64 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Foxc1tm1Blh/Foxc1+ Tyrc-2J/Tyrc-2J B6.Cg-Tyrc-2J Foxc1tm1Blh	abnormal aqueous drainage system morphology	J:82280
	abnormal trabecular meshwork morphology	J:82280
	absent Schlemm's canal	J:82280
	iris synechia	J:82280
Foxc1tm1Blh/Foxc1+ Foxc2tm1Blh/Foxc2+ involves: 129S6/SvEvTac * Black Swiss	abnormal aortic valve morphology	J:57677
	abnormal branching involved in ureteric bud morphogenesis	J:60834
	abnormal canal of Schlemm morphology	J:61775
	abnormal ciliary body morphology	J:61775
	abnormal cornea morphology	J:61775
	abnormal fourth pharyngeal arch artery morphology	J:57677
	abnormal iridocorneal angle	J:61775
	abnormal iris morphology	J:61775
	abnormal mesonephros morphology	J:60834
	abnormal pharyngeal arch artery morphology	J:57677
	abnormal pulmonary valve morphology	J:57677
	abnormal superior vena cava morphology	J:57677
	abnormal trabecular meshwork morphology	J:61775
	absent kidney	J:60834
	aortic arch coarctation	J:57677
	cornea ulcer	J:61775
	corneal vascularization	J:61775
	decreased angiogenesis	J:57677
	double ureter	J:60834
	duplex kidney	J:60834
	ectopic ureteric bud	J:60834
	enlarged liver	J:57677
	eyelids open at birth	J:61775
	hydronephrosis	J:60834
	hydrops fetalis	J:57677
	hydroureter	J:60834
	interrupted aortic arch, type b	J:57677
	iris stroma hypoplasia	J:61775
	lethality throughout fetal growth and development, incomplete penetrance	J:57677
	perimembraneous ventricular septal defect	J:57677
	renal hypoplasia	J:60834
	normal skeleton phenotype	J:57677
	thick aortic valve cusps	J:57677
	thick pulmonary valve cusps	J:57677
	trabecula carnea hypoplasia	J:57677
	ventricle myocardium hypoplasia	J:57677
Foxc1tm1Blh/Foxc1+ Foxc2tm1Blh/Foxc2tm1Blh involves: 129S6/SvEvTac	abnormal mesonephros morphology	J:91443
	abnormal somite shape	J:91443
Foxc1tm1Blh/Foxc1+ Foxc2tm1Blh/Foxc2tm1Blh involves: 129S6/SvEvTac * Black Swiss	abnormal pharyngeal arch artery morphology	J:71693
	abnormal somite shape	J:71693
	abnormal vascular development	J:71693
	absent second pharyngeal arch	J:71693
	decreased somite size	J:71693
	embryonic lethality during organogenesis, complete penetrance	J:71693
	enlarged third pharyngeal arch artery	J:71693
Foxc1tm1Blh/Foxc1tm1Blh Foxc2tm1Blh/Foxc2+ involves: 129S6/SvEvTac	normal embryo phenotype	J:91443
Foxc1tm1Blh/Foxc1tm1Blh Foxc2tm1Blh/Foxc2+ involves: 129S6/SvEvTac * Black Swiss	normal cardiovascular system phenotype	J:71693
	embryonic lethality during organogenesis, complete penetrance	J:71693
Foxc1tm1Blh/Foxc1tm1Blh Foxc2tm1Blh/Foxc2tm1Blh involves: 129S6/SvEvTac	abnormal mesonephros morphology	J:91443
	abnormal somite development	J:91443
	absent somites	J:91443
	normal embryo phenotype	J:91443
Foxc1tm1Blh/Foxc1tm1Blh Foxc2tm1Blh/Foxc2tm1Blh involves: 129S6/SvEvTac * Black Swiss	abnormal dorsal aorta morphology	J:71693
	abnormal dorsal-ventral polarity of the somites	J:71693
	abnormal head development	J:71693
	abnormal heartbeat	J:71693
	abnormal pharyngeal pouch morphology	J:71693
	abnormal vascular development	J:71693
	abnormal vitelline vascular remodeling	J:71693
	absent paraxial mesoderm	J:71693
	absent second pharyngeal arch	J:71693
	absent somites	J:71693
	decreased embryo size	J:71693
	dilated dorsal aorta	J:71693
	disorganized myocardium	J:71693
	embryonic lethality during organogenesis, complete penetrance	J:71693
	enlarged pericardium	J:71693
	head mesenchyme hypoplasia	J:71693
	incomplete rostral neuropore closure	J:71693
	small first pharyngeal arch	J:71693
	small heart	J:71693