GO curators for mouse genes have assigned the following annotations to the gene product of Tph2. (This text reflects annotations as of Wednesday, January 23, 2013.) Summary from NCBI RefSeq
[Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the pterin-dependent aromatic acid hydroxylase family. The encoded protein catalyzes the first and rate limiting step in the biosynthesis of serotonin, an important hormone and neurotransmitter. The human genome contains two related tryptophan hydroxylases, one on chromosome 11p15-p14 and one on chromosome 12q21. This gene is expressed predominantly in the brain stem. Mutations in this gene may be associated with psychiatric diseases such as bipolar affective disorder and major depression. [provided by RefSeq, Jul 2008]Summary text based on GO annotations supported by experimental evidence in mouse
Researchers have inferred from direct assay, that the gene product of Tph2
participates in the following biological processes:
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Quina LA et al. (2009) Brn3a and Nurr1 mediate a gene regulatory pathway for habenula development. J Neurosci, 29:14309-22. (PubMed:19906978)
Walther DJ et al. (2003) Synthesis of serotonin by a second tryptophan hydroxylase isoform. Science, 299:76. (PubMed:12511643)