CDH23 抗体
(Cadherin 23 (CDH23))
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. [provided by RefSeq, Jan 2010].
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Latest Publications for our CDH23 抗体
: "Cadherin-23 mediates heterotypic cell-cell adhesion between breast cancer epithelial cells and fibroblasts." in: PLoS ONE, Vol. 7, Issue 3, pp. e33289, (2012) (PubMed).: "Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%." in: Journal of medical genetics, Vol. 43, Issue 9, pp. 763-8, (2006) (PubMed).
Aliases for CDH23 抗体
cadherin 23 (otocadherin) (Cdh23) 抗体cadherin related 23 (CDH23) 抗体
cadherin-related 23 (Cdh23) 抗体
4930542A03Rik 抗体
ahl 抗体
ahl1 抗体
bob 抗体
bus 抗体
CDHR23 抗体
mdfw 抗体
nmf112 抗体
nmf181 抗体
nmf252 抗体
sals 抗体
USH1D 抗体
v 抗体
W 抗体
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