Activity

Filter

Cancel
Date Panel Item Activity
4 actions
Structural eye disease v0.76 MAB21L2 Nicola Ragge reviewed gene: MAB21L2: Rating: GREEN; Mode of pathogenicity: Other - please provide details in the comments; Publications: 24906020, 25719200; Phenotypes: Microphthalmia, syndromic 14, 615877; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Structural eye disease v0.38 MAB21L2 Ivone Leong reviewed gene: MAB21L2: Rating: GREEN; Mode of pathogenicity: Other - please provide details in the comments; Publications: 24906020, 25719200; Phenotypes: Microphthalmia, syndromic 14, 615877; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Structural eye disease v0.15 MAB21L2 Ivone Leong Source NHS GMS was added to MAB21L2.
Mode of pathogenicity for gene MAB21L2 was changed from to Other - please provide details in the comments
Added phenotypes Microphthalmia, syndromic 14, 615877 for gene: MAB21L2
Structural eye disease v0.2 MAB21L2 Ellen McDonagh gene: MAB21L2 was added
gene: MAB21L2 was added to Structural eye disease. Sources: Expert Review Green
Mode of inheritance for gene: MAB21L2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: MAB21L2 were set to 24906020; 25719200
Phenotypes for gene: MAB21L2 were set to Microphthalmia, syndromic 14, 615877