33 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Dnaaf4b2b811.1Clo/Dnaaf4b2b811.1Clo C57BL/6J-Dnaaf4b2b811.1Clo	abdominal situs ambiguus	J:175213
	abnormal brain ependyma motile cilium physiology	J:205312
	abnormal inferior vena cava morphology	J:205312
	abnormal pancreas morphology	J:205312
	abnormal spleen morphology	J:205312
	abnormal sternum morphology	J:175213
	atrioventricular septal defect	J:205312
	cardiac hypertrophy	J:175213
	coronary fistula	J:205312
	d-loop transposition of the great arteries	J:175213
	dextrocardia	J:205312
	double outlet right ventricle with atrioventricular septal defect	J:205312
	heterotaxia	J:205312
	immotile respiratory cilia	J:175213
	lung situs inversus	J:205312
	muscular ventricular septal defect	J:205312
	neonatal lethality, incomplete penetrance	J:205312
	overriding aortic valve	J:175213
	prenatal lethality, incomplete penetrance	J:205312
	right atrial isomerism	J:205312
	right-sided stomach	J:205312
	situs inversus totalis	J:175213, J:205312
	transposition of great arteries	J:205312
	ventricular septal defect	J:175213, J:205312
Dnaaf4tm1.2Jjlo/Dnaaf4tm1.2Jjlo involves: 129S1/Sv * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J	abnormal brain ependyma motile cilium physiology	J:205312
	abnormal respiratory motile cilium physiology	J:205312
	abnormal spleen morphology	J:205312
	dextrocardia	J:205312
	domed cranium	J:205312
	hydrocephaly	J:205312
	lung situs inversus	J:205312
	postnatal lethality, complete penetrance	J:205312
	prenatal lethality, incomplete penetrance	J:205312
	right-sided stomach	J:205312
	situs ambiguus	J:205312
	situs inversus totalis	J:205312
Dnaaf4tm1b(EUCOMM)Hmgu/Dnaaf4+ C57BL/6N-Dnaaf4tm1b(EUCOMM)Hmgu/J	hyperactivity	J:211773
	impaired pupillary reflex	J:211773
	trunk curl	J:211773
Dnaaf4tm1b(EUCOMM)Hmgu/Dnaaf4tm1b(EUCOMM)Hmgu C57BL/6N-Dnaaf4tm1b(EUCOMM)Hmgu/J	preweaning lethality, incomplete penetrance	J:211773