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Results 1 - 10 of 42 for Tryptophan
  1. YWHAE gene 
    ... kinase C inhibitor protein-1 tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide tyrosine 3/ ...
    https://medlineplus.gov/genetics/gene/ywhae - Genetics
  2. Glutaric acidemia type I 
    ... break down the amino acids lysine, hydroxylysine, and tryptophan, which are building blocks of protein. Excessive levels ... in processing the amino acids lysine, hydroxylysine, and tryptophan.Mutations in the GCDH gene prevent production of ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  3. NPM1 gene 
    ... amino acids). The alterations change the amino acid tryptophan at protein position 290 and often the tryptophan at position 288. These two tryptophans are important ...
    https://medlineplus.gov/genetics/gene/npm1 - Genetics
  4. GCDH gene 
    ... breakdown of the amino acids lysine, hydroxylysine, and tryptophan, which are building blocks of proteins. Mutations in ... role in the breakdown of lysine, hydroxylysine, and tryptophan. This enzyme deficiency allows these amino acids and ...
    https://medlineplus.gov/genetics/gene/gcdh - Genetics
  5. SLC26A2 gene 
    ... the amino acid arginine with the amino acid tryptophan at position 279 in the protein (written as ... the amino acid arginine with the amino acid tryptophan at position 279 in the protein (written as ...
    https://medlineplus.gov/genetics/gene/slc26a2 - Genetics
  6. DDC gene 
    ... and serotonin is produced from the amino acid tryptophan. Both neurotransmitters are produced in two-step processes. ... reactions that convert tyrosine to L-dopa, and tryptophan to 5-hydroxytryptophan. The AADC enzyme then converts ...
    https://medlineplus.gov/genetics/gene/ddc - Genetics
  7. Hartnup disease 
    ... proteins. One particular amino acid transported by B0AT1, tryptophan, is needed to produce vitamin B3 (also known ... these features are related to a deficiency of tryptophan and niacin, specifically. SLC6A19 This condition is inherited ...
    https://medlineplus.gov/genetics/condition/hartnup-disease - Genetics
  8. PTPN22 gene 
    ... block (amino acid) arginine to the amino acid tryptophan at position 620 in the PTPN22 protein sequence, ...
    https://medlineplus.gov/genetics/gene/ptpn22 - Genetics
  9. PPOX gene 
    ... the amino acid arginine with the amino acid tryptophan at position 59 (written as Arg59Trp or R59W). ...
    https://medlineplus.gov/genetics/gene/ppox - Genetics
  10. PAH gene 
    ... the amino acid arginine with the amino acid tryptophan at position 408 (written as Arg408Trp or R408W) ...
    https://medlineplus.gov/genetics/gene/pah - Genetics
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