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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

Gene LinkOut

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