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    DFNB55 deafness, autosomal recessive 55 [ Homo sapiens (human) ]

    Gene ID: 494148, updated on 2-Oct-2019

    Summary

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    Gene symbol
    DFNB55
    Gene description
    deafness, autosomal recessive 55
    Primary source
    MIM:609952
    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:
    4q12-q13.2

    Bibliography

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    Related articles in PubMed

    1. Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2. Irshad S, et al. Clin Genet, 2005 Sep. PMID 16098016, Free PMC Article

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. DFNB55 represents the third autosomal recessive non-syndromic hearing impairment locus mapped to chromosome 4
      Title: Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.
    Submit: New GeneRIF Correction

    Phenotypes

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    deafness, autosomal recessive 55

    General gene information

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    Property

    • phenotype only

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    Molecular Biology Databases