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Symbol
Name
ID
Trim32
tripartite motif-containing 32
MGI:1917057
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Facial palsy
Areflexia
Hyporeflexia
Gait disturbance
Waddling gait
Disease(s) Associated with TRIM32
autosomal recessive limb-girdle muscular dystrophy type 2H

Mouse Phenotypes
abnormal axon morphology
Availability Mouse Genotype
Trim32Gt(BGA355)Byg/Trim32Gt(BGA355)Byg

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
09/10/2019
MGI 6.14
The Jackson Laboratory