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Symbol
Name
ID
C3
complement component 3
MGI:88227
Phenotype annotations related to hematopoietic system
Darker colors indicate more annotations
Human Phenotypes
Pancytopenia
Abnormal erythrocyte enzyme concentration or activity
Persistence of hemoglobin F
Increased mean corpuscular volume
Erythroid hyperplasia
Reticulocytosis
Anemia
Hemolytic anemia
Chronic hemolytic anemia
Increased red cell sickling tendency
Hypochromic anemia
Iron deficiency anemia
Microcytic anemia
Target cells
Leukocytosis
Leukopenia
Arterial thrombosis
Thromboembolism
Venous thrombosis
Deep venous thrombosis
Mesenteric venous thrombosis
Thrombocytopenia
Thrombocytosis
Abnormality of the spleen
Splenic infarction
Splenomegaly
Disease(s) Associated with C3
paroxysmal nocturnal hemoglobinuria
sickle cell anemia
systemic lupus erythematosus

Mouse Phenotypes
decreased susceptibility to autoimmune hemolytic anemia
decreased mast cell number
decreased neutrophil cell number
abnormal neutrophil morphology
decreased osteoclast cell number
abnormal spleen germinal center morphology
decreased spleen germinal center number
decreased spleen germinal center size
abnormal mast cell physiology
Availability Mouse Genotype
C3tm1Crr/C3tm1Crr

Contributing Projects:
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
The Jackson Laboratory