PanelApp (test)
  1. Genes and Genomic Entities
  2. NUP93

NUP93

nucleoporin 93
OMIM: 614351, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green NUP93 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Nephrotic syndrome, type 12 - MIM#616892

Green NUP93 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 Green
    • Expert list
    Phenotypes
    • Nephrotic syndrome, type 12, MIM#616892

    Green NUP93 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Nephrotic syndrome, type 12, 616892 (3), Autosomal recessive

    Green NUP93 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Nephrotic syndrome, type 12, 616892 (3), Autosomal recessive