F13A1 Gene
Coagulation Factor XIII A Chain (F13A1) is a gene involved in fibrin crosslinking that has been studied in relation to immune function, metabolism, and chronic illness. Variants in F13A1 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 F13A1 gene?
F13A1 encodes coagulation factor xiii a chain, a protein involved in fibrin crosslinking. It belongs to the Coagulation category and is part of the Coagulation & Vascular biological cluster. Factor XIII (FXIII) crosslinks fibrin to form a stable clot and protects fibrin from fibrinolysis. The Val34Leu (rs5985) polymorphism affects FXIII activation rate by thrombin.
Biological role and pathway
F13A1 is involved in the fibrin crosslinking 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.
F13A1 and Long COVID / ME-CFS research
FXIII-crosslinked fibrin is resistant to fibrinolysis. Variants affecting FXIII crosslinking efficiency may influence the density of microthrombi in Long COVID. The Val34Leu variant paradoxically reduces fibrin stability and may be protective against microthrombi 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 F13A1 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 F13A1
Research into F13A1 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that F13A1 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 F13A1 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
F13A1 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 F13A1 gene and what does it do?
F13A1 (Coagulation Factor XIII A Chain) is involved in fibrin crosslinking. Factor XIII (FXIII) crosslinks fibrin to form a stable clot and protects fibrin from fibrinolysis. The Val34Leu (rs5985) polymorphism affects FXIII activation rate by thrombin.
How may F13A1 gene variants relate to Long COVID or ME/CFS?
FXIII-crosslinked fibrin is resistant to fibrinolysis. Variants affecting FXIII crosslinking efficiency may influence the density of microthrombi in Long COVID. The Val34Leu variant paradoxically reduces fibrin stability and may be protective against microthrombi in Long COVID.
Can a DNA test reveal information about my F13A1 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 F13A1 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 F13A1. This is not an exhaustive literature review.
- [1]PMID: 27162290
- [2]Blood
- [3]Thrombosis and Haemostasis