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C3

complement C3

HCNC Approved Symbol
C3 (HGNC:1318)
Genomic Coordinates
19:6,677,704 - 6,720,650 (19p13.3)
Synonyms
CPAMD1, ARMD9, C3a, C3b
Disease Associations
This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the C3 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Glomerular c3 deposition
 2 (66.7%)
Glomerulopathy
 2 (66.7%)
Complement deficiency
 1 (33.3%)
Nephropathy
 1 (33.3%)
Proteinuria
 1 (33.3%)
C3 - Gene browser | 3billion