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DFNB13 deafness, autosomal recessive 13 [ Homo sapiens (human) ]

Gene ID: 1705, updated on 31-Aug-2024

Summary

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Official Symbol
DFNB13provided by HGNC
Official Full Name
deafness, autosomal recessive 13provided by HGNC
Primary source
MIM:603098
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:
7q34-q36

Bibliography

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Related articles in PubMed

  1. Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers. Masmoudi S, et al. Clin Genet, 2004 Oct. PMID 15355440
  2. A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36. Mustapha M, et al. Eur J Hum Genet, 1998 May-Jun. PMID 9781028
  3. The search of a genetic basis for noise-induced hearing loss (NIHL). Abreu-Silva RS, et al. Ann Hum Biol, 2011 Mar. PMID 20812880

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Observational study of gene-disease association. (HuGE Navigator)
    Title: The search of a genetic basis for noise-induced hearing loss (NIHL).
  2. In order to identify the DFNB13 gene, we sequenced and eliminated three candidate genes.
    Title: Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
Submit: New GeneRIF Correction

Phenotypes

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Associated conditions

Description Tests
deafness, autosomal recessive 13
OMIM: 603098GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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