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Retinal disorders v3.26 ACO2 Achchuthan Shanmugasundram Tag Q2_22_MOI was removed from gene: ACO2.
Retinal disorders v3.26 ACO2 Achchuthan Shanmugasundram commented on gene: ACO2
Retinal disorders v3.25 ACO2 Achchuthan Shanmugasundram Mode of inheritance for gene ACO2 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Retinal disorders v2.274 ACO2 Sarah Leigh Tag Q2_22_MOI tag was added to gene: ACO2.
Retinal disorders v2.274 ACO2 Sarah Leigh commented on gene: ACO2: New paper (34056600) describing ACO2 as a cause of autosomal dominant optic atrophy - update of inheritance needed.
Tom Cullup (Great Ormond Street Hospital), 17 Feb 2022
Retinal disorders v2.274 ACO2 Sarah Leigh reviewed gene: ACO2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Retinal disorders v2.274 ACO2 Sarah Leigh Publications for gene: ACO2 were set to
Retinal disorders v1.159 ACO2 Gavin Arno reviewed gene: ACO2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v1.137 ACO2 Ivone Leong Source NHS GMS was added to ACO2.
Rating Changed from Green List (high evidence) to Green List (high evidence)