Activity
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13 actions
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| Skeletal dysplasia v7.38 | NPR3 | Eleanor Williams Publications for gene: NPR3 were set to 30032985; 10468599 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v7.37 | NPR3 | Eleanor Williams Phenotypes for gene: NPR3 were changed from Tall stature; arachnodactyly; extra epiphyses; aortic dilatation to Boudin-Mortier syndrome, OMIM:619543; Boudin-Mortier syndrome, MONDO:0859194 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v7.36 | NPR3 |
Eleanor Williams edited their review of gene: NPR3: Added comment: Additional cases reported in: PMID: 35233476 - Lauffer et al 2022 - 2 novel compound heterozygous NPR3 variants c.943G>A p.(Ala315Thr) and c.1294A>T p.(Ile432Phe) in a boy with tall stature and macrodactyly of the halluces. The authors note that compared to other patients with NPR-C (encoded by NPR3) loss-of-function, the phenotype appears to be milder. PMID: 40171685 - Moffat et al 2025 - 3 siblings with a novel homozygous missense variant in NPR3 that in vitro data shows causes loss-of-function. All had tall stature but in addition 1 sibling had severe scoliosis developed and mild scoliosis was observed in the two others. Scoliosis has not been previously reported in NPR3-related tall stature and therefore extends the phenotype.; Changed publications to: 30032985, 10468599, 35233476, 40171685; Changed phenotypes to: Boudin-Mortier syndrome, OMIM:619543 |
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| Skeletal dysplasia v2.177 | NPR3 | Eleanor Williams Tag for-review was removed from gene: NPR3. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.176 | NPR3 | Eleanor Williams commented on gene: NPR3: The rating of this gene has been updated following NHS Genomic Medicine Service approval. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.175 | NPR3 |
Eleanor Williams Source Expert Review Green was added to NPR3. Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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| Skeletal dysplasia v2.75 | NPR3 | Eleanor Williams Classified gene: NPR3 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.75 | NPR3 | Eleanor Williams Added comment: Comment on list classification: Promoting this gene from grey to amber with a recommendation for green rating following GMS review. 3 unrelated cases with a similar phenotype and supporting functional data and mouse model. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.75 | NPR3 | Eleanor Williams Gene: npr3 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.74 | NPR3 | Eleanor Williams Publications for gene: NPR3 were set to PMID: 30032985; 10468599 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.73 | NPR3 | Eleanor Williams Tag for-review tag was added to gene: NPR3. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.73 | NPR3 | Eleanor Williams reviewed gene: NPR3: Rating: GREEN; Mode of pathogenicity: None; Publications: 30032985, 10468599; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v2.3 | NPR3 |
Ian Berry gene: NPR3 was added gene: NPR3 was added to Skeletal dysplasia. Sources: Literature Mode of inheritance for gene: NPR3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NPR3 were set to PMID: 30032985; 10468599 Phenotypes for gene: NPR3 were set to Tall stature; arachnodactyly; extra epiphyses; aortic dilatation Penetrance for gene: NPR3 were set to unknown Review for gene: NPR3 was set to GREEN gene: NPR3 was marked as current diagnostic Added comment: 4 individuals in 3 families reported with striking phenotypic similarity. Functional evidence compelling. Mouse model recapitulates phenotype (including skeletal features). Sources: Literature |
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