NDUFB9 Chromosome 8

NADH:ubiquinone oxidoreductase subunit B9
7 variants 7 Health Risk

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What This Gene Does
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]
Gene Info
Gene Group
"LYR motif containing|NADH:ubiquinone oxidoreductase supernumerary subunits"
Locus Type
gene with protein product
Location
8q24.13
Ensembl
ENSG00000147684
Associated Conditions (3)
NDUFB9-related disorder
Mitochondrial complex I deficiency
nuclear type 24
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS1156454853 Health Risk Conflicting classifications of pathogenicity
RS140417066 Health Risk Conflicting classifications of pathogenicity NDUFB9-related disorder, NDUFB9-related disorder
RS200683472 Health Risk Conflicting classifications of pathogenicity
RS369824948 Health Risk Conflicting classifications of pathogenicity
RS774020236 Health Risk Conflicting classifications of pathogenicity
RS780144498 Health Risk Conflicting classifications of pathogenicity
RS776388520 Health Risk Pathogenic Mitochondrial complex I deficiency, nuclear type 24, Mitochondrial complex I deficiency
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