EFNA1 Back

ephrin-A1

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of EFNA1

This gene encodes a member of the ephrin (EPH) family. The ephrins and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. 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. This gene encodes an EFNA class ephrin which binds to the EPHA2, EPHA4, EPHA5, EPHA6, and EPHA7 receptors. Two transcript variants that encode different isoforms were identified through sequence analysis.

Community Annotation of EFNA1 Add / Edit EFNA1: Annotations

No community annotations yet for EFNA1.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

EFNA1 is highly significantly mutated in
(none)
EFNA1 is significantly mutated in
(none)
EFNA1 is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for EFNA1