|
Symbol Name ID |
C3
complement component 3 MGI:88227 |
| Darker colors indicate more annotations |
| Human Phenotypes | Pericarditis |
Cardiomegaly |
Stroke |
Ischemic stroke |
Hypertension |
Raynaud phenomenon |
Pulmonary arterial hypertension |
Pulmonary embolism |
Budd-Chiari syndrome |
Myocardial infarction |
Abnormality of the vasculature |
Lymphadenopathy |
Abnormality of the spleen |
Splenic infarction |
Splenomegaly |
Recurrent tonsillitis |
| Disease(s) Associated with C3 | ||||||||||||||||
| complement component 3 deficiency | ||||||||||||||||
| paroxysmal nocturnal hemoglobinuria | ||||||||||||||||
| sickle cell anemia | ||||||||||||||||
| systemic lupus erythematosus |
| Mouse Phenotypes | decreased vascular permeability |
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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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