ATP2C1

From WikiMD's Food, Medicine & Wellness Encyclopedia

ATP2C1 is a gene that provides instructions for making a protein that is found in many types of cells, including skin cells. This protein is involved in maintaining the balance of calcium and manganese ions within cells. The ATP2C1 gene is located on the short (p) arm of chromosome 3 at position 21.3.

Function[edit | edit source]

The ATP2C1 gene provides instructions for making a protein that is part of a family of proteins called P-type ATPases. These proteins use energy stored in molecules of adenosine triphosphate (ATP) to transport certain ions across cell membranes. The ATP2C1 protein is found in a cell structure called the Golgi apparatus, which modifies and transports proteins and lipids (fats) to other parts of the cell. The ATP2C1 protein transports calcium and manganese ions out of the Golgi apparatus.

Clinical significance[edit | edit source]

Mutations in the ATP2C1 gene cause Hailey-Hailey disease, a condition that affects the skin. This condition is characterized by outbreaks of rashes and blisters in areas of the skin that rub together, such as the neck, armpits, and groin. The rashes and blisters can be painful and itchy, and they often become infected. The skin abnormalities tend to worsen with heat, sweat, and friction.

See also[edit | edit source]

References[edit | edit source]


External links[edit | edit source]

ATP2C1 Resources
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Contributors: Prab R. Tumpati, MD