U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

DFNB20 deafness, autosomal recessive 20 [ Homo sapiens (human) ]

Gene ID: 1713, updated on 2-Oct-2019

Summary

Go to the top of the page Help
Gene symbol
DFNB20
Gene description
deafness, autosomal recessive 20
Primary source
MIM:604060
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

Go to the top of the page Help
Location:
11q25-qter

Bibliography

Go to the top of the pageHelp

Related articles in PubMed

  1. DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter. Moynihan L, et al. Eur J Hum Genet, 1999 Feb-Mar. PMID 10196710

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help
deafness, autosomal recessive 20

General gene information

Go to the top of the page Help

Property

  • phenotype only

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases