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    DFNA47 deafness, autosomal dominant 47 [ Homo sapiens (human) ]

    Gene ID: 246289, updated on 2-Oct-2019

    Summary

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    Gene symbol
    DFNA47
    Gene description
    deafness, autosomal dominant 47
    Primary source
    MIM:608652
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    DFNB83

    Genomic context

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    Location:
    9p22-p21

    Bibliography

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    Related articles in PubMed

    1. A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family. D'Adamo P, et al. Eur J Hum Genet, 2003 Feb. PMID 12634859

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    deafness, autosomal dominant 47

    General gene information

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    Property

    • phenotype only

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