This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TUFM-20-RE | 20 (40 μL) | 200 μL |  |
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| TUFM-20-OR | 20 (40 μL) | 200 μL |  |
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| TUFM-20-GO | 20 (40 μL) | 200 μL |  |
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| TUFM-20-GR | 20 (40 μL) | 200 μL |  |
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| TUFM-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. [provided by RefSeq, Jul 2008]
Gene Symbol : TUFM
Gene Name : Tu translation elongation factor, mitochondrial
Chromosome : CHR 16: 288,595,61-288,424,10
Locus : 16p11.2
Alt. Genes : RBM12
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