OCRL

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Template:Short description Template:Infobox gene

Inositol polyphosphate 5-phosphatase OCRL-1, also known as Lowe oculocerebrorenal syndrome protein, is an enzyme encoded by the OCRL gene located on the X chromosome in humans.[1]

This gene encodes an inositol polyphosphate 5-phosphatase. The responsible gene locus is at Xq26.1. This phosphatase enzyme is in part responsible for regulating membrane trafficking actin polymerization, and is located in several subcellular parts of the trans-Golgi network.

Deficiencies in OCRL-1 are associated with oculocerebrorenal syndrome[2] and also have been linked to Dent's disease.[3][4]

References

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  3. Online Mendelian Inheritance in Man (OMIM): 300555
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Further reading

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External links

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