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Barth syndrome v1.3 TAZ Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #302060) and the OMIM record was last accessed on 17 December 2025.
Barth syndrome v1.3 TAZ Achchuthan Shanmugasundram Phenotypes for gene: TAZ were changed from to Barth syndrome, OMIM:302060; Barth syndrome, MONDO:0010543
Barth syndrome v1.1 Achchuthan Shanmugasundram Panel version 1.0 has been signed off on 2023-09-14
Barth syndrome v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Barth syndrome v0.3 Achchuthan Shanmugasundram Panel types changed to GMS Rare Disease; GMS signed-off
Barth syndrome v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Barth syndrome v0.1 TAZ Eleanor Williams commented on gene: TAZ
Barth syndrome v0.1 TAZ Achchuthan Shanmugasundram Tag new-gene-name tag was added to gene: TAZ.
Barth syndrome v0.1 TAZ Achchuthan Shanmugasundram reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Barth syndrome v0.1 TAZ Achchuthan Shanmugasundram gene: TAZ was added
gene: TAZ was added to Barth syndrome. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: TAZ was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Barth syndrome v0.0 Achchuthan Shanmugasundram Added Panel Barth syndrome
Set list of related panels to R391
Set panel types to: GMS Rare Disease