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Phenotypes Associated with This Genotype
Genotype
MGI:3608600
Allelic
Composition
Srftm1Rjs/Srftm2.1Nor
Tg(Myh6-cre)2182Mds/0
Genetic
Background
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Srftm1Rjs mutation (0 available); any Srf mutation (27 available)
Srftm2.1Nor mutation (0 available); any Srf mutation (27 available)
Tg(Myh6-cre)2182Mds mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no viable embryos are found beyond E12.5

cardiovascular system
• sarcomere organization is disrupted in hearts
• exhibit less constriction in the atrial ventricular canal at E10.5
• ventricular wall is hypoplastic with fewer trabeculae, ventricular wall compact layer is thinner, and cellular wall expansion is blocked
• intraventricular septation is less developed
• exhibit poorly developed intraventricular groove at E10.5
• dilated pericardial walls at E10.25
• seen at E10.25
• show severe pericardial effusion at E11.5
• lose rhythmic beating between E10.5 and E11.5

embryo
• some embryos arrest at the heart-looping stage (around E10.5-11.5)

muscle
• sarcomere organization is disrupted in hearts

homeostasis/metabolism
• show severe pericardial effusion at E11.5

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
01/20/2026
MGI 6.24
The Jackson Laboratory