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Hearing loss

Gene: EPHB2

Red List (low evidence)

EPHB2 (EPH receptor B2)
EnsemblGeneIds (GRCh38): ENSG00000133216
EnsemblGeneIds (GRCh37): ENSG00000133216
OMIM: 600997, Gene2Phenotype
EPHB2 is in 3 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance
Unknown

Phenotypes
#603688:{Prostate cancer/brain cancer susceptibility, somatic}[<omim version=1.0><clinicalSynopsisList>]

Publications

Details

Sources
  • Expert
OMIM
600997
Clinvar variants
Variants in EPHB2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

EPHB2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert