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TPH1, tryptophan hydroxylase 1

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TPH1, tryptophan hydroxylase 1

  • This gene encodes a member of the aromatic amino acid hydroxylase family. The encoded protein catalyzes the first and rate limiting step in the biosynthesis of serotonin, an important hormone and neurotransmitter. Mutations in this gene have been associated with an elevated risk for a variety of diseases and disorders, including schizophrenia, somatic anxiety, anger-related traits, bipolar disorder, suicidal behavior, addictions, and others.[provided by RefSeq, Apr 2009]

  • Gene Synonyms (tryptophan 5-hydroxylase 1, L-tryptophan hydroxylase, indoleacetic acid-5-hydroxylase, tryptophan 5-monooxygenase 1, tryptophan hydroxylase (tryptophan 5-monooxygenase), TPRH, TRPH,)
  • NCBI Gene ID: 7166
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>P17752
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

tryptophan hydroxylase 1 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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