Entrez gene ID | | 317576 |
Official gene symbol | | Ocrl |
Full name | | oculocerebrorenal syndrome of Lowe |
Aliases | | - |
Gene 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] |
Location | | Chromosome: 0 Locus: Xq35 |
Gene position | | 134271915 - 134322750 Map Viewer |
Gene orientation | | plus |
Gene size | | 50836 bp |
Gene sequence |
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