This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FARS2-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FARS2-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FARS2-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FARS2-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| FARS2-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Gene Symbol : FARS2
Gene Name : Phenylalanyl-tRNA synthetase 2, mitochondrial
Chromosome : CHR 6: 526,100,0-577,159,1
Locus : 6p25.1
Alt. Genes : LRPPRC
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.