ATXN2L Back

ataxin 2-like

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of ATXN2L

This gene encodes an ataxin type 2 related protein of unknown function. This protein is a member of the spinocerebellar ataxia (SCAs) family, which is associated with a complex group of neurodegenerative disorders. Several alternatively spliced transcripts encoding different isoforms have been found for this gene.

Community Annotation of ATXN2L Add / Edit ATXN2L: Annotations

No community annotations yet for ATXN2L.
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

ATXN2L is highly significantly mutated in
(none)
ATXN2L is significantly mutated in
(none)
ATXN2L is near significance in
(none)

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

Data details


Mutation list for ATXN2L