rs876661405

This is a variant in the CEACAM16 gene that changes a glycine to an arginine.

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ClinVar annotation

Pathogenic
1 submitter1 publication

Autosomal dominant nonsyndromic hearing loss 4B

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About CEACAM16

The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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