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| Rare syndromic craniosynostosis or isolated multisuture synostosis v4.126 | FOXO1 |
Achchuthan Shanmugasundram gene: FOXO1 was added gene: FOXO1 was added to Rare syndromic craniosynostosis or isolated multisuture synostosis. Sources: Literature Mode of inheritance for gene: FOXO1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: FOXO1 were set to 35997807; 36980886 Phenotypes for gene: FOXO1 were set to craniosynostosis, MONDO:0015469 Review for gene: FOXO1 was set to RED Added comment: PMID:35997807 reported a cohort of patients with lambdoid synostosis, where a de novo variant (p.Arg180Trp) was identified in FOXO1. Hence, this gene should be added with a red rating. Sources: Literature |
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