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DFNB5 deafness, autosomal recessive 5 [ Homo sapiens (human) ]

Gene ID: 1697, updated on 2-Oct-2019

Summary

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Gene symbol
DFNB5
Gene description
deafness, autosomal recessive 5
Primary source
MIM:600792
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:
14q12

Bibliography

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Related articles in PubMed

  1. Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q. Fukushima K, et al. Hum Mol Genet, 1995 Sep. PMID 8541854

GeneRIFs: Gene References Into Functions

Phenotypes

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deafness, autosomal recessive 5

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases