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Symbol Name ID |
Matr3
matrin 3 MGI:1298379 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Bulbar palsy |
Abnormal lower motor neuron morphology |
Abnormal upper motor neuron morphology |
Amyotrophic lateral sclerosis |
Decreased nerve conduction velocity |
Dysarthria |
Dementia |
Hyperreflexia |
Bulbar signs |
Distal sensory impairment |
| Disease(s) Associated with MATR3 | |||||||||||
| amyotrophic lateral sclerosis type 21 |
| Mouse Phenotypes | increased microglial cell activation |
Purkinje cell degeneration |
small cerebellum |
astrocytosis |
abnormal neuromuscular synapse morphology |
axon degeneration |
axonal spheroids |
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| Availability | Mouse Genotype | |||||||
| Matr3em1Tcp/Matr3em1Tcp | ||||||||
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 04/30/2024 MGI 6.23 |
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