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Ataxia - paediatric v1.16 PRICKLE1 Zornitza Stark Classified gene: PRICKLE1 as Red List (low evidence)
Ataxia - paediatric v1.16 PRICKLE1 Zornitza Stark Gene: prickle1 has been classified as Red List (Low Evidence).
Ataxia - paediatric v1.15 PRICKLE1 Zornitza Stark edited their review of gene: PRICKLE1: Added comment: LIMITED by ClinGen for AR PME.; Changed rating: RED
Ataxia - paediatric v1.15 PRICKLE1 Zornitza Stark Classified gene: PRICKLE1 as Amber List (moderate evidence)
Ataxia - paediatric v1.15 PRICKLE1 Zornitza Stark Gene: prickle1 has been classified as Amber List (Moderate Evidence).
Ataxia - paediatric v1.14 PRICKLE1 Zornitza Stark edited their review of gene: PRICKLE1: Added comment: Note most reported variants are missense with little further supportive evidence and ClinVar variants in this gene are all VOUS/LB/B.; Changed rating: AMBER
Ataxia - paediatric v0.250 PRICKLE1 Zornitza Stark Marked gene: PRICKLE1 as ready
Ataxia - paediatric v0.250 PRICKLE1 Zornitza Stark Gene: prickle1 has been classified as Green List (High Evidence).
Ataxia - paediatric v0.250 PRICKLE1 Zornitza Stark Publications for gene: PRICKLE1 were set to
Ataxia - paediatric v0.249 PRICKLE1 Zornitza Stark reviewed gene: PRICKLE1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301774; Phenotypes: Epilepsy, progressive myoclonic 1B, MIM# 612437; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia - paediatric v0.0 PRICKLE1 Bryony Thompson gene: PRICKLE1 was added
gene: PRICKLE1 was added to Ataxia - paediatric_RMH. Sources: Expert Review Green,Royal Melbourne Hospital
Mode of inheritance for gene: PRICKLE1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: PRICKLE1 were set to Progressive myoclonic epilepsy 1B, 612437; Progressive Myoclonus Epilepsy with Ataxia