75 phenotypes from 6 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Foxh1b2b2662Clo/Foxh1b2b2662Clo C57BL/6J-Foxh1b2b2662Clo	abdominal situs ambiguus	J:175213
	abnormal aortic arch morphology	J:175213
	abnormal cranium morphology	J:175213
	abnormal inferior vena cava morphology	J:175213
	abnormal intestine morphology	J:175213
	abnormal right subclavian artery morphology	J:175213
	abnormal sternum morphology	J:175213
	abnormal thoracic cavity morphology	J:175213
	absent mandible	J:175213
	absent pericardium	J:175213
	absent spleen	J:175213
	acrania	J:175213
	anencephaly	J:175213
	anophthalmia	J:175213
	common atrium	J:175213
	common ventricle	J:175213
	cyclopia	J:175213
	decreased mouth size	J:175213
	dextrocardia	J:175213
	diaphragmatic hernia	J:175213
	double outlet right ventricle with atrioventricular septal defect	J:175213
	double outlet right ventricle, Taussig bing type	J:175213
	heart left ventricle hypoplasia	J:175213
	heterotaxia	J:175213
	lowered ear position	J:175213
	mesocardia	J:175213
	microcephaly	J:175213
	proboscis	J:175213
	right aortic arch	J:175213
	right pulmonary isomerism	J:175213
	right-sided stomach	J:175213
	situs inversus with levocardia	J:175213
	thymus hypoplasia	J:175213
	vascular ring	J:175213
Foxh1tm1Hmd/Foxh1tm1.1Hmd Tg(Leftb-cre)1Hmd/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6Cr	abnormal azygos vein morphology	J:82311
	abnormal heart position or orientation	J:82311
	abnormal hepatic portal vein morphology	J:82311
	abnormal renal vein morphology	J:82311
	atrial septal defect	J:82311
	atrial situs inversus	J:82311
	complete atrioventricular septal defect	J:82311
	dextrocardia	J:82311
	double outlet right ventricle	J:82311
	mesocardia	J:82311
	postnatal lethality, complete penetrance	J:82311
	right atrial isomerism	J:82311
	right pulmonary isomerism	J:82311
	right-sided isomerism	J:82311
	right-sided stomach	J:82311
	spleen hypoplasia	J:82311
	transposition of great arteries	J:82311
	ventricular septal defect	J:82311
Foxh1tm1Jlw/Foxh1tm1Jlw involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal anterior head development	J:69594
	abnormal anterior primitive streak morphology	J:69594
	abnormal cardiac outflow tract development	J:93034
	abnormal heart development	J:93034
	abnormal heart left ventricle morphology	J:93034
	abnormal heart looping	J:93034
	abnormal heart ventricle morphology	J:93034
	abnormal mesendoderm development	J:69594
	abnormal neural plate morphology	J:69594
	abnormal pericardial cavity morphology	J:69594
	abnormal pharyngeal arch artery morphology	J:93034
	absent heart right ventricle	J:93034
	absent neural folds	J:69594
	absent notochord	J:69594
	absent prechordal mesoderm	J:69594
	absent primitive node	J:69594
	decreased embryo size	J:69594
	disorganized myocardium	J:93034
	embryonic growth retardation	J:69594
	embryonic lethality during organogenesis, complete penetrance	J:69594
	embryonic-extraembryonic boundary constriction	J:69594
	failure of heart looping	J:69594
	fused somites	J:69594
	holoprosencephaly	J:69594
	pericardial edema	J:93034
	trabecula carnea hypoplasia	J:93034
Foxh1tm2.1(Foxh1)Cvw/Foxh1tm2.1(Foxh1)Cvw involves: 129S6/SvEvTac * C57BL/6 * SJL	no abnormal phenotype detected	J:217681
Foxh1tm3.1(Foxh1*)Cvw/Foxh1tm3.1(Foxh1*)Cvw involves: 129S6/SvEvTac * C57BL/6 * SJL	no abnormal phenotype detected	J:217681