ULK2 Back

unc-51-like kinase 2 (C. elegans)

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of ULK2

This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified.

Community Annotation of ULK2 Add / Edit ULK2: Annotations

No community annotations yet for ULK2.
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

ULK2 is highly significantly mutated in
(none)
ULK2 is significantly mutated in
(none)
ULK2 is near significance in
(none)

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

Data details


Mutation list for ULK2