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

Hearing loss

Gene: ATF2

Red List (low evidence)

ATF2 (activating transcription factor 2)
EnsemblGeneIds (GRCh38): ENSG00000115966
EnsemblGeneIds (GRCh37): ENSG00000115966
OMIM: 123811, Gene2Phenotype
ATF2 is in 1 panel

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

ATF2 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:05 a.m.
ATF2 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:39 p.m.

Publications

Details

Sources
  • Expert
OMIM
123811
Clinvar variants
Variants in ATF2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

ATF2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert