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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_04455






    Basic information
    locationchr5:90055259-90055259 (hg19)
    gene symbolGPR98 (Reference) 
    band5q14.3
    referenceG
    observedA
    diseaseUsher syndrome
    PubMed ID25404053
    ethnicityNotFound
    descriptionADGRV1:NM_032119:exon58:c.G11974A:p.D3992N (Reference) 
    MGI
    MGI ID1274784
    MGI phenotypemortality/aging
    OMIM
    OMIM ID602851
    OMIM phenotypeUsher syndrome, type 2C, GPR98/PDZD7 digenic
    Genome feature annotation
    segmental duplicationconserved TFBSEncode TFBSDNase I hypersensitivity sites
    -
    wgEncodeBroadHmm feature annotation
    Gm12878H1hescHepg2HmecHsmmHuvecK562NhekNhlf
    Name=13_Heterochrom/lo
    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
    0D1D1D0D1D-4.99
    Conserved and constrained region annotation
    multiz46way
    phastcons46wayScore=439;Name=lod=81
    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