Familial Meniere Disease

Gene: CXCL8

Red List (low evidence)

CXCL8 (C-X-C motif chemokine ligand 8)
EnsemblGeneIds (GRCh38): ENSG00000169429
EnsemblGeneIds (GRCh37): ENSG00000169429
OMIM: 146930, Gene2Phenotype
CXCL8 is in 2 panels

1 review

Eleanor Williams (Genomics England Curator)

Source publication used IL8 gene symbol.
17 Jan 2018, 4:33 p.m.

Details

Sources
  • Literature
OMIM
146930
Clinvar variants
Variants in CXCL8
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)

CXCL8 was added to Familial Meniere Disease panel. Sources: Literature

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

CXCL8 was created by Eleanor Williams