EPHA2

GENERAL INFORMATION

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Gene name

EPHA2

Gene description

EPH receptor A2

Protein class

Cancer-related genes
Disease related genes
Enzymes
FDA approved drug targets
Predicted membrane proteins
RAS pathway related proteins

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (esophagus)
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues showed weak to moderate cytoplasmic positivity. Strong staining was found in parietal cells of stomach, in glandular cells of salivary, thyroid and parathyroid glands and in granular layer of cerebellum. Membranous staining was observed only in the fallopian tube.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
CAB010464
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Thyroid gland

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (esophagus)

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

EPHA2 (HGNC Symbol)

Synonyms

ECK

Description

EPH receptor A2 (HGNC Symbol)

Entrez gene summary

This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene encodes a protein that binds ephrin-A ligands. Mutations in this gene are the cause of certain genetically-related cataract disorders.[provided by RefSeq, May 2010]

Chromosome

1

Cytoband

p36.13

Chromosome location (bp)

16124337 - 16156087

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000142627 (version 78.38)

Entrez gene

1969

UniProt

P29317 (UniProt - Evidence at protein level)

neXtProt

NX_P29317

Antibodypedia

EPHA2 antibodies


PROTEIN BROWSER

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ENST00000358432
 
ENST00000611929
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

EPHA2-001 ENSP00000351209
ENST00000358432
P29317
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Show » Show » 976 108.3 Yes 1
EPHA2-201 ENSP00000484980
ENST00000611929
P29317
Show all »
Show » Show » 976 108.3 Yes 1