Familial Meniere Disease

Gene: MICA

Red List (low evidence)

MICA (MHC class I polypeptide-related sequence A)
EnsemblGeneIds (GRCh38): ENSG00000204520
EnsemblGeneIds (GRCh37): ENSG00000204520
OMIM: 600169, Gene2Phenotype
MICA is in 3 panels

0 reviews

Details

Sources
  • Literature
OMIM
600169
Clinvar variants
Variants in MICA
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)

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

17 Jan 2018, Gel status: 1

Created

Eleanor Williams (Genomics England Curator)

MICA was created by Eleanor Williams