EyeProdb
Ocular Protein Structure Database
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Joint Shantou International Eye Centre of Shantou University and The Chinese University of Hong Kong
By gene
By phenotype
Gene :
MFN2
OMIM :
608507
UniProt :
O95140
AmiGO :
O95140
Phenotype :
Charcot-Marie-Tooth disease, axonal, type 2A2A
Charcot-Marie-Tooth disease, axonal, type 2A2B
Hereditary motor and sensory neuropathy VIA
Lipomatosis, multiple symmetric, with or without peripheral neuropathy
Predicted PDB
WT/mutant
Sequence length
AlphaFold2 pLDDT
RoseTTA B-factor
MFN2R707W
Missense Mutation
757
80.0243_80.0196_78.1052_77.3531_77.0564
4.0057_8.0236_8.0242_8.0243_8.0249
MFN2R94Q
Missense Mutation
757
81.5208_81.4092_78.0577_77.8048_77.4576
3.977_7.4513_8.049_8.0682_8.0692
MFN2WT
Wildtype
757
81.7986_81.2705_77.5396_77.3053_76.9875
3.8694_7.4308_7.92_7.92_8.0479