500218400ENSG00000276130ENSG00000110628ENSMUSG00000000154Q96BI1Q78KK3NM_002555NM_183233NM_001315501NM_001315502NM_001042760NM_008767NP_001302430NP_001302431NP_002546NP_899056NP_001036225NP_032793Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.

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.

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