CRY1 Gene

Cryptochrome Circadian Regulator 1 (CRY1) is a gene involved in circadian clock that has been studied in relation to immune function, metabolism, and chronic illness. Variants in CRY1 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 CRY1 gene?

CRY1 encodes cryptochrome circadian regulator 1, a protein involved in circadian clock. It belongs to the Circadian Rhythm category and is part of the Neurological & Sleep biological cluster. CRY1 encodes a flavoprotein that functions as a transcriptional repressor in the circadian negative feedback loop. CRY1 gain-of-function variants are a cause of familial delayed sleep phase disorder.

Biological role and pathway

CRY1 is involved in the circadian clock pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Neurological & Sleep 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.

CRY1 and Long COVID / ME-CFS research

CRY1 variants affecting sleep phase and duration influence recovery capacity in chronic illness. Circadian rhythm disturbances are prominent in ME/CFS and Long COVID, and CRY1 polymorphisms may contribute to persistent sleep abnormalities.

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 CRY1 gene have been studied in relation to circadian rhythm and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.

Conditions studied in relation to CRY1

Research into CRY1 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that CRY1 causes or treats any condition.

Long CovidSleep DisorderCircadian DisruptionChronic Fatigue

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 CRY1 and related genes in the neurological & sleep 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 Neurological & Sleep pathway

CRY1 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 CRY1 gene and what does it do?

CRY1 (Cryptochrome Circadian Regulator 1) is involved in circadian clock. CRY1 encodes a flavoprotein that functions as a transcriptional repressor in the circadian negative feedback loop. CRY1 gain-of-function variants are a cause of familial delayed sleep phase disorder.

How may CRY1 gene variants relate to Long COVID or ME/CFS?

CRY1 variants affecting sleep phase and duration influence recovery capacity in chronic illness. Circadian rhythm disturbances are prominent in ME/CFS and Long COVID, and CRY1 polymorphisms may contribute to persistent sleep abnormalities.

Can a DNA test reveal information about my CRY1 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 CRY1 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 CRY1. This is not an exhaustive literature review.

  • [1]PMID: 28041889
  • [2]Cell
  • [3]Journal of Clinical Investigation