NOD2
protein-coding gene in the species Homo sapiens
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NOD2
Summary
NOD2 is a gene[1].
Key Facts
- NOD2's instance of is recorded as gene[2].
- NOD2 is a type of protein-coding gene[3].
- NOD2's HomoloGene ID is recorded as 11156[4].
- NOD2's genomic start is recorded as 50727514[5].
- NOD2's genomic start is recorded as 50693588[6].
- NOD2's genomic end is recorded as 50766988[7].
- NOD2's genomic end is recorded as 50734041[8].
- NOD2's ortholog is recorded as Nod2[9].
- NOD2's ortholog is recorded as Nod2[10].
- NOD2's ortholog is recorded as nod2[11].
- NOD2's encodes is recorded as Nucleotide binding oligomerization domain containing 2[12].
- NOD2's encodes is recorded as Nucleotide-binding oligomerization domain-containing protein 2[13].
- NOD2's found in taxon is recorded as Homo sapiens[14].
- NOD2's chromosome is recorded as human chromosome 16[15].
- NOD2's gene insertion association with is recorded as Crohn's disease[16].
- NOD2's genetic association is recorded as Crohn's disease[17].
- NOD2's genetic association is recorded as inflammatory bowel diseases[18].
- NOD2's genetic association is recorded as Blau syndrome[19].
- NOD2's genetic association is recorded as enteritis[20].
- NOD2's genetic association is recorded as ulcerative colitis[21].
- NOD2's strand orientation is recorded as forward strand[22].
- NOD2's exact match is recorded as http://identifiers.org/ncbigene/64127[23].
- NOD2's cytogenetic location is recorded as 16q12.1[24].
- NOD2's expressed in is recorded as monocyte[25].
- NOD2's expressed in is recorded as granulocyte[26].