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- Table of Contents
Facts about Ubiquinone biosynthesis protein COQ9, mitochondrial.
May be required to present its bound-lipid to COQ7. .
| Human | |
|---|---|
| Gene Name: | COQ9 |
| Uniprot: | O75208 |
| Entrez: | 57017 |

| Belongs to: |
|---|
| COQ9 family |

C16orf49DKFZp434K046; chromosome 16 open reading frame 49; coenzyme Q9 homolog (S. cerevisiae); coenzyme Q9 homolog (yeast); DKFZP434K046; ubiquinone biosynthesis protein COQ9, mitochondrial
Mass (kDA):
35.509 kDA

| Human | |
|---|---|
| Location: | 16q21 |
| Sequence: | 16; NC_000016.10 (57447479..57461270) |
Mitochondrion.





PMID: 19375058 by Duncan A.J., et al. A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
PMID: 25339443 by Lohman D.C., et al. Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 to enable coenzyme Q biosynthesis.