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Fetal anomalies v1.211 | IRX4 | Ain Roesley Marked gene: IRX4 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v1.211 | IRX4 | Ain Roesley Gene: irx4 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v1.211 | IRX4 |
Ain Roesley gene: IRX4 was added gene: IRX4 was added to Fetal anomalies. Sources: Literature Mode of inheritance for gene: IRX4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: IRX4 were set to 21544582 Phenotypes for gene: IRX4 were set to Ventricular septal defect Review for gene: IRX4 was set to RED gene: IRX4 was marked as current diagnostic Added comment: Two individuals with novel missense variants identified in a large cohort in 2011. nothing new in punned Sources: Literature |