Folate transporter 1

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SLC19A1
Identifiers
AliasesSLC19A1, CHMD, FOLT, IFC1, REFC, RFC1, solute carrier family 19 member 1, IFC-1, RFC, hRFC, RFT-1, hMEGAF
External IDsOMIM: 600424 MGI: 103182 HomoloGene: 57139 GeneCards: SLC19A1
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001199271
NM_031196

RefSeq (protein)

NP_001186200
NP_112473

Location (UCSC)Chr 21: 45.49 – 45.57 MbChr 10: 77.03 – 77.06 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 19 (folate transporter), member 1, also known as SLC19A1 or RFC1, is a protein which in humans is encoded by the SLC19A1 gene.[5]

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]

Clinical significance

Individuals carrying a specific polymorphism of SLC19A1 (c.80GG) have lower levels of folate.[7] 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.

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000173638Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000001436Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Lapenta V; Sossi V; Gosset P; Vayssettes C; Vitali T; Rabatel N; Tassone F; Blouin JL; Scott HS; Antonarakis SE; Créau N; Brahe C (April 1998). "Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3". Genomics. 49 (1): 1–13. doi:10.1006/geno.1997.5185. PMID 9570943.
  6. ^ "Entrez Gene: SLC19A1 solute carrier family 19 (folate transporter), member 1".
  7. ^ Stanisławska-Sachadyn A; Mitchell LE; Woodside JV; Buckley PT; Kealey C; Young IS; Scott JM; Murray L; Boreham CA; McNulty H; Strain JJ; Whitehead AS (September 2009). "The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women". Ann. Hum. Genet. 73 (Pt 5): 484–491. doi:10.1111/j.1469-1809.2009.00529.x. PMC 2812009. PMID 19650776. {{cite journal}}: Unknown parameter |laysource= ignored (help); Unknown parameter |laysummary= ignored (help)

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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