Gene

NOD2

HGNC: HGNC:5331 | GeneCards: NOD2
Saudi human-genetics coreAll Saudi-affiliated records

Overview

Approved name
Cytogenetic location
-
Locus type
-
In SaudiVarKB
13 articles, 13 mentions

Synonyms

None recorded

External resources

ClinVar ↗PubMed ↗
13Publications6Co-reported phenotypes3Reported variants
0ClinVar pathogenic / likely pathogenic
0Saudi regions
OpenLiterature network

Co-reported phenotypes

Phenotypes named in the same articles as NOD2. Co-mention, not a proven association.

PhenotypeArticlesEvidence
Crohn disease5View sentences
inflammatory bowel disease4View sentences
congenital cataract1View sentences
hepatitis B1View sentences
hepatocellular carcinoma1View sentences
ulcerative colitis1View sentences

Reported variants

Variants linked to NOD2 through dbSNP or LitVar2. ClinVar status is shown for core-subset variants.

VariantrsIDArticlesClinVar
rs2066844rs20668441-
rs2066845rs20668451-
rs5743289rs57432891-

Saudi regions

Regions or cities named in the abstracts of articles that mention NOD2.

No Saudi region named.