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Solute carrier family 61 member 1 is a protein that in humans is encoded by the SLC61A1gene (previously MFSD4).[5]
This protein is responsible for molybdenum uptake instead of the cell.[5] It has previously been described as an atypical SLC, and it is expressed in neuronal plasma membrane.[6] It is a plausible Solute carrier transporter.[7] It transports molybdate anions,[8] and it interacts with GLP-1R.[9] In humans, it is encoded by the gene SLC61A1.[10]
↑Perland E, Fredriksson R (March 2017). "Classification Systems of Secondary Active Transporters". Trends in Pharmacological Sciences. 38 (3): 305–315. doi:10.1016/j.tips.2016.11.008. PMID27939446.