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Phenotypes Associated with This Genotype
Genotype
MGI:2175157
Allelic
Composition
Notch1tm1Con/Notch1tm1Con
Genetic
Background
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Notch1tm1Con mutation (3 available); any Notch1 mutation (116 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most mutants are dead at E10 and all die by E11

embryo
• show a deficit in posterior development at E9
• growth arrest at the 14 somite stage (J:25248)
• embryos are smaller at E9
• neural tube kinks are seen extending posterior to the forelimb
• the notochord degenerates after growth arrest
• mutants exhibit a lack of coordination in segmentation of the somites, leading to variable somite size and misalignment of the somites across the midline of the embryo (J:25248)
• transition from presomitic mesoderm to the somite is disordered (J:25248)
• the most recently formed somites are not as tightly packed as those of wild-type and the epithelialization sometimes appears incomplete (J:25248)
• lack of coordination across the midline in the segmentation of somites, where segmentation is sometimes present on one side but not the other
• variable somite size
• mutants exhibit a delay in segmentation of the somites

growth/size/body
• embryos are smaller at E9

cardiovascular system
• distended pericardia at E9 (J:25248)

cellular
• an increase in cell death is seen in embryos after they arrest

nervous system
• neural tube kinks are seen extending posterior to the forelimb


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
01/20/2026
MGI 6.24
The Jackson Laboratory