SCYL3
Description
The SCYL3 (SCY1 like pseudokinase 3) is a protein-coding gene located on chromosome 1.
SCYL3 is a human gene that encodes a protein that interacts with the carboxyl-terminal domain of ezrin.
May regulate cell adhesion and migration complexes in migrating cells.
SCYL3 is also known as PACE-1, PACE1.
Associated Diseases
- Parkinson disease
- multiple sclerosis
- Alzheimer disease
- lysosomal storage disease
- exercise intolerance, riboflavin-responsive
- GNE myopathy
- inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- tibial muscular dystrophy
- autosomal dominant distal myopathy
- myofibrillar myopathy 3
- tubular aggregate myopathy
- polyglucosan body myopathy type 2
- distal myopathy, Welander type
