UGT2B17 Gene
UDP Glucuronosyltransferase Family 2 Member B17 (UGT2B17) is a gene involved in androgen glucuronidation that has been studied in relation to immune function, metabolism, and chronic illness. Variants in UGT2B17 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 UGT2B17 gene?
UGT2B17 encodes udp glucuronosyltransferase family 2 member b17, a protein involved in androgen glucuronidation. It belongs to the Pharmacogenomics category and is part of the Detox & Medication Sensitivity biological cluster. UGT2B17 encodes a glucuronosyltransferase that conjugates androgens and some NSAIDs for excretion.
Biological role and pathway
UGT2B17 is involved in the androgen glucuronidation pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Detox & Medication Sensitivity 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.
UGT2B17 and Long COVID / ME-CFS research
UGT2B17 deletion variants affect androgen clearance; altered sex hormone levels may influence immune function and symptom severity 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 UGT2B17 gene have been studied in relation to pharmacogenomics and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs59678213— UGT2B17 variant
Conditions studied in relation to UGT2B17
Research into UGT2B17 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that UGT2B17 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 UGT2B17 and related genes in the detox & medication sensitivity 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 Detox & Medication Sensitivity pathway
UGT2B17 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 UGT2B17 gene and what does it do?
UGT2B17 (UDP Glucuronosyltransferase Family 2 Member B17) is involved in androgen glucuronidation. UGT2B17 encodes a glucuronosyltransferase that conjugates androgens and some NSAIDs for excretion.
How may UGT2B17 gene variants relate to Long COVID or ME/CFS?
UGT2B17 deletion variants affect androgen clearance; altered sex hormone levels may influence immune function and symptom severity in Long COVID.
Can a DNA test reveal information about my UGT2B17 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 UGT2B17 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 UGT2B17. This is not an exhaustive literature review.
- [1]PMID: 32296168
- [2]Nature Genetics
- [3]Drug Metabolism and Disposition