Folate transporter 1 is a protein which in humans is encoded by the SLC19A1 gene.[5]
SLC19A1 |
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Identifiers |
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Aliases | SLC19A1, CHMD, FOLT, IFC1, REFC, RFC1, solute carrier family 19 member 1, IFC-1, RFC, hRFC, RFT-1, hMEGAF |
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External IDs | OMIM: 600424; MGI: 103182; HomoloGene: 57139; GeneCards: SLC19A1; OMA:SLC19A1 - orthologs |
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RNA expression pattern |
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Bgee | Human | Mouse (ortholog) |
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Top expressed in | - jejunal mucosa
- blood
- endothelial cell
- Epithelium of choroid plexus
- retinal pigment epithelium
- duodenum
- gallbladder
- stromal cell of endometrium
- right lung
- putamen
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| Top expressed in | - Paneth cell
- right kidney
- retinal pigment epithelium
- vestibular membrane of cochlear duct
- choroid plexus of fourth ventricle
- ciliary body
- Epithelium of choroid plexus
- human kidney
- crypt of lieberkuhn of small intestine
- endothelial cell of lymphatic vessel
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| More reference expression data |
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BioGPS | |
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Wikidata |
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Function
Transport of folate compounds into mammalian cells can occur via receptor-mediated (see folate receptor 1) or carrier-mediated mechanisms. A functional coordination between these 2 mechanisms has been proposed to be the method of folate uptake in certain cell types. Methotrexate (MTX) is an antifolate chemotherapeutic agent that is actively transported by the carrier-mediated uptake system. RFC1 plays a role in maintaining intracellular concentrations of folate.[6] SLC19A1 has also been shown to transport the immune second messenger 2'3'-cGAMP.[7]
Clinical significance
Individuals carrying a specific polymorphism of SLC19A1 (c.80GG) have lower levels of folate.[8] Other studies have also shown that individuals carrying the c.80AA polymorphism who are treated with methotrexate have higher levels of this anti-folate chemotherapeutic agent. Personalized dosing of the drug depending on the patient's genotype may therefore be required.
Alternative names
- Reduced folate carrier 1
- Intestinal folate carrier 1
See also
References
Further reading