| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Congenital ophthalmoplegia v0.21 | REV3L | Zornitza Stark Marked gene: REV3L as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital ophthalmoplegia v0.21 | REV3L | Zornitza Stark Gene: rev3l has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital ophthalmoplegia v0.21 | REV3L | Zornitza Stark Phenotypes for gene: REV3L were changed from möbius syndrome to Möbius syndrome | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital ophthalmoplegia v0.20 | REV3L | Zornitza Stark Classified gene: REV3L as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital ophthalmoplegia v0.20 | REV3L | Zornitza Stark Gene: rev3l has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital ophthalmoplegia v0.8 | REV3L |
Shannon LeBlanc gene: REV3L was added gene: REV3L was added to Congenital fibrosis of the extraocular muscles. Sources: Literature Mode of inheritance for gene: REV3L was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: REV3L were set to PMID: 26068067 Phenotypes for gene: REV3L were set to möbius syndrome Review for gene: REV3L was set to GREEN Added comment: de novo variants in 3 unrelated individuals with möbius syndrome and some functional evidence Sources: Literature |
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