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PEX2 gene

Known as: RNF72, PXMP3, PEX2 
National Institutes of Health

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Zellweger Syndromeperoxisome assembly factor-1

Papers overview

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2014
2014
A deleterious mutation in the PEX2 gene causes Zellweger syndrome in individuals of Ashkenazi Jewish descent
Zellweger syndrome is known to be caused by numerous mutations that occur in at least 12 of the PEX genes. While phenotypes vary… 
2008
2008
Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent
To elucidate molecular and cellular mechanisms of peroxisome biogenesis, we have isolated Chinese hamster ovary (CHO) cell… 
2008
2008
Characterization of the Interaction between Recombinant Human Peroxin Pex3p and Pex19p
Proteins required for peroxisome biogenesis are termed peroxins. The peroxin Pex3p is a peroxisomal membrane protein (PMP… 
2003
2003
The peroxisomal membrane targeting elements of human peroxin 2 (PEX2).
Peroxin 2 (PEX2) is a 35-kDa integral peroxisomal membrane protein with two transmembrane regions and a zinc RING domain within… 
2002
2002
A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import.
2000
2000
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes.
In yeasts, the peroxin Pex3p was identified as a peroxisomal integral membrane protein that presumably plays a role in the early… 
1999
1999
Chromosomal, in silico and in vitro expression analysis of cardiovascular-based genes encoding zinc finger proteins.
Three hundred and sixty expressed sequence tags (ESTs) from human heart cDNA libraries corresponding to one hundred and twenty… 
1995
1995
The Pichia pastoris PER6 Gene Encodes the Yeast Homologue of Human PAF‐1 a
1994
1994
Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization.
The direct mapping method combined with fluorescence in situ suppression hybridization and replicated prometaphase R-bands, which… 
1993
1993
Peroxisome-deficient Chinese hamster ovary cells with point mutations in peroxisome assembly factor-1.
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