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Date	Panel	Item	Activity
Filter activities 6 actions
31 Oct 2022	Genomic newborn screening: BabyScreen+ v0.700	SHANK3	Seb Lunke Marked gene: SHANK3 as ready
31 Oct 2022	Genomic newborn screening: BabyScreen+ v0.700	SHANK3	Seb Lunke Gene: shank3 has been classified as Red List (Low Evidence).
31 Oct 2022	Genomic newborn screening: BabyScreen+ v0.700	SHANK3	Seb Lunke Classified gene: SHANK3 as Red List (low evidence)
31 Oct 2022	Genomic newborn screening: BabyScreen+ v0.700	SHANK3	Seb Lunke Gene: shank3 has been classified as Red List (Low Evidence).
31 Oct 2022	Genomic newborn screening: BabyScreen+ v0.699	SHANK3	Seb Lunke reviewed gene: SHANK3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Phelan-McDermid syndrome, MIM# 606232; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
18 Sep 2022	Genomic newborn screening: BabyScreen+ v0.0	SHANK3	Zornitza Stark gene: SHANK3 was added gene: SHANK3 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: SHANK3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: SHANK3 were set to 17173049; 30842224; 16284256; 20186804; 22892527 Phenotypes for gene: SHANK3 were set to Phelan-McDermid syndrome, MIM# 606232; MONDO:0011652