Familial Meniere Disease

Gene: NOS2

Red List (low evidence)

NOS2 (nitric oxide synthase 2)
EnsemblGeneIds (GRCh38): ENSG00000007171
EnsemblGeneIds (GRCh37): ENSG00000007171
OMIM: 163730, Gene2Phenotype
NOS2 is in 3 panels

0 reviews

Details

Sources
  • Literature
OMIM
163730
Clinvar variants
Variants in NOS2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

27 Mar 2018, Gel status: 1

Panel promoted to version 1.0

Eleanor Williams (Genomics England Curator)

External reviews collated. Internal clinical input. Ready for version 1.

17 Jan 2018, Gel status: 1

Added New Source

Eleanor Williams (Genomics England Curator)

NOS2 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

NOS2 was created by Eleanor Williams