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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Scxtm2Eno
targeted mutation 2, Eric N Olson
MGI:2151296
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Scxtm1Eno/Scxtm2Eno chimera involves: 129S7/SvEvBrd * C57BL/6 * Swiss MGI:3770260


Genotype
MGI:3770260
ht1
Allelic
Composition
Scxtm1Eno/Scxtm2Eno
Genetic
Background
chimera involves: 129S7/SvEvBrd * C57BL/6 * Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scxtm1Eno mutation (0 available); any Scx mutation (15 available)
Scxtm2Eno mutation (0 available); any Scx mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• in two E9.5 chimeric embryos with >95% mutant cells, discernable somites are absent and the somitic region is cell-deficient

cardiovascular system
• n two E9.5 chimeric embryos with >95% mutant cells, the dorsal aortae become dilated to fill the space created by the complete loss of identifiable somites

skeleton
• in chimeric embryos, mutant cells are unable to contribute to (i) the sclerotomal compartment of somites that gives rise to the axial skeleton at E8.5 and E9.5 and (ii) the developing ribs at E14.5 and E16.5





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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
12/10/2024
MGI 6.24
The Jackson Laboratory