Activity

Filter

Cancel
Date Panel Item Activity
10 actions
Severe Paediatric Disorders v0.17 ELOVL5 Louise Daugherty Mode of inheritance for gene ELOVL5 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 ELOVL5 Louise Daugherty reviewed gene: ELOVL5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 ELOVL5 Louise Daugherty Publications for gene ELOVL5 were updated from to 30847515
Severe Paediatric Disorders v0.10 ELOVL5 Louise Daugherty Added phenotypes Spinocerebellar ataxia 38, 615957 for gene: ELOVL5
Severe Paediatric Disorders v0.9 ELOVL5 Louise Daugherty Added phenotypes Spinocerebellar ataxia 38, 615957 for gene: ELOVL5
Severe Paediatric Disorders v0.9 ELOVL5 Louise Daugherty Added phenotypes Spinocerebellar ataxia 38, 615957 for gene: ELOVL5
Severe Paediatric Disorders v0.8 ELOVL5 Louise Daugherty Added phenotypes Spinocerebellar ataxia 38, 615957 for gene: ELOVL5
Severe Paediatric Disorders v0.7 ELOVL5 Louise Daugherty Source Next Generation Children Project was added to ELOVL5.
Severe Paediatric Disorders v0.5 ELOVL5 Louise Daugherty Source Expert Review Green was added to ELOVL5.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 ELOVL5 Louise Daugherty gene: ELOVL5 was added
gene: ELOVL5 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: ELOVL5 was set to