# terms

id: MONDO:0859363
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"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":"spastic paraplegia 79A, autosomal dominant, with ataxia","secondary_identifiers":["UMLS:C5774300","MEDGEN:1824073","DOID:0070455","OMIM:620221"],"termid":"MONDO:0859363","xrefs":{"Monarch":{"xref_id":"0859363"}}}


id: GO:0061337
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Transfer of an organized electrical impulse across the heart to coordinate the contraction of cardiac muscles. The process begins with generation of an action potential (in the sinoatrial node (SA) in humans) and ends with a change in the rate, frequency, or extent of the contraction of the heart muscles.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart contraction","termid":"GO:0008016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac conduction","secondary_identifiers":["Reactome:R-HSA-5576891"],"termid":"GO:0061337"}


id: PR:C6Y4D2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrp49 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4D2"],"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":"54S ribosomal protein MRP49, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1442.19","synonyms":[{"name":"Spom972h-mrp49","type":"exact"}],"termid":"PR:C6Y4D2"}


id: GO:0005272
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the energy-independent facilitated diffusion of a sodium ion through a transmembrane aqueous pore or channel.","definition_xrefs":["ISBN:0815340729","GOC:pr","GOC:mtg_transport","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic cation channel activity","termid":"GO:0005261"},{"relation_name":"is_a","term_name":"sodium ion transmembrane transporter activity","termid":"GO:0015081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"sodium channel activity","secondary_identifiers":["Reactome:R-HSA-9717396","Reactome:R-HSA-9717395","Reactome:R-HSA-2730664","Reactome:R-HSA-3295580","Reactome:R-HSA-9717374","Reactome:R-HSA-9717382"],"termid":"GO:0005272"}


id: GO:0042812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of pheromones, a substance that is secreted and released by an organism and detected by a second organism of the same or a closely related species, in which it causes a specific reaction, such as a definite behavioral reaction or a developmental process.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone catabolic process","termid":"GO:0042447"},{"relation_name":"is_a","term_name":"pheromone metabolic process","termid":"GO:0042810"},{"relation_name":"is_a","term_name":"cellular catabolic process","termid":"GO:0044248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044248"],"is_obsolete":false,"name":"pheromone catabolic process","secondary_identifiers":["GO:0007327","GO:0046614"],"synonyms":[{"name":"pheromone breakdown","type":"exact"},{"name":"pheromone catabolism","type":"exact"},{"name":"pheromone degradation","type":"exact"}],"termid":"GO:0042812"}


id: MONDO:0016254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare variants of adenocarcinoma of the corpus uteri (obsolete MONDO:0016254)","secondary_identifiers":["Orphanet:213574"],"termid":"MONDO:0016254","xrefs":{"Monarch":{"xref_id":"0016254"}}}


id: GO:0055113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of one cell sheet over other cells involved in deuterostomic gastrulation.","definition_xrefs":["ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"is_a","term_name":"epiboly","termid":"GO:0090504"},{"relation_name":"part_of","term_name":"gastrulation with mouth forming second","termid":"GO:0001702"}],"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":"epiboly involved in gastrulation with mouth forming second","termid":"GO:0055113"}


id: PBO:0035983
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_phosphorylation_during_vegetative_growth","termid":"PBO:0035983"}


id: PBO:0026917
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_18S_rRNA_acetylation","termid":"PBO:0026917"}


id: PBO:0072931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small Cajal body-specific RNA 11","termid":"PBO:0072931"}


id: MONDO:0013199
data:
  {"annotated_genes":["SJAG_05346","SJAG_00289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86426,86427],"is_not":false,"summary":null,"term":"MONDO:0013199"}]},"cv_name":"mondo","definition":"Tuberous sclerosis mapped to chromosome 16p13.3 (TSC2 gene).","definition_xrefs":["NCIT:C75331"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete tuberous sclerosis complex (obsolete MONDO:0019341)","termid":"MONDO:0019341"},{"relation_name":"is_a","term_name":"tuberous sclerosis","termid":"MONDO:0001734"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00289":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"tuberous sclerosis 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:15640","DOID:0080325","MESH:C566021","OMIM:613254","UMLS:C1860707","MEDGEN:348170"],"synonyms":[{"name":"TSC2","type":"related"},{"name":"TSC2 Angiomyolipomas, renal, modifier of","type":"related"},{"name":"tuberous sclerosis 2","type":"exact"},{"name":"tuberous sclerosis type 2","type":"exact"},{"name":"tuberous sclerosis, type 2","type":"related"},{"name":"tuberous sclerosis-2","type":"exact"}],"termid":"MONDO:0013199","terms_by_termid":{"MONDO:0013199":null},"xrefs":{"Monarch":{"xref_id":"0013199"}}}


id: PR:Q10201
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- npg1 gene.","definition_xrefs":["UniProtKB:Q10201","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 C17D1.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17D1.07c","synonyms":[{"name":"Spom972h-npg1","type":"exact"}],"termid":"PR:Q10201"}


id: GO:0006667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving sphinganine, D-erythro-2-amino-1,3-octadecanediol.","definition_xrefs":["PMID:29165427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diol metabolic process","termid":"GO:0034311"},{"relation_name":"is_a","term_name":"sphingoid metabolic process","termid":"GO:0046519"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"sphinganine metabolic process","synonyms":[{"name":"dihydrosphingosine metabolic process","type":"exact"},{"name":"dihydrosphingosine metabolism","type":"exact"},{"name":"sphinganine metabolism","type":"exact"}],"termid":"GO:0006667"}


id: MONDO:0023579
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":"Kuster Majewski Hammerstein syndrome","secondary_identifiers":["UMLS:C2931740","MEDGEN:444132","MESH:C538125"],"synonyms":[{"name":"alopecia macular degeneration growth retardation","type":"related"},{"name":"alopecia, macular degeneration, and growth retardation","type":"related"}],"termid":"MONDO:0023579","xrefs":{"Monarch":{"xref_id":"0023579"}}}


id: GO:0035240
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to dopamine, a catecholamine neurotransmitter formed by aromatic-L-amino-acid decarboxylase from 3,4-dihydroxy-L-phenylalanine.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"},{"relation_name":"is_a","term_name":"catecholamine binding","termid":"GO:1901338"}],"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:0005488","GO:0003674"],"is_obsolete":false,"name":"dopamine binding","termid":"GO:0035240"}


id: SO:0000083
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"DNA belonging to the macronuclei of ciliates.","direct_ancestors":[{"relation_name":"is_a","term_name":"organelle_sequence","termid":"SO:0000736"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macronuclear_sequence","synonyms":[{"name":"macronuclear sequence","type":"exact"}],"termid":"SO:0000083"}


id: GO:0046163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of heme C, a derivative of heme found in cytochromes c, b4, and f.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme catabolic process","termid":"GO:0042167"},{"relation_name":"is_a","term_name":"heme C metabolic process","termid":"GO:0046162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"heme C catabolic process","synonyms":[{"name":"haem C catabolic process","type":"exact"},{"name":"haem C catabolism","type":"exact"},{"name":"heme C breakdown","type":"exact"},{"name":"heme C catabolism","type":"exact"},{"name":"heme C degradation","type":"exact"}],"termid":"GO:0046163"}


id: GO:0010359
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of anion channel activity.","definition_xrefs":["PMID:17319842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of monoatomic ion transmembrane transporter activity","termid":"GO:0032412"},{"relation_name":"is_a","term_name":"regulation of monoatomic anion transmembrane transport","termid":"GO:1903959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"regulation of anion channel activity","termid":"GO:0010359"}


id: GO:0003400
data:
  {"annotated_genes":["SJAG_00906","SJAG_04615"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71242,76185],"is_not":false,"summary":null,"term":"GO:0003400"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of the addition of COPII proteins and adaptor proteins to ER membranes during the formation of transport vesicles, forming a vesicle coat.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb","GOC:jp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle organization","termid":"GO:0033043"},{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"regulates","term_name":"COPII vesicle coating","termid":"GO:0048208"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00906":null,"SJAG_04615":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of COPII vesicle coating","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0003400","terms_by_termid":{"GO:0003400":null}}


id: PBO:0113245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein that binds the rDNA replication fork barrier site; required for replication fork blocking and recombinational hotspot activity that results in concerted evolution of the rDNA, termed homogenization; role in recruitment of condensin to the replication fork barrier (RFB), contributing to the faithful segregation of rDNA repeats; proposed role in recovery from low rDNA copy number; related to retroviral integrases","termid":"PBO:0113245"}


id: MONDO:0017303
data:
  {"annotated_genes":["SJAG_04887","SJAG_03145","SJAG_03025","SJAG_03379"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85252],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008070"},{"annotations":[85300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800341"},{"annotations":[85126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012239"},{"annotations":[86685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009725"},{"annotations":[85830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012538"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"}],"gene_count":4,"genes_by_uniquename":{"SJAG_03025":null,"SJAG_03145":null,"SJAG_03379":null,"SJAG_04887":null},"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of tropomyosin","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:284790","UMLS:C5681012","MEDGEN:1842978","GARD:21123"],"termid":"MONDO:0017303","terms_by_termid":{"MONDO:0008070":null,"MONDO:0009725":null,"MONDO:0012239":null,"MONDO:0012538":null,"MONDO:0800341":null},"xrefs":{"Monarch":{"xref_id":"0017303"}}}


id: FYPO:0000046
data:
  {"alleles_by_uniquename":{"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_00409:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00409","name":"gpd1delta","uniquename":"SJAG_00409:allele-1"},"SJAG_00514:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00514","name":"scd1delta","uniquename":"SJAG_00514:allele-1"},"SJAG_01794:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01794","name":"scd2delta","uniquename":"SJAG_01794:allele-1"},"SJAG_01946:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01946","name":"cem1delta","uniquename":"SJAG_01946: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_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_03198:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03198","name":"oar2delta","uniquename":"SJAG_03198:allele-1"},"SJAG_03198:allele-2":{"allele_type":"amino_acid_mutation","description":"Y189D cold sensitive","gene_uniquename":"SJAG_03198","name":"oar2-51","uniquename":"SJAG_03198:allele-2"},"SJAG_03198:allele-3":{"allele_type":"amino_acid_mutation","description":"R72A,L75A,R106A,L109A","gene_uniquename":"SJAG_03198","name":"oar2-dm12","synonyms":[{"name":"destruction box mutations","reference":"PMID:23786411","type":"exact"}],"uniquename":"SJAG_03198:allele-3"},"SJAG_03453:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03453","name":"ras1delta","uniquename":"SJAG_03453:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"},"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"},"SJAG_04703:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04703","name":"for3delta","uniquename":"SJAG_04703:allele-1"},"SJAG_05207:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_05207","name":"cmp7delta","uniquename":"SJAG_05207:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119385,119397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004481"},{"annotations":[119339,119126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000082"},{"annotations":[119308,119322,119194,119306,119307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000080"},{"annotations":[119495,119149,119499,119503,119547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001355"},{"annotations":[119594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001408"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which cell population growth is decreased relative to normal. Decreased growth may reflect a reduced growth rate (i.e. slower growth), growth that occurs to a lesser extent than normal, or both. Cell population growth refers to an increase in the number of cells in the population as individual cells grow and divide.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell population growth","termid":"FYPO:0000045"},{"relation_name":"is_a","term_name":"viable cell population","termid":"FYPO:0002058"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_00409":null,"SJAG_00514":null,"SJAG_01794":null,"SJAG_01946":null,"SJAG_02527":null,"SJAG_02592":null,"SJAG_03198":null,"SJAG_03453":null,"SJAG_04464":null,"SJAG_04697":null,"SJAG_04703":null,"SJAG_05207":null},"genotype_count":15,"genotypes_by_uniquename":{"atf1delta":{"display_name":"atf1delta","display_uniquename":"atf1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00266:allele-1","expression":"Null"}]}]},"cem1delta":{"display_name":"cem1delta","display_uniquename":"cem1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01946:allele-1","expression":"Null"}]}]},"cmp7delta":{"display_name":"cmp7delta","display_uniquename":"cmp7delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]}]},"for3delta":{"display_name":"for3delta","display_uniquename":"for3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04703:allele-1","expression":"Null"}]}]},"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]},"gpd1delta":{"display_name":"gpd1delta","display_uniquename":"gpd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00409: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"}]}]},"oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression":{"display_name":"oar2-51(Y189D cold sensitive)[Overexpression]","display_uniquename":"oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-2","expression":"Overexpression"}]}]},"oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression":{"display_name":"oar2-dm12(R72A,L75A,R106A,L109A aa)[Overexpression]","display_uniquename":"oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-3","expression":"Overexpression"}]}]},"oar2delta":{"display_name":"oar2delta","display_uniquename":"oar2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03198:allele-1","expression":"Null"}]}]},"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]},"ras1delta":{"display_name":"ras1delta","display_uniquename":"ras1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03453:allele-1","expression":"Null"}]}]},"scd1delta":{"display_name":"scd1delta","display_uniquename":"scd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00514:allele-1","expression":"Null"}]}]},"scd2delta":{"display_name":"scd2delta","display_uniquename":"scd2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01794:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002058","FYPO:0001985","FYPO:0002057","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"decreased cell population growth","references_by_uniquename":{"PMID:23786411":null,"PMID:28954740":null,"PMID:29566183":null,"PMID:30726171":null,"PMID:31150379":null,"PMID:32243490":null,"PMID:36058798":null,"PMID:37164017":null,"PMID:37233261":null},"secondary_identifiers":["FYPO:0000222"],"single_locus_annotated_genes":["SJAG_04703","SJAG_03453","SJAG_05207","SJAG_00514","SJAG_00409","SJAG_04697","SJAG_02592","SJAG_03198","SJAG_01946","SJAG_02527","SJAG_01794","SJAG_04464","SJAG_00266"],"single_locus_genotype_uniquenames":["cem1delta","atf1delta","oar2delta","pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","cmp7delta","oar2-51-Y189D_cold_sensitive-amino_acid_mutation-expression-overexpression","gms1delta","lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","scd1delta","ras1delta","for3delta","gpd1delta","sty1delta","scd2delta","oar2-dm12-R72A,L75A,R106A,L109A-amino_acid_mutation-expression-overexpression"],"synonyms":[{"name":"aerobic growth defects","type":"related"},{"name":"decreased aerobic cell population growth","type":"narrow"},{"name":"decreased growth","type":"broad"},{"name":"reduced aerobic cell population growth","type":"narrow"},{"name":"reduced cell population growth","type":"exact"},{"name":"slow aerobic cell population growth","type":"narrow"}],"termid":"FYPO:0000046","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000006":null,"FYECO:0000117":null,"FYECO:0000137":null,"FYPO:0000080":null,"FYPO:0000082":null,"FYPO:0001355":null,"FYPO:0001408":null,"FYPO:0004481":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: FYPO:0006265
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 vacuoles are larger than normal after a cell has been subjected to hypotonic osmotic stress. Normally, vacuoles enlarge during hypotonic stress, and return to the original smaller size when the stress is relieved, either due to shrinking or fission.","definition_xrefs":["PomBase:mah","PMID:28944093"],"direct_ancestors":[{"relation_name":"is_a","term_name":"large vacuoles during vegetative growth","termid":"FYPO:0000123"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"large vacuoles present following cellular hypotonic response","synonyms":[{"name":"enlarged vacuoles present following cellular hypotonic response","type":"exact"},{"name":"large vacuoles large vacuoles present following cellular hypotonic response during mitotic cell cycle","type":"related"},{"name":"large vacuoles present during recovery from cellular hypotonic response","type":"exact"},{"name":"large vacuoles present following cellular hypotonic response during vegetative growth","type":"exact"},{"name":"large vacuoles present following hypotonic stress","type":"exact"}],"termid":"FYPO:0006265"}


id: PR:O42912
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tad1 gene.","definition_xrefs":["UniProtKB:O42912","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":"tRNA-specific adenosine deaminase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16A3.06","synonyms":[{"name":"Spom972h-tad1","type":"exact"},{"name":"tRNA-specific adenosine-37 deaminase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42912"}


id: PBO:0085214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Palmitoylated plasma membrane-bound casein kinase I (CK1) isoform; shares redundant functions with Yck2p in morphogenesis, proper septin assembly, endocytic trafficking, and glucose sensing; stabilized by Sod1p binding in the presence of glucose and oxygen, causing glucose repression of respiratory metabolism; involved in the phosphorylation and regulation of glucose sensor Rgt2p; YCK1 has a paralog, YCK2, that arose from the whole genome duplication","termid":"PBO:0085214"}


id: PBO:0062857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otopetrin 2","termid":"PBO:0062857"}


id: PBO:0045165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal intermediate chain 7","termid":"PBO:0045165"}


id: MONDO:0010899
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNA4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sleep-related hypermotor epilepsy","termid":"MONDO:0000030"},{"relation_name":"is_a","term_name":"autosomal dominant nocturnal frontal lobe epilepsy","termid":"MONDO:0020300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"autosomal dominant nocturnal frontal lobe epilepsy 1","secondary_identifiers":["DOID:0060682","GARD:15319","MEDGEN:324932","MESH:C563930","OMIM:600513","UMLS:C1838049"],"synonyms":[{"name":"CHRNA4 autosomal dominant nocturnal frontal lobe epilepsy","type":"exact"},{"name":"ENFL1","type":"exact"},{"name":"autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA4","type":"exact"},{"name":"autosomal dominant nocturnal frontal lobe epilepsy type 1","type":"exact"},{"name":"epilepsy, nocturnal frontal lobe, 1","type":"related"},{"name":"epilepsy, nocturnal frontal lobe, type 1","type":"exact"},{"name":"nocturnal frontal lobe epilepsy 1","type":"exact"}],"termid":"MONDO:0010899","xrefs":{"Monarch":{"xref_id":"0010899"}}}


id: PBO:0089996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrolipoamide S-succinyltransferase, e2 component of oxoglutarate dehydrogenase complex Kdg2","termid":"PBO:0089996"}


id: GO:0034019
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reactions: violaxanthin = capsorubin, and antheraxanthin = capsanthin.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete capsanthin/capsorubin synthase activity (obsolete GO:0034019)","synonyms":[{"name":"capsanthin/capsorubin synthase activity","type":"exact"}],"termid":"GO:0034019"}


id: PBO:0109464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TENM3 antisense transcript 2","termid":"PBO:0109464"}


id: MONDO:0006301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, well-circumscribed renal cortical neoplasm affecting females more often than males. Polycythemia has been reported in twelve-percent of patients.","definition_xrefs":["NCIT:C27253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal adenoma","termid":"MONDO:0002395"}],"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":"metanephric adenoma","secondary_identifiers":["MEDGEN:266093","UMLS:C1266045","ICDO:8325/0","EFO:1000373","DOID:6404","ICDO:8191/0"],"synonyms":[{"name":"metanephric adenoma","type":"exact"},{"name":"metanephric adenoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0006301","xrefs":{"Monarch":{"xref_id":"0006301"}}}


id: PBO:0000365
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally represses fio1","termid":"PBO:0000365"}


id: PR:O14367
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gti1 gene.","definition_xrefs":["UniProtKB:O14367","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":"gluconate transport inducer 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1751.01c","synonyms":[{"name":"Spom972h-gti1","type":"exact"}],"termid":"PR:O14367"}


id: PBO:0085638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in inserting tail-anchored proteins into ER membranes; forms a complex with Get4p; required for efficient mating; involved in shmoo formation and nuclear migration in the pre-zygote; associates with ribosomes","termid":"PBO:0085638"}


id: FYPO_EXT:1000002
data:
  {"annotation_feature_type":"gene","cv_name":"fypo_extensions","definition":"FYPO extension ontology grouping term for relations relevant to penetrance","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"FYPO extension","termid":"FYPO_EXT:1000000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FYPO penetrance extension","termid":"FYPO_EXT:1000002"}


id: PBO:0085413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane sterol transporter of the ATP-binding cassette family; required, along with Pdr11p, for uptake of exogenous sterols and their incorporation into the plasma membrane; activity is stimulated by phosphatidylserine; sterol uptake is required for anaerobic growth because sterol biosynthesis requires oxygen; AUS1 has a paralog, PDR11, that arose from the whole genome duplication","termid":"PBO:0085413"}


id: PBO:0069721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1001, pseudogene","termid":"PBO:0069721"}


id: PBO:0065457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit ubiquitin receptor, non-ATPase 4","termid":"PBO:0065457"}


id: PBO:0000615
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thiosulfate sulfurtransferase, URM1 activating enzyme (predicted)","termid":"PBO:0000615"}


id: PATO:0001263
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of yellow hue and low brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"yellow","termid":"PATO:0000324"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dark yellow","termid":"PATO:0001263"}


id: GO:0010718
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of epithelial to mesenchymal transition. Epithelial to mesenchymal transition is where an epithelial cell loses apical/basolateral polarity, severs intercellular adhesive junctions, degrades basement membrane components and becomes a migratory mesenchymal cell.","definition_xrefs":["GOC:tb","GOC:dph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial to mesenchymal transition","termid":"GO:0010717"},{"relation_name":"is_a","term_name":"positive regulation of cell differentiation","termid":"GO:0045597"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"epithelial to mesenchymal transition","termid":"GO:0001837"}],"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 epithelial to mesenchymal transition","termid":"GO:0010718"}


id: PBO:0044631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"doublecortin like kinase 2","termid":"PBO:0044631"}


id: PR:Q9P7U7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fub2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7U7"],"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 P4G3.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP4G3.03","synonyms":[{"name":"Spom972h-fub2","type":"exact"}],"termid":"PR:Q9P7U7"}


id: MONDO:0020336
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant form of Emery-Dreifuss muscular dystrophy.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"Emery-Dreifuss muscular dystrophy","termid":"MONDO:0016830"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005336","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant Emery-Dreifuss muscular dystrophy","secondary_identifiers":["GARD:16865","Orphanet:98853"],"synonyms":[{"name":"EDMD2","type":"narrow"},{"name":"Emery-Dreifuss muscular dystrophy, autosomal dominant","type":"exact"},{"name":"autosomal dominant Emery-Dreifuss muscular dystrophy","type":"exact"}],"termid":"MONDO:0020336","xrefs":{"Monarch":{"xref_id":"0020336"}}}


id: PBO:0109023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPRASP3 pseudogene 1","termid":"PBO:0109023"}


id: PBO:0082065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-ketosphinganine reductase; catalyzes the second step in phytosphingosine synthesis; essential for growth in the absence of exogenous dihydrosphingosine or phytosphingosine; localized to lipid droplets; member of short chain dehydrogenase/reductase protein family; mutations in human homolog KDSR cause recessive progressive symmetric erythrokeratoderma","termid":"PBO:0082065"}


id: PBO:0030415
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_spindle_pole_body_duplication","termid":"PBO:0030415"}


id: PBO:0058036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4257","termid":"PBO:0058036"}


id: GO:0102922
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (3R)-3-amino-3-phenylpropanoyl-CoA + baccatin III = 3'-N-debenzoyl-2'-deoxytaxol + CoA.","definition_xrefs":["RHEA:42488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"phenylpropanoyltransferase activity","secondary_identifiers":["MetaCyc:RXN-8857"],"termid":"GO:0102922"}


id: PBO:0085383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane ATP-binding cassette (ABC) transporter; required for the export of a-factor, catalyzes ATP hydrolysis coupled to a-factor transport; contains 12 transmembrane domains and two ATP binding domains; expressed only in MATa cells; human homolog ABCB1 mediates multidrug resistance in many chemotherapy-resistant tumors by effluxing toxic compounds from the cell","termid":"PBO:0085383"}


id: PBO:0083486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene VPH2","termid":"PBO:0083486"}


id: PBO:0031253
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_regulation_of_cytokinesis","termid":"PBO:0031253"}


id: PBO:0005788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudogene wtf element Wtf24","termid":"PBO:0005788"}


id: PBO:0039299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG13 UDP-N-acetylglucosaminyltransferase subunit","termid":"PBO:0039299"}


id: GO:0009098
data:
  {"annotated_genes":["SJAG_03985","SJAG_03562","SJAG_03243","SJAG_04149","SJAG_02841","SJAG_04098","SJAG_06635"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59240,74604,77056,79924,90649,103298,113274],"is_not":false,"summary":null,"term":"GO:0009098"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-leucine, 2-amino-4-methylpentanoic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-leucine metabolic process","termid":"GO:0006551"},{"relation_name":"is_a","term_name":"pyruvate family amino acid biosynthetic process","termid":"GO:0009079"},{"relation_name":"is_a","term_name":"branched-chain amino acid biosynthetic process","termid":"GO:0009082"}],"gene_count":7,"genes_by_uniquename":{"SJAG_02841":null,"SJAG_03243":null,"SJAG_03562":null,"SJAG_03985":null,"SJAG_04098":null,"SJAG_04149":null,"SJAG_06635":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"L-leucine biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:LEUSYN-PWY"],"synonyms":[{"name":"L-leucine anabolism","type":"exact"},{"name":"L-leucine biosynthesis","type":"exact"},{"name":"L-leucine formation","type":"exact"},{"name":"L-leucine synthesis","type":"exact"},{"name":"leucine biosynthetic process","type":"broad"}],"termid":"GO:0009098","terms_by_termid":{"GO:0009098":null}}


id: PBO:0048014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FERM and PDZ domain containing 2B, pseudogene","termid":"PBO:0048014"}


id: PBO:0046074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EIF3M pseudogene 1","termid":"PBO:0046074"}


id: PR:O36017
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lip2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O36017"],"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":"octanoyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F10.05c","synonyms":[{"name":"Spom972h-lip2","type":"exact"},{"name":"lipoate biosynthesis protein (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"lipoate-protein ligase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"lipoyl ligase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"lipoyl/octanoyl transferase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"octanoyl-[acyl-carrier-protein]-protein N-octanoyltransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O36017"}


id: PBO:0051577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17 receptor A","termid":"PBO:0051577"}


id: GO:0071504
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 heparin stimulus.","definition_xrefs":["GOC:mah","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to heparin","termid":"GO:0071503"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"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 heparin","termid":"GO:0071504"}


id: PBO:0072054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 24","termid":"PBO:0072054"}


id: PBO:0077752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target of myb1 like 2 membrane trafficking protein","termid":"PBO:0077752"}


id: PBO:0068286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease H2 subunit C","termid":"PBO:0068286"}


id: GO:2001036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of tongue muscle cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of skeletal muscle fiber differentiation","termid":"GO:1902810"},{"relation_name":"is_a","term_name":"regulation of tongue muscle cell differentiation","termid":"GO:2001035"},{"relation_name":"negatively_regulates","term_name":"tongue muscle cell differentiation","termid":"GO:0035981"}],"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 tongue muscle cell differentiation","termid":"GO:2001036"}


id: PBO:0034319
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-represses_expression_of","termid":"PBO:0034319"}


id: GO:0016191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of the protein coat on a synaptic vesicle following the pinching step at the end of budding from the presynaptic membrane.","definition_xrefs":["PMID:24596248","GOC:curators","PMID:10099709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin coat disassembly","termid":"GO:0072318"},{"relation_name":"part_of","term_name":"synaptic vesicle endocytosis","termid":"GO:0048488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"synaptic vesicle uncoating","synonyms":[{"name":"synaptic vesicle coat depolymerization","type":"exact"},{"name":"synaptic vesicle coat protein depolymerization","type":"exact"}],"termid":"GO:0016191"}


id: PBO:0068233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 18S ribosomal 4","termid":"PBO:0068233"}


id: PBO:0051610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 34","termid":"PBO:0051610"}


id: GO:0031763
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a galanin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide receptor binding","termid":"GO:0071855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"galanin receptor binding","synonyms":[{"name":"galanin receptor ligand","type":"narrow"}],"termid":"GO:0031763"}


id: MONDO:0007165
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spastic ataxia with congenital miosis is a rare hereditary ataxia characterized by an apparently non-progressive or slowly progressive symmetrical ataxia of gait, pyramidal signs in the limbs, spasticity and hyperreflexia (especially in the lower limbs) together with dysarthria and impaired pupillary reaction to light, presenting as a fixed miosis (with pupils that seldom exceed 2 mm in diameter and dilate poorly with mydriatics). Nystagmus may also be present.","definition_xrefs":["Orphanet:1182"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant spastic ataxia","termid":"MONDO:0017846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"spastic ataxia 7","secondary_identifiers":["DOID:0050945","ICD10CM:G11.4","GARD:16560","MEDGEN:354750","MESH:C566247","OMIM:108650","SCTID:763669001","UMLS:C1862441"],"synonyms":[{"name":"SPAX7","type":"exact"},{"name":"autosomal dominant spastic ataxia type 7","type":"exact"},{"name":"miosis, congenital, with spastic ataxia","type":"related"},{"name":"spastic ataxia 7, autosomal dominant","type":"related"},{"name":"spastic ataxia type 7","type":"exact"},{"name":"spastic ataxia with congenital miosis","type":"related"}],"termid":"MONDO:0007165","xrefs":{"Monarch":{"xref_id":"0007165"}}}


id: PBO:0087162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit C11; mediates pol III RNA cleavage activity and is important for termination of transcription; homologous to TFIIS","termid":"PBO:0087162"}


id: MONDO:0011695
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"uveal melanoma","termid":"MONDO:0006486"},{"relation_name":"is_a","term_name":"susceptibility to uveal melanoma","termid":"MONDO:0007966"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanoma, uveal, susceptibility to, 1","secondary_identifiers":["MEDGEN:376198","OMIM:606660","UMLS:C1847724"],"synonyms":[{"name":"UVM1","type":"exact"},{"name":"melanoma, uveal, susceptibility to, 1","type":"exact"},{"name":"melanoma, uveal, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0011695","xrefs":{"Monarch":{"xref_id":"0011695"}}}


id: PBO:0025453
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast cancer","termid":"PBO:0025453"}


id: GO:0005997
data:
  {"annotated_genes":["SJAG_04276"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005998"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving xylulose, the ketopentose threo-2-pentulose.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentose metabolic process","termid":"GO:0019321"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04276":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0005975","GO:0008150"],"is_obsolete":false,"name":"xylulose metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"xylulose metabolism","type":"exact"}],"termid":"GO:0005997","terms_by_termid":{"GO:0005998":null}}


id: MONDO:0015993
data:
  {"annotated_genes":["SJAG_04225","SJAG_01897"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014372"},{"annotations":[85051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014669"}]},"cv_name":"mondo","definition":"Inherited retinal dystrophies that belong to the group of pigmentary retinopathies.","definition_xrefs":["Orphanet:1872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01897":null,"SJAG_04225":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cone-rod dystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D000071700","OMIMPS:120970","MEDGEN:896366","NANDO:1200937","GARD:10790","UMLS:C4085590","DOID:0050572","ICD10CM:H35.5"],"synonyms":[{"name":"CRD","type":"exact"},{"name":"cone rod dystrophy","type":"related"},{"name":"cone-rod retinal dystrophy","type":"exact"}],"termid":"MONDO:0015993","terms_by_termid":{"MONDO:0014372":null,"MONDO:0014669":null},"xrefs":{"Monarch":{"xref_id":"0015993"}}}


id: MONDO:0019228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of histidine metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"inborn disorder of amino acid and other organic acid metabolism","termid":"MONDO:0019189"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid metabolism","termid":"MONDO:0004736"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid and other organic acid metabolism","termid":"MONDO:0019189"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"inborn disorder of histidine metabolism","secondary_identifiers":["MEDGEN:541342","Orphanet:79181","GARD:18959","ICD10CM:E70.40","SCTID:44176004","UMLS:C0268512","icd11.foundation:543162269","DOID:9265","ICD9:270.5"],"synonyms":[{"name":"disorder of histidine metabolic process","type":"exact"},{"name":"disorder of histidine metabolism","type":"exact"},{"name":"disturbance of histidine metabolism","type":"exact"},{"name":"histidine metabolic process disease","type":"exact"},{"name":"histidine metabolism disease","type":"exact"},{"name":"inborn disorder of histidine metabolism","type":"exact"},{"name":"inborn error of histidine metabolic process","type":"exact"},{"name":"inborn error of histidine metabolism","type":"exact"},{"name":"inborn histidine metabolic process disorder","type":"exact"},{"name":"rare inborn error of histidine metabolic process","type":"exact"}],"termid":"MONDO:0019228","xrefs":{"Monarch":{"xref_id":"0019228"}}}


id: PBO:0084225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hsp70 (Ssa1p) nucleotide exchange factor; required for the release of misfolded proteins from the Hsp70 system to the Ub-proteasome machinery for degradation; cytosolic homolog of Sil1p, which is the nucleotide exchange factor for BiP (Kar2p) in the endoplasmic reticulum; protein abundance increases in response to DNA replication stress","termid":"PBO:0084225"}


id: PBO:0041316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 69 pseudogene 2","termid":"PBO:0041316"}


id: PBO:0017967
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked intellectual disability","termid":"PBO:0017967"}


id: PBO:0001185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosidase II Gls2","termid":"PBO:0001185"}


id: GO:0097040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phthiocerol, a lipid-based 1,3-glycol consisting of (3S,4R)-3-methoxy-4-methylnonacosane having (9R)- and (11S)-hydroxy substituents.","definition_xrefs":["GOC:ecd","PMID:9201977","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid biosynthetic process","termid":"GO:0008610"},{"relation_name":"is_a","term_name":"glycol biosynthetic process","termid":"GO:0042845"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"phthiocerol biosynthetic process","synonyms":[{"name":"phthiocerol anabolism","type":"exact"},{"name":"phthiocerol biosynthesis","type":"exact"},{"name":"phthiocerol formation","type":"exact"},{"name":"phthiocerol synthesis","type":"exact"}],"termid":"GO:0097040"}


id: MONDO:0003411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangiopericytoma arising from the breast.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"breast sarcoma","termid":"MONDO:0002490"},{"relation_name":"is_a","term_name":"hemangiopericytoma","termid":"MONDO:0005094"},{"relation_name":"is_a","term_name":"breast neoplasm","termid":"MONDO:0021100"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast hemangiopericytoma","secondary_identifiers":["UMLS:C1511313","MEDGEN:267766","NCIT:C40396","DOID:5370"],"synonyms":[{"name":"breast hemangiopericytoma","type":"exact"},{"name":"breast spindle cell tumor","type":"exact"},{"name":"breast spindle cell tumour","type":"exact"}],"termid":"MONDO:0003411","xrefs":{"Monarch":{"xref_id":"0003411"}}}


id: PBO:0000843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RCC domain protein Ats1 (predicted)","termid":"PBO:0000843"}


id: GO:0042992
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of the movement of a transcription factor from the cytoplasm to the nucleus.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transcription factor import into nucleus (obsolete GO:0042992)","synonyms":[{"name":"down regulation of transcription factor import into nucleus","type":"exact"},{"name":"down-regulation of transcription factor import into nucleus","type":"exact"},{"name":"downregulation of transcription factor import into nucleus","type":"exact"},{"name":"inhibition of transcription factor import into nucleus","type":"narrow"},{"name":"negative regulation of transcription factor import into cell nucleus","type":"exact"},{"name":"negative regulation of transcription factor transport from cytoplasm to nucleus","type":"exact"},{"name":"negative regulation of transcription factor-nucleus import","type":"exact"}],"termid":"GO:0042992"}


id: PBO:0113495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation elongation factor 3; contains two ABC cassettes; binds and hydrolyzes ATP; interacts with mRNA independently of translation; involved in frameshifting at stalled ribosomes; YEF3 has a paralog, HEF3, that arose from the whole genome duplication","termid":"PBO:0113495"}


id: GO:0060303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the number of nucleosomes in a given region of a chromosome.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of nucleosome density (obsolete GO:0060303)","termid":"GO:0060303"}


id: PBO:0062959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(A) binding protein cytoplasmic 1 pseudogene 2","termid":"PBO:0062959"}


id: PBO:0046674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESX homeobox 1","termid":"PBO:0046674"}


id: FYPO:0007793
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which an increase in RNA level that occurs as part of a cellular response to oxidative stress begins later than normal. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah","PMID:10428959"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to oxidative stress during vegetative growth","termid":"FYPO:0001340"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of increase in RNA level during cellular response to oxidative stress","synonyms":[{"name":"delayed increase in RNA level during cellular response to oxidative stress","type":"exact"},{"name":"delayed onset of increase in RNA level during cellular response to oxidative stress during mitotic cell cycle","type":"related"},{"name":"delayed onset of increase in RNA level during cellular response to oxidative stress during vegetative growth","type":"exact"},{"name":"delayed onset of increase in RNA level in response to oxidative stress","type":"exact"},{"name":"delayed onset of increase in transcript level during cellular response to oxidative stress","type":"exact"}],"termid":"FYPO:0007793"}


id: PBO:0001478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"up-frameshift suppressor 3 family protein (predicted)","termid":"PBO:0001478"}


id: PR:O94691
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- jmj3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94691"],"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":"lid2 complex component jmj3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC83.07","synonyms":[{"name":"Lid2C component jmj3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-jmj3","type":"exact"}],"termid":"PR:O94691"}


id: PBO:0046782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EYA2 antisense RNA 1","termid":"PBO:0046782"}


id: GO:1902363
data:
  {"annotated_genes":["SJAG_00883"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902543"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to spindle pole body.","definition_xrefs":["PMID:21131906","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization","termid":"GO:0032880"},{"relation_name":"regulates","term_name":"protein localization to spindle pole body","termid":"GO:0071988"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00883":null},"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 spindle pole body","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of protein localisation to spindle pole body","type":"exact"}],"termid":"GO:1902363","terms_by_termid":{"GO:1902543":null}}


id: GO:0072350
data:
  {"annotated_genes":["SJAG_01922","SJAG_04362","SJAG_04577"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000053"},{"annotations":[62276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006101"},{"annotations":[73748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006102"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving dicarboxylic acids, any organic acid containing three carboxyl (COOH) groups or anions (COO-).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01922":null,"SJAG_04362":null,"SJAG_04577":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"tricarboxylic acid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"tricarboxylic acid metabolism","type":"exact"}],"termid":"GO:0072350","terms_by_termid":{"GO:0000053":null,"GO:0006101":null,"GO:0006102":null}}


id: CHEBI:27641
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":"cycloheximide","termid":"CHEBI:27641"}


id: GO:0000221
data:
  {"annotated_genes":["SJAG_04955","SJAG_01817","SJAG_01397","SJAG_00136","SJAG_04015","SJAG_01471","SJAG_00212","SJAG_01447"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[60538,71000,87989,96591,98911,102674,109885,118754],"is_not":false,"summary":null,"term":"GO:0000221"}]},"cv_name":"cellular_component","definition":"The V1 domain of a proton-transporting V-type ATPase found in the vacuolar membrane.","definition_xrefs":["GOC:mah","PMID:16449553"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton-transporting V-type ATPase, V1 domain","termid":"GO:0033180"},{"relation_name":"part_of","term_name":"vacuolar proton-transporting V-type ATPase complex","termid":"GO:0016471"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00136":null,"SJAG_00212":null,"SJAG_01397":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01817":null,"SJAG_04015":null,"SJAG_04955":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005773","GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"vacuolar proton-transporting V-type ATPase, V1 domain","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"vacuolar hydrogen ion-transporting ATPase V1 domain","type":"exact"}],"termid":"GO:0000221","terms_by_termid":{"GO:0000221":null}}


id: PBO:0000735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin binding protein, coronin Crn1","termid":"PBO:0000735"}


id: PBO:0028695
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_transcription_termination","termid":"PBO:0028695"}


id: GO:0072763
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 hesperadin stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amine stimulus","termid":"GO:0071418"},{"relation_name":"is_a","term_name":"response to hesperadin","termid":"GO:1901595"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"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 hesperadin","termid":"GO:0072763"}


id: PBO:0039157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate kinase 4 pseudogene 4","termid":"PBO:0039157"}


id: PBO:0065769
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"quinoid dihydropteridine reductase","termid":"PBO:0065769"}


id: PBO:0076179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 2B member 1","termid":"PBO:0076179"}


id: PBO:0060383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myelin transcription factor 1","termid":"PBO:0060383"}


id: FYPO:0005482
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of an inositol phosphate phosphatase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phosphatase activity","termid":"FYPO:0004302"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000652","FYPO:0000707","FYPO:0000654"],"is_obsolete":false,"name":"abnormal inositol phosphate phosphatase activity","termid":"FYPO:0005482"}


id: GO:0010129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of cyclohexane-1-carboxylate, a alicyclic acid, in the absence of oxygen.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"}],"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":"anaerobic cyclohexane-1-carboxylate catabolic process","secondary_identifiers":["MetaCyc:PWY-301"],"synonyms":[{"name":"anaerobic cyclohexane-1-carboxylate breakdown","type":"exact"},{"name":"anaerobic cyclohexane-1-carboxylate catabolism","type":"exact"},{"name":"anaerobic cyclohexane-1-carboxylate degradation","type":"exact"}],"termid":"GO:0010129"}


id: MONDO:0001316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infectious meningitis caused by infection with Streptococcus.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial meningitis","termid":"MONDO:0006670"},{"relation_name":"is_a","term_name":"streptococcal infection","termid":"MONDO:0021680"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"streptococcal meningitis","secondary_identifiers":["DOID:11574","ICD9:320.2","ICD10CM:G00.2","SCTID:4510004","UMLS:C0154639","MEDGEN:509616"],"synonyms":[{"name":"Streptococcus caused infectious meningitis","type":"exact"},{"name":"Streptococcus infectious meningitis","type":"exact"}],"termid":"MONDO:0001316","xrefs":{"Monarch":{"xref_id":"0001316"}}}


id: PBO:0072173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S16","termid":"PBO:0072173"}


id: SO:0002298
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An operon whose transcription is coordinated on a single transcription unit.","definition_xrefs":["Bacterial_regulation_working_group:CMA","PMID:32665585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"operon","termid":"SO:0000178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"simple_operon","synonyms":[{"name":"simple operon","type":"exact"}],"termid":"SO:0002298"}


id: PBO:0073821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 7 member 1","termid":"PBO:0073821"}


id: MONDO:0971064
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":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orofacial clefting-cardiac anomalies-facial dysmorphism syndrome","secondary_identifiers":["UMLS:C5925125","MEDGEN:1864391","Orphanet:660021"],"termid":"MONDO:0971064","xrefs":{"Monarch":{"xref_id":"0971064"}}}


id: PBO:0089359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent polydeoxyribonucleotide 5'-hydroxyl-kinase activity implicated in DNA repair","termid":"PBO:0089359"}


id: GO:0070326
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a very-low-density lipoprotein receptor.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle receptor binding","termid":"GO:0070325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"very-low-density lipoprotein particle receptor binding","synonyms":[{"name":"VLDL receptor binding","type":"exact"},{"name":"VLDLR binding","type":"exact"},{"name":"apolipoprotein E receptor binding","type":"related"},{"name":"very-low-density lipoprotein receptor binding","type":"exact"}],"termid":"GO:0070326"}


id: MONDO:0100039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A monogenic disease that has material basis in mutation in the CDKL5 gene.","definition_xrefs":["PMID:27528505","PMID:21154482","PMID:22872100","PMID:27080038"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"pervasive developmental disorder","termid":"MONDO:0000594"},{"relation_name":"excluded_subClassOf","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"relation_name":"excluded_subClassOf","term_name":"obsolete motor stereotypies (obsolete MONDO:0017656)","termid":"MONDO:0017656"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDKL5 disorder","secondary_identifiers":["NORD:904"],"synonyms":[{"name":"CDKL5","type":"related"},{"name":"CDKL5 Deficiency Disorder","type":"exact"},{"name":"CDKL5 disorder","type":"exact"},{"name":"CDKL5 inherited genetic disease","type":"exact"},{"name":"CDKL5-related disorder","type":"related"},{"name":"inherited genetic disease caused by mutation in CDKL5","type":"exact"}],"termid":"MONDO:0100039","xrefs":{"Monarch":{"xref_id":"0100039"}}}


id: MONDO:0021378
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the endocardium.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocardium disorder","termid":"MONDO:0000470"},{"relation_name":"is_a","term_name":"heart neoplasm","termid":"MONDO:0021209"}],"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":"neoplasm of endocardium","secondary_identifiers":["MEDGEN:220938","NCIT:C5346","SCTID:126731002","UMLS:C1290401","ICD9:239.89"],"synonyms":[{"name":"endocardial neoplasm","type":"exact"},{"name":"endocardial tumor","type":"exact"},{"name":"endocardial tumour","type":"exact"},{"name":"endocardium neoplasm","type":"exact"},{"name":"endocardium neoplasm (disease)","type":"exact"},{"name":"endocardium tumor","type":"exact"},{"name":"endocardium tumour","type":"exact"},{"name":"neoplasm of endocardium","type":"exact"},{"name":"neoplasm of the endocardium","type":"exact"},{"name":"tumor of endocardium","type":"exact"},{"name":"tumor of the endocardium","type":"exact"},{"name":"tumour of endocardium","type":"exact"},{"name":"tumour of the endocardium","type":"exact"}],"termid":"MONDO:0021378","xrefs":{"Monarch":{"xref_id":"0021378"}}}


id: MONDO:0054850
data:
  {"annotated_genes":["SJAG_04148"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86360],"is_not":false,"summary":null,"term":"MONDO:0054850"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46 XX gonadal dysgenesis","termid":"MONDO:0009299"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04148":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"ovarian dysgenesis 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618078","UMLS:C4748084","MEDGEN:1648307","DOID:0080498","GARD:18042"],"synonyms":[{"name":"ODG6","type":"related"},{"name":"ovarian dysgenesis 6","type":"exact"}],"termid":"MONDO:0054850","terms_by_termid":{"MONDO:0054850":null},"xrefs":{"Monarch":{"xref_id":"0054850"}}}


id: MONDO:0016335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial disease with dilated cardiomyopathy (obsolete MONDO:0016335)","secondary_identifiers":["Orphanet:217613"],"termid":"MONDO:0016335","xrefs":{"Monarch":{"xref_id":"0016335"}}}


id: PR:P79009
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps2502 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P79009"],"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":"40S ribosomal protein S25-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC694.05c","synonyms":[{"name":"S31-A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rps2502","type":"exact"}],"termid":"PR:P79009"}


id: GO:0009316
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric enzyme complex composed of subunits leuC and leuD. Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate.","definition_xrefs":["MetaCyc:3-ISOPROPYLMALISOM-CPLX","GOC:jl","PMID:7026530"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"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:0005737"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005829","GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"3-isopropylmalate dehydratase complex","synonyms":[{"name":"isopropylmalate isomerase complex","type":"exact"}],"termid":"GO:0009316"}


id: GO:0072494
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A late endosome in which regions of the limiting host cell endosomal membrane invaginate to form internal vesicles; host membrane proteins that enter the internal vesicles are sequestered from the host cytoplasm.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell late endosome","termid":"GO:0044184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host multivesicular body","synonyms":[{"name":"host cell multivesicular body","type":"exact"}],"termid":"GO:0072494"}


id: PBO:0060061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 8","termid":"PBO:0060061"}


id: PBO:0071859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 54","termid":"PBO:0071859"}


id: PBO:0049471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"granzyme A pseudogene 1","termid":"PBO:0049471"}


id: PBO:0036045
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_threonine_phosphorylation_at_Thr-Pro_site_during_vegetative_growth","termid":"PBO:0036045"}


id: GO:0033154
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + oligogalacturonide(out) = ADP + phosphate + oligogalacturonide(in).","definition_xrefs":["PMID:11555291","GOC:mlg","PMID:17451747"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ABC-type oligosaccharide transporter activity","termid":"GO:0015422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"ABC-type oligogalacturonide transporter activity","secondary_identifiers":["GO:0033155","TC:3.A.1.1.11"],"synonyms":[{"name":"ATP-dependent oligogalacturonide transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled oligogalacturonide transmembrane transporter activity","type":"related"},{"name":"oligogalacturonide transmembrane transporter activity","type":"narrow"},{"name":"oligogalacturonide transporting ATPase activity","type":"related"},{"name":"oligogalacturonide-transporting ATPase activity","type":"exact"}],"termid":"GO:0033154"}


id: PBO:0001513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic spindle checkpoint protein Dma1","termid":"PBO:0001513"}


id: PBO:0071541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35a pseudogene 6","termid":"PBO:0071541"}


id: GO:1900994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (-)-secologanin.","definition_xrefs":["GOC:TermGenie","PMID:24104568","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoterpenoid biosynthetic process","termid":"GO:0016099"},{"relation_name":"is_a","term_name":"aldehyde biosynthetic process","termid":"GO:0046184"},{"relation_name":"is_a","term_name":"olefinic compound biosynthetic process","termid":"GO:0120255"},{"relation_name":"is_a","term_name":"beta-glucoside biosynthetic process","termid":"GO:1901806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"(-)-secologanin biosynthetic process","synonyms":[{"name":"(-)-secologanin anabolism","type":"exact"},{"name":"(-)-secologanin biosynthesis","type":"exact"},{"name":"(-)-secologanin formation","type":"exact"},{"name":"(-)-secologanin synthesis","type":"exact"}],"termid":"GO:1900994"}


id: PBO:0016566
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe Unidentified Cyclin","termid":"PBO:0016566"}


id: MONDO:0007163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Episodic ataxia type 2 (EA2) is the most frequent form of Hereditary episodic ataxia (EA) characterized by paroxysmal episodes of ataxia lasting hours, with interictal nystagmus and mildly progressive ataxia.","definition_xrefs":["Orphanet:97"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary episodic ataxia","termid":"MONDO:0016227"},{"relation_name":"is_a","term_name":"CACNA1A-related complex neurodevelopmental disorder","termid":"MONDO:0100254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"episodic ataxia type 2","secondary_identifiers":["MEDGEN:314039","GARD:9602","SCTID:420932006","DOID:0050990","UMLS:C1720416","MESH:C535506","OMIM:108500"],"synonyms":[{"name":"APCA","type":"related"},{"name":"Acetazolamide-responsive episodic ataxia syndrome","type":"related"},{"name":"Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia","type":"related"},{"name":"Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia","type":"related"},{"name":"CACNA1A hereditary episodic ataxia","type":"exact"},{"name":"CAPA","type":"related"},{"name":"Cerebellopathy, hereditary paroxysmal","type":"related"},{"name":"EA2","type":"related"},{"name":"Nystagmus-associated episodic ataxia","type":"related"},{"name":"ataxia, episodic, with Nystagmus","type":"related"},{"name":"ataxia, familial paroxysmal","type":"related"},{"name":"ataxia, familial, paroxysmal","type":"related"},{"name":"cerebellar ataxia, paroxysmal, Acetazolamide-responsive","type":"related"},{"name":"episodic ataxia type 2","type":"exact"},{"name":"episodic ataxia with nystagmus","type":"related"},{"name":"episodic ataxia, Nystagmus-associated","type":"related"},{"name":"episodic ataxia, type 2","type":"related"},{"name":"familial paroxysmal ataxia","type":"related"},{"name":"hereditary episodic ataxia caused by mutation in CACNA1A","type":"exact"}],"termid":"MONDO:0007163","xrefs":{"Monarch":{"xref_id":"0007163"}}}


id: MONDO:0043237
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Painful sensations in the tongue, including a sensation of burning.","definition_xrefs":["MESH:D005926"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tongue disorder","termid":"MONDO:0001165"},{"relation_name":"is_a","term_name":"neurological pain disorder","termid":"MONDO:0700057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glossodynia","secondary_identifiers":["SCTID:30731004","UMLS:C0017672","icd11.foundation:1755751917","MEDGEN:6617"],"synonyms":[{"name":"Glossalgias","type":"related"},{"name":"Glossodynias","type":"related"},{"name":"Glossopyroses","type":"related"},{"name":"glossalgia","type":"related"},{"name":"glossodynia","type":"exact"},{"name":"glossopyrosis","type":"related"},{"name":"painful tongue","type":"related"},{"name":"soreness of tongue","type":"related"}],"termid":"MONDO:0043237","xrefs":{"Monarch":{"xref_id":"0043237"}}}


id: FYPO:0001532
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle phenotype in which the duration of S phase of the mitotic cell cycle is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic S phase progression","termid":"FYPO:0003246"}],"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:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal duration of mitotic S phase","termid":"FYPO:0001532"}


id: PBO:0056826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAX dimerization protein MGA","termid":"PBO:0056826"}


id: PR:Q09789
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC13G6.13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09789"],"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 C13G6.13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G6.13","synonyms":[{"name":"Spom972h-SPAC13G6.13","type":"exact"}],"termid":"PR:Q09789"}


id: PBO:0060657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"natural cytotoxicity triggering receptor 1","termid":"PBO:0060657"}


id: GO:0008113
data:
  {"annotated_genes":["SJAG_00419"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[60657],"is_not":false,"summary":null,"term":"GO:0008113"}]},"cv_name":"molecular_function","definition":"Catalysis of the reactions: peptide-L-methionine + thioredoxin disulfide + H2O = peptide-L-methionine (S)-S-oxide + thioredoxin, and L-methionine + thioredoxin disulfide + H2O = L-methionine (S)-S-oxide + thioredoxin. Can act on oxidized methionine in peptide linkage with specificity for the S enantiomer. Thioredoxin disulfide is the oxidized form of thioredoxin.","definition_xrefs":["GOC:vw","GOC:mah","PMID:11169920","EC:1.8.4.11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00419":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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"peptide-methionine (S)-S-oxide reductase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["GO:0072561","Reactome:R-HSA-1222363","GO:0033742","MetaCyc:RXN-8668","Reactome:R-HSA-5676940","RHEA:14217"],"synonyms":[{"name":"MsrA","type":"related"},{"name":"methionine S-oxide reductase (S-form oxidizing) activity","type":"related"},{"name":"methionine S-oxide reductase activity","type":"broad"},{"name":"methionine sulfoxide (protein) reductase activity","type":"exact"},{"name":"methionine sulfoxide reductase A activity","type":"related"},{"name":"methionine sulfoxide reductase activity","type":"broad"},{"name":"methionine sulphoxide reductase A activity","type":"related"},{"name":"peptide Met(O) reductase activity","type":"related"},{"name":"peptide methionine sulfoxide reductase activity","type":"related"},{"name":"peptide-L-methionine:thioredoxin-disulfide S-oxidoreductase [L-methionine (S)-S-oxide-forming] activity","type":"related"},{"name":"peptide-methionine-(S)-S-oxide reductase activity","type":"exact"},{"name":"protein-methionine-S-oxide reductase activity","type":"exact"}],"termid":"GO:0008113","terms_by_termid":{"GO:0008113":null}}


id: PBO:0017430
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-assayed_substrate","termid":"PBO:0017430"}


id: GO:1900584
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of o-orsellinic acid.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"},{"relation_name":"is_a","term_name":"o-orsellinic acid metabolic process","termid":"GO:1900582"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"o-orsellinic acid biosynthetic process","synonyms":[{"name":"o-orsellinic acid anabolism","type":"exact"},{"name":"o-orsellinic acid biosynthesis","type":"exact"},{"name":"o-orsellinic acid formation","type":"exact"},{"name":"o-orsellinic acid synthesis","type":"exact"}],"termid":"GO:1900584"}


id: PBO:0040666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BBX high mobility group box domain containing","termid":"PBO:0040666"}


id: GO:1901025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of ripoptosome components leading to apoptosis via the extrinsic apoptotic signaling pathway.","definition_xrefs":["GOC:mtg_apoptosis","GOC:TermGenie","PMID:22274400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ripoptosome assembly","termid":"GO:0097343"},{"relation_name":"part_of","term_name":"extrinsic apoptotic signaling pathway","termid":"GO:0097191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"ripoptosome assembly involved in extrinsic apoptotic signaling pathway","termid":"GO:1901025"}


id: PBO:0086428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative high affinity iron transporter; involved in transport of intravacuolar stores of iron; forms complex with Fet5p; expression is regulated by iron; proposed to play indirect role in endocytosis; protein abundance increases in response to DNA replication stress","termid":"PBO:0086428"}


id: PBO:0047023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A26","termid":"PBO:0047023"}


id: MONDO:0010346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MRX52 (obsolete MONDO:0010346)","secondary_identifiers":["OMIM:300504"],"termid":"MONDO:0010346","xrefs":{"Monarch":{"xref_id":"0010346"}}}


id: GO:0060345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of creating a trabecula in the spleen. A trabecula is a tissue element in the form of a small beam, strut or rod.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trabecula formation","termid":"GO:0060343"},{"relation_name":"part_of","term_name":"spleen development","termid":"GO:0048536"}],"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":"spleen trabecula formation","synonyms":[{"name":"spleen trabecula biogenesis","type":"related"},{"name":"spleen trabeculation","type":"exact"}],"termid":"GO:0060345"}


id: MONDO:0012552
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors.","definition_xrefs":["Orphanet:276152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"multiple endocrine neoplasia","termid":"MONDO:0017169"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"multiple endocrine neoplasia type 4","secondary_identifiers":["SCTID:715907003","NCIT:C157449","GARD:17275","OMIM:610755","MEDGEN:373469","MESH:C567059","DOID:0080137","UMLS:C1970712","icd11.foundation:157945677"],"synonyms":[{"name":"CDKN1B multiple endocrine neoplasia","type":"exact"},{"name":"MEN4","type":"exact"},{"name":"multiple endocrine neoplasia caused by mutation in CDKN1B","type":"exact"},{"name":"multiple endocrine neoplasia type 4","type":"exact"},{"name":"multiple endocrine neoplasia, type 4","type":"related"},{"name":"multiple endocrine neoplasia, type IV","type":"exact"}],"termid":"MONDO:0012552","xrefs":{"Monarch":{"xref_id":"0012552"}}}


id: MONDO:0003018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete myotonic disease (obsolete MONDO:0003018)","termid":"MONDO:0003018","xrefs":{"Monarch":{"xref_id":"0003018"}}}


id: GO:0048823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a nucleate erythrocyte over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"erythrocyte development","termid":"GO:0048821"},{"relation_name":"part_of","term_name":"nucleate erythrocyte differentiation","termid":"GO:0043363"}],"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":"nucleate erythrocyte development","synonyms":[{"name":"nucleate RBC development","type":"exact"},{"name":"nucleate red blood cell development","type":"exact"}],"termid":"GO:0048823"}


id: MONDO:1012013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"arthritis deformans, non-human animal","termid":"MONDO:1011936"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arthritis deformans, pig","secondary_identifiers":["OMIA:000065-9823"],"termid":"MONDO:1012013","xrefs":{"Monarch":{"xref_id":"1012013"}}}


id: GO:0071544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a diphosphoinositol polyphosphate, 1,2,3,4,5,6-cyclohexanehexol with one or more diphosphate groups and multiple monophosphate groups attached.","definition_xrefs":["GOC:mah","PMID:12387729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diphosphoinositol polyphosphate metabolic process","termid":"GO:0071543"},{"relation_name":"is_a","term_name":"inositol phosphate catabolic process","termid":"GO:0071545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"diphosphoinositol polyphosphate catabolic process","synonyms":[{"name":"diphosphoinositol polyphosphate breakdown","type":"exact"},{"name":"diphosphoinositol polyphosphate catabolism","type":"exact"},{"name":"diphosphoinositol polyphosphate degradation","type":"exact"}],"termid":"GO:0071544"}


id: PBO:0034353
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_postdisplacement_relationship_with","termid":"PBO:0034353"}


id: GO:0010743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of macrophage derived foam cell differentiation. Macrophage derived foam cell differentiation is the process in which a macrophage acquires the specialized features of a foam cell. A foam cell is a type of cell containing lipids in small vacuoles and typically seen in atherosclerotic lesions, as well as other conditions.","definition_xrefs":["GOC:add","GOC:tb","GOC:dph","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"regulates","term_name":"macrophage derived foam cell differentiation","termid":"GO:0010742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of macrophage derived foam cell differentiation","termid":"GO:0010743"}


id: GO:0060214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of the endocardium of the heart. The endocardium is an anatomical structure comprised of an endothelium and an extracellular matrix that forms the innermost layer of tissue of the heart, and lines the heart chambers.","definition_xrefs":["PMID:17722983","GOC:dph","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"endocardium morphogenesis","termid":"GO:0003160"}],"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":"endocardium formation","termid":"GO:0060214"}


id: MONDO:0007750
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypercholesterolemia","termid":"MONDO:0005439"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"hypercholesterolemia, familial, 1","secondary_identifiers":["OMIM:143890","MEDGEN:152875","NANDO:2200602","SCTID:398036000","UMLS:C0745103"],"synonyms":[{"name":"FHC","type":"related"},{"name":"FHCL1","type":"exact"},{"name":"LDL cholesterol level QTL2","type":"exact"},{"name":"LDL receptor disorder","type":"exact"},{"name":"hyper-low-density-lipoproteinemia","type":"related"},{"name":"hypercholesterolemia, familial","type":"exact"},{"name":"hypercholesterolemia, familial, 1","type":"exact"},{"name":"hypercholesterolemia, familial, due to ldlr defect, modifier of","type":"exact"},{"name":"hypercholesterolemia, familial, modifier of","type":"exact"},{"name":"hypercholesterolemia, susceptibility to","type":"related"},{"name":"hypercholesterolemic xanthomatosis, familial","type":"exact"},{"name":"hyperlipoproteinemia, type 2","type":"exact"},{"name":"hyperlipoproteinemia, type 2A","type":"exact"},{"name":"low density lipoprotein cholesterol level quantitative trait locus 2","type":"related"}],"termid":"MONDO:0007750","xrefs":{"Monarch":{"xref_id":"0007750"}}}


id: GO:0052512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The increase by an organism of the levels of hormones or growth regulators in the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of hormone or growth regulator levels in symbiont (obsolete GO:0052512)","synonyms":[{"name":"positive modulation of hormone or growth regulator levels in symbiont","type":"exact"},{"name":"positive regulation by organism of hormone or growth regulator levels in symbiont","type":"exact"}],"termid":"GO:0052512"}


id: MONDO:1010199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Muscular dystrophy, Duchenne type that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy, non-human animal","termid":"MONDO:0024965"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular dystrophy, Duchenne type, non-human animal","secondary_identifiers":["OMIA:001081"],"termid":"MONDO:1010199","xrefs":{"Monarch":{"xref_id":"1010199"}}}


id: PBO:0006194
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-requires_regulation_by","termid":"PBO:0006194"}


id: PBO:0030592
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_vacuolar_ornithine_level","termid":"PBO:0030592"}


id: PBO:0045240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C19 pseudogene 8","termid":"PBO:0045240"}


id: PBO:0075136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide A","termid":"PBO:0075136"}


id: PBO:0091934
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNase P cleavage specificity not affected by sequences flanking the G+1 cleavage site","termid":"PBO:0091934"}


id: PBO:0028731
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_hercynylselenocysteine_level_during_vegetative_growth","termid":"PBO:0028731"}


id: GO:0001305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that results in changes in chromatin structure contributing to chronological cell aging, occurring in non-dividing cells.","definition_xrefs":["GOC:tb","GOC:jh","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete progressive alteration of chromatin involved in chronological cell aging (obsolete GO:0001305)","synonyms":[{"name":"progressive alteration of chromatin during chronological cell ageing","type":"related"},{"name":"progressive alteration of chromatin during chronological cell aging","type":"related"}],"termid":"GO:0001305"}


id: GO:0050484
data:
  {"annotated_genes":["SJAG_01055"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[117206],"is_not":false,"summary":null,"term":"GO:0050484"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5'-GMP + H2O = guanosine + phosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5'-nucleotidase activity","termid":"GO:0008253"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01055":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"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:0016788","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"GMP 5'-nucleotidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:RXN-7609","RHEA:27714"],"synonyms":[{"name":"GMP 5' nucleotidase activity","type":"exact"},{"name":"IMP-GMP specific 5'-nucleotidase activity","type":"related"}],"termid":"GO:0050484","terms_by_termid":{"GO:0050484":null}}


id: PBO:0051460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 8/OR8-1 (pseudogene)","termid":"PBO:0051460"}


id: MONDO:0010282
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mycobacterium tuberculosis, susceptibility","termid":"MONDO:0000070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mycobacterium tuberculosis, susceptibility to, X-linked","secondary_identifiers":["UMLS:C1866629","OMIM:300259","MEDGEN:357096"],"synonyms":[{"name":"MTBSX","type":"related"},{"name":"Mycobacterium tuberculosis, susceptibility, X-linked","type":"exact"}],"termid":"MONDO:0010282","xrefs":{"Monarch":{"xref_id":"0010282"}}}


id: PBO:0005723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin Nup186","termid":"PBO:0005723"}


id: GO:0045270
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. One of two stalks that connect the catalytic core of the hydrogen-transporting ATP synthase to the plasma membrane-associated Fo proteins; rotates within the catalytic core during catalysis. Examples of this component are found in Bacterial species.","definition_xrefs":["PMID:10838056","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete plasma membrane proton-transporting ATP synthase, central stalk (obsolete GO:0045270)","synonyms":[{"name":"hydrogen-transporting ATP synthase, central stalk","type":"broad"},{"name":"proton-transporting ATP synthase, central stalk","type":"broad"}],"termid":"GO:0045270"}


id: PBO:0071645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36 pseudogene 9","termid":"PBO:0071645"}


id: FYPO:0003292
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 UDP-galactose transmembrane transport is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal UDP-galactose transmembrane transport","synonyms":[{"name":"abnormal UDP-galactose transmembrane transport during mitotic cell cycle","type":"related"},{"name":"abnormal UDP-galactose transmembrane transport during vegetative growth","type":"exact"}],"termid":"FYPO:0003292"}


id: MONDO:0025102
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diseases of Old World and New World monkeys. This term includes diseases of baboons but not of chimpanzees or gorillas (= ape diseases).","definition_xrefs":["MESH:D008992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human primate disease","termid":"MONDO:0025013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monkey disease","synonyms":[{"name":"disease, monkey","type":"related"},{"name":"diseases, monkey","type":"related"},{"name":"monkey disease","type":"exact"}],"termid":"MONDO:0025102","xrefs":{"Monarch":{"xref_id":"0025102"}}}


id: PBO:0061483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuregulin 2","termid":"PBO:0061483"}


id: PBO:0047748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folliculin interacting protein 1","termid":"PBO:0047748"}


id: PBO:0066506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RFX3 divergent transcript","termid":"PBO:0066506"}


id: PBO:0029453
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_multiple_cell_divisions,_elongated_cell","termid":"PBO:0029453"}


id: PBO:0040634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BARX homeobox 1","termid":"PBO:0040634"}


id: PBO:0004172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA repair endonuclease Swi10","termid":"PBO:0004172"}


id: GO:0102876
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+)-marmesin + NADPH + H+ + O2 = psoralen + NADP + acetone + 2 H2O.","definition_xrefs":["EC:1.14.14.141"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"psoralen synthase (NADPH) activity","secondary_identifiers":["RHEA:19281","MetaCyc:RXN-8386"],"termid":"GO:0102876"}


id: GO:0090373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of the directed movement of glycerol into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:tb","GOC:dph","GOC:jh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transmembrane transport","termid":"GO:0034763"},{"relation_name":"is_a","term_name":"regulation of glycerol transport","termid":"GO:0090371"},{"relation_name":"negatively_regulates","term_name":"glycerol transmembrane transport","termid":"GO:0015793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"negative regulation of glycerol transport","termid":"GO:0090373"}


id: MONDO:0007036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic syndrome featuring connective tissue abnormalities. Clinical signs include brachycephaly, arachnodactyly, receding mandible and joint laxity at the hands and feet.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Achard syndrome","secondary_identifiers":["MESH:C536012","OMIM:100700","UMLS:C1332135","MEDGEN:272277","DOID:6686","NCIT:C35809"],"synonyms":[{"name":"Achard syndrome","type":"exact"},{"name":"arachnodactyly, receding lower jaw and joint laxity of hands/feet","type":"related"}],"termid":"MONDO:0007036","xrefs":{"Monarch":{"xref_id":"0007036"}}}


id: FYPO:0002573
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the number of sites at which the protein Ssb1 accumulates is greater than normal.","definition_xrefs":["PomBase:mah","PMID:22927644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased number of Ssb1 foci","synonyms":[{"name":"increased number of RPA foci","type":"exact"},{"name":"increased number of Rad11 foci","type":"exact"},{"name":"increased number of Rpa1 foci","type":"exact"},{"name":"increased number of Ssb1 foci during mitotic cell cycle","type":"related"},{"name":"increased number of Ssb1 foci during vegetative growth","type":"exact"}],"termid":"FYPO:0002573"}


id: GO:0032557
data:
  {"annotated_genes":["SJAG_02370","SJAG_03453","SJAG_02288"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87692,90817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002135"},{"annotations":[90823,91644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002134"}]},"cv_name":"molecular_function","definition":"Binding to a pyrimidine ribonucleotide, any compound consisting of a pyrimidine ribonucleoside that is esterified with (ortho)phosphate or an oligophosphate at any hydroxyl group on the ribose moiety.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleotide binding","termid":"GO:0019103"},{"relation_name":"is_a","term_name":"ribonucleotide binding","termid":"GO:0032553"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02288":null,"SJAG_02370":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"pyrimidine ribonucleotide binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0032557","terms_by_termid":{"GO:0002134":null,"GO:0002135":null}}


id: MONDO:0001348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Lyme disease (obsolete MONDO:0001348)","termid":"MONDO:0001348","xrefs":{"Monarch":{"xref_id":"0001348"}}}


id: PBO:0078140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 19","termid":"PBO:0078140"}


id: MONDO:0016225
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diagnosed when there are specific deficits in an individualbs ability to perceive or process information efficiently and accurately. This disorder first manifests during the years of formal schooling and is characterized by persistent and impairing difficulties with learning foundational academic skills in reading, writing, and/or math. The individualbs performance of the affected academic skills is well below average for age, or acceptable performance levels are achieved only with extraordinary effort. Specific learning disorder may occur in individuals identified as intellectually gifted and manifest only when the learning demands or assessment procedures (e.g., timed tests) pose barriers that cannot be overcome by their innate intelligence and compensatory strategies. For all individuals, specific learning disorder can produce lifelong impairments in activities dependent on the skills, including occupational performance. (from dsm-V)","definition_xrefs":["MESH:D000067559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"specific learning disability","secondary_identifiers":["MEDGEN:871302","Orphanet:211047","UMLS:C4025790"],"synonyms":[{"name":"specific learning difficulty","type":"exact"},{"name":"specific learning disorder","type":"exact"}],"termid":"MONDO:0016225","xrefs":{"Monarch":{"xref_id":"0016225"}}}


id: GO:0061310
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes involved in cardiac neural crest cell differentiation.","definition_xrefs":["GOC:mtg_heart","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete canonical Wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development (obsolete GO:0061310)","synonyms":[{"name":"canonical Wnt receptor signaling pathway involved in cardiac neural crest cell differentiation involved in heart development","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in cardiac neural crest cell differentiation involved in heart development","type":"exact"},{"name":"canonical Wnt-activated signaling pathway involved in cardiac neural crest cell differentiation involved in heart development","type":"exact"}],"termid":"GO:0061310"}


id: GO:0030116
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A growth factor that binds selectively and non-covalently to glial cell-derived neurotrophic factor receptors.","definition_xrefs":["GOC:vw","PMID:11476867"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor receptor binding","termid":"GO:0070851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"glial cell-derived neurotrophic factor receptor binding","synonyms":[{"name":"glial cell line-derived neurotrophic factor receptor binding","type":"related"},{"name":"glial cell line-derived neurotrophic factor receptor ligand","type":"narrow"}],"termid":"GO:0030116"}


id: GO:0032934
data:
  {"annotated_genes":["SJAG_02323","SJAG_01722","SJAG_00355","SJAG_00054","SJAG_01329","SJAG_03718","SJAG_02375","SJAG_01590","SJAG_01407","SJAG_04018"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62188,63763,77092,90386],"is_not":false,"summary":null,"term":"GO:0032934"},{"annotations":[108223,116249,70822,94220,111346,72100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008142"}]},"cv_name":"molecular_function","definition":"Binding to a sterol, a steroid containing a hydroxy group in the 3 position, closely related to cholestan-3-ol.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid binding","termid":"GO:0005496"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00054":null,"SJAG_00355":null,"SJAG_01329":null,"SJAG_01407":null,"SJAG_01590":null,"SJAG_01722":null,"SJAG_02323":null,"SJAG_02375":null,"SJAG_03718":null,"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0008289","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"sterol binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0005498"],"synonyms":[{"name":"sterol carrier activity","type":"related"}],"termid":"GO:0032934","terms_by_termid":{"GO:0008142":null,"GO:0032934":null}}


id: GO:0022619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a generative cell. The generative cell gives rise to the sperm cells in the male gametophyte.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"microgametogenesis","termid":"GO:0055046"}],"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":"generative cell differentiation","termid":"GO:0022619"}


id: GO:0051764
data:
  {"annotated_genes":["SJAG_04621"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89280],"is_not":false,"summary":null,"term":"GO:0051764"}]},"cv_name":"biological_process","definition":"The process in which two or more actin filaments are connected together by proteins that act as crosslinks between the filaments. The crosslinked filaments may be on the same or differing axes.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament organization","termid":"GO:0007015"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0030036","GO:0007010","GO:0008150"],"is_obsolete":false,"name":"actin crosslink formation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"actin bundling","type":"related"},{"name":"actin crosslinking","type":"exact"},{"name":"bridging actin filaments","type":"narrow"},{"name":"formation of actin crosslink","type":"exact"}],"termid":"GO:0051764","terms_by_termid":{"GO:0051764":null}}


id: PBO:0056496
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 1","termid":"PBO:0056496"}


id: PATO:0000319
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of green and blue hue.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color","termid":"PATO:0000014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyan","termid":"PATO:0000319"}


id: MONDO:0004114
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A highly aggressive carcinoma, histologically resembling small cell lung carcinoma. In most cases it is associated with carcinoma in situ.","definition_xrefs":["NCIT:C9461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"urinary bladder carcinoma","termid":"MONDO:0004986"}],"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":"urinary bladder small cell neuroendocrine carcinoma","secondary_identifiers":["EFO:1000129","DOID:7132","UMLS:C1332564","GARD:11923","MEDGEN:231950","Orphanet:284400","ONCOTREE:SCBC"],"synonyms":[{"name":"SCCB","type":"exact"},{"name":"bladder small cell neuroendocrine cancer","type":"exact"},{"name":"bladder small cell neuroendocrine carcinoma","type":"exact"},{"name":"poorly differentiated neuroendocrine carcinoma of the bladder","type":"exact"},{"name":"small cell bladder cancer","type":"exact"},{"name":"small cell bladder carcinoma","type":"exact"},{"name":"small cell carcinoma of the bladder","type":"related"},{"name":"small cell carcinoma of the urinary bladder","type":"exact"},{"name":"small cell carcinoma of urinary bladder","type":"exact"},{"name":"small cell neuroendocrine carcinoma of the urinary bladder","type":"exact"},{"name":"small cell neuroendocrine carcinoma of urinary bladder","type":"exact"},{"name":"small cell/neuroendocrine carcinoma of urinary bladder","type":"exact"},{"name":"urinary bladder small cell carcinoma","type":"exact"}],"termid":"MONDO:0004114","xrefs":{"Monarch":{"xref_id":"0004114"}}}


id: PBO:0069241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 496, pseudogene","termid":"PBO:0069241"}


id: GO:0030085
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A pigment protein complex that forms part of the photosystem II associated light-harvesting complex II; contains two proteins (usually about 28 and 27 kDa), and may contain a third; peripherally located relative to other LHC polypeptides.","definition_xrefs":["PMID:8825475"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chloroplast thylakoid membrane protein complex","termid":"GO:0098807"},{"relation_name":"part_of","term_name":"PSII associated light-harvesting complex II, peripheral complex","termid":"GO:0009656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"PSII associated light-harvesting complex II, peripheral complex, LHCIIb subcomplex","termid":"GO:0030085"}


id: MONDO:0011986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tropical pancreatitis is a rare pancreatic disease of juvenile onset occurring mainly in tropical developing countries and characterized by chronic non-alcoholic pancreatitis manifesting with abdominal pain, steatorrhea and fibrocalculous pancreatopathy. It is also commonly associated with the development of pancreatic calculi and pancreatic cancer at a much higher frequency than seen in ordinary chronic pancreatitis.","definition_xrefs":["Orphanet:103918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary chronic pancreatitis","termid":"MONDO:0008185"}],"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":"tropical pancreatitis","secondary_identifiers":["UMLS:C1842402","GARD:16946","SCTID:724540009","MESH:C564276","icd11.foundation:1645607956","MEDGEN:334069","OMIM:608189"],"synonyms":[{"name":"TCP","type":"exact"},{"name":"fibrocalculous pancreatic diabetes, susceptibility to","type":"related"},{"name":"tropical calcific chronic pancreatitis","type":"exact"},{"name":"tropical calcific pancreatitis","type":"related"}],"termid":"MONDO:0011986","xrefs":{"Monarch":{"xref_id":"0011986"}}}


id: GO:0010657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A form of programmed cell death induced by external or internal signals that trigger the activity of proteolytic caspases, whose actions dismantle a muscle cell and result in its death. A muscle cell is a mature contractile cell, commonly known as a myocyte, that forms one of three kinds of muscle.","definition_xrefs":["CL:0000187","GOC:dph","GOC:mtg_apoptosis","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"}],"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":"muscle cell apoptotic process","synonyms":[{"name":"muscle cell apoptosis","type":"narrow"}],"termid":"GO:0010657"}


id: GO:0034994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a microtubule organizing center attachment site. A microtubule organizing center attachment site is a region of the nuclear envelope to which a microtubule organizing center (MTOC) attaches.","definition_xrefs":["GOC:mah","PMID:18692466"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component organization","termid":"GO:0016043"},{"relation_name":"part_of","term_name":"nuclear envelope organization","termid":"GO:0006998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"microtubule organizing center attachment site organization","synonyms":[{"name":"MAS organization","type":"exact"},{"name":"MTOC attachment site organization","type":"exact"},{"name":"microtubule organising centre attachment site organisation","type":"related"}],"termid":"GO:0034994"}


id: PBO:0061274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADPH oxidase 5","termid":"PBO:0061274"}


id: MONDO:0013042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atypical hemolytic uremic syndrome with complement gene abnormality","termid":"MONDO:0035290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"atypical hemolytic-uremic syndrome with B factor anomaly","secondary_identifiers":["GARD:18554","OMIM:612924","Orphanet:93578","UMLS:C2752038","MEDGEN:416691"],"synonyms":[{"name":"AHUS4","type":"related"},{"name":"D-HUS with B factor anomaly","type":"exact"},{"name":"aHUS with B factor anomaly","type":"exact"},{"name":"aHUS, susceptibility to, 4","type":"related"},{"name":"aHUS4","type":"related"},{"name":"atypical HUS with B factor anomaly","type":"exact"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, 4","type":"related"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, type 4","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhea with B factor anomaly","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhoea with B factor anomaly","type":"exact"},{"name":"susceptibility to atypical hemolytic uremic syndrome 4","type":"related"}],"termid":"MONDO:0013042","xrefs":{"Monarch":{"xref_id":"0013042"}}}


id: PBO:0018248
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae SPO13","termid":"PBO:0018248"}


id: PBO:0048259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactokinase 1","termid":"PBO:0048259"}


id: MONDO:0010338
data:
  {"annotated_genes":["SJAG_02399"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86239],"is_not":false,"summary":null,"term":"MONDO:0010338"}]},"cv_name":"mondo","definition":"X-linked distal spinal muscular atrophy type 3 is a rare distal hereditary motor neuropathy characterized by slowly progressive atrophy and weakness of distal muscles of hands and feet with normal deep tendon reflexes or absent ankle reflexes and minimal or no sensory loss, sometimes mild proximal weakness in the legs and feet and hand deformities in males.","definition_xrefs":["Orphanet:139557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"spinal muscular atrophy","termid":"MONDO:0001516"},{"relation_name":"is_a","term_name":"distal hereditary motor neuropathy","termid":"MONDO:0018894"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02399":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005244"],"is_obsolete":false,"name":"X-linked distal spinal muscular atrophy type 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:766764008","MESH:C564506","OMIM:300489","GARD:16957","DOID:0111196","MEDGEN:335168","UMLS:C1845359"],"synonyms":[{"name":"ATP7A spinal muscular atrophy","type":"exact"},{"name":"ATP7A-related distal motor neuropathy","type":"exact"},{"name":"DSMAX","type":"exact"},{"name":"Dsmax","type":"related"},{"name":"SMAX3","type":"exact"},{"name":"X-linked dHMN type 3","type":"exact"},{"name":"X-linked dHMN3","type":"exact"},{"name":"X-linked dSMA type 3","type":"exact"},{"name":"X-linked dSMA3","type":"exact"},{"name":"X-linked distal hereditary motor neuropathy type 3","type":"exact"},{"name":"spinal muscular atrophy caused by mutation in ATP7A","type":"exact"},{"name":"spinal muscular atrophy, distal, X-linked 3","type":"related"},{"name":"spinal muscular atrophy, distal, X-linked 3, X-linked recessive","type":"exact"},{"name":"spinal muscular atrophy, distal, X-linked recessive","type":"related"},{"name":"spinal muscular atrophy, distal, X-linked type 3","type":"exact"}],"termid":"MONDO:0010338","terms_by_termid":{"MONDO:0010338":null},"xrefs":{"Monarch":{"xref_id":"0010338"}}}


id: PBO:0056093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LYN proto-oncogene, Src family tyrosine kinase","termid":"PBO:0056093"}


id: PBO:0087936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translational elongation factor EF-3; member of the ABC superfamily; stimulates EF-1 alpha-dependent binding of aminoacyl-tRNA by the ribosome; normally expressed in zinc deficient cells; HEF3 has a paralog, YEF3, that arose from the whole genome duplication","termid":"PBO:0087936"}


id: GO:0030906
data:
  {"annotated_genes":["SJAG_01039"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[68976],"is_not":false,"summary":null,"term":"GO:0030906"}]},"cv_name":"cellular_component","definition":"The trimeric subcomplex of the retromer, believed to be closely associated with the membrane. This trimeric complex is responsible for recognizing and binding to cargo molecules. The complex comprises three Vps proteins in both yeast and mammalian cells: Vps35p, Vps29p, and Vps26p in yeast, and VPS35, VPS29 and VPS26A or VPS26B in mammals.","definition_xrefs":["GOC:bf","PMID:11102511","PMID:26220253","PMID:9700157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"retromer complex","termid":"GO:0030904"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01039":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"retromer, cargo-selective complex","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"cargo-selective retromer subcomplex","type":"exact"},{"name":"retromer CSC","type":"exact"},{"name":"retromer complex, inner shell","type":"exact"},{"name":"retromer, CRC","type":"exact"},{"name":"retromer, cargo recognition complex","type":"exact"}],"termid":"GO:0030906","terms_by_termid":{"GO:0030906":null}}


id: PBO:0000936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-mobility group non-histone chromatin protein (predicted)","termid":"PBO:0000936"}


id: PBO:0112744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Telomerase Cajal body protein WRAP53 orthlog, Gnr1","termid":"PBO:0112744"}


id: GO:0050789
data:
  {"annotated_genes":["SJAG_04421","SJAG_03787","SJAG_03089","SJAG_00092","SJAG_03319","SJAG_03869","SJAG_03345","SJAG_04749","SJAG_01181","SJAG_03431","SJAG_03448","SJAG_04373","SJAG_03867","SJAG_02389","SJAG_03421","SJAG_04500","SJAG_01885","SJAG_01149","SJAG_02285","SJAG_02013","SJAG_00854","SJAG_01513","SJAG_02404","SJAG_03599","SJAG_02798","SJAG_00386","SJAG_04655","SJAG_03519","SJAG_02058","SJAG_02392","SJAG_00320","SJAG_04486","SJAG_01625","SJAG_03047","SJAG_03845","SJAG_04213","SJAG_00807","SJAG_01677","SJAG_04818","SJAG_06638","SJAG_02879","SJAG_01517","SJAG_03970","SJAG_00210","SJAG_00678","SJAG_00574","SJAG_04355","SJAG_04522","SJAG_05337","SJAG_02908","SJAG_02846","SJAG_03384","SJAG_02183","SJAG_05335","SJAG_04586","SJAG_03048","SJAG_03081","SJAG_02005","SJAG_00661","SJAG_01320","SJAG_02318","SJAG_04118","SJAG_01521","SJAG_06641","SJAG_04699","SJAG_00425","SJAG_03453","SJAG_01540","SJAG_01754","SJAG_02314","SJAG_01978","SJAG_03283","SJAG_02724","SJAG_00739","SJAG_00452","SJAG_02036","SJAG_03289","SJAG_02066","SJAG_00037","SJAG_00530","SJAG_01044","SJAG_05373","SJAG_03501","SJAG_04009","SJAG_01205","SJAG_04724","SJAG_00973","SJAG_01213","SJAG_02486","SJAG_00526","SJAG_02391","SJAG_03776","SJAG_02684","SJAG_02760","SJAG_00990","SJAG_02923","SJAG_03023","SJAG_03893","SJAG_01331","SJAG_03918","SJAG_03957","SJAG_01622","SJAG_03525","SJAG_01138","SJAG_00883","SJAG_00269","SJAG_00340","SJAG_03883","SJAG_05242","SJAG_03884","SJAG_02244","SJAG_04820","SJAG_03618","SJAG_02447","SJAG_01511","SJAG_02536","SJAG_03097","SJAG_01667","SJAG_00321","SJAG_02703","SJAG_05020","SJAG_03268","SJAG_03635","SJAG_01711","SJAG_03302","SJAG_01740","SJAG_04329","SJAG_00341","SJAG_00156","SJAG_00579","SJAG_05330","SJAG_01146","SJAG_02424","SJAG_02189","SJAG_03405","SJAG_01703","SJAG_04990","SJAG_02549","SJAG_00824","SJAG_03597","SJAG_03371","SJAG_03394","SJAG_03576","SJAG_01553","SJAG_01910","SJAG_01187","SJAG_01050","SJAG_03417","SJAG_03466","SJAG_01956","SJAG_00369","SJAG_01311","SJAG_05978","SJAG_01286","SJAG_04126","SJAG_03655","SJAG_05276","SJAG_02645","SJAG_00545","SJAG_05243","SJAG_03898","SJAG_03137","SJAG_02573","SJAG_04321","SJAG_02945","SJAG_03706","SJAG_03942","SJAG_05203","SJAG_02213","SJAG_03219","SJAG_01894","SJAG_04389","SJAG_02838","SJAG_00961","SJAG_01696","SJAG_00333","SJAG_00052","SJAG_03006","SJAG_02819","SJAG_04879","SJAG_04232","SJAG_02906","SJAG_02569","SJAG_04383","SJAG_03106","SJAG_04597","SJAG_04426","SJAG_04274","SJAG_02303","SJAG_02385","SJAG_04083","SJAG_00226","SJAG_05231","SJAG_01436","SJAG_03128","SJAG_01142","SJAG_02194","SJAG_04771","SJAG_01053","SJAG_01131","SJAG_04682","SJAG_00693","SJAG_01114","SJAG_01254","SJAG_03581","SJAG_01230","SJAG_02255","SJAG_02289","SJAG_04103","SJAG_05153","SJAG_04468","SJAG_00681","SJAG_03113","SJAG_00641","SJAG_03695","SJAG_02500","SJAG_01938","SJAG_01075","SJAG_01111","SJAG_03276","SJAG_02873","SJAG_02474","SJAG_03879","SJAG_01836","SJAG_05290","SJAG_01343","SJAG_03745","SJAG_00892","SJAG_01161","SJAG_06622","SJAG_03601","SJAG_02927","SJAG_01771","SJAG_00244","SJAG_02481","SJAG_03383","SJAG_00756","SJAG_02756","SJAG_04462","SJAG_00247","SJAG_00216","SJAG_01386","SJAG_02439","SJAG_05247","SJAG_01008","SJAG_03799","SJAG_05192","SJAG_03709","SJAG_03591","SJAG_04613","SJAG_01993","SJAG_04712","SJAG_04825","SJAG_02326","SJAG_04200","SJAG_03070","SJAG_04350","SJAG_03366","SJAG_04705","SJAG_03705","SJAG_03548","SJAG_03033","SJAG_04198","SJAG_02258","SJAG_02860","SJAG_02419","SJAG_07011","SJAG_02149","SJAG_00875","SJAG_04671","SJAG_00027","SJAG_00045","SJAG_01901","SJAG_03841","SJAG_03828","SJAG_01403","SJAG_04552","SJAG_02381","SJAG_01768","SJAG_02736","SJAG_04194","SJAG_03557","SJAG_00845","SJAG_02342","SJAG_03982","SJAG_01441","SJAG_02052","SJAG_03897","SJAG_01516","SJAG_02429","SJAG_01584","SJAG_04155","SJAG_00327","SJAG_00993","SJAG_04369","SJAG_00256","SJAG_02605","SJAG_04388","SJAG_03590","SJAG_04452","SJAG_01653","SJAG_00676","SJAG_04507","SJAG_04551","SJAG_04615","SJAG_03677","SJAG_02394","SJAG_02589","SJAG_02165","SJAG_02072","SJAG_02514","SJAG_02383","SJAG_00509","SJAG_03696","SJAG_02765","SJAG_00950","SJAG_00686","SJAG_00410","SJAG_01587","SJAG_04761","SJAG_02608","SJAG_02823","SJAG_00781","SJAG_03623","SJAG_04026","SJAG_00858","SJAG_04280","SJAG_01084","SJAG_02752","SJAG_00664","SJAG_00343","SJAG_02981","SJAG_02169","SJAG_00642","SJAG_01611","SJAG_02494","SJAG_04884","SJAG_04381","SJAG_02409","SJAG_04206","SJAG_01519","SJAG_04457","SJAG_02541","SJAG_02444","SJAG_03664","SJAG_02785","SJAG_01079","SJAG_01016","SJAG_01728","SJAG_00840","SJAG_03637","SJAG_03346","SJAG_03792","SJAG_03611","SJAG_00475","SJAG_00790","SJAG_03026","SJAG_01983","SJAG_02700","SJAG_01253","SJAG_04942","SJAG_00698","SJAG_02135","SJAG_01151","SJAG_04039","SJAG_03441","SJAG_03042","SJAG_04638","SJAG_01942","SJAG_05010","SJAG_04890","SJAG_01672","SJAG_01199","SJAG_01707","SJAG_01489","SJAG_00169","SJAG_00100","SJAG_03940","SJAG_00414","SJAG_04030","SJAG_02921","SJAG_00861","SJAG_03573","SJAG_04100","SJAG_00584","SJAG_04360","SJAG_03538","SJAG_02401","SJAG_04249","SJAG_00163","SJAG_04097","SJAG_01544","SJAG_01799","SJAG_03752","SJAG_01778","SJAG_03340","SJAG_04141","SJAG_03234","SJAG_02232","SJAG_04085","SJAG_01825","SJAG_01720","SJAG_02162","SJAG_05288","SJAG_04283","SJAG_01804","SJAG_04946","SJAG_02594","SJAG_02433","SJAG_02311","SJAG_01429","SJAG_03905","SJAG_03694","SJAG_00266","SJAG_04734","SJAG_05161","SJAG_03692","SJAG_04921","SJAG_01032","SJAG_01952","SJAG_03209","SJAG_01062","SJAG_04839","SJAG_04343","SJAG_00067","SJAG_03628","SJAG_04151","SJAG_00460","SJAG_00124","SJAG_04496","SJAG_00640","SJAG_01166","SJAG_03987","SJAG_03145","SJAG_01212","SJAG_02319","SJAG_00934","SJAG_02620","SJAG_02812","SJAG_06270","SJAG_00073","SJAG_04509","SJAG_06608","SJAG_01906","SJAG_02725","SJAG_01005","SJAG_04987","SJAG_05000","SJAG_03944","SJAG_00712","SJAG_03255","SJAG_04527","SJAG_00114","SJAG_05265","SJAG_00735","SJAG_03508","SJAG_03945","SJAG_01675","SJAG_02938","SJAG_01020","SJAG_03622","SJAG_00150","SJAG_01046","SJAG_01843","SJAG_04056","SJAG_04614","SJAG_02922","SJAG_01867","SJAG_00713","SJAG_03041","SJAG_00786","SJAG_04853","SJAG_02074","SJAG_00704","SJAG_02252","SJAG_00521","SJAG_04407","SJAG_00318","SJAG_03735","SJAG_01376","SJAG_04464","SJAG_01509","SJAG_03529","SJAG_02520","SJAG_02990","SJAG_04999","SJAG_01245","SJAG_02601","SJAG_02768","SJAG_03160","SJAG_01585","SJAG_04601","SJAG_04412","SJAG_03482","SJAG_03753","SJAG_16457","SJAG_03309","SJAG_03386","SJAG_02472","SJAG_00995","SJAG_04765","SJAG_00058","SJAG_04291","SJAG_04910","SJAG_00926","SJAG_03072","SJAG_04140","SJAG_00078","SJAG_01790","SJAG_01000","SJAG_03984","SJAG_03353","SJAG_03624","SJAG_01930","SJAG_04539","SJAG_00551","SJAG_04477","SJAG_03911","SJAG_01714","SJAG_04396","SJAG_02712","SJAG_00797","SJAG_04619","SJAG_03067","SJAG_02613","SJAG_01246","SJAG_03748","SJAG_04768","SJAG_01015","SJAG_01774","SJAG_01583","SJAG_00356","SJAG_01184","SJAG_00342","SJAG_01529","SJAG_00991","SJAG_00349","SJAG_03758","SJAG_00087","SJAG_00507","SJAG_04512","SJAG_04088","SJAG_01823","SJAG_05314","SJAG_01188","SJAG_02022","SJAG_00904","SJAG_00184","SJAG_03193","SJAG_04153","SJAG_04546","SJAG_04322","SJAG_02321","SJAG_03974","SJAG_00439","SJAG_02551","SJAG_00279","SJAG_04758","SJAG_03286","SJAG_02275","SJAG_00561","SJAG_01373","SJAG_01431","SJAG_02458","SJAG_01191","SJAG_04782","SJAG_02730","SJAG_00792","SJAG_04576","SJAG_05187","SJAG_03579","SJAG_01610","SJAG_00440","SJAG_05322","SJAG_02810","SJAG_01601","SJAG_00077","SJAG_00293","SJAG_04855","SJAG_00769","SJAG_04061","SJAG_02329","SJAG_01204","SJAG_02406","SJAG_00680","SJAG_03851","SJAG_00296","SJAG_00028","SJAG_04537","SJAG_02778","SJAG_00581","SJAG_06588","SJAG_01801","SJAG_03931","SJAG_03126","SJAG_03223","SJAG_01787","SJAG_04128","SJAG_05240","SJAG_04394","SJAG_02691","SJAG_02366","SJAG_04471","SJAG_03073","SJAG_02170","SJAG_04503","SJAG_03454","SJAG_01837","SJAG_02044","SJAG_04006","SJAG_01528","SJAG_06621","SJAG_04374","SJAG_03763","SJAG_01658","SJAG_03802","SJAG_00145","SJAG_04259","SJAG_00822","SJAG_04461","SJAG_00143","SJAG_01076","SJAG_03839","SJAG_04793","SJAG_03699","SJAG_01916","SJAG_03488","SJAG_03668","SJAG_02467","SJAG_03689","SJAG_02795","SJAG_03952","SJAG_00906","SJAG_03179","SJAG_01745","SJAG_02817","SJAG_04596","SJAG_04092","SJAG_02498","SJAG_04455","SJAG_03854","SJAG_04980","SJAG_03916","SJAG_02468","SJAG_03342","SJAG_04584","SJAG_04813","SJAG_02869","SJAG_04235","SJAG_00963","SJAG_04332","SJAG_04479","SJAG_02413","SJAG_01243","SJAG_00402","SJAG_01926","SJAG_04574","SJAG_03681","SJAG_01532","SJAG_02576","SJAG_02104","SJAG_03170","SJAG_03258","SJAG_05343","SJAG_00160","SJAG_01255","SJAG_04460","SJAG_06599","SJAG_01157","SJAG_00896","SJAG_02720","SJAG_00285","SJAG_03455","SJAG_01464","SJAG_04871","SJAG_01657","SJAG_00457","SJAG_01830","SJAG_04544","SJAG_04465","SJAG_03844","SJAG_04659","SJAG_01345","SJAG_04647","SJAG_00251","SJAG_01325","SJAG_00364","SJAG_03739","SJAG_03631","SJAG_01150","SJAG_02709","SJAG_03086","SJAG_00142","SJAG_02854","SJAG_01680","SJAG_03592","SJAG_01822","SJAG_04186","SJAG_04253","SJAG_04502","SJAG_00470","SJAG_02218","SJAG_01113","SJAG_01401","SJAG_04756","SJAG_02332","SJAG_00472","SJAG_03248","SJAG_01599","SJAG_05234","SJAG_02336","SJAG_06592","SJAG_00433","SJAG_00602","SJAG_03473","SJAG_00573","SJAG_00613","SJAG_02048","SJAG_02308","SJAG_02878","SJAG_03157","SJAG_00688","SJAG_02098","SJAG_00969","SJAG_00331","SJAG_01218","SJAG_05329","SJAG_01193","SJAG_05304","SJAG_03887","SJAG_01855","SJAG_03438","SJAG_01412","SJAG_01708","SJAG_01605","SJAG_04084","SJAG_02233","SJAG_00117","SJAG_04018","SJAG_04968","SJAG_04640","SJAG_01878","SJAG_01579","SJAG_03263","SJAG_00290","SJAG_00743","SJAG_02566","SJAG_03805","SJAG_01456","SJAG_00004","SJAG_03550","SJAG_04668","SJAG_03061","SJAG_04130","SJAG_02138","SJAG_03907","SJAG_03272","SJAG_00766","SJAG_03132","SJAG_00335","SJAG_03183","SJAG_01176","SJAG_03338","SJAG_02571","SJAG_03969","SJAG_01694","SJAG_03238","SJAG_02000","SJAG_01270","SJAG_00746","SJAG_02231","SJAG_03997","SJAG_02638","SJAG_03036","SJAG_03928","SJAG_00966","SJAG_00209","SJAG_03388","SJAG_01330","SJAG_00910","SJAG_00649","SJAG_01040","SJAG_03130","SJAG_04920","SJAG_03812","SJAG_01307","SJAG_02956","SJAG_02563","SJAG_03627","SJAG_04099","SJAG_02018","SJAG_06576","SJAG_00670","SJAG_02641","SJAG_04191","SJAG_02374","SJAG_01718","SJAG_01082","SJAG_00868","SJAG_04205","SJAG_05289","SJAG_04755","SJAG_01110","SJAG_05346","SJAG_01010","SJAG_00214","SJAG_02621","SJAG_03793","SJAG_04422","SJAG_03241","SJAG_03704","SJAG_02379","SJAG_00909","SJAG_00164","SJAG_04943","SJAG_03279","SJAG_03505","SJAG_00873","SJAG_00979","SJAG_02872","SJAG_02622","SJAG_04025","SJAG_03310","SJAG_04036","SJAG_01863","SJAG_00534","SJAG_04268","SJAG_02045","SJAG_01794","SJAG_02214","SJAG_03484","SJAG_02196","SJAG_03678","SJAG_00701","SJAG_03486","SJAG_02701","SJAG_00996","SJAG_00514","SJAG_03143","SJAG_03981","SJAG_03625","SJAG_16454","SJAG_00302","SJAG_00975","SJAG_02451","SJAG_00623","SJAG_02370","SJAG_04573","SJAG_04611","SJAG_02485","SJAG_00758","SJAG_01699","SJAG_04262","SJAG_02026","SJAG_05286","SJAG_03118","SJAG_04873","SJAG_04159","SJAG_00690","SJAG_02027","SJAG_04287","SJAG_01764","SJAG_03327","SJAG_03680","SJAG_02771","SJAG_02249","SJAG_00666","SJAG_03575","SJAG_00229","SJAG_01873","SJAG_03300","SJAG_01716","SJAG_04038","SJAG_01058","SJAG_05014","SJAG_00429","SJAG_05236","SJAG_00759","SJAG_01465","SJAG_05694","SJAG_00823","SJAG_02254","SJAG_04824","SJAG_03361","SJAG_02416","SJAG_02808","SJAG_02057","SJAG_01118","SJAG_00441","SJAG_03351","SJAG_00855","SJAG_01047","SJAG_04607","SJAG_03720","SJAG_00071","SJAG_01297","SJAG_00304","SJAG_00082","SJAG_03230","SJAG_03886","SJAG_01805","SJAG_00596","SJAG_05006","SJAG_04776","SJAG_03903","SJAG_00600","SJAG_03090","SJAG_00718","SJAG_01936","SJAG_01249","SJAG_05341","SJAG_02698","SJAG_04469","SJAG_01679","SJAG_04435","SJAG_02203","SJAG_04384","SJAG_02723","SJAG_03876","SJAG_02415","SJAG_03543","SJAG_02540","SJAG_04880","SJAG_04005","SJAG_01402","SJAG_03376","SJAG_03967","SJAG_04989","SJAG_02773","SJAG_02382","SJAG_00456","SJAG_03350","SJAG_00236","SJAG_02807","SJAG_02278","SJAG_03927","SJAG_01475","SJAG_05313","SJAG_01252","SJAG_01826","SJAG_02043","SJAG_03355","SJAG_02592","SJAG_02426","SJAG_00317","SJAG_02266","SJAG_00610","SJAG_00737","SJAG_01919","SJAG_03356","SJAG_00297","SJAG_01210","SJAG_00289","SJAG_01821","SJAG_00053","SJAG_02849","SJAG_00167","SJAG_04203","SJAG_04427","SJAG_02898","SJAG_00486","SJAG_00391","SJAG_00424","SJAG_02858","SJAG_04777","SJAG_03936","SJAG_02629","SJAG_04052","SJAG_02671","SJAG_01944","SJAG_02119","SJAG_02239","SJAG_05030","SJAG_02466","SJAG_04312","SJAG_01515","SJAG_00685","SJAG_03850","SJAG_02822","SJAG_00423","SJAG_02380","SJAG_01818","SJAG_01068","SJAG_01725","SJAG_03185","SJAG_00987","SJAG_04666","SJAG_03602","SJAG_01527","SJAG_00802","SJAG_05184"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118343],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:0061158"},{"annotations":[90151,78713,78780,100092],"is_not":false,"rel_names":["negatively_regulates","is_a","regulates"],"summary":null,"term":"GO:0070935"},{"annotations":[89820,94548,95821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051519"},{"annotations":[107982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010846"},{"annotations":[101852,106859,109534,105919,109027,94198,106507,116587,115555],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0010619"},{"annotations":[79113,80016,75582,92293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"},{"annotations":[66011],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0009785"},{"annotations":[72855,79502,98099,92367],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0097720"},{"annotations":[91182,65154,97650,117409],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0019722"},{"annotations":[116167,116505,118256],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0061762"},{"annotations":[90304,95127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051728"},{"annotations":[110775,103492,99740,88009,106867,116506,117933],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051523"},{"annotations":[92231,102146,110991],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000196"},{"annotations":[108463,105544],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007166"},{"annotations":[115609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007267"},{"annotations":[99118,110499,118120,99561,116008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033562"},{"annotations":[113622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140719"},{"annotations":[107246,90686,108268,111975,113799,114288,103895,99589,115926],"is_not":false,"rel_names":["negatively_regulates","is_a","positively_regulates","regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[79677,77386,74263,75761,112018,58524],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000290"},{"annotations":[75889,78950],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031087"},{"annotations":[70528,107190,67971,77157,71104,98713,113824,114095,114228,101240,116055,116803,76199,117253],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0030968"},{"annotations":[91203,59640,93360,116235,65034,118873,68106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0040029"},{"annotations":[116900],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006984"},{"annotations":[103226,94047],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140718"},{"annotations":[62207,63576,58267,72312],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007186"},{"annotations":[80135,109683,99439,69864],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0140469"},{"annotations":[96135,112631,98902,112629,88110,103058,112630,117783,103227,113074,99121,117149,90717,99147,94048,115278],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033696"},{"annotations":[70186,119579,73717,74773,92574,73052,115030,119578,94320,114139,94578,115432,76631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031507"},{"annotations":[70563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071044"},{"annotations":[98415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031141"},{"annotations":[115610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031142"},{"annotations":[116168,106289,89166,87982,116508,118257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010514"},{"annotations":[96527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0012502"},{"annotations":[110938,67835,71032,70122,71189,87802,77167,68354,79884,77360,116346,89881,73222,79093,76418,108465,91454,59360,77126,77528,76144,78218,78843,73811,64931,72065,79026,89823],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0035556"},{"annotations":[93066,77833],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0036498"},{"annotations":[106290],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007254"},{"annotations":[57463,99970],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000165"},{"annotations":[106330,114518],"is_not":false,"rel_names":["regulates","negatively_regulates","part_of","is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[78797],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0044778"},{"annotations":[116085,106628,91396],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[114278,106629,116086,89014],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0051598"},{"annotations":[75209,116694],"is_not":false,"rel_names":["negatively_regulates","part_of","regulates","is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[98690,100136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990949"},{"annotations":[102293,100137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990950"},{"annotations":[72894,70599,78205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007091"},{"annotations":[70420],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031930"},{"annotations":[100537,94378,89952,101440,116030],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0044878"},{"annotations":[111213,114489,77944,116258,93534,116031,79981],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0044773"},{"annotations":[112050,109331,79383,93931,116087,72122,117302,100538,99191,117129,70971,116828,91397,99358,106631,78803,74703],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0033314"},{"annotations":[101625,88898,108905,102362,115928],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031568"},{"annotations":[109684,91273],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031571"},{"annotations":[94510,116032,95824,98425],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031569"},{"annotations":[79246,99360,91398,111745,117043,91761,72120,89075,100539,117741,75153,106632,101053,109332,90171],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007095"},{"annotations":[74252,111746,79137,102363,79251,89076,89121,90408,91399,100860,99361,116089,94511,78802,112051,73783,107680,95986,106633],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031573"},{"annotations":[109921,114521,101802,115580,106332,99433],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a","part_of"],"summary":null,"term":"GO:0007094"},{"annotations":[76280,114874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006402"},{"annotations":[118140],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:0061157"},{"annotations":[89441,70567],"is_not":false,"rel_names":["negatively_regulates","is_a","regulates"],"summary":null,"term":"GO:0048255"},{"annotations":[104380,90372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[100438,107983,92055,92718,116406],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:0110034"},{"annotations":[102364],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905785"},{"annotations":[107984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060195"},{"annotations":[74389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034316"},{"annotations":[111214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[102365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902424"},{"annotations":[72389,76362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010507"},{"annotations":[90689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051517"},{"annotations":[100997,116154],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0106057"},{"annotations":[113380,91183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905949"},{"annotations":[118395,102366,106662,104446,105826,105984,109281],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:0110045"},{"annotations":[118345,99440,95825,103803,107060,107625],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:1903138"},{"annotations":[98573,99294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022408"},{"annotations":[96365,92056,104923,93184,101626,116588,102367,88764],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031138"},{"annotations":[95128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140538"},{"annotations":[98271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000432"},{"annotations":[114875,95563,99441,118258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000766"},{"annotations":[91274,112170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904689"},{"annotations":[69789,75129,94337,115640,99335,109686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"},{"annotations":[101074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045892"},{"annotations":[102368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001033"},{"annotations":[94550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045806"},{"annotations":[77516,78017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904293"},{"annotations":[93851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"},{"annotations":[111775],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904332"},{"annotations":[90926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904846"},{"annotations":[102369,67721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001100"},{"annotations":[70618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045717"},{"annotations":[94028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905569"},{"annotations":[103557,106266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060257"},{"annotations":[99562,116009,118121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070317"},{"annotations":[91707,93299,92127,98873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000134"},{"annotations":[111451,93535,106663,111836,104502,78435,92893,93185,108589,100998,94338,107027,114490,112494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010972"},{"annotations":[70452,78439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110031"},{"annotations":[88765,100910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010629"},{"annotations":[97205,97316,114165,93209,93170,103121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045814"},{"annotations":[102845,102147,89391],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:1902660"},{"annotations":[78839,77122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045719"},{"annotations":[72967,75963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[88043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042997"},{"annotations":[91375,100540,94199,109028,94339,106860,92894,88159,115556,101853,114491,105921,106508,116097,106664,104503,105827],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0010515"},{"annotations":[115504,111388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[117977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905560"},{"annotations":[88044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905533"},{"annotations":[106665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016242"},{"annotations":[88160],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0043409"},{"annotations":[116407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051447"},{"annotations":[98691],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:1902103"},{"annotations":[118032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905707"},{"annotations":[116330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090258"},{"annotations":[102051,106466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010637"},{"annotations":[102370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903500"},{"annotations":[103699],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903472"},{"annotations":[116874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903464"},{"annotations":[92810,102148,99668,107111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902413"},{"annotations":[97761,102372,108909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903467"},{"annotations":[103282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000816"},{"annotations":[94170],"is_not":false,"rel_names":["positively_regulates","is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[102373],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:1902845"},{"annotations":[102374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904537"},{"annotations":[89741],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0120271"},{"annotations":[91636],"is_not":false,"rel_names":["regulates","is_a","negatively_regulates"],"summary":null,"term":"GO:0060212"},{"annotations":[91629,95946,118346,117104,99442,95005],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:1903753"},{"annotations":[107152],"is_not":false,"rel_names":["negatively_regulates","regulates","is_a"],"summary":null,"term":"GO:0180040"},{"annotations":[93294],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0090029"},{"annotations":[109743,112762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071072"},{"annotations":[101446],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062168"},{"annotations":[102375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905757"},{"annotations":[106964,77193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032435"},{"annotations":[105828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042308"},{"annotations":[95827,90927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903067"},{"annotations":[94379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140325"},{"annotations":[107247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902543"},{"annotations":[114492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900181"},{"annotations":[95828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903077"},{"annotations":[72118],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:0046580"},{"annotations":[77209,106666],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0061188"},{"annotations":[107985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045128"},{"annotations":[108508],"is_not":false,"rel_names":["negatively_regulates","regulates","is_a"],"summary":null,"term":"GO:0060906"},{"annotations":[71445],"is_not":false,"rel_names":["negatively_regulates","regulates","is_a"],"summary":null,"term":"GO:0035024"},{"annotations":[72019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902369"},{"annotations":[105052,110185,107555,92895,107248,115929,90690,92811,91699,95613,101278,93429,99591,107112,72680],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:0031030"},{"annotations":[106592,115362,107419,106369,91708,106273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045875"},{"annotations":[91204,111728,105911],"is_not":false,"rel_names":["negatively_regulates","regulates","is_a"],"summary":null,"term":"GO:2000639"},{"annotations":[73037],"is_not":false,"rel_names":["is_a","regulates","negatively_regulates"],"summary":null,"term":"GO:0032007"},{"annotations":[87976,96073,101455,103014,109282,98874,73511,107164,105144,113995,117068,79915,113178,114600,118259,93300,116509,116155,109687,73482,99573],"is_not":false,"rel_names":["negatively_regulates","is_a","regulates"],"summary":null,"term":"GO:1904262"},{"annotations":[116300],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:1903940"},{"annotations":[91149,93266,103958,104261,75299,106267,106742,100999,101854,93852,106762,73683,92128,114282,73590,74037,87545,73106,91221,96260,107986,105922,94200,73859,92104,109029,112107,110737,71684,70419,80401,70134,72177,106509,94612,108247,79568,98884,103558,108590,111158,117397,76717,105829,76916,93364,112992,94696,113847,93710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000122"},{"annotations":[73673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016480"},{"annotations":[101000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010621"},{"annotations":[117963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034244"},{"annotations":[75182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001125"},{"annotations":[88045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905530"},{"annotations":[101456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061192"},{"annotations":[72292,94931,96511,101039,71115,74353,93044,89037,115468,115910,73102,89401,71482,95889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071028"},{"annotations":[109253,104303,111316,118142,96712,87448,91830,92212,90756,107469,109272,90832,99092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033621"},{"annotations":[118143,70098,93414,74517,97232],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071031"},{"annotations":[116356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071032"},{"annotations":[118144,94972,115573,109273,87449,92334,109800,90757,88793,106322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071030"},{"annotations":[106479,97233,102087,115911,115469,93045,95890,105275,107471,104406,92215,118331],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:0071042"},{"annotations":[111266,67799,66386,102173,115352,79838,59186,72937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000956"},{"annotations":[97236,105277,89754,118333,75219,104408,95892,101241,116175,108843,106481,102089,91489,88710,93047,115913,107474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070478"},{"annotations":[98133,79442,76543,99929,59986,98046,115170,70380],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0000288"},{"annotations":[107191,114127,74427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070966"},{"annotations":[93048,115914,101242,117255,118334,95893,97237,108844,107475,104409,62477,116176,105278,102090,106482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070481"},{"annotations":[73277,89860,115401,69770,105906,104767,90271,113599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000184"},{"annotations":[104783,73529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000294"},{"annotations":[94305,89742,116629,92468,78931,95481,90746,70194,75491,115683,73726,79613,92566,77566],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0000289"},{"annotations":[70057,106291,110358,101760,73007,94340],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0038066"},{"annotations":[102782,94050,113314,108172,111286,92040,90172,114007,93415,114438,104093,103229,112122,112638,112639,98249,72180,92794,112640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031508"},{"annotations":[91312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140462"},{"annotations":[89188,92155,96355,106292,93295,97030],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0071507"},{"annotations":[70777],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000750"},{"annotations":[93193,71368,95905,71637,72535],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0048015"},{"annotations":[65387,60724,66171,66312,69250,68601,77701,58100],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000160"},{"annotations":[91637],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036450"},{"annotations":[90747,117256,66385],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:1990074"},{"annotations":[117562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902648"},{"annotations":[88900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[73831,79526],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043065"},{"annotations":[102294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[90691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[118260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075319"},{"annotations":[116035,111976,105192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902425"},{"annotations":[108581,108671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000786"},{"annotations":[97612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901098"},{"annotations":[79913,73479,111858,98875,109688,114602,99444,73507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010508"},{"annotations":[68761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903599"},{"annotations":[102149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905665"},{"annotations":[110992,102150],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0050850"},{"annotations":[116510,118261],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0140648"},{"annotations":[106667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030307"},{"annotations":[92386,102846,90731,88038,117937,89392],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:1903139"},{"annotations":[102151,110993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903340"},{"annotations":[89217,116418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900039"},{"annotations":[104925,107153,111389,101761,98551,99445,100123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031139"},{"annotations":[106668,117155,69597],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000767"},{"annotations":[112052,117303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045739"},{"annotations":[103326,112053,117304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903468"},{"annotations":[70166,79730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032786"},{"annotations":[110199,93853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000781"},{"annotations":[107420],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001034"},{"annotations":[103700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045807"},{"annotations":[64481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903373"},{"annotations":[109865],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070452"},{"annotations":[103701,107626,112488],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061173"},{"annotations":[116610,107627],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:2000784"},{"annotations":[105370,93711,100175],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:2000247"},{"annotations":[89954,102376,93720,111977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031536"},{"annotations":[100176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045921"},{"annotations":[114104,116169,111390,105912,108651,108774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900735"},{"annotations":[106669,109200,117097,105830,105985,102377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1900087"},{"annotations":[103494,108591,94341,88002,73450,93771,98998,94380,70772,92105,116699,110359,101762,116511,111216,88011,91701,98426,107249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010971"},{"annotations":[87803,101390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905287"},{"annotations":[73455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110032"},{"annotations":[89476],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010628"},{"annotations":[89884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035432"},{"annotations":[96557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001172"},{"annotations":[98962],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:0031453"},{"annotations":[108823,104447,107067,103367,99502,87804,100497,101391,116302,108592,119116,119117],"is_not":false,"rel_names":["regulates","is_a","positively_regulates"],"summary":null,"term":"GO:1900237"},{"annotations":[116259,106634,102378,89015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904514"},{"annotations":[116700,102379,89605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905561"},{"annotations":[91709,93301,98876,110554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905589"},{"annotations":[93302,98877,91710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905534"},{"annotations":[93303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905626"},{"annotations":[95052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045834"},{"annotations":[106274,75220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016239"},{"annotations":[103703],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0061361"},{"annotations":[87849,93448,89824,111381,90811],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1902917"},{"annotations":[105709,88169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001178"},{"annotations":[113804],"is_not":false,"rel_names":["regulates","is_a","positively_regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[119118,119119,97031,107068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051446"},{"annotations":[108373,102381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905263"},{"annotations":[95130],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:1905191"},{"annotations":[101855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031117"},{"annotations":[95720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090297"},{"annotations":[108896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090141"},{"annotations":[98703,112689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070131"},{"annotations":[100458],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070134"},{"annotations":[89955,94381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903501"},{"annotations":[87488,94382,94551,110538,113381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903473"},{"annotations":[102382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903465"},{"annotations":[116701],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[102383,116702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903380"},{"annotations":[119286,103704,90732,110780],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903617"},{"annotations":[89825,105193,115495,117921,77861,92387,93773,106397,107061,113382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140281"},{"annotations":[93774,97686,102112,114792,102384,111391,100138],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0045842"},{"annotations":[79404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045951"},{"annotations":[106145,88954,116445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120292"},{"annotations":[116703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905824"},{"annotations":[102385,89957,93775,111217,116704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140429"},{"annotations":[99604,96582,99609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901970"},{"annotations":[89958,94383],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:1902846"},{"annotations":[111452],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0110161"},{"annotations":[89429,118442],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905746"},{"annotations":[74011,92129,110939,75273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048026"},{"annotations":[94384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902854"},{"annotations":[106670],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0120272"},{"annotations":[89653,104926,72692],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0060213"},{"annotations":[111838,108956,108955,108957,95229,118312,108960,117398,108959,108958,108954,112496],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:1900745"},{"annotations":[89647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905857"},{"annotations":[91150],"is_not":false,"rel_names":["positively_regulates","is_a","regulates"],"summary":null,"term":"GO:0090053"},{"annotations":[88097,114646,90812,115612,103705],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0062038"},{"annotations":[92388,94385,87489],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905758"},{"annotations":[61472,68118,65590,66860,68463,67084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901800"},{"annotations":[111729,108910,117098,106671,102386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"},{"annotations":[111188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045732"},{"annotations":[99394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904352"},{"annotations":[93776,111025,100439,101856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046827"},{"annotations":[94342,90813,102388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042307"},{"annotations":[98427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120047"},{"annotations":[89916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045862"},{"annotations":[88409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903931"},{"annotations":[89016],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010845"},{"annotations":[87472,92389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"},{"annotations":[89477],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140501"},{"annotations":[93464,87914,89418,106672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060963"},{"annotations":[89419,93465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090070"},{"annotations":[79418,89664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045899"},{"annotations":[77901,75371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000234"},{"annotations":[87490,89959,110539,93777,102389],"is_not":false,"rel_names":["positively_regulates","regulates","is_a"],"summary":null,"term":"GO:0031031"},{"annotations":[89687,107968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001043"},{"annotations":[110360,91151,94343],"is_not":false,"rel_names":["is_a","positively_regulates","regulates"],"summary":null,"term":"GO:0090055"},{"annotations":[107421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045876"},{"annotations":[78335],"is_not":false,"rel_names":["positively_regulates","regulates","is_a"],"summary":null,"term":"GO:2000640"},{"annotations":[97173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032215"},{"annotations":[111979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904595"},{"annotations":[88992,113702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090180"},{"annotations":[72960,69133],"is_not":false,"rel_names":["positively_regulates","regulates","is_a"],"summary":null,"term":"GO:0032008"},{"annotations":[75811,110555,75224,72391,73968,94290,112879,88264,76364,76742,96074],"is_not":false,"rel_names":["regulates","positively_regulates","is_a"],"summary":null,"term":"GO:1904263"},{"annotations":[91160,97735,107009],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:1904515"},{"annotations":[73039,78485,77899,75987,79321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045943"},{"annotations":[62957,65067,109059,108593,104448,110738,102702,93684,111766,111895,117012,116495,107428,95665,116303,97514,78554,77421,61126,71456,66155,62038,73341,76715,98574,79469,118262,96912,67370,112309,68439,70170,72726,75683,97512,97515,97513,107987,109704,69094,103171,114855,79057,102280,108824,77355,97283,100498,62929,87369,93778,119120,74894,79728,94344,95502,72343,108652,68582,71496,78005,92719,99503,95053,74619,73660,69222,71681,76162,80091,70752,72045,98416,107592,97516,108480,73324,102152,73680,100487,117399,79565,75398,70821,102233,75814,70164,99295,119121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045944"},{"annotations":[117021,79497,106058,71466,70843,78029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032968"},{"annotations":[108739,108766,118961,98673,99025,106384,115321,90643,95353,87407,114754,103677,90327,94419,106059,101960,105710,94309,103418,106251,95837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060261"},{"annotations":[66028,68419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045901"},{"annotations":[72685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045948"},{"annotations":[66029,76381,68420],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045905"},{"annotations":[89145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904775"},{"annotations":[110282,97613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061191"},{"annotations":[119576,119577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016441"},{"annotations":[118009,118122,71147,88329],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990431"},{"annotations":[112489,118815,91105,113067,100177,105372],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0062200"},{"annotations":[111026,105072],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031291"},{"annotations":[108173,104094,113315,70698,92041,72178,112123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000183"},{"annotations":[75039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010510"},{"annotations":[99446,95830,77850,74005,73131,71405,110120,73115,78895,116512,115343,102847,77677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032956"},{"annotations":[107628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032231"},{"annotations":[67781,76691,79262,66896,77228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030833"},{"annotations":[78182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031991"},{"annotations":[97614,111896,109705,94345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903715"},{"annotations":[64809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000381"},{"annotations":[92156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"},{"annotations":[116955],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903023"},{"annotations":[78307,79687,79541,65731,72512,65870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010506"},{"annotations":[87850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032951"},{"annotations":[115073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051516"},{"annotations":[92948,111897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006109"},{"annotations":[69936],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043609"},{"annotations":[106370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901987"},{"annotations":[109060,101628,104927,94514],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0110044"},{"annotations":[119448,119449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008360"},{"annotations":[102848,105930,117938,105358,118063,90733,92373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090334"},{"annotations":[107629,74104,108466,110121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903338"},{"annotations":[102391],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904547"},{"annotations":[75498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045540"},{"annotations":[111684,111034,118886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000369"},{"annotations":[118066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031137"},{"annotations":[71242,76185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003400"},{"annotations":[111176,112410,96053,102582,96197,116847,117485,90227,109721,105263,100270,100719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000765"},{"annotations":[95436,109503,110168,113990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140018"},{"annotations":[95195,103964,103332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990611"},{"annotations":[78183,87851,75339],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032955"},{"annotations":[110341,109096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000018"},{"annotations":[75960,78668,75806,78757,70808,78964,78991,79986,76122,68839,76389,71959,75513,71632,60534,72633,80304,74761,68179,60139,67020,61623,57671,69859,71390,57234,75726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006355"},{"annotations":[72578,90875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000779"},{"annotations":[109333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010569"},{"annotations":[87852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001135"},{"annotations":[89828,113255,77508,102936,78235,92393,92678,113383,90928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030100"},{"annotations":[76556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060628"},{"annotations":[88518,105856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032443"},{"annotations":[111980,94553],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000114"},{"annotations":[102392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000099"},{"annotations":[94554,118816,95635,113068,104538,91106],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:2000100"},{"annotations":[90898,100201,109436,95831,100391,93450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032878"},{"annotations":[92394,102849,87854],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:2000769"},{"annotations":[70030,111027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007096"},{"annotations":[87855,93816,98395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017157"},{"annotations":[98429],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061387"},{"annotations":[89394,92395,102850,94910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070610"},{"annotations":[100179,102154,92679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032995"},{"annotations":[110994,71446,87547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060237"},{"annotations":[111981,71350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010389"},{"annotations":[71351,73526,93971,70254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010468"},{"annotations":[75040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010906"},{"annotations":[69941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006110"},{"annotations":[90776,98564],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0031445"},{"annotations":[87856,91987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033157"},{"annotations":[110201,93855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090006"},{"annotations":[102395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062123"},{"annotations":[118096,76126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019216"},{"annotations":[74654,80393],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0043408"},{"annotations":[101341],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:1905325"},{"annotations":[92106,93268,94346,104333,89768],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051445"},{"annotations":[108374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901993"},{"annotations":[96923],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0040020"},{"annotations":[103706,91107,100180,105374,115344,113069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070507"},{"annotations":[70472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031110"},{"annotations":[89769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010821"},{"annotations":[93779,119382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903499"},{"annotations":[73901],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007346"},{"annotations":[117548,107157,100945,103495,89770,109228,77036,118722,91812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902412"},{"annotations":[111392,101392,87805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902472"},{"annotations":[110940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007088"},{"annotations":[103668,93807],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905557"},{"annotations":[71282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901673"},{"annotations":[111029],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032888"},{"annotations":[115075],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0110162"},{"annotations":[89829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060236"},{"annotations":[116652],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0061013"},{"annotations":[98565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905744"},{"annotations":[75946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050684"},{"annotations":[93713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048024"},{"annotations":[88360],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0043488"},{"annotations":[89756,91491,90154],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:2000815"},{"annotations":[70418,113848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006808"},{"annotations":[98508],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0060211"},{"annotations":[75962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043456"},{"annotations":[97174,100300],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[99395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000185"},{"annotations":[111189],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010967"},{"annotations":[106404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902267"},{"annotations":[107566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000214"},{"annotations":[114651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032434"},{"annotations":[68909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042176"},{"annotations":[107969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905391"},{"annotations":[103327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905634"},{"annotations":[74676,69934],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0032483"},{"annotations":[89123,94348,116311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010520"},{"annotations":[117784],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0010964"},{"annotations":[103230],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:1902681"},{"annotations":[113641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000156"},{"annotations":[93972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051252"},{"annotations":[113385,104504,89921],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0031029"},{"annotations":[101011,93817],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010590"},{"annotations":[89850],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:0023051"},{"annotations":[97175,117785,118147,91831,100301],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:1902801"},{"annotations":[100838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007063"},{"annotations":[116707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904967"},{"annotations":[76874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032210"},{"annotations":[117826,107863,115505,92862,94024],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:1903432"},{"annotations":[108423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006356"},{"annotations":[71612,90551,110489,63748,79077,60787,62069,92469,102052,66254,72710,80175,117643,113426,57681,63023,105405,76396,60463,66724,94180,94104,89169,61894,57914,59021,60202,73444,71490,91571,107938,59902,87609,60322,68576,89064,92263,68303,62626,103368,95810,72502,80022,107456,68828,60503,97809,105787,79054,97043,88445,98498,63467,76015,68890,59221,68404,59311,76467,76037,72919,61398,69758,69111,76495,58603,113149,68429,70830,57283,66680,64698,73877,57309,59466,63912,72499,67107,72675,77753,77368,77797,78033,96558,95866,104039,66587,66551,62726,72080,71772,58110,74256,78315,79601,89293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006357"},{"annotations":[78077,75875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006359"},{"annotations":[103101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990983"},{"annotations":[73843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006449"},{"annotations":[97376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032889"},{"annotations":[91832,92795,118148],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043628"},{"annotations":[92220,89743,87450,115684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031047"},{"annotations":[107368,111874,104095,107796,109132,113076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031048"},{"annotations":[108684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061454"},{"annotations":[106648,99362,108534,103231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0011000"},{"annotations":[115046,102282,99363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031582"},{"annotations":[99364],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090001"},{"annotations":[102283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071807"},{"annotations":[75267],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0007266"},{"annotations":[99449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141014"},{"annotations":[74142,89196,106398,107158,94387,100946],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0031028"},{"annotations":[115363,78521,98528,96366,91153,75242,75867,108425,78358,73917,71936,65435,65343,65803,96304,89170,105832,70711,75106,65210,66065,70732,104264,89885,110096,118043,73733,66367,59085,105137,73114,77197,77676,80027,91712,73130],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0007165"},{"annotations":[90816,106392,111382,115613],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032005"},{"annotations":[97177,118723,100202,92131,118852,95811,106594,111035,92781,111581,111685,97848,113849,87985,104334,92949,87685,107422,98054,117847,107028,106427,118443,110283,118887,97688,106275,105987,115346,117978,93616,109745,105288,87667,108893,112764,102138,88012,109114,115021,97377,91572,93714,92484,89771,105029,108375,111393,91989,102578,105231,105538,105711,106371,115076,116611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0023052"},{"annotations":[96714,111287,108174,99565,113316,114009,116011,117727,71616,111224,95494,104192,110501,113690,112226,118124,118845,94051,99128,103232,107989,112124,92722,104096,91238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030466"},{"annotations":[71148,118125],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990432"},{"annotations":[71509,71830,116012],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030422"},{"annotations":[87451,90759,104193,112125,116562,110502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902794"},{"annotations":[106323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902795"},{"annotations":[114010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141194"},{"annotations":[88788,96715,95310,99567,114325,118846,99129,106563,111225,114592,91239,115448,88733,94063,112227,113691,110669,110503,116013,118011,118126,117728],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"},{"annotations":[116260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062209"},{"annotations":[105194],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0090520"},{"annotations":[64871,112580,116420,68531,112834,63766,103975,89220,88941,92610,118471,93856,89606,102114,118263],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0032933"},{"annotations":[94052,111288,113317,117729,104194,118847,104097,91240,108175,113692,59840,90173,118127,110504,99130,98250,92043,96716,90011,112126,114011,103233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031509"},{"annotations":[90600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090669"},{"annotations":[103965,104310],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0031929"},{"annotations":[98553,75441,92057,114948,79561,106698,106673,113042,93186],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0038202"},{"annotations":[99380,106699,108594,76993,72488,77369],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0038203"},{"annotations":[91378,109592,113169,88113,115032,96424,90659,96633,99142,102783,104572,115412,106915,94091,89238,108481,93749,101566,110490,112994,93483,94181,113339,114415,116563,111768,105639,94105,107344,115426,88296,103122,98666,116374,105044,95867,117596,87610,89065,117994,114326,107895,115280,117574,115730,92264,98231,109081,105788,114242,93980,107696,109360,110625,117297,90673,109484,95446,94153,112567,116931,90552,116313,89751,95421,99392,117644,107457,97072,98499,95860,106763,114740,87757,97811,90028,114253,88829,94125,94278,88446,100978,103369,92762,113150,117481,94613,105036,87936,103851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045815"},{"annotations":[116564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141005"},{"annotations":[74768,91713,76678,115364,108911,115930],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007089"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a biological process. Biological processes are regulated by many means; examples include the control of gene expression, protein modification or interaction with a protein or substrate molecule.","definition_xrefs":["GOC:ai","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological regulation","termid":"GO:0065007"},{"relation_name":"regulates","term_name":"biological_process","termid":"GO:0008150"}],"gene_count":991,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00028":null,"SJAG_00037":null,"SJAG_00045":null,"SJAG_00052":null,"SJAG_00053":null,"SJAG_00058":null,"SJAG_00067":null,"SJAG_00071":null,"SJAG_00073":null,"SJAG_00077":null,"SJAG_00078":null,"SJAG_00082":null,"SJAG_00087":null,"SJAG_00092":null,"SJAG_00100":null,"SJAG_00114":null,"SJAG_00117":null,"SJAG_00124":null,"SJAG_00142":null,"SJAG_00143":null,"SJAG_00145":null,"SJAG_00150":null,"SJAG_00156":null,"SJAG_00160":null,"SJAG_00163":null,"SJAG_00164":null,"SJAG_00167":null,"SJAG_00169":null,"SJAG_00184":null,"SJAG_00209":null,"SJAG_00210":null,"SJAG_00214":null,"SJAG_00216":null,"SJAG_00226":null,"SJAG_00229":null,"SJAG_00236":null,"SJAG_00244":null,"SJAG_00247":null,"SJAG_00251":null,"SJAG_00256":null,"SJAG_00266":null,"SJAG_00269":null,"SJAG_00279":null,"SJAG_00285":null,"SJAG_00289":null,"SJAG_00290":null,"SJAG_00293":null,"SJAG_00296":null,"SJAG_00297":null,"SJAG_00302":null,"SJAG_00304":null,"SJAG_00317":null,"SJAG_00318":null,"SJAG_00320":null,"SJAG_00321":null,"SJAG_00327":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00335":null,"SJAG_00340":null,"SJAG_00341":null,"SJAG_00342":null,"SJAG_00343":null,"SJAG_00349":null,"SJAG_00356":null,"SJAG_00364":null,"SJAG_00369":null,"SJAG_00386":null,"SJAG_00391":null,"SJAG_00402":null,"SJAG_00410":null,"SJAG_00414":null,"SJAG_00423":null,"SJAG_00424":null,"SJAG_00425":null,"SJAG_00429":null,"SJAG_00433":null,"SJAG_00439":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00452":null,"SJAG_00456":null,"SJAG_00457":null,"SJAG_00460":null,"SJAG_00470":null,"SJAG_00472":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00507":null,"SJAG_00509":null,"SJAG_00514":null,"SJAG_00521":null,"SJAG_00526":null,"SJAG_00530":null,"SJAG_00534":null,"SJAG_00545":null,"SJAG_00551":null,"SJAG_00561":null,"SJAG_00573":null,"SJAG_00574":null,"SJAG_00579":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00596":null,"SJAG_00600":null,"SJAG_00602":null,"SJAG_00610":null,"SJAG_00613":null,"SJAG_00623":null,"SJAG_00640":null,"SJAG_00641":null,"SJAG_00642":null,"SJAG_00649":null,"SJAG_00661":null,"SJAG_00664":null,"SJAG_00666":null,"SJAG_00670":null,"SJAG_00676":null,"SJAG_00678":null,"SJAG_00680":null,"SJAG_00681":null,"SJAG_00685":null,"SJAG_00686":null,"SJAG_00688":null,"SJAG_00690":null,"SJAG_00693":null,"SJAG_00698":null,"SJAG_00701":null,"SJAG_00704":null,"SJAG_00712":null,"SJAG_00713":null,"SJAG_00718":null,"SJAG_00735":null,"SJAG_00737":null,"SJAG_00739":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00756":null,"SJAG_00758":null,"SJAG_00759":null,"SJAG_00766":null,"SJAG_00769":null,"SJAG_00781":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00792":null,"SJAG_00797":null,"SJAG_00802":null,"SJAG_00807":null,"SJAG_00822":null,"SJAG_00823":null,"SJAG_00824":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00854":null,"SJAG_00855":null,"SJAG_00858":null,"SJAG_00861":null,"SJAG_00868":null,"SJAG_00873":null,"SJAG_00875":null,"SJAG_00883":null,"SJAG_00892":null,"SJAG_00896":null,"SJAG_00904":null,"SJAG_00906":null,"SJAG_00909":null,"SJAG_00910":null,"SJAG_00926":null,"SJAG_00934":null,"SJAG_00950":null,"SJAG_00961":null,"SJAG_00963":null,"SJAG_00966":null,"SJAG_00969":null,"SJAG_00973":null,"SJAG_00975":null,"SJAG_00979":null,"SJAG_00987":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01005":null,"SJAG_01008":null,"SJAG_01010":null,"SJAG_01015":null,"SJAG_01016":null,"SJAG_01020":null,"SJAG_01032":null,"SJAG_01040":null,"SJAG_01044":null,"SJAG_01046":null,"SJAG_01047":null,"SJAG_01050":null,"SJAG_01053":null,"SJAG_01058":null,"SJAG_01062":null,"SJAG_01068":null,"SJAG_01075":null,"SJAG_01076":null,"SJAG_01079":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01110":null,"SJAG_01111":null,"SJAG_01113":null,"SJAG_01114":null,"SJAG_01118":null,"SJAG_01131":null,"SJAG_01138":null,"SJAG_01142":null,"SJAG_01146":null,"SJAG_01149":null,"SJAG_01150":null,"SJAG_01151":null,"SJAG_01157":null,"SJAG_01161":null,"SJAG_01166":null,"SJAG_01176":null,"SJAG_01181":null,"SJAG_01184":null,"SJAG_01187":null,"SJAG_01188":null,"SJAG_01191":null,"SJAG_01193":null,"SJAG_01199":null,"SJAG_01204":null,"SJAG_01205":null,"SJAG_01210":null,"SJAG_01212":null,"SJAG_01213":null,"SJAG_01218":null,"SJAG_01230":null,"SJAG_01243":null,"SJAG_01245":null,"SJAG_01246":null,"SJAG_01249":null,"SJAG_01252":null,"SJAG_01253":null,"SJAG_01254":null,"SJAG_01255":null,"SJAG_01270":null,"SJAG_01286":null,"SJAG_01297":null,"SJAG_01307":null,"SJAG_01311":null,"SJAG_01320":null,"SJAG_01325":null,"SJAG_01330":null,"SJAG_01331":null,"SJAG_01343":null,"SJAG_01345":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01386":null,"SJAG_01401":null,"SJAG_01402":null,"SJAG_01403":null,"SJAG_01412":null,"SJAG_01429":null,"SJAG_01431":null,"SJAG_01436":null,"SJAG_01441":null,"SJAG_01456":null,"SJAG_01464":null,"SJAG_01465":null,"SJAG_01475":null,"SJAG_01489":null,"SJAG_01509":null,"SJAG_01511":null,"SJAG_01513":null,"SJAG_01515":null,"SJAG_01516":null,"SJAG_01517":null,"SJAG_01519":null,"SJAG_01521":null,"SJAG_01527":null,"SJAG_01528":null,"SJAG_01529":null,"SJAG_01532":null,"SJAG_01540":null,"SJAG_01544":null,"SJAG_01553":null,"SJAG_01579":null,"SJAG_01583":null,"SJAG_01584":null,"SJAG_01585":null,"SJAG_01587":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01605":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01622":null,"SJAG_01625":null,"SJAG_01653":null,"SJAG_01657":null,"SJAG_01658":null,"SJAG_01667":null,"SJAG_01672":null,"SJAG_01675":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01694":null,"SJAG_01696":null,"SJAG_01699":null,"SJAG_01703":null,"SJAG_01707":null,"SJAG_01708":null,"SJAG_01711":null,"SJAG_01714":null,"SJAG_01716":null,"SJAG_01718":null,"SJAG_01720":null,"SJAG_01725":null,"SJAG_01728":null,"SJAG_01740":null,"SJAG_01745":null,"SJAG_01754":null,"SJAG_01764":null,"SJAG_01768":null,"SJAG_01771":null,"SJAG_01774":null,"SJAG_01778":null,"SJAG_01787":null,"SJAG_01790":null,"SJAG_01794":null,"SJAG_01799":null,"SJAG_01801":null,"SJAG_01804":null,"SJAG_01805":null,"SJAG_01818":null,"SJAG_01821":null,"SJAG_01822":null,"SJAG_01823":null,"SJAG_01825":null,"SJAG_01826":null,"SJAG_01830":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01843":null,"SJAG_01855":null,"SJAG_01863":null,"SJAG_01867":null,"SJAG_01873":null,"SJAG_01878":null,"SJAG_01885":null,"SJAG_01894":null,"SJAG_01901":null,"SJAG_01906":null,"SJAG_01910":null,"SJAG_01916":null,"SJAG_01919":null,"SJAG_01926":null,"SJAG_01930":null,"SJAG_01936":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01952":null,"SJAG_01956":null,"SJAG_01978":null,"SJAG_01983":null,"SJAG_01993":null,"SJAG_02000":null,"SJAG_02005":null,"SJAG_02013":null,"SJAG_02018":null,"SJAG_02022":null,"SJAG_02026":null,"SJAG_02027":null,"SJAG_02036":null,"SJAG_02043":null,"SJAG_02044":null,"SJAG_02045":null,"SJAG_02048":null,"SJAG_02052":null,"SJAG_02057":null,"SJAG_02058":null,"SJAG_02066":null,"SJAG_02072":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02119":null,"SJAG_02135":null,"SJAG_02138":null,"SJAG_02149":null,"SJAG_02162":null,"SJAG_02165":null,"SJAG_02169":null,"SJAG_02170":null,"SJAG_02183":null,"SJAG_02189":null,"SJAG_02194":null,"SJAG_02196":null,"SJAG_02203":null,"SJAG_02213":null,"SJAG_02214":null,"SJAG_02218":null,"SJAG_02231":null,"SJAG_02232":null,"SJAG_02233":null,"SJAG_02239":null,"SJAG_02244":null,"SJAG_02249":null,"SJAG_02252":null,"SJAG_02254":null,"SJAG_02255":null,"SJAG_02258":null,"SJAG_02266":null,"SJAG_02275":null,"SJAG_02278":null,"SJAG_02285":null,"SJAG_02289":null,"SJAG_02303":null,"SJAG_02308":null,"SJAG_02311":null,"SJAG_02314":null,"SJAG_02318":null,"SJAG_02319":null,"SJAG_02321":null,"SJAG_02326":null,"SJAG_02329":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02366":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02381":null,"SJAG_02382":null,"SJAG_02383":null,"SJAG_02385":null,"SJAG_02389":null,"SJAG_02391":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02401":null,"SJAG_02404":null,"SJAG_02406":null,"SJAG_02409":null,"SJAG_02413":null,"SJAG_02415":null,"SJAG_02416":null,"SJAG_02419":null,"SJAG_02424":null,"SJAG_02426":null,"SJAG_02429":null,"SJAG_02433":null,"SJAG_02439":null,"SJAG_02444":null,"SJAG_02447":null,"SJAG_02451":null,"SJAG_02458":null,"SJAG_02466":null,"SJAG_02467":null,"SJAG_02468":null,"SJAG_02472":null,"SJAG_02474":null,"SJAG_02481":null,"SJAG_02485":null,"SJAG_02486":null,"SJAG_02494":null,"SJAG_02498":null,"SJAG_02500":null,"SJAG_02514":null,"SJAG_02520":null,"SJAG_02536":null,"SJAG_02540":null,"SJAG_02541":null,"SJAG_02549":null,"SJAG_02551":null,"SJAG_02563":null,"SJAG_02566":null,"SJAG_02569":null,"SJAG_02571":null,"SJAG_02573":null,"SJAG_02576":null,"SJAG_02589":null,"SJAG_02592":null,"SJAG_02594":null,"SJAG_02601":null,"SJAG_02605":null,"SJAG_02608":null,"SJAG_02613":null,"SJAG_02620":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02629":null,"SJAG_02638":null,"SJAG_02641":null,"SJAG_02645":null,"SJAG_02671":null,"SJAG_02684":null,"SJAG_02691":null,"SJAG_02698":null,"SJAG_02700":null,"SJAG_02701":null,"SJAG_02703":null,"SJAG_02709":null,"SJAG_02712":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02724":null,"SJAG_02725":null,"SJAG_02730":null,"SJAG_02736":null,"SJAG_02752":null,"SJAG_02756":null,"SJAG_02760":null,"SJAG_02765":null,"SJAG_02768":null,"SJAG_02771":null,"SJAG_02773":null,"SJAG_02778":null,"SJAG_02785":null,"SJAG_02795":null,"SJAG_02798":null,"SJAG_02807":null,"SJAG_02808":null,"SJAG_02810":null,"SJAG_02812":null,"SJAG_02817":null,"SJAG_02819":null,"SJAG_02822":null,"SJAG_02823":null,"SJAG_02838":null,"SJAG_02846":null,"SJAG_02849":null,"SJAG_02854":null,"SJAG_02858":null,"SJAG_02860":null,"SJAG_02869":null,"SJAG_02872":null,"SJAG_02873":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02898":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_02921":null,"SJAG_02922":null,"SJAG_02923":null,"SJAG_02927":null,"SJAG_02938":null,"SJAG_02945":null,"SJAG_02956":null,"SJAG_02981":null,"SJAG_02990":null,"SJAG_03006":null,"SJAG_03023":null,"SJAG_03026":null,"SJAG_03033":null,"SJAG_03036":null,"SJAG_03041":null,"SJAG_03042":null,"SJAG_03047":null,"SJAG_03048":null,"SJAG_03061":null,"SJAG_03067":null,"SJAG_03070":null,"SJAG_03072":null,"SJAG_03073":null,"SJAG_03081":null,"SJAG_03086":null,"SJAG_03089":null,"SJAG_03090":null,"SJAG_03097":null,"SJAG_03106":null,"SJAG_03113":null,"SJAG_03118":null,"SJAG_03126":null,"SJAG_03128":null,"SJAG_03130":null,"SJAG_03132":null,"SJAG_03137":null,"SJAG_03143":null,"SJAG_03145":null,"SJAG_03157":null,"SJAG_03160":null,"SJAG_03170":null,"SJAG_03179":null,"SJAG_03183":null,"SJAG_03185":null,"SJAG_03193":null,"SJAG_03209":null,"SJAG_03219":null,"SJAG_03223":null,"SJAG_03230":null,"SJAG_03234":null,"SJAG_03238":null,"SJAG_03241":null,"SJAG_03248":null,"SJAG_03255":null,"SJAG_03258":null,"SJAG_03263":null,"SJAG_03268":null,"SJAG_03272":null,"SJAG_03276":null,"SJAG_03279":null,"SJAG_03283":null,"SJAG_03286":null,"SJAG_03289":null,"SJAG_03300":null,"SJAG_03302":null,"SJAG_03309":null,"SJAG_03310":null,"SJAG_03319":null,"SJAG_03327":null,"SJAG_03338":null,"SJAG_03340":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03346":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03353":null,"SJAG_03355":null,"SJAG_03356":null,"SJAG_03361":null,"SJAG_03366":null,"SJAG_03371":null,"SJAG_03376":null,"SJAG_03383":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03388":null,"SJAG_03394":null,"SJAG_03405":null,"SJAG_03417":null,"SJAG_03421":null,"SJAG_03431":null,"SJAG_03438":null,"SJAG_03441":null,"SJAG_03448":null,"SJAG_03453":null,"SJAG_03454":null,"SJAG_03455":null,"SJAG_03466":null,"SJAG_03473":null,"SJAG_03482":null,"SJAG_03484":null,"SJAG_03486":null,"SJAG_03488":null,"SJAG_03501":null,"SJAG_03505":null,"SJAG_03508":null,"SJAG_03519":null,"SJAG_03525":null,"SJAG_03529":null,"SJAG_03538":null,"SJAG_03543":null,"SJAG_03548":null,"SJAG_03550":null,"SJAG_03557":null,"SJAG_03573":null,"SJAG_03575":null,"SJAG_03576":null,"SJAG_03579":null,"SJAG_03581":null,"SJAG_03590":null,"SJAG_03591":null,"SJAG_03592":null,"SJAG_03597":null,"SJAG_03599":null,"SJAG_03601":null,"SJAG_03602":null,"SJAG_03611":null,"SJAG_03618":null,"SJAG_03622":null,"SJAG_03623":null,"SJAG_03624":null,"SJAG_03625":null,"SJAG_03627":null,"SJAG_03628":null,"SJAG_03631":null,"SJAG_03635":null,"SJAG_03637":null,"SJAG_03655":null,"SJAG_03664":null,"SJAG_03668":null,"SJAG_03677":null,"SJAG_03678":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03689":null,"SJAG_03692":null,"SJAG_03694":null,"SJAG_03695":null,"SJAG_03696":null,"SJAG_03699":null,"SJAG_03704":null,"SJAG_03705":null,"SJAG_03706":null,"SJAG_03709":null,"SJAG_03720":null,"SJAG_03735":null,"SJAG_03739":null,"SJAG_03745":null,"SJAG_03748":null,"SJAG_03752":null,"SJAG_03753":null,"SJAG_03758":null,"SJAG_03763":null,"SJAG_03776":null,"SJAG_03787":null,"SJAG_03792":null,"SJAG_03793":null,"SJAG_03799":null,"SJAG_03802":null,"SJAG_03805":null,"SJAG_03812":null,"SJAG_03828":null,"SJAG_03839":null,"SJAG_03841":null,"SJAG_03844":null,"SJAG_03845":null,"SJAG_03850":null,"SJAG_03851":null,"SJAG_03854":null,"SJAG_03867":null,"SJAG_03869":null,"SJAG_03876":null,"SJAG_03879":null,"SJAG_03883":null,"SJAG_03884":null,"SJAG_03886":null,"SJAG_03887":null,"SJAG_03893":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03905":null,"SJAG_03907":null,"SJAG_03911":null,"SJAG_03916":null,"SJAG_03918":null,"SJAG_03927":null,"SJAG_03928":null,"SJAG_03931":null,"SJAG_03936":null,"SJAG_03940":null,"SJAG_03942":null,"SJAG_03944":null,"SJAG_03945":null,"SJAG_03952":null,"SJAG_03957":null,"SJAG_03967":null,"SJAG_03969":null,"SJAG_03970":null,"SJAG_03974":null,"SJAG_03981":null,"SJAG_03982":null,"SJAG_03984":null,"SJAG_03987":null,"SJAG_03997":null,"SJAG_04005":null,"SJAG_04006":null,"SJAG_04009":null,"SJAG_04018":null,"SJAG_04025":null,"SJAG_04026":null,"SJAG_04030":null,"SJAG_04036":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04052":null,"SJAG_04056":null,"SJAG_04061":null,"SJAG_04083":null,"SJAG_04084":null,"SJAG_04085":null,"SJAG_04088":null,"SJAG_04092":null,"SJAG_04097":null,"SJAG_04099":null,"SJAG_04100":null,"SJAG_04103":null,"SJAG_04118":null,"SJAG_04126":null,"SJAG_04128":null,"SJAG_04130":null,"SJAG_04140":null,"SJAG_04141":null,"SJAG_04151":null,"SJAG_04153":null,"SJAG_04155":null,"SJAG_04159":null,"SJAG_04186":null,"SJAG_04191":null,"SJAG_04194":null,"SJAG_04198":null,"SJAG_04200":null,"SJAG_04203":null,"SJAG_04205":null,"SJAG_04206":null,"SJAG_04213":null,"SJAG_04232":null,"SJAG_04235":null,"SJAG_04249":null,"SJAG_04253":null,"SJAG_04259":null,"SJAG_04262":null,"SJAG_04268":null,"SJAG_04274":null,"SJAG_04280":null,"SJAG_04283":null,"SJAG_04287":null,"SJAG_04291":null,"SJAG_04312":null,"SJAG_04321":null,"SJAG_04322":null,"SJAG_04329":null,"SJAG_04332":null,"SJAG_04343":null,"SJAG_04350":null,"SJAG_04355":null,"SJAG_04360":null,"SJAG_04369":null,"SJAG_04373":null,"SJAG_04374":null,"SJAG_04381":null,"SJAG_04383":null,"SJAG_04384":null,"SJAG_04388":null,"SJAG_04389":null,"SJAG_04394":null,"SJAG_04396":null,"SJAG_04407":null,"SJAG_04412":null,"SJAG_04421":null,"SJAG_04422":null,"SJAG_04426":null,"SJAG_04427":null,"SJAG_04435":null,"SJAG_04452":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04462":null,"SJAG_04464":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04471":null,"SJAG_04477":null,"SJAG_04479":null,"SJAG_04486":null,"SJAG_04496":null,"SJAG_04500":null,"SJAG_04502":null,"SJAG_04503":null,"SJAG_04507":null,"SJAG_04509":null,"SJAG_04512":null,"SJAG_04522":null,"SJAG_04527":null,"SJAG_04537":null,"SJAG_04539":null,"SJAG_04544":null,"SJAG_04546":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04573":null,"SJAG_04574":null,"SJAG_04576":null,"SJAG_04584":null,"SJAG_04586":null,"SJAG_04596":null,"SJAG_04597":null,"SJAG_04601":null,"SJAG_04607":null,"SJAG_04611":null,"SJAG_04613":null,"SJAG_04614":null,"SJAG_04615":null,"SJAG_04619":null,"SJAG_04638":null,"SJAG_04640":null,"SJAG_04647":null,"SJAG_04655":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04671":null,"SJAG_04682":null,"SJAG_04699":null,"SJAG_04705":null,"SJAG_04712":null,"SJAG_04724":null,"SJAG_04734":null,"SJAG_04749":null,"SJAG_04755":null,"SJAG_04756":null,"SJAG_04758":null,"SJAG_04761":null,"SJAG_04765":null,"SJAG_04768":null,"SJAG_04771":null,"SJAG_04776":null,"SJAG_04777":null,"SJAG_04782":null,"SJAG_04793":null,"SJAG_04813":null,"SJAG_04818":null,"SJAG_04820":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04839":null,"SJAG_04853":null,"SJAG_04855":null,"SJAG_04871":null,"SJAG_04873":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04884":null,"SJAG_04890":null,"SJAG_04910":null,"SJAG_04920":null,"SJAG_04921":null,"SJAG_04942":null,"SJAG_04943":null,"SJAG_04946":null,"SJAG_04968":null,"SJAG_04980":null,"SJAG_04987":null,"SJAG_04989":null,"SJAG_04990":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05006":null,"SJAG_05010":null,"SJAG_05014":null,"SJAG_05020":null,"SJAG_05030":null,"SJAG_05153":null,"SJAG_05161":null,"SJAG_05184":null,"SJAG_05187":null,"SJAG_05192":null,"SJAG_05203":null,"SJAG_05231":null,"SJAG_05234":null,"SJAG_05236":null,"SJAG_05240":null,"SJAG_05242":null,"SJAG_05243":null,"SJAG_05247":null,"SJAG_05265":null,"SJAG_05276":null,"SJAG_05286":null,"SJAG_05288":null,"SJAG_05289":null,"SJAG_05290":null,"SJAG_05304":null,"SJAG_05313":null,"SJAG_05314":null,"SJAG_05322":null,"SJAG_05329":null,"SJAG_05330":null,"SJAG_05335":null,"SJAG_05337":null,"SJAG_05341":null,"SJAG_05343":null,"SJAG_05346":null,"SJAG_05373":null,"SJAG_05694":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_06576":null,"SJAG_06588":null,"SJAG_06592":null,"SJAG_06599":null,"SJAG_06608":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06638":null,"SJAG_06641":null,"SJAG_07011":null,"SJAG_16454":null,"SJAG_16457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of biological process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:25866389":null,"PMID:30664646":null,"PMID:32915139":null,"PMID:35226668":null},"secondary_identifiers":["GO:0050791"],"synonyms":[{"name":"regulation of physiological process","type":"exact"}],"termid":"GO:0050789","terms_by_termid":{"GO:0000018":null,"GO:0000122":null,"GO:0000160":null,"GO:0000165":null,"GO:0000183":null,"GO:0000184":null,"GO:0000196":null,"GO:0000288":null,"GO:0000289":null,"GO:0000290":null,"GO:0000294":null,"GO:0000381":null,"GO:0000750":null,"GO:0000956":null,"GO:0001100":null,"GO:0003400":null,"GO:0006109":null,"GO:0006110":null,"GO:0006355":null,"GO:0006356":null,"GO:0006357":null,"GO:0006359":null,"GO:0006402":null,"GO:0006449":null,"GO:0006808":null,"GO:0006984":null,"GO:0007063":null,"GO:0007088":null,"GO:0007089":null,"GO:0007091":null,"GO:0007094":null,"GO:0007095":null,"GO:0007096":null,"GO:0007165":null,"GO:0007166":null,"GO:0007186":null,"GO:0007254":null,"GO:0007266":null,"GO:0007267":null,"GO:0007346":null,"GO:0008360":null,"GO:0009785":null,"GO:0010389":null,"GO:0010468":null,"GO:0010506":null,"GO:0010507":null,"GO:0010508":null,"GO:0010510":null,"GO:0010514":null,"GO:0010515":null,"GO:0010520":null,"GO:0010569":null,"GO:0010590":null,"GO:0010619":null,"GO:0010621":null,"GO:0010628":null,"GO:0010629":null,"GO:0010637":null,"GO:0010821":null,"GO:0010845":null,"GO:0010846":null,"GO:0010895":null,"GO:0010906":null,"GO:0010964":null,"GO:0010967":null,"GO:0010971":null,"GO:0010972":null,"GO:0011000":null,"GO:0012502":null,"GO:0016239":null,"GO:0016242":null,"GO:0016441":null,"GO:0016480":null,"GO:0017157":null,"GO:0019216":null,"GO:0019722":null,"GO:0022408":null,"GO:0023051":null,"GO:0023052":null,"GO:0030100":null,"GO:0030307":null,"GO:0030422":null,"GO:0030466":null,"GO:0030833":null,"GO:0030968":null,"GO:0031028":null,"GO:0031029":null,"GO:0031030":null,"GO:0031031":null,"GO:0031047":null,"GO:0031048":null,"GO:0031087":null,"GO:0031110":null,"GO:0031117":null,"GO:0031137":null,"GO:0031138":null,"GO:0031139":null,"GO:0031141":null,"GO:0031142":null,"GO:0031291":null,"GO:0031445":null,"GO:0031453":null,"GO:0031507":null,"GO:0031508":null,"GO:0031509":null,"GO:0031536":null,"GO:0031568":null,"GO:0031569":null,"GO:0031571":null,"GO:0031573":null,"GO:0031582":null,"GO:0031929":null,"GO:0031930":null,"GO:0031991":null,"GO:0032005":null,"GO:0032007":null,"GO:0032008":null,"GO:0032210":null,"GO:0032215":null,"GO:0032231":null,"GO:0032434":null,"GO:0032435":null,"GO:0032436":null,"GO:0032443":null,"GO:0032483":null,"GO:0032786":null,"GO:0032878":null,"GO:0032888":null,"GO:0032889":null,"GO:0032933":null,"GO:0032951":null,"GO:0032955":null,"GO:0032956":null,"GO:0032968":null,"GO:0032995":null,"GO:0033157":null,"GO:0033314":null,"GO:0033315":null,"GO:0033316":null,"GO:0033562":null,"GO:0033621":null,"GO:0033696":null,"GO:0034244":null,"GO:0034307":null,"GO:0034316":null,"GO:0035024":null,"GO:0035432":null,"GO:0035556":null,"GO:0036450":null,"GO:0036498":null,"GO:0038066":null,"GO:0038202":null,"GO:0038203":null,"GO:0040020":null,"GO:0040029":null,"GO:0042176":null,"GO:0042307":null,"GO:0042308":null,"GO:0042997":null,"GO:0043065":null,"GO:0043408":null,"GO:0043409":null,"GO:0043456":null,"GO:0043488":null,"GO:0043609":null,"GO:0043628":null,"GO:0044773":null,"GO:0044778":null,"GO:0044878":null,"GO:0045128":null,"GO:0045540":null,"GO:0045717":null,"GO:0045719":null,"GO:0045732":null,"GO:0045739":null,"GO:0045806":null,"GO:0045807":null,"GO:0045814":null,"GO:0045815":null,"GO:0045820":null,"GO:0045834":null,"GO:0045842":null,"GO:0045862":null,"GO:0045875":null,"GO:0045876":null,"GO:0045892":null,"GO:0045899":null,"GO:0045901":null,"GO:0045905":null,"GO:0045921":null,"GO:0045943":null,"GO:0045944":null,"GO:0045948":null,"GO:0045951":null,"GO:0046580":null,"GO:0046827":null,"GO:0048015":null,"GO:0048024":null,"GO:0048026":null,"GO:0048255":null,"GO:0050684":null,"GO:0050850":null,"GO:0051016":null,"GO:0051252":null,"GO:0051445":null,"GO:0051446":null,"GO:0051447":null,"GO:0051516":null,"GO:0051517":null,"GO:0051519":null,"GO:0051523":null,"GO:0051598":null,"GO:0051728":null,"GO:0060195":null,"GO:0060211":null,"GO:0060212":null,"GO:0060213":null,"GO:0060236":null,"GO:0060237":null,"GO:0060257":null,"GO:0060261":null,"GO:0060628":null,"GO:0060906":null,"GO:0060963":null,"GO:0061013":null,"GO:0061157":null,"GO:0061158":null,"GO:0061173":null,"GO:0061188":null,"GO:0061191":null,"GO:0061192":null,"GO:0061361":null,"GO:0061387":null,"GO:0061454":null,"GO:0061762":null,"GO:0062038":null,"GO:0062123":null,"GO:0062168":null,"GO:0062200":null,"GO:0062209":null,"GO:0070131":null,"GO:0070134":null,"GO:0070317":null,"GO:0070452":null,"GO:0070478":null,"GO:0070481":null,"GO:0070507":null,"GO:0070610":null,"GO:0070935":null,"GO:0070966":null,"GO:0071028":null,"GO:0071030":null,"GO:0071031":null,"GO:0071032":null,"GO:0071042":null,"GO:0071044":null,"GO:0071072":null,"GO:0071507":null,"GO:0071807":null,"GO:0075296":null,"GO:0075297":null,"GO:0075319":null,"GO:0090001":null,"GO:0090006":null,"GO:0090029":null,"GO:0090052":null,"GO:0090053":null,"GO:0090055":null,"GO:0090070":null,"GO:0090141":null,"GO:0090180":null,"GO:0090258":null,"GO:0090267":null,"GO:0090297":null,"GO:0090334":null,"GO:0090520":null,"GO:0090669":null,"GO:0097720":null,"GO:0106057":null,"GO:0110031":null,"GO:0110032":null,"GO:0110034":null,"GO:0110044":null,"GO:0110045":null,"GO:0110161":null,"GO:0110162":null,"GO:0120047":null,"GO:0120271":null,"GO:0120272":null,"GO:0120292":null,"GO:0120306":null,"GO:0140018":null,"GO:0140281":null,"GO:0140325":null,"GO:0140429":null,"GO:0140462":null,"GO:0140469":null,"GO:0140499":null,"GO:0140501":null,"GO:0140538":null,"GO:0140648":null,"GO:0140718":null,"GO:0140719":null,"GO:0140727":null,"GO:0140748":null,"GO:0141005":null,"GO:0141014":null,"GO:0141194":null,"GO:0180040":null,"GO:1900039":null,"GO:1900087":null,"GO:1900181":null,"GO:1900237":null,"GO:1900735":null,"GO:1900745":null,"GO:1901098":null,"GO:1901673":null,"GO:1901800":null,"GO:1901970":null,"GO:1901987":null,"GO:1901993":null,"GO:1902103":null,"GO:1902267":null,"GO:1902369":null,"GO:1902412":null,"GO:1902413":null,"GO:1902424":null,"GO:1902425":null,"GO:1902426":null,"GO:1902472":null,"GO:1902543":null,"GO:1902647":null,"GO:1902648":null,"GO:1902660":null,"GO:1902681":null,"GO:1902794":null,"GO:1902795":null,"GO:1902801":null,"GO:1902845":null,"GO:1902846":null,"GO:1902854":null,"GO:1902917":null,"GO:1903023":null,"GO:1903024":null,"GO:1903067":null,"GO:1903077":null,"GO:1903138":null,"GO:1903139":null,"GO:1903338":null,"GO:1903340":null,"GO:1903373":null,"GO:1903380":null,"GO:1903432":null,"GO:1903464":null,"GO:1903465":null,"GO:1903467":null,"GO:1903468":null,"GO:1903472":null,"GO:1903473":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:1903599":null,"GO:1903617":null,"GO:1903715":null,"GO:1903753":null,"GO:1903931":null,"GO:1903940":null,"GO:1904262":null,"GO:1904263":null,"GO:1904293":null,"GO:1904332":null,"GO:1904352":null,"GO:1904514":null,"GO:1904515":null,"GO:1904537":null,"GO:1904547":null,"GO:1904595":null,"GO:1904689":null,"GO:1904775":null,"GO:1904846":null,"GO:1904967":null,"GO:1905191":null,"GO:1905263":null,"GO:1905287":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:1905391":null,"GO:1905530":null,"GO:1905533":null,"GO:1905534":null,"GO:1905557":null,"GO:1905560":null,"GO:1905561":null,"GO:1905569":null,"GO:1905589":null,"GO:1905626":null,"GO:1905634":null,"GO:1905665":null,"GO:1905707":null,"GO:1905744":null,"GO:1905746":null,"GO:1905757":null,"GO:1905758":null,"GO:1905785":null,"GO:1905786":null,"GO:1905824":null,"GO:1905857":null,"GO:1905949":null,"GO:1990074":null,"GO:1990431":null,"GO:1990432":null,"GO:1990611":null,"GO:1990625":null,"GO:1990949":null,"GO:1990950":null,"GO:1990983":null,"GO:2000099":null,"GO:2000100":null,"GO:2000114":null,"GO:2000134":null,"GO:2000156":null,"GO:2000185":null,"GO:2000214":null,"GO:2000234":null,"GO:2000247":null,"GO:2000369":null,"GO:2000432":null,"GO:2000639":null,"GO:2000640":null,"GO:2000765":null,"GO:2000766":null,"GO:2000767":null,"GO:2000769":null,"GO:2000779":null,"GO:2000781":null,"GO:2000784":null,"GO:2000786":null,"GO:2000815":null,"GO:2000816":null,"GO:2001033":null,"GO:2001034":null,"GO:2001043":null,"GO:2001125":null,"GO:2001135":null,"GO:2001172":null,"GO:2001178":null,"GO:2001211":null}}


id: MONDO:0002067
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"female breast carcinoma","termid":"MONDO:0004379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"female breast upper-inner quadrant cancer","secondary_identifiers":["SCTID:188152004","ICD9:174.2","UMLS:C0153550","MEDGEN:509324","DOID:1647","ICD10CM:C50.2"],"synonyms":[{"name":"malignant neoplasm of upper-inner quadrant of female breast","type":"exact"}],"termid":"MONDO:0002067","xrefs":{"Monarch":{"xref_id":"0002067"}}}


id: GO:1902877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of embryonic pattern specification.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:mr","PMID:16872597"],"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 embryonic pattern specification","termid":"GO:1902875"},{"relation_name":"positively_regulates","term_name":"embryonic pattern specification","termid":"GO:0009880"}],"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 embryonic pattern specification","synonyms":[{"name":"activation of embryonic pattern specification","type":"narrow"},{"name":"activation of ventral/lateral system","type":"related"},{"name":"positive regulation of ventral/lateral system","type":"related"},{"name":"up regulation of embryonic pattern specification","type":"exact"},{"name":"up regulation of ventral/lateral system","type":"related"},{"name":"up-regulation of embryonic pattern specification","type":"exact"},{"name":"up-regulation of ventral/lateral system","type":"related"},{"name":"upregulation of embryonic pattern specification","type":"exact"},{"name":"upregulation of ventral/lateral system","type":"related"}],"termid":"GO:1902877"}


id: GO:0061968
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The organization process that preserves the asymmetry in an organism's body plan or part of an organism with respect to the left and right halves.","definition_xrefs":["GOC:BHF","PMID:18629866"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"}],"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":"maintenance of left/right asymmetry","termid":"GO:0061968"}


id: GO:0035113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring in the embryo, by which the anatomical structures of the appendage are generated and organized. An appendage is an organ or part that is attached to the trunk of an organism, such as a limb or a branch.","definition_xrefs":["ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"appendage morphogenesis","termid":"GO:0035107"},{"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 appendage morphogenesis","termid":"GO:0035113"}


id: MONDO:0850197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A medulloblastoma that is characterized as a molecular subtype by activation of the sonic hedgehog (SHH) pathway and TP53 mutations that may be present or absent.","definition_xrefs":["DOID:0080703"],"direct_ancestors":[{"relation_name":"is_a","term_name":"medulloblastoma","termid":"MONDO:0007959"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"medulloblastoma SHH activated","secondary_identifiers":["NCIT:C129441","MEDGEN:1375478","UMLS:C4330671"],"termid":"MONDO:0850197","xrefs":{"Monarch":{"xref_id":"0850197"}}}


id: PBO:0053957
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 1264","termid":"PBO:0053957"}


id: FYPO:0005297
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"normal 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity","termid":"FYPO:0005297"}


id: PBO:0088715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated WD repeat protein Utp4","termid":"PBO:0088715"}


id: PBO:0068061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 366","termid":"PBO:0068061"}


id: MONDO:0011445
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"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 11","secondary_identifiers":["Orphanet:2822","UMLS:C1858479","GARD:4919","NCIT:C148317","DOID:0110764","MEDGEN:388073","OMIM:604360","SCTID:715491000"],"synonyms":[{"name":"HSP-TCC","type":"exact"},{"name":"Nakamura Osame syndrome","type":"related"},{"name":"Nakamura-Osame syndrome","type":"exact"},{"name":"SPG11","type":"exact"},{"name":"SPG11 hereditary spastic paraplegia","type":"exact"},{"name":"autosomal recessive spastic paraplegia 11","type":"exact"},{"name":"autosomal recessive spastic paraplegia complicated with thin corpus callosum","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 11","type":"exact"},{"name":"autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum","type":"exact"},{"name":"hereditary spastic paraplegia caused by mutation in SPG11","type":"exact"},{"name":"hereditary spastic paraplegia mental impairment and thin corpus callosum","type":"related"},{"name":"hereditary spastic paraplegia type 11","type":"exact"},{"name":"spastic paraplegia - intellectual deficit - thin corpus callosum","type":"related"},{"name":"spastic paraplegia 11","type":"related"},{"name":"spastic paraplegia 11, autosomal recessive","type":"related"},{"name":"spastic paraplegia, autosomal recessive, complicated, with thin corpus callosum","type":"related"},{"name":"spastic paraplegia, autosomal recessive, with mental impairment and thin corpus callosum","type":"related"},{"name":"spastic paraplegia-intellectual disability-thin corpus callosum syndrome","type":"exact"}],"termid":"MONDO:0011445","xrefs":{"Monarch":{"xref_id":"0011445"}}}


id: _global:translates_to
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Inverse of translation _of.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translates_to","termid":"_global:translates_to"}


id: PBO:0068174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 481","termid":"PBO:0068174"}


id: GO:0160013
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N6-(2-hydroxyisobutanoyl)-L-lysyl-[protein] + NAD+ = 2''-O-(2-hydroxyisobutanoyl)-ADP-D-ribose + L-lysyl-[protein] + nicotinamide.","definition_xrefs":["PMID:31328167"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"NAD-dependent protein de-2-hydroxyisobutyrylase activity","secondary_identifiers":["RHEA:24364"],"termid":"GO:0160013"}


id: MONDO:0859341
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypotrichosis","termid":"MONDO:0003037"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis 15","secondary_identifiers":["UMLS:C5774279","MEDGEN:1824052","OMIM:620177","DOID:0060968"],"termid":"MONDO:0859341","xrefs":{"Monarch":{"xref_id":"0859341"}}}


id: GO:0005943
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A class I phosphatidylinositol 3-kinase complex that possesses 1-phosphatidylinositol-4-phosphate 3-kinase activity; comprises a catalytic class IA phosphoinositide 3-kinase (PI3K) subunit and an associated SH2 domain-containing regulatory subunit that is a member of a family of related proteins often called p85 proteins. Through the interaction with the SH2-containing adaptor subunits, Class IA PI3K catalytic subunits are linked to tyrosine kinase signaling pathways.","definition_xrefs":["PMID:9255069","PMID:9759495"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol 3-kinase complex, class I","termid":"GO:0097651"}],"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":"phosphatidylinositol 3-kinase complex, class IA","secondary_identifiers":["GO:0035030"],"synonyms":[{"name":"1-phosphatidylinositol-4-phosphate 3-kinase, class IA complex","type":"exact"},{"name":"1-phosphatidylinositol-4-phosphate kinase, class IA complex","type":"exact"},{"name":"class IA PI3K complex","type":"exact"},{"name":"phosphoinositide 3-kinase complex, class IA","type":"exact"}],"termid":"GO:0005943"}


id: GO:0033806
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-threonine + fluoroacetaldehyde = acetaldehyde + 4-fluoro-L-threonine.","definition_xrefs":["RHEA:11748"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transketolase or transaldolase activity","termid":"GO:0016744"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016744"}],"interesting_parent_ids":["GO:0003824","GO:0016744","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"fluorothreonine transaldolase activity","secondary_identifiers":["EC:2.2.1.8"],"synonyms":[{"name":"fluoroacetaldehyde:L-threonine aldehydetransferase activity","type":"related"}],"termid":"GO:0033806"}


id: FYPO:0005023
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell is inviable, contains one nucleus and one or more septa and is elongated. Cells with this phenotype are inviable, and the nucleus is not in the normal location.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"is_a","term_name":"inviable septated mononucleate vegetative cell","termid":"FYPO:0002000"},{"relation_name":"is_a","term_name":"inviable elongated mononucleate vegetative cell with mislocalized nucleus","termid":"FYPO:0002337"},{"relation_name":"is_a","term_name":"inviable septated vegetative cell with abnormal cell morphology","termid":"FYPO:0002452"},{"relation_name":"is_a","term_name":"elongated septated vegetative cell","termid":"FYPO:0004750"},{"relation_name":"output_of","term_name":"cut","termid":"FYPO:0000229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000337"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000004","FYPO:0000005","FYPO:0005447","FYPO:0000138","FYPO:0000337","FYPO:0000631","FYPO:0000032","FYPO:0000641","FYPO:0000002"],"is_obsolete":false,"name":"inviable elongated septated mononucleate vegetative cell","synonyms":[{"name":"elongated cell with cytokinesis in the absence of nuclear division","type":"related"},{"name":"elongated cell with cytokinesis without nuclear division","type":"related"},{"name":"elongated cell with septation in the absence of nuclear division","type":"related"},{"name":"elongated cell with septation independent of mitosis","type":"related"},{"name":"elongated cell with septation without nuclear division","type":"related"},{"name":"inviable elongated cell with premature septation","type":"related"},{"name":"inviable elongated septated mononucleate cell","type":"exact"},{"name":"inviable elongated septated mononucleate cell during vegetative growth","type":"exact"},{"name":"inviable elongated septated mononucleate vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable elongated septated mononucleate vegetative cell with mislocalized nucleus","type":"exact"},{"name":"inviable septated mononucleate elongated vegetative cell","type":"exact"},{"name":"lethal; elongated septated mononucleate vegetative cell","type":"exact"}],"termid":"FYPO:0005023"}


id: PBO:0028033
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_curved_elongated_mononucleate_vegetative_cell","termid":"PBO:0028033"}


id: GO:0005648
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete importin, beta-subunit (obsolete GO:0005648)","synonyms":[{"name":"importin, beta-subunit","type":"exact"},{"name":"karyopherin-beta1","type":"exact"}],"termid":"GO:0005648"}


id: PBO:0059976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 21","termid":"PBO:0059976"}


id: PBO:0087965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transporter of the ATP-binding cassette (ABC) family; role in plasma membrane sterol incorporation; implicated in pleiotropic drug resistance; provides resistance to ethanol stress and contributes to a decreased intracellular accumulation of ethanol; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0087965"}


id: PBO:0091854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk25","termid":"PBO:0091854"}


id: GO:0000312
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The smaller of the two subunits of a plastid ribosome.","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organellar small ribosomal subunit","termid":"GO:0000314"},{"relation_name":"part_of","term_name":"plastid ribosome","termid":"GO:0009547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"plastid small ribosomal subunit","termid":"GO:0000312"}


id: MONDO:0011569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy.","definition_xrefs":["Orphanet:98856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 2B1","secondary_identifiers":["DOID:0110156","UMLS:C1854154","GARD:8548","icd11.foundation:957134152","OMIM:605588","SCTID:725048002","MESH:C537990","MEDGEN:343064"],"synonyms":[{"name":"AR-CMT2B1","type":"exact"},{"name":"CMT 2B1","type":"related"},{"name":"CMT2B1","type":"exact"},{"name":"Charcot Marie Tooth disease type 2B1","type":"related"},{"name":"Charcot-Marie-Tooth disease neuronal type 2B1","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 2 caused by mutation in LMNA","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, 2B1","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2B1","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2B1","type":"related"},{"name":"Charcot-Marie-Tooth disease, neuronal, type 2B1","type":"related"},{"name":"Charcot-Marie-Tooth disease, type 2B1","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy type 2B1","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, type 2B1","type":"related"},{"name":"LMNA Charcot-Marie-Tooth disease type 2","type":"exact"},{"name":"autosomal recessive Charcot-Marie-Tooth disease type 2B1","type":"exact"},{"name":"autosomal recessive axonal CMT4C1","type":"exact"},{"name":"autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1","type":"exact"}],"termid":"MONDO:0011569","xrefs":{"Monarch":{"xref_id":"0011569"}}}


id: PBO:0109366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 3B","termid":"PBO:0109366"}


id: PBO:0059835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial fission regulator 1","termid":"PBO:0059835"}


id: GO:0002708
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of lymphocyte mediated immunity.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte mediated immunity","termid":"GO:0002705"},{"relation_name":"is_a","term_name":"regulation of lymphocyte mediated immunity","termid":"GO:0002706"},{"relation_name":"positively_regulates","term_name":"lymphocyte mediated immunity","termid":"GO:0002449"}],"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 lymphocyte mediated immunity","synonyms":[{"name":"activation of lymphocyte mediated immunity","type":"narrow"},{"name":"stimulation of lymphocyte mediated immunity","type":"narrow"},{"name":"up regulation of lymphocyte mediated immunity","type":"exact"},{"name":"up-regulation of lymphocyte mediated immunity","type":"exact"},{"name":"upregulation of lymphocyte mediated immunity","type":"exact"}],"termid":"GO:0002708"}


id: PBO:0004869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAG family molecular chaperone regulator Bag101 (predicted)","termid":"PBO:0004869"}


id: PBO:0058699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6827","termid":"PBO:0058699"}


id: GO:0014060
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of epinephrine.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catecholamine secretion","termid":"GO:0050433"},{"relation_name":"regulates","term_name":"epinephrine secretion","termid":"GO:0048242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of epinephrine secretion","synonyms":[{"name":"regulation of adrenaline secretion","type":"exact"}],"termid":"GO:0014060"}


id: PBO:0059332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S6 pseudogene 1","termid":"PBO:0059332"}


id: PBO:0030949
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitochondrial_aggregation_at_cell_tip","termid":"PBO:0030949"}


id: GO:0035134
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring after embryonic development, by which the anatomical structures of the dorsal fin are generated and organized. A dorsal fin is an unpaired medial fin on the dorsal aspect of a fish that provides lateral stability while swimming. Generally fish have one or two dorsal fins.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic medial fin morphogenesis","termid":"GO:0035132"},{"relation_name":"is_a","term_name":"dorsal fin morphogenesis","termid":"GO:0035142"}],"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 dorsal fin morphogenesis","termid":"GO:0035134"}


id: FYPO:0006050
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the rate, or speed, of mitotic sister chromatid separation is normal (i.e. indistinguishable from wild type). Mitotic sister chromatid separation is the process in which sister chromatids are physically detached from each other during mitosis.","definition_xrefs":["PomBase:mah","PMID:27146110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic sister chromatid separation","termid":"FYPO:0004301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal rate of mitotic sister chromatid separation","synonyms":[{"name":"normal mitotic sister chromatid separation rate","type":"exact"},{"name":"normal rate of mitotic sister chromatid separation during vegetative growth","type":"exact"},{"name":"normal rate of sister chromatid separation during mitosis","type":"exact"},{"name":"normal rate of sister chromatid separation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006050"}


id: PBO:0031744
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_intracellular_transport","termid":"PBO:0031744"}


id: PBO:0041380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement C5a receptor 1","termid":"PBO:0041380"}


id: PBO:0046111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4E family member 2 pseudogene 2","termid":"PBO:0046111"}


id: FYPO:0001919
data:
  {"alleles_by_uniquename":{"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119128],"is_not":false,"rel_names":["is_a","has_part"],"summary":null,"term":"FYPO:0003976"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the nucleus is broken into multiple small fragments that are smaller than a normal nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear morphology during vegetative growth","termid":"FYPO:0000062"},{"relation_name":"is_a","term_name":"fragmented nucleus","termid":"FYPO:0006661"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04464":null},"genotype_count":1,"genotypes_by_uniquename":{"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002403","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"fragmented nucleus during vegetative growth","references_by_uniquename":{"PMID:28954740":null},"single_locus_annotated_genes":["SJAG_04464"],"single_locus_genotype_uniquenames":["pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"fragmented nuclear DNA during vegetative growth","type":"related"},{"name":"fragmented nucleus during mitotic cell cycle","type":"related"},{"name":"loss of nuclear integrity during vegetative growth","type":"related"}],"termid":"FYPO:0001919","terms_by_termid":{"FYECO:0000004":null,"FYPO:0003976":null}}


id: FYPO:0005131
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which spores germinate to a lower extent than wild type following exposure to ethanol.","definition_xrefs":["PomBase:mah","PMID:24623719"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell phenotype","termid":"FYPO:0003037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"spores sensitive to ethanol","termid":"FYPO:0005131"}


id: MONDO:0035646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myotonic dystrophy type 1","termid":"MONDO:0008056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005336"],"is_obsolete":false,"name":"congenital-onset Steinert myotonic dystrophy","secondary_identifiers":["GARD:22361","Orphanet:589821","ICD10CM:G71.1","MEDGEN:1842512","UMLS:C5680305"],"synonyms":[{"name":"Congenital-onset Steinert disease","type":"exact"},{"name":"Congenital-onset myotonic dystrophy type 1","type":"exact"}],"termid":"MONDO:0035646","xrefs":{"Monarch":{"xref_id":"0035646"}}}


id: GO:0060845
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of a cell to a venous endothelial cell fate and its capacity to differentiate into an venous endothelial cell.","definition_xrefs":["GOC:dph","GOC:tb","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel endothelial cell fate commitment","termid":"GO:0060846"},{"relation_name":"part_of","term_name":"venous endothelial cell differentiation","termid":"GO:0060843"}],"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":"venous endothelial cell fate commitment","termid":"GO:0060845"}


id: PBO:0075568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spindle and centriole associated protein 1","termid":"PBO:0075568"}


id: PBO:0041933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBX3 pseudogene 1","termid":"PBO:0041933"}


id: PBO:0070044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear","termid":"PBO:0070044"}


id: MOD:00812
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to an O-fucosylserine.","definition_xrefs":["RESID:AA0404","Unimod:295#S","PubMed:1904059","PubMed:1517205","PubMed:10734111","PubMed:11067851","PubMed:3311742","PubMed:15189151","PubMed:3578767","PubMed:12096136","PubMed:11344537"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosyl-L-serine","termid":"MOD:00002"},{"relation_name":"is_a","term_name":"fucosylated","termid":"MOD:00614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-fucosyl-L-serine","synonyms":[{"name":"(2S)-2-amino-3-(6-deoxy-alpha-D-galactopyranosyloxy)propanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (Fuc)","type":"exact"},{"name":"CARBOHYD O-linked (Fuc) serine","type":"exact"},{"name":"CARBOHYD O-linked (dHex)","type":"exact"},{"name":"Fucose","type":"related"},{"name":"O-fucosyl-L-serine","type":"exact"},{"name":"O-glycosylserine","type":"exact"},{"name":"O3-fucosylserine","type":"exact"},{"name":"OFucSer","type":"exact"},{"name":"dHex","type":"related"}],"termid":"MOD:00812"}


id: GO:0042692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a muscle cell.","definition_xrefs":["CL:0000187","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"muscle structure development","termid":"GO:0061061"}],"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":"muscle cell differentiation","synonyms":[{"name":"myogenesis","type":"related"}],"termid":"GO:0042692"}


id: GO:0019044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The perpetuation of a latent state, generally by repressing the viruses own lytic genes expression and ensuring expression of viral genes which function to keep the viral genome from being detected by the host defense mechanisms.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"},{"relation_name":"part_of","term_name":"viral latency","termid":"GO:0019042"}],"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":"maintenance of viral latency","secondary_identifiers":["GO:0075716","GO:0032360"],"synonyms":[{"name":"latent virus maintenance","type":"exact"},{"name":"prophage maintenance","type":"exact"},{"name":"provirus maintenance","type":"exact"}],"termid":"GO:0019044"}


id: PBO:0027312
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_5'_deoxyribonuclease_(pyrimidine_dimer)_activity","termid":"PBO:0027312"}


id: PBO:0076882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 33","termid":"PBO:0076882"}


id: PBO:0087855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional activator essential for nuclear division; localized to the nucleus; essential component of the mechanism that activates the expression of a set of late-S-phase-specific genes; turnover is tightly regulated during cell cycle and in response to DNA damage","termid":"PBO:0087855"}


id: MONDO:0019349
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sotos syndrome is a rare multisystemic genetic disorder characterized by a typical facial appearance, overgrowth of the body in early life with macrocephaly, and mild to severe intellectual disability.","definition_xrefs":["Orphanet:821"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"excluded_subClassOf","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"excluded_subClassOf","term_name":"overgrowth syndrome","termid":"MONDO:0019716"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 5","termid":"MONDO:0016904"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sotos syndrome","secondary_identifiers":["NCIT:C75019","SCTID:75968004","DECIPHER:17","MESH:D058495","icd11.foundation:1887392960","NANDO:1200679","NORD:1727","OMIMPS:117550","MEDGEN:61232","DOID:14748","DOID:0112103","GARD:10091","MedDRA:10064387","NANDO:2200953","OMIM:117550","UMLS:C0175695"],"synonyms":[{"name":"NSD1 Sotos syndrome","type":"exact"},{"name":"SOTOS1","type":"related"},{"name":"Sotos syndrome","type":"exact"},{"name":"Sotos syndrome 1","type":"exact"},{"name":"Sotos syndrome caused by mutation in NSD1","type":"exact"},{"name":"Sotos syndrome type 1","type":"exact"},{"name":"Sotos' syndrome","type":"exact"},{"name":"cerebral gigantism","type":"exact"},{"name":"cerebral gigantism syndrome","type":"exact"},{"name":"chromosome 5q35 deletion syndrome","type":"exact"},{"name":"distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development","type":"related"}],"termid":"MONDO:0019349","xrefs":{"Monarch":{"xref_id":"0019349"}}}


id: PBO:0050707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family B (small) member 3","termid":"PBO:0050707"}


id: GO:1990524
data:
  {"annotated_genes":["SJAG_07008"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[109737],"is_not":false,"summary":null,"term":"GO:1990524"}]},"cv_name":"cellular_component","definition":"A protein complex located in the inner membrane of mitochondria that is involved in the assembly of the peripheral (or stator) stalk of the mitochondrial proton-transporting ATP synthase (also known as the F1F0 ATP synthase). In budding yeast, this complex includes Ina22p and Ina17p.","definition_xrefs":["PMID:24942160","GOC:rn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner mitochondrial membrane protein complex","termid":"GO:0098800"}],"gene_count":1,"genes_by_uniquename":{"SJAG_07008":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005739"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737","GO:0005739"],"is_obsolete":false,"name":"INA complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"INAC","type":"exact"}],"termid":"GO:1990524","terms_by_termid":{"GO:1990524":null}}


id: MONDO:0015342
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute transverse myelitis (ATM) is an inflammatory demyelinating disorder of the spinal cord that can be either idiopathic (IATM) or secondary to a known cause (SATM).","definition_xrefs":["Orphanet:139417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myelitis","termid":"MONDO:0002565"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute transverse myelitis","secondary_identifiers":["ICD9:323.9","ICD9:341.20","MESH:D009188","SCTID:47000000","NCIT:C128378","UMLS:C0270627","GARD:19913","MEDGEN:82847"],"termid":"MONDO:0015342","xrefs":{"Monarch":{"xref_id":"0015342"}}}


id: GO:1990119
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of an RNA helicase.","definition_xrefs":["GOC:rb","PMID:23721653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"},{"relation_name":"is_a","term_name":"ATPase inhibitor activity","termid":"GO:0042030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004857"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0140678","GO:0004857","GO:0098772"],"is_obsolete":false,"name":"RNA helicase inhibitor activity","synonyms":[{"name":"ATP-dependent RNA helicase inhibitor activity","type":"exact"}],"termid":"GO:1990119"}


id: PBO:0053268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukocyte immunoglobulin like receptor A2","termid":"PBO:0053268"}


id: GO:0050436
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a microfibril, any small fibril occurring in biological material.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix binding","termid":"GO:0050840"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"microfibril binding","termid":"GO:0050436"}


id: MONDO:0000786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A allergy involving a Prunus domestica.","definition_xrefs":["MONDO:patterns/allergy"],"gene_count":0,"genotype_count":0,"name":"obsolete plum allergy (obsolete MONDO:0000786)","secondary_identifiers":["DOID:0060511"],"synonyms":[{"name":"Prunus domestica allergic disease","type":"exact"},{"name":"Prunus domestica caused allergic disease","type":"exact"},{"name":"Prunus domestica fruit allergy","type":"exact"},{"name":"allergy of Prunus domestica","type":"exact"}],"termid":"MONDO:0000786","xrefs":{"Monarch":{"xref_id":"0000786"}}}


id: GO:1990248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of DNA damage.","definition_xrefs":["PMID:15660129"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter in response to DNA damage (obsolete GO:1990248)","termid":"GO:1990248"}


id: GO:1900096
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of dosage compensation, by inactivation of X chromosome.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of dosage compensation by inactivation of X chromosome (obsolete GO:1900096)","synonyms":[{"name":"down regulation of Barr body formation","type":"related"},{"name":"down regulation of X chromosome inactivation","type":"exact"},{"name":"down regulation of chromosome inactivation","type":"broad"},{"name":"down regulation of dosage compensation, by inactivation of X chromosome","type":"exact"},{"name":"down-regulation of Barr body formation","type":"related"},{"name":"down-regulation of X chromosome inactivation","type":"exact"},{"name":"down-regulation of chromosome inactivation","type":"broad"},{"name":"down-regulation of dosage compensation, by inactivation of X chromosome","type":"exact"},{"name":"downregulation of Barr body formation","type":"related"},{"name":"downregulation of X chromosome inactivation","type":"exact"},{"name":"downregulation of chromosome inactivation","type":"broad"},{"name":"downregulation of dosage compensation, by inactivation of X chromosome","type":"exact"},{"name":"inhibition of Barr body formation","type":"related"},{"name":"inhibition of X chromosome inactivation","type":"exact"},{"name":"inhibition of chromosome inactivation","type":"broad"},{"name":"inhibition of dosage compensation, by inactivation of X chromosome","type":"narrow"},{"name":"negative regulation of Barr body formation","type":"related"},{"name":"negative regulation of X chromosome inactivation","type":"exact"},{"name":"negative regulation of chromosome inactivation","type":"broad"}],"termid":"GO:1900096"}


id: GO:1904632
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 glucoside stimulus.","definition_xrefs":["PMID:16842873","GOC:TermGenie","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to glucoside","termid":"GO:1904631"}],"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 glucoside","synonyms":[{"name":"cellular response to glucosides","type":"exact"}],"termid":"GO:1904632"}


id: MONDO:0005187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infectious process caused by the human herpesvirus 8. This infection is associated with Kaposi sarcoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human herpesvirus 8 infection","secondary_identifiers":["EFO:0002612","MEDGEN:268211","NCIT:C39291","UMLS:C1512508"],"synonyms":[{"name":"HHV8 infection","type":"exact"},{"name":"Human Herpes Virus 8 infection","type":"exact"},{"name":"Human Herpesvirus 8 infection","type":"exact"}],"termid":"MONDO:0005187","xrefs":{"Monarch":{"xref_id":"0005187"}}}


id: MONDO:0022895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniosynostosis cleft lip palate arthrogryposis","secondary_identifiers":["GARD:1590"],"termid":"MONDO:0022895","xrefs":{"Monarch":{"xref_id":"0022895"}}}


id: GO:0070641
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving vitamin D4, (3S,5Z,7E)-9,10-secoergosta-5,7,10(19)-trien-3-ol.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin D metabolic process","termid":"GO:0042359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0006766"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629","GO:0006766"],"is_obsolete":false,"name":"vitamin D4 metabolic process","synonyms":[{"name":"vitamin D4 metabolism","type":"exact"}],"termid":"GO:0070641"}


id: MOD:00625
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:314"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-methylmaleimide derivatized residue","synonyms":[{"name":"Nmethylmaleimide","type":"related"}],"termid":"MOD:00625"}


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: PBO:0087136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein, subunit of Nrd1 complex (Nrd1p-Nab3p-Sen1p); complex interacts with exosome to mediate 3'-end formation of some mRNAs, snRNAs, snoRNAs, and CUTs; required for termination of non-poly(A) transcripts and efficient splicing; Nrd1-Nab3 pathway appears to have a role in rapid suppression of some genes when cells are shifted to poor growth conditions, indicating role for Nrd1-Nab3 in regulating cellular response to nutrient availability","termid":"PBO:0087136"}


id: GO:0015482
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"gene_count":0,"genotype_count":0,"name":"obsolete voltage-gated anion channel porin activity (obsolete GO:0015482)","synonyms":[{"name":"voltage-dependent anion channel porin activity","type":"exact"},{"name":"voltage-gated anion channel porin activity","type":"exact"}],"termid":"GO:0015482"}


id: GO:0070423
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by the binding of a ligand (such as a bacterial peptidoglycan) to a cytoplasmic nucleotide-binding oligomerization domain containing (NOD) protein receptor, and ending with regulation of a downstream cellular process.","definition_xrefs":["PMID:17944960","GOC:add","PMID:18585455"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleotide-binding oligomerization domain containing signaling pathway (obsolete GO:0070423)","synonyms":[{"name":"NOD signaling pathway","type":"exact"},{"name":"nucleotide-binding oligomerization domain containing signalling pathway","type":"exact"}],"termid":"GO:0070423"}


id: PBO:0080475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vault RNA 1-1","termid":"PBO:0080475"}


id: PR:Q8TFH7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tRNA-splicing endonuclease subunit Sen2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR21227:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-splicing endonuclease subunit sen2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB17E12.07c","secondary_identifiers":["UniProtKB:Q8TFH7"],"synonyms":[{"name":"SPAPB17E12.07c","type":"related"},{"name":"Spom972h-TSEN2","type":"exact"},{"name":"tRNA-intron endonuclease sen2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q8TFH7"}


id: GO:0023025
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a class Ib major histocompatibility complex.","definition_xrefs":["GOC:mtg_signal","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MHC protein complex binding","termid":"GO:0023023"}],"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":"MHC class Ib protein complex binding","termid":"GO:0023025"}


id: MONDO:0033373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 64","secondary_identifiers":["DOID:0070375","MEDGEN:1633501","UMLS:C4693899","OMIM:618004"],"synonyms":[{"name":"DEE64","type":"exact"},{"name":"EIEE64","type":"exact"},{"name":"developmental and epileptic encephalopathy 64","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 64","type":"exact"}],"termid":"MONDO:0033373","xrefs":{"Monarch":{"xref_id":"0033373"}}}


id: GO:0036410
data:
  {"annotated_genes":["SJAG_02629","SJAG_01385","SJAG_02165","SJAG_04815"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90714,99672,104434,105322],"is_not":false,"summary":null,"term":"GO:0036410"}]},"cv_name":"cellular_component","definition":"A protein complex that can catalyze the acetylation of lysine at position 14 in histone H3, and contains Mst2 as the catalytic subunit. In fission yeast, contains at least Mst2, Nto1, Ptf2, Ptf1 and Eaf6.","definition_xrefs":["GOC:vw","PMID:21289066"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3-K14 acetyltransferase complex","termid":"GO:0036409"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01385":null,"SJAG_02165":null,"SJAG_02629":null,"SJAG_04815":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991","GO:0005694"],"is_obsolete":false,"name":"Mst2 histone acetyltransferase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Mst2 H3K14 acetyltransferase complex","type":"exact"},{"name":"Mst2 complex","type":"exact"},{"name":"Mst2 histone H3K14 acetyltransferase complex","type":"exact"}],"termid":"GO:0036410","terms_by_termid":{"GO:0036410":null}}


id: GO:0000335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of DNA transposition.","definition_xrefs":["GOC:tb","GOC:krc","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transposition, DNA-mediated (obsolete GO:0000335)","synonyms":[{"name":"down regulation of DNA transposition","type":"exact"},{"name":"down-regulation of DNA transposition","type":"exact"},{"name":"downregulation of DNA transposition","type":"exact"},{"name":"inhibition of DNA transposition","type":"narrow"},{"name":"negative regulation of DNA transposition","type":"exact"}],"termid":"GO:0000335"}


id: PBO:0064343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plexin A1","termid":"PBO:0064343"}


id: GO:0060479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells, e.g. embryonic or regenerative cells, acquire specialized structural and/or functional features of a mature cell found in the lung. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GOC:mtg_lung","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"lung development","termid":"GO:0030324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lung cell differentiation","synonyms":[{"name":"pulmonary cell differentiation","type":"exact"}],"termid":"GO:0060479"}


id: FYPO:0002582
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of mature mitochondrial transfer RNA (tRNA) measured in a cell is normal (i.e. indistinguishable from wild type). Total tRNA or a specific tRNA may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mature tRNA level","termid":"FYPO:0002580"},{"relation_name":"is_a","term_name":"normal mitochondrial RNA level","termid":"FYPO:0004960"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal mature mitochondrial tRNA level","synonyms":[{"name":"normal mature mitochondrial tRNA accumulation","type":"related"},{"name":"normal mature mitochondrial tRNA level during mitotic cell cycle","type":"related"},{"name":"normal mature mitochondrial tRNA level during vegetative growth","type":"exact"},{"name":"normal mature mitochondrial tRNA transcript level","type":"exact"},{"name":"normal mature mitochondrial transfer RNA level","type":"exact"},{"name":"normal mitochondrial tRNA level","type":"broad"}],"termid":"FYPO:0002582"}


id: MONDO:1012048
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar cortical atrophy, non-human animal","termid":"MONDO:1011836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar cortical atrophy, sheep","secondary_identifiers":["OMIA:000177-9940"],"termid":"MONDO:1012048","xrefs":{"Monarch":{"xref_id":"1012048"}}}


id: PBO:0011146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"di-trans,poly-cis-decaprenylcistransferase (predicted)","termid":"PBO:0011146"}


id: MONDO:0000015
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A genetic deficiency of any early component of the classical pathway (C1q, C1r/s, C2, C4, and C3) that is associated with autoimmune diseases due to the failure of clearance of immune complexes (IC) and apoptotic materials, and the impairment of normal humoral response.","definition_xrefs":["PMID:22773339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complement deficiency","termid":"MONDO:0003832"}],"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":"classic complement early component deficiency","secondary_identifiers":["SCTID:363009005","ICD9:279.8","UMLS:C1285186","GARD:9526","MEDGEN:226929"],"synonyms":[{"name":"genetic deficiency of early component of the classical complement pathway","type":"exact"}],"termid":"MONDO:0000015","xrefs":{"Monarch":{"xref_id":"0000015"}}}


id: GO:0099041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial, indirect interaction between a transport vesicle membrane and the membrane of the Golgi. This interaction is mediated by tethering factors (or complexes), which interact with both membranes. Interaction can occur via direct binding to membrane phospholipids or membrane proteins, or via binding to vesicle coat proteins. This process is distinct from and prior fusion.","definition_xrefs":["PMID:27243008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle tethering","termid":"GO:0099022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"vesicle tethering to Golgi","termid":"GO:0099041"}


id: PBO:0078174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta joining 1-5","termid":"PBO:0078174"}


id: PBO:0059758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 32","termid":"PBO:0059758"}


id: GO:0070642
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving vitamin D5, (1S,3Z)-3-[(2E)-2-[(1R,3aS,7aR)-1-[(1R,4S)-4-ethyl-1,5-dimethylhexyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylene-1-cyclohexanol.","definition_xrefs":["GOC:BHF","GOC:mah","PubChem_Compound:9547700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin D metabolic process","termid":"GO:0042359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0006766"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150","GO:0006766"],"is_obsolete":false,"name":"vitamin D5 metabolic process","synonyms":[{"name":"vitamin D5 metabolism","type":"exact"}],"termid":"GO:0070642"}


id: PBO:0041374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 4 open reading frame 48","termid":"PBO:0041374"}


id: PBO:0058794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7515","termid":"PBO:0058794"}


id: SO:0002088
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript variant occurring within the splice region (1-3 bases of the exon or 3-8 bases of the intron) of a non coding transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_coding_transcript_variant","termid":"SO:0001619"},{"relation_name":"is_a","term_name":"splice_region_variant","termid":"SO:0001630"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non_coding_transcript_splice_region_variant","synonyms":[{"name":"ANNOVAR:ncRNA_splicing","type":"narrow"}],"termid":"SO:0002088"}


id: PBO:0049176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth factor receptor bound protein 14","termid":"PBO:0049176"}


id: PBO:0082007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger SWIM-type containing 5 pseudogene 3","termid":"PBO:0082007"}


id: GO:0019065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any receptor-mediated endocytosis that is involved in the uptake of a virus into a host cell; successive instances of virus endocytosis result in the accumulation of virus particles within the cell.","definition_xrefs":["GOC:bf","GOC:jl","ISBN:0781702534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor-mediated endocytosis","termid":"GO:0006898"},{"relation_name":"is_a","term_name":"endocytosis involved in viral entry into host cell","termid":"GO:0075509"},{"relation_name":"part_of","term_name":"symbiont entry into host cell","termid":"GO:0046718"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"receptor-mediated endocytosis of virus by host cell","secondary_identifiers":["Reactome:R-HSA-168275"],"synonyms":[{"name":"receptor mediated endocytosis by host of virus particle","type":"exact"},{"name":"receptor mediated endocytosis of virus by host","type":"exact"},{"name":"receptor mediated endocytosis of virus particle by host","type":"exact"},{"name":"receptor-mediated endocytosis of virus by host","type":"exact"},{"name":"viral entry into host cell via receptor-mediated endocytosis","type":"related"},{"name":"viral receptor mediated endocytosis","type":"exact"},{"name":"virus receptor-mediated endocytosis by host","type":"exact"}],"termid":"GO:0019065"}


id: PBO:0044820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 109C","termid":"PBO:0044820"}


id: PBO:0003847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Sof1 (predicted)","termid":"PBO:0003847"}


id: MOD:01840
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to L-allo-isoleucine.","definition_xrefs":["ChEBI:43433","RESID:AA0546","PubMed:20805503"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stereoisomerized residue","termid":"MOD:00664"},{"relation_name":"is_a","term_name":"modified L-isoleucine residue","termid":"MOD:00910"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-allo-isoleucine","synonyms":[{"name":"(2S,3R)-2-amino-3-methylpentanoic acid","type":"exact"},{"name":"2-azanyl-3-methylpentanoic acid","type":"exact"},{"name":"3-methyl-norvaline","type":"exact"},{"name":"L-allo-isoleucine","type":"exact"},{"name":"L-threo-isoleucine","type":"exact"},{"name":"MOD_RES L-allo-isoleucine","type":"exact"},{"name":"allo-L-isoleucine","type":"exact"},{"name":"alpha-amino-beta-methylvaleric acid","type":"exact"}],"termid":"MOD:01840"}


id: GO:0010138
data:
  {"annotated_genes":["SJAG_00533","SJAG_04713","SJAG_03708","SJAG_04709","SJAG_04354"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67792,92937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044211"},{"annotations":[87418,67791,91938,92938,88405],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044206"}]},"cv_name":"biological_process","definition":"The pathway by which pyrimidine bases or pyrimidine ribonucleosides from pyrimidine nucleotide breakdown are converted back to pyrimidine ribonucleotides. The salvage pathway is important where there is no de novo pyrimidine nucleotide biosynthesis.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide biosynthetic process","termid":"GO:0009220"},{"relation_name":"is_a","term_name":"pyrimidine nucleotide salvage","termid":"GO:0032262"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00533":null,"SJAG_03708":null,"SJAG_04354":null,"SJAG_04709":null,"SJAG_04713":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:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"pyrimidine ribonucleotide salvage","references_by_uniquename":{"GO_REF:0000041":null,"GO_REF:0000107":null},"termid":"GO:0010138","terms_by_termid":{"GO:0044206":null,"GO:0044211":null}}


id: SO:0000449
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence of nucleotides or amino acids which, by design, has a \\\"random\\\" order of components, given a predetermined input frequency of these components.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synthetic_sequence","termid":"SO:0000351"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"random_sequence","synonyms":[{"name":"random sequence","type":"exact"}],"termid":"SO:0000449"}


id: PBO:0065017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxiredoxin 2 pseudogene 1","termid":"PBO:0065017"}


id: GO:0106256
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A hydroperoxy icosatetraenoate = an oxoicosatetraenoate + H2O.","definition_xrefs":["RHEA:55556","PMID:12881489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"hydroperoxy icosatetraenoate dehydratase activity","secondary_identifiers":["EC:4.2.1.152"],"termid":"GO:0106256"}


id: MONDO:0010328
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alpha-thalassemia-myelodysplastic syndrome (ATMDS) is an acquired form of alpha-thalassemia characterized by a myelodysplastic syndrome (MDS) or more rarely a myeloproliferative disease (MPD) associated with hemoglobin H disease (HbH).","definition_xrefs":["Orphanet:231401"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"acquired","termid":"MONDO:0021141"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"hematologic disorder","termid":"MONDO:0005570"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"alpha-thalassemia-myelodysplastic syndrome","secondary_identifiers":["ICD9:282.49","GARD:17167","ICD10CM:D56.0","MESH:C563023","MEDGEN:108433","SCTID:307343001","DOID:0112125","OMIM:300448","UMLS:C0585216"],"synonyms":[{"name":"ALPHA-thalassemia myelodysplasia syndrome","type":"related"},{"name":"ATMDS","type":"exact"},{"name":"Haemoglobin H disease, acquired","type":"related"},{"name":"Hemoglobin H disease, acquired","type":"related"},{"name":"acquired HbH disease","type":"exact"},{"name":"acquired haemoglobin H disease","type":"exact"},{"name":"acquired hemoglobin H disease","type":"exact"},{"name":"alpha-thalassemia myelodysplasia syndrome, somatic","type":"exact"}],"termid":"MONDO:0010328","xrefs":{"Monarch":{"xref_id":"0010328"}}}


id: FYPO:0002804
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which vacuole organization is abnormal when the cell is subject to nitrogen starvation. Vacuole organization results in the assembly, arrangement of constituent parts, or disassembly of a vacuole.","definition_xrefs":["GO:0007033","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vacuole organization","termid":"FYPO:0002803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal vacuole organization during nitrogen starvation","synonyms":[{"name":"abnormal vacuolar organisation during nitrogen starvation","type":"exact"},{"name":"abnormal vacuolar organization during nitrogen starvation","type":"exact"},{"name":"abnormal vacuole organisation during nitrogen starvation","type":"exact"},{"name":"abnormal vacuole organization during nitrogen depletion","type":"exact"},{"name":"abnormal vacuole organization during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0002804"}


id: PBO:0068491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 75, pseudogene","termid":"PBO:0068491"}


id: PBO:0063059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter of CDKN1A antisense DNA damage activated RNA","termid":"PBO:0063059"}


id: PBO:0089917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multi-spanning vacuolar membrane protease","termid":"PBO:0089917"}


id: PBO:0061792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outer dynein arm docking complex subunit 3","termid":"PBO:0061792"}


id: MONDO:0005623
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammatory disease of the thyroid gland due to autoimmune responses leading to lymphocytic infiltration of the gland. It is characterized by the presence of circulating thyroid antigen-specific T-cells and thyroid autoantibodies. The clinical signs can range from hypothyroidism to thyrotoxicosis depending on the type of autoimmune thyroiditis.","definition_xrefs":["MESH:D013967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of endocrine system","termid":"MONDO:0000569"},{"relation_name":"is_a","term_name":"thyroiditis","termid":"MONDO:0004126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune thyroid disease","secondary_identifiers":["Wikipedia:Autoimmune_thyroiditis","EFO:0006812","UMLS:C0920350","MEDGEN:183088"],"synonyms":[{"name":"autoimmune thyroid gland inflammation","type":"exact"},{"name":"autoimmune thyroiditides","type":"related"},{"name":"autoimmune thyroiditis","type":"related"},{"name":"lymphocytic thyroiditides","type":"related"},{"name":"lymphocytic thyroiditis","type":"related"},{"name":"lymphomatous thyroiditides","type":"related"},{"name":"lymphomatous thyroiditis","type":"related"},{"name":"thyroiditides, autoimmune","type":"related"},{"name":"thyroiditides, lymphocytic","type":"related"},{"name":"thyroiditides, lymphomatous","type":"related"},{"name":"thyroiditis, lymphocytic","type":"related"},{"name":"thyroiditis, lymphomatous","type":"related"}],"termid":"MONDO:0005623","xrefs":{"Monarch":{"xref_id":"0005623"}}}


id: GO:0140004
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H3 serotonylated at glutamine 5.","definition_xrefs":["PMID:34144982"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 reader activity","termid":"GO:0140006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0140566"}],"interesting_parent_ids":["GO:0060090","GO:0140566","GO:0030674","GO:0003674"],"is_obsolete":false,"name":"histone H3Q5ser reader activity","synonyms":[{"name":"H3Q5-serotonin histone reader activity","type":"exact"},{"name":"H3Q5-serotonin modified histone binding","type":"narrow"}],"termid":"GO:0140004"}


id: GO:0072682
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of an eosinophil from the blood vessels into the surrounding tissue.","definition_xrefs":["GOC:mah","GOC:BHF","CL:0000771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular extravasation","termid":"GO:0045123"},{"relation_name":"is_a","term_name":"eosinophil migration","termid":"GO:0072677"}],"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":"eosinophil extravasation","termid":"GO:0072682"}


id: MONDO:0009117
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disorganization, mouse, homolog of (obsolete MONDO:0009117)","secondary_identifiers":["OMIM:223200"],"synonyms":[{"name":"Ds","type":"related"},{"name":"disorganization, mouse, homolog OF","type":"related"}],"termid":"MONDO:0009117","xrefs":{"Monarch":{"xref_id":"0009117"}}}


id: GO:0051387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the neurotrophin TRK receptor signaling pathway.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of neurotrophin TRK receptor signaling pathway","termid":"GO:0051386"},{"relation_name":"is_a","term_name":"negative regulation of cellular response to growth factor stimulus","termid":"GO:0090288"},{"relation_name":"negatively_regulates","term_name":"neurotrophin TRK receptor signaling pathway","termid":"GO:0048011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of neurotrophin TRK receptor signaling pathway","synonyms":[{"name":"down regulation of nerve growth factor receptor signaling pathway","type":"exact"},{"name":"down-regulation of nerve growth factor receptor signaling pathway","type":"exact"},{"name":"downregulation of nerve growth factor receptor signaling pathway","type":"exact"},{"name":"inhibition of nerve growth factor receptor signaling pathway","type":"narrow"},{"name":"negative regulation of NGF receptor signaling pathway","type":"exact"},{"name":"negative regulation of NGF receptor signalling pathway","type":"exact"},{"name":"negative regulation of nerve growth factor receptor signaling pathway","type":"related"},{"name":"negative regulation of nerve growth factor receptor signalling pathway","type":"exact"}],"termid":"GO:0051387"}


id: MONDO:0020292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital anomaly of the great arteries","secondary_identifiers":["MEDGEN:798768","Orphanet:98724","UMLS:C0948632","MedDRA:10061080","GARD:19556"],"synonyms":[{"name":"congenital aorta, aortic arch or pulmonary arteries anomaly","type":"exact"}],"termid":"MONDO:0020292","xrefs":{"Monarch":{"xref_id":"0020292"}}}


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


id: FYPO:0002886
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 transcription occurs to a normal (i.e. indistinguishable from wild type) extent during a cellular response to heavy metal stress. All genes, or a specific subset of genes, may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transcription during vegetative growth","termid":"FYPO:0001855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal transcription during cellular response to heavy metal stress","synonyms":[{"name":"normal transcription during cellular response to heavy metal stress during mitotic cell cycle","type":"related"},{"name":"normal transcription during cellular response to heavy metal stress during vegetative growth","type":"exact"},{"name":"normal transcription in response to heavy metal stress","type":"exact"}],"termid":"FYPO:0002886"}


id: PR:Q9HFF2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC683.02c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HFF2"],"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 C683.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC683.02c","synonyms":[{"name":"Spom972h-SPAC683.02c","type":"exact"}],"termid":"PR:Q9HFF2"}


id: GO:0016527
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 brain-specific angiogenesis inhibitor activity (obsolete GO:0016527)","synonyms":[{"name":"brain-specific angiogenesis inhibitor activity","type":"exact"}],"termid":"GO:0016527"}


id: GO:1905783
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The disaggregation of a CENP-A containing nucleosome into its constituent components.","definition_xrefs":["GO_REF:0000079","GOC:TermGenie","PMID:27666591"],"gene_count":0,"genotype_count":0,"name":"obsolete CENP-A containing nucleosome disassembly (obsolete GO:1905783)","synonyms":[{"name":"centromere specific nucleosome disassembly","type":"related"},{"name":"centromere-specific nucleosome disassembly","type":"related"},{"name":"centromeric nucleosome disassembly","type":"related"}],"termid":"GO:1905783"}


id: PBO:0039760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1","termid":"PBO:0039760"}


id: PBO:0088996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol transfer protein Ltc1","termid":"PBO:0088996"}


id: GO:0006910
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial step in phagocytosis involving adhesion to bacteria, immune complexes and other particulate matter, or an apoptotic cell and based on recognition of factors such as bacterial cell wall components, opsonins like complement and antibody or protein receptors and lipids like phosphatidyl serine, and leading to intracellular signaling in the phagocytosing cell.","definition_xrefs":["GOC:curators","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell recognition","termid":"GO:0008037"},{"relation_name":"part_of","term_name":"phagocytosis","termid":"GO:0006909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"phagocytosis, recognition","synonyms":[{"name":"recognition of phagocytosed substance by phagocytic cell","type":"exact"}],"termid":"GO:0006910"}


id: MONDO:1011093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypospadias that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypospadias, non-human animal","termid":"MONDO:1010269"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypospadias, cattle","secondary_identifiers":["OMIA:001187-9913"],"termid":"MONDO:1011093","xrefs":{"Monarch":{"xref_id":"1011093"}}}


id: MONDO:1011726
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease, non-human animal","termid":"MONDO:1011724"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin A deficiency, non-human animal","secondary_identifiers":["OMIA:000552"],"termid":"MONDO:1011726","xrefs":{"Monarch":{"xref_id":"1011726"}}}


id: PBO:0063202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCBP1 antisense RNA 1","termid":"PBO:0063202"}


id: GO:0000254
data:
  {"annotated_genes":["SJAG_03018"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69704],"is_not":false,"summary":null,"term":"GO:0000254"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 4,4-dimethyl-5alpha-cholest-7-en-3beta-ol + 6 Fe(II)-[cytochrome b5] + 5 H+ + 3 O2 = 4alpha-carboxy-4beta-methyl-5alpha-cholest-7-ene-3beta-ol + 6 Fe(III)-[cytochrome b5] + 4 H2O.","definition_xrefs":["PMID:9811880","RHEA:55220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen","termid":"GO:0016716"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03018":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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"C-4 methylsterol oxidase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-194669","EC:1.14.18.9","MetaCyc:RXN-13188","Reactome:R-HSA-194641"],"synonyms":[{"name":"4-methylsterol oxidase activity","type":"exact"},{"name":"methylsterol hydroxylase activity","type":"related"},{"name":"methylsterol monooxygenase activity","type":"related"}],"termid":"GO:0000254","terms_by_termid":{"GO:0000254":null}}


id: GO:0097717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of copper (Cu) ions passing through the blood-cerebrospinal fluid barrier.","definition_xrefs":["GOC:sl","PMID:24614235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper ion transport","termid":"GO:0006825"},{"relation_name":"is_a","term_name":"transport across blood-cerebrospinal fluid barrier","termid":"GO:0150195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"copper ion transport across blood-cerebrospinal fluid barrier","synonyms":[{"name":"copper ion transport across BCB","type":"related"},{"name":"copper ion transport across BCSFB","type":"exact"},{"name":"copper ion transport across blood-CSF barrier","type":"exact"},{"name":"copper ion transport across blood/CSF barrier","type":"exact"},{"name":"copper ion transport across blood/cerebrospinal fluid barrier","type":"exact"}],"termid":"GO:0097717"}


id: PBO:0061058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitrilase 1","termid":"PBO:0061058"}


id: GO:1900058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of sulfate assimilation.","definition_xrefs":["PMID:7601277","GOC:TermGenie","PMID:7891681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sulfur metabolic process","termid":"GO:0042762"},{"relation_name":"regulates","term_name":"sulfate assimilation","termid":"GO:0000103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0006790"],"is_obsolete":false,"name":"regulation of sulfate assimilation","synonyms":[{"name":"regulation of sulfate assimilation, phosphoadenylyl sulfate reduction by an oxidoreductase, acting on sulfur group of donors, NAD or NADP as acceptor","type":"narrow"},{"name":"regulation of sulphate assimilation","type":"exact"},{"name":"regulation of sulphate assimilation, phosphoadenylyl sulphate reduction by an oxidoreductase, acting on sulphur group of donors, NAD or NADP as acceptor","type":"narrow"}],"termid":"GO:1900058"}


id: PBO:0052365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 13B","termid":"PBO:0052365"}


id: GO:0030957
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to Tat, a viral transactivating regulatory protein from the human immunodeficiency virus, or the equivalent protein from another virus.","definition_xrefs":["GOC:mah","PMID:9094689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II-specific DNA-binding transcription factor binding","termid":"GO:0061629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"Tat protein binding","termid":"GO:0030957"}


id: GO:0034973
data:
  {"annotated_genes":["SJAG_03936","SJAG_04597"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[94377,110537],"is_not":false,"summary":null,"term":"GO:0034973"}]},"cv_name":"cellular_component","definition":"A protein complex that contains a protein kinase (Sid2 in S. pombe) and its regulatory subunit (Mob1). The Sid2p-Mob1p kinase complex is a component of the septation initiation network in fission yeast (called the mitotic exit network in S. cerevisiae) and is required for cytokinesis. The analogous complex in S. cerevisiae is called Dbf2p-Mob1p complex.","definition_xrefs":["PMID:10837231","PMID:15060149","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03936":null,"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"Sid2-Mob1 complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Dbf2p-Mob1p complex","type":"exact"},{"name":"Sid2-Mob1 kinase complex","type":"exact"},{"name":"Sid2p-Mob1p complex","type":"exact"}],"termid":"GO:0034973","terms_by_termid":{"GO:0034973":null}}


id: GO:0102512
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: delphinidin 3-O-beta-D-glucoside + 1-O-vanilloyl-beta-D-glucose = delphinidin 3-O-beta-D-glucoside-5-O-beta-D-glucoside betaine + vanillate + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete delphinidin 3-O-glucoside 5-O-glucosyltransferase (acyl-glucose dependent) activity (obsolete GO:0102512)","termid":"GO:0102512"}


id: PBO:0054786
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 2199","termid":"PBO:0054786"}


id: PATO:0000713
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000713 relative time value (obsolete PATO:0000713)","termid":"PATO:0000713"}


id: PR:O14019
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cyclin-dependent kinase 16 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02128","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":"serine/threonine-protein kinase hal4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.16","secondary_identifiers":["UniProtKB:O14019"],"synonyms":[{"name":"Spom972h-CDK16","type":"exact"},{"name":"halotolerance protein 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"serine/threonine-protein kinase ppk10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14019"}


id: PBO:0028615
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ADP_binding","termid":"PBO:0028615"}


id: GO:2001135
data:
  {"annotated_genes":["SJAG_04509"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87852],"is_not":false,"summary":null,"term":"GO:2001135"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocytic recycling.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular transport","termid":"GO:0032386"},{"relation_name":"is_a","term_name":"regulation of vesicle-mediated transport","termid":"GO:0060627"},{"relation_name":"regulates","term_name":"endocytic recycling","termid":"GO:0032456"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04509":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of endocytic recycling","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of retrograde transport of endocytic vesicles","type":"related"}],"termid":"GO:2001135","terms_by_termid":{"GO:2001135":null}}


id: MONDO:0007753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autonomic disorder characterized by excessive sweating of the forehead, upper lip, perioral region, or sternum subsequent to gustatory stimuli. The auriculotemporal syndrome features facial flushing or sweating limited to the distribution of the auriculotemporal nerve and may develop after trauma to the parotid gland, in association with parotid neoplasms, or following their surgical removal. (From Ann Neurol 1997 Dec;42(6):973-5)","definition_xrefs":["MESH:D013547"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autonomic nervous system disorder","termid":"MONDO:0001292"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Frey syndrome","secondary_identifiers":["DOID:11599","EFO:1000940","MEDGEN:21041","Orphanet:662240","SCTID:238758008","OMIM:144100","UMLS:C0038994"],"synonyms":[{"name":"Baillarger syndrome","type":"exact"},{"name":"Frey syndrome","type":"exact"},{"name":"Frey's syndrome","type":"related"},{"name":"HYPRG","type":"related"},{"name":"auriculotemporal nerve syndrome","type":"related"},{"name":"gustatory hyperhidrosis","type":"exact"},{"name":"gustatory sweating","type":"exact"},{"name":"hyperhidrosis gustatory","type":"related"},{"name":"hyperhidrosis, gustatory","type":"related"}],"termid":"MONDO:0007753","xrefs":{"Monarch":{"xref_id":"0007753"}}}


id: PBO:0066193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBM12B divergent transcript","termid":"PBO:0066193"}


id: PBO:0073182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenoprotein M","termid":"PBO:0073182"}


id: GO:0034272
data:
  {"annotated_genes":["SJAG_04552","SJAG_00114","SJAG_03403","SJAG_01876"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[71367,76595,77179,105728],"is_not":false,"summary":null,"term":"GO:0034272"}]},"cv_name":"cellular_component","definition":"A class III phosphatidylinositol 3-kinase complex that is involved in vacuolar protein sorting (VPS) via endosomes. In budding yeast, this complex consists of Vps30p, Vps34p, Vps38 and Vps15p.","definition_xrefs":["PMID:11157979","PMID:16421251","GOC:rb","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol 3-kinase complex, class III","termid":"GO:0035032"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_01876":null,"SJAG_03403":null,"SJAG_04552":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"phosphatidylinositol 3-kinase complex, class III, type II","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"PtdIns-3-kinase complex II","type":"related"},{"name":"phosphatidylinositol 3-kinase complex II","type":"related"}],"termid":"GO:0034272","terms_by_termid":{"GO:0034272":null}}


id: FYPO:0003119
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 polyadenylated messenger RNA (mRNA) measured in the nucleus is higher than normal. Total mRNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased nuclear RNA level during vegetative growth","termid":"FYPO:0000911"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002403","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"increased nuclear polyadenylated mRNA level during vegetative growth","synonyms":[{"name":"increased nuclear poly(A)+ mRNA level during vegetative growth","type":"exact"},{"name":"increased nuclear polyadenylated mRNA accumulation during vegetative growth","type":"related"},{"name":"increased nuclear polyadenylated mRNA level during mitotic cell cycle","type":"related"},{"name":"increased nuclear polyadenylated mRNA transcript level during vegetative growth","type":"exact"},{"name":"increased nuclear polyadenylated messenger RNA level during vegetative growth","type":"exact"},{"name":"nuclear poly(A)+ mRNA accumulation","type":"related"},{"name":"nuclear poly-A mRNA accumulation","type":"related"}],"termid":"FYPO:0003119"}


id: PBO:0067413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 524, pseudogene","termid":"PBO:0067413"}


id: GO:0034947
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: terephthalate + H2O = benzoate + HCO3-.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete terephthalate decarboxylase activity (obsolete GO:0034947)","termid":"GO:0034947"}


id: PBO:0005107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome-c reductase complex subunit 9 (predicted)","termid":"PBO:0005107"}


id: GO:2000206
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ribosomal small subunit export from nucleus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ribosomal subunit export from nucleus","termid":"GO:2000200"},{"relation_name":"regulates","term_name":"ribosomal small subunit export from nucleus","termid":"GO:0000056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006913"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006913","GO:0006810"],"is_obsolete":false,"name":"regulation of ribosomal small subunit export from nucleus","synonyms":[{"name":"regulation of 30S ribosomal subunit export from nucleus","type":"related"},{"name":"regulation of 40S ribosomal subunit export from nucleus","type":"related"},{"name":"regulation of ribosomal small subunit export from cell nucleus","type":"exact"},{"name":"regulation of ribosomal small subunit export out of nucleus","type":"exact"},{"name":"regulation of ribosomal small subunit transport from nucleus to cytoplasm","type":"exact"},{"name":"regulation of ribosomal small subunit-nucleus export","type":"exact"}],"termid":"GO:2000206"}


id: PBO:0091322
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein substrate KM, thiamine KM 6 uM","termid":"PBO:0091322"}


id: FYPO:0000495
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 mitochondrial transport is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal mitochondrial transport","synonyms":[{"name":"abnormal mitochondrial transport during mitotic cell cycle","type":"related"},{"name":"abnormal mitochondrial transport during vegetative growth","type":"exact"},{"name":"mitochondrial transport: abnormal","type":"related"}],"termid":"FYPO:0000495"}


id: GO:0120506
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysyl79-[histone H3] + 2 S-adenosyl-L-methionine = 2H+ + N6,N6-methyl-L-lysyl79-[histone H3] + 2 S-adenosyl-L-homocysteine.","definition_xrefs":["PMID:14732680","PMID:15371351"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3K79 methyltransferase activity","termid":"GO:0031151"}],"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:0008276"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0016741","GO:0003674","GO:0008276","GO:0016740"],"is_obsolete":false,"name":"histone H3K79 dimethyltransferase activity","termid":"GO:0120506"}


id: MONDO:0015434
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 18 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including hypotonia, neonatal feeding and respiratory difficulties, microcephaly, global developmental delay and intellectual disability, growth hormone deficiency, hypothyroidism, hearing loss, aural atresia, dysmorphic facial features and behavioral characteristics.","definition_xrefs":["Orphanet:1442"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"},{"relation_name":"is_a","term_name":"chromosome 18 disorder","termid":"MONDO:0700125"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 18","secondary_identifiers":["GARD:6077","SCTID:88154004","NORD:943","MEDGEN:539285","MESH:C538304","UMLS:C0265475"],"synonyms":[{"name":"Chromosome 18 Ring","type":"exact"},{"name":"R18","type":"related"},{"name":"Ring 18","type":"related"},{"name":"Ring chromosome 18 syndrome","type":"related"},{"name":"Ring chromosome type 18","type":"exact"},{"name":"chromosome 18 ring","type":"related"}],"termid":"MONDO:0015434","xrefs":{"Monarch":{"xref_id":"0015434"}}}


id: PBO:0056189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member A2B","termid":"PBO:0056189"}


id: RO:0002558
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of is evidence for","direct_ancestors":[{"relation_name":"is_a","term_name":"related_via_evidence_or_inference_to","termid":"RO:0002616"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_evidence","termid":"RO:0002558"}


id: PBO:0075314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor of cytokine signaling 6","termid":"PBO:0075314"}


id: MONDO:0014704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome","secondary_identifiers":["GARD:17860","OMIM:616592","Orphanet:477831","MEDGEN:896409","UMLS:C4225270"],"synonyms":[{"name":"KOGS","type":"related"},{"name":"Kosaki overgrowth syndrome","type":"exact"},{"name":"skeletal overgrowth with Facial Dysmorphism, hyperelastic skin, White matter lesions, and neurologic deterioration","type":"related"}],"termid":"MONDO:0014704","xrefs":{"Monarch":{"xref_id":"0014704"}}}


id: GO:0030905
data:
  {"annotated_genes":["SJAG_00971"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70368],"is_not":false,"summary":null,"term":"GO:0030905"}]},"cv_name":"cellular_component","definition":"The dimeric subcomplex of the retromer, believed to be peripherally associated with the membrane. This dimeric complex is responsible for remodeling endosomal membranes to form a tube-structure to which cargo molecules are selected for recycling. The budding yeast complex comprises Vps5p and Vps17p, and may contain multiple copies of a Vps5p/Vps17p dimer. The mammalian complex contains SNX1 or SNX2 dimerized with SNX5 or SNX6.","definition_xrefs":["PMID:26220253","PMID:9700157","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"retromer complex","termid":"GO:0030904"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00971":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"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":"retromer, tubulation complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"SNX-BAR dimer","type":"exact"},{"name":"heterodimeric membrane-deforming retromer subcomplex","type":"exact"},{"name":"retromer complex, outer shell","type":"exact"}],"termid":"GO:0030905","terms_by_termid":{"GO:0030905":null}}


id: PR:Q12238
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- uvi31 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q12238"],"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":"UV-induced protein uvi31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16E9.06c","synonyms":[{"name":"Spom972h-uvi31","type":"exact"}],"termid":"PR:Q12238"}


id: PBO:0053096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late cornified envelope 3D","termid":"PBO:0053096"}


id: SO:0002092
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A UTR variant of exonic sequence of the 5' UTR.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5_prime_UTR_variant","termid":"SO:0001623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_prime_UTR_exon_variant","synonyms":[{"name":"5 prime UTR exon variant","type":"exact"}],"termid":"SO:0002092"}


id: GO:0140343
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Removes phosphatidylserine from the outer leaflet of a donor membrane, transports it through the aqueous phase while protected in a hydrophobic pocket, and brings it to the outer leaflet of an acceptor membrane.","definition_xrefs":["PMID:26206935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transfer activity","termid":"GO:0120013"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0120013"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0120013","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"phosphatidylserine transfer activity","synonyms":[{"name":"intermembrane phosphatidylserine carrier activity","type":"narrow"}],"termid":"GO:0140343"}


id: PBO:0053808
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 1067","termid":"PBO:0053808"}


id: GO:0071243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arsenic stimulus from compounds containing arsenic, including arsenates, arsenites, and arsenides.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to arsenic-containing substance","termid":"GO:0046685"},{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"}],"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 arsenic-containing substance","synonyms":[{"name":"cellular response to arsenic","type":"exact"}],"termid":"GO:0071243"}


id: PBO:0081505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 408","termid":"PBO:0081505"}


id: PBO:0054178
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 1551","termid":"PBO:0054178"}


id: GO:1990896
data:
  {"annotated_genes":["SJAG_03915","SJAG_01196","SJAG_03011"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91261,114065,116206],"is_not":false,"summary":null,"term":"GO:1990896"}]},"cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, the cell cortex of the cell tip.","definition_xrefs":["PMID:26150232"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to cell cortex","termid":"GO:0072697"},{"relation_name":"is_a","term_name":"protein localization to cell tip","termid":"GO:1990151"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01196":null,"SJAG_03011":null,"SJAG_03915":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to cell cortex of cell tip","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990896","terms_by_termid":{"GO:1990896":null}}


id: PBO:0086880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transcription factor; has homolog in Kluyveromyces lactis","termid":"PBO:0086880"}


id: GO:0033046
data:
  {"annotated_genes":["SJAG_01837","SJAG_04259","SJAG_04999","SJAG_04126","SJAG_02169","SJAG_03126","SJAG_04699","SJAG_01330","SJAG_02336","SJAG_04884","SJAG_03681","SJAG_01297","SJAG_00460","SJAG_00883","SJAG_01082","SJAG_01679","SJAG_02451","SJAG_03353"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90686,111975,103895,115926,108268,99589,113799,114288,107246],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[99433,109921,114521,115580,101802,106332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[103282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000816"},{"annotations":[94170],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[116701],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090267"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of sister chromatid segregation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sister chromatid segregation","termid":"GO:0033045"},{"relation_name":"is_a","term_name":"negative regulation of chromosome segregation","termid":"GO:0051985"},{"relation_name":"is_a","term_name":"negative regulation of chromosome organization","termid":"GO:2001251"},{"relation_name":"negatively_regulates","term_name":"sister chromatid segregation","termid":"GO:0000819"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00460":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01679":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"negative regulation of sister chromatid segregation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0033046","terms_by_termid":{"GO:0007094":null,"GO:0090267":null,"GO:0140499":null,"GO:1902426":null,"GO:2000816":null}}


id: PBO:0088187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc finger protein containing five transmembrane domains; null mutant exhibits strongly fragmented vacuoles and sensitivity to brefeldin A, a drug which is known to affect intracellular transport","termid":"PBO:0088187"}


id: FYPO:0004682
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 polyadenylated 5S rRNA measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal rRNA or precursor level","termid":"FYPO:0006000"}],"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:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal polyadenylated 5S rRNA level","synonyms":[{"name":"normal polyadenylated 5S rRNA accumulation","type":"related"},{"name":"normal polyadenylated 5S rRNA level during mitotic cell cycle","type":"related"},{"name":"normal polyadenylated 5S rRNA level during vegetative growth","type":"exact"},{"name":"normal polyadenylated 5S rRNA transcript level","type":"exact"}],"termid":"FYPO:0004682"}


id: GO:0052198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in peptidase activity, the catalysis of the hydrolysis of peptide bonds in a protein, in a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of peptidase activity in other organism involved in symbiotic interaction (obsolete GO:0052198)","synonyms":[{"name":"modulation of protease activity in other organism during symbiotic interaction","type":"related"},{"name":"modulation of protease activity in other organism involved in symbiotic interaction","type":"narrow"}],"termid":"GO:0052198"}


id: GO:1905688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of diacylglycerol kinase activity.","definition_xrefs":["GO_REF:0000059","PMID:23091060","GOC:PARL","GOC:bc","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of diacylglycerol kinase activity (obsolete GO:1905688)","synonyms":[{"name":"down regulation of 1,2-diacylglycerol kinase (phosphorylating)","type":"exact"},{"name":"down regulation of 1,2-diacylglycerol kinase activity","type":"exact"},{"name":"down regulation of ATP:1,2-diacylglycerol 3-phosphotransferase activity","type":"narrow"},{"name":"down regulation of ATP:diacylglycerol phosphotransferase activity","type":"narrow"},{"name":"down regulation of CTP:diacylglycerol kinase activity","type":"narrow"},{"name":"down regulation of DG kinase activity","type":"exact"},{"name":"down regulation of DGK activity","type":"exact"},{"name":"down regulation of arachidonoyl-specific diacylglycerol kinase activity","type":"exact"},{"name":"down regulation of diacylglycerol kinase activity","type":"exact"},{"name":"down regulation of diacylglycerol:ATP kinase activity","type":"narrow"},{"name":"down regulation of diglyceride kinase activity","type":"exact"},{"name":"down regulation of sn-1,2-diacylglycerol kinase activity","type":"exact"},{"name":"down-regulation of 1,2-diacylglycerol kinase (phosphorylating)","type":"exact"},{"name":"down-regulation of 1,2-diacylglycerol kinase activity","type":"exact"},{"name":"down-regulation of ATP:1,2-diacylglycerol 3-phosphotransferase activity","type":"narrow"},{"name":"down-regulation of ATP:diacylglycerol phosphotransferase activity","type":"narrow"},{"name":"down-regulation of CTP:diacylglycerol kinase activity","type":"narrow"},{"name":"down-regulation of DG kinase activity","type":"exact"},{"name":"down-regulation of DGK activity","type":"exact"},{"name":"down-regulation of arachidonoyl-specific diacylglycerol kinase activity","type":"exact"},{"name":"down-regulation of diacylglycerol kinase activity","type":"exact"},{"name":"down-regulation of diacylglycerol:ATP kinase activity","type":"narrow"},{"name":"down-regulation of diglyceride kinase activity","type":"exact"},{"name":"down-regulation of sn-1,2-diacylglycerol kinase activity","type":"exact"},{"name":"downregulation of 1,2-diacylglycerol kinase (phosphorylating)","type":"exact"},{"name":"downregulation of 1,2-diacylglycerol kinase activity","type":"exact"},{"name":"downregulation of ATP:1,2-diacylglycerol 3-phosphotransferase activity","type":"narrow"},{"name":"downregulation of ATP:diacylglycerol phosphotransferase activity","type":"narrow"},{"name":"downregulation of CTP:diacylglycerol kinase activity","type":"narrow"},{"name":"downregulation of DG kinase activity","type":"exact"},{"name":"downregulation of DGK activity","type":"exact"},{"name":"downregulation of arachidonoyl-specific diacylglycerol kinase activity","type":"exact"},{"name":"downregulation of diacylglycerol kinase activity","type":"exact"},{"name":"downregulation of diacylglycerol:ATP kinase activity","type":"narrow"},{"name":"downregulation of diglyceride kinase activity","type":"exact"},{"name":"downregulation of sn-1,2-diacylglycerol kinase activity","type":"exact"},{"name":"inhibition of 1,2-diacylglycerol kinase (phosphorylating)","type":"narrow"},{"name":"inhibition of 1,2-diacylglycerol kinase activity","type":"narrow"},{"name":"inhibition of ATP:1,2-diacylglycerol 3-phosphotransferase activity","type":"narrow"},{"name":"inhibition of ATP:diacylglycerol phosphotransferase activity","type":"narrow"},{"name":"inhibition of CTP:diacylglycerol kinase activity","type":"narrow"},{"name":"inhibition of DG kinase activity","type":"narrow"},{"name":"inhibition of DGK activity","type":"narrow"},{"name":"inhibition of arachidonoyl-specific diacylglycerol kinase activity","type":"narrow"},{"name":"inhibition of diacylglycerol kinase activity","type":"narrow"},{"name":"inhibition of diacylglycerol:ATP kinase activity","type":"narrow"},{"name":"inhibition of diglyceride kinase activity","type":"narrow"},{"name":"inhibition of sn-1,2-diacylglycerol kinase activity","type":"narrow"},{"name":"negative regulation of 1,2-diacylglycerol kinase (phosphorylating)","type":"exact"},{"name":"negative regulation of 1,2-diacylglycerol kinase activity","type":"exact"},{"name":"negative regulation of ATP:1,2-diacylglycerol 3-phosphotransferase activity","type":"narrow"},{"name":"negative regulation of ATP:diacylglycerol phosphotransferase activity","type":"narrow"},{"name":"negative regulation of CTP:diacylglycerol kinase activity","type":"narrow"},{"name":"negative regulation of DG kinase activity","type":"exact"},{"name":"negative regulation of DGK activity","type":"exact"},{"name":"negative regulation of arachidonoyl-specific diacylglycerol kinase activity","type":"exact"},{"name":"negative regulation of diacylglycerol:ATP kinase activity","type":"narrow"},{"name":"negative regulation of diglyceride kinase activity","type":"exact"},{"name":"negative regulation of sn-1,2-diacylglycerol kinase activity","type":"exact"}],"termid":"GO:1905688"}


id: MONDO:0003963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This is usually an oligoclonal CD8+ lymphocytic infiltration of various organs.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diffuse infiltrative lymphocytosis syndrome","secondary_identifiers":["MEDGEN:232428","NCIT:C35699","UMLS:C1333292","DOID:6677","SCTID:449784008"],"synonyms":[{"name":"diffuse infiltra. lymph. sydrome","type":"exact"},{"name":"diffuse infiltra. lymph. syndrome","type":"exact"}],"termid":"MONDO:0003963","xrefs":{"Monarch":{"xref_id":"0003963"}}}


id: PBO:0007962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphotyrosyl phosphatase activator Ypa2","termid":"PBO:0007962"}


id: PBO:0085577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in 2'-O-methylation of C32 of substrate tRNAs; interacts with 2'-O-ribose methyltransferase Trm7p; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; non-essential gene; yeast null mutant can be functionally complemented by human THADA, mutations in which have been implicated in epithelial thyroid adenomas, type 2 diabetes, and polycystic ovary syndrome (PCOS)","termid":"PBO:0085577"}


id: GO:0004253
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of the Leu-Leu bond in synthetic tetradecapeptide renin substrate, producing angiotensin I, but not active on natural angiotensinogen. Also hydrolyzes BZ-Arg-para-nitroanilide.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete gamma-renin activity (obsolete GO:0004253)","synonyms":[{"name":"gamma-renin activity","type":"exact"}],"termid":"GO:0004253"}


id: GO:1902496
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any protein binding that is involved in negative regulation of telomere maintenance via telomerase.","definition_xrefs":["PMID:24013504","GOC:dph","GOC:TermGenie","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete protein binding involved in negative regulation of telomere maintenance via telomerase (obsolete GO:1902496)","synonyms":[{"name":"protein binding involved in down regulation of telomere maintenance via telomerase activity","type":"exact"},{"name":"protein binding involved in down-regulation of telomere maintenance via telomerase activity","type":"exact"},{"name":"protein binding involved in downregulation of telomere maintenance via telomerase activity","type":"exact"},{"name":"protein binding involved in inhibition of telomere maintenance via telomerase","type":"narrow"}],"termid":"GO:1902496"}


id: FYPO:0002402
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 viable, and has an abnormal shape and a larger volume than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable vegetative cell with abnormal cell shape","termid":"FYPO:0002197"},{"relation_name":"is_a","term_name":"viable swollen vegetative cell","termid":"FYPO:0002377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"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:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000004","FYPO:0000005","FYPO:0001320"],"is_obsolete":false,"name":"viable swollen vegetative cell with abnormal cell shape","synonyms":[{"name":"viable enlarged vegetative cell with abnormal cell shape","type":"related"},{"name":"viable large vegetative cell with abnormal cell shape","type":"related"},{"name":"viable swollen cell with abnormal cell shape during vegetative growth","type":"exact"},{"name":"viable swollen misshapen vegetative cell","type":"related"},{"name":"viable swollen vegetative cell with abnormal cell shape during mitotic cell cycle","type":"related"},{"name":"viable vegetative cell with increased cell size and abnormal cell shape","type":"related"},{"name":"viable vegetative cell with increased cell volume and abnormal cell shape","type":"exact"}],"termid":"FYPO:0002402"}


id: PBO:0108552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 associated factor 1 Laf1","termid":"PBO:0108552"}


id: GO:0030579
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of SMAD signaling proteins by ubiquitination and targeting to the proteasome.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete ubiquitin-dependent SMAD protein catabolic process (obsolete GO:0030579)","synonyms":[{"name":"ubiquitin-dependent SMAD protein breakdown","type":"exact"},{"name":"ubiquitin-dependent SMAD protein catabolism","type":"exact"},{"name":"ubiquitin-dependent SMAD protein degradation","type":"exact"}],"termid":"GO:0030579"}


id: CHEBI:35456
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":"cadmium dichloride","termid":"CHEBI:35456"}


id: PBO:0089283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane peptidase Atp23","termid":"PBO:0089283"}


id: MONDO:0002897
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The secondary stage of syphilis typically that is characterized by generalized rash (including palms and soles), mucocutaneous lesions, and lymphadenopathy. It usually begins one to two months after the primary stage.","definition_xrefs":["NCIT:C128413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syphilis","termid":"MONDO:0005976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary syphilis","secondary_identifiers":["ICD9:091.89","MEDGEN:101776","MESH:C536773","DOID:4157","SCTID:240557004","ICD9:091.9","UMLS:C0149985"],"synonyms":[{"name":"secondary syphilis of viscera or bone","type":"exact"}],"termid":"MONDO:0002897","xrefs":{"Monarch":{"xref_id":"0002897"}}}


id: PBO:0059176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanocortin 2 receptor accessory protein 2","termid":"PBO:0059176"}


id: PBO:0065027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxiredoxin 4 pseudogene 1","termid":"PBO:0065027"}


id: PBO:0108987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm microtubule inner protein 11","termid":"PBO:0108987"}


id: GO:0071223
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 lipoteichoic acid stimulus; lipoteichoic acid is a major component of the cell wall of gram-positive bacteria and typically consists of a chain of glycerol-phosphate repeating units linked to a glycolipid anchor.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipoteichoic acid","termid":"GO:0070391"},{"relation_name":"is_a","term_name":"cellular response to molecule of bacterial origin","termid":"GO:0071219"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"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 lipoteichoic acid","synonyms":[{"name":"cellular response to LTA","type":"exact"}],"termid":"GO:0071223"}


id: GO:0031376
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A fatty acid synthase complex in which each polypeptide chain catalyzes a single activity, located in the cytosol.","definition_xrefs":["GOC:mah","ISBN:0716720094","PMID:12957385","ISBN:0471331309"],"gene_count":0,"genotype_count":0,"name":"obsolete cytosolic type II fatty acid synthase complex (obsolete GO:0031376)","synonyms":[{"name":"cytosolic type II FAS complex","type":"exact"},{"name":"cytosolic type II fatty acid synthase complex","type":"exact"}],"termid":"GO:0031376"}


id: GO:0014843
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of satellite cell proliferation; dependent on specific growth factor activity such as fibroblast growth factors and transforming growth factor beta.","definition_xrefs":["GOC:ef","GOC:mtg_muscle","PMID:16607119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of skeletal muscle satellite cell proliferation","termid":"GO:0014842"}],"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":"growth factor dependent regulation of skeletal muscle satellite cell proliferation","termid":"GO:0014843"}


id: MONDO:0012796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the PROM1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"PROM1-related recessive retinopathy","termid":"MONDO:1040052"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0006025","MONDO:0004736","MONDO:0005328"],"is_obsolete":false,"name":"retinitis pigmentosa 41","secondary_identifiers":["MESH:C567422","ICD10CM:H35.5","MEDGEN:383126","OMIM:612095","UMLS:C2677516","GARD:10379","DOID:0110376"],"synonyms":[{"name":"PROM1 retinitis pigmentosa","type":"exact"},{"name":"RP 41","type":"related"},{"name":"RP41","type":"exact"},{"name":"retinal Degeneration, autosomal recessive, prominin-related","type":"related"},{"name":"retinitis pigmentosa 41","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in PROM1","type":"exact"},{"name":"retinitis pigmentosa type 41","type":"exact"}],"termid":"MONDO:0012796","xrefs":{"Monarch":{"xref_id":"0012796"}}}


id: GO:1902012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly(ribitol phosphate) teichoic acid.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00790","PMID:11882717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teichoic acid biosynthetic process","termid":"GO:0019350"},{"relation_name":"is_a","term_name":"poly(ribitol phosphate) teichoic acid metabolic process","termid":"GO:1902011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0071554","GO:0044281","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"poly(ribitol phosphate) teichoic acid biosynthetic process","synonyms":[{"name":"poly(ribitol phosphate) teichoic acid anabolism","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid biosynthesis","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid formation","type":"exact"},{"name":"poly(ribitol phosphate) teichoic acid synthesis","type":"exact"}],"termid":"GO:1902012"}


id: PR:Q9UUA5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC409.19c gene.","definition_xrefs":["UniProtKB:Q9UUA5","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":"metaxin-like protein C409.19c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC409.19c","synonyms":[{"name":"Spom972h-SPBC409.19c","type":"exact"}],"termid":"PR:Q9UUA5"}


id: PBO:0063940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl cis/trans isomerase, NIMA-interacting 1","termid":"PBO:0063940"}


id: GO:0070990
data:
  {"annotated_genes":["SJAG_03291","SJAG_02558","SJAG_02279","SJAG_04914"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70321,87386],"is_not":false,"summary":null,"term":"GO:0070990"},{"annotations":[113873,70207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990446"},{"annotations":[113874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990447"}]},"cv_name":"molecular_function","definition":"Binding to a small nuclear ribonucleoprotein particle.","definition_xrefs":["GOC:mah","GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonucleoprotein complex binding","termid":"GO:0043021"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02279":null,"SJAG_02558":null,"SJAG_03291":null,"SJAG_04914":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":"snRNP binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0070990","terms_by_termid":{"GO:0070990":null,"GO:1990446":null,"GO:1990447":null}}


id: GO:0035079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The decondensing (loosening) and swelling of the chromosomal sites of target genes on polytene chromosomes following response to a stimulus, to facilitate sudden bursts of transcriptional activity in response to transient environmental signals.","definition_xrefs":["PMID:12543962","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome organization","termid":"GO:0051276"}],"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":"polytene chromosome puffing","termid":"GO:0035079"}


id: GO:0047206
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-D-alanyl-D-alanine + L-alanyl-tRNA(Ala) = UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-N6-(L-alanyl)-L-lysyl-D-alanyl-D-alanine + tRNA(Ala).","definition_xrefs":["EC:2.3.2.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyltransferase activity","termid":"GO:0016755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"UDP-N-acetylmuramoylpentapeptide-lysine N6-alanyltransferase activity","secondary_identifiers":["RHEA:12432","MetaCyc:2.3.2.10-RXN"],"synonyms":[{"name":"UDP-N-acetylmuramoylpentapeptide lysine N(6)-alanyltransferase activity","type":"exact"},{"name":"UDP-N-acetylmuramoylpentapeptide lysine N6-alanyltransferase activity","type":"exact"},{"name":"alanyl-transfer ribonucleate-uridine diphosphoacetylmuramoylpentapeptide transferase activity","type":"exact"},{"name":"uridine diphosphoacetylmuramoylpentapeptide lysine N(6)-alanyltransferase activity","type":"exact"},{"name":"uridine diphosphoacetylmuramoylpentapeptide lysine N6-alanyltransferase activity","type":"exact"}],"termid":"GO:0047206"}


id: PR:O13730
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A muskelin that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01545","PANTHER:PTHR15526:SF5","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":"mei4-dependent protein 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC15A10.10","secondary_identifiers":["UniProtKB:O13730"],"synonyms":[{"name":"Spom972h-MKLN1","type":"exact"}],"termid":"PR:O13730"}


id: PR:O14181
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrpl28 gene.","definition_xrefs":["UniProtKB:O14181","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":"54S ribosomal protein L28, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F8.05c","synonyms":[{"name":"Spom972h-mrpl28","type":"exact"}],"termid":"PR:O14181"}


id: GO:1902009
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of toxin transport.","definition_xrefs":["GOC:dph","GOC:TermGenie","PMID:22792315"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of toxin transport (obsolete GO:1902009)","synonyms":[{"name":"activation of toxin transport","type":"narrow"},{"name":"up regulation of toxin transport","type":"exact"},{"name":"up-regulation of toxin transport","type":"exact"},{"name":"upregulation of toxin transport","type":"exact"}],"termid":"GO:1902009"}


id: MONDO:0007768
data:
  {"annotated_genes":["SJAG_01151"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85631],"is_not":false,"summary":null,"term":"MONDO:0007768"}]},"cv_name":"mondo","definition":"An autosomal dominant inherited syndrome characterized by the development of parathyroid adenoma or carcinoma, ossifying fibroma of the mandible and maxilla, renal neoplasms, and renal cysts.","definition_xrefs":["NCIT:C48287"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"},{"relation_name":"is_a","term_name":"familial primary hyperparathyroidism","termid":"MONDO:0016365"},{"relation_name":"is_a","term_name":"bone neoplasm","termid":"MONDO:0019060"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"abnormal mineralization disorder","termid":"MONDO:0800096"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01151":null},"genotype_count":0,"is_obsolete":false,"name":"hyperparathyroidism 2 with jaw tumors","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:10829","MEDGEN:310065","OMIM:145001","Orphanet:99880","SCTID:702378002","UMLS:C1704981"],"synonyms":[{"name":"HPT-JT","type":"exact"},{"name":"HRPT2","type":"related"},{"name":"familial primary hyperparathyroidism with multiple ossifying jaw fibromas","type":"related"},{"name":"hereditary hyperparathyroidism-jaw tumor syndrome","type":"related"},{"name":"hereditary hyperparathyroidism-jaw tumour syndrome","type":"related"},{"name":"hyperparathyroidism 2","type":"related"},{"name":"hyperparathyroidism 2 with jaw tumors","type":"exact"},{"name":"hyperparathyroidism type 2","type":"exact"},{"name":"hyperparathyroidism, familial primary, with multiple ossifying jaw fibromas","type":"related"},{"name":"hyperparathyroidism-2","type":"exact"},{"name":"hyperparathyroidism-jaw tumor syndrome","type":"exact"},{"name":"hyperparathyroidism-jaw tumor syndrome, hereditary","type":"related"},{"name":"hyperparathyroidism-jaw tumour syndrome","type":"exact"},{"name":"hyperparathyroidism-jaw tumour syndrome, hereditary","type":"related"},{"name":"parathyroid adenoma with cystic changes","type":"exact"},{"name":"parathyroid adenomatosis, familial cystic","type":"related"}],"termid":"MONDO:0007768","terms_by_termid":{"MONDO:0007768":null},"xrefs":{"Monarch":{"xref_id":"0007768"}}}


id: FYPO:0002452
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 contains one or more septa, has abnormal morphology (i.e. size, shape, or structure) and is inviable.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"has_part","term_name":"septated vegetative cell","termid":"FYPO:0002342"},{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell morphology","termid":"FYPO:0002273"},{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000005","FYPO:0001985","FYPO:0000004"],"is_obsolete":false,"name":"inviable septated vegetative cell with abnormal cell morphology","synonyms":[{"name":"lethal; septated vegetative cell with abnormal cell morphology","type":"exact"}],"termid":"FYPO:0002452"}


id: GO:0098519
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: nucleotide + H2O = nucleotide + phosphate.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleotide phosphatase activity, acting on free nucleotides (obsolete GO:0098519)","synonyms":[{"name":"nucleotide phosphatase activity","type":"exact"}],"termid":"GO:0098519"}


id: PBO:0066605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ras homolog family member T2","termid":"PBO:0066605"}


id: PBO:0042641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromodomain Y-linked 16 pseudogene","termid":"PBO:0042641"}


id: PBO:0081089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger DHHC-type palmitoyltransferase 19","termid":"PBO:0081089"}


id: GO:0006234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of TTP, ribosylthymine triphosphate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleoside triphosphate biosynthetic process","termid":"GO:0009209"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide biosynthetic process","termid":"GO:0009220"},{"relation_name":"is_a","term_name":"TTP metabolic process","termid":"GO:0046046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"TTP biosynthetic process","synonyms":[{"name":"TTP anabolism","type":"exact"},{"name":"TTP biosynthesis","type":"exact"},{"name":"TTP formation","type":"exact"},{"name":"TTP synthesis","type":"exact"}],"termid":"GO:0006234"}


id: PBO:0078922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon ACG) 1-1","termid":"PBO:0078922"}


id: GO:0008941
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 NO + 2 O2 + NAD(P)H + H+ = 2 nitrate + NAD(P)+.","definition_xrefs":["EC:1.14.12.17"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of two atoms of oxygen into one donor","termid":"GO:0016708"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"nitric oxide dioxygenase NAD(P)H activity","secondary_identifiers":["MetaCyc:R621-RXN","Reactome:R-HSA-1222723"],"synonyms":[{"name":"NOD activity","type":"related"},{"name":"nitric oxide dioxygenase activity","type":"broad"}],"termid":"GO:0008941"}


id: MOD:00932
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label","definition_xrefs":["PubMed:11821862","Unimod:499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"isotope tagged reagent derivatized residue","termid":"MOD:01426"}],"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":"IDBEST tag for quantitation","synonyms":[{"name":"Heavy IDBEST tag for quantitation","type":"related"},{"name":"IGBP:13C(2)","type":"related"}],"termid":"MOD:00932"}


id: PBO:0046248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELOVL fatty acid elongase 4","termid":"PBO:0046248"}


id: MOD:01433
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue into 1-amino-2-propanone.","definition_xrefs":["PubMed:19196969","ChEBI:17906","PubMed:12715872","RESID:AA0486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dehydrogenated residue","termid":"MOD:00683"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"},{"relation_name":"is_a","term_name":"decarboxylated residue","termid":"MOD:00960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-amino-2-propanone","synonyms":[{"name":"1-amino-2-propanone","type":"exact"},{"name":"1-aminopropan-2-one","type":"exact"},{"name":"1-aminopropanone","type":"exact"},{"name":"MOD_RES 1-amino-2-propanone","type":"exact"},{"name":"aminoacetone","type":"exact"}],"termid":"MOD:01433"}


id: GO:0001983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The increase in nerve impulses from baroreceptors as a result of increased pressure on an artery that results in an inhibition of sympathetic nerve impulses to peripheral blood vessels.","definition_xrefs":["GOC:mtg_cardio","ISBN:0323031951","ISBN:0721643949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of systemic arterial blood pressure by carotid sinus baroreceptor feedback","termid":"GO:0001978"},{"relation_name":"is_a","term_name":"negative regulation of systemic arterial blood pressure","termid":"GO:0003085"}],"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":"baroreceptor response to increased systemic arterial blood pressure","termid":"GO:0001983"}


id: PBO:0072257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 32","termid":"PBO:0072257"}


id: MONDO:0017597
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"T-cell/histiocyte rich large B cell lymphoma (THRLBCL) is a rare variant of diffuse large B-cell lymphoma (DLBCL), mainly affecting middle-aged men and often not being discovered until an advanced disease stage, with involvement of the spleen, liver and bone marrow occurring at a greater frequency than in DLBCL. It is often difficult to diagnose due to its similarity with other lymphoid diseases such as classic Hodgkin lymphoma and nodular lymphocyte-predominant Hodgkin lymphoma and has an aggressive clinical course.","definition_xrefs":["Orphanet:300857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"T-cell/histiocyte rich large B cell lymphoma","secondary_identifiers":["ICDO:9680/3","icd11.foundation:257833622","GARD:12257","ICDO:9688/3","MEDGEN:232943","UMLS:C1321547","ONCOTREE:THRLBCL","NCIT:C9496"],"synonyms":[{"name":"T-cell rich/histiocyte-rich large B-cell lymphoma","type":"exact"},{"name":"T-cell/histiocyte rich lymphoma","type":"exact"},{"name":"T-cell/histiocyte-rich large B-cell lymphoma","type":"exact"},{"name":"THRLBCL","type":"exact"}],"termid":"MONDO:0017597","xrefs":{"Monarch":{"xref_id":"0017597"}}}


id: PBO:0108955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBA5 pseudogene 1","termid":"PBO:0108955"}


id: PBO:0043533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"component of oligomeric golgi complex 1","termid":"PBO:0043533"}


id: MONDO:0003481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell tumor arising from the ovary. Morphologically, it is identical to seminoma and consists of a monotonous population of germ cells with abundant pale cytoplasm and uniform nuclei. The stroma invariably contains chronic inflammatory cells, mostly T-lymphocytes. It responds to chemotherapy or radiotherapy and the prognosis relates to the tumor stage.","definition_xrefs":["NCIT:C8106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysgerminoma","termid":"MONDO:0003002"},{"relation_name":"is_a","term_name":"ovarian primitive germ cell tumor","termid":"MONDO:0003408"}],"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":"dysgerminoma of ovary","secondary_identifiers":["DOID:5511","icd11.foundation:208782658","MEDGEN:83414","ONCOTREE:ODYS","SCTID:254874008","EFO:1000414","UMLS:C0346185"],"synonyms":[{"name":"dysgerminoma","type":"related"},{"name":"dysgerminoma of ovary","type":"exact"},{"name":"dysgerminoma of the ovary","type":"exact"},{"name":"germ cell dysgerminoma of ovary","type":"exact"},{"name":"germ cell dysgerminoma of the ovary","type":"exact"},{"name":"ovarian dysgerminoma","type":"exact"},{"name":"ovarian germ cell dysgerminoma","type":"exact"},{"name":"ovary dysgerminoma (disease)","type":"exact"}],"termid":"MONDO:0003481","xrefs":{"Monarch":{"xref_id":"0003481"}}}


id: GO:0018278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The deamination of N-terminal peptidyl-threonine to form peptidyl-2-oxobutanoic acid.","definition_xrefs":["RESID:AA0129"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal peptidyl-threonine deamination (obsolete GO:0018278)","termid":"GO:0018278"}


id: PBO:0073410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET pseudogene 14","termid":"PBO:0073410"}


id: GO:0060284
data:
  {"annotated_genes":["SJAG_02169","SJAG_04853","SJAG_02392","SJAG_04140","SJAG_00993","SJAG_03581","SJAG_00514"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89820,95821,94548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051519"},{"annotations":[111214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[90689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051517"},{"annotations":[102294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[90691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[92156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of the progression of the cell over time, from its formation to the mature structure. Cell development does not include the steps involved in committing a cell to a specific fate.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell differentiation","termid":"GO:0045595"},{"relation_name":"regulates","term_name":"cell development","termid":"GO:0048468"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_00993":null,"SJAG_02169":null,"SJAG_02392":null,"SJAG_03581":null,"SJAG_04140":null,"SJAG_04853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell development","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0060284","terms_by_termid":{"GO:0034307":null,"GO:0051517":null,"GO:0051519":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


