Symbol Name ID |
Kif5a
kinesin family member 5A MGI:109564 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Ankle clonus |
Lower limb spasticity |
Spastic paraplegia |
Upper limb spasticity |
Spastic gait |
Spastic paraparetic gait |
Amyotrophic lateral sclerosis |
Peripheral axonal neuropathy |
Ataxia |
Parkinsonism |
Knee clonus |
Upper motor neuron dysfunction |
Babinski sign |
Cognitive impairment |
Intellectual disability, moderate |
Hyperreflexia in upper limbs |
Lower limb hyperreflexia |
Sensorimotor neuropathy |
Paresthesia |
Distal sensory impairment |
Impaired distal vibration sensation |
Impaired vibration sensation in the lower limbs |
Disease(s) Associated with KIF5A | ||||||||||||||||||||||
amyotrophic lateral sclerosis type 25 | ||||||||||||||||||||||
hereditary spastic paraplegia 10 |
Mouse Phenotypes | nervous system phenotype |
seizures |
sporadic seizures |
abnormal motor neuron morphology |
axon degeneration |
abnormal axonal transport |
abnormal GABA-mediated receptor currents |
decreased miniature inhibitory postsynaptic current amplitude |
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Availability | Mouse Genotype | ||||||||
Kif5atm1Gsn/Kif5atm1Gsn | * | ||||||||
Kif5atm1.2Noh/Kif5atm1.2Noh Tg(Syn1-cre)671Jxm/0 (conditional) |
* | ||||||||
Kif5atm1Gsn/Kif5atm2Gsn Tg(Syn1-cre)671Jxm/0 (conditional) |
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 05/14/2024 MGI 6.23 |
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