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Fetal anomalies v0.1762 FOLR1 Zornitza Stark Marked gene: FOLR1 as ready
Fetal anomalies v0.1762 FOLR1 Zornitza Stark Gene: folr1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1762 FOLR1 Zornitza Stark Phenotypes for gene: FOLR1 were changed from NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY to Neurodegeneration due to cerebral folate transport deficiency, MIM# 613068
Fetal anomalies v0.1761 FOLR1 Zornitza Stark Publications for gene: FOLR1 were set to
Fetal anomalies v0.1760 FOLR1 Zornitza Stark Classified gene: FOLR1 as Red List (low evidence)
Fetal anomalies v0.1760 FOLR1 Zornitza Stark Gene: folr1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1759 FOLR1 Zornitza Stark changed review comment from: Onset is apparent in late infancy with severe developmental regression, movement disturbances, epilepsy, and leukodystrophy. Recognition and diagnosis of this disorder is critical because folinic acid therapy can reverse the clinical symptoms and improve brain abnormalities and function.; to: Onset is apparent in late infancy with severe developmental regression, movement disturbances, epilepsy, and leukodystrophy. Not pertinent to fetal panel.
Fetal anomalies v0.1759 FOLR1 Zornitza Stark edited their review of gene: FOLR1: Changed rating: RED
Fetal anomalies v0.0 FOLR1 Zornitza Stark gene: FOLR1 was added
gene: FOLR1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: FOLR1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FOLR1 were set to NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY