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. Author manuscript; available in PMC: 2018 May 23.
Published in final edited form as: Mol Genet Metab. 2018 Mar 18;124(1):94–100. doi: 10.1016/j.ymgme.2018.03.005

Table 1.

Mouse mutants of key PCP Genes in a digenic fashion and NTD phenotypes.

Gene and mutant NTD Type Penetrance References
Vangl2Lp/+, Dvl2/ CRN 100% Wang et al. (2006) [25]
Vangl2Lp/+, Dvl3+/ CRN, EX 30% Etheridge et al. (2008) [26]
Vangl2Lp/+,ScribCrc/+ CRN or SB 55% CRN, 5% SB Murdoch et al. (2001) [27]
Vangl2Lp/+,ScribCrc/+ CRN 54% Murdoch et al. (2014) [2]
Vangl2Lp/+,Celsr1Crsh/+ CRN not stated Copp et al. (2003) [41]
Vangl2Lp/+,Celsr1Crsh/+ CRN 54% Murdoch et al. (2014) [2]
Vangl2Lp/+, Ptk7+/ SB 95% Lu et al. (2004) [47]
Vangl2Lp/+,Vangl1+/ CRN 60% Torban et al. (2008) [28]
Dvl2/,Dvl3+/ CRN ~100% Etheridge et al. (2008) [26]
Dvl2+/,Dvl3/ CRN some Etheridge et al. (2008) [26]
ScribCrc/+,Celsr1Crsh/+ CRN 8% Murdoch et al. (2014) [2]

PCP, planar cell polarity; NTD, neural tube defect; CRN, craniorachischisis; SB, spina bifida; EX, exencephaly.