CLIP2 Back

CAP-GLY domain containing linker protein 2

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NCBI Description of CLIP2
The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.

Community Annotation of CLIP2 Add / Edit CLIP2: 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).


Legend

CLIP2 is highly significantly mutated in
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CLIP2 is significantly mutated in
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CLIP2 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 CLIP2