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Hearing loss

Gene: ESR2

Red List (low evidence)

ESR2 (estrogen receptor 2)
EnsemblGeneIds (GRCh38): ENSG00000140009
EnsemblGeneIds (GRCh37): ENSG00000140009
OMIM: 601663, Gene2Phenotype
ESR2 is in 3 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

ESR2 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
ESR2 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:41 p.m.

Publications

Details

Sources
  • Expert
OMIM
601663
Clinvar variants
Variants in ESR2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

ESR2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert