C3 gene homepage

General information
Gene symbol C3
Gene name complement component 3
Chromosome 19
Chromosomal band p13.3-p13.2
Imprinted Unknown
Genomic reference LRG_27
Transcript reference NM_000064.2
Associated with diseases AHUS-5, ARMD-9, C3D
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 59
Unique public DNA variants reported 49
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 1318
Entrez Gene 718
PubMed articles C3
OMIM - Gene 120700
OMIM - Diseases AHUS-5 (hemolytic-uremic syndrome, atypical, type 5 (AHUS-5))
ARMD-9 (macular degeneration, age-related, type 9 (ARMD-9))
C3D (complement component 3 deficiency, autosomal recessive (C3D))

Active transcripts




NCBI ID     

NCBI Protein ID     

00003702 19 complement component 3 NM_000064.2 NP_000055.2 59

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