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Skeletal dysplasia v3.7 WNT1 Achchuthan Shanmugasundram Publications for gene: WNT1 were set to 23499309; 23499310; 23434763; 23656646
Skeletal dysplasia v3.7 WNT1 Achchuthan Shanmugasundram Publications for gene: WNT1 were set to 34875064
Skeletal dysplasia v3.6 WNT1 Achchuthan Shanmugasundram Publications for gene: WNT1 were set to 34875064
Skeletal dysplasia v3.6 WNT1 Achchuthan Shanmugasundram Publications for gene: WNT1 were set to
Skeletal dysplasia v2.112 WNT1 Ivone Leong Phenotypes for gene: WNT1 were changed from {Osteoporosis, early-onset, susceptibility to, autosomal dominant}, OMIM:615221; Osteogenesis imperfecta, type XV, 615220 to {Osteoporosis, early-onset, susceptibility to, autosomal dominant}, OMIM:615221; Osteogenesis imperfecta, type XV, OMIM:615220
Skeletal dysplasia v2.111 WNT1 Ivone Leong Phenotypes for gene: WNT1 were changed from osteogenesis imperfecta; OI/osteoporosis; {Osteoporosis, early-onset, susceptibility to, autosomal dominant}, 615221; Osteogenesis imperfecta, type XV, 615220 to {Osteoporosis, early-onset, susceptibility to, autosomal dominant}, OMIM:615221; Osteogenesis imperfecta, type XV, 615220
Skeletal dysplasia v2.108 WNT10B Ivone Leong Phenotypes for gene: WNT10B were changed from Split-hand/foot malformation 6 225300 to Split-hand/foot malformation 6, OMIM:225300
Skeletal dysplasia v1.153 WNT10B Eleanor Williams Added phenotypes Split-hand/foot malformation 6 225300 for gene: WNT10B
Skeletal dysplasia v1.153 WNT1 Eleanor Williams Added phenotypes osteogenesis imperfecta; OI/osteoporosis; {Osteoporosis, early-onset, susceptibility to, autosomal dominant}, 615221; Osteogenesis imperfecta, type XV, 615220 for gene: WNT1
Skeletal dysplasia v1.147 WNT10B Tracy Lester reviewed gene: WNT10B: Rating: GREEN; Mode of pathogenicity: ; Publications: 24211389; Phenotypes: Split-hand/foot malformation 6 225300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Skeletal dysplasia v1.147 WNT1 Tracy Lester reviewed gene: WNT1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: OI/osteoporosis, Osteogenesis imperfecta, type XV, 615220, {Osteoporosis, early-onset, susceptibility to, autosomal dominant}, 615221, osteogenesis imperfecta; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Skeletal dysplasia v1.146 WNT10B Eleanor Williams reviewed gene: WNT10B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Skeletal dysplasia v1.146 WNT1 Eleanor Williams reviewed gene: WNT1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Skeletal dysplasia v1.145 WNT10B Eleanor Williams Source NHS GMS was added to WNT10B.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Skeletal dysplasia v1.145 WNT1 Eleanor Williams Source NHS GMS was added to WNT1.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Skeletal dysplasia WNT10B Sarah Leigh marked WNT10B as ready
Skeletal dysplasia WNT10B Sarah Leigh commented on WNT10B
Skeletal dysplasia WNT10B Sarah Leigh classified WNT10B as green