This nuclear gene encodes a protein that localizes to the mitochondria, where it catalyzes the transfer of L-arginine to its cognate tRNA, an important step in translation of mitochondrially-encoded proteins. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RARS2-20-RE | 20 (40 μL) | 200 μL |  |
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| RARS2-20-OR | 20 (40 μL) | 200 μL |  |
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| RARS2-20-GO | 20 (40 μL) | 200 μL |  |
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| RARS2-20-GR | 20 (40 μL) | 200 μL |  |
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| RARS2-20-AQ | 20 (40 μL) | 200 μL |  |
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This nuclear gene encodes a protein that localizes to the mitochondria, where it catalyzes the transfer of L-arginine to its cognate tRNA, an important step in translation of mitochondrially-encoded proteins. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Gene Symbol : RARS2
Gene Name : Arginyl-tRNA synthetase 2, mitochondrial
Chromosome : CHR 6: 875,900,31-875,137,43
Locus : 6q15
Alt. Genes : RAD50
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