONDO:0004825
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete encephalitis (obsolete MONDO:0004825)","termid":"MONDO:0004825","xrefs":{"Monarch":{"xref_id":"0004825"}}}


id: PBO:0053449
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 397","termid":"PBO:0053449"}


id: PR:Q10173
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A kinetochore protein Nuf2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR21650:SF2","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":"kinetochore protein nuf2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27F1.04c","secondary_identifiers":["UniProtKB:Q10173"],"synonyms":[{"name":"NMS complex subunit nuf2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC27F1.04c","type":"related"},{"name":"Spom972h-NUF2","type":"exact"}],"termid":"PR:Q10173"}


id: PBO:0049270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GSG1 like","termid":"PBO:0049270"}


id: PBO:0027429
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_rate_of_DNA_strand_elongation_involved_in_mitotic_DNA_replication_at_highly_transcribed_RNA_polymerase_II_genes","termid":"PBO:0027429"}


id: PBO:0000311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerate kinase (predicted)","termid":"PBO:0000311"}


id: PBO:0047863
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(2)(p24.2)","termid":"PBO:0047863"}


id: GO:0052084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a symbiont modulates the frequency, rate or extent of the ethylene-mediated defense response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host defense response","termid":"GO:0052031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated modulation of host ethylene-mediated defense response","secondary_identifiers":["GO:0052441","GO:0052077","GO:0052279"],"synonyms":[{"name":"modulation by organism of defense-related ethylene-mediated signal transduction pathway in other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by organism of ethylene-mediated defense response of other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of defense-related host ethylene-mediated signal transduction pathway","type":"broad"},{"name":"modulation by symbiont of host ethylene-mediated defense response","type":"exact"}],"termid":"GO:0052084"}


id: GO:0004651
data:
  {"annotated_genes":["SJAG_04488"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70222],"is_not":false,"summary":null,"term":"GO:0004651"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 5'-phosphopolynucleotide + H2O = a polynucleotide + phosphate.","definition_xrefs":["EC:3.1.3.33"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04488":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"polynucleotide 5'-phosphatase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["Reactome:R-HSA-77078","MetaCyc:RXN-21861"],"synonyms":[{"name":"5'-polynucleotidase activity","type":"related"},{"name":"polynucleotide 5'-phosphohydrolase activity","type":"related"},{"name":"polynucleotide 5'-triphosphatase activity","type":"related"}],"termid":"GO:0004651","terms_by_termid":{"GO:0004651":null}}


id: FYPO:0003857
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 mevastatin. Cells stop growing (and may die) at a concentration of mevastatin 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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002683","FYPO:0005447","FYPO:0001985","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to mevastatin","synonyms":[{"name":"hypersensitive to mevastatin","type":"exact"},{"name":"sensitive to compactin","type":"exact"},{"name":"sensitive to mevastatin during mitotic cell cycle","type":"related"},{"name":"sensitive to mevastatin during vegetative growth","type":"exact"}],"termid":"FYPO:0003857"}


id: PBO:0091787
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Premature Initiation of Mitosis","termid":"PBO:0091787"}


id: PBO:0030914
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_response_to_chemical_stimulus_during_vegetative_growth","termid":"PBO:0030914"}


id: FYPO:0002756
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of cysteine synthase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal cysteine synthase activity","termid":"FYPO:0002754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0005447","FYPO:0000654","FYPO:0000707","FYPO:0000002","FYPO:0001985","FYPO:0000661"],"is_obsolete":false,"name":"increased cysteine synthase activity","termid":"FYPO:0002756"}


id: FYPO:0003630
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 U2-type prespliceosome assembly is abolished. The U2-type prespliceosome is formed by association of the 5' splice site with the U1 snRNP, while the branch point sequence is recognized by the U2 snRNP, and also contains other proteins.","definition_xrefs":["GO:1903241","PomBase:mah","GO:0071004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mRNA splicing, via spliceosome","termid":"FYPO:0000189"},{"relation_name":"is_a","term_name":"abnormal ribonucleoprotein complex assembly","termid":"FYPO:0003628"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0005447","FYPO:0006551","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished U2-type prespliceosome assembly","synonyms":[{"name":"U2-type prespliceosome assembly abolished","type":"exact"},{"name":"abolished U2-type prespliceosome assembly during mitotic cell cycle","type":"related"},{"name":"abolished U2-type prespliceosome assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0003630"}


id: PBO:0076101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntaxin 6","termid":"PBO:0076101"}


id: SO:0001283
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"2'-O-methylcytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"two_prime_O_methylcytidine","secondary_identifiers":["RNAMOD:022"],"synonyms":[{"name":"2'-O-methylcytidine","type":"exact"},{"name":"Cm","type":"exact"},{"name":"two prime O methylcytidine","type":"exact"}],"termid":"SO:0001283"}


id: PBO:0091254
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 CHS3","termid":"PBO:0091254"}


id: PBO:0001198
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.8.1.4","termid":"PBO:0001198"}


id: GO:0008690
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: CTP + 3-deoxy-D-manno-octulosonate = diphosphate + CMP-3-deoxy-D-manno-octulosonate.","definition_xrefs":["EC:2.7.7.38"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytidylyltransferase activity","termid":"GO:0070567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016779"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016779"],"is_obsolete":false,"name":"3-deoxy-manno-octulosonate cytidylyltransferase activity","secondary_identifiers":["RHEA:23448","MetaCyc:CPM-KDOSYNTH-RXN"],"synonyms":[{"name":"2-keto-3-deoxyoctonate cytidylyltransferase activity","type":"related"},{"name":"3-deoxy-D-manno-octulosonate cytidylyltransferase activity","type":"related"},{"name":"CMP-2-keto-3-deoxyoctulosonic acid synthetase activity","type":"related"},{"name":"CMP-3-deoxy-D-manno-octulosonate diphosphorylase activity","type":"related"},{"name":"CMP-3-deoxy-D-manno-octulosonate pyrophosphorylase activity","type":"related"},{"name":"CMP-3-deoxy-D-manno-octulosonate synthetase activity","type":"related"},{"name":"CMP-KDO synthetase activity","type":"related"},{"name":"CTP:3-deoxy-D-manno-octulosonate cytidylyltransferase activity","type":"related"},{"name":"CTP:3-deoxy-manno-octulosonate cytidylyltransferase activity","type":"exact"},{"name":"CTP:CMP-3-deoxy-D-manno-octulosonate cytidylyltransferase activity","type":"related"},{"name":"cytidine monophospho-3-deoxy-D-manno-octulosonate pyrophosphorylase activity","type":"related"}],"termid":"GO:0008690"}


id: GO:0055108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of proteins from the Golgi to a transport vesicle. Continuously secreted proteins are sorted into transport vesicles that fuse with the plasma membrane, releasing their contents by exocytosis.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular transport","termid":"GO:0046907"},{"relation_name":"part_of","term_name":"Golgi vesicle transport","termid":"GO:0048193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179","GO:0016192"],"is_obsolete":false,"name":"Golgi to transport vesicle transport","termid":"GO:0055108"}


id: PBO:0086761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; regulates PIS1 expression; mutant displays spore wall assembly defect in ether sensitivity screen; YPL077C is not an essential gene; YPL077C has a paralog, YBR197C, that arose from the whole genome duplication","termid":"PBO:0086761"}


id: PBO:0070746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10 pseudogene 2","termid":"PBO:0070746"}


id: PBO:0074762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary ossification center associated regulator of chondrocyte maturation","termid":"PBO:0074762"}


id: GO:1900002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of anthocyanin catabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"positive regulation of anthocyanin metabolic process","termid":"GO:0031539"},{"relation_name":"is_a","term_name":"regulation of anthocyanin catabolic process","termid":"GO:1900000"},{"relation_name":"positively_regulates","term_name":"anthocyanin-containing compound catabolic process","termid":"GO:0046284"}],"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 anthocyanin catabolic process","synonyms":[{"name":"positive regulation of anthocyanin breakdown","type":"exact"},{"name":"positive regulation of anthocyanin catabolism","type":"exact"},{"name":"positive regulation of anthocyanin degradation","type":"exact"},{"name":"up regulation of anthocyanin breakdown","type":"exact"},{"name":"up regulation of anthocyanin catabolic process","type":"related"},{"name":"up regulation of anthocyanin catabolism","type":"exact"},{"name":"up regulation of anthocyanin degradation","type":"exact"}],"termid":"GO:1900002"}


id: MONDO:0011190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any nephronophthisis in which the cause of the disease is a mutation in the INVS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephronophthisis","termid":"MONDO:0019005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005240"],"is_obsolete":false,"name":"nephronophthisis 2","secondary_identifiers":["GARD:18182","MEDGEN:355574","UMLS:C1865872","Orphanet:93591","OMIM:602088","MESH:C566582","DOID:0111113"],"synonyms":[{"name":"INVS nephronophthisis (disease)","type":"exact"},{"name":"NPH2","type":"exact"},{"name":"NPHP2","type":"exact"},{"name":"Nph2","type":"related"},{"name":"infantile nephronophthisis 2","type":"exact"},{"name":"nephronophthisis (disease) caused by mutation in INVS","type":"exact"},{"name":"nephronophthisis 2","type":"exact"},{"name":"nephronophthisis 2, infantile","type":"exact"},{"name":"nephronophthisis type 2","type":"exact"}],"termid":"MONDO:0011190","xrefs":{"Monarch":{"xref_id":"0011190"}}}


id: PBO:0073422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"seizure related 6 homolog like 2","termid":"PBO:0073422"}


id: MOD:00673
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to a methylated asparagine, such as N4-methyl-L-asparagine, or N4,N4-dimethyl-L-asparagine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-asparagine residue","termid":"MOD:00903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated asparagine","synonyms":[{"name":"MeAsn","type":"exact"}],"termid":"MOD:00673"}


id: GO:0075015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a symbiont structure that serves to infect its host organism. It includes physiological, developmental, and morphological changes of the symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"symbiont entry into host","termid":"GO:0044409"}],"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":"formation of infection structure","synonyms":[{"name":"formation by symbiont of infection structure on or near host","type":"related"},{"name":"formation of host infection structure","type":"exact"},{"name":"formation of host penetration structure","type":"related"},{"name":"formation of infection structure on or near host","type":"related"}],"termid":"GO:0075015"}


id: FYPO:0002565
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone methylation does not occur. All histone methylation may be affected, or methylation of specific sites on specific histones may be abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone methylation during vegetative growth","termid":"FYPO:0000457"},{"relation_name":"is_a","term_name":"abolished protein modification during vegetative growth","termid":"FYPO:0000544"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0001320","FYPO:0002274","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished histone methylation during vegetative growth","synonyms":[{"name":"abolished histone methylation during mitotic cell cycle","type":"related"},{"name":"histone methylation abolished during vegetative growth","type":"exact"},{"name":"histone methylation absent during vegetative growth","type":"exact"}],"termid":"FYPO:0002565"}


id: MONDO:0030318
data:
  {"annotated_genes":["SJAG_04533","SJAG_03393"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88165,88166],"is_not":false,"summary":null,"term":"MONDO:0030318"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03393":null,"SJAG_04533":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive 30","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070411","OMIM:619405","MEDGEN:1778853","UMLS:C5543620"],"synonyms":[{"name":"SCAR30","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 30","type":"exact"}],"termid":"MONDO:0030318","terms_by_termid":{"MONDO:0030318":null},"xrefs":{"Monarch":{"xref_id":"0030318"}}}


id: MONDO:0015241
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Arthrogryposis-like syndrome, also known as Kuskokwim disease, is a very rare congenital contracture disorder, reported exclusively in Yup'ik Eskimos of the Kuskokwim River delta region of Alaska, characterized by multiple contractures of large joints (predominantly the knees and ankles) that present at birth or during childhood but are lifelong; deformities of the spine, pelvis and feet; and sometimes proximally or distally displaced patellae and muscle atrophy in the limbs with contractures. Additional radiological features include mild vertebral wedging, elongation of the vertebral pedicle, and clubbing of the distal clavicle. An autosomal recessive pattern of inheritance has been suggested.","definition_xrefs":["Orphanet:1149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arthrogryposis-like syndrome","secondary_identifiers":["GARD:3150","ICD9:719.89","MEDGEN:349229","OMIM:208200","SCTID:702447002","UMLS:C1859709"],"synonyms":[{"name":"Kuskokwim disease","type":"exact"},{"name":"Kuskokwim syndrome","type":"related"},{"name":"arthrogryposis like disorder","type":"related"}],"termid":"MONDO:0015241","xrefs":{"Monarch":{"xref_id":"0015241"}}}


id: PBO:0066876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 176","termid":"PBO:0066876"}


id: PBO:0062505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily G member 7 pseudogene","termid":"PBO:0062505"}


id: PBO:0058479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5586","termid":"PBO:0058479"}


id: GO:1990873
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the plasma membrane surrounding the cell tip consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the plasma membrane surrounding the cell tip or some other covalently attached group such as a GPI anchor that is similarly embedded in the plasma membrane surrounding the cell tip.","definition_xrefs":["PMID:20624220"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of plasma membrane of cell tip (obsolete GO:1990873)","termid":"GO:1990873"}


id: PATO:0000254
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000254 vibrissae reflex (obsolete PATO:0000254)","termid":"PATO:0000254"}


id: GO:0015406
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 ABC-type uptake permease activity (obsolete GO:0015406)","synonyms":[{"name":"ABC-type uptake permease activity","type":"exact"}],"termid":"GO:0015406"}


id: PBO:0071119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 121","termid":"PBO:0071119"}


id: PBO:0047547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast growth factor 7 pseudogene 6","termid":"PBO:0047547"}


id: PBO:0004719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exoribonuclease Rex4 (predicted)","termid":"PBO:0004719"}


id: PBO:0062908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purinergic receptor P2X 1","termid":"PBO:0062908"}


id: GO:0101018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of firing from a late origin of replication involved in mitotic DNA replication.","definition_xrefs":["PMID:26436827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic DNA replication initiation from late origin","termid":"GO:0101017"},{"relation_name":"is_a","term_name":"negative regulation of mitotic DNA replication initiation","termid":"GO:1903467"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"negatively_regulates","termid":"GO:0006260"},{"rel_name":"regulates","termid":"GO:0006260"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006260","GO:0007049","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mitotic DNA replication initiation from late origin","synonyms":[{"name":"negative regulation of late replication origin firing","type":"exact"}],"termid":"GO:0101018"}


id: MONDO:0015924
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease).","definition_xrefs":["Orphanet:182090","PMID:30545973"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary hypertension","termid":"MONDO:0005149"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary arterial hypertension","secondary_identifiers":["GARD:7501","NANDO:1200425","NORD:1634","SCTID:11399002","NANDO:2200298","MedDRA:10064911","icd11.foundation:1931148955","EFO:0001361","MESH:D000081029","NANDO:2100103","MEDGEN:425404","UMLS:C2973725"],"synonyms":[{"name":"PAH","type":"exact"},{"name":"PAH with overt features of venous/capillaries involvement","type":"narrow"},{"name":"PPH","type":"related"},{"name":"PVOD/PCH","type":"narrow"},{"name":"idiopathic pulmonary hypertension","type":"related"},{"name":"pulmonary arterial hypertension","type":"exact"}],"termid":"MONDO:0015924","xrefs":{"Monarch":{"xref_id":"0015924"}}}


id: GO:0030781
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + 6-O-methylnorlaudanosoline = S-adenosyl-L-homocysteine + nororientaline.","definition_xrefs":["EC:2.1.1.121"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016741","GO:0003674"],"is_obsolete":false,"name":"6-O-methylnorlaudanosoline 5'-O-methyltransferase activity","secondary_identifiers":["RHEA:11892","MetaCyc:2.1.1.121-RXN"],"synonyms":[{"name":"S-adenosyl-L-methionine:6-O-methylnorlaudanosoline 5'-O-methyltransferase activity","type":"related"}],"termid":"GO:0030781"}


id: PBO:0054772
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 2184","termid":"PBO:0054772"}


id: PBO:0083672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endoplasmic reticulum zinc transporter; part of a heterodimeric transporter with Msc2p that transfers zinc from the cytosol to the ER lumen; member of the cation diffusion facilitator family of efflux pumps; zinc-regulated directly through Zap1p; transcription induced under conditions of zinc deficiency","termid":"PBO:0083672"}


id: PBO:0080951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger BED-type containing 5","termid":"PBO:0080951"}


id: PBO:0070667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 38","termid":"PBO:0070667"}


id: GO:0016041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 L-glutamate + 2 oxidized ferredoxin = L-glutamine + 2-oxoglutarate + 2 reduced ferredoxin + 2 H+. This is a two-step reaction: (a) L-glutamate + NH3 = L-glutamine + H2O, (b) L-glutamate + 2 oxidized ferredoxin + H2O = NH3 + 2-oxoglutarate + 2 reduced ferredoxin + 2 H+.","definition_xrefs":["EC:1.4.7.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamate synthase activity","termid":"GO:0015930"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors, iron-sulfur protein as acceptor","termid":"GO:0016643"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"glutamate synthase (ferredoxin) activity","secondary_identifiers":["MetaCyc:GLUTAMATE-SYNTHASE-FERREDOXIN-RXN","RHEA:12128"],"synonyms":[{"name":"L-glutamate:ferredoxin oxidoreductase (transaminating)","type":"related"},{"name":"ferredoxin-dependent glutamate synthase activity","type":"related"},{"name":"ferredoxin-glutamate synthase activity","type":"related"},{"name":"glutamate synthase (ferredoxin-dependent)","type":"related"}],"termid":"GO:0016041"}


id: PBO:0069773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1056, pseudogene","termid":"PBO:0069773"}


id: FYPO:0001902
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which cytoplasmic mRNA processing bodies (P-bodies) are smaller than normal when the cell is subject to glucose starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small P-bodies","termid":"FYPO:0001900"}],"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:0000002","FYPO:0001985"],"is_obsolete":false,"name":"small P-bodies during glucose starvation","synonyms":[{"name":"decreased P-body formation during glucose starvation","type":"related"},{"name":"small P bodies during glucose starvation","type":"exact"},{"name":"small P-bodies during glucose depletion","type":"exact"},{"name":"small P-bodies during glucose deprivation","type":"exact"},{"name":"small P-bodies during glucose limitation","type":"related"},{"name":"small P-body during glucose starvation","type":"exact"},{"name":"small cytoplasmic mRNA processing bodies during glucose starvation","type":"exact"}],"termid":"FYPO:0001902"}


id: GO:0005602
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of six subunits of C1q, each formed of the three homologous polypeptide chains C1QA, C1QB, and C1QB, and tetramer of two C1QR and two C1QS polypeptide chains.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular region","termid":"GO:0005576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005576","GO:0005575"],"is_obsolete":false,"name":"complement component C1 complex","synonyms":[{"name":"complement component C1q complex","type":"narrow"}],"termid":"GO:0005602"}


id: PBO:0077898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetrapeptide repeat homeobox like (pseudogene)","termid":"PBO:0077898"}


id: MONDO:0000697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete succinic semialdehyde dehydrogenase deficiency (obsolete MONDO:0000697)","termid":"MONDO:0000697","xrefs":{"Monarch":{"xref_id":"0000697"}}}


id: PBO:0069010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 254, pseudogene","termid":"PBO:0069010"}


id: GO:0006238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that generates CMP, cytidine monophosphate, from derivatives of it without de novo synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CMP biosynthetic process","termid":"GO:0009224"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide salvage","termid":"GO:0010138"}],"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:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"CMP salvage","synonyms":[{"name":"cytidine monophosphate salvage","type":"exact"}],"termid":"GO:0006238"}


id: PBO:0005405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi transport protein Got1 (predicted)","termid":"PBO:0005405"}


id: GO:1901815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of astaxanthin.","definition_xrefs":["GOC:TermGenie","GOC:yaf","PMID:16434154","MetaCyc:PWY-5288","UniPathway:UPA00387"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll biosynthetic process","termid":"GO:0016123"},{"relation_name":"is_a","term_name":"astaxanthin metabolic process","termid":"GO:1901813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"astaxanthin biosynthetic process","synonyms":[{"name":"astaxanthin anabolism","type":"exact"},{"name":"astaxanthin biosynthesis","type":"exact"},{"name":"astaxanthin formation","type":"exact"},{"name":"astaxanthin synthesis","type":"exact"}],"termid":"GO:1901815"}


id: PBO:0016537
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae YPR081C","termid":"PBO:0016537"}


id: GO:0002451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Tolerance induction of mature B cells in the peripheral lymphoid tissues: the blood, lymph nodes, spleen, and mucosal-associated lymphoid tissue.","definition_xrefs":["ISBN:0781735149","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral tolerance induction","termid":"GO:0002465"},{"relation_name":"is_a","term_name":"B cell tolerance induction","termid":"GO:0002514"},{"relation_name":"is_a","term_name":"B cell mediated immunity","termid":"GO:0019724"}],"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":"peripheral B cell tolerance induction","synonyms":[{"name":"peripheral B lymphocyte tolerance induction","type":"exact"},{"name":"peripheral B-cell tolerance induction","type":"exact"},{"name":"peripheral B-lymphocyte tolerance induction","type":"exact"}],"termid":"GO:0002451"}


id: PBO:0078622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 71","termid":"PBO:0078622"}


id: PBO:0028640
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_spore_population","termid":"PBO:0028640"}


id: GO:0010022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a meristem becomes determinate (i.e. ceases to produce lateral organs and may or may not terminally differentiate).","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"meristem maintenance","termid":"GO:0010073"}],"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":"meristem determinacy","termid":"GO:0010022"}


id: PBO:0078329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon CTC) 1-1","termid":"PBO:0078329"}


id: PBO:0040192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"argininosuccinate synthetase 1 pseudogene 5","termid":"PBO:0040192"}


id: PBO:0090356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate-CoA ligase beta subunit Lsc2","termid":"PBO:0090356"}


id: PATO:0000899
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000899 soma dependent fertility value (obsolete PATO:0000899)","termid":"PATO:0000899"}


id: PR:O94579
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proteasome subunit alpha type-2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04818","PANTHER:PTHR11599:SF16","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":"proteasome subunit alpha type-2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1442.06","secondary_identifiers":["UniProtKB:O94579"],"synonyms":[{"name":"Spom972h-PSMA2","type":"exact"}],"termid":"PR:O94579"}


id: MONDO:0014572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025"],"is_obsolete":false,"name":"Lichtenstein-Knorr syndrome","secondary_identifiers":["GARD:17780","MEDGEN:898996","UMLS:C4225383","Orphanet:448251","OMIM:616291","DOID:0080065"],"synonyms":[{"name":"LIKNS","type":"related"},{"name":"Lichtenstein-Knorr syndrome","type":"exact"},{"name":"SCAR19","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia 19","type":"related"},{"name":"autosomal recessive spinocerebellar ataxia type 19","type":"exact"},{"name":"progressive autosomal recessive ataxia-deafness syndrome","type":"related"},{"name":"progressive autosomal recessive ataxia-sensorineural hearing loss syndrome","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 19","type":"related"}],"termid":"MONDO:0014572","xrefs":{"Monarch":{"xref_id":"0014572"}}}


id: MONDO:0015294
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nephrogenic systemic fibrosis (NSF) is a rare systemic fibrosing condition observed in renally impaired patients and characterized by a hardening and thickening of the skin with fibrotic plaques or papules, pruritus, joint pain and stiffness, muscle weakness, limitation of range of motion, and yellowed eyes. It is generally associated with administration of gadolinium-based magnetic resonance imaging contrast agents (GBCA) in patients with kidney disease.","definition_xrefs":["Orphanet:137617"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"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":"nephrogenic systemic fibrosis","secondary_identifiers":["UMLS:C3888044","GARD:9725","MEDGEN:854737","MedDRA:10067467","NORD:1498","ICD9:588.89","MESH:D054989","icd11.foundation:1537082562","NCIT:C84920","SCTID:424114000"],"synonyms":[{"name":"NFD","type":"related"},{"name":"NSF","type":"related"},{"name":"nephrogenic fibrosing dermopathy","type":"exact"}],"termid":"MONDO:0015294","xrefs":{"Monarch":{"xref_id":"0015294"}}}


id: PBO:0014265
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"not functionally complemented by S. cerevisiae RAD24","termid":"PBO:0014265"}


id: PBO:0061438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor 2C2 associated protein","termid":"PBO:0061438"}


id: MONDO:0007186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic disorder characterized by reflux of the gastric and/or duodenal contents into the distal esophagus. It is usually caused by incompetence of the lower esophageal sphincter. Symptoms include heartburn and acid indigestion. It may cause injury to the esophageal mucosa.","definition_xrefs":["NCIT:C26781"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"stomach disorder","termid":"MONDO:0004298"}],"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":"gastroesophageal reflux disease","secondary_identifiers":["ICD9:530.81","EFO:0003948","SCTID:235595009","UMLS:C0017168","DOID:8534","MEDGEN:6553","MESH:D005764","OMIM:109350"],"synonyms":[{"name":"GERD","type":"exact"},{"name":"GERD - gastro-esophageal reflux disease","type":"exact"},{"name":"Gastresophageal reflux","type":"exact"},{"name":"acid reflux","type":"exact"},{"name":"gastro-esophageal reflux","type":"exact"},{"name":"gastroesophageal reflux","type":"exact"},{"name":"gastroesophageal reflux disease","type":"exact"},{"name":"gastroesophageal reflux, paediatric","type":"related"},{"name":"gastroesophageal reflux, pediatric","type":"related"},{"name":"ger","type":"related"}],"termid":"MONDO:0007186","xrefs":{"Monarch":{"xref_id":"0007186"}}}


id: PBO:0067116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 160, pseudogene","termid":"PBO:0067116"}


id: FYPO:0002901
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the kinetochore of a chromosome is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to centromere during vegetative growth","termid":"FYPO:0002574"},{"relation_name":"is_a","term_name":"normal protein localization to kinetochore","termid":"FYPO:0005042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal protein localization to kinetochore during vegetative growth","synonyms":[{"name":"normal protein localisation to kinetochore during vegetative growth","type":"exact"},{"name":"normal protein localization to kinetochore during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002901"}


id: PBO:0085861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the vacuole; YDL211C has a paralog, TDA7, that arose from the whole genome duplication","termid":"PBO:0085861"}


id: MONDO:1010514
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Triploidy that occurs in chicken.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"triploidy, non-human animal","termid":"MONDO:1010031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triploidy, chicken","secondary_identifiers":["OMIA:001180-9031"],"termid":"MONDO:1010514","xrefs":{"Monarch":{"xref_id":"1010514"}}}


id: GO:0000936
data:
  {"annotated_genes":["SJAG_05285","SJAG_01290","SJAG_01835","SJAG_00667"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[58678,65206,102084,117838],"is_not":false,"summary":null,"term":"GO:0000936"}]},"cv_name":"cellular_component","definition":"A cell septum that forms following nuclear division.","definition_xrefs":["GOC:clt","ISBN:0471940526"],"direct_ancestors":[{"relation_name":"is_a","term_name":"division septum","termid":"GO:0000935"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00667":null,"SJAG_01290":null,"SJAG_01835":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0000935"}],"interesting_parent_ids":["GO:0000935","GO:0005575"],"is_obsolete":false,"name":"primary cell septum","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"primary septum","type":"broad"}],"termid":"GO:0000936","terms_by_termid":{"GO:0000936":null}}


id: MONDO:0011160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GIPC3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 15","secondary_identifiers":["MEDGEN:355626","MESH:C566611","OMIM:601869","GARD:22591","DOID:0110470","UMLS:C1866094"],"synonyms":[{"name":"DFNB15","type":"narrow"},{"name":"DFNB72","type":"narrow"},{"name":"DFNB95","type":"narrow"},{"name":"GIPC3 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 15","type":"narrow"},{"name":"autosomal recessive deafness 72","type":"narrow"},{"name":"autosomal recessive deafness 95","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 15","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in GIPC3","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 15","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 15","type":"exact"},{"name":"deafness, autosomal recessive 15","type":"narrow"},{"name":"deafness, autosomal recessive 72","type":"narrow"},{"name":"deafness, autosomal recessive 95","type":"narrow"},{"name":"deafness, autosomal recessive type 15","type":"narrow"}],"termid":"MONDO:0011160","xrefs":{"Monarch":{"xref_id":"0011160"}}}


id: GO:0050332
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pyridine + thiamine = 5-(2-hydroxyethyl)-4-methylthiazole + heteropyrithiamine.","definition_xrefs":["RHEA:17697","EC:2.5.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016765","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"thiamine pyridinylase activity","secondary_identifiers":["MetaCyc:THIAMIN-PYRIDINYLASE-RXN","KEGG_REACTION:R02863"],"synonyms":[{"name":"pyrimidine transferase activity","type":"related"},{"name":"thiamin hydrolase activity","type":"related"},{"name":"thiamin pyridinolase activity","type":"related"},{"name":"thiamin pyridinylase activity","type":"exact"},{"name":"thiamin:base 2-methyl-4-aminopyrimidine-5-methenyltransferase activity","type":"related"},{"name":"thiaminase I activity","type":"narrow"},{"name":"thiamine hydrolase activity","type":"related"},{"name":"thiamine pyridinolase activity","type":"related"},{"name":"thiamine:base 2-methyl-4-aminopyrimidine-5-methenyltransferase activity","type":"related"}],"termid":"GO:0050332"}


id: FYPO:0001486
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 salt stress is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during cellular response to osmotic stress","termid":"FYPO:0003793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal RNA level during cellular response to salt stress","synonyms":[{"name":"normal RNA accumulation during cellular response to salt stress","type":"related"},{"name":"normal RNA level during cellular response to salt stress during mitotic cell cycle","type":"related"},{"name":"normal RNA level during cellular response to salt stress during vegetative growth","type":"exact"},{"name":"normal mRNA level during cellular response to salt stress","type":"narrow"},{"name":"normal transcript level during cellular response to salt stress","type":"exact"}],"termid":"FYPO:0001486"}


id: PBO:0048515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDP dissociation inhibitor 2 pseudogene 2","termid":"PBO:0048515"}


id: PBO:0045068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLG associated protein 1","termid":"PBO:0045068"}


id: MONDO:0044704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that involves the oropharynx.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pharyngeal squamous cell carcinoma","termid":"MONDO:0000536"},{"relation_name":"is_a","term_name":"oropharyngeal carcinoma","termid":"MONDO:0044926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"oropharynx squamous cell carcinoma","secondary_identifiers":["NCIT:C8181","ONCOTREE:OPHSC","MEDGEN:76094","Orphanet:500478","GARD:17928","icd11.foundation:839740136","UMLS:C0280313"],"synonyms":[{"name":"epidermoid carcinoma of oropharynx","type":"exact"},{"name":"epidermoid carcinoma of the oropharynx","type":"exact"},{"name":"oropharyngeal epidermoid carcinoma","type":"exact"},{"name":"oropharyngeal squamous cell carcinoma","type":"exact"},{"name":"oropharyngeal throat squamous cell cancer","type":"exact"},{"name":"squamous cell carcinoma of oropharynx","type":"exact"},{"name":"squamous cell carcinoma of the oropharynx","type":"related"}],"termid":"MONDO:0044704","xrefs":{"Monarch":{"xref_id":"0044704"}}}


id: GO:0004287
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of Pro-Xaa > Ala-Xaa in oligopeptides.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete prolyl oligopeptidase activity (obsolete GO:0004287)","synonyms":[{"name":"endoprolylpeptidase activity","type":"related"},{"name":"post-proline cleaving enzyme activity","type":"related"},{"name":"post-proline endopeptidase activity","type":"related"},{"name":"proline endopeptidase activity","type":"related"},{"name":"proline-specific endopeptidase activity","type":"related"},{"name":"prolyl endopeptidase activity","type":"related"},{"name":"prolyl oligopeptidase activity","type":"exact"}],"termid":"GO:0004287"}


id: MONDO:0004689
data:
  {"annotated_genes":["SJAG_02399","SJAG_04978","SJAG_02117","SJAG_03371"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011417"},{"annotations":[87427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859328"},{"annotations":[87285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010651"},{"annotations":[86829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011301"},{"annotations":[88998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010200"}]},"cv_name":"mondo","definition":"An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals.","definition_xrefs":["DOID:896"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02117":null,"SJAG_02399":null,"SJAG_03371":null,"SJAG_04978":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"inborn metal metabolism disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D008664","UMLS:C0025534","MEDGEN:6325"],"synonyms":[{"name":"metal metabolism disorder","type":"broad"},{"name":"metal metabolism, inborn error","type":"related"}],"termid":"MONDO:0004689","terms_by_termid":{"MONDO:0010200":null,"MONDO:0010651":null,"MONDO:0011301":null,"MONDO:0011417":null,"MONDO:0859328":null},"xrefs":{"Monarch":{"xref_id":"0004689"}}}


id: GO:0061089
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that decreases the rate, frequency, or extent of sequestering of zinc ion. Sequestering of zinc ion is the process of binding or confining zinc ions such that they are separated from other components of a biological system.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of sequestering of zinc ion (obsolete GO:0061089)","termid":"GO:0061089"}


id: MOD:01278
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other -","definition_xrefs":["Unimod:253#K","PubMed:11283024"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crotonaldehyde","termid":"MOD:00576"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crotonaldehyde - site K","synonyms":[{"name":"Crotonaldehyde","type":"related"}],"termid":"MOD:01278"}


id: PATO:0000052
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphological quality inhering in a bearer by virtue of the bearer's ratios of distances between its features (points, edges, surfaces and also holes etc).","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":"shape","secondary_identifiers":["PATO:0001647"],"synonyms":[{"name":"relational shape quality","type":"exact"}],"termid":"PATO:0000052"}


id: PBO:0091191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val","termid":"PBO:0091191"}


id: GO:0002277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a myeloid dendritic cell resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid dendritic cell activation","termid":"GO:0001773"},{"relation_name":"is_a","term_name":"myeloid cell activation involved in immune response","termid":"GO:0002275"}],"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":"myeloid dendritic cell activation involved in immune response","synonyms":[{"name":"myeloid dendritic cell activation during immune response","type":"related"}],"termid":"GO:0002277"}


id: PBO:0044514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CXXC motif containing zinc binding protein","termid":"PBO:0044514"}


id: PBO:0054716
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 2125","termid":"PBO:0054716"}


id: PBO:0028155
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_epirubicin","termid":"PBO:0028155"}


id: GO:0099632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which protein is transported from one region of the plasma membrane to another.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport within lipid bilayer","termid":"GO:0032594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0061024","GO:0051179"],"is_obsolete":false,"name":"protein transport within plasma membrane","termid":"GO:0099632"}


id: MONDO:0010360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"young-onset Parkinson disease","termid":"MONDO:0017279"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parkinson disease 12","secondary_identifiers":["GARD:18604","MEDGEN:337173","MESH:C564486","OMIM:300557","UMLS:C1845165"],"synonyms":[{"name":"PARK12","type":"exact"},{"name":"Parkinson disease 12","type":"related"},{"name":"Parkinson disease, X-linked","type":"related"}],"termid":"MONDO:0010360","xrefs":{"Monarch":{"xref_id":"0010360"}}}


id: PBO:0091672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiosis specific Smp foci lncRNA Sme2, short isoform","termid":"PBO:0091672"}


id: GO:2000187
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of phosphate transmembrane transport.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of inorganic anion transmembrane transport","termid":"GO:1903797"},{"relation_name":"is_a","term_name":"regulation of phosphate transmembrane transport","termid":"GO:2000185"},{"relation_name":"positively_regulates","term_name":"phosphate ion transmembrane transport","termid":"GO:0035435"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of phosphate transmembrane transport","synonyms":[{"name":"positive regulation of phosphate membrane transport","type":"exact"}],"termid":"GO:2000187"}


id: PBO:0047651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP prolyl isomerase 4 pseudogene 7","termid":"PBO:0047651"}


id: PATO:0001247
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of cyan hue and high brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyan","termid":"PATO:0000319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"light cyan","termid":"PATO:0001247"}


id: PBO:0027494
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_wortmannin","termid":"PBO:0027494"}


id: MONDO:0014255
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":"complement factor b deficiency","secondary_identifiers":["NANDO:2200797","MEDGEN:816280","OMIM:615561","UMLS:C3809950"],"synonyms":[{"name":"CFBD","type":"related"},{"name":"complement factor B deficiency","type":"related"},{"name":"complement factor b deficiency","type":"exact"}],"termid":"MONDO:0014255","xrefs":{"Monarch":{"xref_id":"0014255"}}}


id: GO:0031272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the assembly of pseudopodia.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of plasma membrane bounded cell projection assembly","termid":"GO:0120032"},{"relation_name":"regulates","term_name":"pseudopodium assembly","termid":"GO:0031269"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of pseudopodium assembly","synonyms":[{"name":"regulation of pseudopodium formation","type":"related"}],"termid":"GO:0031272"}


id: PBO:0113254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Part of actin cytoskeleton-regulatory complex Pan1p-Sla1p-End3p; associates with actin patches on cell cortex; promotes protein-protein interactions essential for endocytosis; regulates late stages of endocytosis; binds to and activates Arp2/3 complex in vitro; phosphorylation of Thr-1225 is regulated by MAPK Hog1p in response to osmotic stress","termid":"PBO:0113254"}


id: GO:0043051
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the contraction and relaxation movements of the pharyngeal muscle that mediates feeding in nematodes.","definition_xrefs":["PMID:2181052","GOC:cab1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of eating behavior","termid":"GO:1903998"},{"relation_name":"regulates","term_name":"nematode pharyngeal pumping","termid":"GO:0043050"}],"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 nematode pharyngeal pumping","termid":"GO:0043051"}


id: GO:0018881
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving bromoxynil, C7H3Br2NO, a dibrominated phenol derivative with a cyano (-CN) group attached. Bromoxynil is used as a herbicide for post-emergent control of annual broadleaf weeds and works by inhibiting photosynthesis in the target plants.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"nitrile metabolic process","termid":"GO:0050898"},{"relation_name":"is_a","term_name":"organohalogen metabolic process","termid":"GO:0090345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"bromoxynil metabolic process","secondary_identifiers":["UM-BBD_pathwayID:box"],"synonyms":[{"name":"bromoxynil metabolism","type":"exact"}],"termid":"GO:0018881"}


id: PBO:0075451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA3 antisense RNA 1 (head to head)","termid":"PBO:0075451"}


id: PBO:0051778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQ motif containing B1","termid":"PBO:0051778"}


id: GO:1902063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of betaine aldehyde.","definition_xrefs":["GOC:TermGenie","GOC:di","PMID:23563483"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"betaine aldehyde metabolic process","termid":"GO:1902061"}],"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":"betaine aldehyde biosynthetic process","synonyms":[{"name":"betaine aldehyde anabolism","type":"exact"},{"name":"betaine aldehyde biosynthesis","type":"exact"},{"name":"betaine aldehyde formation","type":"exact"},{"name":"betaine aldehyde synthesis","type":"exact"}],"termid":"GO:1902063"}


id: PBO:0088811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi transport protein Sft2","termid":"PBO:0088811"}


id: PBO:0005721
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.2.1.2","termid":"PBO:0005721"}


id: GO:0052830
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: inositol-1,3,4,6-tetrakisphosphate + H2O = inositol-1,3,4-trisphosphate + phosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol tetrakisphosphate phosphatase activity","termid":"GO:0052743"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016788"],"is_obsolete":false,"name":"inositol-1,3,4,6-tetrakisphosphate 6-phosphatase activity","secondary_identifiers":["Reactome:R-HSA-1855171"],"termid":"GO:0052830"}


id: RO:0000058
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between a generically dependent continuant and a specifically dependent continuant, in which the generically dependent continuant depends on some independent continuant in virtue of the fact that the specifically dependent continuant also depends on that same independent continuant. A generically dependent continuant may be concretized as multiple specifically dependent continuants.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_concretized_as","termid":"RO:0000058"}


id: PBO:0091915
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRE1-Like","termid":"PBO:0091915"}


id: PBO:0029261
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_transmembrane_transport_gene_mRNA_during_vegetative_growth","termid":"PBO:0029261"}


id: GO:0045494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process preventing the degeneration of the photoreceptor, a specialized cell type that is sensitive to light.","definition_xrefs":["GOC:rl","CL:0000210","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"retina homeostasis","termid":"GO:0001895"}],"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":"photoreceptor cell maintenance","termid":"GO:0045494"}


id: PBO:0044258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CXADR Ig-like cell adhesion molecule","termid":"PBO:0044258"}


id: GO:0120042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of macrophage proliferation.","definition_xrefs":["GOC:rph","GOC:BHF","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte proliferation","termid":"GO:0070664"},{"relation_name":"is_a","term_name":"regulation of macrophage proliferation","termid":"GO:0120040"},{"relation_name":"negatively_regulates","term_name":"macrophage proliferation","termid":"GO:0061517"}],"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 macrophage proliferation","termid":"GO:0120042"}


id: MONDO:1011694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombasthenia, non-human animal","secondary_identifiers":["OMIA:001000"],"termid":"MONDO:1011694","xrefs":{"Monarch":{"xref_id":"1011694"}}}


id: PBO:0052413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2","termid":"PBO:0052413"}


id: PBO:0070079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 36, pseudogene","termid":"PBO:0070079"}


id: internal:reserved_name
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reserved_name","termid":"internal:reserved_name"}


id: PBO:0064065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 99","termid":"PBO:0064065"}


id: GO:0075094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism activates, maintains or increases the frequency, rate or extent of the symbiont signal transduction mediated by G-protein beta subunit. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by host of symbiont signal transduction mediated by G-protein beta subunit (obsolete GO:0075094)","termid":"GO:0075094"}


id: PBO:0062143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily F member 13 pseudogene","termid":"PBO:0062143"}


id: GO:0036194
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A prolongation or process extending from a muscle cell. A muscle cell is a mature contractile cell, commonly known as a myocyte. This cell has as part of its cytoplasm myofibrils organized in various patterns.","definition_xrefs":["CL:0000187","PMID:15930100","PMID:22464329","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"}],"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":"muscle cell projection","synonyms":[{"name":"muscle arm","type":"narrow"},{"name":"myocyte projection","type":"exact"},{"name":"myopodia","type":"narrow"}],"termid":"GO:0036194"}


id: MONDO:0044282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. The Vel blood group system is defined by the presence of the Vel antigen on red blood cells. Vel is a high frequency antigen that shows variable strength, ranging from strong to weak. The rare Vel-negative blood type is inherited as an autosomal recessive trait and is typically unveiled when Vel-negative individuals develop anti-Vel antibodies after transfusion or pregnancy; Vel alloantibodies are never 'naturally occurring.' Individuals with anti-Vel antibodies may develop severe acute hemolytic transfusion reactions when transfused with Vel-positive blood. Individuals negative for the Vel antigen are rare and are required for the safe transfusion of patients with antibodies to Vel (summary by {3:Daniels, 2002}; {5:Storry et al., 2013}; {2:Cvejic et al., 2013}; {1:Ballif et al., 2013}).","definition_xrefs":["OMIM:615264"],"gene_count":0,"genotype_count":0,"name":"obsolete blood group, vel system (obsolete MONDO:0044282)","synonyms":[{"name":"VEL","type":"related"},{"name":"Vel-null phenotype","type":"related"},{"name":"blood group, VEL system","type":"related"},{"name":"blood group, Vel system","type":"exact"}],"termid":"MONDO:0044282","xrefs":{"Monarch":{"xref_id":"0044282"}}}


id: PBO:0066724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 21","termid":"PBO:0066724"}


id: MONDO:0032839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005267"],"is_obsolete":false,"name":"noonan syndrome 12","secondary_identifiers":["GARD:16369","OMIM:618624","MEDGEN:1684730","NCIT:C177120","UMLS:C5231432","DOID:0112170"],"synonyms":[{"name":"NOONAN SYNDROME 12","type":"related"},{"name":"NS12","type":"related"}],"termid":"MONDO:0032839","xrefs":{"Monarch":{"xref_id":"0032839"}}}


id: MONDO:0003112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell tumor that arises from the stomach. It includes choriocarcinoma and immature teratoma.","definition_xrefs":["NCIT:C5486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastric cancer","termid":"MONDO:0001056"},{"relation_name":"is_a","term_name":"extragonadal germ cell cancer","termid":"MONDO:0003113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"malignant gastric germ cell tumor","secondary_identifiers":["DOID:4716","MEDGEN:233663","UMLS:C1334584"],"synonyms":[{"name":"germ cell tumor of the stomach","type":"exact"},{"name":"germ cell tumour of the stomach","type":"exact"},{"name":"malignant gastric germ cell neoplasm","type":"exact"},{"name":"malignant gastric germ cell tumor","type":"exact"},{"name":"malignant germ cell neoplasm of stomach","type":"exact"},{"name":"malignant germ cell neoplasm of the stomach","type":"exact"},{"name":"malignant germ cell tumor of stomach","type":"exact"},{"name":"malignant germ cell tumor of the stomach","type":"exact"},{"name":"malignant germ cell tumour of stomach","type":"exact"},{"name":"malignant germ cell tumour of the stomach","type":"exact"}],"termid":"MONDO:0003112","xrefs":{"Monarch":{"xref_id":"0003112"}}}


id: PBO:0068523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 119, pseudogene","termid":"PBO:0068523"}


id: PBO:0070209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 137 pseudogene","termid":"PBO:0070209"}


id: GO:0044627
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that modulates the frequency, rate or extent of the classical pathway of complement activation, in a different organism.","definition_xrefs":["PMID:20837040","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of complement activation, classical pathway in another organism (obsolete GO:0044627)","synonyms":[{"name":"modulation of complement activation, classical pathway in other organism","type":"exact"},{"name":"regulation of complement activation, classical pathway in other organism","type":"exact"}],"termid":"GO:0044627"}


id: PBO:0085800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; contains sequence that closely resembles a J domain (typified by the E. coli DnaJ protein)","termid":"PBO:0085800"}


id: GO:0005642
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Stacks of endoplasmic reticulum (ER) membranes containing a high density of nuclear pores, thought to form from excess nuclear membrane components, that have been described in a number of different cells. Annulate lamellar membranes are continuous with and embedded within the ER.","definition_xrefs":["PMID:12631728"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane","termid":"GO:0016020"},{"relation_name":"part_of","term_name":"nuclear outer membrane-endoplasmic reticulum membrane network","termid":"GO:0042175"}],"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":"annulate lamellae","termid":"GO:0005642"}


id: MOD:00994
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3'-bromo-L-tyrosine","termid":"MOD:01025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(79)Br labeled 3'-bromotyrosine","termid":"MOD:00994"}


id: GO:0044488
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism effects a change in the frequency, rate or extent of the activity of a voltage-gated sodium channel in another organism.","definition_xrefs":["PMID:21781281","GOC:jl","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of voltage-gated sodium channel activity in another organism (obsolete GO:0044488)","synonyms":[{"name":"modulation of voltage-gated sodium channel activity in other organism","type":"exact"}],"termid":"GO:0044488"}


id: MONDO:0024757
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007154"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the heart and/or vessels. Representative examples of benign neoplasms include atrial myxoma, hemangioma, and lymphangioma. Representative examples of malignant neoplasms include pericardial malignant mesothelioma and angiosarcoma.","definition_xrefs":["NCIT:C4784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder","termid":"MONDO:0004995"},{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"is_obsolete":false,"name":"cardiovascular neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:721573003","UMLS:C0497243","MEDGEN:105422"],"synonyms":[{"name":"cardiovascular neoplasm","type":"exact"},{"name":"cardiovascular system neoplasm","type":"exact"},{"name":"cardiovascular system tumor","type":"exact"},{"name":"cardiovascular system tumour","type":"exact"},{"name":"cardiovascular tumor","type":"exact"},{"name":"cardiovascular tumour","type":"exact"},{"name":"neoplasm of cardiovascular system","type":"exact"},{"name":"tumor of cardiovascular system","type":"exact"},{"name":"tumour of cardiovascular system","type":"exact"}],"termid":"MONDO:0024757","terms_by_termid":{"MONDO:0007154":null},"xrefs":{"Monarch":{"xref_id":"0024757"}}}


id: GO:0046572
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: versiconal = versicolorin B + H2O.","definition_xrefs":["MetaCyc:RXN-9494","PMID:8784203"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity","termid":"GO:0016835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"versicolorin B synthase activity","secondary_identifiers":["RHEA:33859","EC:4.2.1.143"],"termid":"GO:0046572"}


id: MONDO:0001388
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the glans penis.","direct_ancestors":[{"relation_name":"is_a","term_name":"penile cancer","termid":"MONDO:0001325"}],"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":"glans penis cancer","secondary_identifiers":["ICD9:187.2","MEDGEN:509337","NCIT:C194357","SCTID:363451005","DOID:11839","UMLS:C0153599"],"synonyms":[{"name":"cancer of glans penis","type":"exact"},{"name":"glans penis cancer","type":"exact"},{"name":"malignant glans penis neoplasm","type":"exact"},{"name":"malignant neoplasm of glans penis","type":"exact"},{"name":"malignant tumor of glans penis","type":"exact"},{"name":"malignant tumour of glans penis","type":"exact"}],"termid":"MONDO:0001388","xrefs":{"Monarch":{"xref_id":"0001388"}}}


id: PBO:0073493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingosine-1-phosphate phosphatase 2","termid":"PBO:0073493"}


id: MOD:00001
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with an alkyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkylated residue","synonyms":[{"name":"AlkylRes","type":"exact"}],"termid":"MOD:00001"}


id: GO:0009063
data:
  {"annotated_genes":["SJAG_02901","SJAG_02734","SJAG_00944","SJAG_04842","SJAG_00714","SJAG_03293","SJAG_03434","SJAG_00495","SJAG_04827","SJAG_04145","SJAG_00937","SJAG_02450","SJAG_03743","SJAG_02496","SJAG_03398","SJAG_00674","SJAG_03641","SJAG_03861","SJAG_03671","SJAG_01903","SJAG_02235"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73256,72933,75645],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000949"},{"annotations":[82166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019478"},{"annotations":[80739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036088"},{"annotations":[89300,90292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009450"},{"annotations":[79835,75942,98326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019464"},{"annotations":[70212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042853"},{"annotations":[80190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019544"},{"annotations":[80188,115214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010121"},{"annotations":[72636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006533"},{"annotations":[115951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019450"},{"annotations":[93602,81414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006538"},{"annotations":[72012,79913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010133"},{"annotations":[73887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006567"},{"annotations":[74853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006574"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of amino acids, organic acids containing one or more amino substituents.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolic process","termid":"GO:0006520"},{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00495":null,"SJAG_00674":null,"SJAG_00714":null,"SJAG_00937":null,"SJAG_00944":null,"SJAG_01903":null,"SJAG_02235":null,"SJAG_02450":null,"SJAG_02496":null,"SJAG_02734":null,"SJAG_02901":null,"SJAG_03293":null,"SJAG_03398":null,"SJAG_03434":null,"SJAG_03641":null,"SJAG_03671":null,"SJAG_03743":null,"SJAG_03861":null,"SJAG_04145":null,"SJAG_04827":null,"SJAG_04842":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006520"],"is_obsolete":false,"name":"amino acid catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"amino acid breakdown","type":"exact"},{"name":"amino acid catabolism","type":"exact"},{"name":"amino acid degradation","type":"exact"},{"name":"cellular amino acid catabolic process","type":"exact"}],"termid":"GO:0009063","terms_by_termid":{"GO:0000949":null,"GO:0006533":null,"GO:0006538":null,"GO:0006567":null,"GO:0006574":null,"GO:0009450":null,"GO:0010121":null,"GO:0010133":null,"GO:0019450":null,"GO:0019464":null,"GO:0019478":null,"GO:0019544":null,"GO:0036088":null,"GO:0042853":null}}


id: PBO:0048358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 69","termid":"PBO:0048358"}


id: GO:0098895
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a postsynaptic endosome.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endosome membrane","termid":"GO:0010008"},{"relation_name":"part_of","term_name":"postsynaptic endosome","termid":"GO:0098845"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005768","GO:0031410","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"postsynaptic endosome membrane","termid":"GO:0098895"}


id: PBO:0085605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in control of cell wall structure and stress response; direct inhibitor of the nuclear Dbf2 related (NDR) kinase Cbk1p-Mob2p; overproduction confers resistance to cell-wall degrading enzymes; exhibits genetic interactions with genes involved in the cell wall integrity pathway; LRE1 has a paralog, HLR1, that arose from the whole genome duplication","termid":"PBO:0085605"}


id: PBO:0062758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily N member 3 pseudogene","termid":"PBO:0062758"}


id: GO:0006123
data:
  {"annotated_genes":["SJAG_05629","SJAG_01355","SJAG_02744","SJAG_02504","SJAG_00976","SJAG_01190","SJAG_MIT04","SJAG_MIT20","SJAG_MIT13","SJAG_07007","SJAG_01077"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62493,73602,76018,78225,80671,110266,116246,117480,121080,121102,121131],"is_not":false,"summary":null,"term":"GO:0006123"}]},"cv_name":"biological_process","definition":"The transfer of electrons from cytochrome c to oxygen that occurs during oxidative phosphorylation, mediated by the multisubunit enzyme known as complex IV.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aerobic electron transport chain","termid":"GO:0019646"},{"relation_name":"part_of","term_name":"mitochondrial ATP synthesis coupled electron transport","termid":"GO:0042775"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00976":null,"SJAG_01077":null,"SJAG_01190":null,"SJAG_01355":null,"SJAG_02504":null,"SJAG_02744":null,"SJAG_05629":null,"SJAG_07007":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT20":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0006091"],"is_obsolete":false,"name":"mitochondrial electron transport, cytochrome c to oxygen","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"complex IV (reduction of O2)","type":"related"}],"termid":"GO:0006123","terms_by_termid":{"GO:0006123":null}}


id: PBO:0003149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-AN1 type zinc finger protein","termid":"PBO:0003149"}


id: PBO:0061789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outer dynein arm docking complex subunit 1","termid":"PBO:0061789"}


id: PBO:0060623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NCK associated protein 1","termid":"PBO:0060623"}


id: GO:0030847
data:
  {"annotated_genes":["SJAG_02156","SJAG_04527","SJAG_03179","SJAG_04006"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61944,66363,99171,109439],"is_not":false,"summary":null,"term":"GO:0030847"}]},"cv_name":"biological_process","definition":"The process in which transcription of nonpolyadenylated RNA polymerase II transcripts is terminated; coupled to the maturation of the RNA 3'-end.","definition_xrefs":["GOC:txnOH","PMID:12944462","PMID:18679429","PMID:27371117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"termination of RNA polymerase II transcription","termid":"GO:0006369"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02156":null,"SJAG_03179":null,"SJAG_04006":null,"SJAG_04527":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006351"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006351","GO:0010467"],"is_obsolete":false,"name":"termination of RNA polymerase II transcription, exosome-dependent","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"termination of RNA polymerase II transcription, poly(A)-independent","type":"exact"},{"name":"transcription termination from Pol II promoter, RNA polymerase(A)-independent","type":"exact"},{"name":"transcription termination from Pol II promoter, poly(A)-independent","type":"exact"}],"termid":"GO:0030847","terms_by_termid":{"GO:0030847":null}}


id: GO:0000149
data:
  {"annotated_genes":["SJAG_04023","SJAG_04909","SJAG_00826","SJAG_01748","SJAG_03403","SJAG_01925","SJAG_03536","SJAG_05344","SJAG_03848","SJAG_03499","SJAG_01697","SJAG_04978","SJAG_03963","SJAG_01309","SJAG_05345","SJAG_02349","SJAG_00072","SJAG_02811","SJAG_02241"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73107,73737,75398,76441,76967,77427,77894,77949,78264,78305,79630,80245],"is_not":false,"summary":null,"term":"GO:0000149"},{"annotations":[77089,71540,79783,78256,81428,78369,71713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019905"}]},"cv_name":"molecular_function","definition":"Binding to a SNARE (soluble N-ethylmaleimide-sensitive factor attached protein receptor) protein.","definition_xrefs":["PMID:12642621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00072":null,"SJAG_00826":null,"SJAG_01309":null,"SJAG_01697":null,"SJAG_01748":null,"SJAG_01925":null,"SJAG_02241":null,"SJAG_02349":null,"SJAG_02811":null,"SJAG_03403":null,"SJAG_03499":null,"SJAG_03536":null,"SJAG_03848":null,"SJAG_03963":null,"SJAG_04023":null,"SJAG_04909":null,"SJAG_04978":null,"SJAG_05344":null,"SJAG_05345":null},"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:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"SNARE binding","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-917744","Reactome:R-HSA-374899","Reactome:R-HSA-9023173","Reactome:R-HSA-380869","Reactome:R-HSA-376357","Reactome:R-HSA-372505","Reactome:R-HSA-380905","Reactome:R-HSA-372529","Reactome:R-HSA-210426","Reactome:R-HSA-376369","Reactome:R-HSA-380901","Reactome:R-HSA-265166","Reactome:R-HSA-888589","Reactome:R-HSA-374922","Reactome:R-HSA-380574","Reactome:R-HSA-376364","Reactome:R-HSA-210430"],"synonyms":[{"name":"SNAP receptor binding","type":"exact"}],"termid":"GO:0000149","terms_by_termid":{"GO:0000149":null,"GO:0019905":null}}


id: PBO:0084903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial tryptophanyl-tRNA synthetase","termid":"PBO:0084903"}


id: PBO:0056434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MARK2 pseudogene 7","termid":"PBO:0056434"}


id: GO:1904866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a ventral tegmental area (VTA) over time, from its formation to the mature structure.","definition_xrefs":["GOC:bf","GO_REF:0000094","PMID:26548362","GOC:TermGenie","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"midbrain development","termid":"GO:0030901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"ventral tegmental area development","synonyms":[{"name":"VTA development","type":"broad"},{"name":"a10a development","type":"exact"},{"name":"area tegmentalis ventralis (Tsai) development","type":"related"},{"name":"area tegmentalis ventralis development","type":"related"},{"name":"tegmentum ventrale development","type":"related"},{"name":"ventral brain stem development","type":"related"},{"name":"ventral tegmental area (Tsai) development","type":"related"},{"name":"ventral tegmental area of tsai development","type":"exact"},{"name":"ventral tegmental nucleus (Rioch) development","type":"related"},{"name":"ventral tegmental nucleus (tsai) development","type":"exact"},{"name":"ventral tegmental nucleus of tsai development","type":"exact"},{"name":"ventral tegmentum development","type":"exact"},{"name":"ventromedial mesencephalic tegmentum development","type":"related"}],"termid":"GO:1904866"}


id: MONDO:0009494
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Ketoadipicaciduria (obsolete MONDO:0009494)","termid":"MONDO:0009494","xrefs":{"Monarch":{"xref_id":"0009494"}}}


id: MONDO:1011462
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alzheimer disease that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Alzheimer disease, non-human animal","termid":"MONDO:1011443"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alzheimer disease, domestic cat","secondary_identifiers":["OMIA:000033-9685"],"termid":"MONDO:1011462","xrefs":{"Monarch":{"xref_id":"1011462"}}}


id: GO:0051301
data:
  {"annotated_genes":["SJAG_00442","SJAG_01453","SJAG_00700","SJAG_04621","SJAG_01943","SJAG_03688","SJAG_03704","SJAG_01188","SJAG_02795","SJAG_02392","SJAG_03376","SJAG_04938","SJAG_03123","SJAG_01665","SJAG_01787","SJAG_04850","SJAG_01277","SJAG_03444","SJAG_00526","SJAG_00256","SJAG_06270","SJAG_05285","SJAG_04077","SJAG_02431","SJAG_03564","SJAG_00229","SJAG_01732","SJAG_01837","SJAG_02022","SJAG_03703","SJAG_00082","SJAG_04666","SJAG_00667","SJAG_00996","SJAG_02514","SJAG_02864","SJAG_03508","SJAG_01114","SJAG_04703","SJAG_01464","SJAG_01790","SJAG_03887","SJAG_04597","SJAG_04375","SJAG_01805","SJAG_03025","SJAG_03264","SJAG_00663","SJAG_04001","SJAG_03295","SJAG_03309","SJAG_00279","SJAG_04776","SJAG_04930","SJAG_02592","SJAG_04781","SJAG_00310","SJAG_00807","SJAG_02736","SJAG_00938","SJAG_03048","SJAG_02838","SJAG_03936","SJAG_03592","SJAG_01863","SJAG_03681","SJAG_01143","SJAG_02831","SJAG_00228","SJAG_03342","SJAG_02645","SJAG_04470","SJAG_01889","SJAG_01894","SJAG_03353","SJAG_02657","SJAG_04887","SJAG_02380","SJAG_03915","SJAG_01774","SJAG_05290","SJAG_00845","SJAG_03088","SJAG_02916","SJAG_00268","SJAG_00514","SJAG_04412","SJAG_00883","SJAG_02215","SJAG_04455","SJAG_02232","SJAG_01215","SJAG_04551","SJAG_04690","SJAG_02700","SJAG_02169","SJAG_02753","SJAG_04468","SJAG_04912","SJAG_02807","SJAG_02222","SJAG_03045","SJAG_04498","SJAG_01769","SJAG_01456","SJAG_04358","SJAG_04851","SJAG_04943","SJAG_03581","SJAG_03596","SJAG_05179","SJAG_03631","SJAG_04982","SJAG_03379","SJAG_01386","SJAG_03374","SJAG_03692"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91206,99952,100210,110113],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071520"},{"annotations":[107113],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044837"},{"annotations":[121665],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030995"},{"annotations":[76419,77675,76682],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061640"},{"annotations":[91610],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000917"},{"annotations":[101695,93183],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061796"},{"annotations":[74310,94434,70619,112796,99845,76714,58748,113871,100825,99574,97202,90130,68530,104512,121548,59919,77345,114312,120512,78094],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903475"},{"annotations":[79201],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903479"},{"annotations":[97203,102639,100826,58747,90131,99575,102870,104369,114313,99955],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902404"},{"annotations":[81771,102054,102902,114778,108172,105869,58215,118957,105207,121025,100213],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000281"},{"annotations":[121286,110843,98240,90143],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902408"},{"annotations":[106624,110595,115086,104590,108094,82159,101216],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140278"},{"annotations":[100199],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:2000432"},{"annotations":[97765,92649,96267,104314,105644,112760],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903500"},{"annotations":[105645],"is_not":false,"rel_names":["part_of","negatively_regulates","regulates"],"summary":null,"term":"GO:1903472"},{"annotations":[94735,109071,101598,104089],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1902413"},{"annotations":[104319],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905757"},{"annotations":[92608,112161,94821,107007,101520,93627,109205,94736,117925,109515,95350,74671,97550,103215,109072],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0031030"},{"annotations":[91878,96309],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903501"},{"annotations":[89394,96310,112519,96487,115373],"is_not":false,"rel_names":["positively_regulates","part_of","regulates"],"summary":null,"term":"GO:1903473"},{"annotations":[92651,105650,112762,121287],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903617"},{"annotations":[115374,94311,79724,91749,95699,107146,109018,119922,108358,117494],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140281"},{"annotations":[96313,89395,94312],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905758"},{"annotations":[108078,116404],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031671"},{"annotations":[91613,102088],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030994"},{"annotations":[94219,120691],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904498"},{"annotations":[79992],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031991"},{"annotations":[121207,95705],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903499"},{"annotations":[120743,102883,93741,109115,78689,119547,91695,111204,105439],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902412"},{"annotations":[89719,113378,103336],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902472"},{"annotations":[109933],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905391"},{"annotations":[117842],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990344"},{"annotations":[97573,104189,104199,104200,112631,113459,117672,89309,94053],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000920"}]},"cv_name":"biological_process","definition":"The process resulting in division and partitioning of components of a cell to form more cells; may or may not be accompanied by the physical separation of a cell into distinct, individually membrane-bounded daughter cells.","definition_xrefs":["GOC:di","GOC:go_curators","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"gene_count":117,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00256":null,"SJAG_00268":null,"SJAG_00279":null,"SJAG_00310":null,"SJAG_00442":null,"SJAG_00514":null,"SJAG_00526":null,"SJAG_00663":null,"SJAG_00667":null,"SJAG_00700":null,"SJAG_00807":null,"SJAG_00845":null,"SJAG_00883":null,"SJAG_00938":null,"SJAG_00996":null,"SJAG_01114":null,"SJAG_01143":null,"SJAG_01188":null,"SJAG_01215":null,"SJAG_01277":null,"SJAG_01386":null,"SJAG_01453":null,"SJAG_01456":null,"SJAG_01464":null,"SJAG_01665":null,"SJAG_01732":null,"SJAG_01769":null,"SJAG_01774":null,"SJAG_01787":null,"SJAG_01790":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01863":null,"SJAG_01889":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_02022":null,"SJAG_02169":null,"SJAG_02215":null,"SJAG_02222":null,"SJAG_02232":null,"SJAG_02380":null,"SJAG_02392":null,"SJAG_02431":null,"SJAG_02514":null,"SJAG_02592":null,"SJAG_02645":null,"SJAG_02657":null,"SJAG_02700":null,"SJAG_02736":null,"SJAG_02753":null,"SJAG_02795":null,"SJAG_02807":null,"SJAG_02831":null,"SJAG_02838":null,"SJAG_02864":null,"SJAG_02916":null,"SJAG_03025":null,"SJAG_03045":null,"SJAG_03048":null,"SJAG_03088":null,"SJAG_03123":null,"SJAG_03264":null,"SJAG_03295":null,"SJAG_03309":null,"SJAG_03342":null,"SJAG_03353":null,"SJAG_03374":null,"SJAG_03376":null,"SJAG_03379":null,"SJAG_03444":null,"SJAG_03508":null,"SJAG_03564":null,"SJAG_03581":null,"SJAG_03592":null,"SJAG_03596":null,"SJAG_03631":null,"SJAG_03681":null,"SJAG_03688":null,"SJAG_03692":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03887":null,"SJAG_03915":null,"SJAG_03936":null,"SJAG_04001":null,"SJAG_04077":null,"SJAG_04358":null,"SJAG_04375":null,"SJAG_04412":null,"SJAG_04455":null,"SJAG_04468":null,"SJAG_04470":null,"SJAG_04498":null,"SJAG_04551":null,"SJAG_04597":null,"SJAG_04621":null,"SJAG_04666":null,"SJAG_04690":null,"SJAG_04703":null,"SJAG_04776":null,"SJAG_04781":null,"SJAG_04850":null,"SJAG_04851":null,"SJAG_04887":null,"SJAG_04912":null,"SJAG_04930":null,"SJAG_04938":null,"SJAG_04943":null,"SJAG_04982":null,"SJAG_05179":null,"SJAG_05285":null,"SJAG_05290":null,"SJAG_06270":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell division","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:24699070":null,"PMID:25866389":null,"PMID:27059155":null,"PMID:32915139":null},"secondary_identifiers":["Wikipedia:Cell_division"],"termid":"GO:0051301","terms_by_termid":{"GO:0000281":null,"GO:0000917":null,"GO:0000920":null,"GO:0030994":null,"GO:0030995":null,"GO:0031030":null,"GO:0031671":null,"GO:0031991":null,"GO:0044837":null,"GO:0061640":null,"GO:0061796":null,"GO:0071520":null,"GO:0120306":null,"GO:0140278":null,"GO:0140281":null,"GO:1902404":null,"GO:1902408":null,"GO:1902412":null,"GO:1902413":null,"GO:1902472":null,"GO:1903472":null,"GO:1903473":null,"GO:1903475":null,"GO:1903479":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:1903617":null,"GO:1904498":null,"GO:1905391":null,"GO:1905757":null,"GO:1905758":null,"GO:1990344":null,"GO:2000432":null}}


id: GO:0070931
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a Golgi-associated vesicle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle lumen","termid":"GO:0060205"},{"relation_name":"part_of","term_name":"Golgi apparatus","termid":"GO:0005794"},{"relation_name":"part_of","term_name":"Golgi-associated vesicle","termid":"GO:0005798"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005794"}],"interesting_parent_ids":["GO:0031410","GO:0005794","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"Golgi-associated vesicle lumen","termid":"GO:0070931"}


id: PBO:0069740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1021, pseudogene","termid":"PBO:0069740"}


id: GO:0018767
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-hydroxy-6-oxo-7-methylocta-2,4-dienoate + H2O = cis-2-hydroxypenta-2,4-dienoate + isobutyrate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-hydroxy-6-oxo-7-methylocta-2,4-dienoate hydrolase activity (obsolete GO:0018767)","termid":"GO:0018767"}


id: GO:0051647
data:
  {"annotated_genes":["SJAG_02286","SJAG_03073","SJAG_02509","SJAG_01297","SJAG_00368","SJAG_02737","SJAG_01662","SJAG_00140","SJAG_00397","SJAG_01613","SJAG_03673","SJAG_01370","SJAG_04001","SJAG_00113","SJAG_02431","SJAG_05185","SJAG_04597","SJAG_04143","SJAG_03835","SJAG_02651","SJAG_02561","SJAG_02045","SJAG_00594","SJAG_03264","SJAG_01863","SJAG_04003","SJAG_04387"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110245],"is_not":false,"summary":null,"term":"GO:0051647"},{"annotations":[105205,99502,93739,115962,113404,104914,113053,97121,89623,118972,92877,93274,102666],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030989"},{"annotations":[113227,108562,103380],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032118"},{"annotations":[106503,106835,114779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007097"},{"annotations":[111602,115964,118976,103391,76792,72540,109405],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098863"},{"annotations":[101161,99577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090561"},{"annotations":[89627,78106,99504,93276,101162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000743"},{"annotations":[96312],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902854"}]},"cv_name":"biological_process","definition":"Any process in which the nucleus is transported to, and/or maintained in, a specific location within the cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle localization","termid":"GO:0051640"}],"gene_count":27,"genes_by_uniquename":{"SJAG_00113":null,"SJAG_00140":null,"SJAG_00368":null,"SJAG_00397":null,"SJAG_00594":null,"SJAG_01297":null,"SJAG_01370":null,"SJAG_01613":null,"SJAG_01662":null,"SJAG_01863":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02431":null,"SJAG_02509":null,"SJAG_02561":null,"SJAG_02651":null,"SJAG_02737":null,"SJAG_03073":null,"SJAG_03264":null,"SJAG_03673":null,"SJAG_03835":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04143":null,"SJAG_04387":null,"SJAG_04597":null,"SJAG_05185":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"nucleus localization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"cell nucleus localization","type":"exact"},{"name":"establishment and maintenance of nucleus localization","type":"exact"},{"name":"localization of nucleus","type":"exact"},{"name":"nucleus localisation","type":"exact"}],"termid":"GO:0051647","terms_by_termid":{"GO:0000743":null,"GO:0007097":null,"GO:0030989":null,"GO:0032118":null,"GO:0051647":null,"GO:0090561":null,"GO:0098863":null,"GO:1902854":null}}


id: _global:causally_upstream_of
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","definition":"p is causally upstream of q iff p is causally related to q, the end of p precedes the end of q, and p is not an occurrent part of q.","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_upstream_of_or_within","termid":"_global:causally_upstream_of_or_within"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"},{"relation_name":"is_a","term_name":"precedes","termid":"_global:precedes"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causally_upstream_of","secondary_identifiers":["RO:0002411"],"termid":"_global:causally_upstream_of"}


id: GO:0051121
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving hepoxilins, a class of bioactive icosanoids with roles in the regulation of cell physiology.","definition_xrefs":["PMID:15123652"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid metabolic process","termid":"GO:0001676"}],"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:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"hepoxilin metabolic process","secondary_identifiers":["Reactome:R-HSA-2142696"],"synonyms":[{"name":"hepoxilin metabolism","type":"exact"}],"termid":"GO:0051121"}


id: PBO:0034370
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_upstream_of_sequence_of","termid":"PBO:0034370"}


id: PBO:0109083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA induced by TGF-beta and antagonizes TGF-beta signaling 1","termid":"PBO:0109083"}


id: GO:0010989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of low-density lipoprotein particle clearance. Low-density lipoprotein particle clearance is the process in which a low-density lipoprotein particle is removed from the blood via receptor-mediated endocytosis and its constituent parts degraded.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipoprotein particle clearance","termid":"GO:0010985"},{"relation_name":"is_a","term_name":"regulation of low-density lipoprotein particle clearance","termid":"GO:0010988"},{"relation_name":"negatively_regulates","term_name":"low-density lipoprotein particle clearance","termid":"GO:0034383"}],"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 low-density lipoprotein particle clearance","termid":"GO:0010989"}


id: MONDO:0020112
data:
  {"annotated_genes":["SJAG_03164","SJAG_00694"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87074,87073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009797"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"megaloblastic anemia","termid":"MONDO:0001700"},{"relation_name":"is_a","term_name":"hereditary anemia","termid":"MONDO:0016624"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00694":null,"SJAG_03164":null},"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":"vitamin B12- and folate-independent constitutional megaloblastic anemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842832","ICD10CM:D53.0","UMLS:C5681710","GARD:19464","Orphanet:98415"],"termid":"MONDO:0020112","terms_by_termid":{"MONDO:0009797":null},"xrefs":{"Monarch":{"xref_id":"0020112"}}}


id: GO:0000904
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The change in form (cell shape and size) that occurs when relatively unspecialized cells, e.g. embryonic or regenerative cells, acquire specialized structural and/or functional features that characterize the cells, tissues, or organs of the mature organism or some other relatively stable phase of the organism's life history.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cell morphogenesis involved in differentiation (obsolete GO:0000904)","termid":"GO:0000904"}


id: PBO:0047009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A12, pseudogene","termid":"PBO:0047009"}


id: FYPO:0005332
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 repair of pyrimidine-pyrimidone 6-4 photoproducts by error-prone translesion synthesis does not occur.","definition_xrefs":["PMID:20453833","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal error-prone translesion synthesis","termid":"FYPO:0003892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000293","FYPO:0001985","FYPO:0000298","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abolished error-prone translesion synthesis of pyrimidine-pyrimidone 6-4 photoproducts","synonyms":[{"name":"abolished error-prone translesion synthesis across TT-(6-4)","type":"exact"},{"name":"abolished error-prone translesion synthesis of pyrimidine-pyrimidone 6-4 photoproducts during mitotic cell cycle","type":"related"},{"name":"abolished error-prone translesion synthesis of pyrimidine-pyrimidone 6-4 photoproducts during vegetative growth","type":"exact"},{"name":"error-prone translesion synthesis of pyrimidine-pyrimidone 6-4 photoproducts abolished","type":"exact"}],"termid":"FYPO:0005332"}


id: PBO:0049033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 20","termid":"PBO:0049033"}


id: GO:0070892
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with lipoteichoic acid and transmitting the signal to initiate an innate immune response.","definition_xrefs":["GOC:add","PMID:14665680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern recognition receptor activity","termid":"GO:0038187"}],"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":"lipoteichoic acid immune receptor activity","synonyms":[{"name":"lipoteichoic acid receptor activity","type":"broad"}],"termid":"GO:0070892"}


id: MONDO:0014739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MET gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 97","secondary_identifiers":["GARD:22655","MEDGEN:899875","OMIM:616705","UMLS:C4084709","DOID:0110539"],"synonyms":[{"name":"DFNB97","type":"narrow"},{"name":"MET autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 97","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 97","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in MET","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 97","type":"narrow"},{"name":"deafness, autosomal recessive 97","type":"narrow"},{"name":"deafness, autosomal recessive type 97","type":"narrow"}],"termid":"MONDO:0014739","xrefs":{"Monarch":{"xref_id":"0014739"}}}


id: PBO:0081582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 511","termid":"PBO:0081582"}


id: GO:0034574
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: didemethylisoproturon + H2O = 4'-(2-hydroxyisopropyl)phenylurea + 2 H+ + 2 e-.","definition_xrefs":["UM-BBD_reactionID:r0899"],"gene_count":0,"genotype_count":0,"name":"obsolete didemethylisoproturon dehydrogenase activity (obsolete GO:0034574)","termid":"GO:0034574"}


id: MONDO:0006141
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cervical adenocarcinoma characterized by the presence of a prominent villoglandular pattern.","definition_xrefs":["NCIT:C40208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical mucinous adenocarcinoma","termid":"MONDO:0002742"},{"relation_name":"is_a","term_name":"villous adenocarcinoma","termid":"MONDO:0003204"}],"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":"cervical villoglandular adenocarcinoma","secondary_identifiers":["DOID:8338","ONCOTREE:VGCE","MEDGEN:927340","UMLS:C4289808"],"synonyms":[{"name":"cervical adenocarcinoma, villoglandular variant","type":"exact"},{"name":"cervical villoglandular adenocarcinoma","type":"exact"},{"name":"cervical villoglandular carcinoma","type":"exact"},{"name":"villoglandular adenocarcinoma of the cervix","type":"related"},{"name":"villoglandular variant cervical mucinous adenocarcinoma","type":"exact"}],"termid":"MONDO:0006141","xrefs":{"Monarch":{"xref_id":"0006141"}}}


id: PBO:0070537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 3","termid":"PBO:0070537"}


id: PBO:0064504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II, I and III subunit E","termid":"PBO:0064504"}


id: MONDO:0005170
data:
  {"annotated_genes":["SJAG_03453","SJAG_01349","SJAG_01748","SJAG_01013","SJAG_03905","SJAG_05979","SJAG_02527"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89231,89074,89073,89230,89075,89076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"},{"annotations":[89195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009693"}]},"cv_name":"mondo","definition":"Proliferation of myeloid cells originating from a primitive stem cell.","definition_xrefs":["NCIT:C9290"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lymphoid neoplasm","termid":"MONDO:0005157"},{"relation_name":"is_a","term_name":"hematopoietic and lymphoid cell neoplasm","termid":"MONDO:0044881"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01013":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_02527":null,"SJAG_03453":null,"SJAG_03905":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"myeloid neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ONCOTREE:MYELOID","MEDGEN:445430","DOID:0070004","ICDO:9975/1","UMLS:C2939461","EFO:0002427"],"synonyms":[{"name":"myeloid malignancy","type":"exact"},{"name":"myeloid neoplasm","type":"exact"},{"name":"myeloid tumor","type":"exact"},{"name":"myeloid tumour","type":"exact"}],"termid":"MONDO:0005170","terms_by_termid":{"MONDO:0009693":null,"MONDO:0018874":null},"xrefs":{"Monarch":{"xref_id":"0005170"}}}


id: PBO:0028867
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_mRNA_level_during_vegetative_growth","termid":"PBO:0028867"}


id: MONDO:0000904
data:
  {"annotated_genes":["SJAG_01215","SJAG_04003"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013541"},{"annotations":[87747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014171"},{"annotations":[88467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014337"},{"annotations":[88478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014341"},{"annotations":[87316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012399"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01215":null,"SJAG_04003":null},"genotype_count":0,"is_obsolete":false,"name":"complex cortical dysplasia with other brain malformations","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0090131","OMIMPS:614039"],"synonyms":[{"name":"CDCBM","type":"exact"},{"name":"complex cortical dysplasia with other brain malformations","type":"exact"},{"name":"cortical dysplasia, complex, with other brain malformations","type":"exact"}],"termid":"MONDO:0000904","terms_by_termid":{"MONDO:0012399":null,"MONDO:0013541":null,"MONDO:0014171":null,"MONDO:0014337":null,"MONDO:0014341":null},"xrefs":{"Monarch":{"xref_id":"0000904"}}}


id: GO:0098831
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A specialized region below the presynaptic membrane, characterized by electron-dense material, a specialized cytoskeletal matrix and accumulated (associated) synaptic vesicles.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cortex region","termid":"GO:0099738"},{"relation_name":"part_of","term_name":"presynaptic active zone","termid":"GO:0048786"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005938"},{"rel_name":"is_a","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005575","GO:0005938","GO:0005737"],"is_obsolete":false,"name":"presynaptic active zone cytoplasmic component","synonyms":[{"name":"cortex of presynaptic active zone","type":"exact"},{"name":"presynaptic zone cortex","type":"exact"}],"termid":"GO:0098831"}


id: GO:0004317
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (3R)-hydroxypalmitoyl-[acyl-carrier protein] = 2-hexadecenoyl-[acyl-carrier protein] + H2O.","definition_xrefs":["PMID:8088535"],"gene_count":0,"genotype_count":0,"name":"obsolete (3R)-3-hydroxypalmitoyl-[acyl-carrier-protein] dehydratase activity (obsolete GO:0004317)","synonyms":[{"name":"(3R)-3-hydroxypalmitoyl-acyl-carrier-protein hydro-lyase (hexadec-2-enoyl-acyl-carrier protein-forming)","type":"exact"},{"name":"(3R)-3-hydroxypalmitoyl-acyl-carrier-protein hydro-lyase activity","type":"exact"},{"name":"(3R)-hydroxypalmitoyl-[acyl-carrier-protein] dehydratase activity","type":"exact"},{"name":"3-hydroxypalmitoyl-ACP dehydratase activity","type":"exact"},{"name":"3-hydroxypalmitoyl-[acyl-carrier protein] dehydratase activity","type":"exact"},{"name":"3-hydroxypalmitoyl-[acyl-carrier-protein] dehydratase activity","type":"exact"},{"name":"3-hydroxypalmitoyl-acyl-carrier-protein dehydratase activity","type":"exact"}],"termid":"GO:0004317"}


id: PBO:0053646
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 696","termid":"PBO:0053646"}


id: MONDO:0012111
data:
  {"annotated_genes":["SJAG_00228"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88293],"is_not":false,"summary":null,"term":"MONDO:0012111"}]},"cv_name":"mondo","definition":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00228":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"hypertrophic cardiomyopathy 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:324806","MESH:C563866","OMIM:608751","UMLS:C1837471","DOID:0110314"],"synonyms":[{"name":"CMH8","type":"related"},{"name":"MYL3 hypertrophic cardiomyopathy","type":"exact"},{"name":"cardiomyopathy hypertrophic mid-left ventricular chamber type 1","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 8","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, type 8","type":"exact"},{"name":"cardiomyopathy, hypertrophic, 8","type":"exact"},{"name":"cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1","type":"related"},{"name":"hypertrophic cardiomyopathy 8","type":"exact"},{"name":"hypertrophic cardiomyopathy caused by mutation in MYL3","type":"exact"},{"name":"hypertrophic cardiomyopathy type 8","type":"exact"}],"termid":"MONDO:0012111","terms_by_termid":{"MONDO:0012111":null},"xrefs":{"Monarch":{"xref_id":"0012111"}}}


id: GO:0043199
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to sulfate, SO4(2-), a negatively charged small molecule.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"sulfur compound binding","termid":"GO:1901681"}],"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":"sulfate binding","termid":"GO:0043199"}


id: PBO:0058350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4723","termid":"PBO:0058350"}


id: MONDO:0975756
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"benign vascular tumor","termid":"MONDO:0971115"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reactive angioendotheliomatosis","secondary_identifiers":["UMLS:C2930870","Orphanet:673574","MEDGEN:418935"],"termid":"MONDO:0975756","xrefs":{"Monarch":{"xref_id":"0975756"}}}


id: PBO:0041295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2CD2 like","termid":"PBO:0041295"}


id: MONDO:0800390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Toxicities following administration of chemotherapeutic agents","direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chemotherapy-induced toxicity","termid":"MONDO:0800390","xrefs":{"Monarch":{"xref_id":"0800390"}}}


id: GO:0070771
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaIIb-beta3 integrin complex bound to the cell surface antigen CD47 and the kinase c-Src.","definition_xrefs":["PMID:9169439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"alphaIIb-beta3 integrin-CD47-Src complex","synonyms":[{"name":"ITGA2b-ITGB3-CD47-SRC complex","type":"narrow"}],"termid":"GO:0070771"}


id: FYPO:0006708
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the phosphorylation of one or more specific proteins, or of specific protein sites, does not occur when the cell is subject to glucose starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein phosphorylation","termid":"FYPO:0002678"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002494","FYPO:0005447","FYPO:0001985","FYPO:0002274"],"is_obsolete":false,"name":"abolished protein phosphorylation during glucose starvation","synonyms":[{"name":"abolished protein phosphorylation during cellular response to glucose starvation","type":"exact"},{"name":"abolished protein phosphorylation during glucose deprivation","type":"exact"},{"name":"protein phosphorylation abolished during glucose starvation","type":"exact"}],"termid":"FYPO:0006708"}


id: PBO:0063190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate cancer associated transcript 2","termid":"PBO:0063190"}


id: PBO:0031811
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_biofilm_formation","termid":"PBO:0031811"}


id: MONDO:0100167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing COPD.","definition_xrefs":["MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary disease, chronic obstructive, susceptibility to","secondary_identifiers":["UMLS:C3838076","MEDGEN:854229"],"termid":"MONDO:0100167","xrefs":{"Monarch":{"xref_id":"0100167"}}}


id: PBO:0110168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zpr1 co-chaperone for EF-1 alpha folding","termid":"PBO:0110168"}


id: PBO:0071917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S3 pseudogene 2","termid":"PBO:0071917"}


id: PBO:0048236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G antigen 5","termid":"PBO:0048236"}


id: GO:0035072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process induced by ecdysone that directly activates salivary gland programmed cell death during salivary gland histolysis.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete ecdysone-mediated induction of salivary gland cell autophagic cell death (obsolete GO:0035072)","termid":"GO:0035072"}


id: MONDO:0010267
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":"episodic muscle weakness, X-linked","secondary_identifiers":["OMIM:300211","UMLS:C1846173","MEDGEN:337525","MESH:C564565"],"synonyms":[{"name":"EMWX","type":"exact"},{"name":"episodic muscle weakness, X-linked","type":"exact"}],"termid":"MONDO:0010267","xrefs":{"Monarch":{"xref_id":"0010267"}}}


id: PBO:0069717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 997, pseudogene","termid":"PBO:0069717"}


id: PBO:0016521
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae SST2","termid":"PBO:0016521"}


id: MONDO:0016125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete infectious, fungal or parasitic myopathy (obsolete MONDO:0016125)","secondary_identifiers":["Orphanet:206988"],"termid":"MONDO:0016125","xrefs":{"Monarch":{"xref_id":"0016125"}}}


id: GO:0018812
data:
  {"annotated_genes":["SJAG_01300"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102158"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 3-hydroxy-fatty acyl-CoA = a (2E)-enoyl-CoA + H2O.","definition_xrefs":["RHEA:33767"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enoyl-CoA hydratase activity","termid":"GO:0004300"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01300":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"3-hydroxyacyl-CoA dehydratase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["Reactome:R-HSA-8957389","Reactome:R-HSA-390252","Reactome:R-HSA-2066778","Reactome:R-HSA-2066780","Reactome:R-HSA-389986","Reactome:R-HSA-5676637","Reactome:R-HSA-6809263"],"termid":"GO:0018812","terms_by_termid":{"GO:0102158":null}}


id: PBO:0058702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6830","termid":"PBO:0058702"}


id: GO:0018777
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: alkyl halide + H2O = alcohol + HCl. Substrates are 1,3(R),4,6(R)-tetrachloro-1,4-cyclohexadiene (forms 2,4,5-trichloro-2,5-cyclohexadiene-1-ol) and 2,4,5-trichloro-2,5-cyclohexadiene-1-ol (forms 2,5-dichloro-2,5-cyclohexadiene-1,4-diol).","definition_xrefs":["PMID:10464214"],"gene_count":0,"genotype_count":0,"name":"obsolete 1,3,4,6-tetrachloro-1,4-cyclohexadiene halidohydrolase activity (obsolete GO:0018777)","termid":"GO:0018777"}


id: PBO:0046346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 4","termid":"PBO:0046346"}


id: MONDO:0002732
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm that arises from the lung parenchyma or the bronchi. Representative examples include lung adenoma, lung hamartoma, and endobronchial lipoma.","definition_xrefs":["NCIT:C4454"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system benign neoplasm","termid":"MONDO:0000382"},{"relation_name":"is_a","term_name":"thoracic benign neoplasm","termid":"MONDO:0000634"},{"relation_name":"is_a","term_name":"lung neoplasm","termid":"MONDO:0021117"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lung benign neoplasm","secondary_identifiers":["UMLS:C0345963","DOID:3683","MEDGEN:83393"],"synonyms":[{"name":"benign lung neoplasm","type":"exact"},{"name":"benign lung tumor","type":"exact"},{"name":"benign lung tumour","type":"exact"},{"name":"benign neoplasm of lung","type":"exact"},{"name":"benign neoplasm of the lung","type":"exact"},{"name":"benign tumor of lung","type":"exact"},{"name":"benign tumor of the lung","type":"exact"},{"name":"benign tumour of lung","type":"exact"},{"name":"benign tumour of the lung","type":"exact"},{"name":"lung benign neoplasm","type":"exact"},{"name":"tumor of the lung","type":"broad"},{"name":"tumour of the lung","type":"broad"}],"termid":"MONDO:0002732","xrefs":{"Monarch":{"xref_id":"0002732"}}}


id: PBO:0083409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the dubious ORF YLR366W","termid":"PBO:0083409"}


id: PATO:0002481
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An orientation quality inhering in a bearer by virtue of the bearer having a slanting direction or position : neither perpendicular nor parallel.","definition_xrefs":["merriam-wester:http://www.merriam-webster.com/dictionary/oblique"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orientation","termid":"PATO:0000133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oblique orientation","termid":"PATO:0002481"}


id: PBO:0085030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-ATPase base subunit of the 19S RP of the 26S proteasome; may participate in the recognition of several ligands of the proteasome; contains a leucine-rich repeat (LRR) domain, a site for protein-protein interactions; RP is the acronym for regulatory particle","termid":"PBO:0085030"}


id: MONDO:0013700
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive disorder caused by mutation(s) in the PNLIP gene, encoding pancreatic triacylglycerol lipase. The condition is characterized by absent or reduced pancreatic lipase.","definition_xrefs":["NCIT:C129030"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pancreas disorder","termid":"MONDO:0002356"},{"relation_name":"excluded_subClassOf","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"},{"relation_name":"is_a","term_name":"pancreas disorder","termid":"MONDO:0002356"},{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"pancreatic triacylglycerol lipase deficiency","secondary_identifiers":["MEDGEN:482157","Orphanet:309031","NANDO:2200912","ICD9:277.89","ICD10CM:K90.3","OMIM:614338","SCTID:78960005","UMLS:C3280527","GARD:17401","icd11.foundation:349070670"],"synonyms":[{"name":"PL deficiency","type":"related"},{"name":"PNLIPD","type":"related"},{"name":"colipase, congenital absence of pancreatic","type":"related"},{"name":"lipase and colipase, congenital absence of pancreatic","type":"related"},{"name":"lipase and colipase, deficiency of","type":"related"},{"name":"lipase, congenital absence of pancreatic","type":"related"},{"name":"pancreatic colipase deficiency","type":"related"},{"name":"pancreatic lipase deficiency","type":"related"},{"name":"pancreatic triglyceride lipase deficiency","type":"exact"}],"termid":"MONDO:0013700","xrefs":{"Monarch":{"xref_id":"0013700"}}}


id: PBO:0002545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosyltransferase Alg8 (predicted)","termid":"PBO:0002545"}


id: PBO:0076590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 10C","termid":"PBO:0076590"}


id: PBO:0039280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 9, pseudogene","termid":"PBO:0039280"}


id: GO:0075180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism modulates the frequency, rate or extent of its transcription as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription in response to host (obsolete GO:0075180)","termid":"GO:0075180"}


id: PBO:0074683
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 63E","termid":"PBO:0074683"}


id: MONDO:0032738
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":"gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy","secondary_identifiers":["UMLS:C5193085","MEDGEN:1679397","OMIM:600908","OMIM:618419"],"synonyms":[{"name":"GDRM","type":"related"},{"name":"GONADAL DYSGENESIS, DYSMORPHIC FACIES, RETINAL DYSTROPHY, AND MYOPATHY","type":"exact"},{"name":"KENNERKNECHT syndrome","type":"exact"},{"name":"Kennerknecht syndrome","type":"exact"},{"name":"agonadism, 46,XY, with intellectual disability, short stature, retarded bone age, and multiple extragenital malformations","type":"exact"},{"name":"agonadism, 46,XY, with mental retardation, short stature, retarded bone age, and multiple extragenital malformations","type":"exact"}],"termid":"MONDO:0032738","xrefs":{"Monarch":{"xref_id":"0032738"}}}


id: PBO:0013089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-splicing endonuclease positive effector Dbl8","termid":"PBO:0013089"}


id: PBO:0001468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retromer complex subunit Vps26","termid":"PBO:0001468"}


id: PBO:0064440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich nuclear receptor coactivator 2","termid":"PBO:0064440"}


id: PBO:0029618
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_DNA_damage_checkpoint_during_cellular_response_to_UV","termid":"PBO:0029618"}


id: GO:0005182
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 lipopeptide hormone (obsolete GO:0005182)","synonyms":[{"name":"lipopeptide hormone","type":"exact"}],"termid":"GO:0005182"}


id: GO:0061357
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 a Wnt protein from a cell.","definition_xrefs":["GOC:bf","PMID:19223472"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell communication","termid":"GO:0010647"},{"relation_name":"is_a","term_name":"positive regulation of signaling","termid":"GO:0023056"},{"relation_name":"is_a","term_name":"positive regulation of protein secretion","termid":"GO:0050714"},{"relation_name":"is_a","term_name":"regulation of Wnt protein secretion","termid":"GO:0061356"},{"relation_name":"positively_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":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"positive regulation of Wnt protein secretion","termid":"GO:0061357"}


id: PBO:0040892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bone morphogenetic protein receptor type 1A pseudogene 1","termid":"PBO:0040892"}


id: PBO:0114136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulphite transmembrane transporter Ssu3","termid":"PBO:0114136"}


id: PBO:0055393
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 2823","termid":"PBO:0055393"}


id: PBO:0090243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Rrp7","termid":"PBO:0090243"}


id: PBO:0066526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RANBP2 like and GRIP domain containing 2","termid":"PBO:0066526"}


id: PBO:0078365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 9-1","termid":"PBO:0078365"}


id: PBO:0072726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ryanodine receptor 1","termid":"PBO:0072726"}


id: GO:0047561
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-hydroxyanthranilate + O2 = 6-imino-5-oxocyclohexa-1,3-dienecarboxylate + H2O2.","definition_xrefs":["RHEA:17245","EC:1.10.3.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor","termid":"GO:0016682"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"3-hydroxyanthranilate oxidase activity","secondary_identifiers":["KEGG_REACTION:R02666","MetaCyc:3-HYDROXYANTHRANILATE-OXIDASE-RXN"],"synonyms":[{"name":"3-hydroxyanthranilate:oxygen oxidoreductase activity","type":"related"},{"name":"3-hydroxyanthranilic acid oxidase activity","type":"related"}],"termid":"GO:0047561"}


id: PBO:0029024
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_chromatin_silencing_at_silent_mating-type_cassette","termid":"PBO:0029024"}


id: MONDO:0020841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An an autosomal recessive disorder characterized by intellectual disability associated with ataxia, in which the cause of the disease is a variation in the BRAT1 gene.","definition_xrefs":["OMIM:618056"],"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 cerebellar atrophy and with or without seizures","secondary_identifiers":["MEDGEN:1648373","UMLS:C4748032"],"synonyms":[{"name":"NEDCAS","type":"exact"},{"name":"neurodevelopmental disorder with cerebellar atrophy and with or without seizures","type":"exact"}],"termid":"MONDO:0020841","xrefs":{"Monarch":{"xref_id":"0020841"}}}


id: PBO:0066940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 242","termid":"PBO:0066940"}


id: PBO:0060533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyltransferase 9 (putative)","termid":"PBO:0060533"}


id: PBO:0076777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis development related protein","termid":"PBO:0076777"}


id: SO:0000907
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute to describe a feature that has been predicted using sequence similarity techniques.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"predicted","termid":"SO:0000732"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"supported_by_sequence_similarity","synonyms":[{"name":"supported by sequence similarity","type":"exact"}],"termid":"SO:0000907"}


id: MONDO:0018755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scorpion envenomation is a rare intoxication caused by a scorpion sting which typically manifests with localized pain, edema, erythema, and paresthesias at the site of the sting and, when severe, progresses to produce systemic symptoms of variable severity that include respiratory difficulties, abnormal systemic blood pressure, cardiac arrhythmia, and a combination of parasympathetic (i.e. excessive salivation and lacrimation, diaphoresis, miosis, frequent urination, diarrhea, vomiting, priapism) and sympathetic (e.g. hyperthermia, hyperglycemia, mydriasis) manifestations. Neurological manifestations may also be associated, such as abnormal eye movements, blurred vision, agitation and restlessness, as well as muscle fasciculations and spasms. Signs and symptoms are highly variable and in most severe cases may lead to cardiogenic shock and pulmonary edema.","definition_xrefs":["Orphanet:466677"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scorpion envenomation","secondary_identifiers":["SCTID:217670007","GARD:21939"],"synonyms":[{"name":"poisoning caused by scorpion venom","type":"exact"},{"name":"poisoning due to scorpion venom","type":"exact"},{"name":"toxic effect of venom of scorpion","type":"exact"}],"termid":"MONDO:0018755","xrefs":{"Monarch":{"xref_id":"0018755"}}}


id: PBO:0070386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhophilin associated tail protein 1","termid":"PBO:0070386"}


id: PBO:0003410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Cki2","termid":"PBO:0003410"}


id: PBO:0068424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein with serine rich domain 1","termid":"PBO:0068424"}


id: PBO:0057832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3150a","termid":"PBO:0057832"}


id: PBO:0013003
data:
  {"annotation_feature_type":"gene","cv_name":"feature_relationshipprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curator_email","termid":"PBO:0013003"}


id: MOD:01943
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that crosslinks two adjacent residues by formation of a pyrrolidione ring.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues","termid":"MOD:00033"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyrrolidione ring crosslinked residues","termid":"MOD:01943"}


id: MONDO:0022519
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune myocarditis is an autoimmune disease that affects the heart. The condition is characterized by inflammation of the heart muscle (myocardium). Some people with autoimmune myocarditis have no noticeable symptoms of the condition. When present, signs and symptoms may include chest pain, abnormal heartbeat, shortness of breath, fatigue, signs of infection (i.e. fever, headache, sore throat, diarrhea), and leg swelling. The exact underlying cause of the condition is currently unknown; however, autoimmune conditions, in general, occur when the immune system mistakenly attacks healthy tissue. Treatment is based on the signs and symptoms present in each person. In some cases, medications that suppress the immune system may be recommended.","definition_xrefs":["GARD:0009519"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myocarditis","termid":"MONDO:0004496"},{"relation_name":"is_a","term_name":"autoimmune cardiomyopathy","termid":"MONDO:0030701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005267"],"is_obsolete":false,"name":"autoimmune myocarditis","secondary_identifiers":["GARD:9519","DOID:0080767","UMLS:C1608389","MEDGEN:299070"],"termid":"MONDO:0022519","xrefs":{"Monarch":{"xref_id":"0022519"}}}


id: GO:2000841
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dehydroepiandrosterone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid transport","termid":"GO:0032369"},{"relation_name":"is_a","term_name":"negative regulation of hormone secretion","termid":"GO:0046888"},{"relation_name":"is_a","term_name":"regulation of dehydroepiandrosterone secretion","termid":"GO:2000840"},{"relation_name":"negatively_regulates","term_name":"dehydroepiandrosterone secretion","termid":"GO:0035942"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"negative regulation of dehydroepiandrosterone secretion","synonyms":[{"name":"negative regulation of 3beta-hydroxyandrost-5-en-17-one secretion","type":"exact"},{"name":"negative regulation of DHEA secretion","type":"exact"},{"name":"negative regulation of dehydroisoandrosterone secretion","type":"exact"}],"termid":"GO:2000841"}


id: MONDO:1010669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myeloperoxidase deficiency that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloperoxidase deficiency, non-human animal","termid":"MONDO:1010086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloperoxidase deficiency, dog","secondary_identifiers":["OMIA:002028-9615"],"termid":"MONDO:1010669","xrefs":{"Monarch":{"xref_id":"1010669"}}}


id: MONDO:0020526
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute megakaryoblastic leukemia","termid":"MONDO:0018872"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"acute megakaryoblastic leukemia in down syndrome","secondary_identifiers":["UMLS:C5925108","Orphanet:99887","GARD:19697","MEDGEN:1863778"],"synonyms":[{"name":"DS-AMKL","type":"exact"}],"termid":"MONDO:0020526","xrefs":{"Monarch":{"xref_id":"0020526"}}}


id: GO:0141092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of nodal signaling pathway.","definition_xrefs":["PMID:17239842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of activin receptor signaling pathway","termid":"GO:0032927"},{"relation_name":"is_a","term_name":"regulation of nodal signaling pathway","termid":"GO:1900107"},{"relation_name":"positively_regulates","term_name":"nodal signaling pathway","termid":"GO:0038092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of nodal signaling pathway","termid":"GO:0141092"}


id: MONDO:0012351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndactyly type 1","termid":"MONDO:0008512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zygodactyly type 1","secondary_identifiers":["Orphanet:295187","DOID:0111820","GARD:17357","icd11.foundation:1671375617","MESH:C565223","OMIM:609815","MEDGEN:377870","UMLS:C1853294"],"synonyms":[{"name":"SD1, Weidenreich type","type":"exact"},{"name":"SD1a","type":"exact"},{"name":"ZYGODACTYLY 1","type":"related"},{"name":"Zd1","type":"related"},{"name":"Zygodactyly, Weidenreich type","type":"exact"},{"name":"syndactyly type 1, Weidenreich type","type":"exact"},{"name":"syndactyly type 1a","type":"exact"},{"name":"zygodactyly type 1","type":"exact"}],"termid":"MONDO:0012351","xrefs":{"Monarch":{"xref_id":"0012351"}}}


id: GO:0008255
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action characteristic of ecdysis-triggering hormone, a peptide hormone that, upon receptor binding, initiates pre-ecdysis and ecdysis (i.e. cuticle shedding) through direct action on the central nervous system.","definition_xrefs":["PMID:9020043","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide hormone activity","termid":"GO:0005184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0140677","GO:0005515","GO:0098772"],"is_obsolete":false,"name":"ecdysis-triggering hormone activity","termid":"GO:0008255"}


id: GO:0032537
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specific behavior of an organism that are associated with finding a host organism; may include behavioral responses to light, temperature, or chemical emanations from the prospective host.","definition_xrefs":["PMID:11931033","GOC:mah","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavior","termid":"GO:0007610"}],"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":"host-seeking behavior","synonyms":[{"name":"host-seeking behaviour","type":"exact"}],"termid":"GO:0032537"}


id: GO:0039619
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The protein coat that surrounds the infective nucleic acid in some virus particles where the subunits (capsomeres) are arranged to form an icosahedron with T=4 symmetry. The T=4 capsid is composed of 12 pentameric and 30 hexameric capsomeres.","definition_xrefs":["VZ:808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"icosahedral viral capsid","termid":"GO:0019030"}],"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":"T=4 icosahedral viral capsid","termid":"GO:0039619"}


id: PBO:0024823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ath1 complex protein Ath2 nuclease, XP-G family (predicted)","termid":"PBO:0024823"}


id: PBO:0034685
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_intergenic_meiotic_recombination","termid":"PBO:0034685"}


id: FYPO:0001450
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 cells show decreased sensitivity to cold.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"resistance to stress during vegetative growth","termid":"FYPO:0000850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"resistance to cold","synonyms":[{"name":"increased growth during cellular response to cold","type":"exact"},{"name":"increased vegetative cell population growth during cellular response to cold","type":"exact"},{"name":"resistance to cold during mitotic cell cycle","type":"related"},{"name":"resistance to cold during vegetative growth","type":"exact"},{"name":"resistance to low temperature","type":"exact"},{"name":"resistant to cold","type":"exact"}],"termid":"FYPO:0001450"}


id: PBO:0041561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 19 open reading frame 73","termid":"PBO:0041561"}


id: PBO:0005668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell end marker Tea1","termid":"PBO:0005668"}


id: PBO:0062033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily T member 2","termid":"PBO:0062033"}


id: PBO:0086063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function that contains 2 PY motifs; ubiquinated by Rsp5p; overexpression confers resistance to arsenite; green fluorescent protein (GFP)-fusion protein localizes it to the cytoplasm; non-essential gene","termid":"PBO:0086063"}


id: PBO:0033773
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_site-specific_DNA_replication_termination_at_RTS1_barrier","termid":"PBO:0033773"}


id: PBO:0036013
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_acetylation_during_vegetative_growth","termid":"PBO:0036013"}


id: FYPO:0003278
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 position, morphology, or physical characteristics of all or part of the plasma membrane is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"output_of","term_name":"abnormal plasma membrane organization","termid":"FYPO:0000813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal plasma membrane during vegetative growth","synonyms":[{"name":"abnormal plasma membrane during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003278"}


id: PBO:0058462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5191","termid":"PBO:0058462"}


id: FYPO:0005543
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 duration of actomyosin contractile ring contraction is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring contraction","termid":"FYPO:0001364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0004803","FYPO:0000631","FYPO:0000032"],"is_obsolete":false,"name":"increased duration of actomyosin contractile ring contraction","synonyms":[{"name":"increased duration of actomyosin contractile ring contraction during mitotic cell cycle","type":"related"},{"name":"increased duration of actomyosin contractile ring contraction during vegetative growth","type":"exact"},{"name":"increased duration of mitotic actomyosin contractile ring contraction","type":"exact"},{"name":"prolonged actomyosin contractile ring contraction","type":"exact"}],"termid":"FYPO:0005543"}


id: GO:0045858
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any heritable epigenetic process that increases the frequency, rate or extent of protein function by self-perpetuating conformational conversions of normal proteins in healthy cells. This is distinct from, though mechanistically analogous to, disease states associated with prion propagation and amyloidogenesis. A single protein, if it carries a glutamine/asparagine-rich ('prion') domain, can sometimes stably exist in at least two distinct physical states, each associated with a different phenotype; propagation of one of these traits is achieved by a self-perpetuating change in the protein from one form to the other, mediated by conformational changes in the glutamine/asparagine-rich domain. Prion domains are both modular and transferable to other proteins, on which they can confer a heritable epigenetic alteration of function; existing bioinformatics data indicate that they are rare in non-eukarya, but common in eukarya.","definition_xrefs":["GOC:dph","GOC:tb","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of molecular function, epigenetic (obsolete GO:0045858)","synonyms":[{"name":"activation of protein activity, epigenetic","type":"narrow"},{"name":"positive regulation of protein activity, epigenetic","type":"exact"},{"name":"stimulation of protein activity, epigenetic","type":"narrow"},{"name":"up regulation of protein activity, epigenetic","type":"exact"},{"name":"up-regulation of protein activity, epigenetic","type":"exact"},{"name":"upregulation of protein activity, epigenetic","type":"exact"}],"termid":"GO:0045858"}


id: PR:000037300
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein complex composed of two subunits of Schizosaccharomyces pombe serine/threonine-protein kinase cds1 primed by rad3-rad26 complex and activated by autophosphorylation.","definition_xrefs":["PMID:19357077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine/threonine-protein kinase cds1 (Schizosaccharomyces pombe)","termid":"PR:000030002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein kinase cds1 homodimer, phosphorylated 2 (Schizosaccharomyces pombe)","pombase_gene_id":"SPCC18B5.11c","termid":"PR:000037300"}


id: PBO:0029472
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_acid_phosphatase_activity","termid":"PBO:0029472"}


id: SO:1000084
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Sequence variant decreases the stability (half-life) of the transcript.","definition_xrefs":["EBI:www.ebi.ac.uk/mutations/recommendations/mutevent.html"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000084 sequence_variant_decreasing_transcript_stability (obsolete SO:1000084)","synonyms":[{"name":"mutation decreasing transcript stability","type":"related"},{"name":"sequence variant decreasing transcript stability","type":"exact"}],"termid":"SO:1000084"}


id: MONDO:0008587
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tracheobronchopathia osteochondroplastica (TO) is an idiopathic and benign disease of the large airways characterized by submucosal osteocartilaginous nodules presenting in the trachea with or without the involvement of the major bronchi.","definition_xrefs":["Orphanet:3348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tracheobronchopathia osteochondroplastica","secondary_identifiers":["OMIM:189961","SCTID:54675009","MESH:C536977","icd11.foundation:1797446244","UMLS:C3887588","GARD:5235","MEDGEN:854438"],"synonyms":[{"name":"cartilaginous or bony projections into the tracheobronchial lumen","type":"related"},{"name":"tracheobronchopathia osteochondroplastica","type":"exact"},{"name":"tracheobronchopathia osteoplastica","type":"related"},{"name":"tracheopathia osteoplastica","type":"exact"}],"termid":"MONDO:0008587","xrefs":{"Monarch":{"xref_id":"0008587"}}}


id: MONDO:0054561
data:
  {"annotated_genes":["SJAG_04582"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88739],"is_not":false,"summary":null,"term":"MONDO:0054561"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"anauxetic dysplasia","termid":"MONDO:0011773"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04582":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"anauxetic dysplasia 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1384439","OMIM:617396","UMLS:C4479357","DOID:0080962"],"synonyms":[{"name":"ANXD2","type":"related"},{"name":"anauxetic dysplasia 2","type":"exact"}],"termid":"MONDO:0054561","terms_by_termid":{"MONDO:0054561":null},"xrefs":{"Monarch":{"xref_id":"0054561"}}}


id: MOD:00566
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Unimod","termid":"MOD:00003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"label cysteine with IGBP reagent","synonyms":[{"name":"IGBP","type":"related"},{"name":"Light IDBEST tag for quantitation","type":"related"}],"termid":"MOD:00566"}


id: PBO:0062635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 11 subfamily J member 2 pseudogene","termid":"PBO:0062635"}


id: PBO:0074459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingomyelin phosphodiesterase 4","termid":"PBO:0074459"}


id: PBO:0059561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1E","termid":"PBO:0059561"}


id: PBO:0071384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L30 pseudogene 7","termid":"PBO:0071384"}


id: PBO:0061542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSUN5 pseudogene 2","termid":"PBO:0061542"}


id: PBO:0000513
data:
  {"annotation_feature_type":"gene","cv_name":"sequence_feature","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLS","termid":"PBO:0000513"}


id: PBO:0032702
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9K14_acetylation","termid":"PBO:0032702"}


id: PBO:0088440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pumilio family RNA-binding protein Puf1","termid":"PBO:0088440"}


id: GO:0071652
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of chemokine (C-C motif) ligand 1.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemokine production","termid":"GO:0032642"},{"relation_name":"regulates","term_name":"chemokine (C-C motif) ligand 1 production","termid":"GO:0071610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of chemokine (C-C motif) ligand 1 production","synonyms":[{"name":"regulation of CCL1 production","type":"exact"},{"name":"regulation of T cell activation 3 production","type":"exact"},{"name":"regulation of TCA-3 production","type":"exact"}],"termid":"GO:0071652"}


id: GO:0021844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment and response to guidance cues that distribute interneurons to different cerebral cortex structures.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:jid","GOC:dph","GOC:dgh","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"taxis","termid":"GO:0042330"},{"relation_name":"part_of","term_name":"substrate-independent telencephalic tangential interneuron migration","termid":"GO:0021843"}],"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":"interneuron sorting involved in substrate-independent cerebral cortex tangential migration","termid":"GO:0021844"}


id: GO:0062156
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the ATP-dependent diffusion of a potassium ion across the mitochondrial inner membrane.","definition_xrefs":["PMID:31435016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium channel activity","termid":"GO:0005267"},{"relation_name":"is_a","term_name":"ATP-gated ion channel activity","termid":"GO:0035381"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic cation channel activity","termid":"GO:0099094"}],"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:0003674","GO:0022857"],"is_obsolete":false,"name":"mitochondrial ATP-gated potassium channel activity","synonyms":[{"name":"mitoK-ATP activity","type":"exact"},{"name":"mitochondrial potassium channel activity","type":"exact"}],"termid":"GO:0062156"}


id: MONDO:0003949
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cervical adenoma malignum (obsolete MONDO:0003949)","termid":"MONDO:0003949","xrefs":{"Monarch":{"xref_id":"0003949"}}}


id: GO:0034279
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9-alpha-copalyl diphosphate = 9-beta-pimara-7,15-diene + diphosphate.","definition_xrefs":["RHEA:25560"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"syn-pimara-7,15-diene synthase activity","secondary_identifiers":["EC:4.2.3.35","MetaCyc:RXN-4883","KEGG_REACTION:R09117"],"synonyms":[{"name":"9alpha-copalyl-diphosphate diphosphate-lyase (9beta-pimara-7,15-diene-forming) activity","type":"exact"}],"termid":"GO:0034279"}


id: GO:0098657
data:
  {"annotated_genes":["SJAG_03010","SJAG_03777","SJAG_03987","SJAG_01373","SJAG_00991","SJAG_03591","SJAG_00800","SJAG_03250","SJAG_02511","SJAG_02463","SJAG_03088","SJAG_03268","SJAG_00114","SJAG_01353","SJAG_04465","SJAG_04343","SJAG_04466","SJAG_03086","SJAG_01017","SJAG_01964","SJAG_03718","SJAG_04666","SJAG_03596","SJAG_01406","SJAG_00514","SJAG_00938","SJAG_02684","SJAG_02707","SJAG_02245","SJAG_04886","SJAG_03146","SJAG_05209","SJAG_00355","SJAG_03970","SJAG_00402","SJAG_00104","SJAG_03137","SJAG_00700","SJAG_04668","SJAG_00521","SJAG_01268","SJAG_03119","SJAG_04551","SJAG_02779","SJAG_04637","SJAG_04718","SJAG_02104","SJAG_01206","SJAG_02857","SJAG_05175","SJAG_01748","SJAG_02572","SJAG_02735","SJAG_02075","SJAG_04905","SJAG_02177","SJAG_00907","SJAG_00152","SJAG_04506","SJAG_02780","SJAG_02789","SJAG_04714","SJAG_01686","SJAG_04673","SJAG_00296","SJAG_05296","SJAG_02626","SJAG_02605","SJAG_04479","SJAG_00032","SJAG_04051","SJAG_04724","SJAG_00137","SJAG_01493","SJAG_04001","SJAG_01030","SJAG_04931","SJAG_00546","SJAG_00185","SJAG_05011","SJAG_04246","SJAG_03044","SJAG_00922","SJAG_00649","SJAG_04185","SJAG_02805","SJAG_02883","SJAG_02877","SJAG_04509","SJAG_03504","SJAG_01732","SJAG_02282","SJAG_01981","SJAG_01090","SJAG_04052","SJAG_04830","SJAG_00405","SJAG_01167","SJAG_00803","SJAG_03404","SJAG_03608","SJAG_04100","SJAG_03960","SJAG_03667","SJAG_03643","SJAG_01379","SJAG_03145","SJAG_03465","SJAG_00970","SJAG_02968","SJAG_01983","SJAG_00057","SJAG_04457","SJAG_02384","SJAG_03631","SJAG_05229","SJAG_03581","SJAG_01258","SJAG_01722","SJAG_01384","SJAG_04050","SJAG_03011","SJAG_04644","SJAG_04554","SJAG_03072","SJAG_01660","SJAG_05198","SJAG_03595","SJAG_02320","SJAG_05346","SJAG_04517","SJAG_02834","SJAG_02166","SJAG_02228","SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098702"},{"annotations":[81015,73551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905135"},{"annotations":[68214,76221,94292,116455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098703"},{"annotations":[94481,114919,110039,104688,119551,94098,112683,76226,120924,107684,93436,113678,114318,98209,110319,96805,75396,80053,58573,81528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072583"},{"annotations":[89806,116608],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098705"},{"annotations":[119240],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098708"},{"annotations":[93955],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905136"},{"annotations":[73648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140206"},{"annotations":[74017,90021,81086,72146,71552,74067,81572,73212,92627,112256,80362,100837,76127,101798,101616,108827,79474,107114,77755,107131,73953,77137,107886,95940,73111,75593,81372,91707,79532,95916,73324,75074,103663,110963,75724,81823,99843,101644,100765,77029,71930,104064,73577,120885,81953,104460,111053,118212,92556,81593,101400,103396,89500,106577,105263,89993,105014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006897"},{"annotations":[89857],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120207"},{"annotations":[112641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140425"},{"annotations":[94384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140270"},{"annotations":[97437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098709"},{"annotations":[114555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098710"},{"annotations":[115222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098711"},{"annotations":[102295],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097638"},{"annotations":[102296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097639"},{"annotations":[103599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098714"},{"annotations":[103600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098715"},{"annotations":[97678],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106081"},{"annotations":[73791,74790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904679"},{"annotations":[93105,115372],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905949"},{"annotations":[96486],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045806"},{"annotations":[89956],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905533"},{"annotations":[89957],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905530"},{"annotations":[81721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098716"},{"annotations":[74231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098717"},{"annotations":[104090],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905665"},{"annotations":[105646],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045807"},{"annotations":[100804,95222,112535,93637],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905589"},{"annotations":[93638,95223,100805],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905534"},{"annotations":[95224],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905626"},{"annotations":[72425,73985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990573"},{"annotations":[102289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905647"},{"annotations":[74856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031623"},{"annotations":[113023,120907,113670],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000369"},{"annotations":[94317,92847,104882,115245,115375,94603,80198,91752,79283],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0030100"},{"annotations":[62894,62566,71068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033214"},{"annotations":[103601],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098720"},{"annotations":[97679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106082"},{"annotations":[67084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902434"},{"annotations":[109965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901583"},{"annotations":[102616],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140125"},{"annotations":[104961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140207"},{"annotations":[74798,113029,107685,120917,80981,81021,80308,94099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070086"},{"annotations":[97450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098721"},{"annotations":[106125,115223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071578"}]},"cv_name":"biological_process","definition":"The directed movement of some substance from outside of a cell into a cell. This may occur via transport across the plasma membrane or via endocytosis.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"}],"gene_count":135,"genes_by_uniquename":{"SJAG_00032":null,"SJAG_00057":null,"SJAG_00104":null,"SJAG_00114":null,"SJAG_00137":null,"SJAG_00152":null,"SJAG_00185":null,"SJAG_00296":null,"SJAG_00355":null,"SJAG_00402":null,"SJAG_00405":null,"SJAG_00514":null,"SJAG_00521":null,"SJAG_00546":null,"SJAG_00649":null,"SJAG_00700":null,"SJAG_00800":null,"SJAG_00803":null,"SJAG_00845":null,"SJAG_00907":null,"SJAG_00922":null,"SJAG_00938":null,"SJAG_00970":null,"SJAG_00991":null,"SJAG_01017":null,"SJAG_01030":null,"SJAG_01090":null,"SJAG_01167":null,"SJAG_01206":null,"SJAG_01258":null,"SJAG_01268":null,"SJAG_01353":null,"SJAG_01373":null,"SJAG_01379":null,"SJAG_01384":null,"SJAG_01406":null,"SJAG_01493":null,"SJAG_01660":null,"SJAG_01686":null,"SJAG_01722":null,"SJAG_01732":null,"SJAG_01748":null,"SJAG_01964":null,"SJAG_01981":null,"SJAG_01983":null,"SJAG_02075":null,"SJAG_02104":null,"SJAG_02166":null,"SJAG_02177":null,"SJAG_02228":null,"SJAG_02245":null,"SJAG_02282":null,"SJAG_02320":null,"SJAG_02384":null,"SJAG_02463":null,"SJAG_02511":null,"SJAG_02572":null,"SJAG_02605":null,"SJAG_02626":null,"SJAG_02684":null,"SJAG_02707":null,"SJAG_02735":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_02789":null,"SJAG_02805":null,"SJAG_02834":null,"SJAG_02857":null,"SJAG_02877":null,"SJAG_02883":null,"SJAG_02968":null,"SJAG_03010":null,"SJAG_03011":null,"SJAG_03044":null,"SJAG_03072":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03119":null,"SJAG_03137":null,"SJAG_03145":null,"SJAG_03146":null,"SJAG_03250":null,"SJAG_03268":null,"SJAG_03404":null,"SJAG_03465":null,"SJAG_03504":null,"SJAG_03581":null,"SJAG_03591":null,"SJAG_03595":null,"SJAG_03596":null,"SJAG_03608":null,"SJAG_03631":null,"SJAG_03643":null,"SJAG_03667":null,"SJAG_03718":null,"SJAG_03777":null,"SJAG_03960":null,"SJAG_03970":null,"SJAG_03987":null,"SJAG_04001":null,"SJAG_04050":null,"SJAG_04051":null,"SJAG_04052":null,"SJAG_04100":null,"SJAG_04185":null,"SJAG_04246":null,"SJAG_04343":null,"SJAG_04457":null,"SJAG_04465":null,"SJAG_04466":null,"SJAG_04479":null,"SJAG_04506":null,"SJAG_04509":null,"SJAG_04517":null,"SJAG_04551":null,"SJAG_04554":null,"SJAG_04637":null,"SJAG_04644":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04673":null,"SJAG_04714":null,"SJAG_04718":null,"SJAG_04724":null,"SJAG_04830":null,"SJAG_04886":null,"SJAG_04905":null,"SJAG_04931":null,"SJAG_05011":null,"SJAG_05175":null,"SJAG_05198":null,"SJAG_05209":null,"SJAG_05229":null,"SJAG_05296":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"import into cell","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"uptake","type":"broad"}],"termid":"GO:0098657","terms_by_termid":{"GO:0006897":null,"GO:0030100":null,"GO:0031623":null,"GO:0033214":null,"GO:0045806":null,"GO:0045807":null,"GO:0070086":null,"GO:0071578":null,"GO:0072583":null,"GO:0097638":null,"GO:0097639":null,"GO:0098702":null,"GO:0098703":null,"GO:0098705":null,"GO:0098708":null,"GO:0098709":null,"GO:0098710":null,"GO:0098711":null,"GO:0098714":null,"GO:0098715":null,"GO:0098716":null,"GO:0098717":null,"GO:0098720":null,"GO:0098721":null,"GO:0106081":null,"GO:0106082":null,"GO:0120207":null,"GO:0140125":null,"GO:0140206":null,"GO:0140207":null,"GO:0140270":null,"GO:0140425":null,"GO:1901583":null,"GO:1902434":null,"GO:1904679":null,"GO:1905135":null,"GO:1905136":null,"GO:1905530":null,"GO:1905533":null,"GO:1905534":null,"GO:1905589":null,"GO:1905626":null,"GO:1905647":null,"GO:1905665":null,"GO:1905949":null,"GO:1990573":null,"GO:2000369":null}}


id: MOD:01920
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to 3-hydroxy-L-histidine.","definition_xrefs":["ChEBI:138021","RESID:AA0580","PubMed:21251231"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydroxylated residue","termid":"MOD:00677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxy-L-histidine","synonyms":[{"name":"(2S)-2-amino-3-hydroxy-3-(1H-imidazol-4-yl)propanoic acid","type":"exact"},{"name":"3-hydroxy-L-histidine","type":"exact"},{"name":"MOD_RES (3S)-3-hydroxyhistidine","type":"exact"}],"termid":"MOD:01920"}


id: PBO:0091423
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-Factor precursor","termid":"PBO:0091423"}


id: PBO:0070014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1311, pseudogene","termid":"PBO:0070014"}


id: MONDO:0018834
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete adenylosuccinate synthetase-like 1-related distal myopathy (obsolete MONDO:0018834)","termid":"MONDO:0018834","xrefs":{"Monarch":{"xref_id":"0018834"}}}


id: MONDO:0015144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An inflammatory disease involving a pathogenic inflammatory response in the brain.","definition_xrefs":["MONDO:patterns/inflammatory_disease_by_site"],"gene_count":0,"genotype_count":0,"name":"obsolete brain inflammatory disease (obsolete MONDO:0015144)","secondary_identifiers":["Orphanet:102005"],"synonyms":[{"name":"brain inflammation","type":"exact"},{"name":"inflammation of brain","type":"exact"}],"termid":"MONDO:0015144","xrefs":{"Monarch":{"xref_id":"0015144"}}}


id: GO:0022882
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + beta-glucoside(out) = protein histidine + beta-glucoside phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"},{"relation_name":"is_a","term_name":"beta-glucoside transmembrane transporter activity","termid":"GO:0015573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0016740","GO:0022857","GO:0003824","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-beta-glucoside phosphotransferase system transporter activity","synonyms":[{"name":"beta-glucoside PTS transporter activity","type":"exact"}],"termid":"GO:0022882"}


id: PBO:0048712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutaredoxin 3 pseudogene 1","termid":"PBO:0048712"}


id: MONDO:0017394
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ketamine-induced biliary dilatation is an acquired biliary tract disease caused by the abusive consumption of ketamine, which results in the fusiform dilatation of the common bile ducts (CBD) without obstructive lesions or dilatation of the intrahepatic biliary ducts. Possible manifestations of the underlying cholangiopathy include epigastric pain and impaired liver function. Severity of CBD dilatation appears to correlate with the duration of ketamine consumption and the condition has been reported to be reversible in abstinent patients.","definition_xrefs":["Orphanet:293807"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biliary tract disorder","termid":"MONDO:0004868"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"ketamine-induced biliary dilatation","secondary_identifiers":["SCTID:726613003","UMLS:C4512018","MEDGEN:1380193"],"termid":"MONDO:0017394","xrefs":{"Monarch":{"xref_id":"0017394"}}}


id: PBO:0059215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MRNIP divergent transcript","termid":"PBO:0059215"}


id: MONDO:0018771
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A congenital heart malformation that involves the interventricular septum.","definition_xrefs":["MONDO:patterns/location"],"gene_count":0,"genotype_count":0,"name":"obsolete congenital anomaly of ventricular septum (obsolete MONDO:0018771)","secondary_identifiers":["Orphanet:474347"],"synonyms":[{"name":"congenital anomaly of interventricular communication","type":"exact"},{"name":"congenital heart malformation of interventricular septum","type":"exact"},{"name":"congenital ventricular septal anomaly","type":"exact"},{"name":"interventricular septum congenital heart malformation","type":"exact"},{"name":"rare congenital anomaly of ventricular septum","type":"related"}],"termid":"MONDO:0018771","xrefs":{"Monarch":{"xref_id":"0018771"}}}


id: MONDO:0013680
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":"cognitive impairment with or without cerebellar ataxia","secondary_identifiers":["OMIM:614306","MEDGEN:482045","UMLS:C3280415"],"synonyms":[{"name":"CIAT","type":"related"},{"name":"cognitive impairment with or without cerebellar ataxia","type":"exact"}],"termid":"MONDO:0013680","xrefs":{"Monarch":{"xref_id":"0013680"}}}


id: PBO:0040083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARSD antisense RNA 1","termid":"PBO:0040083"}


id: GO:0030350
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an iron-responsive element, a regulatory sequence found in the 5'- and 3'-untranslated regions of mRNAs encoding many iron-binding proteins.","definition_xrefs":["PMID:3198610","PMID:8710843"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA binding","termid":"GO:0003729"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0003723","GO:0005488"],"is_obsolete":false,"name":"iron-responsive element binding","synonyms":[{"name":"IRE binding","type":"exact"}],"termid":"GO:0030350"}


id: GO:0044341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of phosphate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore, by a mechanism dependent upon sodium ions.","definition_xrefs":["GOC:BHF","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate ion transport","termid":"GO:0006817"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"sodium-dependent phosphate transport","termid":"GO:0044341"}


id: PBO:0062485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily B member 1 pseudogene","termid":"PBO:0062485"}


id: PR:Q9UUH2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- bmt2 gene.","definition_xrefs":["UniProtKB:Q9UUH2","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":"25S rRNA adenine-N(1) methyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC630.10","synonyms":[{"name":"Spom972h-bmt2","type":"exact"}],"termid":"PR:Q9UUH2"}


id: PBO:0076399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAF1A antisense RNA 1","termid":"PBO:0076399"}


id: GO:1904175
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone demethylase activity (H3-K4 specific).","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","PMID:24843136","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone demethylase activity (H3-K4 specific) (obsolete GO:1904175)","synonyms":[{"name":"activation of histone demethylase activity (H3-K4 specific)","type":"narrow"},{"name":"up regulation of histone demethylase activity (H3-K4 specific)","type":"exact"},{"name":"up-regulation of histone demethylase activity (H3-K4 specific)","type":"exact"},{"name":"upregulation of histone demethylase activity (H3-K4 specific)","type":"exact"}],"termid":"GO:1904175"}


id: GO:0004068
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate = beta-alanine + CO2.","definition_xrefs":["EC:4.1.1.11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"aspartate 1-decarboxylase activity","secondary_identifiers":["RHEA:19497","MetaCyc:ASPDECARBOX-RXN"],"synonyms":[{"name":"L-aspartate 1-carboxy-lyase (beta-alanine-forming)","type":"related"},{"name":"L-aspartate 1-carboxy-lyase activity","type":"related"},{"name":"L-aspartate alpha-decarboxylase activity","type":"related"},{"name":"aspartate alpha-decarboxylase activity","type":"related"},{"name":"aspartic alpha-decarboxylase","type":"broad"}],"termid":"GO:0004068"}


id: MONDO:0007320
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chondrocalcinosis","termid":"MONDO:0001314"}],"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":"chondrocalcinosis due to apatite crystal deposition","secondary_identifiers":["MEDGEN:349317","MESH:C535939","UMLS:C1861580","OMIM:118610"],"synonyms":[{"name":"chondrocalcinosis due to apatite crystal deposition","type":"exact"},{"name":"familial apatite disease","type":"related"}],"termid":"MONDO:0007320","xrefs":{"Monarch":{"xref_id":"0007320"}}}


id: PBO:0000899
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds STREP motif","termid":"PBO:0000899"}


id: GO:0047453
data:
  {"annotated_genes":["SJAG_03669"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79294],"is_not":false,"summary":null,"term":"GO:0047453"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (6S)-6beta-hydroxy-1,4,5,6-tetrahydronicotinamide adenine dinucleotide + ATP = ADP + H+ + NAD(P)H + phosphate.","definition_xrefs":["EC:4.2.1.93","PMID:3061454"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03669":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"ATP-dependent NAD(P)H-hydrate dehydratase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R00129","Reactome:R-HSA-6806967","MetaCyc:4.2.1.93-RXN"],"synonyms":[{"name":"(6S)-beta-6-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine-dinucleotide hydro-lyase (ATP-hydrolysing)","type":"related"},{"name":"(6S)-beta-6-hydroxy-1,4,5,6-tetrahydronicotinamide-adenine-dinucleotide hydro-lyase(ATP-hydrolysing; NADH-forming)","type":"related"},{"name":"ATP-dependent H(4)NAD(P)OH dehydratase activity","type":"exact"},{"name":"ATP-dependent H4NAD(P)OH dehydratase activity","type":"exact"},{"name":"reduced nicotinamide adenine dinucleotide hydrate dehydratase activity","type":"broad"}],"termid":"GO:0047453","terms_by_termid":{"GO:0047453":null}}


id: PBO:0000443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRCT domain","termid":"PBO:0000443"}


id: GO:0120256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of an olefinic compound, any compound which contains a carbon-carbon double bond (aka C=C).","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"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":"olefinic compound catabolic process","synonyms":[{"name":"alkene substituted compound breakdown","type":"exact"},{"name":"alkene substituted compound catabolic process","type":"exact"},{"name":"alkene substituted compound catabolism","type":"exact"},{"name":"alkene substituted compound degradation","type":"exact"}],"termid":"GO:0120256"}


id: GO:0051826
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of synapse structural plasticity.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"is_a","term_name":"regulation of synapse structural plasticity","termid":"GO:0051823"}],"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 synapse structural plasticity","synonyms":[{"name":"down regulation of synapse structural plasticity","type":"exact"},{"name":"down-regulation of synapse structural plasticity","type":"exact"},{"name":"downregulation of synapse structural plasticity","type":"exact"},{"name":"inhibition of synapse structural plasticity","type":"narrow"}],"termid":"GO:0051826"}


id: PBO:0089086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane copper transporter complex subunit Ctr5","termid":"PBO:0089086"}


id: PBO:0086684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; identified by homology to uncharacterized proteins in other fungi","termid":"PBO:0086684"}


id: MONDO:0001144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"paralytic strabismus","termid":"MONDO:0001143"},{"relation_name":"is_a","term_name":"oculomotor nerve paralysis","termid":"MONDO:0001309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial third-nerve palsy","secondary_identifiers":["UMLS:C0271370","DOID:10864","SCTID:194118007","MEDGEN:75745","ICD9:378.51"],"synonyms":[{"name":"partial third nerve palsy","type":"exact"},{"name":"third nerve palsy with pupil sparing","type":"exact"},{"name":"third or oculomotor nerve palsy, partial","type":"exact"}],"termid":"MONDO:0001144","xrefs":{"Monarch":{"xref_id":"0001144"}}}


id: MONDO:0011477
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any tooth agenesis in which the cause of the disease is a mutation in the PAX9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tooth agenesis","termid":"MONDO:0005486"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth agenesis, selective, 3","secondary_identifiers":["OMIM:604625","MEDGEN:410035","GARD:18247","UMLS:C1970291","MESH:C567036"],"synonyms":[{"name":"PAX9 tooth agenesis","type":"exact"},{"name":"STHAG3","type":"related"},{"name":"hypodontia/oligodontia 3","type":"related"},{"name":"tooth agenesis caused by mutation in PAX9","type":"exact"},{"name":"tooth agenesis, selective, 3","type":"exact"},{"name":"tooth agenesis, selective, type 3","type":"exact"}],"termid":"MONDO:0011477","xrefs":{"Monarch":{"xref_id":"0011477"}}}


id: PBO:0004712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tel2 interacting protein Tti2, predicted ASTRA complex subunit","termid":"PBO:0004712"}


id: PBO:0047781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FOXD2 adjacent opposite strand RNA 1","termid":"PBO:0047781"}


id: GO:0031531
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a receptor for thyrotropin-releasing hormone, a tripeptide hormone that is produced by the hypothalamus and stimulates the release of thyroid-stimulating hormone (TSH) and prolactin by the anterior pituitary.","definition_xrefs":["PMID:8592728"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"},{"relation_name":"is_a","term_name":"peptide hormone receptor binding","termid":"GO:0051428"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"thyrotropin-releasing hormone receptor binding","secondary_identifiers":["GO:0031888"],"synonyms":[{"name":"thyrotropin releasing hormone receptor binding","type":"exact"},{"name":"thyrotropin-releasing hormone receptor ligand","type":"narrow"}],"termid":"GO:0031531"}


id: MONDO:0011068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing type 1 diabetes mellitus in which the cause of the disease is a mutation in the CTLA4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene","MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"},{"relation_name":"is_a","term_name":"diabetes mellitus, insulin-dependent, X-linked, susceptibility to","termid":"MONDO:0010255"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 1 diabetes mellitus 12","secondary_identifiers":["UMLS:C1832392","MESH:C563326","OMIM:601388","DOID:0110751","MEDGEN:318618"],"synonyms":[{"name":"CTLA4 type 1 diabetes mellitus","type":"exact"},{"name":"IDDM12","type":"exact"},{"name":"diabetes mellitus, insulin-dependent, 12","type":"related"},{"name":"diabetes mellitus, insulin-dependent, type 12","type":"exact"},{"name":"insulin-dependent diabetes mellitus 12","type":"exact"},{"name":"type 1 diabetes mellitus caused by mutation in CTLA4","type":"exact"}],"termid":"MONDO:0011068","xrefs":{"Monarch":{"xref_id":"0011068"}}}


id: PBO:0054632
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 2037","termid":"PBO:0054632"}


id: GO:0060512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a prostate gland are generated and organized.","definition_xrefs":["PMID:18977204","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"gland morphogenesis","termid":"GO:0022612"},{"relation_name":"part_of","term_name":"prostate gland development","termid":"GO:0030850"}],"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":"prostate gland morphogenesis","termid":"GO:0060512"}


id: PBO:0075131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein U5 subunit 40","termid":"PBO:0075131"}


id: GO:0050023
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-fuconate = 2-dehydro-3-deoxy-L-fuconate + H2O.","definition_xrefs":["EC:4.2.1.68","RHEA:22772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"L-fuconate dehydratase activity","secondary_identifiers":["KEGG_REACTION:R03688","MetaCyc:L-FUCONATE-HYDRATASE-RXN"],"synonyms":[{"name":"L-fuconate hydratase activity","type":"exact"},{"name":"L-fuconate hydro-lyase (2-dehydro-3-deoxy-L-fuconate-forming)","type":"related"},{"name":"L-fuconate hydro-lyase activity","type":"related"}],"termid":"GO:0050023"}


id: PBO:0048951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GOT2 pseudogene 2","termid":"PBO:0048951"}


id: GO:0030009
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A cofactor for the serine protease complement factor I.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete complement factor H activity (obsolete GO:0030009)","synonyms":[{"name":"complement factor H activity","type":"exact"}],"termid":"GO:0030009"}


id: GO:0102909
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: NAD + 2-hydroxyglutarate = H+ + 2-oxoglutarate + NADH.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete alpha-ketoglutarate reductase activity (NADH-dependent) (obsolete GO:0102909)","termid":"GO:0102909"}


id: PBO:0072605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal L24 domain containing 1","termid":"PBO:0072605"}


id: PBO:0058576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6513","termid":"PBO:0058576"}


id: PBO:0058746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6870","termid":"PBO:0058746"}


id: GO:0032199
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The synthesis of DNA from an RNA transposon intermediate.","definition_xrefs":["GOC:txnOH","GOC:jp","ISBN:1555812090"],"gene_count":0,"genotype_count":0,"name":"obsolete reverse transcription involved in RNA-mediated transposition (obsolete GO:0032199)","synonyms":[{"name":"reverse transcription during retrotransposition","type":"exact"}],"termid":"GO:0032199"}


id: MONDO:0008710
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Carpenter syndrome in which the cause of the disease is a mutation in the RAB23 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Carpenter syndrome","termid":"MONDO:0019012"}],"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":"RAB23-related Carpenter syndrome","secondary_identifiers":["SCTID:205813009","MEDGEN:1644017","GARD:15128","UMLS:C4551510","OMIM:201000"],"synonyms":[{"name":"ACPS 2","type":"broad"},{"name":"CARPENTER syndrome 1","type":"related"},{"name":"CRPT1","type":"related"},{"name":"Carpenter syndrome","type":"broad"},{"name":"Carpenter syndrome 1","type":"exact"},{"name":"Carpenter syndrome caused by mutation in RAB23","type":"exact"},{"name":"Carpenter syndrome type 1","type":"exact"},{"name":"RAB23 Carpenter syndrome","type":"exact"},{"name":"RAB23-related Carpenter syndrome","type":"exact"},{"name":"acrocephalopolysyndactyly type 2","type":"broad"}],"termid":"MONDO:0008710","xrefs":{"Monarch":{"xref_id":"0008710"}}}


id: PBO:0027655
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_cycle_regulation_during_cellular_response_to_ionizing_radiation_during_mitotic_G2_phase","termid":"PBO:0027655"}


id: FYPO:0006809
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 shortening of the poly(A) tail of a messenger RNA (mRNA) molecule is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA catabolic process during vegetative growth","termid":"FYPO:0002137"},{"relation_name":"is_a","term_name":"abnormal deadenylation-dependent decay","termid":"FYPO:0006808"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000294","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased nuclear-transcribed mRNA poly(A) tail shortening","synonyms":[{"name":"decreased nuclear-transcribed mRNA poly(A) tail shortening during mitotic cell cycle","type":"related"},{"name":"decreased nuclear-transcribed mRNA poly(A) tail shortening during vegetative growth","type":"exact"},{"name":"reduced nuclear-transcribed mRNA poly(A) tail shortening","type":"exact"}],"termid":"FYPO:0006809"}


id: PBO:0063333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2","termid":"PBO:0063333"}


id: PBO:0027507
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-spores_sensitive_to_acetone","termid":"PBO:0027507"}


id: PBO:0090269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP II complex subunit Trs65","termid":"PBO:0090269"}


id: MONDO:1012133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin G deficiency, non-human animal","termid":"MONDO:1011727"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin G deficiency, horse","secondary_identifiers":["OMIA:000554-9796"],"termid":"MONDO:1012133","xrefs":{"Monarch":{"xref_id":"1012133"}}}


id: PBO:0064417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenylethanolamine N-methyltransferase","termid":"PBO:0064417"}


id: FYPO:0001208
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 a specific substance measured in a cell is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"},{"relation_name":"is_a","term_name":"substance absent from cell","termid":"FYPO:0001888"}],"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:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"substance absent from cell during vegetative growth","synonyms":[{"name":"substance absent from cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001208"}


id: MONDO:0000611
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease of cellular proliferation that results in abnormal growths in the body, which do not invade or destroy the surrounding tissue but, given enough time, will transform into a cancer.","definition_xrefs":["DOID:0060071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"},{"relation_name":"is_a","term_name":"precancerous condition","termid":"MONDO:0021074"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-malignant neoplasm","secondary_identifiers":["UMLS:C5817154","MEDGEN:1837212"],"termid":"MONDO:0000611","xrefs":{"Monarch":{"xref_id":"0000611"}}}


id: GO:1901448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of response to butan-1-ol.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to alcohol","termid":"GO:1901419"},{"relation_name":"regulates","term_name":"response to butan-1-ol","termid":"GO:1901422"}],"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 response to butan-1-ol","termid":"GO:1901448"}


id: GO:0014038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Schwann cell differentiation.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glial cell differentiation","termid":"GO:0045685"},{"relation_name":"regulates","term_name":"Schwann cell differentiation","termid":"GO:0014037"}],"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 Schwann cell differentiation","termid":"GO:0014038"}


id: MONDO:0008424
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":"sella turcica, bridged","secondary_identifiers":["MEDGEN:356654","OMIM:182200","UMLS:C1866959","MESH:C566689"],"synonyms":[{"name":"sella turcica, bridged","type":"exact"}],"termid":"MONDO:0008424","xrefs":{"Monarch":{"xref_id":"0008424"}}}


id: MONDO:0044784
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign soft tissue neoplasm characterized by the presence of spindle and stellate cells, lobulated growth pattern, and myxoid stroma formation.","definition_xrefs":["NCIT:C6577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign soft tissue neoplasm","termid":"MONDO:0044335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myxoma","secondary_identifiers":["MEDGEN:10160","ONCOTREE:MYXO","MESH:D009232","UMLS:C0027149","SCTID:404082003"],"synonyms":[{"name":"MYXOMA, BENIGN","type":"exact"},{"name":"Myxoma","type":"exact"}],"termid":"MONDO:0044784","xrefs":{"Monarch":{"xref_id":"0044784"}}}


id: GO:0010339
data:
  {"annotated_genes":["SJAG_04864","SJAG_04720","SJAG_00239","SJAG_01755","SJAG_01975","SJAG_04723"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90562],"is_not":false,"summary":null,"term":"GO:0010339"},{"annotations":[104920,108829,104921,118589,104666],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070263"}]},"cv_name":"cellular_component","definition":"The side of the cell wall that is opposite to the side that faces the cell and its contents.","definition_xrefs":["GOC:mtg_sensu","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cell wall","termid":"GO:0005618"},{"relation_name":"part_of","term_name":"cell surface","termid":"GO:0009986"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00239":null,"SJAG_01755":null,"SJAG_01975":null,"SJAG_04720":null,"SJAG_04723":null,"SJAG_04864":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0009986"},{"rel_name":"part_of","termid":"GO:0005618"}],"interesting_parent_ids":["GO:0005575","GO:0009986","GO:0005618"],"is_obsolete":false,"name":"external side of cell wall","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010339","terms_by_termid":{"GO:0010339":null,"GO:0070263":null}}


id: PBO:0017618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic cohesin-associated protein Pds5","termid":"PBO:0017618"}


id: FYPO:0002333
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_01143:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"711-723","gene_uniquename":"SJAG_01143","name":"mid1-delta(711-723 a.a.)","uniquename":"SJAG_01143:allele-2"},"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_03250:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03250","name":"sst4delta","uniquename":"SJAG_03250:allele-1"},"SJAG_03596:allele-1":{"allele_type":"amino_acid_mutation","description":"L264P,P442T","gene_uniquename":"SJAG_03596","name":"cdc15-A","uniquename":"SJAG_03596:allele-1"},"SJAG_03783:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03783","name":"vps24delta","uniquename":"SJAG_03783:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"},"SJAG_03892:allele-2":{"allele_type":"amino_acid_mutation","description":"E233Q","gene_uniquename":"SJAG_03892","name":"Vps4-EQ","uniquename":"SJAG_03892:allele-2"},"SJAG_03892:allele-3":{"allele_type":"amino_acid_mutation","description":"I307T L327S","gene_uniquename":"SJAG_03892","name":"vps4-ts","uniquename":"SJAG_03892:allele-3"},"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"},"SJAG_04349:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04349","name":"vps28delta","uniquename":"SJAG_04349:allele-1"},"SJAG_04489:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04489","name":"did4delta","uniquename":"SJAG_04489:allele-1"},"SJAG_04912:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04912","name":"vps25delta","uniquename":"SJAG_04912:allele-1"},"SJAG_05207:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_05207","name":"cmp7delta","uniquename":"SJAG_05207:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007771"},{"annotations":[121281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005503"},{"annotations":[121596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"},{"annotations":[121283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"},{"annotations":[121279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003946"}],"single_locus_phenotype":[{"annotations":[121583,121582,121581],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001440"},{"annotations":[121592,121593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001370"},{"annotations":[121595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004718"},{"annotations":[121302,121301],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000731"},{"annotations":[121568,121590,121591,121589,121571,121570,121586,121587,121561,121560,121567,121584,121588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007771"},{"annotations":[121275,121683,121686,121684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005503"},{"annotations":[121337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001375"},{"annotations":[121273,121280,121284,121272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"},{"annotations":[121564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007073"},{"annotations":[121685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002870"},{"annotations":[121276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000644"},{"annotations":[121563],"is_not":false,"rel_names":["is_a","output_of"],"summary":null,"term":"FYPO:0003657"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype that affects the localization of a protein in a cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization phenotype","termid":"FYPO:0000138"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00030":null,"SJAG_01050":null,"SJAG_01143":null,"SJAG_01665":null,"SJAG_01745":null,"SJAG_01794":null,"SJAG_02392":null,"SJAG_03250":null,"SJAG_03581":null,"SJAG_03596":null,"SJAG_03703":null,"SJAG_03783":null,"SJAG_03892":null,"SJAG_04280":null,"SJAG_04349":null,"SJAG_04489":null,"SJAG_04498":null,"SJAG_04522":null,"SJAG_04912":null,"SJAG_05207":null},"genotype_count":19,"genotypes_by_uniquename":{"Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"Vps4-EQ(E233Q aa)","display_uniquename":"Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-2","expression":"Not assayed or wild type"}]}]},"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta":{"display_name":"cdc15-A(L264P,P442T aa) mid1delta","display_uniquename":"cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type__mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03596:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"cmp7delta":{"display_name":"cmp7delta","display_uniquename":"cmp7delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]}]},"cmp7delta__vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cmp7delta vps4-ts(I307T L327S aa)","display_uniquename":"cmp7delta__vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-3","expression":"Not assayed or wild type"}]}]},"did4delta":{"display_name":"did4delta","display_uniquename":"did4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04489:allele-1","expression":"Null"}]}]},"lem2delta":{"display_name":"lem2delta","display_uniquename":"lem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01745:allele-1","expression":"Null"}]}]},"mid1-delta(711-723_a.a.)-711-723-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"mid1-delta(711-723 a.a.)(aa)","display_uniquename":"mid1-delta(711-723_a.a.)-711-723-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-2","expression":"Not assayed or wild type"}]}]},"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"nur1delta":{"display_name":"nur1delta","display_uniquename":"nur1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]}]},"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"sst4delta":{"display_name":"sst4delta","display_uniquename":"sst4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03250:allele-1","expression":"Null"}]}]},"vps24delta":{"display_name":"vps24delta","display_uniquename":"vps24delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03783:allele-1","expression":"Null"}]}]},"vps25delta":{"display_name":"vps25delta","display_uniquename":"vps25delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04912:allele-1","expression":"Null"}]}]},"vps28delta":{"display_name":"vps28delta","display_uniquename":"vps28delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04349:allele-1","expression":"Null"}]}]},"vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"vps4-ts(I307T L327S aa)","display_uniquename":"vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-3","expression":"Not assayed or wild type"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]},"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"wee1-as8(T582G aa)","display_uniquename":"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_02392","SJAG_03596","SJAG_03892","SJAG_01050","SJAG_01143","SJAG_05207"],"name":"protein localization phenotype","references_by_uniquename":{"PMID:25866389":null,"PMID:30664646":null,"PMID:32109380":null,"PMID:32243490":null},"single_locus_annotated_genes":["SJAG_03783","SJAG_03250","SJAG_04912","SJAG_05207","SJAG_01050","SJAG_02392","SJAG_04349","SJAG_01745","SJAG_04280","SJAG_01143","SJAG_04489","SJAG_03892"],"single_locus_genotype_uniquenames":["mid1delta","sst4delta","vps25delta","vps24delta","vps28delta","did4delta","Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type","cmp7delta","nur1delta","mid1-delta(711-723_a.a.)-711-723-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","lem2delta","pom1delta","vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","vps4delta"],"synonyms":[{"name":"cellular protein localization phenotype","type":"exact"},{"name":"fission yeast protein localization phenotype","type":"exact"},{"name":"protein localisation phenotype","type":"exact"}],"termid":"FYPO:0002333","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000137":null,"FYECO:0000338":null,"FYPO:0000644":null,"FYPO:0000731":null,"FYPO:0001132":null,"FYPO:0001370":null,"FYPO:0001375":null,"FYPO:0001440":null,"FYPO:0002870":null,"FYPO:0003657":null,"FYPO:0003946":null,"FYPO:0004718":null,"FYPO:0005503":null,"FYPO:0007073":null,"FYPO:0007177":null,"FYPO:0007771":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null,"GO:0000815":null}}


id: MONDO:1012166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitral valve disease, non-human animal","termid":"MONDO:1011643"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitral valve disease, dog","secondary_identifiers":["OMIA:000654-9615"],"termid":"MONDO:1012166","xrefs":{"Monarch":{"xref_id":"1012166"}}}


id: GO:0033102
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding an acidocalcisome.","definition_xrefs":["GOC:ecd","PMID:11378195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bounding membrane of organelle","termid":"GO:0098588"},{"relation_name":"part_of","term_name":"acidocalcisome","termid":"GO:0020022"}],"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":"acidocalcisome membrane","termid":"GO:0033102"}


id: MOD:01558
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ8plex-117 reporter+balance group.","definition_xrefs":["Unimod:730#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ8plex-117 reporter+balance reagent acylated residue","termid":"MOD:01556"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent N-acylated residue","termid":"MOD:01710"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"iTRAQ8plex-117 reporter+balance reagent N6-acylated lysine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"Representative mass and accurate mass for 113, 114, 116 & 117","type":"related"},{"name":"iTRAQ8plex","type":"related"},{"name":"iTRAQ8plex:13C(7)15N(1)","type":"related"}],"termid":"MOD:01558"}


id: MONDO:1012246
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"rod-cone dysplasia, non-human animal","termid":"MONDO:1011982"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rod-cone dysplasia, dog","secondary_identifiers":["OMIA:000881-9615"],"termid":"MONDO:1012246","xrefs":{"Monarch":{"xref_id":"1012246"}}}


id: GO:0098767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. M phase during meiosis II.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete meiosis II M phase (obsolete GO:0098767)","termid":"GO:0098767"}


id: PBO:0044640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decapping mRNA 2","termid":"PBO:0044640"}


id: GO:0061962
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency or rate of heme oxygenase activity.","definition_xrefs":["PMID:24844779","GOC:BHF_miRNA","GOC:BHF","GOC:rph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of heme oxygenase activity (obsolete GO:0061962)","termid":"GO:0061962"}


id: PBO:0069501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 768, pseudogene","termid":"PBO:0069501"}


id: MONDO:0014784
data:
  {"annotated_genes":["SJAG_04500"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87610],"is_not":false,"summary":null,"term":"MONDO:0014784"}]},"cv_name":"mondo","definition":"Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome is a rare, genetic, non-dystrophic congenital myopathy disorder characterized by a neonatal-onset of severe generalized hypotonia associated with mild psychomotor delay, congenital strabismus with abducens nerve palsy, and atrial and/or ventricular septal defects. Cryptorchidism is commonly reported in male patients and muscle biopsy typically reveals increased variability in muscle fiber size.","definition_xrefs":["Orphanet:467176"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04500":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005267"],"is_obsolete":false,"name":"severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:902080","UMLS:C4225196","GARD:17840","OMIM:616816"],"synonyms":[{"name":"IHPMR","type":"exact"},{"name":"hypotonia, infantile, with psychomotor retardation","type":"exact"}],"termid":"MONDO:0014784","terms_by_termid":{"MONDO:0014784":null},"xrefs":{"Monarch":{"xref_id":"0014784"}}}


id: PBO:0065372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"presenilin enhancer, gamma-secretase subunit","termid":"PBO:0065372"}


id: PBO:0038553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABHD17A pseudogene 8","termid":"PBO:0038553"}


id: PBO:0111892
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain","termid":"PBO:0111892"}


id: PBO:0088063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-protein ligase subunit of the CCR4-NOT complex; with Ubc4p, ubiquitinates nascent polypeptide-associated complex subunits and histone demethyase Jhd2p; CCR4-NOT has roles in transcription regulation, mRNA degradation, and post-transcriptional modifications; regulates levels of DNA Polymerase-{alpha} to promote efficient and accurate DNA replication","termid":"PBO:0088063"}


id: GO:0001909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed killing of a target cell by a leukocyte.","definition_xrefs":["GO_REF:0000022","ISBN:0781735149","PMID:11911826","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell killing","termid":"GO:0001906"},{"relation_name":"is_a","term_name":"leukocyte mediated immunity","termid":"GO:0002443"}],"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":"leukocyte mediated cytotoxicity","synonyms":[{"name":"immune cell mediated cell death","type":"exact"},{"name":"immune cell mediated cell killing","type":"exact"},{"name":"immune cell mediated cytotoxicity","type":"exact"},{"name":"leucocyte mediated cytotoxicity","type":"exact"}],"termid":"GO:0001909"}


id: PBO:0085972
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 contain a single transmembrane domain; mutant has increased aneuploidy tolerance; localized to both the mitochondrial outer membrane and the plasma membrane; protein abundance increases in response to DNA replication stress","termid":"PBO:0085972"}


id: GO:0120549
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->6)-alpha-D-glucosidic linkages to branches with degrees of polymerization of three or four glucose residues in limit dextrin.","definition_xrefs":["EC:3.2.1.196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016798"],"is_obsolete":false,"name":"limit dextrin alpha-1,6-maltotetraose-hydrolase activity","secondary_identifiers":["MetaCyc:RXN0-5146"],"synonyms":[{"name":"glycogen debranching enzyme","type":"exact"}],"termid":"GO:0120549"}


id: GO:0004087
data:
  {"annotated_genes":["SJAG_00392","SJAG_00412","SJAG_00964"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73060,95314,113084],"is_not":false,"summary":null,"term":"GO:0004087"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 ATP + hydrogencarbonate + NH4+ = 2 ADP + carbamoyl phosphate + 2 H+ + phosphate.","definition_xrefs":["EC:6.3.4.16","RHEA:18029"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00392":null,"SJAG_00412":null,"SJAG_00964":null},"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:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"carbamoyl-phosphate synthase (ammonia) activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-70555","KEGG_REACTION:R00149","MetaCyc:RXN-13202"],"synonyms":[{"name":"CPS I activity","type":"narrow"},{"name":"carbamoyl phosphate synthase (ammonia) activity","type":"exact"},{"name":"carbamoyl-phosphate synthetase (ammonia) activity","type":"related"},{"name":"carbamoyl-phosphate synthetase I activity","type":"related"},{"name":"carbamoylphosphate synthase (ammonia)","type":"related"},{"name":"carbamoylphosphate synthase activity","type":"related"},{"name":"carbamoylphosphate synthetase (ammonia) activity","type":"related"},{"name":"carbamylphosphate synthetase I","type":"related"},{"name":"carbamylphosphate synthetase activity","type":"related"},{"name":"carbmoylphosphate synthetase activity","type":"related"},{"name":"carbon-dioxide--ammonia ligase activity","type":"related"},{"name":"carbon-dioxide:ammonia ligase (ADP-forming, carbamate-phosphorylating)","type":"related"}],"termid":"GO:0004087","terms_by_termid":{"GO:0004087":null}}


id: PBO:0024801
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-involved_in","termid":"PBO:0024801"}


id: PBO:0044669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dimethylarginine dimethylaminohydrolase 2","termid":"PBO:0044669"}


id: PBO:0049901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hes family bHLH transcription factor 2","termid":"PBO:0049901"}


id: PBO:0080582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WDR5B divergent transcript","termid":"PBO:0080582"}


id: GO:1901711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of homoserine biosynthetic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of homoserine biosynthetic process","termid":"GO:1901710"},{"relation_name":"is_a","term_name":"negative regulation of amino acid biosynthetic process","termid":"GO:2000283"},{"relation_name":"negatively_regulates","term_name":"homoserine biosynthetic process","termid":"GO:0009090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"negative regulation of homoserine biosynthetic process","synonyms":[{"name":"down regulation of homoserine anabolism","type":"exact"},{"name":"down regulation of homoserine biosynthesis","type":"exact"},{"name":"down regulation of homoserine biosynthetic process","type":"exact"},{"name":"down regulation of homoserine formation","type":"exact"},{"name":"down regulation of homoserine synthesis","type":"exact"},{"name":"down-regulation of homoserine anabolism","type":"exact"},{"name":"down-regulation of homoserine biosynthesis","type":"exact"},{"name":"down-regulation of homoserine biosynthetic process","type":"exact"},{"name":"down-regulation of homoserine formation","type":"exact"},{"name":"down-regulation of homoserine synthesis","type":"exact"},{"name":"downregulation of homoserine anabolism","type":"exact"},{"name":"downregulation of homoserine biosynthesis","type":"exact"},{"name":"downregulation of homoserine biosynthetic process","type":"exact"},{"name":"downregulation of homoserine formation","type":"exact"},{"name":"downregulation of homoserine synthesis","type":"exact"},{"name":"inhibition of homoserine anabolism","type":"exact"},{"name":"inhibition of homoserine biosynthesis","type":"exact"},{"name":"inhibition of homoserine biosynthetic process","type":"narrow"},{"name":"inhibition of homoserine formation","type":"exact"},{"name":"inhibition of homoserine synthesis","type":"exact"},{"name":"negative regulation of homoserine anabolism","type":"exact"},{"name":"negative regulation of homoserine biosynthesis","type":"exact"},{"name":"negative regulation of homoserine formation","type":"exact"},{"name":"negative regulation of homoserine synthesis","type":"exact"}],"termid":"GO:1901711"}


id: PBO:0018062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 Ubc8 (predicted)","termid":"PBO:0018062"}


id: FYPO:0003929
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which spores germinate to a lower extent than wild type following exposure to ionizing radiation.","definition_xrefs":["PMID:24847916","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell phenotype","termid":"FYPO:0003037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"spores sensitive to ionizing radiation","synonyms":[{"name":"sensitive to ionizing radiation in the spore phase","type":"exact"},{"name":"spores sensitive to IR","type":"exact"}],"termid":"FYPO:0003929"}


id: MONDO:0010668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Skeletal dysplasia-intellectual disability syndrome combines skeletal anomalies (short stature, ridging of the metopic suture, fusion of cervical vertebrae, thoracic hemivertebrae, scoliosis, sacral hypoplasia and short middle phalanges) and mild intellectual deficit. It has been described in four male cousins in three sibships. Glucose intolerance was present in three cases, and imperforated anus in one case. Carrier females had minor manifestations (fusion of cervical vertebrae and glucose intolerance). Transmission seems to be X-linked.","definition_xrefs":["Orphanet:1436"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"spondylodysplastic dysplasia","termid":"MONDO:0019694"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"skeletal dysplasia-intellectual disability syndrome","secondary_identifiers":["MEDGEN:326949","OMIM:309620","MESH:C564101","UMLS:C1839729","SCTID:722478008","GARD:3520"],"synonyms":[{"name":"Christian syndrome","type":"exact"},{"name":"MRSD","type":"related"},{"name":"X-linked skeletal dysplasia-intellectual disability syndrome","type":"related"},{"name":"intellectual disability skeletal dysplasia abducens palsy","type":"related"},{"name":"intellectual disability, skeletal dysplasia, and abducens palsy","type":"related"},{"name":"mental retardation skeletal dysplasia abducens palsy","type":"related"},{"name":"mental retardation, skeletal dysplasia, and abducens palsy","type":"related"},{"name":"mental retardation-skeletal dysplasia","type":"exact"}],"termid":"MONDO:0010668","xrefs":{"Monarch":{"xref_id":"0010668"}}}


id: MONDO:0015660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sporadic fetal brain disruption sequence is a rare, non-syndromic, central nervous system malformation disorder characterized by severe microcephaly (average occipitofrontal circumference -5.8 SD), overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly.","definition_xrefs":["Orphanet:1665"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system disorder","termid":"MONDO:0002602"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sporadic fetal brain disruption sequence","secondary_identifiers":["SCTID:763717004","MEDGEN:1636968","UMLS:C4706553","GARD:18734"],"termid":"MONDO:0015660","xrefs":{"Monarch":{"xref_id":"0015660"}}}


id: GO:2001067
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to pullulan.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide binding","termid":"GO:0030247"}],"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":"pullulan binding","termid":"GO:2001067"}


id: PBO:0086422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative GTPase with a role in biogenesis of RNA pol II and polIII; may be involved in assembly of RNA polymerases II and III and in their transport into the nucleus; may have a role in sister chromatid cohesion; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum and vacuole respectively; contains a Gly-Pro-Asn motif in the G domain; similar to Npa3p and Gpn2p","termid":"PBO:0086422"}


id: GO:1902952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of dendritic spine maintenance.","definition_xrefs":["GOC:sjp","GO_REF:0000058","PMID:24328732","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell projection organization","termid":"GO:0031346"},{"relation_name":"is_a","term_name":"regulation of dendritic spine maintenance","termid":"GO:1902950"},{"relation_name":"positively_regulates","term_name":"dendritic spine maintenance","termid":"GO:0097062"}],"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 dendritic spine maintenance","synonyms":[{"name":"activation of dendritic spine maintenance","type":"narrow"},{"name":"up regulation of dendritic spine maintenance","type":"exact"},{"name":"up-regulation of dendritic spine maintenance","type":"exact"},{"name":"upregulation of dendritic spine maintenance","type":"exact"}],"termid":"GO:1902952"}


id: PBO:0074940
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 105","termid":"PBO:0074940"}


id: GO:0033076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving isoquinoline alkaloids, alkaloid compounds that contain bicyclic N-containing aromatic rings and are derived from a 3,4-dihydroxytyramine (dopamine) precursor that undergoes a Schiff base addition with aldehydes of different origin.","definition_xrefs":["PMID:26503307","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaloid metabolic process","termid":"GO:0009820"}],"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":"isoquinoline alkaloid metabolic process","synonyms":[{"name":"ipecac alkaloid metabolism","type":"related"},{"name":"isoquinoline alkaloid metabolism","type":"exact"}],"termid":"GO:0033076"}


id: GO:0070007
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of internal peptide bonds in a polypeptide chain by a mechanism involving a glutamate/glutamine catalytic dyad.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endopeptidase activity","termid":"GO:0004175"},{"relation_name":"is_a","term_name":"glutamic-type peptidase activity","termid":"GO:0070002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0008233"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0008233","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"glutamic-type endopeptidase activity","termid":"GO:0070007"}


id: MONDO:0042911
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":"Schwartz-Cohen-addad-Lambert syndrome","secondary_identifiers":["UMLS:C2931036","MEDGEN:443962","MESH:C535835"],"synonyms":[{"name":"Schwartz Cohen-Addad Lambert syndrome","type":"related"},{"name":"congenital melanocytosis with myelomeningocele and hydrocephalus","type":"related"}],"termid":"MONDO:0042911","xrefs":{"Monarch":{"xref_id":"0042911"}}}


id: GO:0008949
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + oxalyl-CoA = CO2 + formyl-CoA.","definition_xrefs":["RHEA:19333","EC:4.1.1.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"oxalyl-CoA decarboxylase activity","secondary_identifiers":["KEGG_REACTION:R01908","MetaCyc:OXALYL-COA-DECARBOXYLASE-RXN"],"synonyms":[{"name":"oxalyl coenzyme A decarboxylase activity","type":"related"},{"name":"oxalyl-CoA carboxy-lyase (formyl-CoA-forming)","type":"related"},{"name":"oxalyl-CoA carboxy-lyase activity","type":"related"}],"termid":"GO:0008949"}


id: GO:0034066
data:
  {"annotated_genes":["SJAG_00143","SJAG_06588"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[77569,79047],"is_not":false,"summary":null,"term":"GO:0034066"}]},"cv_name":"cellular_component","definition":"A protein complex that acts as a nucleotide exchange factor for the GTPase Ypt6p, and is required for fusion of endosome-derived vesicles with the Golgi.","definition_xrefs":["GOC:jh","GOC:mah","PMID:10990452"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanyl-nucleotide exchange factor complex","termid":"GO:0032045"},{"relation_name":"part_of","term_name":"Golgi apparatus","termid":"GO:0005794"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00143":null,"SJAG_06588":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005794","GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Ric1-Rgp1 guanyl-nucleotide exchange factor complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"Ric1p-Rgp1p complex","type":"related"}],"termid":"GO:0034066","terms_by_termid":{"GO:0034066":null}}


id: PATO:0000525
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000525 soil composition sensitivity value (obsolete PATO:0000525)","termid":"PATO:0000525"}


id: PBO:0059996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 16","termid":"PBO:0059996"}


id: PBO:0075724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermidine synthase","termid":"PBO:0075724"}


id: PBO:0040074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin domain containing 2","termid":"PBO:0040074"}


id: MONDO:0010583
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked form of Dyggve-Melchior-Clausen disease.","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":"Dyggve-Melchior-Clausen disease","termid":"MONDO:0009130"}],"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":"Dyggve-Melchior-Clausen syndrome, X-linked","secondary_identifiers":["GARD:15290","MEDGEN:337052","UMLS:C1844654","OMIM:304950"],"synonyms":[{"name":"Dyggve-Melchior-Clausen disease, X-linked","type":"exact"},{"name":"Dyggve-Melchior-Clausen syndrome, X-linked","type":"exact"},{"name":"X-linked Dyggve-Melchior-Clausen disease","type":"exact"}],"termid":"MONDO:0010583","xrefs":{"Monarch":{"xref_id":"0010583"}}}


id: GO:0046394
data:
  {"annotated_genes":["SJAG_03679","SJAG_03485","SJAG_03553","SJAG_04156","SJAG_03313","SJAG_00305","SJAG_04577","SJAG_00495","SJAG_00832","SJAG_00518","SJAG_00432","SJAG_05007","SJAG_04404","SJAG_04107","SJAG_03914","SJAG_00396","SJAG_03972","SJAG_01935","SJAG_00660","SJAG_05283","SJAG_01300","SJAG_00902","SJAG_00234","SJAG_00337","SJAG_03306","SJAG_00309","SJAG_01126","SJAG_03152","SJAG_03671","SJAG_02313","SJAG_01404","SJAG_01346","SJAG_00248","SJAG_04459","SJAG_05200","SJAG_02689","SJAG_03055","SJAG_04149","SJAG_02007","SJAG_06635","SJAG_03130","SJAG_04425","SJAG_00412","SJAG_03943","SJAG_03275","SJAG_03243","SJAG_00106","SJAG_00635","SJAG_02769","SJAG_00630","SJAG_02450","SJAG_02717","SJAG_01766","SJAG_01592","SJAG_03856","SJAG_01356","SJAG_02225","SJAG_02841","SJAG_02791","SJAG_01238","SJAG_03198","SJAG_02388","SJAG_01574","SJAG_00830","SJAG_00869","SJAG_04145","SJAG_00673","SJAG_00502","SJAG_02400","SJAG_00359","SJAG_01880","SJAG_03526","SJAG_03124","SJAG_04674","SJAG_03312","SJAG_01271","SJAG_04747","SJAG_00107","SJAG_03266","SJAG_00582","SJAG_00592","SJAG_03712","SJAG_02293","SJAG_01946","SJAG_01019","SJAG_02988","SJAG_01137","SJAG_03614","SJAG_01461","SJAG_04972","SJAG_00099","SJAG_02832","SJAG_00392","SJAG_03562","SJAG_04054","SJAG_00815","SJAG_02106","SJAG_01458","SJAG_02972","SJAG_04481","SJAG_04098","SJAG_03167","SJAG_04449","SJAG_00695","SJAG_03985","SJAG_03786","SJAG_04007","SJAG_00636","SJAG_01630","SJAG_00395","SJAG_04688","SJAG_02885","SJAG_03141","SJAG_01061","SJAG_01466","SJAG_03881","SJAG_03457","SJAG_00224","SJAG_00120","SJAG_00881","SJAG_03580","SJAG_04549","SJAG_02290","SJAG_02408","SJAG_01955","SJAG_00529","SJAG_04652","SJAG_04305","SJAG_03180","SJAG_01455","SJAG_02505","SJAG_03775","SJAG_04042"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62030,69930,113093,66747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071266"},{"annotations":[114420,110328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009257"},{"annotations":[74769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008153"},{"annotations":[70140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019413"},{"annotations":[74487,80007,60344,76739,78702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009073"},{"annotations":[79486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006532"},{"annotations":[77960,81123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009102"},{"annotations":[91717,116108,92987,96495,103196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009423"},{"annotations":[80276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019240"},{"annotations":[112501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019344"},{"annotations":[77927,60971,67692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006535"},{"annotations":[70010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006761"},{"annotations":[113539,105574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052699"},{"annotations":[69079,79145,96920,65080,78718,103997,109449,110699,71977,93329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006633"},{"annotations":[113323,75442,81536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030497"},{"annotations":[93837,79514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034625"},{"annotations":[79518,93838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019367"},{"annotations":[70640,114421,110329,61212,106751,57126,108053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046656"},{"annotations":[73236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006542"},{"annotations":[73886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006545"},{"annotations":[75098,73838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019264"},{"annotations":[75369,72904,117806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009090"},{"annotations":[113234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042852"},{"annotations":[104570,113081,100083,72076,108491,113911,112460,120435,80274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042450"},{"annotations":[112788,104106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070981"},{"annotations":[60118,119765,113236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097054"},{"annotations":[58061,60403,72899,78385,82100,65351,77464,80211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000105"},{"annotations":[112502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071269"},{"annotations":[92566,105725,110299,112428,115263,105242,113098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901705"},{"annotations":[92567,59634,78930,81616,105243,115264,76569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009098"},{"annotations":[102609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019280"},{"annotations":[59106,82097,79591,81009,78665,80146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019509"},{"annotations":[100448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019284"},{"annotations":[79720,100268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009094"},{"annotations":[68786,92766,65687,79655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0055129"},{"annotations":[81377,61498,118935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006564"},{"annotations":[75946,75218,70062,79014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000162"},{"annotations":[81617,78813,65024,58873,77837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009099"},{"annotations":[60993,61425,63263,59613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019249"},{"annotations":[99788,76789,99086],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009107"},{"annotations":[74027,106273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042759"},{"annotations":[78448,115462,98278,65968,79240,78012,71922,65303,76800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019878"},{"annotations":[73616,80852,113974,76322,72673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009086"},{"annotations":[72606],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045717"},{"annotations":[74141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006592"},{"annotations":[99611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900535"},{"annotations":[79448,64025,74133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015940"},{"annotations":[65477,113975,71421,78784,62028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009088"},{"annotations":[78449,80533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006571"},{"annotations":[71995,76976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006636"},{"annotations":[76697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006780"},{"annotations":[93841,75439,105419,74387,79516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042761"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of carboxylic acids, any organic acid containing one or more carboxyl (-COOH) groups.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic acid biosynthetic process","termid":"GO:0016053"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":133,"genes_by_uniquename":{"SJAG_00099":null,"SJAG_00106":null,"SJAG_00107":null,"SJAG_00120":null,"SJAG_00224":null,"SJAG_00234":null,"SJAG_00248":null,"SJAG_00305":null,"SJAG_00309":null,"SJAG_00337":null,"SJAG_00359":null,"SJAG_00392":null,"SJAG_00395":null,"SJAG_00396":null,"SJAG_00412":null,"SJAG_00432":null,"SJAG_00495":null,"SJAG_00502":null,"SJAG_00518":null,"SJAG_00529":null,"SJAG_00582":null,"SJAG_00592":null,"SJAG_00630":null,"SJAG_00635":null,"SJAG_00636":null,"SJAG_00660":null,"SJAG_00673":null,"SJAG_00695":null,"SJAG_00815":null,"SJAG_00830":null,"SJAG_00832":null,"SJAG_00869":null,"SJAG_00881":null,"SJAG_00902":null,"SJAG_01019":null,"SJAG_01061":null,"SJAG_01126":null,"SJAG_01137":null,"SJAG_01238":null,"SJAG_01271":null,"SJAG_01300":null,"SJAG_01346":null,"SJAG_01356":null,"SJAG_01404":null,"SJAG_01455":null,"SJAG_01458":null,"SJAG_01461":null,"SJAG_01466":null,"SJAG_01574":null,"SJAG_01592":null,"SJAG_01630":null,"SJAG_01766":null,"SJAG_01880":null,"SJAG_01935":null,"SJAG_01946":null,"SJAG_01955":null,"SJAG_02007":null,"SJAG_02106":null,"SJAG_02225":null,"SJAG_02290":null,"SJAG_02293":null,"SJAG_02313":null,"SJAG_02388":null,"SJAG_02400":null,"SJAG_02408":null,"SJAG_02450":null,"SJAG_02505":null,"SJAG_02689":null,"SJAG_02717":null,"SJAG_02769":null,"SJAG_02791":null,"SJAG_02832":null,"SJAG_02841":null,"SJAG_02885":null,"SJAG_02972":null,"SJAG_02988":null,"SJAG_03055":null,"SJAG_03124":null,"SJAG_03130":null,"SJAG_03141":null,"SJAG_03152":null,"SJAG_03167":null,"SJAG_03180":null,"SJAG_03198":null,"SJAG_03243":null,"SJAG_03266":null,"SJAG_03275":null,"SJAG_03306":null,"SJAG_03312":null,"SJAG_03313":null,"SJAG_03457":null,"SJAG_03485":null,"SJAG_03526":null,"SJAG_03553":null,"SJAG_03562":null,"SJAG_03580":null,"SJAG_03614":null,"SJAG_03671":null,"SJAG_03679":null,"SJAG_03712":null,"SJAG_03775":null,"SJAG_03786":null,"SJAG_03856":null,"SJAG_03881":null,"SJAG_03914":null,"SJAG_03943":null,"SJAG_03972":null,"SJAG_03985":null,"SJAG_04007":null,"SJAG_04042":null,"SJAG_04054":null,"SJAG_04098":null,"SJAG_04107":null,"SJAG_04145":null,"SJAG_04149":null,"SJAG_04156":null,"SJAG_04305":null,"SJAG_04404":null,"SJAG_04425":null,"SJAG_04449":null,"SJAG_04459":null,"SJAG_04481":null,"SJAG_04549":null,"SJAG_04577":null,"SJAG_04652":null,"SJAG_04674":null,"SJAG_04688":null,"SJAG_04747":null,"SJAG_04972":null,"SJAG_05007":null,"SJAG_05200":null,"SJAG_05283":null,"SJAG_06635":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"carboxylic acid biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000043":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"synonyms":[{"name":"carboxylic acid anabolism","type":"exact"},{"name":"carboxylic acid biosynthesis","type":"exact"},{"name":"carboxylic acid formation","type":"exact"},{"name":"carboxylic acid synthesis","type":"exact"}],"termid":"GO:0046394","terms_by_termid":{"GO:0000105":null,"GO:0000162":null,"GO:0006532":null,"GO:0006535":null,"GO:0006542":null,"GO:0006545":null,"GO:0006564":null,"GO:0006571":null,"GO:0006592":null,"GO:0006633":null,"GO:0006636":null,"GO:0006761":null,"GO:0006780":null,"GO:0008153":null,"GO:0009073":null,"GO:0009086":null,"GO:0009088":null,"GO:0009090":null,"GO:0009094":null,"GO:0009098":null,"GO:0009099":null,"GO:0009102":null,"GO:0009107":null,"GO:0009257":null,"GO:0009423":null,"GO:0015940":null,"GO:0019240":null,"GO:0019249":null,"GO:0019264":null,"GO:0019280":null,"GO:0019284":null,"GO:0019344":null,"GO:0019367":null,"GO:0019413":null,"GO:0019509":null,"GO:0019878":null,"GO:0030497":null,"GO:0034625":null,"GO:0042450":null,"GO:0042759":null,"GO:0042761":null,"GO:0042852":null,"GO:0045717":null,"GO:0046656":null,"GO:0052699":null,"GO:0055129":null,"GO:0070981":null,"GO:0071266":null,"GO:0071269":null,"GO:0097054":null,"GO:1900535":null,"GO:1901705":null}}


id: RO:0002513
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of ribosomal translation of","direct_ancestors":[{"relation_name":"is_a","term_name":"genomically_related_to","termid":"RO:0002330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomally_translates_to","termid":"RO:0002513"}


id: PBO:0069995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1290, pseudogene","termid":"PBO:0069995"}


id: PBO:0089212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE binding protein Sec1","termid":"PBO:0089212"}


id: PBO:0077703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"troponin C2, fast skeletal type","termid":"PBO:0077703"}


id: FYPO:0009098
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is increased relative to normal in a medium containing mannitol as the carbon source.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002057","FYPO:0002058","FYPO:0000139","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"increased cell population growth on mannitol carbon source","synonyms":[{"name":"increased growth on mannitol carbon source","type":"broad"},{"name":"increased vegetative cell growth on mannitol carbon source","type":"exact"}],"termid":"FYPO:0009098"}


id: GO:0019895
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The activity of linking kinesins, cytoplasmic proteins responsible for moving vesicles and organelles towards the distal end of microtubules, to mitochondria.","definition_xrefs":["PMID:12495622"],"gene_count":0,"genotype_count":0,"name":"obsolete kinesin-associated mitochondrial adaptor activity (obsolete GO:0019895)","termid":"GO:0019895"}


id: PBO:0017058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sSchizosaccharomyces pombe specific protein, similar to a region of alpha-galactosidase","termid":"PBO:0017058"}


id: GO:0004727
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: prenylated-protein tyrosine phosphate + H2O = prenylated-protein tyrosine + phosphate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete prenylated protein tyrosine phosphatase activity (obsolete GO:0004727)","termid":"GO:0004727"}


id: PATO:0001463
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a cell's plasma membrane by virtue of a brief fluctuation in the bearer's potential caused by the rapid opening and closing of voltage-gated ion channels.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Action_potential"],"direct_ancestors":[{"relation_name":"is_a","term_name":"electric potential","termid":"PATO:0001464"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"action potential","termid":"PATO:0001463"}


id: GO:0005524
data:
  {"annotated_genes":["SJAG_04650","SJAG_04114","SJAG_03077","SJAG_04230","SJAG_04597","SJAG_03209","SJAG_02592","SJAG_01315","SJAG_04772","SJAG_00649","SJAG_04757","SJAG_01179","SJAG_04655","SJAG_04849","SJAG_05231","SJAG_04589","SJAG_02295","SJAG_05290","SJAG_01040","SJAG_02889","SJAG_05276","SJAG_04622","SJAG_02720","SJAG_01181","SJAG_03376","SJAG_02236","SJAG_00857","SJAG_03892","SJAG_03789","SJAG_05019","SJAG_03479","SJAG_02058","SJAG_00500","SJAG_00048","SJAG_02249","SJAG_01082","SJAG_01373","SJAG_04081","SJAG_00999","SJAG_01669","SJAG_02206","SJAG_01787","SJAG_02364","SJAG_01679","SJAG_01311","SJAG_01718","SJAG_00597","SJAG_03780","SJAG_02521","SJAG_04394","SJAG_04665","SJAG_01825","SJAG_01613","SJAG_01615","SJAG_00381","SJAG_01129","SJAG_02721","SJAG_02077","SJAG_02991","SJAG_00475","SJAG_03224","SJAG_00729","SJAG_02875","SJAG_00136","SJAG_03475","SJAG_00947","SJAG_00533","SJAG_04372","SJAG_00564","SJAG_03950","SJAG_00798","SJAG_00198","SJAG_01254","SJAG_00516","SJAG_00853","SJAG_02704","SJAG_03036","SJAG_02394","SJAG_01024","SJAG_03362","SJAG_01799","SJAG_04874","SJAG_01268","SJAG_05295","SJAG_01724","SJAG_01953","SJAG_04692","SJAG_01084","SJAG_04121","SJAG_00583","SJAG_02558","SJAG_04001","SJAG_00963","SJAG_01383","SJAG_02468","SJAG_00114","SJAG_01152","SJAG_02618","SJAG_01805","SJAG_00704","SJAG_06642","SJAG_02342","SJAG_04669","SJAG_03421","SJAG_01052","SJAG_01575","SJAG_04277","SJAG_03982","SJAG_02712","SJAG_04094","SJAG_02082","SJAG_02680","SJAG_02738","SJAG_04334","SJAG_03157","SJAG_00529","SJAG_03753","SJAG_02838","SJAG_03658","SJAG_00845","SJAG_01159","SJAG_04700","SJAG_04409","SJAG_04038","SJAG_01002","SJAG_00881","SJAG_02370","SJAG_03887","SJAG_05022","SJAG_04857","SJAG_16456","SJAG_06597","SJAG_02187","SJAG_01544","SJAG_02267","SJAG_03785","SJAG_04206","SJAG_02872","SJAG_01618","SJAG_04468","SJAG_02022","SJAG_02421","SJAG_01018","SJAG_03676","SJAG_00931","SJAG_03613","SJAG_02879","SJAG_03854","SJAG_03497","SJAG_01221","SJAG_02690","SJAG_00039","SJAG_02183","SJAG_00898","SJAG_04150","SJAG_03660","SJAG_04552","SJAG_03557","SJAG_03659","SJAG_02923","SJAG_00342","SJAG_01680","SJAG_01376","SJAG_02906","SJAG_00757","SJAG_02878","SJAG_03048","SJAG_01400","SJAG_01471","SJAG_00964","SJAG_02429","SJAG_03703","SJAG_01855","SJAG_00403","SJAG_03813","SJAG_01877","SJAG_05313","SJAG_02015","SJAG_00790","SJAG_02287","SJAG_01474","SJAG_04551","SJAG_03501","SJAG_00256","SJAG_03206","SJAG_03927","SJAG_04167","SJAG_02428","SJAG_04777","SJAG_03529","SJAG_00488","SJAG_02226","SJAG_04577","SJAG_04276","SJAG_05209","SJAG_04435","SJAG_00995","SJAG_04634","SJAG_01351","SJAG_00984","SJAG_04970","SJAG_03449","SJAG_00356","SJAG_01405","SJAG_01510","SJAG_04469","SJAG_03730","SJAG_04189","SJAG_00243","SJAG_00168","SJAG_00712","SJAG_04473","SJAG_03946","SJAG_00661","SJAG_04840","SJAG_01546","SJAG_02200","SJAG_00779","SJAG_02498","SJAG_03069","SJAG_03799","SJAG_01807","SJAG_00378","SJAG_00084","SJAG_03689","SJAG_00541","SJAG_01176","SJAG_03720","SJAG_01500","SJAG_02517","SJAG_02378","SJAG_02084","SJAG_02835","SJAG_01577","SJAG_03237","SJAG_03071","SJAG_03585","SJAG_00855","SJAG_00690","SJAG_00887","SJAG_03495","SJAG_02199","SJAG_01863","SJAG_04187","SJAG_00863","SJAG_01344","SJAG_03486","SJAG_04734","SJAG_00616","SJAG_03967","SJAG_04287","SJAG_01186","SJAG_00392","SJAG_00718","SJAG_00988","SJAG_00252","SJAG_03096","SJAG_04745","SJAG_00427","SJAG_04974","SJAG_03570","SJAG_01677","SJAG_05010","SJAG_05353","SJAG_03011","SJAG_01489","SJAG_04856","SJAG_05213","SJAG_01942","SJAG_02598","SJAG_02698","SJAG_04865","SJAG_01731","SJAG_00636","SJAG_02897","SJAG_01611","SJAG_00786","SJAG_03160","SJAG_04755","SJAG_00106","SJAG_02926","SJAG_03708","SJAG_03129","SJAG_03533","SJAG_01235","SJAG_01000","SJAG_04760","SJAG_02074","SJAG_03141","SJAG_03811","SJAG_01945","SJAG_02602","SJAG_01762","SJAG_00042","SJAG_04125","SJAG_01081","SJAG_04355","SJAG_00996","SJAG_03897","SJAG_03567","SJAG_02725","SJAG_00650","SJAG_00638","SJAG_00300","SJAG_04312","SJAG_01791","SJAG_00678","SJAG_02748","SJAG_02457","SJAG_04156","SJAG_02760","SJAG_04845","SJAG_03909","SJAG_01352","SJAG_01664","SJAG_00633","SJAG_01938","SJAG_03832","SJAG_01499","SJAG_04738","SJAG_02615","SJAG_01198","SJAG_04147","SJAG_01653","SJAG_01937","SJAG_03438","SJAG_00111","SJAG_00851","SJAG_00169","SJAG_00464","SJAG_01197","SJAG_01918","SJAG_01530","SJAG_01587","SJAG_04549","SJAG_00815","SJAG_03277","SJAG_04285","SJAG_04537","SJAG_03061","SJAG_04882","SJAG_00332","SJAG_00412","SJAG_00337","SJAG_00773","SJAG_00653","SJAG_02619","SJAG_03987","SJAG_02571","SJAG_02895","SJAG_02564","SJAG_02643","SJAG_00933","SJAG_01410","SJAG_01704","SJAG_02563","SJAG_01240","SJAG_03886","SJAG_00610","SJAG_04232","SJAG_03193","SJAG_03545","SJAG_04747","SJAG_01885","SJAG_00980","SJAG_04486","SJAG_01402","SJAG_03798","SJAG_02426","SJAG_01837","SJAG_04507","SJAG_02713","SJAG_02392","SJAG_01070","SJAG_01131","SJAG_03349","SJAG_02825","SJAG_02604","SJAG_01080","SJAG_00293","SJAG_00330","SJAG_02950","SJAG_03932","SJAG_04511","SJAG_04544","SJAG_02460","SJAG_05105","SJAG_00486","SJAG_02431","SJAG_02286","SJAG_04657","SJAG_01684","SJAG_00329","SJAG_04183","SJAG_03363","SJAG_00331","SJAG_02736","SJAG_02887","SJAG_01182","SJAG_02242","SJAG_01297","SJAG_01047","SJAG_04482","SJAG_03534","SJAG_03709","SJAG_03017","SJAG_04980","SJAG_01616","SJAG_00604","SJAG_04055","SJAG_03313","SJAG_04761","SJAG_04203","SJAG_04320","SJAG_01816","SJAG_02723","SJAG_04288","SJAG_03336","SJAG_00875","SJAG_01571","SJAG_01644","SJAG_16455","SJAG_03451","SJAG_00878","SJAG_03140","SJAG_04465","SJAG_03471","SJAG_04457","SJAG_03602","SJAG_03345","SJAG_00443","SJAG_00359","SJAG_05025","SJAG_04052","SJAG_00986","SJAG_05024","SJAG_03257","SJAG_02997","SJAG_04258","SJAG_00364","SJAG_03174","SJAG_00402","SJAG_00884","SJAG_04064","SJAG_04118","SJAG_00244","SJAG_04461","SJAG_05340","SJAG_04210","SJAG_00938","SJAG_05249","SJAG_02808","SJAG_04762","SJAG_00930","SJAG_03496","SJAG_01010","SJAG_04599","SJAG_01522","SJAG_02545","SJAG_02708","SJAG_00208","SJAG_00871","SJAG_01595","SJAG_01259","SJAG_03457","SJAG_03145","SJAG_00766","SJAG_00436","SJAG_04154","SJAG_01164","SJAG_03669","SJAG_02420","SJAG_01447","SJAG_02858","SJAG_03923","SJAG_02336","SJAG_04495","SJAG_02104","SJAG_02400","SJAG_05304","SJAG_03526","SJAG_03409","SJAG_02796","SJAG_03355","SJAG_02348","SJAG_02294","SJAG_02399","SJAG_04566","SJAG_00390","SJAG_01354","SJAG_01435","SJAG_03386","SJAG_02596","SJAG_00358","SJAG_01148","SJAG_03866","SJAG_03850","SJAG_02785","SJAG_01944","SJAG_05372","SJAG_04477","SJAG_01874","SJAG_05018","SJAG_01419","SJAG_01797","SJAG_01831","SJAG_03626","SJAG_00669","SJAG_00353","SJAG_00956","SJAG_03728","SJAG_02382","SJAG_02741","SJAG_02610","SJAG_03898","SJAG_03846","SJAG_04612","SJAG_02061","SJAG_00609","SJAG_05173","SJAG_03067","SJAG_02575","SJAG_03948","SJAG_01620","SJAG_04573","SJAG_02182","SJAG_03213","SJAG_02994","SJAG_03436","SJAG_02686","SJAG_03384","SJAG_02527","SJAG_04268","SJAG_00605","SJAG_01878","SJAG_03896","SJAG_03592","SJAG_00599","SJAG_04946","SJAG_05194","SJAG_04693","SJAG_03679","SJAG_00447","SJAG_00420","SJAG_00103","SJAG_03320","SJAG_04480","SJAG_00993","SJAG_04282","SJAG_04126","SJAG_04280","SJAG_02038","SJAG_02977","SJAG_00150","SJAG_00004","SJAG_01964","SJAG_02822"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57002,57029,57072,57120,57164,57188,57196,57271,57280,57329,57356,57364,57380,57410,57415,57435,57459,57469,57474,57495,57505,57523,57536,57572,57589,57618,57654,57660,57671,57676,57718,57730,57756,57770,57832,57861,57906,57918,57930,57940,57958,58076,58082,58137,58154,58183,58223,58253,58268,58304,58307,58334,58343,58430,58486,58490,58509,58536,58540,58585,58614,58628,58638,58654,58661,58703,58711,58737,58761,58784,58823,58830,58856,58893,58913,58935,58944,58954,58968,59000,59011,59028,59041,59053,59065,59129,59155,59161,59192,59199,59216,59257,59272,59286,59321,59330,59342,59345,59353,59409,59420,59444,59476,59517,59564,59579,59598,59619,59621,59645,59655,59662,59666,59751,59771,59857,59864,59867,59874,60000,60022,60038,60058,60096,60131,60135,60155,60174,60210,60273,60293,60300,60309,60317,60357,60400,60422,60438,60454,60482,60527,60548,60593,60631,60637,60658,60702,60725,60744,60759,60787,60824,60922,60945,60996,61026,61058,61085,61101,61125,61156,61224,61273,61279,61300,61307,61314,61372,61377,61480,61571,61591,61607,61641,61666,61688,61694,61705,61729,61755,61790,61840,61855,61971,62008,62026,62031,62039,62045,62052,62055,62183,62197,62213,62274,62332,62359,62383,62425,62437,62486,62497,62501,62548,62586,62615,62635,62666,62711,62767,62771,62836,62854,62919,62999,63009,63017,63043,63071,63077,63082,63146,63199,63308,63332,63400,63417,63459,63463,63517,63526,63541,63550,63575,63591,63636,63645,63668,63676,63770,63832,63945,63995,64046,64057,64123,64129,64148,64164,64209,64216,64230,64242,64316,64327,64357,64378,64390,64405,64434,64545,64568,64578,64625,64694,64719,64742,64799,64849,64857,64859,64866,64880,64949,64980,65043,65070,65093,65130,65214,65220,65230,65241,65330,65354,65383,65395,65539,65556,65583,65588,65614,65640,65694,65706,65724,65766,65788,65806,65874,65893,65993,65997,66016,66056,66085,66104,66147,66154,66172,66239,66275,66287,66300,66388,66390,66409,66431,66436,66442,66468,66476,66506,66531,66582,66605,66639,66672,66679,66773,66808,66828,66835,66838,66894,66935,66992,67002,67020,67135,67145,67149,67171,67218,67237,67263,67309,67325,67366,67381,67399,67428,67446,67486,67506,67507,67519,67527,67534,67656,67672,67718,67723,67735,67815,67822,67841,67862,67891,67915,67927,67969,67993,68014,68035,68056,68090,68102,68179,68241,68256,68266,68286,68325,68343,68367,68394,68410,68463,68499,68543,68600,68710,68787,68815,68823,68850,68880,68962,68975,68983,69001,69006,69021,69037,69067,69086,69114,69126,69149,69217,69346,69351,69371,69393,69435,69438,69450,69460,69492,69524,69540,69562,69567,69581,69585,69597,69604,69632,69719,69726,69776,69778,69790,69813,69834,69850,69861,69933,70005,70043,70069,70081,70087,70157,70164,70189,70228,70300,70309,70328,70330,70348,70358,70361,70403,70427,70449,70471,70501,70532,70576,70604,70639,70660,70667,70707,70711,70747,70838,70861,70863,70871,70946,70979,70997,71061,71120,71129,71137,71153,71163,71191,71260,71263,71270,71276,71311,71317,71398,71416,71485,71499,71512,71516,71715,73485,73864,74214,74434,74501,74718,75862,76095,78241,79215,79564,82012,90252,90679,90954,91097,91380,91727,93051,93447,94040,95594,98411,99422,100725,101070,101271,101621,102033,103046,104209,104618,105272,105775,106274,106601,107201,107462,107560,109922,110147,110487,110529,112529,113083,113389,114963,114964,114967,115099,115188,115433,115602,116076,116130,116535,117721,117786,118043,119957,120018],"is_not":false,"summary":null,"term":"GO:0005524"}]},"cv_name":"molecular_function","definition":"Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenyl ribonucleotide binding","termid":"GO:0032559"},{"relation_name":"is_a","term_name":"purine ribonucleoside triphosphate binding","termid":"GO:0035639"}],"gene_count":557,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00039":null,"SJAG_00042":null,"SJAG_00048":null,"SJAG_00084":null,"SJAG_00103":null,"SJAG_00106":null,"SJAG_00111":null,"SJAG_00114":null,"SJAG_00136":null,"SJAG_00150":null,"SJAG_00168":null,"SJAG_00169":null,"SJAG_00198":null,"SJAG_00208":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00252":null,"SJAG_00256":null,"SJAG_00293":null,"SJAG_00300":null,"SJAG_00329":null,"SJAG_00330":null,"SJAG_00331":null,"SJAG_00332":null,"SJAG_00337":null,"SJAG_00342":null,"SJAG_00353":null,"SJAG_00356":null,"SJAG_00358":null,"SJAG_00359":null,"SJAG_00364":null,"SJAG_00378":null,"SJAG_00381":null,"SJAG_00390":null,"SJAG_00392":null,"SJAG_00402":null,"SJAG_00403":null,"SJAG_00412":null,"SJAG_00420":null,"SJAG_00427":null,"SJAG_00436":null,"SJAG_00443":null,"SJAG_00447":null,"SJAG_00464":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00488":null,"SJAG_00500":null,"SJAG_00516":null,"SJAG_00529":null,"SJAG_00533":null,"SJAG_00541":null,"SJAG_00564":null,"SJAG_00583":null,"SJAG_00597":null,"SJAG_00599":null,"SJAG_00604":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00610":null,"SJAG_00616":null,"SJAG_00633":null,"SJAG_00636":null,"SJAG_00638":null,"SJAG_00649":null,"SJAG_00650":null,"SJAG_00653":null,"SJAG_00661":null,"SJAG_00669":null,"SJAG_00678":null,"SJAG_00690":null,"SJAG_00704":null,"SJAG_00712":null,"SJAG_00718":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00773":null,"SJAG_00779":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00798":null,"SJAG_00815":null,"SJAG_00845":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00855":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00875":null,"SJAG_00878":null,"SJAG_00881":null,"SJAG_00884":null,"SJAG_00887":null,"SJAG_00898":null,"SJAG_00930":null,"SJAG_00931":null,"SJAG_00933":null,"SJAG_00938":null,"SJAG_00947":null,"SJAG_00956":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00980":null,"SJAG_00984":null,"SJAG_00986":null,"SJAG_00988":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_00999":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01010":null,"SJAG_01018":null,"SJAG_01024":null,"SJAG_01040":null,"SJAG_01047":null,"SJAG_01052":null,"SJAG_01070":null,"SJAG_01080":null,"SJAG_01081":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01148":null,"SJAG_01152":null,"SJAG_01159":null,"SJAG_01164":null,"SJAG_01176":null,"SJAG_01179":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01186":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01221":null,"SJAG_01235":null,"SJAG_01240":null,"SJAG_01254":null,"SJAG_01259":null,"SJAG_01268":null,"SJAG_01297":null,"SJAG_01311":null,"SJAG_01315":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01383":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01435":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01474":null,"SJAG_01489":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01510":null,"SJAG_01522":null,"SJAG_01530":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01571":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01587":null,"SJAG_01595":null,"SJAG_01611":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01616":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01644":null,"SJAG_01653":null,"SJAG_01664":null,"SJAG_01669":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01684":null,"SJAG_01704":null,"SJAG_01718":null,"SJAG_01724":null,"SJAG_01731":null,"SJAG_01762":null,"SJAG_01787":null,"SJAG_01791":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01816":null,"SJAG_01825":null,"SJAG_01831":null,"SJAG_01837":null,"SJAG_01855":null,"SJAG_01863":null,"SJAG_01874":null,"SJAG_01877":null,"SJAG_01878":null,"SJAG_01885":null,"SJAG_01918":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_01953":null,"SJAG_01964":null,"SJAG_02015":null,"SJAG_02022":null,"SJAG_02038":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02104":null,"SJAG_02182":null,"SJAG_02183":null,"SJAG_02187":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02206":null,"SJAG_02226":null,"SJAG_02236":null,"SJAG_02242":null,"SJAG_02249":null,"SJAG_02267":null,"SJAG_02286":null,"SJAG_02287":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02348":null,"SJAG_02364":null,"SJAG_02370":null,"SJAG_02378":null,"SJAG_02382":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02399":null,"SJAG_02400":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02429":null,"SJAG_02431":null,"SJAG_02457":null,"SJAG_02460":null,"SJAG_02468":null,"SJAG_02498":null,"SJAG_02517":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02545":null,"SJAG_02558":null,"SJAG_02563":null,"SJAG_02564":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02592":null,"SJAG_02596":null,"SJAG_02598":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02610":null,"SJAG_02615":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02643":null,"SJAG_02680":null,"SJAG_02686":null,"SJAG_02690":null,"SJAG_02698":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02720":null,"SJAG_02721":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02741":null,"SJAG_02748":null,"SJAG_02760":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02808":null,"SJAG_02822":null,"SJAG_02825":null,"SJAG_02835":null,"SJAG_02838":null,"SJAG_02858":null,"SJAG_02872":null,"SJAG_02875":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02906":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02950":null,"SJAG_02977":null,"SJAG_02991":null,"SJAG_02994":null,"SJAG_02997":null,"SJAG_03011":null,"SJAG_03017":null,"SJAG_03036":null,"SJAG_03048":null,"SJAG_03061":null,"SJAG_03067":null,"SJAG_03069":null,"SJAG_03071":null,"SJAG_03077":null,"SJAG_03096":null,"SJAG_03129":null,"SJAG_03140":null,"SJAG_03141":null,"SJAG_03145":null,"SJAG_03157":null,"SJAG_03160":null,"SJAG_03174":null,"SJAG_03193":null,"SJAG_03206":null,"SJAG_03209":null,"SJAG_03213":null,"SJAG_03224":null,"SJAG_03237":null,"SJAG_03257":null,"SJAG_03277":null,"SJAG_03313":null,"SJAG_03320":null,"SJAG_03336":null,"SJAG_03345":null,"SJAG_03349":null,"SJAG_03355":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03376":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03409":null,"SJAG_03421":null,"SJAG_03436":null,"SJAG_03438":null,"SJAG_03449":null,"SJAG_03451":null,"SJAG_03457":null,"SJAG_03471":null,"SJAG_03475":null,"SJAG_03479":null,"SJAG_03486":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03501":null,"SJAG_03526":null,"SJAG_03529":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03545":null,"SJAG_03557":null,"SJAG_03567":null,"SJAG_03570":null,"SJAG_03585":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03613":null,"SJAG_03626":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03669":null,"SJAG_03676":null,"SJAG_03679":null,"SJAG_03689":null,"SJAG_03703":null,"SJAG_03708":null,"SJAG_03709":null,"SJAG_03720":null,"SJAG_03728":null,"SJAG_03730":null,"SJAG_03753":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03789":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03811":null,"SJAG_03813":null,"SJAG_03832":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03854":null,"SJAG_03866":null,"SJAG_03886":null,"SJAG_03887":null,"SJAG_03892":null,"SJAG_03896":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03909":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03932":null,"SJAG_03946":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03967":null,"SJAG_03982":null,"SJAG_03987":null,"SJAG_04001":null,"SJAG_04038":null,"SJAG_04052":null,"SJAG_04055":null,"SJAG_04064":null,"SJAG_04081":null,"SJAG_04094":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04154":null,"SJAG_04156":null,"SJAG_04167":null,"SJAG_04183":null,"SJAG_04187":null,"SJAG_04189":null,"SJAG_04203":null,"SJAG_04206":null,"SJAG_04210":null,"SJAG_04230":null,"SJAG_04232":null,"SJAG_04258":null,"SJAG_04268":null,"SJAG_04276":null,"SJAG_04277":null,"SJAG_04280":null,"SJAG_04282":null,"SJAG_04285":null,"SJAG_04287":null,"SJAG_04288":null,"SJAG_04312":null,"SJAG_04320":null,"SJAG_04334":null,"SJAG_04355":null,"SJAG_04372":null,"SJAG_04394":null,"SJAG_04409":null,"SJAG_04435":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04473":null,"SJAG_04477":null,"SJAG_04480":null,"SJAG_04482":null,"SJAG_04486":null,"SJAG_04495":null,"SJAG_04507":null,"SJAG_04511":null,"SJAG_04537":null,"SJAG_04544":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04566":null,"SJAG_04573":null,"SJAG_04577":null,"SJAG_04589":null,"SJAG_04597":null,"SJAG_04599":null,"SJAG_04612":null,"SJAG_04622":null,"SJAG_04634":null,"SJAG_04650":null,"SJAG_04655":null,"SJAG_04657":null,"SJAG_04665":null,"SJAG_04669":null,"SJAG_04692":null,"SJAG_04693":null,"SJAG_04700":null,"SJAG_04734":null,"SJAG_04738":null,"SJAG_04745":null,"SJAG_04747":null,"SJAG_04755":null,"SJAG_04757":null,"SJAG_04760":null,"SJAG_04761":null,"SJAG_04762":null,"SJAG_04772":null,"SJAG_04777":null,"SJAG_04840":null,"SJAG_04845":null,"SJAG_04849":null,"SJAG_04856":null,"SJAG_04857":null,"SJAG_04865":null,"SJAG_04874":null,"SJAG_04882":null,"SJAG_04946":null,"SJAG_04970":null,"SJAG_04974":null,"SJAG_04980":null,"SJAG_05010":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05022":null,"SJAG_05024":null,"SJAG_05025":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05194":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05231":null,"SJAG_05249":null,"SJAG_05276":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05304":null,"SJAG_05313":null,"SJAG_05340":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_06597":null,"SJAG_06642":null,"SJAG_16455":null,"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"ATP binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-265682"],"synonyms":[{"name":"Mg-ATP binding","type":"exact"},{"name":"MgATP binding","type":"exact"}],"termid":"GO:0005524","terms_by_termid":{"GO:0005524":null}}


id: PBO:0083581
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; transcription is AZF1 dependent in glycerol-lactate medium and SLT2 dependent in response to the lipid hydroperoxides","termid":"PBO:0083581"}


id: PBO:0109052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MSL3 pseudogene 3","termid":"PBO:0109052"}


id: MONDO:0035112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"acute myeloid leukemia with BCR-ABL1","secondary_identifiers":["MEDGEN:1377153","NCIT:C129785","Orphanet:585867","UMLS:C4329268","DOID:0080976","GARD:22340"],"synonyms":[{"name":"AML with BCR-ABL1","type":"exact"},{"name":"AML with t(9;22)(q34.1;q11.2)","type":"exact"},{"name":"acute myeloid leukaemia with t(9;22)(q34.1;q11.2)","type":"exact"},{"name":"acute myeloid leukemia with t(9;22)(q34.1;q11.2)","type":"exact"}],"termid":"MONDO:0035112","xrefs":{"Monarch":{"xref_id":"0035112"}}}


id: MONDO:0012420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive disorder caused by mutations in the MARVELD2 gene, encoding MARVEL domain-containing protein 2. The condition is characterized by profound prelingual deafness.","definition_xrefs":["NCIT:C129024"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 49","secondary_identifiers":["MESH:C565717","OMIM:610153","UMLS:C1857811","DOID:0110506","GARD:22619","MEDGEN:346670"],"synonyms":[{"name":"DFNB49","type":"narrow"},{"name":"MARVELD2 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 49","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 49","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in MARVELD2","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 49","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 49","type":"exact"},{"name":"deafness, autosomal recessive 49","type":"narrow"},{"name":"deafness, autosomal recessive type 49","type":"narrow"}],"termid":"MONDO:0012420","xrefs":{"Monarch":{"xref_id":"0012420"}}}


id: FYPO:0002128
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 plasma membrane is abolished, and the protein is present in the cytoplasm instead.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"protein mislocalized to cytoplasm during vegetative growth","termid":"FYPO:0000783"},{"relation_name":"is_a","term_name":"protein mislocalized to cytoplasm during vegetative growth","termid":"FYPO:0000783"},{"relation_name":"is_a","term_name":"abolished protein localization to plasma membrane during vegetative growth","termid":"FYPO:0002126"},{"relation_name":"is_a","term_name":"abolished protein localization to cell periphery during vegetative growth","termid":"FYPO:0005571"},{"relation_name":"is_a","term_name":"abolished protein localization to membrane during vegetative growth","termid":"FYPO:0005757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to plasma membrane, with protein mislocalized to cytoplasm, during vegetative growth","synonyms":[{"name":"abolished protein localisation to plasma membrane, with protein mislocalised to cytoplasm, during vegetative growth","type":"exact"},{"name":"abolished protein localization in plasma membrane, with protein mislocalized to cytoplasm, during vegetative growth","type":"exact"},{"name":"abolished protein localization to cell membrane, with protein mislocalized to cytoplasm, during vegetative growth","type":"exact"},{"name":"abolished protein localization to plasma membrane, with protein mislocalized to cytoplasm during mitotic cell cycle","type":"related"},{"name":"protein localization to plasma membrane abolished, with protein mislocalized to cytoplasm, during vegetative growth","type":"exact"}],"termid":"FYPO:0002128"}


id: PBO:0047619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FIG4 phosphoinositide 5-phosphatase","termid":"PBO:0047619"}


id: MONDO:0008910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive condition caused by mutation(s) in the CPN1 gene, encoding carboxypeptidase N catalytic chain. It may be characterized by episodic angioedema, chronic urticaria, asthma and/or allergic hypersensitivity.","definition_xrefs":["NCIT:C132196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxypeptidase N deficiency","secondary_identifiers":["DOID:0111583","MEDGEN:98312","ICD9:279.8","MESH:C562876","OMIM:212070","UMLS:C0398782","SCTID:234627009"],"synonyms":[{"name":"carboxypeptidase N deficiency","type":"exact"}],"termid":"MONDO:0008910","xrefs":{"Monarch":{"xref_id":"0008910"}}}


id: GO:0005963
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An intracellular enzyme complex that catalyzes the removal of serine- or threonine-bound phosphate groups from a wide range of phosphoproteins, including a number of enzymes that have been phosphorylated under the action of a kinase.","definition_xrefs":["PMID:17517611","PMID:22343722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine phosphatase complex","termid":"GO:0008287"},{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"magnesium-dependent protein serine/threonine phosphatase complex","termid":"GO:0005963"}


id: PBO:0070914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 22","termid":"PBO:0070914"}


id: MOD:01344
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical with MOD:00835. Remap to MOD:00835.","definition_xrefs":["Unimod:401","PubMed:9252331","PubMed:9276974"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01344 dehydrogenated residue - site S (obsolete MOD:01344)","synonyms":[{"name":"2-amino-3-oxo-butanoic_acid","type":"related"},{"name":"Didehydro","type":"related"}],"termid":"MOD:01344"}


id: MOD:00521
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod N-linked glycosylation","definition_xrefs":["Unimod:153","RESID:AA0151#var"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N4-glycosyl-L-asparagine","termid":"MOD:00160"},{"relation_name":"is_a","term_name":"complex glycosylation","termid":"MOD:00725"}],"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":"Hex2HexNAc2 N4-glycosylated asparagine","synonyms":[{"name":"Hex(2)HexNAc(2)","type":"related"},{"name":"Hex2HexNAc2","type":"related"}],"termid":"MOD:00521"}


id: PBO:0049967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIG1 hypoxia inducible domain family member 1A pseudogene 13","termid":"PBO:0049967"}


id: GO:0031746
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 cysteinyl leukotriene receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteinyl leukotriene receptor binding","termid":"GO:0031745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"type 1 cysteinyl leukotriene receptor binding","synonyms":[{"name":"type 1 cysteinyl leukotriene receptor ligand","type":"narrow"}],"termid":"GO:0031746"}


id: MONDO:0007565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Brooke-Spiegler syndrome","termid":"MONDO:0011512"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"familial cylindromatosis","secondary_identifiers":["UMLS:C1851526","GARD:9707","NCIT:C43352","Orphanet:211","MEDGEN:343593","MESH:C536611","OMIM:132700"],"synonyms":[{"name":"'turban tumor' syndrome","type":"related"},{"name":"Ancell-Spiegler Cylindromas","type":"related"},{"name":"Ancell-Spiegler syndrome","type":"exact"},{"name":"CYLD","type":"related"},{"name":"Cylindromas, dermal eccrine","type":"related"},{"name":"cylindromatosis, familial","type":"related"},{"name":"turban tumor","type":"exact"},{"name":"turban tumor syndrome","type":"exact"},{"name":"turban tumors","type":"related"},{"name":"turban tumour","type":"exact"},{"name":"turban tumour syndrome","type":"exact"},{"name":"turban tumours","type":"related"}],"termid":"MONDO:0007565","xrefs":{"Monarch":{"xref_id":"0007565"}}}


id: GO:0062196
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the size of a lysosome.","definition_xrefs":["PMID:31314175"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component size","termid":"GO:0032535"}],"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 lysosome size","termid":"GO:0062196"}


id: PBO:0074376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMG1 pseudogene 2","termid":"PBO:0074376"}


id: PATO:0001991
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's disposition to being capable of indefinite growth or division.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viability","termid":"PATO:0000169"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immortal","termid":"PATO:0001991"}


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


id: MONDO:0011999
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"otosclerosis","termid":"MONDO:0005349"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otosclerosis 3","secondary_identifiers":["MEDGEN:334054","DOID:0060922","OMIM:608244","MESH:C564268","UMLS:C1842353"],"synonyms":[{"name":"OTSC3","type":"exact"},{"name":"otosclerosis 3","type":"exact"}],"termid":"MONDO:0011999","xrefs":{"Monarch":{"xref_id":"0011999"}}}


id: MONDO:0014274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"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":"L-ferritin deficiency","secondary_identifiers":["GARD:17748","Orphanet:440731","MEDGEN:816420","UMLS:C3810090","OMIM:615604"],"synonyms":[{"name":"L-ferritin deficiency","type":"exact"},{"name":"L-ferritin deficiency, dominant and recessive","type":"exact"},{"name":"LFTD","type":"related"}],"termid":"MONDO:0014274","xrefs":{"Monarch":{"xref_id":"0014274"}}}


id: PBO:0026969
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-actin_cortical_patches_present_in_decreased_numbers","termid":"PBO:0026969"}


id: PBO:0029191
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-excess_intracellular_endomembrane_system_present","termid":"PBO:0029191"}


id: MONDO:0971005
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 1","secondary_identifiers":["OMIM:209920"],"termid":"MONDO:0971005","xrefs":{"Monarch":{"xref_id":"0971005"}}}


id: GO:0006933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disassembly of adhesions at the front and rear of a migrating cell. At the leading edge, adhesion disassembly accompanies the formation of new protrusions; at the cell rear, it promotes tail retraction.","definition_xrefs":["GOC:tb","ISBN:0815316194","PMID:11944043","GOC:dph","PMID:14657486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell adhesion","termid":"GO:0007162"},{"relation_name":"part_of","term_name":"substrate-dependent cell migration","termid":"GO:0006929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of cell adhesion involved in substrate-bound cell migration","synonyms":[{"name":"substrate-bound cell migration, cell release from substrate","type":"exact"}],"termid":"GO:0006933"}


id: GO:0090087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of peptides, compounds of two or more amino acids where the alpha carboxyl group of one is bound to the alpha amino group of another, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"peptide transport","termid":"GO:0015833"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of peptide transport","termid":"GO:0090087"}


id: GO:0036399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a TCR signalosome.","definition_xrefs":["GOC:krc","PMID:22426112"],"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":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"TCR signalosome assembly","synonyms":[{"name":"LAT signalosome assembly","type":"exact"},{"name":"linker for activation of T cells signalosome assembly","type":"exact"}],"termid":"GO:0036399"}


id: PBO:0031058
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_mixed_population_including_spores_and_divided_germinated_spores_(obsolete_FYPO:0000319)","termid":"PBO:0031058"}


id: MONDO:0009161
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of Ehlers-Danlos syndrome (EDS) characterized by extreme skin fragility and laxity, a prominent facial gestalt, excessive bruising and, sometimes, major complications due to visceral and vascular fragility.","definition_xrefs":["Orphanet:1901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ehlers-Danlos syndrome, dermatosparaxis type","secondary_identifiers":["icd11.foundation:445808781","MEDGEN:397792","OMIM:225410","MESH:C567527","NANDO:1200651","NANDO:2201261","SCTID:55711009","DOID:0080733","GARD:2089","UMLS:C2700425"],"synonyms":[{"name":"EDS 7C","type":"related"},{"name":"EDS VIIC","type":"exact"},{"name":"EDS7C","type":"related"},{"name":"EDSDERMS","type":"related"},{"name":"Ehlers-Danlos syndrome type 7C","type":"exact"},{"name":"Ehlers-Danlos syndrome type 7C (formerly)","type":"related"},{"name":"Ehlers-Danlos syndrome, dermatosparaxis type","type":"exact"},{"name":"Ehlers-Danlos syndrome, type VII, autosomal recessive","type":"related"},{"name":"dEDS","type":"related"},{"name":"dermatosparaxis","type":"related"},{"name":"dermatosparaxis EDS","type":"related"},{"name":"dermatosparaxis Ehlers-Danlos syndrome","type":"related"}],"termid":"MONDO:0009161","xrefs":{"Monarch":{"xref_id":"0009161"}}}


id: MONDO:0015230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome is a multiple congenital anomalies syndrome, reported in the offsprings of a consanguineous couple and characterized by multiple congenital skeletal (dolichocephaly, skull asymmetry, camptodactyly, clubfoot), muscular (muscle hypoplasia), ocular (anophthalmia, buphthalmos, retinal detachment, aniridia) and cardiac (prolapse of tricuspid valves, mitral and tricuspid insufficiency) abnormalities. An autosomal recessive inheritance with variable expressivity was suspected. There have been no further descriptions in the literature since 1992.","definition_xrefs":["Orphanet:1101"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome","secondary_identifiers":["UMLS:C4304035","MEDGEN:929704","SCTID:720495005","GARD:717"],"synonyms":[{"name":"Cassia Stocco dos Santos syndrome","type":"exact"},{"name":"anophthalmia megalocornea cardiopathy skeletal anomalies","type":"exact"}],"termid":"MONDO:0015230","xrefs":{"Monarch":{"xref_id":"0015230"}}}


id: PATO:0000876
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000876 respiratory rate value (obsolete PATO:0000876)","termid":"PATO:0000876"}


id: PBO:0064755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 91","termid":"PBO:0064755"}


id: FYPO:0000471
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 occurrence of mating type switching is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating type switching","termid":"FYPO:0000468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000293"],"is_obsolete":false,"name":"increased mating type switching","synonyms":[{"name":"increased mating type switching during mitotic cell cycle","type":"related"},{"name":"increased mating type switching during vegetative growth","type":"exact"},{"name":"mating type switching: increased","type":"related"}],"termid":"FYPO:0000471"}


id: GO:0046381
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving CMP-N-acetylneuraminate, a substance composed of 5-(acetylamino)-3,5-dideoxy-D-glycero-D-galacto-non-3-ulosonic acid in glycosidic linkage with cytidine monophosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar metabolic process","termid":"GO:0009225"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"CMP-N-acetylneuraminate metabolic process","synonyms":[{"name":"CMP-N-acetylneuraminate metabolism","type":"exact"}],"termid":"GO:0046381"}


id: MONDO:0019045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare form of sleep disorder.","gene_count":0,"genotype_count":0,"name":"obsolete rare sleep disorder (obsolete MONDO:0019045)","secondary_identifiers":["Orphanet:68354","MedDRA:10040984","MESH:D012893"],"synonyms":[{"name":"rare sleep disorder","type":"exact"},{"name":"rare sleep wake disorder","type":"exact"},{"name":"rare sleep-wake disorder","type":"exact"}],"termid":"MONDO:0019045","xrefs":{"Monarch":{"xref_id":"0019045"}}}


id: PBO:0068710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 91, pseudogene","termid":"PBO:0068710"}


id: PBO:0033788
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_metaphase_chromosome_recapture","termid":"PBO:0033788"}


id: PBO:0072838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAP30BP antisense RNA 1","termid":"PBO:0072838"}


id: PBO:0065476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, non-ATPase 13","termid":"PBO:0065476"}


id: PR:Q9C0Y6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An NADPH-dependent curcumin reductase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc-type alcohol dehydrogenase-like protein PB24D3.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB24D3.08c","secondary_identifiers":["UniProtKB:Q9C0Y6"],"synonyms":[{"name":"Spom972h-curA","type":"exact"}],"termid":"PR:Q9C0Y6"}


id: PBO:0005085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unconventional prefoldin involved in translation initiation (predicted)","termid":"PBO:0005085"}


id: MONDO:0018358
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"secondary neonatal autoimmune disease","termid":"MONDO:0018356"},{"relation_name":"is_a","term_name":"autoimmune hemolytic anemia","termid":"MONDO:0020108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"neonatal autoimmune hemolytic anemia","secondary_identifiers":["UMLS:C4751517","GARD:21645","Orphanet:398109","MEDGEN:1662969"],"synonyms":[{"name":"neonatal AHA","type":"exact"},{"name":"neonatal AIHA","type":"exact"}],"termid":"MONDO:0018358","xrefs":{"Monarch":{"xref_id":"0018358"}}}


id: PBO:0051264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (III)-82 (pseudogene)","termid":"PBO:0051264"}


id: GO:0071960
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the association between sister chromatids of a replicated chromosome along the length of the centromeric region is maintained as chromosomes condense, attach to the spindle in a bipolar orientation, and congress to the metaphase plate during a mitotic cell cycle.","definition_xrefs":["GOC:mah","PMID:1708436"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"},{"relation_name":"part_of","term_name":"mitotic sister chromatid cohesion, centromeric","termid":"GO:0071962"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"maintenance of mitotic sister chromatid cohesion, centromeric","synonyms":[{"name":"maintenance of centromeric mitotic sister chromatin cohesion","type":"exact"},{"name":"maintenance of mitotic sister chromatin cohesion at centromere","type":"exact"},{"name":"maintenance of sister chromatin cohesion at centromere at mitosis","type":"exact"}],"termid":"GO:0071960"}


id: GO:0100055
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that positively regulates phosphatidylserine biosynthetic process.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of phosphatidylserine biosynthetic process by transcription from RNA polymerase II promoter (obsolete GO:0100055)","termid":"GO:0100055"}


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


id: GO:0009314
data:
  {"annotated_genes":["SJAG_01010","SJAG_05242","SJAG_04877","SJAG_02182","SJAG_05197","SJAG_03898","SJAG_04791","SJAG_00208","SJAG_01648","SJAG_02828","SJAG_00272","SJAG_02818","SJAG_00729","SJAG_02199","SJAG_04150","SJAG_02334","SJAG_00814","SJAG_02860","SJAG_04190","SJAG_00863","SJAG_02200","SJAG_01262"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79759],"is_not":false,"summary":null,"term":"GO:0009314"},{"annotations":[67594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009785"},{"annotations":[121376,121375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071483"},{"annotations":[78659,104775,97150,111095],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[66022,106180,107912,60750,114840,67868,70512,99045,95554,77445,89878,97931,69013,71793,66914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an electromagnetic radiation stimulus. Electromagnetic radiation is a propagating wave in space with electric and magnetic components. These components oscillate at right angles to each other and to the direction of propagation.","definition_xrefs":["GOC:jl","Wikipedia:Electromagnetic_radiation"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to abiotic stimulus","termid":"GO:0009628"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00208":null,"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_01010":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02334":null,"SJAG_02818":null,"SJAG_02828":null,"SJAG_02860":null,"SJAG_03898":null,"SJAG_04150":null,"SJAG_04190":null,"SJAG_04791":null,"SJAG_04877":null,"SJAG_05197":null,"SJAG_05242":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to radiation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:23873862":null},"synonyms":[{"name":"response to electromagnetic radiation stimulus","type":"exact"},{"name":"response to radiation stimulus","type":"exact"}],"termid":"GO:0009314","terms_by_termid":{"GO:0009314":null,"GO:0009785":null,"GO:0070914":null,"GO:0071483":null,"GO:1904161":null}}


id: GO:0060197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The separation of the single opening of the digestive, urinary, and reproductive tracts, the cloaca, into multiple isolated openings during development.","definition_xrefs":["GOC:dph","GOC:st"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tube morphogenesis","termid":"GO:0035239"},{"relation_name":"part_of","term_name":"cloaca development","termid":"GO:0035844"}],"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":"cloacal septation","synonyms":[{"name":"cloaca septation","type":"exact"}],"termid":"GO:0060197"}


id: SO:0000601
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000601 edited_by_G_addition (obsolete SO:0000601)","termid":"SO:0000601"}


id: PBO:0026710
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_MCM_complex_binding","termid":"PBO:0026710"}


id: FYPO:0002384
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which acetylation of lysine at positions 5, 8, 12 and 16 of histone H4 in centromere outer repeat regions occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah","PMID:23851719"],"gene_count":0,"genotype_count":0,"name":"obsolete increased histone H4-K5, H4-K8, H4-K12 and H4-K16 acetylation at centromere outer repeat during vegetative growth (obsolete FYPO:0002384)","synonyms":[{"name":"increased histone H4 acetylation (K5, K8, K12 and K16) at centromere outer repeat during vegetative growth","type":"exact"},{"name":"increased histone H4-K5, H4-K8, H4-K12 and H4-K16 acetylation at centromere otr during vegetative growth","type":"exact"},{"name":"increased histone H4-K5, H4-K8, H4-K12 and H4-K16 acetylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"increased histone H4-K5, H4-K8, H4-K12 and H4-K16 acetylation at centromeric outer repeat region during vegetative growth","type":"exact"},{"name":"increased histone H4-K5, H4-K8, H4-K12 and H4-K16 acetylation at pericentric region during vegetative growth","type":"related"},{"name":"increased histone H4-K5, H4-K8, H4-K12 and H4-K16 acetylation at pericentromeric region during vegetative growth","type":"related"},{"name":"increased histone H4-K5/8/12/16 acetylation at centromere outer repeat during vegetative growth","type":"exact"},{"name":"increased histone H4K5, H4K8, H4K12 and H4K16 acetylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0002384"}


id: PR:O60059
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- puf1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60059"],"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":"pumilio domain-containing protein C56F2.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC56F2.08c","synonyms":[{"name":"Spom972h-puf1","type":"exact"}],"termid":"PR:O60059"}


id: PR:O94514
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nucleolar protein 56 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02646","PANTHER:PTHR10894: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":"nucleolar protein 56 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC646.10c","secondary_identifiers":["UniProtKB:O94514"],"synonyms":[{"name":"Spom972h-NOP56","type":"exact"},{"name":"ribosome biosynthesis protein sik1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94514"}


id: PBO:0034296
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_endoparasite","termid":"PBO:0034296"}


id: PBO:0028034
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_post-anaphase_microtubule_array_organization","termid":"PBO:0028034"}


id: MONDO:0009899
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyhydramnios, chronic idiopathic","secondary_identifiers":["MESH:C564876","UMLS:C1849720","MEDGEN:340402","OMIM:263610"],"synonyms":[{"name":"Lactogen receptor defect of chorion","type":"related"},{"name":"polyhydramnios, chronic idiopathic","type":"exact"}],"termid":"MONDO:0009899","xrefs":{"Monarch":{"xref_id":"0009899"}}}


id: PBO:0061981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily AT member 2 pseudogene","termid":"PBO:0061981"}


id: PBO:0084639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mg2+-dependent phosphatidate (PA) phosphatase; dephosphorylates PA to yield diacylglycerol; regulates phospholipid synthesis, nuclear/ER membrane growth, lipid droplet formation, triacylglycerol synthesis, vacuolar homeostasis and cell wall integrity; phosphorylated by Pho85p/Pho80p, Cdc28p/Cyclin B, PKA, PKC, and CKII, regulating activity, localization, and proteosomal degradation; homolog of mammalian lipins 1 and 2; human homologs LPIN1, LPIN2, LPIN3 complement the null","termid":"PBO:0084639"}


id: PBO:0050344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 46","termid":"PBO:0050344"}


id: PATO:0005004
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape that is almost an ellipse.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"superelliptic","termid":"PATO:0002318"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subelliptical","termid":"PATO:0005004"}


id: PBO:0004018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-amino-4-deoxychorismate lyase (predicted)","termid":"PBO:0004018"}


id: PBO:0001719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomere length regulator protein Rif1","termid":"PBO:0001719"}


id: GO:0050225
data:
  {"annotated_genes":["SJAG_03213"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107463],"is_not":false,"summary":null,"term":"GO:0050225"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + pseudouridine = ADP + 2 H+ + pseudouridine 5'-phosphate.","definition_xrefs":["EC:2.7.1.83","RHEA:22448"],"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":1,"genes_by_uniquename":{"SJAG_03213":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016301","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"pseudouridine kinase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R03315","MetaCyc:PSEUDOURIDINE-KINASE-RXN"],"synonyms":[{"name":"ATP:pseudouridine 5'-phosphotransferase activity","type":"related"},{"name":"pseudouridine kinase (phosphorylating)","type":"related"}],"termid":"GO:0050225","terms_by_termid":{"GO:0050225":null}}


id: PBO:0040324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase inhibitory factor subunit 1","termid":"PBO:0040324"}


id: FYPO:0004456
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the nucleus is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to nucleus","termid":"FYPO:0002956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"increased protein localization to nucleus","synonyms":[{"name":"increased protein localisation to nucleus","type":"exact"}],"termid":"FYPO:0004456"}


id: FYPO:0000345
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transport phenotype observed in the vegetative growth phase of the life cycle in which the export of protein from the nucleus is abnormal. Export of all proteins or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal intracellular protein transport during vegetative growth","termid":"FYPO:0000215"},{"relation_name":"is_a","term_name":"abnormal nuclear export","termid":"FYPO:0000506"},{"relation_name":"is_a","term_name":"abnormal protein export from nucleus","termid":"FYPO:0005745"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein export from nucleus during vegetative growth","synonyms":[{"name":"abnormal protein export from nucleus during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000345"}


id: GO:0070614
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of tungstate (WO4 2-) ions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Tungstate is a bivalent oxoanion of tungsten.","definition_xrefs":["GOC:dh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic anion transport","termid":"GO:0015698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"tungstate ion transport","termid":"GO:0070614"}


