KLHL1

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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