This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PLEKHG5-20-RE | 20 (40 μL) | 200 μL |  |
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| PLEKHG5-20-OR | 20 (40 μL) | 200 μL |  |
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| PLEKHG5-20-GO | 20 (40 μL) | 200 μL |  |
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| PLEKHG5-20-GR | 20 (40 μL) | 200 μL |  |
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| PLEKHG5-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]
Gene Symbol : PLEKHG5
Gene Name : Pleckstrin homology and RhoGEF domain containing G5
Chromosome : CHR 1: 652,006,0-646,609,1
Locus : 1p36.31
Alt. Genes : RBM12
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