Solute Carrier Family 67 Member A1

**Semantic type:** Amino Acid, Peptide, or Protein

**Definition:** Solute carrier family 67 member A1 (424 aa, ~45 kDa) is encoded by the human SLC67A1 gene. This protein is involved in the transport of cations, quinidine-related compounds and protons.

**Synonyms:** - Beckwith-Wiedemann Syndrome Chromosomal Region 1 Candidate Gene A Protein - Efflux Transporter-Like Protein - Imprinted Multi-Membrane-Spanning Polyspecific Transporter-Related Protein 1 - Imprinted Polyspecific Membrane Transporter 1 - ORCTL-2 - Organic Cation Transporter-Like 2 - Organic Cation Transporter-Like 2 Protein - Organic Cation Transporter-Like Protein 2 - SLC22A18 - SLC22A1L - SLC67A1 - Solute Carrier Family 22 Member 1-Like - Solute Carrier Family 22 Member 18 - Solute Carrier Family 67 Member 1 - TSSC5 - Tumor Suppressing Subtransferable Candidate 5 Protein - Tumor-Suppressing STF CDNA 5 Protein - Tumor-Suppressing STF cDNA 5 Protein - Tumor-Suppressing Subchromosomal Transferable Fragment Candidate Gene 5 Protein - p45 Beckwith-Wiedemann Region 1A - p45-BWR1A - p45-Beckwith-Wiedemann Region 1 A