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

Gene : ACO2
    
OMIM : 100850
    
UniProt : Q99798
    
AmiGO : Q99798
    
WT/mutant : Missense Mutation
    
Phenotype : Infantile cerebellar-retinal degeneration Optic atrophy 9
Protein sequence ( length = 753 ) :
Alphafold2:

pLDDT : 97.4411
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RoseTTA:

B-factor : 4.753
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