KLHL32
Description
The KLHL32 (kelch like family member 32) is a protein-coding gene located on chromosome 6.
KLHL32 is also known as BKLHD5, KIAA1900, UG0030H05, dJ21F7.1.
Associated Diseases
- Griscelli syndrome type 3
- diabetes mellitus, transient neonatal, 2
- type 2 diabetes mellitus
- type 1 diabetes mellitus
- uncombable hair syndrome
- hyperinsulinism due to glucokinase deficiency
- oculocutaneous albinism type 3
- 3-hydroxy-3-methylglutaryl-CoA synthase deficiency
- exercise-induced hyperinsulinism
- glycogen storage disorder due to hepatic glycogen synthase deficiency
- hypotrichosis simplex
