Symbol Name ID |
Pmp22
peripheral myelin protein 22 MGI:97631 |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
Profound sensorineural hearing impairment |
Hearing impairment |
Tinnitus |
Disease(s) Associated with PMP22 | ||||
Charcot-Marie-Tooth disease type 1A | ||||
Charcot-Marie-Tooth disease type 1E |
Mouse Phenotypes | increased or absent threshold for auditory brainstem response |
impaired hearing |
deafness |
|
Availability | Mouse Genotype | |||
Pmp22Tr-2J/Pmp22+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|