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Fetal anomalies v0.3639 FBXO11 Zornitza Stark Marked gene: FBXO11 as ready
Fetal anomalies v0.3639 FBXO11 Zornitza Stark Gene: fbxo11 has been classified as Red List (Low Evidence).
Fetal anomalies v0.3639 FBXO11 Zornitza Stark Phenotypes for gene: FBXO11 were changed from Variable Neurodevelopmental Disorder to Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, MIM# 618089
Fetal anomalies v0.3638 FBXO11 Zornitza Stark Publications for gene: FBXO11 were set to 30057029
Fetal anomalies v0.3637 FBXO11 Zornitza Stark Mode of inheritance for gene: FBXO11 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.3636 FBXO11 Zornitza Stark reviewed gene: FBXO11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, MIM# 618089; Mode of inheritance: None
Fetal anomalies v0.0 FBXO11 Zornitza Stark gene: FBXO11 was added
gene: FBXO11 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: FBXO11 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: FBXO11 were set to 30057029
Phenotypes for gene: FBXO11 were set to Variable Neurodevelopmental Disorder