|
Symbol Name ID |
Klc2
kinesin light chain 2 MGI:107953 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ankle clonus |
Absent Achilles reflex |
Hyporeflexia of lower limbs |
Spastic paraplegia |
Progressive spastic paraplegia |
Difficulty walking |
Decreased number of peripheral myelinated nerve fibers |
Peripheral axonal neuropathy |
Motor axonal neuropathy |
Sensory axonal neuropathy |
Abnormality of extrapyramidal motor function |
Exaggerated startle response |
Babinski sign |
Dysarthria |
Proximal hyperreflexia |
Inability to walk |
Motor delay |
Delayed gross motor development |
Impaired vibration sensation in the lower limbs |
| Disease(s) Associated with KLC2 | |||||||||||||||||||
| SPOAN syndrome |
| Mouse Phenotypes | decreased cochlear outer hair cell number |
abnormal cochlear inner hair cell morphology |
abnormal cochlear outer hair cell morphology |
cochlear outer hair cell degeneration |
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| Availability | Mouse Genotype | ||||
| Klc2em1Jgao/Klc2em1Jgao | |||||
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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