SLCO1B3 deficiency in Rotor syndrome

Type

Disease
Gene
- SLCO1B3 / Solute Carrier Organic Anion Transporter Family Member 1B3
  12p12.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Solute carrier organic anion transporter family member 1B3
Parent entry
- Rotor syndrome