PanelApp (test)
  1. Genes and Genomic Entities
  2. SLCO1B1

SLCO1B1

solute carrier organic anion transporter family member 1B1
OMIM: 604843, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green SLCO1B1 in Mendeliome


Version 1.1902

review Other
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperbilirubinemia, Rotor type, digenic 237450

Green SLCO1B1 in Haem degradation and bilirubin metabolism defects


Level 2: Metabolic disorders
Version 0.17

Component of the following Super Panels:

  • Liverome Superpanel
  • Metabolic Disorders Superpanel

    		•  review Other
    Sources
    • Expert Review Green
    Phenotypes
    • Rotor syndrome MONDO:0009379 (MIM#237450), Disorders of bilirubin metabolism and biliary transport

    No list SLCO1B1 in Pharmacogenomics_Paediatric


    Level 2: Screening
    Version 0.50

    		review Other
    Sources
    • Other
    Phenotypes
    • Risk for simvastatin-induced myopathy

    Red SLCO1B1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Hyperbilirubinemia, Rotor type, digenic

    Red SLCO1B1 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Hyperbilirubinemia, Rotor type, digenic

    Green SLCO1B1 in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    		review Other
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Hyperbilirubinemia, Rotor type, digenic MIM# 237450