|
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 | Neurofibrillary tangles |
Long-tract signs |
Alzheimer disease |
Senile plaques |
Parkinsonism |
Apraxia |
Cognitive impairment |
Memory impairment |
Dementia |
Sleep-wake cycle disturbance |
Parietal hypometabolism in FDG PET |
| Disease(s) Associated with APOE | |||||||||||
| Alzheimer's disease 2 | |||||||||||
| Alzheimer's disease 4 |
| Mouse Phenotypes | nervous system phenotype |
abnormal kindling response |
abnormal blood-brain barrier function |
hypopituitarism |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
abnormal response to CNS ischemic injury |
decreased cerebral infarction 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 |
|
| Availability | Mouse Genotype | ||||||||||||||||||
| Apoetm1Bres/Apoetm1Bres | |||||||||||||||||||
| Apoetm1Unc/Apoetm1Unc | * | ||||||||||||||||||
| Apoetm2(APOE_i2)Sfu/Apoetm2(APOE_i2)Sfu | |||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 02/16/2021 MGI 6.16 |
|
|
|
||
Analysis Tools