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| Congenital Heart Defect v1.0 | PRMT9 | Gene migrated from ENSG00000164169 to ENSG00000164169 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.510 | Lucy Spencer Copied gene PRMT9 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.510 | PRMT9 |
Lucy Spencer gene: PRMT9 was added gene: PRMT9 was added to Congenital Heart Defect. Sources: Expert Review Green,Literature Mode of inheritance for gene: PRMT9 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PRMT9 were set to 38561334; 41260215 Phenotypes for gene: PRMT9 were set to Neurodevelopmental disorder, MONDO:0700092, PRMT9-related |
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