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SLCO1B1

solute carrier organic anion transporter family member 1B1
3 disorders 1 no genetic record 1 susceptibility 1 causative 12p12.1 gene with protein product
HGNC:10959MonarchNCBI Gene 10599ENSG00000134538UniProt Q9Y6L6OMIM 604843

Previous symbols: SLC21A6. Aliases: OATP-C, LST-1, OATP1B1.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Methotrexate Toxicity susceptibility
mechanism: Systemic Methotrexate Exposure
Rotor Syndrome causative
mechanism: Combined OATP1B1 and OATP1B3 Deficiency
Hypercholanemia Familial 2 no genetic record
mechanism: Residual Enterohepatic Cycling via Auxiliary Transporters
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.