Symbol Name ID |
Prx
periaxin MGI:108176 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Vocal cord paresis |
Disease(s) Associated with PRX | |
Charcot-Marie-Tooth disease type 4F |
Mouse Phenotypes | behavior/neurological phenotype |
aphagia |
hyporesponsive to tactile stimuli |
limb grasping |
impaired coordination |
abnormal gait |
abnormal touch/ nociception |
decreased thermal nociceptive threshold |
|
Availability | Mouse Genotype | ||||||||
Prxtm1Brp/Prxtm1Brp | |||||||||
Prxtm2.1Brp/Prxtm2.1Brp | * |
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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