Varaico: Literature-Extracted Genetic Variants

Gene:CXCL16
Variant:p.A181V
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CXCL16

NM_001386809.1:p.A181V

Associated Papers

Involvement of CXCL10 rs4256246, CXCR4 rs2228014, CCR2 rs1799864 and CXCL16 rs2277680 in the Predisposition to Schizophrenia.

Saoud H et al.

Journal of Molecular Neuroscience : Mn, 2024

A Functional Variant of CXCL16 Is Associated With Predisposition to Sepsis and MODS in Trauma Patients: Genetic Association Studies.

Sun J et al.

Frontiers in Genetics, 2021

Human genetic basis of fulminant viral hepatitis.

Jouanguy E

Human Genetics, 2020

Association of NOD1, CXCL16, STAT6 and TLR4 gene polymorphisms with Malaysian patients with Crohn's disease.

Chua KH et al.

Peerj, 2016

CXCL16 haplotypes in patients with human carotid atherosclerosis: preliminary results.

Zivković M et al.

Journal of Atherosclerosis and Thrombosis, 2015

The gender-specific association of CXCL16 A181V gene polymorphism with susceptibility to multiple sclerosis, and its effects on PBMC mRNA and plasma soluble CXCL16 levels: preliminary findings.

Stojković L et al.

Journal of Neurology, 2014

The CXCL16 A181V mutation selectively inhibits monocyte adhesion to CXCR6 but is not associated with human coronary heart disease.

Petit SJ et al.

Arteriosclerosis, Thrombosis, and Vascular Biology, 2011

Chemokine CXC Ligand 16 serum concentration but not A181V genotype is associated with atherosclerotic stroke.

Wang KD et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2010

Atherogenic lipids induce high-density lipoprotein uptake and cholesterol efflux in human macrophages by up-regulating transmembrane chemokine CXCL16 without engaging CXCL16-dependent cell adhesion.

Barlic J et al.

Journal of Immunology (baltimore, Md. : 1950), 2009

rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.

Glas J et al.

The American Journal of Gastroenterology, 2009

Genotype-phenotype analysis of the CXCL16 p.Ala181Val polymorphism in inflammatory bowel disease.

Seiderer J et al.

Clinical Immunology (orlando, Fla.), 2008

Genetic factors for obesity.

Yamada Y et al.

International Journal of Molecular Medicine, 2006

Assessment of genetic factors for type 2 diabetes mellitus.

Yamada Y et al.

International Journal of Molecular Medicine, 2006

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."