Database of mammalian genes
Home

Home Search Browse RAGs User guide FAQs Links Questions Contribute

Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for DFNA5 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID1687
Official gene symbolDFNA5
Full namedeafness, autosomal dominant 5
Aliases,ICERE-1,
Gene summaryHearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq]
LocationChromosome: 7   Locus: 7p15
Gene position24797639 - 24737974  Map Viewer
Gene orientationminus
Gene size59666 bp
Gene sequence
OMIM ID608798