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Fetal anomalies v1.511 SCYL2 Zornitza Stark Publications for gene: SCYL2 were set to 31960134; 26203146
Fetal anomalies v1.510 SCYL2 Zornitza Stark Classified gene: SCYL2 as Green List (high evidence)
Fetal anomalies v1.510 SCYL2 Zornitza Stark Gene: scyl2 has been classified as Green List (High Evidence).
Fetal anomalies v1.509 SCYL2 Zornitza Stark reviewed gene: SCYL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 40243816, 39169672, 31960134; Phenotypes: Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum, MIM# 618766; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.664 SCYL2 Zornitza Stark Marked gene: SCYL2 as ready
Fetal anomalies v0.664 SCYL2 Zornitza Stark Gene: scyl2 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.664 SCYL2 Zornitza Stark Classified gene: SCYL2 as Amber List (moderate evidence)
Fetal anomalies v0.664 SCYL2 Zornitza Stark Gene: scyl2 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.612 SCYL2 Krithika Murali gene: SCYL2 was added
gene: SCYL2 was added to Fetal anomalies. Sources: Expert list,Literature
Mode of inheritance for gene: SCYL2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SCYL2 were set to 31960134; 26203146
Phenotypes for gene: SCYL2 were set to Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum - #618766
Review for gene: SCYL2 was set to AMBER
Added comment: 2 unrelated consanguineous families reported with AMC (PMID: 31960134).
Constitutive mouse knockout of Scyl2 results in neonatal lethality and severe motor and sensory deficits (PMID: 26203146).
Sources: Expert list, Literature