Activity
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6 actions
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| Rare syndromic craniosynostosis or isolated multisuture synostosis v2.40 | ACTG2 | Zornitza Stark Deleted their review | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v2.31 | ACTG2 | Eleanor Williams Classified gene: ACTG2 as No list | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v2.31 | ACTG2 | Eleanor Williams Added comment: Comment on list classification: Keeping this gene grey as it is not the correct gene for the panel (should be ACTG1). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v2.31 | ACTG2 | Eleanor Williams Gene: actg2 has been removed from the panel. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v2.30 | ACTG2 | Eleanor Williams commented on gene: ACTG2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v2.9 | ACTG2 |
Zornitza Stark gene: ACTG2 was added gene: ACTG2 was added to Craniosynostosis. Sources: Expert list Mode of inheritance for gene: ACTG2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: ACTG2 were set to Baraitser-Winter syndrome 2, MIM# 614583 Review for gene: ACTG2 was set to GREEN Added comment: Metopic ridging is a key feature of this condition. Sources: Expert list |
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