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Congenital myopathy v3.50 KBTBD13 Arina Puzriakova Phenotypes for gene: KBTBD13 were changed from Nemaline Myopathy, Dominant; Nemaline myopathy 6, autosomal dominant, 609273 to Nemaline myopathy 6, autosomal dominant, OMIM:609273
Congenital myopathy v1.120 KBTBD13 Rachael Mein edited their review of gene: KBTBD13: Changed publications: 21109227; Changed phenotypes: Nemaline Myopathy, Dominant, Nemaline myopathy 6, autosomal dominant, 609273
Congenital myopathy v1.76 KBTBD13 Louise Daugherty reviewed gene: KBTBD13: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Congenital myopathy v1.75 KBTBD13 Rachael Mein reviewed gene: KBTBD13: Rating: GREEN; Mode of pathogenicity: ; Publications: 23222957; Phenotypes: vacuolar myopathy?; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes
Congenital myopathy v1.74 KBTBD13 Louise Daugherty Source NHS GMS was added to KBTBD13.
Congenital myopathy v1.73 KBTBD13 Louise Daugherty Source London South GLH was added to KBTBD13.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Congenital myopathy KBTBD13 Anna Sarkozy reviewed KBTBD13
Congenital myopathy KBTBD13 Helen Brittain marked KBTBD13 as ready
Congenital myopathy KBTBD13 Helen Brittain reviewed KBTBD13