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Phenotypes Associated with This Genotype
Genotype
MGI:6110152
Allelic
Composition
Myh10ehc/Myh10ehc
Genetic
Background
involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myh10ehc mutation (0 available); any Myh10 mutation (95 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• in the ventricles
• does not display organized clusters of smooth muscle cells or vascular structures unlike wild-type myocardium
• completely penetrant at E16.5
• distended, abnormally positioned relative to the ventricle
• rounded without apex
• reduced trabeculation, thinner compact myocardium and disorganized ventricular myocardium
• reduced myocardial cytokinesis
• with tearing of the membranous region at E14.5
• thin with tearing of the membranous region at E14.5
• however, initial development is normal unlike in null mice
• on the surface of the heart at E11.5 and persisting until death at E16.5
• at E11.5

homeostasis/metabolism
• at E11.5
• at E15.5 in the spinal cord region

nervous system
• prominent in the mesencephalic vesicle at E13.5, persisting at E15.5

skeleton
• in mice that survive beyond E16.5

muscle
• in the ventricles
• does not display organized clusters of smooth muscle cells or vascular structures unlike wild-type myocardium
• reduced trabeculation, thinner compact myocardium and disorganized ventricular myocardium
• reduced myocardial cytokinesis

craniofacial
• in mice that survive beyond E16.5


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
03/18/2025
MGI 6.24
The Jackson Laboratory