DCAF17 Back

DDB1 and CUL4 associated factor 17

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NCBI Description of DCAF17

This gene encodes a nuclear transmembrane protein that associates with cullin 4A/damaged DNA binding protein 1 ubiquitin ligase complex. Mutations in this gene are associated with Woodhouse-Sakati syndrome. Alternate splicing results in multiple transcript variants.

Community Annotation of DCAF17 Add / Edit DCAF17: Annotations

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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).


DCAF17 is highly significantly mutated in
DCAF17 is significantly mutated in
DCAF17 is near significance in

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

Data details

Mutation list for DCAF17