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Polymicrogyria and Schizencephaly v0.53 EMX2 Zornitza Stark Marked gene: EMX2 as ready
Polymicrogyria and Schizencephaly v0.53 EMX2 Zornitza Stark Gene: emx2 has been classified as Amber List (Moderate Evidence).
Polymicrogyria and Schizencephaly v0.53 EMX2 Zornitza Stark Phenotypes for gene: EMX2 were changed from to Schizencephaly MIM# 269160
Polymicrogyria and Schizencephaly v0.52 EMX2 Zornitza Stark Publications for gene: EMX2 were set to 8528262; 9359037; 9153481
Polymicrogyria and Schizencephaly v0.51 EMX2 Zornitza Stark Publications for gene: EMX2 were set to
Polymicrogyria and Schizencephaly v0.50 EMX2 Zornitza Stark Mode of inheritance for gene: EMX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Polymicrogyria and Schizencephaly v0.49 EMX2 Zornitza Stark Classified gene: EMX2 as Amber List (moderate evidence)
Polymicrogyria and Schizencephaly v0.49 EMX2 Zornitza Stark Gene: emx2 has been classified as Amber List (Moderate Evidence).
Polymicrogyria and Schizencephaly v0.48 EMX2 Zornitza Stark Tag disputed tag was added to gene: EMX2.
Polymicrogyria and Schizencephaly v0.45 EMX2 Lauren Akesson reviewed gene: EMX2: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 8528262, 9359037, 9153481; Phenotypes: Schizencephaly MIM# 269160; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Polymicrogyria and Schizencephaly v0.0 EMX2 Zornitza Stark gene: EMX2 was added
gene: EMX2 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green
Mode of inheritance for gene: EMX2 was set to Unknown