This gene encodes a leucine-rich protein that has multiple pentatricopeptide repeats (PPR). The precise role of this protein is unknown but studies suggest it may play a role in cytoskeletal organization, vesicular transport, or in transcriptional regulation of both nuclear and mitochondrial genes. The protein localizes primarily to mitochondria and is predicted to have an N-terminal mitochondrial targeting sequence. Mutations in this gene are associated with the French-Canadian type of Leigh syndrome. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LRPPRC-20-RE | 20 (40 μL) | 200 μL |  |
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| LRPPRC-20-OR | 20 (40 μL) | 200 μL |  |
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| LRPPRC-20-GO | 20 (40 μL) | 200 μL |  |
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| LRPPRC-20-GR | 20 (40 μL) | 200 μL |  |
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| LRPPRC-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a leucine-rich protein that has multiple pentatricopeptide repeats (PPR). The precise role of this protein is unknown but studies suggest it may play a role in cytoskeletal organization, vesicular transport, or in transcriptional regulation of both nuclear and mitochondrial genes. The protein localizes primarily to mitochondria and is predicted to have an N-terminal mitochondrial targeting sequence. Mutations in this gene are associated with the French-Canadian type of Leigh syndrome. [provided by RefSeq, Mar 2012]
Gene Symbol : LRPPRC
Gene Name : Leucine rich pentatricopeptide repeat containing
Chromosome : CHR 2: 439,960,04-438,862,23
Locus : 2p21
Alt. Genes : FEM1B
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