C7 Chromosome 5

Complement C7
53 variants 53 Health Risk

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What This Gene Does
This gene encodes a serum glycoprotein that forms a membrane attack complex together with complement components C5b, C6, C8, and C9 as part of the terminal complement pathway of the innate immune system. The protein encoded by this gene contains a cholesterol-dependent cytolysin/membrane attack complex/perforin-like (CDC/MACPF) domain and belongs to a large family of structurally related molecules that form pores involved in host immunity and bacterial pathogenesis. This protein initiates membrane attack complex formation by binding the C5b-C6 subcomplex and inserts into the phospholipid bilayer, serving as a membrane anchor. Mutations in this gene are associated with a rare disorder called C7 deficiency. [provided by RefSeq, Nov 2016]
Gene Info
Gene Group
"Sushi domain containing|Complement system activation components|Membrane Attack complex"
Locus Type
gene with protein product
Location
5p13.1
Ensembl
ENSG00000112936
Associated Conditions (6)
Complement component 7 deficiency
C7 and C6 deficiency
combined subtotal
C7-related disorder
Inborn genetic diseases
Ovarian serous cystadenocarcinoma
Key Variants
All Variants (53)
RSID Category Clinical Significance Conditions
RS769923441 Health Risk Pathogenic/Likely pathogenic C7-related disorder, C7-related disorder
RS769984570 Health Risk Pathogenic/Likely pathogenic Complement component 7 deficiency, Complement component 7 deficiency
RS770367814 Health Risk Pathogenic/Likely pathogenic Complement component 7 deficiency, Complement component 7 deficiency
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