FADD Back

Fas (TNFRSF6)-associated via death domain

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of FADD

The protein encoded by this gene is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis factor receptor, TNFRSF25, and TNFSF10/TRAIL-receptor, and thus it participates in the death signaling initiated by these receptors. Interaction of this protein with the receptors unmasks the N-terminal effector domain of this protein, which allows it to recruit caspase-8, and thereby activate the cysteine protease cascade. Knockout studies in mice also suggest the importance of this protein in early T cell development.

Community Annotation of FADD Add / Edit FADD: Annotations

No community annotations yet for FADD.
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

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

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

Data details


Mutation list for FADD