The protein encoded by this gene belongs to the evolutionary conserved sif2 family of proteins that share the DUF155 domain in common. This protein is thought to be localized in the mitochondria and involved in mitochondrial translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-11. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RMND1-20-RE | 20 (40 μL) | 200 μL |  |
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| RMND1-20-OR | 20 (40 μL) | 200 μL |  |
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| RMND1-20-GO | 20 (40 μL) | 200 μL |  |
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| RMND1-20-GR | 20 (40 μL) | 200 μL |  |
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| RMND1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene belongs to the evolutionary conserved sif2 family of proteins that share the DUF155 domain in common. This protein is thought to be localized in the mitochondria and involved in mitochondrial translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-11. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012]
Gene Symbol : RMND1
Gene Name : Required for meiotic nuclear division 1 homolog
Chromosome : CHR 6: 151,452,180-151,404,547
Locus : 6q25.1
Alt. Genes : ZNF263
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