PRMT5 and congenital bilateral aplasia of vas deferens from CFTR mutation: The only exception was protein arginine N-methyltransferase 5 (PRMT5, O14744) which was downregulated in control VIC from patients with CAVD by proteomics data compared to VIC from healthy aortic valves (Log2FC = −20.16; adjusted P-value < 0.001).