Adarem1Stsn/Adartm1.1Phs
Ifih1tm1.1Cln/Ifih1tm1.1Cln
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J
|
normal
growth/size/body region phenotype |
J:308678
|
|
normal
mortality/aging |
J:308678
|
Adarem1Stsn/Adartm1.1Phs
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J
|
decreased body size |
J:308678
|
|
lethality, complete penetrance |
J:308678
|
Atmtm2Pmc/Atmtm2Pmc
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * C57BL/6J
|
decreased cellular sensitivity to ionizing radiation |
J:181920
|
Braftm1Sva/Braftm1.1Sva
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
|
lethality at weaning, complete penetrance |
J:105998
|
|
postnatal growth retardation |
J:105998
|
Capn1tm1Ahc/Capn1tm1Ahc
Capn2tm1Tcs/Capn2tm2.1Tcs
Meox2tm1(cre)Sor/Meox2+
B6.129-Capn2tm1Tcs/Capn2tm2.1Tcs Meox2tm1(cre)Sor Capn1tm1Ahc
|
abnormal survival |
J:175868
|
Capn2tm1Tcs/Capn2tm2.1Tcs
Meox2tm1(cre)Sor/Meox2+
B6.129S-Capn2tm1Tcs/Capn2tm2.1Tcs Meox2tm1(cre)Sor
|
abnormal survival |
J:175868
|
Cubntm1Rkoz/Cubntm1Rkoz
Lrp2tm1Tew/Lrp2tm1Tew
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6
|
abnormal kidney morphology |
J:164025
|
|
abnormal renal reabsorption |
J:164025
|
|
albuminuria |
J:164025
|
|
neonatal lethality, incomplete penetrance |
J:164025
|
Cubntm1Rkoz/Cubntm1Rkoz
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6
|
abnormal renal reabsorption |
J:164025
|
|
abnormal vitamin B12 level |
J:164025
|
|
albuminuria |
J:164025
|
|
postnatal lethality, incomplete penetrance |
J:164025
|
Dab2tm1Cpr/Dab2tm1.1Cpr
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * C57BL/6
|
abnormal proximal convoluted tubule morphology |
J:75911
|
|
increased urine protein level |
J:75911
|
Dab2tm2.1Xxx/Dab2tm2.2Xxx
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J
|
normal
mortality/aging |
J:205046
|
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/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
|
Elmo2tm1c(EUCOMM)Hmgu/Elmo2tm1c(EUCOMM)Hmgu
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * C57BL/6N
|
preweaning lethality, complete penetrance |
J:331473
|
Ern1tm2.1Tiw/Ern1tm2.2Tiw
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJae * C57BL/6
|
normal
embryo phenotype |
J:153222
|
|
normal
liver/biliary system phenotype |
J:153222
|
Espl1tm2Pzg/Espl1+
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129S7/SvEvBrd
|
abnormal centrosome morphology |
J:131838
|
|
abnormal gonadal ridge morphology |
J:131838
|
|
abnormal male germ cell morphology |
J:131838
|
|
abnormal mitosis |
J:131838
|
|
abnormal spermatid morphology |
J:131838
|
|
abnormal spermatocyte morphology |
J:131838
|
|
abnormal spermatogenesis |
J:131838
|
|
abnormal spermatogonia morphology |
J:131838
|
|
absent primordial germ cells |
J:131838
|
|
aneuploidy |
J:131838
|
|
decreased primordial germ cell proliferation |
J:131838
|
|
female infertility |
J:131838
|
|
increased mitotic index |
J:131838
|
|
infertility |
J:131838
|
|
male infertility |
J:131838
|
|
small testis |
J:131838
|
Ets1tm1Jml/Ets1tm1Jml
Ets2tm5.1Rgo/Ets2tm5.1Rgo
Meox2tm1(cre)Sor/Meox2+
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * FVB/N
|
edema |
J:151187
|
|
hemorrhage |
J:151187
|
|
prenatal lethality, complete penetrance |
J:151187
|
Ets2tm2Rgo/Ets2tm3Rgo
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
|
prenatal lethality, complete penetrance |
J:128952
|
Ets2tm3Rgo/Ets2+
Meox2tm1(cre)Sor/?
Tg(MMTV-cre)7Mul/?
involves: 129S4/SvJaeSor * FVB/N
|
increased mammary gland tumor incidence |
J:102368
|
Ets2tm3Rgo/Ets2+
Meox2tm1(cre)Sor/?
Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?
involves: 129S4/SvJae * C57BL/6 * FVB/N
|
increased mammary gland tumor incidence |
J:102368
|
Ets2tm3Rgo/Ets2tm3.1Rgo
Meox2tm1(cre)Sor/?
Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?
involves: 129S4/SvJae * C57BL/6 * FVB/N
|
increased mammary gland tumor incidence |
J:102368
|
|
mammary gland hyperplasia |
J:102368
|
Ets2tm3Rgo/Ets2tm3Rgo
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
|
abnormal visceral yolk sac morphology |
J:128952
|
|
decreased embryo size |
J:128952
|
|
embryonic lethality between somite formation and embryo turning, complete penetrance |
J:128952
|
Ets2tm3Rgo/Ets2tm3Rgo
Meox2tm1(cre)Sor/?
Tg(MMTV-cre)7Mul/?
involves: 129S4/SvJaeSor * FVB/N
|
increased mammary gland tumor incidence |
J:102368
|
Ets2tm5.1Rgo/Ets2tm5.1Rgo
Meox2tm1(cre)Sor/Meox2+
involves: 129/Sv * 129S4/SvJaeSor * C57BL/6 * FVB/N
|
normal
mortality/aging |
J:151187
|
|
waved hair |
J:151187
|
Fosl1tm2Wag/Fosl1tm2Wag
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
|
abnormal osteoblast physiology |
J:93053
|
|
normal
cardiovascular system phenotype |
J:95691
|
|
decreased bone mass |
J:93053
|
|
normal
liver/biliary system phenotype |
J:213764
|
|
osteoporosis |
J:93053
|
Fosl2tm2Wag/Fosl2tm2Wag
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
|
normal
skeleton phenotype |
J:137646
|
Junbtm3Wag/Junbtm3Wag
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
|
abnormal bone ossification |
J:88126
|
|
abnormal osteoclast differentiation |
J:88126
|
|
abnormal skeleton development |
J:88126
|
|
abnormal skeleton physiology |
J:88126
|
|
decreased bone mineral density |
J:88126
|
|
decreased bone resorption |
J:88126
|
|
decreased bone strength |
J:88126
|
|
decreased compact bone thickness |
J:88126
|
|
decreased osteoblast cell number |
J:88126
|
|
decreased osteoclast cell number |
J:88126
|
|
increased chronic myelocytic leukemia incidence |
J:88126
|
|
short tibia |
J:88126
|
Kcnq1ot1tm2.1Ckan/Kcnq1ot1+
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SD7
|
abnormal imprinting |
J:185569
|
|
decreased body weight |
J:185569
|
|
postnatal growth retardation |
J:185569
|
Krastm4Tyj/Kras+
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJae * 129S4/SvJaeSor
|
abnormal atrioventricular valve morphology |
J:119477
|
|
abnormal branching involved in lung morphogenesis |
J:119477
|
|
abnormal bronchus morphology |
J:119477
|
|
abnormal cardiovascular system physiology |
J:119477
|
|
abnormal embryonic erythrocyte morphology |
J:119477
|
|
abnormal embryonic erythropoiesis |
J:119477
|
|
conotruncal ridge hyperplasia |
J:119477
|
|
dilated respiratory conducting tube |
J:119477
|
|
double outlet right ventricle |
J:119477
|
|
edema |
J:119477
|
|
normal
embryo phenotype |
J:119477
|
|
embryonic lethality during organogenesis, incomplete penetrance |
J:119477
|
|
hemorrhage |
J:119477
|
|
impaired branching involved in bronchus morphogenesis |
J:119477
|
|
impaired branching involved in terminal bronchiole morphogenesis |
J:119477
|
|
increased hepatocyte apoptosis |
J:119477
|
|
lethality throughout fetal growth and development, complete penetrance |
J:119477
|
|
liver hypoplasia |
J:119477
|
|
pallor |
J:119477
|
|
ventricular septal defect |
J:119477
|
Krastm4Tyj/Kras+
Spry2tm1.1Mrt/Spry2tm1.1Mrt
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * FVB/N
|
impaired branching involved in bronchus morphogenesis |
J:119477
|
Lamtor2tm1.1Lah/Lamtor2tm1.1Lah
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
|
embryonic lethality during organogenesis, complete penetrance |
J:119075
|
Lig4tm1Pmc/Lig4tm1Pmc
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor
|
abnormal nervous system development |
J:144617
|
Llgl1tm1Vv/Llgl1tm1Vv
Meox2tm1(cre)Sor/Meox2+
involves: 129 * 129S4/SvJaeSor * C57BL/6J
|
abnormal brain vasculature morphology |
J:89028
|
|
abnormal cerebral cortex morphology |
J:89028
|
|
abnormal embryonic neuroepithelial layer differentiation |
J:89028
|
|
abnormal embryonic neuroepithelium morphology |
J:89028
|
|
abnormal neuron differentiation |
J:89028
|
|
abnormal neuronal precursor proliferation |
J:89028
|
|
abnormal striatum morphology |
J:89028
|
|
decreased neuron number |
J:89028
|
|
dilated brain ventricle |
J:89028
|
|
dilated lateral ventricle |
J:89028
|
|
domed cranium |
J:89028
|
|
hydrocephaly |
J:89028
|
|
increased neuronal precursor cell number |
J:89028
|
|
intraventricular hemorrhage |
J:89028
|
|
neonatal lethality, complete penetrance |
J:89028
|
Lrp2tm1Tew/Lrp2tm1Tew
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor
|
abnormal renal reabsorption |
J:164025
|
Map2k1tm1Bacc/Map2k1tm1.1Bacc
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
|
normal
mortality/aging |
J:199705
|
Mef2dtm3Eno/Mef2dtm3Eno
Meox2tm1(cre)Sor/Meox2+
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL
|
abnormal heart morphology |
J:130825
|
|
abnormal heart size |
J:130825
|
|
abnormal myocardial fiber morphology |
J:130825
|
|
decreased cardiac muscle contractility |
J:130825
|
Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnh
Meox2tm1Vpa/Meox2tm1Vpa
involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6
|
abnormal skeletal muscle morphology |
J:84754
|
|
abnormal somite development |
J:84754
|
|
absent ribs |
J:84754
|
|
absent vertebrae |
J:84754
|
|
decreased body length |
J:84754
|
|
neonatal lethality, complete penetrance |
J:84754
|
|
vestigial tail |
J:84754
|
Meox1tm1Bmk/Meox1+
Meox2tm1Vpa/Meox2tm1Vpa
involves: 129P2/OlaHsd * C57BL/6
|
abnormal axial skeleton morphology |
J:84754
|
|
abnormal vertebrae morphology |
J:84754
|
|
caudal vertebral fusion |
J:84754
|
Meox1tm1Bmk/Meox1tm1Bmk
Meox2tm1Vpa/Meox2+
involves: 129P2/OlaHsd * C57BL/6
|
abnormal vertebrae development |
J:84754
|
|
abnormal vertebral body morphology |
J:84754
|
|
caudal vertebral fusion |
J:84754
|
|
rib fusion |
J:84754
|
Meox1tm1Bmk/Meox1tm1Bmk
Meox2tm1Vpa/Meox2tm1Vpa
involves: 129P2/OlaHsd * C57BL/6
|
abnormal axial skeleton morphology |
J:84754
|
|
abnormal dermomyotome development |
J:84754
|
|
abnormal dorsal root ganglion morphology |
J:84754
|
|
abnormal dorsal-ventral polarity of the somites |
J:84754
|
|
abnormal epaxial muscle morphology |
J:84754
|
|
abnormal hypaxial muscle morphology |
J:84754
|
|
abnormal myotome development |
J:84754
|
|
abnormal sclerotome morphology |
J:84754
|
|
abnormal skeletal muscle morphology |
J:84754
|
|
abnormal somite development |
J:84754
|
|
abnormal somite shape |
J:84754
|
|
abnormal somite size |
J:84754
|
|
abnormal spinal nerve morphology |
J:84754
|
|
abnormal sternum morphology |
J:84754
|
|
abnormal vertebrae morphology |
J:84754
|
|
abnormal vertebral column morphology |
J:84754
|
|
absent caudal vertebrae |
J:84754
|
|
absent ribs |
J:84754
|
|
cyanosis |
J:84754
|
|
decreased body length |
J:84754
|
|
decreased brown adipose tissue amount |
J:84754
|
|
fused dorsal root ganglion |
J:84754
|
|
loose skin |
J:84754
|
|
neonatal lethality, complete penetrance |
J:84754
|
|
occipital bone hypoplasia |
J:84754
|
|
vestigial tail |
J:84754
|
Meox2tm1(cre)Sor/Meox2+
Smad1tm2Rob/Smad1tm2Sor
involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6
|
abnormal stomach epithelium morphology |
J:90769
|
|
abnormal stomach morphology |
J:90769
|
|
abnormal stomach muscularis externa morphology |
J:90769
|
|
meteorism |
J:90769
|
|
perinatal lethality, incomplete penetrance |
J:90769
|
Meox2tm1(cre)Sor/Meox2+
Nodaltm1Rob/Nodaltm5Rob
involves: 129S/SvEv * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6
|
abnormal developmental patterning |
J:93140
|
|
abnormal proximal-distal axis patterning |
J:93140
|
|
abnormal visceral yolk sac morphology |
J:93140
|
|
rostral body truncation |
J:93140
|
Meox2tm1(cre)Sor/Meox2+
Snai1tm1Grid/Snai1tm2Grid
involves: 129S1/Sv * 129S4/SvJaeSor
|
abnormal allantois morphology |
J:111702
|
|
abnormal cardiac outflow tract development |
J:111702
|
|
abnormal direction of embryo turning |
J:111702
|
|
abnormal direction of heart looping |
J:111702
|
|
abnormal fetal atrioventricular canal morphology |
J:111702
|
|
abnormal heart development |
J:111702
|
|
abnormal primitive streak morphology |
J:111702
|
|
embryonic lethality during organogenesis, complete penetrance |
J:111702
|
|
increased allantois apoptosis |
J:111702
|
Meox2tm1(cre)Sor/Meox2+
Snai1tm1Grid/Snai1tm2Grid
Snai2tm2Grid/Snai2tm2Grid
involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6
|
embryonic growth retardation |
J:111702
|
|
normal
nervous system phenotype |
J:111702
|
|
open neural tube |
J:111702
|
Meox2tm1(cre)Sor/Meox2+
Procrtm1Cte/Procrtm2Cte
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * Black Swiss * C57BL/6
|
prenatal lethality, complete penetrance |
J:119529
|
Meox2tm1(cre)Sor/Meox2+
Mfn1tm1Dcc/Mfn1tm2Dcc
involves: 129S/SvEv * 129S4/SvJaeSor * Black Swiss
|
no abnormal phenotype detected |
J:132329
|
Meox2tm1(cre)Sor/Meox2+
Mfn1tm1Dcc/Mfn1tm2Dcc
Mfn2tm1Dcc/Mfn2tm3Dcc
involves: 129S/SvEv * 129S4/SvJaeSor * Black Swiss
|
neonatal lethality, complete penetrance |
J:132329
|
Meox2tm1(cre)Sor/Meox2+
Mfn1tm1Dcc/Mfn1tm2Dcc
Mfn2tm3Dcc/Mfn2+
involves: 129S/SvEv * 129S4/SvJaeSor * Black Swiss
|
neonatal lethality, complete penetrance |
J:132329
|
Meox2tm1(cre)Sor/Meox2+
Mfn2tm1Dcc/Mfn2tm3Dcc
involves: 129S/SvEv * 129S4/SvJaeSor * Black Swiss
|
decreased body size |
J:132329
|
|
impaired limb coordination |
J:132329
|
|
impaired righting response |
J:132329
|
|
neonatal lethality, incomplete penetrance |
J:132329
|
|
postnatal lethality, complete penetrance |
J:132329
|
|
small cerebellum |
J:132329
|
Meox2tm1(cre)Sor/Meox2+
Raf1tm2Bacc/Raf1tm2.1Bacc
involves: 129P2/OlaHsd * 129S4/SvJaeSor
|
prenatal lethality, complete penetrance |
J:105998
|
Meox2tm1(cre)Sor/Meox2+
Rasgrf1tm4.1Pds/Rasgrf1+
involves: 129S4/SvJaeSor * C57BL/6
|
normal
cellular phenotype |
J:117666
|
Meox2tm1(cre)Sor/Meox2+
Thoc1tm2.1Dwg/Thoc1tm2.1Dwg
involves: 129S4/SvJae * C57BL/6J
|
abnormal embryonic tissue morphology |
J:117869
|
|
embryonic lethality before implantation, complete penetrance |
J:117869
|
Meox2tm1(cre)Sor/Meox2+
Procrtm2Cte/Procrtm2Cte
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * Black Swiss * C57BL/6
|
abnormal hematopoietic system morphology/development |
J:119529
|
|
decreased circulating fibrinogen level |
J:119529
|
|
increased circulating C-reactive protein level |
J:119529
|
|
thrombocytopenia |
J:119529
|
Meox2tm1(cre)Sor/Meox2+
Tead4tm1Bnno/Tead4tm1Bnno
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6
|
no abnormal phenotype detected |
J:126338
|
Meox2tm1(cre)Sor/Meox2+
Slc40a1tm2Nca/Slc40a1tm2Nca
involves: 129S4/SvJae * 129S6/SvEvTac
|
abnormal erythrocyte morphology |
J:129846
|
|
abnormal liver iron level |
J:129846
|
|
anemia |
J:129846
|
|
anisocytosis |
J:129846
|
|
decreased body size |
J:129846
|
|
decreased hemoglobin content |
J:129846
|
|
decreased mean corpuscular hemoglobin |
J:129846
|
|
decreased mean corpuscular volume |
J:129846
|
|
increased intestinal iron level |
J:129846
|
|
increased spleen iron level |
J:129846
|
|
normal
mortality/aging |
J:129846
|
|
pallor |
J:129846
|
|
poikilocytosis |
J:129846
|
|
reticulocytosis |
J:129846
|
Meox2tm1(cre)Sor/Meox2+
Ptrh2tm1Eruo/Ptrh2tm1.1Eruo
B6.Cg-Ptrh2tm1Eruo Ptrh2tm1.1Eruo Meox2tm1(cre)Sor
|
abnormal cerebral cortex morphology |
J:220518
|
|
abnormal hepatocyte morphology |
J:220518
|
|
abnormal muscle fiber morphology |
J:220518
|
|
abnormal pancreatic acinar cell morphology |
J:220518
|
|
ataxia |
J:220518
|
|
cachexia |
J:220518
|
|
cerebellum atrophy |
J:220518
|
|
decreased brain weight |
J:220518
|
|
exocrine pancreatic insufficiency |
J:220518
|
|
muscle weakness |
J:220518
|
|
postnatal growth retardation |
J:220518
|
|
postnatal lethality, complete penetrance |
J:220518
|
Meox2tm1(cre)Sor/Meox2+
Mfn1tm2Dcc/Mfn1+
Mfn2tm1Dcc/Mfn2tm3Dcc
involves: 129S/SvEv * 129S4/SvJaeSor * Black Swiss
|
decreased body size |
J:132329
|
|
impaired limb coordination |
J:132329
|
|
impaired righting response |
J:132329
|
|
neonatal lethality, incomplete penetrance |
J:132329
|
|
postnatal lethality, complete penetrance |
J:132329
|
Meox2tm1(cre)Sor/Meox2+
Pcsk5tm2Prat/Pcsk5tm2.1Prat
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ
|
abnormal heart morphology |
J:136243
|
|
abnormal palate morphology |
J:136243
|
|
abnormal skeleton morphology |
J:136243
|
|
abnormal spinal cord morphology |
J:136243
|
|
abnormal vertebral column morphology |
J:136243
|
|
absent kidney |
J:136243
|
|
absent tail |
J:136243
|
|
atrial septal defect |
J:136243
|
|
dextrocardia |
J:136243
|
|
double outlet right ventricle |
J:136243
|
|
omphalocele |
J:136243
|
|
pulmonary hypoplasia |
J:136243
|
|
right aortic arch |
J:136243
|
|
short hindlimb |
J:136243
|
|
short tail |
J:136243
|
|
tracheoesophageal fistula |
J:136243
|
|
transposition of great arteries |
J:136243
|
|
vascular ring |
J:136243
|
|
ventricular septal defect |
J:136243
|
Meox2tm1(cre)Sor/Meox2+
Xrcc1tm1Pmc/Xrcc1tm1Pmc
involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6
|
abnormal embryonic tissue morphology |
J:152528
|
|
embryonic lethality during organogenesis, complete penetrance |
J:152528
|
|
increased embryonic tissue cell apoptosis |
J:152528
|
Meox2tm1(cre)Sor/Meox2+
Ptpn11tm6Bgn/Ptpn11+
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6
|
abnormal heart morphology |
J:147154
|
|
atrial septal defect |
J:147154
|
|
double outlet right ventricle |
J:147154
|
|
heart valve hyperplasia |
J:147154
|
|
thin myocardium |
J:147154
|
|
ventricular septal defect |
J:147154
|
Meox2tm1(cre)Sor/Meox2+
Zfp568Gt(P103E09)Wrst/Zfp568Gt(RRU161)Byg
involves: 129P2/OlaHsd * 129S2/SvPas * 129S4/SvJaeSor
|
abnormal embryo development |
J:168015
|
Meox2tm1(cre)Sor/Meox2+
Pak4tm2.1Amin/Pak4tm2.2Amin
involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * FVB/N
|
abnormal placenta labyrinth morphology |
J:152821
|
|
abnormal visceral yolk sac morphology |
J:152821
|
Meox2tm1(cre)Sor/Meox2+
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
involves: 129S4/SvJaeSor * C57BL/6 * SJL
|
preweaning lethality, complete penetrance |
J:232065
|
Meox2tm1(cre)Sor/Meox2+
Tg(CAG-lacZ,-FUS,-EGFP)629Gyu/0
involves: 129S4/SvJaeSor * C57BL/6
|
abnormal gait |
J:216672
|
|
abnormal neuromuscular synapse morphology |
J:216672
|
|
astrocytosis |
J:216672
|
|
decreased body weight |
J:216672
|
|
decreased grip strength |
J:216672
|
|
impaired righting response |
J:216672
|
|
limb grasping |
J:216672
|
|
microgliosis |
J:216672
|
|
muscular atrophy |
J:216672
|
|
premature death |
J:216672
|
Meox2tm1(cre)Sor/Meox2+
Tg(CAG-lacZ,-FUS*R521G,-EGFP)682Gyu/0
involves: 129S4/SvJaeSor * C57BL/6
|
abnormal dendrite morphology |
J:216672
|
|
abnormal dendritic spine morphology |
J:216672
|
|
abnormal gait |
J:216672
|
|
abnormal motor capabilities/coordination/movement |
J:216672
|
|
abnormal neuromuscular synapse morphology |
J:216672
|
|
abnormal social investigation |
J:216672
|
|
astrocytosis |
J:216672
|
|
decreased body weight |
J:216672
|
|
decreased grip strength |
J:216672
|
|
decreased locomotor activity |
J:216672
|
|
impaired coordination |
J:216672
|
|
impaired righting response |
J:216672
|
|
limb grasping |
J:216672
|
|
microgliosis |
J:216672
|
|
muscular atrophy |
J:216672
|
|
premature death |
J:216672
|
|
normal
taste/olfaction phenotype |
J:216672
|
Meox2tm1(cre)Sor/?
Nrastm1Zhng/Nrastm1Zhng
involves: 129S4/SvJae * C57BL/6
|
normal
neoplasm |
J:174880
|
Meox2tm1(cre)Sor/0
Pcsk5tm2Prat/Pcsk5tm2.1Prat
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SJL
|
abnormal sternocostal joint morphology |
J:134264
|
|
absent kidney |
J:134264
|
|
absent tail |
J:134264
|
|
asymmetric sternocostal joints |
J:134264
|
|
atelectasis |
J:134264
|
|
decreased body size |
J:134264
|
|
delayed bone ossification |
J:134264
|
|
hemorrhage |
J:134264
|
|
herniated intestine |
J:134264
|
|
increased rib number |
J:134264
|
|
neonatal lethality, complete penetrance |
J:134264
|
|
respiratory failure |
J:134264
|
|
short tail |
J:134264
|
|
vertebral transformation |
J:134264
|
Nrastm1Tyj/Nras+
Meox2tm1(cre)Sor/Meox2+
B6.Cg-Nrastm1Tyj Meox2tm1(cre)Sor
|
abnormal definitive hematopoiesis |
J:305401
|
|
abnormal fetal liver hematopoietic progenitor cell morphology |
J:305401
|
|
abnormal heart development |
J:305401
|
|
abnormal heart morphology |
J:305401
|
|
abnormal myocardial trabeculae morphology |
J:305401
|
|
abnormal pulmonary valve development |
J:305401
|
|
decreased fetal size |
J:305401
|
|
double outlet right ventricle |
J:305401
|
|
hepatic necrosis |
J:305401
|
|
hydrops fetalis |
J:305401
|
|
increased erythroid progenitor cell number |
J:305401
|
|
increased hematopoietic stem cell number |
J:305401
|
|
lethality throughout fetal growth and development, complete penetrance |
J:305401
|
|
pallor |
J:305401
|
|
pulmonary valve stenosis |
J:305401
|
|
small liver |
J:305401
|
|
thin myocardium |
J:305401
|
|
thin ventricle myocardium compact layer |
J:305401
|
|
thin ventricular wall |
J:305401
|
|
ventricular septal defect |
J:305401
|
Nrastm1Tyj/Nras+
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * C57BL/6
|
prenatal lethality, complete penetrance |
J:174880
|
Pdgfrbtm12(Pdgfrb)Sor/Pdgfrb+
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * C57BL/6
|
no abnormal phenotype detected |
J:173602
|
Pdgfrbtm13(Pdgfrb)Sor/Pdgfrb+
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * C57BL/6
|
postnatal growth retardation |
J:173602
|
|
postnatal lethality, complete penetrance |
J:173602
|
Pdgfrbtm14(Pdgfrb)Sor/Pdgfrb+
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * C57BL/6
|
postnatal growth retardation |
J:173602
|
|
postnatal lethality, complete penetrance |
J:173602
|
Pkd1tm1Ggg/Pkd1tm2Ggg
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJae * 129S4/SvJaeSor
|
abnormal placenta morphology |
J:165114
|
|
abnormal placenta vasculature |
J:165114
|
|
normal
cardiovascular system phenotype |
J:165114
|
|
edema |
J:165114
|
|
kidney cyst |
J:165114
|
|
lethality throughout fetal growth and development, incomplete penetrance |
J:165114
|
|
neonatal lethality, complete penetrance |
J:165114
|
|
polyhydramnios |
J:165114
|
|
respiratory failure |
J:165114
|
Pkd2tm1.1Tjwt/Pkd2tm1.2Tjwt
Meox2tm1(cre)Sor/Meox2+
involves: 129S/Sv * 129X1/SvJ * C57BL/6 * SJL
|
dextrocardia |
J:165114
|
|
edema |
J:165114
|
|
kidney cyst |
J:165114
|
|
neonatal lethality |
J:165114
|
|
pancreas cyst |
J:165114
|
|
situs inversus |
J:165114
|
Procrtm2Cte/Procrtm3Cte
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6
|
normal
mortality/aging |
J:144388
|
Rictortm1.1Mgn/Rictortm1.2Mgn
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL
|
lethality throughout fetal growth and development, incomplete penetrance |
J:119564
|
Zfxtm1.1Reiz/Y
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129S6/SvEvTac
|
neonatal lethality, complete penetrance |
J:149654
|
Zfxtm1.1Reiz/Zfxtm1.1Reiz
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129S6/SvEvTac
|
neonatal lethality, complete penetrance |
J:149654
|
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