The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SEM1-20-RE | 20 (40 μL) | 200 μL |  |
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| SEM1-20-OR | 20 (40 μL) | 200 μL |  |
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| SEM1-20-GO | 20 (40 μL) | 200 μL |  |
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| SEM1-20-GR | 20 (40 μL) | 200 μL |  |
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| SEM1-20-AQ | 20 (40 μL) | 200 μL |  |
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The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]
Gene Symbol : SEM1
Gene Name : SEM1, 26S proteasome complex subunit
Chromosome : CHR 7: 967,098,90-966,887,66
Locus : 7q21.3
Alt. Genes : ALG3
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