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Optic neuropathy v3.3 SLC25A46 Achchuthan Shanmugasundram Phenotypes for gene: SLC25A46 were changed from Neuropathy, hereditary motor and sensory, type VIB 616505 to Optic atrophy, MONDO:0003608; Neuropathy, hereditary motor and sensory, type VIB, MIM# 616505; Pontocerebellar hypoplasia, type 1E, MIM# 619303, MONDO:0030260
Optic neuropathy v3.2 SLC25A46 Achchuthan Shanmugasundram Publications for gene: SLC25A46 were set to 26168012; 28369803
Optic neuropathy v3.1 SLC25A46 Achchuthan Shanmugasundram reviewed gene: SLC25A46: Rating: GREEN; Mode of pathogenicity: None; Publications: 26168012, 27430653, 28369803, 28376086, 28558379, 28934388, 30178502, 33816684; Phenotypes: Optic atrophy, MONDO:0003608, Neuropathy, hereditary motor and sensory, type VIB, MIM# 616505, Pontocerebellar hypoplasia, type 1E, MIM# 619303, MONDO:0030260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Optic neuropathy v1.28 SLC25A46 Tom Cullup reviewed gene: SLC25A46: Rating: GREEN; Mode of pathogenicity: ; Publications: 26168012, 28369803; Phenotypes: Neuropathy, hereditary motor and sensory, type VIB, 616505; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Optic neuropathy v1.27 SLC25A46 Ivone Leong Source London North GLH was added to SLC25A46.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Optic neuropathy SLC25A46 Sarah Leigh classified SLC25A46 as green
Optic neuropathy SLC25A46 Sarah Leigh edited their review of SLC25A46
Optic neuropathy SLC25A46 Sarah Leigh added SLC25A46 to panel
Optic neuropathy SLC25A46 Sarah Leigh reviewed SLC25A46