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Aliases for NOD2 Gene

Aliases for NOD2 Gene

  • Nucleotide Binding Oligomerization Domain Containing 2 2 3 5
  • Nucleotide-Binding Oligomerization Domain, Leucine Rich Repeat And CARD Domain Containing 2 2 3
  • Caspase Recruitment Domain-Containing Protein 15 3 4
  • Caspase Recruitment Domain Family, Member 15 2 3
  • NLR Family, CARD Domain Containing 2 2 3
  • Inflammatory Bowel Disease Protein 1 3 4
  • NOD-Like Receptor C2 2 3
  • CARD15 3 4
  • IBD1 3 4
  • Nucleotide-Binding Oligomerization Domain-Containing Protein 2 3
  • Nucleotide-Binding Oligomerization Domain 2 3
  • Caspase Recruitment Domain Protein 15 3
  • CLR16.3 3
  • PSORAS1 3
  • BLAUS 3
  • NLRC2 3
  • NOD2B 3
  • ACUG 3
  • BLAU 3
  • YAOS 3
  • CD 3

External Ids for NOD2 Gene

Previous HGNC Symbols for NOD2 Gene

  • IBD1
  • CARD15

Previous GeneCards Identifiers for NOD2 Gene

  • GC16P049289
  • GC16P050731
  • GC16P036618
  • GC16P050729

Summaries for NOD2 Gene

Entrez Gene Summary for NOD2 Gene

  • This gene is a member of the Nod1/Apaf-1 family and encodes a protein with two caspase recruitment (CARD) domains and six leucine-rich repeats (LRRs). The protein is primarily expressed in the peripheral blood leukocytes. It plays a role in the immune response to intracellular bacterial lipopolysaccharides (LPS) by recognizing the muramyl dipeptide (MDP) derived from them and activating the NFKB protein. Mutations in this gene have been associated with Crohn disease and Blau syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jun 2014]

GeneCards Summary for NOD2 Gene

NOD2 (Nucleotide Binding Oligomerization Domain Containing 2) is a Protein Coding gene. Diseases associated with NOD2 include Blau Syndrome and Yao Syndrome. Among its related pathways are Ovarian tumor domain proteases and Activated TLR4 signalling. GO annotations related to this gene include protein kinase binding and peptidoglycan binding. An important paralog of this gene is NOD1.

UniProtKB/Swiss-Prot for NOD2 Gene

  • Involved in gastrointestinal immunity. Upon stimulation by muramyl dipeptide (MDP), a fragment of bacterial peptidoglycan, binds the proximal adapter receptor-interacting RIPK2, which recruits ubiquitin ligases as XIAP, BIRC2, BIRC3 and the LUBAC complex, triggering activation of MAP kinases and activation of NF-kappa-B signaling. This in turn leads to the transcriptional activation of hundreds of genes involved in immune response. Required for MDP-induced NLRP1-dependent CASP1 activation and IL1B release in macrophages (PubMed:18511561).

Gene Wiki entry for NOD2 Gene

Additional gene information for NOD2 Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for NOD2 Gene

Genomics for NOD2 Gene

Regulatory Elements for NOD2 Gene

Enhancers for NOD2 Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH16H050695 1.9 FANTOM5 Ensembl ENCODE dbSUPER 62 +4.4 4366 5 HDGF PKNOX1 ATF1 SIN3A DMAP1 ZNF766 ZNF207 ATF7 RUNX3 REST NOD2 SNX20 CYLD ADCY7 GC16P050707 PIR45400
GH16H050678 1.8 FANTOM5 Ensembl ENCODE dbSUPER 59.4 -11.0 -10978 8 HDGF PKNOX1 FOXA2 TBL1XR1 RB1 SIN3A BATF RAD21 GATA2 SCRT2 NOD2 SNX20 BRD7 CYLD ADCY7
GH16H050740 1.9 FANTOM5 Ensembl ENCODE dbSUPER 38.3 +50.9 50904 7 HDGF PKNOX1 FOXA2 ARID4B SIN3A DMAP1 YY1 SLC30A9 ZNF143 ZNF207 NOD2 PAPD5 SNX20 CYLD LOC102724907 BRD7 ADCY7 LOC105371251
GH16H050702 1 FANTOM5 ENCODE dbSUPER 16.2 +9.5 9465 2 MAX MYC SETDB1 NOD2 CYLD SNX20 ADCY7 PIR45400 GC16P050707
GH16H050708 1.2 Ensembl ENCODE dbSUPER 12.4 +15.7 15720 1 CTCF MAX BATF POLR2A EED ZNF207 ETV6 RUNX3 IKZF2 ZNF687 NOD2 ENSG00000270120 GC16P050707 PIR45400
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around NOD2 on UCSC Golden Path with GeneCards custom track

Promoters for NOD2 Gene
Ensembl Regulatory Elements (ENSRs) TSS Distance (bp) Size (bp) Binding Sites for Transcription Factors within promoters
ENSR00000085822 119 601 ZNF792 INSM2 MAX ZNF223 ZNF2 ZNF157 POLR2A EED ZBTB20 MAZ

Transcription factor binding sites by QIAGEN in the NOD2 gene promoter:

Genomic Location for NOD2 Gene

Chromosome:
16
Start:
50,693,581 bp from pter
End:
50,734,041 bp from pter
Size:
40,461 bases
Orientation:
Plus strand

Genomic View for NOD2 Gene

Genes around NOD2 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
NOD2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for NOD2 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for NOD2 Gene

Proteins for NOD2 Gene

  • Protein details for NOD2 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Q9HC29-NOD2_HUMAN
    Recommended name:
    Nucleotide-binding oligomerization domain-containing protein 2
    Protein Accession:
    Q9HC29
    Secondary Accessions:
    • E2JEQ6
    • Q96RH5
    • Q96RH6
    • Q96RH8

    Protein attributes for NOD2 Gene

    Size:
    1040 amino acids
    Molecular mass:
    115283 Da
    Quaternary structure:
    • Component of a signaling complex consisting of ARHGEF2, NOD2 and RIPK2 (PubMed:21887730). Interacts (via CARD domain) with RIPK2 (via CARD domain) (PubMed:19592251, PubMed:21887730). Interacts with ATG16L1 (PubMed:23376921). Interacts (via NACHT domain) with CARD9 (PubMed:24960071). Interacts with ANKRD17 (via N-terminus) (PubMed:23711367). Interacts with HSPA1A; the interaction enhances NOD2 stability (PubMed:24790089). Interacts (via both CARD domains) with HSP90; the interaction enhances NOD2 stability (PubMed:23019338). Interacts (via CARD domain) with SOCS3; the interaction promotes NOD2 degradation (PubMed:23019338). Interacts (via CARD domain) with ERBBI2P; the interaction inhibits activation of NOD2 (PubMed:16203728). Interacts (via CARD domain) with CASP1; this interaction leads to IL1B processing. Also interacts with CASP4. Interacts with NLRP1; this interaction is enhanced in the presence of muramyl dipeptide (MDP) and leads to increased IL1B release (PubMed:18511561). Interacts with MAPKBP1; the interaction is enhanced in the presence of muramyl dipeptide (MDP) (PubMed:22700971).

    Alternative splice isoforms for NOD2 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for NOD2 Gene

Post-translational modifications for NOD2 Gene

  • Polyubiquitinated following MDP stimulation, leading to proteasome-mediated degradation (PubMed:23019338).
  • Modification sites at PhosphoSitePlus
  • Modification sites at neXtProt

No data available for DME Specific Peptides for NOD2 Gene

Domains & Families for NOD2 Gene

Gene Families for NOD2 Gene

HGNC:
IUPHAR :
Human Protein Atlas (HPA):
  • Disease related genes
  • Predicted intracellular proteins

Suggested Antigen Peptide Sequences for NOD2 Gene

Graphical View of Domain Structure for InterPro Entry

Q9HC29

UniProtKB/Swiss-Prot:

NOD2_HUMAN :
  • The ATG16L1-binding motif mediates interaction with ATG16L1.
Domain:
  • The ATG16L1-binding motif mediates interaction with ATG16L1.
  • Intramolecular interactions between the N-terminal moiety and the leucine-rich repeats (LRR) may be important for autoinhibition in the absence of activating signal. In the absence of LRRs, the protein becomes a constitutive activator of CASP1 cleavage and proIL1B processing.
genes like me logo Genes that share domains with NOD2: view

Function for NOD2 Gene

Molecular function for NOD2 Gene

UniProtKB/Swiss-Prot Function:
Involved in gastrointestinal immunity. Upon stimulation by muramyl dipeptide (MDP), a fragment of bacterial peptidoglycan, binds the proximal adapter receptor-interacting RIPK2, which recruits ubiquitin ligases as XIAP, BIRC2, BIRC3 and the LUBAC complex, triggering activation of MAP kinases and activation of NF-kappa-B signaling. This in turn leads to the transcriptional activation of hundreds of genes involved in immune response. Required for MDP-induced NLRP1-dependent CASP1 activation and IL1B release in macrophages (PubMed:18511561).

Phenotypes From GWAS Catalog for NOD2 Gene

Gene Ontology (GO) - Molecular Function for NOD2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0003779 actin binding IDA 24790089
GO:0005515 protein binding IPI 11087742
GO:0005524 ATP binding IEA --
GO:0019899 enzyme binding IPI 15753091
GO:0019901 protein kinase binding IPI 15075345
genes like me logo Genes that share ontologies with NOD2: view
genes like me logo Genes that share phenotypes with NOD2: view

Human Phenotype Ontology for NOD2 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for NOD2 Gene

MGI Knock Outs for NOD2:

Animal Model Products

CRISPR Products

miRNA for NOD2 Gene

miRTarBase miRNAs that target NOD2

Inhibitory RNA Products

Clone Products

  • Applied Biological Materials Clones for NOD2
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

No data available for Enzyme Numbers (IUBMB) , Transcription Factor Targets and HOMER Transcription for NOD2 Gene

Localization for NOD2 Gene

Subcellular locations from UniProtKB/Swiss-Prot for NOD2 Gene

Cytoplasm. Membrane. Basolateral cell membrane.

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for NOD2 gene
Compartment Confidence
plasma membrane 5
cytoskeleton 5
cytosol 5
golgi apparatus 4
nucleus 3
extracellular 2
lysosome 1
endosome 1

Subcellular locations from the

Human Protein Atlas (HPA)
  • Cytosol (2)
  • Golgi apparatus (1)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for NOD2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005737 cytoplasm TAS 15967716
GO:0005794 Golgi apparatus IDA --
GO:0005829 cytosol TAS --
GO:0005856 cytoskeleton IDA 21887730
GO:0005886 plasma membrane IDA,IEA 15998797
genes like me logo Genes that share ontologies with NOD2: view

Pathways & Interactions for NOD2 Gene

genes like me logo Genes that share pathways with NOD2: view

Gene Ontology (GO) - Biological Process for NOD2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000187 activation of MAPK activity TAS --
GO:0002367 cytokine production involved in immune response IMP 16260731
GO:0002374 cytokine secretion involved in immune response IMP 20441518
GO:0002376 immune system process IEA --
GO:0002606 positive regulation of dendritic cell antigen processing and presentation ISS --
genes like me logo Genes that share ontologies with NOD2: view

No data available for SIGNOR curated interactions for NOD2 Gene

Drugs & Compounds for NOD2 Gene

(13) Drugs for NOD2 Gene - From: PharmGKB, DGIdb, IUPHAR, and Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Tacrolimus Approved, Investigational Pharma 1125
muramyl dipeptide Pharma Agonist 0

(5) Additional Compounds for NOD2 Gene - From: Novoseek

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
genes like me logo Genes that share compounds with NOD2: view

Transcripts for NOD2 Gene

Unigene Clusters for NOD2 Gene

Nucleotide-binding oligomerization domain containing 2:
Representative Sequences:

CRISPR Products

Inhibitory RNA Products

Clone Products

  • Applied Biological Materials Clones for NOD2
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

Alternative Splicing Database (ASD) splice patterns (SP) for NOD2 Gene

ExUns: 1a · 1b ^ 2 ^ 3 ^ 4 ^ 5a · 5b · 5c ^ 6 ^ 7 ^ 8 ^ 9 ^ 10a · 10b ^ 11 ^ 12 ^ 13
SP1: - - -
SP2: -
SP3: - - -
SP4: - - -
SP5: - - - -
SP6: - - -
SP7:
SP8: - - - - -
SP9: - - - -
SP10: - - -

Relevant External Links for NOD2 Gene

GeneLoc Exon Structure for
NOD2
ECgene alternative splicing isoforms for
NOD2

Expression for NOD2 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for NOD2 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for NOD2 Gene

This gene is overexpressed in Whole Blood (x13.2), Skin - Sun Exposed (Lower leg) (x4.7), Esophagus - Mucosa (x4.2), and Skin - Not Sun Exposed (Suprapubic) (x4.1).

Protein differential expression in normal tissues from HIPED for NOD2 Gene

This gene is overexpressed in Adipocyte (65.8).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, and MOPED for NOD2 Gene



Protein tissue co-expression partners for NOD2 Gene

- Elite partner

NURSA nuclear receptor signaling pathways regulating expression of NOD2 Gene:

NOD2

SOURCE GeneReport for Unigene cluster for NOD2 Gene:

Hs.592072

mRNA Expression by UniProt/SwissProt for NOD2 Gene:

Q9HC29-NOD2_HUMAN
Tissue specificity: Expressed in intestinal mucosa, mainly in Paneth cells and, at lower extent, in the glandular epithelium.

Evidence on tissue expression from TISSUES for NOD2 Gene

  • Blood(4.6)
  • Intestine(3.2)
  • Lymph node(2.4)
  • Spleen(2.3)
  • Skin(2.1)

Phenotype-based relationships between genes and organs from Gene ORGANizer for NOD2 Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
Systems:
  • cardiovascular
  • digestive
  • immune
  • integumentary
  • lymphatic
  • nervous
  • reproductive
  • skeletal muscle
  • skeleton
Organs:
Head and neck:
  • brain
  • cranial nerve
  • ear
  • eye
  • face
  • head
  • jaw
  • mandible
  • maxilla
  • meninges
  • mouth
  • neck
  • skull
Thorax:
  • chest wall
  • clavicle
  • esophagus
  • rib
  • rib cage
  • scapula
  • sternum
Abdomen:
  • intestine
  • large intestine
  • small intestine
  • stomach
Pelvis:
  • pelvis
  • penis
  • testicle
  • vagina
Limb:
  • ankle
  • arm
  • digit
  • elbow
  • femur
  • fibula
  • finger
  • foot
  • forearm
  • hand
  • hip
  • humerus
  • knee
  • lower limb
  • radius
  • shin
  • shoulder
  • thigh
  • tibia
  • toe
  • ulna
  • upper limb
  • wrist
General:
  • blood
  • blood vessel
  • bone marrow
  • coagulation system
  • hair
  • peripheral nerve
  • peripheral nervous system
  • skin
  • spinal column
  • spinal cord
  • vertebrae
  • white blood cell
genes like me logo Genes that share expression patterns with NOD2: view

Primer Products

Orthologs for NOD2 Gene

This gene was present in the common ancestor of chordates.

Orthologs for NOD2 Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia NOD2 33 34
  • 99.23 (n)
dog
(Canis familiaris)
Mammalia NOD2 33 34
  • 85.39 (n)
cow
(Bos Taurus)
Mammalia NOD2 33 34
  • 83.55 (n)
mouse
(Mus musculus)
Mammalia Nod2 33 16 34
  • 80.75 (n)
rat
(Rattus norvegicus)
Mammalia Nod2 33
  • 80.69 (n)
oppossum
(Monodelphis domestica)
Mammalia NOD2 34
  • 68 (a)
OneToOne
platypus
(Ornithorhynchus anatinus)
Mammalia NOD2 34
  • 63 (a)
OneToOne
zebrafish
(Danio rerio)
Actinopterygii nod2 33 34
  • 54.42 (n)
Species where no ortholog for NOD2 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • chicken (Gallus gallus)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • fruit fly (Drosophila melanogaster)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • lizard (Anolis carolinensis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • tropical clawed frog (Silurana tropicalis)
  • wheat (Triticum aestivum)
  • worm (Caenorhabditis elegans)

Evolution for NOD2 Gene

ENSEMBL:
Gene Tree for NOD2 (if available)
TreeFam:
Gene Tree for NOD2 (if available)

Paralogs for NOD2 Gene

Variants for NOD2 Gene

Sequence variations from dbSNP and Humsavar for NOD2 Gene

SNP ID Clin Chr 16 pos Sequence Context AA Info Type
rs104895420 untested, Inflammatory bowel disease 1 (IBD1) [MIM:266600] 50,699,883(+) TGGCA(C/T)GGGAG intron-variant, nc-transcript-variant, upstream-variant-2KB, reference, missense, utr-variant-5-prime
rs104895422 untested, Inflammatory bowel disease 1 (IBD1) [MIM:266600] 50,710,614(+) AGTCT(C/T)GCTTC nc-transcript-variant, reference, missense
rs104895423 untested, Inflammatory bowel disease 1 (IBD1) [MIM:266600] 50,710,654(+) CTGCC(G/T)GGAGG nc-transcript-variant, reference, missense
rs104895424 untested, Inflammatory bowel disease 1 (IBD1) [MIM:266600] 50,710,782(+) ATGAC(A/G)ATGCG nc-transcript-variant, reference, missense
rs104895425 untested, Inflammatory bowel disease 1 (IBD1) [MIM:266600] 50,710,792(+) GGACA(C/G)TGTGC nc-transcript-variant, reference, missense

Structural Variations from Database of Genomic Variants (DGV) for NOD2 Gene

Variant ID Type Subtype PubMed ID
esv3638608 CNV gain 21293372

Variation tolerance for NOD2 Gene

Residual Variation Intolerance Score: 97.8% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 4.63; 65.54% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for NOD2 Gene

Human Gene Mutation Database (HGMD)
NOD2
SNPedia medical, phenotypic, and genealogical associations of SNPs for
NOD2

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for NOD2 Gene

Disorders for NOD2 Gene

MalaCards: The human disease database

(52) MalaCards diseases for NOD2 Gene - From: HGMD, OMIM, ClinVar, GeneTests, Swiss-Prot, DISEASES, Novoseek, and GeneCards

Disorder Aliases PubMed IDs
blau syndrome
  • arthrocutaneouveal granulomatosis
yao syndrome
  • yaos
crohn disease-associated growth failure
  • inflammatory bowel disease 1, crohn disease
behcet syndrome
  • behcet's disease
crohn's disease
  • crohn disease
- elite association - COSMIC cancer census association via MalaCards
Search NOD2 in MalaCards View complete list of genes associated with diseases

UniProtKB/Swiss-Prot

NOD2_HUMAN
  • Blau syndrome (BLAUS) [MIM:186580]: An autosomal dominant inflammatory disorder characterized by the formation of immune granulomas invading the skin, joints and eye. Other organs may be involved. Clinical manifestations are variable and include early-onset granulomatous arthritis, uveitis and skin rash. Blindness, joint destruction and visceral involvement have been reported in severe cases. {ECO:0000269 PubMed:11528384, ECO:0000269 PubMed:15459013, ECO:0000269 PubMed:15812565, ECO:0000269 PubMed:19116920, ECO:0000269 PubMed:19169908, ECO:0000269 PubMed:19359344, ECO:0000269 PubMed:19479837, ECO:0000269 PubMed:20199415, ECO:0000269 PubMed:24960071, ECO:0000269 PubMed:25093298, ECO:0000269 PubMed:25692065, ECO:0000269 PubMed:25724124}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Inflammatory bowel disease 1 (IBD1) [MIM:266600]: A chronic, relapsing inflammation of the gastrointestinal tract with a complex etiology. It is subdivided into Crohn disease and ulcerative colitis phenotypes. Crohn disease may affect any part of the gastrointestinal tract from the mouth to the anus, but most frequently it involves the terminal ileum and colon. Bowel inflammation is transmural and discontinuous; it may contain granulomas or be associated with intestinal or perianal fistulas. In contrast, in ulcerative colitis, the inflammation is continuous and limited to rectal and colonic mucosal layers; fistulas and granulomas are not observed. Both diseases include extraintestinal inflammation of the skin, eyes, or joints. {ECO:0000269 PubMed:11385576, ECO:0000269 PubMed:15024686, ECO:0000269 PubMed:16485124, ECO:0000269 PubMed:24790089, ECO:0000269 PubMed:24960071}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
  • Yao syndrome (YAOS) [MIM:617321]: An autoinflammatory disease characterized by periodic fever, dermatitis, polyarthritis, leg swelling, and gastrointestinal and sicca-like symptoms. YAOS is a complex disease with multifactorial inheritance. {ECO:0000269 PubMed:21914217, ECO:0000269 PubMed:26070941}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.

Relevant External Links for NOD2

Genetic Association Database (GAD)
NOD2
Human Genome Epidemiology (HuGE) Navigator
NOD2
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
NOD2
genes like me logo Genes that share disorders with NOD2: view

No data available for Genatlas for NOD2 Gene

Publications for NOD2 Gene

  1. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis. (PMID: 19116920) Okafuji I … Nakahata T (Arthritis and rheumatism 2009) 3 4 22 45 60
  2. Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease. (PMID: 16485124) Schnitzler F … Lohse P (Immunogenetics 2006) 3 4 22 45 60
  3. NOD2 polymorphisms predict severe acute graft-versus-host and treatment-related mortality in T-cell-depleted haematopoietic stem cell transplantation. (PMID: 19219079) van der Velden WJ … Donnelly JP (Bone marrow transplantation 2009) 3 22 45 60
  4. CARD15 gene variants and risk of reoperation in Crohn's disease patients. (PMID: 19638967) Maconi G … Annese V (The American journal of gastroenterology 2009) 3 22 45 60
  5. Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer. (PMID: 19843337) Möckelmann N … Hampe J (BMC gastroenterology 2009) 3 22 45 60

Products for NOD2 Gene

Sources for NOD2 Gene

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