This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NDUFA12-20-RE | 20 (40 μL) | 200 μL |  |
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| NDUFA12-20-OR | 20 (40 μL) | 200 μL |  |
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| NDUFA12-20-GO | 20 (40 μL) | 200 μL |  |
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| NDUFA12-20-GR | 20 (40 μL) | 200 μL |  |
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| NDUFA12-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012]
Gene Symbol : NDUFA12
Gene Name : NADH:ubiquinone oxidoreductase subunit A12
Chromosome : CHR 12: 950,037,12-949,713,27
Locus : 12q22
Alt. Genes : MKRN3-AS1
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