SLC52A3 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLC52A3 wild-type allele is located in the vicinity of 20p13 and is approximately 20 kb in length. This allele, which encodes solute carrier family 52, riboflavin transporter, member 3 protein, plays a role in vitamin B2 transport. Mutation of the gene is associated with Brown-Vialetto-Van Laere syndrome 1 and Fazio-Londe disease.

**Synonyms:** - BVVLS - BVVLS1 - C20orf54 - Chromosome 20 Open Reading Frame 54 Gene - Hypothetical Protein LOC113278 Gene - RFT2 - RFVT3 - Solute Carrier Family 52 (Riboflavin Transporter), Member 3 Gene - Solute Carrier Family 52 Member 3 wt Allele - Solute Carrier Family 52, Riboflavin Transporter, Member 3 Gene - bA371L19.1 - hRFT2