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Hearing loss

Gene: HES1

Red List (low evidence)

HES1 (hes family bHLH transcription factor 1)
EnsemblGeneIds (GRCh38): ENSG00000114315
EnsemblGeneIds (GRCh37): ENSG00000114315
OMIM: 139605, Gene2Phenotype
HES1 is in 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

HES1 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
HES1 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:42 p.m.

Publications

Details

Sources
  • Expert
OMIM
139605
Clinvar variants
Variants in HES1
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

HES1 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert