1. Gene
  2. Slc52a3 - solute carrier protein family 52, member 3 Gene

Slc52a3 - solute carrier protein family 52, member 3 Gene

Mus musculus

Also known as RFT2; 2310046K01Rik

Gene ID: 69698 | Gene type: protein coding

About Slc52a3

Summary

Predicted to enable riboflavin transmembrane transporter activity. Acts upstream of or within cellular response to heat. Predicted to be located in cytoplasm; nucleus; and plasma membrane. Predicted to be integral component of plasma membrane. Is expressed in several structures, including extraembryonic component; genitourinary system; gut; and inner ear vestibular component. 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(3)

mRNA Protein Name
NM_001164819.1 NP_001158291.1 solute carrier family 52, riboflavin transporter, member 3 isoform 1 precursor
NM_001164820.1 NP_001158292.1 solute carrier family 52, riboflavin transporter, member 3 isoform 2
NM_027172.3 NP_081448.2 solute carrier family 52, riboflavin transporter, member 3 isoform 1 precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables riboflavin transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
26660539 MGI
Biological Process GO Annotation Evidence Reference Source
acts upstream of or within cellular response to heat IDA
IDA: Inferred from direct assay
18755693 MGI
involved in flavin adenine dinucleotide biosynthetic process IMP
IMP: Inferred from mutant phenotype
33116204 MGI
involved in riboflavin metabolic process IMP
IMP: Inferred from mutant phenotype
33116204 MGI
Cellular Component GO Annotation Evidence Reference Source
is active in plasma membrane IMP
IMP: Inferred from mutant phenotype
26660539 MGI
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

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc52a3 NCBI NCBI:113278