# terms

id: PR:O13873
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A PCI domain-containing protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02053"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein CSN12 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B3.08","secondary_identifiers":["UniProtKB:O13873"],"synonyms":[{"name":"Spom972h-PCID2","type":"exact"}],"termid":"PR:O13873"}


id: MONDO:0001497
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male genital organ vascular disease","secondary_identifiers":["SCTID:198057005","MEDGEN:508280","DOID:12335","ICD9:608.83","UMLS:C0042374"],"synonyms":[{"name":"vascular disorder of male genital organs","type":"exact"}],"termid":"MONDO:0001497","xrefs":{"Monarch":{"xref_id":"0001497"}}}


id: MONDO:0014355
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome associated with dilated cardiomyopathy (obsolete MONDO:0016337)","termid":"MONDO:0016337"},{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited odontologic disease (obsolete MONDO:0019183)","termid":"MONDO:0019183"},{"relation_name":"is_a","term_name":"arrhythmogenic cardiomyopathy with wooly hair and keratoderma","termid":"MONDO:0011581"},{"relation_name":"is_a","term_name":"erythrokeratoderma","termid":"MONDO:0019270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis","secondary_identifiers":["MEDGEN:862830","Orphanet:476096","UMLS:C4014393","GARD:16014","OMIM:615821"],"synonyms":[{"name":"DCWHKTA","type":"related"},{"name":"EKC syndrome","type":"exact"},{"name":"cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis","type":"exact"},{"name":"dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis","type":"exact"},{"name":"dilated cardiomyopathy with wooly hair, keratoderma, and tooth agenesis","type":"exact"},{"name":"erythrokeratodermia-cardiomyopathy syndrome","type":"exact"}],"termid":"MONDO:0014355","xrefs":{"Monarch":{"xref_id":"0014355"}}}


id: MONDO:0034217
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta (obsolete MONDO:0034217)","secondary_identifiers":["Orphanet:566243"],"termid":"MONDO:0034217","xrefs":{"Monarch":{"xref_id":"0034217"}}}


id: GO:0019449
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-cysteine into other compounds, including hypotaurine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-cysteine catabolic process","termid":"GO:0019448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"L-cysteine catabolic process to hypotaurine","synonyms":[{"name":"L-cysteine breakdown to hypotaurine","type":"exact"},{"name":"L-cysteine degradation to hypotaurine","type":"exact"}],"termid":"GO:0019449"}


id: GO:0042803
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an identical protein to form a homodimer.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"identical protein binding","termid":"GO:0042802"},{"relation_name":"is_a","term_name":"protein dimerization activity","termid":"GO:0046983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"protein homodimerization activity","synonyms":[{"name":"dimerization activity","type":"broad"}],"termid":"GO:0042803"}


id: MONDO:0005925
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bovine respiratory disease found in animals that have been shipped or exposed to cattle recently transported. The major agent responsible for the disease is mannheimia haemolytica and less commonly, pasteurella multocida or haemophilus somnus. All three agents are normal inhabitants of the bovine nasal pharyngeal mucosa but not the lung. They are considered opportunistic pathogens following stress, physiological and/or a viral infection. The resulting bacterial fibrinous bronchopneumonia is often fatal.","definition_xrefs":["MESH:D012766"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumonic pasteurellosis","secondary_identifiers":["MEDGEN:11408","EFO:0007449","UMLS:C0036969"],"termid":"MONDO:0005925","xrefs":{"Monarch":{"xref_id":"0005925"}}}


id: GO:0044514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism initiates, promotes, or enhances a G protein-coupled receptor signaling pathway in another organism via the action of a venom.","definition_xrefs":["GOC:jl","GOC:fj","PMID:8405712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of G protein-coupled receptor signaling pathway","termid":"GO:0044513"}],"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":"venom-mediated activation of G protein-coupled receptor signaling pathway","synonyms":[{"name":"envenomation resulting in positive regulation of G protein-coupled receptor activity in another organism","type":"exact"},{"name":"envenomation resulting in positive regulation of G protein-coupled receptor activity in other organism","type":"exact"},{"name":"envenomation resulting in positive regulation of G-protein coupled receptor activity in other organism","type":"exact"}],"termid":"GO:0044514"}


id: GO:0019033
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structure lying between the capsid and envelope of a virus, varying in thickness and often distributed asymmetrically.","definition_xrefs":["ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"virion component","termid":"GO:0044423"}],"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":"viral tegument","secondary_identifiers":["Wikipedia:Viral_tegument"],"termid":"GO:0019033"}


id: PBO:0068452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 28, pseudogene","termid":"PBO:0068452"}


id: PBO:0059257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L22 pseudogene 1","termid":"PBO:0059257"}


id: MONDO:0017967
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular agenesis","secondary_identifiers":["SCTID:371015003","MEDGEN:98344","Orphanet:325124","icd11.foundation:1382370664","GARD:5819","UMLS:C0405582"],"synonyms":[{"name":"absence of testes","type":"related"},{"name":"anorchia","type":"related"},{"name":"bilateral anorchia","type":"exact"},{"name":"congenital absence of testes","type":"related"},{"name":"empty scrotum","type":"related"}],"termid":"MONDO:0017967","xrefs":{"Monarch":{"xref_id":"0017967"}}}


id: FYECO:0000282
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which aminolevulinic acid was added to the medium or assay buffers in a limiting quantity compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping limited","termid":"FYECO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ limited aminolevulinic acid","secondary_identifiers":["PMID:7565608"],"synonyms":[{"name":"+ limited ALA","type":"exact"}],"termid":"FYECO:0000282"}


id: GO:0051513
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of monopolar cell growth, polarized growth from one end of a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of unidimensional cell growth","termid":"GO:0051510"},{"relation_name":"regulates","term_name":"monopolar cell growth","termid":"GO:0042814"}],"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 monopolar cell growth","termid":"GO:0051513"}


id: GO:0023004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that initiates the dopamine receptor protein signaling pathway through stimulation of the dopamine receptor.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of dopamine receptor signaling pathway (obsolete GO:0023004)","synonyms":[{"name":"activation of dopamine receptor signaling pathway","type":"exact"},{"name":"activation of dopamine receptor signalling pathway","type":"exact"},{"name":"initiation of dopamine receptor signaling pathway","type":"related"},{"name":"stimulation of dopamine receptor signaling pathway","type":"exact"}],"termid":"GO:0023004"}


id: MONDO:0100160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute disease characterized by severe ketoacidosis in the absence of diabetes mellitus and occurring in individuals with a history of prolonged excessive alcohol consumption. Disease manifestations include nausea, intractable vomiting, and abdominal pain. When treated, AKA resolves rapidly and completely with no apparent sequelae.","definition_xrefs":["PMID:16714496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acidosis disorder","termid":"MONDO:0006022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"alcoholic ketoacidosis","secondary_identifiers":["UMLS:C0268039","DOID:0080949","MEDGEN:541151"],"synonyms":[{"name":"alcoholic acidosis","type":"exact"},{"name":"alcoholic ketosis","type":"exact"}],"termid":"MONDO:0100160","xrefs":{"Monarch":{"xref_id":"0100160"}}}


id: GO:0039524
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts mRNA processing in its host. mRNA processing is the conversion of a primary mRNA transcript into one or more mature mRNA(s) prior to translation into polypeptide. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["VZ:903","GOC:bf","PMID:16571812","GOC:sp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host gene expression","termid":"GO:0039656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host mRNA processing","secondary_identifiers":["Reactome:R-HSA-168315"],"synonyms":[{"name":"inhibition by virus of host mRNA processing","type":"narrow"},{"name":"inhibition of host mRNA processing","type":"exact"},{"name":"inhibition of host pre-mRNA processing by virus","type":"narrow"},{"name":"negative regulation of host mRNA processing","type":"broad"},{"name":"suppression by virus of host mRNA processing","type":"narrow"}],"termid":"GO:0039524"}


id: PBO:0079755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urocortin","termid":"PBO:0079755"}


id: MOD:01093
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isopropyl lysyl","termid":"MOD:01093"}


id: FYPO:0007790
data:
  {"alleles_by_uniquename":{"SJAG_00601:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00601","name":"rip1delta","uniquename":"SJAG_00601:allele-1"},"SJAG_01355:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01355","name":"cox6delta","uniquename":"SJAG_01355:allele-1"},"SJAG_01680:allele-2":{"allele_type":"amino_acid_mutation","description":"P470L","gene_uniquename":"SJAG_01680","name":"chk1-P470L","synonyms":[{"name":"chk1- hyperactive (chk1-hyp)","reference":"PMID:23090706","type":"exact"},{"name":"chk1-hyperactive (chk1-hyp)","reference":"PMID:20368354","type":"exact"}],"uniquename":"SJAG_01680:allele-2"},"SJAG_02266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02266","name":"rad24delta","uniquename":"SJAG_02266:allele-1"},"SJAG_02486:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02486","name":"ste6delta","uniquename":"SJAG_02486:allele-1"},"SJAG_04287:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04287","name":"cds1delta","uniquename":"SJAG_04287:allele-1"},"SJAG_04671:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04671","name":"mrc1delta","uniquename":"SJAG_04671:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121393],"is_not":false,"summary":null,"term":"FYPO:0007790"}],"single_locus_phenotype":[{"annotations":[121223,121383,121390,121510,121511],"is_not":false,"summary":null,"term":"FYPO:0007790"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which hyphal growth is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:31150379"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"},{"relation_name":"is_a","term_name":"biological process phenotype","termid":"FYPO:0000300"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00601":null,"SJAG_01355":null,"SJAG_01680":null,"SJAG_02266":null,"SJAG_02486":null,"SJAG_04287":null,"SJAG_04671":null},"genotype_count":6,"genotypes_by_uniquename":{"cds1delta":{"display_name":"cds1delta","display_uniquename":"cds1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04287:allele-1","expression":"Null"}]}]},"chk1-P470L-P470L-amino_acid_mutation-expression-not_assayed_or_wild_type__rad24delta":{"display_name":"chk1-P470L(aa) rad24delta","display_uniquename":"chk1-P470L-P470L-amino_acid_mutation-expression-not_assayed_or_wild_type__rad24delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01680:allele-2","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02266:allele-1","expression":"Null"}]}]},"cox6delta":{"display_name":"cox6delta","display_uniquename":"cox6delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01355:allele-1","expression":"Null"}]}]},"mrc1delta":{"display_name":"mrc1delta","display_uniquename":"mrc1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04671:allele-1","expression":"Null"}]}]},"rip1delta":{"display_name":"rip1delta","display_uniquename":"rip1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00601:allele-1","expression":"Null"}]}]},"ste6delta":{"display_name":"ste6delta","display_uniquename":"ste6delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02486:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01680","SJAG_02266"],"name":"normal hyphal growth","references_by_uniquename":{"PMID:23090706":null,"PMID:29566183":null,"PMID:31150379":null,"PMID:37164017":null},"single_locus_annotated_genes":["SJAG_00601","SJAG_04671","SJAG_01355","SJAG_02486","SJAG_04287"],"single_locus_genotype_uniquenames":["mrc1delta","cox6delta","ste6delta","cds1delta","rip1delta"],"synonyms":[{"name":"hyphal growth abolished","type":"exact"}],"termid":"FYPO:0007790","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000015":null,"FYECO:0000137":null,"FYPO:0007790":null}}


id: MONDO:0005930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete postpoliomyelitis syndrome (obsolete MONDO:0005930)","termid":"MONDO:0005930","xrefs":{"Monarch":{"xref_id":"0005930"}}}


id: PBO:0042986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"checkpoint kinase 1","termid":"PBO:0042986"}


id: PBO:0039273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 1, pseudogene","termid":"PBO:0039273"}


id: PBO:0055778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lon peptidase 2, peroxisomal","termid":"PBO:0055778"}


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


id: MONDO:0017941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection that is caused by the Chikungunya virus, which is transmitted by mosquitoes; it is characterized by fever and severe arthralgia.","definition_xrefs":["NCIT:C128422"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Alphavirus infectious disease","termid":"MONDO:0005643"},{"relation_name":"is_a","term_name":"arbovirus fever","termid":"MONDO:0018093"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chikungunya","secondary_identifiers":["GARD:6038","UMLS:C0008055","Orphanet:324625","MESH:D065632","SCTID:111864006","MEDGEN:3362","icd11.foundation:900389391","NORD:924","DOID:0050012"],"synonyms":[{"name":"CHIK","type":"related"},{"name":"CHIKV infection","type":"related"},{"name":"CK","type":"related"},{"name":"Chikungunya fever","type":"exact"},{"name":"Chikungunya virus caused disease or disorder","type":"exact"},{"name":"Chikungunya virus disease or disorder","type":"exact"},{"name":"Chikungunya virus infection","type":"related"},{"name":"Chikungunya virus infectious disease","type":"exact"},{"name":"arbovirus A Chikungunya type","type":"related"}],"termid":"MONDO:0017941","xrefs":{"Monarch":{"xref_id":"0017941"}}}


id: PBO:0085581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in 60S assembly and pre-40S AFs recycling; has sequence similarity to human MybBP1A and weak sequence similarity to B-type DNA polymerases; not required for chromosomal DNA replication","termid":"PBO:0085581"}


id: PBO:0059963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 8","termid":"PBO:0059963"}


id: MONDO:0024277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thrombocytopenia","termid":"MONDO:0002049"}],"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":"neonatal thrombocytopenia","secondary_identifiers":["MEDGEN:526130","SCTID:82835005","UMLS:C0221028","MESH:D054098"],"synonyms":[{"name":"neonatal purpura","type":"related"},{"name":"neonatal thrombocytopenia","type":"exact"},{"name":"purpura of newborn","type":"related"}],"termid":"MONDO:0024277","xrefs":{"Monarch":{"xref_id":"0024277"}}}


id: GO:0005803
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A small subcellular vesicle, or granule, surrounded by a single-layered membrane; formed from the Golgi apparatus and contains a highly concentrated protein destined for secretion.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete secretory vesicle (obsolete GO:0005803)","synonyms":[{"name":"secretory vesicle","type":"exact"},{"name":"transition vesicle","type":"narrow"}],"termid":"GO:0005803"}


id: PBO:0076316
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SYNM antisense RNA 2","termid":"PBO:0076316"}


id: MONDO:0008387
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring dermoid of cornea is characterized by annular limbal dermoids (growths with a skin-like structure) with corneal and conjunctival extension. Less than 30 cases have been described. Transmission is autosomal dominant and mutations in the PITX2 gene have been suggested as a potential cause of the condition.","definition_xrefs":["Orphanet:91481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"eye neoplasm","termid":"MONDO:0021220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"ring dermoid of cornea","secondary_identifiers":["icd11.foundation:271430543","MEDGEN:357922","GARD:9696","UMLS:C1867155","SCTID:723499000","DOID:0111548","MESH:C535684","OMIM:180550"],"synonyms":[{"name":"RDC","type":"related"},{"name":"RING dermoid of cornea","type":"related"},{"name":"Ring dermoid syndrome","type":"exact"},{"name":"bilateral, annular limbal dermoids with corneal and conjunctival extension","type":"related"},{"name":"ring dermoid of cornea","type":"exact"}],"termid":"MONDO:0008387","xrefs":{"Monarch":{"xref_id":"0008387"}}}


id: MONDO:0022613
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":"bruyn scheltens syndrome","termid":"MONDO:0022613","xrefs":{"Monarch":{"xref_id":"0022613"}}}


id: SO:0000663
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that can be transcribed into a transfer RNA (tRNA).","direct_ancestors":[{"relation_name":"is_a","term_name":"non_protein_coding","termid":"SO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA_encoding","synonyms":[{"name":"tRNA encoding","type":"exact"}],"termid":"SO:0000663"}


id: PBO:0077544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 255A","termid":"PBO:0077544"}


id: MONDO:0001978
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Carcinoma of the ureter without spread to any other region.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ureter carcinoma","termid":"MONDO:0006481"}],"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":"regional ureteric cancer","secondary_identifiers":["UMLS:C0854921","DOID:14491","MEDGEN:167733","NCIT:C9356"],"synonyms":[{"name":"regional malignant ureteral tumor","type":"exact"},{"name":"regional malignant ureteral tumour","type":"exact"},{"name":"regional ureter carcinoma","type":"exact"},{"name":"regional ureteric carcinoma","type":"exact"}],"termid":"MONDO:0001978","xrefs":{"Monarch":{"xref_id":"0001978"}}}


id: PBO:0030971
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_dimethylation_at_centromere","termid":"PBO:0030971"}


id: _global:causal_agent_in_process
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"A relationship between a material entity and a process where the material entity has some causal role that influences the process","direct_ancestors":[{"relation_name":"is_a","term_name":"causal_relation_between_material_entity_and_a_process","termid":"_global:causal_relation_between_material_entity_and_a_process"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causal_agent_in_process","secondary_identifiers":["RO:0002500"],"termid":"_global:causal_agent_in_process"}


id: PBO:0063380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 1","termid":"PBO:0063380"}


id: PBO:0086166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for spore wall formation; subunit of leading edge protein (LEP) complex (Ssp1-Ady3-Don1-Irc10) that forms ring-like structure at leading edge of prospore membrane during meiosis II; mediates assembly of LEP complex, formation of ring-like structure via interaction with spindle pole body components, and prospore membrane maturation; potentially phosphorylated by Cdc28p; ADY3 has a paralog, CNM67, that arose from the whole genome duplication","termid":"PBO:0086166"}


id: MONDO:0010780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial myopathy","termid":"MONDO:0009637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066","MONDO:0005336"],"is_obsolete":false,"name":"mitochondrial myopathy with reversible cytochrome C oxidase deficiency","secondary_identifiers":["UMLS:C3151898","MEDGEN:463248","OMIM:500009","Orphanet:254864","GARD:17227","icd11.foundation:723205095"],"synonyms":[{"name":"Cox deficiency myopathy, infantile, transient","type":"related"},{"name":"MMIT","type":"related"},{"name":"benign COX deficiency","type":"exact"},{"name":"infantile reversible cytochrome C oxidase deficiency myopathy","type":"exact"},{"name":"mitochondrial myopathy with reversible COX deficiency","type":"exact"},{"name":"mitochondrial myopathy with reversible complex IV deficiency","type":"exact"},{"name":"mitochondrial myopathy, infantile, transient","type":"related"},{"name":"mitochondrial myopathy, infantile, transient, due to respiratory chain deficiency","type":"related"},{"name":"respiratory chain deficiency, infantile, transient","type":"related"},{"name":"reversible infantile cytochrome C oxidase deficiency","type":"exact"},{"name":"reversible infantile respiratory chain deficiency","type":"exact"}],"termid":"MONDO:0010780","xrefs":{"Monarch":{"xref_id":"0010780"}}}


id: PBO:0072672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor transporter protein 5 (putative)","termid":"PBO:0072672"}


id: PBO:0058120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4422 host gene","termid":"PBO:0058120"}


id: GO:0045100
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A type of intermediate filament.","definition_xrefs":["ISBN:0815316194"],"gene_count":0,"genotype_count":0,"name":"obsolete desmin (obsolete GO:0045100)","synonyms":[{"name":"desmin","type":"exact"}],"termid":"GO:0045100"}


id: GO:0047868
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2R,3S)-2,3-dimethylmalate = dimethylmaleate + H2O.","definition_xrefs":["RHEA:20253","EC:4.2.1.85"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"dimethylmaleate hydratase activity","secondary_identifiers":["KEGG_REACTION:R03069","MetaCyc:DIMETHYLMALEATE-HYDRATASE-RXN"],"synonyms":[{"name":"(2R,3S)-2,3-dimethylmalate hydro-lyase (dimethylmaleate-forming)","type":"related"},{"name":"(2R,3S)-2,3-dimethylmalate hydro-lyase activity","type":"related"}],"termid":"GO:0047868"}


id: MONDO:0002377
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of breast fibroadenoma without clinical significance. It is characterized by distortion and compression of the ducts by proliferating stromal cells.","definition_xrefs":["NCIT:C4271"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast fibroadenoma","termid":"MONDO:0002056"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast intracanalicular fibroadenoma","secondary_identifiers":["ICDO:9011/0","MEDGEN:137772","DOID:2656","UMLS:C0334496"],"synonyms":[{"name":"breast intracanalicular fibroadenoma","type":"exact"},{"name":"intracanalicular breast fibroadenoma","type":"exact"},{"name":"intracanalicular fibroadenoma","type":"exact"},{"name":"intracanalicular fibroadenoma of breast","type":"exact"},{"name":"intracanalicular fibroadenoma of the breast","type":"exact"}],"termid":"MONDO:0002377","xrefs":{"Monarch":{"xref_id":"0002377"}}}


id: GO:0018688
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane + O2 + 2 H+ + 2 e- = cis-2,3-dihydrodiol DDT. 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane is also known as DDT.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete DDT 2,3-dioxygenase activity (obsolete GO:0018688)","termid":"GO:0018688"}


id: MONDO:0017481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"amelia of lower limb","termid":"MONDO:0017438"}],"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":"amelia of lower limb, bilateral","secondary_identifiers":["icd11.foundation:1627185647","MEDGEN:1775586","UMLS:C2910294","Orphanet:295059"],"termid":"MONDO:0017481","xrefs":{"Monarch":{"xref_id":"0017481"}}}


id: PBO:0070905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 13","termid":"PBO:0070905"}


id: PBO:0072963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretogranin V","termid":"PBO:0072963"}


id: FYPO:0000691
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of DNA-1,N6-ethenoadenine 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:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal DNA-1,N6-ethenoadenine N-glycosylase activity","termid":"FYPO:0000691"}


id: FYPO:0005469
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, and eventually lyses.","definition_xrefs":["PMID:8978670","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division","termid":"FYPO:0001991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000004","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, lysed cell","synonyms":[{"name":"inviable after spore germination, undivided lysed cell","type":"exact"},{"name":"inviable following spore germination, without cell division, with cell lysis","type":"exact"},{"name":"inviable germinated spore, without cell division, with cell lysis","type":"exact"},{"name":"lethal after spore germination, without cell division, with cell lysis","type":"exact"}],"termid":"FYPO:0005469"}


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


id: PBO:0080843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 1 pseudogene 7","termid":"PBO:0080843"}


id: FYPO:0008060
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to a ubiquitin monomer is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:16138082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein-protein interaction","termid":"FYPO:0000703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000702","FYPO:0000652"],"is_obsolete":false,"name":"normal mono ubiquitin binding","termid":"FYPO:0008060"}


id: MONDO:0015697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"}],"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":"immunoglobulin heavy chain deficiency","secondary_identifiers":["UMLS:C0398692","icd11.foundation:960006636","GARD:20111","ICD9:279.03","MEDGEN:98309","Orphanet:169110","SCTID:234539005"],"termid":"MONDO:0015697","xrefs":{"Monarch":{"xref_id":"0015697"}}}


id: GO:0035965
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Remodeling the acyl chains of premature (de novo synthesized) cardiolipin (1,3-bis(3-phosphatidyl)glycerol), through sequential deacylation and re-acylation reactions, to generate mature cardiolipin containing high-levels of unsaturated fatty acids.","definition_xrefs":["GOC:rb","GOC:bf","PMID:19244244"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiolipin metabolic process","termid":"GO:0032048"}],"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:0008150","GO:0006629"],"is_obsolete":false,"name":"cardiolipin acyl-chain remodeling","secondary_identifiers":["Reactome:R-HSA-1482798"],"synonyms":[{"name":"cardiolipin acyl-chain remodelling","type":"exact"},{"name":"cardiolipin maturation","type":"broad"},{"name":"diphosphatidylglycerol remodeling","type":"related"}],"termid":"GO:0035965"}


id: GO:0006412
data:
  {"annotated_genes":["SJAG_05573","SJAG_00799","SJAG_02071","SJAG_02762","SJAG_00148","SJAG_04756","SJAG_02285","SJAG_00544","SJAG_03034","SJAG_04020","SJAG_02840","SJAG_03433","SJAG_00338","SJAG_04847","SJAG_00060","SJAG_03364","SJAG_00860","SJAG_01734","SJAG_04174","SJAG_04207","SJAG_04873","SJAG_04762","SJAG_00733","SJAG_00786","SJAG_03277","SJAG_00662","SJAG_04130","SJAG_03262","SJAG_01517","SJAG_02746","SJAG_02871","SJAG_03425","SJAG_00384","SJAG_04490","SJAG_04635","SJAG_03122","SJAG_01536","SJAG_01117","SJAG_03335","SJAG_03919","SJAG_01643","SJAG_02283","SJAG_02015","SJAG_03732","SJAG_02786","SJAG_02452","SJAG_04753","SJAG_03192","SJAG_02723","SJAG_02292","SJAG_02856","SJAG_00423","SJAG_03550","SJAG_02184","SJAG_00243","SJAG_05003","SJAG_04695","SJAG_01954","SJAG_04176","SJAG_03629","SJAG_01045","SJAG_04160","SJAG_00497","SJAG_04476","SJAG_00466","SJAG_00940","SJAG_04085","SJAG_01296","SJAG_02891","SJAG_03922","SJAG_02331","SJAG_03762","SJAG_00465","SJAG_01364","SJAG_01387","SJAG_01608","SJAG_00507","SJAG_01851","SJAG_00503","SJAG_02531","SJAG_01259","SJAG_03996","SJAG_01074","SJAG_04409","SJAG_00269","SJAG_01352","SJAG_00226","SJAG_03322","SJAG_00629","SJAG_00844","SJAG_04216","SJAG_01551","SJAG_02046","SJAG_00086","SJAG_03568","SJAG_04378","SJAG_01727","SJAG_04893","SJAG_02428","SJAG_04351","SJAG_01942","SJAG_02510","SJAG_07009","SJAG_00488","SJAG_02682","SJAG_00443","SJAG_00513","SJAG_02592","SJAG_04738","SJAG_01249","SJAG_00188","SJAG_01565","SJAG_01591","SJAG_04029","SJAG_03040","SJAG_01322","SJAG_00749","SJAG_04862","SJAG_05218","SJAG_02081","SJAG_04204","SJAG_02493","SJAG_03658","SJAG_05265","SJAG_02597","SJAG_02755","SJAG_03422","SJAG_00944","SJAG_02353","SJAG_16456","SJAG_04383","SJAG_05221","SJAG_00726","SJAG_02096","SJAG_01568","SJAG_00898","SJAG_04746","SJAG_03094","SJAG_02615","SJAG_02390","SJAG_01719","SJAG_01463","SJAG_01522","SJAG_04248","SJAG_02206","SJAG_02340","SJAG_02312","SJAG_01197","SJAG_04772","SJAG_03383","SJAG_04493","SJAG_02201","SJAG_02263","SJAG_07013","SJAG_01520","SJAG_00286","SJAG_02335","SJAG_01580","SJAG_04304","SJAG_04066","SJAG_00690","SJAG_01047","SJAG_02738","SJAG_03794","SJAG_01226","SJAG_00155","SJAG_05320","SJAG_02803","SJAG_02236","SJAG_00069","SJAG_03859","SJAG_00103","SJAG_03863","SJAG_03678","SJAG_01366","SJAG_03147","SJAG_04891","SJAG_03545","SJAG_04019","SJAG_01079","SJAG_02280","SJAG_00166","SJAG_05008","SJAG_04157","SJAG_03626","SJAG_04534","SJAG_04168","SJAG_02585","SJAG_04285","SJAG_02522","SJAG_00220","SJAG_02471","SJAG_02628","SJAG_02777","SJAG_03284","SJAG_03232","SJAG_03065","SJAG_01676","SJAG_02977","SJAG_01235","SJAG_03402","SJAG_00315","SJAG_00034","SJAG_04414","SJAG_03428","SJAG_02026","SJAG_01365","SJAG_04473","SJAG_00508","SJAG_01696","SJAG_02243","SJAG_02477","SJAG_05248","SJAG_04672","SJAG_03043","SJAG_02802","SJAG_02180","SJAG_03159","SJAG_03053","SJAG_04889","SJAG_00468","SJAG_01478","SJAG_00782","SJAG_01630","SJAG_06253","SJAG_04856","SJAG_00523","SJAG_04244","SJAG_01269","SJAG_03869","SJAG_00169","SJAG_02164","SJAG_04494","SJAG_03133","SJAG_01468","SJAG_03459","SJAG_01436","SJAG_03189","SJAG_02812","SJAG_01806","SJAG_00308","SJAG_02017","SJAG_04164","SJAG_04482","SJAG_02121","SJAG_01438","SJAG_04452","SJAG_02904","SJAG_03326","SJAG_02020","SJAG_01767","SJAG_03424","SJAG_00251","SJAG_01058","SJAG_04814","SJAG_00579","SJAG_01497","SJAG_04173","SJAG_00077","SJAG_03501","SJAG_00105","SJAG_03197","SJAG_06284","SJAG_02861","SJAG_03472","SJAG_04918","SJAG_00892","SJAG_00642","SJAG_02061","SJAG_04283","SJAG_01248","SJAG_02704","SJAG_03127","SJAG_04367","SJAG_01548","SJAG_03176","SJAG_02721","SJAG_05216","SJAG_03071","SJAG_01411","SJAG_02638","SJAG_02324","SJAG_01715","SJAG_04324","SJAG_02253","SJAG_02601","SJAG_05244","SJAG_05000","SJAG_04890","SJAG_05271","SJAG_03636","SJAG_03423","SJAG_02546","SJAG_01512","SJAG_01202","SJAG_02870","SJAG_01659","SJAG_05560","SJAG_02836","SJAG_04291","SJAG_02611","SJAG_03666","SJAG_00541","SJAG_02359","SJAG_00887","SJAG_04959","SJAG_00653","SJAG_04744","SJAG_02995","SJAG_06110","SJAG_03971","SJAG_03949","SJAG_16454","SJAG_01487","SJAG_02894","SJAG_01026","SJAG_01853","SJAG_05332","SJAG_03584","SJAG_02749","SJAG_02307","SJAG_01797","SJAG_04788","SJAG_01287","SJAG_00600","SJAG_03677","SJAG_01303","SJAG_02643","SJAG_00628","SJAG_01632","SJAG_01721","SJAG_00921","SJAG_01588","SJAG_01159","SJAG_01609","SJAG_04981","SJAG_03297","SJAG_03585","SJAG_04897","SJAG_00420","SJAG_04689","SJAG_07014","SJAG_01518","SJAG_00748","SJAG_00765","SJAG_00912","SJAG_04544","SJAG_01576","SJAG_04281","SJAG_03534","SJAG_04998","SJAG_03649","SJAG_01368","SJAG_04093","SJAG_01473","SJAG_04663","SJAG_01128","SJAG_00889","SJAG_04929","SJAG_02072","SJAG_04900","SJAG_03254","SJAG_02535","SJAG_01413","SJAG_03223","SJAG_06612","SJAG_04188","SJAG_03106","SJAG_04256","SJAG_03461","SJAG_01829","SJAG_02467","SJAG_02189","SJAG_04475","SJAG_00936","SJAG_02067","SJAG_02043","SJAG_04626","SJAG_00537","SJAG_04159","SJAG_03788","SJAG_01132","SJAG_02479","SJAG_02517","SJAG_02207","SJAG_05270","SJAG_01577","SJAG_02890","SJAG_01087","SJAG_01194","SJAG_02376","SJAG_02224","SJAG_04342","SJAG_04478"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63614,103056],"is_not":false,"summary":null,"term":"GO:0006412"},{"annotations":[116271],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140708"},{"annotations":[71563,73947,100980,104302,116058,116341,102267,108544,106256,115354,90970,109049,114961,74982,101610,104287,105926,118288,119277,100981,98381,103375,114243,115908,78393,92867,75546,97386,71934,98168,92843,109119,113264,120150,114052,97718,96574,116899,115770,107502,78533,98972,73833,77934,78895,114242,114498,100474,119463,118747,115292,78959,119821,80081,105925,80138,62310,99253,76976,103490,113263,119464,81869,78210,109708,101865,92845,107037,109750,111140,112582,116386,116387,79692,107256,98816,107376,107918,115883,72801,92844,101471,107197,119272,101866,95436,115293,100475,81558,103491,110212,79327,117035,95334,96859,107510,93419,105676,112963,92136,109749,79094,111383,111384,114053,116059,71002,93180,106904,114960,75347,115884,119296,63154,115771,94011,112583,117036,107509,103374,116412,120585,95333,111830,99254,79154,95531,102726,115291,99013,107255,120151,92866,98888,112962,104952,102290,73780,79903,107501,101470,101609,98167,104301,72054,106493,116340,116413,91419,104286,75223,119510,74505,80890,107750,72061,76503,79977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002181"},{"annotations":[118155,100144,97160,120835,69185,107386,115728,100143,120353,106925,58450,118156,107232,120787,120836,116584,107231,111001,70648,98518,109731,117580,118816,111002,120786,67464],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0002182"},{"annotations":[78933,102324,105214,98475,89331,75658,120390,105035,107438,106584,115832,91717,105348,108850,109143,100189,112462,92173,99038],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0002183"},{"annotations":[98296,111003,60451,96623,75585,117887,60860,111004],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0002184"},{"annotations":[100744,64939,64701,60316,60160,63226,71313,73757,70260,76905,59471,98665],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001732"},{"annotations":[119927,97902,75201,73132,79757,80197],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001731"},{"annotations":[114149,76224,97607],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990145"},{"annotations":[73537,104132,98044,93278,109922,91695,77469,90165,90837,109918,81153,114317,93387,114580,117454,115309,118014,118864,112232,112954,96002,119910,99801,72546,111204,111980,103280,117539,104085,116173,105152,80373,93472,95532,95628,96286,98818,98410,99774,110426,114080,112514,116452,97164,77052,91774,107865,79865,104903,70831,99800,106185,107534,78114,109979,119781,58356,100031,76884,61002,108230,109781,110067,98442,111687,117276,119259,120277,110017,104438,118123,93895,99482,114216,116569,105755,108949,102912,105503,112626,108590,97061,91294,71493,77129,91747,96291,117874,79812,100908,63246,79040,114750,110312,105823,119949,71367,67730,98707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032543"},{"annotations":[75387,93803,81860,81711],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070125"},{"annotations":[103730,110182,80258,109111,75856,100517,107413,92809,103118],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070124"},{"annotations":[97316,103888,106530,100462,97753],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070126"},{"annotations":[116711,120097,97406,101253],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2000766"},{"annotations":[93121,114008],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1904689"},{"annotations":[71679,76982,96178,101147,117478,111518],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1990625"},{"annotations":[77097],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2001125"},{"annotations":[71520,108487,118994],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2000767"},{"annotations":[114530,100518],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0070131"},{"annotations":[102279],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0070134"},{"annotations":[70301,67841],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045901"},{"annotations":[74472],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045948"},{"annotations":[67842,70302,78279],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0045905"},{"annotations":[118682,102091,107078,97896,102535,114249,92080,98039,104399,111554,119318,113016],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000765"},{"annotations":[115828,97280,111999,111334],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0140018"},{"annotations":[105149,97041,105781],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1990611"},{"annotations":[104920],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1990983"},{"annotations":[75762],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006449"},{"annotations":[77098,104953,71582,79942,65402,78365,105431,107463,117947],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0072344"},{"annotations":[101261],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0141014"},{"annotations":[76906,75202],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0002188"},{"annotations":[65709,62389],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006414"},{"annotations":[67845,70305],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006452"},{"annotations":[73431],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006413"},{"annotations":[62762,79179],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006415"},{"annotations":[96479],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070127"}]},"cv_name":"biological_process","definition":"The cellular metabolic process in which a protein is formed, using the sequence of a mature mRNA or circRNA molecule to specify the sequence of amino acids in a polypeptide chain. Translation is mediated by the ribosome, and begins with the formation of a ternary complex between aminoacylated initiator methionine tRNA, GTP, and initiation factor 2, which subsequently associates with the small subunit of the ribosome and an mRNA or circRNA. Translation ends with the release of a polypeptide chain from the ribosome.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"is_a","term_name":"protein metabolic process","termid":"GO:0019538"},{"relation_name":"part_of","term_name":"gene expression","termid":"GO:0010467"}],"gene_count":394,"genes_by_uniquename":{"SJAG_00034":null,"SJAG_00060":null,"SJAG_00069":null,"SJAG_00077":null,"SJAG_00086":null,"SJAG_00103":null,"SJAG_00105":null,"SJAG_00148":null,"SJAG_00155":null,"SJAG_00166":null,"SJAG_00169":null,"SJAG_00188":null,"SJAG_00220":null,"SJAG_00226":null,"SJAG_00243":null,"SJAG_00251":null,"SJAG_00269":null,"SJAG_00286":null,"SJAG_00308":null,"SJAG_00315":null,"SJAG_00338":null,"SJAG_00384":null,"SJAG_00420":null,"SJAG_00423":null,"SJAG_00443":null,"SJAG_00465":null,"SJAG_00466":null,"SJAG_00468":null,"SJAG_00488":null,"SJAG_00497":null,"SJAG_00503":null,"SJAG_00507":null,"SJAG_00508":null,"SJAG_00513":null,"SJAG_00523":null,"SJAG_00537":null,"SJAG_00541":null,"SJAG_00544":null,"SJAG_00579":null,"SJAG_00600":null,"SJAG_00628":null,"SJAG_00629":null,"SJAG_00642":null,"SJAG_00653":null,"SJAG_00662":null,"SJAG_00690":null,"SJAG_00726":null,"SJAG_00733":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00765":null,"SJAG_00782":null,"SJAG_00786":null,"SJAG_00799":null,"SJAG_00844":null,"SJAG_00860":null,"SJAG_00887":null,"SJAG_00889":null,"SJAG_00892":null,"SJAG_00898":null,"SJAG_00912":null,"SJAG_00921":null,"SJAG_00936":null,"SJAG_00940":null,"SJAG_00944":null,"SJAG_01026":null,"SJAG_01045":null,"SJAG_01047":null,"SJAG_01058":null,"SJAG_01074":null,"SJAG_01079":null,"SJAG_01087":null,"SJAG_01117":null,"SJAG_01128":null,"SJAG_01132":null,"SJAG_01159":null,"SJAG_01194":null,"SJAG_01197":null,"SJAG_01202":null,"SJAG_01226":null,"SJAG_01235":null,"SJAG_01248":null,"SJAG_01249":null,"SJAG_01259":null,"SJAG_01269":null,"SJAG_01287":null,"SJAG_01296":null,"SJAG_01303":null,"SJAG_01322":null,"SJAG_01352":null,"SJAG_01364":null,"SJAG_01365":null,"SJAG_01366":null,"SJAG_01368":null,"SJAG_01387":null,"SJAG_01411":null,"SJAG_01413":null,"SJAG_01436":null,"SJAG_01438":null,"SJAG_01463":null,"SJAG_01468":null,"SJAG_01473":null,"SJAG_01478":null,"SJAG_01487":null,"SJAG_01497":null,"SJAG_01512":null,"SJAG_01517":null,"SJAG_01518":null,"SJAG_01520":null,"SJAG_01522":null,"SJAG_01536":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01565":null,"SJAG_01568":null,"SJAG_01576":null,"SJAG_01577":null,"SJAG_01580":null,"SJAG_01588":null,"SJAG_01591":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01630":null,"SJAG_01632":null,"SJAG_01643":null,"SJAG_01659":null,"SJAG_01676":null,"SJAG_01696":null,"SJAG_01715":null,"SJAG_01719":null,"SJAG_01721":null,"SJAG_01727":null,"SJAG_01734":null,"SJAG_01767":null,"SJAG_01797":null,"SJAG_01806":null,"SJAG_01829":null,"SJAG_01851":null,"SJAG_01853":null,"SJAG_01942":null,"SJAG_01954":null,"SJAG_02015":null,"SJAG_02017":null,"SJAG_02020":null,"SJAG_02026":null,"SJAG_02043":null,"SJAG_02046":null,"SJAG_02061":null,"SJAG_02067":null,"SJAG_02071":null,"SJAG_02072":null,"SJAG_02081":null,"SJAG_02096":null,"SJAG_02121":null,"SJAG_02164":null,"SJAG_02180":null,"SJAG_02184":null,"SJAG_02189":null,"SJAG_02201":null,"SJAG_02206":null,"SJAG_02207":null,"SJAG_02224":null,"SJAG_02236":null,"SJAG_02243":null,"SJAG_02253":null,"SJAG_02263":null,"SJAG_02280":null,"SJAG_02283":null,"SJAG_02285":null,"SJAG_02292":null,"SJAG_02307":null,"SJAG_02312":null,"SJAG_02324":null,"SJAG_02331":null,"SJAG_02335":null,"SJAG_02340":null,"SJAG_02353":null,"SJAG_02359":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02428":null,"SJAG_02452":null,"SJAG_02467":null,"SJAG_02471":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02493":null,"SJAG_02510":null,"SJAG_02517":null,"SJAG_02522":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02546":null,"SJAG_02585":null,"SJAG_02592":null,"SJAG_02597":null,"SJAG_02601":null,"SJAG_02611":null,"SJAG_02615":null,"SJAG_02628":null,"SJAG_02638":null,"SJAG_02643":null,"SJAG_02682":null,"SJAG_02704":null,"SJAG_02721":null,"SJAG_02723":null,"SJAG_02738":null,"SJAG_02746":null,"SJAG_02749":null,"SJAG_02755":null,"SJAG_02762":null,"SJAG_02777":null,"SJAG_02786":null,"SJAG_02802":null,"SJAG_02803":null,"SJAG_02812":null,"SJAG_02836":null,"SJAG_02840":null,"SJAG_02856":null,"SJAG_02861":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02890":null,"SJAG_02891":null,"SJAG_02894":null,"SJAG_02904":null,"SJAG_02977":null,"SJAG_02995":null,"SJAG_03034":null,"SJAG_03040":null,"SJAG_03043":null,"SJAG_03053":null,"SJAG_03065":null,"SJAG_03071":null,"SJAG_03094":null,"SJAG_03106":null,"SJAG_03122":null,"SJAG_03127":null,"SJAG_03133":null,"SJAG_03147":null,"SJAG_03159":null,"SJAG_03176":null,"SJAG_03189":null,"SJAG_03192":null,"SJAG_03197":null,"SJAG_03223":null,"SJAG_03232":null,"SJAG_03254":null,"SJAG_03262":null,"SJAG_03277":null,"SJAG_03284":null,"SJAG_03297":null,"SJAG_03322":null,"SJAG_03326":null,"SJAG_03335":null,"SJAG_03364":null,"SJAG_03383":null,"SJAG_03402":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03428":null,"SJAG_03433":null,"SJAG_03459":null,"SJAG_03461":null,"SJAG_03472":null,"SJAG_03501":null,"SJAG_03534":null,"SJAG_03545":null,"SJAG_03550":null,"SJAG_03568":null,"SJAG_03584":null,"SJAG_03585":null,"SJAG_03626":null,"SJAG_03629":null,"SJAG_03636":null,"SJAG_03649":null,"SJAG_03658":null,"SJAG_03666":null,"SJAG_03677":null,"SJAG_03678":null,"SJAG_03732":null,"SJAG_03762":null,"SJAG_03788":null,"SJAG_03794":null,"SJAG_03859":null,"SJAG_03863":null,"SJAG_03869":null,"SJAG_03919":null,"SJAG_03922":null,"SJAG_03949":null,"SJAG_03971":null,"SJAG_03996":null,"SJAG_04019":null,"SJAG_04020":null,"SJAG_04029":null,"SJAG_04066":null,"SJAG_04085":null,"SJAG_04093":null,"SJAG_04130":null,"SJAG_04157":null,"SJAG_04159":null,"SJAG_04160":null,"SJAG_04164":null,"SJAG_04168":null,"SJAG_04173":null,"SJAG_04174":null,"SJAG_04176":null,"SJAG_04188":null,"SJAG_04204":null,"SJAG_04207":null,"SJAG_04216":null,"SJAG_04244":null,"SJAG_04248":null,"SJAG_04256":null,"SJAG_04281":null,"SJAG_04283":null,"SJAG_04285":null,"SJAG_04291":null,"SJAG_04304":null,"SJAG_04324":null,"SJAG_04342":null,"SJAG_04351":null,"SJAG_04367":null,"SJAG_04378":null,"SJAG_04383":null,"SJAG_04409":null,"SJAG_04414":null,"SJAG_04452":null,"SJAG_04473":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04478":null,"SJAG_04482":null,"SJAG_04490":null,"SJAG_04493":null,"SJAG_04494":null,"SJAG_04534":null,"SJAG_04544":null,"SJAG_04626":null,"SJAG_04635":null,"SJAG_04663":null,"SJAG_04672":null,"SJAG_04689":null,"SJAG_04695":null,"SJAG_04738":null,"SJAG_04744":null,"SJAG_04746":null,"SJAG_04753":null,"SJAG_04756":null,"SJAG_04762":null,"SJAG_04772":null,"SJAG_04788":null,"SJAG_04814":null,"SJAG_04847":null,"SJAG_04856":null,"SJAG_04862":null,"SJAG_04873":null,"SJAG_04889":null,"SJAG_04890":null,"SJAG_04891":null,"SJAG_04893":null,"SJAG_04897":null,"SJAG_04900":null,"SJAG_04918":null,"SJAG_04929":null,"SJAG_04959":null,"SJAG_04981":null,"SJAG_04998":null,"SJAG_05000":null,"SJAG_05003":null,"SJAG_05008":null,"SJAG_05216":null,"SJAG_05218":null,"SJAG_05221":null,"SJAG_05244":null,"SJAG_05248":null,"SJAG_05265":null,"SJAG_05270":null,"SJAG_05271":null,"SJAG_05320":null,"SJAG_05332":null,"SJAG_05560":null,"SJAG_05573":null,"SJAG_06110":null,"SJAG_06253":null,"SJAG_06284":null,"SJAG_06612":null,"SJAG_07009":null,"SJAG_07013":null,"SJAG_07014":null,"SJAG_16454":null,"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"translation","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0006416","GO:0043037","GO:0006453","Reactome:R-HSA-72766","Wikipedia:Translation_(genetics)"],"synonyms":[{"name":"protein anabolism","type":"exact"},{"name":"protein biosynthesis","type":"exact"},{"name":"protein biosynthetic process","type":"exact"},{"name":"protein formation","type":"exact"},{"name":"protein synthesis","type":"exact"},{"name":"protein translation","type":"exact"}],"termid":"GO:0006412","terms_by_termid":{"GO:0001731":null,"GO:0001732":null,"GO:0002181":null,"GO:0002182":null,"GO:0002183":null,"GO:0002184":null,"GO:0002188":null,"GO:0006412":null,"GO:0006413":null,"GO:0006414":null,"GO:0006415":null,"GO:0006449":null,"GO:0006452":null,"GO:0032543":null,"GO:0045901":null,"GO:0045905":null,"GO:0045948":null,"GO:0070124":null,"GO:0070125":null,"GO:0070126":null,"GO:0070127":null,"GO:0070131":null,"GO:0070134":null,"GO:0072344":null,"GO:0140018":null,"GO:0140708":null,"GO:0141014":null,"GO:1904689":null,"GO:1990145":null,"GO:1990611":null,"GO:1990625":null,"GO:1990983":null,"GO:2000765":null,"GO:2000766":null,"GO:2000767":null,"GO:2001125":null}}


id: PBO:0051421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 2-28 (pseudogene)","termid":"PBO:0051421"}


id: PBO:0071157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 22","termid":"PBO:0071157"}


id: GO:0046867
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of carotenoids into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Carotenoids are tetraterpenoid compounds in which two units of 4 isoprenoid residues joined head-to-tail are themselves joined tail-to-tail.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tetraterpenoid transport","termid":"GO:0046866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"carotenoid transport","termid":"GO:0046867"}


id: GO:0014869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a muscle inactivity stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of inactivity","termid":"GO:0014863"},{"relation_name":"is_a","term_name":"response to muscle inactivity","termid":"GO:0014870"}],"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":"detection of muscle inactivity","termid":"GO:0014869"}


id: MONDO:0020283
data:
  {"annotated_genes":["SJAG_01756","SJAG_00856"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009624"},{"annotations":[87036],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014592"}]},"cv_name":"mondo","definition":"An inflammatory process affecting a part of or the entire uvea. Causes include inflammatory agents (e.g., herpes simplex, herpes zoster, leptospirosis) and systemic diseases (e.g., inflammatory bowel disease, multiple sclerosis, systemic lupus erythematosus, ankylosing spondylitis). Patients present with pain and redness in the eye, light sensitivity, and blurred and decreased vision.","definition_xrefs":["NCIT:C26909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uveal disorder","termid":"MONDO:0002661"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00856":null,"SJAG_01756":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"uveitis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:13141","GARD:19549","MedDRA:10046851","MESH:D014605","UMLS:C0042164","EFO:1001231","HP:0000554","Orphanet:98715","SCTID:128473001","MEDGEN:52961"],"synonyms":[{"name":"inflammation of uvea","type":"exact"},{"name":"uvea inflammation","type":"exact"},{"name":"uveitis","type":"exact"},{"name":"uveitis (disease)","type":"exact"}],"termid":"MONDO:0020283","terms_by_termid":{"MONDO:0009624":null,"MONDO:0014592":null},"xrefs":{"Monarch":{"xref_id":"0020283"}}}


id: GO:1901828
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving zeaxanthin bis(beta-D-glucoside).","definition_xrefs":["PMID:20075616","GOC:yaf","GOC:TermGenie","MetaCyc:PWY-6288","UniPathway:UPA00798"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid metabolic process","termid":"GO:0016116"},{"relation_name":"is_a","term_name":"beta-glucoside metabolic process","termid":"GO:1901804"}],"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":"zeaxanthin bis(beta-D-glucoside) metabolic process","synonyms":[{"name":"zeaxanthin bis(beta-D-glucoside) metabolism","type":"exact"},{"name":"zeaxanthin diglucoside metabolism","type":"exact"}],"termid":"GO:1901828"}


id: MONDO:0023258
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease due to glucose-6-phosphatase deficiency in which the cause of the disease is a mutation in the SLC37A4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease I","termid":"MONDO:0002413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"glycogen storage disease type 1 due to SLC37A4 mutation","secondary_identifiers":["GARD:2501","UMLS:C2931345","MEDGEN:419390","MESH:C536831","NANDO:1200841","HGNC:4061"],"synonyms":[{"name":"G6P translocase deficiency","type":"broad"},{"name":"SLC37A4 glycogen storage disease I","type":"exact"},{"name":"glucose-6-phosphate translocase deficiency","type":"exact"},{"name":"glycogen storage disease I caused by mutation in SLC37A4","type":"exact"}],"termid":"MONDO:0023258","xrefs":{"Monarch":{"xref_id":"0023258"}}}


id: MONDO:0012910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"},{"relation_name":"is_a","term_name":"presbycusis","termid":"MONDO:0043765"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"age-related hearing impairment 1","secondary_identifiers":["MEDGEN:382794","UMLS:C2676230","OMIM:612448","MESH:C567305"],"synonyms":[{"name":"ARHI1","type":"exact"},{"name":"age-related hearing impairment 1","type":"exact"},{"name":"presbycusis 1","type":"related"}],"termid":"MONDO:0012910","xrefs":{"Monarch":{"xref_id":"0012910"}}}


id: GO:0047470
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-[(1->4)-alpha-D-glucosyl](n-1)-D-glucose = 1-alpha-D-[(1->4)-alpha-D-glucosyl](n-1)-alpha-D-glucopyranoside.","definition_xrefs":["EC:5.4.99.15","MetaCyc:5.4.99.15-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"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:0016853"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"(1,4)-alpha-D-glucan 1-alpha-D-glucosylmutase activity","secondary_identifiers":["RHEA:13621"],"synonyms":[{"name":"(1->4)-alpha-D-glucan 1-alpha-D-glucosylmutase","type":"broad"},{"name":"malto-oligosyltrehalose synthase activity","type":"related"},{"name":"maltodextrin alpha-D-glucosyltransferase activity","type":"related"}],"termid":"GO:0047470"}


id: PBO:0079585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 D1","termid":"PBO:0079585"}


id: PBO:0000913
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.3.5.3","termid":"PBO:0000913"}


id: PBO:0088109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar alpha mannosidase; involved in free oligosaccharide (fOS) degradation; upregulated under glucose starvation; delivered to the vacuole in a novel pathway separate from the secretory pathway","termid":"PBO:0088109"}


id: PR:P87058
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sla1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87058"],"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":"La protein homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A10.10c","synonyms":[{"name":"La autoantigen homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"La ribonucleoprotein (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-sla1","type":"exact"}],"termid":"PR:P87058"}


id: MONDO:0006499
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008097"}]},"cv_name":"mondo","definition":"A benign and excessive tumor-like growth of mature cells and normal tissues which grow in a disorganized pattern.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"is_obsolete":false,"name":"hamartoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C3075","SCTID:400006008","UMLS:C0018552","MESH:D006222","HP:0010566","ICD9:759.6","MEDGEN:6713","EFO:1000634"],"synonyms":[{"name":"hamartoma","type":"exact"},{"name":"hamartoma (disease)","type":"exact"}],"termid":"MONDO:0006499","terms_by_termid":{"MONDO:0008097":null},"xrefs":{"Monarch":{"xref_id":"0006499"}}}


id: MONDO:0002769
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Whitish or yellowish mucosal vaginal discharge.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal discharge","termid":"MONDO:0002770"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukorrhea","secondary_identifiers":["UMLS:C0023533","MEDGEN:44134","MESH:D007973","DOID:3766"],"synonyms":[{"name":"discharge - leukorrhea","type":"exact"},{"name":"leukorrhea of vagina","type":"exact"}],"termid":"MONDO:0002769","xrefs":{"Monarch":{"xref_id":"0002769"}}}


id: MONDO:0012607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any inherited susceptibility to asthma in which the cause of the disease is a mutation in the IRAK3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited susceptibility to asthma","termid":"MONDO:0010940"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asthma-related traits, susceptibility to, 5","secondary_identifiers":["UMLS:C1970224","MEDGEN:370858","OMIM:611064"],"synonyms":[{"name":"ASRT5","type":"related"},{"name":"IRAK3 inherited susceptibility to asthma","type":"exact"},{"name":"asthma susceptibility 5","type":"exact"},{"name":"asthma-related traits, susceptibility to, 5","type":"exact"},{"name":"asthma-related traits, susceptibility to, type 5","type":"exact"},{"name":"inherited susceptibility to asthma caused by mutation in IRAK3","type":"exact"}],"termid":"MONDO:0012607","xrefs":{"Monarch":{"xref_id":"0012607"}}}


id: PBO:0040948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein 3 pseudogene 19","termid":"PBO:0040948"}


id: GO:0032539
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of any behavior associated with finding a host organism.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of host-seeking behavior","termid":"GO:0032538"},{"relation_name":"is_a","term_name":"negative regulation of behavior","termid":"GO:0048521"},{"relation_name":"negatively_regulates","term_name":"host-seeking behavior","termid":"GO:0032537"}],"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 host-seeking behavior","synonyms":[{"name":"down regulation of host-seeking behavior","type":"exact"},{"name":"down-regulation of host-seeking behavior","type":"exact"},{"name":"downregulation of host-seeking behavior","type":"exact"},{"name":"inhibition of host-seeking behavior","type":"narrow"},{"name":"negative regulation of host-seeking behaviour","type":"exact"}],"termid":"GO:0032539"}


id: PBO:0034290
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_target_end_location","termid":"PBO:0034290"}


id: MONDO:0003973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of testicular seminoma characterized by the presence of seminoma cells arranged in tubular patterns and few lymphocytes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular seminoma","termid":"MONDO:0003669"}],"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":"tubular variant testicular seminoma","secondary_identifiers":["DOID:6706","UMLS:C1515294","NCIT:C40959","MEDGEN:308259"],"synonyms":[{"name":"testicular seminoma, tubular variant","type":"exact"}],"termid":"MONDO:0003973","xrefs":{"Monarch":{"xref_id":"0003973"}}}


id: PBO:0079545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBA6 divergent transcript","termid":"PBO:0079545"}


id: GO:0033576
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of a carbohydrate or carbohydrate derivative unit to a protein amino acid in the cytosol.","definition_xrefs":["GOC:mah","GOC:pr","PMID:12042244"],"gene_count":0,"genotype_count":0,"name":"obsolete protein glycosylation in cytosol (obsolete GO:0033576)","synonyms":[{"name":"protein amino acid glycosylation in cytosol","type":"exact"}],"termid":"GO:0033576"}


id: PBO:0076403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 1 like","termid":"PBO:0076403"}


id: MONDO:0002022
data:
  {"annotated_genes":["SJAG_02286","SJAG_02712","SJAG_03677","SJAG_04995","SJAG_02885","SJAG_04745","SJAG_00856","SJAG_02951","SJAG_00531","SJAG_04008","SJAG_02848","SJAG_02384","SJAG_02150","SJAG_00750","SJAG_00995","SJAG_02828","SJAG_04553","SJAG_04601","SJAG_03592","SJAG_04225","SJAG_03603","SJAG_03786","SJAG_01784","SJAG_02623","SJAG_04495","SJAG_04529","SJAG_02362","SJAG_02889","SJAG_00390","SJAG_03827","SJAG_03453","SJAG_04938","SJAG_03588","SJAG_00404","SJAG_03497","SJAG_02954","SJAG_04819","SJAG_00570","SJAG_01756","SJAG_03818","SJAG_01634","SJAG_03258","SJAG_01422","SJAG_02163","SJAG_00643","SJAG_04681","SJAG_03024","SJAG_02955","SJAG_03199","SJAG_04567","SJAG_00702","SJAG_01356","SJAG_03081","SJAG_02509","SJAG_04387","SJAG_00742","SJAG_02031","SJAG_00495","SJAG_03795","SJAG_MIT13","SJAG_00737","SJAG_04637","SJAG_01868","SJAG_02946","SJAG_01745","SJAG_00845","SJAG_04865","SJAG_01630","SJAG_02645","SJAG_02878","SJAG_00516","SJAG_04199","SJAG_01242","SJAG_03557","SJAG_02063","SJAG_02919","SJAG_04114","SJAG_00624","SJAG_02194","SJAG_00582","SJAG_00638","SJAG_04631","SJAG_01183","SJAG_04003","SJAG_01298","SJAG_01474","SJAG_02641","SJAG_01897","SJAG_MIT03","SJAG_03815","SJAG_04016","SJAG_01526","SJAG_03581","SJAG_05342","SJAG_01998","SJAG_02295","SJAG_02656","SJAG_04497","SJAG_02947","SJAG_04296","SJAG_03375","SJAG_04334","SJAG_01152","SJAG_00326","SJAG_02200","SJAG_03233","SJAG_MIT15"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89102,89103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012419"},{"annotations":[88392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[88982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"},{"annotations":[87551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008134"},{"annotations":[88183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009815"},{"annotations":[87674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008858"},{"annotations":[88716,88718,88717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013411"},{"annotations":[88731],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011547"},{"annotations":[88100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013859"},{"annotations":[87218],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014565"},{"annotations":[86874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014673"},{"annotations":[87773],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008925"},{"annotations":[88923,88924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032735"},{"annotations":[87174,87172,87173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011413"},{"annotations":[88659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008955"},{"annotations":[87466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012553"},{"annotations":[86779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014696"},{"annotations":[87467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012554"},{"annotations":[88668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015026"},{"annotations":[88351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957264"},{"annotations":[87604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013644"},{"annotations":[88727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010557"},{"annotations":[87746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009258"},{"annotations":[87110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009352"},{"annotations":[88223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014372"},{"annotations":[86869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014669"},{"annotations":[87881],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014872"},{"annotations":[88561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010912"},{"annotations":[88190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007376"},{"annotations":[87821,87822,87820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009257"},{"annotations":[87256,87257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009737"},{"annotations":[88234,88235],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013802"},{"annotations":[88240],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013805"},{"annotations":[86892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014050"},{"annotations":[87776,87777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054771"},{"annotations":[88961,88962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100119"},{"annotations":[88710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013454"},{"annotations":[87231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012990"},{"annotations":[88768],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032794"},{"annotations":[87409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012056"},{"annotations":[86887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060650"},{"annotations":[87330,87329,87331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010788"},{"annotations":[87667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008097"},{"annotations":[87742,87741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024552"},{"annotations":[86843,86842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012481"},{"annotations":[89071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009624"},{"annotations":[87036],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014592"},{"annotations":[88264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007918"},{"annotations":[86782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014698"},{"annotations":[88471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013783"},{"annotations":[87740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010671"},{"annotations":[88647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0975809"},{"annotations":[87075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014611"},{"annotations":[87285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032941"},{"annotations":[87831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012154"},{"annotations":[88721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009756"},{"annotations":[89039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010645"},{"annotations":[87404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958176"},{"annotations":[87248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008133"},{"annotations":[87456,87457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012543"},{"annotations":[88418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007429"},{"annotations":[88873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009796"},{"annotations":[88352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957262"},{"annotations":[88113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008379"},{"annotations":[87862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010828"},{"annotations":[88002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010806"},{"annotations":[87918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011075"},{"annotations":[88995],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010723"},{"annotations":[88467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012363"},{"annotations":[86836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012477"},{"annotations":[88552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013468"},{"annotations":[87249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013516"},{"annotations":[87629,87630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013611"},{"annotations":[87613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014256"},{"annotations":[88382,88386,88384,88385,88381,88388,88389,88383,88387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014323"},{"annotations":[88066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014400"},{"annotations":[88631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015013"},{"annotations":[88505,88506],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044320"},{"annotations":[88028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032604"},{"annotations":[87828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008972"},{"annotations":[87673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014743"},{"annotations":[86831,86832],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0016369"},{"annotations":[89033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010035"},{"annotations":[87361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031007"},{"annotations":[87889,87890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010819"},{"annotations":[87422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014296"},{"annotations":[87039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010485"},{"annotations":[88379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010216"}]},"cv_name":"mondo","definition":"A disease that involves the orbital region.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete sensory system disease (obsolete MONDO:0005128)","termid":"MONDO:0005128"},{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":107,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00390":null,"SJAG_00404":null,"SJAG_00495":null,"SJAG_00516":null,"SJAG_00531":null,"SJAG_00570":null,"SJAG_00582":null,"SJAG_00624":null,"SJAG_00638":null,"SJAG_00643":null,"SJAG_00702":null,"SJAG_00737":null,"SJAG_00742":null,"SJAG_00750":null,"SJAG_00845":null,"SJAG_00856":null,"SJAG_00995":null,"SJAG_01152":null,"SJAG_01183":null,"SJAG_01242":null,"SJAG_01298":null,"SJAG_01356":null,"SJAG_01422":null,"SJAG_01474":null,"SJAG_01526":null,"SJAG_01630":null,"SJAG_01634":null,"SJAG_01745":null,"SJAG_01756":null,"SJAG_01784":null,"SJAG_01868":null,"SJAG_01897":null,"SJAG_01998":null,"SJAG_02031":null,"SJAG_02063":null,"SJAG_02150":null,"SJAG_02163":null,"SJAG_02194":null,"SJAG_02200":null,"SJAG_02286":null,"SJAG_02295":null,"SJAG_02362":null,"SJAG_02384":null,"SJAG_02509":null,"SJAG_02623":null,"SJAG_02641":null,"SJAG_02645":null,"SJAG_02656":null,"SJAG_02712":null,"SJAG_02828":null,"SJAG_02848":null,"SJAG_02878":null,"SJAG_02885":null,"SJAG_02889":null,"SJAG_02919":null,"SJAG_02946":null,"SJAG_02947":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_02955":null,"SJAG_03024":null,"SJAG_03081":null,"SJAG_03199":null,"SJAG_03233":null,"SJAG_03258":null,"SJAG_03375":null,"SJAG_03453":null,"SJAG_03497":null,"SJAG_03557":null,"SJAG_03581":null,"SJAG_03588":null,"SJAG_03592":null,"SJAG_03603":null,"SJAG_03677":null,"SJAG_03786":null,"SJAG_03795":null,"SJAG_03815":null,"SJAG_03818":null,"SJAG_03827":null,"SJAG_04003":null,"SJAG_04008":null,"SJAG_04016":null,"SJAG_04114":null,"SJAG_04199":null,"SJAG_04225":null,"SJAG_04296":null,"SJAG_04334":null,"SJAG_04387":null,"SJAG_04495":null,"SJAG_04497":null,"SJAG_04529":null,"SJAG_04553":null,"SJAG_04567":null,"SJAG_04601":null,"SJAG_04631":null,"SJAG_04637":null,"SJAG_04681":null,"SJAG_04745":null,"SJAG_04819":null,"SJAG_04865":null,"SJAG_04938":null,"SJAG_04995":null,"SJAG_05342":null,"SJAG_MIT03":null,"SJAG_MIT13":null,"SJAG_MIT15":null},"genotype_count":0,"is_obsolete":false,"name":"disorder of orbital region","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:1492","SCTID:371409005","ICD9:362.10","ICD10CM:H00-H59","UMLS:C5886742","MEDGEN:1863347"],"synonyms":[{"name":"disease of orbital region","type":"exact"},{"name":"disease or disorder of orbital region","type":"exact"},{"name":"disorder of eye region","type":"exact"},{"name":"disorder of orbital region","type":"exact"},{"name":"eye and adnexa disease","type":"related"},{"name":"ophthalmological disorder","type":"related"},{"name":"orbital region disease","type":"exact"},{"name":"orbital region disease or disorder","type":"exact"}],"termid":"MONDO:0002022","terms_by_termid":{"MONDO:0007376":null,"MONDO:0007429":null,"MONDO:0007918":null,"MONDO:0008097":null,"MONDO:0008133":null,"MONDO:0008134":null,"MONDO:0008379":null,"MONDO:0008858":null,"MONDO:0008925":null,"MONDO:0008955":null,"MONDO:0008972":null,"MONDO:0009257":null,"MONDO:0009258":null,"MONDO:0009352":null,"MONDO:0009624":null,"MONDO:0009737":null,"MONDO:0009756":null,"MONDO:0009796":null,"MONDO:0009815":null,"MONDO:0010035":null,"MONDO:0010216":null,"MONDO:0010485":null,"MONDO:0010557":null,"MONDO:0010645":null,"MONDO:0010671":null,"MONDO:0010723":null,"MONDO:0010788":null,"MONDO:0010806":null,"MONDO:0010819":null,"MONDO:0010828":null,"MONDO:0010912":null,"MONDO:0011075":null,"MONDO:0011413":null,"MONDO:0011547":null,"MONDO:0012056":null,"MONDO:0012099":null,"MONDO:0012154":null,"MONDO:0012363":null,"MONDO:0012419":null,"MONDO:0012477":null,"MONDO:0012481":null,"MONDO:0012543":null,"MONDO:0012553":null,"MONDO:0012554":null,"MONDO:0012990":null,"MONDO:0013411":null,"MONDO:0013454":null,"MONDO:0013468":null,"MONDO:0013516":null,"MONDO:0013611":null,"MONDO:0013644":null,"MONDO:0013783":null,"MONDO:0013802":null,"MONDO:0013805":null,"MONDO:0013859":null,"MONDO:0014050":null,"MONDO:0014256":null,"MONDO:0014296":null,"MONDO:0014323":null,"MONDO:0014372":null,"MONDO:0014400":null,"MONDO:0014565":null,"MONDO:0014592":null,"MONDO:0014611":null,"MONDO:0014669":null,"MONDO:0014673":null,"MONDO:0014696":null,"MONDO:0014698":null,"MONDO:0014743":null,"MONDO:0014872":null,"MONDO:0014937":null,"MONDO:0015013":null,"MONDO:0015026":null,"MONDO:0016369":null,"MONDO:0024552":null,"MONDO:0031007":null,"MONDO:0032604":null,"MONDO:0032735":null,"MONDO:0032794":null,"MONDO:0032941":null,"MONDO:0044320":null,"MONDO:0054771":null,"MONDO:0060650":null,"MONDO:0100119":null,"MONDO:0957262":null,"MONDO:0957264":null,"MONDO:0958176":null,"MONDO:0975809":null},"xrefs":{"Monarch":{"xref_id":"0002022"}}}


id: PBO:0064521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit B","termid":"PBO:0064521"}


id: FYPO:0001518
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of diethyl maleate than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002682","FYPO:0001985","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"resistance to diethyl maleate","synonyms":[{"name":"resistance to DEM","type":"exact"},{"name":"resistance to diethyl maleate during mitotic cell cycle","type":"related"},{"name":"resistance to diethyl maleate during vegetative growth","type":"exact"},{"name":"resistant to diethyl maleate","type":"exact"}],"termid":"FYPO:0001518"}


id: PBO:0087728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Set3 complex; complex is a meiotic-specific repressor of sporulation specific genes that contains deacetylase activity; potential Cdc28p substrate","termid":"PBO:0087728"}


id: GO:1905343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of cohesin unloading.","definition_xrefs":["PMID:26687354","GOC:TermGenie","GO_REF:0000058"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cohesin unloading (obsolete GO:1905343)","termid":"GO:1905343"}


id: PBO:0085575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in 20S proteasome assembly; forms a heterodimer with Add66p that binds to proteasome precursors; interaction with Pba1p-Add66p may affect function of the mature proteasome and its role in maintaining respiratory metabolism; similar to human PAC1 constituent of the PAC1-PAC2 complex involved in proteasome assembly","termid":"PBO:0085575"}


id: PBO:0054976
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 2390","termid":"PBO:0054976"}


id: FYPO:0008375
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of phosphatidylinositol-4-phosphate measured in the Golgi is higher than normal.","direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular phosphoinositide level","termid":"FYPO:0001286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased phosphatidylinositol-4-phosphate level in the Golgi","termid":"FYPO:0008375"}


id: GO:0102320
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,8-cineole + NADPH + H+ + O2 = 2-exo-hydroxy-1,8-cineole + NADP + H2O.","definition_xrefs":["GOC:pz","RHEA:32895"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"1,8-cineole 2-exo-monooxygenase activity","secondary_identifiers":["MetaCyc:RXN-4342","EC:1.14.14.56"],"termid":"GO:0102320"}


id: MONDO:0012286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked myopathy with excessive autophagy","termid":"MONDO:0010684"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myopathy, autophagic vacuolar, infantile-onset","secondary_identifiers":["UMLS:C2931230","MEDGEN:419364","OMIM:609500"],"synonyms":[{"name":"myopathy, autophagic vacuolar, infantile-onset","type":"exact"}],"termid":"MONDO:0012286","xrefs":{"Monarch":{"xref_id":"0012286"}}}


id: PR:O13953
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mortality factor 4-like protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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":"chromatin modification-related protein eaf3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23H4.12","secondary_identifiers":["UniProtKB:O13953"],"synonyms":[{"name":"ESA1-associated factor 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC23H4.12","type":"related"},{"name":"Spom972h-MORF4L1","type":"exact"},{"name":"altered polarity protein 13 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eaf3","type":"related"}],"termid":"PR:O13953"}


id: MONDO:0100531
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked Emery-Dreifuss muscular dystrophy","termid":"MONDO:0010680"}],"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:0005336","MONDO:0005267"],"is_obsolete":false,"name":"Emery-Dreifuss muscular dystrophy 1, X-linked","secondary_identifiers":["MEDGEN:1720295","NCIT:C168730","DOID:0070246","OMIM:310300","UMLS:C5243475"],"synonyms":[{"name":"EDMD1","type":"exact"},{"name":"EMD1","type":"exact"},{"name":"Ehlers-Danlos syndrome, classic-like, 1","type":"related"},{"name":"Emery-Dreifuss muscular dystrophy 1, X-linked","type":"exact"},{"name":"Humeroperoneal neuromuscular disease","type":"related"},{"name":"Humeroperoneal neuromuscular disease, formerly","type":"related"},{"name":"humeroperoneal neuromuscular disease","type":"exact"},{"name":"scapuloperoneal syndrome, X-linked","type":"exact"},{"name":"scapuloperoneal syndrome, X-linked, formerly","type":"related"}],"termid":"MONDO:0100531","xrefs":{"Monarch":{"xref_id":"0100531"}}}


id: MONDO:0001127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tendinitis that involves the tibialis.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tendinitis","termid":"MONDO:0004857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"tibialis tendinitis","secondary_identifiers":["UMLS:C0158321","DOID:10810","ICD9:726.72","SCTID:50127006","MEDGEN:510515"],"synonyms":[{"name":"tendinitis of tibialis","type":"exact"},{"name":"tibialis tendinitis","type":"exact"}],"termid":"MONDO:0001127","xrefs":{"Monarch":{"xref_id":"0001127"}}}


id: PBO:0085552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the synaptonemal complex axial elements; involved in chromosome segregation during the first meiotic division; critical for coupling checkpoint signaling to SC formation; promotes interhomolog recombination by phosphorylating Hop1p; also interacts with Mec3p and Ddc1p","termid":"PBO:0085552"}


id: PBO:0031573
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-swollen_vegetative_cell","termid":"PBO:0031573"}


id: GO:0005892
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A homo- or hetero-pentameric protein complex that forms a transmembrane channel through which ions may pass in response to acetylcholine binding.","definition_xrefs":["GOC:mah","PMID:15579462","PMID:12381728","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic ion channel complex","termid":"GO:0034702"},{"relation_name":"is_a","term_name":"plasma membrane signaling receptor complex","termid":"GO:0098802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"acetylcholine-gated channel complex","synonyms":[{"name":"nicotinic acetylcholine receptor","type":"broad"},{"name":"nicotinic acetylcholine-gated receptor-channel complex","type":"exact"}],"termid":"GO:0005892"}


id: MONDO:0032873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"RPE65-related dominant retinopathy","termid":"MONDO:0100452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0000426","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 87 with choroidal involvement","secondary_identifiers":["MEDGEN:1684667","OMIM:618697","GARD:16374","UMLS:C5231465"],"synonyms":[{"name":"RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT","type":"related"},{"name":"RP87","type":"related"}],"termid":"MONDO:0032873","xrefs":{"Monarch":{"xref_id":"0032873"}}}


id: PBO:0072251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 26","termid":"PBO:0072251"}


id: FYPO:0001570
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 glutathione (GSH) measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased cellular glutathione level during vegetative growth","synonyms":[{"name":"decreased cellular GSH level during vegetative growth","type":"exact"},{"name":"decreased cellular L-gamma-glutamyl-L-cysteinylglycine level during vegetative growth","type":"exact"},{"name":"decreased cellular glutathione level during mitotic cell cycle","type":"related"},{"name":"decreased cellular reduced glutathione level during vegetative growth","type":"exact"},{"name":"decreased glutathione accumulation during vegetative growth","type":"related"},{"name":"reduced cellular glutathione level during vegetative growth","type":"exact"}],"termid":"FYPO:0001570"}


id: MONDO:0100519
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epilepsy, idiopathic generalized, susceptibility to, 17","secondary_identifiers":["MEDGEN:1794141","OMIM:602477","UMLS:C5561931"],"synonyms":[{"name":"EIG17","type":"exact"}],"termid":"MONDO:0100519","xrefs":{"Monarch":{"xref_id":"0100519"}}}


id: GO:0008796
data:
  {"annotated_genes":["SJAG_04169","SJAG_04870"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90529],"is_not":false,"summary":null,"term":"GO:0008796"},{"annotations":[79906],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004081"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of P(1),P(4)-bis(5'-nucleosyl)tetraphosphate into two nucleotides.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04169":null,"SJAG_04870":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"bis(5'-nucleosyl)-tetraphosphatase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0008796","terms_by_termid":{"GO:0004081":null,"GO:0008796":null}}


id: GO:0046014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of resting T cell proliferation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell proliferation","termid":"GO:0042130"},{"relation_name":"is_a","term_name":"regulation of T cell homeostatic proliferation","termid":"GO:0046013"},{"relation_name":"negatively_regulates","term_name":"T cell homeostatic proliferation","termid":"GO:0001777"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of T cell homeostatic proliferation","synonyms":[{"name":"down regulation of T cell homeostatic proliferation","type":"exact"},{"name":"down-regulation of T cell homeostatic proliferation","type":"exact"},{"name":"downregulation of T cell homeostatic proliferation","type":"exact"},{"name":"inhibition of T cell homeostatic proliferation","type":"narrow"},{"name":"negative regulation of T lymphocyte homeostatic proliferation","type":"exact"},{"name":"negative regulation of T-cell homeostatic proliferation","type":"exact"},{"name":"negative regulation of T-lymphocyte homeostatic proliferation","type":"exact"},{"name":"negative regulation of resting T cell proliferation","type":"exact"}],"termid":"GO:0046014"}


id: GO:0051106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of DNA ligation, the re-formation of a broken phosphodiester bond in the DNA backbone, carried out by DNA ligase.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of DNA ligation (obsolete GO:0051106)","synonyms":[{"name":"activation of DNA ligation","type":"narrow"},{"name":"stimulation of DNA ligation","type":"narrow"},{"name":"up regulation of DNA ligation","type":"exact"},{"name":"up-regulation of DNA ligation","type":"exact"},{"name":"upregulation of DNA ligation","type":"exact"}],"termid":"GO:0051106"}


id: GO:0106118
data:
  {"annotated_genes":["SJAG_02044","SJAG_01307","SJAG_04018","SJAG_02104"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"},{"annotations":[111697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070452"},{"annotations":[77234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045540"},{"annotations":[107666,90379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032443"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a sterol biosynthetic process.","definition_xrefs":["GOC:rph","GOC:BHF_miRNA","PMID:16459310","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid biosynthetic process","termid":"GO:0050810"},{"relation_name":"regulates","term_name":"sterol biosynthetic process","termid":"GO:0016126"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01307":null,"SJAG_02044":null,"SJAG_02104":null,"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of sterol biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0106118","terms_by_termid":{"GO:0010895":null,"GO:0032443":null,"GO:0045540":null,"GO:0070452":null}}


id: GO:0018936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving nitrilotriacetate, the aminotricarboxylic acid N(CH2COO-)3, that occur in the absence of oxygen.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrilotriacetate metabolic process","termid":"GO:0018934"}],"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:0008150","GO:0044281"],"is_obsolete":false,"name":"anaerobic nitrilotriacetate metabolic process","synonyms":[{"name":"anaerobic nitrilotriacetate metabolism","type":"exact"}],"termid":"GO:0018936"}


id: GO:0016744
data:
  {"annotated_genes":["SJAG_03934","SJAG_03985","SJAG_04263"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003984"},{"annotations":[74864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004801"},{"annotations":[81417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004802"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an aldehyde or ketonic group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity","termid":"GO:0016740"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03934":null,"SJAG_03985":null,"SJAG_04263":null},"genotype_count":0,"in_subsets":["mf_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"transketolase or transaldolase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:2.2.1.-","GO:0016745"],"synonyms":[{"name":"transferase activity, transferring aldehyde or ketonic groups","type":"exact"}],"termid":"GO:0016744","terms_by_termid":{"GO:0003984":null,"GO:0004801":null,"GO:0004802":null}}


id: MONDO:0100331
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A poisoning that is caused by exposure to a nerve agent or gas.","definition_xrefs":["MONDO:patterns/patterns/poisoning"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nerve agent poisoning","termid":"MONDO:0100331","xrefs":{"Monarch":{"xref_id":"0100331"}}}


id: PBO:0079090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (anticodon GTA) 5-3","termid":"PBO:0079090"}


id: PBO:0048194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GABPB1 antisense RNA 1","termid":"PBO:0048194"}


id: MONDO:0005365
data:
  {"annotated_genes":["SJAG_01941","SJAG_04703","SJAG_03007","SJAG_04882","SJAG_02139","SJAG_01253","SJAG_01538","SJAG_05175","SJAG_04558","SJAG_02348","SJAG_05330","SJAG_03943","SJAG_01400","SJAG_03536","SJAG_05282","SJAG_04554","SJAG_03703","SJAG_05213","SJAG_00279","SJAG_04619","SJAG_00082","SJAG_00301","SJAG_04856","SJAG_04613","SJAG_00164","SJAG_02016","SJAG_04719","SJAG_03088","SJAG_02155","SJAG_03145","SJAG_01943","SJAG_05182","SJAG_04706","SJAG_01722","SJAG_04409","SJAG_00244","SJAG_02431","SJAG_01926","SJAG_01344","SJAG_03811","SJAG_00488","SJAG_00358","SJAG_00365","SJAG_02463","SJAG_03785","SJAG_04115","SJAG_04295"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012196"},{"annotations":[87122,87123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007424"},{"annotations":[87334,87335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011350"},{"annotations":[87640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011480"},{"annotations":[87290,87288,87286,87287,87289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011568"},{"annotations":[87064],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014603"},{"annotations":[88541,88542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010915"},{"annotations":[87045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014594"},{"annotations":[87417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014853"},{"annotations":[89139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011067"},{"annotations":[88410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012091"},{"annotations":[87105,87106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010933"},{"annotations":[88553,88554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013471"},{"annotations":[88836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013386"},{"annotations":[87592,87593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014237"},{"annotations":[88520,88519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013489"},{"annotations":[89077,86796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010799"},{"annotations":[88569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0027048"},{"annotations":[87138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033258"},{"annotations":[88495,88494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032911"},{"annotations":[88503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032917"},{"annotations":[87134,87135,87133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030058"},{"annotations":[87556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033668"},{"annotations":[88892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030719"},{"annotations":[88373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859524"},{"annotations":[88370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859525"},{"annotations":[88927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032740"},{"annotations":[87166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033199"},{"annotations":[88043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032639"},{"annotations":[88957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032761"},{"annotations":[88960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032762"},{"annotations":[88932],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958277"},{"annotations":[88937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032749"},{"annotations":[87168,87167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010577"},{"annotations":[87621,87620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009479"},{"annotations":[88992],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010378"}]},"cv_name":"mondo","definition":"A partial or complete loss of hearing in one or both ears. It is classified as conductive, sensory, or central.","definition_xrefs":["NCIT:C35731"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing disorder","termid":"MONDO:0021945"}],"gene_count":47,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00164":null,"SJAG_00244":null,"SJAG_00279":null,"SJAG_00301":null,"SJAG_00358":null,"SJAG_00365":null,"SJAG_00488":null,"SJAG_01253":null,"SJAG_01344":null,"SJAG_01400":null,"SJAG_01538":null,"SJAG_01722":null,"SJAG_01926":null,"SJAG_01941":null,"SJAG_01943":null,"SJAG_02016":null,"SJAG_02139":null,"SJAG_02155":null,"SJAG_02348":null,"SJAG_02431":null,"SJAG_02463":null,"SJAG_03007":null,"SJAG_03088":null,"SJAG_03145":null,"SJAG_03536":null,"SJAG_03703":null,"SJAG_03785":null,"SJAG_03811":null,"SJAG_03943":null,"SJAG_04115":null,"SJAG_04295":null,"SJAG_04409":null,"SJAG_04554":null,"SJAG_04558":null,"SJAG_04613":null,"SJAG_04619":null,"SJAG_04703":null,"SJAG_04706":null,"SJAG_04719":null,"SJAG_04856":null,"SJAG_04882":null,"SJAG_05175":null,"SJAG_05182":null,"SJAG_05213":null,"SJAG_05282":null,"SJAG_05330":null},"genotype_count":0,"is_obsolete":false,"name":"hearing loss disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:H90","MEDGEN:235586","MESH:D034381","EFO:0004238","ICD9:389.8","UMLS:C1384666","ICD9:389","ICD9:389.9","SCTID:15188001"],"synonyms":[{"name":"deafness","type":"narrow"},{"name":"hearing impairment","type":"related"},{"name":"hearing loss","type":"exact"},{"name":"hypoacuses","type":"exact"},{"name":"hypoacusis","type":"exact"},{"name":"loss of hearing","type":"exact"},{"name":"loss, hearing","type":"exact"}],"termid":"MONDO:0005365","terms_by_termid":{"MONDO:0007424":null,"MONDO:0009479":null,"MONDO:0010378":null,"MONDO:0010577":null,"MONDO:0010799":null,"MONDO:0010915":null,"MONDO:0010933":null,"MONDO:0011067":null,"MONDO:0011350":null,"MONDO:0011480":null,"MONDO:0011568":null,"MONDO:0012091":null,"MONDO:0012196":null,"MONDO:0013386":null,"MONDO:0013471":null,"MONDO:0013489":null,"MONDO:0014237":null,"MONDO:0014594":null,"MONDO:0014603":null,"MONDO:0014853":null,"MONDO:0027048":null,"MONDO:0030058":null,"MONDO:0030719":null,"MONDO:0032639":null,"MONDO:0032740":null,"MONDO:0032749":null,"MONDO:0032761":null,"MONDO:0032762":null,"MONDO:0032911":null,"MONDO:0032917":null,"MONDO:0033199":null,"MONDO:0033258":null,"MONDO:0033668":null,"MONDO:0859524":null,"MONDO:0859525":null,"MONDO:0958277":null},"xrefs":{"Monarch":{"xref_id":"0005365"}}}


id: PBO:0053980
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 1293","termid":"PBO:0053980"}


id: GO:0036012
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The inner, i.e. lumen-facing, lipid bilayer of the cyanelle envelope; also faces the cyanelle stroma.","definition_xrefs":["PMID:18976493","GOC:aa"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid inner membrane","termid":"GO:0009528"},{"relation_name":"is_a","term_name":"cyanelle membrane","termid":"GO:0033113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"cyanelle inner membrane","synonyms":[{"name":"cyanelle inner envelope membrane","type":"exact"}],"termid":"GO:0036012"}


id: MONDO:0009333
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mullerian derivatives-lymphangiectasia-polydactyly syndrome is characterized by prenatal linear growth deficiency, hypertrophied alveolar ridges, redundant nuchal skin, postaxial polydactyly and cryptorchidism. Mullerian duct remnants, lymphangiectasis, and renal anomalies are also present. Three cases have been described. A small penis was observed in two of these cases. The syndrome is likely to be an autosomal recessive or X-linked trait. All the reported patients died neonatally of hepatic failure.","definition_xrefs":["Orphanet:1655"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"primary lymphedema","termid":"MONDO:0019175"}],"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":"mullerian derivatives-lymphangiectasia-polydactyly syndrome","secondary_identifiers":["OMIM:235255","MESH:C536478","GARD:5430","UMLS:C1856159","MEDGEN:343489"],"synonyms":[{"name":"MULLERIAN derivatives, persistence of, with lymphangiectasia and postaxial polydactyly","type":"related"},{"name":"Müllerian derivatives-lymphangiectasia-polydactyly syndrome","type":"related"},{"name":"Urioste syndrome","type":"related"},{"name":"persistence of mullerian derivatives with lymphangiectasia and postaxial polydactyly","type":"related"},{"name":"renal and craniofacial anomalies with persistence of mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly","type":"related"}],"termid":"MONDO:0009333","xrefs":{"Monarch":{"xref_id":"0009333"}}}


id: GO:0038138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of a ligand to the tyrosine kinase receptor ERBB4, followed by ligand-induced homodimerization of ERBB4 and transmission of the signal into the cell by the homodimeric ERBB4 complex. The pathway ends with regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","PMID:16460914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ERBB4 signaling pathway","termid":"GO:0038130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"ERBB4-ERBB4 signaling pathway","synonyms":[{"name":"ERBB4 homodimeric signaling pathway","type":"exact"},{"name":"ERBB4-ERBB4 signalling pathway","type":"exact"},{"name":"HER4-HER4 signaling pathway","type":"exact"}],"termid":"GO:0038138"}


id: MONDO:0022173
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of chromosome 11","termid":"MONDO:0016932"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 11q trisomy","secondary_identifiers":["GARD:20882","Orphanet:262923","MESH:C538297","MEDGEN:167075","UMLS:C0795842"],"synonyms":[{"name":"11q duplication","type":"exact"},{"name":"11q trisomy","type":"exact"},{"name":"Duplication 11q","type":"exact"},{"name":"chromosome 11q duplication","type":"exact"},{"name":"partial duplication of chromosome 11q","type":"exact"},{"name":"partial duplication of the long arm of chromosome 11","type":"exact"},{"name":"partial duplication of the long arm of chromosome type 11","type":"exact"},{"name":"partial trisomy 11q","type":"exact"},{"name":"partial trisomy of chromosome 11q","type":"exact"},{"name":"partial trisomy of the long arm of chromosome 11","type":"exact"},{"name":"trisomy 11q","type":"exact"}],"termid":"MONDO:0022173","xrefs":{"Monarch":{"xref_id":"0022173"}}}


id: PBO:0053782
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 1033","termid":"PBO:0053782"}


id: MONDO:0018388
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare male infertility due to testicular endocrine disorder (obsolete MONDO:0018388)","secondary_identifiers":["Orphanet:399685"],"termid":"MONDO:0018388","xrefs":{"Monarch":{"xref_id":"0018388"}}}


id: PBO:0059785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 11","termid":"PBO:0059785"}


id: FYPO:0004224
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 trimethylation of lysine at position 20 of histone H4 occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H4-K20 methylation during vegetative growth","termid":"FYPO:0004215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0002274","FYPO:0001985","FYPO:0005447","FYPO:0002494"],"is_obsolete":false,"name":"decreased histone H4-K20 trimethylation during vegetative growth","synonyms":[{"name":"decreased H4K20me3 during vegetative growth","type":"exact"},{"name":"decreased histone H4-K20 trimethylation during mitotic cell cycle","type":"related"},{"name":"decreased histone H4K20 trimethylation during vegetative growth","type":"exact"},{"name":"decreased histone lysine H4-K20 trimethylation during vegetative growth","type":"exact"},{"name":"reduced histone H4-K20 trimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0004224"}


id: PBO:0072578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRN3 pseudogene 1","termid":"PBO:0072578"}


id: MONDO:0700001
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare pulmonary complication of an underlying autoimmune disorder that is reported in association with systemic lupus erythematosus (SLE). Reduced lung volumes result in restrictive ventilatory defect and a preserved carbon monoxide transfer coefficient.","definition_xrefs":["PMID:21686610","PMID:24836585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung disorder","termid":"MONDO:0005275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shrinking lung syndrome","secondary_identifiers":["MEDGEN:743060","UMLS:C1960277"],"synonyms":[{"name":"SLS","type":"exact"},{"name":"shrinking of the lung","type":"broad"},{"name":"small lungs","type":"related"}],"termid":"MONDO:0700001","xrefs":{"Monarch":{"xref_id":"0700001"}}}


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


id: MONDO:0004714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of primary or secondary disorders affecting the muscles. It is characterized by an abnormal reduction in the muscle volume and atrophy. The atrophy may be caused by diseases of the muscle tissues or diseases of the peripheral nerves.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle tissue disorder","termid":"MONDO:0003939"},{"relation_name":"is_a","term_name":"neuromuscular disease","termid":"MONDO:0019056"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrophic muscular disease","secondary_identifiers":["MEDGEN:156267","DOID:913","NCIT:C84574","UMLS:C0752352"],"synonyms":[{"name":"atrophic muscular disorder","type":"exact"}],"termid":"MONDO:0004714","xrefs":{"Monarch":{"xref_id":"0004714"}}}


id: PBO:0029651
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mislocalized_nucleus","termid":"PBO:0029651"}


id: PBO:0046810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F11 antisense RNA 1","termid":"PBO:0046810"}


id: PBO:0063183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PBX3 divergent transcript","termid":"PBO:0063183"}


id: GO:0034939
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 5-hydroxypyrrole-2-carboxylate = 5-oxo-4,5-dihydropyrrole-2-carboxylate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 5-hydroxypyrrole-2-carboxylate tautomerase activity (obsolete GO:0034939)","termid":"GO:0034939"}


id: GO:0050956
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive an electrical stimulus, convert it to a molecular signal, and recognize and characterize the signal. Many fish possess an electroception sense; for example, the electric eel uses low voltage pulses of electricity for navigation and prey location.","definition_xrefs":["Wikipedia:Electroreception","GOC:ai","PMID:10210663"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory perception of electrical stimulus","termid":"GO:0050952"}],"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":"electroception","synonyms":[{"name":"electroception sense","type":"exact"},{"name":"electroceptive sense","type":"exact"}],"termid":"GO:0050956"}


id: MONDO:0008441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spastic paraplegia with associated extrapyramidal signs","secondary_identifiers":["MESH:C566681","MEDGEN:355815","UMLS:C1866852","OMIM:182800"],"synonyms":[{"name":"spastic paraplegia with associated extrapyramidal signs","type":"exact"}],"termid":"MONDO:0008441","xrefs":{"Monarch":{"xref_id":"0008441"}}}


id: MONDO:0014906
data:
  {"annotated_genes":["SJAG_00031"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87928],"is_not":false,"summary":null,"term":"MONDO:0014906"}]},"cv_name":"mondo","definition":"An autosomal recessive sub-type of Charcot-Marie-Tooth disease caused by compound heterozygous or homozygous mutation(s) in the MFN2 gene, encoding mitofusin-2. This condition is more severe and has an earlier onset as compared to Charcot-Marie-Tooth disease type 2A2A.","definition_xrefs":["NCIT:C150647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00031":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4310725","MEDGEN:934692","OMIM:617087","DOID:0111557"],"synonyms":[{"name":"CMT2A2B","type":"related"},{"name":"Charcot-Marie-Tooth disease type 2A2B","type":"exact"},{"name":"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B","type":"related"},{"name":"Charcot-Marie-Tooth disease, axonal, type 2A2B","type":"exact"}],"termid":"MONDO:0014906","terms_by_termid":{"MONDO:0014906":null},"xrefs":{"Monarch":{"xref_id":"0014906"}}}


id: GO:0006958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the activation of any of the steps of the classical pathway of the complement cascade which allows for the direct killing of microbes, the disposal of immune complexes, and the regulation of other immune processes.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complement activation","termid":"GO:0006956"},{"relation_name":"part_of","term_name":"humoral immune response mediated by circulating immunoglobulin","termid":"GO:0002455"}],"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":"complement activation, classical pathway","secondary_identifiers":["Reactome:R-HSA-173623"],"synonyms":[{"name":"complement cascade, classical pathway","type":"exact"}],"termid":"GO:0006958"}


id: PBO:0091232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane heme transmembrane transporter Str3","termid":"PBO:0091232"}


id: MONDO:0008850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cooper-Wang-Jabs syndrome is a multiple malformation syndrome characterized by atresia of the auditory canal together with ventricular septal defect, anteriorly displaced anus, mild clubfoot, and intellectual deficit. It has been described only once, in two sisters. The mode of inheritance is most likely autosomal recessive.","definition_xrefs":["Orphanet:1488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cooper-Jabs syndrome","secondary_identifiers":["OMIM:209770","SCTID:720748007","GARD:16567","UMLS:C1859591","MEDGEN:347912","MESH:C565923"],"synonyms":[{"name":"aural atresia, multiple congenital anomalies, and intellectual disability","type":"related"},{"name":"aural atresia, multiple congenital anomalies, and mental retardation","type":"related"},{"name":"aural atresia-multiple congenital anomalies-intellectual disability syndrome","type":"exact"}],"termid":"MONDO:0008850","xrefs":{"Monarch":{"xref_id":"0008850"}}}


id: GO:1902836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of proline import into cell.","definition_xrefs":["GO_REF:0000058","PMID:24344203","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organic acid transport","termid":"GO:0032892"},{"relation_name":"is_a","term_name":"positive regulation of transmembrane transport","termid":"GO:0034764"},{"relation_name":"is_a","term_name":"positive regulation of amino acid transport","termid":"GO:0051957"},{"relation_name":"is_a","term_name":"regulation of proline import across plasma membrane","termid":"GO:1902834"},{"relation_name":"positively_regulates","term_name":"proline import across plasma membrane","termid":"GO:1905647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"positive regulation of proline import across plasma membrane","synonyms":[{"name":"activation of proline import into cell","type":"narrow"},{"name":"positive regulation of proline import into cell","type":"exact"},{"name":"up regulation of proline import into cell","type":"exact"},{"name":"up-regulation of proline import into cell","type":"exact"},{"name":"upregulation of proline import into cell","type":"exact"}],"termid":"GO:1902836"}


id: PBO:0062661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 13 subfamily D member 2 pseudogene","termid":"PBO:0062661"}


id: GO:0014048
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the controlled release of glutamate.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organic acid transport","termid":"GO:0032890"},{"relation_name":"is_a","term_name":"regulation of amino acid transport","termid":"GO:0051955"},{"relation_name":"is_a","term_name":"regulation of secretion by cell","termid":"GO:1903530"},{"relation_name":"regulates","term_name":"glutamate secretion","termid":"GO:0014047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of glutamate secretion","termid":"GO:0014048"}


id: PBO:0077124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIMP metallopeptidase inhibitor 3","termid":"PBO:0077124"}


id: MONDO:0025263
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of horses with parasitic nematodes of the superfamily strongyloidea. Characteristics include the development of hemorrhagic nodules on the abdominal peritoneum.","definition_xrefs":["MESH:D013319"],"direct_ancestors":[{"relation_name":"is_a","term_name":"horse disease","termid":"MONDO:0024950"},{"relation_name":"is_a","term_name":"helminthiasis, animal","termid":"MONDO:0025082"},{"relation_name":"is_a","term_name":"Strongylida infectious disease, non-human animal","termid":"MONDO:0700209"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"strongyle infections, equine","synonyms":[{"name":"Strongyloses, equine","type":"related"},{"name":"Strongylosis, equine","type":"related"},{"name":"equine Strongyloses","type":"related"},{"name":"equine Strongylosis","type":"related"},{"name":"equine strongyle infection","type":"related"},{"name":"equine strongyle infections","type":"related"},{"name":"infection, equine strongyle","type":"related"},{"name":"infections, equine strongyle","type":"related"},{"name":"strongyle infection, equine","type":"related"}],"termid":"MONDO:0025263","xrefs":{"Monarch":{"xref_id":"0025263"}}}


id: PR:O74175
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 60S ribosomal protein L13 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11722: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":"60S ribosomal protein L13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC664.05","secondary_identifiers":["UniProtKB:O74175"],"synonyms":[{"name":"SPAC664.05","type":"related"},{"name":"Spom972h-RPL13","type":"exact"}],"termid":"PR:O74175"}


id: MONDO:0010321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autism, susceptiblity to","termid":"MONDO:0020836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autism, susceptibility to, X-linked 1","secondary_identifiers":["OMIM:300425","MEDGEN:335205","UMLS:C1845540"],"synonyms":[{"name":"AUTSX1","type":"related"},{"name":"autism susceptibility, X-linked 1","type":"exact"},{"name":"autism, susceptibility to, X-linked 1","type":"exact"},{"name":"autism, susceptibility to, X-linked type 1","type":"exact"},{"name":"susceptibility to X-linked autism 1","type":"related"}],"termid":"MONDO:0010321","xrefs":{"Monarch":{"xref_id":"0010321"}}}


id: MONDO:0015699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"immunodeficiency due to a classical component pathway complement deficiency","secondary_identifiers":["GARD:15025","icd11.foundation:327609494","UMLS:C0398750","Orphanet:169147","MEDGEN:585054"],"synonyms":[{"name":"immunodeficiency due to C1, C4, or C2 component complement deficiency","type":"exact"},{"name":"immunodeficiency due to a C1, C4, or C2 component complement deficiency","type":"exact"},{"name":"immunodeficiency due to an early component of complement deficiency","type":"exact"}],"termid":"MONDO:0015699","xrefs":{"Monarch":{"xref_id":"0015699"}}}


id: MONDO:0007875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Larsen syndrome (LS) is a rare skeletal dysplasia characterized by congenital dislocation of large joints, foot deformities, cervical spine dysplasia, scoliosis, spatula-shaped distal phalanges and distinctive craniofacial abnormalities, including cleft palate.","definition_xrefs":["Orphanet:503"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"filamin-related bone disorder","termid":"MONDO:0019690"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"}],"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":"Larsen syndrome","secondary_identifiers":["MEDGEN:104500","UMLS:C0175778","OMIM:150250","GARD:6860","icd11.foundation:607849551","NANDO:2201019","MESH:C580241","SCTID:63387002","DOID:14764","NORD:1349","ICD9:759.89"],"synonyms":[{"name":"LRS","type":"related"},{"name":"Larsen syndrome","type":"exact"},{"name":"autosomal dominant Larsen syndrome","type":"related"},{"name":"dominant Larsen syndrome","type":"exact"}],"termid":"MONDO:0007875","xrefs":{"Monarch":{"xref_id":"0007875"}}}


id: MONDO:0006046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant serous cystic epithelial neoplasm arising from the ovary. It is characterized by the presence of glandular, papillary, or solid structures. Psammoma bodies may be present. In well differentiated cases the malignant epithelial cells resemble the cells of fallopian tube epithelium. In poorly differentiated cases the malignant epithelial cells show anaplastic features.","definition_xrefs":["NCIT:C7978"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian cystadenocarcinoma","termid":"MONDO:0002702"},{"relation_name":"is_a","term_name":"ovarian serous adenocarcinoma","termid":"MONDO:0005211"},{"relation_name":"is_a","term_name":"serous cystadenocarcinoma","termid":"MONDO:0024621"}],"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":"ovarian serous cystadenocarcinoma","secondary_identifiers":["DOID:5746","EFO:1000043","MEDGEN:83541","UMLS:C0279663"],"synonyms":[{"name":"ovarian serous cystadenocarcinoma","type":"exact"}],"termid":"MONDO:0006046","xrefs":{"Monarch":{"xref_id":"0006046"}}}


id: GO:0072463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about whether spindle is correctly assembled and chromosomes are attached to the spindle is received and converted into a molecular signal, contributing to a meiotic spindle assembly checkpoint.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of stimulus involved in meiotic spindle assembly checkpoint (obsolete GO:0072463)","synonyms":[{"name":"meiotic spindle assembly checkpoint sensor mechanism","type":"related"},{"name":"meiotic spindle assembly checkpoint sensor process","type":"related"},{"name":"sensing involved in meiotic spindle assembly checkpoint","type":"related"}],"termid":"GO:0072463"}


id: GO:0015755
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of fructose into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Fructose exists in a open chain form or as a ring compound. D-fructose is the sweetest of the sugars and is found free in a large number of fruits and honey.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexose transmembrane transport","termid":"GO:0008645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"fructose transmembrane transport","synonyms":[{"name":"fructose transport","type":"related"}],"termid":"GO:0015755"}


id: MONDO:0018643
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"functional neutrophil defect","termid":"MONDO:0015978"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"susceptibility to localized juvenile periodontitis","secondary_identifiers":["UMLS:C5681199","MEDGEN:1812489","Orphanet:447740"],"termid":"MONDO:0018643","xrefs":{"Monarch":{"xref_id":"0018643"}}}


id: PBO:0057203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 374b","termid":"PBO:0057203"}


id: PBO:0045929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EF-hand domain containing 2","termid":"PBO:0045929"}


id: MOD:01103
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00503. Remap to MOD:00503.","definition_xrefs":["DeltaMass:0"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01103 myristoleylation (one double bond) (obsolete MOD:01103)","termid":"MOD:01103"}


id: PBO:0041655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel auxiliary subunit gamma 1","termid":"PBO:0041655"}


id: GO:0006161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of deoxyguanosine, a nucleoside consisting of the base guanine and the sugar deoxyribose.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyguanosine metabolic process","termid":"GO:0042453"},{"relation_name":"is_a","term_name":"purine deoxyribonucleoside catabolic process","termid":"GO:0046124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"deoxyguanosine catabolic process","synonyms":[{"name":"deoxyguanosine breakdown","type":"exact"},{"name":"deoxyguanosine catabolism","type":"exact"},{"name":"deoxyguanosine degradation","type":"exact"}],"termid":"GO:0006161"}


id: PBO:0073529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain containing GRB2 like 1, endophilin A2 pseudogene 2","termid":"PBO:0073529"}


id: MONDO:0000937
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An encephalitis caused by infection with Treponema.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Treponema infectious disease","termid":"MONDO:0007000"},{"relation_name":"is_a","term_name":"infectious encephalitis","termid":"MONDO:0020067"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syphilitic encephalitis","secondary_identifiers":["ICD9:094.81","SCTID:26135000","DOID:10081","MEDGEN:509177","UMLS:C0153168"],"synonyms":[{"name":"Treponema caused encephalitis","type":"exact"},{"name":"Treponema encephalitis","type":"exact"}],"termid":"MONDO:0000937","xrefs":{"Monarch":{"xref_id":"0000937"}}}


id: PBO:0041620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium binding protein 7","termid":"PBO:0041620"}


id: MONDO:0020717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"isolated familial wooly hair disorder","termid":"MONDO:0008686"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal dominant wooly hair","secondary_identifiers":["DOID:0111573","MEDGEN:348571","UMLS:C1860238","OMIM:194300"],"synonyms":[{"name":"ADWH","type":"related"},{"name":"woolly hair, autosomal dominant","type":"exact"},{"name":"wooly hair, autosomal dominant","type":"exact"}],"termid":"MONDO:0020717","xrefs":{"Monarch":{"xref_id":"0020717"}}}


id: GO:0014005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a microglial cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:dgh","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell development","termid":"GO:0021782"},{"relation_name":"is_a","term_name":"myeloid cell development","termid":"GO:0061515"},{"relation_name":"part_of","term_name":"microglia differentiation","termid":"GO:0014004"}],"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":"microglia development","synonyms":[{"name":"microglial cell development","type":"exact"}],"termid":"GO:0014005"}


id: GO:0060328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The actin filament-based movement by which cytoplasmic actin filaments slide past one another resulting in a contraction that propels the cell in the direction that has been defined as the front of the cell.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic actin-based contraction involved in cell motility","termid":"GO:0060327"}],"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":"cytoplasmic actin-based contraction involved in forward cell motility","synonyms":[{"name":"cytoplasmic actin-based contraction involved in forward cell locomotion","type":"related"}],"termid":"GO:0060328"}


id: PBO:0068695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 76, pseudogene","termid":"PBO:0068695"}


id: PBO:0078045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 35 (non-functional)","termid":"PBO:0078045"}


id: MONDO:0020831
data:
  {"annotated_genes":["SJAG_02618"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030077"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02618":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0006025"],"is_obsolete":false,"name":"congenital vertebral-cardiac-renal anomalies syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1814457","GARD:17961","OMIMPS:617660","Orphanet:521438","UMLS:C5680183"],"synonyms":[{"name":"VCRL","type":"exact"},{"name":"vertebral, cardiac, renal, and limb defects syndrome","type":"exact"}],"termid":"MONDO:0020831","terms_by_termid":{"MONDO:0030077":null},"xrefs":{"Monarch":{"xref_id":"0020831"}}}


id: PBO:0069792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1078, pseudogene","termid":"PBO:0069792"}


id: MONDO:0011131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"tricho-oculo-dermo-vertebral syndrome","secondary_identifiers":["MESH:C537441","OMIM:601701","icd11.foundation:1206025469","UMLS:C1866427","MEDGEN:355714","Orphanet:3354"],"synonyms":[{"name":"Alves syndrome","type":"related"},{"name":"Alves-dos Santos-Castelo syndrome","type":"exact"},{"name":"Todv syndrome","type":"related"},{"name":"Trichooculodermovertebral syndrome","type":"related"},{"name":"arthrogryposis and ectodermal dysplasia","type":"related"},{"name":"ectodermal dysplasia - cataracts - kyphoscoliosis","type":"related"},{"name":"ectodermal dysplasia-cataracts-kyphoscoliosis syndrome","type":"exact"}],"termid":"MONDO:0011131","xrefs":{"Monarch":{"xref_id":"0011131"}}}


id: PBO:0050081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group AT-hook 1 pseudogene 1","termid":"PBO:0050081"}


id: FYPO:0006357
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which chromatin remodeling, i.e. any dynamic structural change to chromatin, occurs to a lower extent than normal when the cell is subject to glucose starvation.","definition_xrefs":["GO:0006338","PMID:28674280","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000641","FYPO:0000002"],"is_obsolete":false,"name":"decreased chromatin remodeling during glucose starvation","synonyms":[{"name":"decreased chromatin modeling during glucose starvation","type":"exact"},{"name":"decreased chromatin remodeling during glucose depletion","type":"exact"},{"name":"decreased chromatin remodeling during glucose deprivation","type":"related"},{"name":"decreased chromatin remodeling during glucose limitation","type":"related"},{"name":"decreased chromatin remodelling during glucose starvation","type":"exact"},{"name":"reduced decreased chromatin remodeling during glucose starvation","type":"exact"}],"termid":"FYPO:0006357"}


id: PBO:0057255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 466","termid":"PBO:0057255"}


id: PATO:0001431
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An emergent molecular quality that arises by virtue of the bearer's disposition to exhibit molecular attraction to another entity in contact.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesivity","synonyms":[{"name":"adhesiveness","type":"exact"},{"name":"stickiness","type":"related"}],"termid":"PATO:0001431"}


id: PBO:0108570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Las1","termid":"PBO:0108570"}


id: GO:0098745
data:
  {"annotated_genes":["SJAG_01746","SJAG_05694","SJAG_05010"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[93138,93366,111729],"is_not":false,"summary":null,"term":"GO:0098745"}]},"cv_name":"cellular_component","definition":"A protein complex consisting of a Dcp1 regulatory subunit and a Dcp2 catalytic subunit that has mRNA cap binding activity and is involved in decapping of nuclear-transcribed mRNA.","definition_xrefs":["GOC:dos","GOC:vw","PMID:22323607"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01746":null,"SJAG_05010":null,"SJAG_05694":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":"RNA decapping complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Dcp1-Dcp2 complex","type":"exact"}],"termid":"GO:0098745","terms_by_termid":{"GO:0098745":null}}


id: GO:0002645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of tolerance induction.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tolerance induction","termid":"GO:0002643"},{"relation_name":"is_a","term_name":"positive regulation of immune system process","termid":"GO:0002684"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"tolerance induction","termid":"GO:0002507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of tolerance induction","synonyms":[{"name":"activation of tolerance induction","type":"narrow"},{"name":"stimulation of tolerance induction","type":"narrow"},{"name":"up regulation of tolerance induction","type":"exact"},{"name":"up-regulation of tolerance induction","type":"exact"},{"name":"upregulation of tolerance induction","type":"exact"}],"termid":"GO:0002645"}


id: FYPO:0002229
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of ergosterol measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal cellular ergosterol level","synonyms":[{"name":"normal cellular ergosterol accumulation","type":"related"},{"name":"normal cellular ergosterol level during mitotic cell cycle","type":"related"},{"name":"normal cellular ergosterol level during vegetative growth","type":"exact"}],"termid":"FYPO:0002229"}


id: GO:1901760
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of beta-L-Ara4N-lipid A which occurs as a result of modification of the lipid A moiety of lipopolysaccharide by the addition of the sugar 4-amino-4-deoxy-L-arabinose (L-Ara4N). This strategy is adopted by pathogenic Gram-negative bacteria to evade cationic antimicrobial peptides produced by the innate immune system.","definition_xrefs":["GOC:TermGenie","GOC:yaf","PMID:17928292","UniPathway:UPA00037","PMID:19166326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid biosynthetic process","termid":"GO:0008654"},{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"},{"relation_name":"is_a","term_name":"lipooligosaccharide biosynthetic process","termid":"GO:1901271"},{"relation_name":"is_a","term_name":"beta-L-Ara4N-lipid A metabolic process","termid":"GO:1901759"}],"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:0008150","GO:0006629"],"is_obsolete":false,"name":"beta-L-Ara4N-lipid A biosynthetic process","synonyms":[{"name":"4-amino-4-deoxy-beta-L-arabinose-lipid A biosynthesis","type":"exact"},{"name":"4-amino-4-deoxy-beta-L-arabinose-lipid A biosynthetic process","type":"exact"},{"name":"beta-L-Ara4N-lipid A anabolism","type":"exact"},{"name":"beta-L-Ara4N-lipid A biosynthesis","type":"exact"},{"name":"beta-L-Ara4N-lipid A formation","type":"exact"},{"name":"beta-L-Ara4N-lipid A synthesis","type":"exact"}],"termid":"GO:1901760"}


id: PBO:0002389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial RNA polymerase Rpo41","termid":"PBO:0002389"}


id: MONDO:1011617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Waardenburg syndrome that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg syndrome, non-human animal","termid":"MONDO:1011447"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Waardenburg syndrome, domestic cat","secondary_identifiers":["OMIA:001059-9685"],"termid":"MONDO:1011617","xrefs":{"Monarch":{"xref_id":"1011617"}}}


id: GO:0070521
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha4-beta1 integrin complex bound to membrane protein CD82, a member of the tetraspan family.","definition_xrefs":["PMID:8757325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"alpha4-beta1 integrin-CD82 complex","termid":"GO:0070521"}


id: PR:000049784
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A myosin regulatory light chain 1 (Schizosaccharomyces pombe 972h-) that has been phosphorylated on two consecutive residues equivalent to Ser-35 and Ser-36 in the sequence represented by UniProtKB:Q9UUG5-1. Example: UniProtKB:Q9UUG5-1, Ser-35/Ser-36, MOD:00046.","definition_xrefs":["PomBase:MAH","PMID:19029336","PMID:19570908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myosin regulatory light chain 1 (Schizosaccharomyces pombe 972h-)","termid":"PR:Q9UUG5"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rlc1/Phos(S35,S36)","pombase_gene_id":"SPAC926.03","synonyms":[{"name":"PomBase_original_PRO_term_name: myosin regulatory light chain 1 phosphorylated 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Rlc1p phosphorylated 1","type":"broad"},{"name":"myosin II regulatory light chain Rlc1p Ser-35/Ser-36 phosphorylated","type":"related"},{"name":"rlc1/Phos(S35,S36)","type":"exact"}],"termid":"PR:000049784"}


id: SO:0001163
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A promoter motif with consensus sequence TCATTCG.","definition_xrefs":["PMID:16827941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA_motif","termid":"SO:0000713"},{"relation_name":"part_of","term_name":"RNApol_II_promoter","termid":"SO:0000170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INR1_motif","synonyms":[{"name":"DMp3","type":"exact"},{"name":"INR1 motif","type":"exact"},{"name":"directional motif p3","type":"exact"},{"name":"directional promoter motif 3","type":"exact"}],"termid":"SO:0001163"}


id: PBO:0042515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell death inducing p53 target 1","termid":"PBO:0042515"}


id: PBO:0036438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RhoGAP, GTPase activating protein Rga5","termid":"PBO:0036438"}


id: PBO:0120358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DIP2C antisense RNA 3","termid":"PBO:0120358"}


id: PBO:0026998
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_exit_from_mitosis","termid":"PBO:0026998"}


id: MONDO:0006114
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bladder squamous cell carcinoma (obsolete MONDO:0006114)","termid":"MONDO:0006114","xrefs":{"Monarch":{"xref_id":"0006114"}}}


id: PBO:0042475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin 2","termid":"PBO:0042475"}


id: GO:0098735
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the force of heart muscle contraction.","definition_xrefs":["GOC:BHF","GOC:rl","GOC:mtg_cardiac_conduct_nov11","GOC:dos","PMID:17242280"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of the force of heart contraction","termid":"GO:0002026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of the force of heart contraction","termid":"GO:0098735"}


id: MONDO:0010490
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of congenital disorders of N-linked glycosylation characterized by neurologic abnormalities (global developmental delay in language, social skills and fine and gross motor development, intellectual disability, hypotonia, microcephaly, seizures/epilepsy), facial dysmorphism (deep set eyes, large ears, hypoplastic vermillion of upper lip, large mouth with widely spaced teeth), feeding problems often due to chewing difficulties and aversion to food with certain textures, failure to thrive, gastrointestinal abnormalities (reflux or vomiting) and strabismus. The disease is caused by mutations in the gene SSR4(Xq28).","definition_xrefs":["Orphanet:370927"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type I","termid":"MONDO:0005500"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"SSR4-congenital disorder of glycosylation","secondary_identifiers":["DOID:0080574","GARD:12405","SCTID:733115009","OMIM:300934","UMLS:C4012395","MEDGEN:860832"],"synonyms":[{"name":"CDG 1Y","type":"related"},{"name":"CDG Iy","type":"related"},{"name":"CDG syndrome type Iy","type":"exact"},{"name":"CDG-Iy","type":"exact"},{"name":"CDG1Y","type":"exact"},{"name":"CDGIy","type":"related"},{"name":"SSR4-CDG","type":"exact"},{"name":"SSR4-congenital disorder of glycosylation","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type Iy","type":"exact"},{"name":"congenital disorder of glycosylation type 1y","type":"exact"},{"name":"congenital disorder of glycosylation type Iy","type":"exact"},{"name":"congenital disorder of glycosylation, type Iy","type":"related"},{"name":"congenital disorder of glycosylation, type Iy, X-linked recessive","type":"exact"}],"termid":"MONDO:0010490","xrefs":{"Monarch":{"xref_id":"0010490"}}}


id: MONDO:0004399
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epithelial malignant thymoma (obsolete MONDO:0004399)","termid":"MONDO:0004399","xrefs":{"Monarch":{"xref_id":"0004399"}}}


id: GO:1901761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving oxytetracycline.","definition_xrefs":["GOC:TermGenie","GOC:yaf","PMID:8163168"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide metabolic process","termid":"GO:0030638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"oxytetracycline metabolic process","synonyms":[{"name":"oxytetracycline metabolism","type":"exact"}],"termid":"GO:1901761"}


id: PBO:0055852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LDL receptor related protein 2","termid":"PBO:0055852"}


id: PBO:0059038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MMP25 antisense RNA 1","termid":"PBO:0059038"}


id: GO:0009965
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the leaf are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant organ morphogenesis","termid":"GO:1905392"},{"relation_name":"part_of","term_name":"shoot system morphogenesis","termid":"GO:0010016"},{"relation_name":"part_of","term_name":"leaf development","termid":"GO:0048366"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"leaf morphogenesis","termid":"GO:0009965"}


id: PBO:0083806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein that forms a dimer with Ntr2p; also forms a trimer, with Ntr2p and Prp43p, that is involved in spliceosome disassembly; found also in a multisubunit complex with the splicing factor Clf1p; suppressor of prp38-1 mutation","termid":"PBO:0083806"}


id: MONDO:0012145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any age-related macular degeneration in which the cause of the disease is a mutation in the FBLN5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"age-related macular degeneration","termid":"MONDO:0005150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"macular degeneration, age-related, 3","secondary_identifiers":["MEDGEN:373276","UMLS:C1837187","MESH:C563838","OMIM:608895"],"synonyms":[{"name":"ARMD3","type":"related"},{"name":"FBLN5 age-related macular degeneration","type":"exact"},{"name":"HNARMD","type":"related"},{"name":"age-related macular degeneration caused by mutation in FBLN5","type":"exact"},{"name":"macular Degeneration, age-related, type 3","type":"exact"},{"name":"macular degeneration, age-related, 3","type":"exact"},{"name":"neuropathy, hereditary, with or without age-related macular Degeneration","type":"related"},{"name":"neuropathy, hereditary, with or without age-related macular degeneration","type":"related"}],"termid":"MONDO:0012145","xrefs":{"Monarch":{"xref_id":"0012145"}}}


id: GO:0005388
data:
  {"annotated_genes":["SJAG_03850","SJAG_01400"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73173,81976],"is_not":false,"summary":null,"term":"GO:0005388"}]},"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 + Ca2+(in) = ADP + phosphate + Ca2+(out).","definition_xrefs":["RHEA:18105"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium ion transmembrane transporter activity","termid":"GO:0015085"},{"relation_name":"is_a","term_name":"P-type ion transporter activity","termid":"GO:0015662"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01400":null,"SJAG_03850":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"P-type calcium transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-427910","MetaCyc:TRANS-RXN-194","Reactome:R-HSA-418309","EC:7.2.2.10","Reactome:R-HSA-9662114","Reactome:R-HSA-9664214","Reactome:R-HSA-418365","Reactome:R-HSA-936883"],"synonyms":[{"name":"ATP-dependent calcium transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled calcium transmembrane transporter activity","type":"related"},{"name":"Ca(2+)-transporting ATPase activity","type":"related"},{"name":"Ca2+-transporting ATPase activity","type":"related"},{"name":"calcium efflux ATPase","type":"narrow"},{"name":"calcium pump","type":"broad"},{"name":"calcium transmembrane transporter activity, phosphorylative mechanism","type":"exact"},{"name":"calcium transporting ATPase activity","type":"exact"},{"name":"calcium-translocating P-type ATPase activity","type":"narrow"},{"name":"calcium-transporting ATPase activity","type":"exact"},{"name":"sarco(endo)plasmic reticulum Ca2+-ATPase","type":"narrow"}],"termid":"GO:0005388","terms_by_termid":{"GO:0005388":null}}


id: PBO:0080639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 87","termid":"PBO:0080639"}


id: PBO:0071944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 21","termid":"PBO:0071944"}


id: MOD:01436
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to cyclo[(prolylserin)-O-yl] cysteinate.","definition_xrefs":["PubMed:7961166","RESID:AA0489#CYS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclo[(prolylserin)-O-yl] cysteinate","termid":"MOD:01629"}],"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":"cyclo[(prolylserin)-O-yl] cysteinate (Cys)","synonyms":[{"name":"(3,6-dioxopyrrolo[4,5-a]piperazin-2-yl)methyl cysteinate","type":"exact"},{"name":"MOD_RES Cyclo[(prolylserin)-O-yl] cysteinate","type":"exact"},{"name":"[(3S,8aS)-1,4-dioxooctahydropyrrolo[1,2-a]pyrazin-3-yl]methyl (2R)-2-amino-3-sulfanylpropanoate","type":"exact"},{"name":"cyclo[(prolylserin)-O-yl] cysteinate","type":"exact"}],"termid":"MOD:01436"}


id: FYPO:0007314
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 acetylation of lysine at position 12 of histone H4 at the central core of the centromeric regions occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H4-K12 acetylation at centromere during vegetative growth","termid":"FYPO:0007306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0000002","FYPO:0002274","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"increased histone H4-K12 acetylation at centromere central core during vegetative growth","synonyms":[{"name":"increased histone H4-K12 acetylation at centromere central core during mitotic cell cycle","type":"related"},{"name":"increased histone H4-K12 acetylation at centromeric central core during vegetative growth","type":"exact"},{"name":"increased histone H4K12 acetylation at centromere central core during vegetative growth","type":"exact"}],"termid":"FYPO:0007314"}


id: FYPO:0009109
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell growth phenotype in which cell population growth is decreased relative to normal after short incubation in hydroxyurea.","direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"},{"relation_name":"is_a","term_name":"increased sensitivity to chemical","termid":"FYPO:0002683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0002057","FYPO:0002683","FYPO:0005447","FYPO:0002058","FYPO:0000139","FYPO:0002060"],"is_obsolete":false,"name":"decreased vegetative cell population growth after short incubation in hydroxyurea","secondary_identifiers":["PMID:37200372"],"synonyms":[{"name":"decreased vegetative cell population growth after acute hydroxyurea treatment","type":"exact"}],"termid":"FYPO:0009109"}


id: PBO:0056510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallo-beta-lactamase domain containing 2","termid":"PBO:0056510"}


id: PBO:0031682
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_peroxisome_degradation","termid":"PBO:0031682"}


id: PBO:0002293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial single-stranded DNA binding protein Rim1","termid":"PBO:0002293"}


id: PBO:0031525
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_DNA-1,N6-ethenoadenine_N-glycosylase_activity","termid":"PBO:0031525"}


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


id: PBO:0076338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin 6","termid":"PBO:0076338"}


id: FYPO:0002544
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of serine residues three positions C-terminal to arginine residues (i.e. in Arg-X-X-Ser, or RxxS, sequences) does not occur during a cellular response to hydrogen peroxide.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete abolished protein serine phosphorylation at RxxS site during cellular response to hydrogen peroxide (obsolete FYPO:0002544)","synonyms":[{"name":"abolished protein serine phosphorylation at Arg-X-X-Ser site during cellular response to hydrogen peroxide","type":"exact"},{"name":"abolished protein serine phosphorylation at PAS site during cellular response to hydrogen peroxide","type":"exact"},{"name":"abolished protein serine phosphorylation at RxxS site during cellular response to H2O2","type":"exact"},{"name":"abolished protein serine phosphorylation at RxxS site during cellular response to hydrogen peroxide during mitotic cell cycle","type":"related"},{"name":"abolished protein serine phosphorylation at RxxS site during cellular response to hydrogen peroxide during vegetative growth","type":"exact"},{"name":"abolished protein serine phosphorylation at arginine-X-X-serine site during cellular response to hydrogen peroxide","type":"exact"},{"name":"abolished protein serine phosphorylation at phospho-Akt site during cellular response to hydrogen peroxide","type":"exact"},{"name":"protein serine phosphorylation abolished at RxxS site during cellular response to hydrogen peroxide","type":"exact"}],"termid":"FYPO:0002544"}


id: PBO:0085660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in mRNA turnover and ribosome assembly; required at post-transcriptional step for efficient retrotransposition; localizes to the nucleolus","termid":"PBO:0085660"}


id: PBO:0089880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor Spf30","termid":"PBO:0089880"}


id: PBO:0083673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endoplasmic reticulum zinc transporter; part of a heterodimeric transporter with Zrg17p that transfers zinc from the cytosol to the ER lumen; member of the cation diffusion facilitator family of efflux pumps; localizes to ER and nucleus; mutations affect the cellular distribution of zinc and also confer defects in meiotic recombination between homologous chromatids","termid":"PBO:0083673"}


id: GO:0004820
data:
  {"annotated_genes":["SJAG_01352"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74687],"is_not":false,"summary":null,"term":"GO:0004820"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + glycine + tRNA(Gly) = AMP + diphosphate + glycyl-tRNA(Gly).","definition_xrefs":["EC:6.1.1.14"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyl-tRNA ligase activity","termid":"GO:0004812"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01352":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824","GO:0140098","GO:0140101"],"is_obsolete":false,"name":"glycine-tRNA ligase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-380240","MetaCyc:GLYCINE--TRNA-LIGASE-RXN","Reactome:R-HSA-380048","RHEA:16013"],"synonyms":[{"name":"glycine:tRNAGly ligase (AMP-forming) activity","type":"related"},{"name":"glycyl translase activity","type":"related"},{"name":"glycyl-tRNA synthetase activity","type":"exact"},{"name":"glycyl-transfer RNA synthetase activity","type":"related"},{"name":"glycyl-transfer ribonucleate synthetase activity","type":"related"},{"name":"glycyl-transfer ribonucleic acid synthetase activity","type":"related"}],"termid":"GO:0004820","terms_by_termid":{"GO:0004820":null}}


id: MONDO:1011143
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Choanal atresia that occurs in llama.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choanal atresia, non-human animal","termid":"MONDO:1010289"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choanal atresia, llama","secondary_identifiers":["OMIA:001764-9844"],"termid":"MONDO:1011143","xrefs":{"Monarch":{"xref_id":"1011143"}}}


id: PBO:0044021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"casein kinase 1 gamma 3","termid":"PBO:0044021"}


id: GO:0007601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive a visual stimulus, convert it to a molecular signal, and recognize and characterize the signal. Visual stimuli are detected in the form of photons and are processed to form an image.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory perception of light stimulus","termid":"GO:0050953"}],"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":"visual perception","secondary_identifiers":["Wikipedia:Visual_perception"],"synonyms":[{"name":"sense of sight","type":"exact"},{"name":"sensory visual perception","type":"exact"},{"name":"vision","type":"exact"}],"termid":"GO:0007601"}


id: GO:0097658
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A nuclear ubiquitin ligase multiprotein complex located in the inner nuclear membrane (INM) that recognizes and ubiquitinates misfolded INM proteins and also some proteins involved in sterol biosynthesis, during ER-associated protein degradation (ERAD). In S. cerevisiae, this complex contains the ubiquitin ligases Asi1p and Asi3p.","definition_xrefs":["PMID:25236469","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear ubiquitin ligase complex","termid":"GO:0000152"},{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"nuclear inner membrane","termid":"GO:0005637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"Asi complex","termid":"GO:0097658"}


id: GO:0060602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The growth process in which a branch increases in length from its base to its tip.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axis elongation","termid":"GO:0003401"},{"relation_name":"part_of","term_name":"morphogenesis of a branching epithelium","termid":"GO:0061138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"branch elongation of an epithelium","termid":"GO:0060602"}


id: PBO:0076895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 49","termid":"PBO:0076895"}


id: GO:1990188
data:
  {"annotated_genes":["SJAG_03689","SJAG_00471"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107214,117853],"is_not":false,"summary":null,"term":"GO:1990188"}]},"cv_name":"molecular_function","definition":"Binding to euchromatin, a dispersed and relatively uncompacted form of chromatin.","definition_xrefs":["GOC:vw","PMID:22431512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatin binding","termid":"GO:0003682"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00471":null,"SJAG_03689":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":"euchromatin binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990188","terms_by_termid":{"GO:1990188":null}}


id: MONDO:0060774
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A superficial polypoid lesion that arises from the vagina. It is characterized by the presence of a fibroblastic stroma which is often myxoid, covered by squamous epithelial cells.","definition_xrefs":["NCIT:C4948"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyp of vagina","termid":"MONDO:0021394"},{"relation_name":"is_a","term_name":"fibroepithelial polyp","termid":"MONDO:0060765"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginal fibroepithelial polyp","secondary_identifiers":["MEDGEN:152894","UMLS:C0750071"],"synonyms":[{"name":"fibroepithelial polyp of the vagina","type":"exact"},{"name":"fibroepithelial polyp of vagina","type":"exact"},{"name":"vaginal fibroepithelial polyp","type":"exact"},{"name":"vaginal fibroepithelial stromal polyp","type":"exact"}],"termid":"MONDO:0060774","xrefs":{"Monarch":{"xref_id":"0060774"}}}


id: GO:0033296
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to the D- or L-enantiomer of rhamnose.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide binding","termid":"GO:0048029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"rhamnose binding","termid":"GO:0033296"}


id: MONDO:0005052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Irritable bowel syndrome (IBS) is a chronic functional condition of the lower gastrointestinal (GI) tract characterized by abdominal pain or discomfort and disordered bowel habit (diarrhea, constipation, or fluctuation between the two).","definition_xrefs":["PMID:2174034","PMID:28657875"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"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":"irritable bowel syndrome","secondary_identifiers":["ICD9:564.1","DOID:9778","icd11.foundation:1158238623","ICD10CM:K58","EFO:0000555","NCIT:C82343","MESH:D043183","SCTID:10743008","UMLS:C0022104","MEDGEN:5897"],"synonyms":[{"name":"IBD","type":"exact"},{"name":"IBS","type":"exact"},{"name":"irritable bowel syndrome","type":"exact"},{"name":"irritable colon","type":"exact"},{"name":"mucus colitis","type":"exact"},{"name":"psychogenic IBS","type":"related"},{"name":"spastic colon","type":"exact"}],"termid":"MONDO:0005052","xrefs":{"Monarch":{"xref_id":"0005052"}}}


id: FYPO:0007080
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the initial release of duplicated spindle pole bodies that begins with the nucleation of microtubules from each SPB within the nucleus, and occurs as part of the first meiotic nuclear division, is abnormal.","definition_xrefs":["PomBase:mah","PMID:31532702"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body organization","termid":"FYPO:0003560"},{"relation_name":"is_a","term_name":"abnormal meiosis I","termid":"FYPO:0003603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0000054"],"is_obsolete":false,"name":"abnormal initial meiotic spindle pole body separation in meiosis I","synonyms":[{"name":"abnormal initial meiotic spindle pole body separation in first meiotic nuclear division","type":"exact"},{"name":"abnormal initial mitotic SPB separation in meiosis I","type":"exact"}],"termid":"FYPO:0007080"}


id: GO:0071732
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 nitric oxide stimulus.","definition_xrefs":["GOC:yaf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitric oxide","termid":"GO:0071731"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"cellular response to reactive nitrogen species","termid":"GO:1902170"}],"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 nitric oxide","termid":"GO:0071732"}


id: PBO:0046012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 1 pseudogene 7","termid":"PBO:0046012"}


id: PATO:0001460
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A sensitivity of a process inhering in a biological process by virtue of the process unfolding in a location without oxygen.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitivity of a process to oxygen","termid":"PATO:0001458"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaerobic (for occurrence)","termid":"PATO:0001460"}


id: FYPO:0003816
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell requires histidine or lysine in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxotrophy","termid":"FYPO:0000128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"growth auxotrophic for histidine or lysine","synonyms":[{"name":"growth auxotrophic for histidine or lysine during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for histidine or lysine during vegetative growth","type":"exact"},{"name":"growth auxotrophic for lysine or histidine","type":"exact"},{"name":"histidine or lysine auxotrophy","type":"exact"}],"termid":"FYPO:0003816"}


id: GO:1905356
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of snRNA pseudouridine synthesis.","definition_xrefs":["PMID:27268497","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of RNA metabolic process","termid":"GO:0051252"},{"relation_name":"regulates","term_name":"snRNA pseudouridine synthesis","termid":"GO:0031120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016073"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016073","GO:0008150"],"is_obsolete":false,"name":"regulation of snRNA pseudouridine synthesis","termid":"GO:1905356"}


id: FYPO:0002645
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of threonine residues in one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete decreased protein threonine phosphorylation during vegetative growth (obsolete FYPO:0002645)","synonyms":[{"name":"decreased peptidyl-threonine phosphorylation during vegetative growth","type":"exact"},{"name":"decreased protein threonine phosphorylation during mitotic cell cycle","type":"related"},{"name":"decreased threonine phosphorylation during vegetative growth","type":"exact"},{"name":"reduced protein threonine phosphorylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002645"}


id: PBO:0060567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NBPF member 3","termid":"PBO:0060567"}


id: PR:Q9Y803
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An RNA-binding protein EIF1AD that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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":"S1-like domain-containing protein C146.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC146.08c","secondary_identifiers":["UniProtKB:Q9Y803"],"synonyms":[{"name":"Spom972h-EIF1AD","type":"exact"}],"termid":"PR:Q9Y803"}


id: MONDO:0012215
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, late adult-onset myofibrillar myopathy characterized by progressive distal muscle weakness associated with peripheral neuropathy and hyporeflexia. Ambulation may be lost within a few years.","definition_xrefs":["Orphanet:98911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"muscular dystrophy, limb-girdle, autosomal dominant","termid":"MONDO:0015151"},{"relation_name":"is_a","term_name":"autosomal dominant distal myopathy","termid":"MONDO:0016108"},{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"myofibrillar myopathy 3","secondary_identifiers":["UMLS:C3714934","GARD:16871","MESH:C563775","MESH:C535906","Orphanet:268129","MEDGEN:811509","DOID:0080094","OMIM:609200","OMIM:182920","DOID:0110300","MESH:C000598645","Orphanet:266","SCTID:765196004","SCTID:765092004","OMIM:159000","SCTID:719985001"],"synonyms":[{"name":"LGMD1","type":"related"},{"name":"LGMD1A","type":"exact"},{"name":"MFM3","type":"related"},{"name":"MYOT autosomal dominant distal myopathy","type":"exact"},{"name":"MYOT autosomal dominant limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal dominant distal myopathy caused by mutation in MYOT","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy caused by mutation in MYOT","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy type 1A","type":"exact"},{"name":"autosomal dominant spheroid body myopathy","type":"related"},{"name":"distal myotilinopathy","type":"exact"},{"name":"limb-girdle muscular dystrophy due to myotilin deficiency","type":"exact"},{"name":"limb-girdle muscular dystrophy type 1A","type":"related"},{"name":"muscular dystrophy limb-girdle type 1A","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 1A","type":"related"},{"name":"muscular dystrophy, proximal, type 1A","type":"related"},{"name":"myofibrillar myopathy type 3","type":"exact"},{"name":"myopathy, myofibrillar, 3","type":"related"},{"name":"myopathy, myofibrillar, myotilin-related","type":"related"},{"name":"myopathy, myofibrillar, type 3","type":"exact"},{"name":"myopathy, spheroid body","type":"related"},{"name":"myotilinopathy","type":"exact"},{"name":"proximal muscular dystrophy type 1A","type":"exact"},{"name":"spheroid body myopathy","type":"exact"}],"termid":"MONDO:0012215","xrefs":{"Monarch":{"xref_id":"0012215"}}}


id: PBO:0051995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"junctional adhesion molecule 3","termid":"PBO:0051995"}


id: PBO:0001659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SM22/transgelin-like actin modulating protein Stg1","termid":"PBO:0001659"}


id: GO:0019479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-alanine to D-lactate and ammonia.","definition_xrefs":["MetaCyc:ALACAT2-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-alanine catabolic process","termid":"GO:0042853"}],"gene_count":0,"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:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"L-alanine oxidation to D-lactate and ammonia","termid":"GO:0019479"}


id: MONDO:1012132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin G deficiency, non-human animal","termid":"MONDO:1011727"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin G deficiency, dog","secondary_identifiers":["OMIA:000554-9615"],"termid":"MONDO:1012132","xrefs":{"Monarch":{"xref_id":"1012132"}}}


id: GO:0002570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of variable numbers of random nucleotides by terminal deoxytransferase in the N regions of heavy chain immunoglobulin genes. N regions are found at the V-D and D-J recombinational junctions.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immune receptors by N region addition","termid":"GO:0002569"},{"relation_name":"is_a","term_name":"somatic diversification of immunoglobulins","termid":"GO:0016445"},{"relation_name":"part_of","term_name":"somatic recombination of immunoglobulin gene segments","termid":"GO:0016447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006310","GO:0006259","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"somatic diversification of immunoglobulin genes by N region addition","synonyms":[{"name":"somatic diversification of antibody genes by N region addition","type":"exact"}],"termid":"GO:0002570"}


id: PBO:0030576
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vacuolar_methionine_level","termid":"PBO:0030576"}


id: GO:1905017
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of isoleucine-tRNA ligase activity.","definition_xrefs":["PMID:1665486","GO_REF:0000059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of isoleucine-tRNA ligase activity (obsolete GO:1905017)","synonyms":[{"name":"activation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"narrow"},{"name":"activation of isoleucine translase activity","type":"narrow"},{"name":"activation of isoleucine-tRNA ligase activity","type":"narrow"},{"name":"activation of isoleucine-tRNA synthetase activity","type":"narrow"},{"name":"activation of isoleucine-transfer RNA ligase activity","type":"narrow"},{"name":"activation of isoleucyl-tRNA synthetase activity","type":"narrow"},{"name":"activation of isoleucyl-transfer RNA synthetase activity","type":"narrow"},{"name":"activation of isoleucyl-transfer ribonucleate synthetase activity","type":"narrow"},{"name":"positive regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"positive regulation of isoleucine translase activity","type":"exact"},{"name":"positive regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"positive regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"positive regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"positive regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"positive regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"up regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"up regulation of isoleucine translase activity","type":"exact"},{"name":"up regulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"up regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"up regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"up regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"up regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"up regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"up-regulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"up-regulation of isoleucine translase activity","type":"exact"},{"name":"up-regulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"up-regulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"up-regulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"up-regulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"up-regulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"up-regulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"},{"name":"upregulation of L-isoleucine:tRNAIle ligase (AMP-forming)","type":"exact"},{"name":"upregulation of isoleucine translase activity","type":"exact"},{"name":"upregulation of isoleucine-tRNA ligase activity","type":"exact"},{"name":"upregulation of isoleucine-tRNA synthetase activity","type":"exact"},{"name":"upregulation of isoleucine-transfer RNA ligase activity","type":"exact"},{"name":"upregulation of isoleucyl-tRNA synthetase activity","type":"exact"},{"name":"upregulation of isoleucyl-transfer RNA synthetase activity","type":"exact"},{"name":"upregulation of isoleucyl-transfer ribonucleate synthetase activity","type":"exact"}],"termid":"GO:1905017"}


id: PBO:0003312
data:
  {"annotation_feature_type":"gene","cv_name":"pathway","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functions coordinately with the protein kinase C pathway","termid":"PBO:0003312"}


id: MONDO:0957921
data:
  {"annotated_genes":["SJAG_02701"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88040],"is_not":false,"summary":null,"term":"MONDO:0957921"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Cornelia de Lange syndrome","termid":"MONDO:0016033"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02701":null},"genotype_count":0,"is_obsolete":false,"name":"Cornelia de Lange syndrome 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5882712","MEDGEN:1848930","OMIM:620568","DOID:0060970"],"termid":"MONDO:0957921","terms_by_termid":{"MONDO:0957921":null},"xrefs":{"Monarch":{"xref_id":"0957921"}}}


id: GO:0003687
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA replication factor (obsolete GO:0003687)","synonyms":[{"name":"DNA replication factor","type":"exact"}],"termid":"GO:0003687"}


id: PBO:0060760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 4","termid":"PBO:0060760"}


id: FYPO:0001496
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is viable, is elongated, and contain more than one septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated multiseptate vegetative cell","termid":"FYPO:0000223"},{"relation_name":"is_a","term_name":"viable elongated vegetative cell","termid":"FYPO:0001492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000004","FYPO:0000005","FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0000032"],"is_obsolete":false,"name":"viable elongated multiseptate vegetative cell","synonyms":[{"name":"elongated multiseptate viable vegetative cell","type":"exact"},{"name":"elongated viable multiseptate cell during vegetative growth","type":"exact"},{"name":"viable elongated multiseptate vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001496"}


id: GO:0050862
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of signaling pathways initiated by the cross-linking of an antigen receptor on a T cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T cell receptor signaling pathway","termid":"GO:0050856"},{"relation_name":"is_a","term_name":"positive regulation of antigen receptor-mediated signaling pathway","termid":"GO:0050857"},{"relation_name":"positively_regulates","term_name":"T cell receptor signaling pathway","termid":"GO:0050852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of T cell receptor signaling pathway","synonyms":[{"name":"activation of T cell receptor signaling pathway","type":"narrow"},{"name":"positive regulation of T cell receptor signalling pathway","type":"exact"},{"name":"positive regulation of T lymphocyte receptor signaling pathway","type":"exact"},{"name":"positive regulation of T lymphocyte receptor signalling pathway","type":"exact"},{"name":"positive regulation of T-cell receptor signaling pathway","type":"exact"},{"name":"positive regulation of T-lymphocyte receptor signaling pathway","type":"exact"},{"name":"positive regulation of T-lymphocyte receptor signalling pathway","type":"exact"},{"name":"positive regulation of TCR signaling pathway","type":"exact"},{"name":"stimulation of T cell receptor signaling pathway","type":"narrow"},{"name":"up regulation of T cell receptor signaling pathway","type":"exact"},{"name":"up-regulation of T cell receptor signaling pathway","type":"exact"},{"name":"upregulation of T cell receptor signaling pathway","type":"exact"}],"termid":"GO:0050862"}


id: PATO:0002024
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's location of features or characteristics along the anterior-posterior axis.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positional polarity","termid":"PATO:0001769"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anterior-posterior polarity","synonyms":[{"name":"rostral-caudal polarity ","type":"exact"},{"name":"superior-caudal polarity (human torso)","type":"exact"}],"termid":"PATO:0002024"}


id: PBO:0000738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LEA domain protein","termid":"PBO:0000738"}


id: GO:0003253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a neural crest cell from one site to another that will contribute to the morphogenesis of the outflow tract.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural crest cell migration","termid":"GO:0001755"},{"relation_name":"is_a","term_name":"cell migration involved in heart development","termid":"GO:0060973"},{"relation_name":"part_of","term_name":"cardiac neural crest cell development involved in outflow tract morphogenesis","termid":"GO:0061309"}],"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 neural crest cell migration involved in outflow tract morphogenesis","termid":"GO:0003253"}


id: FYPO:0000656
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of DNA binding by a gene product is abnormal, when a gene or the bound DNA sequence is mutated. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA binding phenotype","termid":"FYPO:0000653"},{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000653"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000653","FYPO:0000652","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"abnormal DNA binding","termid":"FYPO:0000656"}


id: GO:0042802
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an identical protein or proteins.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"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:0005488","GO:0005515"],"is_obsolete":false,"name":"identical protein binding","synonyms":[{"name":"isoform-specific homophilic binding","type":"exact"},{"name":"protein homopolymerization","type":"related"}],"termid":"GO:0042802"}


id: GO:0043450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an alkene, any acyclic branched or unbranched hydrocarbon having one carbon-carbon double bond and the general formula CnH2n.","definition_xrefs":["Wikipedia:Alkene","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkene metabolic process","termid":"GO:0043449"},{"relation_name":"is_a","term_name":"olefin biosynthetic process","termid":"GO:1900674"}],"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":"alkene biosynthetic process","synonyms":[{"name":"alkene anabolism","type":"exact"},{"name":"alkene biosynthesis","type":"exact"},{"name":"alkene formation","type":"exact"},{"name":"alkene synthesis","type":"exact"}],"termid":"GO:0043450"}


id: PBO:0036451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear export factor family protein, human LENG8 ortholog","termid":"PBO:0036451"}


id: GO:0160232
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex containing Integrator and protein phosphatase 2A core enzyme (PP2A-AC) that stably associates with the C-terminus of RNA polymerase II and promotes premature RNA polymerase II transcription termination.","definition_xrefs":["PMID:38570683","PMID:33243860"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"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:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"INTAC complex","synonyms":[{"name":"integrator-PP2A complex","type":"exact"}],"termid":"GO:0160232"}


id: GO:0006937
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of muscle contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle system process","termid":"GO:0090257"},{"relation_name":"regulates","term_name":"muscle contraction","termid":"GO:0006936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of muscle contraction","termid":"GO:0006937"}


id: PBO:0050089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group AT-hook 2","termid":"PBO:0050089"}


id: PR:O74822
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC337.11 gene.","definition_xrefs":["UniProtKB:O74822","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":"zinc-type alcohol dehydrogenase-like protein C337.11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC337.11","synonyms":[{"name":"Spom972h-SPBC337.11","type":"exact"}],"termid":"PR:O74822"}


id: PBO:0076706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor 7","termid":"PBO:0076706"}


id: PBO:0016586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transthyretin/hydroxyisourate hydrolase (predicted)","termid":"PBO:0016586"}


id: PBO:0039425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiopoietin like 5","termid":"PBO:0039425"}


id: GO:0019759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of glycosinolates, substituted thioglycosides found in rapeseed products and related cruciferae.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete glycosinolate catabolic process (obsolete GO:0019759)","synonyms":[{"name":"glycosinolate breakdown","type":"exact"},{"name":"glycosinolate catabolism","type":"exact"},{"name":"glycosinolate degradation","type":"exact"}],"termid":"GO:0019759"}


id: PBO:0090344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hsp40 family DNAJ domain protein Psi1","termid":"PBO:0090344"}


id: MONDO:0044970
data:
  {"annotated_genes":["SJAG_16456","SJAG_02480","SJAG_00354","SJAG_04094","SJAG_01865","SJAG_03563","SJAG_03310","SJAG_02324","SJAG_02201","SJAG_04568","SJAG_03553","SJAG_02007","SJAG_01589","SJAG_02721","SJAG_04843","SJAG_04560","SJAG_02398","SJAG_01190","SJAG_01490","SJAG_04738","SJAG_04317","SJAG_03222","SJAG_02658","SJAG_02977","SJAG_04019","SJAG_03550","SJAG_03046","SJAG_01405","SJAG_02848","SJAG_00186","SJAG_00532","SJAG_01147","SJAG_02302","SJAG_02384","SJAG_01820","SJAG_02229","SJAG_04473","SJAG_00133","SJAG_00547","SJAG_00308","SJAG_MIT15","SJAG_04588","SJAG_01004","SJAG_01368","SJAG_05560","SJAG_01355","SJAG_01174","SJAG_06046","SJAG_03114","SJAG_03490","SJAG_04183","SJAG_06002","SJAG_02265","SJAG_04816","SJAG_02158","SJAG_MIT04","SJAG_06392","SJAG_04378","SJAG_03296","SJAG_03104","SJAG_MIT13","SJAG_02895","SJAG_03064","SJAG_01575","SJAG_00997","SJAG_02353","SJAG_01866","SJAG_00634","SJAG_00522","SJAG_04885","SJAG_07005","SJAG_03332","SJAG_02452","SJAG_02397","SJAG_03322","SJAG_00459","SJAG_04016","SJAG_01797","SJAG_04849","SJAG_04367","SJAG_03014","SJAG_04397","SJAG_00721","SJAG_03290","SJAG_01417","SJAG_00885","SJAG_00933","SJAG_00513","SJAG_01063","SJAG_04862","SJAG_01164","SJAG_01524","SJAG_00088","SJAG_00319","SJAG_00894","SJAG_03461","SJAG_03773","SJAG_02016","SJAG_00217","SJAG_04639","SJAG_00358","SJAG_03585","SJAG_02564","SJAG_01303","SJAG_MIT20","SJAG_02548","SJAG_04348","SJAG_04285","SJAG_01671","SJAG_00852","SJAG_01179","SJAG_00103","SJAG_05199","SJAG_01077","SJAG_01890","SJAG_05271","SJAG_00866","SJAG_00260","SJAG_01924","SJAG_03155","SJAG_03173","SJAG_03641","SJAG_02615","SJAG_02306","SJAG_06022","SJAG_05218","SJAG_02006","SJAG_05305","SJAG_04450","SJAG_02428","SJAG_00797","SJAG_03813","SJAG_03099","SJAG_01503","SJAG_02050","SJAG_04000","SJAG_02464","SJAG_04856","SJAG_00755","SJAG_02641","SJAG_00080","SJAG_02646","SJAG_00653","SJAG_03071","SJAG_04665","SJAG_01647","SJAG_02656","SJAG_01649","SJAG_01413","SJAG_00255","SJAG_04553","SJAG_03584","SJAG_MIT03","SJAG_00601","SJAG_03701","SJAG_02643","SJAG_02504","SJAG_02457","SJAG_01640","SJAG_07003","SJAG_00404","SJAG_06603","SJAG_01577","SJAG_03992","SJAG_03782","SJAG_01043"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87315],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013111"},{"annotations":[87004],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060582"},{"annotations":[87551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008134"},{"annotations":[88096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012784"},{"annotations":[87674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008858"},{"annotations":[88890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009872"},{"annotations":[87140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011451"},{"annotations":[86893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014051"},{"annotations":[86872],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014667"},{"annotations":[86870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014668"},{"annotations":[87478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012557"},{"annotations":[88663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014455"},{"annotations":[88679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014467"},{"annotations":[87724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014733"},{"annotations":[88238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011829"},{"annotations":[88088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013838"},{"annotations":[87654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033615"},{"annotations":[89010,89011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013969"},{"annotations":[88846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013986"},{"annotations":[88845],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013987"},{"annotations":[87711,87710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014190"},{"annotations":[87765],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012510"},{"annotations":[88062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014397"},{"annotations":[88063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014398"},{"annotations":[88523],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014525"},{"annotations":[87200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014547"},{"annotations":[87021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014636"},{"annotations":[86882],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014684"},{"annotations":[87644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012534"},{"annotations":[89056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013306"},{"annotations":[87752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013570"},{"annotations":[88248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013811"},{"annotations":[87438],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014269"},{"annotations":[88683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020727"},{"annotations":[87720,87719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014775"},{"annotations":[87001,87002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054677"},{"annotations":[86884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054741"},{"annotations":[86883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054742"},{"annotations":[87782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054781"},{"annotations":[87902],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032712"},{"annotations":[87924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032726"},{"annotations":[87292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030006"},{"annotations":[87293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030007"},{"annotations":[87297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030008"},{"annotations":[87304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030017"},{"annotations":[87150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033533"},{"annotations":[87152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033534"},{"annotations":[87151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033537"},{"annotations":[88357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030311"},{"annotations":[88921],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859228"},{"annotations":[87497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859323"},{"annotations":[87381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859337"},{"annotations":[87849],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957992"},{"annotations":[87317,87318],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013116"},{"annotations":[89077,86796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010799"},{"annotations":[88087],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013837"},{"annotations":[88824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015003"},{"annotations":[87311,87310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013726"},{"annotations":[88085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013840"},{"annotations":[88084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[87756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012512"},{"annotations":[87209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011730"},{"annotations":[87733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011308"},{"annotations":[87617],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014261"},{"annotations":[87223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012191"},{"annotations":[86851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009706"},{"annotations":[87066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014020"},{"annotations":[87907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014882"},{"annotations":[87875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014869"},{"annotations":[88713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013458"},{"annotations":[87744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014162"},{"annotations":[87329,87330,87331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010788"},{"annotations":[88798],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014976"},{"annotations":[88719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012622"},{"annotations":[89016],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013971"},{"annotations":[88439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013762"},{"annotations":[87226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014576"},{"annotations":[87937,87936,87938,87939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010789"},{"annotations":[88033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032617"},{"annotations":[88039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032630"},{"annotations":[88041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032631"},{"annotations":[88027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032609"},{"annotations":[88030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032612"},{"annotations":[87368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030935"},{"annotations":[87369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030937"},{"annotations":[87341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030974"},{"annotations":[88490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032909"},{"annotations":[87498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859321"},{"annotations":[87523],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033639"},{"annotations":[87525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033645"},{"annotations":[87524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033649"},{"annotations":[87536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033651"},{"annotations":[87530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033653"},{"annotations":[87532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033654"},{"annotations":[87533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033655"},{"annotations":[87539,87537,87538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033656"},{"annotations":[87515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033635"},{"annotations":[87512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033636"},{"annotations":[87521],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033637"},{"annotations":[87522],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033638"},{"annotations":[88141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020858"},{"annotations":[88672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032869"},{"annotations":[87989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100294"},{"annotations":[88259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007415"},{"annotations":[86914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014063"},{"annotations":[86915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014064"},{"annotations":[86913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014065"},{"annotations":[86917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014066"},{"annotations":[87718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014194"},{"annotations":[88207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014356"},{"annotations":[88213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014364"},{"annotations":[88493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014496"},{"annotations":[89025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0700250"},{"annotations":[88333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859160"},{"annotations":[88369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859520"},{"annotations":[86891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014091"},{"annotations":[87278],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011421"},{"annotations":[88341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957254"},{"annotations":[88340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957255"},{"annotations":[86912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014062"},{"annotations":[87143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011283"},{"annotations":[89004],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014959"},{"annotations":[87698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014175"},{"annotations":[87612],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014820"},{"annotations":[88991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014943"},{"annotations":[88805,88804],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032815"},{"annotations":[87281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032932"},{"annotations":[86861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0976132"},{"annotations":[88862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008758"},{"annotations":[88864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013350"},{"annotations":[87421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009747"},{"annotations":[88109],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012792"},{"annotations":[89034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009504"},{"annotations":[88108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012791"},{"annotations":[87934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013865"},{"annotations":[87473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020714"},{"annotations":[87046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044714"},{"annotations":[87722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010779"},{"annotations":[87949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013877"},{"annotations":[86927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011582"},{"annotations":[88648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0975806"},{"annotations":[87454],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013675"},{"annotations":[87810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014132"},{"annotations":[87075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014611"},{"annotations":[87141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033282"},{"annotations":[87783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054785"},{"annotations":[88134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957382"},{"annotations":[88803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971174"},{"annotations":[88693,88694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024553"},{"annotations":[89059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013307"},{"annotations":[86786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010794"},{"annotations":[87217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014562"},{"annotations":[87248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008133"},{"annotations":[88418],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007429"},{"annotations":[88819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008759"},{"annotations":[87232],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012992"},{"annotations":[89015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013972"},{"annotations":[87790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014126"},{"annotations":[86827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0976232"},{"annotations":[87098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012683"},{"annotations":[87682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014754"},{"annotations":[88323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024528"},{"annotations":[86945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012238"},{"annotations":[87316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013117"},{"annotations":[88135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009783"},{"annotations":[86907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014656"},{"annotations":[88206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020845"},{"annotations":[87848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957993"},{"annotations":[88228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010717"},{"annotations":[87709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013580"},{"annotations":[88570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009502"},{"annotations":[86994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009529"},{"annotations":[88571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009503"},{"annotations":[88226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012120"},{"annotations":[87470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008922"},{"annotations":[88220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011835"},{"annotations":[88712],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010437"},{"annotations":[87584],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014804"},{"annotations":[87273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012664"},{"annotations":[88870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013354"},{"annotations":[88461],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013776"},{"annotations":[87583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014803"},{"annotations":[86966],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012450"},{"annotations":[87531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010524"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":166,"genes_by_uniquename":{"SJAG_00080":null,"SJAG_00088":null,"SJAG_00103":null,"SJAG_00133":null,"SJAG_00186":null,"SJAG_00217":null,"SJAG_00255":null,"SJAG_00260":null,"SJAG_00308":null,"SJAG_00319":null,"SJAG_00354":null,"SJAG_00358":null,"SJAG_00404":null,"SJAG_00459":null,"SJAG_00513":null,"SJAG_00522":null,"SJAG_00532":null,"SJAG_00547":null,"SJAG_00601":null,"SJAG_00634":null,"SJAG_00653":null,"SJAG_00721":null,"SJAG_00755":null,"SJAG_00797":null,"SJAG_00852":null,"SJAG_00866":null,"SJAG_00885":null,"SJAG_00894":null,"SJAG_00933":null,"SJAG_00997":null,"SJAG_01004":null,"SJAG_01043":null,"SJAG_01063":null,"SJAG_01077":null,"SJAG_01147":null,"SJAG_01164":null,"SJAG_01174":null,"SJAG_01179":null,"SJAG_01190":null,"SJAG_01303":null,"SJAG_01355":null,"SJAG_01368":null,"SJAG_01405":null,"SJAG_01413":null,"SJAG_01417":null,"SJAG_01490":null,"SJAG_01503":null,"SJAG_01524":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01589":null,"SJAG_01640":null,"SJAG_01647":null,"SJAG_01649":null,"SJAG_01671":null,"SJAG_01797":null,"SJAG_01820":null,"SJAG_01865":null,"SJAG_01866":null,"SJAG_01890":null,"SJAG_01924":null,"SJAG_02006":null,"SJAG_02007":null,"SJAG_02016":null,"SJAG_02050":null,"SJAG_02158":null,"SJAG_02201":null,"SJAG_02229":null,"SJAG_02265":null,"SJAG_02302":null,"SJAG_02306":null,"SJAG_02324":null,"SJAG_02353":null,"SJAG_02384":null,"SJAG_02397":null,"SJAG_02398":null,"SJAG_02428":null,"SJAG_02452":null,"SJAG_02457":null,"SJAG_02464":null,"SJAG_02480":null,"SJAG_02504":null,"SJAG_02548":null,"SJAG_02564":null,"SJAG_02615":null,"SJAG_02641":null,"SJAG_02643":null,"SJAG_02646":null,"SJAG_02656":null,"SJAG_02658":null,"SJAG_02721":null,"SJAG_02848":null,"SJAG_02895":null,"SJAG_02977":null,"SJAG_03014":null,"SJAG_03046":null,"SJAG_03064":null,"SJAG_03071":null,"SJAG_03099":null,"SJAG_03104":null,"SJAG_03114":null,"SJAG_03155":null,"SJAG_03173":null,"SJAG_03222":null,"SJAG_03290":null,"SJAG_03296":null,"SJAG_03310":null,"SJAG_03322":null,"SJAG_03332":null,"SJAG_03461":null,"SJAG_03490":null,"SJAG_03550":null,"SJAG_03553":null,"SJAG_03563":null,"SJAG_03584":null,"SJAG_03585":null,"SJAG_03641":null,"SJAG_03701":null,"SJAG_03773":null,"SJAG_03782":null,"SJAG_03813":null,"SJAG_03992":null,"SJAG_04000":null,"SJAG_04016":null,"SJAG_04019":null,"SJAG_04094":null,"SJAG_04183":null,"SJAG_04285":null,"SJAG_04317":null,"SJAG_04348":null,"SJAG_04367":null,"SJAG_04378":null,"SJAG_04397":null,"SJAG_04450":null,"SJAG_04473":null,"SJAG_04553":null,"SJAG_04560":null,"SJAG_04568":null,"SJAG_04588":null,"SJAG_04639":null,"SJAG_04665":null,"SJAG_04738":null,"SJAG_04816":null,"SJAG_04843":null,"SJAG_04849":null,"SJAG_04856":null,"SJAG_04862":null,"SJAG_04885":null,"SJAG_05199":null,"SJAG_05218":null,"SJAG_05271":null,"SJAG_05305":null,"SJAG_05560":null,"SJAG_06002":null,"SJAG_06022":null,"SJAG_06046":null,"SJAG_06392":null,"SJAG_06603":null,"SJAG_07003":null,"SJAG_07005":null,"SJAG_16456":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT15":null,"SJAG_MIT20":null},"genotype_count":0,"is_obsolete":false,"name":"mitochondrial disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2100163","UMLS:C0751651","NANDO:1200173","MEDGEN:155901"],"termid":"MONDO:0044970","terms_by_termid":{"MONDO:0007415":null,"MONDO:0007429":null,"MONDO:0008133":null,"MONDO:0008134":null,"MONDO:0008758":null,"MONDO:0008759":null,"MONDO:0008858":null,"MONDO:0008922":null,"MONDO:0009502":null,"MONDO:0009503":null,"MONDO:0009504":null,"MONDO:0009529":null,"MONDO:0009706":null,"MONDO:0009747":null,"MONDO:0009783":null,"MONDO:0009872":null,"MONDO:0010437":null,"MONDO:0010524":null,"MONDO:0010717":null,"MONDO:0010779":null,"MONDO:0010788":null,"MONDO:0010789":null,"MONDO:0010794":null,"MONDO:0010799":null,"MONDO:0011283":null,"MONDO:0011308":null,"MONDO:0011421":null,"MONDO:0011451":null,"MONDO:0011582":null,"MONDO:0011730":null,"MONDO:0011829":null,"MONDO:0011835":null,"MONDO:0012120":null,"MONDO:0012191":null,"MONDO:0012238":null,"MONDO:0012450":null,"MONDO:0012510":null,"MONDO:0012512":null,"MONDO:0012534":null,"MONDO:0012557":null,"MONDO:0012622":null,"MONDO:0012664":null,"MONDO:0012683":null,"MONDO:0012784":null,"MONDO:0012791":null,"MONDO:0012792":null,"MONDO:0012992":null,"MONDO:0013111":null,"MONDO:0013116":null,"MONDO:0013117":null,"MONDO:0013306":null,"MONDO:0013307":null,"MONDO:0013350":null,"MONDO:0013354":null,"MONDO:0013458":null,"MONDO:0013570":null,"MONDO:0013580":null,"MONDO:0013675":null,"MONDO:0013726":null,"MONDO:0013762":null,"MONDO:0013776":null,"MONDO:0013811":null,"MONDO:0013836":null,"MONDO:0013837":null,"MONDO:0013838":null,"MONDO:0013840":null,"MONDO:0013865":null,"MONDO:0013877":null,"MONDO:0013969":null,"MONDO:0013971":null,"MONDO:0013972":null,"MONDO:0013986":null,"MONDO:0013987":null,"MONDO:0014020":null,"MONDO:0014051":null,"MONDO:0014062":null,"MONDO:0014063":null,"MONDO:0014064":null,"MONDO:0014065":null,"MONDO:0014066":null,"MONDO:0014091":null,"MONDO:0014126":null,"MONDO:0014132":null,"MONDO:0014162":null,"MONDO:0014175":null,"MONDO:0014190":null,"MONDO:0014194":null,"MONDO:0014261":null,"MONDO:0014269":null,"MONDO:0014356":null,"MONDO:0014364":null,"MONDO:0014397":null,"MONDO:0014398":null,"MONDO:0014455":null,"MONDO:0014467":null,"MONDO:0014496":null,"MONDO:0014525":null,"MONDO:0014547":null,"MONDO:0014562":null,"MONDO:0014576":null,"MONDO:0014611":null,"MONDO:0014636":null,"MONDO:0014656":null,"MONDO:0014667":null,"MONDO:0014668":null,"MONDO:0014684":null,"MONDO:0014733":null,"MONDO:0014754":null,"MONDO:0014775":null,"MONDO:0014803":null,"MONDO:0014804":null,"MONDO:0014820":null,"MONDO:0014869":null,"MONDO:0014882":null,"MONDO:0014943":null,"MONDO:0014959":null,"MONDO:0014976":null,"MONDO:0015003":null,"MONDO:0020714":null,"MONDO:0020727":null,"MONDO:0020845":null,"MONDO:0020858":null,"MONDO:0024528":null,"MONDO:0024553":null,"MONDO:0030006":null,"MONDO:0030007":null,"MONDO:0030008":null,"MONDO:0030017":null,"MONDO:0030311":null,"MONDO:0030935":null,"MONDO:0030937":null,"MONDO:0030974":null,"MONDO:0032609":null,"MONDO:0032612":null,"MONDO:0032617":null,"MONDO:0032630":null,"MONDO:0032631":null,"MONDO:0032712":null,"MONDO:0032726":null,"MONDO:0032815":null,"MONDO:0032869":null,"MONDO:0032909":null,"MONDO:0032932":null,"MONDO:0033282":null,"MONDO:0033533":null,"MONDO:0033534":null,"MONDO:0033537":null,"MONDO:0033615":null,"MONDO:0033635":null,"MONDO:0033636":null,"MONDO:0033637":null,"MONDO:0033638":null,"MONDO:0033639":null,"MONDO:0033645":null,"MONDO:0033649":null,"MONDO:0033651":null,"MONDO:0033653":null,"MONDO:0033654":null,"MONDO:0033655":null,"MONDO:0033656":null,"MONDO:0044714":null,"MONDO:0054677":null,"MONDO:0054741":null,"MONDO:0054742":null,"MONDO:0054781":null,"MONDO:0054785":null,"MONDO:0060582":null,"MONDO:0100294":null,"MONDO:0700250":null,"MONDO:0859160":null,"MONDO:0859228":null,"MONDO:0859321":null,"MONDO:0859323":null,"MONDO:0859337":null,"MONDO:0859520":null,"MONDO:0957254":null,"MONDO:0957255":null,"MONDO:0957382":null,"MONDO:0957992":null,"MONDO:0957993":null,"MONDO:0971174":null,"MONDO:0975806":null,"MONDO:0976132":null,"MONDO:0976232":null},"xrefs":{"Monarch":{"xref_id":"0044970"}}}


id: PBO:0040678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCAR3 adaptor protein, NSP family member","termid":"PBO:0040678"}


id: _global:enables_subfunction
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"Holds between an entity and an process P where the entity enables some larger compound process, and that larger process has-part P.","direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_related_to","termid":"_global:functionally_related_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enables_subfunction","secondary_identifiers":["RO:0004031"],"termid":"_global:enables_subfunction"}


id: PBO:0025467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family plus-end microtubule motor Cut7","termid":"PBO:0025467"}


id: PBO:0050025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class II, DQ alpha 1","termid":"PBO:0050025"}


id: GO:0043829
data:
  {"annotated_genes":["SJAG_04380"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73361],"is_not":false,"summary":null,"term":"GO:0043829"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosine-37 + H2O = inosine-37 + NH3, in a tRNA-Ala molecule.","definition_xrefs":["PMID:8915538","PMID:9707437","RHEA:50968"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA-specific adenosine deaminase activity","termid":"GO:0008251"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04380":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016810","GO:0140101","GO:0016787","GO:0003674","GO:0140098","GO:0003824"],"is_obsolete":false,"name":"tRNA-specific adenosine-37 deaminase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:3.5.4.34"],"synonyms":[{"name":"TAD1","type":"related"},{"name":"tRNA(Ala)-A37 deaminase activity","type":"exact"},{"name":"tRNA-specific adenosine deaminase 1","type":"exact"}],"termid":"GO:0043829","terms_by_termid":{"GO:0043829":null}}


id: PBO:0054002
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 1327","termid":"PBO:0054002"}


id: MONDO:0016621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Juvenile Huntington disease (JHD) is a form of Huntington disease (HD), characterized by onset of signs and symptoms before 20 years of age.","definition_xrefs":["Orphanet:248111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Huntington disease","termid":"MONDO:0007739"}],"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":"juvenile Huntington disease","secondary_identifiers":["MEDGEN:155518","NCIT:C147072","UMLS:C0751208","GARD:10510","SCTID:230299004"],"synonyms":[{"name":"Huntington disease, juvenile onset","type":"related"},{"name":"JHD","type":"exact"},{"name":"juvenile Huntington chorea","type":"exact"},{"name":"juvenile onset HD","type":"related"}],"termid":"MONDO:0016621","xrefs":{"Monarch":{"xref_id":"0016621"}}}


id: PR:Q09948
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rsc4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09948"],"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":"chromatin structure-remodeling complex subunit rsc4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.15","synonyms":[{"name":"RSC complex subunit rsc4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rsc4","type":"exact"},{"name":"bromodomain-containing protein brd1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09948"}


id: MOD:00676
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively adds oxygen atoms to a residue with or without the removal of hydrogen atoms.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidized residue","termid":"MOD:00675"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxygenated residue","synonyms":[{"name":"OxyRes","type":"exact"}],"termid":"MOD:00676"}


id: FYPO:0006896
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of mitochondria to the cell tip is decreased during one or both meiotic nuclear divisions.","definition_xrefs":["PMID:30649994","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"abnormal protein localization to cell tip","termid":"FYPO:0005987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"decreased mitochondrion localization to cell tip during meiosis","synonyms":[{"name":"decreased mitochondrial localization to cell tip during meiosis","type":"exact"},{"name":"decreased mitochondrion localisation to cell tip during meiosis","type":"exact"},{"name":"decreased mitochondrion localization to cell end during meiosis","type":"exact"},{"name":"decreased mitochondrion localization to cell tip during meiotic nuclear division","type":"exact"},{"name":"reduced mitochondrion localization to cell tip during meiosis","type":"exact"}],"termid":"FYPO:0006896"}


id: MONDO:0030089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"permanent neonatal diabetes mellitus","termid":"MONDO:0100164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005015"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005015","MONDO:0019254","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"diabetes mellitus, permanent neonatal 4","secondary_identifiers":["UMLS:C5394307","GARD:16390","MEDGEN:1711191","OMIM:618858"],"synonyms":[{"name":"DIABETES MELLITUS, PERMANENT NEONATAL 4","type":"exact"},{"name":"PNDM4","type":"exact"},{"name":"diabetes mellitus, permanent neonatal 4","type":"exact"}],"termid":"MONDO:0030089","xrefs":{"Monarch":{"xref_id":"0030089"}}}


id: PBO:0039430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin 1","termid":"PBO:0039430"}


id: GO:0052200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of detecting the defenses of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to host","termid":"GO:0075136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated response to host defenses","secondary_identifiers":["GO:0075145","GO:0075140"],"synonyms":[{"name":"maintenance of symbiont tolerance to host defense molecules","type":"narrow"},{"name":"response of symbiont to host defense molecules","type":"narrow"},{"name":"response to host defense molecules","type":"narrow"},{"name":"response to host defenses","type":"exact"}],"termid":"GO:0052200"}


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


id: GO:0005700
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A type of chromosome in a polyploid cell, formed when multiple copies of homologous chromosomes are aligned side by side to give a giant chromosome in which distinct chromosome bands are readily visible.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome","termid":"GO:0005694"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005575","GO:0005694"],"is_obsolete":false,"name":"polytene chromosome","secondary_identifiers":["Wikipedia:Polytene_chromosome"],"termid":"GO:0005700"}


id: FYPO:0004348
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing methylglyoxal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0002060","FYPO:0002058","FYPO:0000003","FYPO:0000139","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on methylglyoxal","synonyms":[{"name":"normal cell population growth in presence of methylglyoxal","type":"exact"},{"name":"normal cell population growth on methylglyoxal","type":"exact"},{"name":"normal cellular response to methylglyoxal","type":"related"},{"name":"normal vegetative cell population growth on methylglyoxal","type":"exact"}],"termid":"FYPO:0004348"}


id: GO:0033715
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: inosine + O2 = 9-riburonosylhypoxanthine + 2 H2O; (1a) 2 inosine + O2 = 2 5'-dehydroinosine + 2 H2O, and (1b) 2 5'-dehydroinosine + O2 = 2 9-riburonosylhypoxanthine + 2 H2O.","definition_xrefs":["RHEA:28651","EC:1.1.3.28"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"nucleoside oxidase activity","secondary_identifiers":["MetaCyc:NUCLEOSIDE-OXIDASE-RXN"],"synonyms":[{"name":"nucleoside:oxygen 5'-oxidoreductase activity","type":"related"}],"termid":"GO:0033715"}


id: PBO:0052205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel subfamily Q member 2","termid":"PBO:0052205"}


id: PBO:0054352
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 1745","termid":"PBO:0054352"}


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


id: MONDO:0700122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any BAFopathy in which the cause of the disease is a mutation in the PBRM1 gene.","definition_xrefs":["PMID:30580808","MONDO:patterns/OMIM_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PBRM1-related BAFopathy","termid":"MONDO:0700122","xrefs":{"Monarch":{"xref_id":"0700122"}}}


id: GO:0036108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate, a precursor of 4-amino-4-deoxy-L-arabinose (L-Ara4N).","definition_xrefs":["GOC:yaf","PMID:15695810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid biosynthetic process","termid":"GO:0008654"},{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"},{"relation_name":"is_a","term_name":"terpenoid biosynthetic process","termid":"GO:0016114"},{"relation_name":"is_a","term_name":"4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate metabolic process","termid":"GO:0036107"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate biosynthetic process","synonyms":[{"name":"4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate anabolism","type":"exact"},{"name":"4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate biosynthesis","type":"exact"},{"name":"4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate formation","type":"exact"},{"name":"4-amino-4-deoxy-alpha-L-arabinopyranosyl undecaprenyl phosphate synthesis","type":"exact"},{"name":"undecaprenyl phosphate alpha-L-Ara4N biosynthesis","type":"exact"}],"termid":"GO:0036108"}


id: PBO:0086993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Reticulon-interacting protein; ER integral membrane protein involved in the generation of tubular ER morphology; promotes membrane curvature; forms tubules in vitro; regulates the ER asymmetry-induced inheritance block during ER stress; role in ER-derived peroxisomal biogenesis; interacts with Yip1p to mediate membrane traffic and with Sey1p to maintain ER morphology; facilitates lipid exchange between the ER and mitochondria; forms ER foci upon DNA replication stress","termid":"PBO:0086993"}


id: GO:0009151
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving purine deoxyribonucleotide, a compound consisting of deoxyribonucleoside (a purine base linked to a deoxyribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide metabolic process","termid":"GO:0006163"},{"relation_name":"is_a","term_name":"2'-deoxyribonucleotide metabolic process","termid":"GO:0009394"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"purine deoxyribonucleotide metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"purine deoxyribonucleotide metabolism","type":"exact"}],"termid":"GO:0009151","terms_by_termid":{"GO:0035863":null}}


id: GO:0005769
data:
  {"annotated_genes":["SJAG_01309","SJAG_01135","SJAG_01448","SJAG_01382","SJAG_02240","SJAG_04616","SJAG_01112","SJAG_00314","SJAG_03250","SJAG_01379"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[74831,74855,76408,81792,81839,101727,104479],"is_not":false,"summary":null,"term":"GO:0005769"},{"annotations":[97711,101526,82053],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031901"}]},"cv_name":"cellular_component","definition":"A membrane-bounded organelle that receives incoming material from primary endocytic vesicles that have been generated by clathrin-dependent and clathrin-independent endocytosis; vesicles fuse with the early endosome to deliver cargo for sorting into recycling or degradation pathways.","definition_xrefs":["PMID:19696797","GOC:mah","NIF_Subcellular:nlx_subcell_20090701"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endosome","termid":"GO:0005768"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00314":null,"SJAG_01112":null,"SJAG_01135":null,"SJAG_01309":null,"SJAG_01379":null,"SJAG_01382":null,"SJAG_01448":null,"SJAG_02240":null,"SJAG_03250":null,"SJAG_04616":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005768","GO:0005575"],"is_obsolete":false,"name":"early endosome","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0005769","terms_by_termid":{"GO:0005769":null,"GO:0031901":null}}


id: PBO:0069026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 271, pseudogene","termid":"PBO:0069026"}


id: PBO:0000003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene characterisation status","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved unknown","termid":"PBO:0000003"}


id: PBO:0017540
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Copper regulated Meiotic gene","termid":"PBO:0017540"}


id: GO:0090614
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5'methyl thioadenosine + H2O = 5'methyl thioinosine + NH3.","definition_xrefs":["RHEA:25025","PMID:23968233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","termid":"GO:0016814"},{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0016810","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"5'-methylthioadenosine deaminase activity","secondary_identifiers":["EC:3.5.4.31"],"termid":"GO:0090614"}


id: PBO:0072467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 31","termid":"PBO:0072467"}


id: GO:1990171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of the SCF ubiquitin ligase complex in response to cadmium stress.","definition_xrefs":["GOC:rb","PMID:23000173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"part_of","term_name":"cellular response to cadmium ion","termid":"GO:0071276"}],"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":"SCF complex disassembly in response to cadmium stress","termid":"GO:1990171"}


id: GO:0071924
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of chemokine (C-C motif) ligand 22 (CCL22) due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah","PMID:18832724"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine production","termid":"GO:0032602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"chemokine (C-C motif) ligand 22 production","synonyms":[{"name":"C-C motif chemokine 22 production","type":"exact"},{"name":"CCL-22 production","type":"exact"},{"name":"CCL22 production","type":"exact"}],"termid":"GO:0071924"}


id: FYPO:0007391
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A viability phenotype in which an aneuploid spore is unable to survive under conditions in which wild type spores survive. An inviable spore does not germinate.","definition_xrefs":["PMID:22737087","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable spore","termid":"FYPO:0002151"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"inviable aneuploid spore","synonyms":[{"name":"abolished aneuploid spore germination","type":"exact"},{"name":"aneuploid spore germination abolished","type":"exact"},{"name":"decreased aneuploid spore viability","type":"exact"},{"name":"decreased viability of aneuploid cells","type":"related"},{"name":"decreased viability of aneuploid spores","type":"related"},{"name":"lethal in aneuploid spore","type":"related"}],"termid":"FYPO:0007391"}


id: PBO:0052428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIT ligand","termid":"PBO:0052428"}


id: PBO:0061021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleolar protein interacting with the FHA domain of MKI67 pseudogene 4","termid":"PBO:0061021"}


id: PBO:0079439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tu translation elongation factor, mitochondrial","termid":"PBO:0079439"}


id: PBO:0065416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome subunit beta 3 pseudogene 2","termid":"PBO:0065416"}


id: PBO:0080010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP12 pseudogene Y-linked","termid":"PBO:0080010"}


id: FYPO:0004028
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 5' deoxyribonuclease (pyrimidine dimer) activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000654","FYPO:0000661"],"is_obsolete":false,"name":"abnormal 5' deoxyribonuclease (pyrimidine dimer) activity","termid":"FYPO:0004028"}


id: PBO:0069446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 711, pseudogene","termid":"PBO:0069446"}


id: MONDO:0012625
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the NR2E3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"retinitis pigmentosa 37","secondary_identifiers":["MESH:C567005","OMIM:611131","UMLS:C1970163","MEDGEN:410004","DOID:0110399","GARD:15508","ICD10CM:H35.5"],"synonyms":[{"name":"NR2E3 retinitis pigmentosa","type":"exact"},{"name":"RP37","type":"exact"},{"name":"retinitis pigmentosa 37","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in NR2E3","type":"exact"},{"name":"retinitis pigmentosa type 37","type":"exact"}],"termid":"MONDO:0012625","xrefs":{"Monarch":{"xref_id":"0012625"}}}


id: PBO:0091183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orf307","termid":"PBO:0091183"}


id: PBO:0035928
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_phosphorylation_during_vegetative_growth","termid":"PBO:0035928"}


id: PBO:0005077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine-dependent NAD(+) synthetase (predicted)","termid":"PBO:0005077"}


id: MONDO:0004770
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The anterior displacement of the eye within the orbit, giving a bulging appearance.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"exophthalmos","secondary_identifiers":["DOID:9370","NCIT:C118763","MEDGEN:41917","HP:0000520","MESH:D005094","SCTID:18265008","ICD9:376.30","UMLS:C0015300"],"synonyms":[{"name":"exophthalmos","type":"exact"},{"name":"exophthalmos (disease)","type":"exact"},{"name":"proptosis","type":"exact"}],"termid":"MONDO:0004770","xrefs":{"Monarch":{"xref_id":"0004770"}}}


id: MONDO:0007224
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly type E","termid":"MONDO:0019677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly, type E, with atrial septal defect, type 2","secondary_identifiers":["UMLS:C1862101","MEDGEN:354662","MESH:C566193","OMIM:113301"],"synonyms":[{"name":"brachydactyly, type E, with atrial septal defect, type II","type":"related"}],"termid":"MONDO:0007224","xrefs":{"Monarch":{"xref_id":"0007224"}}}


id: MOD:01771
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"The farnesyl cation protein modification reporter fragment produced by fragmentation of some farnesyl modified residues.","definition_xrefs":["PubMed:15609361","PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"farnesylated residue","termid":"MOD:00437"},{"relation_name":"is_a","term_name":"modification reporter fragment","termid":"MOD:01520"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"farnesyl reporter fragment","synonyms":[{"name":"(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ylium","type":"exact"},{"name":"Farn+","type":"exact"},{"name":"farnesyl cation","type":"exact"}],"termid":"MOD:01771"}


id: PBO:0057497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 615","termid":"PBO:0057497"}


id: MONDO:0003491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rectum squamous cell carcinoma (obsolete MONDO:0003491)","termid":"MONDO:0003491","xrefs":{"Monarch":{"xref_id":"0003491"}}}


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


id: PBO:0079544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin like modifier activating enzyme 6","termid":"PBO:0079544"}


id: GO:0018208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of peptidyl-proline.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptidyl-proline modification","termid":"GO:0018208"}


id: PBO:0059567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1J, pseudogene","termid":"PBO:0059567"}


id: GO:0060023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of the soft palate from an initial condition to its mature state. This process begins with the formation of the structure and ends with the mature structure, whatever form that may be including its natural destruction. The soft palate is the posterior portion of the palate extending from the posterior edge of the hard palate.","definition_xrefs":["GOC:dph","ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"secondary palate development","termid":"GO:0062009"}],"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":"soft palate development","synonyms":[{"name":"palatum molle development","type":"exact"},{"name":"velum palatum development","type":"exact"}],"termid":"GO:0060023"}


id: PBO:0061560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-nucleotidase domain containing 2","termid":"PBO:0061560"}


id: PBO:0044710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 10 pseudogene 1","termid":"PBO:0044710"}


id: PBO:0059513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded major H-strand promoter","termid":"PBO:0059513"}


id: PBO:0028279
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_localization_to_pericentric_heterochromatin","termid":"PBO:0028279"}


id: MOD:01425
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that crosslinks three residues by formation of a pyridinyl ring, such as pyridine-2,5-dicarboxylic acid or 5-aminopiperideine-2,5-dicarboxylic acid.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues","termid":"MOD:00033"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridinyl ring crosslinked residues","termid":"MOD:01425"}


id: PBO:0080430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS51 pseudogene 14","termid":"PBO:0080430"}


id: GO:0045797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of uptake of cholesterol into the blood by absorption from the intestine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intestinal cholesterol absorption","termid":"GO:0030300"},{"relation_name":"is_a","term_name":"positive regulation of intestinal lipid absorption","termid":"GO:1904731"},{"relation_name":"positively_regulates","term_name":"intestinal cholesterol absorption","termid":"GO:0030299"}],"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 intestinal cholesterol absorption","synonyms":[{"name":"activation of cholesterol absorption","type":"narrow"},{"name":"stimulation of cholesterol absorption","type":"narrow"},{"name":"up regulation of cholesterol absorption","type":"exact"},{"name":"up-regulation of cholesterol absorption","type":"exact"},{"name":"upregulation of cholesterol absorption","type":"exact"}],"termid":"GO:0045797"}


id: PBO:0043311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride intracellular channel 4","termid":"PBO:0043311"}


id: PBO:0076536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 63 pseudogene","termid":"PBO:0076536"}


id: PBO:0041835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer susceptibility 15","termid":"PBO:0041835"}


id: GO:0050607
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: formaldehyde + mycothiol + NAD+ = S-formylmycothiol + NADH + H+.","definition_xrefs":["EC:1.1.1.306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"mycothiol-dependent formaldehyde dehydrogenase activity","secondary_identifiers":["MetaCyc:1.2.1.66-RXN","RHEA:28502"],"synonyms":[{"name":"NAD/factor-dependent formaldehyde dehydrogenase activity","type":"related"},{"name":"formaldehyde:NAD+ oxidoreductase (mycothiol-formylating)","type":"exact"}],"termid":"GO:0050607"}


id: GO:0035023
data:
  {"annotated_genes":["SJAG_04462"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73283],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035024"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Rho protein signal transduction.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of small GTPase mediated signal transduction","termid":"GO:0051056"},{"relation_name":"regulates","term_name":"Rho protein signal transduction","termid":"GO:0007266"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04462":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of Rho protein signal transduction","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0035023","terms_by_termid":{"GO:0035024":null}}


id: GO:0007295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Growth of the egg chamber between the time it leaves the germarium and the onset of vitellogenesis. During this time both nurse cells and the oocyte undergo developmental changes including nuclear organization and cytoplasmic growth. An example of this is found in Drosophila melanogaster.","definition_xrefs":["GOC:mtg_sensu","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"developmental growth","termid":"GO:0048589"},{"relation_name":"part_of","term_name":"oogenesis","termid":"GO:0048477"}],"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 of a germarium-derived egg chamber","synonyms":[{"name":"egg chamber growth","type":"exact"}],"termid":"GO:0007295"}


id: PBO:0069557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 829, pseudogene","termid":"PBO:0069557"}


id: PBO:0072138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 15","termid":"PBO:0072138"}


id: FYPO:0002847
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of a protein measured in the proteasome is lower than normal.","definition_xrefs":["PMID:22906049","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"},{"relation_name":"is_a","term_name":"abnormal protein complex composition","termid":"FYPO:0005003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein level in proteasome","synonyms":[{"name":"decreased proteasomal protein level during vegetative growth","type":"exact"},{"name":"decreased protein level in proteasome during mitotic cell cycle","type":"related"},{"name":"decreased protein level in proteasome during vegetative growth","type":"exact"},{"name":"reduced protein level in proteasome","type":"exact"}],"termid":"FYPO:0002847"}


id: PBO:0068012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 317","termid":"PBO:0068012"}


id: GO:1903934
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of DNA primase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:14766746"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of DNA primase activity (obsolete GO:1903934)","synonyms":[{"name":"activation of DNA primase activity","type":"narrow"},{"name":"up regulation of DNA primase activity","type":"exact"},{"name":"up-regulation of DNA primase activity","type":"exact"},{"name":"upregulation of DNA primase activity","type":"exact"}],"termid":"GO:1903934"}


id: PBO:0045807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"embryonic ectoderm development","termid":"PBO:0045807"}


id: PBO:0038494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily C member 5","termid":"PBO:0038494"}


id: CHEBI:16761
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":"ADP","termid":"CHEBI:16761"}


id: GO:0005858
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A dynein complex found in eukaryotic cilia and flagella; the motor domain heads interact with adjacent microtubules to generate a sliding force which is converted to a bending motion.","definition_xrefs":["ISBN:0815316194","GOC:cilia","GOC:hla","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dynein complex","termid":"GO:0030286"},{"relation_name":"part_of","term_name":"axoneme","termid":"GO:0005930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0032991","GO:0015630","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"axonemal dynein complex","synonyms":[{"name":"axonemal dynein heavy chain","type":"narrow"},{"name":"axonemal dynein intermediate chain","type":"narrow"},{"name":"axonemal dynein intermediate light chain","type":"narrow"},{"name":"axonemal dynein light chain","type":"narrow"}],"termid":"GO:0005858"}


id: PBO:0056725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix extracellular phosphoglycoprotein","termid":"PBO:0056725"}


id: SO:0000920
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An edit to insert a cytidine.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000920 insert_C (obsolete SO:0000920)","synonyms":[{"name":"insert C","type":"exact"}],"termid":"SO:0000920"}


id: MONDO:0044144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder in which an individual experiences recurrent, unexpected panic attacks and persistent concern about having additional panic attacks. Agoraphobia is a component of this disorder.","definition_xrefs":["NCIT:C97194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"agoraphobia","termid":"MONDO:0003709"},{"relation_name":"is_a","term_name":"panic disorder","termid":"MONDO:0005383"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"panic disorder with agoraphobia","secondary_identifiers":["SCTID:35607004","MEDGEN:472969","ICD10CM:F40.01","UMLS:C0236800"],"synonyms":[{"name":"panic disorder with agoraphobia","type":"exact"}],"termid":"MONDO:0044144","xrefs":{"Monarch":{"xref_id":"0044144"}}}


id: PBO:0054489
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 1889","termid":"PBO:0054489"}


id: GO:0048681
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of axon regeneration.","definition_xrefs":["GOC:jid","GOC:dgh","GOC:dph","GOC:lm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to external stimulus","termid":"GO:0032102"},{"relation_name":"is_a","term_name":"regulation of axon regeneration","termid":"GO:0048679"},{"relation_name":"is_a","term_name":"negative regulation of neuron projection regeneration","termid":"GO:0070571"},{"relation_name":"is_a","term_name":"negative regulation of response to wounding","termid":"GO:1903035"},{"relation_name":"negatively_regulates","term_name":"axon regeneration","termid":"GO:0031103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of axon regeneration","synonyms":[{"name":"down regulation of axon regeneration","type":"exact"},{"name":"down-regulation of axon regeneration","type":"exact"},{"name":"downregulation of axon regeneration","type":"exact"},{"name":"inhibition of axon regeneration","type":"narrow"}],"termid":"GO:0048681"}


id: GO:0050609
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + NAD+ + phosphonate = 2 H+ + NADH + phosphate.","definition_xrefs":["RHEA:13173","EC:1.20.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on phosphorus or arsenic in donors, with NAD(P)+ as acceptor","termid":"GO:0050499"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"phosphonate dehydrogenase activity","secondary_identifiers":["UM-BBD_reactionID:r1055","KEGG_REACTION:R05746","MetaCyc:1.20.1.1-RXN"],"synonyms":[{"name":"NAD-dependent phosphite dehydrogenas activity","type":"related"},{"name":"NAD:phosphite oxidoreductase activity","type":"related"},{"name":"phosphite dehydrogenase activity","type":"related"},{"name":"phosphonate:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0050609"}


id: MOD:01245
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-aspartic acid residue to the potassium aspartate salt.","definition_xrefs":["Unimod:530#D"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-aspartic acid residue","termid":"MOD:00904"},{"relation_name":"is_a","term_name":"monopotassium salt","termid":"MOD:01072"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium L-aspartate","synonyms":[{"name":"Cation:K","type":"related"},{"name":"Replacement of proton by potassium","type":"related"}],"termid":"MOD:01245"}


id: PBO:0057869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3179-2","termid":"PBO:0057869"}


id: PBO:0080267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 30 pseudogene","termid":"PBO:0080267"}


id: PBO:0003746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L35 (predicted)","termid":"PBO:0003746"}


id: GO:0009432
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An error-prone process for repairing damaged microbial DNA.","definition_xrefs":["PMID:16000023","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA damage response","termid":"GO:0006974"}],"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":"SOS response","secondary_identifiers":["Wikipedia:SOS_response"],"termid":"GO:0009432"}


id: PBO:0003132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC50 domain protein, implicated in signal transduction (predicted)","termid":"PBO:0003132"}


id: PBO:0041881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CATR tumorigenicity conversion 1","termid":"PBO:0041881"}


id: PBO:0082791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Trk1p-Trk2p potassium transport system; contributes to K(+) supply and maintenance of plasma-membrane potential; TRK2 has a paralog, TRK1, that arose from the whole genome duplication","termid":"PBO:0082791"}


id: PBO:0074151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 35 member E1","termid":"PBO:0074151"}


id: MOD:00892
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to D-serine.","definition_xrefs":["PubMed:18025465","PubMed:6893271","RESID:AA0195#CYS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-serine","termid":"MOD:00891"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"D-serine (Cys)","synonyms":[{"name":"(R)-2-amino-3-hydroxypropanoic acid","type":"exact"},{"name":"D-serine","type":"exact"},{"name":"MOD_RES D-serine (Cys)","type":"exact"}],"termid":"MOD:00892"}


id: GO:0106074
data:
  {"annotated_genes":["SJAG_01248","SJAG_04738","SJAG_02015","SJAG_03545","SJAG_00443","SJAG_01259","SJAG_01797","SJAG_02428","SJAG_04285"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[57173,57477,58321,59245,62061,64481,65263,65289,68280],"is_not":false,"summary":null,"term":"GO:0106074"}]},"cv_name":"biological_process","definition":"Any process which detects an amino-acid acetylated tRNA is charged with the correct amino acid, or removes incorrect amino acids from a charged tRNA. This process can be performed by tRNA synthases, or by subsequent reactions after tRNA aminoacylation.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA metabolic process","termid":"GO:0006399"},{"relation_name":"is_a","term_name":"regulation of translational fidelity","termid":"GO:0006450"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00443":null,"SJAG_01248":null,"SJAG_01259":null,"SJAG_01797":null,"SJAG_02015":null,"SJAG_02428":null,"SJAG_03545":null,"SJAG_04285":null,"SJAG_04738":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0006399","GO:0008150"],"is_obsolete":false,"name":"aminoacyl-tRNA metabolism involved in translational fidelity","references_by_uniquename":{"GO_REF:0000108":null},"synonyms":[{"name":"aminoacyl-tRNA correction","type":"related"},{"name":"aminoacyl-tRNA editin","type":"related"},{"name":"aminoacyl-tRNA proofreading","type":"related"}],"termid":"GO:0106074","terms_by_termid":{"GO:0106074":null}}


id: PBO:0062987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PACRG antisense RNA 2","termid":"PBO:0062987"}


id: MONDO:0013607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"GATA2 deficiency with susceptibility to MDS/AML","termid":"MONDO:0042982"}],"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":"monocytopenia with susceptibility to infections","secondary_identifiers":["UMLS:C3280030","OMIM:614172","GARD:10934","DOID:0111947","icd11.foundation:1077753382","Orphanet:228423","MEDGEN:481660"],"synonyms":[{"name":"DCML","type":"related"},{"name":"Dendritic cell, monocyte, B and NK lymphoid deficiency","type":"exact"},{"name":"Dendritic cell, monocyte, B lymphocyte, and natural Killer lymphocyte deficiency","type":"related"},{"name":"GATA2 deficiency","type":"related"},{"name":"IMD21","type":"related"},{"name":"MonoMAC","type":"exact"},{"name":"combined immunodeficiency with susceptibility to mycobacterial, viral and fungal infections","type":"exact"},{"name":"combined immunodeficiency with susceptibility to mycobacterial, viral, and fungal infections","type":"related"},{"name":"immunodeficiency 21","type":"related"},{"name":"immunodeficiency type 21","type":"exact"},{"name":"monocyte - B - natural killer - dendritic cell deficiency","type":"related"},{"name":"monocyte-B-natural killer-dendritic cell deficiency syndrome","type":"exact"},{"name":"monocytopenia and mycobacterial infection syndrome","type":"exact"},{"name":"monocytopenia with susceptibility to mycobacterial, fungal, and Papillomavirus infections and myelodysplasia","type":"related"}],"termid":"MONDO:0013607","xrefs":{"Monarch":{"xref_id":"0013607"}}}


id: MONDO:0008436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sneddon's syndrome (SS) is a rare non-inflammatory thrombotic vasculopathy characterized by the combination of cerebrovascular disease with livedo racemosa.","definition_xrefs":["Orphanet:820"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arterial disorder","termid":"MONDO:0000473"},{"relation_name":"is_a","term_name":"skin vascular disease","termid":"MONDO:0019293"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"},{"relation_name":"is_a","term_name":"deficiency of adenosine deaminase 2","termid":"MONDO:0100317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"Sneddon syndrome","secondary_identifiers":["NORD:1726","icd11.foundation:1474816492","OMIM:182410","MEDGEN:76449","MESH:D018860","UMLS:C0282492","EFO:1001186","MedDRA:10053841","SCTID:238776001","DOID:13096","GARD:7664"],"synonyms":[{"name":"Ehrmann-Sneddon syndrome","type":"exact"},{"name":"Sneddon syndrome","type":"exact"},{"name":"Sneddon's syndrome","type":"related"},{"name":"cerebro-vascular lesions and livedo reticularis","type":"related"},{"name":"idiopathic livedo reticularis with systemic involvement","type":"exact"},{"name":"livedo racemosa and cerebrovascular accidents","type":"related"},{"name":"livedo racemosa-cerebrovascular accident syndrome","type":"exact"},{"name":"livedo reticularis and cerebrovascular accidents","type":"related"},{"name":"livedo reticularis-cerebrovascular accident syndrome","type":"exact"}],"termid":"MONDO:0008436","xrefs":{"Monarch":{"xref_id":"0008436"}}}


id: MONDO:0001175
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract disease in which the cataract contains some transparent protein","definition_xrefs":["Wikipedia:Cataract"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"senile cataract","termid":"MONDO:0004847"},{"relation_name":"is_a","term_name":"cataract","termid":"MONDO:0005129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"immature cataract","secondary_identifiers":["MEDGEN:755282","DOID:10997","UMLS:C2960113","icd11.foundation:1444156961","SCTID:446474007"],"synonyms":[{"name":"incipient cataract","type":"exact"},{"name":"incipient senile cataract","type":"exact"},{"name":"water clefts","type":"exact"}],"termid":"MONDO:0001175","xrefs":{"Monarch":{"xref_id":"0001175"}}}


id: GO:1900114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone H3-K9 trimethylation.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone H3-K9 trimethylation (obsolete GO:1900114)","synonyms":[{"name":"activation of histone H3-K9 trimethylation","type":"narrow"},{"name":"up regulation of histone H3-K9 trimethylation","type":"exact"},{"name":"up-regulation of histone H3-K9 trimethylation","type":"exact"},{"name":"upregulation of histone H3-K9 trimethylation","type":"exact"}],"termid":"GO:1900114"}


id: MONDO:0100213
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An X-linked multiple congenital anomaly disorder with variable severity. The classic triad, which defines IFAP, is ichthyosis follicularis, atrichia, and photophobia. Some patients have additional features, including mental retardation, brain anomalies, Hirschsprung disease, corneal opacifications, kidney dysplasia, cryptorchidism, cleft palate, and skeletal malformations, particularly of the vertebrae, which constitutes BRESHECK syndrome.","definition_xrefs":["OMIM:308205"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete malformation syndrome with skin/mucosae involvement (obsolete MONDO:0015331)","termid":"MONDO:0015331"},{"relation_name":"excluded_subClassOf","term_name":"X-linked ichthyosis syndrome","termid":"MONDO:0017269"},{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary alopecia (obsolete MONDO:0021034)","termid":"MONDO:0021034"},{"relation_name":"is_a","term_name":"X-linked recessive disease","termid":"MONDO:0020605"},{"relation_name":"is_a","term_name":"IFAP syndrome","termid":"MONDO:0100212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"IFAP syndrome 1, with or without BRESHECK syndrome","secondary_identifiers":["MESH:C536085","DOID:0111821","GARD:15297","NANDO:2200999","MEDGEN:1746744","UMLS:C5399971"],"synonyms":[{"name":"IFAP syndrome with or without BRESHECK syndrome","type":"exact"},{"name":"IFAP syndrome with or without BRESHECK syndrome, X-linked recessive","type":"exact"},{"name":"IFAP/BRESHECK syndrome","type":"exact"},{"name":"ichthyosis follicularis atrichia photophobia syndrome","type":"related"},{"name":"ichthyosis follicularis, atrichia, and photophobia with or without brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, Ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia","type":"exact"},{"name":"ichthyosis follicularis-alopecia-photophobia syndrome","type":"broad"}],"termid":"MONDO:0100213","xrefs":{"Monarch":{"xref_id":"0100213"}}}


id: PBO:0001882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pho88 family protein (predicted)","termid":"PBO:0001882"}


id: PBO:0045680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein light chain LC8-type 1","termid":"PBO:0045680"}


id: MONDO:0016494
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete regional variant of Guillain-Barre syndrome (obsolete MONDO:0016494)","secondary_identifiers":["Orphanet:231416"],"synonyms":[{"name":"regional variant of GBS","type":"exact"},{"name":"regional variant of Guillain-Barré syndrome","type":"related"}],"termid":"MONDO:0016494","xrefs":{"Monarch":{"xref_id":"0016494"}}}


id: PBO:0088802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin, WD repeat Nup146","termid":"PBO:0088802"}


id: GO:0021607
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the accessory nerve is generated and organized. The spinal branch of this motor nerve innervates the trapezius and the sternocleidomastoid muscles. The cranial branch joins the vagus nerve and innervates the same targets as the vagus nerve.","definition_xrefs":["GOC:cls","GOC:dgh","GOC:dph","ISBN:0838580343","GOC:jid","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve morphogenesis","termid":"GO:0021602"},{"relation_name":"part_of","term_name":"accessory nerve development","termid":"GO:0021565"}],"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":"accessory nerve morphogenesis","synonyms":[{"name":"CN XI morphogenesis","type":"related"}],"termid":"GO:0021607"}


id: GO:1904120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of otic vesicle morphogenesis.","definition_xrefs":["PMID:25677106","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of animal organ morphogenesis","termid":"GO:0110110"},{"relation_name":"is_a","term_name":"regulation of otic vesicle morphogenesis","termid":"GO:1904118"},{"relation_name":"is_a","term_name":"positive regulation of morphogenesis of an epithelium","termid":"GO:1905332"},{"relation_name":"positively_regulates","term_name":"otic vesicle morphogenesis","termid":"GO:0071600"}],"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 otic vesicle morphogenesis","synonyms":[{"name":"activation of otic vesicle morphogenesis","type":"narrow"},{"name":"up regulation of otic vesicle morphogenesis","type":"exact"},{"name":"up-regulation of otic vesicle morphogenesis","type":"exact"},{"name":"upregulation of otic vesicle morphogenesis","type":"exact"}],"termid":"GO:1904120"}


id: MONDO:0014311
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome in which the cause of the disease is a mutation in the RUBCN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome","termid":"MONDO:0018446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0005559","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive spinocerebellar ataxia 15","secondary_identifiers":["UMLS:C3810326","DOID:0080057","GARD:17678","OMIM:615705","Orphanet:404499","MEDGEN:816656"],"synonyms":[{"name":"RUBCN autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome","type":"exact"},{"name":"RUBCN autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome","type":"exact"},{"name":"SCAR15","type":"exact"},{"name":"Salih ataxia","type":"related"},{"name":"autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome caused by mutation in RUBCN","type":"exact"},{"name":"autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to KIAA0226 deficiency","type":"related"},{"name":"autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in RUBCN","type":"exact"},{"name":"autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency","type":"related"},{"name":"autosomal recessive spinocerebellar ataxia type 15","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 15","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 15","type":"exact"}],"termid":"MONDO:0014311","xrefs":{"Monarch":{"xref_id":"0014311"}}}


id: PBO:0078209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 7-2","termid":"PBO:0078209"}


id: FYPO:0005539
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of telomerase RNA reverse transcriptase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abnormal telomerase RNA reverse transcriptase activity","synonyms":[{"name":"abnormal telomerase activity","type":"broad"}],"termid":"FYPO:0005539"}


id: PBO:0045008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DIO2 antisense RNA 1","termid":"PBO:0045008"}


id: PBO:0041738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cathelicidin antimicrobial peptide","termid":"PBO:0041738"}


id: PBO:0078141
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 20","termid":"PBO:0078141"}


id: PATO:0001525
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A sound frequency in the range of 20 to 20.000 Hz.","direct_ancestors":[{"relation_name":"is_a","term_name":"sound frequency","termid":"PATO:0001520"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sonic","termid":"PATO:0001525"}


id: SO:0000936
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in partially rearranged genomic DNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immune_system_gene_recombination_feature","termid":"SO:0000301"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_segment","synonyms":[{"name":"vertebrate immunoglobulin T cell receptor rearranged segment","type":"exact"}],"termid":"SO:0000936"}


id: PBO:0113354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for production of 4-hydroxy-5-methylfuran-3(2H)-one (MHF); cupin superfamily protein; has structural resemblance to plant storage and ligand binding proteins (canavalin, glycinin, auxin binding protein) and to some enzymes (epimerase, germin); localizes to nucleus and cytoplasm","termid":"PBO:0113354"}


id: PBO:0077442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 176B","termid":"PBO:0077442"}


id: MONDO:1012815
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Laryngeal paralysis that occurs in dogs due to a mutation in the RAPGEF6 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"laryngeal paralysis, dog","termid":"MONDO:1012322"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laryngeal paralysis, RAPGEF6-related, dog","secondary_identifiers":["OMIA:002222-9615"],"termid":"MONDO:1012815","xrefs":{"Monarch":{"xref_id":"1012815"}}}


id: GO:0086099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An angiotensin-mediated signaling pathway that contributes to a circulatory system process carried out by the heart, where the activated receptor transmits the signal via Gq-mediated activation of phospholipase C (PLC). PLC hydrolyses phosphatidylinositol 4,5-bisphosphate (PIP2) into the second messengers inositol-1,4,5,-triphosphate (IP3) and diacylglycerol (DAG). DAG activates protein kinase C (PKC), whilst IP3 binds intracellular receptors to induce the release of Ca2+ from intracellular stores.","definition_xrefs":["PMID:17376402","GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase C-activating angiotensin-activated signaling pathway","termid":"GO:0086097"},{"relation_name":"is_a","term_name":"angiotensin-activated signaling pathway involved in heart process","termid":"GO:0086098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"phospholipase C-activating angiotensin-activated signaling pathway involved in heart process","synonyms":[{"name":"Gq-coupled angiotensin receptor signaling pathway involved in heart process","type":"exact"},{"name":"PLC-activating angiotensin receptor signaling pathway involved in heart process","type":"exact"},{"name":"angiotensin receptor signaling pathway via activation of phospholipase C involved in heart process","type":"exact"},{"name":"cardiac angiotensin receptor signaling pathway via activation of PLC","type":"exact"},{"name":"phospholipase C-activating angiotensin-mediated signaling pathway involved in heart process","type":"related"}],"termid":"GO:0086099"}


id: PBO:0082183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alanine:glyoxylate aminotransferase (AGT); catalyzes the synthesis of glycine from glyoxylate, which is one of three pathways for glycine biosynthesis in yeast; similar to mammalian and plant alanine:glyoxylate aminotransferases; human homolog AGXT complements yeast null mutant","termid":"PBO:0082183"}


id: PATO:0000904
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000904 wild abortive value (obsolete PATO:0000904)","termid":"PATO:0000904"}


id: MONDO:0007843
data:
  {"annotated_genes":["SJAG_00861"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87663],"is_not":false,"summary":null,"term":"MONDO:0007843"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Kabuki syndrome","termid":"MONDO:0016512"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00861":null},"genotype_count":0,"is_obsolete":false,"name":"Kabuki syndrome 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:147920"],"synonyms":[{"name":"KABUK1","type":"related"},{"name":"KABUKI syndrome 1","type":"related"},{"name":"Kabuki make-Up syndrome","type":"related"},{"name":"Kabuki syndrome","type":"related"},{"name":"Kabuki syndrome 1","type":"exact"},{"name":"Kabuki syndrome type 1","type":"exact"},{"name":"Niikawa-Kuroki syndrome","type":"related"}],"termid":"MONDO:0007843","terms_by_termid":{"MONDO:0007843":null},"xrefs":{"Monarch":{"xref_id":"0007843"}}}


id: GO:0019019
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A segmented viral genome consisting of three sub-genomic nucleic acids but each nucleic acid is packaged into a different virion.","definition_xrefs":["ISBN:0121585336"],"gene_count":0,"genotype_count":0,"name":"obsolete tripartite viral genome (obsolete GO:0019019)","termid":"GO:0019019"}


id: PBO:0053411
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 348","termid":"PBO:0053411"}


id: PBO:0036424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chaperone activator Aha1","termid":"PBO:0036424"}


id: CHEBI:28938
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":"ammonium","termid":"CHEBI:28938"}


id: PBO:0075919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST13, Hsp70 interacting protein pseudogene 11","termid":"PBO:0075919"}


id: PBO:0113551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase complex epsilon subunit, Ost2","termid":"PBO:0113551"}


id: PBO:0034701
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-2 adaptor complex mu subunit Apm4 (predicted)","termid":"PBO:0034701"}


id: MONDO:0007973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mental and growth retardation with amblyopia","secondary_identifiers":["MEDGEN:331885","MESH:C563591","OMIM:156190","UMLS:C1835028"],"synonyms":[{"name":"mental and growth retardation with amblyopia","type":"exact"}],"termid":"MONDO:0007973","xrefs":{"Monarch":{"xref_id":"0007973"}}}


id: MONDO:0859339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth agenesis","termid":"MONDO:0005486"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth agenesis, selective, 10","secondary_identifiers":["UMLS:C5774277","OMIM:620173","MEDGEN:1824050"],"termid":"MONDO:0859339","xrefs":{"Monarch":{"xref_id":"0859339"}}}


id: MONDO:0014900
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive limb-girdle muscular dystrophy type 2Y (LGMD2Y) is a form of limb-girdle muscular dystrophy, presenting in the first or second decades of life, characterized by slowly progressive proximal and distal muscle weakness and atrophy. Additional manifestations include contractures of the proximal and distal interphalangeal hand joints, rigid spine, restricted pulmonary function, and mild cardiomyopathy.","definition_xrefs":["Orphanet:424261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"TOR1AIP1-related myopathy","termid":"MONDO:0100582"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"autosomal recessive limb-girdle muscular dystrophy type 2Y","secondary_identifiers":["SCTID:725907002","MEDGEN:1385152","GARD:17708","NCIT:C181000","UMLS:C4511482","OMIM:617072","DOID:0110289"],"synonyms":[{"name":"LGMD2Y","type":"exact"},{"name":"TOR1AIP1 autosomal recessive limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy caused by mutation in TOR1AIP1","type":"exact"},{"name":"autosomal recessive muscular dystrophy due to LAP1B deficiency","type":"exact"},{"name":"autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency","type":"exact"},{"name":"muscular dystrophy with progressive weakness, distal contractures and rigid spine","type":"exact"},{"name":"muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 2Y","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 2y","type":"exact"}],"termid":"MONDO:0014900","xrefs":{"Monarch":{"xref_id":"0014900"}}}


id: GO:0032153
data:
  {"annotated_genes":["SJAG_04012","SJAG_01146","SJAG_03655","SJAG_01799","SJAG_01889","SJAG_03596","SJAG_03753","SJAG_01720","SJAG_02169","SJAG_01756","SJAG_04455","SJAG_03637","SJAG_03375","SJAG_03158","SJAG_04960","SJAG_01353","SJAG_03011","SJAG_01135","SJAG_00589","SJAG_02444","SJAG_04287","SJAG_02132","SJAG_00800","SJAG_03936","SJAG_02700","SJAG_02222","SJAG_02797","SJAG_03331","SJAG_03131","SJAG_02333","SJAG_03746","SJAG_00245","SJAG_04280","SJAG_00063","SJAG_03453","SJAG_01281","SJAG_00152","SJAG_04050","SJAG_02422","SJAG_00845","SJAG_01453","SJAG_03631","SJAG_03172","SJAG_01956","SJAG_02716","SJAG_04901","SJAG_00700","SJAG_05179","SJAG_01317","SJAG_01943","SJAG_01460","SJAG_02065","SJAG_03705","SJAG_00229","SJAG_01658","SJAG_00661","SJAG_04358","SJAG_04001","SJAG_05205","SJAG_01196","SJAG_00028","SJAG_04498","SJAG_01171","SJAG_04315","SJAG_00610","SJAG_02379","SJAG_01255","SJAG_04058","SJAG_03602","SJAG_01787","SJAG_01769","SJAG_02957","SJAG_00018","SJAG_01360","SJAG_01590","SJAG_05264","SJAG_03938","SJAG_01095","SJAG_02657","SJAG_02609","SJAG_00663","SJAG_02266","SJAG_03688","SJAG_03353","SJAG_04077","SJAG_00666","SJAG_00546","SJAG_00228","SJAG_01863","SJAG_03887","SJAG_01181","SJAG_01732","SJAG_04624","SJAG_02864","SJAG_04051","SJAG_02737","SJAG_02004","SJAG_02412","SJAG_04771","SJAG_03052","SJAG_04421","SJAG_02581","SJAG_05315","SJAG_01189","SJAG_01319","SJAG_02186","SJAG_03731","SJAG_03795","SJAG_01350","SJAG_05978","SJAG_04074","SJAG_04931","SJAG_04322","SJAG_04781","SJAG_01894","SJAG_02943","SJAG_01703","SJAG_04621","SJAG_01738","SJAG_00514","SJAG_02322","SJAG_00993","SJAG_04668","SJAG_02215","SJAG_04887","SJAG_00268","SJAG_04522","SJAG_05001","SJAG_00185","SJAG_04765","SJAG_02602","SJAG_04062","SJAG_04690","SJAG_02104","SJAG_02848","SJAG_02838","SJAG_03915","SJAG_02278","SJAG_04509","SJAG_04706","SJAG_03793","SJAG_04044","SJAG_00910","SJAG_03581","SJAG_02062","SJAG_03986","SJAG_04828","SJAG_00318","SJAG_03606","SJAG_03564","SJAG_04609","SJAG_02431","SJAG_05290","SJAG_03374","SJAG_01003","SJAG_04461","SJAG_02760","SJAG_00331","SJAG_01277","SJAG_00072","SJAG_00101","SJAG_01774","SJAG_01993","SJAG_04597","SJAG_05004","SJAG_00551","SJAG_02075","SJAG_01459","SJAG_02572","SJAG_01754","SJAG_01071","SJAG_00236","SJAG_02550","SJAG_05210","SJAG_03429","SJAG_03748","SJAG_04566","SJAG_00938","SJAG_01456","SJAG_00264","SJAG_00692","SJAG_02729","SJAG_03536","SJAG_03703","SJAG_03025","SJAG_03088","SJAG_04703","SJAG_04258","SJAG_02902","SJAG_04776","SJAG_04470","SJAG_01215","SJAG_05232","SJAG_00850","SJAG_02730","SJAG_03119","SJAG_02114","SJAG_01898","SJAG_01983","SJAG_00030","SJAG_04724","SJAG_02508","SJAG_02753","SJAG_03537","SJAG_02761","SJAG_03005","SJAG_01631","SJAG_03338","SJAG_00856","SJAG_01384","SJAG_03229","SJAG_04013","SJAG_01901","SJAG_00805","SJAG_04591","SJAG_04268","SJAG_02712","SJAG_02022","SJAG_02058","SJAG_00279","SJAG_00162","SJAG_05285","SJAG_00587","SJAG_01888","SJAG_02368","SJAG_02241","SJAG_02733","SJAG_04551","SJAG_00137","SJAG_02968","SJAG_03010","SJAG_00521","SJAG_00445","SJAG_03891","SJAG_02511","SJAG_01143","SJAG_03123","SJAG_03704","SJAG_03625","SJAG_03681","SJAG_04829","SJAG_01665","SJAG_02645","SJAG_05198","SJAG_01268","SJAG_03146","SJAG_00807","SJAG_01686","SJAG_03086","SJAG_01817","SJAG_02684","SJAG_01770","SJAG_00472","SJAG_04486","SJAG_00743","SJAG_01114","SJAG_02916","SJAG_03432","SJAG_00667","SJAG_03074","SJAG_00280","SJAG_01571","SJAG_04069","SJAG_04655","SJAG_03708","SJAG_00442","SJAG_02228","SJAG_04375","SJAG_00750","SJAG_01855","SJAG_03145","SJAG_01288","SJAG_00773","SJAG_04666","SJAG_03754","SJAG_01794","SJAG_04620","SJAG_02576","SJAG_03760","SJAG_01448","SJAG_04673","SJAG_02277","SJAG_04917","SJAG_03486","SJAG_01822","SJAG_01118","SJAG_01848","SJAG_02152","SJAG_04462","SJAG_03407","SJAG_00082","SJAG_04479","SJAG_07018","SJAG_04460","SJAG_01978","SJAG_03264","SJAG_02392","SJAG_00104","SJAG_03246","SJAG_03835","SJAG_02366","SJAG_04982","SJAG_00916","SJAG_04457","SJAG_03126","SJAG_04787","SJAG_03380","SJAG_04935","SJAG_01964","SJAG_04595","SJAG_03073","SJAG_02831","SJAG_01835","SJAG_02202","SJAG_03379","SJAG_01290","SJAG_01373","SJAG_02886","SJAG_00333","SJAG_02320","SJAG_00424","SJAG_02727","SJAG_05185","SJAG_00724","SJAG_00652","SJAG_00575","SJAG_04167","SJAG_00669","SJAG_01925","SJAG_01718","SJAG_02166","SJAG_00317","SJAG_03600","SJAG_03643","SJAG_01167","SJAG_04637","SJAG_00677","SJAG_00118","SJAG_03810","SJAG_00289","SJAG_01697","SJAG_01247","SJAG_00216","SJAG_02566"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[59512,66945,67223,67828,70185,77199,80833,89263,89868,89947,90050,90067,90432,90592,91145,91179,91244,91422,91518,91637,92020,92153,92274,92275,92276,92277,92278,92279,92280,92281,92282,92768,92877,92943,92967,93070,93285,93406,93450,93566,93658,93919,93926,93994,94079,94140,94517,94841,95280,95307,95458,95651,95684,95940,96032,96193,96207,96759,96807,97510,97768,98085,98123,98144,98228,98282,98384,98502,98606,98745,98833,99361,100039,100183,100622,100631,100646,100721,101097,101400,101493,101951,101989,102205,102261,102422,102736,102768,103168,103240,103290,103565,103733,103954,104039,104259,104429,104543,104559,104580,104828,105128,105267,105279,105325,105341,105529,105552,106439,106469,106549,106649,106987,107441,107458,107740,108182,108307,108312,108497,108503,108519,108673,108682,108842,108935,108989,109013,109054,109893,110019,110130,110173,110203,110448,110476,110592,110632,111213,111359,111367,112010,112020,112533,112708,112769,112899,113107,113278,113321,113345,113505,113525,113780,113798,113862,113990,114015,114322,114331,114852,115064,115095,115300,115516,115519,115628,115685,116009,116024,116177,116687,116771,116782,116808,116920,117149,117182,117501,117914,117925,117937,118046,118336,118590,118690,118780,118876,119364,119382,119587,119856,119874,120202,120203,120302,120401,120419,120447,120462,120602,120623,120663,120741,120852],"is_not":false,"summary":null,"term":"GO:0032153"},{"annotations":[120982,121145,121146,121147,121148,120990,121144],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005826"},{"annotations":[105300,100234,117859,100808],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110115"},{"annotations":[108868,107927,117668,91671,89694,94204,101573],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032154"},{"annotations":[89803,93091],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090689"},{"annotations":[69406,89340,90279,113214,91545,98673,102747,104460,92526,90088,97471,101555,73384,108103,111949,95368,115896,119748,105304,119762,118421,103756,114931,116234,112827,94205,107928,89322,95544,71884,92650,96387,92555,106487,92575,103755,102005,94074,94224],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000935"},{"annotations":[121361,121368,95171,120991,121363,121370],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990753"},{"annotations":[103244,101900,118797,119050,104138,112423,114618,110681,111441,102184,102799,108274],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000923"},{"annotations":[101718,89341,75694,73925,94349,107170,97183,90281,112366,101131,120752,89962,66335,94226,100708,99533,70366,106971,57604,104883,114901,104480,63143,112604,109441,96389,112645,119749,99727],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031097"},{"annotations":[102776,114630,99628,105735,109791,119730,58303,120514,101930,103584],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036391"},{"annotations":[98137,92528,95671,90084,103076,108028,118892,119731,107005,90765,94396,102513,94132,99836],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071341"},{"annotations":[102492,102173,116236,94397,114196,98805,94208],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032178"},{"annotations":[107179,108722,94350,91628,117673,121362,95634,100096,103084,89701,121367,119501,112606,121371,76684,96390,121498,117757,121369,92530,121364,78057,120713,103077,91139],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110085"},{"annotations":[102350,110898,102515,119733,106972],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120106"},{"annotations":[97659,96753,119751,105511,92577,108030,91800,90086,114157,102749,115213,96217,112647,119734,110899,98139,99007],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120105"},{"annotations":[99838,102778,118894,99459,105737,109968,79966,101933,108872,110900,118801,81509,94134,58834,58302],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120104"},{"annotations":[101967,117676,58768,65242],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000936"},{"annotations":[117828,107841,101936,96316],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032169"}]},"cv_name":"cellular_component","definition":"The eventual plane of cell division (also known as cell cleavage or cytokinesis) in a dividing cell. In Eukaryotes, the cleavage apparatus, composed of septin structures and the actomyosin contractile ring, forms along this plane, and the mitotic, or meiotic, spindle is aligned perpendicular to the division plane. In bacteria, the cell division site is generally located at mid-cell and is the site at which the cytoskeletal structure, the Z-ring, assembles.","definition_xrefs":["GOC:imk","PMID:12101122","PMID:15380095","PMID:16983191","PMID:18165305","GOC:bf","GOC:krc","GOC:ns"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"gene_count":344,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00028":null,"SJAG_00030":null,"SJAG_00063":null,"SJAG_00072":null,"SJAG_00082":null,"SJAG_00101":null,"SJAG_00104":null,"SJAG_00118":null,"SJAG_00137":null,"SJAG_00152":null,"SJAG_00162":null,"SJAG_00185":null,"SJAG_00216":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00236":null,"SJAG_00245":null,"SJAG_00264":null,"SJAG_00268":null,"SJAG_00279":null,"SJAG_00280":null,"SJAG_00289":null,"SJAG_00317":null,"SJAG_00318":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00424":null,"SJAG_00442":null,"SJAG_00445":null,"SJAG_00472":null,"SJAG_00514":null,"SJAG_00521":null,"SJAG_00546":null,"SJAG_00551":null,"SJAG_00575":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00610":null,"SJAG_00652":null,"SJAG_00661":null,"SJAG_00663":null,"SJAG_00666":null,"SJAG_00667":null,"SJAG_00669":null,"SJAG_00677":null,"SJAG_00692":null,"SJAG_00700":null,"SJAG_00724":null,"SJAG_00743":null,"SJAG_00750":null,"SJAG_00773":null,"SJAG_00800":null,"SJAG_00805":null,"SJAG_00807":null,"SJAG_00845":null,"SJAG_00850":null,"SJAG_00856":null,"SJAG_00910":null,"SJAG_00916":null,"SJAG_00938":null,"SJAG_00993":null,"SJAG_01003":null,"SJAG_01071":null,"SJAG_01095":null,"SJAG_01114":null,"SJAG_01118":null,"SJAG_01135":null,"SJAG_01143":null,"SJAG_01146":null,"SJAG_01167":null,"SJAG_01171":null,"SJAG_01181":null,"SJAG_01189":null,"SJAG_01196":null,"SJAG_01215":null,"SJAG_01247":null,"SJAG_01255":null,"SJAG_01268":null,"SJAG_01277":null,"SJAG_01281":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01317":null,"SJAG_01319":null,"SJAG_01350":null,"SJAG_01353":null,"SJAG_01360":null,"SJAG_01373":null,"SJAG_01384":null,"SJAG_01448":null,"SJAG_01453":null,"SJAG_01456":null,"SJAG_01459":null,"SJAG_01460":null,"SJAG_01571":null,"SJAG_01590":null,"SJAG_01631":null,"SJAG_01658":null,"SJAG_01665":null,"SJAG_01686":null,"SJAG_01697":null,"SJAG_01703":null,"SJAG_01718":null,"SJAG_01720":null,"SJAG_01732":null,"SJAG_01738":null,"SJAG_01754":null,"SJAG_01756":null,"SJAG_01769":null,"SJAG_01770":null,"SJAG_01774":null,"SJAG_01787":null,"SJAG_01794":null,"SJAG_01799":null,"SJAG_01817":null,"SJAG_01822":null,"SJAG_01835":null,"SJAG_01848":null,"SJAG_01855":null,"SJAG_01863":null,"SJAG_01888":null,"SJAG_01889":null,"SJAG_01894":null,"SJAG_01898":null,"SJAG_01901":null,"SJAG_01925":null,"SJAG_01943":null,"SJAG_01956":null,"SJAG_01964":null,"SJAG_01978":null,"SJAG_01983":null,"SJAG_01993":null,"SJAG_02004":null,"SJAG_02022":null,"SJAG_02058":null,"SJAG_02062":null,"SJAG_02065":null,"SJAG_02075":null,"SJAG_02104":null,"SJAG_02114":null,"SJAG_02132":null,"SJAG_02152":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02186":null,"SJAG_02202":null,"SJAG_02215":null,"SJAG_02222":null,"SJAG_02228":null,"SJAG_02241":null,"SJAG_02266":null,"SJAG_02277":null,"SJAG_02278":null,"SJAG_02320":null,"SJAG_02322":null,"SJAG_02333":null,"SJAG_02366":null,"SJAG_02368":null,"SJAG_02379":null,"SJAG_02392":null,"SJAG_02412":null,"SJAG_02422":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02508":null,"SJAG_02511":null,"SJAG_02550":null,"SJAG_02566":null,"SJAG_02572":null,"SJAG_02576":null,"SJAG_02581":null,"SJAG_02602":null,"SJAG_02609":null,"SJAG_02645":null,"SJAG_02657":null,"SJAG_02684":null,"SJAG_02700":null,"SJAG_02712":null,"SJAG_02716":null,"SJAG_02727":null,"SJAG_02729":null,"SJAG_02730":null,"SJAG_02733":null,"SJAG_02737":null,"SJAG_02753":null,"SJAG_02760":null,"SJAG_02761":null,"SJAG_02797":null,"SJAG_02831":null,"SJAG_02838":null,"SJAG_02848":null,"SJAG_02864":null,"SJAG_02886":null,"SJAG_02902":null,"SJAG_02916":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_02968":null,"SJAG_03005":null,"SJAG_03010":null,"SJAG_03011":null,"SJAG_03025":null,"SJAG_03052":null,"SJAG_03073":null,"SJAG_03074":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03119":null,"SJAG_03123":null,"SJAG_03126":null,"SJAG_03131":null,"SJAG_03145":null,"SJAG_03146":null,"SJAG_03158":null,"SJAG_03172":null,"SJAG_03229":null,"SJAG_03246":null,"SJAG_03264":null,"SJAG_03331":null,"SJAG_03338":null,"SJAG_03353":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03379":null,"SJAG_03380":null,"SJAG_03407":null,"SJAG_03429":null,"SJAG_03432":null,"SJAG_03453":null,"SJAG_03486":null,"SJAG_03536":null,"SJAG_03537":null,"SJAG_03564":null,"SJAG_03581":null,"SJAG_03596":null,"SJAG_03600":null,"SJAG_03602":null,"SJAG_03606":null,"SJAG_03625":null,"SJAG_03631":null,"SJAG_03637":null,"SJAG_03643":null,"SJAG_03655":null,"SJAG_03681":null,"SJAG_03688":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03705":null,"SJAG_03708":null,"SJAG_03731":null,"SJAG_03746":null,"SJAG_03748":null,"SJAG_03753":null,"SJAG_03754":null,"SJAG_03760":null,"SJAG_03793":null,"SJAG_03795":null,"SJAG_03810":null,"SJAG_03835":null,"SJAG_03887":null,"SJAG_03891":null,"SJAG_03915":null,"SJAG_03936":null,"SJAG_03938":null,"SJAG_03986":null,"SJAG_04001":null,"SJAG_04012":null,"SJAG_04013":null,"SJAG_04044":null,"SJAG_04050":null,"SJAG_04051":null,"SJAG_04058":null,"SJAG_04062":null,"SJAG_04069":null,"SJAG_04074":null,"SJAG_04077":null,"SJAG_04167":null,"SJAG_04258":null,"SJAG_04268":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04315":null,"SJAG_04322":null,"SJAG_04358":null,"SJAG_04375":null,"SJAG_04421":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04462":null,"SJAG_04470":null,"SJAG_04479":null,"SJAG_04486":null,"SJAG_04498":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04551":null,"SJAG_04566":null,"SJAG_04591":null,"SJAG_04595":null,"SJAG_04597":null,"SJAG_04609":null,"SJAG_04620":null,"SJAG_04621":null,"SJAG_04624":null,"SJAG_04637":null,"SJAG_04655":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04673":null,"SJAG_04690":null,"SJAG_04703":null,"SJAG_04706":null,"SJAG_04724":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04776":null,"SJAG_04781":null,"SJAG_04787":null,"SJAG_04828":null,"SJAG_04829":null,"SJAG_04887":null,"SJAG_04901":null,"SJAG_04917":null,"SJAG_04931":null,"SJAG_04935":null,"SJAG_04960":null,"SJAG_04982":null,"SJAG_05001":null,"SJAG_05004":null,"SJAG_05179":null,"SJAG_05185":null,"SJAG_05198":null,"SJAG_05205":null,"SJAG_05210":null,"SJAG_05232":null,"SJAG_05264":null,"SJAG_05285":null,"SJAG_05290":null,"SJAG_05315":null,"SJAG_05978":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"cell division site","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:25866389":null,"PMID:27059155":null,"PMID:27734801":null,"PMID:28655757":null,"PMID:36148799":null},"synonyms":[{"name":"cell division plane","type":"exact"}],"termid":"GO:0032153","terms_by_termid":{"GO:0000085":null,"GO:0000923":null,"GO:0000935":null,"GO:0000936":null,"GO:0005826":null,"GO:0031097":null,"GO:0032153":null,"GO:0032154":null,"GO:0032169":null,"GO:0032178":null,"GO:0036391":null,"GO:0051325":null,"GO:0051329":null,"GO:0071341":null,"GO:0090689":null,"GO:0110085":null,"GO:0110115":null,"GO:0120104":null,"GO:0120105":null,"GO:0120106":null,"GO:1990753":null}}


id: GO:0100006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that positively regulates sulfite transport.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of sulfite transport by transcription from RNA polymerase II promoter (obsolete GO:0100006)","termid":"GO:0100006"}


id: PBO:0090421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane chaperone for multipass membrane proteins, PAT complex subunit, and TMCO1 translocon subunit (human CCDC47 ortholog)","termid":"PBO:0090421"}


id: GO:2000357
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of kidney smooth muscle cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of smooth muscle cell differentiation","termid":"GO:0051151"},{"relation_name":"is_a","term_name":"regulation of kidney smooth muscle cell differentiation","termid":"GO:2000356"},{"relation_name":"negatively_regulates","term_name":"kidney smooth muscle cell differentiation","termid":"GO:0072195"}],"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 kidney smooth muscle cell differentiation","termid":"GO:2000357"}


id: GO:0009938
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of gibberellic acid mediated signaling activity.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gibberellic acid mediated signaling pathway","termid":"GO:0009937"},{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"negatively_regulates","term_name":"gibberellic acid mediated signaling pathway","termid":"GO:0009740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of gibberellic acid mediated signaling pathway","synonyms":[{"name":"down regulation of gibberellic acid mediated signaling","type":"exact"},{"name":"down-regulation of gibberellic acid mediated signaling","type":"exact"},{"name":"downregulation of gibberellic acid mediated signaling","type":"exact"},{"name":"inhibition of gibberellic acid mediated signaling","type":"narrow"},{"name":"negative regulation of gibberellic acid mediated signalling","type":"exact"}],"termid":"GO:0009938"}


id: MONDO:0007836
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"IVIC syndrome is a very rare genetic malformation syndrome characterized by upper limb anomalies (radial ray defects, carpal bone fusion), extraocular motor disturbances, and congenital bilateral non-progressive mixed hearing loss.","definition_xrefs":["Orphanet:2307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"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":"IVIC syndrome","secondary_identifiers":["MEDGEN:233003","OMIM:147750","DOID:0111381","MESH:C535544","UMLS:C1327918","SCTID:722019000","GARD:269"],"synonyms":[{"name":"IVIC syndrome","type":"exact"},{"name":"Instituto venezolano de Investigaciones Cientificas syndrome","type":"related"},{"name":"OORS","type":"related"},{"name":"oculo-oto-radial syndrome","type":"exact"},{"name":"oculootoradial syndrome","type":"related"},{"name":"radial Ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia","type":"related"},{"name":"radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia","type":"exact"}],"termid":"MONDO:0007836","xrefs":{"Monarch":{"xref_id":"0007836"}}}


id: MONDO:0044709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"middle ear anomaly","termid":"MONDO:0015604"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cochleovestibular dysplasia","secondary_identifiers":["UMLS:C5761642","MEDGEN:1818562","GARD:22044","Orphanet:502305"],"termid":"MONDO:0044709","xrefs":{"Monarch":{"xref_id":"0044709"}}}


id: MONDO:0000175
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ataxia-telangiectasia-like disorder (obsolete MONDO:0000175)","termid":"MONDO:0000175","xrefs":{"Monarch":{"xref_id":"0000175"}}}


id: PBO:0082728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Rix1 complex and pre-replicative complexes (pre-RCs); required for processing of ITS2 sequences from 35S pre-rRNA; component of the pre-60S ribosomal particle with the dynein-related AAA-type ATPase Mdn1p; required for pre-RC formation and maintenance during DNA replication licensing; highly conserved protein which contains several WD40 motifs; IPI3 is an essential gene; other members include Rix1p, Ipi1p, and Ipi3p","termid":"PBO:0082728"}


id: PBO:0012291
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae YOR341W","termid":"PBO:0012291"}


id: MONDO:0002140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm that arises from the vagina. Representative examples include botryoid-type embryonal rhabdomyosarcoma, leiomyosarcoma, and endometrioid stromal sarcoma.","definition_xrefs":["NCIT:C7737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal cancer","termid":"MONDO:0001402"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"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":"vagina sarcoma","secondary_identifiers":["UMLS:C0238519","DOID:1901","MEDGEN:65971"],"synonyms":[{"name":"sarcoma of the vagina","type":"exact"},{"name":"sarcoma of vagina","type":"exact"},{"name":"vagina sarcoma","type":"exact"},{"name":"vaginal sarcoma","type":"exact"}],"termid":"MONDO:0002140","xrefs":{"Monarch":{"xref_id":"0002140"}}}


id: PBO:0066190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 12","termid":"PBO:0066190"}


id: PBO:0078808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 25-1","termid":"PBO:0078808"}


id: PBO:0079658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2V1 pseudogene 6","termid":"PBO:0079658"}


id: GO:0043083
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The narrow gap that separates the presynaptic and postsynaptic membranes, into which neurotransmitter is released.","definition_xrefs":["GOC:jl","PMID:30784960"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular region","termid":"GO:0005576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005576","GO:0005575"],"is_obsolete":false,"name":"synaptic cleft","secondary_identifiers":["NIF_Subcellular:sao243541954"],"termid":"GO:0043083"}


id: PBO:0046498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERH pseudogene 1","termid":"PBO:0046498"}


id: PBO:0056846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-6-methylguanine-DNA methyltransferase","termid":"PBO:0056846"}


id: PBO:0042082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 149","termid":"PBO:0042082"}


id: PBO:0056239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mago homolog, exon junction complex subunit","termid":"PBO:0056239"}


id: PR:000035411
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A BUB1 CDK-consensus sites phosphorylated form in Schizosaccharomyces pombe 972h-. The exact combination of phosphorylated sites is not known but may involve Thr-340, Thr-423, Thr-455, and/or Ser-466 in UniProtKB:O94751. Phosphorylation occurs during Meiosis I or spindle disruption (tubulin mutant). UniProtKB:O94751, Thr-340/Thr-423/Thr-455, MOD:00047|Ser-466, MOD:00046.","definition_xrefs":["PMID:12606573","PRO:KER"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic checkpoint serine/threonine-protein kinase BUB1 phosphorylated 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1322.12c","synonyms":[{"name":"Spom972h-BUB1/Phos:6","type":"exact"}],"termid":"PR:000035411"}


id: GO:0042004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Promotion of female sex and sexual phenotypes in the hermaphroditic soma. An example of this is found in Caenorhabditis elegans.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hermaphrodite somatic sex determination","termid":"GO:0042001"}],"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":"feminization of hermaphrodite soma","termid":"GO:0042004"}


id: PBO:0052779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 19 pseudogene 2","termid":"PBO:0052779"}


id: MONDO:1011766
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"warts between hooves, non-human animal","secondary_identifiers":["OMIA:001060"],"termid":"MONDO:1011766","xrefs":{"Monarch":{"xref_id":"1011766"}}}


id: PBO:0001332
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inherited protein folding defects","termid":"PBO:0001332"}


id: GO:0004111
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + creatine = N-phosphocreatine + ADP + 2 H+.","definition_xrefs":["RHEA:17157","EC:2.7.3.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, nitrogenous group as acceptor","termid":"GO:0016775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016301","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"creatine kinase activity","secondary_identifiers":["Reactome:R-HSA-200326","MetaCyc:CREATINE-KINASE-RXN","Reactome:R-HSA-200318","KEGG_REACTION:R01881"],"synonyms":[{"name":"ATP:creatine N-phosphotransferase activity","type":"related"},{"name":"ATP:creatine phosphotransferase activity","type":"related"},{"name":"BB-CK","type":"related"},{"name":"CK","type":"related"},{"name":"CK-BB","type":"related"},{"name":"CK-MB","type":"related"},{"name":"CK-MM","type":"related"},{"name":"CKMiMi","type":"related"},{"name":"MB-CK","type":"related"},{"name":"MM-CK","type":"related"},{"name":"Mi-CK","type":"related"},{"name":"MiMi-CK","type":"related"},{"name":"adenosine triphosphate-creatine transphosphorylase activity","type":"related"},{"name":"creatine phosphokinase activity","type":"related"},{"name":"creatine phosphotransferase activity","type":"related"},{"name":"phosphocreatine kinase activity","type":"related"}],"termid":"GO:0004111"}


id: PBO:0003430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically upregulated gene Mug97","termid":"PBO:0003430"}


id: PBO:0002379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar import and degradation protein Vid28 (predicted)","termid":"PBO:0002379"}


id: PBO:0002318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-amylase homolog (predicted)","termid":"PBO:0002318"}


id: PR:O94639
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- zrt1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc-regulated transporter 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.06","synonyms":[{"name":"Spom972h-zrt1","type":"exact"},{"name":"high-affinity zinc transport protein zrt1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94639"}


id: MONDO:0013507
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chronic granulomatous disease","termid":"MONDO:0018305"}],"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":"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3","secondary_identifiers":["DOID:0070194","GARD:15736","NANDO:2201283","MEDGEN:462759","UMLS:C3151409","OMIM:613960"],"synonyms":[{"name":"CDG3","type":"related"},{"name":"CGD, autosomal recessive cytochrome B-positive, type 3","type":"related"},{"name":"chronic granulomatous disease 3, autosomal recessive","type":"exact"},{"name":"granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type III","type":"related"},{"name":"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3","type":"exact"},{"name":"granulomatous disease, chronic, due to Ncf4 deficiency","type":"related"}],"termid":"MONDO:0013507","xrefs":{"Monarch":{"xref_id":"0013507"}}}


id: GO:0048865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a stem cell.","definition_xrefs":["CL:0000034","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate commitment","termid":"GO:0045165"},{"relation_name":"part_of","term_name":"stem cell differentiation","termid":"GO:0048863"}],"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":"stem cell fate commitment","termid":"GO:0048865"}


id: PBO:0046351
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleotide pyrophosphatase/phosphodiesterase 7 pseudogene 9","termid":"PBO:0046351"}


id: GO:0140677
data:
  {"annotated_genes":["SJAG_04509","SJAG_00071","SJAG_01121","SJAG_02982","SJAG_01401","SJAG_03268","SJAG_03371","SJAG_01213","SJAG_00028","SJAG_03957","SJAG_04074","SJAG_02277","SJAG_04968","SJAG_03936","SJAG_04391","SJAG_02332","SJAG_00901","SJAG_03681","SJAG_00824","SJAG_04013","SJAG_05219","SJAG_02026","SJAG_03353","SJAG_00369","SJAG_01270","SJAG_03045","SJAG_04462","SJAG_03085","SJAG_03655","SJAG_01708","SJAG_03221","SJAG_00424","SJAG_05346","SJAG_01411","SJAG_04910","SJAG_04080","SJAG_01386","SJAG_04679","SJAG_00236","SJAG_00142","SJAG_02920","SJAG_05338","SJAG_02231","SJAG_03809","SJAG_04614","SJAG_02390","SJAG_02278","SJAG_01600","SJAG_04498","SJAG_04896","SJAG_00078","SJAG_04200","SJAG_04890","SJAG_03699","SJAG_02379","SJAG_02232","SJAG_00686","SJAG_00864","SJAG_02666","SJAG_00092","SJAG_02638","SJAG_00666","SJAG_00289","SJAG_02520","SJAG_03338","SJAG_02785","SJAG_04938","SJAG_04950","SJAG_04638","SJAG_02765","SJAG_04522","SJAG_05017","SJAG_00457","SJAG_04190","SJAG_00333","SJAG_00296","SJAG_04853","SJAG_04020","SJAG_04776","SJAG_00591","SJAG_01142","SJAG_00526","SJAG_02045","SJAG_00467","SJAG_01526","SJAG_01076","SJAG_03751","SJAG_00551","SJAG_03618","SJAG_01048","SJAG_03453","SJAG_03021","SJAG_04484","SJAG_02057","SJAG_05252","SJAG_03695","SJAG_03793","SJAG_03858","SJAG_02199","SJAG_02605","SJAG_00837","SJAG_04682","SJAG_00439","SJAG_04211","SJAG_00991","SJAG_00990","SJAG_04140","SJAG_04724","SJAG_03748","SJAG_03340","SJAG_04943","SJAG_02625","SJAG_01011","SJAG_00066","SJAG_01605","SJAG_00939","SJAG_01184","SJAG_01823","SJAG_00318","SJAG_03090","SJAG_00095","SJAG_04502","SJAG_04179","SJAG_01597","SJAG_01051","SJAG_02845","SJAG_02012","SJAG_01114","SJAG_04733","SJAG_02444","SJAG_02539","SJAG_05212","SJAG_05000","SJAG_01746","SJAG_04428","SJAG_04666","SJAG_00796","SJAG_04400","SJAG_04765","SJAG_04548","SJAG_05694","SJAG_01857","SJAG_03153"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[93032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098744"},{"annotations":[72383,71767,77705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010698"},{"annotations":[96040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010856"},{"annotations":[75759,57570,109502,68413,93203,98063,80824,112152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001671"},{"annotations":[67367,72004,81565,118939,75812,103444,114824,113057],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061575"},{"annotations":[117268,72938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030337"},{"annotations":[118672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140656"},{"annotations":[79901,75990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061133"},{"annotations":[111897,97562,96448,80322,95363,108554,109958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008047"},{"annotations":[91516,106750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044692"},{"annotations":[69468,71931,60663,72642,73581,72979,66944,73363,75285,76664,71921,76744,89347,107118,97917,59025,79347,77376,80153,74907,72396,73282,95136,69968,75164,112811,116860,70804,72098,74645,78522,67705,74535,67222,79350,97686,74064,98371,95786,67827,72570,78481,80011,66475,95144,71850,81399,79159,78841,80963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005096"},{"annotations":[111733,93140,114012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0170008"},{"annotations":[80801,78675,72566,77033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016504"},{"annotations":[120455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019211"},{"annotations":[113290,74019,71892,91035,74660,118179,93122,80182,72200,101006,108977,114338],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030295"},{"annotations":[80630,76467,78251,94742,74370,116841,119812,99513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072542"},{"annotations":[111116,70560,106955,77202,120248,93002,77197,91257,89721,91049,112396,94244,92669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043539"},{"annotations":[73453,77574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008160"},{"annotations":[80570,90301],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120230"},{"annotations":[79573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061632"},{"annotations":[101265],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030546"},{"annotations":[77137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141106"},{"annotations":[78322,80872,82133,80846,81695],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990757"},{"annotations":[119021,100385],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097027"},{"annotations":[78672,78712,73574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018237"}]},"cv_name":"molecular_function","definition":"A molecular function regulator that activates or increases the activity of its target via non-covalent binding that does not result in covalent modification to the target.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular function regulator activity","termid":"GO:0098772"}],"gene_count":143,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_00066":null,"SJAG_00071":null,"SJAG_00078":null,"SJAG_00092":null,"SJAG_00095":null,"SJAG_00142":null,"SJAG_00236":null,"SJAG_00289":null,"SJAG_00296":null,"SJAG_00318":null,"SJAG_00333":null,"SJAG_00369":null,"SJAG_00424":null,"SJAG_00439":null,"SJAG_00457":null,"SJAG_00467":null,"SJAG_00526":null,"SJAG_00551":null,"SJAG_00591":null,"SJAG_00666":null,"SJAG_00686":null,"SJAG_00796":null,"SJAG_00824":null,"SJAG_00837":null,"SJAG_00864":null,"SJAG_00901":null,"SJAG_00939":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_01011":null,"SJAG_01048":null,"SJAG_01051":null,"SJAG_01076":null,"SJAG_01114":null,"SJAG_01121":null,"SJAG_01142":null,"SJAG_01184":null,"SJAG_01213":null,"SJAG_01270":null,"SJAG_01386":null,"SJAG_01401":null,"SJAG_01411":null,"SJAG_01526":null,"SJAG_01597":null,"SJAG_01600":null,"SJAG_01605":null,"SJAG_01708":null,"SJAG_01746":null,"SJAG_01823":null,"SJAG_01857":null,"SJAG_02012":null,"SJAG_02026":null,"SJAG_02045":null,"SJAG_02057":null,"SJAG_02199":null,"SJAG_02231":null,"SJAG_02232":null,"SJAG_02277":null,"SJAG_02278":null,"SJAG_02332":null,"SJAG_02379":null,"SJAG_02390":null,"SJAG_02444":null,"SJAG_02520":null,"SJAG_02539":null,"SJAG_02605":null,"SJAG_02625":null,"SJAG_02638":null,"SJAG_02666":null,"SJAG_02765":null,"SJAG_02785":null,"SJAG_02845":null,"SJAG_02920":null,"SJAG_02982":null,"SJAG_03021":null,"SJAG_03045":null,"SJAG_03085":null,"SJAG_03090":null,"SJAG_03153":null,"SJAG_03221":null,"SJAG_03268":null,"SJAG_03338":null,"SJAG_03340":null,"SJAG_03353":null,"SJAG_03371":null,"SJAG_03453":null,"SJAG_03618":null,"SJAG_03655":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03699":null,"SJAG_03748":null,"SJAG_03751":null,"SJAG_03793":null,"SJAG_03809":null,"SJAG_03858":null,"SJAG_03936":null,"SJAG_03957":null,"SJAG_04013":null,"SJAG_04020":null,"SJAG_04074":null,"SJAG_04080":null,"SJAG_04140":null,"SJAG_04179":null,"SJAG_04190":null,"SJAG_04200":null,"SJAG_04211":null,"SJAG_04391":null,"SJAG_04400":null,"SJAG_04428":null,"SJAG_04462":null,"SJAG_04484":null,"SJAG_04498":null,"SJAG_04502":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04548":null,"SJAG_04614":null,"SJAG_04638":null,"SJAG_04666":null,"SJAG_04679":null,"SJAG_04682":null,"SJAG_04724":null,"SJAG_04733":null,"SJAG_04765":null,"SJAG_04776":null,"SJAG_04853":null,"SJAG_04890":null,"SJAG_04896":null,"SJAG_04910":null,"SJAG_04938":null,"SJAG_04943":null,"SJAG_04950":null,"SJAG_04968":null,"SJAG_05000":null,"SJAG_05017":null,"SJAG_05212":null,"SJAG_05219":null,"SJAG_05252":null,"SJAG_05338":null,"SJAG_05346":null,"SJAG_05694":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0098772","GO:0003674"],"is_obsolete":false,"name":"molecular function activator activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0140677","terms_by_termid":{"GO:0001671":null,"GO:0005096":null,"GO:0008047":null,"GO:0008160":null,"GO:0010698":null,"GO:0010856":null,"GO:0016504":null,"GO:0018237":null,"GO:0019211":null,"GO:0030295":null,"GO:0030337":null,"GO:0030546":null,"GO:0043539":null,"GO:0044692":null,"GO:0061133":null,"GO:0061575":null,"GO:0061632":null,"GO:0072542":null,"GO:0097027":null,"GO:0098744":null,"GO:0120230":null,"GO:0140656":null,"GO:0141106":null,"GO:0170008":null,"GO:1990757":null}}


id: GO:0018415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The incorporation of iron into a 3Fe-2S cluster via tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino nickel triiron disulfide trioxide.","definition_xrefs":["RESID:AA0292"],"gene_count":0,"genotype_count":0,"name":"obsolete iron incorporation into iron-sulfur cluster via tris-L-cysteinyl L-cysteine persulfido bis-L-glutamato L-histidino nickel triiron disulfide trioxide (obsolete GO:0018415)","synonyms":[{"name":"iron incorporation into iron-sulphur cluster via tris-L-cysteinyl L-cysteine persulphido bis-L-glutamato L-histidino nickel triiron disulphide trioxide","type":"exact"}],"termid":"GO:0018415"}


id: PBO:0058318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4691","termid":"PBO:0058318"}


id: MONDO:0043199
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":"short limb dwarf lethal colavita kozlowski type","secondary_identifiers":["MESH:C537597","UMLS:C2931544","MEDGEN:419106"],"synonyms":[{"name":"Colavita Kozlowski syndrome","type":"related"}],"termid":"MONDO:0043199","xrefs":{"Monarch":{"xref_id":"0043199"}}}


id: MONDO:0006077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hyperplasia that involves the adrenal medulla.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperplasia","termid":"MONDO:0005043"},{"relation_name":"is_a","term_name":"adrenal gland disorder","termid":"MONDO:0005495"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adrenal medullary hyperplasia","secondary_identifiers":["UMLS:C1332177","MEDGEN:231356","EFO:1000076","NCIT:C35838"],"synonyms":[{"name":"adrenal medulla hyperplasia","type":"exact"}],"termid":"MONDO:0006077","xrefs":{"Monarch":{"xref_id":"0006077"}}}


id: MONDO:0016118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete muscular glycogenosis (obsolete MONDO:0016118)","secondary_identifiers":["ICD10CM:E74.0","NANDO:1200823","Orphanet:206959"],"synonyms":[{"name":"glycogen storage myopathy","type":"exact"}],"termid":"MONDO:0016118","xrefs":{"Monarch":{"xref_id":"0016118"}}}


id: GO:0009381
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within deoxyribonucleic acid at sites flanking regions of damaged DNA to which the Uvr ABC excinuclease complexes bind.","definition_xrefs":["PMID:15192705","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA endonuclease activity","termid":"GO:0004520"},{"relation_name":"is_a","term_name":"hydrolase activity, acting on ester bonds","termid":"GO:0016788"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140097"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0140097","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"excinuclease ABC activity","termid":"GO:0009381"}


id: GO:0032158
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A diffuse ring composed of a series of septin bars that run parallel to the long axis of the cell. This type of septin structure has been observed in a number of locations associated with polarized grown and/or deposition of new membrane, but not with cytokinesis, such as at the shmoo (mating projection) neck, at the junction between the mother cell and the germ tube (hypha) of a fungal cell growing filamentously.","definition_xrefs":["PMID:16151244","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"septin cytoskeleton","termid":"GO:0032156"}],"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":"septin band","termid":"GO:0032158"}


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


id: PBO:0054943
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 2357","termid":"PBO:0054943"}


id: MONDO:0024410
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Bifidobacterium.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bifidobacteriales infectious disease","termid":"MONDO:0006706"},{"relation_name":"is_a","term_name":"gram-positive bacterial infections","termid":"MONDO:0021679"},{"relation_name":"is_a","term_name":"anaerobic bacteria infectious disease","termid":"MONDO:0024389"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infection caused by Bifidobacterium","secondary_identifiers":["MEDGEN:923145","SCTID:721759009","UMLS:C1096283"],"synonyms":[{"name":"Bifidobacterium caused disease or disorder","type":"exact"},{"name":"Bifidobacterium disease or disorder","type":"exact"},{"name":"Bifidobacterium infection","type":"related"},{"name":"Bifidobacterium infectious disease","type":"exact"},{"name":"infection caused by Bifidobacterium","type":"exact"}],"termid":"MONDO:0024410","xrefs":{"Monarch":{"xref_id":"0024410"}}}


id: PBO:0069085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 332, pseudogene","termid":"PBO:0069085"}


id: GO:0032393
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an MHC class I protein complex to initiate a change in cellular activity. Class I here refers to classical class I molecules.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"},{"relation_name":"is_a","term_name":"immune receptor activity","termid":"GO:0140375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"MHC class I receptor activity","synonyms":[{"name":"T cell receptor activity","type":"related"},{"name":"alpha-beta T cell receptor activity","type":"related"},{"name":"gamma-delta T cell receptor activity","type":"related"}],"termid":"GO:0032393"}


id: GO:0007490
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the tergite are generated and organized. The tergite is the primary plate or sclerite forming the dorsal surface of any insect body segment.","definition_xrefs":["PMID:16451739","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"histoblast morphogenesis","termid":"GO:0007488"}],"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":"tergite morphogenesis","termid":"GO:0007490"}


id: GO:1905214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of RNA binding.","definition_xrefs":["GOC:TermGenie","GOC:PARL","GOC:bf","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of RNA binding (obsolete GO:1905214)","termid":"GO:1905214"}


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:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"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: PBO:0052450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kruppel like factor 3 pseudogene 1","termid":"PBO:0052450"}


id: MONDO:0020469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"48,XYYY syndrome is a rare Y chromosome number anomaly that affects only males and is characterized by mild-moderate developmental delay (especially speech), normal to mild intellectual disability, large, irregular teeth with poor enamel, tall stature and acne. Radioulnar stenosis and clinodactyly have also been associated. Boys generally present normal genitalia, while hypogonadism and infertility is frequently reported in adult males.","definition_xrefs":["Orphanet:99329"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"tetrasomy","termid":"MONDO:0030502"},{"relation_name":"is_a","term_name":"chromosome Y disorder","termid":"MONDO:0700028"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"48,XYYY syndrome","secondary_identifiers":["GARD:11985","MEDGEN:1371767","SCTID:733625003","UMLS:C4518082"],"synonyms":[{"name":"48,XYYY","type":"related"}],"termid":"MONDO:0020469","xrefs":{"Monarch":{"xref_id":"0020469"}}}


id: PBO:0070952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18a pseudogene 7","termid":"PBO:0070952"}


id: PR:Q9HDY5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPB1A10.05 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HDY5"],"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 PB1A10.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB1A10.05","synonyms":[{"name":"Spom972h-SPAPB1A10.05","type":"exact"}],"termid":"PR:Q9HDY5"}


id: PBO:0070716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 21","termid":"PBO:0070716"}


id: GO:0005754
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The hexamer, comprising three alpha and three beta subunits, that possesses the catalytic activity of the mitochondrial hydrogen-transporting ATP synthase.","definition_xrefs":["GOC:mtg_sensu","PMID:10838056"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial proton-transporting ATP synthase, catalytic core (obsolete GO:0005754)","termid":"GO:0005754"}


id: MONDO:0001224
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atopic conjunctivitis that is of relatively short duration and that has a rapid onset.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute conjunctivitis","termid":"MONDO:0001214"},{"relation_name":"is_a","term_name":"atopic conjunctivitis","termid":"MONDO:0005642"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005046"],"is_obsolete":false,"name":"Angelucci syndrome","secondary_identifiers":["UMLS:C0001309","ICD9:372.05","ICD10CM:H10.1","SCTID:67678004","MEDGEN:1316","NCIT:C34353","DOID:11203"],"synonyms":[{"name":"Angelucci syndrome","type":"exact"},{"name":"Angelucci's syndrome","type":"exact"},{"name":"acute atopic conjunctivitis","type":"exact"}],"termid":"MONDO:0001224","xrefs":{"Monarch":{"xref_id":"0001224"}}}


id: PBO:0077904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tryptase pseudogene 2","termid":"PBO:0077904"}


id: MONDO:0001035
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypopyon","termid":"MONDO:0001036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"hypopyon ulcer","secondary_identifiers":["UMLS:C0155070","SCTID:6395007","DOID:10442","ICD9:370.04","MEDGEN:509768"],"termid":"MONDO:0001035","xrefs":{"Monarch":{"xref_id":"0001035"}}}


id: GO:0000460
data:
  {"annotated_genes":["SJAG_02250","SJAG_03425","SJAG_00955","SJAG_02993","SJAG_04916","SJAG_03012","SJAG_04174","SJAG_00882","SJAG_03796","SJAG_03952","SJAG_04321","SJAG_04818","SJAG_04524","SJAG_02644","SJAG_03179","SJAG_01581","SJAG_06613","SJAG_04153","SJAG_00854","SJAG_03234","SJAG_00772","SJAG_04006","SJAG_04369","SJAG_16455","SJAG_02275","SJAG_01551","SJAG_04824","SJAG_04330","SJAG_00689","SJAG_00722","SJAG_00897","SJAG_01431","SJAG_01818","SJAG_01521","SJAG_02374","SJAG_02547","SJAG_01191","SJAG_01623","SJAG_01811","SJAG_02553","SJAG_04188","SJAG_00965","SJAG_02861","SJAG_04582","SJAG_04084","SJAG_03745","SJAG_00081","SJAG_04289","SJAG_04492","SJAG_02830","SJAG_03789"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73390,76961,80796,81111,81230,102855],"is_not":false,"summary":null,"term":"GO:0000460"},{"annotations":[93513,96775,105934,73267],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000448"},{"annotations":[110845,106382,107483,115346,60879,76268,107484,106599,104948,117165,117253,116061,96522,74656,80041,98601,98312,120472,72095,73649,72962],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000447"},{"annotations":[109288,73065,79431,100755,74185,103897,99051,72367,81200,117742,108296,76820,117303,73360,91793],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000467"},{"annotations":[109289],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000465"},{"annotations":[80475,79957,99790,63813,62234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000466"}]},"cv_name":"biological_process","definition":"Any process involved in the maturation of a precursor 5.8S ribosomal RNA (rRNA) molecule into a mature 5.8S rRNA molecule.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA processing","termid":"GO:0006364"}],"gene_count":51,"genes_by_uniquename":{"SJAG_00081":null,"SJAG_00689":null,"SJAG_00722":null,"SJAG_00772":null,"SJAG_00854":null,"SJAG_00882":null,"SJAG_00897":null,"SJAG_00955":null,"SJAG_00965":null,"SJAG_01191":null,"SJAG_01431":null,"SJAG_01521":null,"SJAG_01551":null,"SJAG_01581":null,"SJAG_01623":null,"SJAG_01811":null,"SJAG_01818":null,"SJAG_02250":null,"SJAG_02275":null,"SJAG_02374":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_02644":null,"SJAG_02830":null,"SJAG_02861":null,"SJAG_02993":null,"SJAG_03012":null,"SJAG_03179":null,"SJAG_03234":null,"SJAG_03425":null,"SJAG_03745":null,"SJAG_03789":null,"SJAG_03796":null,"SJAG_03952":null,"SJAG_04006":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04174":null,"SJAG_04188":null,"SJAG_04289":null,"SJAG_04321":null,"SJAG_04330":null,"SJAG_04369":null,"SJAG_04492":null,"SJAG_04524":null,"SJAG_04582":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_04916":null,"SJAG_06613":null,"SJAG_16455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0044085","GO:0008150","GO:0042254"],"is_obsolete":false,"name":"maturation of 5.8S rRNA","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0000460","terms_by_termid":{"GO:0000447":null,"GO:0000448":null,"GO:0000460":null,"GO:0000465":null,"GO:0000466":null,"GO:0000467":null}}


id: GO:1904045
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 aldosterone stimulus.","definition_xrefs":["GOC:TermGenie","PMID:17644563","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to mineralocorticoid stimulus","termid":"GO:0071389"},{"relation_name":"is_a","term_name":"cellular response to alcohol","termid":"GO:0097306"},{"relation_name":"is_a","term_name":"cellular response to aldehyde","termid":"GO:0110096"},{"relation_name":"is_a","term_name":"cellular response to ketone","termid":"GO:1901655"},{"relation_name":"is_a","term_name":"response to aldosterone","termid":"GO:1904044"}],"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 aldosterone","termid":"GO:1904045"}


id: MONDO:0019871
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 2p is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 2, with a highly variable phenotype principally characterized by pre- and post-natal growth failure, global developmental delay, facial dysmorphism (incl. high forehead/frontal bossing, abnormal ear shape and/or position, hypertelorism/telecanthus, broad/depressed nasal bridge) and ocular anomalies (e.g. exophthalmos, retinal hypopigmentation, optic nerve and foveal hypoplasia). Other reported anomalies include generalized hypotonia, pectus excavatum, long fingers and toes, syndactyly, congenital heart (e.g. ventricular and atrial septal defects) and neural tube defects, seizures, pulmonary hypoplasia, diaphragmatic hernia and urogenital anomalies.","definition_xrefs":["Orphanet:96070"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete chromosomal anomaly with cataract (obsolete MONDO:0020226)","termid":"MONDO:0020226"},{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 2","termid":"MONDO:0016939"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 2p","secondary_identifiers":["MEDGEN:1646233","UMLS:C4706937","SCTID:764518004","GARD:19304"],"synonyms":[{"name":"distal duplication 2p","type":"exact"},{"name":"distal trisomy type 2p","type":"exact"},{"name":"telomeric duplication 2p","type":"exact"},{"name":"trisomy 2pter","type":"exact"}],"termid":"MONDO:0019871","xrefs":{"Monarch":{"xref_id":"0019871"}}}


id: MONDO:0020535
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"House allergic alveolitis is a hypersensitivity pneumonitis resulting from the inhalation of an antigen to which an individual has been previously sensitized in his/her domestic environment. House allergic alveolitis encompasses summer hypersensitivity pneumonitis, humidifier-induced lung diseases, hot tub lung and legionellosis.","definition_xrefs":["Orphanet:99907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity pneumonitis","termid":"MONDO:0017853"}],"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":"house allergic alveolitis","secondary_identifiers":["SCTID:725415009","UMLS:C4511048","GARD:19703","icd11.foundation:1985023223","MEDGEN:1387737"],"termid":"MONDO:0020535","xrefs":{"Monarch":{"xref_id":"0020535"}}}


id: PBO:0065209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA processing factor 40 homolog A","termid":"PBO:0065209"}


id: GO:0048335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of mesoderm cell fate determination.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesodermal cell fate determination","termid":"GO:0048334"},{"relation_name":"is_a","term_name":"negative regulation of cell fate determination","termid":"GO:1905934"},{"relation_name":"negatively_regulates","term_name":"mesodermal cell fate determination","termid":"GO:0007500"}],"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 mesodermal cell fate determination","synonyms":[{"name":"down regulation of mesodermal cell fate determination","type":"exact"},{"name":"down-regulation of mesodermal cell fate determination","type":"exact"},{"name":"downregulation of mesodermal cell fate determination","type":"exact"},{"name":"inhibition of mesodermal cell fate determination","type":"narrow"}],"termid":"GO:0048335"}


id: SO:1000027
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transversion from guanine to thymine.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine_to_pyrimidine_transversion","termid":"SO:1000023"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G_to_T_transversion","synonyms":[{"name":"G to T transversion","type":"exact"}],"termid":"SO:1000027"}


id: PBO:0029268
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_serine_phosphorylation_during_vegetative_growth","termid":"PBO:0029268"}


id: GO:2000024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of leaf development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"leaf development","termid":"GO:0048366"}],"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 leaf development","termid":"GO:2000024"}


id: PBO:0029365
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_tRNA_level","termid":"PBO:0029365"}


id: GO:0010893
data:
  {"annotated_genes":["SJAG_04018"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070452"}]},"cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of steroids, compounds with a 1,2,cyclopentanoperhydrophenanthrene nucleus.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of steroid metabolic process","termid":"GO:0045940"},{"relation_name":"is_a","term_name":"positive regulation of lipid biosynthetic process","termid":"GO:0046889"},{"relation_name":"is_a","term_name":"regulation of steroid biosynthetic process","termid":"GO:0050810"},{"relation_name":"positively_regulates","term_name":"steroid biosynthetic process","termid":"GO:0006694"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"positive regulation of steroid biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010893","terms_by_termid":{"GO:0070452":null}}


