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Severe Paediatric Disorders v0.12 WNT10B Louise Daugherty reviewed gene: WNT10B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.12 WNT10A Louise Daugherty reviewed gene: WNT10A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.12 WNT1 Louise Daugherty reviewed gene: WNT1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 WNT10B Louise Daugherty Publications for gene WNT10B were updated from to 30847515
Severe Paediatric Disorders v0.11 WNT10A Louise Daugherty Publications for gene WNT10A were updated from to 30847515
Severe Paediatric Disorders v0.11 WNT1 Louise Daugherty Publications for gene WNT1 were updated from to 30847515
Severe Paediatric Disorders v0.10 WNT10B Louise Daugherty Added phenotypes Split-hand/foot malformation 6, 225300; Tooth agenesis, selective, 8, 617073 for gene: WNT10B
Severe Paediatric Disorders v0.10 WNT10A Louise Daugherty Added phenotypes Tooth agenesis, selective, 4, 150400; Schopf-Schulz-Passarge syndrome, 224750; Odontoonychodermal dysplasia, 257980 for gene: WNT10A
Severe Paediatric Disorders v0.10 WNT1 Louise Daugherty Added phenotypes Osteogenesis imperfecta, type XV, 615220 for gene: WNT1
Severe Paediatric Disorders v0.9 WNT10B Louise Daugherty Added phenotypes Split-hand/foot malformation 6, 225300; Tooth agenesis, selective, 8, 617073 for gene: WNT10B
Severe Paediatric Disorders v0.9 WNT10A Louise Daugherty Added phenotypes Tooth agenesis, selective, 4, 150400; Schopf-Schulz-Passarge syndrome, 224750; Odontoonychodermal dysplasia, 257980 for gene: WNT10A
Severe Paediatric Disorders v0.9 WNT1 Louise Daugherty Added phenotypes Osteogenesis imperfecta, type XV, 615220 for gene: WNT1
Severe Paediatric Disorders v0.9 WNT10B Louise Daugherty Added phenotypes Split-hand/foot malformation 6, 225300; Tooth agenesis, selective, 8, 617073 for gene: WNT10B
Severe Paediatric Disorders v0.9 WNT10A Louise Daugherty Added phenotypes Tooth agenesis, selective, 4, 150400; Schopf-Schulz-Passarge syndrome, 224750; Odontoonychodermal dysplasia, 257980 for gene: WNT10A
Severe Paediatric Disorders v0.9 WNT1 Louise Daugherty Added phenotypes Osteogenesis imperfecta, type XV, 615220 for gene: WNT1
Severe Paediatric Disorders v0.8 WNT10B Louise Daugherty Added phenotypes Split-hand/foot malformation 6, 225300; Tooth agenesis, selective, 8, 617073 for gene: WNT10B
Severe Paediatric Disorders v0.8 WNT10A Louise Daugherty Added phenotypes Schopf-Schulz-Passarge syndrome, 224750; Tooth agenesis, selective, 4, 150400; Odontoonychodermal dysplasia, 257980 for gene: WNT10A
Severe Paediatric Disorders v0.8 WNT1 Louise Daugherty Added phenotypes Osteogenesis imperfecta, type XV, 615220 for gene: WNT1
Severe Paediatric Disorders v0.8 WNT10B Louise Daugherty Mode of inheritance for gene WNT10B was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Split-hand/foot malformation 6, 225300; Tooth agenesis, selective, 8, 617073 for gene: WNT10B
Severe Paediatric Disorders v0.8 WNT10A Louise Daugherty Mode of inheritance for gene WNT10A was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Tooth agenesis, selective, 4, 150400; Schopf-Schulz-Passarge syndrome, 224750; Odontoonychodermal dysplasia, 257980 for gene: WNT10A
Severe Paediatric Disorders v0.8 WNT1 Louise Daugherty Mode of inheritance for gene WNT1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Osteogenesis imperfecta, type XV, 615220 for gene: WNT1
Severe Paediatric Disorders v0.7 WNT10B Louise Daugherty Source Next Generation Children Project was added to WNT10B.
Severe Paediatric Disorders v0.7 WNT10A Louise Daugherty Source Next Generation Children Project was added to WNT10A.
Severe Paediatric Disorders v0.7 WNT1 Louise Daugherty Source Next Generation Children Project was added to WNT1.
Severe Paediatric Disorders v0.5 WNT10B Louise Daugherty Source Expert Review Green was added to WNT10B.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.5 WNT10A Louise Daugherty Source Expert Review Green was added to WNT10A.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.5 WNT1 Louise Daugherty Source Expert Review Green was added to WNT1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 WNT10B Louise Daugherty gene: WNT10B was added
gene: WNT10B was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: WNT10B was set to
Severe Paediatric Disorders v0.4 WNT10A Louise Daugherty gene: WNT10A was added
gene: WNT10A was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: WNT10A was set to
Severe Paediatric Disorders v0.4 WNT1 Louise Daugherty gene: WNT1 was added
gene: WNT1 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: WNT1 was set to