heme A: farnesyltransferase [Homo sapiens]

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A Novel COX10 Deletion Polymorphism as a Susceptibility Factor for Sudden Cardiac Death Risk in Chinese Populations. [DNA Cell Biol. 2021]
A Novel COX10 Deletion Polymorphism as a Susceptibility Factor for Sudden Cardiac Death Risk in Chinese Populations.
Yang Z, Zhang Q, Yu H, Li L, He Y, Zhu S, Li C, Zhang S, Luo B, Gao Y. DNA Cell Biol. 2021 Jan; 40(1):10-17. Epub 2020 Nov 11.
Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene. [Ann Neurol. 2004]
Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene.
Coenen MJ, van den Heuvel LP, Ugalde C, Ten Brinke M, Nijtmans LG, Trijbels FJ, Beblo S, Maier EM, Muntau AC, Smeitink JA. Ann Neurol. 2004 Oct; 56(4):560-4.
The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs. [Hum Mol Genet. 1997]
The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs.
Reiter LT, Murakami T, Koeuth T, Gibbs RA, Lupski JR. Hum Mol Genet. 1997 Sep; 6(9):1595-603.

RefSeq genomic sequence
See the genomic reference sequence for the COX10 gene (NG_008034.1).
RefSeq protein
See the reference protein sequence for protoheme IX farnesyltransferase, mitochondrial (NP_001294.2).

Nucleotide
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Transcript/Protein Information [PANTHER Classification System]
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