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Hearing loss

Gene: GBX2

Red List (low evidence)

GBX2 (gastrulation brain homeobox 2)
EnsemblGeneIds (GRCh38): ENSG00000168505
EnsemblGeneIds (GRCh37): ENSG00000168505
OMIM: 601135, Gene2Phenotype
GBX2 is in 1 panel

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

GBX2 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
GBX2 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:42 p.m.

Publications

Details

Sources
  • Expert
OMIM
601135
Clinvar variants
Variants in GBX2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

GBX2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert