CLRN2

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Description

The CLRN2 (clarin 2) is a protein-coding gene located on chromosome 4.

CLRN2, also known as Clarin-2, is essential for normal hearing. It plays a crucial role in maintaining the organized structure of the stereocilia bundle, which is vital for converting sound vibrations into electrical signals in the inner ear.

CLRN2 is also known as DFNB117.

Associated Diseases

• Deafness, autosomal recessive 117