MED13L Back

mediator complex subunit 13-like

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of MED13L
The protein encoded by this gene is a subunit of the Mediator complex, a large complex of proteins that functions as a transcriptional coactivator for most RNA polymerase II-transcribed genes. The encoded protein is involved in early development of the heart and brain. Defects in this gene are a cause of transposition of the great arteries, dextro-looped (DTGA).

Community Annotation of MED13L Add / Edit MED13L: Annotations

No community annotations yet for MED13L.
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

MED13L is highly significantly mutated in
(none)
MED13L is significantly mutated in
(none)
MED13L is near significance in
(none)

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

Data details


• Mutation list for MED13L