SATB2 Back

SATB homeobox 2

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of SATB2

This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and mental retardation. Alternate splicing results in multiple transcript variants that encode the same protein.

Community Annotation of SATB2 Add / Edit SATB2: Annotations

No community annotations yet for SATB2.
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

SATB2 is highly significantly mutated in
(none)
SATB2 is significantly mutated in
(none)
SATB2 is near significance in
(none)

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

Data details


Mutation list for SATB2