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DFNB45 deafness, autosomal recessive 45 [ Homo sapiens (human) ]

Gene ID: 449483, updated on 2-Oct-2019

Summary

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Gene symbol
DFNB45
Gene description
deafness, autosomal recessive 45
Primary source
MIM:612433
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:
1q43-q44

Bibliography

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Related articles in PubMed

  1. Mapping of a new autosomal recessive non-syndromic hearing impairment locus (DFNB45) to chromosome 1q43-q44. Bhatti A, et al. Clin Genet, 2008 Apr. PMID 18325041, Free PMC Article

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. The locus responsible for non-syndromic hearing impairment in six generations of a consanguineous Pakistani family was localized to chromosome 1q43-q44.
    Title: Mapping of a new autosomal recessive non-syndromic hearing impairment locus (DFNB45) to chromosome 1q43-q44.
Submit: New GeneRIF Correction

Phenotypes

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deafness, autosomal recessive 45

General gene information

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Property

  • phenotype only

Gene LinkOut

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