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peroxisome biogenesis disorder, (zellweger)
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PEX3
The peroxin pex3p initiates membrane assembly in peroxisome biogenesis
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G
PEX13
Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene
PEX19
Interaction of a farnesylated protein with renal type IIa Na/Pi co-transporter in response to parathyroid hormone and dietary phosphate
PEX19 is a predominantly cytosolic chaperone and import receptor for class 1 peroxisomal membrane proteins
Interaction of PEX3 and PEX19 visualized by fluorescence resonance energy transfer (FRET)
PEX14
Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways
Pex17p of Saccharomyces cerevisiae is a novel peroxin and component of the peroxisomal protein translocation machinery
Identification and characterization of the human orthologue of yeast Pex14p
PEX1
The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes
PEX5
Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor
Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
PEX12
Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences
PEX6
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor
PEX10
Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences
PEX26
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation
PEX16
Peroxisome Synthesis in the Absence of Preexisting Peroxisomes
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ABC-family proteins mediated transport
species not specified
2 genes