SLC6A19 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLC6A19 wild-type allele is located in the vicinity of 5p15.33 and is approximately 24 kb in length. This allele, which encodes sodium-dependent neutral amino acid transporter B(0)AT1 protein, plays a role in epithelial cell uptake of neutral amino acids. Mutation of the gene is associated with iminoglycinuria, hyperglycinuria and Hartnup disorder.

**Synonyms:** - B0AT1 - HND - Hartnup Disease Gene - Solute Carrier Family 6 (Neurotransmitter Transporter), Member 19 Gene - Solute Carrier Family 6 (Neutral Amino Acid Transporter), Member 19 Gene - Solute Carrier Family 6 Member 19 wt Allele