1. Genes and Genomic Entities
  2. NOS1AP

NOS1AP

nitric oxide synthase 1 adaptor protein
OMIM: 605551, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red NOS1AP in Short QT syndrome


Level 2: Cardiology
Version 3.16
Latest signed off version: v3.14 (30 Apr 2025)

Component of the following Super Panels:

  • Cardiac arrhythmias
  • Sudden unexplained death or survivors of a cardiac event
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review Not set
    Sources
    • Long QT syndrome (Version 1.5)
    Red NOS1AP in Long QT syndrome


    Level 2: Cardiology
    Version 3.12
    Latest signed off version: v3.10 (30 Apr 2025)

    Component of the following Super Panels:

  • Cardiac arrhythmias
  • Sudden unexplained death or survivors of a cardiac event
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review Unknown
    Sources
    • South West GLH
    • Expert list
    Green NOS1AP in Proteinuric renal disease


    Level 2: Renal
    Version 5.7
    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
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Nephrotic syndrome, type 22, OMIM:619155
    Green NOS1AP in Unexplained young onset end-stage renal disease - additional genes


    Level 2: Renal
    Version 1.4
    Latest signed off version: v1.1 (30 Apr 2025)

    Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Nephrotic syndrome, type 22, OMIM:619155