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    Data summary

    • Publications : 1001
    • Phenotypes : 178
    • Genes : 207
    • Mutations : 4631
    • SNVs : 3422
    • InDels : 1209
    • Last Update : 22/02/2019

    Detailed information for C21orf2






    Basic information
    Official symbolC21orf2
    Official full namechromosome 21 open reading frame 2
    Location21q22.3
    Gene typeprotein-coding
    SynonymsYF5/A2
    Quick linksEntrez ID:755; HGNC:1260; MIM:603191; Ensembl:ENSG00000160226; HPRD:OTTHUMG00000086909; Vega:
    GO related
    GO term accessionGO term nameNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-Value
    GO:0009653anatomical structure morphogenesis20557025.562.741.99e-167.08e-15
    GO:0030030cell projection organization9344611.623.962.85e-169.84e-15
    GO:0048856anatomical structure development403010250.132.034.19e-161.33e-14
    GO:0000902cell morphogenesis9454211.763.572.49e-137.69e-12
    GO:0032502developmental process457210456.881.833.53e-131.04e-11
    Pathway related
    TermSurceNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    PPI related
    IDNumber of reference genesNumber of genesExpected numberRatio of enrichmentP-valueAdjusted P-value
    OMIM related
    chromosomebeginenddisorder MIM numberdisorderphene mapping keygene/locus MIM numbercytogenetic loaction
    MGI related
    chromosomebeginendgene IDgene symbol of mouseMGIMPphenotype description
    chr2145747826457592217551810043G02RikMGI:1915134--
    Mutation spectrum

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    Gene-disease network

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