Slc52a3 - solute carrier family 52 member 3 Gene

Also Known as Rft2; rRFT2; RGD1304644

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 311536

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 1 and Fazio-Londe disease. Orthologous to human SLC52A3 (solute carrier family 52 member 3). [provided by Alliance of Genome Resources, Apr 2022]

Slc52a3 Products (1)

mRNA Protein Name
NM_001037198.1 NP_001032275.1 solute carrier family 52, riboflavin transporter, member 3

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables riboflavin transmembrane transporter activity IDA
IDA: Inferred from direct assay
19122205 RGD
Biological Process GO Annotation Evidence References Source
involved in riboflavin transport IDA
IDA: Inferred from direct assay
19122205 RGD
Cellular Component GO Annotation Evidence References Source
located in plasma membrane IDA
IDA: Inferred from direct assay
19122205 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 3

  • riboflavin transporter 2

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13279 SLC52A3 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc52a3 NCBI NCBI:113278