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pex1

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Official Full Name
peroxisomal biogenesis factor 1
Background
This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.
Synonyms
PEX1; peroxisomal biogenesis factor 1; peroxisome biogenesis factor 1 , Zellweger syndrome , Zellweger syndrome 1 , ZWS, ZWS1; peroxisome biogenesis factor 1; Highly similar to ATPase [H.sapiens]; Peroxin 1; Peroxin-1; peroxin1; Peroxisome biogenesis disorder protein 1; PEX1_HUMAN; ZWS1; Zellweger syndrome; ZWS