CEP152 Back

centrosomal protein 152kDa

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of CEP152
This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants.

Community Annotation of CEP152 Add / Edit CEP152: Annotations

No community annotations yet for CEP152.
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

CEP152 is highly significantly mutated in
(none)
CEP152 is significantly mutated in
(none)
CEP152 is near significance in
(none)

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

Data details


• Mutation list for CEP152