This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| REEP1-20-RE | 20 (40 μL) | 200 μL |  |
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| REEP1-20-OR | 20 (40 μL) | 200 μL |  |
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| REEP1-20-GO | 20 (40 μL) | 200 μL |  |
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| REEP1-20-GR | 20 (40 μL) | 200 μL |  |
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| REEP1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Gene Symbol : REEP1
Gene Name : Receptor accessory protein 1
Chromosome : CHR 2: 863,380,82-862,139,92
Locus : 2p11.2
Alt. Genes : TRAP1
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