The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PEX16-20-RE | 20 (40 μL) | 200 μL |  |
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| PEX16-20-OR | 20 (40 μL) | 200 μL |  |
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| PEX16-20-GO | 20 (40 μL) | 200 μL |  |
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| PEX16-20-GR | 20 (40 μL) | 200 μL |  |
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| PEX16-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described. [provided by RefSeq, Jul 2008]
Gene Symbol : PEX16
Gene Name : Peroxisomal biogenesis factor 16
Chromosome : CHR 11: 459,181,22-459,096,68
Locus : 11p11.2
Alt. Genes : RAD50
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