Symbol Name ID |
Reep1
receptor accessory protein 1 MGI:1098827 |
Darker colors indicate more annotations |
Human Phenotypes | Ankle clonus |
Absent Achilles reflex |
Decreased patellar reflex |
Dysphagia |
Lower limb spasticity |
Spastic paraplegia |
Spastic tetraparesis |
Spastic gait |
Difficulty walking |
Babinski sign |
Decreased motor nerve conduction velocity |
Dysarthria |
Hyperreflexia |
Brisk reflexes |
Hyperreflexia in upper limbs |
Lower limb hyperreflexia |
Gait disturbance |
Bulbar signs |
Distal sensory impairment |
Impaired proprioception |
Disease(s) Associated with REEP1 | ||||||||||||||||||||
autosomal dominant distal hereditary motor neuronopathy 12 | ||||||||||||||||||||
hereditary spastic paraplegia 31 |
Mouse Phenotypes | abnormal cerebral cortex morphology |
abnormal motor neuron morphology |
abnormal axon morphology |
axon degeneration |
demyelination |
abnormal nervous system electrophysiology |
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Availability | Mouse Genotype | ||||||
Reep1Gt(OST398247)Tigm/Reep1Gt(OST398247)Tigm | |||||||
Reep1tm1.1Cahb/Reep1tm1.1Cahb | |||||||
Reep1tm1.1Cahb/Reep1+ |
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 04/16/2024 MGI 6.23 |
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