EFNB2
Ephrin-B2
Also known as: EFNB2_HUMAN, EPLG5, Htk-L, HTKL, LERK5, MGC126226, MGC126227, MGC126228
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P52799
- Gene
- EFNB2
- Ensembl
- ENSG00000125266
- Chromosome
- 13
- Canonical length
- 333 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. This gene encodes an EFNB class ephrin which binds to the EPHB4 and EPHA3 receptors. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
333 residues, UniProt reviewed canonical sequence.
>P52799|EFNB2
1 MAVRRDSVWK YCWGVLMVLC RTAISKSIVL EPIYWNSSNS KFLPGQGLVL YPQIGDKLDI
61 ICPKVDSKTV GQYEYYKVYM VDKDQADRCT IKKENTPLLN CAKPDQDIKF TIKFQEFSPN
121 LWGLEFQKNK DYYIISTSNG SLEGLDNQEG GVCQTRAMKI LMKVGQDASS AGSTRNKDPT
181 RRPELEAGTN GRSSTTSPFV KPNPGSSTDG NSAGHSGNNI LGSEVALFAG IASGCIIFIV
241 IIITLVVLLL KYRRRHRKHS PQHTTTLSLS TLATPKRSGN NNGSEPSDII IPLRTADSVF
301 CPHYEKVSGD YGHPVYIVQE MPPQSPANIY YKVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EFNB2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- placenta: 15 nTPM
- stomach: 14 nTPM
- colon: 14 nTPM
- lung: 13 nTPM
- seminal vesicle: 9.9 nTPM
- rectum: 9.3 nTPM
Single-cell type
- vascular endothelial cells: 298 nCPM
- prostatic glandular cells: 225 nCPM
- foveolar cells: 209 nCPM
- suprabasal keratinocytes: 202 nCPM
- lymphatic endothelial cells: 192 nCPM
- salivary basal cells: 182 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 23 nTPM
- cerebral cortex: 22 nTPM
- hypothalamus: 21 nTPM
- hippocampal formation: 20 nTPM
- white matter: 20 nTPM
- amygdala: 16 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.22
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 1.83
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adherens junction organization
- anatomical structure morphogenesis
- angiogenesis
- animal organ morphogenesis
- axon guidance
- blood vessel morphogenesis
- cell adhesion
- cell migration involved in sprouting angiogenesis
- cellular response to lipopolysaccharide
- ephrin receptor signaling pathway
- keratinocyte proliferation
- lymph vessel development
- negative regulation of keratinocyte proliferation
- negative regulation of neuron projection development
- nephric duct morphogenesis
- positive regulation of aorta morphogenesis
- positive regulation of cardiac muscle cell differentiation
- positive regulation of cell population proliferation
- positive regulation of leukocyte adhesion to arterial endothelial cell
- presynapse assembly
- regulation of chemotaxis
- regulation of postsynaptic membrane neurotransmitter receptor levels
- regulation of postsynaptic neurotransmitter receptor internalization
- T cell costimulation
- venous blood vessel morphogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EFNB2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads EFNB2 as an antibody target. Whether an autoantibody or antibody against EFNB2 could matter depends on whether native EFNB2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EFNB2 is annotated at the cell surface, where native EFNB2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label EFNB2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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