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Phenotypes Associated with This Genotype
Genotype
MGI:3831190
Allelic
Composition
Ctnnb1tm2Kem/Ctnnb1tm2.1Kem
Kdrtm1(cre)Sato/Kdr+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctnnb1tm2.1Kem mutation (0 available); any Ctnnb1 mutation (49 available)
Ctnnb1tm2Kem mutation (1 available); any Ctnnb1 mutation (49 available)
Kdrtm1(cre)Sato mutation (1 available); any Kdr mutation (73 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all embryos die by E12.5 due to severe hemorrhaging within the central nervous system

cardiovascular system
• in E12.5 embryos, endothelial cells and pericytes are entirely absent from the neuroepithelium
• hemorrhaging is detected throughout the developing brain of E12.5 embryos
• hemorrhaging is detected throughout the developing spine of E12.5 embryos
• hemorrhaging and downregulation of the endothelial marker GLUT-1 suggest a defect in the blood brain barrier of developing embryos

nervous system
• hemorrhaging is detected throughout the developing brain of E12.5 embryos
• hemorrhaging is detected throughout the developing spine of E12.5 embryos
• hemorrhaging and downregulation of the endothelial marker GLUT-1 suggest a defect in the blood brain barrier of developing embryos


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
06/12/2024
MGI 6.13
The Jackson Laboratory