38 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt Osr2tm5(cre)Jian/Osr2+ involves: 129X1/SvJ	abnormal dental mesenchyme morphology	J:153554
	abnormal tooth development	J:153554
	cleft palate	J:153554
	neonatal lethality	J:153554
Ctnnb1tm2Kem/Ctnnb1+ Osr2tm2(cre)Jian/Osr2+ involves: 129S1/Sv * 129X1/SvJ	abnormal enamel knot morphology	J:153554
	cleft secondary palate	J:153554
	growth retardation of incisors	J:153554
	growth retardation of molars	J:153554
	neonatal lethality	J:153554
Ctnnb1tm2Kem/Ctnnb1tm2Kem Osr2tm2(cre)Jian/Osr2+ involves: 129S1/Sv * 129X1/SvJ	abnormal joint morphology	J:171478
Gsk3btm1.1Ypc/Gsk3btm1.1Ypc Osr2tm2(cre)Jian/Osr2+ involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6	normal craniofacial phenotype	J:166721
	normal mortality/aging	J:166721
Hand2tm1Cse/Hand2tm1Cse Osr2tm2(cre)Jian/Osr2+ involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	mandible hypoplasia	J:149232
Mapk1tm1Gela/Mapk1tm1Gela Osr2tm2(cre)Jian/Osr2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	normal craniofacial phenotype	J:239772
Osr1tm2Jian/Osr1tm2Jian Osr2tm1Jian/Osr2tm1Jian Tg(Prrx1-cre)1Cjt/0 involves: 129S1/Sv * C57BL/6J * SJL/J	abnormal bone mineralization	J:171478
	abnormal joint morphology	J:171478
	failure of eyelid fusion	J:171478
	fused synovial joints	J:171478
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
Osr2tm1Jian/Osr2tm3(Osr1)Jian involves: 129S1/Sv * C57BL/6J	abnormal tympanic ring morphology	J:149458
	normal craniofacial phenotype	J:149458
	eyelids open at birth	J:149458
Osr2tm1Jian/Osr2tm4(Osr2*)Jian involves: 129S1/Sv * C57BL/6J	normal craniofacial phenotype	J:149458
	eyelids open at birth	J:149458
	normal hearing/vestibular/ear phenotype	J:149458
Osr2tm2(cre)Jian/Osr2+ Tg(CAG-Nog)1Ych/0 involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	abnormal mandible morphology	J:149232
	cleft palate	J:149232
Osr2tm2(cre)Jian/Osr2+ Tg(CAG-Bmp4,-EGFP)1Ypc/0 involves: 129S1/Sv * C57BL/6J * CD-1	cleft palate	J:214763
	palatal shelf fusion with tongue or mandible	J:214763
	palatal shelves fail to meet at midline	J:214763
Osr2tm3(Osr1)Jian/Osr2tm3(Osr1)Jian involves: 129S1/Sv * C57BL/6J	abnormal eye development	J:149458
	abnormal eyelid fusion	J:149458
	normal craniofacial phenotype	J:149458
	eyelids open at birth	J:149458
	normal hearing/vestibular/ear phenotype	J:149458
Osr2tm4(Osr2*)Jian/Osr2tm4(Osr2*)Jian involves: 129S1/Sv * C57BL/6J	normal craniofacial phenotype	J:149458
	eyelids open at birth	J:149458
	normal hearing/vestibular/ear phenotype	J:149458
Osr2tm5(cre)Jian/Osr2+ Tg(CAG-Nog)1Ych/0 Not Specified	abnormal palatine aponeurosis morphology	J:310908
	abnormal palatopharyngeus muscle morphology	J:310908
	abnormal secondary palate development	J:310908
	abnormal superior pharyngeal constrictor muscle morphology	J:310908
	palatal shelf hypoplasia	J:310908
	small levator veli palatini muscle	J:310908
	small tensor veli palatini muscle	J:310908
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