This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PEX1-20-RE | 20 (40 μL) | 200 μL |  |
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| PEX1-20-OR | 20 (40 μL) | 200 μL |  |
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| PEX1-20-GO | 20 (40 μL) | 200 μL |  |
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| PEX1-20-GR | 20 (40 μL) | 200 μL |  |
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| PEX1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]
Gene Symbol : PEX1
Gene Name : Peroxisomal biogenesis factor 1
Chromosome : CHR 7: 925,285,30-924,870,22
Locus : 7q21.2
Alt. Genes : ENAM
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