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- Table of Contents
Facts about Peroxisome biogenesis factor 1.
.
Human | |
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Gene Name: | PEX1 |
Uniprot: | O43933 |
Entrez: | 5189 |
Belongs to: |
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AAA ATPase family |
peroxin-1; peroxisomal biogenesis factor 1; Peroxisome biogenesis disorder protein 1; peroxisome biogenesis factor 1; Zellweger syndrome 1; Zellweger syndrome; ZWS; ZWS1
Mass (kDA):
142.867 kDA
Human | |
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Location: | 7q21.2 |
Sequence: | 7; NC_000007.14 (92487023..92528520, complement) |
Cytoplasm. Peroxisome membrane. Associated with peroxisomal membranes.
PMID: 9398848 by Portsteffen H., et al. Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders.
PMID: 9398847 by Reuber B.E., et al. Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.