TBXA2R Gene

Thromboxane A2 Receptor (TBXA2R) is a gene involved in platelet activation that has been studied in relation to immune function, metabolism, and chronic illness. Variants in TBXA2R 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 TBXA2R gene?

TBXA2R encodes thromboxane a2 receptor, a protein involved in platelet activation. It belongs to the Coagulation category and is part of the Coagulation & Vascular biological cluster. TBXA2R mediates platelet aggregation, vasoconstriction, and bronchoconstriction in response to thromboxane A2 produced by COX enzymes. Variants affect aspirin antiplatelet efficacy and platelet responsiveness.

Biological role and pathway

TBXA2R is involved in the platelet activation 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.

TBXA2R and Long COVID / ME-CFS research

TXA2-mediated platelet activation contributes to COVID-19-associated thrombosis. TBXA2R variants affecting platelet TXA2 responsiveness may influence the degree of platelet hyperactivation and microthrombi formation in Long COVID coagulopathy.

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 TBXA2R gene have been studied in relation to coagulation and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.

Conditions studied in relation to TBXA2R

Research into TBXA2R variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that TBXA2R 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 TBXA2R 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

TBXA2R 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 TBXA2R gene and what does it do?

TBXA2R (Thromboxane A2 Receptor) is involved in platelet activation. TBXA2R mediates platelet aggregation, vasoconstriction, and bronchoconstriction in response to thromboxane A2 produced by COX enzymes. Variants affect aspirin antiplatelet efficacy and platelet responsiveness.

How may TBXA2R gene variants relate to Long COVID or ME/CFS?

TXA2-mediated platelet activation contributes to COVID-19-associated thrombosis. TBXA2R variants affecting platelet TXA2 responsiveness may influence the degree of platelet hyperactivation and microthrombi formation in Long COVID coagulopathy.

Can a DNA test reveal information about my TBXA2R 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 TBXA2R 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 TBXA2R. This is not an exhaustive literature review.

  • [1]PMID: 27568270
  • [2]Arteriosclerosis Thrombosis and Vascular Biology
  • [3]Journal of Thrombosis and Haemostasis