Symbol Name ID |
Apoe
apolipoprotein E MGI:88057 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Stroke |
Dysphagia |
Spasticity |
Spastic tetraparesis |
Fatigable weakness of bulbar muscles |
Fatigable weakness of swallowing muscles |
Fatigable weakness of respiratory muscles |
Motor neuron atrophy |
Amyotrophic lateral sclerosis |
Morphological central nervous system abnormality |
Cerebral cortical atrophy |
Neurofibrillary tangles |
Spinal cord compression |
Alzheimer disease |
Neurodegeneration |
Optic ataxia |
Abnormality of extrapyramidal motor function |
Parkinsonism |
Apraxia |
Fasciculations |
Myoclonus |
Paralysis |
Babinski sign |
Long-tract signs |
Dysarthria |
Language impairment |
Depression |
Emotional lability |
Disturbed sensory perception |
Anxiety |
Atypical behavior |
Personality changes |
Agitation |
Cognitive impairment |
Memory impairment |
Dementia |
Frontotemporal dementia |
Reduced consciousness |
Sleep abnormality |
Hyperreflexia |
Jaw hyperreflexia |
Lower limb hyperreflexia |
Dystonia |
Gait disturbance |
Gait imbalance |
Headache |
Seizure |
Paresthesia |
Disease(s) Associated with APOE | ||||||||||||||||||||||||||||||||||||||||||||||||
Alzheimer's disease 2 | ||||||||||||||||||||||||||||||||||||||||||||||||
Alzheimer's disease 3 | ||||||||||||||||||||||||||||||||||||||||||||||||
amyotrophic lateral sclerosis | ||||||||||||||||||||||||||||||||||||||||||||||||
cerebral infarction | ||||||||||||||||||||||||||||||||||||||||||||||||
malaria | ||||||||||||||||||||||||||||||||||||||||||||||||
multiple myeloma |
Mouse Phenotypes | nervous system phenotype |
abnormal kindling response |
impaired blood-brain barrier function |
hypopituitarism |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
decreased cerebral infarct size |
abnormal hippocampus morphology |
abnormal cerebral cortex morphology |
abnormal neuron morphology |
abnormal myelin sheath morphology |
abnormal dendrite morphology |
abnormal synapse morphology |
abnormal synaptic vesicle morphology |
cochlear ganglion degeneration |
abnormal sciatic nerve morphology |
abnormal astrocyte physiology |
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Availability | Mouse Genotype | |||||||||||||||||
Apoetm1Bres/Apoetm1Bres | ||||||||||||||||||
Apoetm1Unc/Apoetm1Unc | * |
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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