Gene: MFN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.110 GeneticVariation disease BEFREE Dominant optic atrophy (DOA) and axonal peripheral neuropathy (Charcot-Marie-Tooth type 2, or CMT2) are hereditary neurodegenerative disorders most commonly caused by mutations in the canonical mitochondrial fusion genes OPA1 and MFN2, respectively. 26168012 2015
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.110 GeneticVariation disease CLINVAR
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.110 Biomarker disease HPO