Solute carrier family 22 member 18 Products

Description

Solute carrier family 22 member 18 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.

Bioinformatics

Entrez	5002 Human
Uniprot	NP_002546 Human NP_899056 Human Q96BI1 Human
Product By Gene ID	5002
Alternate Names	BWR1AORCTL2 BWSCR1Asolute carrier family 22 (organic cation transporter), member 1-like Efflux transporter-like protein HET imprinted multi-membrane spanning polyspecific transporter-related protein 1 Imprinted multi-membrane-spanning polyspecific transporter-related protein 1 IMPT1DKFZp667A184 ITMp45-BWR1A ORCTL-2 organic cation transporter-like 2 Organic cation transporter-like protein 2 p45 Beckwith-Wiedemann region 1A SLC22A1Lcandidate A solute carrier family 22 member 18 Solute carrier family 22 member 1-like solute carrier family 22, member 18 TSSC5p45-Beckwith-Wiedemann region 1 A Tumor-suppressing STF cDNA 5 protein Tumor-suppressing subchromosomal transferable fragment candidate gene 5 protein