43 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf3tm1Mrc/Fgf3+ Fgf10tm1Wss/Fgf10tm1Wss involves: 129S7/SvEvBrd * 129X1/SvJ	small otic vesicle	J:83659
Fgf3tm1Mrc/Fgf3tm1Mrc Fgf10tm1Wss/Fgf10+ involves: 129S7/SvEvBrd * 129X1/SvJ	abnormal otic vesicle development	J:83659
	small otic vesicle	J:83659
Fgf3tm1Mrc/Fgf3tm1Mrc Fgf10tm1Wss/Fgf10tm1Wss involves: 129S7/SvEvBrd * 129X1/SvJ	absent inner ear	J:83659
	absent limbs	J:83659
	absent otic vesicle	J:83659
	curly tail	J:83659
	short tail	J:83659
Fgf3tm1Sng/Fgf3tm1Sng Fgf10tm1Ska/Fgf10tm1Ska involves: 129P2/OlaHsd * C57BL/6 * CBA	abnormal ear development	J:87221
	absent vestibulocochlear ganglion	J:87221
	embryonic lethality during organogenesis, complete penetrance	J:87221
	small otic vesicle	J:87221
Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1Sms Gt(ROSA)26Sortm9(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	abnormal cecum development	J:187831
	abnormal lung bud morphology	J:187831
	interdigital webbing	J:187831
Fgf10tm1.1Sms/Fgf10tm1.1Sms Fgf3tm1.1Sms/Fgf3tm1.1Sms involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ	absent limbs	J:160254
	absent otic vesicle	J:160254
	short tail	J:160254
	small otic vesicle	J:160254
Fgf10tm1.2Sms/Fgf10tm1.2Sms Fgf3tm1.2Sms/Fgf3tm1.2Sms involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ	no abnormal phenotype detected	J:160254
Fgf10tm1Ska/Fgf10+ Fgf8tm1Moon/Fgf8tm1Moon Mesp1tm2(cre)Ysa/Mesp1+ involves: C57BL/6NCrlj * CBA/JNCrlj	aberrant origin of the right subclavian artery	J:170879
	abnormal aortic arch morphology	J:170879
	abnormal cardiac outflow tract development	J:170879
	abnormal cardiovascular development	J:170879
	abnormal common carotid artery morphology	J:170879
	abnormal fourth pharyngeal arch artery morphology	J:170879
	abnormal pharyngeal arch artery morphology	J:170879
	abnormal sixth pharyngeal arch artery morphology	J:170879
	abnormal third pharyngeal arch artery morphology	J:170879
	decreased heart right ventricle size	J:170879
	double outlet right ventricle	J:170879
	right aortic arch	J:170879
	second pharyngeal arch hypoplasia	J:170879
	third pharyngeal arch hypoplasia	J:170879
	ventricular septal defect	J:170879
Fgf10tm1Ska/Fgf10tm1Ska Fgf8tm1Moon/Fgf8tm1Moon Mesp1tm2(cre)Ysa/Mesp1+ involves: C57BL/6NCrlj * CBA/JNCrlj	aberrant origin of the right subclavian artery	J:170879
	abnormal aortic arch morphology	J:170879
	abnormal cardiac epithelial to mesenchymal transition	J:170879
	abnormal cardiac neural crest cell migration	J:170879
	abnormal cardiac outflow tract development	J:170879
	abnormal cardiovascular development	J:170879
	abnormal common carotid artery morphology	J:170879
	abnormal fourth pharyngeal arch artery morphology	J:170879
	abnormal pharyngeal arch artery morphology	J:170879
	abnormal sixth pharyngeal arch artery morphology	J:170879
	abnormal third pharyngeal arch artery morphology	J:170879
	decreased heart right ventricle size	J:170879
	double outlet right ventricle	J:170879
	second pharyngeal arch hypoplasia	J:170879
	third pharyngeal arch hypoplasia	J:170879
	ventricular septal defect	J:170879
Fgf10tm1Ska/Fgf10tm1Sms Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Twist2tm1(cre)Dor/Twist2+ involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA	abnormal lung development	J:150706
	abnormal lung lobe morphology	J:150706
	abnormal right lung accessory lobe morphology	J:150706
	abnormal right lung cranial lobe morphology	J:150706
	abnormal right lung middle lobe morphology	J:150706
	impaired branching involved in bronchus morphogenesis	J:150706
	lung hemorrhage	J:150706
	pulmonary hypoplasia	J:150706
	small lung	J:150706
	small lung lobe	J:150706
Fgf10tm1Wss/Fgf10+ Fgfr2tm2Dsn/Fgfr2+ Tg(Pgk1-cre)1Lni/0 involves: 129 * 129X1/SvJ * BALB/c * C57BL/6	abnormal submandibular duct morphology	J:119849
	decreased submandibular gland size	J:119849