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 |
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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 09/03/2024 MGI 6.24 |
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