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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Eomestm1.1Rob
targeted mutation 1.1, Elizabeth J Robertson
MGI:3774028
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Eomestm1.1Rob/Eomestm1.1Rob involves: 129S/SvEv * C57BL/6 * CBA MGI:3775736
cn2
Eomestm1Rob/Eomestm1.1Rob
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * CBA MGI:3775735
cn3
Eomestm1Rob/Eomestm1.1Rob
Tg(T-cre)1Lwd/0
involves: 129S/SvEv * C3H * C57BL/6 * CBA MGI:3775734
cn4
Eomestm1Rob/Eomestm1.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * CBA MGI:3775733
cx5
Eomestm1.1Rob/Eomes+
Wnt3tm1Brd/Wnt3+
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA MGI:3775738
cx6
Eomestm1.1Rob/Eomes+
Nodaltm1Rob/Nodal+
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA MGI:3775732
cx7
Eomestm1.1Rob/Eomes+
Nodaltm4Rob/Nodaltm4Rob
involves: 129S/SvEv * C57BL/6 * CBA MGI:3775739


Genotype
MGI:3775736
hm1
Allelic
Composition
Eomestm1.1Rob/Eomestm1.1Rob
Genetic
Background
involves: 129S/SvEv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eomestm1.1Rob mutation (0 available); any Eomes mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• E7.5 blastocysts after 72 hours in culture either fail to form a a trophoblast outgrowth, or at best, form a rudimentary outgrowth with a few trophoblast giant cells; thus recapitulating the null phenotype




Genotype
MGI:3775735
cn2
Allelic
Composition
Eomestm1Rob/Eomestm1.1Rob
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background
involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (43 available)
Eomestm1.1Rob mutation (0 available); any Eomes mutation (44 available)
Eomestm1Rob mutation (0 available); any Eomes mutation (44 available)
Gt(ROSA)26Sortm1Sor mutation (7 available); any Gt(ROSA)26Sor mutation (993 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• specification of the definitive endoderm is disrupted
• visceral endoderm fails to displace proximally at E7.5




Genotype
MGI:3775734
cn3
Allelic
Composition
Eomestm1Rob/Eomestm1.1Rob
Tg(T-cre)1Lwd/0
Genetic
Background
involves: 129S/SvEv * C3H * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eomestm1.1Rob mutation (0 available); any Eomes mutation (44 available)
Eomestm1Rob mutation (0 available); any Eomes mutation (44 available)
Tg(T-cre)1Lwd mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
N
• Mendelian numbers of conditionally null embryos are recovered around E6.5




Genotype
MGI:3775733
cn4
Allelic
Composition
Eomestm1Rob/Eomestm1.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background
involves: 129S/SvEv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (43 available)
Eomestm1.1Rob mutation (0 available); any Eomes mutation (44 available)
Eomestm1Rob mutation (0 available); any Eomes mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• by late headfold stages, embryos have multiple cystic epiblast invaginations and completely lack a discrete mesoderm layer
• at E7.5, there is complete absence of mesodermal cells between the visceral endoderm and the epiblast
• mutant embryos display abnormal thickening of the primitive streak at E7.0, resulting in an abnormal embryo shape
• there is accumulation of cells with mesenchymal morphology in the primitive streak




Genotype
MGI:3775738
cx5
Allelic
Composition
Eomestm1.1Rob/Eomes+
Wnt3tm1Brd/Wnt3+
Genetic
Background
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eomestm1.1Rob mutation (0 available); any Eomes mutation (44 available)
Wnt3tm1Brd mutation (0 available); any Wnt3 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• no phenotypic abnormalities are observed at E9.5




Genotype
MGI:3775732
cx6
Allelic
Composition
Eomestm1.1Rob/Eomes+
Nodaltm1Rob/Nodal+
Genetic
Background
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eomestm1.1Rob mutation (0 available); any Eomes mutation (44 available)
Nodaltm1Rob mutation (2 available); any Nodal mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• AVE is correctly induced but fails to migrate anteriorly
• heart patterning abnormalities are observed by E9.5 due to loss of midline structures
• embryos lack visible germ layers
• left-right patterning abnormalities are observed by E9.5 due to loss of midline structures
• floor plate expansion results in increased spacing between somite rows at E9.5
• by E9.5, mutants lack head structures rostral to the otic placodes
• in the most severely affected embryos, relatively complete duplications of the posterior body axis are observed, including extra somite rows
• node abnormalities result in expansion of the floor plate of the neural tube
• node duplications are accompanied by formation of an accessory notochord
• at E8.5, development of the node is severely disturbed in a subset of mutants
• complete node duplications are observed in some mutants
• the most severely affected double heterozygotes show abnormalities around E7 and fail to form a primitive streak
• addition rows of somites are observed in the most severely affected embryos
• by late gastrulation stages, embryos are grossly disorganized
• the most severely affected embryos develop pronounced constrictions between the embryonic and extraembryonic regions of the conceptus
• embryos frequently show tissue accumulation within the amniotic cavity

nervous system
• node abnormalities result in expansion of the floor plate of the neural tube

cellular
• AVE is correctly induced but fails to migrate anteriorly




Genotype
MGI:3775739
cx7
Allelic
Composition
Eomestm1.1Rob/Eomes+
Nodaltm4Rob/Nodaltm4Rob
Genetic
Background
involves: 129S/SvEv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eomestm1.1Rob mutation (0 available); any Eomes mutation (44 available)
Nodaltm4Rob mutation (0 available); any Nodal mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• normal Mendelian numbers are recovered during embryogenesis





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory