This gene encodes a mitochondrial complex I assembly protein that interacts with complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency, a fatal neonatal disorder of the oxidative phosphorylation system. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NDUFAF3-20-RE | 20 (40 μL) | 200 μL |  |
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| NDUFAF3-20-OR | 20 (40 μL) | 200 μL |  |
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| NDUFAF3-20-GO | 20 (40 μL) | 200 μL |  |
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| NDUFAF3-20-GR | 20 (40 μL) | 200 μL |  |
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| NDUFAF3-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a mitochondrial complex I assembly protein that interacts with complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency, a fatal neonatal disorder of the oxidative phosphorylation system. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2009]
Gene Symbol : NDUFAF3
Gene Name : NADH:ubiquinone oxidoreductase complex assembly factor 3
Chromosome : CHR 3: 490,204,74-490,234,94
Locus : 3p21.31
Alt. Genes : ENAM
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