EPHB2

EPH Receptor B2: A Key Regulator in Cell Positioning, Migration, and Cancer Progression

Gene Information Card

Symbol EPHB2
Full Name EPH Receptor B2
Gene Type protein-coding
Chromosomal Location 1p36.12
NCBI Gene ID 2048 ncbi.nlm.nih.gov/gene/2048
Ensembl ID ENSG00000133216
UniProt ID P29323
OMIM ID 600997
HGNC ID 3393
Aliases CAPB, DRT, EPHT3, ERK, Hek5, PCBC, Tyro5

Description

EPHB2 (EPH receptor B2) is a member of the Eph receptor tyrosine kinase family, which mediates bidirectional signaling upon binding to ephrin-B ligands. It plays critical roles in cell positioning, migration, axon guidance, and angiogenesis. EPHB2 is frequently altered in various cancers, including colorectal, prostate, and breast cancers, where it can act as either a tumor suppressor or oncogene depending on the cellular context.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal Cancer Loss of EPHB2 expression disrupts intestinal epithelial cell positioning and promotes tumor progression. ClinVar, COSMIC
Prostate Cancer EPHB2 mutations and reduced expression are associated with aggressive disease and metastasis. COSMIC, NCBI Gene
Breast Cancer EPHB2 overexpression correlates with poor prognosis and invasive phenotype. NCBI Gene, COSMIC
Gastric Cancer EPHB2 downregulation is linked to tumor invasion and lymph node metastasis. NCBI Gene
Lung Cancer EPHB2 alterations contribute to tumor growth and resistance to therapy. COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 Medium
Colon 8.3 Medium
Prostate 7.1 Medium
Breast 6.4 Low
Lung 5.2 Low
Liver 3.8 Low
Cell Line Expression
Cell Line nTPM Notes
HEK 293 15.2 High expression
HeLa 10.1 Moderate expression
MCF7 7.8 Moderate expression
PC3 6.5 Low expression
A549 4.3 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
p.Gly787Arg Missense <1% Alters kinase domain; potential loss of function
p.Arg524* Nonsense <1% Truncation; loss of function
p.Val105Ile Missense <1% Unknown significance
p.Pro707Leu Missense <1% Unknown significance
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations leading to truncated protein or reduced kinase activity.

Gain of Function (GOF)

Missense mutations in the kinase domain that enhance signaling have been reported in some cancers.

Dominant Negative (DN)

Truncated receptors lacking the kinase domain can interfere with wild-type EPHB2 signaling.

Gene Ontology (GO)

• receptor tyrosine kinase activity • transmembrane signaling receptor activity
• protein binding • ATP binding
• axon guidance • cell migration
• angiogenesis • cell adhesion
• ephrin receptor signaling pathway

Pathways

Ephrin B-EPHB forward signaling
Ephrin B reverse signaling
Axon guidance
Signaling by Receptor Tyrosine Kinases
EPH-ephrin mediated repulsion of cells

Protein Summary

EPHB2 is a single-pass type I transmembrane receptor with an N-terminal ephrin-binding domain, a cysteine-rich region, two fibronectin type III repeats, a transmembrane segment, and a cytoplasmic tyrosine kinase domain. Upon binding ephrin-B ligands, it undergoes autophosphorylation and activates downstream signaling pathways, including MAPK and PI3K/AKT, regulating cytoskeletal dynamics and cell adhesion. EPHB2 also mediates reverse signaling through its ligand ephrin-B.

Related Products

Product name Cat.No. Species Gene ID
EPHB2 Knockout HEK293 Cell Line EDJ-KQ2329 Human 2048 Details Get a Quote
EPHB2 Knockout HCT 116 Cell Line EDJ-KQ21402 Human 2048 Details Get a Quote
EPHB2 Knockout A-549 Cell Line EDJ-KQ22725 Human 2048 Details Get a Quote
EPHB2 Knockout HeLa Cell Line EDJ-KQ22727 Human 2048 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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