# terms

id: GO:0030813
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of nucleotides.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"regulation of nucleotide catabolic process","termid":"GO:0030811"},{"relation_name":"is_a","term_name":"positive regulation of nucleotide metabolic process","termid":"GO:0045981"},{"relation_name":"positively_regulates","term_name":"nucleotide catabolic process","termid":"GO:0009166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"positively_regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"positive regulation of nucleotide catabolic process","synonyms":[{"name":"activation of nucleotide catabolic process","type":"narrow"},{"name":"positive regulation of nucleotide breakdown","type":"exact"},{"name":"positive regulation of nucleotide catabolism","type":"exact"},{"name":"positive regulation of nucleotide degradation","type":"exact"},{"name":"stimulation of nucleotide catabolic process","type":"narrow"},{"name":"up regulation of nucleotide catabolic process","type":"exact"},{"name":"up-regulation of nucleotide catabolic process","type":"exact"},{"name":"upregulation of nucleotide catabolic process","type":"exact"}],"termid":"GO:0030813"}


id: PBO:0067080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 113, pseudogene","termid":"PBO:0067080"}


id: _global:results_in_maturation_of
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","definition":"The relationship that links an entity with a process that results in the progression of the entity over time that is independent of changes in it's shape and results in an end point state of that entity.","direct_ancestors":[{"relation_name":"is_a","term_name":"has_participant","termid":"RO:0000057"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"},{"relation_name":"is_a","term_name":"results_in_changes_to_anatomical_or_cellular_structure","termid":"_global:results_in_changes_to_anatomical_or_cellular_structure"},{"relation_name":"is_a","term_name":"results_in_developmental_progression_of","termid":"_global:results_in_developmental_progression_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_maturation_of","secondary_identifiers":["GOREL:0001013","RO:0002299"],"termid":"_global:results_in_maturation_of"}


id: GO:0009637
data:
  {"annotated_genes":["SJAG_02860","SJAG_05242"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009785"},{"annotations":[121261,121262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071483"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a blue light stimulus. Blue light is electromagnetic radiation with a wavelength of between 440 and 500nm.","definition_xrefs":["GOC:ai","GOC:mtg_far_red"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to light stimulus","termid":"GO:0009416"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02860":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 blue light","references_by_uniquename":{"GO_REF:0000108":null,"PMID:23873862":null},"synonyms":[{"name":"blue light response","type":"exact"},{"name":"blue-light response","type":"exact"},{"name":"response to blue light stimulus","type":"exact"}],"termid":"GO:0009637","terms_by_termid":{"GO:0009785":null,"GO:0071483":null}}


id: GO:1901746
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of prephenate(2-).","definition_xrefs":["GOC:yaf","GOC:TermGenie","PMID:16752890"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid catabolic process","termid":"GO:0043649"},{"relation_name":"is_a","term_name":"prephenate(2-) metabolic process","termid":"GO:1901745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"prephenate(2-) catabolic process","synonyms":[{"name":"prephenate breakdown","type":"exact"},{"name":"prephenate catabolism","type":"exact"},{"name":"prephenate degradation","type":"exact"},{"name":"prephenate(2-) breakdown","type":"exact"},{"name":"prephenate(2-) catabolism","type":"exact"},{"name":"prephenate(2-) degradation","type":"exact"}],"termid":"GO:1901746"}


id: PBO:0077451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM183A pseudogene 1","termid":"PBO:0077451"}


id: PBO:0057400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548h-2","termid":"PBO:0057400"}


id: PBO:0002276
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.2.14","termid":"PBO:0002276"}


id: PBO:0070216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 148 pseudogene","termid":"PBO:0070216"}


id: MONDO:0016251
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete salivary gland type cancer of the breast (obsolete MONDO:0016251)","termid":"MONDO:0016251","xrefs":{"Monarch":{"xref_id":"0016251"}}}


id: PBO:0029505
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_microcolony,_tapered_cells_(obsolete_FYPO:0002210)","termid":"PBO:0029505"}


id: FYPO:0004959
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 the mitochondrion 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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal level of substance in mitochondrion","synonyms":[{"name":"normal level of substance in mitochondria","type":"exact"},{"name":"normal level of substance in mitochondrion during mitotic cell cycle","type":"related"},{"name":"normal level of substance in mitochondrion during vegetative growth","type":"exact"},{"name":"normal mitochondrial level of substance","type":"exact"}],"termid":"FYPO:0004959"}


id: PBO:0056498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyl-CpG binding domain protein 3 like 2B","termid":"PBO:0056498"}


id: _global:results_in_formation_of
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","definition":"The relationship linking a entity and its participation in a process whereby at the beginning of the process the entity does not exist and at the end of the process the entity exists.","definition_xrefs":["GOC:mtg_berkeley_2013"],"direct_ancestors":[{"relation_name":"is_a","term_name":"has_output","termid":"RO:0002234"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"},{"relation_name":"is_a","term_name":"has_output","termid":"_global:has_output"},{"relation_name":"is_a","term_name":"results_in_developmental_progression_of","termid":"_global:results_in_developmental_progression_of"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"results_in_formation_of","secondary_identifiers":["RO:0002297","GOREL:0001020"],"termid":"_global:results_in_formation_of"}


id: MONDO:0850225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune hepatitis that is characterized by primary biliary cirrhosis clinical, biochemical, and histologic characteristics with antinuclear antibody positive sera.","definition_xrefs":["DOID:0080742"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholangitis","termid":"MONDO:0004789"},{"relation_name":"is_a","term_name":"autoimmune hepatitis","termid":"MONDO:0016264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"autoimmune cholangitis","secondary_identifiers":["UMLS:C4075851","MEDGEN:881331"],"termid":"MONDO:0850225","xrefs":{"Monarch":{"xref_id":"0850225"}}}


id: GO:0005018
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with platelet-derived growth factor isoform PDGF-AA, PDGF-BB or PDGF-AB to initiate a change in cell activity.","definition_xrefs":["PMID:1657917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"platelet-derived growth factor receptor activity","termid":"GO:0005017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016301","GO:0140096","GO:0003674","GO:0004672","GO:0016740","GO:0003824","GO:0038023"],"is_obsolete":false,"name":"platelet-derived growth factor alpha-receptor activity","synonyms":[{"name":"PDGF alpha-receptor activity","type":"exact"},{"name":"alphaPDGF receptor activity","type":"exact"}],"termid":"GO:0005018"}


id: PBO:0056838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MGAT4 family member C","termid":"PBO:0056838"}


id: SO:0002203
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A nucleotide site from which replication initiates.","definition_xrefs":["NCBI:cf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"origin_of_replication","termid":"SO:0000296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication_start_site","synonyms":[{"name":"INSDC_feature:misc_feature","type":"broad"},{"name":"INSDC_note:replication_start_site","type":"exact"},{"name":"replication start site","type":"exact"}],"termid":"SO:0002203"}


id: MONDO:0019674
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"postaxial polydactyly of fingers","termid":"MONDO:0017426"},{"relation_name":"is_a","term_name":"postaxial polydactyly","termid":"MONDO:0020927"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly type B","secondary_identifiers":["icd11.foundation:366939273","MEDGEN:357425","Orphanet:93335","SCTID:715707008","UMLS:C1868120","GARD:16818"],"synonyms":[{"name":"PAPB","type":"exact"}],"termid":"MONDO:0019674","xrefs":{"Monarch":{"xref_id":"0019674"}}}


id: PBO:0070787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 17","termid":"PBO:0070787"}


id: FYPO:0003327
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells form cytoplasmic microtubules that are curved, i.e. follow a smooth bend rather than a straight line, during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton morphology during mitotic interphase","termid":"FYPO:0003625"},{"relation_name":"is_a","term_name":"curved microtubules","termid":"FYPO:0004862"},{"relation_name":"is_a","term_name":"abnormal interphase microtubules","termid":"FYPO:0006101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002399","FYPO:0000054","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"curved interphase microtubules","synonyms":[{"name":"curved cytoplasmic microtubules during mitotic interphase","type":"exact"},{"name":"curved interphase cytoplasmic microtubules","type":"exact"},{"name":"curved interphase microtubules during mitotic cell cycle","type":"related"},{"name":"curved interphase microtubules during vegetative growth","type":"exact"}],"termid":"FYPO:0003327"}


id: FYPO:0000755
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutathione gamma-glutamylcysteinyltransferase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal glutathione gamma-glutamylcysteinyltransferase activity","termid":"FYPO:0000754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000707","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"decreased glutathione gamma-glutamylcysteinyltransferase activity","synonyms":[{"name":"reduced glutathione gamma-glutamylcysteinyltransferase activity","type":"exact"}],"termid":"FYPO:0000755"}


id: PR:G2TRS3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein kish-A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02592","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":"protein kish (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC530.16","secondary_identifiers":["UniProtKB:G2TRS3"],"synonyms":[{"name":"Spom972h-TMEM167A","type":"exact"}],"termid":"PR:G2TRS3"}


id: PBO:0063759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyhomeotic homolog 1","termid":"PBO:0063759"}


id: GO:0035936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of testosterone into the circulatory system. Testosterone is an androgen having 17beta-hydroxy and 3-oxo groups, together with unsaturation at C-4-C-5.","definition_xrefs":["GOC:sl","PMID:12606499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"},{"relation_name":"is_a","term_name":"hormone secretion","termid":"GO:0046879"},{"relation_name":"is_a","term_name":"lipid export from cell","termid":"GO:0140353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"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:0051179","GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"testosterone secretion","termid":"GO:0035936"}


id: GO:0106025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of onset of pupariation.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of pupariation","termid":"GO:0106023"},{"relation_name":"positively_regulates","term_name":"pupariation","termid":"GO:0035073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of pupariation","termid":"GO:0106025"}


id: MONDO:0054593
data:
  {"annotated_genes":["SJAG_05245"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87257],"is_not":false,"summary":null,"term":"MONDO:0054593"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal recessive primary microcephaly","termid":"MONDO:0016660"},{"relation_name":"is_a","term_name":"autosomal dominant primary microcephaly","termid":"MONDO:0007988"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05245":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0000426","MONDO:0002320"],"is_obsolete":false,"name":"microcephaly 18, primary, autosomal dominant","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617520","GARD:16233","DOID:0070295","MEDGEN:1391110","UMLS:C4479608"],"synonyms":[{"name":"MCPH18","type":"related"},{"name":"microcephaly 18, primary, autosomal dominant","type":"exact"},{"name":"primary autosomal dominant microcephaly 18","type":"related"}],"termid":"MONDO:0054593","terms_by_termid":{"MONDO:0054593":null},"xrefs":{"Monarch":{"xref_id":"0054593"}}}


id: PBO:0000758
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tandem duplication","termid":"PBO:0000758"}


id: PBO:0050038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class II, DR beta 6 (pseudogene)","termid":"PBO:0050038"}


id: PBO:0073235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO peptidase family member, NEDD8 specific","termid":"PBO:0073235"}


id: FYPO:0005073
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 mitotic chromosome condensation occurs to a lower extent than normal along the chromosome arms.","definition_xrefs":["GO:1990892","PMID:21633354","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased mitotic chromosome condensation","termid":"FYPO:0003286"}],"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:0000337"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000641","FYPO:0000337","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000293","FYPO:0001985"],"is_obsolete":false,"name":"decreased mitotic chromosome arm condensation","synonyms":[{"name":"decreased chromosome arm condensation during mitotic cell cycle","type":"related"},{"name":"decreased mitotic chromosome arm chromatin condensation","type":"exact"},{"name":"decreased mitotic chromosome arm condensation during vegetative growth","type":"exact"},{"name":"decreased mitotic chromosome condensation along chromosome arms","type":"exact"},{"name":"reduced mitotic chromosome arm condensation","type":"exact"}],"termid":"FYPO:0005073"}


id: PBO:0027620
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_cell_population_growth_on_urea_nitrogen_source","termid":"PBO:0027620"}


id: PBO:0044799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 1","termid":"PBO:0044799"}


id: MONDO:0015963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete inherited renal tumor (obsolete MONDO:0015963)","secondary_identifiers":["Orphanet:183595"],"synonyms":[{"name":"genetic renal tumor","type":"related"}],"termid":"MONDO:0015963","xrefs":{"Monarch":{"xref_id":"0015963"}}}


id: PBO:0048409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GASK1B antisense RNA 1","termid":"PBO:0048409"}


id: PBO:0000463
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulated by oleic acid","termid":"PBO:0000463"}


id: PBO:0059076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"molybdenum cofactor synthesis 3 pseudogene 2","termid":"PBO:0059076"}


id: GO:0098567
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of a plasma membrane that faces the periplasm, and all proteins embedded in it or attached to its surface.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"external side of plasma membrane","termid":"GO:0009897"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"part_of","termid":"GO:0009986"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0009986","GO:0005886"],"is_obsolete":false,"name":"periplasmic side of plasma membrane","termid":"GO:0098567"}


id: PR:Q9P6R2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- leo1 gene.","definition_xrefs":["UniProtKB:Q9P6R2","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C13E7.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC13E7.08c","synonyms":[{"name":"Spom972h-leo1","type":"exact"}],"termid":"PR:Q9P6R2"}


id: MONDO:0800413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antisocial behavior, susceptibility to","secondary_identifiers":["MEDGEN:934798","UMLS:C4310831"],"termid":"MONDO:0800413","xrefs":{"Monarch":{"xref_id":"0800413"}}}


id: PBO:0067155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 205, pseudogene","termid":"PBO:0067155"}


id: PBO:0043066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor muscarinic 2","termid":"PBO:0043066"}


id: GO:0031622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of fever generation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of acute inflammatory response","termid":"GO:0002675"},{"relation_name":"is_a","term_name":"regulation of fever generation","termid":"GO:0031620"},{"relation_name":"is_a","term_name":"positive regulation of heat generation","termid":"GO:0031652"},{"relation_name":"positively_regulates","term_name":"fever generation","termid":"GO:0001660"}],"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 fever generation","synonyms":[{"name":"activation of fever","type":"narrow"},{"name":"positive regulation of pyrexia","type":"exact"},{"name":"stimulation of fever","type":"narrow"},{"name":"up regulation of fever","type":"exact"},{"name":"up-regulation of fever","type":"exact"},{"name":"upregulation of fever","type":"exact"}],"termid":"GO:0031622"}


id: PBO:0091238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane transporter Mfs2","termid":"PBO:0091238"}


id: PBO:0050973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon omega 1 pseudogene 18","termid":"PBO:0050973"}


id: PBO:0087359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Splicing protein; required for splicing of two mitochondrial group I introns (BI3 in COB and AI5beta in COX1); forms a splicing complex, containing four subunits of Mrs1p and two subunits of the BI3-encoded maturase, that binds to the BI3 RNA; MRS1 has a paralog, CCE1, that arose from the whole genome duplication","termid":"PBO:0087359"}


id: MONDO:0003760
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor that arises from the ovary and occurs in children.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood germ cell tumor","termid":"MONDO:0003751"},{"relation_name":"is_a","term_name":"ovarian germ cell tumor","termid":"MONDO:0011366"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pediatric ovarian germ cell tumor","secondary_identifiers":["DOID:6084","MEDGEN:162990","UMLS:C0796664","NCIT:C8588"],"synonyms":[{"name":"childhood ovarian germ cell neoplasm","type":"exact"},{"name":"childhood ovarian germ cell tumor","type":"exact"},{"name":"childhood ovarian germ cell tumour","type":"exact"},{"name":"ovarian germ cell tumor","type":"broad"},{"name":"ovarian germ cell tumor of childhood","type":"exact"},{"name":"ovarian germ cell tumour","type":"broad"},{"name":"ovarian germ cell tumour of childhood","type":"exact"},{"name":"paediatric ovarian germ cell neoplasm","type":"exact"},{"name":"pediatric ovarian germ cell neoplasm","type":"exact"},{"name":"pediatric ovarian germ cell tumor","type":"exact"}],"termid":"MONDO:0003760","xrefs":{"Monarch":{"xref_id":"0003760"}}}


id: GO:0061559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of a cranial ganglion is generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ganglion morphogenesis","termid":"GO:0061552"},{"relation_name":"part_of","term_name":"cranial nerve morphogenesis","termid":"GO:0021602"},{"relation_name":"part_of","term_name":"cranial ganglion development","termid":"GO:0061550"}],"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":"cranial ganglion morphogenesis","synonyms":[{"name":"cranial ganglia morphogenesis","type":"related"}],"termid":"GO:0061559"}


id: PR:Q10163
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- smb1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10163"],"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":"small nuclear ribonucleoprotein-associated protein B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26A3.08","synonyms":[{"name":"Sm protein B (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Sm-B (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SmB (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-smb1","type":"exact"},{"name":"snRNP-B (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10163"}


id: PBO:0082958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic protein involved in the regulation of enolase (ENO1); mRNA expression is induced by calcium shortage, copper deficiency (via Mac1p) and the presence of galactose (via Gal4p); mRNA expression is also regulated by the cell cycle","termid":"PBO:0082958"}


id: PBO:0068717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4atac small nuclear 6, pseudogene","termid":"PBO:0068717"}


id: GO:0007343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the egg becomes metabolically active, initiates protein and DNA synthesis and undergoes structural changes to its cortex and/or cytoplasm.","definition_xrefs":["GOC:bf","PMID:9630751"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell activation","termid":"GO:0001775"},{"relation_name":"part_of","term_name":"single fertilization","termid":"GO:0007338"}],"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":"egg activation","secondary_identifiers":["Wikipedia:Egg_activation"],"termid":"GO:0007343"}


id: FYPO:0000582
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the rate, or speed, of spore germination is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spore germination","termid":"FYPO:0000305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased rate of spore germination","synonyms":[{"name":"reduced rate of spore germination","type":"exact"},{"name":"spore germination: decreased rate","type":"related"}],"termid":"FYPO:0000582"}


id: PBO:0049525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A.Z variant histone 1","termid":"PBO:0049525"}


id: GO:1901381
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of potassium ion transmembrane transport.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of potassium ion transport","termid":"GO:0043268"},{"relation_name":"is_a","term_name":"regulation of potassium ion transmembrane transport","termid":"GO:1901379"},{"relation_name":"is_a","term_name":"positive regulation of cation transmembrane transport","termid":"GO:1904064"},{"relation_name":"positively_regulates","term_name":"potassium ion transmembrane transport","termid":"GO:0071805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of potassium ion transmembrane transport","secondary_identifiers":["Reactome:R-HSA-1296041","Reactome:R-HSA-1296052"],"synonyms":[{"name":"activation of potassium ion transmembrane transport","type":"narrow"},{"name":"positive regulation of potassium ion membrane transport","type":"exact"},{"name":"up regulation of potassium ion transmembrane transport","type":"exact"},{"name":"up-regulation of potassium ion transmembrane transport","type":"exact"},{"name":"upregulation of potassium ion transmembrane transport","type":"exact"}],"termid":"GO:1901381"}


id: MONDO:0019647
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital megacalycosis","termid":"MONDO:0019639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"congenital bilateral megacalycosis","secondary_identifiers":["GARD:19180","MEDGEN:1842447","Orphanet:93177","UMLS:C5681455"],"termid":"MONDO:0019647","xrefs":{"Monarch":{"xref_id":"0019647"}}}


id: GO:0036207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of expression of a histone-encoding gene. Gene expression is the process in which a gene's coding sequence is converted into a mature gene product or products (proteins or RNA). This includes the production of an RNA transcript as well as any processing to produce a mature RNA product or an mRNA (for protein-coding genes) and the translation of that mRNA into protein.","definition_xrefs":["GOC:krc","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone gene expression (obsolete GO:0036207)","synonyms":[{"name":"activation of histone gene expression","type":"narrow"},{"name":"positive regulation of expression of histone-encoding gene","type":"exact"},{"name":"up-regulation of histone gene expression","type":"exact"},{"name":"upregulation of histone gene expression","type":"exact"}],"termid":"GO:0036207"}


id: PBO:0088855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 histone deacetylase associated PHD-finger protein Cph2","termid":"PBO:0088855"}


id: PBO:0085014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Neutral trehalase, degrades trehalose; required for thermotolerance and may mediate resistance to other cellular stresses; phosphorylated and activated by Cdc28p at the G1/S phase transition to coordinately regulate carbohydrate metabolism and the cell cycle; inhibited by Dcs1p; NTH1 has a paralog, NTH2, that arose from the whole genome duplication","termid":"PBO:0085014"}


id: PBO:0048288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galanin like peptide","termid":"PBO:0048288"}


id: PBO:0040322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase F1 subunit epsilon pseudogene 1","termid":"PBO:0040322"}


id: MONDO:0014607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the KCNA2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undetermined early-onset epileptic encephalopathy","termid":"MONDO:0018614"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005027","MONDO:0700092","MONDO:0005066"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 32","secondary_identifiers":["MEDGEN:909501","OMIM:616366","DOID:0080416","GARD:16096","UMLS:C4225350"],"synonyms":[{"name":"DEE32","type":"exact"},{"name":"EIEE32","type":"exact"},{"name":"KCNA2 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 32","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in KCNA2","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 32","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 32","type":"exact"}],"termid":"MONDO:0014607","xrefs":{"Monarch":{"xref_id":"0014607"}}}


id: MONDO:0003616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Formation of nodules in the isthmus of the fallopian tube due to fallopian tube diverticulosis. It may cause infertility or ectopic pregnancy.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic salpingitis","termid":"MONDO:0003617"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"salpingitis isthmica nodosa","secondary_identifiers":["UMLS:C0269043","NCIT:C40119","SCTID:36742000","DOID:5730","icd11.foundation:1586025352","MEDGEN:82840"],"termid":"MONDO:0003616","xrefs":{"Monarch":{"xref_id":"0003616"}}}


id: SO:0001503
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript for which no open reading frame has been identified and for which no other function has been determined.","definition_xrefs":["MGI:hdeen"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"processed_transcript","synonyms":[{"name":"processed transcript","type":"exact"}],"termid":"SO:0001503"}


id: MONDO:0004056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive or non-invasive papillary transitional cell carcinoma of the urinary bladder. It is classified as low - or high-grade. -- 2003","definition_xrefs":["NCIT:C7383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder papillary urothelial neoplasm","termid":"MONDO:0003442"},{"relation_name":"is_a","term_name":"bladder transitional cell carcinoma","termid":"MONDO:0005611"},{"relation_name":"is_a","term_name":"papillary transitional cell carcinoma","termid":"MONDO:0006350"}],"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":"bladder papillary urothelial carcinoma","secondary_identifiers":["MEDGEN:309552","DOID:6975","UMLS:C1518882"],"synonyms":[{"name":"bladder papillary urothelial carcinoma","type":"exact"},{"name":"bladder urothelial papillary carcinoma","type":"related"},{"name":"urinary bladder papillary transitional cell carcinoma","type":"exact"},{"name":"urothelial papillary carcinoma of the bladder","type":"exact"}],"termid":"MONDO:0004056","xrefs":{"Monarch":{"xref_id":"0004056"}}}


id: GO:0001855
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a C4b product of the classical complement cascade.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opsonin binding","termid":"GO:0001846"},{"relation_name":"is_a","term_name":"complement binding","termid":"GO:0001848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"complement component C4b binding","termid":"GO:0001855"}


id: MONDO:0020160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete secondary entropion (obsolete MONDO:0020160)","secondary_identifiers":["Orphanet:98569"],"termid":"MONDO:0020160","xrefs":{"Monarch":{"xref_id":"0020160"}}}


id: PBO:0044156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTD small phosphatase 1","termid":"PBO:0044156"}


id: GO:1904903
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of an ESCRT III complex into its constituent components.","definition_xrefs":["GOC:PARL","GOC:TermGenie","GO_REF:0000079","GOC:pad","PMID:20588296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ESCRT complex disassembly","termid":"GO:1904896"}],"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":"ESCRT III complex disassembly","termid":"GO:1904903"}


id: PBO:0029752
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_modification","termid":"PBO:0029752"}


id: PBO:0077162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TLE family member 3, transcriptional corepressor","termid":"PBO:0077162"}


id: GO:0071486
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a high light intensity stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to high light intensity","termid":"GO:0009644"},{"relation_name":"is_a","term_name":"cellular response to light intensity","termid":"GO:0071484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to high light intensity","termid":"GO:0071486"}


id: GO:0008998
data:
  {"annotated_genes":["SJAG_02948"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73661],"is_not":false,"summary":null,"term":"GO:0008998"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: [thioredoxin]-disulfide + a 2'-deoxyribonucleoside 5'-triphosphate + H2O = [thioredoxin]-dithiol + a ribonucleoside 5'-triphosphate.","definition_xrefs":["RHEA:12701"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups, disulfide as acceptor","termid":"GO:0016728"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02948":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:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"ribonucleoside-triphosphate reductase (thioredoxin) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:1.17.4.2","MetaCyc:1.17.4.2-RXN"],"synonyms":[{"name":"2'-deoxyribonucleoside-triphosphate:oxidized-thioredoxin 2'-oxidoreductase activity","type":"related"},{"name":"2'-deoxyribonucleoside-triphosphate:thioredoxin-disulfide 2'-oxidoreductase activity","type":"related"},{"name":"ribonucleoside-triphosphate reductase activity","type":"exact"},{"name":"ribonucleotide reductase activity","type":"broad"}],"termid":"GO:0008998","terms_by_termid":{"GO:0008998":null}}


id: MONDO:0001887
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by laceration in the posterior leaf of broad ligament along with abnormally mobile cervix.","definition_xrefs":["doi:10.1007/s10620-006-9237-7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"},{"relation_name":"is_a","term_name":"disorder of uterine broad ligament","termid":"MONDO:0045043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Allen-Masters syndrome","secondary_identifiers":["UMLS:C0152079","DOID:14133","SCTID:69186005","MEDGEN:508875","ICD9:620.6"],"synonyms":[{"name":"Broad ligament laceration syndrome","type":"exact"},{"name":"Masters-Allen syndrome","type":"exact"}],"termid":"MONDO:0001887","xrefs":{"Monarch":{"xref_id":"0001887"}}}


id: MONDO:0030966
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":"neurofacioskeletal syndrome with or without renal agenesis","secondary_identifiers":["OMIM:619194","UMLS:C5543070","MEDGEN:1778926"],"synonyms":[{"name":"NFSRA","type":"exact"},{"name":"Neurodevelopmental Disorder With Corpus Callosum Agenesis, Craniofacial Dysmorphism, and Skeletal Anomalies, With or Without Renal Agenesis","type":"exact"}],"termid":"MONDO:0030966","xrefs":{"Monarch":{"xref_id":"0030966"}}}


id: MONDO:0020617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blood group--ok (obsolete MONDO:0020617)","secondary_identifiers":["OMIM:111380"],"synonyms":[{"name":"BLOOD GROUP--OK","type":"related"},{"name":"OK","type":"related"},{"name":"blood group, OK","type":"exact"}],"termid":"MONDO:0020617","xrefs":{"Monarch":{"xref_id":"0020617"}}}


id: GO:0043198
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Cylindric portion of the dendrite, directly stemming from the perikaryon, and carrying the dendritic spines.","definition_xrefs":["GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"dendrite","termid":"GO:0030425"}],"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":"dendritic shaft","secondary_identifiers":["NIF_Subcellular:sao2034472720"],"synonyms":[{"name":"trunk","type":"related"}],"termid":"GO:0043198"}


id: PBO:0028708
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_number_of_double-strand_break_sites","termid":"PBO:0028708"}


id: GO:0072130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process in which the identity of the renal capsule is specified. Identity is considered to be the aggregate of characteristics by which a structure is recognized.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"is_a","term_name":"pattern specification involved in kidney development","termid":"GO:0061004"},{"relation_name":"part_of","term_name":"renal capsule formation","termid":"GO:0072129"}],"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":"renal capsule specification","termid":"GO:0072130"}


id: GO:0045807
data:
  {"annotated_genes":["SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105493],"is_not":false,"summary":null,"term":"GO:0045807"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of endocytosis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of endocytosis","termid":"GO:0030100"},{"relation_name":"is_a","term_name":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"positively_regulates","term_name":"endocytosis","termid":"GO:0006897"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00845":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"positive regulation of endocytosis","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of endocytosis","type":"narrow"},{"name":"stimulation of endocytosis","type":"narrow"},{"name":"up regulation of endocytosis","type":"exact"},{"name":"up-regulation of endocytosis","type":"exact"},{"name":"upregulation of endocytosis","type":"exact"}],"termid":"GO:0045807","terms_by_termid":{"GO:0045807":null}}


id: PBO:0083267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; not conserved in closely related Saccharomyces species; 85% of ORF overlaps the uncharacterized gene CUE5; deletion in cyr1 mutant results in loss of stress resistance","termid":"PBO:0083267"}


id: PBO:0080045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 18","termid":"PBO:0080045"}


id: PBO:0041360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C4BPA pseudogene 3","termid":"PBO:0041360"}


id: GO:0003079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of natriuresis.","definition_xrefs":["GOC:mtg_cardio"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of natriuresis (obsolete GO:0003079)","synonyms":[{"name":"positive regulation of natriuresis","type":"exact"}],"termid":"GO:0003079"}


id: MONDO:0006416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Burkitt lymphoma that arises from the small intestine.","definition_xrefs":["NCIT:C27409"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"small intestine lymphoma","termid":"MONDO:0001852"},{"relation_name":"is_a","term_name":"Burkitt lymphoma","termid":"MONDO:0007243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570","MONDO:0004335"],"is_obsolete":false,"name":"small intestinal Burkitt lymphoma","secondary_identifiers":["UMLS:C1335991","MEDGEN:277650"],"synonyms":[{"name":"Burkitt lymphoma of small intestine","type":"exact"},{"name":"Burkitts lymphoma of small intestine","type":"exact"},{"name":"primary small intestinal Burkitt's lymphoma","type":"exact"},{"name":"small intestinal Burkitt lymphoma","type":"exact"},{"name":"small intestinal Burkitt's lymphoma","type":"exact"},{"name":"small intestine Burkitt lymphoma","type":"exact"},{"name":"small intestine Burkitt's lymphoma","type":"exact"},{"name":"small intestine Burkitts lymphoma","type":"exact"}],"termid":"MONDO:0006416","xrefs":{"Monarch":{"xref_id":"0006416"}}}


id: MONDO:0015278
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87576],"is_not":false,"summary":null,"term":"MONDO:0015278"}]},"cv_name":"mondo","definition":"Familial pancreatic carcinoma is defined by the presence of pancreatic cancer (PC) in two or more first-degree relatives.","definition_xrefs":["Orphanet:1333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"exocrine pancreatic carcinoma","termid":"MONDO:0005192"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"familial pancreatic carcinoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C2931038","MEDGEN:419700","icd11.foundation:1385362916","NCIT:C43298","GARD:4206","OMIM:260350","SCTID:715414009","MESH:C535837"],"synonyms":[{"name":"familial pancreatic cancer","type":"exact"},{"name":"familial pancreatic carcinoma","type":"exact"},{"name":"hereditary exocrine pancreatic carcinoma","type":"exact"},{"name":"hereditary pancreatic cancer","type":"exact"},{"name":"hereditary pancreatic carcinoma","type":"exact"},{"name":"pancreatic acinar carcinoma","type":"related"},{"name":"pancreatic cancer, somatic","type":"exact"},{"name":"pancreatic carcinoma, somatic","type":"exact"}],"termid":"MONDO:0015278","terms_by_termid":{"MONDO:0015278":null},"xrefs":{"Monarch":{"xref_id":"0015278"}}}


id: PBO:0055436
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 2866","termid":"PBO:0055436"}


id: GO:0048295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of isotype switching to IgE isotypes.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of isotype switching","termid":"GO:0045830"},{"relation_name":"is_a","term_name":"regulation of isotype switching to IgE isotypes","termid":"GO:0048293"},{"relation_name":"positively_regulates","term_name":"isotype switching to IgE isotypes","termid":"GO:0048289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"positively_regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0006259","GO:0006310","GO:0008150"],"is_obsolete":false,"name":"positive regulation of isotype switching to IgE isotypes","synonyms":[{"name":"activation of isotype switching to IgE isotypes","type":"narrow"},{"name":"positive regulation of class switch recombination to IgE isotypes","type":"exact"},{"name":"positive regulation of class switching to IgE isotypes","type":"exact"},{"name":"positive regulation of isotype switch recombination to IgE isotypes","type":"exact"},{"name":"stimulation of isotype switching to IgE isotypes","type":"narrow"},{"name":"up regulation of isotype switching to IgE isotypes","type":"exact"},{"name":"up-regulation of isotype switching to IgE isotypes","type":"exact"},{"name":"upregulation of isotype switching to IgE isotypes","type":"exact"}],"termid":"GO:0048295"}


id: MONDO:0017954
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pyogenic autoinflammatory syndrome (obsolete MONDO:0017954)","secondary_identifiers":["Orphanet:324927"],"termid":"MONDO:0017954","xrefs":{"Monarch":{"xref_id":"0017954"}}}


id: MOD:00418
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with an (pyridin-3-yl)acetyl group.","definition_xrefs":["Unimod:25","PubMed:9276974"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylated residue","termid":"MOD:00649"},{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridylacetylated residue","synonyms":[{"name":"Pyridylacetyl","type":"related"},{"name":"pyridylacetyl","type":"related"}],"termid":"MOD:00418"}


id: PBO:0075624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPRING1 pseudogene 1","termid":"PBO:0075624"}


id: FYPO:0004553
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cut phenotype that is observed when a cell is exposed to ionizing radiation during mitotic S phase. In a cut phenotype, a cell undergoes septation despite abnormal chromosome segregation.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cut during cellular response to ionizing radiation during mitotic S phase (obsolete FYPO:0004553)","synonyms":[{"name":"cut during cellular response to IR during mitotic S phase","type":"exact"},{"name":"cut during cellular response to ionizing radiation during S phase of mitotic cell cycle","type":"related"},{"name":"cut during cellular response to ionizing radiation during mitotic S phase during vegetative growth","type":"exact"},{"name":"septation following abnormal mitotic chromosome segregation during cellular response to ionizing radiation during mitotic S phase","type":"exact"}],"termid":"FYPO:0004553"}


id: PATO:0001880
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's having a tail or tail-like projection.","definition_xrefs":["PATOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exserted","termid":"PATO:0000623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caudate","synonyms":[{"name":"caudal","type":"exact"},{"name":"tailed","type":"related"}],"termid":"PATO:0001880"}


id: GO:0098851
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to double-stranded miRNA. double-stranded miRNA is formed by processing of pre-miRNA stem-loop structures.","definition_xrefs":["PMID:19966796","GOC:BHF_miRNA","GOC:BHF","GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"double-stranded RNA binding","termid":"GO:0003725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003723"],"is_obsolete":false,"name":"double-stranded miRNA binding","synonyms":[{"name":"miRNA duplex binding","type":"exact"}],"termid":"GO:0098851"}


id: GO:0033643
data:
  {"annotated_genes":["SJAG_02392"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[121254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0085039"}]},"cv_name":"cellular_component","definition":"Any constituent part of a host cell. 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":"host cellular component","termid":"GO:0018995"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02392":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell part","references_by_uniquename":{"PMID:30726171":null},"termid":"GO:0033643","terms_by_termid":{"GO:0085039":null}}


id: PR:Q9UUF3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC17A3.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UUF3"],"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":"tyrosine-protein phosphatase C17A3.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17A3.03c","synonyms":[{"name":"Spom972h-SPBC17A3.03c","type":"exact"}],"termid":"PR:Q9UUF3"}


id: GO:1990899
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process following clipping in double-strand break processing of SPO11 induced breaks, where long-tract single-stranded 3'-end DNA is generated from naked (SPO11 has been removed) 5' ends.","definition_xrefs":["PMID:26130711"],"gene_count":0,"genotype_count":0,"name":"obsolete meiotic DNA double-strand break resectioning (obsolete GO:1990899)","termid":"GO:1990899"}


id: PBO:0091280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial F1-FO ATP synthase chaperone Atp10","termid":"PBO:0091280"}


id: PBO:0048317
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 28","termid":"PBO:0048317"}


id: SO:0001231
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A modified RNA base in which guanine is methylated at the 7- position.","definition_xrefs":["RSC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_RNA_base_feature","termid":"SO:0000250"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"seven_methylguanine","synonyms":[{"name":"7-methylguanine","type":"exact"},{"name":"seven methylguanine","type":"exact"}],"termid":"SO:0001231"}


id: PBO:0027578
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transposon-derived_cDNA_recombination","termid":"PBO:0027578"}


id: PBO:0053708
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 911","termid":"PBO:0053708"}


id: GO:0044009
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transfer of virions by means of an organism (often an insect or other animal) in order to create new infection.","definition_xrefs":["GOC:cc"],"gene_count":0,"genotype_count":0,"name":"obsolete viral transmission by vector (obsolete GO:0044009)","termid":"GO:0044009"}


id: PBO:0058149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4444-2","termid":"PBO:0058149"}


id: PATO:0001593
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature which is relatively low.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"curved","termid":"PATO:0000406"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased curvature","termid":"PATO:0001593"}


id: PATO:0001314
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A variability quality inhering in a bearer by virtue of the bearer's having or exhibiting variation of temperature.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"variability of temperature","termid":"PATO:0001304"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variant temperature","termid":"PATO:0001314"}


id: FYPO:0006657
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which acid phosphatase activity is absent during a cellular response to phosphate starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished acid phosphatase activity","termid":"FYPO:0002244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0000654","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"abolished acid phosphatase activity during cellular response to phosphate starvation","synonyms":[{"name":"acid phosphatase activity abolished during cellular response to phosphate starvation","type":"exact"}],"termid":"FYPO:0006657"}


id: PBO:0092019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Tryptophan (cca), mitochondrial","termid":"PBO:0092019"}


id: MONDO:0024238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurodegenerative disease that involves the telencephalon.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"cerebral degeneration","secondary_identifiers":["MEDGEN:56343","SCTID:418143002","UMLS:C0154671","ICD9:331.9"],"synonyms":[{"name":"cerebral degeneration","type":"exact"},{"name":"neurodegenerative disease of telencephalon","type":"exact"},{"name":"telencephalon neurodegenerative disease","type":"exact"}],"termid":"MONDO:0024238","xrefs":{"Monarch":{"xref_id":"0024238"}}}


id: MONDO:0018610
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset partial cataract","termid":"MONDO:0020377"}],"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":"early-onset posterior subcapsular cataract","secondary_identifiers":["GARD:21846","MEDGEN:1842187","Orphanet:441447","UMLS:C5681190"],"termid":"MONDO:0018610","xrefs":{"Monarch":{"xref_id":"0018610"}}}


id: PBO:0079506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin pseudogene 4","termid":"PBO:0079506"}


id: GO:0047900
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + formate = ADP + formyl phosphate + H+.","definition_xrefs":["RHEA:16009","EC:2.7.2.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, carboxyl group as acceptor","termid":"GO:0016774"}],"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:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016301","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"formate kinase activity","secondary_identifiers":["KEGG_REACTION:R00518","MetaCyc:FORMATE-KINASE-RXN"],"synonyms":[{"name":"ATP:formate phosphotransferase activity","type":"related"}],"termid":"GO:0047900"}


id: MONDO:0034103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemolytic-uremic syndrome","termid":"MONDO:0001549"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"}],"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":"infection-related hemolytic uremic syndrome","secondary_identifiers":["MEDGEN:1826072","GARD:22234","Orphanet:544482","UMLS:C5680165"],"termid":"MONDO:0034103","xrefs":{"Monarch":{"xref_id":"0034103"}}}


id: MOD:00493
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with a formyl group.","definition_xrefs":["DeltaMass:0","Unimod:122","PubMed:15799070"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylated residue","termid":"MOD:00649"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formylated residue","synonyms":[{"name":"FoRes","type":"exact"},{"name":"Formyl","type":"related"},{"name":"Formylation","type":"related"},{"name":"Formylation (CHO)","type":"exact"}],"termid":"MOD:00493"}


id: PR:Q10196
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC11C11.05 gene.","definition_xrefs":["UniProtKB:Q10196","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C11C11.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC11C11.05","synonyms":[{"name":"Spom972h-SPBC11C11.05","type":"exact"}],"termid":"PR:Q10196"}


id: GO:1902676
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any ciliary basal body that is part of a right ventral flagellum found in Giardia species (trophozoite stage).","definition_xrefs":["PMID:5961344","GO_REF:0000064","PMID:16607022","GOC:giardia","GOC:TermGenie","ISBN:9780124260207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary basal body","termid":"GO:0036064"},{"relation_name":"part_of","term_name":"right ventral flagellum","termid":"GO:0097559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0015630","GO:0005575"],"is_obsolete":false,"name":"right ventral basal body","synonyms":[{"name":"cilial basal body of right ventral cilium","type":"exact"},{"name":"cilial basal body of right ventral flagellum","type":"exact"},{"name":"ciliary basal body of right ventral cilium","type":"exact"},{"name":"ciliary basal body of right ventral flagellum","type":"exact"},{"name":"cilium basal body of right ventral cilium","type":"exact"},{"name":"cilium basal body of right ventral flagellum","type":"exact"},{"name":"microtubule basal body of right ventral cilium","type":"exact"},{"name":"microtubule basal body of right ventral flagellum","type":"exact"},{"name":"right ventral flagellum ciliary basal body","type":"exact"}],"termid":"GO:1902676"}


id: PBO:0053201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase","termid":"PBO:0053201"}


id: SO:0000021
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An internal RNA loop where one of the strands includes more bases than the corresponding region on the other strand.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA_internal_loop","termid":"SO:0000020"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asymmetric_RNA_internal_loop","synonyms":[{"name":"asymmetric RNA internal loop","type":"exact"}],"termid":"SO:0000021"}


id: MONDO:1010560
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spina bifida that occurs in rabbit.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spina bifida, non-human animal","termid":"MONDO:1010047"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spina bifida, rabbit","secondary_identifiers":["OMIA:000933-9986"],"termid":"MONDO:1010560","xrefs":{"Monarch":{"xref_id":"1010560"}}}


id: GO:0034334
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The maintenance of an adherens junction. An adherens junction is a cell-cell junction composed of the epithelial cadherin-catenin complex at which the cytoplasmic face of the plasma membrane is attached to actin filaments.","definition_xrefs":["GOC:bc","GOC:mah","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adherens junction organization","termid":"GO:0034332"},{"relation_name":"is_a","term_name":"cell-cell junction maintenance","termid":"GO:0045217"}],"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":"adherens junction maintenance","termid":"GO:0034334"}


id: PBO:0042203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin G2 pseudogene 1","termid":"PBO:0042203"}


id: GO:0061015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of snRNA, small nuclear ribonucleic acid into the nucleus.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA import into nucleus","termid":"GO:0006404"},{"relation_name":"is_a","term_name":"snRNA transport","termid":"GO:0051030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006913"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006913","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"snRNA import into nucleus","termid":"GO:0061015"}


id: PBO:0085325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatidylinositol:ceramide phosphoinositol transferase; required for sphingolipid synthesis; can mutate to confer aureobasidin A resistance; also known as IPC synthase","termid":"PBO:0085325"}


id: MONDO:0007078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of pseudohypoparathyroidism (PHP) characterized by renal resistance to parathyroid hormone (PTH), resulting in hypocalcemia, hyperphosphatemia, and elevated PTH; resistance to other hormones including thydroid stimulating hormone (TSH), gonadotropins and growth-hormone-releasing hormone (GHRH); and a constellation of clinical features known as Albright hereditary osteodystrophy (AHO).","definition_xrefs":["Orphanet:79443"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"excluded_subClassOf","term_name":"dermis disorder","termid":"MONDO:0021154"},{"relation_name":"is_a","term_name":"acromelic dysplasia","termid":"MONDO:0019695"},{"relation_name":"is_a","term_name":"pseudohypoparathyroidism","termid":"MONDO:0019992"},{"relation_name":"is_a","term_name":"disorder of GNAS inactivation","termid":"MONDO:0800466"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0005066"],"is_obsolete":false,"name":"pseudohypoparathyroidism type 1A","secondary_identifiers":["UMLS:C3494506","icd11.foundation:1513156369","NANDO:1201075","GARD:7486","ICD9:275.49","DOID:0080053","MEDGEN:488447","NCIT:C129721","OMIM:103580","SCTID:58833000","MESH:C537045"],"synonyms":[{"name":"AHO","type":"related"},{"name":"AHO-PHP syndrome Ia","type":"exact"},{"name":"Albright hereditary osteodystrophy","type":"exact"},{"name":"Albright hereditary osteodystrophy with multiple hormone resistance","type":"exact"},{"name":"Albright hereditary osteodystrophy-PHP syndrome Ia","type":"exact"},{"name":"Albright's hereditary osteodystrophy","type":"exact"},{"name":"PHP 1A","type":"related"},{"name":"PHP1A","type":"exact"},{"name":"Pseudohypoparathyroidism Ia","type":"exact"},{"name":"Pseudohypoparathyroidism type 1A","type":"exact"},{"name":"Pseudohypoparathyroidism, type 1A","type":"related"},{"name":"Pseudohypoparathyroidism, type IA","type":"related"}],"termid":"MONDO:0007078","xrefs":{"Monarch":{"xref_id":"0007078"}}}


id: PBO:0047947
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(16)(q23.2)","termid":"PBO:0047947"}


id: PBO:0085270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peroxisomal cystathionine beta-lyase; converts cystathionine into homocysteine; may be redox regulated by Gto1p; involved in the release of the aromatic thiol 3-mercaptohexanol during wine fermentation","termid":"PBO:0085270"}


id: FYPO:0007648
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to pericentric heterochromatin is abnormal.","definition_xrefs":["GO:1902682","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to heterochromatin","termid":"FYPO:0004718"},{"relation_name":"is_a","term_name":"abnormal protein localization to centromere","termid":"FYPO:0005597"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to pericentric heterochromatin","synonyms":[{"name":"abnormal protein localization to centromeric heterochromatin","type":"exact"},{"name":"abnormal protein localization to nuclear centromeric heterochromatin","type":"exact"}],"termid":"FYPO:0007648"}


id: GO:0035473
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a lipase.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"lipase binding","termid":"GO:0035473"}


id: PBO:0064204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLAG1 zinc finger","termid":"PBO:0064204"}


id: PBO:0031642
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_shmoo_formation","termid":"PBO:0031642"}


id: MONDO:0012762
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the CASQ2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catecholaminergic polymorphic ventricular tachycardia","termid":"MONDO:0017990"}],"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":"catecholaminergic polymorphic ventricular tachycardia 2","secondary_identifiers":["ICD10CM:I47.2","DOID:0060676","UMLS:C2677794","GARD:15535","MEDGEN:393837","NCIT:C148368","OMIM:611938"],"synonyms":[{"name":"CASQ2 catecholaminergic polymorphic ventricular tachycardia","type":"exact"},{"name":"CPVT2","type":"related"},{"name":"CVPT2","type":"exact"},{"name":"catecholaminergic polymorphic ventricular tachycardia 2","type":"exact"},{"name":"catecholaminergic polymorphic ventricular tachycardia caused by mutation in CASQ2","type":"exact"},{"name":"catecholaminergic polymorphic ventricular tachycardia type 2","type":"exact"},{"name":"ventricular tachycardia, catecholaminergic polymorphic, 2","type":"related"},{"name":"ventricular tachycardia, catecholaminergic polymorphic, type 2","type":"exact"},{"name":"ventricular tachycardia, stress-induced polymorphic","type":"related"}],"termid":"MONDO:0012762","xrefs":{"Monarch":{"xref_id":"0012762"}}}


id: PBO:0111646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative cofactor 2 complex subunit Bur6","termid":"PBO:0111646"}


id: PBO:0041619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium binding protein 5","termid":"PBO:0041619"}


id: GO:0010172
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the embryonic soma are generated and organized.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"body morphogenesis","termid":"GO:0010171"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"embryonic body morphogenesis","termid":"GO:0010172"}


id: FYPO:0002294
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an elongated germ tube, but does not go on to form a viable dividing cell, and instead lyses.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"vegetative cell lysis","termid":"FYPO:0000647"},{"relation_name":"is_a","term_name":"vegetative cell lysis","termid":"FYPO:0000647"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, with elongated germ tube","termid":"FYPO:0002379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000005","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"inviable after spore germination with elongated germ tube and cell lysis","synonyms":[{"name":"inviable after spore germination with elongated cell and cell lysis","type":"exact"},{"name":"inviable after spore germination, without cell division, with elongated germ tube and cell lysis","type":"exact"},{"name":"inviable germinated spore with elongated germ tube and cell lysis","type":"exact"},{"name":"lethal after spore germination with elongated germ tube and cell lysis","type":"exact"},{"name":"lysed cell after spore germination with elongated germ tube","type":"exact"}],"termid":"FYPO:0002294"}


id: GO:0016443
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the digestion of double-stranded RNAs into 20 to 30-nucleotide products. These products typically associate to the RNA-induced silencing complex and serve as guide RNAs for posttranslational RNA interference.","definition_xrefs":["PMID:15242644"],"gene_count":0,"genotype_count":0,"name":"obsolete bidentate ribonuclease III activity (obsolete GO:0016443)","synonyms":[{"name":"bidentate RNase III activity","type":"exact"}],"termid":"GO:0016443"}


id: PBO:0109047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 histone deacetylase complex MRG family subunit Alp13/Eaf3","termid":"PBO:0109047"}


id: MONDO:0800043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare autosomal recessive congenital primary skeletal dysplasia, characterized by small stature, bowing of the long bones, camptodactyly, hyperthermic episodes, respiratory distress/apneic episodes and feeding difficulties that usually lead to early mortality.","definition_xrefs":["Orphanet:3206"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schwartz-Jampel syndrome","termid":"MONDO:0009717"},{"relation_name":"is_a","term_name":"bent bone dysplasia","termid":"MONDO:0019698"},{"relation_name":"is_a","term_name":"Stuve-Wiedemann syndrome","termid":"MONDO:0031280"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0006025"],"is_obsolete":false,"name":"Stüve-Wiedemann syndrome 1","secondary_identifiers":["GARD:5045","OMIM:601559","SCTID:254097005","UMLS:C5676888","MEDGEN:1803541","MESH:C537502"],"synonyms":[{"name":"SJS2","type":"exact"},{"name":"STUVE-Wiedemann syndrome","type":"broad"},{"name":"STWS","type":"exact"},{"name":"SWS","type":"broad"},{"name":"Schwartz-Jampel syndrome neonatal","type":"exact"},{"name":"Schwartz-Jampel syndrome type 2","type":"exact"},{"name":"Schwartz-Jampel syndrome, neonatal","type":"exact"},{"name":"Schwartz-Jampel syndrome, type 2","type":"related"},{"name":"Stuve-Wiedemann syndrome","type":"broad"},{"name":"Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome","type":"exact"},{"name":"Stuve-Wiedemann/Schwartz-Jampel type 2 syndrome","type":"related"},{"name":"Stws","type":"broad"},{"name":"Stüve-Wiedemann dysplasia","type":"exact"},{"name":"Stüve-Wiedemann syndrome","type":"broad"},{"name":"Stüve-Wiedemann/Schwartz-Jampel type 2 syndrome","type":"exact"},{"name":"neonatal Schwartz-Jampel syndrome","type":"exact"},{"name":"neonatal Schwartz-Jampel syndrome type 2","type":"related"}],"termid":"MONDO:0800043","xrefs":{"Monarch":{"xref_id":"0800043"}}}


id: MONDO:0019022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sensorineural hearing loss-early graying-essential tremor syndrome is characterized by the combination of sensorineural hearing loss, early graying of scalp hair and adult onset essential tremor.","definition_xrefs":["Orphanet:66633"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sensorineural hearing loss-early graying-essential tremor syndrome","secondary_identifiers":["GARD:18869","UMLS:C4510044","MEDGEN:1389497"],"termid":"MONDO:0019022","xrefs":{"Monarch":{"xref_id":"0019022"}}}


id: GO:0075283
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a multicellular or syncytial spore via septations over time, from its initiation to the mature structure.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sporulation","termid":"GO:0043934"}],"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":"sporulation resulting in formation of a multicellular or syncytial spore","synonyms":[{"name":"multicellular or syncytial spore formation by sporulation","type":"exact"}],"termid":"GO:0075283"}


id: GO:0010776
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A system for the identification and correction of base-base mismatches, small insertion-deletion loops, and regions of heterology that are present in duplex DNA formed with strands from two recombining molecules resulting in meiotic gene conversion. Meiotic gene conversion is the cell cycle process in which genetic information is transferred from one helix to another.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic mismatch repair","termid":"GO:0000710"},{"relation_name":"part_of","term_name":"meiotic gene conversion","termid":"GO:0006311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0006281"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0006310","GO:0006281","GO:0007049"],"is_obsolete":false,"name":"meiotic mismatch repair involved in meiotic gene conversion","termid":"GO:0010776"}


id: PBO:0089381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malate transmembrane transporter","termid":"PBO:0089381"}


id: PBO:0028539
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_primary_cell_septum_thickness","termid":"PBO:0028539"}


id: PBO:0011095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOPs/CORVET complex subunit Pep5/Vps11 (predicted)","termid":"PBO:0011095"}


id: GO:0016614
data:
  {"annotated_genes":["SJAG_02313","SJAG_00409","SJAG_02960","SJAG_02010","SJAG_00337","SJAG_01850","SJAG_02488","SJAG_03370","SJAG_03198","SJAG_01036","SJAG_01012","SJAG_00237","SJAG_00242","SJAG_02176","SJAG_01690","SJAG_00240","SJAG_00593","SJAG_00281","SJAG_00396","SJAG_02855","SJAG_01492","SJAG_00502","SJAG_01137","SJAG_02696","SJAG_05033","SJAG_04027","SJAG_04972","SJAG_03235","SJAG_03196","SJAG_03804","SJAG_03958","SJAG_01298","SJAG_03821","SJAG_01414","SJAG_04458","SJAG_04362","SJAG_03822","SJAG_04660","SJAG_00265","SJAG_01753","SJAG_04376","SJAG_03098","SJAG_02297","SJAG_01457","SJAG_02963","SJAG_03152","SJAG_02142","SJAG_01869","SJAG_00491","SJAG_03715","SJAG_02148","SJAG_01543","SJAG_03852","SJAG_00038","SJAG_03562","SJAG_03492","SJAG_04048","SJAG_00630","SJAG_01432"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70945],"is_not":false,"summary":null,"term":"GO:0016614"},{"annotations":[113600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099615"},{"annotations":[65917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047545"},{"annotations":[72603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000253"},{"annotations":[111910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000252"},{"annotations":[74679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047560"},{"annotations":[76482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003862"},{"annotations":[58735,98945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004316"},{"annotations":[67107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008703"},{"annotations":[73172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000140"},{"annotations":[72849,79835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004022"},{"annotations":[108349,79203,94244,108350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008106"},{"annotations":[93590,75991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004032"},{"annotations":[77869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003885"},{"annotations":[82100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004458"},{"annotations":[82099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008720"},{"annotations":[97534,102975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032866"},{"annotations":[106859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046526"},{"annotations":[100516,100515,116456,116455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120542"},{"annotations":[80782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047935"},{"annotations":[69610,63459,60247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004345"},{"annotations":[75191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008888"},{"annotations":[70756,63794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141152"},{"annotations":[76836,76965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030267"},{"annotations":[81999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004399"},{"annotations":[72434],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047046"},{"annotations":[72825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004412"},{"annotations":[73422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004420"},{"annotations":[76963,76834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016618"},{"annotations":[76588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003938"},{"annotations":[93593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047018"},{"annotations":[93594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047019"},{"annotations":[75536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004450"},{"annotations":[78717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004455"},{"annotations":[70512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045703"},{"annotations":[97535,102976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032867"},{"annotations":[74300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003939"},{"annotations":[75789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030060"},{"annotations":[74934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004471"},{"annotations":[69829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050085"},{"annotations":[106856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043892"},{"annotations":[66758,79937,70631,67223,105724,65873,60196,72141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016616"},{"annotations":[82062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004616"},{"annotations":[65915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004617"},{"annotations":[116236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050236"},{"annotations":[105273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106322"},{"annotations":[105274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106321"},{"annotations":[105275],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080007"},{"annotations":[110341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004757"},{"annotations":[60346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004764"},{"annotations":[70514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141040"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a CH-OH group act as a hydrogen or electron donor and reduces a hydrogen or electron acceptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":59,"genes_by_uniquename":{"SJAG_00038":null,"SJAG_00237":null,"SJAG_00240":null,"SJAG_00242":null,"SJAG_00265":null,"SJAG_00281":null,"SJAG_00337":null,"SJAG_00396":null,"SJAG_00409":null,"SJAG_00491":null,"SJAG_00502":null,"SJAG_00593":null,"SJAG_00630":null,"SJAG_01012":null,"SJAG_01036":null,"SJAG_01137":null,"SJAG_01298":null,"SJAG_01414":null,"SJAG_01432":null,"SJAG_01457":null,"SJAG_01492":null,"SJAG_01543":null,"SJAG_01690":null,"SJAG_01753":null,"SJAG_01850":null,"SJAG_01869":null,"SJAG_02010":null,"SJAG_02142":null,"SJAG_02148":null,"SJAG_02176":null,"SJAG_02297":null,"SJAG_02313":null,"SJAG_02488":null,"SJAG_02696":null,"SJAG_02855":null,"SJAG_02960":null,"SJAG_02963":null,"SJAG_03098":null,"SJAG_03152":null,"SJAG_03196":null,"SJAG_03198":null,"SJAG_03235":null,"SJAG_03370":null,"SJAG_03492":null,"SJAG_03562":null,"SJAG_03715":null,"SJAG_03804":null,"SJAG_03821":null,"SJAG_03822":null,"SJAG_03852":null,"SJAG_03958":null,"SJAG_04027":null,"SJAG_04048":null,"SJAG_04362":null,"SJAG_04376":null,"SJAG_04458":null,"SJAG_04660":null,"SJAG_04972":null,"SJAG_05033":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"oxidoreductase activity, acting on CH-OH group of donors","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-1500781","EC:1.1.-.-"],"synonyms":[{"name":"oxidoreductase activity, acting on the CH-OH group of donors, other acceptors","type":"narrow"}],"termid":"GO:0016614","terms_by_termid":{"GO:0000140":null,"GO:0000252":null,"GO:0000253":null,"GO:0003862":null,"GO:0003885":null,"GO:0003938":null,"GO:0003939":null,"GO:0004022":null,"GO:0004032":null,"GO:0004316":null,"GO:0004345":null,"GO:0004399":null,"GO:0004412":null,"GO:0004420":null,"GO:0004450":null,"GO:0004455":null,"GO:0004458":null,"GO:0004471":null,"GO:0004616":null,"GO:0004617":null,"GO:0004757":null,"GO:0004764":null,"GO:0008106":null,"GO:0008703":null,"GO:0008720":null,"GO:0008888":null,"GO:0016614":null,"GO:0016616":null,"GO:0016618":null,"GO:0030060":null,"GO:0030267":null,"GO:0032866":null,"GO:0032867":null,"GO:0043892":null,"GO:0045703":null,"GO:0046526":null,"GO:0047018":null,"GO:0047019":null,"GO:0047046":null,"GO:0047545":null,"GO:0047560":null,"GO:0047935":null,"GO:0050085":null,"GO:0050236":null,"GO:0080007":null,"GO:0099615":null,"GO:0106321":null,"GO:0106322":null,"GO:0120542":null,"GO:0141040":null,"GO:0141152":null}}


id: GO:1990162
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H3 N6-acetyl-L-lysine (position 4) + H2O = histone H3 L-lysine (position 4) + acetate. This reaction represents the removal of an acetyl group from lysine at position 4 of the histone H3 protein.","definition_xrefs":["PMID:28450737","PMID:23771057","GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3K deacetylase activity","termid":"GO:0141050"},{"relation_name":"is_a","term_name":"histone deacetylase activity, hydrolytic mechanism","termid":"GO:0141221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0033558"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0019213"}],"interesting_parent_ids":["GO:0033558","GO:0140096","GO:0003824","GO:0016810","GO:0003674","GO:0016787","GO:0019213"],"is_obsolete":false,"name":"histone H3K4 deacetylase activity, hydrolytic mechanism","synonyms":[{"name":"histone H3-K4 deacetylase activity","type":"exact"},{"name":"histone H3K14 deacetylase activity","type":"broad"},{"name":"histone deacetylase activity (H3-K4 specific)","type":"broad"}],"termid":"GO:1990162"}


id: PBO:0046683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation termination factor 1 pseudogene 1","termid":"PBO:0046683"}


id: PBO:0053839
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 1104","termid":"PBO:0053839"}


id: PBO:0028609
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_urease_activity","termid":"PBO:0028609"}


id: PBO:0066138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RB transcriptional corepressor 1","termid":"PBO:0066138"}


id: GO:0001744
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Establishment of the optic lobe placode. In Drosophila, for example, the placode appears in the dorsolateral region of the head in late stage 11 embryos and is the precursor to the larval visual system.","definition_xrefs":["PMID:8402833","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal placode formation","termid":"GO:0060788"},{"relation_name":"part_of","term_name":"insect visual primordium development","termid":"GO:0001748"}],"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":"insect visual primordium formation","secondary_identifiers":["GO:0007457"],"synonyms":[{"name":"optic lobe and Bolwig's organ precursor formation","type":"exact"},{"name":"optic lobe placode formation","type":"exact"}],"termid":"GO:0001744"}


id: MONDO:0014710
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the RORC gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited susceptibility to mycobacterial diseases","termid":"MONDO:0019146"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency","secondary_identifiers":["MEDGEN:1799070","UMLS:C5567647","DOID:0111940","OMIM:616622","Orphanet:477857"],"synonyms":[{"name":"IMD42","type":"exact"},{"name":"RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency","type":"exact"},{"name":"autosomal recessive MSMD due to complete RORgamma receptor defiency","type":"exact"},{"name":"autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in RORC","type":"exact"},{"name":"autosomal recessive primary immunodeficiency due to RORC mutation","type":"exact"},{"name":"immunodeficiency 42","type":"exact"},{"name":"immunodeficiency type 42","type":"exact"}],"termid":"MONDO:0014710","xrefs":{"Monarch":{"xref_id":"0014710"}}}


id: PBO:0044296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CXXC finger protein 5","termid":"PBO:0044296"}


id: PBO:0080944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger B-box domain containing","termid":"PBO:0080944"}


id: GO:1901389
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of transforming growth factor beta activation.","definition_xrefs":["GOC:sl","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transforming growth factor beta activation (obsolete GO:1901389)","synonyms":[{"name":"down regulation of L-TGF-beta activation","type":"exact"},{"name":"down regulation of TGF-B activation","type":"exact"},{"name":"down regulation of TGF-beta activation","type":"exact"},{"name":"down regulation of TGFB activation","type":"exact"},{"name":"down regulation of TGFbeta activation","type":"exact"},{"name":"down regulation of latent TGF-beta activation","type":"exact"},{"name":"down regulation of transforming growth factor beta activation","type":"exact"},{"name":"down-regulation of L-TGF-beta activation","type":"exact"},{"name":"down-regulation of TGF-B activation","type":"exact"},{"name":"down-regulation of TGF-beta activation","type":"exact"},{"name":"down-regulation of TGFB activation","type":"exact"},{"name":"down-regulation of TGFbeta activation","type":"exact"},{"name":"down-regulation of latent TGF-beta activation","type":"exact"},{"name":"down-regulation of transforming growth factor beta activation","type":"exact"},{"name":"downregulation of L-TGF-beta activation","type":"exact"},{"name":"downregulation of TGF-B activation","type":"exact"},{"name":"downregulation of TGF-beta activation","type":"exact"},{"name":"downregulation of TGFB activation","type":"exact"},{"name":"downregulation of TGFbeta activation","type":"exact"},{"name":"downregulation of latent TGF-beta activation","type":"exact"},{"name":"downregulation of transforming growth factor beta activation","type":"exact"},{"name":"inhibition of L-TGF-beta activation","type":"exact"},{"name":"inhibition of TGF-B activation","type":"exact"},{"name":"inhibition of TGF-beta activation","type":"exact"},{"name":"inhibition of TGFB activation","type":"exact"},{"name":"inhibition of TGFbeta activation","type":"exact"},{"name":"inhibition of latent TGF-beta activation","type":"exact"},{"name":"inhibition of transforming growth factor beta activation","type":"narrow"},{"name":"negative regulation of L-TGF-beta activation","type":"exact"},{"name":"negative regulation of TGF-B activation","type":"exact"},{"name":"negative regulation of TGF-beta activation","type":"exact"},{"name":"negative regulation of TGFB activation","type":"exact"},{"name":"negative regulation of TGFbeta activation","type":"exact"},{"name":"negative regulation of latent TGF-beta activation","type":"exact"}],"termid":"GO:1901389"}


id: PBO:0043030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"charged multivesicular body protein 4A","termid":"PBO:0043030"}


id: GO:0035039
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The conversion at fertilization of the inactive sperm nucleus into a male pronucleus with its chromosomes processed for the first zygotic division.","definition_xrefs":["PMID:11735001","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus organization","termid":"GO:0006997"},{"relation_name":"is_a","term_name":"organelle assembly","termid":"GO:0070925"},{"relation_name":"part_of","term_name":"single fertilization","termid":"GO:0007338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"male pronucleus assembly","synonyms":[{"name":"male pronucleus formation","type":"related"}],"termid":"GO:0035039"}


id: PBO:0091470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centaurin ADP ribosylation factor GTPase activating protein family","termid":"PBO:0091470"}


id: PBO:0031621
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_sporulation","termid":"PBO:0031621"}


id: PBO:0074881
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 60","termid":"PBO:0074881"}


id: GO:0015911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a long-chain fatty acid from outside of a cell, across the plasma membrane and into the cytosol. A long-chain fatty acid has an aliphatic tail containing 13 to 22 carbons.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid import into cell","termid":"GO:0044539"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"fatty acid transmembrane transport","termid":"GO:1902001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"long-chain fatty acid import across plasma membrane","synonyms":[{"name":"plasma membrane long-chain fatty acid transport","type":"exact"}],"termid":"GO:0015911"}


id: MONDO:0010286
data:
  {"annotated_genes":["SJAG_03664"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88418],"is_not":false,"summary":null,"term":"MONDO:0010286"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03664":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"syndromic X-linked intellectual disability Siderius type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060812","GARD:9704","MESH:C537333","OMIM:300263","MEDGEN:337375","Orphanet:85287","UMLS:C1846055"],"synonyms":[{"name":"MRXSSD","type":"exact"},{"name":"Siderius Hamel syndrome","type":"related"},{"name":"Siderius X-linked intellectual disability syndrome","type":"exact"},{"name":"Siderius X-linked mental retardation syndrome","type":"exact"},{"name":"Siderius-Hamel syndrome","type":"exact"},{"name":"X-linked intellectual disability Hamel type","type":"related"},{"name":"X-linked intellectual disability, Siderius type","type":"related"},{"name":"X-linked mental retardation Hamel type","type":"related"},{"name":"intellectual deficit X-linked Siderius type","type":"related"},{"name":"intellectual developmental disorder, X-linked, syndromic, Siderius type, X-linked recessive","type":"exact"},{"name":"intellectual disability X-linked Siderius type","type":"related"},{"name":"intellectual disability syndrome, X-linked, Siderius type","type":"exact"},{"name":"intellectual disability, X-linked, syndromic, Siderius type","type":"related"},{"name":"mental retardation X-linked Siderius type","type":"related"},{"name":"mental retardation syndrome, X-linked, Siderius type","type":"exact"},{"name":"mental retardation, X-linked, syndromic, Siderius type","type":"related"},{"name":"syndromic X-linked intellectual disability Siderius type","type":"exact"}],"termid":"MONDO:0010286","terms_by_termid":{"MONDO:0010286":null},"xrefs":{"Monarch":{"xref_id":"0010286"}}}


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


id: PBO:0001953
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates adg2","termid":"PBO:0001953"}


id: GO:0033301
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A mitotic cell cycle in which mitosis is completed but cytokinesis does not occur, resulting in a cell containing multiple nuclei each with a chromosomal complement of the original ploidy (usually 2N).","definition_xrefs":["GOC:mah","GOC:expert_vm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic cell cycle","termid":"GO:0000278"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"cell cycle comprising mitosis without cytokinesis","termid":"GO:0033301"}


id: PATO:0000062
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A sleep quality defined by the mathematic properties of the relative time frames of the sleep cycle.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavioral quality of a process","termid":"PATO:0001530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sleep pattern","termid":"PATO:0000062"}


id: GO:0052020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in the structure or function of the host cell wall. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete modification by symbiont of host cell wall (obsolete GO:0052020)","synonyms":[{"name":"metabolism of host cell wall by organism","type":"exact"}],"termid":"GO:0052020"}


id: FYPO:0007330
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 formaldehyde. Cells stop growing (and may die) at a concentration of formaldehyde 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:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0000139","FYPO:0005447","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to formaldehyde","synonyms":[{"name":"hypersensitive to formaldehyde","type":"exact"},{"name":"sensitive to formaldehyde during mitotic cell cycle","type":"related"},{"name":"sensitive to formaldehyde during vegetative growth","type":"exact"}],"termid":"FYPO:0007330"}


id: GO:0052135
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism towards a lower concentration of environmental oxygen within its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative aerotaxis in host (obsolete GO:0052135)","synonyms":[{"name":"negative aerotaxis within host","type":"exact"}],"termid":"GO:0052135"}


id: FYPO:0006674
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 abolished during conjugation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus","termid":"FYPO:0003450"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to nucleus during mating","synonyms":[{"name":"abolished protein localisation to nucleus during mating","type":"exact"},{"name":"abolished protein localization to nucleus during conjugation","type":"exact"},{"name":"nuclear exclusion during mating","type":"related"},{"name":"nuclear protein exclusion during mating","type":"related"},{"name":"protein localization to nucleus abolished during mating","type":"exact"}],"termid":"FYPO:0006674"}


id: GO:0090583
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 S-phosphocysteine + D-sorbitol(out) = protein cysteine + D-sorbitol-1-phosphate(in).","definition_xrefs":["PMID:8875915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-phosphocysteine-sugar phosphotransferase activity","termid":"GO:0090563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0005215","GO:0022857","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"protein-phosphocysteine-D-sorbitol-phosphotransferase system transporter activity","termid":"GO:0090583"}


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


id: MONDO:0010195
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Weissenbacher-Zweymuller syndrome (obsolete MONDO:0010195)","termid":"MONDO:0010195","xrefs":{"Monarch":{"xref_id":"0010195"}}}


id: PBO:0076162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUGT1P4-STRA6LP-CCDC180 readthrough","termid":"PBO:0076162"}


id: PBO:0087758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the tRNA splicing endonuclease; tRNA splicing endonuclease (Sen complex) is composed of Sen2p, Sen15p, Sen34p, and Sen54p; Sen complex also cleaves the CBP1 mRNA at the mitochondrial surface; Sen34p contains the active site for tRNA 3' splice site cleavage and has similarity to Sen2p and to Archaeal tRNA splicing endonuclease","termid":"PBO:0087758"}


id: MONDO:0030697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopia","termid":"MONDO:0001384"}],"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":"myopia 28, autosomal recessive","secondary_identifiers":["OMIM:619781","UMLS:C5676935","MEDGEN:1806812"],"synonyms":[{"name":"MYP28","type":"exact"},{"name":"myopia 28, autosomal recessive","type":"exact"}],"termid":"MONDO:0030697","xrefs":{"Monarch":{"xref_id":"0030697"}}}


id: PBO:0053062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"linker for activation of T cells","termid":"PBO:0053062"}


id: MONDO:1011018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"L-2-hydroxyglutaricacidemia that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-2-hydroxyglutaricacidemia, non-human animal","termid":"MONDO:1010244"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-2-hydroxyglutaricacidemia, dog","secondary_identifiers":["OMIA:001371-9615"],"termid":"MONDO:1011018","xrefs":{"Monarch":{"xref_id":"1011018"}}}


id: SO:0000461
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosomal deletion whereby a chromosome generated by recombination between two inversions; has a deficiency at each end of the inversion.","definition_xrefs":["FB:km"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal_deletion","termid":"SO:1000029"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inversion_derived_bipartite_deficiency","synonyms":[{"name":"inversion derived bipartite deficiency","type":"exact"}],"termid":"SO:0000461"}


id: MONDO:0013805
data:
  {"annotated_genes":["SJAG_02286"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88193],"is_not":false,"summary":null,"term":"MONDO:0013805"}]},"cv_name":"mondo","definition":"Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant syndromic intellectual disability","termid":"MONDO:0100601"},{"relation_name":"is_a","term_name":"dyneinopathy","termid":"MONDO:1040031"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02286":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005328"],"is_obsolete":false,"name":"intellectual disability, autosomal dominant 13","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070043","GARD:16462","UMLS:C3281202","OMIM:614563","MEDGEN:482832"],"synonyms":[{"name":"DYNC1H1 autosomal dominant non-syndromic intellectual disability","type":"exact"},{"name":"MRD13","type":"exact"},{"name":"autosomal dominant intellectual disability 13","type":"exact"},{"name":"autosomal dominant mental retardation 13","type":"exact"},{"name":"autosomal dominant non-syndromic intellectual disability 13","type":"related"},{"name":"autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1","type":"exact"},{"name":"intellectual disability, autosomal dominant 13","type":"exact"},{"name":"intellectual disability, autosomal dominant 13, with neuronal migration defects","type":"exact"},{"name":"intellectual disability, autosomal dominant type 13","type":"exact"},{"name":"intellectual disability, autosomal dominant, 13, with neuronal migration defects","type":"related"},{"name":"mental retardation, autosomal dominant 13","type":"related"},{"name":"mental retardation, autosomal dominant 13, with neuronal migration defects","type":"exact"},{"name":"mental retardation, autosomal dominant type 13","type":"exact"},{"name":"mental retardation, autosomal dominant, 13, with neuronal migration defects","type":"related"}],"termid":"MONDO:0013805","terms_by_termid":{"MONDO:0013805":null},"xrefs":{"Monarch":{"xref_id":"0013805"}}}


id: GO:0045640
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of basophil differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of granulocyte differentiation","termid":"GO:0030852"},{"relation_name":"regulates","term_name":"basophil differentiation","termid":"GO:0030221"}],"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 basophil differentiation","termid":"GO:0045640"}


id: PBO:0073121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEBOX homeobox","termid":"PBO:0073121"}


id: MONDO:0005254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A heart failure which results in symptoms such as shortness of breath, fatigue, inability to exerciseb& etc","definition_xrefs":["EFO:0003146"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart failure","termid":"MONDO:0005252"}],"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":"symptomatic heart failure","termid":"MONDO:0005254","xrefs":{"Monarch":{"xref_id":"0005254"}}}


id: PBO:0012827
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-added_during","termid":"PBO:0012827"}


id: GO:2000083
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of L-ascorbic acid biosynthetic process.","definition_xrefs":["PMID:19395407"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"negative regulation of vitamin metabolic process","termid":"GO:0046137"},{"relation_name":"is_a","term_name":"regulation of L-ascorbic acid biosynthetic process","termid":"GO:2000082"},{"relation_name":"negatively_regulates","term_name":"L-ascorbic acid biosynthetic process","termid":"GO:0019853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006766"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0006766"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0044281","GO:0005975","GO:0006766","GO:0008150"],"is_obsolete":false,"name":"negative regulation of L-ascorbic acid biosynthetic process","synonyms":[{"name":"negative regulation of L-ascorbic acid anabolism","type":"exact"},{"name":"negative regulation of L-ascorbic acid biosynthesis","type":"exact"},{"name":"negative regulation of L-ascorbic acid formation","type":"exact"},{"name":"negative regulation of L-ascorbic acid synthesis","type":"exact"},{"name":"negative regulation of ascorbate biosynthesis","type":"exact"},{"name":"negative regulation of ascorbate biosynthetic process","type":"exact"},{"name":"negative regulation of vitamin C biosynthesis","type":"exact"},{"name":"negative regulation of vitamin C biosynthetic process","type":"exact"}],"termid":"GO:2000083"}


id: PBO:0038981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenoceptor alpha 1A","termid":"PBO:0038981"}


id: PBO:0066068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid receptor beta","termid":"PBO:0066068"}


id: MONDO:0003407
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ovarian yolk sac tumor (obsolete MONDO:0003407)","termid":"MONDO:0003407","xrefs":{"Monarch":{"xref_id":"0003407"}}}


id: PBO:0078070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 60 (pseudogene)","termid":"PBO:0078070"}


id: MONDO:0014483
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies","secondary_identifiers":["Orphanet:397758","GARD:17640","ICD10CM:H35.5","MEDGEN:863583","OMIM:616079","UMLS:C4015146"],"synonyms":[{"name":"RDGCA","type":"related"},{"name":"retinal dystrophy with inner nuclear layer and ganglion cell anomalies","type":"exact"},{"name":"retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities","type":"related"}],"termid":"MONDO:0014483","xrefs":{"Monarch":{"xref_id":"0014483"}}}


id: GO:0097585
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein dimer complex that possesses dolichyl-phosphate-mannose-protein mannosyltransferase activity and, in S. cerevisiae, is composed of Pmt5p-Pmt3p.","definition_xrefs":["PMID:12551906","GOC:jd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dolichyl-phosphate-mannose-protein mannosyltransferase complex","termid":"GO:0031502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005789","GO:0005783","GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"dolichyl-phosphate-mannose-protein mannosyltransferase Pmt5p-Pmt3p dimer complex","synonyms":[{"name":"Pmt5p-Pmt3p complex","type":"narrow"}],"termid":"GO:0097585"}


id: PBO:0071900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 38","termid":"PBO:0071900"}


id: GO:0004052
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: arachidonate + O2 = (5Z,8Z,10E,12S,14Z)-12-hydroperoxyicosa-5,8,10,14-tetraenoate.","definition_xrefs":["EC:1.13.11.31","RHEA:10428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"arachidonate 12(S)-lipoxygenase activity","secondary_identifiers":["Reactome:R-HSA-2161964","KEGG_REACTION:R01596","Reactome:R-HSA-9025957","Reactome:R-HSA-9026007","Reactome:R-HSA-2161948","MetaCyc:ARACHIDONATE-12-LIPOXYGENASE-RXN","Reactome:R-HSA-9024983","Reactome:R-HSA-9026006","Reactome:R-HSA-2161950"],"synonyms":[{"name":"12-lipoxygenase activity","type":"related"},{"name":"12Delta-lipoxygenase activity","type":"related"},{"name":"12S-lipoxygenase activity","type":"related"},{"name":"C-12 lipoxygenase activity","type":"related"},{"name":"LTA4 synthase activity","type":"related"},{"name":"arachidonate:oxygen 12-oxidoreductase activity","type":"related"},{"name":"delta12-lipoxygenase activity","type":"related"},{"name":"leukotriene A4 synthase","type":"broad"}],"termid":"GO:0004052"}


id: SO:0001298
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"2prime_O_methyladenosine is a modified adenosine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_adenosine","termid":"SO:0001273"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"two_prime_O_methyladenosine","secondary_identifiers":["RNAMOD:004"],"synonyms":[{"name":"2'-O-methyladenosine","type":"exact"},{"name":"Am","type":"exact"},{"name":"two prime O methyladenosine","type":"exact"}],"termid":"SO:0001298"}


id: GO:0019836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cytolytic destruction of red blood cells, with the release of intracellular hemoglobin, in the host organism by a symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["UniProtKB-KW:KW-0354","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated cytolysis of host cell","termid":"GO:0001897"}],"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 hemolysis of host erythrocyte","synonyms":[{"name":"haemolysis in host","type":"exact"},{"name":"hemolysin activity","type":"related"},{"name":"hemolysis by symbiont of host RBCs","type":"exact"},{"name":"hemolysis by symbiont of host erythrocytes","type":"exact"},{"name":"hemolysis by symbiont of host red blood cells","type":"exact"},{"name":"pathogenesis","type":"broad"},{"name":"regulation of cytolysis of host cells by symbiont","type":"exact"}],"termid":"GO:0019836"}


id: PBO:0031476
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_actin_cortical_patch_internalization","termid":"PBO:0031476"}


id: MONDO:1010935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary generalized muscle atrophy characterized by the histological presence of rod-like inclusion bodies in skeletal muscle fibers in dogs due a variation in the NEB gene.","definition_xrefs":["PMID:27215641"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nemaline myopathy, NEB-related, dog","secondary_identifiers":["OMIA:002137-9615"],"termid":"MONDO:1010935","xrefs":{"Monarch":{"xref_id":"1010935"}}}


id: MONDO:0006272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low grade, late-metastasizing variant of fibrosarcoma characterized by alternating fibrous and myxoid areas and a whorling growth pattern. The neoplastic cells have a spindle morphology, and lack hyperchromasia or significant nuclear atypia. Approximately 40% of cases show the focal presence of collagen rosettes. A t(7;16)(q33;p11) translocation has been identified in the majority of cases, associated with the presence of FUS-CREB3L2 fusion protein. Rare cases carry the t(11;16)(p11;p11) translocation which is associated with the presence of the FUS-CREB3L1 fusion protein.","definition_xrefs":["NCIT:C45202"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrosarcoma","termid":"MONDO:0005164"}],"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":"low grade fibromyxoid sarcoma","secondary_identifiers":["MEDGEN:224814","ONCOTREE:LGFMS","SCTID:404088004","UMLS:C1275282","ICD9:171.9"],"synonyms":[{"name":"low grade fibromyxoid sarcoma","type":"exact"},{"name":"low-grade fibromyxoid sarcoma","type":"related"}],"termid":"MONDO:0006272","xrefs":{"Monarch":{"xref_id":"0006272"}}}


id: MONDO:0800134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An immunodeficiency disease caused by a variation in the CRACR2A gene.","definition_xrefs":["PMID:34908525","PMID:35151051"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"primary immunodeficiency due to calcium channel deficiency","termid":"MONDO:0800134","xrefs":{"Monarch":{"xref_id":"0800134"}}}


id: PBO:0088869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-type ATPase","termid":"PBO:0088869"}


id: GO:1904213
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of iodide transmembrane transport.","definition_xrefs":["GOC:TermGenie","PMID:20392814","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of inorganic anion transmembrane transport","termid":"GO:1903796"},{"relation_name":"is_a","term_name":"negative regulation of anion transmembrane transport","termid":"GO:1903960"},{"relation_name":"is_a","term_name":"negative regulation of iodide transport","termid":"GO:1904202"},{"relation_name":"is_a","term_name":"regulation of iodide transmembrane transport","termid":"GO:1904212"},{"relation_name":"negatively_regulates","term_name":"iodide transmembrane transport","termid":"GO:1904200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of iodide transmembrane transport","synonyms":[{"name":"down regulation of iodide transmembrane transport","type":"exact"},{"name":"down-regulation of iodide transmembrane transport","type":"exact"},{"name":"downregulation of iodide transmembrane transport","type":"exact"},{"name":"inhibition of iodide transmembrane transport","type":"narrow"}],"termid":"GO:1904213"}


id: PBO:0060455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglutamate synthase","termid":"PBO:0060455"}


id: MOD:00620
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:301","PubMed:7856876"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"cysteine monobromobimane derivative","synonyms":[{"name":"Bromobimane","type":"related"},{"name":"Monobromobimane derivative","type":"related"}],"termid":"MOD:00620"}


id: FYPO:0005562
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which stable microtubule bundles are shorter than normal. Stable microtubule bundles, also called Q-MT bundles, are found in quiescent cells.","definition_xrefs":["PMID:26124291","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"short microtubule bundle","termid":"FYPO:0005797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0002399","FYPO:0001320","FYPO:0000054","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"short stable microtubule bundle","synonyms":[{"name":"decreased stable microtubule bundle length","type":"exact"},{"name":"short Q-MT bundles","type":"exact"},{"name":"short quiescent cell MT bundle","type":"exact"},{"name":"short quiescent cell microtubule bundle","type":"exact"},{"name":"short stable microtubule array","type":"related"},{"name":"short static microtubule bundle","type":"exact"}],"termid":"FYPO:0005562"}


id: GO:0015332
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 leucine/valine/isoleucine permease activity (obsolete GO:0015332)","synonyms":[{"name":"leucine/valine/isoleucine permease activity","type":"exact"}],"termid":"GO:0015332"}


id: PR:O94573
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1773.16c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94573"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized transcriptional regulatory protein C1773.16c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1773.16c","synonyms":[{"name":"Spom972h-SPBC1773.16c","type":"exact"}],"termid":"PR:O94573"}


id: FYPO:0002014
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 iron ion starvation is higher than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"},{"relation_name":"is_a","term_name":"altered RNA level during cellular response to iron ion starvation","termid":"FYPO:0003196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"increased RNA level during cellular response to iron ion starvation","synonyms":[{"name":"increased RNA accumulation during cellular response to iron ion starvation","type":"related"},{"name":"increased RNA level during cellular response to iron ion depletion","type":"exact"},{"name":"increased RNA level during cellular response to iron ion deprivation","type":"exact"},{"name":"increased RNA level during cellular response to iron ion starvation during mitotic cell cycle","type":"related"},{"name":"increased RNA level during cellular response to iron ion starvation during vegetative growth","type":"exact"},{"name":"increased RNA level during cellular response to iron starvation","type":"exact"},{"name":"increased RNA level during iron ion starvation","type":"exact"},{"name":"increased mRNA level during cellular response to iron ion starvation","type":"narrow"},{"name":"increased transcript level during cellular response to iron ion starvation","type":"exact"}],"termid":"FYPO:0002014"}


id: MOD:00284
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct between an aspartic acid residue, a glutamic acid residue, and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron.","definition_xrefs":["RESID:AA0279","PubMed:10447690"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin modified residue","termid":"MOD:00699"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-aspartic acid residue","termid":"MOD:02066"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-glutamic acid residue","termid":"MOD:02068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydroxyheme-L-aspartate ester-L-glutamate ester","synonyms":[{"name":"1,5-bishydroxymethyl protoporphyrin IX 1-glutamate ester 5-aspartate ester","type":"exact"},{"name":"BINDING Heme (covalent; via 2 links)","type":"exact"},{"name":"[13-[(S)-(4-amino-4-carboxy)butanoyloxymethyl]-3-[(S)-(3-amino-3-carboxy)propanoyloxymethyl]-7,12-diethenyl-8,17-dimethyl-21H,23H-porphine-2,18-bis(2-carboxyethyl)-N21,N22,N23,N24]-ferrate","type":"exact"},{"name":"dihydroxyheme-L-aspartate ester-L-glutamate ester","type":"exact"},{"name":"peroxidase heme cofactor","type":"exact"}],"termid":"MOD:00284"}


id: GO:0015839
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of cadaverine, 1,5-pentanediamine, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"cadaverine transport","termid":"GO:0015839"}


id: GO:1990627
data:
  {"annotated_genes":["SJAG_02656"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106712],"is_not":false,"summary":null,"term":"GO:1990627"}]},"cv_name":"biological_process","definition":"The membrane organization process that joins two mitochondrial inner membranes to form a single membrane.","definition_xrefs":["PMID:17055438","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner mitochondrial membrane organization","termid":"GO:0007007"},{"relation_name":"part_of","term_name":"mitochondrial fusion","termid":"GO:0008053"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02656":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0007005"},{"rel_name":"part_of","termid":"GO:0007005"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024","GO:0007005"],"is_obsolete":false,"name":"mitochondrial inner membrane fusion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mitochondrion inner membrane fusion","type":"exact"}],"termid":"GO:1990627","terms_by_termid":{"GO:1990627":null}}


id: PBO:0005038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fun thirty related protein Fft2 (predicted)","termid":"PBO:0005038"}


id: PBO:0086028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; YET3 null mutant decreases the level of secreted invertase; homolog of human BAP31 protein; protein abundance increases in response to DNA replication stress","termid":"PBO:0086028"}


id: PBO:0081664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 586","termid":"PBO:0081664"}


id: MONDO:0700155
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Adeonocarcinoma of the thyroid gland occurring in a dog.","definition_xrefs":["NCIT:C132275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma, non-human animal","termid":"MONDO:0700099"},{"relation_name":"is_a","term_name":"endocrine system disorder, non-human animal","termid":"MONDO:1011317"},{"relation_name":"is_a","term_name":"cancer, dog","termid":"MONDO:1012570"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine thyroid adenocarcinoma","termid":"MONDO:0700155","xrefs":{"Monarch":{"xref_id":"0700155"}}}


id: PBO:0060205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial E3 ubiquitin protein ligase 1","termid":"PBO:0060205"}


id: MONDO:0017927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Severe lateral tibial bowing with short stature is a rare, genetic, primary bent bone dysplasia characterized by significant, uni-/bilateral, lateral tibial bowing localized to the distal two-thirds of the tibia, with respective cortical thickening and thinning of the inner and outer tibial curve, loss of normal trabecular bone, bilateral abnormalities of the tibial epiphyses and growth plates, as well as foot abnormalities, including abnormally high arches. Affected individuals have short stature with absence of other skeletal abnormalities.","definition_xrefs":["Orphanet:324307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bent bone dysplasia","termid":"MONDO:0019698"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"severe lateral tibial bowing with short stature","secondary_identifiers":["GARD:21436","UMLS:C4707850","SCTID:766819001","MEDGEN:1634340"],"termid":"MONDO:0017927","xrefs":{"Monarch":{"xref_id":"0017927"}}}


id: FYPO:0001438
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing tetracycline.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0000257","FYPO:0000003","FYPO:0002058","FYPO:0000139","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on tetracycline","synonyms":[{"name":"normal cell population growth in presence of tetracycline","type":"exact"},{"name":"normal cell population growth on tetracycline","type":"exact"},{"name":"normal cellular response to tetracycline","type":"related"},{"name":"normal vegetative cell population growth on tetracycline","type":"exact"}],"termid":"FYPO:0001438"}


id: GO:0016432
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a uridine in tRNA + S-adenosyl-L-methionine = a 3-[(3S)-3-amino-3-carboxypropyl]uridine in tRNA + S-methyl-5'-thioadenosine + H+.","definition_xrefs":["RHEA:62432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"}],"interesting_parent_ids":["GO:0016740","GO:0016765","GO:0140101","GO:0003674","GO:0140098","GO:0003824"],"is_obsolete":false,"name":"tRNA-uridine aminocarboxypropyltransferase activity","secondary_identifiers":["MetaCyc:RXN-21179","EC:2.5.1.25"],"synonyms":[{"name":"S-adenosyl-L-methionine:tRNA-uridine 3-(3-amino-3-carboxypropyl)transferase activity","type":"related"}],"termid":"GO:0016432"}


id: GO:1902564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of neutrophil activation.","definition_xrefs":["GOC:TermGenie","PMID:17588661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte activation","termid":"GO:0002695"},{"relation_name":"is_a","term_name":"regulation of neutrophil activation","termid":"GO:1902563"},{"relation_name":"negatively_regulates","term_name":"neutrophil activation","termid":"GO:0042119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of neutrophil activation","synonyms":[{"name":"down regulation of neutrophil activation","type":"exact"},{"name":"down-regulation of neutrophil activation","type":"exact"},{"name":"downregulation of neutrophil activation","type":"exact"},{"name":"inhibition of neutrophil activation","type":"narrow"}],"termid":"GO:1902564"}


id: FYPO:0005257
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-proline measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular amino acid level","termid":"FYPO:0003985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased cellular proline level","synonyms":[{"name":"decreased cellular L-proline level","type":"exact"},{"name":"decreased cellular proline level during mitotic cell cycle","type":"related"},{"name":"decreased cellular proline level during vegetative growth","type":"exact"},{"name":"decreased level of proline in cell","type":"exact"},{"name":"reduced cellular proline level","type":"exact"},{"name":"reduced level of proline in cell","type":"exact"}],"termid":"FYPO:0005257"}


id: GO:0050216
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD+ + propane-1,2-diol 1-phosphate = H+ + hydroxyacetone phosphate + NADH.","definition_xrefs":["RHEA:21584","EC:1.1.1.7"],"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":"propanediol-phosphate dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R04236","MetaCyc:PROPANEDIOL-PHOSPHATE-DEHYDROGENASE-RXN"],"termid":"GO:0050216"}


id: GO:0004013
data:
  {"annotated_genes":["SJAG_03556"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79174],"is_not":false,"summary":null,"term":"GO:0004013"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-homocysteine + H2O = adenosine + L-homocysteine.","definition_xrefs":["RHEA:21708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-sulfur bonds","termid":"GO:0046508"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03556":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"adenosylhomocysteinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:ADENOSYLHOMOCYSTEINASE-RXN","Reactome:R-HSA-5579084","EC:3.13.2.1","Reactome:R-HSA-174401"],"synonyms":[{"name":"AdoHcyase activity","type":"related"},{"name":"S-adenosyl-L-homocysteine hydrolase activity","type":"related"},{"name":"S-adenosylhomocysteinase activity","type":"related"},{"name":"S-adenosylhomocysteine hydrolase activity","type":"broad"},{"name":"S-adenosylhomocysteine synthase activity","type":"related"},{"name":"SAHase activity","type":"related"},{"name":"adenosylhomocysteine hydrolase activity","type":"related"}],"termid":"GO:0004013","terms_by_termid":{"GO:0004013":null}}


id: MONDO:0014448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited autosomal dominant trait characterized by abnormally elevated levels of total serum thyroxine; (T4) in euthyroid patients with abnormal serum albumin that binds T4 with enhanced affinity. The serum levels of free T4, free T3, and tsh are normal. It is one of several T4 abnormalities produced by non-thyroid disorder. This condition is due to mutations of the alb gene on chromosome 4.","definition_xrefs":["MESH:D050010"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"hyperthyroidism","termid":"MONDO:0004425"},{"relation_name":"is_a","term_name":"hyperthyroxinemia","termid":"MONDO:0005333"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperthyroxinemia, familial dysalbuminemic","secondary_identifiers":["MEDGEN:90974","Orphanet:276271","UMLS:C0342185","SCTID:237547004","NCIT:C131813","OMIM:615999"],"synonyms":[{"name":"FDAH","type":"related"},{"name":"FDH","type":"related"},{"name":"bisalbuminemia","type":"exact"},{"name":"dysalbuminemic hyperthyroxinemia","type":"exact"},{"name":"dysalbuminemic hypertriiodothyroninemia","type":"exact"},{"name":"euthyroid hyperthyroxinemia 1","type":"related"},{"name":"familial Dysalbuminemic hyperthyroidism","type":"exact"},{"name":"familial Dysalbuminemic hyperthyroxinemia","type":"exact"},{"name":"hyperthyroxinemia, familial Dysalbuminemic","type":"exact"},{"name":"hyperthyroxinemia, familial dysalbuminemic","type":"exact"}],"termid":"MONDO:0014448","xrefs":{"Monarch":{"xref_id":"0014448"}}}


id: PBO:0036360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human CCNDBP1 ortholog","termid":"PBO:0036360"}


id: FYPO:0002415
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, and has an abnormal shape and a larger volume than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable swollen vegetative cell","termid":"FYPO:0002414"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell shape","termid":"FYPO:0002451"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000005","FYPO:0000002","FYPO:0000004","FYPO:0001320"],"is_obsolete":false,"name":"inviable swollen vegetative cell with abnormal cell shape","synonyms":[{"name":"inviable enlarged vegetative cell with abnormal cell shape","type":"related"},{"name":"inviable large vegetative cell with abnormal cell shape","type":"related"},{"name":"inviable swollen cell with abnormal cell shape during vegetative growth","type":"exact"},{"name":"inviable swollen misshapen vegetative cell","type":"related"},{"name":"inviable swollen vegetative cell with abnormal cell shape during mitotic cell cycle","type":"related"},{"name":"inviable vegetative cell with increased cell size and abnormal cell shape","type":"related"},{"name":"inviable vegetative cell with increased cell volume and abnormal cell shape","type":"exact"},{"name":"lethal; swollen vegetative cell with abnormal cell shape","type":"exact"}],"termid":"FYPO:0002415"}


id: PBO:0080774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XK related 5","termid":"PBO:0080774"}


id: PBO:0034488
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_chromatin_at_boundary_element_IRC1L","termid":"PBO:0034488"}


id: SO:0000286
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence directly repeated at both ends of a defined sequence, of the sort typically found in retroviruses.","direct_ancestors":[{"relation_name":"is_a","term_name":"repeat_region","termid":"SO:0000657"},{"relation_name":"part_of","term_name":"LTR_retrotransposon","termid":"SO:0000186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long_terminal_repeat","secondary_identifiers":["http://en.wikipedia.org/wiki/Long_terminal_repeat"],"synonyms":[{"name":"INSDC_feature:repeat_region","type":"broad"},{"name":"INSDC_qualifier:long_terminal_repeat","type":"exact"},{"name":"LTR","type":"exact"},{"name":"direct terminal repeat","type":"related"},{"name":"long terminal repeat","type":"exact"}],"termid":"SO:0000286"}


id: MONDO:1011415
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Amyloidosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloidosis, non-human animal","secondary_identifiers":["OMIA:000037"],"termid":"MONDO:1011415","xrefs":{"Monarch":{"xref_id":"1011415"}}}


id: MONDO:0000217
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Frontometaphyseal dysplasia (obsolete MONDO:0000217)","termid":"MONDO:0000217","xrefs":{"Monarch":{"xref_id":"0000217"}}}


id: GO:0016563
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any transcription regulator activity required for initiation or upregulation of transcription.","definition_xrefs":["GOC:jl","ISBN:0124325653"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription activator activity (obsolete GO:0016563)","synonyms":[{"name":"transcription activating factor","type":"narrow"},{"name":"transcription activator activity","type":"exact"},{"name":"transcriptional activator activity","type":"exact"}],"termid":"GO:0016563"}


id: GO:0032291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a glial cell membrane closes around an axon in the central nervous system. This can be a myelinating or a non-myelinating neuron-glial interaction.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon ensheathment","termid":"GO:0008366"}],"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 ensheathment in central nervous system","synonyms":[{"name":"ensheathment of axons in central nervous system","type":"exact"}],"termid":"GO:0032291"}


id: PBO:0062426
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 86 pseudogene","termid":"PBO:0062426"}


id: PBO:0076576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 3 pseudogene 4","termid":"PBO:0076576"}


id: FYPO:0008269
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 total amount of phosphate (Pi) measured in the cell is lower than normal.","definition_xrefs":["PMID:37949217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular phosphate (Pi) level","termid":"FYPO:0008268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased total cellular phosphate (Pi) level","termid":"FYPO:0008269"}


id: GO:1902130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (+)-lariciresinol.","definition_xrefs":["GOC:TermGenie","PMID:8910615","PMID:9872995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan metabolic process","termid":"GO:0009806"},{"relation_name":"is_a","term_name":"ether metabolic process","termid":"GO:0018904"},{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"primary alcohol metabolic process","termid":"GO:0034308"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"(+)-lariciresinol metabolic process","synonyms":[{"name":"(+)-lariciresinol metabolism","type":"exact"}],"termid":"GO:1902130"}


id: CHEBI:35176
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc sulfate","termid":"CHEBI:35176"}


id: PBO:0004120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-C3HC4 type zinc finger","termid":"PBO:0004120"}


id: MONDO:0012017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Parkes Weber syndrome (obsolete MONDO:0012017)","termid":"MONDO:0012017","xrefs":{"Monarch":{"xref_id":"0012017"}}}


id: GO:0071420
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a histamine stimulus. Histamine, the biogenic amine 2-(1H-imidazol-4-yl)ethanamine, is involved in local immune responses as well as regulating physiological function in the gut and acting as a neurotransmitter.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to histamine","termid":"GO:0034776"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to histamine","synonyms":[{"name":"cellular response to histamine stimulus","type":"exact"}],"termid":"GO:0071420"}


id: PBO:0074878
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 58C","termid":"PBO:0074878"}


id: MONDO:0016792
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA (obsolete MONDO:0016792)","secondary_identifiers":["Orphanet:254767"],"synonyms":[{"name":"OXPHOS disease due to a large-scale single deletion of mitochondrial DNA","type":"exact"},{"name":"OXPHOS disease due to a large-scale single deletion of mtDNA","type":"exact"},{"name":"mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mtDNA","type":"exact"}],"termid":"MONDO:0016792","xrefs":{"Monarch":{"xref_id":"0016792"}}}


id: PBO:0054234
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 1616","termid":"PBO:0054234"}


id: PBO:0068027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 332","termid":"PBO:0068027"}


id: PBO:0073517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain binding glutamate rich protein like 2","termid":"PBO:0073517"}


id: PBO:0078280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 13-1","termid":"PBO:0078280"}


id: PBO:0111896
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin bimC subfamily","termid":"PBO:0111896"}


id: PBO:0070186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 104 pseudogene","termid":"PBO:0070186"}


id: GO:0000820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving amino acids of the glutamine family, comprising arginine, glutamate, glutamine and proline.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amino acid metabolic process","termid":"GO:0006521"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"regulates","term_name":"glutamine family amino acid metabolic process","termid":"GO:0009064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"regulation of glutamine family amino acid metabolic process","synonyms":[{"name":"regulation of glutamine family amino acid metabolism","type":"exact"}],"termid":"GO:0000820"}


id: PBO:0057129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 212","termid":"PBO:0057129"}


id: PBO:0081578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF503 antisense RNA 2","termid":"PBO:0081578"}


id: GO:0052125
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism on or near its host organism in response to physical parameters involved in energy generation, such as light, oxygen, and oxidizable substrates. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete energy taxis on or near host (obsolete GO:0052125)","termid":"GO:0052125"}


id: PBO:0084023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycosyltransferase involved in protein glycosylation; transfers GDP-mannose to methyl-alpha-mannoside in vitro; member of the KRE2/MNT1 mannosyltransferase family of type II membrane proteins with a short cytoplasmic N-terminus, a membrane-spanning region and a highly conserved catalytic lumenal domain","termid":"PBO:0084023"}


id: PBO:0003482
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIng-localized protein with homology to Diaphanous GTPase-binding domain","termid":"PBO:0003482"}


id: GO:0016254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The stepwise addition of the components of the GPI anchor on to phosphatidylinositol lipids in the endoplasmic reticulum membrane.","definition_xrefs":["ISBN:0879695595"],"gene_count":0,"genotype_count":0,"name":"obsolete preassembly of GPI anchor in ER membrane (obsolete GO:0016254)","synonyms":[{"name":"preassembly of GPI anchor in endoplasmic reticulum membrane","type":"exact"}],"termid":"GO:0016254"}


id: PBO:0063213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCCA antisense RNA 1","termid":"PBO:0063213"}


id: PBO:0113522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Upstream serine/threonine kinase for the SNF1 complex; plays a role in pseudohyphal growth; partially redundant with Elm1p and Tos3p; members of this family have functional orthology with LKB1, a mammalian kinase associated with Peutz-Jeghers cancer-susceptibility syndrome; SAK1 has a paralog, TOS3, that arose from the whole genome duplication","termid":"PBO:0113522"}


id: PBO:0069203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 457, pseudogene","termid":"PBO:0069203"}


id: PBO:0113442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Substrate adaptor for Cdc48p; ubiquitin regulatory X (UBX) and Ub-associated (UBA) domain-containing protein that acts as a substrate recruiting cofactor; K48-specific Ub chain binding protein involved in ER-associated degradation (ERAD); positively regulates Glc7p protein phosphatase activity to promote growth and mitotic progression in complex with Cdc48p; regulated by nuclear Ub-dependent degradation (INMAD pathway) independent of the Asi and Doa10 complexes; homolog of human p47 (NSFL1C)","termid":"PBO:0113442"}


id: PBO:0081445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 302","termid":"PBO:0081445"}


id: PBO:0060013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 1","termid":"PBO:0060013"}


id: GO:0060047
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multicellular organismal process in which the heart decreases in volume in a characteristic way to propel blood through the body.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart process","termid":"GO:0003015"},{"relation_name":"part_of","term_name":"blood circulation","termid":"GO:0008015"}],"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":"heart contraction","synonyms":[{"name":"cardiac contraction","type":"related"},{"name":"heart beating","type":"exact"},{"name":"hemolymph circulation","type":"related"}],"termid":"GO:0060047"}


id: PBO:0054745
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 2154","termid":"PBO:0054745"}


id: MONDO:0100187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A constipation disorder caused by use of opioids. OIC may present immediately when a patient takes the opioid, or it may present gradually during opioid therapy.","direct_ancestors":[{"relation_name":"is_a","term_name":"constipation disorder","termid":"MONDO:0002203"}],"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":"opioid-induced constipation","secondary_identifiers":["MEDGEN:1641995","UMLS:C3160897"],"synonyms":[{"name":"OIC","type":"exact"}],"termid":"MONDO:0100187","xrefs":{"Monarch":{"xref_id":"0100187"}}}


id: MONDO:0859319
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dyskeratosis congenita","termid":"MONDO:0015780"}],"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":"dyskeratosis congenita, autosomal recessive 8","secondary_identifiers":["UMLS:C5774257","MEDGEN:1824030","OMIM:620133"],"termid":"MONDO:0859319","xrefs":{"Monarch":{"xref_id":"0859319"}}}


id: GO:0072686
data:
  {"annotated_genes":["SJAG_03731","SJAG_00207","SJAG_00526","SJAG_00800","SJAG_02209","SJAG_01775","SJAG_04745","SJAG_00245","SJAG_00943","SJAG_03846","SJAG_00930","SJAG_02761","SJAG_04841","SJAG_03387","SJAG_05319","SJAG_03540","SJAG_03116","SJAG_00514","SJAG_05205","SJAG_01832","SJAG_01849","SJAG_00082","SJAG_00879","SJAG_01837","SJAG_00918","SJAG_02624","SJAG_02821","SJAG_02336","SJAG_01557","SJAG_01546","SJAG_01232","SJAG_03569","SJAG_02311","SJAG_00724","SJAG_00666","SJAG_02098","SJAG_05315","SJAG_02542","SJAG_04412","SJAG_00883","SJAG_04931","SJAG_01211","SJAG_01613","SJAG_04884","SJAG_02045","SJAG_01224","SJAG_01371","SJAG_02248","SJAG_03437","SJAG_02025","SJAG_01391","SJAG_05266","SJAG_03062","SJAG_05313","SJAG_00692","SJAG_03901","SJAG_03911","SJAG_03073","SJAG_00723","SJAG_04140","SJAG_01805","SJAG_03906","SJAG_02608","SJAG_04257","SJAG_00646","SJAG_00163","SJAG_04010","SJAG_04074","SJAG_03592","SJAG_04940","SJAG_04607","SJAG_04623","SJAG_01887","SJAG_01330","SJAG_03048","SJAG_02695","SJAG_01634","SJAG_00773","SJAG_02807","SJAG_02460","SJAG_01110","SJAG_01297","SJAG_01429","SJAG_00697","SJAG_00140","SJAG_02266"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[64442,64515,66087,70413,74619,77496,89357,89765,90050,91060,91130,91383,91634,93083,93503,94521,94696,95710,96988,97325,97664,97818,98053,98252,98546,99156,100154,101420,101613,101614,101924,102307,104239,104692,104844,105508,106053,107785,107972,108020,109041,109556,109903,110516,110842,110910,111033,111570,112392,113271,113328,113335,113510,113761,115242,116379,116523,116846,116903],"is_not":false,"summary":null,"term":"GO:0072686"},{"annotations":[63003,80530,93149],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061673"},{"annotations":[98753],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905721"},{"annotations":[109314],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990941"},{"annotations":[103222,66654,108122,102158],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990498"},{"annotations":[102838,113723,110065,96546,119419,77933,104147,78855,91760,120556,95565,91393,93150,105335,80526,118507,102323,92747,113019],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990023"},{"annotations":[119995,109315,100397,100998],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990537"},{"annotations":[102159,119996],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097431"}]},"cv_name":"cellular_component","definition":"A spindle that forms as part of mitosis. Mitotic and meiotic spindles contain distinctive complements of proteins associated with microtubules.","definition_xrefs":["GOC:mah","PMID:11408572","PMID:8027178","GOC:vw","PMID:18367542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle","termid":"GO:0005819"}],"gene_count":86,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00140":null,"SJAG_00163":null,"SJAG_00207":null,"SJAG_00245":null,"SJAG_00514":null,"SJAG_00526":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00692":null,"SJAG_00697":null,"SJAG_00723":null,"SJAG_00724":null,"SJAG_00773":null,"SJAG_00800":null,"SJAG_00879":null,"SJAG_00883":null,"SJAG_00918":null,"SJAG_00930":null,"SJAG_00943":null,"SJAG_01110":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01232":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01371":null,"SJAG_01391":null,"SJAG_01429":null,"SJAG_01546":null,"SJAG_01557":null,"SJAG_01613":null,"SJAG_01634":null,"SJAG_01775":null,"SJAG_01805":null,"SJAG_01832":null,"SJAG_01837":null,"SJAG_01849":null,"SJAG_01887":null,"SJAG_02025":null,"SJAG_02045":null,"SJAG_02098":null,"SJAG_02209":null,"SJAG_02248":null,"SJAG_02266":null,"SJAG_02311":null,"SJAG_02336":null,"SJAG_02460":null,"SJAG_02542":null,"SJAG_02608":null,"SJAG_02624":null,"SJAG_02695":null,"SJAG_02761":null,"SJAG_02807":null,"SJAG_02821":null,"SJAG_03048":null,"SJAG_03062":null,"SJAG_03073":null,"SJAG_03116":null,"SJAG_03387":null,"SJAG_03437":null,"SJAG_03540":null,"SJAG_03569":null,"SJAG_03592":null,"SJAG_03731":null,"SJAG_03846":null,"SJAG_03901":null,"SJAG_03906":null,"SJAG_03911":null,"SJAG_04010":null,"SJAG_04074":null,"SJAG_04140":null,"SJAG_04257":null,"SJAG_04412":null,"SJAG_04607":null,"SJAG_04623":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04884":null,"SJAG_04931":null,"SJAG_04940":null,"SJAG_05205":null,"SJAG_05266":null,"SJAG_05313":null,"SJAG_05315":null,"SJAG_05319":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0015630"],"is_obsolete":false,"name":"mitotic spindle","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0072686","terms_by_termid":{"GO:0061673":null,"GO:0072686":null,"GO:0097431":null,"GO:1905721":null,"GO:1990023":null,"GO:1990498":null,"GO:1990537":null,"GO:1990941":null}}


id: MONDO:0018262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fetal anticonvulsant syndrome (obsolete MONDO:0018262)","secondary_identifiers":["Orphanet:370068"],"synonyms":[{"name":"FACS","type":"exact"},{"name":"fetal AEDS","type":"exact"},{"name":"fetal antiepileptic drug syndrome","type":"exact"},{"name":"foetal AEDS","type":"exact"},{"name":"foetal antiepileptic drug syndrome","type":"exact"}],"termid":"MONDO:0018262","xrefs":{"Monarch":{"xref_id":"0018262"}}}


id: PBO:0110100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tbasic amino acid ransmembrane transporter","termid":"PBO:0110100"}


id: GO:1904739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A posttranscriptional regulation of gene expression that results in regulation of synapse organization.","definition_xrefs":["GO_REF:0000063","GOC:rb","GOC:TermGenie","PMID:20729808"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of synapse organization by posttranscriptional regulation of gene expression (obsolete GO:1904739)","synonyms":[{"name":"regulation of synapse development by posttranscriptional regulation of gene expression","type":"exact"},{"name":"regulation of synapse morphogenesis by posttranscriptional regulation of gene expression","type":"related"},{"name":"regulation of synapse organisation by posttranscriptional regulation of gene expression","type":"exact"},{"name":"regulation of synapse organization and biogenesis by posttranscriptional regulation of gene expression","type":"related"}],"termid":"GO:1904739"}


id: PBO:0055280
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 2707","termid":"PBO:0055280"}


id: PBO:0111485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II CTD S5 small phosphatase Psr1","termid":"PBO:0111485"}


id: GO:1902543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to mitotic spindle pole body.","definition_xrefs":["GOC:TermGenie","PMID:22809626"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein localization to spindle pole body","termid":"GO:1902364"},{"relation_name":"is_a","term_name":"regulation of protein localization to mitotic spindle pole body","termid":"GO:1902542"},{"relation_name":"negatively_regulates","term_name":"protein localization to mitotic spindle pole body","termid":"GO:1902440"}],"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 protein localization to mitotic spindle pole body","synonyms":[{"name":"down regulation of protein localisation to mitotic spindle pole body","type":"exact"},{"name":"down regulation of protein localization to mitotic spindle pole body","type":"exact"},{"name":"down-regulation of protein localisation in mitotic spindle pole body","type":"exact"},{"name":"down-regulation of protein localisation to mitotic spindle pole body","type":"exact"},{"name":"down-regulation of protein localization to mitotic spindle pole body","type":"exact"},{"name":"downregulation of protein localisation to mitotic spindle pole body","type":"exact"},{"name":"downregulation of protein localization to mitotic spindle pole body","type":"exact"},{"name":"inhibition of protein localisation to mitotic spindle pole body","type":"narrow"},{"name":"inhibition of protein localization to mitotic spindle pole body","type":"narrow"},{"name":"negative regulation of protein localisation to mitotic spindle pole body","type":"exact"}],"termid":"GO:1902543"}


id: PBO:0119958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial cytochrome c oxidase Cox2 assembly protein, Cox16","termid":"PBO:0119958"}


id: MONDO:0005676
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An encephalomyelitis of horses, sheep and cattle caused by borna disease virus.","definition_xrefs":["MESH:D001890"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"},{"relation_name":"is_a","term_name":"acute disease, non-human animal","termid":"MONDO:1011300"},{"relation_name":"is_a","term_name":"inflammatory disease, non-human animal","termid":"MONDO:1011327"},{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"borna disease","secondary_identifiers":["EFO:0007178"],"synonyms":[{"name":"enzootic encephalomyelitis","type":"related"}],"termid":"MONDO:0005676","xrefs":{"Monarch":{"xref_id":"0005676"}}}


id: PBO:0071324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L27a pseudogene 8","termid":"PBO:0071324"}


id: MONDO:0012267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A holoprosencephaly that has material basis in variation in the chromosome region 14q13.","definition_xrefs":["DOID:0110879","PMID:15820313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"holoprosencephaly","termid":"MONDO:0016296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"holoprosencephaly 8","secondary_identifiers":["MESH:C563723","MEDGEN:322873","OMIM:609408","UMLS:C1836254"],"synonyms":[{"name":"HPE8","type":"exact"},{"name":"holoprosencephaly 8","type":"exact"},{"name":"holoprosencephaly type 8","type":"exact"}],"termid":"MONDO:0012267","xrefs":{"Monarch":{"xref_id":"0012267"}}}


id: MONDO:0004414
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spectrum of endometrial abnormalities that occur in women who use tamoxifen to treat or prevent the development of breast cancer. These abnormalities include endometrial polyps, endometrial hyperplasia, and endometrial carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrial disorder","termid":"MONDO:0000931"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tamoxifen-related endometrial lesion","secondary_identifiers":["NCIT:C40159","DOID:7962","MEDGEN:271571","UMLS:C1515212"],"synonyms":[{"name":"tamoxifen-related endometrial disorder","type":"exact"}],"termid":"MONDO:0004414","xrefs":{"Monarch":{"xref_id":"0004414"}}}


id: PBO:0085221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Palmitoyltransferase with autoacylation activity; required for palmitoylation of amino acid permeases containing a C-terminal Phe-Trp-Cys site; required for modification of Chs3p; member of the DHHC family of putative palmitoyltransferases","termid":"PBO:0085221"}


id: MONDO:0010171
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of Usher syndrome type I that is caused by homozygous or compound heterozygous mutation in the gene encoding harmonin on chromosome 11p15. It is inherited in an autosomal recessive manner.","definition_xrefs":["OMIM:276904"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Usher syndrome type 1","termid":"MONDO:0010168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Usher syndrome type 1C","secondary_identifiers":["DOID:0110830","UMLS:C1848604","ICD10CM:H35.5","GARD:5437","MEDGEN:338506"],"synonyms":[{"name":"USH1C","type":"exact"},{"name":"USHER syndrome, type IC","type":"related"},{"name":"Usher syndrome type 1C","type":"exact"},{"name":"Usher syndrome type I Acadian variety","type":"exact"},{"name":"Usher syndrome type IC","type":"exact"},{"name":"Usher syndrome, Acadian variety","type":"related"},{"name":"Usher syndrome, type 1C","type":"related"},{"name":"Usher syndrome, type I, Acadian variety","type":"related"}],"termid":"MONDO:0010171","xrefs":{"Monarch":{"xref_id":"0010171"}}}


id: GO:0140672
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A chromatin remodeling complex that regulates transcription via acetylation primarily of nucleosomal histones H3 and possibly H4. Shares the histone acetylation (HAT) module of GCN5/PCAF-ADA2-ADA3-SGF29 (or orthologs) with the related SAGA complex (GO:0000124). Contains HAT subunits GCN5 or PCAF in a mutually exclusive manner. In addition to the HAT module contains DR1/NC2B, KAT14, MBIP, WDR5, YEATS2 and ZZZ3 or orthologs. Also regulates the activity of non-histone targets and orchestrates mitotic progression by regulating Cyclin A degradation through acetylation.","definition_xrefs":["PMID:19936620","GOC:bhm","PMID:28966424","PMID:20562830"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SAGA-type complex","termid":"GO:0070461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0032991","GO:0005694","GO:0005575"],"is_obsolete":false,"name":"ATAC complex","synonyms":[{"name":"ADA2A-containing complex","type":"exact"},{"name":"Ada Two-A containing complex","type":"exact"},{"name":"Ada two A containing complex","type":"exact"},{"name":"Ada-Two-A-containing complex","type":"exact"},{"name":"G-ATAC complex","type":"exact"},{"name":"KAT2A-containing ATAC complex","type":"exact"},{"name":"KAT2B-containing ATAC complex","type":"exact"}],"termid":"GO:0140672"}


id: PBO:0056881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MICOS10 pseudogene 1","termid":"PBO:0056881"}


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


id: MONDO:1010487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ventricular septal defect 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":"ventricular septal defect, non-human animal","termid":"MONDO:1010022"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ventricular septal defect, chicken","secondary_identifiers":["OMIA:001041-9031"],"termid":"MONDO:1010487","xrefs":{"Monarch":{"xref_id":"1010487"}}}


id: GO:1905793
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a pericentriolar material.","definition_xrefs":["PMID:24385583","GOC:TermGenie","GO_REF:0000087","PMID:21694707"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to centrosome","termid":"GO:0071539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to pericentriolar material","synonyms":[{"name":"protein localisation in pericentriolar material","type":"exact"},{"name":"protein localisation to pericentriolar material","type":"exact"},{"name":"protein localization in pericentriolar material","type":"exact"}],"termid":"GO:1905793"}


id: FYPO:0000614
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through S phase of the mitotic cell cycle is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic S phase progression","termid":"FYPO:0000610"},{"relation_name":"is_a","term_name":"increased duration of mitotic cell cycle phase","termid":"FYPO:0001069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"name":"increased duration of mitotic S phase","secondary_identifiers":["FYPO:0000612","FYPO:0000613"],"synonyms":[{"name":"decreased rate of mitotic S phase progression","type":"related"},{"name":"delayed mitotic S phase progression","type":"related"},{"name":"delayed mitotic S phase progression during vegetative growth","type":"related"},{"name":"increased S phase index","type":"related"},{"name":"increased duration of S phase during mitotic cell cycle","type":"exact"},{"name":"increased duration of mitotic S phase during vegetative growth","type":"exact"},{"name":"mitotic cell cycle progression in S phase: decreased rate","type":"related"},{"name":"mitotic cell cycle progression in S phase: delayed","type":"related"},{"name":"mitotic cell cycle progression in S phase: increased duration","type":"related"},{"name":"prolonged mitotic S phase","type":"exact"},{"name":"reduced rate of mitotic S phase progression","type":"related"}],"termid":"FYPO:0000614"}


id: FYPO:0007776
data:
  {"alleles_by_uniquename":{"SJAG_00124:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00124","name":"SJAG_00124delta","uniquename":"SJAG_00124:allele-1"},"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_02013:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02013","name":"pyp1delta","uniquename":"SJAG_02013:allele-1"},"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"},"SJAG_04551:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04551","name":"pmk1delta","uniquename":"SJAG_04551:allele-1"},"SJAG_04551:allele-2":{"allele_type":"amino_acid_insertion","description":"82-NITCIYDLDIIINPYNFNEVYIYEE-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sj(ins82-105)","uniquename":"SJAG_04551:allele-2"},"SJAG_04551:allele-3":{"allele_type":"other","description":"Pmk1 from S. pombe","gene_uniquename":"SJAG_04551","name":"Pmk1Sp","uniquename":"SJAG_04551:allele-3"},"SJAG_04551:allele-4":{"allele_type":"partial_amino_acid_deletion","description":"Pmk1 from S. pombe with deleted residues 82-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sp(delta82-105)","uniquename":"SJAG_04551:allele-4"},"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[120973,121209,121221,121225,121230,121233,121338,121341,121464],"is_not":false,"summary":null,"term":"FYPO:0007776"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which hyphae are shorter than normal.","definition_xrefs":["PMID:31150379","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal hyphal growth","termid":"FYPO:0007773"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00124":null,"SJAG_00610":null,"SJAG_02013":null,"SJAG_02527":null,"SJAG_04551":null,"SJAG_04697":null},"genotype_count":9,"genotypes_by_uniquename":{"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sj(ins82-105)(82-NITCIYDLDIIINPYNFNEVYIYEE-105)","display_uniquename":"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-2","expression":"Not assayed or wild type"}]}]},"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(delta82-105)(Pmk1 from S. pombe with deleted residues 82-105 Δaa)","display_uniquename":"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-4","expression":"Not assayed or wild type"}]}]},"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(Pmk1 from S. pombe)","display_uniquename":"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-3","expression":"Not assayed or wild type"}]}]},"SJAG_00124delta":{"display_name":"SJAG_00124delta","display_uniquename":"SJAG_00124delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00124:allele-1","expression":"Null"}]}]},"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]},"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]},"pck2delta":{"display_name":"pck2delta","display_uniquename":"pck2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00610:allele-1","expression":"Null"}]}]},"pmk1delta":{"display_name":"pmk1delta","display_uniquename":"pmk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-1","expression":"Null"}]}]},"pyp1delta":{"display_name":"pyp1delta","display_uniquename":"pyp1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02013:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0007773"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0007773","FYPO:0000002"],"is_obsolete":false,"name":"decreased hyphal length","references_by_uniquename":{"PMID:31150379":null,"PMID:34198697":null,"PMID:36058798":null,"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_04697","SJAG_04551","SJAG_02527","SJAG_00610","SJAG_02013","SJAG_00124"],"single_locus_genotype_uniquenames":["pck2delta","Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","pmk1delta","Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","gms1delta","SJAG_00124delta","pyp1delta"],"synonyms":[{"name":"short hyphae","type":"exact"}],"termid":"FYPO:0007776","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000314":null,"FYPO:0007776":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: MOD:00934
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Post-translational","definition_xrefs":["Unimod:506"],"direct_ancestors":[{"relation_name":"is_a","term_name":"levuglandinyl (prostaglandin H2) adduct","termid":"MOD:00846"},{"relation_name":"is_a","term_name":"modified L-arginine residue","termid":"MOD:00902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Levuglandinyl - arginine hydroxylactam adduct","synonyms":[{"name":"LG-Hlactam-R","type":"related"},{"name":"Levuglandinyl - arginine hydroxylactam adduct","type":"related"}],"termid":"MOD:00934"}


id: MONDO:0100193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Liver failure that develops slowly and gradually for some time, possibly for years, often as the result of cirrhosis, or malnutrition.","direct_ancestors":[{"relation_name":"is_a","term_name":"liver failure","termid":"MONDO:0100192"}],"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":"chronic liver failure","secondary_identifiers":["UMLS:C2936476","ICD10CM:K72.1","MEDGEN:423539","NCIT:C84428"],"synonyms":[{"name":"ESLD","type":"exact"},{"name":"end stage liver disease","type":"exact"},{"name":"end stage liver disease (decompensated liver disease)","type":"exact"},{"name":"end-stage liver disease","type":"exact"}],"termid":"MONDO:0100193","xrefs":{"Monarch":{"xref_id":"0100193"}}}


id: PBO:0046453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPS8 like 1","termid":"PBO:0046453"}


id: MONDO:0022873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corpus callosum dysgenesis cleft spasm","termid":"MONDO:0022873","xrefs":{"Monarch":{"xref_id":"0022873"}}}


id: GO:0061287
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of a mesonephric capsule from unspecified parts. The mesonephric capsule is the tough fibrous layer surrounding the mesonephros, covered in a thick layer of perinephric adipose tissue. It provides some protection from trauma and damage.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal capsule formation","termid":"GO:0072129"},{"relation_name":"part_of","term_name":"mesonephric capsule morphogenesis","termid":"GO:0061286"}],"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":"mesonephric capsule formation","termid":"GO:0061287"}


id: MONDO:0030366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dilated cardiomyopathy that is characterized by neonatal or early childhood onset of dilated cardiomyopathy, with rapid progression to cardiac failure and death unless patients undergo cardiac transplantation and that has material basis in homozygous or compound heterozygous mutation in the JPH2 gene on chromosome 20q13.","definition_xrefs":["DOID:0081161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"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":"cardiomyopathy, dilated, 2E","secondary_identifiers":["OMIM:619492","UMLS:C5561970","MEDGEN:1794180"],"synonyms":[{"name":"CMD2E","type":"exact"},{"name":"cardiomyopathy, dilated, 2E","type":"exact"}],"termid":"MONDO:0030366","xrefs":{"Monarch":{"xref_id":"0030366"}}}


id: MOD:00957
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Covalent modification of, or a change resulting in an alteration of the measured molecular mass of, a peptide or protein amino acid residue with a secondary loss of a neutral carbon dioxide molecular fragment.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue with a secondary neutral loss","termid":"MOD:00431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified residue with neutral loss of carbon dioxide","synonyms":[{"name":"dCO2ModRes","type":"exact"}],"termid":"MOD:00957"}


id: MONDO:1012869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any heart disorder characterized by pathologically prolonged ventricular action potential duration with sudden cardiac death due to polymorphic vetricular tachycardia that occurs in rabbits due to a mutation in the KCNH2 gene created by genetic engineering or gene editing.","definition_xrefs":["PMID:18464931"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"heart disorder, non-human animal","termid":"MONDO:1012982"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long QT syndrome, KCNH2-related, rabbit","secondary_identifiers":["OMIA:002333-9986"],"termid":"MONDO:1012869","xrefs":{"Monarch":{"xref_id":"1012869"}}}


id: GO:0140433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to a meiotic spindle pole body.","definition_xrefs":["PMID:22438582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to spindle pole body","termid":"GO:1902363"},{"relation_name":"regulates","term_name":"protein localization to meiotic spindle pole body","termid":"GO:1902441"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein localization to meiotic spindle pole body","termid":"GO:0140433"}


id: GO:0018589
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: dibutyltin + O2 + 2 H+ + 2 e- = H2O + beta-hydroxybutylbutyltin.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete di-n-butyltin dioxygenase activity (obsolete GO:0018589)","synonyms":[{"name":"DBT dioxygenase activity","type":"exact"}],"termid":"GO:0018589"}


id: MONDO:0018249
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":"finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome","secondary_identifiers":["UMLS:C5190599","Orphanet:369979","GARD:21584","MEDGEN:1673147"],"termid":"MONDO:0018249","xrefs":{"Monarch":{"xref_id":"0018249"}}}


id: GO:0015541
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of cyanate from one side of a membrane to the other.","definition_xrefs":["TC:2.A.1.17.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyanate transmembrane transporter activity","termid":"GO:0015110"},{"relation_name":"is_a","term_name":"secondary active transmembrane transporter activity","termid":"GO:0015291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"secondary active cyanate transmembrane transporter activity","synonyms":[{"name":"cyanate porter activity","type":"related"}],"termid":"GO:0015541"}


id: GO:0008628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by the detection of a hormone, and which triggers the apoptotic signaling pathway in a cell. The pathway starts with reception of a hormone signal, and ends when the execution phase of apoptosis is triggered.","definition_xrefs":["GOC:bf","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"is_a","term_name":"apoptotic signaling pathway","termid":"GO:0097190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"hormone-mediated apoptotic signaling pathway","synonyms":[{"name":"apoptotic signaling pathway in response to hormone","type":"related"},{"name":"induction of apoptosis by hormones","type":"related"}],"termid":"GO:0008628"}


id: GO:1902689
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of NAD metabolic process.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:di","PMID:19846558"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of purine nucleotide metabolic process","termid":"GO:1900543"},{"relation_name":"is_a","term_name":"regulation of NAD metabolic process","termid":"GO:1902688"},{"relation_name":"negatively_regulates","term_name":"NAD+ metabolic process","termid":"GO:0019674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055086"},{"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:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"negative regulation of NAD metabolic process","synonyms":[{"name":"down regulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"down regulation of NAD (oxidized) metabolism","type":"exact"},{"name":"down regulation of NAD metabolic process","type":"exact"},{"name":"down regulation of NAD metabolism","type":"exact"},{"name":"down regulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"down regulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down regulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"down regulation of oxidized NAD metabolic process","type":"exact"},{"name":"down regulation of oxidized NAD metabolism","type":"exact"},{"name":"down regulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down regulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"down-regulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"down-regulation of NAD (oxidized) metabolism","type":"exact"},{"name":"down-regulation of NAD metabolic process","type":"exact"},{"name":"down-regulation of NAD metabolism","type":"exact"},{"name":"down-regulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"down-regulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down-regulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"down-regulation of oxidized NAD metabolic process","type":"exact"},{"name":"down-regulation of oxidized NAD metabolism","type":"exact"},{"name":"down-regulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down-regulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"downregulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"downregulation of NAD (oxidized) metabolism","type":"exact"},{"name":"downregulation of NAD metabolic process","type":"exact"},{"name":"downregulation of NAD metabolism","type":"exact"},{"name":"downregulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"downregulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"downregulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"downregulation of oxidized NAD metabolic process","type":"exact"},{"name":"downregulation of oxidized NAD metabolism","type":"exact"},{"name":"downregulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"downregulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"inhibition of NAD (oxidized) metabolic process","type":"narrow"},{"name":"inhibition of NAD (oxidized) metabolism","type":"narrow"},{"name":"inhibition of NAD metabolic process","type":"narrow"},{"name":"inhibition of NAD metabolism","type":"narrow"},{"name":"inhibition of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"inhibition of nicotinamide adenine dinucleotide metabolic process","type":"narrow"},{"name":"inhibition of nicotinamide adenine dinucleotide metabolism","type":"narrow"},{"name":"inhibition of oxidized NAD metabolic process","type":"narrow"},{"name":"inhibition of oxidized NAD metabolism","type":"narrow"},{"name":"inhibition of oxidized nicotinamide adenine dinucleotide metabolic process","type":"narrow"},{"name":"inhibition of oxidized nicotinamide adenine dinucleotide metabolism","type":"narrow"},{"name":"negative regulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"negative regulation of NAD (oxidized) metabolism","type":"exact"},{"name":"negative regulation of NAD metabolism","type":"exact"},{"name":"negative regulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"negative regulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"negative regulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"negative regulation of oxidized NAD metabolic process","type":"exact"},{"name":"negative regulation of oxidized NAD metabolism","type":"exact"},{"name":"negative regulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"negative regulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"}],"termid":"GO:1902689"}


id: MONDO:0012707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"febrile seizures, familial","termid":"MONDO:0000032"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial febrile seizures 9","secondary_identifiers":["MESH:C566901","MEDGEN:369868","DOID:0111303","OMIM:611634","UMLS:C1968846"],"synonyms":[{"name":"FEB9","type":"exact"},{"name":"febrile convulsions, familial, 9","type":"related"},{"name":"febrile seizures, familial, 9","type":"related"}],"termid":"MONDO:0012707","xrefs":{"Monarch":{"xref_id":"0012707"}}}


id: PBO:0028098
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_index","termid":"PBO:0028098"}


id: GO:0035665
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by a ligand binding to a toll-like receptor 4 where the TIRAP/MAL adaptor mediates transduction of the signal. Toll-like 4 receptors are pattern recognition receptors that bind bacterial lipopolysaccharide (LPS) to initiate an innate immune response.","definition_xrefs":["GOC:BHF","PMID:12447441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toll-like receptor 4 signaling pathway","termid":"GO:0034142"},{"relation_name":"is_a","term_name":"TIRAP-dependent toll-like receptor signaling pathway","termid":"GO:0035664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"TIRAP-dependent toll-like receptor 4 signaling pathway","synonyms":[{"name":"MAL-dependent toll-like receptor 4 signaling pathway","type":"exact"},{"name":"MyD88 adapter-like dependent toll-like receptor 4 signaling pathway","type":"exact"},{"name":"TIRAP-dependent TLR4 signaling pathway","type":"exact"},{"name":"TIRAP-dependent toll-like receptor 4 signalling pathway","type":"exact"}],"termid":"GO:0035665"}


id: GO:0060193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of lipase activity, the hydrolysis of a lipid or phospholipid.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of hydrolase activity","termid":"GO:0051345"}],"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 lipase activity","termid":"GO:0060193"}


id: MONDO:0006516
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles.","definition_xrefs":["MESH:D055948"],"gene_count":0,"genotype_count":0,"name":"obsolete sarcopenia (obsolete MONDO:0006516)","secondary_identifiers":["ICD10CM:M62.84","MedDRA:10063024"],"termid":"MONDO:0006516","xrefs":{"Monarch":{"xref_id":"0006516"}}}


id: MONDO:0957533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukoencephalopathy, megalencephalic","termid":"MONDO:0000137"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megalencephalic leukoencephalopathy with subcortical cysts 3","secondary_identifiers":["OMIM:620447","UMLS:C5830625","MEDGEN:1841261"],"termid":"MONDO:0957533","xrefs":{"Monarch":{"xref_id":"0957533"}}}


id: GO:0009124
data:
  {"annotated_genes":["SJAG_03708","SJAG_04487","SJAG_04882","SJAG_01661","SJAG_03140","SJAG_00964","SJAG_00044","SJAG_04845","SJAG_04709","SJAG_01081","SJAG_06634","SJAG_04681","SJAG_00533","SJAG_02850","SJAG_04354","SJAG_00197","SJAG_03811","SJAG_04970","SJAG_04627","SJAG_03355","SJAG_00444","SJAG_02364","SJAG_03164","SJAG_04634","SJAG_01070","SJAG_04713","SJAG_01298","SJAG_01859","SJAG_03771","SJAG_00694","SJAG_04123","SJAG_01814"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78671,80656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044208"},{"annotations":[60487,71601,57133,66731,78446,58273,73275,65365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006189"},{"annotations":[62631,59781,57252,59407,61633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044205"},{"annotations":[75623,57284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"},{"annotations":[69536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009224"},{"annotations":[71588,81164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006231"},{"annotations":[71587,81187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006226"},{"annotations":[74526],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009398"},{"annotations":[63836,59780],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006177"},{"annotations":[102986,77324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"},{"annotations":[65881,77325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032264"},{"annotations":[60470,64351,62400],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009156"},{"annotations":[90219,69537,93746,89225,94744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044206"},{"annotations":[110090,77326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a nucleoside monophosphate, a compound consisting of a nucleobase linked to a deoxyribose or ribose sugar esterified with phosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside monophosphate metabolic process","termid":"GO:0009123"},{"relation_name":"is_a","term_name":"nucleoside phosphate biosynthetic process","termid":"GO:1901293"}],"gene_count":32,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00197":null,"SJAG_00444":null,"SJAG_00533":null,"SJAG_00694":null,"SJAG_00964":null,"SJAG_01070":null,"SJAG_01081":null,"SJAG_01298":null,"SJAG_01661":null,"SJAG_01814":null,"SJAG_01859":null,"SJAG_02364":null,"SJAG_02850":null,"SJAG_03140":null,"SJAG_03164":null,"SJAG_03355":null,"SJAG_03708":null,"SJAG_03771":null,"SJAG_03811":null,"SJAG_04123":null,"SJAG_04354":null,"SJAG_04487":null,"SJAG_04627":null,"SJAG_04634":null,"SJAG_04681":null,"SJAG_04709":null,"SJAG_04713":null,"SJAG_04845":null,"SJAG_04882":null,"SJAG_04970":null,"SJAG_06634":null},"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:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"nucleoside monophosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"nucleoside monophosphate anabolism","type":"exact"},{"name":"nucleoside monophosphate biosynthesis","type":"exact"},{"name":"nucleoside monophosphate formation","type":"exact"},{"name":"nucleoside monophosphate synthesis","type":"exact"}],"termid":"GO:0009124","terms_by_termid":{"GO:0006177":null,"GO:0006189":null,"GO:0006226":null,"GO:0006231":null,"GO:0009156":null,"GO:0009224":null,"GO:0009398":null,"GO:0032263":null,"GO:0032264":null,"GO:0032265":null,"GO:0044205":null,"GO:0044206":null,"GO:0044208":null,"GO:0044209":null}}


id: PBO:0002033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-splicing endonuclease subunit Sen15 (predicted)","termid":"PBO:0002033"}


id: PBO:0051783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQ motif containing F1","termid":"PBO:0051783"}


id: PBO:0003532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCAAT-binding factor complex subunit Php2","termid":"PBO:0003532"}


id: PBO:0049686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine ammonia-lyase","termid":"PBO:0049686"}


id: GO:0018570
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: p-cumate + NADH + H+ + O2 = NAD+ + cis-2,3-dihydroxy-2,3-dihydro-p-cumate.","definition_xrefs":["RHEA:42344"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"p-cumate 2,3-dioxygenase activity","secondary_identifiers":["UM-BBD_reactionID:r0395","EC:1.14.12.25","MetaCyc:RXN-664"],"termid":"GO:0018570"}


id: PBO:0024807
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-contributes_to","termid":"PBO:0024807"}


id: MONDO:0859376
data:
  {"annotated_genes":["SJAG_02447","SJAG_02589"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89058,89059],"is_not":false,"summary":null,"term":"MONDO:0859376"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"congenital hydrocephalus","termid":"MONDO:0016349"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02447":null,"SJAG_02589":null},"genotype_count":0,"is_obsolete":false,"name":"hydrocephalus, congenital, 5, susceptibility to","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1840908","OMIM:620241","UMLS:C5830272"],"termid":"MONDO:0859376","terms_by_termid":{"MONDO:0859376":null},"xrefs":{"Monarch":{"xref_id":"0859376"}}}


id: GO:0120285
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of tyrosine.","definition_xrefs":["GOC:krc","PMID:31498992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid sensor activity","termid":"GO:0140785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140299"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140299","GO:0098772"],"is_obsolete":false,"name":"tyrosine sensor activity","synonyms":[{"name":"tyrosine sensing activity","type":"exact"}],"termid":"GO:0120285"}


id: PBO:0050053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class I, T (pseudogene)","termid":"PBO:0050053"}


id: PBO:0061864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxidized low density lipoprotein receptor 1","termid":"PBO:0061864"}


id: PR:O13766
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mde10 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13766"],"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 metalloprotease mde10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17A5.04c","synonyms":[{"name":"Spom972h-mde10","type":"exact"},{"name":"meiotically up-regulated gene 139 protein (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"sporulation protein mde10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13766"}


id: MOD:00417
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-carboxamidoethyl-L-cysteine.","definition_xrefs":["OMSSA:5","DeltaMass:72","PubMed:1481983","Unimod:24#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-carboxamidoethyl-L-cysteine","synonyms":[{"name":"Acrylamide adduct","type":"related"},{"name":"PAM-Cys","type":"exact"},{"name":"Propionamide","type":"related"},{"name":"Propionamide or Acrylamide adduct","type":"exact"},{"name":"S-(3-amino-3-oxopropyl)cysteine","type":"exact"},{"name":"S-carbamoylethyl-L-cysteine","type":"exact"},{"name":"S-propanamide-L-cysteine","type":"exact"},{"name":"propionamidec","type":"exact"}],"termid":"MOD:00417"}


id: PBO:0072705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RWD domain containing 1 pseudogene 1","termid":"PBO:0072705"}


id: GO:0008159
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any activity that increases the rate of transcription elongation, the addition of ribonucleotides to an RNA molecule following transcription initiation.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive transcription elongation factor activity (obsolete GO:0008159)","synonyms":[{"name":"positive transcription elongation factor activity","type":"exact"}],"termid":"GO:0008159"}


id: PBO:0071597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 14","termid":"PBO:0071597"}


id: PBO:0003796
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chediak-Higashi syndrome","termid":"PBO:0003796"}


id: PBO:0065354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPN13 like Y-linked pseudogene 4","termid":"PBO:0065354"}


id: PBO:0073191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenoprotein T pseudogene 2","termid":"PBO:0073191"}


id: MONDO:1011567
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neurofibromatosis that occurs in teleost fishes.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibromatosis, non-human animal","termid":"MONDO:1011437"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurofibromatosis, teleost fishes","secondary_identifiers":["OMIA:000716-32443"],"termid":"MONDO:1011567","xrefs":{"Monarch":{"xref_id":"1011567"}}}


id: PBO:0051573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17B","termid":"PBO:0051573"}


id: FYPO:0002600
data:
  {"alleles_by_uniquename":{"SJAG_02621:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02621","name":"ago1delta","uniquename":"SJAG_02621:allele-1"},"SJAG_03118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03118","name":"leo1delta","uniquename":"SJAG_03118:allele-1"},"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121286,121285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}],"single_locus_phenotype":[{"annotations":[121278],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0006989"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone modification is normal. All histone modification may be assayed, or modification of specific sites on specific histones may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein modification during vegetative growth","termid":"FYPO:0000549"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02621":null,"SJAG_03118":null,"SJAG_03689":null},"genotype_count":3,"genotypes_by_uniquename":{"ago1delta__leo1delta":{"display_name":"ago1delta leo1delta","display_uniquename":"ago1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02621:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]},"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]},"dcr1delta__leo1delta":{"display_name":"dcr1delta leo1delta","display_uniquename":"dcr1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_02621","SJAG_03689","SJAG_03118"],"name":"normal histone modification during vegetative growth","references_by_uniquename":{"PMID:35226668":null},"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"normal histone modification during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002600","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0006989":null}}


id: PBO:0063381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 1 ligand 2","termid":"PBO:0063381"}


id: GO:0061100
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuroendocrine cell of the lung epithelium.","definition_xrefs":["PMID:9126746","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroendocrine cell differentiation","termid":"GO:0061101"},{"relation_name":"is_a","term_name":"lung secretory cell differentiation","termid":"GO:0061140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lung neuroendocrine cell differentiation","termid":"GO:0061100"}


id: GO:0070147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of coupling cysteine to cysteinyl-tRNA in a mitochondrion, catalyzed by cysteinyl-tRNA synthetase. In tRNA aminoacylation, the amino acid is first activated by linkage to AMP and then transferred to either the 2'- or the 3'-hydroxyl group of the 3'-adenosine residue of the tRNA.","definition_xrefs":["GOC:mah","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteinyl-tRNA aminoacylation","termid":"GO:0006423"},{"relation_name":"is_a","term_name":"tRNA aminoacylation for mitochondrial protein translation","termid":"GO:0070127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0140053"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0006399","GO:0006520","GO:0008150","GO:0140053","GO:0010467"],"is_obsolete":false,"name":"mitochondrial cysteinyl-tRNA aminoacylation","termid":"GO:0070147"}


id: MONDO:0002236
data:
  {"annotated_genes":["SJAG_03677"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm affecting the structures of the eye.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory system cancer","termid":"MONDO:0000649"},{"relation_name":"is_a","term_name":"head and neck cancer","termid":"MONDO:0005627"},{"relation_name":"is_a","term_name":"eye neoplasm","termid":"MONDO:0021220"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03677":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"ocular cancer","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:190.8","ICD9:239.89","MESH:D005134","UMLS:C0496836","DOID:2174","MEDGEN:105418","NCIT:C4767","SCTID:371486001"],"synonyms":[{"name":"cancer of eye","type":"exact"},{"name":"cancer of eyeball of camera-type eye","type":"exact"},{"name":"cancer of the eye","type":"exact"},{"name":"eye cancer","type":"exact"},{"name":"eye neoplasm","type":"broad"},{"name":"eye neoplasm, malignant","type":"exact"},{"name":"eyeball of camera-type eye cancer","type":"exact"},{"name":"malignant eye neoplasm","type":"exact"},{"name":"malignant eye tumor","type":"exact"},{"name":"malignant eye tumour","type":"exact"},{"name":"malignant eyeball of camera-type eye neoplasm","type":"exact"},{"name":"malignant neoplasm of eye","type":"exact"},{"name":"malignant neoplasm of eyeball of camera-type eye","type":"exact"},{"name":"malignant neoplasm of the eye","type":"exact"},{"name":"malignant ocular neoplasm","type":"exact"},{"name":"malignant ocular tumor","type":"exact"},{"name":"malignant ocular tumour","type":"exact"},{"name":"malignant tumor of eye","type":"exact"},{"name":"malignant tumor of the eye","type":"exact"},{"name":"malignant tumour of eye","type":"exact"},{"name":"malignant tumour of the eye","type":"exact"},{"name":"neoplasm of eye","type":"broad"},{"name":"neoplasm of eye proper","type":"related"},{"name":"ocular tumor","type":"broad"},{"name":"ocular tumour","type":"broad"}],"termid":"MONDO:0002236","terms_by_termid":{"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0002236"}}}


id: PBO:0086884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transcription factor containing a zinc finger; overexpression increases salt tolerance through increased expression of the ENA1 (Na+/Li+ extrusion pump) gene while gene disruption decreases both salt tolerance and ENA1 expression; HAL9 has a paralog, TBS1, that arose from the whole genome duplication","termid":"PBO:0086884"}


id: PBO:0072299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 17","termid":"PBO:0072299"}


id: GO:0008612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of peptidyl-lysine to form hypusine, peptidyl-N6-(4-amino-2-hydroxybutyl)-L-lysine.","definition_xrefs":["GOC:ma","ISBN:0198547684","RESID:AA0116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"peptidyl-lysine modification","termid":"GO:0018205"},{"relation_name":"is_a","term_name":"protein maturation","termid":"GO:0051604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"peptidyl-lysine modification to peptidyl-hypusine","secondary_identifiers":["GO:0046515","Reactome:R-HSA-204626"],"synonyms":[{"name":"hypusine anabolism","type":"exact"},{"name":"hypusine anabolism from peptidyl-lysine","type":"exact"},{"name":"hypusine biosynthesis","type":"exact"},{"name":"hypusine biosynthetic process","type":"exact"},{"name":"hypusine biosynthetic process from peptidyl-lysine","type":"exact"},{"name":"hypusine formation","type":"exact"},{"name":"hypusine formation from peptidyl-lysine","type":"exact"},{"name":"hypusine synthesis","type":"exact"},{"name":"hypusine synthesis from peptidyl-lysine","type":"exact"},{"name":"hypusinylation","type":"exact"},{"name":"protein hypusination","type":"exact"}],"termid":"GO:0008612"}


id: MONDO:0020113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acquired aplastic anemia","termid":"MONDO:0015610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"primary acquired red cell aplasia","secondary_identifiers":["GARD:19465","MedDRA:10038184","Orphanet:98421"],"synonyms":[{"name":"primary autoimmune red cell aplasia","type":"exact"},{"name":"red cell aplasia","type":"broad"}],"termid":"MONDO:0020113","xrefs":{"Monarch":{"xref_id":"0020113"}}}


id: PBO:0070825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13a pseudogene 3","termid":"PBO:0070825"}


id: PBO:0028389
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_methylglyoxal","termid":"PBO:0028389"}


id: PBO:0068435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 5, pseudogene","termid":"PBO:0068435"}


id: PBO:0038465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily A member 4","termid":"PBO:0038465"}


id: MONDO:0013081
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition of decreased or absent presence or activity of IL2-inducible t-cell kinase. Deficiency of this protein is associated with lymphoproliferative syndrome 1, an autosomal recessive primary immunodeficiency characterized by onset in early childhood of Epstein-Barr virus (EBV)-associated immune dysregulation, manifest as lymphoma, lymphomatoid granulomatosis, hemophagocytic lymphohistiocytosis, Hodgkin disease, and/or hypogammaglobulinemia..","definition_xrefs":["NCIT:C126344"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"disease","termid":"MONDO:0000001"},{"relation_name":"excluded_subClassOf","term_name":"obsolete autosomal recessive lymphoproliferative disease (obsolete MONDO:0016536)","termid":"MONDO:0016536"},{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"lymphoproliferative syndrome","termid":"MONDO:0016537"},{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"lymphoproliferative syndrome 1","secondary_identifiers":["UMLS:C3552634","DOID:0060707","NANDO:2200734","Orphanet:538963","MEDGEN:765548","MESH:C567815","GARD:17979","OMIM:613011"],"synonyms":[{"name":"ITK deficiency","type":"exact"},{"name":"ITK lymphoproliferative syndrome","type":"exact"},{"name":"LPFS1","type":"exact"},{"name":"lymphoproliferative syndrome 1","type":"exact"},{"name":"lymphoproliferative syndrome caused by mutation in ITK","type":"exact"},{"name":"lymphoproliferative syndrome type 1","type":"exact"}],"termid":"MONDO:0013081","xrefs":{"Monarch":{"xref_id":"0013081"}}}


id: PBO:0091165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-classical export protein Nce101","termid":"PBO:0091165"}


id: PBO:0029666
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_phosphorylation_during_vegetative_growth","termid":"PBO:0029666"}


id: GO:0005534
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to aldohexose galactose (galacto-hexose), a common constituent of many oligo- and polysaccharides.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide binding","termid":"GO:0048029"}],"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":"galactose binding","synonyms":[{"name":"galactose binding lectin","type":"related"}],"termid":"GO:0005534"}


id: MONDO:0005654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection that is caused by the roundworm Ascaris lumbricoides, many cases of which remain asymptomatic. During the transient larval migratory phase, shortness of breath, fever, and eosinophilia can occur. Depending on the intestinal worm burden, a spectrum of gastrointestinal tract symptoms can occur.","definition_xrefs":["NCIT:C128392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ascaridida infectious disease","termid":"MONDO:0005656"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ascariasis","secondary_identifiers":["ICD10CM:B77","icd11.foundation:17842540","MEDGEN:2087","MESH:D001196","CSP:1248-7284","DOID:456","SCTID:2435008","EFO:0007154","ICD9:127.0","UMLS:C0003950"],"synonyms":[{"name":"Ascaris lumbricoides caused disease or disorder","type":"exact"},{"name":"Ascaris lumbricoides disease or disorder","type":"exact"},{"name":"Ascaris lumbricoides infection","type":"related"},{"name":"Ascaris lumbricoides infectious disease","type":"exact"},{"name":"ascariasis - roundworm","type":"exact"}],"termid":"MONDO:0005654","xrefs":{"Monarch":{"xref_id":"0005654"}}}


id: _global:singly_occurring_form_of
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"singly_occurring_form_of","synonyms":[{"name":"monadic_form_of","type":"exact"}],"termid":"_global:singly_occurring_form_of"}


id: MONDO:0008320
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":"Protrusio acetabuli","secondary_identifiers":["UMLS:C0409495","OMIM:177050","HP:0003179","ICD10CM:M24.7","MEDGEN:98369","SCTID:59606006"],"synonyms":[{"name":"PROTRUSIO acetabuli","type":"related"},{"name":"Protrusio acetabuli","type":"exact"},{"name":"Protrusio acetabuli (disease)","type":"exact"}],"termid":"MONDO:0008320","xrefs":{"Monarch":{"xref_id":"0008320"}}}


id: PBO:0086718
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; non-essential gene; expression directly regulated by the metabolic and meiotic transcriptional regulator Ume6p","termid":"PBO:0086718"}


id: GO:0001040
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to an RNA polymerase III (Pol III) complex, typically composed of seventeen subunits, and with another protein, macromolecule, or complex, permitting those molecules to function in a coordinated way. Once recruited to an RNA polymerase III hybrid type promoter, binds to DNA, recruits RNA polymerase III and facilitates the transition from the closed to the open complex.","definition_xrefs":["GOC:txnOH-2018","PMID:12381659"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA polymerase III hybrid type promoter TFIIIB-type transcription factor activity (obsolete GO:0001040)","termid":"GO:0001040"}


id: MONDO:0000679
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An agnosia that is a loss of the ability to perceive facial expression, body language and intonation, rendering them unable to non-verbally perceive people's emotions and limiting that aspect of social interaction.","definition_xrefs":["DOID:0060149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"agnosia","termid":"MONDO:0005638"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"social emotional agnosia","synonyms":[{"name":"expressive agnosia","type":"exact"}],"termid":"MONDO:0000679","xrefs":{"Monarch":{"xref_id":"0000679"}}}


id: GO:0035303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of removal of phosphate groups from a molecule.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phosphate metabolic process","termid":"GO:0019220"},{"relation_name":"regulates","term_name":"dephosphorylation","termid":"GO:0016311"}],"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 dephosphorylation","termid":"GO:0035303"}


id: PR:Q9USW4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An acetyl-coenzyme A transporter 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02941","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C21B10.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21B10.09","secondary_identifiers":["UniProtKB:Q9USW4"],"synonyms":[{"name":"Spom972h-SLC33A1","type":"exact"}],"termid":"PR:Q9USW4"}


id: MONDO:0001116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the mesenteric lymph nodes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphadenitis","termid":"MONDO:0002052"}],"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":"mesenteric lymphadenitis","secondary_identifiers":["ICD10CM:I88.0","MESH:D008640","DOID:10782","UMLS:C0025469","SCTID:44897000","MEDGEN:6318","ICD9:289.2","NCIT:C26830"],"synonyms":[{"name":"lymphadenitis (disease) of mesentery","type":"exact"},{"name":"mesenteric adenitis","type":"exact"},{"name":"mesenteric lymphadenitis","type":"exact"},{"name":"mesentery lymphadenitis (disease)","type":"exact"}],"termid":"MONDO:0001116","xrefs":{"Monarch":{"xref_id":"0001116"}}}


id: PBO:0002486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-acyldihydroxyacetone phosphate reductase (predicted)","termid":"PBO:0002486"}


id: PBO:0084864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the small subunit; contains twin cysteine-x9-cysteine motifs; oxidized by Mia40p during import into mitochondria","termid":"PBO:0084864"}


id: FYPO:0004827
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell dies as it goes through mitosis, usually as a result of abnormal chromosome and spindle dynamics.","definition_xrefs":["PMID:16824200","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"}],"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:0000004"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"inviable vegetative cell with cell death during mitosis","synonyms":[{"name":"inviable cell with cell death during mitosis during vegetative growth","type":"exact"},{"name":"inviable vegetative cell with cell death during mitosis during mitotic cell cycle","type":"related"},{"name":"lethal; vegetative cell with cell death during mitosis","type":"exact"}],"termid":"FYPO:0004827"}


id: PBO:0064456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein O-glucosyltransferase 2","termid":"PBO:0064456"}


id: PR:O14110
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An aminomethyltransferase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01259","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":"aminomethyltransferase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC31G5.14","secondary_identifiers":["UniProtKB:O14110"],"synonyms":[{"name":"GCVT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-AMT","type":"exact"},{"name":"glycine cleavage system T protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14110"}


id: GO:0097135
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of cyclin E2 and cyclin-dependent kinase 2 (CDK2). Cyclins are characterized by periodicity in protein abundance throughout the cell cycle. Cyclin-dependent kinases represent a family of serine/threonine protein kinases that become active upon binding to a cyclin regulatory partner.","definition_xrefs":["GOC:so","PMID:15935619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent protein kinase holoenzyme complex","termid":"GO:0000307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cyclin E2-CDK2 complex","termid":"GO:0097135"}


id: PBO:0000061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudogene","termid":"PBO:0000061"}


id: MONDO:0030028
data:
  {"annotated_genes":["SJAG_00763"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87130],"is_not":false,"summary":null,"term":"MONDO:0030028"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00763":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618868","UMLS:C5394335","MEDGEN:1715031"],"synonyms":[{"name":"CONATOC","type":"exact"},{"name":"neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline","type":"exact"}],"termid":"MONDO:0030028","terms_by_termid":{"MONDO:0030028":null},"xrefs":{"Monarch":{"xref_id":"0030028"}}}


id: PBO:0000460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S24 (predicted)","termid":"PBO:0000460"}


id: MONDO:0007528
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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, autosomal dominant, type unspecified","secondary_identifiers":["MESH:C562424","UMLS:C0220679","MEDGEN:65083","OMIM:130090"],"synonyms":[{"name":"EDS, unspecified type","type":"related"},{"name":"Ehlers-Danlos syndrome, Friedman-Harrod type","type":"related"},{"name":"Ehlers-Danlos syndrome, autosomal dominant, type unspecified","type":"exact"}],"termid":"MONDO:0007528","xrefs":{"Monarch":{"xref_id":"0007528"}}}


id: PBO:0086093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein phosphotyrosine phosphatase of unknown cellular role; activated by adenine","termid":"PBO:0086093"}


id: MONDO:0013974
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pure hair and nail ectodermal dysplasia","termid":"MONDO:0019071"}],"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":"ectodermal dysplasia 6, hair/nail type","secondary_identifiers":["GARD:18064","UMLS:C3554111","MEDGEN:767025","DOID:0111659","OMIM:614928"],"synonyms":[{"name":"ECTD6","type":"exact"},{"name":"ectodermal dysplasia 6, hair/nail type","type":"exact"}],"termid":"MONDO:0013974","xrefs":{"Monarch":{"xref_id":"0013974"}}}


id: PBO:0080392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS26 retromer complex component A","termid":"PBO:0080392"}


id: PBO:0005191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanine deaminase (predicted)","termid":"PBO:0005191"}


id: PBO:0027346
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_menadione","termid":"PBO:0027346"}


id: GO:0060743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process, independent of morphogenetic (shape) change, that is required for an epithelial cell of the prostate gland to attain its fully functional state. An epithelial cell is a cell usually found in a two-dimensional sheet with a free surface.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell maturation","termid":"GO:0002070"},{"relation_name":"part_of","term_name":"epithelial cell differentiation involved in prostate gland development","termid":"GO:0060742"}],"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":"epithelial cell maturation involved in prostate gland development","synonyms":[{"name":"prostate gland epithelial cell development","type":"exact"}],"termid":"GO:0060743"}


id: MONDO:1010835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Wilson disease that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Wilson disease, non-human animal","termid":"MONDO:1010164"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wilson disease, cattle","secondary_identifiers":["OMIA:001071-9913"],"termid":"MONDO:1010835","xrefs":{"Monarch":{"xref_id":"1010835"}}}


id: PBO:0066952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 254","termid":"PBO:0066952"}


id: PBO:0052153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNJ2 antisense RNA 1","termid":"PBO:0052153"}


id: MONDO:0010072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive form of spondyloepiphyseal dysplasia tarda.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloepiphyseal dysplasia with congenital joint dislocations","termid":"MONDO:0007738"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia tarda","termid":"MONDO:0019667"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005497"],"is_obsolete":false,"name":"spondyloepiphyseal dysplasia tarda, autosomal recessive","secondary_identifiers":["OMIM:271600","UMLS:C1849054","MESH:C564797","MEDGEN:338604","DOID:0112293","GARD:15237"],"synonyms":[{"name":"autosomal recessive spondyloepiphyseal dysplasia tarda","type":"exact"},{"name":"spondyloepiphyseal dysplasia tarda, autosomal recessive","type":"exact"}],"termid":"MONDO:0010072","xrefs":{"Monarch":{"xref_id":"0010072"}}}


id: GO:0015613
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 galactose/glucose (methylgalactoside) porter activity (obsolete GO:0015613)","synonyms":[{"name":"galactose/glucose (methylgalactoside) porter activity","type":"exact"}],"termid":"GO:0015613"}


id: RO:0002452
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relation that holds between a disease or an organism and a phenotype","direct_ancestors":[{"relation_name":"is_a","term_name":"has_phenotype","termid":"RO:0002200"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_symptom","termid":"RO:0002452"}


id: PBO:0001631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"threonine aspartase (predicted)","termid":"PBO:0001631"}


id: MONDO:0010142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypothyroidism due to thyroid-stimulating hormone (TSH) receptor mutations is a type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth due to thyroid resistance to TSH.","definition_xrefs":["Orphanet:90673"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypothyroidism, congenital, nongoitrous","termid":"MONDO:0000045"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypothyroidism due to TSH receptor mutations","secondary_identifiers":["DOID:0070126","GARD:16793","UMLS:C3493776","MEDGEN:487729","OMIM:275200"],"synonyms":[{"name":"CHNG1","type":"exact"},{"name":"TSH resistance","type":"exact"},{"name":"congenital nongoitrous hypothyroidism 1","type":"related"},{"name":"hypothyroidism due to unresponsiveness to thyrotropin","type":"related"},{"name":"hypothyroidism, Nonautoimmune","type":"related"},{"name":"hypothyroidism, congenital, due to TSH resistance","type":"related"},{"name":"hypothyroidism, congenital, nongoitrous, 1","type":"related"},{"name":"hypothyroidism, congenital, nongoitrous, type 1","type":"exact"},{"name":"thyroid-stimulating hormone, resistance to","type":"related"},{"name":"thyrotropin resistance","type":"related"}],"termid":"MONDO:0010142","xrefs":{"Monarch":{"xref_id":"0010142"}}}


id: PBO:0087227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Secreted alpha-galactosidase; required for catabolic conversion of melibiose to glucose and galactose","termid":"PBO:0087227"}


id: PBO:0079656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2V1 pseudogene 4","termid":"PBO:0079656"}


id: GO:0034907
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: acetanilide + O2 + 2 H+ + NADH = catechol + NAD+ + acetamide.","definition_xrefs":["UM-BBD_reactionID:r0723"],"gene_count":0,"genotype_count":0,"name":"obsolete acetanilide 1,2-dioxygenase activity (obsolete GO:0034907)","termid":"GO:0034907"}


id: MONDO:0010474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the COX7B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"linear skin defects with multiple congenital anomalies","termid":"MONDO:0010672"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005093"],"is_obsolete":false,"name":"linear skin defects with multiple congenital anomalies 2","secondary_identifiers":["MEDGEN:763835","DOID:0111877","OMIM:300887","GARD:15272","UMLS:C3550921"],"synonyms":[{"name":"COX7B microphthalmia with linear skin defects syndrome","type":"exact"},{"name":"LSDMCA2","type":"related"},{"name":"aplasia cutis congenita, Reticulolinear, with microcephaly, Facial Dysmorphism, and Other congenital anomalies","type":"related"},{"name":"linear skin defects with multiple congenital anomalies 2","type":"exact"},{"name":"linear skin defects with multiple congenital anomalies 2, X-linked dominant","type":"exact"},{"name":"linear skin defects with multiple congenital anomalies type 2","type":"exact"},{"name":"microphthalmia with linear skin defects syndrome caused by mutation in COX7B","type":"exact"}],"termid":"MONDO:0010474","xrefs":{"Monarch":{"xref_id":"0010474"}}}


id: MONDO:0014636
data:
  {"annotated_genes":["SJAG_16456"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86973],"is_not":false,"summary":null,"term":"MONDO:0014636"}]},"cv_name":"mondo","definition":"Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the MARS2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 25","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:616430","DOID:0111468","UMLS:C5567742","GARD:17775","MEDGEN:1799165","Orphanet:447954"],"synonyms":[{"name":"COXPD25","type":"exact"},{"name":"MARS2 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 25","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in MARS2","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 25","type":"exact"}],"termid":"MONDO:0014636","terms_by_termid":{"MONDO:0014636":null},"xrefs":{"Monarch":{"xref_id":"0014636"}}}


id: MONDO:0012149
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"attention deficit-hyperactivity disorder","termid":"MONDO:0007743"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"attention deficit-hyperactivity disorder, susceptibility to, 1","secondary_identifiers":["OMIM:608903","UMLS:C1837153","MEDGEN:323087"],"synonyms":[{"name":"ADHD1","type":"exact"},{"name":"attention deficit-hyperactivity disorder, susceptibility to, 1","type":"exact"},{"name":"attention deficit-hyperactivity disorder, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0012149","xrefs":{"Monarch":{"xref_id":"0012149"}}}


id: PBO:0089451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gfo/Idh/MocA-like oxidoreductase, N-terminal","termid":"PBO:0089451"}


id: SO:0000110
data:
  {"annotated_genes":["SJAG_02093","SJAG_04924","SJAG_04571","SJAG_04922","SJAG_03749","SJAG_04046","SJAG_00771","SJAG_04723","SJAG_00239","SJAG_01858","SJAG_03727","SJAG_00096","SJAG_01985","SJAG_04785","SJAG_04905","SJAG_00530","SJAG_01705","SJAG_02949","SJAG_02877","SJAG_01755","SJAG_03650","SJAG_02217","SJAG_02827","SJAG_01846","SJAG_01959","SJAG_04090","SJAG_03820","SJAG_00357","SJAG_04598","SJAG_02131","SJAG_01388","SJAG_03138","SJAG_04247","SJAG_03178","SJAG_03057","SJAG_02435","SJAG_00310","SJAG_02582","SJAG_02301","SJAG_02173","SJAG_00981","SJAG_04419","SJAG_00876","SJAG_00415","SJAG_04821","SJAG_02875","SJAG_04363","SJAG_00708","SJAG_02260","SJAG_01445","SJAG_04808","SJAG_02432","SJAG_04906","SJAG_03148","SJAG_00403","SJAG_04796","SJAG_02495","SJAG_00751","SJAG_02959","SJAG_00109","SJAG_04927","SJAG_04067","SJAG_01965","SJAG_04851","SJAG_05271","SJAG_00570","SJAG_03930","SJAG_01363","SJAG_03640","SJAG_05291","SJAG_04193","SJAG_04789","SJAG_03414","SJAG_03204","SJAG_01416","SJAG_01675","SJAG_05001","SJAG_00161","SJAG_04799","SJAG_04209","SJAG_00906","SJAG_02389","SJAG_01970","SJAG_02102","SJAG_04096","SJAG_00131","SJAG_02580","SJAG_04677","SJAG_04435","SJAG_01948","SJAG_01223","SJAG_04904","SJAG_00340","SJAG_02694","SJAG_02193","SJAG_01189","SJAG_04073","SJAG_01595","SJAG_05353","SJAG_00593","SJAG_03202","SJAG_01458","SJAG_00554","SJAG_04864","SJAG_00659","SJAG_03030","SJAG_01835","SJAG_00975","SJAG_01968","SJAG_03444","SJAG_05189","SJAG_03521","SJAG_00667","SJAG_05008","SJAG_04797","SJAG_05261","SJAG_01290","SJAG_00517","SJAG_00254","SJAG_04301","SJAG_02145","SJAG_00810","SJAG_00288","SJAG_02944","SJAG_03483","SJAG_03800","SJAG_01069","SJAG_02489","SJAG_03280","SJAG_03824","SJAG_00784","SJAG_03282","SJAG_01407","SJAG_03816","SJAG_03295","SJAG_01038","SJAG_03201","SJAG_00490","SJAG_02958","SJAG_01321","SJAG_04875","SJAG_00481","SJAG_01086","SJAG_01171","SJAG_00620","SJAG_04345","SJAG_00680","SJAG_01861","SJAG_04770","SJAG_02676","SJAG_03203","SJAG_04106","SJAG_00218","SJAG_04685","SJAG_04807","SJAG_00222","SJAG_00852","SJAG_01991","SJAG_03672","SJAG_02823","SJAG_04833","SJAG_02987","SJAG_00781","SJAG_04525","SJAG_00484","SJAG_04238","SJAG_00057","SJAG_03814","SJAG_04398","SJAG_00860","SJAG_02134","SJAG_04786","SJAG_01709","SJAG_02091","SJAG_04184","SJAG_02537","SJAG_03606","SJAG_02353","SJAG_02076","SJAG_01421","SJAG_16452","SJAG_00286","SJAG_01028","SJAG_01006","SJAG_02049","SJAG_01128","SJAG_00025","SJAG_02437","SJAG_03239","SJAG_00709","SJAG_01689","SJAG_00732","SJAG_04835","SJAG_04483","SJAG_01029","SJAG_02190","SJAG_00110","SJAG_04850","SJAG_06600","SJAG_03535","SJAG_04720","SJAG_04196","SJAG_05272","SJAG_02478","SJAG_00790","SJAG_00437","SJAG_00367","SJAG_05279","SJAG_02191","SJAG_01136","SJAG_05327","SJAG_04975","SJAG_00780","SJAG_01488","SJAG_04819","SJAG_05013","SJAG_01626","SJAG_01868","SJAG_06425","SJAG_02839","SJAG_03270","SJAG_00846","SJAG_01999","SJAG_04236","SJAG_02568","SJAG_02192","SJAG_02258","SJAG_02413","SJAG_03333","SJAG_00695","SJAG_01427"],"annotation_feature_type":"gene","cv_annotations":{"sequence":[{"annotations":[82331,82386,82296,82355,82283],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"SO:0001808"},{"annotations":[82183,82244,82218,82173,82202,82382,82426,82477,82201,82450,82263,82231,82254,82216,82417,82170,82176,82257,82270,82288,82306,82438,82401,82387,82346,82179,82210,82330,82388,82439,82221,82196,82332,82180,82354,82449,82398,82422,82161,82384,82177,82338,82316,82447,82347,82290,82325,82446,82466,82396,82279,82255,82158,82425,82322,82259,82165,82475,82373,82175,82198,82395,82308,82416,82367,82213,82368,82164,82284,82459,82295,82318,82278,82349,82454,82440,82397,82260,82315,82264,82282,82235,82374,82311,82162,82436,82376,82171,82182,82280,82437,82442,82321,82160,82471,82480,82375,82411,82378,82328,82267,82245,82391,82219,82363,82385,82163,82215,82305,82239,82479,82369,82159,82377,82172,82272,82465,82291,82379,82472,82197,82345,82262,82234,82360,82256,82483,82428,82370,82275,82341,82265,82312,82462,82214,82233,82350,82434,82348,82240,82310,82294,82184,82207,82251,82241,82451,82246,82467,82269,82242,82248,82430,82309,82441,82399,82227,82482,82268,82415,82250,82478,82274,82307,82185,82418,82252,82410,82342,82400,82406,82199,82261,82381,82281,82167,82431,82461,82365,82408,82178,82448,82463,82304,82457,82247,82409,82435,82352,82458,82481,82314,82174,82258,82220,82429,82253,82206,82327,82351,82333,82326,82293,82273,82452,82353,82403,82362,82419,82445,82474,82249,82444,82412,82200,82334,82243,82211,82320,82456,82228,82313,82319,82339,82169,82371],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"SO:0000418"}]},"cv_name":"sequence","definition":"Any extent of continuous biological sequence.","definition_xrefs":["SO:ke","LAMHDI:mb"],"gene_count":231,"genes_by_uniquename":{"SJAG_00025":null,"SJAG_00057":null,"SJAG_00096":null,"SJAG_00109":null,"SJAG_00110":null,"SJAG_00131":null,"SJAG_00161":null,"SJAG_00218":null,"SJAG_00222":null,"SJAG_00239":null,"SJAG_00254":null,"SJAG_00286":null,"SJAG_00288":null,"SJAG_00310":null,"SJAG_00340":null,"SJAG_00357":null,"SJAG_00367":null,"SJAG_00403":null,"SJAG_00415":null,"SJAG_00437":null,"SJAG_00481":null,"SJAG_00484":null,"SJAG_00490":null,"SJAG_00517":null,"SJAG_00530":null,"SJAG_00554":null,"SJAG_00570":null,"SJAG_00593":null,"SJAG_00620":null,"SJAG_00659":null,"SJAG_00667":null,"SJAG_00680":null,"SJAG_00695":null,"SJAG_00708":null,"SJAG_00709":null,"SJAG_00732":null,"SJAG_00751":null,"SJAG_00771":null,"SJAG_00780":null,"SJAG_00781":null,"SJAG_00784":null,"SJAG_00790":null,"SJAG_00810":null,"SJAG_00846":null,"SJAG_00852":null,"SJAG_00860":null,"SJAG_00876":null,"SJAG_00906":null,"SJAG_00975":null,"SJAG_00981":null,"SJAG_01006":null,"SJAG_01028":null,"SJAG_01029":null,"SJAG_01038":null,"SJAG_01069":null,"SJAG_01086":null,"SJAG_01128":null,"SJAG_01136":null,"SJAG_01171":null,"SJAG_01189":null,"SJAG_01223":null,"SJAG_01290":null,"SJAG_01321":null,"SJAG_01363":null,"SJAG_01388":null,"SJAG_01407":null,"SJAG_01416":null,"SJAG_01421":null,"SJAG_01427":null,"SJAG_01445":null,"SJAG_01458":null,"SJAG_01488":null,"SJAG_01595":null,"SJAG_01626":null,"SJAG_01675":null,"SJAG_01689":null,"SJAG_01705":null,"SJAG_01709":null,"SJAG_01755":null,"SJAG_01835":null,"SJAG_01846":null,"SJAG_01858":null,"SJAG_01861":null,"SJAG_01868":null,"SJAG_01948":null,"SJAG_01959":null,"SJAG_01965":null,"SJAG_01968":null,"SJAG_01970":null,"SJAG_01985":null,"SJAG_01991":null,"SJAG_01999":null,"SJAG_02049":null,"SJAG_02076":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02102":null,"SJAG_02131":null,"SJAG_02134":null,"SJAG_02145":null,"SJAG_02173":null,"SJAG_02190":null,"SJAG_02191":null,"SJAG_02192":null,"SJAG_02193":null,"SJAG_02217":null,"SJAG_02258":null,"SJAG_02260":null,"SJAG_02301":null,"SJAG_02353":null,"SJAG_02389":null,"SJAG_02413":null,"SJAG_02432":null,"SJAG_02435":null,"SJAG_02437":null,"SJAG_02478":null,"SJAG_02489":null,"SJAG_02495":null,"SJAG_02537":null,"SJAG_02568":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02676":null,"SJAG_02694":null,"SJAG_02823":null,"SJAG_02827":null,"SJAG_02839":null,"SJAG_02875":null,"SJAG_02877":null,"SJAG_02944":null,"SJAG_02949":null,"SJAG_02958":null,"SJAG_02959":null,"SJAG_02987":null,"SJAG_03030":null,"SJAG_03057":null,"SJAG_03138":null,"SJAG_03148":null,"SJAG_03178":null,"SJAG_03201":null,"SJAG_03202":null,"SJAG_03203":null,"SJAG_03204":null,"SJAG_03239":null,"SJAG_03270":null,"SJAG_03280":null,"SJAG_03282":null,"SJAG_03295":null,"SJAG_03333":null,"SJAG_03414":null,"SJAG_03444":null,"SJAG_03483":null,"SJAG_03521":null,"SJAG_03535":null,"SJAG_03606":null,"SJAG_03640":null,"SJAG_03650":null,"SJAG_03672":null,"SJAG_03727":null,"SJAG_03749":null,"SJAG_03800":null,"SJAG_03814":null,"SJAG_03816":null,"SJAG_03820":null,"SJAG_03824":null,"SJAG_03930":null,"SJAG_04046":null,"SJAG_04067":null,"SJAG_04073":null,"SJAG_04090":null,"SJAG_04096":null,"SJAG_04106":null,"SJAG_04184":null,"SJAG_04193":null,"SJAG_04196":null,"SJAG_04209":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04247":null,"SJAG_04301":null,"SJAG_04345":null,"SJAG_04363":null,"SJAG_04398":null,"SJAG_04419":null,"SJAG_04435":null,"SJAG_04483":null,"SJAG_04525":null,"SJAG_04571":null,"SJAG_04598":null,"SJAG_04677":null,"SJAG_04685":null,"SJAG_04720":null,"SJAG_04723":null,"SJAG_04770":null,"SJAG_04785":null,"SJAG_04786":null,"SJAG_04789":null,"SJAG_04796":null,"SJAG_04797":null,"SJAG_04799":null,"SJAG_04807":null,"SJAG_04808":null,"SJAG_04819":null,"SJAG_04821":null,"SJAG_04833":null,"SJAG_04835":null,"SJAG_04850":null,"SJAG_04851":null,"SJAG_04864":null,"SJAG_04875":null,"SJAG_04904":null,"SJAG_04905":null,"SJAG_04906":null,"SJAG_04922":null,"SJAG_04924":null,"SJAG_04927":null,"SJAG_04975":null,"SJAG_05001":null,"SJAG_05008":null,"SJAG_05013":null,"SJAG_05189":null,"SJAG_05261":null,"SJAG_05271":null,"SJAG_05272":null,"SJAG_05279":null,"SJAG_05291":null,"SJAG_05327":null,"SJAG_05353":null,"SJAG_06425":null,"SJAG_06600":null,"SJAG_16452":null},"genotype_count":0,"is_obsolete":false,"name":"sequence_feature","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"INSDC_feature:misc_feature","type":"exact"},{"name":"INSDC_note:other","type":"exact"},{"name":"INSDC_note:sequence_feature","type":"exact"},{"name":"located sequence feature","type":"related"},{"name":"located_sequence_feature","type":"exact"},{"name":"sequence feature","type":"exact"}],"termid":"SO:0000110","terms_by_termid":{"SO:0000418":null,"SO:0001808":null}}


id: PBO:0080289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 53 pseudogene","termid":"PBO:0080289"}


id: GO:0032668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-24 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-24 production","termid":"GO:0032628"}],"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:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-24 production","secondary_identifiers":["GO:0045528"],"synonyms":[{"name":"regulation of IL-24 production","type":"exact"},{"name":"regulation of interleukin-24 biosynthetic process","type":"narrow"}],"termid":"GO:0032668"}


id: MONDO:0017585
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"benign peripheral nerve sheath tumor","termid":"MONDO:0016752"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"painful orbital and systemic neurofibromas-marfanoid habitus syndrome","secondary_identifiers":["MEDGEN:1650687","UMLS:C4751109","Orphanet:300501","GARD:11006"],"synonyms":[{"name":"multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus","type":"related"}],"termid":"MONDO:0017585","xrefs":{"Monarch":{"xref_id":"0017585"}}}


id: MONDO:1010688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AA amyloidosis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AA amyloidosis, non-human animal","termid":"MONDO:1010092"},{"relation_name":"is_a","term_name":"cardiomyopathy, domestic cat","termid":"MONDO:1010442"},{"relation_name":"is_a","term_name":"amyloidosis, domestic cat","termid":"MONDO:1011468"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AA amyloidosis, domestic cat","secondary_identifiers":["OMIA:000038-9685"],"termid":"MONDO:1010688","xrefs":{"Monarch":{"xref_id":"1010688"}}}


id: MONDO:0007207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Book syndrome is a rare autosomal dominant ectodermal dysplasia syndrome reported in a Swedish family (25 cases from 4 generations), and one isolated case, and is characterized by premolar aplasia, hyperhidrosis, and premature graying of the hair. Additional features reported in the isolated case include a narrow palate, hypoplastic nails, eyebrow anomalies, a unilateral simian crease, and poorly formed dermatoglyphics.","definition_xrefs":["Orphanet:1262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"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":"Böök syndrome","secondary_identifiers":["MESH:C562993","OMIM:112300","SCTID:722296002","UMLS:C0457014","MEDGEN:99140","GARD:932"],"synonyms":[{"name":"Böök syndrome","type":"exact"},{"name":"PHC syndrome","type":"related"},{"name":"book syndrome","type":"exact"},{"name":"premolar aplasia, hyperhidrosis, and canities prematura","type":"related"}],"termid":"MONDO:0007207","xrefs":{"Monarch":{"xref_id":"0007207"}}}


id: PBO:0049816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone deacetylase 8","termid":"PBO:0049816"}


id: GO:0061549
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a sympathetic ganglion over time, from its formation to the mature structure.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ganglion development","termid":"GO:0061548"},{"relation_name":"part_of","term_name":"sympathetic nervous system development","termid":"GO:0048485"}],"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":"sympathetic ganglion development","synonyms":[{"name":"sympathetic ganglia development","type":"related"}],"termid":"GO:0061549"}


id: PBO:0086501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative poly(U)-specific 3'-to-5' RNA exonuclease; involved in 3'-end processing of U6 snRNA removing uridines and generating a terminal 2&#8242;,3&#8242; cyclic phosphate; essential protein that localizes to the nucleus and mitochondria; overexpression suppresses the respiratory defects of oxa1 and mtf2 mutants; homolog of S.pombe gene, mpn1 and human gene, hUSB1; mutations in hUSB1 are associated with a rare genodermatosis, poikiloderma with neutropenia (OMIM 604173)","termid":"PBO:0086501"}


id: PBO:0086498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative plasma membrane permease; proposed to be involved in carboxylic acid uptake and repressed by thiamine; substrate of Dbf2p/Mob1p kinase; transcription is altered if mitochondrial dysfunction occurs","termid":"PBO:0086498"}


id: PR:000085738
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerase II subunit rpb1 CTD-phosphorylated form (Schizosaccharomyces pombe) that has been post-translationally modified to include phosphoserine at the second and fifth positions of one or more of the C-terminal heptad repeats (YSPTSPS).","definition_xrefs":["PRO:DAN","PomBase:VW","PMID:11387325"],"direct_ancestors":[{"relation_name":"has_part","term_name":"O-phospho-L-serine","termid":"MOD:00046"},{"relation_name":"is_a","term_name":"rpb1/Phos(CTD-S2,S5,S7)","termid":"PR:000050494"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rpb1/Phos(CTD-S2,S5)","pombase_gene_id":"SPBC28F2.12","synonyms":[{"name":"PomBase_original_PRO_term_name: DNA-directed RNA polymerase II subunit rpb1 phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-rpb1/Phos:1","type":"exact"},{"name":"rpb1/Phos(CTD-S2,S5)","type":"exact"}],"termid":"PR:000085738"}


id: GO:0007612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in an organism in which a relatively long-lasting adaptive behavioral change occurs as the result of experience.","definition_xrefs":["ISBN:0582227089","ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"learning or memory","termid":"GO:0007611"}],"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":"learning","secondary_identifiers":["Wikipedia:Learning"],"termid":"GO:0007612"}


id: GO:0042764
data:
  {"annotated_genes":["SJAG_01825","SJAG_02368","SJAG_02076","SJAG_04275","SJAG_03145","SJAG_04948","SJAG_03688","SJAG_01867","SJAG_04001","SJAG_03250","SJAG_00821","SJAG_01697","SJAG_04470","SJAG_04781","SJAG_04483","SJAG_03721","SJAG_03483","SJAG_03587","SJAG_00971","SJAG_03013","SJAG_03638","SJAG_04184","SJAG_02169","SJAG_03746","SJAG_04922","SJAG_02736","SJAG_00826","SJAG_00405","SJAG_00974","SJAG_01084","SJAG_01855","SJAG_03536","SJAG_03915","SJAG_03079","SJAG_01469","SJAG_01769","SJAG_00663","SJAG_00430","SJAG_04080"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[93542,116302,117174],"is_not":false,"summary":null,"term":"GO:0042764"},{"annotations":[93633,114867],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905754"},{"annotations":[103279,105965,119354,103502,92490,89977,93060,106781,102637,110881,118771,95637,109197,98407,105100,95333,115919,97151,93272,111121,99334,120882,94659,105052,118081,96239],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005628"},{"annotations":[104715,100611,120397],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070056"},{"annotations":[107091,120398,104716],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070057"},{"annotations":[96279,101906,107819,117809],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032169"}]},"cv_name":"cellular_component","definition":"An immature spore undergoing development. The spore usually consists of nucleic acid, prospore membrane(s) that encase the nucleic acid, and ultimately a cell wall that covers the membrane(s). This type of spore is observed in ascospore-forming fungi.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular immature spore","termid":"GO:0042763"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00405":null,"SJAG_00430":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00971":null,"SJAG_00974":null,"SJAG_01084":null,"SJAG_01469":null,"SJAG_01697":null,"SJAG_01769":null,"SJAG_01825":null,"SJAG_01855":null,"SJAG_01867":null,"SJAG_02076":null,"SJAG_02169":null,"SJAG_02368":null,"SJAG_02736":null,"SJAG_03013":null,"SJAG_03079":null,"SJAG_03145":null,"SJAG_03250":null,"SJAG_03483":null,"SJAG_03536":null,"SJAG_03587":null,"SJAG_03638":null,"SJAG_03688":null,"SJAG_03721":null,"SJAG_03746":null,"SJAG_03915":null,"SJAG_04001":null,"SJAG_04080":null,"SJAG_04184":null,"SJAG_04275":null,"SJAG_04470":null,"SJAG_04483":null,"SJAG_04781":null,"SJAG_04922":null,"SJAG_04948":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"ascospore-type prospore","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0042764","terms_by_termid":{"GO:0005628":null,"GO:0032169":null,"GO:0042764":null,"GO:0070056":null,"GO:0070057":null,"GO:1905754":null}}


id: PBO:0046326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enolase 4","termid":"PBO:0046326"}


id: GO:1902983
data:
  {"annotated_genes":["SJAG_02182","SJAG_00814","SJAG_03780","SJAG_03495","SJAG_05197","SJAG_04879","SJAG_02818","SJAG_01010","SJAG_00874","SJAG_01823","SJAG_00729","SJAG_04190","SJAG_02908","SJAG_02667","SJAG_00272","SJAG_00863","SJAG_02199","SJAG_04877"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66863,68951,72040,111767,114352,115406,117246],"is_not":false,"summary":null,"term":"GO:1902983"},{"annotations":[106023,120042,104626,110928,106741,97020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903459"},{"annotations":[106024,109164,95739,97053,108795,97021,91349,106742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903460"}]},"cv_name":"biological_process","definition":"Any DNA strand elongation involved in mitotic cell cycle DNA replication.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA strand elongation involved in nuclear cell cycle DNA replication","termid":"GO:1902319"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic DNA replication","termid":"GO:1902969"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_00874":null,"SJAG_01010":null,"SJAG_01823":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02667":null,"SJAG_02818":null,"SJAG_02908":null,"SJAG_03495":null,"SJAG_03780":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_05197":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0007049","GO:0006260"],"is_obsolete":false,"name":"DNA strand elongation involved in mitotic DNA replication","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"DNA strand elongation involved in mitotic cell cycle DNA replication","type":"exact"}],"termid":"GO:1902983","terms_by_termid":{"GO:1902983":null,"GO:1903459":null,"GO:1903460":null}}


id: MONDO:0000307
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Ichthyosporea.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic infectious disease","termid":"MONDO:0005135"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parasitic Ichthyosporea infectious disease","secondary_identifiers":["DOID:0050291"],"synonyms":[{"name":"Ichthyosporea caused disease or disorder","type":"exact"},{"name":"Ichthyosporea disease or disorder","type":"exact"},{"name":"Ichthyosporea infectious disease","type":"exact"}],"termid":"MONDO:0000307","xrefs":{"Monarch":{"xref_id":"0000307"}}}


id: MONDO:0011344
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":"parotitis, juvenile recurrent","secondary_identifiers":["MESH:C566359","OMIM:603588","MEDGEN:350954","UMLS:C1863691"],"synonyms":[{"name":"parotitis, juvenile recurrent","type":"exact"}],"termid":"MONDO:0011344","xrefs":{"Monarch":{"xref_id":"0011344"}}}


id: GO:0043912
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: D-lysine + H2O + O2 = 6-amino-2-oxohexanoate + H2O2 + NH4+.","definition_xrefs":["PMID:17259313"],"gene_count":0,"genotype_count":0,"name":"obsolete D-lysine oxidase activity (obsolete GO:0043912)","termid":"GO:0043912"}


id: MONDO:0016944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 7p duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the short arm (p) of chromosome 7. The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. Features that often occur in people with chromosome 7p duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Most cases are not inherited, but people can pass the duplication on to their children. Treatment is based on the signs and symptoms present in each person.","definition_xrefs":["GARD:0005355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of chromosome 7","termid":"MONDO:0016928"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial duplication of the short arm of chromosome 7","secondary_identifiers":["icd11.foundation:79901143","MESH:C537819","Orphanet:262749","GARD:5355","UMLS:C0795820","MEDGEN:162875"],"synonyms":[{"name":"7p duplication","type":"related"},{"name":"7p trisomy","type":"related"},{"name":"Duplication 7p","type":"related"},{"name":"chromosome 7p duplication","type":"related"},{"name":"partial duplication of chromosome 7p","type":"exact"},{"name":"partial duplication of the short arm of chromosome type 7","type":"exact"},{"name":"partial trisomy 7p","type":"related"},{"name":"partial trisomy of chromosome 7p","type":"exact"},{"name":"partial trisomy of the short arm of chromosome 7","type":"exact"},{"name":"trisomy 7p","type":"related"}],"termid":"MONDO:0016944","xrefs":{"Monarch":{"xref_id":"0016944"}}}


id: GO:0004818
data:
  {"annotated_genes":["SJAG_03277","SJAG_03071"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71966,74549],"is_not":false,"summary":null,"term":"GO:0004818"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + L-glutamate + tRNA(Glu) = AMP + diphosphate + L-glutamyl-tRNA(Glu).","definition_xrefs":["EC:6.1.1.17"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyl-tRNA ligase activity","termid":"GO:0004812"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03071":null,"SJAG_03277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140101","GO:0003824","GO:0016874","GO:0140098","GO:0003674"],"is_obsolete":false,"name":"glutamate-tRNA ligase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-379861","RHEA:23540","MetaCyc:GLURS-RXN","Reactome:R-HSA-380216"],"synonyms":[{"name":"L-glutamate:tRNAGlu ligase (AMP-forming) activity","type":"related"},{"name":"glutamate-tRNA synthetase activity","type":"related"},{"name":"glutamic acid translase activity","type":"related"},{"name":"glutamyl-tRNA synthetase activity","type":"exact"},{"name":"glutamyl-transfer RNA synthetase activity","type":"related"},{"name":"glutamyl-transfer ribonucleate synthetase activity","type":"related"},{"name":"glutamyl-transfer ribonucleic acid synthetase activity","type":"related"}],"termid":"GO:0004818","terms_by_termid":{"GO:0004818":null}}


id: MONDO:0011729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stroke, susceptibility to, 1","secondary_identifiers":["MEDGEN:335696","OMIM:606799","UMLS:C1847482"],"synonyms":[{"name":"Strk1","type":"related"},{"name":"stroke, susceptibility to, 1","type":"exact"},{"name":"stroke, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0011729","xrefs":{"Monarch":{"xref_id":"0011729"}}}


id: PBO:0090372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane P-type ATPase, calcium transporting Pmr1","termid":"PBO:0090372"}


id: MOD:00971
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:38"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oxohistidine (from histidine)","termid":"MOD:00971"}


id: GO:0098643
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A supramolecular assembly of fibrillar collagen complexes in the form of a long fiber (fibril) with transverse striations (bands).","definition_xrefs":["PMID:21421911","PMID:29853175","GOC:dos","PMID:20386646"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex of collagen trimers","termid":"GO:0098644"}],"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":"fibrillar collagen","synonyms":[{"name":"banded collagen fibril","type":"exact"}],"termid":"GO:0098643"}


id: RO:0002600
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Holds between a material entity c and a pathological process p if and only if c is capable of some activity a, where a negatively regulates p.","direct_ancestors":[{"relation_name":"is_a","term_name":"capable_of_positively_regulating","termid":"RO:0002598"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capable_of_upregulating_or_causing_pathological_process","termid":"RO:0002600"}


id: FYPO:0001845
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 kinetochore organization is normal (i.e. indistinguishable from wild type). Kinetochore organization is the assembly, arrangement of constituent parts, or disassembly of kinetochores and their associated proteins.","definition_xrefs":["GO:0051383","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal kinetochore organization","synonyms":[{"name":"normal kinetochore organisation","type":"exact"},{"name":"normal kinetochore organization during mitotic cell cycle","type":"related"},{"name":"normal kinetochore organization during vegetative growth","type":"exact"}],"termid":"FYPO:0001845"}


id: MONDO:0004499
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lung carcinoma arising from the hilum of the lung.","definition_xrefs":["NCIT:C7454"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung hilum cancer","termid":"MONDO:0004332"},{"relation_name":"is_a","term_name":"lung carcinoma","termid":"MONDO:0005138"}],"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":"lung hilum carcinoma","secondary_identifiers":["MEDGEN:235266","UMLS:C1334445","DOID:8207"],"synonyms":[{"name":"carcinoma of lung hilus","type":"exact"},{"name":"hilar lung carcinoma","type":"exact"},{"name":"lung hilum cancer","type":"broad"},{"name":"lung hilum carcinoma","type":"exact"},{"name":"lung hilus carcinoma","type":"exact"}],"termid":"MONDO:0004499","xrefs":{"Monarch":{"xref_id":"0004499"}}}


id: MOD:00132
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-serine residue and an L-lysine residue to release water and form 2-amino-6-(2-amino-2-carboxyethylamino)hexanoic acid.","definition_xrefs":["DeltaMass:0","PubMed:2544544","RESID:AA0123#KSX"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"L-lysinoalanine","termid":"MOD:01853"},{"relation_name":"is_a","term_name":"crosslinked L-lysine residue","termid":"MOD:02051"},{"relation_name":"is_a","term_name":"crosslinked L-serine residue","termid":"MOD:02055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-lysinoalanine (Lys-Ser)","synonyms":[{"name":"(2R,9S)-lysinoalanine","type":"exact"},{"name":"(2S)-2-amino-6-([(2R)-2-amino-2-carboxyethyl]amino)hexanoic acid","type":"exact"},{"name":"CROSSLNK Lysinoalanine (Ser-Lys)","type":"exact"},{"name":"L-lysinoalanine","type":"exact"},{"name":"LAL","type":"exact"},{"name":"Lysinoalanine (from Cysteine)","type":"exact"},{"name":"N-epsilon-(2-amino-2-carboxyethyl)-L-lysine","type":"exact"},{"name":"N6-(2-amino-2-carboxyethyl)-L-lysine","type":"exact"},{"name":"XLNK-N6Lys-3Dha(Ser)","type":"exact"},{"name":"alaninolysine","type":"exact"}],"termid":"MOD:00132"}


id: PBO:0047667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKTN antisense RNA 1","termid":"PBO:0047667"}


id: PR:Q10138
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- csr102 gene.","definition_xrefs":["UniProtKB:Q10138","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":"CRAL-TRIO domain-containing protein C3H8.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3H8.02","synonyms":[{"name":"Spom972h-csr102","type":"exact"}],"termid":"PR:Q10138"}


id: PBO:0055717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipase maturation factor 2","termid":"PBO:0055717"}


id: PBO:0113751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tudor domain superfamily protein, potential role in central carbon metabolism based on C. neoformans metabolic data, see PF11160","termid":"PBO:0113751"}


id: PBO:0072577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRN3 homolog, RNA polymerase I transcription factor","termid":"PBO:0072577"}


id: PBO:0039723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3D","termid":"PBO:0039723"}


id: PR:Q9USV6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC27B12.14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USV6"],"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":"assembly factor cbp4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC27B12.14","synonyms":[{"name":"Spom972h-SPBC27B12.14","type":"exact"},{"name":"cytochrome b mRNA-processing protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USV6"}


id: RO:0002450
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Holds between molecular entities A and B where A can physically interact with B and in doing so positively regulates a process that B is capable of.  For example, A and B may be gene products and binding of B by A positively regulates the kinase activity of B.","direct_ancestors":[{"relation_name":"is_a","term_name":"activity_directly_regulates_activity_of","termid":"RO:0002448"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activity_directly_positively_regulates_activity_of","synonyms":[{"name":"molecularly increases activity of","type":"exact"}],"termid":"RO:0002450"}


id: GO:0048015
data:
  {"annotated_genes":["SJAG_01519","SJAG_00114","SJAG_00321","SJAG_04537","SJAG_05330"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73245,73458,74429,94998,97712],"is_not":false,"summary":null,"term":"GO:0048015"}]},"cv_name":"biological_process","definition":"The series of molecular signals in which a cell uses a phosphatidylinositol-mediated signaling to convert a signal into a response. Phosphatidylinositols include phosphatidylinositol (PtdIns) and its phosphorylated derivatives.","definition_xrefs":["GOC:ceb","GOC:bf","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signal transduction","termid":"GO:0035556"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00321":null,"SJAG_01519":null,"SJAG_04537":null,"SJAG_05330":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"phosphatidylinositol-mediated signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"inositol phospholipid-mediated signaling","type":"broad"},{"name":"phosphatidylinositol-mediated signal transduction","type":"exact"},{"name":"phosphatidylinositol-mediated signalling","type":"exact"},{"name":"phosphoinositide-mediated signaling","type":"exact"},{"name":"phosphoinositide-mediated signalling","type":"exact"}],"termid":"GO:0048015","terms_by_termid":{"GO:0048015":null}}


id: PBO:0065377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pregnancy specific beta-1-glycoprotein 5","termid":"PBO:0065377"}


id: PBO:0003595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spindle pole body protein Sfi1","termid":"PBO:0003595"}


id: PBO:0080848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YBX2 pseudogene 1","termid":"PBO:0080848"}


id: MONDO:0008096
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":"nevus flammeus of nape of neck","secondary_identifiers":["UMLS:C2697447","MEDGEN:437278","OMIM:163100","MESH:C567524"],"synonyms":[{"name":"Unna Nevus","type":"related"},{"name":"erythema nuchae","type":"related"},{"name":"nevus flammeus of nape of neck","type":"exact"}],"termid":"MONDO:0008096","xrefs":{"Monarch":{"xref_id":"0008096"}}}


id: MONDO:0007802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypospadias","termid":"MONDO:0005345"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypospadias 3, autosomal","secondary_identifiers":["UMLS:C2675154","MEDGEN:382538","MESH:C567191","GARD:18184","OMIM:146450"],"synonyms":[{"name":"HYSP3","type":"related"},{"name":"hypospadias 3, autosomal","type":"exact"},{"name":"hypospadias 3, autosomal, multifactorial","type":"exact"}],"termid":"MONDO:0007802","xrefs":{"Monarch":{"xref_id":"0007802"}}}


id: PBO:0073318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine incorporator 1","termid":"PBO:0073318"}


id: GO:0048616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the anterior midgut (ectodermal) are generated and organized, during the post-embryonic phase.","definition_xrefs":["GOC:jid","GOC:rc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"anterior midgut (ectodermal) morphogenesis","termid":"GO:0007441"},{"relation_name":"part_of","term_name":"post-embryonic ectodermal digestive tract morphogenesis","termid":"GO:0048614"}],"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":"post-embryonic anterior midgut (ectodermal) morphogenesis","termid":"GO:0048616"}


id: MONDO:0019667
data:
  {"annotated_genes":["SJAG_03467"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010737"}]},"cv_name":"mondo","definition":"Spondyloepiphyseal dysplasia tarda (SEDT) is characterized by disproportionate short stature in adolescence or adulthood, associated with a short trunk and arms and barrel-shaped chest.","definition_xrefs":["Orphanet:93284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03467":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"spondyloepiphyseal dysplasia tarda","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:51952004","ICD9:756.9","DOID:0112284","NORD:1732"],"termid":"MONDO:0019667","terms_by_termid":{"MONDO:0010737":null},"xrefs":{"Monarch":{"xref_id":"0019667"}}}


id: MONDO:0017692
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"galactose epimerase deficiency","termid":"MONDO:0009257"},{"relation_name":"is_a","term_name":"disorder of galactose and fructose metabolism","termid":"MONDO:0800152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0005328"],"is_obsolete":false,"name":"generalized galactose epimerase deficiency","secondary_identifiers":["SCTID:297237003","GARD:17393","MEDGEN:657804","Orphanet:308487","UMLS:C0574089"],"synonyms":[{"name":"generalised GALE deficiency","type":"exact"},{"name":"generalised GALE-D","type":"exact"},{"name":"generalised UDP-galactose-4-epimerase deficiency","type":"exact"},{"name":"generalised epimerase deficiency galactosemia","type":"exact"},{"name":"generalised uridine diphosphate galactose-4-epimerase deficiency","type":"exact"},{"name":"generalized GALE deficiency","type":"exact"},{"name":"generalized GALE-D","type":"exact"},{"name":"generalized UDP-galactose-4-epimerase deficiency","type":"exact"},{"name":"generalized epimerase deficiency galactosemia","type":"exact"},{"name":"generalized uridine diphosphate galactose-4-epimerase deficiency","type":"exact"}],"termid":"MONDO:0017692","xrefs":{"Monarch":{"xref_id":"0017692"}}}


id: GO:0031396
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the addition of ubiquitin groups to a protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification by small protein conjugation or removal","termid":"GO:1903320"},{"relation_name":"regulates","term_name":"protein ubiquitination","termid":"GO:0016567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"regulation of protein ubiquitination","termid":"GO:0031396"}


id: MONDO:0019451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare chronic myeloproliferative neoplasm characterized by neutrophilic leukocytosis. There is no detectable Philadelphia chromosome or BCR/ABL fusion gene.","definition_xrefs":["NCIT:C3179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic leukemia","termid":"MONDO:0001014"},{"relation_name":"is_a","term_name":"myeloproliferative neoplasm","termid":"MONDO:0020076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"chronic neutrophilic leukemia","secondary_identifiers":["EFO:1000179","SCTID:188734009","ONCOTREE:CNL","ICDO:9963/3","DOID:0080187","icd11.foundation:426734182","GARD:10585","MEDGEN:6061","MESH:D015467","Orphanet:86829","UMLS:C0023481"],"synonyms":[{"name":"CNL","type":"related"},{"name":"chronic neutrophilic leukemia","type":"exact"},{"name":"neutrophilic leukaemia","type":"exact"},{"name":"neutrophilic leukemia","type":"exact"}],"termid":"MONDO:0019451","xrefs":{"Monarch":{"xref_id":"0019451"}}}


id: MONDO:0003894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanotic schwannoma that affects the mediastinum.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanotic neurilemmoma","termid":"MONDO:0002558"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediastinal melanocytic neurilemmoma","secondary_identifiers":["DOID:6484","NCIT:C6635","UMLS:C1334668","MEDGEN:277352"],"synonyms":[{"name":"mediastinal melanocytic schwannoma","type":"exact"},{"name":"mediastinal melanotic schwannoma","type":"exact"},{"name":"melanocytic neurilemmoma of mediastinum","type":"exact"},{"name":"melanocytic neurilemmoma of the mediastinum","type":"exact"},{"name":"melanocytic schwannoma of mediastinum","type":"exact"},{"name":"melanocytic schwannoma of the mediastinum","type":"exact"}],"termid":"MONDO:0003894","xrefs":{"Monarch":{"xref_id":"0003894"}}}


id: GO:1901691
data:
  {"annotated_genes":["SJAG_01669","SJAG_01129"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89474,89475],"is_not":false,"summary":null,"term":"GO:1901691"}]},"cv_name":"molecular_function","definition":"Binding to proton.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01129":null,"SJAG_01669":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"proton binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"hydrogen ion binding","type":"exact"}],"termid":"GO:1901691","terms_by_termid":{"GO:1901691":null}}


id: GO:0043190
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex for the transport of metabolites into and out of the cell, typically comprised of four domains; two membrane-associated domains and two ATP-binding domains at the intracellular face of the membrane, that form a central pore through the plasma membrane. Each of the four core domains may be encoded as a separate polypeptide or the domains can be fused in any one of a number of ways into multidomain polypeptides. In Bacteria and Archaebacteria, ABC transporters also include substrate binding proteins to bind substrate external to the cytoplasm and deliver it to the transporter.","definition_xrefs":["PMID:15111107","GOC:jl","PMID:11421269","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase dependent transmembrane transport complex","termid":"GO:0098533"},{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"ATP-binding cassette (ABC) transporter complex","secondary_identifiers":["GO:0043191","GO:0043192"],"synonyms":[{"name":"ABC-type efflux permease complex","type":"narrow"},{"name":"ABC-type efflux porter complex","type":"narrow"},{"name":"ABC-type uptake permease complex","type":"narrow"},{"name":"mating pheromone exporter","type":"narrow"}],"termid":"GO:0043190"}


id: PBO:0079406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin beta 8B","termid":"PBO:0079406"}


id: PR:O94408
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U6 snRNA-associated Sm-like protein LSm2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04961","PRO:DNx","PANTHER:PTHR13829:SF2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U6 snRNA-associated Sm-like protein LSm2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.01c","secondary_identifiers":["UniProtKB:O94408"],"synonyms":[{"name":"Spom972h-LSM2","type":"exact"}],"termid":"PR:O94408"}


id: GO:0004641
data:
  {"annotated_genes":["SJAG_03140"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72441],"is_not":false,"summary":null,"term":"GO:0004641"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-(formamido)-N(1)-(5-phospho-D-ribosyl)acetamidine + ATP = 5-amino-1-(5-phospho-D-ribosyl)imidazole + ADP + 2 H+ + phosphate.","definition_xrefs":["RHEA:23032","EC:6.3.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclo-ligase activity","termid":"GO:0016882"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03140":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"phosphoribosylformylglycinamidine cyclo-ligase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:AIRS-RXN","Reactome:R-HSA-73810","KEGG_REACTION:R04208"],"synonyms":[{"name":"2-(formamido)-1-N-(5-phosphoribosyl)acetamidine cyclo-ligase (ADP-forming)","type":"related"},{"name":"2-(formamido)-N1-(5-phosphoribosyl)acetamidine cyclo-ligase (ADP-forming)","type":"related"},{"name":"5'-aminoimidazole ribonucleotide synthetase activity","type":"related"},{"name":"AIR synthase activity","type":"related"},{"name":"AIR synthetase activity","type":"related"},{"name":"AIRS activity","type":"related"},{"name":"phosphoribosyl-aminoimidazole synthetase activity","type":"related"},{"name":"phosphoribosylaminoimidazole synthetase activity","type":"related"}],"termid":"GO:0004641","terms_by_termid":{"GO:0004641":null}}


id: PBO:0055747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA activating regulator of DKK1","termid":"PBO:0055747"}


id: MONDO:0015985
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Bone dysplasia Azouz type is a form of generalized enchondromatosis with involvement of the spine (so called spondyloenchondromatosis). Spondyloenchondromatosis is a very rare skeletal dysplasia characterized by severe platyspondyly, and mild involvement of hands and feet.","definition_xrefs":["Orphanet:1844"],"gene_count":0,"genotype_count":0,"name":"obsolete bone dysplasia, Azouz type (obsolete MONDO:0015985)","secondary_identifiers":["GARD:920","SCTID:720566004","icd11.foundation:2054115498"],"synonyms":[{"name":"bone dysplasia Azouz type","type":"related"}],"termid":"MONDO:0015985","xrefs":{"Monarch":{"xref_id":"0015985"}}}


id: PBO:0065466
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 8","termid":"PBO:0065466"}


id: MONDO:0002487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually benign neoplasm that arises from the breast. It presents as a single, firm, and painless mass. It is characterized by the presence of neoplastic cells with eosinophilic granular cytoplasm.","definition_xrefs":["NCIT:C40400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"granular cell tumor","termid":"MONDO:0006235"},{"relation_name":"is_a","term_name":"breast neoplasm","termid":"MONDO:0021100"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast granular cell tumor","secondary_identifiers":["DOID:3011","MEDGEN:307309","UMLS:C1511312"],"synonyms":[{"name":"breast granular cell tumor","type":"exact"},{"name":"granular cell tumor of breast","type":"exact"},{"name":"granular cell tumour of breast","type":"exact"}],"termid":"MONDO:0002487","xrefs":{"Monarch":{"xref_id":"0002487"}}}


id: GO:1904188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of transformation of host cell by virus.","definition_xrefs":["GOC:TermGenie","PMID:12200142","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biological process","termid":"GO:0048519"},{"relation_name":"is_a","term_name":"regulation of transformation of host cell by virus","termid":"GO:1904187"},{"relation_name":"negatively_regulates","term_name":"symbiont-mediated transformation of host cell","termid":"GO:0019087"}],"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 transformation of host cell by virus","synonyms":[{"name":"down regulation of transformation of host cell by virus","type":"exact"},{"name":"down regulation of viral transformation","type":"exact"},{"name":"down regulation of viral transformation of host cell","type":"exact"},{"name":"down-regulation of transformation of host cell by virus","type":"exact"},{"name":"down-regulation of viral transformation","type":"exact"},{"name":"down-regulation of viral transformation of host cell","type":"exact"},{"name":"downregulation of transformation of host cell by virus","type":"exact"},{"name":"downregulation of viral transformation","type":"exact"},{"name":"downregulation of viral transformation of host cell","type":"exact"},{"name":"inhibition of transformation of host cell by virus","type":"narrow"},{"name":"inhibition of viral transformation","type":"narrow"},{"name":"inhibition of viral transformation of host cell","type":"narrow"},{"name":"negative regulation of viral transformation","type":"exact"},{"name":"negative regulation of viral transformation of host cell","type":"exact"}],"termid":"GO:1904188"}


id: GO:1905213
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mitotic chromosome condensation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:23219725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"negative regulation of chromosome condensation","termid":"GO:1902340"},{"relation_name":"is_a","term_name":"regulation of mitotic chromosome condensation","termid":"GO:1903379"},{"relation_name":"negatively_regulates","term_name":"mitotic chromosome condensation","termid":"GO:0007076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mitotic chromosome condensation","termid":"GO:1905213"}


id: MONDO:0009260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis with variable neurological and systemic manifestations.","definition_xrefs":["Orphanet:79255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic dyslipidemia","termid":"MONDO:0015905"},{"relation_name":"is_a","term_name":"GM1 gangliosidosis","termid":"MONDO:0018149"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005066","MONDO:0002561","MONDO:0002525"],"is_obsolete":false,"name":"GM1 gangliosidosis type 1","secondary_identifiers":["NANDO:1200067","NANDO:2201196","DOID:0080502","GARD:6479","icd11.foundation:466200180","MEDGEN:75665","MONDO:0023211","OMIM:230500","SCTID:238026007","UMLS:C0268271"],"synonyms":[{"name":"Beta galactosidase deficiency type 1","type":"related"},{"name":"Beta-galactosidase-1 deficiency","type":"related"},{"name":"GLB deficiency type 1","type":"related"},{"name":"GM1-gangliosidosis, type 1","type":"related"},{"name":"GM1-gangliosidosis, type I","type":"related"},{"name":"GM1-gangliosidosis, type I, with Cardiac involvement","type":"related"},{"name":"Glb1 deficiency","type":"related"},{"name":"Norman-Landing disease","type":"exact"},{"name":"gangliosidosis generalised GM1 infantile form","type":"related"},{"name":"gangliosidosis generalised GM1 type 1","type":"related"},{"name":"gangliosidosis generalized GM1 infantile form","type":"related"},{"name":"gangliosidosis generalized GM1 type 1","type":"related"},{"name":"gangliosidosis, generalised GM1, infantile form","type":"related"},{"name":"gangliosidosis, generalised GM1, type 1","type":"related"},{"name":"gangliosidosis, generalised GM1, type I, with Cardiac involvement","type":"related"},{"name":"gangliosidosis, generalized GM1, infantile form","type":"related"},{"name":"gangliosidosis, generalized GM1, type 1","type":"related"},{"name":"gangliosidosis, generalized GM1, type I, with Cardiac involvement","type":"related"},{"name":"infantile GM1 gangliosidosis","type":"exact"}],"termid":"MONDO:0009260","xrefs":{"Monarch":{"xref_id":"0009260"}}}


id: MONDO:0010857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Semantic dementia (SD) is a form of frontotemporal dementia (FTD), characterized by the progressive, amodal and profound loss of semantic knowledge (combination of visual associative agnosia, anomia, surface dyslexia or dysgraphia and disrupted comprehension of word meaning) and behavioral abnormalities, attributable to the degeneration of the anterior temporal lobes.","definition_xrefs":["Orphanet:100069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive non-fluent aphasia","termid":"MONDO:0015059"},{"relation_name":"is_a","term_name":"behavioral variant of frontotemporal dementia","termid":"MONDO:0017160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"semantic dementia","secondary_identifiers":["MEDGEN:83268","OMIM:600274","NANDO:1200550","UMLS:C0338462","GARD:10792","DOID:0081391"],"synonyms":[{"name":"FTD","type":"related"},{"name":"Ftdp17","type":"related"},{"name":"Ftld with Tau inclusions","type":"related"},{"name":"Pallidopontonigral Degeneration","type":"related"},{"name":"Pick Complex","type":"related"},{"name":"Wilhelmsen-Lynch disease","type":"related"},{"name":"dementia, frontotemporal","type":"exact"},{"name":"dementia, frontotemporal, with Parkinsonism","type":"related"},{"name":"dementia, frontotemporal, with or without parkinsonism","type":"exact"},{"name":"disinhibition-dementia-Parkinsonism-amyotrophy Complex","type":"related"},{"name":"frontotemporal dementia","type":"related"},{"name":"frontotemporal dementia with Parkinsonism","type":"related"},{"name":"frontotemporal lobar Degeneration with Tau inclusions","type":"related"},{"name":"frontotemporal lobe dementia","type":"related"},{"name":"multiple system tauopathy with presenile dementia","type":"related"},{"name":"semantic primary progressive aphasia","type":"exact"},{"name":"semantic variant PPA","type":"exact"}],"termid":"MONDO:0010857","xrefs":{"Monarch":{"xref_id":"0010857"}}}


id: MONDO:0005463
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Calcification of the aortic valve","definition_xrefs":["EFO:0005239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aortic valve disorder","termid":"MONDO:0003803"}],"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":"aortic valve calcification","secondary_identifiers":["MEDGEN:140899","UMLS:C0428791","HP:0004380","SCTID:250978003"],"synonyms":[{"name":"aortic valve calcification","type":"exact"},{"name":"aortic valve calcification (disease)","type":"exact"}],"termid":"MONDO:0005463","xrefs":{"Monarch":{"xref_id":"0005463"}}}


id: MONDO:1010812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polydactyly that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polydactyly, non-human animal","termid":"MONDO:1010158"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polydactyly, domestic cat","secondary_identifiers":["OMIA:000810-9685"],"termid":"MONDO:1010812","xrefs":{"Monarch":{"xref_id":"1010812"}}}


id: PBO:0028256
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_ornithine_carbamoyltransferase_activity","termid":"PBO:0028256"}


id: PBO:0117023
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 3144","termid":"PBO:0117023"}


id: PR:Q9UU99
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC23B6.04c gene.","definition_xrefs":["UniProtKB:Q9UU99","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":"CRAL-TRIO domain-containing protein C23B6.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC23B6.04c","synonyms":[{"name":"Spom972h-SPCC23B6.04c","type":"exact"}],"termid":"PR:Q9UU99"}


id: GO:0071501
data:
  {"annotated_genes":["SJAG_04018","SJAG_00718","SJAG_04573","SJAG_03568","SJAG_02104","SJAG_01253","SJAG_00293","SJAG_04384","SJAG_02682","SJAG_01657","SJAG_03302","SJAG_03345","SJAG_03501","SJAG_02703","SJAG_05304","SJAG_04151","SJAG_01632","SJAG_01150","SJAG_01585","SJAG_05286","SJAG_01307","SJAG_00642"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107702,93011,113544],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:2000639"},{"annotations":[115276,115277,62215,80120],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:2000640"},{"annotations":[105768,114402,120089,65968,64664,91038,91425,90756,103904,94415,114655,118234,95662,120308,70408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032933"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus indicating deprivation of sterols. Sterols are a group of steroids characterized by the presence of one or more hydroxyl groups and a hydrocarbon side-chain in the molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to sterol depletion","termid":"GO:0006991"},{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00293":null,"SJAG_00642":null,"SJAG_00718":null,"SJAG_01150":null,"SJAG_01253":null,"SJAG_01307":null,"SJAG_01585":null,"SJAG_01632":null,"SJAG_01657":null,"SJAG_02104":null,"SJAG_02682":null,"SJAG_02703":null,"SJAG_03302":null,"SJAG_03345":null,"SJAG_03501":null,"SJAG_03568":null,"SJAG_04018":null,"SJAG_04151":null,"SJAG_04384":null,"SJAG_04573":null,"SJAG_05286":null,"SJAG_05304":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to sterol depletion","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"cellular sterol depletion response","type":"exact"}],"termid":"GO:0071501","terms_by_termid":{"GO:0032933":null,"GO:2000639":null,"GO:2000640":null}}


id: MONDO:0020243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete colobomatous and areolar dystrophy (obsolete MONDO:0020243)","secondary_identifiers":["Orphanet:98665"],"termid":"MONDO:0020243","xrefs":{"Monarch":{"xref_id":"0020243"}}}


id: GO:0090250
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of one cell to another cell via adhesion molecules that contributes to the establishment of planar cell polarity.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"},{"relation_name":"part_of","term_name":"establishment of planar polarity","termid":"GO:0001736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"cell-cell adhesion involved in establishment of planar polarity","termid":"GO:0090250"}


id: MONDO:0004480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pancreatic invasive intraductal papillary-mucinous carcinoma (obsolete MONDO:0004480)","termid":"MONDO:0004480","xrefs":{"Monarch":{"xref_id":"0004480"}}}


id: PBO:0069320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 578, pseudogene","termid":"PBO:0069320"}


id: PBO:0017084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific protein Mug150","termid":"PBO:0017084"}


id: GO:0016171
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cell surface antigen (obsolete GO:0016171)","synonyms":[{"name":"cell surface antigen","type":"exact"}],"termid":"GO:0016171"}


id: PBO:0044583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysbindin domain containing 1","termid":"PBO:0044583"}


id: PBO:0054336
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 1729","termid":"PBO:0054336"}


id: GO:0033376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a protein to a location within a secretory granule in a T cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein transport","termid":"GO:0006886"},{"relation_name":"part_of","term_name":"protein localization to T cell secretory granule","termid":"GO:0033374"}],"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":"establishment of protein localization to T cell secretory granule","synonyms":[{"name":"establishment of protein localisation in T cell secretory granule","type":"exact"},{"name":"establishment of protein localization in T cell secretory granule","type":"exact"},{"name":"establishment of protein localization in T lymphocyte secretory granule","type":"exact"},{"name":"establishment of protein localization in T-cell secretory granule","type":"exact"},{"name":"establishment of protein localization in T-lymphocyte secretory granule","type":"exact"}],"termid":"GO:0033376"}


id: PR:Q9UUK7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phosphoribosylglycinamide formyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO05064","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":"phosphoribosylglycinamide formyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC569.08c","secondary_identifiers":["UniProtKB:Q9UUK7"],"synonyms":[{"name":"5'-phosphoribosylglycinamide transformylase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GAR transformylase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GART (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-purN","type":"exact"}],"termid":"PR:Q9UUK7"}


id: MONDO:0004345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant peripheral nerve sheath tumor occurring in children.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"},{"relation_name":"is_a","term_name":"malignant peripheral nerve sheath tumor","termid":"MONDO:0017827"}],"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":"childhood malignant schwannoma","secondary_identifiers":["NCIT:C8094","UMLS:C0279987","DOID:7732","MEDGEN:83582"],"synonyms":[{"name":"childhood MPNST","type":"exact"},{"name":"childhood malignant neoplasm of peripheral nerve sheath","type":"exact"},{"name":"childhood malignant neoplasm of the peripheral nerve sheath","type":"exact"},{"name":"childhood malignant neurilemmoma","type":"exact"},{"name":"childhood malignant peripheral nerve sheath neoplasm","type":"exact"},{"name":"childhood malignant peripheral nerve sheath tumor","type":"exact"},{"name":"childhood malignant peripheral nerve sheath tumour","type":"exact"},{"name":"childhood malignant schwannoma","type":"exact"},{"name":"childhood malignant tumor of peripheral nerve sheath","type":"exact"},{"name":"childhood malignant tumor of the peripheral nerve sheath","type":"exact"},{"name":"childhood malignant tumour of peripheral nerve sheath","type":"exact"},{"name":"childhood malignant tumour of the peripheral nerve sheath","type":"exact"},{"name":"childhood neurofibrosarcoma","type":"exact"},{"name":"childhood neurogenic sarcoma","type":"exact"},{"name":"malignant peripheral nerve sheath tumor","type":"broad"},{"name":"malignant peripheral nerve sheath tumour","type":"broad"},{"name":"paediatric MPNST","type":"exact"},{"name":"paediatric malignant neoplasm of peripheral nerve sheath","type":"exact"},{"name":"paediatric malignant neoplasm of the peripheral nerve sheath","type":"exact"},{"name":"paediatric malignant neurilemmoma","type":"exact"},{"name":"paediatric malignant peripheral nerve sheath neoplasm","type":"exact"},{"name":"paediatric malignant peripheral nerve sheath tumour","type":"exact"},{"name":"paediatric malignant schwannoma","type":"exact"},{"name":"paediatric malignant tumour of peripheral nerve sheath","type":"exact"},{"name":"paediatric malignant tumour of the peripheral nerve sheath","type":"exact"},{"name":"pediatric MPNST","type":"exact"},{"name":"pediatric malignant neoplasm of peripheral nerve sheath","type":"exact"},{"name":"pediatric malignant neoplasm of the peripheral nerve sheath","type":"exact"},{"name":"pediatric malignant neurilemmoma","type":"exact"},{"name":"pediatric malignant peripheral nerve sheath neoplasm","type":"exact"},{"name":"pediatric malignant peripheral nerve sheath tumor","type":"exact"},{"name":"pediatric malignant schwannoma","type":"exact"},{"name":"pediatric malignant tumor of peripheral nerve sheath","type":"exact"},{"name":"pediatric malignant tumor of the peripheral nerve sheath","type":"exact"}],"termid":"MONDO:0004345","xrefs":{"Monarch":{"xref_id":"0004345"}}}


id: MONDO:0005309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Traumatic or pathological injury to the spine in which the continuity of a vertebral bone is broken. Symptoms include back pain and difficulty bending and twisting.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone fracture","termid":"MONDO:0005315"},{"relation_name":"is_a","term_name":"spinal injury","termid":"MONDO:0037747"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal fracture","secondary_identifiers":["SCTID:50448004","MESH:D016103","EFO:0003902"],"synonyms":[{"name":"bone fracture of vertebral column","type":"exact"},{"name":"vertebral column bone fracture","type":"exact"}],"termid":"MONDO:0005309","xrefs":{"Monarch":{"xref_id":"0005309"}}}


id: PBO:0029417
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_palmitoylation_during_meiosis","termid":"PBO:0029417"}


id: MONDO:1011159
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteoarthritis that occurs in koala.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteoarthritis, non-human animal","termid":"MONDO:1010297"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoarthritis, koala","secondary_identifiers":["OMIA:000747-38626"],"termid":"MONDO:1011159","xrefs":{"Monarch":{"xref_id":"1011159"}}}


id: PR:Q09927
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- aca1 gene.","definition_xrefs":["UniProtKB:Q09927","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":"L-azetidine-2-carboxylic acid acetyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC21E11.04","synonyms":[{"name":"Spom972h-aca1","type":"exact"}],"termid":"PR:Q09927"}


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


id: GO:1904241
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of VCP-NPL4-UFD1 AAA ATPase complex assembly.","definition_xrefs":["GOC:PARL","GOC:TermGenie","GO_REF:0000058","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of VCP-NPL4-UFD1 AAA ATPase complex assembly","termid":"GO:1904239"},{"relation_name":"positively_regulates","term_name":"VCP-NPL4-UFD1 AAA ATPase complex assembly","termid":"GO:1904210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"positive regulation of VCP-NPL4-UFD1 AAA ATPase complex assembly","synonyms":[{"name":"activation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex assembly","type":"narrow"},{"name":"activation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex formation","type":"narrow"},{"name":"activation of VCP-NPL4-UFD1 AAA ATPase complex assembly","type":"narrow"},{"name":"activation of VCP-NPL4-UFD1 AAA ATPase complex formation","type":"narrow"},{"name":"activation of p97-Ufd1-Npl4 complex assembly","type":"narrow"},{"name":"activation of p97-Ufd1-Npl4 complex formation","type":"narrow"},{"name":"positive regulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex assembly","type":"narrow"},{"name":"positive regulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex formation","type":"narrow"},{"name":"positive regulation of VCP-NPL4-UFD1 AAA ATPase complex formation","type":"exact"},{"name":"positive regulation of p97-Ufd1-Npl4 complex assembly","type":"exact"},{"name":"positive regulation of p97-Ufd1-Npl4 complex formation","type":"exact"},{"name":"up regulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex assembly","type":"narrow"},{"name":"up regulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex formation","type":"narrow"},{"name":"up regulation of VCP-NPL4-UFD1 AAA ATPase complex assembly","type":"exact"},{"name":"up regulation of VCP-NPL4-UFD1 AAA ATPase complex formation","type":"exact"},{"name":"up regulation of p97-Ufd1-Npl4 complex assembly","type":"exact"},{"name":"up regulation of p97-Ufd1-Npl4 complex formation","type":"exact"},{"name":"up-regulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex assembly","type":"narrow"},{"name":"up-regulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex formation","type":"narrow"},{"name":"up-regulation of VCP-NPL4-UFD1 AAA ATPase complex assembly","type":"exact"},{"name":"up-regulation of VCP-NPL4-UFD1 AAA ATPase complex formation","type":"exact"},{"name":"up-regulation of p97-Ufd1-Npl4 complex assembly","type":"exact"},{"name":"up-regulation of p97-Ufd1-Npl4 complex formation","type":"exact"},{"name":"upregulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex assembly","type":"narrow"},{"name":"upregulation of Cdc48p-Npl4p-Ufd1p AAA ATPase complex formation","type":"narrow"},{"name":"upregulation of VCP-NPL4-UFD1 AAA ATPase complex assembly","type":"exact"},{"name":"upregulation of VCP-NPL4-UFD1 AAA ATPase complex formation","type":"exact"},{"name":"upregulation of p97-Ufd1-Npl4 complex assembly","type":"exact"},{"name":"upregulation of p97-Ufd1-Npl4 complex formation","type":"exact"}],"termid":"GO:1904241"}


id: MONDO:0011495
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Langerhans-cell histiocytosis (obsolete MONDO:0011495)","termid":"MONDO:0011495","xrefs":{"Monarch":{"xref_id":"0011495"}}}


id: PBO:0086244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that may be involved in nonsense-mediated mRNA decay; interacts with Nam7p, relocalizes from nucleus to cytoplasmic foci upon DNA replication stress","termid":"PBO:0086244"}


id: GO:0018110
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: histone L-arginine + ATP = histone N(omega)-phospho-L-arginine + ADP + 2 H+.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone arginine kinase activity (obsolete GO:0018110)","synonyms":[{"name":"histone-arginine kinase activity","type":"exact"}],"termid":"GO:0018110"}


id: PR:Q09862
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC29E6.09 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C29E6.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29E6.09","synonyms":[{"name":"Spom972h-SPAC29E6.09","type":"exact"}],"termid":"PR:Q09862"}


id: PBO:0086456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative membrane protein upregulated in toxic manganese levels; mRNA identified as translated by ribosome profiling data; partially overlaps dubious ORF YBR056C-B; YBR056W-A has a paralog, YDR034W-B, that arose from the whole genome duplication","termid":"PBO:0086456"}


id: MONDO:0002941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the perianal skin","direct_ancestors":[{"relation_name":"is_a","term_name":"skin carcinoma","termid":"MONDO:0002656"},{"relation_name":"is_a","term_name":"anal carcinoma","termid":"MONDO:0003199"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093","MONDO:0004335"],"is_obsolete":false,"name":"anal margin carcinoma","secondary_identifiers":["DOID:4284","MEDGEN:87604","NCIT:C7472","UMLS:C0349534"],"synonyms":[{"name":"anal margin cancer","type":"exact"},{"name":"anal margin carcinoma","type":"exact"},{"name":"carcinoma of anal margin","type":"exact"},{"name":"carcinoma of perianal skin","type":"exact"},{"name":"carcinoma of the anal margin","type":"exact"},{"name":"perianal skin carcinoma","type":"exact"}],"termid":"MONDO:0002941","xrefs":{"Monarch":{"xref_id":"0002941"}}}


id: PBO:0040707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 like 12 pseudogene 1","termid":"PBO:0040707"}


id: PBO:0003040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adducin","termid":"PBO:0003040"}


id: PBO:0043829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CPSF1 pseudogene 2","termid":"PBO:0043829"}


id: MONDO:0009176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare inherited genodermatosis characterized by chronic infection with human papillomavirus (HPV) leading to polymorphous cutaneous lesions and high risk of developing non melanoma skin cancer.","definition_xrefs":["Orphanet:302"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"epidermodysplasia verruciformis","secondary_identifiers":["icd11.foundation:1191479808","SCTID:19138001","MedDRA:10052339","UMLS:C0014522","NANDO:2200768","MESH:D004819","GARD:6357","DOID:13777","NCIT:C126877","ICD9:757.8","ICD9:078.19","MEDGEN:41831"],"synonyms":[{"name":"EV","type":"related"},{"name":"Lewandowsky-Lutz dysplasia","type":"exact"},{"name":"Lewandowsky-Lutz syndrome","type":"exact"},{"name":"Lutz-Lewandowsky epidermodysplasia verruciformis","type":"exact"},{"name":"epidermodysplasia verruciformis","type":"exact"},{"name":"ever","type":"related"}],"termid":"MONDO:0009176","xrefs":{"Monarch":{"xref_id":"0009176"}}}


id: GO:0034847
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: naphthyl-2-hydroxymethyl-succinyl-CoA = naphthyl-2-oxomethyl-succinyl-CoA + 2 H+ + 2 e-.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete naphthyl-2-hydroxymethyl-succinyl-CoA dehydrogenase activity (obsolete GO:0034847)","termid":"GO:0034847"}


id: PBO:0063474
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein disulfide isomerase family A member 3 pseudogene 1","termid":"PBO:0063474"}


id: GO:0061255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a mesonephric glomerular parietal epithelial cell. Mesonephric glomerular parietal epithelial cells are specialized epithelial cells that form tight junctions as a barrier to protein transport. These cells may also give rise to podocytes.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesonephric glomerular epithelial cell fate commitment","termid":"GO:0061252"},{"relation_name":"is_a","term_name":"glomerular parietal epithelial cell fate commitment","termid":"GO:0072147"},{"relation_name":"part_of","term_name":"mesonephric glomerular parietal epithelial cell differentiation","termid":"GO:0061253"}],"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":"mesonephric glomerular parietal epithelial cell fate commitment","termid":"GO:0061255"}


id: PBO:0070572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 38","termid":"PBO:0070572"}


id: PBO:0062411
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 38 pseudogene","termid":"PBO:0062411"}


id: PBO:0079063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon TAC) 3-1","termid":"PBO:0079063"}


id: FYPO:0007030
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 levels and proportions of monosaccharides in the cell wall are normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:30389790","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal cell wall monosaccharide composition during vegetative growth","synonyms":[{"name":"normal cell wall monosaccharide composition during mitotic cell cycle","type":"related"}],"termid":"FYPO:0007030"}


id: PR:000028992
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An sre1-type sterol regulatory element-binding protein 1 cleaved 1 in Schizosaccharomyces pombe. This form is the N-terminal domain of the membrane protein sre1 that is cleaved off upon activation (e.g. by hypoxia). UniProtKB:Q9UUD1-1, 1-440.","definition_xrefs":["PMID:22017871","PomBase:AL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sre1/Clv:(1-440)","pombase_gene_id":"SPBC19C2.09","synonyms":[{"name":"PomBase_original_PRO_term_name: Sre1N (Schizosaccharomyces pombe)","type":"exact"},{"name":"sre1/Clv:(1-440)","type":"exact"}],"termid":"PR:000028992"}


id: PBO:0060758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 2","termid":"PBO:0060758"}


id: MONDO:0008998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cockayne syndrome type III, also known as the mild form of Cockayne syndrome, is a rare genetic disorder that causes early (premature) aging. Unlike the more severe forms of this condition, individuals with Cockayne syndrome type III can have normal growth and development. Symptoms may include sunlight sensitivity (photosensitivity), hearing loss, eye and bone abnormalities, and changes to the brain that can be seen on imaging (brain MRIs). In general, symptoms of Cockayne syndrome type III are usually not noticeable until later in childhood.","direct_ancestors":[{"relation_name":"is_a","term_name":"Cockayne syndrome","termid":"MONDO:0016006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0019303"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0019303","MONDO:0021190","MONDO:0006025"],"is_obsolete":false,"name":"Cockayne syndrome type 3","secondary_identifiers":["OMIM:216411","icd11.foundation:1401163130","MEDGEN:196713","Orphanet:90324","UMLS:C0751037","GARD:1417"],"synonyms":[{"name":"Cockayne syndrome type 3","type":"exact"},{"name":"Cockayne syndrome type C","type":"related"},{"name":"Cockayne syndrome type III","type":"exact"},{"name":"Cockayne syndrome, type III","type":"related"}],"termid":"MONDO:0008998","xrefs":{"Monarch":{"xref_id":"0008998"}}}


id: PR:Q9UTA9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC25B8.09 gene.","definition_xrefs":["UniProtKB:Q9UTA9","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized methyltransferase C25B8.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25B8.09","synonyms":[{"name":"Spom972h-SPAC25B8.09","type":"exact"}],"termid":"PR:Q9UTA9"}


id: PBO:0069489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 756, pseudogene","termid":"PBO:0069489"}


id: GO:0072225
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metanephric late distal convoluted tubule over time, from its formation to the mature structure. The metanephric late distal convoluted tubule contains metanephric DCT cells and intercalated (IC) alpha and beta cells and is vasopressin-sensitive.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"late distal convoluted tubule development","termid":"GO:0072068"},{"relation_name":"is_a","term_name":"metanephric nephron epithelium development","termid":"GO:0072243"},{"relation_name":"part_of","term_name":"metanephric distal convoluted tubule development","termid":"GO:0072221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric late distal convoluted tubule development","termid":"GO:0072225"}


id: PBO:0047824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box O4","termid":"PBO:0047824"}


id: GO:0060013
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A reflex process in which an animal immediately tries to turn over after being placed in a supine position.","definition_xrefs":["GOC:dph","PMID:8635460"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reflex","termid":"GO:0060004"}],"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":"righting reflex","synonyms":[{"name":"righting response","type":"exact"}],"termid":"GO:0060013"}


id: GO:0007304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The construction of a chorion-containing eggshell. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mah","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eggshell formation","termid":"GO:0030703"},{"relation_name":"part_of","term_name":"follicle cell of egg chamber development","termid":"GO:0030707"}],"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":"chorion-containing eggshell formation","synonyms":[{"name":"eggshell formation","type":"broad"}],"termid":"GO:0007304"}


id: PBO:0004486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"16 small nucleolar RNA","termid":"PBO:0004486"}


id: PBO:0078801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (GTT) 19-1","termid":"PBO:0078801"}


id: GO:1901253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of intracellular transport of viral material.","definition_xrefs":["GOC:TermGenie","GOC:jl","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular transport of viral material","termid":"GO:1901252"},{"relation_name":"is_a","term_name":"negative regulation of viral life cycle","termid":"GO:1903901"},{"relation_name":"negatively_regulates","term_name":"intracellular transport of virus","termid":"GO:0075733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of intracellular transport of viral material","synonyms":[{"name":"down regulation of egress of virus within host cell","type":"exact"},{"name":"down regulation of movement of virus within host cell","type":"exact"},{"name":"down regulation of viral egress","type":"exact"},{"name":"down-regulation of egress of virus within host cell","type":"exact"},{"name":"down-regulation of movement of virus within host cell","type":"exact"},{"name":"down-regulation of viral egress","type":"exact"},{"name":"downregulation of egress of virus within host cell","type":"exact"},{"name":"downregulation of movement of virus within host cell","type":"exact"},{"name":"downregulation of viral egress","type":"exact"},{"name":"inhibition of egress of virus within host cell","type":"narrow"},{"name":"inhibition of movement of virus within host cell","type":"exact"},{"name":"inhibition of viral egress","type":"exact"},{"name":"negative regulation of egress of virus within host cell","type":"related"},{"name":"negative regulation of movement of virus within host cell","type":"exact"},{"name":"negative regulation of viral egress","type":"exact"}],"termid":"GO:1901253"}


id: PBO:0014606
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae Fen2","termid":"PBO:0014606"}


id: MONDO:0013666
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive Stickler syndrome in which the cause of the disease is a mutation in the COL9A2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Stickler syndrome","termid":"MONDO:0019354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005497"],"is_obsolete":false,"name":"Stickler syndrome, type 5","secondary_identifiers":["UMLS:C3280342","OMIM:614284","GARD:18359","MEDGEN:481972"],"synonyms":[{"name":"COL9A2 autosomal recessive Stickler syndrome","type":"exact"},{"name":"STICKLER syndrome, type V","type":"related"},{"name":"STL5","type":"related"},{"name":"autosomal recessive Stickler syndrome caused by mutation in COL9A2","type":"exact"}],"termid":"MONDO:0013666","xrefs":{"Monarch":{"xref_id":"0013666"}}}


id: MONDO:1011259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinitis pigmentosa that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa, non-human animal","termid":"MONDO:1010334"},{"relation_name":"is_a","term_name":"retinal degeneration, cattle","termid":"MONDO:1011247"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa, cattle","secondary_identifiers":["OMIA:001413-9913"],"termid":"MONDO:1011259","xrefs":{"Monarch":{"xref_id":"1011259"}}}


id: GO:0051499
data:
  {"annotated_genes":["SJAG_01248"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051500"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a D-aminoacyl-tRNA + H2O = a D-alpha-amino acid + a tRNA + H+.  Removal of a D-amino acid from a charged tRNA.","definition_xrefs":["PMID:14527667","RHEA:13953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyl-tRNA deacylase activity","termid":"GO:0002161"},{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"},{"relation_name":"is_a","term_name":"deacylase activity","termid":"GO:0160215"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01248":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0140098","GO:0140101","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"D-aminoacyl-tRNA deacylase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:RXN-15041","EC:3.1.1.96"],"termid":"GO:0051499","terms_by_termid":{"GO:0051500":null}}


id: PBO:0078651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon CTT) 4-1","termid":"PBO:0078651"}


id: GO:0051135
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of natural killer T cell activation.","definition_xrefs":["PMID:12154375","PMID:9133426","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of alpha-beta T cell activation","termid":"GO:0046635"},{"relation_name":"is_a","term_name":"regulation of NK T cell activation","termid":"GO:0051133"},{"relation_name":"positively_regulates","term_name":"NK T cell activation","termid":"GO:0051132"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"positive regulation of NK T cell activation","synonyms":[{"name":"activation of NK T cell activation","type":"narrow"},{"name":"positive regulation of NK T lymphocyte activation","type":"exact"},{"name":"positive regulation of NK T-cell activation","type":"exact"},{"name":"positive regulation of NK T-lymphocyte activation","type":"exact"},{"name":"positive regulation of NKT cell activation","type":"exact"},{"name":"positive regulation of NT cell activation","type":"exact"},{"name":"positive regulation of natural T cell activation","type":"exact"},{"name":"positive regulation of natural killer T cell activation","type":"exact"},{"name":"stimulation of NK T cell activation","type":"narrow"},{"name":"up regulation of NK T cell activation","type":"exact"},{"name":"up-regulation of NK T cell activation","type":"exact"},{"name":"upregulation of NK T cell activation","type":"exact"}],"termid":"GO:0051135"}


id: MONDO:0006053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A leiomyoma that involves the kidney.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"kidney benign neoplasm","termid":"MONDO:0002513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal leiomyoma","secondary_identifiers":["MEDGEN:1691847","UMLS:C5204259","EFO:1000050","NCIT:C159209"],"synonyms":[{"name":"kidney leiomyoma","type":"exact"},{"name":"leiomyoma of kidney","type":"exact"}],"termid":"MONDO:0006053","xrefs":{"Monarch":{"xref_id":"0006053"}}}


id: PBO:0072516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 45","termid":"PBO:0072516"}


id: PBO:0087835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Thiol-specific peroxiredoxin; reduces hydroperoxides to protect against oxidative damage; function in vivo requires covalent conjugation to Urm1p","termid":"PBO:0087835"}


id: PBO:0065184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline and serine rich 2","termid":"PBO:0065184"}


id: MONDO:0009892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chuvash erythrocytosis is a rare, genetic, congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death.","definition_xrefs":["Orphanet:238557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial polycythemia","termid":"MONDO:0001115"},{"relation_name":"is_a","term_name":"congenital secondary polycythemia","termid":"MONDO:0016540"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"Chuvash polycythemia","secondary_identifiers":["UMLS:C1837915","MESH:C563918","GARD:17176","MEDGEN:332974","OMIM:263400","DOID:0060474"],"synonyms":[{"name":"Chuvash erythrocytosis","type":"related"},{"name":"Chuvash erythromatosis","type":"exact"},{"name":"Chuvash polycythemia","type":"exact"},{"name":"Chuvash type polycythemia","type":"exact"},{"name":"ECYT2","type":"related"},{"name":"VHL familial polycythemia","type":"exact"},{"name":"Von Hippel-Lindau-dependent polycythemia","type":"exact"},{"name":"autosomal recessive benign erythrocytosis","type":"exact"},{"name":"erythrocytosis, autosomal recessive benign","type":"related"},{"name":"erythrocytosis, familial, 2","type":"related"},{"name":"erythrocytosis, familial, type 2","type":"exact"},{"name":"familial erythrocytosis 2","type":"exact"},{"name":"familial polycythemia caused by mutation in VHL","type":"exact"},{"name":"polycythemia, Chuvash type","type":"related"},{"name":"polycythemia, VHL-dependent","type":"related"}],"termid":"MONDO:0009892","xrefs":{"Monarch":{"xref_id":"0009892"}}}


id: PBO:0028167
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_crossover_junction_endodeoxyribonuclease_activity","termid":"PBO:0028167"}


id: PBO:0059019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix metallopeptidase 8","termid":"PBO:0059019"}


id: GO:0030846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An RNA polymerase II transcription termination process in which cleavage and polyadenylylation of the mRNA 3' end are coupled to transcription termination.","definition_xrefs":["PMID:12944462","PMID:18679429","PMID:27371117","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"termination of RNA polymerase II transcription","termid":"GO:0006369"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006351"],"is_obsolete":false,"name":"termination of RNA polymerase II transcription, poly(A)-coupled","synonyms":[{"name":"termination of RNA polymerase II transcription, polyadenylation-coupled","type":"related"},{"name":"transcription termination from Pol II promoter, RNA polymerase(A) coupled","type":"related"},{"name":"transcription termination from Pol II promoter, poly(A) coupled","type":"related"}],"termid":"GO:0030846"}


id: PBO:0057158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"miR-302/367 cluster host gene","termid":"PBO:0057158"}


id: PBO:0043720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6B2","termid":"PBO:0043720"}


id: MONDO:0013841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"stutter disorder","termid":"MONDO:0000723"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stuttering, familial persistent, 3","secondary_identifiers":["OMIM:614655","MEDGEN:766295","UMLS:C3553381"],"synonyms":[{"name":"STUT3","type":"exact"},{"name":"stuttering, familial persistent, 3","type":"exact"}],"termid":"MONDO:0013841","xrefs":{"Monarch":{"xref_id":"0013841"}}}


id: PBO:0086200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that associates with mitochondrial ribosome; green fluorescent protein (GFP)-fusion protein localizes to the mitochondrion; null mutation results in a decrease in plasma membrane electron transport","termid":"PBO:0086200"}


id: PBO:0005070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase alpha B-subunit","termid":"PBO:0005070"}


id: PBO:0062429
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 90 pseudogene","termid":"PBO:0062429"}


id: MONDO:0003706
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"adult astrocytic tumor","termid":"MONDO:0002503"},{"relation_name":"is_a","term_name":"adult brainstem glioma","termid":"MONDO:0003153"},{"relation_name":"is_a","term_name":"brain stem astrocytic neoplasm","termid":"MONDO:0003173"}],"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":"adult brainstem astrocytoma","secondary_identifiers":["UMLS:C1332191","NCIT:C6954","DOID:5922","MEDGEN:233962"],"synonyms":[{"name":"adult brain stem astrocytoma","type":"exact"},{"name":"adult brainstem astrocytoma","type":"exact"}],"termid":"MONDO:0003706","xrefs":{"Monarch":{"xref_id":"0003706"}}}


id: GO:0008237
data:
  {"annotated_genes":["SJAG_01004","SJAG_02809","SJAG_00662","SJAG_04651","SJAG_03648","SJAG_00451","SJAG_03009","SJAG_04103","SJAG_03744","SJAG_03393","SJAG_01430","SJAG_03407","SJAG_00795","SJAG_01896","SJAG_00720","SJAG_00730","SJAG_03022","SJAG_00764","SJAG_01816","SJAG_01321","SJAG_02900","SJAG_03396","SJAG_01312","SJAG_00546","SJAG_03147","SJAG_00573","SJAG_04514","SJAG_02419","SJAG_04858","SJAG_04215","SJAG_02503","SJAG_02341","SJAG_00762","SJAG_01088","SJAG_02033","SJAG_03686","SJAG_01542","SJAG_03586","SJAG_02397","SJAG_00181","SJAG_03752","SJAG_01838","SJAG_04497","SJAG_00742","SJAG_01281","SJAG_00406","SJAG_00479","SJAG_01528","SJAG_00969","SJAG_06636","SJAG_02244","SJAG_03429","SJAG_04533","SJAG_01179","SJAG_04641"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[63145,65454,67993,73907,78064,100595,108785,116488],"is_not":false,"summary":null,"term":"GO:0008237"},{"annotations":[112161,64230,95913,90263,75902,69754,115463,98324,101659,117081,107608,116652,97084,106421,117009,107440,57326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140492"},{"annotations":[116293,76156,57898,65526,64732,60601,99625,74324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"},{"annotations":[76080,58368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004181"},{"annotations":[61916,60938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070573"},{"annotations":[109892,100090,71334,71515,60448,79811,79320,71757,77556,76582,79881,78990,68448,111020,78559,99106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004222"},{"annotations":[69392,70708],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008235"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of peptide bonds by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidase activity","termid":"GO:0008233"}],"gene_count":55,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_00406":null,"SJAG_00451":null,"SJAG_00479":null,"SJAG_00546":null,"SJAG_00573":null,"SJAG_00662":null,"SJAG_00720":null,"SJAG_00730":null,"SJAG_00742":null,"SJAG_00762":null,"SJAG_00764":null,"SJAG_00795":null,"SJAG_00969":null,"SJAG_01004":null,"SJAG_01088":null,"SJAG_01179":null,"SJAG_01281":null,"SJAG_01312":null,"SJAG_01321":null,"SJAG_01430":null,"SJAG_01528":null,"SJAG_01542":null,"SJAG_01816":null,"SJAG_01838":null,"SJAG_01896":null,"SJAG_02033":null,"SJAG_02244":null,"SJAG_02341":null,"SJAG_02397":null,"SJAG_02419":null,"SJAG_02503":null,"SJAG_02809":null,"SJAG_02900":null,"SJAG_03009":null,"SJAG_03022":null,"SJAG_03147":null,"SJAG_03393":null,"SJAG_03396":null,"SJAG_03407":null,"SJAG_03429":null,"SJAG_03586":null,"SJAG_03648":null,"SJAG_03686":null,"SJAG_03744":null,"SJAG_03752":null,"SJAG_04103":null,"SJAG_04215":null,"SJAG_04497":null,"SJAG_04514":null,"SJAG_04533":null,"SJAG_04641":null,"SJAG_04651":null,"SJAG_04858":null,"SJAG_06636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0003674","GO:0008233","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"metallopeptidase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-3928660","Reactome:R-HSA-5211356","Reactome:R-HSA-8986181","Reactome:R-HSA-9759522","Reactome:R-HSA-193679","Reactome:R-HSA-2022393","Reactome:R-HSA-2220976","Reactome:R-HSA-2730752","Reactome:R-HSA-5211340","Reactome:R-HSA-5211387","Reactome:R-HSA-5211391","Reactome:R-HSA-5211400","Reactome:R-HSA-157629","Reactome:R-HSA-157632","Reactome:R-HSA-2022399","Reactome:R-HSA-2220944","Reactome:R-HSA-5211405","Reactome:R-HSA-9662837","Reactome:R-HSA-9013284","Reactome:R-HSA-9604264","Reactome:R-HSA-2666278","Reactome:R-HSA-2022368","Reactome:R-HSA-2022396"],"synonyms":[{"name":"metalloprotease activity","type":"narrow"},{"name":"metalloproteinase activity","type":"narrow"}],"termid":"GO:0008237","terms_by_termid":{"GO:0004181":null,"GO:0004222":null,"GO:0008235":null,"GO:0008237":null,"GO:0070006":null,"GO:0070573":null,"GO:0140492":null}}


id: PBO:0083638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eIF3j component of translation initiation factor 3 (eIF3); dual function protein involved in translation initiation as a substoichiometric component (eIF3j) of eIF3; required for 20S pre-rRNA processing; required at post-transcriptional step for efficient retrotransposition; absence decreases Ty1 Gag:GFP protein levels; binds eIF3 subunits Rpg1p, Prt1p and 18S rRNA; eIF3 also involved in programmed stop codon read through; human homolog EIF3J can complement yeast hcr1 mutant","termid":"PBO:0083638"}


id: GO:0009485
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: 4 ferrocytochrome c + O2 = 4 ferricytochrome c + 2 H2O.","definition_xrefs":["EC:1.9.3.1"],"gene_count":0,"genotype_count":0,"name":"obsolete cbb3-type cytochrome c oxidase (obsolete GO:0009485)","synonyms":[{"name":"cbb3-type cytochrome c oxidase","type":"exact"}],"termid":"GO:0009485"}


id: GO:0061071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the urethra epithelium over time from its initial formation to the mature structure. The urethra is a renal system organ that carries urine from the bladder to outside the body. The epithelium is the tubular, planar layer of cells through which the urine passes.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tube development","termid":"GO:0035295"},{"relation_name":"is_a","term_name":"epithelium development","termid":"GO:0060429"},{"relation_name":"part_of","term_name":"urethra development","termid":"GO:0061068"}],"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":"urethra epithelium development","termid":"GO:0061071"}


id: MONDO:0014295
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare, complex type of hereditary spastic paraplegia, characterized by onset in infancy of pronounced leg spasticity (leading to the inability to walk independently), reduced visual acuity due to optic atrophy, and distal wasting of the hands and feet due to an axonal demyelinating sensorimotor neuropathy. SPG57 is caused by mutations in the TFG gene (3q12.2) encoding protein TFG, which is thought to play a role in ER microtubular architecture and function.","definition_xrefs":["Orphanet:431329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 57","secondary_identifiers":["DOID:0110809","SCTID:723826007","OMIM:615658","GARD:17712","UMLS:C3714897","MEDGEN:811490"],"synonyms":[{"name":"SPG57","type":"exact"},{"name":"TFG hereditary spastic paraplegia","type":"exact"},{"name":"autosomal recessive spastic paraplegia 57","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 57","type":"exact"},{"name":"hereditary spastic paraplegia caused by mutation in TFG","type":"exact"},{"name":"hereditary spastic paraplegia type 57","type":"exact"},{"name":"spastic paraplegia 57, autosomal recessive","type":"related"},{"name":"spastic paraplegia due to partial TFG deficiency","type":"exact"}],"termid":"MONDO:0014295","xrefs":{"Monarch":{"xref_id":"0014295"}}}


