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| Limb disorders v5.4 | FBXW11 | Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Limb disorders v5.4 | FBXW11 |
Achchuthan Shanmugasundram Tag Q4_21_NHS_review was removed from gene: FBXW11. Tag Q4_23_promote_green was removed from gene: FBXW11. |
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| Limb disorders v5.4 | FBXW11 | Eleanor Williams edited their review of gene: FBXW11: Added comment: The rating of this gene has been updated togreenand the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown'following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Limb disorders v5.3 | FBXW11 |
Achchuthan Shanmugasundram Source NHS GMS was added to FBXW11. Source Expert Review Green was added to FBXW11. Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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| Limb disorders v4.14 | FBXW11 | Sarah Leigh Entity copied from Skeletal dysplasia v4.35 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Limb disorders v4.14 | FBXW11 |
Sarah Leigh gene: FBXW11 was added gene: FBXW11 was added to Limb disorders. Sources: Literature,Expert Review Amber Q4_21_NHS_review, Q4_23_promote_green tags were added to gene: FBXW11. Mode of inheritance for gene: FBXW11 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: FBXW11 were set to 31402090 Phenotypes for gene: FBXW11 were set to Neurodevelopmental, jaw, eye, and digital syndrome, OMIM:618914; neurodevelopmental, jaw, eye, and digital syndrome, MONDO:0030057 Penetrance for gene: FBXW11 were set to unknown |
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