Gene: AFG3L2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10939
Gene Symbol: AFG3L2
AFG3L2 		0.110 GeneticVariation phenotype BEFREE Because the same genotype was described in six cases from a Tunisian family with a typical AOA2 without myoclonus, we speculate this latter feature is associated with a second mutated gene, namely AFG3L2 (p.Gly116Arg variant). 25927548 2015
Entrez Id: 10939
Gene Symbol: AFG3L2
AFG3L2 		0.110 Biomarker phenotype HPO