SNX7 Back

sorting nexin 7

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NCBI Description of SNX7

This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region like some family members, and its exact function is unknown. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11.

Community Annotation of SNX7 Add / Edit SNX7: 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

SNX7 is highly significantly mutated in
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SNX7 is significantly mutated in
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SNX7 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 SNX7