Familial Meniere Disease

Gene: CCL2

Red List (low evidence)

CCL2 (C-C motif chemokine ligand 2)
EnsemblGeneIds (GRCh38): ENSG00000108691
EnsemblGeneIds (GRCh37): ENSG00000108691
OMIM: 158105, Gene2Phenotype
CCL2 is in 3 panels

0 reviews

Details

Sources
  • Literature
OMIM
158105
Clinvar variants
Variants in CCL2
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)

CCL2 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

CCL2 was created by Eleanor Williams