Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Optic Atrophy v0.49 ATAD3A Zornitza Stark Marked gene: ATAD3A as ready
Optic Atrophy v0.49 ATAD3A Zornitza Stark Added comment: Comment when marking as ready: Optic atrophy reported in individuals with the recurrent de novo missense p.Arg528Trp only at this stage.
Optic Atrophy v0.49 ATAD3A Zornitza Stark Gene: atad3a has been classified as Green List (High Evidence).
Optic Atrophy v0.46 ATAD3A Zornitza Stark Phenotypes for gene: ATAD3A were changed from to Harel-Yoon syndrome, MIM#617183
Optic Atrophy v0.45 ATAD3A Zornitza Stark Publications for gene: ATAD3A were set to 27640307; 28652416
Optic Atrophy v0.43 ATAD3A Zornitza Stark Publications for gene: ATAD3A were set to
Optic Atrophy v0.41 ATAD3A Zornitza Stark Mode of pathogenicity for gene: ATAD3A was changed from to Other
Optic Atrophy v0.40 ATAD3A Zornitza Stark Mode of inheritance for gene: ATAD3A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Optic Atrophy v0.11 ATAD3A Elena Savva reviewed gene: ATAD3A: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 27640307, 28652416; Phenotypes: Harel-Yoon syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Optic Atrophy v0.0 ATAD3A Zornitza Stark gene: ATAD3A was added
gene: ATAD3A was added to Optic Atrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ATAD3A was set to Unknown