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Date	Panel	Item	Activity
Filter activities 5 actions
25 May 2020	Syndromic Retinopathy v0.54	PEX26	Bryony Thompson Marked gene: PEX26 as ready
25 May 2020	Syndromic Retinopathy v0.54	PEX26	Bryony Thompson Gene: pex26 has been classified as Amber List (Moderate Evidence).
25 May 2020	Syndromic Retinopathy v0.54	PEX26	Bryony Thompson Classified gene: PEX26 as Amber List (moderate evidence)
25 May 2020	Syndromic Retinopathy v0.54	PEX26	Bryony Thompson Gene: pex26 has been classified as Amber List (Moderate Evidence).
25 May 2020	Syndromic Retinopathy v0.53	PEX26	Bryony Thompson gene: PEX26 was added gene: PEX26 was added to Syndromic Retinopathy. Sources: Expert list Mode of inheritance for gene: PEX26 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PEX26 were set to 28944237 Phenotypes for gene: PEX26 were set to Peroxisome biogenesis disorder 7A (Zellweger) MIM#614872; Peroxisome biogenesis disorder 7B MIM#614873 Review for gene: PEX26 was set to AMBER Added comment: Two cases reported with retinitis pigmentosa as a feature of the condition. Sources: Expert list