Slc52a2 - solute carrier family 52 member 2 Gene

Also Known as rRFT1; Gpr172a; Gpr172b; RGD1560410

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 362942

Summary

Enables riboflavin transmembrane transporter activity. Involved in riboflavin transport. Is integral component of plasma membrane. Human ortholog(s) of this gene implicated in Brown-Vialetto-Van Laere syndrome 2 and riboflavin deficiency. Orthologous to several human genes including SLC52A2 (solute carrier family 52 member 2). [provided by Alliance of Genome Resources, Apr 2022]

Slc52a2 Products (1)

mRNA Protein Name
NM_001109670.1 NP_001103140.1 solute carrier family 52, riboflavin transporter, member 2
Molecular Function GO Annotation Evidence References Source
enables riboflavin transmembrane transporter activity IDA
IDA: Inferred from direct assay
18632736 RGD
Biological Process GO Annotation Evidence References Source
involved in riboflavin transport IDA
IDA: Inferred from direct assay
18632736 RGD
Cellular Component GO Annotation Evidence References Source
located in plasma membrane IDA
IDA: Inferred from direct assay
18632736 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

solute carrier family 52, riboflavin transporter, member 2

  • G protein-coupled receptor 172A

  • G protein-coupled receptor 172B

  • porcine endogenous retrovirus A receptor 2

  • riboflavin transporter 1

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc52a2 NCBI NCBI:79581