SLFN12L
Description
The SLFN12L (schlafen family member 12 like) is a protein-coding gene located on chromosome 17.
The SLFN12L gene encodes a protein called Schlafen family member 12 like. This protein is found in humans and plays a role in regulating cell growth and development.
The SLFN12L gene encodes a protein belonging to the Schlafen family. This family of proteins is known to play a role in regulating cell growth and development, potentially by influencing the cell cycle. However, the specific function of SLFN12L protein remains to be fully characterized.
SLFN12L is also known as -.
Associated Diseases
- isolated agammaglobulinemia
- familial atrial fibrillation
- Brugada syndrome
- common variable immunodeficiency
- severe combined immunodeficiency due to CARD11 deficiency
