WDR62 Back

WD repeat domain 62

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of WDR62
This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and mental retardation. Alternative splicing results in multiple transcript variants.

Community Annotation of WDR62 Add / Edit WDR62: Annotations

No community annotations yet for WDR62.
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

WDR62 is highly significantly mutated in
(none)
WDR62 is significantly mutated in
(none)
WDR62 is near significance in
(none)

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

Data details


• Mutation list for WDR62