Short QT syndrome

Gene: NOS1AP

Red List (low evidence)

NOS1AP (nitric oxide synthase 1 adaptor protein)
EnsemblGeneIds (GRCh38): ENSG00000198929
EnsemblGeneIds (GRCh37): ENSG00000198929
OMIM: 605551, Gene2Phenotype
NOS1AP is in 3 panels

1 review

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

Not associated with Short QT phenotype in OMIM or in Gen2Phen. Listed on the Long QT syndrome panel (Version 1.5).
Created: 15 Nov 2018, 12:10 p.m.


  • Long QT syndrome (Version 1.5)
Clinvar variants
Variants in NOS1AP
Panels with this gene

History Filter Activity

20 Nov 2018, Gel status: 1

Panel promoted to version 1.0

Sarah Leigh (Genomics England Curator)

Sarah Leigh: Not associated with Short QT p

15 Nov 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance

Sarah Leigh (Genomics England Curator)

gene: NOS1AP was added gene: NOS1AP was added to Short QT syndrome. Sources: Long QT syndrome (Version 1.5) Mode of inheritance for gene: NOS1AP was set to