SLC23A1 explained

Solute carrier family 23 member 1 is a protein that in humans is encoded by the SLC23A1 gene.[1] [2] [3]

Function

The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters. The encoded protein is active in bulk vitamin C transport involving epithelial surfaces. Previously, this gene had an official symbol of SLC23A2.

See also

Further reading

Notes and References

  1. Faaland CA, Race JE, Ricken G, Warner FJ, Williams WJ, Holtzman EJ . Molecular characterization of two novel transporters from human and mouse kidney and from LLC-PK1 cells reveals a novel conserved family that is homologous to bacterial and Aspergillus nucleobase transporters . Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression . 1442 . 2–3 . 353–60 . November 1998 . 9804989 . 10.1016/S0167-4781(98)00151-1 .
  2. Tsukaguchi H, Tokui T, Mackenzie B, Berger UV, Chen XZ, Wang Y, Brubaker RF, Hediger MA . A family of mammalian Na+-dependent L-ascorbic acid transporters . Nature . 399 . 6731 . 70–5 . May 1999 . 10331392 . 10.1038/19986 . 1999Natur.399...70T . 4425479 .
  3. Web site: Entrez Gene: SLC23A1 solute carrier family 23 (nucleobase transporters), member 1.