This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ABHD11-20-RE | 20 (40 μL) | 200 μL |  |
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| ABHD11-20-OR | 20 (40 μL) | 200 μL |  |
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| ABHD11-20-GO | 20 (40 μL) | 200 μL |  |
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| ABHD11-20-GR | 20 (40 μL) | 200 μL |  |
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| ABHD11-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]
Gene Symbol : ABHD11
Gene Name : Abhydrolase domain containing 11
Chromosome : CHR 7: 737,388,66-737,360,93
Locus : 7q11.23
Alt. Genes : G3BP1
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