The NOD2 gene homepage

General information
Gene symbol NOD2
Gene name nucleotide-binding oligomerization domain containing 2
Chromosome 16
Chromosomal band q12
Imprinted Unknown
Genomic reference LRG_177
Transcript reference NM_022162.1, XM_005256084.1
Associated with diseases Blau, IBD-1, arthritis, psoriatic, susceptibility to, sarcoidosis, early-onset
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 76
Unique public DNA variants reported 15
Individuals with public variants 32
Hidden variants 34
Date created November 30, -0001
Date last updated September 28, 2016
Version NOD2:160928

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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:5331
Entrez Gene 64127
PubMed articles NOD2
OMIM - Gene 605956
OMIM - Diseases Blau (Blau syndrome)
IBD-1 (bowel disease, inflammatory, type 1 (IBD-1))
arthritis, psoriatic, susceptibility to
sarcoidosis, early-onset


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00022204 16 nucleotide-binding oligomerization domain containing 2 NM_022162.1 NP_071445.1 76
00037762 16 transcript variant X1 XM_005256084.1 XP_005256141.1 -