Harmonizome 3.0

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]

CDH23 antisense RNA 1

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cdh23 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From Pathway Commons Protein-Protein Interactions

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

From CORUM Protein Complexes

proteins in the Cdh23-Myo1c complex protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the CDH23-harmonin transmembrane complex protein complex from the CORUM Protein Complexes dataset.

From DisGeNET Gene-Disease Associations

genes associated with the disease Ush1D/F, Cdh23/Pcdh15, Digenic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.