|
Symbol Name ID |
C3
complement component 3 MGI:88227 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Macular degeneration |
Retinopathy |
| Disease(s) Associated with C3 | ||
| age related macular degeneration 7 | ||
| sickle cell anemia | ||
| systemic lupus erythematosus |
| Mouse Phenotypes | vision/eye phenotype |
abnormal retina rod bipolar cell morphology |
abnormal retina horizontal cell morphology |
decreased b-wave amplitude |
abnormal c-wave shape |
abnormal eye electrophysiology |
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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 04/16/2024 MGI 6.23 |
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