SELE Gene

Selectin E (SELE) is a gene involved in leukocyte rolling that has been studied in relation to immune function, metabolism, and chronic illness. Variants in SELE may influence how the body responds to infection, inflammation, and long-term recovery.

This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.

What is the SELE gene?

SELE encodes selectin e, a protein involved in leukocyte rolling. It belongs to the Cell Adhesion category and is part of the Coagulation & Vascular biological cluster. E-selectin (CD62E) mediates the initial tethering and rolling of leukocytes on activated endothelium during acute inflammation. It is induced by cytokines and is stored with von Willebrand factor in Weibel-Palade bodies.

Biological role and pathway

SELE is involved in the leukocyte rolling pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Coagulation & Vascular cluster work together to maintain balanced function across interconnected biological systems.

Variants in genes within this pathway may influence an individual's predisposition to altered function in these systems — particularly under conditions of physiological stress such as viral infection or prolonged illness.

SELE and Long COVID / ME-CFS research

E-selectin is elevated in COVID-19 endothelial activation and contributes to the leukocyte trafficking underlying vascular inflammation. SELE variants (Ser128Arg) are associated with acute coronary syndromes; elevated E-selectin in Long COVID may indicate sustained endothelial activation.

This information is based on published research and does not constitute medical advice. See references below.

Known genetic variants

The following variants (SNPs) in the SELE gene have been studied in relation to cell adhesion and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.

Conditions studied in relation to SELE

Research into SELE variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that SELE causes or treats any condition.

Genetic insights from DNA data

Consumer DNA files from 23andMe, AncestryDNA, and MyHeritage contain raw SNP data. When you upload your file to ChronicDNA, the analysis engine checks your genotype against a curated panel of 80+ genes selected for their relevance to Long COVID, ME/CFS, and connected biological pathways - some of which may include SELE and related genes in the coagulation & vascular pathway.

The report is educational - it explains which variants you carry, what the research says about them, and how they fit into the biological pathways most relevant to chronic illness. Results are presented in plain English with appropriate scientific context, no medical jargon, no scare tactics. All results should be discussed with a qualified healthcare provider.

Related genes in the Coagulation & Vascular pathway

SELE does not act in isolation. The following genes are functionally related and may be analysed together for a more complete picture of your genetic predispositions.

Frequently asked questions

What is the SELE gene and what does it do?

SELE (Selectin E) is involved in leukocyte rolling. E-selectin (CD62E) mediates the initial tethering and rolling of leukocytes on activated endothelium during acute inflammation. It is induced by cytokines and is stored with von Willebrand factor in Weibel-Palade bodies.

How may SELE gene variants relate to Long COVID or ME/CFS?

E-selectin is elevated in COVID-19 endothelial activation and contributes to the leukocyte trafficking underlying vascular inflammation. SELE variants (Ser128Arg) are associated with acute coronary syndromes; elevated E-selectin in Long COVID may indicate sustained endothelial activation.

Can a DNA test reveal information about my SELE gene?

Consumer DNA data from 23andMe, AncestryDNA, and MyHeritage includes SNP variants for many genes. ChronicDNA analyses your raw DNA file and reports on variants that have been studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.

Explore your SELE genetic insights

Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.

Get Your Personalised DNA Report

Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for SELE. This is not an exhaustive literature review.

  • [1]PMID: 29445268
  • [2]Nature Reviews Immunology
  • [3]Arteriosclerosis Thrombosis and Vascular Biology