1. Genes and Genomic Entities
  2. PTPRO

PTPRO

protein tyrosine phosphatase, receptor type O
OMIM: 600579, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red PTPRO in Unexplained kidney failure in young people

Level 3: Disorders of function
Level 2: Renal and urinary tract disorders
Version 1.125

review Not set
Sources
  • Eligibility statement prior genetic testing
Amber PTPRO in Proteinuric renal disease


Level 2: Renal
Version 6.22
Latest signed off version: v6.13 (12 Aug 2026)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • NHS GMS
    • Eligibility statement prior genetic testing
    Phenotypes
    • Nephrotic syndrome, type 6, OMIM:614196
    • nephrotic syndrome, type 6, MONDO:0013619
    Tags
    • watchlist