PanelApp (stage)
  1. Genes and Genomic Entities
  2. NUP205

NUP205

nucleoporin 205
OMIM: 614352, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NUP205 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Nephrotic syndrome, type 13, MIM#616893

Red NUP205 in Proteinuria


Level 2: Renal and urinary tract disorders
Version 0.225

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Nephrotic syndrome, type 13, MIM#616893