Activity

Filter

Cancel
Date Panel Item Activity
15 actions
Holoprosencephaly and septo-optic dysplasia v1.14 DISP1 Bryony Thompson Publications for gene: DISP1 were set to 19184110; 26748417; 23542665
Holoprosencephaly and septo-optic dysplasia v1.13 DISP1 Bryony Thompson Mode of inheritance for gene: DISP1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Holoprosencephaly and septo-optic dysplasia v1.12 DISP1 Bryony Thompson Classified gene: DISP1 as Green List (high evidence)
Holoprosencephaly and septo-optic dysplasia v1.12 DISP1 Bryony Thompson Gene: disp1 has been classified as Green List (High Evidence).
Holoprosencephaly and septo-optic dysplasia v1.3 DISP1 Zornitza Stark Phenotypes for gene: DISP1 were changed from Holoprosencephaly to Holoprosencephaly, MONDO:0016296
Holoprosencephaly and septo-optic dysplasia v0.61 DISP1 Zornitza Stark Marked gene: DISP1 as ready
Holoprosencephaly and septo-optic dysplasia v0.61 DISP1 Zornitza Stark Gene: disp1 has been classified as Amber List (Moderate Evidence).
Holoprosencephaly and septo-optic dysplasia v0.61 DISP1 Zornitza Stark Phenotypes for gene: DISP1 were changed from to Holoprosencephaly
Holoprosencephaly and septo-optic dysplasia v0.60 DISP1 Zornitza Stark Mode of inheritance for gene: DISP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Holoprosencephaly and septo-optic dysplasia v0.59 DISP1 Zornitza Stark Mode of pathogenicity for gene: DISP1 was changed from to Other
Holoprosencephaly and septo-optic dysplasia v0.58 DISP1 Zornitza Stark Publications for gene: DISP1 were set to
Holoprosencephaly and septo-optic dysplasia v0.57 DISP1 Zornitza Stark Classified gene: DISP1 as Amber List (moderate evidence)
Holoprosencephaly and septo-optic dysplasia v0.57 DISP1 Zornitza Stark Gene: disp1 has been classified as Amber List (Moderate Evidence).
Holoprosencephaly and septo-optic dysplasia v0.56 DISP1 Zornitza Stark reviewed gene: DISP1: Rating: AMBER; Mode of pathogenicity: Other; Publications: 19184110, 26748417, 23542665; Phenotypes: Holoprosencephaly; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Holoprosencephaly and septo-optic dysplasia v0.0 DISP1 Zornitza Stark gene: DISP1 was added
gene: DISP1 was added to Holoprosencephaly and septo-optic dysplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: DISP1 was set to Unknown