SYNPO2

synaptopodin 2
OMIM: 620941, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SYNPO2 in Mendeliome


Version 2.22

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Nephrotic Syndrome MONDO:0005377

Red SYNPO2 in Proteinuria


Level 2: Renal and urinary tract disorders
Version 1.0

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    • Literature
    Phenotypes
    • Nephrotic Syndrome MONDO:0005377