2. Gene
  3. Slc5a6 - solute carrier family 5 (sodium-dependent vitamin transporter), member 6 Gene

Slc5a6 - solute carrier family 5 (sodium-dependent vitamin transporter), member 6 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Mus musculus

Also known as E430023I20

Gene ID: 330064 | Gene type: protein coding

About Slc5a6

Summary

Predicted to enable biotin transmembrane transporter activity; pantothenate transmembrane transporter activity; and sodium-dependent multivitamin transmembrane transporter activity. Predicted to be involved in anion transmembrane transport; sodium ion transport; and transport across blood-brain barrier. Predicted to act upstream of or within ion transport. Predicted to be located in brush border membrane and vesicle membrane. Is expressed in several structures, including 4-cell stage embryo; choroid plexus; pericardium; pituitary gland; and skeletal musculature. Orthologous to human SLC5A6 (solute carrier family 5 member 6). [provided by Alliance of Genome Resources, Apr 2022]

Slc5a6 Products(4)

mRNA Protein Name
NM_001177621.1 NP_001171092.1 sodium-dependent multivitamin transporter
NM_001177622.1 NP_001171093.1 sodium-dependent multivitamin transporter
NM_001360022.1 NP_001346951.1 sodium-dependent multivitamin transporter
NM_177870.5 NP_808538.1 sodium-dependent multivitamin transporter
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables amide transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
23104561 MGI
enables monocarboxylate:sodium symporter activity IMP
IMP: Inferred from mutant phenotype
23104561 MGI
enables pantothenate transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
23104561 MGI
enables pantothenate:sodium symporter activity IMP
IMP: Inferred from mutant phenotype
23104561 MGI
enables sodium-dependent multivitamin transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
23104561 MGI
enables sulfur compound transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
23104561 MGI
enables vitamin transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
23104561 MGI
Biological Process GO Annotation Evidence Reference Source
involved in biotin metabolic process IMP
IMP: Inferred from mutant phenotype
23104561 MGI
involved in pantothenate transmembrane transport IMP
IMP: Inferred from mutant phenotype
23104561 MGI
Cellular Component GO Annotation Evidence Reference Source
is active in plasma membrane IMP
IMP: Inferred from mutant phenotype
23104561 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

sodium-dependent multivitamin transporter

Na(+)-dependent multivitamin transporter

solute carrier family 5 member 6

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS13292 SLC5A6 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc5a6 NCBI NCBI:8884