| Gene ID | 5002 |
| Symbol | SLC22A18 |
| Synonymous | BWR1A|BWSCR1A|HET|IMPT1|ITM|ORCTL2|SLC22A1L|TSSC5|p45-BWR1A |
| Full name | solute carrier family 22, member 18 |
| Gene description | Beckwith-Wiedemann syndrome chromosome region 1, candidate A|ORCTL-2|beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein|efflux transporter-like protein|imprinted multi-membrane spanning polyspecific transporter-related protein 1|imp |
| Cytoband | 11p15.5 |
| Gene type | protein-coding |
| Synonymous | MIM:602631; HGNC:HGNC:10964; Ensembl:ENSG00000110628; HPRD:04024; Vega:OTTHUMG00000010037 |
There is no record for SLC22A18 |