SLC67A1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLC67A1 wild-type allele is located in the vicinity of 11p15.4 and is approximately 424 kb in length. This allele, which encodes solute carrier family 67 member A1 protein, plays a role in tumor suppression and the transport of protons and organic cations. Somatic mutations in the gene are associated with breast cancer, lung cancer and rhabdomyosarcoma.

**Synonyms:** - BWR1A - BWSCR1A - Beckwith-Wiedemann Region 1A Gene - Beckwith-Wiedemann Syndrome Chromosome Region 1, Candidate A Gene - HET - IMPT1 - ITM - Imprinted Multi-Membrane-Spanning Polyspecific Transporter-Like Gene 1 - Imprinted Polyspecific Membrane Transporter 1 Gene - ORCTL2 - Organic Cation Transporter-Like 2 Gene - SLC22A18 - SLC22A1L - SLC22A1L Gene - Solute Carrier Family 22 (Organic Cation Transporter), Member 18 Gene - Solute Carrier Family 22 Member 18 Gene - Solute Carrier Family 22, Member 18 Gene - Solute Carrier Family 22, Organic Cation Transporter, Member 1-Like Gene - Solute Carrier Family 67 Member 1 wt Allele - TSSC5 - Tumor-Suppressing STF cDNA 5 Gene - Tumor-Suppressing Subchromosomal Transferable Fragment Candidate Gene 5 - p45-BWR1A