PanelApp (staging)
  1. Genes and Genomic Entities
  2. APOL1

APOL1

apolipoprotein L1
OMIM: 603743, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber APOL1 in Mendeliome


Version 1.2302

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • {Glomerulosclerosis, focal segmental, 4, susceptibility to} 612551
  • {End-stage renal disease, nondiabetic, susceptibility to} OMIM:612551

Amber APOL1 in Proteinuria


Level 2: Renal and urinary tract disorders
Version 0.229

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel

    		•  4 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • {Glomerulosclerosis, focal segmental, 4, susceptibility to}, MIM#612551

    Red APOL1 in Defects of intrinsic and innate immunity


    Level 2: Immunological disorders
    Version 1.19

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • {Glomerulosclerosis, focal segmental, 4, susceptibility to} 612551