PDE4DIP Back

phosphodiesterase 4D interacting protein (myomegalin)

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NCBI Description of PDE4DIP
The protein encoded by this gene serves to anchor phosphodiesterase 4D to the Golgi/centrosome region of the cell. Defects in this gene may be a cause of myeloproliferative disorder (MBD) associated with eosinophilia. Several transcript variants encoding different isoforms have been found for this gene.

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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

PDE4DIP is highly significantly mutated in
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PDE4DIP is significantly mutated in
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PDE4DIP is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for PDE4DIP