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Symbol
Name
ID
Capn3
calpain 3
MGI:107437
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
!Indicates phenotype varies with strain background.
Darker colors indicate more annotations
Human Phenotypes
Facial palsy
Congenital finger flexion contractures
Ankle flexion contracture
Calf muscle hypertrophy
Scapular muscle atrophy
Scapular winging
Lower limb muscle weakness
Limb-girdle muscular dystrophy
Pelvic girdle amyotrophy
Elbow flexion contracture
Wrist flexion contracture
Myositis
Flexion contracture
Hamstring contractures
Difficulty climbing stairs
Difficulty walking
Muscle weakness
Generalized muscle weakness
Proximal muscle weakness
Myotonia
Central core regions in muscle fibers
Pectoralis amyotrophy
Proximal amyotrophy
Muscle eosinophilia
Muscular dystrophy
Myopathy
Disease(s) Associated with CAPN3
autosomal recessive limb-girdle muscular dystrophy type 2A
muscular dystrophy

Mouse Phenotypes
muscle phenotype
abnormal gastrocnemius morphology
abnormal soleus morphology
abnormal tibialis anterior morphology
abnormal muscle morphology
abnormal sarcolemma morphology
abnormal A band morphology
abnormal skeletal muscle fiber morphology
decreased skeletal muscle fiber diameter
centrally nucleated skeletal muscle fibers
abnormal diaphragm morphology
decreased skeletal muscle mass
skeletal muscle degeneration
dystrophic muscle
Availability Mouse Genotype
Capn3Gt(OST141731)Lex/Capn3Gt(OST141731)Lex
Capn3tm1.1Hiso/Capn3tm1.1Hiso
Capn3tm1Jsb/Capn3tm1Jsb !
Tg(ACTA1-Capn3)7.2Spc/0 *
Tg(ACTA1-Capn3*)10.3Spc/0
Tg(ACTA1-Capn3*)27.10Spc/0
Tg(ACTA1-Capn3*)37.3Spc/0
Tg(ACTA1-Capn3*)37.9Spc/0
Tg(ACTA1-Capn3*)39.1Spc/0
Tg(ACTA1-Capn3*)41.1Spc/0
Tg(ACTA1-Capn3*)42Spc/0

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
04/16/2024
MGI 6.23
The Jackson Laboratory