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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Meox2
mesenchyme homeobox 2
MGI:103219
249 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
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 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
myocardial hypertrabeculation 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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12/10/2024
MGI 6.24 		The Jackson Laboratory