Familial Meniere Disease

Gene: CCND1

Red List (low evidence)

CCND1 (cyclin D1)
EnsemblGeneIds (GRCh38): ENSG00000110092
EnsemblGeneIds (GRCh37): ENSG00000110092
OMIM: 168461, Gene2Phenotype
CCND1 is in 2 panels

0 reviews

Details

Sources
  • Literature
OMIM
168461
Clinvar variants
Variants in CCND1
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)

CCND1 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

CCND1 was created by Eleanor Williams