Tryptophan hydroxylase 2

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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]

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".

neuroendocrine relating to hormones that influence the nervous system

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.