CLDN5 Gene
Claudin 5 (CLDN5) is a gene involved in tight junction / blood-brain barrier integrity that has been studied in relation to immune function, metabolism, and chronic illness. Variants in CLDN5 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 CLDN5 gene?
CLDN5 encodes claudin 5, a protein involved in tight junction / blood-brain barrier integrity. It belongs to the Vascular category and is part of the Coagulation & Microcirculation biological cluster. CLDN5 encodes claudin-5, a critical tight junction protein at the blood-brain barrier that restricts paracellular passage.
Biological role and pathway
CLDN5 is involved in the tight junction / blood-brain barrier integrity pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Coagulation & Microcirculation 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.
CLDN5 and Long COVID / ME-CFS research
Blood-brain barrier disruption in Long COVID may involve claudin-5 downregulation; CLDN5 variants may affect BBB integrity and susceptibility to neurological complications.
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 CLDN5 gene have been studied in relation to vascular and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs6539267— CLDN5 variant
Conditions studied in relation to CLDN5
Research into CLDN5 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that CLDN5 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 CLDN5 and related genes in the coagulation & microcirculation 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 & Microcirculation pathway
CLDN5 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 CLDN5 gene and what does it do?
CLDN5 (Claudin 5) is involved in tight junction / blood-brain barrier integrity. CLDN5 encodes claudin-5, a critical tight junction protein at the blood-brain barrier that restricts paracellular passage.
How may CLDN5 gene variants relate to Long COVID or ME/CFS?
Blood-brain barrier disruption in Long COVID may involve claudin-5 downregulation; CLDN5 variants may affect BBB integrity and susceptibility to neurological complications.
Can a DNA test reveal information about my CLDN5 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 CLDN5 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 ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for CLDN5. This is not an exhaustive literature review.
- [1]PMID: 33664986
- [2]Nature Neuroscience
- [3]Journal of Neuroinflammation