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DFNA31 deafness, autosomal dominant 31 [ Homo sapiens (human) ]

Gene ID: 347737, updated on 31-Aug-2024

Summary

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Official Symbol
DFNA31provided by HGNC
Official Full Name
deafness, autosomal dominant 31provided by HGNC
Primary source
MIM:608645
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:
6p21

Bibliography

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Related articles in PubMed

  1. A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3. Snoeckx RL, et al. J Med Genet, 2004 Jan. PMID 14729819, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
deafness, autosomal dominant 31
OMIM: 608645GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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