frizzled-related protein

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NCBI Description of FRZB

The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility.

Community Annotation of FRZB Add / Edit FRZB: Annotations

No community annotations yet for FRZB.
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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).


FRZB is highly significantly mutated in
FRZB is significantly mutated in
FRZB is near significance in

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

Data details

Mutation list for FRZB