TBXA2R Back

thromboxane A2 receptor

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of TBXA2R

This gene encodes a member of the G protein-coupled receptor family. The protein interacts with thromboxane A2 to induce platelet aggregation and regulate hemostasis. A mutation in this gene results in a bleeding disorder. Multiple transcript variants encoding different isoforms have been found for this gene.

Community Annotation of TBXA2R Add / Edit TBXA2R: Annotations

No community annotations yet for TBXA2R.
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

TBXA2R is highly significantly mutated in
(none)
TBXA2R is significantly mutated in
(none)
TBXA2R is near significance in
(none)

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

Data details


Mutation list for TBXA2R