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Severe Paediatric Disorders v0.12 SAMD9L Louise Daugherty reviewed gene: SAMD9L: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.12 SAMD9 Louise Daugherty reviewed gene: SAMD9: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 SAMD9L Louise Daugherty Publications for gene SAMD9L were updated from to 30847515
Severe Paediatric Disorders v0.11 SAMD9 Louise Daugherty Publications for gene SAMD9 were updated from to 30847515
Severe Paediatric Disorders v0.10 SAMD9L Louise Daugherty Added phenotypes Ataxia-pancytopenia syndrome, 159550 for gene: SAMD9L
Severe Paediatric Disorders v0.10 SAMD9 Louise Daugherty Added phenotypes Tumoral calcinosis, familial, normophosphatemic, 610455; MIRAGE syndrome, 617053 for gene: SAMD9
Severe Paediatric Disorders v0.9 SAMD9L Louise Daugherty Added phenotypes Ataxia-pancytopenia syndrome, 159550 for gene: SAMD9L
Severe Paediatric Disorders v0.9 SAMD9 Louise Daugherty Added phenotypes Tumoral calcinosis, familial, normophosphatemic, 610455; MIRAGE syndrome, 617053 for gene: SAMD9
Severe Paediatric Disorders v0.9 SAMD9L Louise Daugherty Added phenotypes Ataxia-pancytopenia syndrome, 159550 for gene: SAMD9L
Severe Paediatric Disorders v0.9 SAMD9 Louise Daugherty Added phenotypes Tumoral calcinosis, familial, normophosphatemic, 610455; MIRAGE syndrome, 617053 for gene: SAMD9
Severe Paediatric Disorders v0.8 SAMD9L Louise Daugherty Added phenotypes Ataxia-pancytopenia syndrome, 159550 for gene: SAMD9L
Severe Paediatric Disorders v0.8 SAMD9 Louise Daugherty Added phenotypes MIRAGE syndrome, 617053; Tumoral calcinosis, familial, normophosphatemic, 610455 for gene: SAMD9
Severe Paediatric Disorders v0.8 SAMD9L Louise Daugherty Mode of inheritance for gene SAMD9L was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Ataxia-pancytopenia syndrome, 159550 for gene: SAMD9L
Severe Paediatric Disorders v0.8 SAMD9 Louise Daugherty Mode of inheritance for gene SAMD9 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Tumoral calcinosis, familial, normophosphatemic, 610455; MIRAGE syndrome, 617053 for gene: SAMD9
Severe Paediatric Disorders v0.7 SAMD9L Louise Daugherty Source Next Generation Children Project was added to SAMD9L.
Severe Paediatric Disorders v0.7 SAMD9 Louise Daugherty Source Next Generation Children Project was added to SAMD9.
Severe Paediatric Disorders v0.5 SAMD9L Louise Daugherty Source Expert Review Green was added to SAMD9L.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.5 SAMD9 Louise Daugherty Source Expert Review Green was added to SAMD9.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 SAMD9L Louise Daugherty gene: SAMD9L was added
gene: SAMD9L was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: SAMD9L was set to
Severe Paediatric Disorders v0.4 SAMD9 Louise Daugherty gene: SAMD9 was added
gene: SAMD9 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: SAMD9 was set to