| GENE NAME | SLCO1B3 |
| CHROMOSOME | 12 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000111700 |
| UNIPROT ACCESSION NUMBER | Q9NPD5 |
| GO MOLECULAR FUNCTION | ['organic anion transmembrane transporter activity', 'sodium-independent organic anion transmembrane transporter activity', 'bile acid transmembrane transporter activity'] |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | 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-5619058; R-HSA-5619102; R-HSA-5619115; R-HSA-879518; R-HSA-8957322 |
| 4 combinations linked to SLCO1B3 | OLI1018; OLI1017; OLI1479; OLI1007 |
| 4 variants linked to SLCO1B3 | Copy Number Variant insertion on chromosome 12 of the L1 in the gene SLCO1B3; Copy Number Variant deletion on chromosome 12 of the exon12 in the gene SLCO1B3; Copy Number Variant insertion on chromosome 12 of the exon3 in the gene SLCO1B3; SLCO1B3:c.1747+1G>A, |
| 1 disease linked to SLCO1B3 | Rotor syndrome |