Regional enteritis: genes and variants

Regional enteritis is linked to 1 analyzed protein (NOD2). 9 DNA variants are known to cause it; 131 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Genes linked to Regional enteritis

Where Regional enteritis variants cluster

Known disease-causing variants in Regional enteritis

VariantPositionProtein partClinical label
NOD2 R334Q334NACHTDisease-causing (★★)
NOD2 R334W334NACHTDisease-causing (★★)
NOD2 N670K670Disease-causing (★★)
NOD2 M513T513NACHTDisease-causing (★★)
NOD2 R587C587NACHTDisease-causing (★★)
NOD2 E383K383NACHTDisease-causing (★)
NOD2 E383D383NACHTDisease-causing (★)
NOD2 D382E382NACHTDisease-causing (★)
NOD2 G481D481NACHTDisease-causing (★)

Which prediction tools work for Regional enteritis

How often each tool ranks a disease-causing variant above a harmless one (AUROC × 100).

Same protein, different disease

Diseases related to Regional enteritis

Frequently asked questions

Which genes are linked to Regional enteritis?

In CATVariant, Regional enteritis is linked to 1 analyzed protein: NOD2 (Nucleotide-binding oligomerization domain-containing protein 2).

How many genetic variants are linked to Regional enteritis?

153 variants: 9 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 131 are of uncertain significance or have conflicting reports.

Which uncertain variants in Regional enteritis look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

Which variant effect predictor works best for Regional enteritis?

Among tools not trained on clinical labels, AlphaMissense separates this disease's known disease-causing variants from harmless ones best (AUROC 0.93, based on 8 disease-causing and 16 harmless variants).

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

Download every variant as CSV · Browse all diseases · Methods · About the Center