KCNH8
Description
The KCNH8 (potassium voltage-gated channel subfamily H member 8) is a protein-coding gene located on chromosome 3.
KCNH8 is a gene that codes for a protein called potassium voltage-gated channel subfamily H member 8. This protein is a subunit of a voltage-gated potassium channel.
KCNH8 is also known as ELK, ELK1, Kv12.1, elk3.
Associated Diseases
- multiple sclerosis
- transverse myelitis
- Brugada syndrome
- spinal cord injury
- action myoclonus-renal failure syndrome
