39 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Isl1tm1(cre)Sev/Isl1+ Msx1tm1Rilm/Msx1+ Pax9tm1Rbal/Pax9tm1.1Hpt involves: 129 * CD-1	aberrant origin of the right subclavian artery	J:311535
	abnormal hyoid bone greater horn morphology	J:311535
	abnormal hyoid bone lesser horn morphology	J:311535
	abnormal hyoid bone morphology	J:311535
	abnormal inferior horn of thyroid cartilage morphology	J:311535
	abnormal superior horn of thyroid cartilage morphology	J:311535
	craniofacial phenotype	J:311535
	neonatal lethality, complete penetrance	J:311535
	preaxial polydactyly	J:311535
Msx1tm1Rilm/Msx1+ Pax9tm1Rbal/Pax9+ involves: 129 * CD-1	decreased tooth number	J:311535
Msx1tm1Rilm/Msx1+ Pax9tm1Rbal/Pax9tm1Rbal involves: 129 * CD-1	aberrant origin of the right subclavian artery	J:311535
	abnormal aorta morphology	J:311535
	abnormal common carotid artery morphology	J:311535
	abnormal first pharyngeal arch artery morphology	J:311535
	abnormal fourth pharyngeal arch artery morphology	J:311535
	abnormal second pharyngeal arch artery morphology	J:311535
	abnormal third pharyngeal arch artery morphology	J:311535
	cleft secondary palate	J:311535
	decreased neural crest cell number	J:311535
	double outlet right ventricle	J:311535
	ectopic thymus	J:311535
	fourth pharyngeal arch artery hypoplasia	J:311535
	interrupted aortic arch	J:311535
	neonatal lethality	J:311535
	preaxial polydactyly	J:311535
	third pharyngeal arch artery hypoplasia	J:311535
	thymus hypoplasia	J:311535
Msx1tm1Rilm/Msx1tm1Rilm Pax9tm1Rbal/Pax9+ involves: 129 * CD-1	cleft palate	J:311535
Msx1tm1Rilm/Msx1tm1Rilm Pax9tm1Rbal/Pax9tm1Rbal involves: 129 * CD-1	aberrant origin of the right subclavian artery	J:311535
	abnormal pharyngeal arch artery morphology	J:311535
	double outlet right ventricle	J:311535
	interrupted aortic arch, type b	J:311535
	normal limbs/digits/tail phenotype	J:311535
Osr2tm1Jian/Osr2tm1Jian Pax9tm1.1(Osr2)Jian/Pax9+ involves: 129S1/Sv * C57BL/6J * FVB/N	abnormal tooth development	J:173121
	cleft secondary palate	J:173121
Osr2tm1Jian/Osr2tm1Jian Pax9tm1.2(Osr2)Jian/Pax9+ involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6J * FVB/N	cleft secondary palate	J:173121
	normal craniofacial phenotype	J:173121
Pax9tm1(Osr2)Jian/Pax9tm1(Osr2)Jian involves: 129S1/Sv * C57BL/6J	abnormal lower incisor morphology	J:173121
Pax9tm1.1(Osr2)Jian/Pax9tm1.1(Osr2)Jian involves: 129S1/Sv * C57BL/6J * FVB/N	abnormal craniofacial bone morphology	J:173121
	abnormal mandible morphology	J:173121
	abnormal palatal shelf morphology	J:173121
	absent mandibular coronoid process	J:173121
	arrest of tooth development	J:173121
	cleft secondary palate	J:173121
	decreased tympanic ring size	J:173121
	neonatal lethality, complete penetrance	J:173121
	palatal shelves fail to meet at midline	J:173121
	preaxial polydactyly	J:173121
	small mandible	J:173121