KCNT1

Potassium channel subfamily T, member 1, also known as KCNT1 or SLACK is a human gene that encodes the K_Ca4.1 protein. K_Ca4.1 is a member of the calcium-activated potassium channel protein family

Associated Conditions

Mutations in the KCNT1 gene has been shown to be a cause of Ohtahara syndrome and other congenital neurodegenerative diseases.

See also

• SK channel
• Voltage-gated potassium channel

References

Further reading