Peroxisomal Biogenesis Factor 2
                             
                            
                            
                                
                                    
                                            
	"Peroxisomal Biogenesis Factor 2" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, 
	MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, 
	which enables searching at various levels of specificity.
	
	
		
			
			
				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.
    
			
			
				
				
					
						| Descriptor ID | D000074428 | 
					
						| MeSH Number(s) | D12.776.157.635.500 D12.776.543.689 | 
					
						| Concept/Terms | Peroxisomal Biogenesis Factor 2Peroxisomal Biogenesis Factor 2PMP35Peroxisome Biogenesis Factor 2Peroxin-2Peroxin 2Peroxisome Assembly Factor-1Peroxisome Assembly Factor 1Peroxisomal Membrane Protein 35
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				Below are MeSH descriptors whose meaning is more general than "Peroxisomal Biogenesis Factor 2".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Peroxisomal Biogenesis Factor 2".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
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				Below are the most recent publications written about "Peroxisomal Biogenesis Factor 2" by people in Profiles.