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Phenotypes Associated with This Genotype
Genotype
MGI:4950916
Allelic
Composition
\Ppp2catm1.1Nju/\Ppp2catm1.1Nju
\Tg(Tek-cre)12Flv/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppp2catm1.1Nju mutation (0 available); any Ppp2ca mutation (24 available)
Tg(Tek-cre)12Flv mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a further loss of mice is seen between E12.5 and E14.5
• however, some mice survive to adulthood
• the expected number of mice are found at E10.5 but fewer than expected are found at E12.5

hematopoietic system
• fetal livers contain very few erythrocytes but numbers of other hematopoietic lineage cells are similar to controls at E12.5
• severe impairment in the differentiation of proerythroblasts into erythroblasts in the fetal liver at E14.5
• total numbers of BFU-E and CFU-E are dramatically lower in fetal livers compared to controls
• however, embryonic erythropoiesis is similar to controls
• severe in embryos
• however, surviving adults have normal steady-state hematocrit
• dramatic reduction in the number of erythrocytes in the fetal liver at E14.5
• increase in the number of LSK cells in the fetal liver at E14.5
• cultured erythroid cells are more sensitive to apoptotic stimulation compared to control cells

liver/biliary system
• enlarged fetal liver cells and reduced total liver cellularity at E12.5 and E14.5
• livers contain very few hematopoietic cells unlike in controls at E12.5
• at E12.5

cardiovascular system
N
• despite recombination in endothelial cells, no obvious vascular defects are detected

integument
• at E12.5


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
03/25/2025
MGI 6.24
The Jackson Laboratory