LXN
Description
The LXN (latexin) is a protein-coding gene located on chromosome 3.
LXN is a human gene that encodes a protein known as Latexin. It's a potent, non-competitive, and hardly reversible inhibitor of CPA1, CPA2, and CPA4. It may play a role in inflammation.
LXN is also known as ECI, TCI.
Associated Diseases
- hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
- combined oxidative phosphorylation deficiency
- cancer
- cryopyrin-associated periodic syndrome
