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Date	Panel	Item	Activity
Filter activities 7 actions
16 Apr 2020	Ataxia - paediatric v0.74	TMEM138	Zornitza Stark Marked gene: TMEM138 as ready
16 Apr 2020	Ataxia - paediatric v0.74	TMEM138	Zornitza Stark Gene: tmem138 has been classified as Amber List (Moderate Evidence).
16 Apr 2020	Ataxia - paediatric v0.74	TMEM138	Zornitza Stark Phenotypes for gene: TMEM138 were changed from Joubert syndrome 16 to Joubert syndrome 16, MIM# 614465
16 Apr 2020	Ataxia - paediatric v0.73	TMEM138	Zornitza Stark Classified gene: TMEM138 as Amber List (moderate evidence)
16 Apr 2020	Ataxia - paediatric v0.73	TMEM138	Zornitza Stark Gene: tmem138 has been classified as Amber List (Moderate Evidence).
16 Apr 2020	Ataxia - paediatric v0.72	TMEM138	Zornitza Stark reviewed gene: TMEM138: Rating: AMBER; Mode of pathogenicity: None; Publications: 22282472; Phenotypes: Joubert syndrome 16, MIM# 614465; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
19 Dec 2019	Ataxia - paediatric v0.0	TMEM138	Bryony Thompson gene: TMEM138 was added gene: TMEM138 was added to Ataxia - paediatric_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: TMEM138 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TMEM138 were set to Joubert syndrome 16