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    DFNA43 deafness, autosomal dominant 43 [ Homo sapiens (human) ]

    Gene ID: 192676, updated on 2-Oct-2019

    Summary

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    Gene symbol
    DFNA43
    Gene description
    deafness, autosomal dominant 43
    Primary source
    MIM:608394
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

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    Location:
    2p12-p11.1

    Bibliography

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    Related articles in PubMed

    1. Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12. Flex E, et al. J Med Genet, 2003 Apr. PMID 12676899, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    deafness, autosomal dominant 43

    General gene information

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    Markers

    Other Names

    • deafness, autosomal dominant 40

    Property

    • phenotype only

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