Concept information
Preferred term
Peroxisomal Biogenesis Factor 2
Type
-
mesh:Descriptor
Definition
- 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.
Broader concept
Entry terms
- 135847-86-8
- Peroxin-2
- Peroxisomal Membrane Protein 35
- Peroxisome Assembly Factor-1
- Peroxisome Biogenesis Factor 2
- PMP35
Allowable Qualifier(s)
- administration & dosage (Qualifier)
- adverse effects (Qualifier)
- agonists (Qualifier)
- analysis (Qualifier)
- antagonists & inhibitors (Qualifier)
- biosynthesis (Qualifier)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemical synthesis (Qualifier)
- chemistry (Qualifier)
- classification (Qualifier)
- deficiency (Qualifier)
- drug effects (Qualifier)
- economics (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- isolation & purification (Qualifier)
- metabolism (Qualifier)
- pharmacokinetics (Qualifier)
- pharmacology (Qualifier)
- physiology (Qualifier)
- poisoning (Qualifier)
- radiation effects (Qualifier)
- standards (Qualifier)
- supply & distribution (Qualifier)
- therapeutic use (Qualifier)
- toxicity (Qualifier)
- ultrastructure (Qualifier)
- urine (Qualifier)
In other languages
-
French
-
135847-86-8
-
Facteur-1 d'assemblage des péroxysomes
-
Facteur-1 d'assemblage du péroxysome
-
Facteur-2 de biogénèse des péroxysomes
-
Facteur-2 de biogénèse du péroxysome
-
Péroxine-2
-
Péroxyne-2
-
PMP35
-
Protéine 35 de la membrane péroxysomale
URI
http://data.loterre.fr/ark:/67375/JVR-R6LN31KF-R
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