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Date	Panel	Item	Activity
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31 Mar 2020	Hereditary Neuropathy_CMT - isolated v0.13	FBXO38	Zornitza Stark Marked gene: FBXO38 as ready
31 Mar 2020	Hereditary Neuropathy_CMT - isolated v0.13	FBXO38	Zornitza Stark Gene: fbxo38 has been classified as Amber List (Moderate Evidence).
31 Mar 2020	Hereditary Neuropathy_CMT - isolated v0.13	FBXO38	Zornitza Stark Classified gene: FBXO38 as Amber List (moderate evidence)
31 Mar 2020	Hereditary Neuropathy_CMT - isolated v0.13	FBXO38	Zornitza Stark Gene: fbxo38 has been classified as Amber List (Moderate Evidence).
31 Mar 2020	Hereditary Neuropathy_CMT - isolated v0.12	FBXO38	Zornitza Stark reviewed gene: FBXO38: Rating: AMBER; Mode of pathogenicity: None; Publications: 24207122, 31420593; Phenotypes: Neuronopathy, distal hereditary motor, type IID, MIM# 615575; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
13 Jan 2020	Hereditary Neuropathy_CMT - isolated v0.0	FBXO38	Bryony Thompson gene: FBXO38 was added gene: FBXO38 was added to Hereditary Neuropathy - isolated_RMH. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: FBXO38 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: FBXO38 were set to Neuronopathy, distal hereditary motor, type IID, 615575; dHMN/dSMA