PEX26 Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description peroxisomal biogenesis factor 26|This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010] (NCBI Entrez Gene Database, 55670)
External Link http://www.ncbi.nlm.nih.gov/gene/55670
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Genes

9 interacting proteins for PEX26 from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
ELAVL1 ELAV like RNA binding protein 1
HNF4A hepatocyte nuclear factor 4, alpha
PEX1 peroxisomal biogenesis factor 1
PEX16 peroxisomal biogenesis factor 16
PEX19 peroxisomal biogenesis factor 19
PEX3 peroxisomal biogenesis factor 3
PEX6 peroxisomal biogenesis factor 6
SUFU suppressor of fused homolog (Drosophila)
UBC ubiquitin C