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
|