PECAM1 Gene
Platelet And Endothelial Cell Adhesion Molecule 1 (PECAM1) is a gene involved in endothelial junction that has been studied in relation to immune function, metabolism, and chronic illness. Variants in PECAM1 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 PECAM1 gene?
PECAM1 encodes platelet and endothelial cell adhesion molecule 1, a protein involved in endothelial junction. It belongs to the Cell Adhesion category and is part of the Coagulation & Vascular biological cluster. PECAM-1 (CD31) mediates leukocyte transendothelial migration through homophilic interactions at endothelial cell junctions. It also provides anti-apoptotic and anti-thrombotic signals in endothelial cells.
Biological role and pathway
PECAM1 is involved in the endothelial junction 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.
PECAM1 and Long COVID / ME-CFS research
PECAM-1 is expressed on endothelium, platelets, and monocytes, integrating coagulation and inflammation. Variants in PECAM1 affect leukocyte transendothelial migration and endothelial survival, potentially influencing vascular integrity in Long COVID.
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 PECAM1 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 PECAM1
Research into PECAM1 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that PECAM1 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 PECAM1 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
PECAM1 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 PECAM1 gene and what does it do?
PECAM1 (Platelet And Endothelial Cell Adhesion Molecule 1) is involved in endothelial junction. PECAM-1 (CD31) mediates leukocyte transendothelial migration through homophilic interactions at endothelial cell junctions. It also provides anti-apoptotic and anti-thrombotic signals in endothelial cells.
How may PECAM1 gene variants relate to Long COVID or ME/CFS?
PECAM-1 is expressed on endothelium, platelets, and monocytes, integrating coagulation and inflammation. Variants in PECAM1 affect leukocyte transendothelial migration and endothelial survival, potentially influencing vascular integrity in Long COVID.
Can a DNA test reveal information about my PECAM1 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 PECAM1 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.
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References
The following publications were used in compiling the research context for PECAM1. This is not an exhaustive literature review.
- [1]PMID: 28286069
- [2]Arteriosclerosis Thrombosis and Vascular Biology
- [3]Journal of Clinical Investigation