LGI4
Description
The LGI4 (leucine rich repeat LGI family member 4) is a protein-coding gene located on chromosome 19.
LGI4 is involved in Schwann cell signaling pathways, which are essential for controlling how axons are separated and how myelin is formed around them.
LGI4 is also known as AMC1, AMCNMY, LGIL3.
Associated Diseases
- Hypomyelination neuropathy-arthrogryposis syndrome
- Arthrogryposis multiplex congenita, neurogenic, with myelin defect
