This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| VWA3B-20-RE | 20 (40 μL) | 200 μL |  |
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| VWA3B-20-OR | 20 (40 μL) | 200 μL |  |
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| VWA3B-20-GO | 20 (40 μL) | 200 μL |  |
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| VWA3B-20-GR | 20 (40 μL) | 200 μL |  |
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| VWA3B-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2017]
Gene Symbol : VWA3B
Gene Name : Von Willebrand factor A domain containing 3B
Chromosome : CHR 2: 980,871,31-983,306,74
Locus : 2q11.2
Alt. Genes : RBM12
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