This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC4A11-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC4A11-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC4A11-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC4A11-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC4A11-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]
Gene Symbol : SLC4A11
Gene Name : Solute carrier family 4 member 11
Chromosome : CHR 20: 324,148,2-322,741,6
Locus : 20p13
Alt. Genes : LRPPRC
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