Activity

Filter

Cancel
Date Panel Item Activity
9 actions
Fetal anomalies v0.3130 PSAT1 Zornitza Stark Marked gene: PSAT1 as ready
Fetal anomalies v0.3130 PSAT1 Zornitza Stark Gene: psat1 has been classified as Green List (High Evidence).
Fetal anomalies v0.3130 PSAT1 Zornitza Stark Publications for gene: PSAT1 were set to 25152457; 31903955
Fetal anomalies v0.3129 PSAT1 Zornitza Stark Classified gene: PSAT1 as Green List (high evidence)
Fetal anomalies v0.3129 PSAT1 Zornitza Stark Gene: psat1 has been classified as Green List (High Evidence).
Fetal anomalies v0.3128 PSAT1 Zornitza Stark edited their review of gene: PSAT1: Changed phenotypes: Neu-Laxova syndrome 2, MIM# 616038
Fetal anomalies v0.3128 PSAT1 Zornitza Stark changed review comment from: Neu-Laxova syndrome: severe perinatal presentation with high mortality, not relevant to this panel. PSAT1 deficiency: single family described, ID is part of the phenotype. There is probably a spectrum of disorders related to this gene, downgrade to Amber on this panel for now.; to: Neu-Laxova syndrome: severe perinatal presentation with high mortality.
Fetal anomalies v0.3128 PSAT1 Zornitza Stark edited their review of gene: PSAT1: Changed rating: GREEN
Fetal anomalies v0.0 PSAT1 Zornitza Stark gene: PSAT1 was added
gene: PSAT1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: PSAT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PSAT1 were set to 25152457; 31903955
Phenotypes for gene: PSAT1 were set to Neu-Laxova syndrome 2, MONDO:0014466; Neu-Laxova syndrome 2, OMIM:616038