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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

Limb-girdle muscular dystrophy

Shoulder girdle muscle atrophy

Pelvic girdle muscle weakness

Spasticity

EMG abnormality

EMG: myopathic abnormalities

Muscle weakness

Neck flexor weakness

Proximal muscle weakness

Gowers sign

Myotonia

Pelvic girdle muscle atrophy

Increased variability in muscle fiber diameter

Central core regions in muscle fibers

Centrally nucleated skeletal muscle fibers

Skeletal muscle atrophy

Proximal amyotrophy

Muscular dystrophy

Myopathy

Disease(s) Associated with TRIM32

autosomal recessive limb-girdle muscular dystrophy type 2H

Bardet-Biedl syndrome

muscular dystrophy

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

delayed skeletal muscle regeneration

myopathy

Availability

Mouse Genotype

Trim32^{Gt(BGA355)Byg}/Trim32^{Gt(BGA355)Byg}

*

Trim32^tm1Hdin/Trim32^tm1Hdin

Trim32^tm1Spc/Trim32^tm1Spc

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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