XPO5

exportin 5
OMIM: 607845, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red XPO5 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Nephrotic syndrome

Red XPO5 in Proteinuria


Level 2: Renal and urinary tract disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Nephrotic syndrome