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Severe Paediatric Disorders v0.12 SLC19A3 Louise Daugherty reviewed gene: SLC19A3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 SLC19A3 Louise Daugherty Publications for gene SLC19A3 were updated from to 30847515
Severe Paediatric Disorders v0.10 SLC19A3 Louise Daugherty Added phenotypes Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 for gene: SLC19A3
Severe Paediatric Disorders v0.9 SLC19A3 Louise Daugherty Added phenotypes Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 for gene: SLC19A3
Severe Paediatric Disorders v0.9 SLC19A3 Louise Daugherty Added phenotypes Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 for gene: SLC19A3
Severe Paediatric Disorders v0.8 SLC19A3 Louise Daugherty Added phenotypes Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 for gene: SLC19A3
Severe Paediatric Disorders v0.8 SLC19A3 Louise Daugherty Mode of inheritance for gene SLC19A3 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 for gene: SLC19A3
Severe Paediatric Disorders v0.7 SLC19A3 Louise Daugherty Source Next Generation Children Project was added to SLC19A3.
Severe Paediatric Disorders v0.5 SLC19A3 Louise Daugherty Source Expert Review Green was added to SLC19A3.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 SLC19A3 Louise Daugherty gene: SLC19A3 was added
gene: SLC19A3 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: SLC19A3 was set to