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Date	Panel	Item	Activity
Filter activities 7 actions
19 Dec 2022	Mendeliome v1.563	WDFY3	Zornitza Stark Phenotypes for gene: WDFY3 were changed from Microcephaly 18, primary, autosomal dominant, MIM#617520 to Microcephaly 18, primary, autosomal dominant, MIM#617520; Neurodevelopmental disorder with macrocephaly
26 Nov 2019	Mendeliome v0.87	WDFY3	Zornitza Stark Marked gene: WDFY3 as ready
26 Nov 2019	Mendeliome v0.87	WDFY3	Zornitza Stark Gene: wdfy3 has been classified as Green List (High Evidence).
26 Nov 2019	Mendeliome v0.87	WDFY3	Zornitza Stark Phenotypes for gene: WDFY3 were changed from to Microcephaly 18, primary, autosomal dominant, MIM#617520
26 Nov 2019	Mendeliome v0.86	WDFY3	Zornitza Stark Publications for gene: WDFY3 were set to
26 Nov 2019	Mendeliome v0.85	WDFY3	Zornitza Stark Mode of inheritance for gene: WDFY3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
17 Nov 2019	Mendeliome v0.0	WDFY3	Zornitza Stark gene: WDFY3 was added gene: WDFY3 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: WDFY3 was set to Unknown