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Date	Panel	Item	Activity
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13 Feb 2019	Likely inborn error of metabolism v1.47	DPAGT1	Ivone Leong Source NHS GMS was added to DPAGT1. Source London North GLH was added to DPAGT1.
16 Dec 2018	Likely inborn error of metabolism v0.4	DPAGT1	Ellen McDonagh Added phenotypes Myasthenic syndrome, congenital, 13, with tubular aggregates 614750; UDP-GlcNAc:Dol-P-GlcNac-P transferase deficiency (Disorders of protein N-glycosylation); Congenital disorder of glycosylation, type Ij 608093 for gene: DPAGT1 Publications for gene DPAGT1 were changed from 12872255; 22304930 to 27604308
16 Dec 2018	Likely inborn error of metabolism v0.4	DPAGT1	Ellen McDonagh gene: DPAGT1 was added gene: DPAGT1 was added to Inborn errors of metabolism. Sources: Expert Review Green Mode of inheritance for gene: DPAGT1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DPAGT1 were set to 12872255; 22304930 Phenotypes for gene: DPAGT1 were set to Myasthenic syndrome, congenital, 13, with tubular aggregates 614750; UDP-GlcNAc:Dol-P-GlcNac-P transferase deficiency (Disorders of protein N-glycosylation); Congenital disorder of glycosylation, type Ij 608093