This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LAT2-20-RE | 20 (40 μL) | 200 μL |  |
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| LAT2-20-OR | 20 (40 μL) | 200 μL |  |
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| LAT2-20-GO | 20 (40 μL) | 200 μL |  |
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| LAT2-20-GR | 20 (40 μL) | 200 μL |  |
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| LAT2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]
Gene Symbol : LAT2
Gene Name : Linker for activation of T-cells family member 2
Chromosome : CHR 7: 742,097,56-742,298,33
Locus : 7q11.23
Alt. Genes : RBM6
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