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Severe Paediatric Disorders v0.17 DNMT1 Louise Daugherty Mode of inheritance for gene DNMT1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 DNMT1 Louise Daugherty reviewed gene: DNMT1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 DNMT1 Louise Daugherty Publications for gene DNMT1 were updated from to 30847515
Severe Paediatric Disorders v0.10 DNMT1 Louise Daugherty Added phenotypes Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121; Neuropathy, hereditary sensory, type IE, 614116 for gene: DNMT1
Severe Paediatric Disorders v0.9 DNMT1 Louise Daugherty Added phenotypes Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121; Neuropathy, hereditary sensory, type IE, 614116 for gene: DNMT1
Severe Paediatric Disorders v0.9 DNMT1 Louise Daugherty Added phenotypes Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121; Neuropathy, hereditary sensory, type IE, 614116 for gene: DNMT1
Severe Paediatric Disorders v0.8 DNMT1 Louise Daugherty Added phenotypes Neuropathy, hereditary sensory, type IE, 614116; Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121 for gene: DNMT1
Severe Paediatric Disorders v0.7 DNMT1 Louise Daugherty Source Next Generation Children Project was added to DNMT1.
Severe Paediatric Disorders v0.5 DNMT1 Louise Daugherty Source Expert Review Green was added to DNMT1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 DNMT1 Louise Daugherty gene: DNMT1 was added
gene: DNMT1 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: DNMT1 was set to