View gene C3

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 ARMD-9, C3D, hemolytic-uremic syndrome, atypical, type 5
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

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


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00003702 19 complement component 3 NM_000064.2 NP_000055.2 0