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Fetal anomalies v0.472 MAFB Zornitza Stark Marked gene: MAFB as ready
Fetal anomalies v0.472 MAFB Zornitza Stark Gene: mafb has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.472 MAFB Zornitza Stark Phenotypes for gene: MAFB were changed from MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects to Multicentric carpotarsal osteolysis syndrome (MIM#166300)
Fetal anomalies v0.471 MAFB Zornitza Stark Publications for gene: MAFB were set to
Fetal anomalies v0.470 MAFB Zornitza Stark Classified gene: MAFB as Amber List (moderate evidence)
Fetal anomalies v0.470 MAFB Zornitza Stark Gene: mafb has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.448 MAFB Daniel Flanagan reviewed gene: MAFB: Rating: AMBER; Mode of pathogenicity: None; Publications: 23956186, 30208859; Phenotypes: Multicentric carpotarsal osteolysis syndrome (MIM#166300); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.0 MAFB Zornitza Stark gene: MAFB was added
gene: MAFB was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: MAFB was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: MAFB were set to MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects