This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PEX2-20-RE | 20 (40 μL) | 200 μL |  |
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| PEX2-20-OR | 20 (40 μL) | 200 μL |  |
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| PEX2-20-GO | 20 (40 μL) | 200 μL |  |
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| PEX2-20-GR | 20 (40 μL) | 200 μL |  |
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| PEX2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
Gene Symbol : PEX2
Gene Name : Peroxisomal biogenesis factor 2
Chromosome : CHR 8: 770,010,43-769,802,57
Locus : 8q21.13
Alt. Genes : LRPPRC
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