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Symbol
Name
ID
Trim32
tripartite motif-containing 32
MGI:1917057
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Facial palsy
Calf muscle pseudohypertrophy
Shoulder girdle muscle weakness
Proximal muscle weakness in lower limbs
Quadriceps muscle weakness
Shoulder girdle muscle atrophy
Pelvic girdle muscle weakness
EMG abnormality
EMG: myopathic abnormalities
Neck flexor weakness
Gowers sign
Pelvic girdle muscle atrophy
Increased variability in muscle fiber diameter
Centrally nucleated skeletal muscle fibers
Muscular dystrophy
Myopathy
Disease(s) Associated with TRIM32
autosomal recessive limb-girdle muscular dystrophy type 2H

Mouse Phenotypes
muscle phenotype
abnormal skeletal muscle fiber morphology
decreased skeletal muscle fiber diameter
increased variability of skeletal muscle fiber size
centrally nucleated skeletal muscle fibers
decreased muscle weight
abnormal skeletal muscle morphology
abnormal skeletal muscle fiber type ratio
increased satellite cell number
dystrophic muscle
abnormal muscle physiology
impaired skeletal muscle regeneration
myopathy
Availability Mouse Genotype
Trim32Gt(BGA355)Byg/Trim32Gt(BGA355)Byg *
Trim32tm1Hdin/Trim32tm1Hdin
Trim32tm1Spc/Trim32tm1Spc

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
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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory