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Phenotypes Associated with This Genotype
Genotype
MGI:5613023
Allelic
Composition
Sox2tm1.1Knd/Sox2tm1.1Knd
Tbx6tm1Pa/Tbx6tm1Pa
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sox2tm1.1Knd mutation (0 available); any Sox2 mutation (56 available)
Tbx6tm1Pa mutation (1 available); any Tbx6 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• absence of genes associated with neural tube development in the paraxial compartment concomitant with absence of tubular structures at E9.5
• expression analysis indicates absence of markers for the paraxial mesoderm, intermediate mesoderm and endoderm
• however, unlike mice homozygous for the Tbx6 mutation alone, no ectopic expression of Sox2 is seen in the neural tube

nervous system
• absence of genes associated with neural tube development in the paraxial compartment concomitant with absence of tubular structures at E9.5
• expression analysis indicates absence of markers for the paraxial mesoderm, intermediate mesoderm and endoderm
• however, unlike mice homozygous for the Tbx6 mutation alone, no ectopic expression of Sox2 is seen in the neural tube


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
05/07/2024
MGI 6.23
The Jackson Laboratory