SLC26A1

solute carrier family 26 member 1
OMIM: 610130, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC26A1 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Nephrolithiasis, calcium oxalate, MIM#167030
Tags
  • disputed

Red SLC26A1 in Renal Tubulopathies and related disorders


Level 2: Renal and urinary tract disorders
Version 1.14

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • KidGen_MetabolicRenal v38.1.0
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Nephrolithiasis, calcium oxalate, MIM#167030