40 phenotypes from 8 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Efnb1tm1.1Jwu/Efnb1tm1.1Jwu Tg(Lck-cre)I540Jxm/0 B6.Cg-Efnb1tm1.1Jwu Tg(Lck-cre)I540Jxm	normal immune system phenotype	J:178148
Efnb1tm1.1Rha/Efnb1tm1.1Rha involves: 129P2/OlaHsd * BALB/c * C57BL/6	cleft palate	J:110732
	decreased cranium height	J:110732
	edema	J:110732
	neonatal lethality, incomplete penetrance	J:110732
	omphalocele	J:110732
Efnb1tm1.1Sor/Efnb1+ involves: 129S4/SvJaeSor	abnormal axon morphology	J:176056
	frontal bone foramen	J:150043
	polydactyly	J:150043
Efnb1tm1.1Sor/Y involves: 129S4/SvJaeSor	abnormal axon morphology	J:176056
	abnormal corpus callosum morphology	J:150043
	abnormal rib morphology	J:150043
	abnormal tympanic ring morphology	J:150043
	absent corpus callosum	J:150043
	cleft secondary palate	J:150043
Efnb1tm1.1Sor/Efnb1+ involves: 129S4/SvJaeSor * C57BL/6	abnormal frontal bone morphology	J:115952
	abnormal vibrissa morphology	J:115952
	frontal bone foramen	J:115952
	normal nervous system phenotype	J:150043
Efnb1tm1.1Sor/Efnb1tm1.1Sor involves: 129S4/SvJaeSor	abnormal cardiac neural crest cell migration	J:89008
	abnormal corpus callosum morphology	J:150043
	abnormal cranial ganglia morphology	J:89008
	abnormal cranial neural crest cell migration	J:89008
	abnormal oculomotor nerve morphology	J:89008
	abnormal rib morphology	J:150043
	abnormal tympanic ring morphology	J:89008, J:150043
	absent corpus callosum	J:150043
	absent palatal shelf	J:89008
	cleft secondary palate	J:89008, J:150043
Efnb1tm1Rha/Y involves: 129P2/OlaHsd	cleft palate	J:110732
	neonatal lethality, incomplete penetrance	J:110732
Efnb1tm1Rha/Efnb1+ involves: 129P2/OlaHsd	asymmetric rib joints	J:110732
	preaxial polydactyly	J:110732
	sternebra fusion	J:110732
Efnb1tm1Rha/Efnb1+ Tg(Pgk1-cre)1Lni/? involves: 129P2/OlaHsd * BALB/c * C57BL/6	abnormal carpal bone morphology	J:110732
	abnormal cartilage development	J:110732
	asymmetric rib joints	J:110732
	fused carpal bones	J:110732
	omphalocele	J:110732
	polydactyly	J:110732
	postnatal lethality, incomplete penetrance	J:110732
Efnb1tm1Rha/Efnb1+ Tg(Prrx1-cre)1Cjt/? involves: 129P2/OlaHsd * C57BL/6J * SJL/J	polydactyly	J:110732
Efnb1tm1Rha/Efnb1tm1Rha involves: 129P2/OlaHsd	cleft palate	J:110732
	neonatal lethality, incomplete penetrance	J:110732
Efnb1tm1Rha/Y Tg(Pgk1-cre)1Lni/? involves: 129P2/OlaHsd * BALB/c * C57BL/6	abnormal autopod morphology	J:110732
	abnormal axial skeleton morphology	J:110732
	abnormal bone ossification	J:110732
	abnormal carpal bone morphology	J:110732
	abnormal cartilage development	J:110732
	abnormal sternebra morphology	J:110732
	asymmetric sternocostal joints	J:110732
	cleft palate	J:110732
	decreased cranium height	J:110732
	edema	J:110732
	fused carpal bones	J:110732
	omphalocele	J:110732
	polydactyly	J:110732
	polysyndactyly	J:110732
	postnatal lethality, incomplete penetrance	J:110732
	normal reproductive system phenotype	J:110732
	short sternum	J:110732
	sternebra fusion	J:110732
Efnb1tm1Sor/Efnb1+ Meox2tm1(cre)Sor/Meox2+ involves: 129S4/SvJaeSor	polydactyly	J:89008
	postnatal lethality, incomplete penetrance	J:89008
Efnb1tm1Sor/Efnb1+ Meox2tm1(cre)Sor/Meox2+ involves: 129S4/SvJaeSor * C57BL/6	abnormal perichondrium morphology	J:89008
	polydactyly	J:89008
	postnatal lethality, incomplete penetrance	J:89008
Efnb1tm1Sor/Efnb1+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * C57BL/6 * CBA	abnormal tympanic ring morphology	J:89008
	cleft palate	J:89008
	failure of palatal shelf elevation	J:89008
Efnb1tm1Sor/Efnb1tm1Sor Meox2tm1(cre)Sor/Meox2+ involves: 129S4/SvJaeSor	postnatal lethality, incomplete penetrance	J:89008
Efnb1tm1Sor/Y Meox2tm1(cre)Sor/Meox2+ involves: 129S4/SvJaeSor	postnatal lethality, incomplete penetrance	J:89008
Efnb1tm1Sor/Y Meox2tm1(cre)Sor/Meox2+ involves: 129S4/SvJaeSor * C57BL/6	postnatal lethality, incomplete penetrance	J:89008
Efnb1tm2.2Sor/Y involves: 129S4/SvJaeSor	normal nervous system phenotype	J:150043
	normal skeleton phenotype	J:150043
Efnb1tm2.2Sor/Efnb1+ involves: 129S4/SvJaeSor	normal skeleton phenotype	J:150043
Efnb1tm2.2Sor/Efnb1tm2.2Sor involves: 129S4/SvJaeSor	normal nervous system phenotype	J:150043
	normal skeleton phenotype	J:150043
Efnb1tm3.2Sor/Y involves: 129S4/SvJaeSor	abnormal corpus callosum morphology	J:150043
	absent corpus callosum	J:150043
	normal skeleton phenotype	J:150043
Efnb1tm3.2Sor/Efnb1+ involves: 129S4/SvJaeSor	absent corpus callosum	J:150043
	normal skeleton phenotype	J:150043
Efnb1tm3.2Sor/Efnb1+ involves: 129S4/SvJaeSor * C57BL/6	normal nervous system phenotype	J:150043
Efnb1tm3.2Sor/Y involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	normal nervous system phenotype	J:150043
Efnb1tm3.2Sor/Efnb1tm3.2Sor involves: 129S4/SvJaeSor	abnormal corpus callosum morphology	J:150043
	absent corpus callosum	J:150043
	normal skeleton phenotype	J:150043
Efnb1tm3.2Sor/Efnb1tm3.2Sor involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	normal nervous system phenotype	J:150043
Efnb1tm4.2Sor/Y involves: 129S4/SvJaeSor	absent corpus callosum	J:150043
	normal nervous system phenotype	J:150043
	normal skeleton phenotype	J:150043
Efnb1tm4.2Sor/Efnb1+ involves: 129S4/SvJaeSor	absent corpus callosum	J:150043
	normal skeleton phenotype	J:150043
Efnb1tm4.2Sor/Efnb1tm4.2Sor involves: 129S4/SvJaeSor	absent corpus callosum	J:150043
	normal nervous system phenotype	J:150043
	normal skeleton phenotype	J:150043