PSPH

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Template:Cs1 config Template:Short description Template:Infobox gene Phosphoserine phosphatase is an enzyme that in humans is encoded by the PSPH gene.[1][2][3]

Function

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.[3]

Clinical significance

Homozygous or compound heterozygous mutations in PSPH cause Neu–Laxova syndrome[4] and Phosphoserine phosphatase deficiency.[5][6]

References

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Further reading

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External links

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