Familial Meniere Disease

Gene: CASP3

Red List (low evidence)

CASP3 (caspase 3)
EnsemblGeneIds (GRCh38): ENSG00000164305
EnsemblGeneIds (GRCh37): ENSG00000164305
OMIM: 600636, Gene2Phenotype
CASP3 is in 2 panels

0 reviews

Details

Sources
  • Literature
OMIM
600636
Clinvar variants
Variants in CASP3
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)

CASP3 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

CASP3 was created by Eleanor Williams