Myl2tm1(cre)Krc/Myl2+
Ptk2tm1.1Guan/Ptk2tm1.1Guan
involves: 129P2/OlaHsd * 129S4/SvJae
|
abnormal myocardial fiber morphology |
J:105371
|
|
abnormal myocardium layer morphology |
J:105371
|
|
cardiac hypertrophy |
J:105371
|
|
cardiac interstitial fibrosis |
J:105371
|
|
dilated heart left ventricle |
J:105371
|
|
disorganized myocardium |
J:105371
|
Ptk2tm1.1Guan/Ptk2tm1.1Guan
Tg(Tek-cre)12Flv/0
involves: 129P2/OlaHsd * C3H * C57BL/6
|
abnormal blood vessel morphology |
J:162690
|
|
abnormal placenta vasculature |
J:162690
|
|
abnormal vitelline vasculature morphology |
J:162690
|
|
decreased embryo size |
J:162690
|
|
dilated vasculature |
J:162690
|
|
edema |
J:162690
|
|
embryonic lethality during organogenesis, complete penetrance |
J:162690
|
|
hemorrhage |
J:162690
|
|
increased apoptosis |
J:162690
|
|
increased vascular permeability |
J:162690
|
|
thin placenta labyrinth |
J:162690
|
Ptk2tm1.1Guan/Ptk2tm1.2Guan
Tg(Tek-cre)12Flv/0
involves: 129P2/OlaHsd * C3H * C57BL/6 * C57BL/6J
|
abnormal amnion morphology |
J:99637
|
|
abnormal capillary morphology |
J:99637
|
|
abnormal placenta vasculature |
J:99637
|
|
abnormal vascular branching morphogenesis |
J:99637
|
|
abnormal vascular endothelial cell morphology |
J:99637
|
|
abnormal vitelline vasculature morphology |
J:99637
|
|
decreased embryo size |
J:99637
|
|
edema |
J:99637
|
|
embryonic growth retardation |
J:99637
|
|
hemorrhage |
J:99637
|
|
lethality throughout fetal growth and development, incomplete penetrance |
J:99637
|
|
thick dermal layer |
J:99637
|
|
thin placenta labyrinth |
J:99637
|
Ptk2tm1.1Itl/Ptk2tm1.1Itl
involves: 129S/SvEv * C57BL/6 * SJL
|
abnormal cell physiology |
J:165360
|
|
abnormal fibroblast migration |
J:165360
|
|
abnormal head morphology |
J:165360
|
|
abnormal heart morphology |
J:165360
|
|
abnormal vascular development |
J:165360
|
|
abnormal vitelline vascular remodeling |
J:165360
|
|
abnormal vitelline vasculature morphology |
J:165360
|
|
absent heartbeat |
J:165360
|
|
absent somites |
J:165360
|
|
embryonic lethality during organogenesis, complete penetrance |
J:165360
|
|
enlarged allantois |
J:165360
|
|
failure of chorioallantoic fusion |
J:165360
|
|
hemorrhage |
J:165360
|
Ptk2tm1.1Jtpa/Ptk2tm1.1Jtpa
B6.129P2-Ptk2tm1.1Jtpa
|
increased physiological sensitivity to xenobiotic |
J:142317
|
Ptk2tm1.1Jtpa/Ptk2tm1.1Jtpa
involves: 129P2/OlaHsd * C57BL/6
|
normal
muscle phenotype |
J:142495
|
Ptk2tm1.2Guan/Ptk2tm1.2Guan
involves: 129P2/OlaHsd * C57BL/6J
|
embryonic growth retardation |
J:99637
|
|
embryonic lethality during organogenesis, complete penetrance |
J:99637
|
Ptk2tm1Gwm/Ptk2tm1Gwm
Tg(KRT14-cre/ERT2)1Ipc/0
involves: 129P2/OlaHsd * FVB
|
decreased incidence of tumors by chemical induction |
J:94680
|
|
decreased keratinocyte migration |
J:94680
|
|
decreased tumor growth/size |
J:94680
|
|
increased keratinocyte apoptosis |
J:94680
|
Ptk2tm1Heen/Ptk2tm1Heen
involves: 129/Sv * C57BL/6
|
abnormal blood vessel morphology |
J:157804
|
|
abnormal heart development |
J:157804
|
|
abnormal limb development |
J:157804
|
|
abnormal liver development |
J:157804
|
|
abnormal lung development |
J:157804
|
|
abnormal vitelline vasculature morphology |
J:157804
|
|
decreased embryo size |
J:157804
|
|
decreased fibroblast cell migration |
J:157804
|
|
decreased fibroblast proliferation |
J:157804
|
|
decreased survivor rate |
J:157804
|
|
delayed heart development |
J:157804
|
|
delayed hepatic development |
J:157804
|
|
disorganized yolk sac vascular plexus |
J:157804
|
|
edema |
J:157804
|
|
embryonic growth retardation |
J:157804
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:157804
|
|
hemorrhage |
J:157804
|
|
lethality throughout fetal growth and development, incomplete penetrance |
J:157804
|
|
liver hemorrhage |
J:157804
|
|
normal
reproductive system phenotype |
J:157804
|
Ptk2tm1Imeg/Ptk2+
CBA.Cg-Ptk2tm1Imeg
|
abnormal dorsal aorta morphology |
J:82150
|
|
abnormal vascular development |
J:82150
|
|
decreased embryo size |
J:82150
|
Ptk2tm1Imeg/Ptk2tm1Imeg
CBA.Cg-Ptk2tm1Imeg
|
abnormal blood vessel morphology |
J:82150
|
|
abnormal vascular endothelial cell development |
J:82150
|
|
absent vitelline blood vessels |
J:82150
|
|
embryonic lethality between somite formation and embryo turning, complete penetrance |
J:82150
|
|
hemorrhage |
J:82150
|
Ptk2tm1Imeg/Ptk2tm1Imeg
involves: C57BL/6 * CBA
|
abnormal allantois morphology |
J:29978
|
|
abnormal amnion morphology |
J:29978
|
|
abnormal aorta morphology |
J:29978
|
|
abnormal blood circulation |
J:29978
|
|
abnormal blood vessel morphology |
J:29978
|
|
abnormal cell migration |
J:29273
|
|
abnormal cell morphology |
J:29273
|
|
abnormal developmental patterning |
J:29978
|
|
abnormal dorsal aorta morphology |
J:29273
|
|
abnormal ectoderm development |
J:29273
|
|
abnormal embryonic neuroepithelium morphology |
J:29978
|
|
abnormal embryonic tissue morphology |
J:29978
|
|
abnormal endocardium morphology |
J:29273
|
|
abnormal extraembryonic tissue morphology |
J:29978
|
|
abnormal foregut morphology |
J:29978
|
|
abnormal head fold morphology |
J:29978
|
|
abnormal head mesenchyme morphology |
J:29978
|
|
abnormal heart development |
J:29273,
J:29978
|
|
abnormal mesocardium morphology |
J:29273
|
|
abnormal mesoderm development |
J:29273,
J:29978
|
|
abnormal notochord morphology |
J:29273,
J:29978
|
|
abnormal rostral-caudal axis patterning |
J:29273,
J:29978
|
|
abnormal somite development |
J:29273,
J:29978
|
|
abnormal visceral yolk sac cavity morphology |
J:29978
|
|
abnormal vitelline artery morphology |
J:29273
|
|
decreased embryo size |
J:29978
|
|
embryonic lethality during organogenesis, complete penetrance |
J:29978
|
|
failure of chorioallantoic fusion |
J:29978
|
|
failure of initiation of embryo turning |
J:29978
|
|
hemorrhage |
J:29978
|
|
small amniotic cavity |
J:29978
|
|
small visceral yolk sac |
J:29978
|
|
thick myocardium |
J:29978
|
Ptk2tm1Itl/Ptk2+
involves: 129S/SvEv * C57BL/6
|
decreased body size |
J:165360
|
Ptk2tm1Itl/Ptk2tm1Itl
involves: 129S/SvEv * C57BL/6
|
prenatal lethality, complete penetrance |
J:165360
|
Ptk2tm1Lfr/Ptk2tm1Ilic
Tg(KRT5-cre)5132Jlj/0
involves: 129X1/SvJ * C57BL/6 * CBA * DBA/2J
|
abnormal hair cycle |
J:107206
|
|
abnormal hair follicle orientation |
J:107206
|
|
decreased hair follicle number |
J:107206
|
|
decreased keratinocyte proliferation |
J:107206
|
|
decreased sebaceous gland number |
J:107206
|
|
sparse hair |
J:107206
|
|
thin epidermis |
J:107206
|
Ptk2tm1Lfr/Ptk2tm1Lfr
Tg(Tek-cre)1Rwng/0
involves: 129X1/SvJ * FVB/N
|
abnormal blood vessel morphology |
J:104401
|
|
abnormal capillary morphology |
J:104401
|
|
abnormal vascular endothelial cell morphology |
J:104401
|
|
abnormal vascular regression |
J:104401
|
|
abnormal vitelline vasculature morphology |
J:104401
|
|
decreased angiogenesis |
J:104401
|
|
decreased embryo size |
J:104401
|
|
disorganized yolk sac vascular plexus |
J:104401
|
|
embryonic lethality during organogenesis, complete penetrance |
J:104401
|
|
hemorrhage |
J:104401
|
Ptk2tm1Mmsh/Ptk2tm1Mmsh
Tg(Nes-cre)1Sasa/0
B6.Cg-Ptk2tm1Mmsh Tg(Nes-cre)1Sasa
|
abnormal innervation |
J:132715
|
|
abnormal Purkinje cell innervation |
J:132715
|
|
ectopic Bergmann glia cells |
J:132715
|
|
reduced cerebellar foliation |
J:132715
|
Ptk2tm2.1Guan/Ptk2tm1.1Guan
Tg(Tek-cre)12Flv/0
involves: 129P2/OlaHsd * C3H * C57BL/6 * FVB/N
|
abnormal blood vessel morphology |
J:162690
|
|
dilated vasculature |
J:162690
|
|
increased apoptosis |
J:162690
|
|
increased vascular permeability |
J:162690
|
|
lethality throughout fetal growth and development, complete penetrance |
J:162690
|
Ptk2tm2.1Guan/Ptk2tm2.1Guan
involves: 129P2/OlaHsd * C57BL/6J * FVB/N
|
embryonic lethality during organogenesis, complete penetrance |
J:162690
|
Ptk2tm3.1Guan/Ptk2tm3.1Guan
involves: 129P2/OlaHsd * C57BL/6J * FVB/N
|
no abnormal phenotype detected |
J:195658
|
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