OnlineIMD

SLCO1B1 deficiency in Rotor syndrome

  • Type
    Disease
  • Gene
    • SLCO1B1 / Solute Carrier Organic Anion Transporter Family Member 1B1
      • 12p12.1
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Solute carrier organic anion transporter family member 1B1
  • Parent entry
    • Rotor syndrome