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EPHB2

EPH receptor B2

HCNC Approved Symbol
EPHB2 (HGNC:3393)
Genomic Coordinates
1:22,710,838 - 22,921,500 (1p36.12)
Synonyms
Hek5, Tyro5, DRT, ERK, EPHT3
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Bleeding disorder, platelet-type, 22
618462AR
{Prostate cancer/brain cancer susceptibility, somatic}
603688-

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the EPHB2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results