Non-syndromic hearing impairment protein 5 is a protein that in humans is encoded by the DFNA5 gene.
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, Jul 2008].
via MyGene.info
Non-syndromic hearing impairment protein 5 is a protein that in humans is encoded by the DFNA5 gene.
== Function ==
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).