This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RD3-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RD3-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RD3-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RD3-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| RD3-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Gene Symbol : RD3
Gene Name : Retinal degeneration 3
Chromosome : CHR 1: 211,492,916-211,476,521
Locus : 1q32.3
Alt. Genes : PREB
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.