|
Symbol Name ID |
Prph
peripherin MGI:97774 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Pseudobulbar paralysis |
Spasticity |
Degeneration of anterior horn cells |
Amyotrophic lateral sclerosis |
Degeneration of the lateral corticospinal tracts |
Fasciculations |
Dysarthria |
Sleep apnea |
Hyperreflexia |
| Disease(s) Associated with PRPH | ||||||||||
| amyotrophic lateral sclerosis type 1 |
| Mouse Phenotypes | nervous system phenotype |
abnormal axon morphology |
abnormal sensory neuron morphology |
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| Availability | Mouse Genotype | |||
| Prphtm1Jpj/Prphtm1Jpj | * | |||
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 05/21/2024 MGI 6.23 |
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