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Optic neuropathy v2.63 MFN2 Arina Puzriakova Phenotypes for gene: MFN2 were changed from Optic Atrophy; Hereditary motor and sensory neuropathy VIA; Charcot-Marie-Tooth disease, axonal, type 2A2A (AD), 609260; Charcot-Marie-Tooth disease, axonal, type 2A2B (AR), 617087; Hereditary motor and sensory neuropathy VIA (AD), 601152 to Charcot-Marie-Tooth disease, axonal, type 2A2A, OMIM:609260; Charcot-Marie-Tooth disease, axonal, type 2A2B, OMIM:617087; Hereditary motor and sensory neuropathy VIA, OMIM:601152
Optic neuropathy v1.28 MFN2 Tom Cullup reviewed gene: MFN2: Rating: GREEN; Mode of pathogenicity: ; Publications: 26955893, 26306937, 21715711; Phenotypes: Optic Atrophy, Hereditary motor and sensory neuropathy VIA, Charcot-Marie-Tooth disease, axonal, type 2A2A (AD), 609260, Charcot-Marie-Tooth disease, axonal, type 2A2B (AR), 617087, Hereditary motor and sensory neuropathy VIA (AD), 601152; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Optic neuropathy v1.27 MFN2 Ivone Leong Source London North GLH was added to MFN2.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Optic neuropathy MFN2 Panagiotis Sergouniotis reviewed gene: MFN2
Optic neuropathy MFN2 Ellen Thomas marked MFN2 as ready
Optic neuropathy MFN2 Ellen Thomas classified MFN2 as green
Optic neuropathy MFN2 Ellen Thomas commented on MFN2
Optic neuropathy MFN2 Ellen McDonagh classified MFN2 as amber
Optic neuropathy MFN2 Ellen McDonagh commented on MFN2