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Symbol Name ID |
C3
complement component 3 MGI:88227 |
| Darker colors indicate more annotations |
| Human Phenotypes | Stroke |
Ischemic stroke |
Anorexia |
Dysphagia |
Abnormality of the nervous system |
Chorea |
Depression |
Psychosis |
Lethargy |
Headache |
Seizure |
| Disease(s) Associated with C3 | |||||||||||
| paroxysmal nocturnal hemoglobinuria | |||||||||||
| sickle cell anemia | |||||||||||
| systemic lupus erythematosus |
| Mouse Phenotypes | decreased cerebral infarct size |
brain inflammation |
abnormal hippocampus CA3 region morphology |
abnormal dendritic spine morphology |
increased neuron number |
abnormal retina rod bipolar cell morphology |
abnormal retina horizontal cell morphology |
abnormal synaptic vesicle number |
enhanced central nervous system regeneration |
abnormal synaptic plasticity |
enhanced long-term potentiation |
enhanced paired-pulse facilitation |
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| Availability | Mouse Genotype | ||||||||||||
| C3tm1Crr/C3tm1Crr | |||||||||||||
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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