background:
SLC5A6 (Solute Carrier Family 5 (Sodium/Multivitamin And Iodide Cotransporter), Member 6) is a Protein Coding gene. Diseases associated with SLC5A6 include thiamine metabolism dysfunction syndrome 2 and urinary tract obstruction. Among its related pathways are Metabolism and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds. GO annotations related to this gene include transporter activity and sodium-dependent multivitamin transmembrane transporter activity. An important paralog of this gene is SLC5A10.
Function:
Transports pantothenate, biotin and lipoate in the presence of sodium.
Subcellular Location:
Membrane.
Similarity:
Belongs to the sodium:solute symporter (SSF) (TC 2.A.21) family.
Database links:
Entrez Gene: 8884 Human
Entrez Gene: 100009326 Rabbit
Entrez Gene: 170551 Rat
Omim: 604024 Human
SwissProt: Q9Y289 Human
SwissProt: Q9XT77 Rabbit
SwissProt: O70247 Rat
Unigene: 435735 Human
Unigene: 11105 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
|
|