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Ataxia - paediatric v0.143 SLC9A1 Zornitza Stark Marked gene: SLC9A1 as ready
Ataxia - paediatric v0.143 SLC9A1 Zornitza Stark Gene: slc9a1 has been classified as Amber List (Moderate Evidence).
Ataxia - paediatric v0.143 SLC9A1 Zornitza Stark Phenotypes for gene: SLC9A1 were changed from Lichtenstein-Knorr Syndrome to Lichtenstein-Knorr Syndrome, MIM# 616291
Ataxia - paediatric v0.142 SLC9A1 Zornitza Stark Publications for gene: SLC9A1 were set to
Ataxia - paediatric v0.141 SLC9A1 Zornitza Stark Classified gene: SLC9A1 as Amber List (moderate evidence)
Ataxia - paediatric v0.141 SLC9A1 Zornitza Stark Gene: slc9a1 has been classified as Amber List (Moderate Evidence).
Ataxia - paediatric v0.140 SLC9A1 Zornitza Stark reviewed gene: SLC9A1: Rating: AMBER; Mode of pathogenicity: None; Publications: 25205112, 30018422, 25760855; Phenotypes: Lichtenstein-Knorr syndrome, MIM# 616291; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia - paediatric v0.0 SLC9A1 Bryony Thompson gene: SLC9A1 was added
gene: SLC9A1 was added to Ataxia - paediatric_RMH. Sources: Expert Review Green,Royal Melbourne Hospital
Mode of inheritance for gene: SLC9A1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SLC9A1 were set to Lichtenstein-Knorr Syndrome