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Fetal anomalies v0.3055 MYO5A Zornitza Stark Marked gene: MYO5A as ready
Fetal anomalies v0.3055 MYO5A Zornitza Stark Gene: myo5a has been classified as Red List (Low Evidence).
Fetal anomalies v0.3055 MYO5A Zornitza Stark Phenotypes for gene: MYO5A were changed from GRISCELLI SYNDROME TYPE 3; ELEJALDE SYNDROME to Griscelli syndrome, type 1 MIM#214450
Fetal anomalies v0.3054 MYO5A Zornitza Stark Publications for gene: MYO5A were set to
Fetal anomalies v0.2948 MYO5A Ain Roesley reviewed gene: MYO5A: Rating: RED; Mode of pathogenicity: None; Publications: 32275080, 22711375, 25283056; Phenotypes: Griscelli syndrome, type 1 MIM#214450; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 MYO5A Zornitza Stark gene: MYO5A was added
gene: MYO5A was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: MYO5A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MYO5A were set to GRISCELLI SYNDROME TYPE 3; ELEJALDE SYNDROME