This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IMPAD1-20-RE | 20 (40 μL) | 200 μL |  |
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| IMPAD1-20-OR | 20 (40 μL) | 200 μL |  |
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| IMPAD1-20-GO | 20 (40 μL) | 200 μL |  |
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| IMPAD1-20-GR | 20 (40 μL) | 200 μL |  |
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| IMPAD1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011]
Gene Symbol : IMPAD1
Gene Name : Inositol monophosphatase domain containing 1
Chromosome : CHR 8: 569,938,73-569,579,28
Locus : 8q12.1
Alt. Genes : ENAM
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