Molekulargenetisches Labor
Zentrum für Nephrologie und Stoffwechsel
Moldiag Erkrankungen Gene Support Kontakt

Komplement-Komponente C5

Das C5-Gen kodiert die Komplement-Komponente C5, die eine wichtige Rolle bei der Aktivierung des Membran-Attack-Complexes (MAC) spielt. Da dieses protein der Angriffspunkt des Medikamentes Eculizumab spielt, sind bereits genetische Variationen entdeckt worden, die das Ansprechen auf den im Eculizumab vorhandenen monoklonalen Antikörper beeinflussen können. Des weiteren sind Assoziationen von Variationen mit Leberfibrose und rheumatischer Arthrtis beschrieben.

Gentests:

Klinisch Untersuchungsmethoden Familienuntersuchung
Bearbeitungszeit 5 Tage
Probentyp genomische DNS
Klinisch Untersuchungsmethoden Hochdurchsatz-Sequenzierung
Bearbeitungszeit 25 Tage
Probentyp genomische DNS
Klinisch Untersuchungsmethoden Direkte Sequenzierung der proteinkodierenden Bereiche eines Gens
Bearbeitungszeit 25 Tage
Probentyp genomische DNS

Verknüpfte Erkrankungen:

Schlechtes Ansprechen auf Eculizumab
C5
Komplement C5-Mangel
C5
Meningokokken-Infektanfälligkeit
C3
C5
C7
C8A
C8B
C8G
C9
CD46
CFB
CFD
CFH
CFP

Referenzen:

1.

None (1997) A genome-wide search for asthma susceptibility loci in ethnically diverse populations. The Collaborative Study on the Genetics of Asthma (CSGA).

external link
2.

Halangk J et al. (2008) Evaluation of complement factor 5 variants as genetic risk factors for the development of advanced fibrosis in chronic hepatitis C infection.

external link
3.

Plenge RM et. al. (2007) TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.

external link
4.

Pickering MC et al. (2006) Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice.

external link
5.

Hillebrandt S et al. (2005) Complement factor 5 is a quantitative trait gene that modifies liver fibrogenesis in mice and humans.

external link
6.

Peng T et al. (2005) Role of C5 in the development of airway inflammation, airway hyperresponsiveness, and ongoing airway response.

external link
7.

Pfarr N et al. (2005) Linking C5 deficiency to an exonic splicing enhancer mutation.

external link
8.

Delgado-Cerviño E et al. (2005) C5 complement deficiency in a Spanish family. Molecular characterization of the double mutation responsible for the defect.

external link
9.

Hillebrandt S et al. (2002) Genome-wide analysis of hepatic fibrosis in inbred mice identifies the susceptibility locus Hfib1 on chromosome 15.

external link
10.

Wetsel RA et al. (1988) Molecular analysis of human complement component C5: localization of the structural gene to chromosome 9.

external link
11.

Jeremiah SJ et al. (1988) The assignment of the human gene coding for complement C5 to chromosome 9q22-9q33.

external link
12.

Haviland DL et al. (1991) Complete cDNA sequence of human complement pro-C5. Evidence of truncated transcripts derived from a single copy gene.

external link
13.

Carney DF et al. (1991) Structural aspects of the human C5 gene. Intron/exon organization, 5'-flanking region features, and characterization of two truncated cDNA clones.

external link
14.

Tack BF et al. (1979) Fifth component of human complement: purification from plasma and polypeptide chain structure.

external link
15.

Nishimura J et al. (2014) Genetic variants in C5 and poor response to eculizumab.

external link
16.

Wang X et al. (1995) Inherited human complement C5 deficiency. Nonsense mutations in exons 1 (Gln1 to Stop) and 36 (Arg1458 to Stop) and compound heterozygosity in three African-American families.

external link
17.

Wetsel RA et al. (1990) Deficiency of the murine fifth complement component (C5). A 2-base pair gene deletion in a 5'-exon.

external link
18.

Karp CL et al. (2000) Identification of complement factor 5 as a susceptibility locus for experimental allergic asthma.

external link
19.

Wjst M et al. (1999) A genome-wide search for linkage to asthma. German Asthma Genetics Group.

external link
20.

Ober C et al. (1998) Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma.

external link
21.

Gavett SH et al. (1995) Interleukin 12 inhibits antigen-induced airway hyperresponsiveness, inflammation, and Th2 cytokine expression in mice.

external link
22.

Orphanet article

Orphanet ID 160093 external link
23.

NCBI article

NCBI 727 external link
24.

OMIM.ORG article

Omim 120900 external link
25.

Wikipedia Artikel

Wikipedia DE (Komplementkomponente_C5) external link
Update: 14. August 2020
Copyright © 2005-2020 Zentrum für Nephrologie und Stoffwechsel, Dr. Mato Nagel
Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Deutschland, Tel.: +49-3576-287922, Fax: +49-3576-287944
Seitenüberblick | Webmail | Haftungsausschluss | Datenschutz