This gene encodes a member of the G protein-coupled receptors, as well as the EDG family of proteins. The encoded protein is a receptor for sphingosine 1-phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in this gene have been associated with congenital profound deafness. [provided by RefSeq, Mar 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| S1PR2-20-RE | 20 (40 μL) | 200 μL |  |
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| S1PR2-20-OR | 20 (40 μL) | 200 μL |  |
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| S1PR2-20-GO | 20 (40 μL) | 200 μL |  |
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| S1PR2-20-GR | 20 (40 μL) | 200 μL |  |
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| S1PR2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the G protein-coupled receptors, as well as the EDG family of proteins. The encoded protein is a receptor for sphingosine 1-phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in this gene have been associated with congenital profound deafness. [provided by RefSeq, Mar 2016]
Gene Symbol : S1PR2
Gene Name : Sphingosine-1-phosphate receptor 2
Chromosome : CHR 19: 102,312,71-102,214,32
Locus : 19p13.2
Alt. Genes : RBM12
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