Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
CDH23 cadherin related 23 PITA5 , USH1D , CDHR23 Homo sapiens 71 protein-coding CDHR3 , CDH7 , CDH8 , CDH15 , CDH13 , CDH17 , CDH26 , CDH24 , CDH2 , CDH20 , CDH19 , CDH9 , CDH6 , CDH10 , CDH4 , CDH18 , CDH5 , CDH1 , CDH3 , CDH12 , CDH22 , CDH11 , DCHS1 605516

Summary

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]

GeneOntology

Gene Loss events - CDH23 (1 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_2YMMEM Trichechus manatus Sirenia LOF (frameshift, premature stop, ss) Full No 10.1093/icb/icy004