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EPHB4

EPH receptor B4

HCNC Approved Symbol
EPHB4 (HGNC:3395)
Genomic Coordinates
7:100,802,565 - 100,827,523 (7q22.1)
Synonyms
Tyro11, HTK
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

6Patients

In total, 6 patients were diagnosed with a variant in the EPHB4 gene.

Frequently observed phenotypes

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

Telangiectasia
 3 (50.0%)
Dysmorphism
 1 (16.7%)
Fetal hydrops
 1 (16.7%)
Asthma
 1 (16.7%)
Chronic gastritis
 1 (16.7%)
EPHB4 - Gene browser | 3billion