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DFNB27 deafness, autosomal recessive 27 [ Homo sapiens (human) ]

Gene ID: 23713, updated on 31-Aug-2024

Summary

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Official Symbol
DFNB27provided by HGNC
Official Full Name
deafness, autosomal recessive 27provided by HGNC
Primary source
MIM:605818
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:
2q24

Bibliography

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Related articles in PubMed

  1. A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31. Pulleyn LJ, et al. Eur J Hum Genet, 2000 Dec. PMID 11175289

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
deafness, autosomal recessive 27
OMIM: 605818GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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