Fig. 2From: A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplicationSubcellular localization of wild-type and variant RIPPLY3 proteins in the HEK293T cells. The wild-type and variant RIPPLY3 (P30L, T52S, D113N and V179D) were located in both cytoplasm and nucleus, and there seems no significant difference between themBack to article page