STK38L
Description
The STK38L (serine/threonine kinase 38 like) is a protein-coding gene located on chromosome 12.
STK38L is an enzyme that in humans is encoded by the STK38L gene. It is a serine/threonine-protein kinase.
STK38L plays a role in regulating structural processes within both developing and mature nerve cells.
STK38L is also known as NDR2.
Associated Diseases
- multiple sclerosis
- Parkinson disease
- Alzheimer disease
- lysosomal storage disease
- X-linked retinal dysplasia
- severe early-childhood-onset retinal dystrophy
- retinitis pigmentosa
