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 |