NOD2
protein-coding gene in the species Homo sapiens
Facts
14 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 16[12]
- Cytogenetic location
- 16q12.1[20]
- Encodes
- Nucleotide binding oligomerization domain containing 2, Nucleotide-binding oligomerization domain-containing protein 2[9][10]
- Expressed in
- monocyte, granulocyte, blood, skin of leg, skin of abdomen, vulva, human penis, cartilage tissue, bone marrow cell, vagina[21][22][23][24][25][26][27][28][29][30]
- Found in taxon
- Homo sapiens[11]
- Gene insertion association with
- Crohn's disease[13]
- Genetic association
- Crohn's disease, inflammatory bowel diseases, Blau syndrome, enteritis, ulcerative colitis[14][15][16][17][18]
- HomoloGene ID
- 11156[3]
- Strand orientation
- forward strand[19]
🏷️ Also known as
en ACUG
en BLAU
en BLAUS
en CARD15
en CD
en CLR16.3
en IBD1
en NLRC2
en NOD2
en NOD2B
en nucleotide binding oligomerization domain containing 2
en PSORAS1
en YAOS
🔖 Identifiers · 10
- Image (Wikimedia Commons)
- NOD2 protein.png ↗
- Ensembl gene ID
- ENSG00000167207
- Ensembl transcript ID
- ENST00000534067, ENST00000300589, ENST00000524712, ENST00000526417, ENST00000527052, ENST00000527070, ENST00000529633, ENST00000531674, ENST00000532206, ENST00000534057, ENST00000641284, ENST00000647318, ENST00000646677
- Entrez Gene ID
- 64127
- Exact match
- identifiers.org
- HGNC ID
- 5331
- HGNC gene symbol
- NOD2
- OMIM ID
- 605956
- RefSeq RNA ID
- XR_933387, NM_001293557, NM_022162, XM_006721242, XM_006721243, XM_011523259, XM_011523260, XM_011523261, XR_429725, XR_429726, XM_017023535, XM_017023536, XM_017023537, XM_017023538, NM_001370466, NR_163434
- UMLS CUI
- C1826449
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