BAZ1B Back

bromodomain adjacent to zinc finger domain, 1B

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NCBI Description of BAZ1B

This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.

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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).


BAZ1B is highly significantly mutated in
BAZ1B is significantly mutated in
BAZ1B is near significance in

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

Data details

Mutation list for BAZ1B