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Date	Panel	Item	Activity
Filter activities 8 actions
21 May 2019	Childhood onset hereditary spastic paraplegia v1.166	WDR48	Louise Daugherty reviewed gene: WDR48: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
21 May 2019	Childhood onset hereditary spastic paraplegia v1.165	WDR48	Louise Daugherty Source Expert Review Amber was added to WDR48. Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
13 May 2019	Childhood onset hereditary spastic paraplegia v1.86	WDR48	Louise Daugherty Phenotypes for gene: WDR48 were changed from to spastic paraplegia
13 May 2019	Childhood onset hereditary spastic paraplegia v1.85	WDR48	Louise Daugherty Publications for gene: WDR48 were set to Novarino et al. (2014)
13 May 2019	Childhood onset hereditary spastic paraplegia v1.76	WDR48	Louise Daugherty Source NHS GMS was added to WDR48.
13 May 2019	Childhood onset hereditary spastic paraplegia v1.75	WDR48	Louise Daugherty Source Yorkshire and North East GLH was added to WDR48.
10 May 2019	Childhood onset hereditary spastic paraplegia v1.74	WDR48	Nick Beauchamp reviewed gene: WDR48: Rating: AMBER; Mode of pathogenicity: None; Publications: 24482476, 24482476; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
19 Dec 2018	Childhood onset hereditary spastic paraplegia v0.6	WDR48	Sarah Leigh gene: WDR48 was added gene: WDR48 was added to Hereditary spastic paraplegia - childhood onset. Sources: Expert list,Expert Review Red Mode of inheritance for gene: WDR48 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: WDR48 were set to Novarino et al. (2014)