Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Hearing loss

Gene: HES5

Red List (low evidence)

HES5 (hes family bHLH transcription factor 5)
EnsemblGeneIds (GRCh38): ENSG00000197921
EnsemblGeneIds (GRCh37): ENSG00000197921
OMIM: 607348, Gene2Phenotype
HES5 is in 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

HES5 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:07 a.m.
HES5 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:42 p.m.

Publications

Details

Sources
  • Expert
OMIM
607348
Clinvar variants
Variants in HES5
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

HES5 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert