30 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Daam1Gt(RRT390)Byg/Daam1Gt(RRT390)Byg involves: 129P2/OlaHsd * C57BL/6J	abnormal cell adhesion	J:167714
	abnormal fetal cardiomyocyte morphology	J:167714
	abnormal fibroblast physiology	J:167714
	abnormal heart left ventricle morphology	J:167714
	abnormal heart ventricle morphology	J:167714
	abnormal muscle physiology	J:167714
	abnormal sarcomere morphology	J:167714
	normal cardiovascular system phenotype	J:167714
	cyanosis	J:167714
	decreased fetal size	J:167714
	decreased survivor rate	J:167714
	double outlet right ventricle	J:167714
	fetal cardiomyocyte disarray	J:167714
	impaired wound healing	J:167714
	lethality throughout fetal growth and development, incomplete penetrance	J:167714
	neonatal lethality, incomplete penetrance	J:167714
	pericardial effusion	J:167714
	ventricular septal defect	J:167714
Daam1Gt(RRT390)Byg/Daam1Gt(RRT390)Byg Nkx2-5tm1(cre)Rjs/Nkx2-5+ involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	normal cardiovascular system phenotype	J:167714
	decreased body size	J:167714
	decreased embryo size	J:167714
	normal mortality/aging	J:167714
Daam1tm1.1Tpy/Daam1tm1.1Tpy Nkx2-5tm1(cre)Rjs/Nkx2-5+ involves: 129S1/Sv * 129S7/SvEvBrd	abnormal diastolic filling velocity	J:228507
	abnormal heart left ventricle morphology	J:228507
	abnormal heart right ventricle morphology	J:228507
	abnormal myocardial trabeculae morphology	J:228507
	abnormal pulmonary pressure	J:228507
	normal cardiovascular system phenotype	J:228507
	decreased right ventricle systolic pressure	J:228507
	thin ventricle myocardium compact layer	J:228507
Daam1tm1b(EUCOMM)Hmgu/Daam1+ C57BL/6N-Daam1tm1b(EUCOMM)Hmgu/H	increased blood urea nitrogen level	J:211773
	increased circulating amylase level	J:211773
Daam1tm1b(EUCOMM)Hmgu/Daam1tm1b(EUCOMM)Hmgu C57BL/6N-Daam1tm1b(EUCOMM)Hmgu/H	preweaning lethality, complete penetrance	J:211773