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Fetal anomalies v0.3203 FRRS1L Zornitza Stark Marked gene: FRRS1L as ready
Fetal anomalies v0.3203 FRRS1L Zornitza Stark Gene: frrs1l has been classified as Red List (Low Evidence).
Fetal anomalies v0.3203 FRRS1L Zornitza Stark Phenotypes for gene: FRRS1L were changed from Epileptic encephalopathy with continuous spike-and-wave during sleep to Epileptic encephalopathy, early infantile, 37, MIM#616981
Fetal anomalies v0.3202 FRRS1L Zornitza Stark Publications for gene: FRRS1L were set to
Fetal anomalies v0.3201 FRRS1L Zornitza Stark Classified gene: FRRS1L as Red List (low evidence)
Fetal anomalies v0.3201 FRRS1L Zornitza Stark Gene: frrs1l has been classified as Red List (Low Evidence).
Fetal anomalies v0.3200 FRRS1L Zornitza Stark changed review comment from: Five unrelated individuals reported.
Sources: Expert list; to: Five unrelated individuals reported. Presentation is typically post-natal.
Sources: Expert list
Fetal anomalies v0.3200 FRRS1L Zornitza Stark edited their review of gene: FRRS1L: Changed rating: RED
Fetal anomalies v0.0 FRRS1L Zornitza Stark gene: FRRS1L was added
gene: FRRS1L was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: FRRS1L was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FRRS1L were set to Epileptic encephalopathy with continuous spike-and-wave during sleep