VPS13B Back

vacuolar protein sorting 13 homolog B (yeast)

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NCBI Description of VPS13B

This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene.

Community Annotation of VPS13B Add / Edit VPS13B: 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).


VPS13B is highly significantly mutated in
VPS13B is significantly mutated in
VPS13B is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for VPS13B