NDUFA1 Chromosome X

NADH:ubiquinone oxidoreductase subunit A1
3 variants 3 Health Risk

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What This Gene Does
The human NDUFA1 gene codes for an essential component of complex I of the respiratory chain, which transfers electrons from NADH to ubiquinone. It has been noted that the N-terminal hydrophobic domain has the potential to be folded into an alpha-helix spanning the inner mitochondrial membrane with a C-terminal hydrophilic domain interacting with globular subunits of complex I. The highly conserved two-domain structure suggests that this feature is critical for the protein function and might act as an anchor for the NADH:ubiquinone oxidoreductase complex at the inner mitochondrial membrane. However, the NDUFA1 peptide is one of about 31 components of the "hydrophobic protein" (HP) fraction of complex I which is involved in proton translocation. Thus the NDUFA1 peptide may also participate in that function. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
NADH:ubiquinone oxidoreductase supernumerary subunits
Locus Type
gene with protein product
Location
Xq24
Ensembl
ENSG00000125356
Associated Conditions (3)
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 12
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS797044914 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS104894884 Health Risk Pathogenic Mitochondrial complex I deficiency, nuclear type 12, Mitochondrial complex I deficiency
RS104894885 Health Risk Pathogenic Mitochondrial complex I deficiency, nuclear type 12, Mitochondrial complex I deficiency
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