CDH23 Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description cadherin-related 23|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. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described. [provided by RefSeq, May 2013] (NCBI Entrez Gene Database, 64072)
External Link http://www.ncbi.nlm.nih.gov/gene/64072
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Genes

16 interacting proteins for CDH23 from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
CSNK2A1 casein kinase 2, alpha 1 polypeptide
CSNK2A2 casein kinase 2, alpha prime polypeptide
CSNK2B casein kinase 2, beta polypeptide
CTNND1 catenin (cadherin-associated protein), delta 1
CTNND2 catenin (cadherin-associated protein), delta 2
EGFR epidermal growth factor receptor
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB3 erb-b2 receptor tyrosine kinase 3
ERBB4 erb-b2 receptor tyrosine kinase 4
FER fer (fps/fes related) tyrosine kinase
FYN FYN proto-oncogene, Src family tyrosine kinase
LYN LYN proto-oncogene, Src family tyrosine kinase
MYO7A myosin VIIA
PTPN1 protein tyrosine phosphatase, non-receptor type 1
SRC SRC proto-oncogene, non-receptor tyrosine kinase
USH1C Usher syndrome 1C (autosomal recessive, severe)