EPHA8

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

Ephrin type-A receptor 8 is a protein that in humans is encoded by the EPHA8 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesEPHA8, EEK, EK3, HEK3, EPH receptor A8
Quick facts Available structures, PDB ...
EPHA8
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesEPHA8, EEK, EK3, HEK3, EPH receptor A8
External IDsOMIM: 176945; MGI: 109378; HomoloGene: 22436; GeneCards: EPHA8; OMA:EPHA8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001006943
NM_020526

NM_007939

RefSeq (protein)

NP_001006944
NP_065387

NP_031965

Location (UCSC)Chr 1: 22.56 – 22.6 MbChr 4: 136.93 – 136.96 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

Function

This gene encodes a member of 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. The protein encoded by this gene functions as a receptor for ephrin A2, A3 and A5 and plays a role in short-range contact-mediated axonal guidance during development of the mammalian nervous system.[6]

Interactions

EPHA8 has been shown to interact with FYN.[7]

References

Further reading

Related Articles

Wikiwand AI