Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Ataxia and cerebellar anomalies - narrow panel v3.30 PI4KA Eleanor Williams Tag Q3_21_rating was removed from gene: PI4KA.
Ataxia and cerebellar anomalies - narrow panel v3.30 PI4KA Eleanor Williams reviewed gene: PI4KA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Ataxia and cerebellar anomalies - narrow panel v3.29 PI4KA Eleanor Williams Source Expert Review Green was added to PI4KA.
Source NHS GMS was added to PI4KA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v2.233 PI4KA Ivone Leong Tag Q3_21_rating tag was added to gene: PI4KA.
Ataxia and cerebellar anomalies - narrow panel v2.233 PI4KA Ivone Leong Phenotypes for gene: PI4KA were changed from Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis , 616531 to Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, OMIM:616531
Ataxia and cerebellar anomalies - narrow panel v2.232 PI4KA Ivone Leong Publications for gene: PI4KA were set to 25855803
Ataxia and cerebellar anomalies - narrow panel v2.231 PI4KA Ivone Leong Classified gene: PI4KA as Amber List (moderate evidence)
Ataxia and cerebellar anomalies - narrow panel v2.231 PI4KA Ivone Leong Gene: pi4ka has been classified as Amber List (Moderate Evidence).
Ataxia and cerebellar anomalies - narrow panel v2.230 PI4KA Ivone Leong reviewed gene: PI4KA: Rating: GREEN; Mode of pathogenicity: None; Publications: 25855803, 34415322, 34415310; Phenotypes: ; Mode of inheritance: None
Ataxia and cerebellar anomalies - narrow panel v0.5 PI4KA Ellen McDonagh gene: PI4KA was added
gene: PI4KA was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Red
Mode of inheritance for gene: PI4KA was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PI4KA were set to 25855803
Phenotypes for gene: PI4KA were set to Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis , 616531