SLC26A1

solute carrier family 26 member 1
OMIM: 610130, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SLC26A1 in Nephrocalcinosis or nephrolithiasis


Level 2: Renal
Version 5.5
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Nephrolithiasis, calcium oxalate, MIM#167030