- Concept UI
- M0185701
- Scope Note
- 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.
- Terms
-
Peroxisomal Biogenesis Factor 2
Preferred Term
Term UI
T000915885
Date02/16/2017
LexicalTag
NON
ThesaurusID
NLM (2018)
-
Peroxisome Assembly Factor-1
Term UI
T000915886
Date02/16/2017
LexicalTag
NON
ThesaurusID
NLM (1991)
-
Peroxisomal Membrane Protein 35
Term UI
T000915887
Date02/16/2017
LexicalTag
NON
ThesaurusID
NLM (1991)
-
Peroxisome Biogenesis Factor 2
Term UI
T000915888
Date02/16/2017
LexicalTag
NON
ThesaurusID
NLM (2018)
-
Peroxin-2
Term UI
T000915889
Date02/16/2017
LexicalTag
NON
ThesaurusID
NLM (1991)
-
PMP35
Term UI
T215703
Date01/01/1955
LexicalTag
ABB
ThesaurusID
NLM (1991)