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| Genetic Epilepsy v0.2220 | SOX11 | Elena Savva Mode of pathogenicity for gene: SOX11 was changed from None to None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2219 | SOX11 | Elena Savva Marked gene: SOX11 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2219 | SOX11 | Elena Savva Gene: sox11 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2219 | SOX11 |
Elena Savva gene: SOX11 was added gene: SOX11 was added to Genetic Epilepsy. Sources: Literature Mode of inheritance for gene: SOX11 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: SOX11 were set to Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism MIM#615866 Review for gene: SOX11 was set to RED Added comment: No reports found of patients with seizures/epilepsy. Gene was listed in the Oliver list Sources: Literature |
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