Varaico: Literature-Extracted Genetic Variants

Gene:NOD1
Variant:p.E266K
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NOD1

NM_006092.4:p.E266K

Associated Papers

Human iPSC-based breast cancer model identifies S100P-dependent cancer stemness induced by BRCA1 mutation.

Liu J et al.

Science Advances, 2025

40712032 (PubMed )
Supplement: sciadv.adi2370_tables_s8_and_s9.zip › adi2370_table_s9.xlsx › BRCA1-mutant_corrected_iPSC

NOD1 and NOD2 genetic variants: Impact on hepatocellular carcinoma susceptibility and progression in Moroccan population.

Zerrad C et al.

Gene, 2024

Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.

Villa M et al.

British Journal of Cancer, 2024

39478125 (PubMed )
Supplement: 41416_2024_2881_MOESM1_ESM.pdf

Association between genetic polymorphisms of NOD1, Interleukin-1B, and cagA strain with low-grade duodenal eosinophilia in Helicobacter pylori-related dyspepsia.

Barreyro FJ et al.

Helicobacter, 2023

Association of NOD1 and NOD2 Polymorphisms With Susceptibility to Subacute Sclerosing Panencephalitis.

Kocaaga A et al.

Journal of Child Neurology, 2023

Nucleotide oligomerization domain polymorphism confers no risk to Guillain-Barré syndrome.

Hayat S et al.

Acta Neurologica Scandinavica, 2022

Association of NOD1, NOD2, PYDC1 and PYDC2 genes with Behcet's disease susceptibility and clinical manifestations.

Kocaaga A et al.

Ophthalmic Genetics, 2021

NOD1 rs2075820 (p.E266K) polymorphism is associated with gastric cancer among individuals infected with cagPAI-positive H. pylori.

Gonzalez-Hormazabal P et al.

Biological Research, 2021

A novel mutation in early-onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes.

Okazaki F et al.

Pediatric Rheumatology Online Journal, 2021

Pattern recognition receptor polymorphisms in early periodontitis.

Leite FRM et al.

Journal of Periodontology, 2019

Gene Variants, mRNA and NOD1/2 Protein Levels in Tunisian Childhood Asthma.

Belhaj R et al.

Lung, 2019

The different roles of innate immune receptors in inflammation and carcinogenesis between races.

Yamaguchi N et al.

Environmental Health and Preventive Medicine, 2017

Homology modeling and in silico prediction of Ulcerative colitis associated polymorphisms of NOD1.

Majumdar I et al.

Molecular and Cellular Probes, 2017

Effects of genetic variations in the genes encoding NOD1 and NOD2 on type 2 diabetes mellitus and insulin resistance.

Ozbayer C et al.

Journal of Clinical Pharmacy and Therapeutics, 2017

NOD1CARD Might Be Using Multiple Interfaces for RIP2-Mediated CARD-CARD Interaction: Insights from Molecular Dynamics Simulation.

Maharana J et al.

Plos One, 2017

Role of nucleotide-binding oligomerization domain 1 (NOD1) and its variants in human cytomegalovirus control in vitro and in vivo.

Fan YH et al.

Proceedings of the National Academy of Sciences of the United States of America, 2016

Association of NOD1 and NOD2 polymorphisms with Guillain-Barré syndrome in Northern Indian population.

Kharwar NK et al.

Journal of the Neurological Sciences, 2016

The role of NOD1/CARD4 and NOD2/CARD15 genetic variations in lung cancer risk.

Ozbayer C et al.

Inflammation Research : Official Journal of the European Histamine Research Society ... [et Al.], 2015

NOD1 and NOD2 Genetic Variants in Association with Risk of Gastric Cancer and Its Precursors in a Chinese Population.

Li ZX et al.

Plos One, 2015

The nucleotide-binding oligomerization domain-containing protein 1 (NOD1) polymorphism S7N does not affect receptor function.

Mayle S et al.

Bmc Research Notes, 2014

The genetics of innate immunity sensors and human disease.

Pothlichet J et al.

International Reviews of Immunology, 2013

Effects of polymorphisms in nucleotide-binding oligomerization domains 1 and 2 on biomarkers of the metabolic syndrome and type II diabetes.

Cuda C et al.

Genes & Nutrition, 2012

Association of NOD1 and NOD2 genes polymorphisms with Helicobacter pylori related gastric cancer in a Chinese population.

Wang P et al.

World Journal of Gastroenterology, 2012

Structure and functional characterization of the RNA-binding element of the NLRX1 innate immune modulator.

Hong M et al.

Immunity, 2012

Variants of NOD1 and NOD2 genes display opposite associations with familial risk of Crohn's disease and anti-saccharomyces cerevisiae antibody levels.

Vasseur F et al.

Inflammatory Bowel Diseases, 2012

Lack of association between gene polymorphisms of Angiotensin converting enzyme, Nod-like receptor 1, Toll-like receptor 4, FAS/FASL and the presence of Helicobacter pylori-induced premalignant gastric lesions and gastric cancer in Caucasians.

Kupcinskas J et al.

Bmc Medical Genetics, 2011

[Barrier- and autophagic functions of the intestinal epithelia: role of disturbances in the pathogenesis of Crohn's disease].

Lapis K

Orvosi Hetilap, 2010

The significance of E266K polymorphism in the NOD1 gene on Helicobacter pylori infection: an effective force on pathogenesis?

Kara B et al.

Clinical and Experimental Medicine, 2010

Relevance of the genetic polymorphism of NOD1 in Chlamydia pneumoniae seropositive stroke patients.

Tiszlavicz Z et al.

European Journal of Neurology, 2009

Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer.

Möckelmann N et al.

Bmc Gastroenterology, 2009

No involvement of the NOD1 polymorphism Glu266Lys in Japanese leprosy patients.

Li HJ et al.

Journal of Dermatological Science, 2009

Frequency of single nucleotide polymorphisms in NOD1 gene of ulcerative colitis patients: a case-control study in the Indian population.

Verma R et al.

Bmc Medical Genetics, 2009

[Genetic involvement of bacterial sensor molecules in Japanese leprosy].

Kanazawa N et al.

Nihon Hansenbyo Gakkai Zasshi = Japanese Journal of Leprosy : Official Organ of the Japanese Leprosy Association, 2009

Multiple sclerosis and polymorphisms of innate pattern recognition receptors TLR1-10, NOD1-2, DDX58, and IFIH1.

Enevold C et al.

Journal of Neuroimmunology, 2009

Nucleotide-binding oligomerization domain containing 1 (NOD1) haplotypes and single nucleotide polymorphisms modify susceptibility to inflammatory bowel diseases in a New Zealand caucasian population: a case-control study.

Huebner C et al.

Bmc Research Notes, 2009

Interaction between seroreactivity to microbial antigens and genetics in Crohn's disease: is there a role for defensins?

Lakatos PL et al.

Tissue Antigens, 2008

NOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease.

Molnar T et al.

Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 2007

Genetic polymorphisms of NOD1 and IL-8, but not polymorphisms of TLR4 genes, are associated with Helicobacter pylori-induced duodenal ulcer and gastritis.

Hofner P et al.

Helicobacter, 2007

Complex insertion/deletion polymorphism in NOD1 (CARD4) is not associated with inflammatory bowel disease susceptibility in East Anglia panel.

Tremelling M et al.

Inflammatory Bowel Diseases, 2006

Sarcoidosis and NOD1 variation with impaired recognition of intracellular Propionibacterium acnes.

Tanabe T et al.

Biochimica Et Biophysica Acta, 2006

NOD2/CARD15, NOD1/CARD4, and ICAM-1 gene polymorphisms in Turkish patients with inflammatory bowel disease.

Ozen SC et al.

Journal of Gastroenterology, 2006

Association between a complex insertion/deletion polymorphism in NOD1 (CARD4) and susceptibility to inflammatory bowel disease.

McGovern DP et al.

Human Molecular Genetics, 2005

Visceral manifestations in hereditary haemorrhagic telangiectasia type 2.

Abdalla SA et al.

Journal of Medical Genetics, 2003

[Analysis of polymorphisms on Lewis blood group antigen related SE gene in the populations in Shandong with high-risk of gastric cancer and Beijing].

Jiang JM et al.

Yi Chuan = Hereditas, 2003

CARD4/NOD1 is not involved in inflammatory bowel disease.

Zouali H et al.

Gut, 2003

[Association of polymorphisms in toll-like receptor genes with atopic dermatitis in the Republic of Bashkortostan].

Gimalova GF et al.

Molekuliarnaia Biologiia, 0

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