About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Synmtm1.1(KOMP)Vlcg
targeted mutation 1.1, Velocigene
MGI:5548847
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Synmtm1.1(KOMP)Vlcg/Synmtm1.1(KOMP)Vlcg C57BL/6N-Synmtm1.1(KOMP)Vlcg/Ucd MGI:5701008
hm2
Synmtm1.1(KOMP)Vlcg/Synmtm1.1(KOMP)Vlcg involves: C57BL/6NTac MGI:5750322


Genotype
MGI:5701008
hm1
Allelic
Composition
Synmtm1.1(KOMP)Vlcg/Synmtm1.1(KOMP)Vlcg
Genetic
Background
C57BL/6N-Synmtm1.1(KOMP)Vlcg/Ucd
Cell Lines 14923A-H9
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Synmtm1.1(KOMP)Vlcg mutation (1 available); any Synm mutation (58 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological




Genotype
MGI:5750322
hm2
Allelic
Composition
Synmtm1.1(KOMP)Vlcg/Synmtm1.1(KOMP)Vlcg
Genetic
Background
involves: C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Synmtm1.1(KOMP)Vlcg mutation (1 available); any Synm mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• 31% increase in the mass of 12 month old hearts
• however, heart muscles show normal sarcomere and costamere architecture
• modest enlargement of cardiomyocytes at 12 months of age
• in 12 month old mice
• hearts show modest hypertrophy including a 20% increase in the number of nuclei at 12 months
• old hearts have greater left ventricle mass, suggesting left ventricle myocardial hypertrophy
• old hearts have greater left ventricle mass, suggesting left ventricle myocardial hypertrophy
• young hearts show lower left ventricle posterior wall thickness
• old hearts have lower left ventricle fractional shortening and left ventricle ejection fraction and greater left ventricle end-diastolic dimension and greater left ventricular dimension during diastole, indicating left ventricle dilation
• hearts show a small increase in fibrosis at 12 months of age
• 12 month old mice show decreased cardiac output
• 12 month old mice show decreased stroke volume
• young (3 months) and old (12 months) hearts have lower left ventricle fractional shortening and left ventricle ejection fraction, indicating decreased left ventricle contractility
• PV loop studies of 3 month old mice show lower left ventricle ejection fraction, maximal rate of left ventricular pressure rise (+dP/dt), slope of left ventricular end-systolic pressure-volume relationship (Ees), preload recruitable stroke work (PRSW), and +dp/dt-end-diastolic pressure, indicating impaired left ventricular systolic function
• PV loops studies of 12 month old mice show significant increases in left ventricle end diastolic pressure and decreases in Ees, PRSW, +dP/dt-EDP and left ventricle ejection fraction
• echocardiography shows that young (3 months) and old (12 months) hearts have greater left ventricular dimension during systole and decreased left ventricle fractional shortening and ejection fraction
• echocardiogarphy shows that old hearts also exhibit increased left ventricular dimension during diastole and left ventricle mass
• heart rate is increased in 12 month old mice compared to 3 month old mice
• in response to contractions elicited by action potentials under no-load conditions, cardiomyocytes from 3 and 12 month old mice show a decrease in the magnitude of sarcomeric shortening and in the rate of shortening, however relaxation is normal
• cardiomyocytes from 12 month, but not 3 month old mice, show a decrease in the calcium transient amplitude
• 12 month old hearts show patterns of hypertrophic cardiomyopathy

muscle
• old hearts have greater left ventricle mass, suggesting left ventricle myocardial hypertrophy
• old hearts have greater left ventricle mass, suggesting left ventricle myocardial hypertrophy
• more fibers with centrally located nuclei in tibialis anterior and extensor digitorum longus
• contractile apparatus appears normal
• sarcolemma, costamere, associated myofibrils are more deformable than in controls
• modest enlargement of cardiomyocytes at 12 months of age
• separation of sarcolemma from myofibrils occurs more readily
• sarcolemma is less stable
• tibialis anterior muscle is more susceptible to loss of function due to injury caused by lengthening contractions
• more necrotic fibers are found three days after injury than are found in controls
• significantly reduced muscle mass of the tibialis anterior
• smaller diameter of tibialis anterior and quadriceps muscle but normal size for extensor digitorum longus and soleus
• young (3 months) and old (12 months) hearts have lower left ventricle fractional shortening and left ventricle ejection fraction, indicating decreased left ventricle contractility
• PV loop studies of 3 month old mice show lower left ventricle ejection fraction, maximal rate of left ventricular pressure rise (+dP/dt), slope of left ventricular end-systolic pressure-volume relationship (Ees), preload recruitable stroke work (PRSW), and +dp/dt-end-diastolic pressure, indicating impaired left ventricular systolic function
• PV loops studies of 12 month old mice show significant increases in left ventricle end diastolic pressure and decreases in Ees, PRSW, +dP/dt-EDP and left ventricle ejection fraction
• 12 month old hearts show patterns of hypertrophic cardiomyopathy
• fatigue increases relative to controls later in testing but is similar to controls earlier in testing
• ability to run uphill on a treadmill is less than controls but not significantly
• 25% decrease in twitch specific force in isolated tibialis anterior fibers
• tetanic contractions less significantly affected

growth/size/body
• in 12 month old mice
• hearts show modest hypertrophy including a 20% increase in the number of nuclei at 12 months
• old hearts have greater left ventricle mass, suggesting left ventricle myocardial hypertrophy
• old hearts have greater left ventricle mass, suggesting left ventricle myocardial hypertrophy
• in 12 month old mice

cellular
• tibialis anterior muscle is more susceptible to loss of function due to injury caused by lengthening contractions
• more necrotic fibers are found three days after injury than are found in controls





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory