27 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wdpcpcys40/Wdpcpcys40 involves: C57BL/6J	abnormal cell physiology	J:205269
	abnormal cilium morphology	J:205269
	abnormal cochlear hair cell morphology	J:205269
	abnormal embryonic neuroepithelium morphology	J:205269
	abnormal heart development	J:205269
	abnormal intestine morphology	J:205269
	abnormal kidney collecting duct morphology	J:205269
	abnormal kinocilium morphology	J:205269
	abnormal podocyte motility	J:205269
	abnormal septation of the cloaca	J:205269
	abnormal truncus arteriosus septation	J:205269
	anophthalmia	J:205269
	atrioventricular septal defect	J:205269
	cleft palate	J:205269
	duplex kidney	J:205269
	normal embryo phenotype	J:205269
	facial cleft	J:205269
	impaired fibroblast cell migration	J:205269
	kidney cyst	J:205269
	persistent truncus arteriosus	J:205269
	polydactyly	J:205269
	pulmonary valve atresia	J:205269
	renal glomerulus cyst	J:205269
	normal respiratory system phenotype	J:205269
	tracheoesophageal fistula	J:205269
Wdpcptm1.1Clo/Wdpcptm1.1Clo involves: 129	abnormal cardiac outflow tract development	J:205269
	abnormal intestine morphology	J:205269
	anophthalmia	J:205269
	cleft palate	J:205269
	duplex kidney	J:205269
	kidney cyst	J:205269
	perinatal lethality, complete penetrance	J:205269
	polydactyly	J:205269