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Fetal anomalies v0.4491 RAPSN Zornitza Stark Marked gene: RAPSN as ready
Fetal anomalies v0.4491 RAPSN Zornitza Stark Gene: rapsn has been classified as Green List (High Evidence).
Fetal anomalies v0.4491 RAPSN Zornitza Stark Phenotypes for gene: RAPSN were changed from FETAL AKINESIA DEFORMATION SEQUENCE; CONGENITAL MYASTHENIC SYNDROME WITH ACETYLCHOLINE RECEPTOR DEFICIENCY to Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency, MIM#616326; Fetal akinesia deformation sequence 2, MIM# 618388
Fetal anomalies v0.4490 RAPSN Zornitza Stark edited their review of gene: RAPSN: Changed phenotypes: Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency, MIM#616326, Fetal akinesia deformation sequence 2, MIM# 618388
Fetal anomalies v0.4490 RAPSN Zornitza Stark changed review comment from: ID is not part of the phenotype.; to: Fetal akinesia, contractures.
Fetal anomalies v0.4490 RAPSN Zornitza Stark edited their review of gene: RAPSN: Changed rating: GREEN
Fetal anomalies v0.0 RAPSN Zornitza Stark gene: RAPSN was added
gene: RAPSN was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: RAPSN was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: RAPSN were set to FETAL AKINESIA DEFORMATION SEQUENCE; CONGENITAL MYASTHENIC SYNDROME WITH ACETYLCHOLINE RECEPTOR DEFICIENCY