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Phenotypes Associated with This Genotype
Genotype
MGI:3700177
Allelic
Composition
Supt20Gt(RRK304)Byg/Supt20Gt(RRK304)Byg
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Supt20Gt(RRK304)Byg mutation (0 available); any Supt20 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• E9.5 and E10.5 embryos are developmentally delayed

embryo
• yolk sac membranes are poorly vascularized
• midline marker analysis indicates that midline is present in embryos but is often severely disrupted and discontinuous
• mesoderm is properly specified at E8.5, as indicated by marker analysis, but it is disorganized
• mutant mesoderm undergoes a partial epithelial to mesenchymal transition (EMT), however it fails to complete EMT
• often the paraxial mesoderm is not divided into discrete left and right domains
• E9.5 and E10.5 embryos are developmentally delayed
• often the paraxial mesoderm is not divided into discrete left and right domains
• mutants exhibit misshapen head folds
• a significant proportion of the mesoderm fails to migrate away from the primitive streak
• E7.5 primitive streak mesoderm cells do not migrate away from explants when grown in culture
• homozygotes fail to form somites or form only a few anterior somites; presomitic mesoderm is specified as indicated by marker analysis, although it is not organized into somitomeres
• embryos develop a malformed allantois
• yolk sac membranes are wrinkled
• embryos develop a malformed allantois that fails to fuse to the chorion

nervous system

cardiovascular system
• yolk sac membranes are poorly vascularized

cellular


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
04/16/2024
MGI 6.23
The Jackson Laboratory