Retinoschisin 1 抗体
(Retinoschisin 1 (RS1))
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].
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Aliases for Retinoschisin 1 抗体
regulatory solute carrier protein, family 1, member 1 (Rsc1a1) 抗体retinoschisin 1 (RS1) 抗体
retinoschisin 1 S homeolog (rs1.S) 抗体
retinoschisin 1 (rs1) 抗体
retinoschisis (X-linked, juvenile) 1 (human) (Rs1) 抗体
retinoschisin 1a (rs1a) 抗体
retinoschisin 1 (Rs1) 抗体
1700027M01Rik 抗体
OTTMUSG00000010365 抗体
RS 抗体
Rs1 抗体
rs1 抗体
Rs1h 抗体
tmgc1 抗体
XLRS1 抗体
Xlrs1 抗体
zgc:92703 抗体
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