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Phenotypes Associated with This Genotype
Genotype
MGI:4366947
Allelic
Composition
Tln1tm4.1Crit/Tln1tm4.1Crit
Tln2tm1.1Crit/Tln2tm1.1Crit
Tg(ACTA1-cre)1Mll/0
Genetic
Background
involves: 129P2/OlaHsd * BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(ACTA1-cre)1Mll mutation (0 available)
Tln1tm4.1Crit mutation (2 available); any Tln1 mutation (145 available)
Tln2tm1.1Crit mutation (0 available); any Tln2 mutation (151 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die shortly after birth

muscle
• at E18.5, muscle fibers are disorganized with variation in fiber size unlike in wild-type mice
• myofilaments are detached from the myotendinous junction and necrotic material accumulates in gaps unlike in wild-type mice
• at E18.5, unfused myoblasts are observed in developing muscle unlike in wild-type mice
• myoblasts fail to fuse in culture unlike wild-type cells
• unlike in wild-type mice, myotomes form only occasionally but are short with rudimentary cytoskeletons
• myofilament organization is disrupted and the Z-bands appear rudimentary unlike in wild-type mice
• myofilaments are detached from the myotendinous junction and necrotic material accumulates in gaps unlike in wild-type mice
• Z-bands appear rudimentary

behavior/neurological
• mice exhibit a contracted posture at birth

cellular
• unlike in wild-type mice, myotomes form only occasionally but are short with rudimentary cytoskeletons
• at E18.5, unfused myoblasts are observed in developing muscle unlike in wild-type mice
• myoblasts fail to fuse in culture unlike wild-type cells


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
03/31/2026
MGI 6.24
The Jackson Laboratory