FZD9 Back

frizzled homolog 9 (Drosophila)

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NCBI Description of FZD9

Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.

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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

FZD9 is highly significantly mutated in
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FZD9 is significantly mutated in
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FZD9 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 FZD9