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Phenotypes Associated with This Genotype
Genotype
MGI:2656914
Allelic
Composition
Sgcatm1Eeng/Sgcatm1Eeng
Genetic
Background
involves: 129S/SvEv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sgcatm1Eeng mutation (0 available); any Sgca mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• muscle extensibility is decreased in skeletal muscle
• muscle force-generating capacity of diaphragm muscle is depressed
• mice show a loss of coupling between transverse passive stress and contractile muscle force
• skeletal muscles are stiffer in the axial, as well as in the transverse, direction to the muscle fibers

Mouse Models of Human Disease
OMIM ID Ref(s)
Muscular Dystrophy, Limb-Girdle, Type 2D; LGMD2D 608099 J:83034


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
05/17/2016
MGI 6.03
The Jackson Laboratory