# terms

id: PBO:0071411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 17","termid":"PBO:0071411"}


id: PATO:0000561
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000561 length value (obsolete PATO:0000561)","termid":"PATO:0000561"}


id: PBO:0076838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TERF1 pseudogene 5","termid":"PBO:0076838"}


id: GO:0044561
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism effects a change in the frequency, rate or extent of the activity of an ion channel in another organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of ion channel activity in another organism (obsolete GO:0044561)","synonyms":[{"name":"modulation of ion channel activity in other organism","type":"exact"},{"name":"regulation of ion channel activity in other organism","type":"exact"}],"termid":"GO:0044561"}


id: MONDO:0016606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Prenatal benign hypophosphatasia (PB-HPP) is a very rare form of hypophosphatasia characterized by prenatal skeletal manifestations (limb shortening and bowing) that slowly resolve spontaneously and later develop into the milder infantile, childhood or adult forms of the disease.","definition_xrefs":["Orphanet:247638"],"gene_count":0,"genotype_count":0,"name":"obsolete prenatal benign hypophosphatasia (obsolete MONDO:0016606)","secondary_identifiers":["ICD10CM:E83.3"],"synonyms":[{"name":"prenatal benign Rathburn disease","type":"exact"},{"name":"prenatal benign phosphoethanolaminuria","type":"exact"}],"termid":"MONDO:0016606","xrefs":{"Monarch":{"xref_id":"0016606"}}}


id: FYPO:0000291
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype that affects translation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression phenotype","termid":"FYPO:0000142"},{"relation_name":"is_a","term_name":"cellular metabolism phenotype during vegetative growth","termid":"FYPO:0001348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"translation phenotype","synonyms":[{"name":"fission yeast translation phenotype","type":"exact"},{"name":"translation phenotype during mitotic cell cycle","type":"related"},{"name":"translation phenotype during vegetative growth","type":"exact"}],"termid":"FYPO:0000291"}


id: PBO:0087444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit III of cytochrome c oxidase (Complex IV); Complex IV is the terminal member of the mitochondrial inner membrane electron transport chain; one of three mitochondrially-encoded subunits","termid":"PBO:0087444"}


id: PBO:0117143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THUMP domain 2 tRNA and snRNA guanosine methyltransferase","termid":"PBO:0117143"}


id: PBO:0051226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (II)-15-1 (pseudogene)","termid":"PBO:0051226"}


id: GO:0060468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The negative regulation of fertilization process that takes place as part of egg activation, ensuring that only a single sperm fertilizes the egg.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of fertilization","termid":"GO:0060467"},{"relation_name":"part_of","term_name":"egg activation","termid":"GO:0007343"}],"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":"prevention of polyspermy","synonyms":[{"name":"negative regulation of fertilization involved in egg activation","type":"exact"},{"name":"polyspermy block","type":"exact"}],"termid":"GO:0060468"}


id: PBO:0067054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 75, pseudogene","termid":"PBO:0067054"}


id: GO:2001303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lipoxin A4. Lipoxin A4 is a C20 hydroxy fatty acid having (5S)-, (6R)- and (15S)-hydroxy groups as well as (7E)- (9E)-, (11Z)- and (13E)-double bonds.","definition_xrefs":["GOC:mw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unsaturated fatty acid biosynthetic process","termid":"GO:0006636"},{"relation_name":"is_a","term_name":"long-chain fatty acid biosynthetic process","termid":"GO:0042759"},{"relation_name":"is_a","term_name":"lipoxin biosynthetic process","termid":"GO:2001301"},{"relation_name":"is_a","term_name":"lipoxin A4 metabolic process","termid":"GO:2001302"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"lipoxin A4 biosynthetic process","synonyms":[{"name":"LXA4 anabolism","type":"exact"},{"name":"LXA4 biosynthesis","type":"exact"},{"name":"LXA4 biosynthetic process","type":"exact"},{"name":"LXA4 formation","type":"exact"},{"name":"LXA4 synthesis","type":"exact"},{"name":"lipoxin A4 anabolism","type":"exact"},{"name":"lipoxin A4 biosynthesis","type":"exact"},{"name":"lipoxin A4 formation","type":"exact"},{"name":"lipoxin A4 synthesis","type":"exact"}],"termid":"GO:2001303"}


id: PATO:0001667
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An attachment quality inhering in a bearer by virtue of the bearer's connection or association with another entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment quality","termid":"PATO:0001435"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"attached to","synonyms":[{"name":"affixed to","type":"related"},{"name":"attached","type":"exact"}],"termid":"PATO:0001667"}


id: GO:0002124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Aggressive behavior performed in defence of a fixed area against intruders, typically conspecifics.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aggressive behavior","termid":"GO:0002118"}],"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":"territorial aggressive behavior","synonyms":[{"name":"territorial aggression","type":"exact"}],"termid":"GO:0002124"}


id: GO:0070699
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type II activin receptor.","definition_xrefs":["GOC:BHF","GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activin receptor binding","termid":"GO:0070697"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type II activin receptor binding","termid":"GO:0070699"}


id: GO:0042175
data:
  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continuous network of membranes encompassing the nuclear outer membrane and the endoplasmic reticulum membrane.","definition_xrefs":["GOC:vw","GOC:bf","GOC:pr","GOC:mah","GOC:mcc","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane","termid":"GO:0016020"},{"relation_name":"part_of","term_name":"endomembrane 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id: PR:O43052
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rga1 gene.","definition_xrefs":["UniProtKB:O43052","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":"rho-type GTPase-activating protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3F6.05","synonyms":[{"name":"Spom972h-rga1","type":"exact"}],"termid":"PR:O43052"}


id: RO:0002381
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  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x main_stem_of y if y is a branching structure and x is a channel that traces a linear path through y, such that x has higher capacity than any other such path.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_branching_relationship_with","termid":"RO:0002375"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"main_stem_of","termid":"RO:0002381"}


id: RO:0002260
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  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c has-biological-role r iff c has-role r and r is a biological role (CHEBI:24432)","direct_ancestors":[{"relation_name":"is_a","term_name":"has_role","termid":"RO:0000087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_biological_role","termid":"RO:0002260"}


id: GO:0150180
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of phosphatidylserine metabolic process.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:30074985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phosphatidylserine metabolic process","termid":"GO:0150178"},{"relation_name":"is_a","term_name":"negative regulation of phospholipid metabolic process","termid":"GO:1903726"},{"relation_name":"negatively_regulates","term_name":"phosphatidylserine metabolic process","termid":"GO:0006658"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of phosphatidylserine metabolic process","termid":"GO:0150180"}


id: FYPO:0002870
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  {"alleles_by_uniquename":{"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121558],"is_not":false,"summary":null,"term":"FYPO:0002870"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to a non-growing cell tip is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to new cell tip","termid":"FYPO:0004977"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04280":null,"SJAG_04522":null},"genotype_count":1,"genotypes_by_uniquename":{"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"wee1-as8(T582G aa)","display_uniquename":"wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to non-growing cell tip","references_by_uniquename":{"PMID:30664646":null},"single_locus_annotated_genes":["SJAG_04280"],"single_locus_genotype_uniquenames":["wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"increased protein localisation to non-growing cell tip","type":"exact"},{"name":"increased protein localization to new non-growing cell tip","type":"exact"},{"name":"increased protein localization to non-growing cell end","type":"exact"},{"name":"increased protein localization to non-growing cell tip during mitotic cell cycle","type":"related"},{"name":"increased protein localization to non-growing cell tip during vegetative growth","type":"exact"}],"termid":"FYPO:0002870","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYECO:0000338":null,"FYPO:0002870":null}}


id: MONDO:0025699
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Coffin-Siris syndrome","termid":"MONDO:0015452"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coffin-Siris syndrome 12","secondary_identifiers":["UMLS:C5444111","MEDGEN:1782096","DOID:0112370","GARD:16443","OMIM:619325"],"synonyms":[{"name":"CSS12","type":"exact"}],"termid":"MONDO:0025699","xrefs":{"Monarch":{"xref_id":"0025699"}}}


id: SO:0002277
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  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Crypton is a superfamily of DNA transposons that use tyrosine recombinase (YR) to cut and rejoin the recombining DNA molecules.","definition_xrefs":["PMID:22011512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA_transposon","termid":"SO:0000182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Crypton_YR_transposon","synonyms":[{"name":"Crypton YR transposon","type":"exact"},{"name":"Crypton transposon","type":"exact"},{"name":"DYC transposon","type":"exact"}],"termid":"SO:0002277"}


id: PBO:0066034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAN pseudogene 3","termid":"PBO:0066034"}


id: GO:2000875
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glyoxylate cycle.","definition_xrefs":["GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of glyoxylate cycle","termid":"GO:2000874"},{"relation_name":"negatively_regulates","term_name":"glyoxylate cycle","termid":"GO:0006097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"negative regulation of glyoxylate cycle","synonyms":[{"name":"negative regulation of glyoxylate bypass","type":"exact"}],"termid":"GO:2000875"}


id: GO:0023003
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Migration of one of the four nuclei at each pole of the eight-nucleate embryo sac, to the center of the cell.","definition_xrefs":["GOC:mtg_plant","ISBN:047186840X","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryo sac nuclear migration","termid":"GO:0009562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"nuclear migration to the embryo sac center","synonyms":[{"name":"nuclear migration to the embryo sac centre","type":"exact"},{"name":"nuclear migration to the female gametophyte center","type":"exact"},{"name":"nuclear migration to the female gametophyte centre","type":"exact"},{"name":"nuclear migration to the megagametophyte center","type":"exact"},{"name":"nuclear migration to the megagametophyte centre","type":"exact"},{"name":"nucleus migration to the female gametophyte center","type":"exact"},{"name":"nucleus migration to the female gametophyte centre","type":"exact"}],"termid":"GO:0023003"}


id: MONDO:0018658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"19p13.3 microduplication syndrome is a rare, genetic, syndromic intellectual disability characterized by intrauterine growth retardation, microcephaly, hypotonia, motor and neurodevelopmental delay, speech delay, intellectual disability, and mild dysmorphic features.","definition_xrefs":["Orphanet:447980"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 19","termid":"MONDO:0018659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19p13.3 microduplication syndrome","secondary_identifiers":["GARD:21875","MEDGEN:1807189","UMLS:C5679996"],"synonyms":[{"name":"dup(19)(p13.13)","type":"exact"}],"termid":"MONDO:0018658","xrefs":{"Monarch":{"xref_id":"0018658"}}}


id: GO:1903534
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lactose biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mr","PMID:12018418","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of carbohydrate biosynthetic process","termid":"GO:0043255"},{"relation_name":"regulates","term_name":"lactose biosynthetic process","termid":"GO:0005989"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of lactose biosynthetic process","synonyms":[{"name":"regulation of lactose anabolism","type":"exact"},{"name":"regulation of lactose biosynthesis","type":"exact"},{"name":"regulation of lactose formation","type":"exact"},{"name":"regulation of lactose synthesis","type":"exact"}],"termid":"GO:1903534"}


id: GO:0042308
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  {"annotated_genes":["SJAG_01311"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107733],"is_not":false,"summary":null,"term":"GO:0042308"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the movement of proteins from the cytoplasm into the nucleus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein import into nucleus","termid":"GO:0042306"},{"relation_name":"is_a","term_name":"negative regulation of nucleocytoplasmic transport","termid":"GO:0046823"},{"relation_name":"is_a","term_name":"negative regulation of intracellular protein transport","termid":"GO:0090317"},{"relation_name":"is_a","term_name":"negative regulation of protein localization to nucleus","termid":"GO:1900181"},{"relation_name":"negatively_regulates","term_name":"protein import into nucleus","termid":"GO:0006606"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01311":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006913"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006913"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006913","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of protein import into nucleus","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of protein import into nucleus","type":"exact"},{"name":"down-regulation of protein import into nucleus","type":"exact"},{"name":"downregulation of protein import into nucleus","type":"exact"},{"name":"inhibition of protein import into nucleus","type":"narrow"},{"name":"negative regulation of protein import into cell nucleus","type":"exact"},{"name":"negative regulation of protein transport from cytoplasm to nucleus","type":"exact"},{"name":"negative regulation of protein-nucleus import","type":"exact"}],"termid":"GO:0042308","terms_by_termid":{"GO:0042308":null}}


id: PBO:0045560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 9","termid":"PBO:0045560"}


id: GO:0100027
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that regulates cell separation after cytokinesis.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cell separation after cytokinesis by transcription from RNA polymerase II promoter (obsolete GO:0100027)","termid":"GO:0100027"}


id: MONDO:0002011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary angioedema (obsolete MONDO:0002011)","termid":"MONDO:0002011","xrefs":{"Monarch":{"xref_id":"0002011"}}}


id: PR:Q10289
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fas2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10289"],"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":"fatty acid synthase subunit alpha (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.11c","synonyms":[{"name":"Spom972h-fas2","type":"exact"},{"name":"p190/210 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10289"}


id: GO:2000084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mesenchymal to epithelial transition involved in mesonephros morphogenesis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell differentiation involved in kidney development","termid":"GO:2000696"},{"relation_name":"regulates","term_name":"mesenchymal to epithelial transition involved in mesonephros morphogenesis","termid":"GO:0061261"}],"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 mesenchymal to epithelial transition involved in mesonephros morphogenesis","synonyms":[{"name":"regulation of mesonephric mesenchyme to epithelial transition","type":"related"}],"termid":"GO:2000084"}


id: GO:1902700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of pentose to butan-1-ol.","definition_xrefs":["PMID:19539744","GOC:mengo_curators","GO_REF:0000093","PMID:18727018","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete pentose catabolic process to butan-1-ol (obsolete GO:1902700)","synonyms":[{"name":"pentose breakdown to butan-1-ol","type":"exact"},{"name":"pentose catabolic process to 1-butanol","type":"exact"},{"name":"pentose catabolic process to butanol","type":"exact"},{"name":"pentose catabolism to butan-1-ol","type":"exact"},{"name":"pentose degradation to butan-1-ol","type":"exact"},{"name":"solventogenesis","type":"broad"}],"termid":"GO:1902700"}


id: MONDO:0018607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"combined hamartoma of the retina and retinal pigment epithelium","secondary_identifiers":["NCIT:C174548","Orphanet:440727","UMLS:C1862062","GARD:21843","MEDGEN:396281"],"synonyms":[{"name":"CHR-RPE","type":"exact"},{"name":"combined hamartoma of the retina and RPE","type":"exact"}],"termid":"MONDO:0018607","xrefs":{"Monarch":{"xref_id":"0018607"}}}


id: PBO:0078114
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 3","termid":"PBO:0078114"}


id: GO:0070089
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a potassium cation by a channel that opens when a chloride ion has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["GOC:mtg_transport","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium channel activity","termid":"GO:0005267"},{"relation_name":"is_a","term_name":"monoatomic ion-gated channel activity","termid":"GO:0022839"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic cation channel activity","termid":"GO:0099094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"chloride-activated potassium channel activity","termid":"GO:0070089"}


id: PBO:0066287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein Y-linked family 2 member M, pseudogene","termid":"PBO:0066287"}


id: MONDO:0009157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any split hand-foot malformation in which the cause of the disease is a mutation in the WNT10B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"split hand-foot malformation","termid":"MONDO:0016576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"split hand-foot malformation 6","secondary_identifiers":["DOID:0090026","GARD:15166","MESH:C567616","UMLS:C2749665","OMIM:225300","MEDGEN:440845"],"synonyms":[{"name":"SHFM6","type":"exact"},{"name":"WNT10B split hand-foot malformation","type":"exact"},{"name":"ectrodactyly, autosomal recessive","type":"related"},{"name":"split hand-foot malformation caused by mutation in WNT10B","type":"exact"},{"name":"split hand-foot malformation type 6","type":"exact"},{"name":"split-hand/foot malformation 6","type":"related"},{"name":"split-hand/foot malformation type 6","type":"exact"}],"termid":"MONDO:0009157","xrefs":{"Monarch":{"xref_id":"0009157"}}}


id: PBO:0065717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Prader Willi/Angelman region RNA 1","termid":"PBO:0065717"}


id: PBO:0044866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENN domain containing 2A","termid":"PBO:0044866"}


id: GO:0052583
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of an oxidation-reduction in which a halogen in the donor substance acts as a hydrogen or electron donor and reduces a hydrogen or electron acceptor.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidoreductase activity, acting on halogen in donors (obsolete GO:0052583)","termid":"GO:0052583"}


id: GO:0043045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A epigenetic process that happens during embryonic development that modulates gene expression potential at later stages of development of the organism, including the adult. Epigenetic regulation takes place via chromatin remodeling either by modifying higher order chromatin fiber structure, nucleosomal histones, or cytosine DNA methylation.","definition_xrefs":["PMID:12138111","PMID:22868271","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epigenetic regulation of gene expression","termid":"GO:0040029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006325"],"is_obsolete":false,"name":"epigenetic programming of gene expression","synonyms":[{"name":"DNA methylation involved in embryo development","type":"related"},{"name":"de novo DNA methylation","type":"related"},{"name":"epigenetic regulation of embryonic gene expression","type":"related"},{"name":"post-fertilization epigenetic regulation of gene expression","type":"related"}],"termid":"GO:0043045"}


id: PBO:0091865
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ring-type zinc finger protein","termid":"PBO:0091865"}


id: PBO:0086888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transmembrane polyol transporter; supports growth on and uptake of mannitol and sorbitol with moderate affinity when overexpressed in a strain deleted for hexose family members; minor hexose transport activity when overexpressed in a similar strain; induced by raffinose and galactose at pH 7.7 versus pH 4.7, repressed by high levels of glucose; HXT17 has a paralog, HXT13, that arose from a segmental duplication","termid":"PBO:0086888"}


id: PBO:0043526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly factor 7","termid":"PBO:0043526"}


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


id: MONDO:0005617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually aggressive malignant epithelial neoplasm composed of atypical cells which do not display evidence of glandular, squamous, or transitional cell differentiation.","definition_xrefs":["NCIT:C3692"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"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":"undifferentiated carcinoma","secondary_identifiers":["ICDO:8021/3","EFO:0006772","MEDGEN:60010","ICDO:8020/3","UMLS:C0205698"],"synonyms":[{"name":"anaplastic carcinoma","type":"exact"},{"name":"carcinoma, undifferentiated","type":"exact"},{"name":"carcinoma, undifferentiated, malignant","type":"exact"},{"name":"undifferentiated carcinoma","type":"exact"}],"termid":"MONDO:0005617","xrefs":{"Monarch":{"xref_id":"0005617"}}}


id: MONDO:0006847
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neoplasms composed of lymphoid tissue, a lattice work of reticular tissue the interspaces of which contain lymphocytes. The concept does not refer to neoplasms located in lymphatic vessels.","definition_xrefs":["MESH:D018190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoid neoplasm","termid":"MONDO:0005157"}],"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":"malignant lymphatic vessel tumor","termid":"MONDO:0006847","xrefs":{"Monarch":{"xref_id":"0006847"}}}


id: PBO:0088710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF2457 family conserved fungal protein","termid":"PBO:0088710"}


id: MONDO:0012760
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"idiopathic generalized epilepsy","termid":"MONDO:0005579"},{"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, 5","secondary_identifiers":["DOID:0111320","MEDGEN:393842","UMLS:C2677808","OMIM:611934"],"synonyms":[{"name":"EIG5","type":"exact"},{"name":"epilepsy, idiopathic generalized, susceptibility to, 5","type":"exact"},{"name":"epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 10","type":"related"}],"termid":"MONDO:0012760","xrefs":{"Monarch":{"xref_id":"0012760"}}}


id: GO:0045643
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of eosinophil differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of granulocyte differentiation","termid":"GO:0030852"},{"relation_name":"regulates","term_name":"eosinophil differentiation","termid":"GO:0030222"}],"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 eosinophil differentiation","termid":"GO:0045643"}


id: PBO:0045660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decapping exoribonuclease","termid":"PBO:0045660"}


id: GO:0072247
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 metanephric glomerular parietal epithelial cell. Metanephric glomerular parietal epithelial cells are specialized epithelial cells that form tight junctions as a barrier to protein transport. These cells may also give rise to podocytes.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular parietal epithelial cell fate commitment","termid":"GO:0072147"},{"relation_name":"is_a","term_name":"metanephric glomerular epithelial cell fate commitment","termid":"GO:0072315"},{"relation_name":"part_of","term_name":"metanephric glomerular parietal epithelial cell differentiation","termid":"GO:0072245"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric glomerular parietal epithelial cell fate commitment","synonyms":[{"name":"metanephric Bowman's capsule cell fate commitment","type":"exact"}],"termid":"GO:0072247"}


id: FYPO:0008404
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the degradation a protein which is normally degraded during meiosis does not occur. Protein degradation, also known as protein catabolism, is any metabolic process that results in the destruction of the native, active configuration of a protein, with or without the hydrolysis of peptide bonds.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein degradation","termid":"FYPO:0002275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein degradation during meiosis","termid":"FYPO:0008404"}


id: PR:Q09735
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cytosol aminopeptidase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00229","PANTHER:PTHR11963:SF3","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":"aminopeptidase C13A11.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13A11.05","secondary_identifiers":["UniProtKB:Q09735"],"synonyms":[{"name":"Spom972h-LAP3","type":"exact"}],"termid":"PR:Q09735"}


id: PBO:0049957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HIG1 hypoxia inducible domain family member 1A pseudogene 3","termid":"PBO:0049957"}


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


id: GO:1990512
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Nuclear transcriptional repressor complex that is capable of negatively regulating CLOCK-BMAL-dependent transactivation of genes in a delayed negative feedback manner which generates circadian rhythms.","definition_xrefs":["GOC:bhm","PMID:24855952"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription repressor complex","termid":"GO:0017053"},{"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:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Cry-Per complex","termid":"GO:1990512"}


id: MONDO:0006411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, highly aggressive carcinoma that arises from the sinonasal tract. It is characterized by the presence of small to medium size malignant cells. The prognosis is poor.","definition_xrefs":["NCIT:C54294"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undifferentiated carcinoma","termid":"MONDO:0005617"}],"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":"sinonasal undifferentiated carcinoma","secondary_identifiers":["DOID:0080799","SCTID:697993003","UMLS:C1710096","EFO:1000527","MEDGEN:313704","MESH:C537344","ONCOTREE:SNUC"],"synonyms":[{"name":"SNUC","type":"related"},{"name":"Sinonasal anaplastic carcinoma","type":"exact"},{"name":"highly aggressive undifferentiated carcinoma of the nasal cavity and paranasal sinuses","type":"related"},{"name":"sinonasal undifferentiated carcinoma","type":"exact"},{"name":"undifferentiated Sinonasal cancer","type":"exact"}],"termid":"MONDO:0006411","xrefs":{"Monarch":{"xref_id":"0006411"}}}


id: PATO:0000290
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000290 absolute respiratory rate (obsolete PATO:0000290)","termid":"PATO:0000290"}


id: PBO:0058677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6805","termid":"PBO:0058677"}


id: MONDO:0012085
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAH5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 3","secondary_identifiers":["DOID:0110599","GARD:15436","MEDGEN:325210","MESH:C535278","NCIT:C172392","OMIM:608644","UMLS:C1837618"],"synonyms":[{"name":"CILD3","type":"exact"},{"name":"DNAH5 primary ciliary dyskinesia","type":"exact"},{"name":"ciliary dyskinesia, primary, 3","type":"related"},{"name":"ciliary dyskinesia, primary, 3, with or without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 3","type":"exact"},{"name":"primary ciliary dyskinesia 3","type":"exact"},{"name":"primary ciliary dyskinesia 3 with or without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in DNAH5","type":"exact"},{"name":"primary ciliary dyskinesia type 3","type":"exact"}],"termid":"MONDO:0012085","xrefs":{"Monarch":{"xref_id":"0012085"}}}


id: MONDO:0017013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 8p is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 8, with highly variable phenotype ranging from no dysmorphic features and only mild intellectual disability to patients with severe developmental delay, neonatal hypotonia, short stature, profound intellectual disability, mild dysmorphic features (e.g. mild ptosis, hypertelorism, down-slanting palpebral fissures, broad nasal bridge, short, prominent philtrum, abnormal dentition) and structural brain abnormalities. Autism, epilepsy, and spastic paraplegia have also been reported.","definition_xrefs":["Orphanet:264450"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 8","termid":"MONDO:0016945"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trisomy 8p","secondary_identifiers":["MESH:C538019","UMLS:C0795825","GARD:20920","MEDGEN:167072"],"synonyms":[{"name":"Duplication 8p","type":"exact"},{"name":"trisomy type 8p","type":"exact"}],"termid":"MONDO:0017013","xrefs":{"Monarch":{"xref_id":"0017013"}}}


id: GO:0042726
data:
  {"annotated_genes":["SJAG_00491","SJAG_00376","SJAG_01054","SJAG_02491","SJAG_01937","SJAG_02360","SJAG_00480","SJAG_04711","SJAG_04845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006747"},{"annotations":[74598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009398"},{"annotations":[116089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046444"},{"annotations":[119164,60578,72987,67140,80494,79732,78198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009231"},{"annotations":[74599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006771"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving a flavin, any derivative of the dimethylisoalloxazine (7,8-dimethylbenzo[g]pteridine-2,4(3H,10H)-dione) skeleton, with a substituent on the 10 position.","definition_xrefs":["GOC:mah","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00376":null,"SJAG_00480":null,"SJAG_00491":null,"SJAG_01054":null,"SJAG_01937":null,"SJAG_02360":null,"SJAG_02491":null,"SJAG_04711":null,"SJAG_04845":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"flavin-containing compound metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"flavin-containing compound metabolism","type":"exact"},{"name":"riboflavin and derivative metabolic process","type":"related"},{"name":"riboflavin and derivative metabolism","type":"related"},{"name":"vitamin B2 and derivative metabolic process","type":"related"},{"name":"vitamin B2 and derivative metabolism","type":"related"}],"termid":"GO:0042726","terms_by_termid":{"GO:0006747":null,"GO:0006771":null,"GO:0009231":null,"GO:0009398":null,"GO:0046444":null}}


id: GO:0000912
data:
  {"annotated_genes":["SJAG_01732","SJAG_02431","SJAG_04498","SJAG_03048","SJAG_04703","SJAG_02838","SJAG_01943","SJAG_01787","SJAG_01894","SJAG_02864","SJAG_04982","SJAG_00082","SJAG_00700","SJAG_02592","SJAG_02392","SJAG_04621","SJAG_00279","SJAG_04887","SJAG_03596","SJAG_03025","SJAG_00938","SJAG_03045","SJAG_04597","SJAG_04930","SJAG_00845","SJAG_01805","SJAG_02795","SJAG_01143","SJAG_02831","SJAG_02700","SJAG_00228","SJAG_03703","SJAG_00268","SJAG_04077"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91150,100160,110072,99902],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071520"},{"annotations":[100775,76705,99524,58727,121498,74300,59898,68511,77336,90073,97151,112757,78085,113831,70600,120474,99795,94383,104464,114272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903475"},{"annotations":[79192],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903479"},{"annotations":[100149],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:2000432"},{"annotations":[92594,96216,104264,105598,97714,112721],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903500"},{"annotations":[96258,91822],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903501"},{"annotations":[95654,121444],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903499"}]},"cv_name":"biological_process","definition":"The assembly and arrangement of an apparatus composed of actin, myosin, and associated proteins that will function in cytokinesis.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"cytokinetic process","termid":"GO:0032506"},{"relation_name":"part_of","term_name":"cytoskeleton-dependent cytokinesis","termid":"GO:0061640"}],"gene_count":34,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00228":null,"SJAG_00268":null,"SJAG_00279":null,"SJAG_00700":null,"SJAG_00845":null,"SJAG_00938":null,"SJAG_01143":null,"SJAG_01732":null,"SJAG_01787":null,"SJAG_01805":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_02392":null,"SJAG_02431":null,"SJAG_02592":null,"SJAG_02700":null,"SJAG_02795":null,"SJAG_02831":null,"SJAG_02838":null,"SJAG_02864":null,"SJAG_03025":null,"SJAG_03045":null,"SJAG_03048":null,"SJAG_03596":null,"SJAG_03703":null,"SJAG_04077":null,"SJAG_04498":null,"SJAG_04597":null,"SJAG_04621":null,"SJAG_04703":null,"SJAG_04887":null,"SJAG_04930":null,"SJAG_04982":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"assembly of actomyosin apparatus involved in cytokinesis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:27059155":null,"PMID:32915139":null},"synonyms":[{"name":"actomyosin apparatus assembly involved in cytokinesis","type":"exact"},{"name":"cytokinesis, formation of actomyosin apparatus","type":"exact"},{"name":"formation of actomyosin apparatus involved in cytokinesis","type":"related"}],"termid":"GO:0000912","terms_by_termid":{"GO:0071520":null,"GO:0120306":null,"GO:1903475":null,"GO:1903479":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:2000432":null}}


id: PBO:0064531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit H","termid":"PBO:0064531"}


id: MONDO:0002472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising in a pre-existing pleomorphic adenoma. It most often occurs in the parotid gland and less often in the submandibular gland and minor salivary gland. Patients usually present with a history of a long-standing mass which recently had undergone rapid growth. The prognosis depends on the invasiveness of the malignant component. Patients with non-invasive or minimally invasive tumors usually have a good prognosis following surgical resection. Invasive tumors are usually aggressive and are associated with recurrences and metastases.","definition_xrefs":["NCIT:C4397"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myoepithelial tumor","termid":"MONDO:0002380"},{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"},{"relation_name":"is_a","term_name":"malignant mixed neoplasm","termid":"MONDO:0005853"}],"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":"carcinoma ex pleomorphic adenoma","secondary_identifiers":["ICDO:8941/3","UMLS:C0344460","MEDGEN:87486"],"synonyms":[{"name":"carcinoma ex pleomorphic adenoma","type":"exact"},{"name":"carcinoma ex pleomorphic adenoma (morphologic abnormality)","type":"exact"},{"name":"carcinoma in pleomorphic adenoma","type":"exact"}],"termid":"MONDO:0002472","xrefs":{"Monarch":{"xref_id":"0002472"}}}


id: GO:0034618
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 2-amino-5-(carbamimidamido)pentanoic acid.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid binding","termid":"GO:0016597"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"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":"arginine binding","synonyms":[{"name":"Arg binding","type":"exact"},{"name":"aminopentanoic acid binding","type":"related"}],"termid":"GO:0034618"}


id: FYPO:0001923
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 protein dephosphorylation is normal (i.e. indistinguishable from wild type) during the G2/M phase transition of the mitotic cell cycle. Protein dephosphorylation is the removal of a phosphate group from a protein amino acid.","definition_xrefs":["PomBase:mah","GO:0006470"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein dephosphorylation during vegetative growth","termid":"FYPO:0001922"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein dephosphorylation during mitotic G2/M transition","synonyms":[{"name":"normal protein dephosphorylation during G2/M phase transition","type":"exact"},{"name":"normal protein dephosphorylation during G2/M transition during vegetative growth","type":"exact"},{"name":"normal protein dephosphorylation during G2/M transition of mitotic cell cycle","type":"exact"},{"name":"normal protein/peptide dephosphorylation during mitotic G2/M transition","type":"exact"}],"termid":"FYPO:0001923"}


id: PBO:0058582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6715b","termid":"PBO:0058582"}


id: MONDO:0012233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any Li-Fraumeni syndrome in which the cause of the disease is a mutation in the CHEK2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"gene_count":0,"genotype_count":0,"name":"obsolete Li-Fraumeni syndrome 2 (obsolete MONDO:0012233)","secondary_identifiers":["OMIM:609265","MESH:C563755","DOID:0111504"],"synonyms":[{"name":"CHEK2 Li-Fraumeni syndrome","type":"exact"},{"name":"LFS2","type":"related"},{"name":"Li-Fraumeni syndrome 2","type":"exact"},{"name":"Li-Fraumeni syndrome caused by mutation in CHEK2","type":"exact"},{"name":"Li-Fraumeni syndrome type 2","type":"exact"}],"termid":"MONDO:0012233","xrefs":{"Monarch":{"xref_id":"0012233"}}}


id: PBO:0046421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPHA5 antisense RNA 1","termid":"PBO:0046421"}


id: PBO:0003438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexed with Cdc5 protein Cwf15","termid":"PBO:0003438"}


id: PBO:0069781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1066, pseudogene","termid":"PBO:0069781"}


id: PBO:0038533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 8","termid":"PBO:0038533"}


id: GO:0045882
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of sulfur utilization.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sulfur utilization","termid":"GO:0006792"},{"relation_name":"is_a","term_name":"negative regulation of response to nutrient levels","termid":"GO:0032108"},{"relation_name":"negatively_regulates","term_name":"sulfur utilization","termid":"GO:0006791"}],"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 sulfur utilization","synonyms":[{"name":"down regulation of sulfur utilization","type":"exact"},{"name":"down-regulation of sulfur utilization","type":"exact"},{"name":"downregulation of sulfur utilization","type":"exact"},{"name":"inhibition of sulfur utilization","type":"narrow"},{"name":"negative regulation of sulphur utilization","type":"exact"}],"termid":"GO:0045882"}


id: GO:0045095
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A filament composed of acidic and basic keratins (types I and II), typically expressed in epithelial cells. The keratins are the most diverse classes of IF proteins, with a large number of keratin isoforms being expressed. Each type of epithelium always expresses a characteristic combination of type I and type II keratins.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament","termid":"GO:0005882"}],"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":"keratin filament","synonyms":[{"name":"acidic keratin","type":"related"},{"name":"basic/neutral keratin","type":"related"}],"termid":"GO:0045095"}


id: MONDO:0025513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune form of urticaria (disease).","definition_xrefs":["MONDO:patterns/autoimmune"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urticaria","termid":"MONDO:0005492"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"autoimmune urticaria","secondary_identifiers":["ICD9:708.8","MEDGEN:725554","SCTID:402397006","UMLS:C1304191"],"synonyms":[{"name":"autoimmune urticaria","type":"exact"},{"name":"autoimmune urticaria (disease)","type":"exact"}],"termid":"MONDO:0025513","xrefs":{"Monarch":{"xref_id":"0025513"}}}


id: FYPO:0003377
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to nitrosative stress is lower than normal. Total RNA or a specific RNA may be affected. Nitrosative stress often results from exposure to high levels of nitric oxide (NO) or the highly reactive oxidant peroxynitrite, which is produced following interaction of NO with superoxide anions.","definition_xrefs":["PomBase:mah","GO:0071500","PMID:20204527"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased RNA level during cellular response to nitrosative stress","synonyms":[{"name":"decreased RNA accumulation during cellular response to nitrosative stress","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to nitrosative stress during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to nitrosative stress","type":"narrow"},{"name":"decreased transcript level during cellular response to nitrosative stress","type":"exact"},{"name":"reduced RNA level during cellular response to nitrosative stress","type":"exact"}],"termid":"FYPO:0003377"}


id: PBO:0072932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small Cajal body-specific RNA 12","termid":"PBO:0072932"}


id: MONDO:0005367
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Physical and psychological dependence on the drug heroin.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opiate dependence","termid":"MONDO:0005530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heroin dependence","secondary_identifiers":["DOID:9976","NCIT:C34694","icd11.foundation:443161089","UMLS:C0019337","EFO:0004240","SCTID:231477003","MEDGEN:5532","MESH:D006556"],"synonyms":[{"name":"Heroin addiction","type":"exact"}],"termid":"MONDO:0005367","xrefs":{"Monarch":{"xref_id":"0005367"}}}


id: GO:0018095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of one or more alpha-linked glutamyl units to the gamma carboxyl group of peptidyl-glutamic acid.","definition_xrefs":["RESID:AA0202"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-glutamic acid modification","termid":"GO:0018200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein polyglutamylation","termid":"GO:0018095"}


id: GO:0061869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hepatic stellate cell migration.","definition_xrefs":["PMID:24204762"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of fibroblast migration","termid":"GO:0010762"},{"relation_name":"regulates","term_name":"hepatic stellate cell migration","termid":"GO:0061868"}],"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 hepatic stellate cell migration","termid":"GO:0061869"}


id: GO:0030878
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the thyroid gland over time, from its formation to the mature structure. The thyroid gland is an endoderm-derived gland that produces thyroid hormone.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gland development","termid":"GO:0048732"},{"relation_name":"part_of","term_name":"endocrine system development","termid":"GO:0035270"}],"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":"thyroid gland development","termid":"GO:0030878"}


id: GO:1990346
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex consisting of BID and BCL-xl, members of the Bcl-2 family of anti- and proapoptotic regulators.","definition_xrefs":["GOC:bhm","PMID:14634621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"BID-BCL-xl complex","termid":"GO:1990346"}


id: MONDO:0005668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypersensitivity granulomatous pneumonitis caused by the inhalation of avian antigens that are present in the dust of the droppings and feathers of many species of birds. In the acute phase it manifests as fever, chills, dyspnea, cough, and chest tightness. Chronic exposure may lead to interstitial lung fibrosis.","definition_xrefs":["NCIT:C34425"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity pneumonitis","termid":"MONDO:0017853"},{"relation_name":"is_a","term_name":"occupational lung disease","termid":"MONDO:0022736"}],"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":"bird fancier's lung","secondary_identifiers":["icd11.foundation:912113736","GARD:16924","SCTID:69339004","DOID:13891","MedDRA:10004941","MEDGEN:586","MESH:D001716","ICD10CM:J67.2","Orphanet:99908","ICD9:495.2","UMLS:C0005592"],"synonyms":[{"name":"Avian hypersensitivity pneumonitis","type":"exact"},{"name":"bird breeder's lung","type":"exact"},{"name":"bird fancier lung","type":"exact"},{"name":"bird fancier's lung","type":"exact"},{"name":"bird-breeder's lung","type":"related"},{"name":"bird-fancier's lung","type":"exact"},{"name":"bird-fanciers' lung","type":"exact"},{"name":"pigeon breeder's lung","type":"exact"},{"name":"pigeon-breeder lung disease","type":"exact"},{"name":"pigeon-breeder's lung","type":"exact"},{"name":"poultry worker's lung","type":"related"}],"termid":"MONDO:0005668","xrefs":{"Monarch":{"xref_id":"0005668"}}}


id: PR:Q09195
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A delta(14)-sterol reductase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04051","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":"delta(14)-sterol reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16G5.18","secondary_identifiers":["UniProtKB:Q09195"],"synonyms":[{"name":"C-14 sterol reductase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-TM7SF2","type":"exact"},{"name":"sterol C14-reductase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09195"}


id: PBO:0044016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"casein kinase 1 epsilon","termid":"PBO:0044016"}


id: PBO:0052216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel modifier subfamily S member 3","termid":"PBO:0052216"}


id: GO:0045028
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a purine nucleotide and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["GOC:mah","PMID:9755289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purinergic nucleotide receptor activity","termid":"GO:0001614"},{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"G protein-coupled purinergic nucleotide receptor activity","synonyms":[{"name":"G protein coupled purinergic nucleotide receptor activity","type":"exact"},{"name":"G-protein coupled purinergic nucleotide receptor activity","type":"exact"},{"name":"P2Y","type":"related"},{"name":"P2Y receptor","type":"related"},{"name":"purinergic nucleotide receptor activity, G protein coupled","type":"exact"},{"name":"purinergic nucleotide receptor activity, G-protein coupled","type":"exact"}],"termid":"GO:0045028"}


id: MONDO:0005777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition resulting from infection by Klebsiella granulomati, which is characterized by ulcerative lesions of the genitalia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"bacterial sexually transmitted disease","termid":"MONDO:0005323"},{"relation_name":"is_a","term_name":"Klebsiella infectious disease","termid":"MONDO:0030603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"granuloma inguinale","secondary_identifiers":["UMLS:C0018190","DOID:9113","EFO:0007291","NCIT:C3065","SCTID:28867007","MESH:D006100","ICD9:099.2","icd11.foundation:764124124","ICD10CM:A58","MEDGEN:42291"],"synonyms":[{"name":"donovanosis","type":"exact"},{"name":"granuloma inguinale","type":"exact"},{"name":"pudendal ulcer","type":"exact"}],"termid":"MONDO:0005777","xrefs":{"Monarch":{"xref_id":"0005777"}}}


# genes

id: HGNC:100
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"ASIC1","product":"acid sensing ion channel subunit 1","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:100"}


id: HGNC:10000
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS4","product":"regulator of G protein signaling 4","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10000"}


id: HGNC:10001
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS5","product":"regulator of G protein signaling 5","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10001"}


id: HGNC:10002
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS6","product":"regulator of G protein signaling 6","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10002"}


id: HGNC:10003
data:
  {"cv_annotations":{},"deletion_viability":"unknown","feature_so_termid":"SO:0000704","feature_type":"gene","flags":["not_load_organism"],"has_protein_features":false,"name":"RGS7","product":"regulator of G protein signaling 7","split_by_parent_groups":{},"taxonid":9606,"taxonomic_distribution":"not curated","transcript_so_termid":null,"uniquename":"HGNC:10003"}


id: HGNC:10004
data:
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id: HGNC:10006
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id: HGNC:10007
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id: HGNC:10008
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id: HGNC:10009
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id: HGNC:1001
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id: HGNC:10010
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id: HGNC:10011
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id: HGNC:10012
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id: HGNC:10013
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id: HGNC:10017
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id: HGNC:10018
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id: HGNC:10019
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id: HGNC:1002
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id: HGNC:10020
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id: HGNC:10021
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id: HGNC:10023
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id: HGNC:10024
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id: HGNC:10025
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id: HGNC:10026
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id: HGNC:10027
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id: HGNC:10031
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id: HGNC:10037
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id: HGNC:10038
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id: HGNC:10039
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id: HGNC:1004
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id: HGNC:10040
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id: HGNC:10041
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id: HGNC:10042
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id: HGNC:10043
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id: HGNC:10044
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id: HGNC:10045
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id: HGNC:10046
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id: HGNC:10047
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id: HGNC:10048
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id: HGNC:10049
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id: HGNC:1005
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id: HGNC:10050
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id: HGNC:10055
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id: HGNC:10056
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id: HGNC:10057
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id: HGNC:10058
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id: HGNC:10059
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id: HGNC:1006
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id: HGNC:10060
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id: HGNC:10061
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id: HGNC:10062
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id: HGNC:10063
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id: HGNC:10064
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id: HGNC:10065
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id: HGNC:10066
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id: HGNC:10067
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id: HGNC:10068
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id: HGNC:10069
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id: HGNC:1007
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id: HGNC:10070
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id: HGNC:10071
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id: HGNC:10072
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id: HGNC:10073
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id: HGNC:10074
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id: HGNC:10075
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id: HGNC:10078
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id: HGNC:10079
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id: HGNC:1008
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id: HGNC:10080
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id: HGNC:10082
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id: HGNC:10083
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id: HGNC:10084
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id: HGNC:10085
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id: HGNC:10086
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id: HGNC:10096
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id: HGNC:10097
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id: HGNC:10098
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id: HGNC:10099
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id: HGNC:101
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id: HGNC:10100
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id: HGNC:10101
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id: HGNC:10103
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id: HGNC:10104
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id: HGNC:10105
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id: HGNC:10106
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id: HGNC:10107
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id: HGNC:10108
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id: HGNC:10109
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id: HGNC:10110
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id: HGNC:10111
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id: HGNC:10112
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id: HGNC:10113
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id: HGNC:10114
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id: HGNC:10115
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id: HGNC:10116
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id: HGNC:10118
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id: HGNC:10119
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id: HGNC:1012
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id: HGNC:10120
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id: HGNC:10123
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id: HGNC:10128
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id: HGNC:10130
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id: HGNC:10133
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id: HGNC:10137
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id: HGNC:10139
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id: HGNC:1014
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id: HGNC:10140
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id: HGNC:10142
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id: HGNC:10143
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id: HGNC:10144
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id: HGNC:10145
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id: HGNC:10146
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id: HGNC:10147
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id: HGNC:10148
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id: HGNC:10149
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id: HGNC:1015
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id: HGNC:10150
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id: HGNC:10151
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id: HGNC:10152
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id: HGNC:10153
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id: HGNC:10154
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id: HGNC:10155
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id: HGNC:10157
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id: HGNC:10158
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id: HGNC:10159
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id: HGNC:1016
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id: HGNC:10160
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id: HGNC:10161
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id: HGNC:10162
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id: HGNC:10163
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id: HGNC:10164
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id: HGNC:10165
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id: HGNC:10166
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id: HGNC:10168
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id: HGNC:1017
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id: HGNC:10175
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id: HGNC:10177
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id: HGNC:10178
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id: HGNC:10179
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id: HGNC:1018
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id: HGNC:10180
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id: HGNC:10181
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id: HGNC:10182
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id: HGNC:10183
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id: HGNC:10184
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id: HGNC:10185
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id: HGNC:10186
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id: HGNC:10187
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id: HGNC:10188
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id: HGNC:10189
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id: HGNC:10192
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id: HGNC:10193
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id: HGNC:10194
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id: HGNC:10195
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id: HGNC:10196
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id: HGNC:10197
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id: HGNC:10198
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id: HGNC:10199
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id: HGNC:102
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id: HGNC:1020
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id: HGNC:10200
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id: HGNC:10201
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id: HGNC:10202
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id: HGNC:10203
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id: HGNC:10204
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id: HGNC:10205
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id: HGNC:10206
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id: HGNC:10207
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id: HGNC:10208
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id: HGNC:10209
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id: HGNC:10210
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id: HGNC:10211
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id: HGNC:10212
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id: HGNC:10214
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id: HGNC:10215
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id: HGNC:10216
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id: HGNC:10217
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id: HGNC:10218
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id: HGNC:10219
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id: HGNC:1022
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id: HGNC:10220
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id: HGNC:10221
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id: HGNC:10222
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id: HGNC:10223
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id: HGNC:10224
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id: HGNC:10225
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id: HGNC:10226
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id: HGNC:10227
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id: HGNC:10228
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id: HGNC:10229
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id: HGNC:1023
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id: HGNC:10230
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id: HGNC:10231
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id: HGNC:10232
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id: HGNC:10233
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id: HGNC:10234
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id: HGNC:10235
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id: HGNC:10236
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id: HGNC:10237
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id: HGNC:10239
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id: HGNC:1024
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id: HGNC:10240
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id: HGNC:10241
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id: HGNC:10242
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id: HGNC:10243
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id: HGNC:10244
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id: HGNC:10245
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id: HGNC:10246
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id: HGNC:10247
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id: HGNC:10248
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id: HGNC:10249
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id: HGNC:10250
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id: HGNC:10251
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id: HGNC:10252
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id: HGNC:10253
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id: HGNC:10254
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id: HGNC:10256
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id: HGNC:10257
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id: HGNC:10258
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id: HGNC:10259
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id: HGNC:10260
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id: HGNC:10261
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id: HGNC:10263
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id: HGNC:1027
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id: HGNC:10274
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id: HGNC:10288
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id: HGNC:10289
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id: HGNC:1029
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id: HGNC:10290
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id: HGNC:10291
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id: HGNC:10293
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id: HGNC:10294
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id: HGNC:10295
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id: HGNC:10296
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id: HGNC:10297
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id: HGNC:10298
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id: HGNC:10299
data:
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id: HGNC:103
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id: HGNC:1030
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id: HGNC:10300
data:
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id: HGNC:10301
data:
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id: HGNC:10302
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id: HGNC:10303
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id: HGNC:10304
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id: HGNC:10305
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id: HGNC:10306
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id: HGNC:10307
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id: HGNC:10310
data:
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id: HGNC:10311
data:
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id: HGNC:10312
data:
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id: HGNC:10313
data:
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id: HGNC:10314
data:
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id: HGNC:10315
data:
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id: HGNC:10316
data:
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id: HGNC:10317
data:
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id: HGNC:10318
data:
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id: HGNC:10319
data:
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id: HGNC:10320
data:
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id: HGNC:10321
data:
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id: HGNC:10322
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id: HGNC:10324
data:
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id: HGNC:10325
data:
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id: HGNC:10327
data:
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id: HGNC:10328
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id: HGNC:10329
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id: HGNC:1033
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id: HGNC:10330
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id: HGNC:10331
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id: HGNC:10332
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id: HGNC:10333
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id: HGNC:10334
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id: HGNC:10335
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id: HGNC:10336
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id: HGNC:10337
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id: HGNC:10338
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id: HGNC:10339
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id: HGNC:1034
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id: HGNC:10340
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id: HGNC:10341
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id: HGNC:10342
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id: HGNC:10343
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id: HGNC:10344
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id: HGNC:10345
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id: HGNC:10346
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id: HGNC:10347
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id: HGNC:10348
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id: HGNC:10349
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id: HGNC:10350
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id: HGNC:10351
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id: HGNC:10352
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id: HGNC:10353
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id: HGNC:10354
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id: HGNC:10355
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id: HGNC:10356
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id: HGNC:10357
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id: HGNC:10358
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id: HGNC:10359
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id: HGNC:1036
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id: HGNC:10360
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id: HGNC:10361
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id: HGNC:10362
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id: HGNC:10363
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id: HGNC:10364
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id: HGNC:10367
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id: HGNC:10368
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id: HGNC:10369
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id: HGNC:1037
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id: HGNC:10371
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id: HGNC:10372
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id: HGNC:10377
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id: HGNC:10378
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id: HGNC:10379
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id: HGNC:10380
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id: HGNC:10381
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id: HGNC:10382
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id: HGNC:10383
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id: HGNC:10384
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id: HGNC:10385
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id: HGNC:10386
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id: HGNC:10387
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id: HGNC:10388
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id: HGNC:10389
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id: HGNC:10396
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id: HGNC:10397
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id: HGNC:10398
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id: HGNC:10399
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id: HGNC:104
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id: HGNC:1040
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id: HGNC:10401
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id: HGNC:10402
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id: HGNC:10404
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id: HGNC:10405
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id: HGNC:10406
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id: HGNC:10407
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id: HGNC:10408
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id: HGNC:10409
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id: HGNC:1041
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id: HGNC:10410
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id: HGNC:10411
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id: HGNC:10412
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id: HGNC:10413
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id: HGNC:10414
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id: HGNC:10415
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id: HGNC:10416
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id: HGNC:10417
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id: HGNC:10418
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id: HGNC:10419
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id: HGNC:10420
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id: HGNC:10421
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id: HGNC:10422
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id: HGNC:10424
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id: HGNC:10425
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id: HGNC:10426
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id: HGNC:10427
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id: HGNC:10428
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id: HGNC:10429
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id: HGNC:1043
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id: HGNC:10430
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id: HGNC:10431
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id: HGNC:10432
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id: HGNC:10433
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id: HGNC:10434
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id: HGNC:10435
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id: HGNC:10436
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id: HGNC:10437
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id: HGNC:10439
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id: HGNC:1044
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id: HGNC:10440
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id: HGNC:10441
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id: HGNC:10442
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id: HGNC:10443
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id: HGNC:10445
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id: HGNC:10446
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id: HGNC:10447
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id: HGNC:10448
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id: HGNC:10449
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id: HGNC:10450
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id: HGNC:10451
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id: HGNC:10452
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id: HGNC:10454
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id: HGNC:10455
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id: HGNC:10456
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id: HGNC:10457
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id: HGNC:10458
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id: HGNC:1046
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id: HGNC:10461
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id: HGNC:10464
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id: HGNC:10466
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id: HGNC:10467
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id: HGNC:10468
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id: HGNC:10469
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id: HGNC:1047
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id: HGNC:10471
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id: HGNC:10472
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id: HGNC:10473
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id: HGNC:10474
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id: HGNC:10475
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id: HGNC:10477
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id: HGNC:10478
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id: HGNC:10479
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id: HGNC:1048
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id: HGNC:10480
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id: HGNC:10481
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id: HGNC:10482
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id: HGNC:10483
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id: HGNC:10484
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id: HGNC:10485
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id: HGNC:10486
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id: HGNC:10487
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id: HGNC:10488
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id: HGNC:10489
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id: HGNC:1049
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id: HGNC:10490
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id: HGNC:10491
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id: HGNC:10492
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id: HGNC:10493
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id: HGNC:10494
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id: HGNC:10495
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id: HGNC:10496
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id: HGNC:10497
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id: HGNC:10498
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id: HGNC:10499
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id: HGNC:105
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id: HGNC:1050
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id: HGNC:10500
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id: HGNC:10504
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id: HGNC:1051
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id: HGNC:10513
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id: HGNC:10514
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id: HGNC:10515
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id: HGNC:10516
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id: HGNC:10518
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id: HGNC:10519
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id: HGNC:1052
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id: HGNC:10520
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id: HGNC:10521
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id: HGNC:10522
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id: HGNC:10524
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id: HGNC:10525
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id: HGNC:10526
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id: HGNC:10527
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id: HGNC:10528
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id: HGNC:1053
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id: HGNC:10530
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id: HGNC:10532
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id: HGNC:10534
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id: HGNC:10535
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id: HGNC:10536
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id: HGNC:10537
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id: HGNC:10538
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id: HGNC:10539
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id: HGNC:1054
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id: HGNC:10540
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id: HGNC:10541
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id: HGNC:10542
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id: HGNC:10545
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id: HGNC:10546
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id: HGNC:10547
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id: HGNC:10548
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id: HGNC:10549
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id: HGNC:1055
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id: HGNC:10555
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id: HGNC:10560
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id: HGNC:10561
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id: HGNC:10563
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id: HGNC:10564
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id: HGNC:10565
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id: HGNC:10566
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id: HGNC:10567
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id: HGNC:10569
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id: HGNC:1057
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id: HGNC:10570
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id: HGNC:10571
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id: HGNC:10572
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id: HGNC:10573
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id: HGNC:10575
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id: HGNC:10576
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id: HGNC:10577
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id: HGNC:1058
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id: HGNC:10580
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id: HGNC:10581
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id: HGNC:10582
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id: HGNC:10583
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id: HGNC:10585
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id: HGNC:10586
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id: HGNC:10588
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id: HGNC:10589
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id: HGNC:1059
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id: HGNC:10590
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id: HGNC:10591
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id: HGNC:10592
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id: HGNC:10593
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id: HGNC:10594
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id: HGNC:10596
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id: HGNC:10597
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id: HGNC:10599
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id: HGNC:1060
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id: HGNC:10600
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id: HGNC:10601
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id: HGNC:10602
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id: HGNC:10603
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id: HGNC:10604
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id: HGNC:10606
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id: HGNC:10607
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id: HGNC:10608
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id: HGNC:10609
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id: HGNC:10610
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id: HGNC:10611
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id: HGNC:10612
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id: HGNC:10613
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id: HGNC:10614
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id: HGNC:10615
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id: HGNC:10616
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id: HGNC:10617
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id: HGNC:10618
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id: HGNC:10619
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id: HGNC:1062
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id: HGNC:10620
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id: HGNC:10621
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id: HGNC:10622
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id: HGNC:10623
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id: HGNC:10624
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id: HGNC:10625
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id: HGNC:10626
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id: HGNC:10627
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id: HGNC:10628
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id: HGNC:10629
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id: HGNC:1063
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id: HGNC:10630
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id: HGNC:10631
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id: HGNC:10632
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id: HGNC:10634
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id: HGNC:10635
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id: HGNC:10637
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id: HGNC:10638
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id: HGNC:10639
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id: HGNC:10640
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id: HGNC:10641
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id: HGNC:10642
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id: HGNC:10643
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id: HGNC:10645
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id: HGNC:10646
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id: HGNC:10647
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id: HGNC:10648
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id: HGNC:1065
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id: HGNC:10658
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id: HGNC:10659
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id: HGNC:1066
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id: HGNC:10660
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id: HGNC:10661
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id: HGNC:10662
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id: HGNC:10663
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id: HGNC:10664
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id: HGNC:10665
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id: HGNC:10666
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id: HGNC:10667
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id: HGNC:10668
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id: HGNC:10669
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id: HGNC:1067
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id: HGNC:10671
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id: HGNC:10672
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id: HGNC:10675
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id: HGNC:10676
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id: HGNC:1068
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id: HGNC:10680
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id: HGNC:10681
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id: HGNC:10682
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id: HGNC:10683
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id: HGNC:10684
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id: HGNC:10685
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id: HGNC:10686
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id: HGNC:10687
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id: HGNC:10688
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id: HGNC:10689
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id: HGNC:1069
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id: HGNC:10690
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id: HGNC:10691
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id: HGNC:10696
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id: HGNC:10697
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id: HGNC:10698
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id: HGNC:10699
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id: HGNC:1070
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id: HGNC:10700
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id: HGNC:10701
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id: HGNC:10702
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id: HGNC:10703
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id: HGNC:10704
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id: HGNC:10705
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id: HGNC:10706
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id: HGNC:10707
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id: HGNC:1071
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id: HGNC:10710
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id: HGNC:10711
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id: HGNC:10712
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id: HGNC:10713
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id: HGNC:10714
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id: HGNC:10715
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id: HGNC:10716
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id: HGNC:10717
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id: HGNC:10718
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id: HGNC:10719
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id: HGNC:1072
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id: HGNC:10720
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id: HGNC:10721
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id: HGNC:10722
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id: HGNC:10723
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id: HGNC:10724
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id: HGNC:10725
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id: HGNC:10726
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id: HGNC:10727
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id: HGNC:10728
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id: HGNC:10729
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id: HGNC:1073
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id: HGNC:10730
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id: HGNC:10731
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id: HGNC:10732
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id: HGNC:10734
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id: HGNC:10735
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id: HGNC:10736
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id: HGNC:10737
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id: HGNC:10738
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id: HGNC:10739
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id: HGNC:1074
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id: HGNC:10740
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id: HGNC:10741
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id: HGNC:10742
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id: HGNC:10743
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id: HGNC:1075
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id: HGNC:10750
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id: HGNC:10751
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id: HGNC:10752
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id: HGNC:10753
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id: HGNC:10755
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id: HGNC:10756
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id: HGNC:10757
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id: HGNC:10759
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id: HGNC:1076
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id: HGNC:10760
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id: HGNC:10761
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id: HGNC:10762
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id: HGNC:10763
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id: HGNC:10765
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