25 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wfdc2em1(IMPC)H/Wfdc2+ C57BL/6NTac-Wfdc2em1(IMPC)H/H	enlarged heart	J:211773
	increased circulating amylase level	J:211773
Wfdc2em1(IMPC)H/Wfdc2em1(IMPC)H C57BL/6NTac-Wfdc2em1(IMPC)H/H	preweaning lethality, incomplete penetrance	J:211773
Wfdc2em1Fcw/Wfdc2em1Fcw involves: C57	abnormal lung interstitium morphology	J:293623
	abnormal lung morphology	J:293623
	abnormal pulmonary alveolar system morphology	J:293623
	normal cardiovascular system phenotype	J:293623
	cyanosis	J:293623
	decreased blood oxygen saturation level	J:293623
	decreased pulmonary endothelial cell surface	J:293623
	decreased type I pneumocyte number	J:293623
	normal growth/size/body region phenotype	J:293623
	normal hematopoietic system phenotype	J:293623
	neonatal lethality, complete penetrance	J:293623
	respiratory distress	J:293623
Wfdc2tm1.1Ohbo/Wfdc2tm1.1Ohbo involves: C57BL/6NCrlj * CBA/JNCrlj	abnormal alveolar lamellar body morphology	J:282576
	abnormal cytokine level	J:282576
	abnormal lung morphology	J:282576
	abnormal phospholipid level	J:282576
	abnormal respiratory epithelium physiology	J:282576
	abnormal respiratory motile cilium morphology	J:282576
	atelectasis	J:282576
	normal cardiovascular system phenotype	J:282576
	cyanosis	J:282576
	decreased respiratory motile cilia number	J:282576
	lung inflammation	J:282576
	postnatal lethality, complete penetrance	J:282576
	respiratory distress	J:282576
Wfdc2tm1.1Ohbo/Wfdc2tm1b(EUCOMM)Hmgu involves: C57BL/6N * C57BL/6NCrlj * CBA/JNCrlj	absent club cells	J:282576