This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FANCB-20-RE | 20 (40 μL) | 200 μL |  |
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| FANCB-20-OR | 20 (40 μL) | 200 μL |  |
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| FANCB-20-GO | 20 (40 μL) | 200 μL |  |
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| FANCB-20-GR | 20 (40 μL) | 200 μL |  |
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| FANCB-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
Gene Symbol : FANCB
Gene Name : Fanconi anemia complementation group B
Chromosome : CHR X: 148,732,54-146,908,62
Locus : Xp22.2
Alt. Genes : ENAM
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