靶标：
NDUFB9
产品别名：
B22； CI-B22； LYRM3； MC1DN24； UQOR22； NDUFB9； NADH:ubiquinone oxidoreductase subunit B9； NADH:ubiquinone oxidoreductase subunit B9； NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9； LYR motif-containing protein 3； NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa； NADH-ubiquinone oxidoreductase B22 subunit； complex I B22 subunit； NDUFB9蛋白；
背景信息：
The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015],
