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Phenotypes Associated with This Genotype
Genotype
MGI:3838168
Allelic
Composition
Cbfbtm1Ppl/Cbfb+
Genetic
Background
either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cbfbtm1Ppl mutation (0 available); any Cbfb mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all embryos normal at E11.5
• lethality between E11.5 and E13.5

cardiovascular system
• multiple hemorrhages begin to develop at E12
• sometimes
• sometimes
• hemorrhages mostly in the central nervous system, 100% of E12.5 embryos
• periventricular regions of the striatum, pons, medulla
• intraparenchymal hemorrhage frequent at the ganglia of cranial nerves VII and VIII
• blood often accumulates in the ventricles

cellular
• observed in areas susceptible to hemorrhage

liver/biliary system
• from E11.5 to E13.5
• few or no erythropoietic cells
• no megakaryocytes

hematopoietic system
• no definitive hematopoietic cells in the hepatic cords at E11.5-E13.5
• mostly immature yolk sac derived erythrocytes in the circulation at E12.5, about 78%
• reduced ability of fetal liver and yolk cells to proliferate and differentiate in vitro

nervous system
• hemorrhages mostly in the central nervous system, 100% of E12.5 embryos
• periventricular regions of the striatum, pons, medulla
• intraparenchymal hemorrhage frequent at the ganglia of cranial nerves VII and VIII
• blood often accumulates in the ventricles

homeostasis/metabolism
• sometimes


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
04/30/2024
MGI 6.23
The Jackson Laboratory