SLC5A6 (Solute Carrier Family 5 Member 6) is a Protein Coding gene. Diseases associated with SLC5A6 include Biotin Deficiency and Retinitis Pigmentosa 50. Among its related pathways are Metabolism of water-soluble vitamins and cofactors and NRF2 pathway. Gene Ontology (GO) annotations related to this gene include transporter activity and sodium-dependent multivitamin transmembrane transporter activity. An important paralog of this gene is SLC5A8.
Immunogen Information
Immunogen
A synthetic peptide of human SLC5A6 (NP_066918.2).