Peroxisomal Biogenesis Factor 2
A multi-pass transmembrane protein that contains a C-terminal RING finger domain. It localizes to the PEROXISOME membrane and is essential for peroxisome biogenesis. Mutations in the PEX2 gene are associated with ZELLWEGER SYNDROME and INFANTILE REFSUM DISEASE.
Year introduced: 2018 (1991)
PubMed search builder options
Subheadings:
Tree Number(s): D12.776.157.635.500, D12.776.543.689
MeSH Unique ID: D000074428
Registry Number: 135847-86-8
Entry Terms:
- Peroxisome Assembly Factor-1
- Peroxisome Assembly Factor 1
- Peroxisomal Membrane Protein 35
- Peroxisome Biogenesis Factor 2
- Peroxin-2
- Peroxin 2
- PMP35
See Also: