Symbol Name ID |
Hspb8
heat shock protein 8 MGI:2135756 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Decreased number of large peripheral myelinated nerve fibers |
Peripheral axonal neuropathy |
Decreased amplitude of sensory action potentials |
Areflexia |
Hyporeflexia |
Distal sensory impairment |
Disease(s) Associated with HSPB8 | ||||||
Charcot-Marie-Tooth disease axonal type 2L |
Mouse Phenotypes | nervous system phenotype |
amyloid beta deposits |
abnormal sciatic nerve morphology |
axon degeneration |
abnormal action potential |
|
Availability | Mouse Genotype | |||||
Hspb8tm1.1Vti/Hspb8tm1.1Vti | * | |||||
Hspb8tm1Vti/Hspb8tm1Vti | ||||||
Hspb8tm1Vti/Hspb8+ | ||||||
Tg(Myh6*/tetO-Hspb8*K141N)#Atsa/0 Tg(Myh6-tTA)55Rbns/0 |
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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