This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of proline to tRNA molecules. Mutations have been found in this gene in some patients with Alpers syndrome. [provided by RefSeq, Mar 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PARS2-20-RE | 20 (40 μL) | 200 μL |  |
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| PARS2-20-OR | 20 (40 μL) | 200 μL |  |
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| PARS2-20-GO | 20 (40 μL) | 200 μL |  |
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| PARS2-20-GR | 20 (40 μL) | 200 μL |  |
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| PARS2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of proline to tRNA molecules. Mutations have been found in this gene in some patients with Alpers syndrome. [provided by RefSeq, Mar 2015]
Gene Symbol : PARS2
Gene Name : Prolyl-tRNA synthetase 2, mitochondrial
Chromosome : CHR 1: 547,645,52-547,568,97
Locus : 1p32.3
Alt. Genes : ZNF263
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