This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PEX10-20-RE | 20 (40 μL) | 200 μL |  |
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| PEX10-20-OR | 20 (40 μL) | 200 μL |  |
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| PEX10-20-GO | 20 (40 μL) | 200 μL |  |
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| PEX10-20-GR | 20 (40 μL) | 200 μL |  |
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| PEX10-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Symbol : PEX10
Gene Name : Peroxisomal biogenesis factor 10
Chromosome : CHR 1: 241,262,1-240,480,1
Locus : 1p36.32
Alt. Genes : KIF20A
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