24 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Vangl1Gt(XL802)Byg/Vangl1+ Vangl2Lp/Vangl2+ involves: 129P2/OlaHsd * C57BL/6J * LPT/LeJ	abnormal cochlea morphology	J:132697
	abnormal cochlear hair cell stereociliary bundle morphology	J:132697
	abnormal orientation of inner hair cell stereociliary bundles	J:132697
	abnormal orientation of outer hair cell stereociliary bundles	J:132697
	normal cardiovascular system phenotype	J:132697
	craniorachischisis	J:132697
	curly tail	J:132697
	perinatal lethality, incomplete penetrance	J:132697
	retroesophageal right subclavian artery	J:132697
Vangl1Gt(XL802)Byg/Vangl1+ Vangl2ska17/Vangl2+ involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J	no abnormal phenotype detected	J:169664
Vangl1Gt(XL802)Byg/Vangl1Gt(XL802)Byg Vangl2Lp/Vangl2+ involves: 129P2/OlaHsd * A	abnormal cochlear inner hair cell morphology	J:162640
	abnormal cochlear outer hair cell morphology	J:162640
	female infertility	J:162640
	short tail	J:162640
	vagina atresia	J:162640
Vangl1Gt(XL802)Byg/Vangl1Gt(XL802)Byg Vangl2tm1.2Yy/Vangl2+ involves: 129P2/OlaHsd * C57BL/6 * CBA	abnormal cochlear outer hair cell morphology	J:162640
	long tail	J:162640
Vangl1Gt(XL802)Byg/Vangl1Gt(XL802)Byg Vangl2tm1.2Yy/Vangl2tm1.2Yy involves: 129P2/OlaHsd * C57BL/6 * CBA	abnormal cochlear inner hair cell morphology	J:162640
	abnormal cochlear outer hair cell morphology	J:162640
	abnormal embryo turning	J:162640
	abnormal embryonic cilium location or orientation	J:162640
	abnormal motile primary cilium physiology	J:162640
	abnormal notochord morphology	J:162640
	abnormal prenatal body size	J:162640
	failure of heart looping	J:162640
	heterotaxia	J:162640
	left pulmonary isomerism	J:162640