Members

 PEX1
 PEX2
 PEX3
 PEX4
 PEX5
 PEX6
 PEX7 - peroxin-7 - mutations in Refsum disease and rhizomelic chondrodysplasia punctata type 1
 PEX8
 PEX9
 PEX10 - peroxin-10 (MIM.602859) - Zelleweger's syndrome complementation group 7, neonatal adrenoleukodystrophy
 PEX11
 PEX12
 PEX13
 PEX14
 PEX15
 PEX16
 PEX17
 PEX18
 PEX19
 PEX20
 PEX21
 PEX22
 PEX23
 PEX24
 PEX25
 PEX26 - peroxin-26 - peroxisome-biogenesis disorders complementation group 8
 PEX27
 PEX28
 PEX29