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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: age related hearing loss 1; bobby; bustling; Cadherin; cadherin 23; cadherin 23 (otocadherin); cadherin-23-like; cadherin-like 23; cadherin-related family member 23; DFNB12; DKFZp434P2350; FLJ00233; FLJ36499; member of cadherin superfamily; MGC102761; modifier of deaf waddler; otocadherin; OTTHUMP00000044780; unnamed protein product; USH1H; waltzer; Waltzing
Gene Aliases: 4930542A03Rik; ahl; ahl1; bob; bus; CDHR23; mdfw; nmf112; nmf181; nmf252; PITA5; sals; USH1D; v
UniProt ID: (Human) Q9H251, (Mouse) Q99PF4, (Rat) P58365
Entrez Gene ID: (Human) 64072, (Mouse) 22295, (Rat) 114102
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