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| Congenital Heart Defect v1.0 | MEF2C | Gene migrated from ENSG00000081189 to ENSG00000081189 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.4 | MEF2C | Zornitza Stark Marked gene: MEF2C as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.4 | MEF2C | Zornitza Stark Gene: mef2c has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.4 | MEF2C |
Zornitza Stark gene: MEF2C was added gene: MEF2C was added to Congenital Heart Defect_VCGS. Sources: Expert list Mode of inheritance for gene: MEF2C was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MEF2C were set to 29104469; 22498567; 26811383 Phenotypes for gene: MEF2C were set to Congenital heart disease Review for gene: MEF2C was set to RED Added comment: Two families described and an animal model. This is very low level of evidence considering the prevalence of CHD. Sources: Expert list |
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