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Nuclear receptor subfamily 3 group C member 1
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
 | This article is a stub. |
NR3C1 or nuclear receptor subfamily 3, group C, member 1 or glucocorticoid receptor is a gene that may be associated with the development of chronic fatigue syndrome.[1][2]
Function[edit | edit source]
ME/CFS[edit | edit source]
Goertzel et al. (2006) concluded:
Three genes were found to be common in a group of people with Chronic Fatigue Syndrome compared to the general population; TPH2 - neuronal tryptophan hydroxylase, COMT - catechol-O-methyltransferase, and NR3C1 - nuclear receptor subfamily 3, group C, member 1 glucocorticoid receptor, together these three have an accuracy of 76%.[2]
Notable studies[edit | edit source]
- 2006, Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes[2] - (Full text)
See also[edit | edit source]
Learn more[edit | edit source]
- Nuclear receptor subfamily 3 group C member 1 - Genecards.org
- Wikipedia
References[edit | edit source]
- ↑ "Nuclear receptor subfamily 3 group C member 1". Gene cards. Retrieved April 1, 2025.
- ↑ Jump up to: 2.0 2.1 2.2 Goertzel, Benjamin N.; Pennachin, Cassio; de Souza Coelho, Lucio; Gurbaxani, Brian; Maloney, Elizabeth M.; Jones, James F. (April 2006). "Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome". Pharmacogenomics. 7 (3): 475–483. doi:10.2217/14622416.7.3.475. ISSN 1462-2416. PMID 16610957.
