Tryptophan hydroxylase 2

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
(Redirected from TPH2)

Tryptophan Hydroxylase 2 or neuronal tryptophan hydroxylase or TPH2 or ADHD7 is a gene found by Goertzel et al. (2006) to be associated with the development of chronic fatigue syndrome.[1][2]

Function[edit | edit source]

ME/CFS[edit | edit source]

Notable studies[edit | edit source]

  • 2006, Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes[1] - (Full text)

See also[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]

  1. ↑ 1.0 1.1 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.
  2. ↑ "TPH2 Gene card". Gene cards. Retrieved March 18, 2022.

single nucleotide polymorphism (SNP) - A single nucleotide polymorphism (SNP, pronounced "snip") is a potential genetic mutation that occurs in a single spot in the human genome; a difference in a single DNA building block. SNPs are often represented by an "rs" number, such as "rs53576".

relating to hormones that influence the nervous system[1]

neuroendocrine relating to hormones that influence the nervous system

Retrieved from "https://me-pedia.org/w/index.php?title=Tryptophan_hydroxylase_2&oldid=236757"