Coenzyme Q10 Deficiency Gene Set
Genes
22 genes associated with the disease Coenzyme Q10 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AFP
|
alpha-fetoprotein
|
|
ANO10
|
anoctamin 10
|
|
APTX
|
aprataxin
|
|
ATG5
|
autophagy related 5
|
|
COQ2
|
coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
|
|
COQ4
|
coenzyme Q4
|
|
COQ6
|
coenzyme Q6 monooxygenase
|
|
COQ7
|
coenzyme Q7 homolog, ubiquinone (yeast)
|
|
COQ8A
|
coenzyme Q8A
|
|
COQ8B
|
coenzyme Q8B
|
|
COQ9
|
coenzyme Q9
|
|
ENTPD5
|
ectonucleoside triphosphate diphosphohydrolase 5
|
|
ETFDH
|
electron-transferring-flavoprotein dehydrogenase
|
|
MPV17
|
MpV17 mitochondrial inner membrane protein
|
|
MT-ATP6
|
ATP synthase F0 subunit 6
|
|
PDSS1
|
prenyl (decaprenyl) diphosphate synthase, subunit 1
|
|
PDSS2
|
prenyl (decaprenyl) diphosphate synthase, subunit 2
|
|
PIK3C2A
|
phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
SLC2A1
|
solute carrier family 2 (facilitated glucose transporter), member 1
|
|
SQOR
|
sulfide quinone oxidoreductase
|
|
TK2
|
thymidine kinase 2, mitochondrial
|
