Gene: NDUFB9
Alternate names for this Gene: B22|CI-B22|LYRM3|MC1DN24|UQOR22
Gene Summary: 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.
Gene is located in Chromosome: 8
Location in Chromosome : 8q24.13
Description of this Gene: NADH:ubiquinone oxidoreductase subunit B9
Type of Gene: protein-coding
Gene: MTSS1
Alternate names for this Gene:
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