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DFNB38 deafness, autosomal recessive 38 [ Homo sapiens (human) ]

Gene ID: 337991, updated on 31-Aug-2024

Summary

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Official Symbol
DFNB38provided by HGNC
Official Full Name
deafness, autosomal recessive 38provided by HGNC
Primary source
MIM:608219
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:
6q25.3-q27

Bibliography

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Related articles in PubMed

  1. Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan. Ansar M, et al. Hum Hered, 2003. PMID 12890929, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
deafness, autosomal recessive 38
OMIM: 608219GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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