This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| WIPF1-20-RE | 20 (40 μL) | 200 μL |  |
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| WIPF1-20-OR | 20 (40 μL) | 200 μL |  |
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| WIPF1-20-GO | 20 (40 μL) | 200 μL |  |
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| WIPF1-20-GR | 20 (40 μL) | 200 μL |  |
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| WIPF1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : WIPF1
Gene Name : WAS/WASL interacting protein family member 1
Chromosome : CHR 2: 174,682,898-174,559,573
Locus : 2q31.1
Alt. Genes : ENAM
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