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DFNB85 deafness, autosomal recessive 85 [ Homo sapiens (human) ]

Gene ID: 100359399, updated on 31-Aug-2024

Summary

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Official Symbol
DFNB85provided by HGNC
Official Full Name
deafness, autosomal recessive 85provided by HGNC
Primary source
MIM:613392
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
This locus was defined by homozygosity mapping in a kindred of 42 enrolled individuals, between FAM18B2 and NF1. [provided by RefSeq, Feb 2010]

Genomic context

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Location:
17p12-q11.2

Bibliography

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Related articles in PubMed

  1. Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. Shahin H, et al. Eur J Hum Genet, 2010 Apr. PMID 19888295, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
deafness, autosomal recessive 85
OMIM: 613392GeneReviews: Not available

General gene information

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Property

  • phenotype only

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