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Mitochondrial disease v0.1225 MFN2 Zornitza Stark Marked gene: MFN2 as ready
Mitochondrial disease v0.1225 MFN2 Zornitza Stark Gene: mfn2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.1225 MFN2 Zornitza Stark Phenotypes for gene: MFN2 were changed from to Charcot-Marie-Tooth disease, axonal, type 2A2A 609260; Charcot-Marie-Tooth disease, axonal, type 2A2B, MIM# 617087; Hereditary motor and sensory neuropathy VIA, MIM# 601152
Mitochondrial disease v0.1224 MFN2 Zornitza Stark Publications for gene: MFN2 were set to
Mitochondrial disease v0.1223 MFN2 Zornitza Stark Mode of inheritance for gene: MFN2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mitochondrial disease v0.0 MFN2 Zornitza Stark gene: MFN2 was added
gene: MFN2 was added to Mitochondrial_AGHA_VCGS. Sources: Expert Review Green,Australian Genomics Health Alliance Mitochondrial Flagship,Victorian Clinical Genetics Services
Mode of inheritance for gene: MFN2 was set to Unknown