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Hearing loss

Gene: DLX2

Red List (low evidence)

DLX2 (distal-less homeobox 2)
EnsemblGeneIds (GRCh38): ENSG00000115844
EnsemblGeneIds (GRCh37): ENSG00000115844
OMIM: 126255, Gene2Phenotype
DLX2 is in 2 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

DLX2 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
DLX2 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:41 p.m.

Publications

Details

Sources
  • Expert
OMIM
126255
Clinvar variants
Variants in DLX2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

DLX2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert