SLC9A3

solute carrier family 9 member A3
OMIM: 182307, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green SLC9A3 in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.13

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Diarrhoea 8, secretory sodium, congenital 616868

Amber SLC9A3 in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.121

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert Review
    Phenotypes
    • Diarrhoea 8, secretory sodium, congenital 616868
    • Very Early Onset Inflammatory Bowel Disease

    Green SLC9A3 in Mendeliome


    Version 1.1902

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diarrhoea 8, secretory sodium, congenital 616868

    Green SLC9A3 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Diarrhea 8, secretory sodium, congenital, 616868 (3), Autosomal recessive

    Green SLC9A3 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Diarrhea 8, secretory sodium, congenital, 616868 (3), Autosomal recessive

    Amber SLC9A3 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Diarrhoea 8, secretory sodium, congenital, MiM# 616868
    Tags
    • for review