DRP2 Back

dystrophin related protein 2

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of DRP2

Members of the dystrophin family of proteins perform a critical role in the maintenance of membrane-associated complexes at points of intercellular contact in vertebrate cells. The protein encoded by this gene is predicted to resemble certain short C-terminal isoforms of dystrophin and dystrophin-related protein 1 (DRP1 or utrophin). DRP2 is expressed principally in the brain and spinal cord. Two transcript variants encoding different isoforms have been found for this gene.

Community Annotation of DRP2 Add / Edit DRP2: Annotations

No community annotations yet for DRP2.
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

DRP2 is highly significantly mutated in
(none)
DRP2 is significantly mutated in
(none)
DRP2 is near significance in
(none)

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

Data details


Mutation list for DRP2