Familial Meniere Disease

Gene: KCNE3

Red List (low evidence)

KCNE3 (potassium voltage-gated channel subfamily E regulatory subunit 3)
EnsemblGeneIds (GRCh38): ENSG00000175538
EnsemblGeneIds (GRCh37): ENSG00000175538
OMIM: 604433, Gene2Phenotype
KCNE3 is in 3 panels

0 reviews

Details

Sources
  • Literature
OMIM
604433
Clinvar variants
Variants in KCNE3
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)

KCNE3 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

KCNE3 was created by Eleanor Williams