PanelApp (test)
  1. Genes and Genomic Entities
  2. SLC10A2

SLC10A2

solute carrier family 10 member 2
OMIM: 601295, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red SLC10A2 in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.13

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Bile acid malabsorption, primary, MIM# 613291

Red SLC10A2 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Bile acid malabsorption, primary, MIM# 613291

Red SLC10A2 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 BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    Phenotypes
    • bile acid malabsorption, primary, 1 MONDO:0013214
    • Disorders of bile acid metabolism