6 genes annotated in human
A mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis.
In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "coenzyme q10 deficiency disease"
|Name||Description||Probability||Func Analog Organism|
|AIFM1||apoptosis-inducing factor, mitochondrion-associated, 1||0.123|
|GOT1||glutamic-oxaloacetic transaminase 1, soluble (aspartate aminotransferase 1)||0.040|
|SDHA||succinate dehydrogenase complex, subunit A, flavoprotein (Fp)||0.018|
|SUCLG1||succinate-CoA ligase, alpha subunit||0.014|
|NDUFS2||NADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase)||0.011|
|COQ6||coenzyme Q6 homolog, monooxygenase (S. cerevisiae)||0.004|
|COQ2||coenzyme Q2 homolog, prenyltransferase (yeast)||0.002|
|PDSS1||prenyl (decaprenyl) diphosphate synthase, subunit 1||0.002|
|ADCK3||aarF domain containing kinase 3||0.001|
|COQ9||coenzyme Q9 homolog (S. cerevisiae)||0.001|
|PDSS2||prenyl (decaprenyl) diphosphate synthase, subunit 2||0.001|