This gene encodes a transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
SLC46A1-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
SLC46A1-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
SLC46A1-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
SLC46A1-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
SLC46A1-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013]
Gene Symbol : SLC46A1
Gene Name : Solute carrier family 46 member 1
Chromosome : CHR 17: 284,066,29-283,946,41
Locus : 17q11.2
Alt. Genes : ENAM
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