SLC52A1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLC52A1 wild-type allele is located in the vicinity of 17p13.2 and is approximately 19 kb in length. This allele, which encodes solute carrier family 52, riboflavin transporter, member 1 protein, plays a role in the uptake of vitamin B2. Maternal haploinsufficiency of this gene is associated with transient neonatal riboflavin deficiency.

**Synonyms:** - FLJ10060 - G Protein-Coupled Receptor 172B Gene - G-Protein Coupled Receptor 42 Gene - GPCR42 - GPR172B - PAR2 - Porcine Endogenous Retrovirus, Subgroup A, Receptor 2 Gene - RBFVD - RFT1 - RFVT1 - Solute Carrier Family 52 (Riboflavin Transporter), Member 1 Gene - Solute Carrier Family 52 Member 1 wt Allele - Solute Carrier Family 52, Riboflavin Transporter, Member 1 Gene - hRFT1 - huPAR-2