VIPAR Back

VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of VIPAR

This gene encodes a protein involved in the sorting of lysosomal proteins. Mutations in this gene are associated with ARCS2 (arthrogryposis, renal dysfunction, and cholestasis-2). Alternative splicing results in multiple transcript variants.

Community Annotation of VIPAR Add / Edit VIPAR: Annotations

No community annotations yet for VIPAR.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

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

VIPAR is highly significantly mutated in
(none)
VIPAR is significantly mutated in
(none)
VIPAR is near significance in
(none)

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

Data details


Mutation list for VIPAR