Neha Patil (Editor)

SLC22A18

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Species
  
Entrez
  
5002

Human
  
Ensembl
  
n/a

SLC22A18

Aliases
  
SLC22A18, BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5, p45-BWR1A, solute carrier family 22 member 18

External IDs
  
MGI: 1336884 HomoloGene: 1918 GeneCards: SLC22A18

Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.

Function

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.

References

SLC22A18 Wikipedia


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