The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RLBP1-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RLBP1-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RLBP1-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RLBP1-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RLBP1-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens. [provided by RefSeq, Jul 2008]
Gene Symbol : RLBP1
Gene Name : Retinaldehyde binding protein 1
Chromosome : CHR 15: 892,231,78-892,098,66
Locus : 15q26.1
Alt. Genes : FEM1B
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.