NUP205

nucleoporin 205
OMIM: 614352, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green NUP205 in Mendeliome


Version 2.0

3 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Nephrotic syndrome, type 13, MIM#616893
  • Visceral heterotaxy MONDO:0018677
  • Premature ovarian failure, MONDO:0019852, NUP205-related

Amber NUP205 in Proteinuria


Level 2: Renal and urinary tract disorders
Version 1.0

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel
  • 2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Nephrotic syndrome, type 13, MIM#616893

    Green NUP205 in Primary Ovarian Insufficiency_Premature Ovarian Failure

    Level 3: Gonadal and sex development disorders
    Level 2: Endocrine disorders
    Version 1.0

    1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Premature ovarian failure, MONDO:0019852, NUP205-related

    Green NUP205 in Infertility and Recurrent Pregnancy Loss


    Version 2.0

    1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Premature ovarian failure, MONDO:0019852, NUP205-related