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CFI / Complement Factor I

complement factor I

CFI / Complement Factor I is a serine proteinase that is essential for regulating the complement cascade. The encoded preproprotein is cleaved to produce both heavy and light chains, which are linked by disulfide bonds to form a heterodimeric glycoprotein. This heterodimer can cleave and inactivate the complement components C4b and C3b, and it prevents the assembly of the C3 and C5 convertase enzymes. Defects in this gene cause complement factor I deficiency, an autosomal recessive disease associated with a susceptibility to pyogenic infections. Mutations in this gene have been associated with a predisposition to atypical hemolytic uraemic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immmune deposits is another condition associated with mutation of this gene.

Gene Name: complement factor I
Family/Subfamily: Protease , Serine S1
Synonyms: CFI, AHUS3, C3BINA, C3b-inactivator, C3B/C4B inactivator, Complement component I, Complement component factor i, Factor I, FI, KAF, I factor, I factor (complement), C3b-INA, Complement factor I, Light chain of factor I
Target Sequences: NM_000204 NP_000195.2 P05156

Publications (1)

1
The imbalance in the complement system and its possible physiological mechanisms in patients with lung cancer. Zhao P, Wu J, Lu F, Peng X, Liu C, Zhou N, Ying M. BMC cancer. 2019 March;19:201. [Full Text Article] [PubMed:30841875] [PMC:PMC6404310]

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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).