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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Efnb1
ephrin B1
MGI:102708
40 phenotypes from 8 alleles in 8 genetic backgrounds
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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
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory