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SLCO1B3

solute carrier organic anion transporter family member 1B3
3 disorders 2 no genetic record 1 causative 12p12.2 gene with protein product
HGNC:10961MonarchNCBI Gene 28234ENSG00000111700UniProt Q9NPD5OMIM 605495

Previous symbols: SLC21A8. Aliases: OATP8, OATP1B3.

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
Rotor Syndrome causative
mechanism: Combined OATP1B1 and OATP1B3 Deficiency
Amatoxin Poisoning no genetic record
mechanism: OATP1B3-Mediated Hepatocyte Uptake of Alpha-Amanitin
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.