Activity

Filter

Cancel
Date Panel Item Activity
12 actions
Fetal anomalies v1.836 PNPLA1 Arina Puzriakova Tag for-review was removed from gene: PNPLA1.
Fetal anomalies v1.836 PNPLA1 Arina Puzriakova commented on gene: PNPLA1: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Fetal anomalies v1.835 PNPLA1 Arina Puzriakova Source Expert Review Green was added to PNPLA1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Fetal anomalies v1.495 PNPLA1 Arina Puzriakova Phenotypes for gene: PNPLA1 were changed from CONGENITAL ICHTHYOSIS to Ichthyosis, congenital, autosomal recessive 10, OMIM:615024; Autosomal recessive congenital ichthyosis 10, MONDO:0014011
Fetal anomalies v1.492 PNPLA1 Arina Puzriakova Classified gene: PNPLA1 as Amber List (moderate evidence)
Fetal anomalies v1.492 PNPLA1 Arina Puzriakova Added comment: Comment on list classification: Following curation and clinical review at GOSH it has been agreed that the associated phenotype is fetally-relevant. Therefore this gene should be promoted to Green at the next GMS panel update (added 'for-review' tag)
Fetal anomalies v1.492 PNPLA1 Arina Puzriakova Gene: pnpla1 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v1.491 PNPLA1 Arina Puzriakova Tag for-review tag was added to gene: PNPLA1.
Fetal anomalies v1.205 PNPLA1 Rhiannon Mellis reviewed gene: PNPLA1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ichthyosis, congenital, autosomal recessive 10; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.9 PNPLA1 Rebecca Foulger commented on gene: PNPLA1: DDG2P rating in original PAGE list: Probable for CONGENITAL ICHTHYOSIS
Fetal anomalies v0.3 PNPLA1 Rebecca Foulger reviewed gene: PNPLA1: Rating: AMBER; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: ; Mode of inheritance:
Fetal anomalies v0.1 PNPLA1 Rebecca Foulger gene: PNPLA1 was added
gene: PNPLA1 was added to Fetal anomalies. Sources: PAGE DD-Gene2Phenotype,Expert Review Amber
Mode of inheritance for gene: PNPLA1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: PNPLA1 were set to CONGENITAL ICHTHYOSIS