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Date	Panel	Item	Activity
Filter activities 7 actions
17 Apr 2020	Ataxia - paediatric v0.207	ARMC9	Zornitza Stark Marked gene: ARMC9 as ready
17 Apr 2020	Ataxia - paediatric v0.207	ARMC9	Zornitza Stark Gene: armc9 has been classified as Red List (Low Evidence).
17 Apr 2020	Ataxia - paediatric v0.207	ARMC9	Zornitza Stark Phenotypes for gene: ARMC9 were changed from Joubert syndrome 30 to Joubert syndrome 30, MIM#617622
17 Apr 2020	Ataxia - paediatric v0.206	ARMC9	Zornitza Stark Classified gene: ARMC9 as Red List (low evidence)
17 Apr 2020	Ataxia - paediatric v0.206	ARMC9	Zornitza Stark Gene: armc9 has been classified as Red List (Low Evidence).
27 Dec 2019	Ataxia - paediatric v0.5	ARMC9	Zornitza Stark reviewed gene: ARMC9: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Joubert syndrome 30, MIM#617622; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
19 Dec 2019	Ataxia - paediatric v0.0	ARMC9	Bryony Thompson gene: ARMC9 was added gene: ARMC9 was added to Ataxia - paediatric_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: ARMC9 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ARMC9 were set to Joubert syndrome 30