SCEL
Description
The SCEL (sciellin) is a protein-coding gene located on chromosome 13.
SCEL is a human gene.
SCEL may play a role in the organization or control of proteins within the cornified envelope. Its LIM domain potentially facilitates interactions with other SCEL proteins or different proteins, and might help guide SCEL to the cornified envelope.
SCEL is also known as -.
Associated Diseases
- cancer
- congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency
- breast cancer
- pachyonychia congenita
