NUP133

nucleoporin 133
OMIM: 607613, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green NUP133 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Nephrotic syndrome, type 18, MIM#618177

Green NUP133 in Proteinuria


Level 2: Renal and urinary tract disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Nephrotic syndrome, type 18, MIM#618177