CLCNKB : chloride voltage-gated channel Kb


Headline: The Vital Role of CLCNKB in Health and Disease

Description:

The CLC family of genes is responsible for producing chloride channels, which facilitate the transport of chloride ions across cell membranes. Among them, the CLCNKB gene holds a crucial role in the kidneys and inner ear.

Associated Diseases:

Mutations in the CLCNKB gene can lead to disorders such as:

  • Bartter syndrome type 3
  • Gitelman syndrome
  • Hypokalemic alkalosis
  • Sensorineural hearing loss

These conditions primarily affect kidney function, electrolyte balance, and hearing ability.

Did you Know ?

Bartter syndrome type 3, caused by CLCNKB mutations, affects approximately 1 in 500,000 individuals.


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.