Date Panel Item Activity
3 actions
Short QT syndrome v1.4 SNTA1 James Eden reviewed gene: SNTA1: Rating: RED; Mode of pathogenicity: ; Publications: 19862833, 30420954, 16301704; Phenotypes: Long QT syndrome 12 (612955); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Short QT syndrome v1.3 SNTA1 Ellen McDonagh Source North West GLH was added to SNTA1.
Added phenotypes Long QT syndrome 12 (612955) for gene: SNTA1
Publications for gene SNTA1 were changed from to 30420954; 19862833; 16301704
Short QT syndrome v0.2 SNTA1 Sarah Leigh gene: SNTA1 was added
gene: SNTA1 was added to Short QT syndrome. Sources: Long QT syndrome (Version 1.5),Emory Genetics Laboratory
Mode of inheritance for gene: SNTA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted