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Symbol Name ID |
Pmp2
peripheral myelin protein 2 MGI:102667 |
| Darker colors indicate more annotations |
| Human Phenotypes | Absent patellar reflexes |
Absent Achilles reflex |
Difficulty walking |
Frequent falls |
Onion bulb formation |
Peripheral demyelination |
Hand tremor |
Babinski sign |
Decreased compound muscle action potential amplitude |
Steppage gait |
Impaired pain sensation |
Distal sensory impairment |
Impaired distal vibration sensation |
| Disease(s) Associated with PMP2 | |||||||||||||
| Charcot-Marie-Tooth disease type 1G |
| Mouse Phenotypes | decreased nerve conduction velocity |
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| Availability | Mouse Genotype | |
| Pmp2tm1.1(KOMP)Vlcg/Pmp2tm1.1(KOMP)Vlcg | ||
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 04/23/2024 MGI 6.23 |
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