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

Hearing loss

Gene: EPHB3

Red List (low evidence)

EPHB3 (EPH receptor B3)
EnsemblGeneIds (GRCh38): ENSG00000182580
EnsemblGeneIds (GRCh37): ENSG00000182580
OMIM: 601839, Gene2Phenotype
EPHB3 is in 1 panel

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

EPHB3 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
EPHB3 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:41 p.m.

Publications

Details

Sources
  • Expert
OMIM
601839
Clinvar variants
Variants in EPHB3
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

EPHB3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert