RAMP1 Gene

Receptor Activity Modifying Protein 1 (RAMP1) is a gene involved in CGRP receptor / migraine that has been studied in relation to immune function, metabolism, and chronic illness. Variants in RAMP1 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 RAMP1 gene?

RAMP1 encodes receptor activity modifying protein 1, a protein involved in CGRP receptor / migraine. It belongs to the Neurological category and is part of the Neurological & Cognitive Function biological cluster. RAMP1 encodes a receptor accessory protein that forms the CGRP receptor with CALCRL; it is required for high-affinity CGRP binding and migraine signaling.

Biological role and pathway

RAMP1 is involved in the CGRP receptor / migraine pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Neurological & Cognitive Function 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.

RAMP1 and Long COVID / ME-CFS research

RAMP1/CALCRL CGRP receptor mediates headache and migraine; RAMP1 variants may affect CGRP sensitivity and susceptibility to the migraine and headache phenotype of 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 RAMP1 gene have been studied in relation to neurological and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.

Conditions studied in relation to RAMP1

Research into RAMP1 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that RAMP1 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 RAMP1 and related genes in the neurological & cognitive function 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 & Cognitive Function pathway

RAMP1 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 RAMP1 gene and what does it do?

RAMP1 (Receptor Activity Modifying Protein 1) is involved in CGRP receptor / migraine. RAMP1 encodes a receptor accessory protein that forms the CGRP receptor with CALCRL; it is required for high-affinity CGRP binding and migraine signaling.

How may RAMP1 gene variants relate to Long COVID or ME/CFS?

RAMP1/CALCRL CGRP receptor mediates headache and migraine; RAMP1 variants may affect CGRP sensitivity and susceptibility to the migraine and headache phenotype of Long COVID.

Can a DNA test reveal information about my RAMP1 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 RAMP1 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 RAMP1. This is not an exhaustive literature review.

  • [1]PMID: 33664986
  • [2]Nature Genetics
  • [3]Cephalalgia