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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

EFNA5 Protein Structure

Ephrin

Ephrin: Ephrin (27 - 163)

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

ephrin-A5

AL-1

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