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COQ2

coenzyme Q2, polyprenyltransferase

HCNC Approved Symbol
COQ2 (HGNC:25223)
Genomic Coordinates
4:83,263,824 - 83,285,134 (4q21.23)
Synonyms
CL640, FLJ26072
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
{Multiple system atrophy, susceptibility to}
146500AD; AR
Coenzyme Q10 deficiency, primary, 1
607426AR

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the COQ2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Ataxia, progressive
 1 (100.0%)