CCDC22 Back

coiled-coil domain containing 22

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NCBI Description of CCDC22
This gene encodes a protein containing a coiled-coil domain. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. Localization of the orthologous rat protein suggests that it may play a role in neuronal injury response. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability.

Community Annotation of CCDC22 Add / Edit CCDC22: 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

CCDC22 is highly significantly mutated in
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CCDC22 is significantly mutated in
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CCDC22 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 CCDC22