There is currently no genetic test available to predict which people are likely to develop ME/CFS. A number of studies have found a combination of several different genes to be more common in people with ME/CFS.
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- Acid sensing ion channel 3 (ASIC3) research
- Purinergic receptor P2 4 (P2RX4, P2RX4 or purinergic receptor P2 X, ligand-gated ion channel 4) research
- Transient receptor potential vanilloid receptor 1 (TRPV1, Transient receptor potential cation channel subfamily V member 1) research
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Angiotensin I converting enzyme II, Angiotensin-converting enzyme, Ankyrin Repeat And Death Domain Containing 1B, Armadillo Like Helical Domain Containing 4, ATP-Dependent RNA Helicase DDX51, Brain-derived neurotrophic factor, CD1d, CD24, COMT, COX, Cystathionine beta synthase, Cytochrome P450 2D6, Gene expression, Genetic testing, Histamine N-methyltransferase, Human leukocyte antigen genes, Indoleamine-2,3-dioxygenase, Indoleamine-2,3-dioxygenase 1, Indoleamine-2,3-dioxygenase 2, Lymphotoxin-alpha, NLRP3, NR3C1, Nrf2, NTRK, Proline-rich transmembrane protein 4, Serine Protease 56, SIRT1, Transient Receptor Potential Melastatin 3
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- ► Clusters of differentiation (4 P)
Pages in category "Genes"
The following 62 pages are in this category, out of 62 total.