COCH


Description

The COCH (cochlin) is a protein-coding gene located on chromosome 14.

COCH, also known as Coch, is a human gene.

COCH plays a crucial role in regulating the shape and movement of cells within the trabecular meshwork.

COCH is also known as COCH-5B2, COCH5B2, DFNA9, DFNB110.

Associated Diseases


Disclaimer: The information provided here is not exhaustive by any means. Always consult your doctor or other qualified healthcare provider with any questions you may have regarding a medical condition, procedure, or treatment, whether it is a prescription medication, over-the-counter drug, vitamin, supplement, or herbal alternative.