KLHL1
Description
The KLHL1 (kelch like family member 1) is a protein-coding gene located on chromosome 13.
Kelch-like protein 1 is a protein that in humans is encoded by the KLHL1 gene.
KLHL1 is also known as MRP2.
Associated Diseases
- childhood onset asthma
- upper respiratory tract disorder
- autosomal dominant sensory ataxia 1
- spinocerebellar ataxia type 11
- Sandhoff disease
- spinocerebellar ataxia type 8
