This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RPGRIP1-20-RE | 20 (40 μL) | 200 μL |  |
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| RPGRIP1-20-OR | 20 (40 μL) | 200 μL |  |
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| RPGRIP1-20-GO | 20 (40 μL) | 200 μL |  |
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| RPGRIP1-20-GR | 20 (40 μL) | 200 μL |  |
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| RPGRIP1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008]
Gene Symbol : RPGRIP1
Gene Name : RPGR interacting protein 1
Chromosome : CHR 14: 212,879,76-213,513,15
Locus : 14q11.2
Alt. Genes : CEBPZ
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