C5 Chromosome 9

Complement C5
52 variants 52 Health Risk

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What This Gene Does
This gene encodes a component of the complement system, a part of the innate immune system that plays an important role in inflammation, host homeostasis, and host defense against pathogens. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the C5 alpha chain, C5 beta chain, C5a anaphylatoxin and C5b. The C5 protein is comprised of the C5 alpha and beta chains, which are linked by a disulfide bridge. Cleavage of the alpha chain by a convertase enzyme results in the formation of the C5a anaphylatoxin, which possesses potent spasmogenic and chemotactic activity, and the C5b macromolecular cleavage product, a subunit of the membrane attack complex (MAC). Mutations in this gene cause complement component 5 deficiency, a disease characterized by recurrent bacterial infections. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]
Gene Info
Gene Group
"Receptor ligands|C3 and PZP like, alpha-2-macroglobulin domain containing|Complement system activation components|Membrane Attack complex"
Locus Type
gene with protein product
Location
9q33.2
Ensembl
ENSG00000106804
Associated Conditions (7)
Complement component 5 deficiency
Eculizumab
poor response to
C5-related disorder
Colon adenocarcinoma
Gastric cancer
Lathosterolosis
Key Variants
All Variants (52)
RSID Category Clinical Significance Conditions
RS867527050 Health Risk Pathogenic
RS1408798589 Health Risk Pathogenic/Likely pathogenic Eculizumab, poor response to, Complement component 5 deficiency
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