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DFNB65 deafness, autosomal recessive 65 [ Homo sapiens (human) ]

Gene ID: 692219, updated on 31-Aug-2024

Summary

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Official Symbol
DFNB65provided by HGNC
Official Full Name
deafness, autosomal recessive 65provided by HGNC
Primary source
MIM:610248
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:
20q13.2-q13.32

Bibliography

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Related articles in PubMed

  1. Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32. Tariq A, et al. J Mol Med (Berl), 2006 Jun. PMID 16596430, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
deafness, autosomal recessive 65
OMIM: 610248GeneReviews: Not available

General gene information

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Property

  • phenotype only

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