| GENE NAME | SLCO1B1 |
| CHROMOSOME | 12 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000134538 |
| UNIPROT ACCESSION NUMBER | Q9Y6L6 |
| GO MOLECULAR FUNCTION | ['thyroid hormone transmembrane transporter activity', 'sodium-independent organic anion transmembrane transporter activity', 'bile acid transmembrane transporter activity'] |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | hsa04976; hsa04976; hsa04976; R-HSA-1430728; R-HSA-159418; R-HSA-1643685; R-HSA-189445; R-HSA-189483; R-HSA-194068; R-HSA-382551; R-HSA-425397; R-HSA-425407; R-HSA-556833; R-HSA-5619102; R-HSA-5619110; R-HSA-5619115; R-HSA-879518; R-HSA-8957322 |
| 4 combinations linked to SLCO1B1 | OLI1018; OLI1017; OLI1479; OLI1007 |
| 3 variants linked to SLCO1B1 | SLCO1B1:c.1738C>T, p.Arg580Ter; SLCO1B1:c.757C>T, p.Arg253Ter; SLCO1B1:c.1738C>T, p.Arg580Ter |
| 1 disease linked to SLCO1B1 | Rotor syndrome |