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    Data summary

    • Publications : 991
    • Phenotypes : 178
    • Genes : 207
    • Mutations : 4583
    • SNVs : 3411
    • InDels : 1172
    • Last Update : 05/11/2017

    Detailed information for RetinalMD_04477






    Basic information
    locationchr17:26875685-26875685 (hg19)
    gene symbolUNC119 (Reference) 
    band17q11.2
    referenceC
    observedT
    diseaseCone-rod dystrophy
    PubMed ID23563732
    ethnicityChinese
    descriptionUNC119:NM_005148:exon2:c.G259A:p.D87N,UNC119:NM_054035:exon2:c.G259A:p.D87N (Reference) 
    MGI
    MGI ID
    MGI phenotype
    OMIM
    OMIM ID
    OMIM phenotype
    Genome feature annotation
    segmental duplicationconserved TFBSEncode TFBSDNase I hypersensitivity sites
    Score=879;Name=V$EVI1_06
    wgEncodeBroadHmm feature annotation
    Gm12878H1hescHepg2HmecHsmmHuvecK562NhekNhlf
    Name=4_Strong_Enhancer
    ESP and CG annotation
    ESP5400ESP5400_aaESP5400_eaESP6500ESP6500_aaESP6500_eaESP6500siESP6500si_aaESP6500si_eaCG46CG69
    --
    dbSNP annotation
    snp137snp135snp132snp131snp130snp129snp137_NonFlaggedsnp135_NonFlaggedsnp132_NonFlaggedsnp131_NonFlaggedsnp130_NonFlagged
    1000 genomes annotation
    2012apr2012apr_eur2012apr_amr2012apr_asn2012apr_afr2012feb2011may2010nov
    Functional prediction
    SIFTSIFT predictPolyPhen2PolyPhen2 predictphyloPphyloP predictLRTLRT predictMTMT predictGERP++GERP++ predictGERP++elemGERP++gt2
    0.08T0.872P0.318B0D1D-5.49
    Conserved and constrained region annotation
    multiz46way
    phastcons46wayScore=614;Name=lod=417
    phylop46way
    RNA function annotation
    human_predictions_S_C_aug2010human_predictions_S_0_aug2010human_predictions_0_C_aug2010human_predictions_0_0_aug2010circRNAs sebastian memczakconserved functional RNA