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C2

complement C2

HCNC Approved Symbol
C2 (HGNC:1248)
Genomic Coordinates
6:31,897,783 - 31,945,672 (6p21.33)
Synonyms
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the C2 gene.

Frequently observed phenotypes

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

Systemic lupus erythematosus
 3 (75.0%)
Arthritis
 2 (50.0%)
Photosensitivity
 2 (50.0%)
Glomerulonephritis
 1 (25.0%)
Glomerulopathy
 1 (25.0%)
C2 - Gene browser | 3billion