This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| OCRL-20-RE | 20 (40 μL) | 200 μL |  |
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| OCRL-20-OR | 20 (40 μL) | 200 μL |  |
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| OCRL-20-GO | 20 (40 μL) | 200 μL |  |
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| OCRL-20-GR | 20 (40 μL) | 200 μL |  |
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| OCRL-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Gene Symbol : OCRL
Gene Name : OCRL, inositol polyphosphate-5-phosphatase
Chromosome : CHR X: 129,532,736-129,592,560
Locus : Xq26.1
Alt. Genes : HIPK3
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