About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Edil3
EGF-like repeats and discoidin I-like domains 3
MGI:1329025
387 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Abcb7tm1Mdf/Abcb7+
Edil3Tg(Sox2-cre)1Amc/Edil3+
either: B6.Cg-Edil3Tg(Sox2-cre)1Amc Abcb7tm1Mdf or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * CBA) 		normal mortality/aging J:106838
Abcb7tm1Mdf/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
either: B6.Cg-Edil3Tg(Sox2-cre)1Amc Abcb7tm1Mdf or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * CBA) 		embryonic lethality between somite formation and embryo turning, complete penetrance J:106838
Adgrg6em2Jlp/Adgrg6em2Jlp
Edil3Tg(Sox2-cre)1Amc/Edil3+
Gt(ROSA)26Sortm1(ADGRG6)Jlp/Gt(ROSA)26Sor+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl * CBA 		embryonic lethality during organogenesis, complete penetrance J:315981
lethality throughout fetal growth and development, incomplete penetrance J:315981
normal nervous system phenotype J:315981
Adgrg6em3Jlp/Adgrg6em3Jlp
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		decreased body size J:315981
embryonic lethality during organogenesis, complete penetrance J:315981
joint contracture J:315981
lethality throughout fetal growth and development, incomplete penetrance J:315981
small heart J:315981
Ankmy2tm1a(EUCOMM)Hmgu/Ankmy2tm1a(EUCOMM)Hmgu
Edil3Tg(Sox2-cre)1Amc/0
involves: C57BL/6 * C57BL/6N * CBA 		abnormal embryonic neuroepithelial layer differentiation J:297055
embryonic lethality between somite formation and embryo turning, complete penetrance J:297055
Arap3tm1.1Sve/Arap3tm1.2Sve
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * CBA * SJL 		abnormal placenta labyrinth morphology J:185401
abnormal placenta vasculature J:185401
decreased embryo size J:185401
decreased placental labyrinth size J:185401
embryonic growth arrest J:185401
embryonic lethality during organogenesis, complete penetrance J:185401
excessive folding of visceral yolk sac J:185401
pale yolk sac J:185401
pallor J:185401
Arhgef7tm1c(EUCOMM)Wtsi/Arhgef7tm1c(EUCOMM)Wtsi
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6N * CBA 		normal embryo phenotype J:217373
Casz1tm1.1Flc/Casz1tm1.1Flc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA * SJL 		abnormal heart development J:221324
embryonic lethality during organogenesis, complete penetrance J:221324
heart hypoplasia J:221324
thin ventricular wall J:221324
ventricular septal defect J:221324
Cdx2tm1Fbe/Cdx2tm2Fbe
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA 		caudal body truncation J:179732
Chd1tm1c(KOMP)Rsan/Chd1tm1c(KOMP)Rsan
Edil3Tg(Sox2-cre)1Amc/?
involves: 129P2/OlaHsd * C57BL/6J * CBA 		embryonic lethality, complete penetrance J:217689
Chd3tm1.1Cya/Chd3tm1.1Cya
Edil3Tg(Sox2-cre)1Amc/0
involves: C57BL/6 * C57BL/6J * CBA 		embryonic lethality, incomplete penetrance J:294633
normal reproductive system phenotype J:294633
Cited2tm1Bha/Cited2tm2Bha
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * CBA * SJL 		abnormal heart left ventricle morphology J:137951
abnormal inferior vena cava morphology J:137951
absent adrenal gland J:137951
absent coronary sinus J:137951
common atrioventricular valve J:137951
dextrocardia J:137951
double outlet right ventricle J:137951
exencephaly J:137951
lethality throughout fetal growth and development, incomplete penetrance J:137951
ostium primum atrial septal defect J:137951
postnatal lethality, complete penetrance J:137951
right aortic arch J:137951
right atrial isomerism J:137951
right pulmonary isomerism J:137951
transposition of great arteries J:137951
ventricular septal defect J:137951
Commd9tm1c(KOMP)Wtsi/Commd9tm1c(KOMP)Wtsi
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6N 		prenatal lethality, complete penetrance J:230747
Ctnnb1tm2Kem/Ctnnb1tm2.1Kem
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * CBA 		abnormal embryonic tissue morphology J:187739
prenatal lethality, complete penetrance J:187739
Ctnnb1tm2Kem/Ctnnb1tm2.1Kem
Gt(ROSA)26Sortm1(Ctnnb1)Kem/Gt(ROSA)26Sortm1.1(Ctnnb1)Kem
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * CBA 		abnormal embryonic tissue morphology J:187739
abnormal germ layer development J:187739
failure to gastrulate J:187739
prenatal lethality, complete penetrance J:187739
Ctsdtm1.1Thre/Ctsdtm1.1Thre
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * C57BL/6N * CBA * SJL 		astrocytosis J:227618
decreased body weight J:227618
decreased double-positive T cell number J:227618
decreased small intestinal villus height J:227618
gliosis J:227618
microgliosis J:227618
neuron degeneration J:227618
premature death J:227618
small intestinal villus atrophy J:227618
thymus atrophy J:227618
weight loss J:227618
Cul4btm1.1Pz/Cul4b+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * C57BL/6J * CBA 		normal mortality/aging J:199210
Cul4btm1.1Pz/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * C57BL/6J * CBA 		no abnormal phenotype detected J:199210
Cul4btm1Swl/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
B6.Cg-Edil3Tg(Sox2-cre)1Amc Cul4btm1Swl 		abnormal dendrite morphology J:187403
abnormal dendritic spine morphology J:187403
abnormal spatial learning J:187403
decreased neuron number J:187403
impaired spatial working memory J:187403
increased susceptibility to pharmacologically induced seizures J:187403
Dab2tm2.1Xxx/Dab2tm2.2Xxx
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA 		normal embryo phenotype J:205046
increased circulating cholesterol level J:205046
increased circulating LDL cholesterol level J:205046
normal mortality/aging J:205046
Dag1tm1Kcam/Dag1tm2.1Kcam
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL 		abnormal axon fasciculation J:194150
abnormal axon guidance J:194150
abnormal basement membrane morphology J:194150
abnormal spinal cord dorsal column morphology J:194150
abnormal spinal cord ventral commissure morphology J:194150
radial glial endfoot detachment J:194150
Ddx3xtm1.1Lyou/Ddx3x+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * CBA 		no abnormal phenotype detected J:231798
Ddx3xtm1.1Lyou/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * CBA 		abnormal allantois morphology J:231798
abnormal brain development J:231798
abnormal cell cycle J:231798
abnormal cell physiology J:231798
abnormal developmental patterning J:231798
abnormal embryo turning J:231798
abnormal head fold morphology J:231798
abnormal myocardial trabeculae morphology J:231798
abnormal neural tube closure J:231798
embryonic growth retardation J:231798
embryonic lethality prior to tooth bud stage J:231798
failure of chorioallantoic fusion J:231798
increased embryonic tissue cell apoptosis J:231798
increased mitotic index J:231798
microcephaly J:231798
pericardial effusion J:231798
preweaning lethality, complete penetrance J:231798
small allantois J:231798
Dicer1tm1Bdh/Dicer1tm1Bdh
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * CBA 		spina bifida J:244791
Disp1icb/Disp1icb
Shhtm1Amc/Shhtm5Amc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129/Sv * C57BL/6J * SWR 		abnormal frontonasal prominence morphology J:94270
perinatal lethality, complete penetrance J:94270
Disp1tm1Pab/Disp1tm1Pab
Shhtm2Chg/Shh+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal digit morphology J:109101
perinatal lethality, complete penetrance J:109101
preaxial polydactyly J:109101
Dph1tm1.1Cmch/Dph1tm1.1Cmch
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA 		abnormal tongue position J:214744
absent palatine bone J:214744
cleft palate J:214744
edema J:214744
fetal growth retardation J:214744
mandible hypoplasia J:214744
neonatal lethality, complete penetrance J:214744
palatal shelves fail to meet at midline J:214744
pallor J:214744
short mandible J:214744
small cranium J:214744
E2f7tm1Gle/E2f7tm1Gle
E2f8tm1Gle/E2f8tm1Gle
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * SJL 		abnormal embryonic tissue morphology J:183999
abnormal respiratory system morphology J:183999
normal embryo phenotype J:183999
neonatal lethality J:183999
Edil3Tg(Sox2-cre)1Amc/Edil3+
Wnt7atm1Amc/Wnt7atm1Amc
Wnt7btm1Parr/Wnt7btm2Amc
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal blood-brain barrier function J:142352
abnormal vasculogenesis J:142352
embryonic lethality during organogenesis, complete penetrance J:142352
intracranial hemorrhage J:142352
spinal hemorrhage J:142352
Edil3Tg(Sox2-cre)1Amc/Edil3+
Tgif1tm1Caw/Tgif1tm1Caw
Tgif2tm1Dwot/Tgif2tm1Dwot
involves: 129S/SvEv * C57BL/6 * C57BL/6J * CBA 		abnormal cephalic neural fold morphology J:183402
abnormal direction of heart looping J:157256
abnormal forebrain development J:183402
abnormal forebrain morphology J:183402
abnormal heart looping J:157256
abnormal left-right axis patterning J:157256
abnormal olfactory epithelium morphology J:183402
abnormal optic vesicle formation J:183402
abnormal primitive streak elongation J:157256
cyclopia J:183402
decreased embryonic neuroepithelial cell proliferation J:183402
decreased embryonic neuroepithelium thickness J:183402
decreased forebrain size J:183402
embryonic lethality during organogenesis, complete penetrance J:157256
embryonic lethality during organogenesis, incomplete penetrance J:183402
failure of heart looping J:157256
heterotaxia J:183402
incomplete rostral neuropore closure J:183402
increased apoptosis J:183402
proboscis J:183402
Edil3Tg(Sox2-cre)1Amc/Edil3+
Hapstr1tm1.1Menm/Hapstr1tm1.2Menm
Trp53tm1Tyj/Trp53tm1Tyj
involves: 129S2/SvPas * C57BL/6 * C57BL/6J * CBA 		prenatal lethality, complete penetrance J:348964
Edil3tm1Tq/Edil3tm1Tq
Itgaltm1Bll/Itgaltm1Bll
involves: 129 * C57BL/6 		abnormal cellular extravasation J:141063
abnormal neutrophil physiology J:141063
Eef1a1tm1Tcrl/Eef1a1+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * CBA 		holoprosencephaly J:225273
lethality throughout fetal growth and development, incomplete penetrance J:225273
open neural tube J:225273
postnatal lethality, complete penetrance J:225273
spina bifida J:225273
Elavl1tm1Dkon/Elavl1tm1Dkon
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA 		abnormal craniofacial bone morphology J:149149
abnormal lung development J:149149
abnormal spleen development J:149149
abnormal vertebrae development J:149149
absent spleen J:149149
delayed endochondral bone ossification J:149149
lethality throughout fetal growth and development, complete penetrance J:149149
midline facial cleft J:149149
short limbs J:149149
small limb buds J:149149
split xiphoid process J:149149
syndactyly J:149149
synostosis J:149149
Enpp2tm1Vart/Enpp2tm1Vart
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		embryonic lethality J:159118
Eomestm1Rob/Eomes+
Nodaltm1Rob/Nodal+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * CBA 		prenatal lethality J:131055
rostral body truncation J:131055
Eomestm1Rob/Eomestm1.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * CBA 		abnormal embryonic epiblast morphology J:131055
abnormal primitive streak morphology J:131055
absent mesoderm J:131055
Eomestm1Rob/Eomestm1.1Rob
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * CBA 		abnormal endoderm development J:131055
abnormal visceral endoderm morphology J:131055
Eomestm1Rob/Eomestm2.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * CBA 		abnormal embryonic epiblast morphology J:154785
abnormal primitive streak morphology J:154785
failure to gastrulate J:154785
Erbb3tm1.1Dwt/Erbb3tm2.1Dwt
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * CBA 		preweaning lethality, complete penetrance J:152703
Esrrbtm1.1Nat/Esrrbtm1.2Nat
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL 		abnormal scala media morphology J:124941
abnormal semicircular canal ampulla morphology J:124941
abnormal semicircular canal morphology J:124941
absent startle reflex J:124941
circling J:124941
decreased endolymph production J:124941
head bobbing J:124941
increased or absent threshold for auditory brainstem response J:124941
small scala media J:124941
Evc2tm2.1Mis/Evc2tm2.1Mis
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129X1/SvJ * C57BL/6 * CBA 		disproportionate dwarf J:226455
Fam20ctm1.1Cqi/Fam20ctm1.1Cqi
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * CBA 		abnormal chondrocyte differentiation J:185208
abnormal circulating protein level J:185208
abnormal limb long bone morphology J:185208
abnormal long bone diaphysis morphology J:185208
abnormal long bone epiphyseal plate morphology J:185208
abnormal long bone epiphyseal plate proliferative zone J:185208
abnormal osteocyte morphology J:185208
abnormal skeleton morphology J:185208
abnormal vertebral column morphology J:185208
abnormal vitamin D level J:185208
decreased body size J:185208
decreased body weight J:185208
decreased bone mineral density J:185208
decreased bone mineralization J:185208
decreased chondrocyte apoptosis J:185208
decreased chondrocyte proliferation J:185208
decreased circulating phosphate level J:185208
decreased compact bone thickness J:185208
delayed bone ossification J:185208
delayed cranial suture closure J:185208
delayed endochondral bone ossification J:185208
female infertility J:185208
flat face J:185208
fragile skeleton J:185208
impaired osteoblast differentiation J:185208
increased circulating parathyroid hormone level J:185208
increased width of hypertrophic chondrocyte zone J:185208
male infertility J:185208
osteomalacia J:185208
postnatal growth retardation J:185208
rickets J:185208
short snout J:185208
small cranium J:185208
Fnip1m1Btlr/Fnip1m1Btlr
Prkag2tm1.1Geno/Prkag2tm1.1Geno
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129 * C57BL/6 * C57BL/6J * CBA 		normal cardiovascular system phenotype J:256296
Foxp2tm1Sfis/Foxp2tm1.2Sfis
Edil3Tg(Sox2-cre)1Amc/?
involves: C57BL/6 * CBA * SJL 		decreased body weight J:125023
delayed eyelid opening J:125023
impaired righting response J:125023
lethality at weaning, complete penetrance J:125023
reduced cerebellar foliation J:125023
small cerebellum J:125023
Fzd4tm1Nat/Fzd4+
Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat/Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat
Edil3Tg(Sox2-cre)1Amc/?
involves: 129 * C57BL/6 * CBA 		abnormal angiogenesis J:154020
abnormal descending aorta morphology J:154020
embryonic growth retardation J:154020
embryonic lethality, incomplete penetrance J:154020
Fzd4tm1Nat/Fzd4tm1Nat
Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat/Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat
Edil3Tg(Sox2-cre)1Amc/?
involves: 129 * C57BL/6 * CBA 		normal cardiovascular system phenotype J:154020
normal growth/size/body region phenotype J:154020
normal mortality/aging J:154020
Fzd5tm1Nat/Fzd5tm2Nat
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL 		abnormal thalamus morphology J:136390
decreased body size J:136390
decreased body weight J:136390
impaired coordination J:136390
retina degeneration J:136390
Fzr1tm1Mama/Fzr1tm1.1Mama
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: BALB/cJ * C57BL/6 * SJL 		normal embryo phenotype J:137456
normal mortality/aging J:137456
Fzr1tm1Mama/Fzr1tm1Mama
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA * SJL 		normal embryo phenotype J:137456
normal mortality/aging J:137456
Gli3tm1Alj/Gli3+
Tgif1tm1Caw/Tgif1tm1Caw
Tgif2tm1Dwot/Tgif2tm1Dwot
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J * CBA 		abnormal cephalic neural fold morphology J:183402
abnormal forebrain development J:183402
abnormal olfactory epithelium morphology J:183402
decreased embryonic neuroepithelial cell proliferation J:183402
exencephaly J:183402
Gt(ROSA)26Sortm1(Wnk1)Clhu/Gt(ROSA)26Sor+
Wnk1Gt(OST38262)Lex/Wnk1Gt(OST38262)Lex
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S5/SvEvBrd * C57BL/6 * CBA 		embryonic lethality during organogenesis J:152906
Gt(ROSA)26Sortm1.1(DUX4*)Plj/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/0
involves: C57BL/6 * CBA 		embryonic lethality, complete penetrance J:256652
Gt(ROSA)26Sortm3(Snai2)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		embryonic lethality J:194078
hemorrhage J:194078
pallor J:194078
Gt(ROSA)26Sortm4(Snai1)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		abnormal embryo development J:194078
embryonic lethality during organogenesis, complete penetrance J:194078
Gt(ROSA)26Sortm5(CAG-Mdm4,-EGFP)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		no abnormal phenotype detected J:194078
Gt(ROSA)26Sortm6(Vegfa*)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		embryonic lethality J:194078
Gt(ROSA)26Sortm8(Aifm1)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		normal mortality/aging J:194078
Gt(ROSA)26Sortm9(Aifm1*)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		normal mortality/aging J:194078
Gt(ROSA)26Sortm10(Gata2)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		embryonic lethality J:194078
Gt(ROSA)26Sortm11(Gata3)Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		normal mortality/aging J:194078
Gt(ROSA)26Sortm14Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		normal mortality/aging J:194078
Gt(ROSA)26Sortm16Jhai/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA 		normal cellular phenotype J:195147
Hapstr1tm1.1Menm/Hapstr1tm1.2Menm
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * C57BL/6J * CBA 		decreased fetal size J:348964
decreased fibroblast proliferation J:348964
lethality throughout fetal growth and development, complete penetrance J:348964
Hcfc1tm1Lwh/Hcfc1+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		abnormal embryo morphology J:231596
abnormal extraembryonic tissue morphology J:231596
decreased body length J:231596
decreased cell proliferation J:231596
decreased embryo size J:231596
decreased lean body mass J:231596
embryonic lethality prior to organogenesis J:231596
embryonic lethality, complete penetrance J:231596
increased apoptosis J:231596
Hcfc1tm1Lwh/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		decreased embryo size J:231596
embryonic lethality prior to organogenesis J:231596
embryonic lethality, complete penetrance J:231596
Hcfc1tm1Lwh/Hcfc1tm1Lwh
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		abnormal embryo morphology J:231596
abnormal extraembryonic tissue morphology J:231596
decreased cell proliferation J:231596
decreased embryo size J:231596
embryonic lethality prior to organogenesis J:231596
embryonic lethality, complete penetrance J:231596
increased apoptosis J:231596
Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat/Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat
Edil3Tg(Sox2-cre)1Amc/?
involves: 129 * C57BL/6 * CBA 		abnormal angiogenesis J:154020
abnormal aorta smooth muscle morphology J:154020
embryonic growth retardation J:154020
prenatal lethality, complete penetrance J:154020
Igs1tm11(CAG-Bgeo,-Edn2)Nat/Igs1+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal vascular development J:201133
embryonic growth retardation J:201133
enlarged heart J:201133
internal hemorrhage J:201133
open neural tube J:201133
prenatal lethality J:201133
Kdm6atm1c(EUCOMM)Wtsi/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
either: (involves: C57BL/6 * CBA * CD-1) or (involves: 129 * C57BL/6 * CBA * CD-1) 		normal mortality/aging J:201868
Kdm6atm1c(EUCOMM)Wtsi/Kdm6atm1c(EUCOMM)Wtsi
Edil3Tg(Sox2-cre)1Amc/Edil3+
either: (involves: C57BL/6 * CBA * CD-1) or (involves: 129 * C57BL/6 * CBA * CD-1) 		lethality throughout fetal growth and development, complete penetrance J:201868
Lama1tm1.1Arhi/Lama1tm1.2Arhi
Edil3Tg(Sox2-cre)1Amc/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal Bergmann glial cell morphology J:184432
abnormal brain meninges morphology J:184432
abnormal brain pia mater morphology J:184432
abnormal cerebellar foliation J:184432
abnormal cerebellar granule layer morphology J:184432
abnormal cerebellar Purkinje cell layer J:184432
abnormal cerebellum morphology J:184432
abnormal Purkinje cell dendrite morphology J:184432
abnormal radial glial cell morphology J:184432
impaired coordination J:184432
limb grasping J:184432
normal mortality/aging J:184432
short stride length J:184432
small cerebellum J:184432
Lama1tm1Olf/Lama1tm1Olf
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S2/SvPas * C57BL/6J * CBA * CD-1 * Swiss Webster 		abnormal Muller cell morphology J:160722
abnormal ocular fundus morphology J:160722
abnormal retina blood vessel morphology J:160722
abnormal retina blood vessel pattern J:160722
abnormal retina inner limiting membrane morphology J:160722
abnormal retina neuronal layer morphology J:160722
abnormal retina vasculature morphology J:160722
decreased birth weight J:160722
macrophthalmia J:160722
normal mortality/aging J:160722
persistence of hyaloid vascular system J:160722
normal reproductive system phenotype J:160722
retina outer nuclear layer degeneration J:160722
retina spots J:160722
thin retina inner nuclear layer J:160722
thin retina inner plexiform layer J:160722
vitreal fibroplasia J:160722
Lhx1tm1Bhr/Lhx1tm2.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * C57BL/6N * CBA 		abnormal endoderm development J:226614
abnormal heart looping J:226614
abnormal heart morphology J:226614
abnormal nervous system development J:226614
abnormal primitive node morphology J:226614
cardia bifida J:226614
cellular necrosis J:226614
embryonic growth retardation J:226614
enlarged pericardium J:226614
Lrp5tm1Kry/Lrp5tm1Kry
Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat/Igs1tm2(CAG-Bgeo,-Ndp,-EGFP)Nat
Edil3Tg(Sox2-cre)1Amc/?
involves: 129 * C57BL/6 * CBA 		abnormal angiogenesis J:154020
abnormal descending aorta morphology J:154020
embryonic growth retardation J:154020
embryonic lethality, incomplete penetrance J:154020
Map2k1tm1Bacc/Map2k1tm1.1Bacc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA 		no abnormal phenotype detected J:199705
Map2k1tm1Chrn/Map2k1tm1.1Chrn
Edil3Tg(Sox2-cre)1Amc/?
involves: 129S/SvEv * C57BL/6 * CBA * FVB/N 		normal reproductive system phenotype J:112223
Mapk11tm1Jsca/Mapk11+
Mapk14tm2Nbr/Mapk14tm2Nbr
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA 		primary sex reversal J:191096
Mapk11tm1Jsca/Mapk11tm1Jsca
Mapk14tm2Nbr/Mapk14tm2Nbr
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA 		abnormal fetal cardiomyocyte proliferation J:176023
abnormal liver morphology J:176023
abnormal neuron proliferation J:176023
exencephaly J:176023
increased hepatocyte apoptosis J:176023
lethality throughout fetal growth and development, complete penetrance J:176023
primary sex reversal J:191096
small liver J:176023
spina bifida J:176023
ventricular septal defect J:176023
Mapk11tm1Jsca/Mapk11tm1Jsca
Mapk14tm2Nbr/Mapk14tm3.1(Mapk11)Nbr
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA 		normal nervous system phenotype J:176023
postnatal lethality, complete penetrance J:176023
ventricular septal defect J:176023
Mapk14tm2Nbr/Mapk14tm3.1(Mapk11)Nbr
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		postnatal lethality, incomplete penetrance J:176023
Myctm2.1Atp/Myctm2.1Atp
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA 		abnormal common myeloid progenitor cell morphology J:137630
abnormal proerythroblast morphology J:137630
normal cardiovascular system phenotype J:137630
decreased embryo size J:137630
decreased erythroid progenitor cell number J:137630
embryonic lethality during organogenesis, complete penetrance J:137630
impaired hematopoiesis J:137630
liver hypoplasia J:137630
pale yolk sac J:137630
Nodaltm1Rob/Nodal+
Edil3Tg(Sox2-cre)1Amc/Edil3+
Tgif1tm1Caw/Tgif1tm1Caw
Tgif2tm1Dwot/Tgif2tm1Dwot
involves: 129S/SvEv * C57BL/6 * C57BL/6J * CBA 		abnormal embryonic neuroepithelium morphology J:183402
abnormal forebrain development J:183402
abnormal left-right axis patterning J:157256
normal cardiovascular system phenotype J:157256
decreased forebrain size J:183402
embryonic growth retardation J:183402
holoprosencephaly J:183402
rostral body truncation J:183402
Nodaltm1Rob/Nodaltm5Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 		abnormal developmental patterning J:93140
abnormal distal visceral endoderm morphology J:93140
abnormal germ layer development J:93140
absent mesoderm J:93140
Nsdhltm1.1Hrm/Nsdhl+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA 		abnormal hair growth J:220990
abnormal skeleton morphology J:220990
decreased body size J:220990
hyperkeratosis J:220990
Nsdhltm1.1Hrm/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA 		postnatal growth retardation J:220990
Nuggctm1Diaz/Nuggctm1Diaz
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * C57BL/6J * CBA 		abnormal somatic hypermutation frequency J:190402
normal immune system phenotype J:190402
Orc1tm1.1Gle/Orc1tm1.2Gle
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA * SJL 		embryonic lethality, complete penetrance J:272584
Pak4tm2.1Amin/Pak4tm2.2Amin
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S2/SvPas * C57BL/6 * CBA * FVB/N 		abnormal placenta labyrinth morphology J:152821
abnormal visceral yolk sac morphology J:152821
embryonic growth retardation J:152821
preweaning lethality, complete penetrance J:152821
Pdgfrbtm12(Pdgfrb)Sor/Pdgfrb+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJae * C57BL/6 * CBA 		no abnormal phenotype detected J:173602
Pdgfrbtm13(Pdgfrb)Sor/Pdgfrb+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJae * C57BL/6 * CBA 		increased aorta wall thickness J:173602
postnatal growth retardation J:173602
postnatal lethality, complete penetrance J:173602
Pdgfrbtm14(Pdgfrb)Sor/Pdgfrb+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJaeSor * C57BL/6 * CBA 		abnormal ascending aorta morphology J:173602
abnormal hypodermis fat layer morphology J:173602
abnormal inguinal fat pad morphology J:173602
abnormal mesenteric fat pad morphology J:173602
abnormal white adipose tissue morphology J:173602
abnormal white fat cell differentation J:173602
normal adipose tissue phenotype J:173602
increased white fat cell number J:173602
postnatal growth retardation J:173602
postnatal lethality, complete penetrance J:173602
Pnkptm1.1Pmc/Pnkptm1.1Pmc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * C57BL/6 * CBA 		embryonic lethality, complete penetrance J:226703
Porcntm1.1Lcm/Porcn+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal autopod morphology J:173672
abnormal hair follicle development J:173672
abnormal tail morphology J:173672
absent ulna J:173672
caudal body truncation J:173672
cleft palate J:173672
decreased body size J:173672
hairless J:173672
normal integument phenotype J:173672
omphalocele J:173672
perinatal lethality, complete penetrance J:173672
short tail J:173672
sternum hypoplasia J:173672
thin dermal layer J:173672
Porcntm1.1Lcm/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal mesoderm development J:173672
lethality throughout fetal growth and development, complete penetrance J:173672
Prdm15tm1c(EUCOMM)Wtsi/Prdm15tm1c(EUCOMM)Wtsi
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6J * C57BL/6N 		abnormal brain morphology J:285408
decreased embryo size J:285408
prenatal lethality, complete penetrance J:285408
Prickle1tm1.2Asw/Prickle1tm1.3Asw
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		abnormal hair follicle development J:213772
abnormal hair follicle orientation J:213772
Prickle1tm1.3Asw/Prickle1tm1.3Asw
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		postnatal lethality, complete penetrance J:213772
Prkag2tm1.1Geno/Prkag2tm1.1Geno
Edil3Tg(Sox2-cre)1Amc/Edil3+
B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc 		abnormal sinoatrial node conduction J:256296
increased heart rate J:256296
Psip1tm1Eng/Psip1tm1Eng
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * CBA 		abnormal cell physiology J:177408
Ptentm1Ppp/Pten+
Rac1tm1Tyb/Rac1tm2Tyb
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/Sv * C3H * C57BL/6 * CBA 		abnormal apoptosis J:173526
abnormal embryo development J:173526
Rac1tm1Tyb/Rac1tm2Tyb
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJae * C3H * C57BL/6 * CBA 		abnormal cell adhesion J:173526
abnormal developmental patterning J:173526
abnormal mesoderm development J:173526
abnormal neural tube closure J:173526
abnormal notochordal plate morphology J:173526
abnormal primitive node morphology J:173526
abnormal primitive streak morphology J:173526
cardia bifida J:173526
decreased cell proliferation J:173526
decreased embryo size J:173526
impaired somite development J:173526
increased embryonic tissue cell apoptosis J:173526
prenatal lethality, complete penetrance J:166095
Sall4tm2Tre/Sall4tm2.1Tre
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * CD-1 		embryonic growth arrest J:115635
embryonic lethality between implantation and somite formation, complete penetrance J:115635
Shhtm1Chg/Shhtm2Chg
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal carpal bone morphology J:109101
abnormal digit morphology J:109101
abnormal tarsal bone morphology J:109101
perinatal lethality J:125109
Shhtm2Chg/Shh+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA 		abnormal choroid plexus morphology J:125109
abnormal corpus callosum morphology J:125109
abnormal embryonic/fetal subventricular zone morphology J:125109
abnormal hippocampus development J:125109
abnormal lateral ganglionic eminence morphology J:125109
abnormal maxillary shelf morphology J:125109
abnormal medial ganglionic eminence morphology J:125109
abnormal neurocranium morphology J:125109
abnormal telencephalon development J:125109
abnormal telencephalon morphology J:125109
absent olfactory bulb J:125109
cleft secondary palate J:125109
enlarged brain ventricles J:125109
holoprosencephaly J:125109
increased forebrain size J:125109
increased midbrain size J:125109
palatal shelves fail to meet at midline J:125109
perinatal lethality, complete penetrance J:125109
polydactyly J:109101
Slc13a4tm1c(EUCOMM)Wtsi/Slc13a4tm1d(EUCOMM)Wtsi
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		normal embryo phenotype J:239786
lethality throughout fetal growth and development, complete penetrance J:239786
normal mortality/aging J:239786
Smad2tm1Rob/Smad2tm2Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * CBA * CD-1 		abnormal anterior definitive endoderm morphology J:84300
abnormal heart looping J:84300
abnormal rostral-caudal axis patterning J:84300
absent forebrain J:84300
absent midbrain J:84300
enlarged pericardium J:84300
pericardial edema J:84300
truncated foregut J:84300
Smad2tm1Rob/Smad2tm2Rob
Smad3tm1Xfw/Smad3+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129/Sv * 129S/SvEv * C57BL/6 * CBA * CD-1 		abnormal heart development J:84300
absent foregut J:84300
fused somites J:84300
rostral body truncation J:84300
Smad4tm1Rob/Smad4tm1.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * CD-1 		abnormal allantois morphology J:92066
abnormal dorsal-ventral axis patterning J:92066
abnormal hindbrain development J:92066
abnormal rhombomere morphology J:92066
abnormal rostral-caudal axis patterning J:92066
absent foregut J:92066
absent hindgut J:92066
absent primordial germ cells J:92066
embryonic lethality during organogenesis, complete penetrance J:92066
fused somites J:92066
Sppl3tm1Itl/Sppl3tm1Itl
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * CBA 		decreased birth body size J:280182
neonatal lethality, incomplete penetrance J:280182
postnatal lethality, incomplete penetrance J:280182
Strip1tm1b(KOMP)Wtsi/Strip1tm1c(KOMP)Wtsi
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6N * CBA * FVB/NJ * SJL 		abnormal head fold morphology J:251816
abnormal mesoderm development J:251816
cardia bifida J:251816
normal embryo phenotype J:251816
short rostral-caudal axis J:251816
Tlk2tm1.1Strc/Tlk2tm1.2Strc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C3H * C57BL/6 		no abnormal phenotype detected J:268910
Trim28tm1.1Ipc/Trim28tm1.2Ipc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S2/SvPas * C57BL/6 * CBA 		abnormal digestive system development J:178936
abnormal lateral plate mesoderm morphology J:178936
abnormal vitelline vasculature morphology J:178936
normal embryo phenotype J:178936
embryonic growth arrest J:178936
short rostral-caudal axis J:178936
wavy neural tube J:178936
Trim33tm1.1Los/Trim33tm1.2Los
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S2/SvPas * C57BL/6 * CBA * SJL 		abnormal brain development J:163858
abnormal endoderm development J:163858
abnormal mesendoderm development J:163858
abnormal primitive node morphology J:163858
abnormal primitive streak elongation J:163858
decreased embryo size J:163858
normal embryo phenotype J:163858
embryonic lethality, incomplete penetrance J:163858
incomplete rostral neuropore closure J:163858
Trpm7tm1Clph/Trpm7tm1.1Clph
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJae * C57BL/6 * CBA 		embryonic lethality, complete penetrance J:140630
Ubr4tm1.2Nkt/Ubr4tm1.2Nkt
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL 		abnormal atrioventricular cushion morphology J:203460
abnormal brain morphology J:203460
abnormal cell death J:203460
abnormal fourth ventricle morphology J:203460
abnormal head morphology J:203460
abnormal heart development J:203460
abnormal interventricular septum morphology J:203460
abnormal lateral ganglionic eminence morphology J:203460
abnormal liver parenchyma morphology J:203460
abnormal liver vasculature morphology J:203460
abnormal medial ganglionic eminence morphology J:203460
decreased brain size J:203460
dilated liver sinusoidal space J:203460
normal embryo phenotype J:203460
embryonic growth retardation J:203460
increased cell proliferation J:203460
lethality throughout fetal growth and development, complete penetrance J:203460
liver hypoplasia J:203460
thin ventricular wall J:203460
Vps52tm1.1Kab/Vps52tm1.2Kab
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL * C57BL/6 * CBA * DBA 		abnormal embryonic tissue morphology J:190873
abnormal vitelline vasculature morphology J:190873
disorganized yolk sac vascular plexus J:190873
embryonic lethality J:190873
Wnt7btm2Amc/Wnt7btm2.1Amc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129X1/SvJ * C57BL/6 * CBA 		abnormal kidney cell proliferation J:142685
abnormal kidney collecting duct epithelium morphology J:142685
abnormal kidney medulla development J:142685
abnormal kidney morphology J:142685
abnormal lung development J:134483
abnormal right lung middle lobe morphology J:134483
abnormal tracheal cartilage morphology J:134483
absent kidney medulla J:142685
atelectasis J:134483
cyanosis J:134483
decreased kidney cell proliferation J:142685
decreased lung weight J:134483
decreased mesenchymal cell proliferation involved in lung development J:134483
hydroureter J:142685
increased kidney apoptosis J:142685
lung hemorrhage J:134483
neonatal lethality, complete penetrance J:134483
small lung J:134483
thin lung-associated mesenchyme J:134483
truncated loop of Henle J:142685
Yy1tm1Yshi/Yy1tm2.1Yshi
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJae * C57BL/6 * CBA 		abnormal endoderm development J:186556
abnormal extraembryonic ectoderm morphology J:186556
abnormal extraembryonic tissue morphology J:186556
abnormal gastrulation J:186556
abnormal gastrulation movements J:186556
abnormal mesoderm development J:186556
abnormal primitive streak elongation J:186556
abnormal primitive streak formation J:186556
abnormal rostral-caudal axis patterning J:186556
abnormal visceral endoderm morphology J:186556
absent head fold J:186556
absent notochord J:186556
absent primitive node J:186556
decreased embryo size J:186556
Zfp568Gt(P103E09)Wrst/Zfp568Gt(RRU161)Byg
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * CBA 		abnormal embryo development J:168015
Zic3tm1.1Smwa/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: C57BL/6 * CBA 		abnormal gastrulation J:194989
abnormal heart looping J:194989
abnormal heart morphology J:194989
abnormal neural tube morphology J:194989
Zic3tm2.1Jwb/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6 * CBA 		abnormal anus morphology J:192577
abnormal axial skeleton morphology J:192577
abnormal direction of heart looping J:192577
abnormal embryo development J:192577
abnormal eye morphology J:192577
abnormal heart looping J:192577
abnormal heart position or orientation J:192577
abnormal inferior vena cava morphology J:192577
abnormal lung position or orientation J:192577
abnormal neural tube morphology J:192577
abnormal stomach position or orientation J:192577
atrial septal defect J:192577
cleft palate J:192577
dextrocardia J:192577
embryonic growth retardation J:192577
exencephaly J:192577
heterotaxia J:192577
hindlimb paralysis J:192577
kinked tail J:192577
lethality throughout fetal growth and development, incomplete penetrance J:192577
right-sided stomach J:192577
ventricular septal defect J:192577
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory