Symbol Name ID |
C3
complement component 3 MGI:88227 |
Darker colors indicate more annotations |
Human Phenotypes | Diarrhea |
Dysphagia |
Esophageal spasms |
Odynophagia |
Disease(s) Associated with C3 | ||||
paroxysmal nocturnal hemoglobinuria |
Mouse Phenotypes | abnormal intestine morphology |
abnormal intestinal lipid absorption |
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Availability | Mouse Genotype | ||
C3tm1Crr/C3tm1Crr | |||
C3tm1Hrc/C3tm1Hrc |
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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