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Fetal anomalies v2.0 BIN1 Gene migrated from ENSG00000136717 to ENSG00000136717 (gene set migration)
Fetal anomalies v0.320 BIN1 Zornitza Stark Publications for gene: BIN1 were set to 17676042; 17676042
Fetal anomalies v0.319 BIN1 Zornitza Stark Marked gene: BIN1 as ready
Fetal anomalies v0.319 BIN1 Zornitza Stark Gene: bin1 has been classified as Green List (High Evidence).
Fetal anomalies v0.319 BIN1 Zornitza Stark Phenotypes for gene: BIN1 were changed from CENTRONUCLEAR MYOPATHY 2 to Centronuclear myopathy 2, MIM# 255200
Fetal anomalies v0.318 BIN1 Zornitza Stark Publications for gene: BIN1 were set to
Fetal anomalies v0.317 BIN1 Zornitza Stark changed review comment from: ID is generally not part of the phenotype of this myopathy, mild ID reported in one individual only.; to: Variable onset from congenital to childhood. Congenital contractures reported.
Fetal anomalies v0.317 BIN1 Zornitza Stark edited their review of gene: BIN1: Changed publications: 17676042, 17676042
Fetal anomalies v0.317 BIN1 Zornitza Stark edited their review of gene: BIN1: Changed rating: GREEN
Fetal anomalies v0.0 BIN1 Zornitza Stark gene: BIN1 was added
gene: BIN1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: BIN1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: BIN1 were set to CENTRONUCLEAR MYOPATHY 2