This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LCA5-20-RE | 20 (40 μL) | 200 μL |  |
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| LCA5-20-OR | 20 (40 μL) | 200 μL |  |
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| LCA5-20-GO | 20 (40 μL) | 200 μL |  |
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| LCA5-20-GR | 20 (40 μL) | 200 μL |  |
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| LCA5-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]
Gene Symbol : LCA5
Gene Name : LCA5, lebercilin
Chromosome : CHR 6: 795,374,29-794,849,90
Locus : 6q14.1
Alt. Genes : TRAP1
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