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| Genetic Epilepsy v2.0 | CECR2 | Gene migrated from ENSG00000099954 to ENSG00000099954 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v1.419 | Lucy Spencer Copied gene CECR2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v1.419 | CECR2 |
Lucy Spencer gene: CECR2 was added gene: CECR2 was added to Genetic Epilepsy. Sources: Expert Review Green,Literature Mode of inheritance for gene: CECR2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CECR2 were set to 41964217; 37424722 Phenotypes for gene: CECR2 were set to Neurodevelopmental disorder, MONDO:0700092, CECR2-related; neural tube defects, susceptibility to MONDO:0020705, CECR2-related |
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