Symbol Name ID |
Trim2
tripartite motif-containing 2 MGI:1933163 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased number of peripheral myelinated nerve fibers |
Axonal degeneration |
Peripheral axonal neuropathy |
Vocal cord paralysis |
Decreased motor nerve conduction velocity |
Areflexia |
Broad-based gait |
Inability to walk |
Delayed ability to walk |
Disease(s) Associated with TRIM2 | |||||||||
Charcot-Marie-Tooth disease type 2R |
Mouse Phenotypes | seizures |
decreased Purkinje cell number |
abnormal cerebellum deep nucleus morphology |
abnormal axon morphology |
decreased retina ganglion cell number |
retina ganglion cell degeneration |
neurodegeneration |
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Availability | Mouse Genotype | |||||||
Trim2Gt(IRESBetageo)11Pgr/Trim2Gt(IRESBetageo)11Pgr |
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 09/03/2024 MGI 6.24 |
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