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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(ACTA1*D286G)#Kjno
transgene insertion, Kristen J Nowak
MGI:5566909
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Acta1tm1Jll/Acta1+
Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno
involves: C57BL/6 * CBA MGI:5566913
tg2
Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno involves: C57BL/6 * CBA MGI:5566910


Genotype
MGI:5566913
cx1
Allelic
Composition
Acta1tm1Jll/Acta1+
Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Acta1tm1Jll mutation (0 available); any Acta1 mutation (16 available)
Tg(ACTA1*D286G)#Kjno mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only about 18% of mice survive to sexual maturity

growth/size/body
• between P10 and P12, pups show reduced body mass

behavior/neurological
• about 82% of mutants develop severe hindlimb paralysis and immobility between P8 and P17

muscle
• about 20% of muscle fibers display widespread myofibril disorganization
• subsarcolemmal accumulations of fine filaments and atrophic fibers
• fast-twitch predominant and slow-twitch soleus muscle of adults shows large aggregates that correspond to regions of nemaline bodies
• Ringbinden are prominent in fast-twitch muscle of surviving mutants
• Z-band fragmentation and streaming
• skeletal muscles show numerous aggregates of filamentous actin and the presence of nemaline bodies
• large variations in myofiber size

reproductive system
• the mutants that survive to sexual maturity are poor breeders, producing no, or only a few small litters

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
nemaline myopathy 3 DOID:0110927 OMIM:161800
J:209273




Genotype
MGI:5566910
tg2
Allelic
Composition
Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• 8 month old mice spend less time traveling, cover a reduced distance and average speed is diminished during a 30 min interval in a novel environment
• 8 month old mice do not perform as well as wild-type mice on a 5 min trial on an accelerating rotarod but perform normally during shorter 2 min trials
• one-month and four-month old mice are less active when housed with a voluntary running wheel, traveling a reduced distance over a 1 week period
• 8 month old mice spend less time traveling, cover a reduced distance and average speed is diminished during a 30 min interval in a novel environment

growth/size/body
• mice have reduced body mass at 1 month of age but no longer at 4 months of age

muscle
• fast- and slow-twitch predominant muscles exhibit regions with complete loss of sarcomeric organization
• fast- and slow-twitch predominant muscles exhibit Z-band widening, and slipping and fragmentation
• nemaline bodies are seen in skeletal muscle at 1 and 4 months of age
• skeletal muscle exhibits filamentous actin accumulation
• tubular aggregates are common in fast twitch muscles at 4 months of age
• fast twitch muscles from mice older than 4 months of age contain ringbinden fibers
• quadriceps, gastrocnemius, and soleus muscle show aggregates of alphaB-crystallin and desmin
• myofibrillar disorganization
• maximal specific force produced by EDL and soleus muscles is reduced in 1 month old mice
• skinned EDL muscle fibers are less sensitive to calcium
• EDL and soleus muscles are weak; EDL muscle fibers produce less force at 3, 6, and 9 months of age, EDL and soleus muscles produce less maximal specific force, and have right shifted force-stimulation frequency relationships, with differences seen at 10, 20, 40, and 60 Hz of stimulation, both EDL and soleus muscles have lower twitch-specific force production, and the maximum rate of rise of the twitch responses is 50% slower in muscles
• the twitch responses are slower relative to wild-type muscles

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
nemaline myopathy 3 DOID:0110927 OMIM:161800
J:209273





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last database update
11/05/2024
MGI 6.24
The Jackson Laboratory