SLC25A37 Gene

Solute Carrier Family 25 Member 37 (Mitoferrin-1) (SLC25A37) is a gene involved in mitochondrial iron import that has been studied in relation to immune function, metabolism, and chronic illness. Variants in SLC25A37 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 SLC25A37 gene?

SLC25A37 encodes solute carrier family 25 member 37 (mitoferrin-1), a protein involved in mitochondrial iron import. It belongs to the Metabolic category and is part of the Mitochondrial Energy Production & PEM biological cluster. SLC25A37 encodes mitoferrin-1, the mitochondrial inner membrane iron transporter essential for heme and iron-sulfur cluster biosynthesis in erythroid cells.

Biological role and pathway

SLC25A37 is involved in the mitochondrial iron import pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Mitochondrial Energy Production & PEM 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.

SLC25A37 and Long COVID / ME-CFS research

Mitochondrial iron import for heme synthesis is critical for erythropoiesis; variants may affect red blood cell production and hemoglobin synthesis impaired in Long COVID anemia.

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 SLC25A37 gene have been studied in relation to metabolic and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.

Conditions studied in relation to SLC25A37

Research into SLC25A37 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that SLC25A37 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 SLC25A37 and related genes in the mitochondrial energy production & pem 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 Energy Production & PEM pathway

SLC25A37 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 SLC25A37 gene and what does it do?

SLC25A37 (Solute Carrier Family 25 Member 37 (Mitoferrin-1)) is involved in mitochondrial iron import. SLC25A37 encodes mitoferrin-1, the mitochondrial inner membrane iron transporter essential for heme and iron-sulfur cluster biosynthesis in erythroid cells.

How may SLC25A37 gene variants relate to Long COVID or ME/CFS?

Mitochondrial iron import for heme synthesis is critical for erythropoiesis; variants may affect red blood cell production and hemoglobin synthesis impaired in Long COVID anemia.

Can a DNA test reveal information about my SLC25A37 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 SLC25A37 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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Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for SLC25A37. This is not an exhaustive literature review.

  • [1]PMID: 34316049
  • [2]Nature Genetics
  • [3]Blood