MAVS Gene

Mitochondrial Antiviral Signaling Protein (MAVS) is a gene involved in RLR signaling that has been studied in relation to immune function, metabolism, and chronic illness. Variants in MAVS 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 MAVS gene?

MAVS encodes mitochondrial antiviral signaling protein, a protein involved in RLR signaling. It belongs to the Innate Immunity category and is part of the Innate Immunity & Interferons biological cluster. MAVS is the mitochondrial outer membrane adaptor protein that aggregates upon RIG-I or MDA5 activation, serving as a signaling platform for IRF3/IRF7 and NF-κB activation. MAVS aggregates are prion-like and self-amplifying.

Biological role and pathway

MAVS is involved in the RLR signaling pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Innate Immunity & Interferons 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.

MAVS and Long COVID / ME-CFS research

SARS-CoV-2 protease NSP3 cleaves MAVS to evade antiviral immunity. MAVS variants affecting aggregation dynamics or cleavage susceptibility may alter the efficiency of initial SARS-CoV-2 interferon induction relevant to Long COVID pathogenesis.

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

Conditions studied in relation to MAVS

Research into MAVS variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that MAVS 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 MAVS and related genes in the innate immunity & interferons 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 Innate Immunity & Interferons pathway

MAVS 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 MAVS gene and what does it do?

MAVS (Mitochondrial Antiviral Signaling Protein) is involved in RLR signaling. MAVS is the mitochondrial outer membrane adaptor protein that aggregates upon RIG-I or MDA5 activation, serving as a signaling platform for IRF3/IRF7 and NF-κB activation. MAVS aggregates are prion-like and self-amplifying.

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

SARS-CoV-2 protease NSP3 cleaves MAVS to evade antiviral immunity. MAVS variants affecting aggregation dynamics or cleavage susceptibility may alter the efficiency of initial SARS-CoV-2 interferon induction relevant to Long COVID pathogenesis.

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

  • [1]PMID: 33514933
  • [2]Cell
  • [3]Science