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Severe Paediatric Disorders v0.17 FKBP10 Louise Daugherty Mode of inheritance for gene FKBP10 was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.12 FKBP10 Louise Daugherty reviewed gene: FKBP10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 FKBP10 Louise Daugherty Publications for gene FKBP10 were updated from to 30847515
Severe Paediatric Disorders v0.10 FKBP10 Louise Daugherty Added phenotypes Bruck syndrome 1, 259450; Osteogenesis imperfecta, type XI, 610968 for gene: FKBP10
Severe Paediatric Disorders v0.9 FKBP10 Louise Daugherty Added phenotypes Bruck syndrome 1, 259450; Osteogenesis imperfecta, type XI, 610968 for gene: FKBP10
Severe Paediatric Disorders v0.9 FKBP10 Louise Daugherty Added phenotypes Bruck syndrome 1, 259450; Osteogenesis imperfecta, type XI, 610968 for gene: FKBP10
Severe Paediatric Disorders v0.8 FKBP10 Louise Daugherty Added phenotypes Osteogenesis imperfecta, type XI, 610968; Bruck syndrome 1, 259450 for gene: FKBP10
Severe Paediatric Disorders v0.7 FKBP10 Louise Daugherty Source Next Generation Children Project was added to FKBP10.
Severe Paediatric Disorders v0.5 FKBP10 Louise Daugherty Source Expert Review Green was added to FKBP10.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 FKBP10 Louise Daugherty gene: FKBP10 was added
gene: FKBP10 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: FKBP10 was set to