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Phenotypes Associated with This Genotype
Genotype
MGI:3687952
cn2
Allelic
Composition
Tfap2atm1Hsv/Tfap2atm2Will
Tfap2ctm1Will/Tfap2ctm2Will
Tg(Zp3-cre)3Mrt/0
Genetic
Background
involves: 129S1/Sv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tfap2atm1Hsv mutation (1 available); any Tfap2a mutation (39 available)
Tfap2atm2Will mutation (1 available); any Tfap2a mutation (39 available)
Tfap2ctm1Will mutation (0 available); any Tfap2c mutation (28 available)
Tfap2ctm2Will mutation (1 available); any Tfap2c mutation (28 available)
Tg(Zp3-cre)3Mrt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a significant reduction in number of double-null embryos (5.5% vs 25% expected) compared to 3 other possible genotypic combinations results in earlier lethality than loss of either allele alone (~E7.5)

embryo
N
• double-null embryos are found at ~expected frequencies (~25%) at E3.5; embryos are detected in both the morula (~75%) and blastocyst (~25%) stages, indicating that deficiency of both Tcfap2a and Tcfap2c does not affect the zygote prior to E3.5;
• other genotypic combinations are all found at similar frequencies (~25%) at E7.5, indicating that loss of any combination of 3 of 4 wild-type Tcfap2a and Tcfap2c alleles allows embryo survival to ~E7.5


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)
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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory