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Fetal anomalies v0.515 CHUK Zornitza Stark Marked gene: CHUK as ready
Fetal anomalies v0.515 CHUK Zornitza Stark Gene: chuk has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.515 CHUK Zornitza Stark Phenotypes for gene: CHUK were changed from COCOON SYNDROME to Popliteal pterygium syndrome, Bartsocas-Papas type 2, MIM# 619339; Cocoon syndrome, MIM# 613630; AEC-like syndrome
Fetal anomalies v0.514 CHUK Zornitza Stark Publications for gene: CHUK were set to
Fetal anomalies v0.513 CHUK Zornitza Stark Mode of inheritance for gene: CHUK was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Fetal anomalies v0.512 CHUK Zornitza Stark Classified gene: CHUK as Amber List (moderate evidence)
Fetal anomalies v0.512 CHUK Zornitza Stark Gene: chuk has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.511 CHUK Zornitza Stark reviewed gene: CHUK: Rating: AMBER; Mode of pathogenicity: None; Publications: 25691407, 20961246, 10195895, 10195896, 29523099, 28513979; Phenotypes: Popliteal pterygium syndrome, Bartsocas-Papas type 2, MIM# 619339, Cocoon syndrome, MIM# 613630, AEC-like syndrome; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Fetal anomalies v0.0 CHUK Zornitza Stark gene: CHUK was added
gene: CHUK was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: CHUK was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CHUK were set to COCOON SYNDROME