CDH23 / USH1D polyclonal, anti-human

Background:
This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described.

Other Names:
Cadherin-23, Otocadherin, CDH23, KIAA1774, KIAA1812

Antigen Types:
Synthetic Peptide

Gene Name:
CDH23 {ECO:0000303|PubMed:11138009, ECO:0000312|HGNC:HGNC:13733}
Gene ID:
64072
Primary Accession: Q9H251
Other Accession: NP_443068;64072;