OXSM
Description
The OXSM (3-oxoacyl-ACP synthase, mitochondrial) is a protein-coding gene located on chromosome 3.
OXSM is believed to be involved in the production of lipoic acid, a vital component for various metabolic processes, as well as the synthesis of longer chain fatty acids that are crucial for optimal mitochondrial function.
OXSM is also known as CEM1, FASN2D, KASI, KS.
Associated Diseases
- congenital disorder of deglycosylation
- congenital disorder of deglycosylation 1
- benign adult familial myoclonic epilepsy
