Gene:
oculocerebrorenal syndrome of Lowe (mapped)
Gene ID:
133762
Symbol:
Ocrl_mapped
Species:
1182
Description:
mutation in human OCRL causes Lowe syndrome, also known as oculocerebrorenal syndrome; mouse homolog RIKEN cDNA 9530014D17 possesses an inositol polyphosphate phosphatase domain [RGD]