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    DFNA16 deafness, autosomal dominant 16 [ Homo sapiens (human) ]

    Gene ID: 1694, updated on 31-Aug-2024

    Summary

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    Official Symbol
    DFNA16provided by HGNC
    Official Full Name
    deafness, autosomal dominant 16provided by HGNC
    Primary source
    MIM:603964
    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:
    2q24

    Bibliography

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    Related articles in PubMed

    1. A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3. Fukushima K, et al. Am J Hum Genet, 1999 Jul. PMID 10364526, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    deafness, autosomal dominant 16
    OMIM: 603964GeneReviews: Not available

    General gene information

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    Markers

    Property

    • phenotype only

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