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  2. EFNA5 - ephrin A5 Gene

EFNA5 - ephrin A5 Gene

Homo sapiens

Also known as AF1; EFL5; RAGS; EPLG7; GLC1M; LERK7

Gene ID: 1946 | Gene type: protein coding

About EFNA5

Cytogenetic location: 5q21.3 Genomic coordinates (GRCh38): 5:107,376,894-107,670,937 (from NCBI)

This gene has 5 transcripts (splice variants), 289 orthologues and 7 paralogues. Ubiquitous expression in skin (RPKM 2.4), brain (RPKM 1.7) and 22 other tissues.

Summary

Ephrin-A5, a member of the ephrin gene family, prevents axon bundling in cocultures of cortical neurons with astrocytes, a model of late stage nervous system development and differentiation. The EPH and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, particularly in the nervous system. Eph Receptors typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin ligands and receptors have been named by the Eph Nomenclature Committee (1997). 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. The Eph family of receptors are similarly divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. [provided by RefSeq, Jul 2008]

EFNA5 Products(2)

mRNA Protein Name
NM_001410773.1 NP_001397702.1 ephrin-A5 isoform 2 precursor
NM_001962.3 NP_001953.1 ephrin-A5 isoform 1 precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables ephrin receptor binding IPI
IPI: Inferred from physical interaction
11519828 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19836338 GOA
Biological Process GO Annotation Evidence Reference Source
NOT involved in apoptotic process IDA
IDA: Inferred from direct assay
11870224 GOA
involved in ephrin receptor signaling pathway IDA
IDA: Inferred from direct assay
11870224 GOA
acts upstream of or within negative regulation of substrate adhesion-dependent cell spreading IDA
IDA: Inferred from direct assay
23242526 GOA
involved in regulation of GTPase activity IDA
IDA: Inferred from direct assay
11870224 GOA
involved in regulation of actin cytoskeleton organization IDA
IDA: Inferred from direct assay
11870224 GOA
acts upstream of or within regulation of cell morphogenesis IDA
IDA: Inferred from direct assay
23242526 GOA
involved in regulation of cell-cell adhesion IDA
IDA: Inferred from direct assay
11870224 GOA
involved in regulation of focal adhesion assembly IDA
IDA: Inferred from direct assay
11870224 GOA
involved in regulation of microtubule cytoskeleton organization IDA
IDA: Inferred from direct assay
11870224 GOA
Cellular Component GO Annotation Evidence Reference Source
located in external side of plasma membrane IDA
IDA: Inferred from direct assay
11870224 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

EFNA5 Protein Structure

Ephrin

Ephrin: Ephrin (27 - 163)

  • 0
  • 100
  • 200
  • 228 a.a.
Protein Preferred Names Protein Names

ephrin-A5

AL-1

EFNA5 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
EFNA5 P52803 SGPL1 Homo sapiens O95470 32296183
Intra
EFNA5 P52803 SGPL1 Homo sapiens O95470 32296183
Intra
EFNA5 P52803 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
EFNA5 P52803 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
EFNA5 P52803 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
EFNA5 P52803 HIBADH Homo sapiens P31937 32296183
Intra
EFNA5 P52803 HIBADH Homo sapiens P31937 32296183
Intra
EFNA5 P52803 GPR151 Homo sapiens Q8TDV0 32296183
Intra
EFNA5 P52803 GPR151 Homo sapiens Q8TDV0 32296183
Intra
EFNA5 P52803 GPR151 Homo sapiens Q8TDV0 32296183
Intra
EFNA5 P52803 TSPO2 Homo sapiens Q5TGU0 32296183
Intra
EFNA5 P52803 TSPO2 Homo sapiens Q5TGU0 32296183
Intra
EFNA5 P52803 TSPO2 Homo sapiens Q5TGU0 32296183
Intra
EFNA5 P52803 AQP2 Homo sapiens P41181 32296183
Intra
EFNA5 P52803 AQP2 Homo sapiens P41181 32296183
Intra
EFNA5 P52803 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
EFNA5 P52803 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
EFNA5 P52803 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
EFNA5 P52803 SLC13A4 Homo sapiens Q9UKG4 32296183
Intra
EFNA5 P52803 SLC13A4 Homo sapiens Q9UKG4 32296183
Intra
EFNA5 P52803 SLC13A4 Homo sapiens Q9UKG4 32296183
Intra
EFNA5 P52803 AQP6 Homo sapiens Q13520 32296183
Intra
EFNA5 P52803 AQP6 Homo sapiens Q13520 32296183
Intra
EFNA5 P52803 AQP6 Homo sapiens Q13520 32296183
Intra
EFNA5 P52803 GPR152 Homo sapiens Q8TDT2 32296183
Intra
EFNA5 P52803 GPR152 Homo sapiens Q8TDT2 32296183
Intra
EFNA5 P52803 GPR152 Homo sapiens Q8TDT2 32296183
Intra
EFNA5 P52803 TM4SF18 Homo sapiens Q96CE8 32296183
Intra
EFNA5 P52803 TM4SF18 Homo sapiens Q96CE8 32296183
Intra
EFNA5 P52803 TM4SF18 Homo sapiens Q96CE8 32296183
Intra
EFNA5 P52803 ACKR2 Homo sapiens O00590 32296183
Intra
EFNA5 P52803 ACKR2 Homo sapiens O00590 32296183
Intra
EFNA5 P52803 EPHA7 Homo sapiens Q15375 33961781
Intra
EFNA5 P52803 RHCG Homo sapiens Q9UBD6 32296183
Intra
EFNA5 P52803 RHCG Homo sapiens Q9UBD6 32296183
Intra
EFNA5 P52803 RHCG Homo sapiens Q9UBD6 32296183
Intra
EFNA5 P52803 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
EFNA5 P52803 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
EFNA5 P52803 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
EFNA5 P52803 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
EFNA5 P52803 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
EFNA5 P52803 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
EFNA5 P52803 GJB1 Homo sapiens P08034 32296183
Intra
EFNA5 P52803 GJB1 Homo sapiens P08034 32296183
Intra
EFNA5 P52803 FFAR3 Homo sapiens O14843 32296183
Intra
EFNA5 P52803 FFAR3 Homo sapiens O14843 32296183
Intra
EFNA5 P52803 TRHR Homo sapiens P34981 32296183
Intra
EFNA5 P52803 TRHR Homo sapiens P34981 32296183
Intra
EFNA5 P52803 GPR42 Homo sapiens O15529 32296183
Intra
EFNA5 P52803 GPR42 Homo sapiens O15529 32296183
Intra
EFNA5 P52803 SLC10A2 Homo sapiens Q12908 32296183
Intra
EFNA5 P52803 SLC10A2 Homo sapiens Q12908 32296183
Intra
EFNA5 P52803 SLC10A2 Homo sapiens Q12908 32296183
Intra
EFNA5 P52803 CLDN5 Homo sapiens O00501 32296183
Intra
EFNA5 P52803 CLDN5 Homo sapiens O00501 32296183
Intra
EFNA5 P52803 BEST2 Homo sapiens Q8NFU1 32296183
Intra
EFNA5 P52803 BEST2 Homo sapiens Q8NFU1 32296183
Intra
EFNA5 P52803 BEST2 Homo sapiens Q8NFU1 32296183
Intra
EFNA5 P52803 HERPUD2 Homo sapiens Q9BSE4 32296183
Intra
EFNA5 P52803 HERPUD2 Homo sapiens Q9BSE4 32296183
Intra
EFNA5 P52803 HERPUD2 Homo sapiens Q9BSE4 32296183
Intra
EFNA5 P52803 EPHA4 Homo sapiens P54764 33961781
Intra
EFNA5 P52803 GPR161 Homo sapiens Q8N6U8 32296183
Intra
EFNA5 P52803 GPR161 Homo sapiens Q8N6U8 32296183
Intra
EFNA5 P52803 GPR161 Homo sapiens Q8N6U8 32296183
Intra
EFNA5 P52803 CD53 Homo sapiens P19397 32296183
Intra
EFNA5 P52803 CD53 Homo sapiens P19397 32296183
Intra
EFNA5 P52803 EPHA2 Homo sapiens P29317 33961781
Intra
EFNA5 P52803 KASH5 Homo sapiens Q8N6L0 32296183
Intra
EFNA5 P52803 KASH5 Homo sapiens Q8N6L0 32296183
Intra
EFNA5 P52803 KASH5 Homo sapiens Q8N6L0 32296183
Intra
EFNA5 P52803 YIPF6 Homo sapiens Q96EC8 32296183
Intra
EFNA5 P52803 YIPF6 Homo sapiens Q96EC8 32296183
Intra
EFNA5 P52803 YIPF6 Homo sapiens Q96EC8 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant EFNA5 Proteins

Cat. No. Product Name Accession Purity
HY-P70379 Ephrin-A5/EFNA5 Protein, Human (HEK293, Fc) P52803 (Q21-N203) ≥95%
HY-P73012 Ephrin-A5/EFNA5 Protein, Human (HEK293, His) P52803 (Q21-N203) ≥95%

Related Diseases

Diseases Alias
Cortical Senile Cataract
Persistent Hyperplastic Primary Vitreous

Congenital Retinal Detachment

Ncrna Disease

Non-Syndromic Congenital Retinal Non-Attachment

Pfvs

Phpv

Persistent Fetal Vasculature Syndrome

Omenn Syndrome

Histiocytic Medullary Reticulosis

Severe Combined Immunodeficiency With Hypereosinophilia

Combined Immunodeficiency With Hypereosinophilia

Reticuloendotheliosis, Familial, With Eosinophilia

Reticuloendotheliosis Familial With Eosinophilia

Familial Reticuloendotheliosis

Omenn'S Syndrome

OS

Malignant Histiocytosis

Cataract

Cataracts

Cat - [Cataract]

Cataract Form

Lens Opacity

Lens Opacities

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus EFNA5 MGD MGI:107444
Felis catus EFNA5 VGNC VGNC:102192
Rattus norvegicus EFNA5 RGD RGD:620391
Bos taurus EFNA5 VGNC VGNC:28358
Macaca mulatta EFNA5 VGNC VGNC:72168
Canis familiaris EFNA5 VGNC VGNC:53168
Others EFNA5 NCBI