Homo sapiens nucleotide binding oligomerization domain containing 2 (N - Nucleotide

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Identifying functional dysregulation of NOD2 variant Q902K in patients with Yao syndrome. [Arthritis Res Ther. 2024]
Identifying functional dysregulation of NOD2 variant Q902K in patients with Yao syndrome.
Zhang J, Luo Y, Wu B, Huang X, Zhao M, Wu N, Miao J, Li J, Zhu L, Wu D, et al. Arthritis Res Ther. 2024 Feb 23; 26(1):58. Epub 2024 Feb 23.
The expanding clinical spectrum of autoinflammatory diseases with NOD2 variants: a case series and literature review. [Front Immunol. 2024]
The expanding clinical spectrum of autoinflammatory diseases with NOD2 variants: a case series and literature review.
Karamanakos A, Vougiouka O, Sapountzi E, Venetsanopoulou AI, Tektonidou MG, Germenis AE, Sfikakis PP, Laskari K. Front Immunol. 2024; 15:1342668. Epub 2024 Jan 29.
Distinct NOD2 mutations reported in three families with Blau syndrome (BS) from a single center in India - Case series and review of literature. [Clin Immunol. 2023]
Distinct NOD2 mutations reported in three families with Blau syndrome (BS) from a single center in India - Case series and review of literature.
Baisya R, Manthri R, Tyagi M, Uppin SG, Rajasekhar L. Clin Immunol. 2023 Oct; 255:109743. Epub 2023 Aug 20.

RefSeq alternative splicing
See 27 reference mRNA sequence splice variants for the NOD2 gene.
RefSeq protein product
See the reference protein sequence for nucleotide-binding oligomerization domain-containing protein 2 isoform 2 (NP_001357395.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
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Nucleotide