Joint Shantou International Eye Centre of Shantou University and The Chinese University of Hong Kong

Gene : PEX7
    
OMIM : 601757
    
UniProt : O00628
    
AmiGO : O00628
    
WT/mutant : Missense Mutation
    
Phenotype : Peroxisome biogenesis disorder 9B Rhizomelic chondrodysplasia punctata, type 1
Protein sequence ( length = 323 ) :
Alphafold2:

pLDDT : 94.0247
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RoseTTA:

B-factor : 8.1695
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