Familial Meniere Disease

Gene: FCHO2

Red List (low evidence)

FCHO2 (FCH domain only 2)
EnsemblGeneIds (GRCh38): ENSG00000157107
EnsemblGeneIds (GRCh37): ENSG00000157107
OMIM: 613438, Gene2Phenotype
FCHO2 is in 1 panel

0 reviews

Details

Sources
  • Literature
OMIM
613438
Clinvar variants
Variants in FCHO2
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)

FCHO2 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

FCHO2 was created by Eleanor Williams