ⓘ SLC22A18

                                     

ⓘ SLC22A18

This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene may play a role in malignancies and disease that involve this region as well as the transport of chloroquine- and quinidine-related compounds in the kidney. Two alternative transcripts encoding the same isoform have been described.

                                     
  • 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:
  • 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:
  • member 18 also known as SLC 6A 18 is a protein which in humans is encoded by the SLC 6A 18 gene. The SLC 6 family of proteins, which includes SLC 6A 18 acts
  • 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 2 also termed OCT2 or organic cation transporter - 2 is a protein that in humans is encoded by the SLC 22 A2 gene. Polyspecific
  • Solute carrier family 22 member 1 is a protein that in humans is encoded by the gene SLC 22 A1. Polyspecific organic cation transporters in the liver, kidney
  • family 22 organic anion cation transporter member 12, also known as SLC 22 A12 and URAT1, is a protein which in humans is encoded by the SLC 22 A12 gene
  • Solute carrier family 22 member 3 SLC 22 A3 also known as the organic cation transporter 3 OCT3 or extraneuronal monoamine transporter EMT is a protein
  • 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
  • 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
  • SLC 22 A5 is a membrane transport protein associated with primary carnitine deficiency. This protein is involved in the active cellular uptake of carnitine