Entrez gene ID | | 1687 |
Official gene symbol | | DFNA5 |
Full name | | deafness, autosomal dominant 5 |
Aliases | | ,ICERE-1, |
Gene summary | | Hearing 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] |
Location | | Chromosome: 7 Locus: 7p15 |
Gene position | | 24797639 - 24737974 Map Viewer |
Gene orientation | | minus |
Gene size | | 59666 bp |
Gene sequence |
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OMIM ID | | 608798 |
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