COQ2 Chromosome 4

Coenzyme Q2, polyprenyltransferase
52 variants 52 Health Risk

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What This Gene Does
This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme, which is part of the coenzyme Q10 pathway, catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency, a mitochondrial encephalomyopathy, and also COQ2 nephropathy, an inherited form of mitochondriopathy with primary renal involvement. [provided by RefSeq, Oct 2009]
Associated Conditions (13)
Coenzyme Q10 deficiency
primary
1
Nephrotic syndrome
Inborn genetic diseases
COQ2-related disorder
Multiple system atrophy 1
susceptibility to
Focal segmental glomerulosclerosis
Multiple system atrophy
Uterine corpus endometrial carcinoma
Kidney disorder
Neonatal encephalopathy
Key Variants
All Variants (52)
RSID Category Clinical Significance Conditions
RS397514727 Health Risk risk factor Multiple system atrophy, Multiple system atrophy
RS751185256 Health Risk risk factor Multiple system atrophy, Coenzyme Q10 deficiency, Multiple system atrophy
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