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DDG2P v3.52 MAGEL2 Achchuthan Shanmugasundram Phenotypes for gene: MAGEL2 were changed from Schaaf-Yang syndrome, OMIM:615547 to Schaaf-Yang syndrome, OMIM:615547
DDG2P v3.52 MAGEL2 Achchuthan Shanmugasundram Phenotypes for gene: MAGEL2 were changed from Schaaf-Yang syndrome; ARTHROGRYPOSIS MULTIPLEX CONGENITA to Schaaf-Yang syndrome, OMIM:615547
DDG2P v3.51 MAGEL2 Achchuthan Shanmugasundram Tag watchlist was removed from gene: MAGEL2.
DDG2P v3.12 MAGEL2 Achchuthan Shanmugasundram reviewed gene: MAGEL2: Rating: GREEN; Mode of pathogenicity: ; Publications: 27195816, 26365340, 24076603; Phenotypes: Schaaf-Yang syndrome, OMIM:615547; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
DDG2P v3.11 MAGEL2 Achchuthan Shanmugasundram Publications for gene: MAGEL2 were updated from 26365340 to 27195816; 26365340; 24076603
DDG2P v0.79 MAGEL2 Rebecca Foulger Classified gene: MAGEL2 as Green List (high evidence)
DDG2P v0.79 MAGEL2 Rebecca Foulger Gene: magel2 has been classified as Green List (High Evidence).
DDG2P v0.55 MAGEL2 Rebecca Foulger edited their review of gene: MAGEL2: Added comment: Multiple DD-Gene2Phenotype ratings (confirmed; probable). Changed rating to Green to reflect highest DD-G2P Disease confidence: confirmed for Schaaf-Yang syndrome.; Changed rating: GREEN
DDG2P v0.4 MAGEL2 Rebecca Foulger commented on gene: MAGEL2: Added watchlist tag to highlight different DD-G2P ratings for different gene:disorder associations.
DDG2P v0.4 MAGEL2 Rebecca Foulger Tag watchlist tag was added to gene: MAGEL2.
DDG2P v0.2 MAGEL2 Rebecca Foulger reviewed gene: MAGEL2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
DDG2P v0.1 MAGEL2 Rebecca Foulger Added phenotypes ARTHROGRYPOSIS MULTIPLEX CONGENITA for gene: MAGEL2
Publications for gene MAGEL2 were changed from 27195816; 24076603 to 26365340
DDG2P v0.1 MAGEL2 Rebecca Foulger gene: MAGEL2 was added
gene: MAGEL2 was added to DDG2P. Sources: Expert Review Amber,DD-Gene2Phenotype
Mode of inheritance for gene: MAGEL2 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Publications for gene: MAGEL2 were set to 27195816; 24076603
Phenotypes for gene: MAGEL2 were set to Schaaf-Yang syndrome