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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Wnt3tm1Brd
targeted mutation 1, Allan Bradley
MGI:2178826
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Wnt3tm1Brd/Wnt3tm1Brd involves: 129S7/SvEvBrd * C57BL/6J MGI:3640124
cx2
Lrp6Gw/Lrp6+
Wnt3tm1Brd/Wnt3+
involves: 101/H * 129S7/SvEvBrd * BALB/c * C3H MGI:4947304
cx3
Ctdnep1tm1Ryn/Ctdnep1+
Wnt3tm1Brd/Wnt3+
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 MGI:5510852
cx4
Eomestm1.1Rob/Eomes+
Wnt3tm1Brd/Wnt3+
involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA MGI:3775738


Genotype
MGI:3640124
hm1
Allelic
Composition
Wnt3tm1Brd/Wnt3tm1Brd
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Wnt3tm1Brd mutation (0 available); any Wnt3 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no homozygous mutant embryos are recovered after E10.5

embryo
• at E7.0, wild-type embryos consist of three germ layers and are developing the posterior amniotic fold, whereas mutant embryos remain as bi-layered structures with one cavity resembling a pre-gastrula
• at E7.0, the mutant ectoderm is thick, except for a small region immediately adjacent to the ectoplacental cone composed of a thinner layer of cells that most likely is extra-embryonic ectoderm
• by E8.5, the ectoderm and visceral endoderm continue to proliferate and excess ectoderm causes folding of the mutant embryos; extra-embryonic ectoderm is reduced
• homozygotes fail to gastrulate
• homozygotes lack anterior-posterior neural patterning
• at E7.5, homozygous mutant embryos are of variable size
• at E8.5, the mutant ectoderm fails to differentiate beyond the epiblast state, suggesting impaired epiblast patterning
• at E6.5-E8.5, homozygotes consist of only ectoderm and visceral endoderm; no mesoderm is formed
• at E7.5, homozygotes appear to lack nodal tissue
• at E7.0, homozygotes lack an identifiable primitive streak
• at E7.5, homozygotes lack distinct embryonic structures
• at E8.5, homozygotes lack an identifiable allantois
• at E8.5, homozygotes lack an identifiable amnion
• at E7.0, homozygous mutant embryos fail to develop the posterior amniotic fold
• at E8.5, homozygotes lack an identifiable chorion
• at E8.5, homozygotes lack an identifiable yolk sac
• at E6.5 and E7.5, initial development of the anterior visceral endoderm (AVE) appears to occur normally, but the overlying ectoderm does not acquire anterior neural identity

growth/size/body
• at E7.5, homozygous mutant embryos are of variable size

limbs/digits/tail
• homozygotes never develop limbs




Genotype
MGI:4947304
cx2
Allelic
Composition
Lrp6Gw/Lrp6+
Wnt3tm1Brd/Wnt3+
Genetic
Background
involves: 101/H * 129S7/SvEvBrd * BALB/c * C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lrp6Gw mutation (0 available); any Lrp6 mutation (95 available)
Wnt3tm1Brd mutation (0 available); any Wnt3 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• in 22% of mice




Genotype
MGI:5510852
cx3
Allelic
Composition
Ctdnep1tm1Ryn/Ctdnep1+
Wnt3tm1Brd/Wnt3+
Genetic
Background
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctdnep1tm1Ryn mutation (0 available); any Ctdnep1 mutation (20 available)
Wnt3tm1Brd mutation (0 available); any Wnt3 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Decrease in the number of Dppa3+ primordial germ cells in Ctdnep1tm1Ryn/Ctdnep1+ Wnt3tm1Brd/Wnt3+ embryos

cellular
• half as many Dppa3+ primordial germ cells as in wild-type mice

reproductive system
• half as many Dppa3+ primordial germ cells as in wild-type mice

embryo
N
• mice do not exhibit morphological defects




Genotype
MGI:3775738
cx4
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





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory