Multidrug and toxin extrusion protein 1
Template:PBB Solute carrier family 47, member 1, also known as SLC47A1, is a protein which in humans is encoded by the SLC47A1 gene.[1][2]
Function
This gene is located within the Smith-Magenis syndrome region on chromosome 17.[1]
SLC47A1 belongs to a MATE (multidrug and toxic compound extrusion) family of transporters that excrete endogenous and exogenous toxic electrolytes through urine and bile.[2]
See also
References
- ^ a b "Entrez Gene: FLJ10847 hypothetical protein FLJ10847".
- ^ a b Otsuka M, Matsumoto T, Morimoto R, Arioka S, Omote H, Moriyama Y (2005). "A human transporter protein that mediates the final excretion step for toxic organic cations". Proc. Natl. Acad. Sci. U.S.A. 102 (50): 17923–8. doi:10.1073/pnas.0506483102. PMC 1312386. PMID 16330770.
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Further reading
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