Symbol Name ID |
Hc
hemolytic complement MGI:96031 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal erythrocyte enzyme concentration or activity |
Decreased circulating iron concentration |
Unconjugated hyperbilirubinemia |
Increased blood urea nitrogen |
Reduced haptoglobin level |
Increased circulating lactate dehydrogenase concentration |
Renal Fanconi syndrome |
Glycosuria |
Proteinuria |
Hemoglobinuria |
Paroxysmal nocturnal hemoglobinuria |
Hemosiderinuria |
Disease(s) Associated with C5 | ||||||||||||
paroxysmal nocturnal hemoglobinuria |
Mouse Phenotypes | homeostasis/metabolism phenotype |
decreased fasting circulating glucose level |
decreased susceptibility to injury |
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Availability | Mouse Genotype | |||
Hc0/Hc0 | * | |||
Hctm1b(EUCOMM)Wtsi/Hctm1b(EUCOMM)Wtsi |
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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