1. Genes and Genomic Entities
  2. GON7

GON7

GON7, KEOPS complex subunit
OMIM: 617436, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green GON7 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.181
Latest signed off version: v6.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Galloway-Mowat syndrome 9, OMIM:619603
Green GON7 in Proteinuric renal disease


Level 2: Renal
Version 5.9
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Galloway-Mowat syndrome MONDO:0009627
    Tags
    • founder-effect