Familial Meniere Disease

Gene: CCR5

Red List (low evidence)

CCR5 (C-C motif chemokine receptor 5 (gene/pseudogene))
EnsemblGeneIds (GRCh38): ENSG00000160791
EnsemblGeneIds (GRCh37): ENSG00000160791
OMIM: 601373, Gene2Phenotype
CCR5 is in 1 panel

0 reviews

Details

Sources
  • Literature
OMIM
601373
Clinvar variants
Variants in CCR5
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)

CCR5 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

CCR5 was created by Eleanor Williams