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Arrhythmogenic Cardiomyopathy v0.29 TGFB3 Zornitza Stark changed review comment from: Two families reported, variants in UTRs in both. One of the variants is present in 10 individuals in gnomad and was also present in unaffected family members in the original family reported, so effectively one family only. Gene is associated with LDS.; to: Two families reported, variants in UTRs in both. One of the variants is present in 10 individuals in gnomad and was also present in unaffected family members in the original family reported, so effectively one family only. Rated as LIMITED by ClinGen. Gene is associated with LDS.
Arrhythmogenic Cardiomyopathy v0.21 TGFB3 Zornitza Stark Marked gene: TGFB3 as ready
Arrhythmogenic Cardiomyopathy v0.21 TGFB3 Zornitza Stark Gene: tgfb3 has been classified as Red List (Low Evidence).
Arrhythmogenic Cardiomyopathy v0.21 TGFB3 Zornitza Stark Phenotypes for gene: TGFB3 were changed from to Arrhythmogenic right ventricular dysplasia 1, MIM# 107970
Arrhythmogenic Cardiomyopathy v0.20 TGFB3 Zornitza Stark Publications for gene: TGFB3 were set to
Arrhythmogenic Cardiomyopathy v0.19 TGFB3 Zornitza Stark Mode of inheritance for gene: TGFB3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arrhythmogenic Cardiomyopathy v0.18 TGFB3 Zornitza Stark Classified gene: TGFB3 as Red List (low evidence)
Arrhythmogenic Cardiomyopathy v0.18 TGFB3 Zornitza Stark Gene: tgfb3 has been classified as Red List (Low Evidence).
Arrhythmogenic Cardiomyopathy v0.17 TGFB3 Zornitza Stark Tag 5'UTR tag was added to gene: TGFB3.
Arrhythmogenic Cardiomyopathy v0.17 TGFB3 Zornitza Stark reviewed gene: TGFB3: Rating: RED; Mode of pathogenicity: None; Publications: 15639475; Phenotypes: Arrhythmogenic right ventricular dysplasia 1, MIM# 107970; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arrhythmogenic Cardiomyopathy v0.0 TGFB3 Zornitza Stark gene: TGFB3 was added
gene: TGFB3 was added to Arrhythmogenic right ventricular cardiomyopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: TGFB3 was set to Unknown