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Date	Panel	Item	Activity
Filter activities 6 actions
22 Oct 2020	Mendeliome v0.5067	TCF21	Bryony Thompson Marked gene: TCF21 as ready
22 Oct 2020	Mendeliome v0.5067	TCF21	Bryony Thompson Gene: tcf21 has been classified as Red List (Low Evidence).
22 Oct 2020	Mendeliome v0.5067	TCF21	Bryony Thompson Classified gene: TCF21 as Red List (low evidence)
22 Oct 2020	Mendeliome v0.5067	TCF21	Bryony Thompson Gene: tcf21 has been classified as Red List (Low Evidence).
22 Oct 2020	Mendeliome v0.5066	TCF21	Bryony Thompson reviewed gene: TCF21: Rating: RED; Mode of pathogenicity: None; Publications: 16156022, 10769282, 24875298; Phenotypes: Sensorineural hearing loss, dilated cardiomyopathy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
17 Nov 2019	Mendeliome v0.0	TCF21	Zornitza Stark gene: TCF21 was added gene: TCF21 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: TCF21 was set to Unknown