CGGBP1 Back

CGG triplet repeat binding protein 1

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NCBI Description of CGGBP1
CGGBP1 influences expression of the FMR1 gene (MIM 309550), which is associated with the fragile X mental retardation syndrome (MIM 300624), by specifically interacting with the 5-prime (CGG)n-3-prime repeat in its 5-prime UTR.[supplied by OMIM, Mar 2008].

Community Annotation of CGGBP1 Add / Edit CGGBP1: Annotations

No community annotations yet for CGGBP1.
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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

CGGBP1 is highly significantly mutated in
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CGGBP1 is significantly mutated in
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CGGBP1 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 CGGBP1