CYP7A1 Gene
Cytochrome P450 Family 7 Subfamily A Member 1 (CYP7A1) is a gene involved in bile acid synthesis that has been studied in relation to immune function, metabolism, and chronic illness. Variants in CYP7A1 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 CYP7A1 gene?
CYP7A1 encodes cytochrome p450 family 7 subfamily a member 1, a protein involved in bile acid synthesis. It belongs to the Metabolism category and is part of the Mitochondrial & Metabolic biological cluster. CYP7A1 (cholesterol 7α-hydroxylase) catalyzes the rate-limiting step in the classical bile acid synthesis pathway, converting cholesterol to 7α-hydroxycholesterol. It is regulated by FXR, LXR, and thyroid hormone.
Biological role and pathway
CYP7A1 is involved in the bile acid synthesis pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Mitochondrial & Metabolic 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.
CYP7A1 and Long COVID / ME-CFS research
Bile acid metabolism is disrupted in COVID-19 liver disease, and bile acids regulate immune function through FXR. CYP7A1 promoter variants affecting bile acid synthesis rate may influence liver disease severity and FXR-mediated immune regulation relevant to 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 CYP7A1 gene have been studied in relation to metabolism and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
Conditions studied in relation to CYP7A1
Research into CYP7A1 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that CYP7A1 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 CYP7A1 and related genes in the mitochondrial & metabolic 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 Mitochondrial & Metabolic pathway
CYP7A1 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 CYP7A1 gene and what does it do?
CYP7A1 (Cytochrome P450 Family 7 Subfamily A Member 1) is involved in bile acid synthesis. CYP7A1 (cholesterol 7α-hydroxylase) catalyzes the rate-limiting step in the classical bile acid synthesis pathway, converting cholesterol to 7α-hydroxycholesterol. It is regulated by FXR, LXR, and thyroid hormone.
How may CYP7A1 gene variants relate to Long COVID or ME/CFS?
Bile acid metabolism is disrupted in COVID-19 liver disease, and bile acids regulate immune function through FXR. CYP7A1 promoter variants affecting bile acid synthesis rate may influence liver disease severity and FXR-mediated immune regulation relevant to Long COVID.
Can a DNA test reveal information about my CYP7A1 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 CYP7A1 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 CYP7A1. This is not an exhaustive literature review.
- [1]PMID: 25556481
- [2]Journal of Lipid Research
- [3]Cell Metabolism