|
Symbol Name ID |
C3
complement component 3 MGI:88227 |
| Darker colors indicate more annotations |
| Human Phenotypes | Renal Fanconi syndrome |
Hematuria |
Pyuria |
Glycosuria |
Proteinuria |
Hemoglobinuria |
Paroxysmal nocturnal hemoglobinuria |
Hemosiderinuria |
Abnormality of the kidney |
Lupus nephritis |
Membranoproliferative glomerulonephritis |
Abnormal renal physiology |
Nephritis |
Nephrotic syndrome |
Renal insufficiency |
Acute kidney injury |
Chronic kidney disease |
| Disease(s) Associated with C3 | |||||||||||||||||
| complement component 3 deficiency | |||||||||||||||||
| paroxysmal nocturnal hemoglobinuria | |||||||||||||||||
| sickle cell anemia | |||||||||||||||||
| systemic lupus erythematosus |
| Mouse Phenotypes | decreased urine albumin level |
glomerulonephritis |
|
| 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) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools