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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cdx2tm1Fbe
targeted mutation 1, F Beck
MGI:1857928
Summary 10 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cdx2tm1Fbe/Cdx2tm1Fbe involves: 129S1/Sv * C57BL/6J MGI:2175777
hm2
Cdx2tm1Fbe/Cdx2tm1Fbe involves: ICR MGI:3580005
ht3
Cdx2tm1Fbe/Cdx2+ involves: 129S1/Sv * C57BL/6 * CBA MGI:3613766
ht4
Cdx2tm1Fbe/Cdx2+ involves: 129S1/Sv * C57BL/6J MGI:2175778
ht5
Cdx2tm1Fbe/Cdx2tm2.1Fbe involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ MGI:5308976
ht6
Cdx2tm1.2Aral/Cdx2tm1Fbe involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL MGI:5445753
cn7
Cdx2tm1Fbe/Cdx2tm2Fbe
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA MGI:5308975
cn8
Cdx2tm1.1Aral/Cdx2tm1Fbe
Tg(Zp3-cre)93Knw/0
involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL MGI:5445751
cx9
Cdx2tm1Fbe/Cdx2+
Cdx4tm1.1Jdes/Cdx4+
involves: 129 * C57BL/6 * CBA * FVB MGI:3613771
cx10
Cdx2tm1Fbe/Cdx2+
Cdx4tm1.1Jdes/Y
involves: 129 * C57BL/6 * CBA * FVB MGI:3613767


Genotype
MGI:2175777
hm1
Allelic
Composition
Cdx2tm1Fbe/Cdx2tm1Fbe
Genetic
Background
involves: 129S1/Sv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die between E3.5 and E5.5

reproductive system




Genotype
MGI:3580005
hm2
Allelic
Composition
Cdx2tm1Fbe/Cdx2tm1Fbe
Genetic
Background
involves: ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes die around implantation

embryo
• a 3-fold increase in cell death is seen in the inner cell mass at E4.5
• an 8-fold increase in cell death is seen in the trophoectoderm at E4.5
• at E4.5 embryos are still in the zona pellucida
• at E4.5, little or no blastocoelic cavity is seen
• the blastocoel is initially formed but collapses
• after 72 hours in culture (starting at the 8-cell stage) trophoectodermal cells appear rounded and non-epithelial
• tight and adherens junctions appear abnormal at the late blastocyst stage and it appears that the polarity and integrity of the trophoectoderm are not maintained
• trophoblast giant cells are not formed and trophoblast stem cell lines can not be established
• trophoblast differentiation is impaired beyond the expanded blastocyst stage

cellular
• a 3-fold increase in cell death is seen in the inner cell mass at E4.5
• an 8-fold increase in cell death is seen in the trophoectoderm at E4.5




Genotype
MGI:3613766
ht3
Allelic
Composition
Cdx2tm1Fbe/Cdx2+
Genetic
Background
involves: 129S1/Sv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• 6 of 62 embryos that do undergo normal chorioallantoic fusion display deficient placental labyrinth development at E10.5
• allantois of 3 of 54 heterozygotes has not fused with the chorion at E9.5




Genotype
MGI:2175778
ht4
Allelic
Composition
Cdx2tm1Fbe/Cdx2+
Genetic
Background
involves: 129S1/Sv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body

skeleton
• anterior homeotic shift of the cervical and thoracic spine such as an 8th rib attached to the sternum, or the second rib attached to the sternum at the top of the manubrium together with the first rib
• T3 shows morphological features characteristic of the immediately cranial vertebrae in the wild-type
• C6 and C7 show morphological features characteristic of the immediately cranial vertebrae in the wild-type

limbs/digits/tail
• 50-60% exhibit a short or kinked tail
• 50-60% exhibit a short or kinked tail

neoplasm
• presence of multiple adenomatous polyps at 12-28 weeks of age
• tumors are found predominately in the proximal colon and occasionally in the small intestine
• tumors are found predominately in the proximal colon
• largest tumors are pedunculated tubulovillous colonic adenomata

digestive/alimentary system
• presence of multiple adenomatous polyps at 12-28 weeks of age
• tumors are found predominately in the proximal colon and occasionally in the small intestine
• tumors are found predominately in the proximal colon
• largest tumors are pedunculated tubulovillous colonic adenomata




Genotype
MGI:5308976
ht5
Allelic
Composition
Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
Cdx2tm2.1Fbe mutation (0 available); any Cdx2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• at E10.5 in embryos grown on tetraploid trophoblast




Genotype
MGI:5445753
ht6
Allelic
Composition
Cdx2tm1.2Aral/Cdx2tm1Fbe
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1.2Aral mutation (0 available); any Cdx2 mutation (22 available)
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• reach the blastocyst stage then collapse around implantation

embryo
• reach the blastocyst stage then collapse around implantation




Genotype
MGI:5308975
cn7
Allelic
Composition
Cdx2tm1Fbe/Cdx2tm2Fbe
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
Cdx2tm2Fbe mutation (0 available); any Cdx2 mutation (22 available)
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo




Genotype
MGI:5445751
cn8
Allelic
Composition
Cdx2tm1.1Aral/Cdx2tm1Fbe
Tg(Zp3-cre)93Knw/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * CD-1 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1.1Aral mutation (0 available); any Cdx2 mutation (22 available)
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
Tg(Zp3-cre)93Knw mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• reach the blastocyst stage then collapse around implantation

embryo
• reach the blastocyst stage then collapse around implantation




Genotype
MGI:3613771
cx9
Allelic
Composition
Cdx2tm1Fbe/Cdx2+
Cdx4tm1.1Jdes/Cdx4+
Genetic
Background
involves: 129 * C57BL/6 * CBA * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
Cdx4tm1.1Jdes mutation (0 available); any Cdx4 mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• 2 of 11 embryos that do undergo normal chorioallantoic fusion display deficient placental labyrinth development at E10.5
• allantois of 2 of 28 mutants has not fused with the chorion at E9.5




Genotype
MGI:3613767
cx10
Allelic
Composition
Cdx2tm1Fbe/Cdx2+
Cdx4tm1.1Jdes/Y
Genetic
Background
involves: 129 * C57BL/6 * CBA * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdx2tm1Fbe mutation (0 available); any Cdx2 mutation (22 available)
Cdx4tm1.1Jdes mutation (0 available); any Cdx4 mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

growth/size/body
• exhibit developmental retardation at E10.5

embryo
• truncation of embryonic structures posterior to the hindlimbs that results in a more anteriorly located tail bud
• exhibit developmental retardation at E10.5
• allantoic endothelial cells often exhibit, to a variable extent, a poorer degree of primary vessel organization around the time of chorioallantoic fusion
• at E10.5, maternal blood pools and embryonic blood vessels are widely separated
• the hemotrichorial membrane is almost completely absent
• all embryos that do undergo chorioallantoic fusion display deficient placental labyrinth development at E10.5
• fail to properly extend the allantoic vascular network into the chorionic ectoderm and do not develop a functional placental labyrinth
• allantois of 7 of 35 mutants has not fused with the chorion at E9.5

skeleton
• have 14 ribs due to the partial or complete bilateral rib attachment to V21
• 4 of 4 have the 8th pair of ribs attached to the sternum, indicating anterior transformation at the level of V15
• 4 of 4 have a partial or complete rib attached to V21 bilaterally, at the position normally corresponding to the first lumbar vertebrae

homeostasis/metabolism
• thoracic edema at E10.5

limbs/digits/tail
• truncation of embryonic structures posterior to the hindlimbs that results in a more anteriorly located tail bud

cardiovascular system
• at E10.5, maternal blood pools and embryonic blood vessels are widely separated





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory