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DFNB46 deafness, autosomal recessive 46 [ Homo sapiens (human) ]

Gene ID: 449488, updated on 31-Aug-2024

Summary

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Official Symbol
DFNB46provided by HGNC
Official Full Name
deafness, autosomal recessive 46provided by HGNC
Primary source
MIM:609647
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:
18p11.32-p11.31

Bibliography

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Related articles in PubMed

  1. Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31. Mir A, et al. Am J Med Genet A, 2005 Feb 15. PMID 15637723, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
deafness, autosomal recessive 46
OMIM: 609647GeneReviews: Not available

General gene information

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Property

  • phenotype only

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