This gene encodes an extracellular protein that plays a crucial role in the cellular organization of the retina. The encoded protein is assembled and secreted from photoreceptors and bipolar cells as a homo-oligomeric protein complex. Mutations in this gene are responsible for X-linked retinoschisis, a common, early-onset macular degeneration in males that results in a splitting of the inner layers of the retina and severe loss in vision. [provided by RefSeq, Oct 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RS1-20-RE | 20 (40 μL) | 200 μL |  |
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| RS1-20-OR | 20 (40 μL) | 200 μL |  |
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| RS1-20-GO | 20 (40 μL) | 200 μL |  |
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| RS1-20-GR | 20 (40 μL) | 200 μL |  |
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| RS1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an extracellular protein that plays a crucial role in the cellular organization of the retina. The encoded protein is assembled and secreted from photoreceptors and bipolar cells as a homo-oligomeric protein complex. Mutations in this gene are responsible for X-linked retinoschisis, a common, early-onset macular degeneration in males that results in a splitting of the inner layers of the retina and severe loss in vision. [provided by RefSeq, Oct 2008]
Gene Symbol : RS1
Gene Name : Retinoschisin 1
Chromosome : CHR X: 186,721,02-186,396,87
Locus : Xp22.13
Alt. Genes : CELA3A
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