The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PSPH-20-RE | 20 (40 μL) | 200 μL |  |
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| PSPH-20-OR | 20 (40 μL) | 200 μL |  |
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| PSPH-20-GO | 20 (40 μL) | 200 μL |  |
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| PSPH-20-GR | 20 (40 μL) | 200 μL |  |
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| PSPH-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008]
Gene Symbol : PSPH
Gene Name : Phosphoserine phosphatase
Chromosome : CHR 7: 560,516,03-560,103,62
Locus : 7p11.2
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