EPH receptor A4

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

EPH receptor A4

EPH receptor A4 (ephrin type-A receptor 4) is a protein that in humans is encoded by the EPHA4 gene.[5][6]

Quick Facts EPHA4, Available structures ...
EPHA4
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesEPHA4, Epha4, 2900005C20Rik, AI385584, Cek8, Hek8, Sek, Sek1, Tyro1, rb, EPH receptor A4, HEK8, SEK, TYRO1, EK8
External IDsOMIM: 602188; MGI: 98277; HomoloGene: 20933; GeneCards: EPHA4; OMA:EPHA4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001304536
NM_001304537
NM_004438
NM_001363748

NM_007936

RefSeq (protein)

NP_001291465
NP_001291466
NP_004429
NP_001350677

NP_031962

Location (UCSC)Chr 2: 221.42 – 221.57 MbChr 1: 77.34 – 77.49 Mb
PubMed search[3][4]
Wikidata
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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.[6]

In 2012, a publication in Nature Medicine revealed a connection between EPHA4 and the neurodegenerative disease Amyotrophic lateral sclerosis (ALS), where a defective gene allows ALS patients to live considerably longer than patients with an intact gene. This opens up for development of treatment for this currently untreatable disease.

References

Further reading

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