Gene Symbol | Ocrl |
Entrez Gene ID | 317576 |
Full Name | OCRL, inositol polyphosphate-5-phosphatase |
General protein information |
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Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome | |
Summary | mutation in human OCRL causes Lowe syndrome, also known as oculocerebrorenal syndrome; mouse homolog RIKEN cDNA 9530014D17 possesses an inositol polyphosphate phosphatase domain [RGD, Feb 2006]. |