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| Genetic Epilepsy v2.0 | NCOR1 | Gene migrated from ENSG00000141027 to ENSG00000141027 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v1.432 | Bryony Thompson Copied gene NCOR1 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v1.432 | NCOR1 |
Bryony Thompson gene: NCOR1 was added gene: NCOR1 was added to Genetic Epilepsy. Sources: Expert Review Green,Literature Mode of inheritance for gene: NCOR1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: NCOR1 were set to 32034166; 31849593; 30664766; 30289594; 29483668 Phenotypes for gene: NCOR1 were set to complex neurodevelopmental disorder, MONDO:0100038 |
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