1. Genes and Genomic Entities
  2. NOS1AP

NOS1AP

nitric oxide synthase 1 adaptor protein
OMIM: 605551, Gene2Phenotype

3 panels

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


Version 3.10
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

  • Cardiac arrhythmias
  • Sudden unexplained death or survivors of a cardiac event

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

    Level 3: Cardiac arrhythmia
    Level 2: Cardiovascular disorders
    Version 3.7
    Latest signed off version: v3.1 (22 Mar 2023)

    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
    Amber NOS1AP in Proteinuric renal disease

    Level 3: Syndromes with prominent renal abnormalities
    Level 2: Renal and urinary tract disorders
    Version 4.12
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Renal superpanel - broad
  • Renal superpanel - narrow

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Nephrotic syndrome, type 22, OMIM:619155
    Tags
    • Q1_24_promote_green