ⓘ SLC22A1

                                     

ⓘ SLC22A1

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter.

It is also necessary for the introduction of Metformin to the cells.

                                     
  • carrier family 22 member 25 SLC 22 A25 also known as organic anion transporter UST6, is a protein that in humans is encoded by the SLC 22 A25 gene. GRCh38:
  • SLC22A1 and SLC 22 A2 are located on chromosome 6q26 Cytogenet Cell Genet. 79 3 4 198 200. doi: 10.1159 000134720. PMID 9605850. Entrez Gene: SLC 22A2
  • famotidine toward human organic cation transporter 1 hOCT 1 SLC22A1 hOCT2 SLC 22 A2 and hOCT3 SLC 22 A3 J. Pharmacol. Exp. Ther. 315 3 1288 1297
  • family 22 organic anion cation transporter member 12, also known as SLC 22 A12 and URAT 1 is a protein which in humans is encoded by the SLC 22 A12 gene
  • carrier family 22 member 10 SLC 22 A10 also known as organic anion transporter 5 OAT5 is a protein that in humans is encoded by the SLC 22 A10 gene. GRCh38:
  • Solute carrier family 22 member 4, also known as SLC 22 A4, is a human gene the encoded protein is known as the ergothioneine transporter. The encoded
  • Solute carrier family 22 member 9 is a protein that in humans is encoded by the SLC 22 A9 gene. SLC 22 A9 protein, human at the US National Library of Medicine
  • Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC 22 A18 gene. This gene is one of several tumor - suppressing subtransferable
  • Solute carrier family 22 member 7 is a protein that in humans is encoded by the gene SLC 22 A7. The protein encoded by this gene is involved in the sodium - independent
  • SLC 22 A5 is a membrane transport protein associated with primary carnitine deficiency. This protein is involved in the active cellular uptake of carnitine
  • Glucose - 6 - phosphate exchanger SLC 37A 1 is a protein that in humans is encoded by the SLC 37A 1 gene. SLC 37A 1 locates to the membrane of the endoplasmic reticulum
  • Solute carrier family 22 member 8, or organic anion transporter 3 OAT3 is a protein that in humans is encoded by the SLC 22 A8 gene. OAT3 is involved