WDR65 Back

WD repeat domain 65

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NCBI Description of WDR65
This protein encoded by this gene belongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of biological pathways. This family member is thought to function in craniofacial development, possibly in the fusion of lip and palate. A missense mutation in this gene is associated with Van der Woude syndrome 2. Alternative splicing of this gene results in multiple transcript variants.

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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

WDR65 is highly significantly mutated in
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WDR65 is significantly mutated in
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WDR65 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 WDR65