ERCC4 Back

excision repair cross-complementing rodent repair deficiency, complementation group 4

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of ERCC4

The protein encoded by this gene forms a complex with ERCC1 and is involved in the 5' incision made during nucleotide excision repair. This complex is a structure specific DNA repair endonuclease that interacts with EME1. Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F), or xeroderma pigmentosum VI (XP6).

Community Annotation of ERCC4 Add / Edit ERCC4: Annotations

No community annotations yet for ERCC4.
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

ERCC4 is highly significantly mutated in
(none)
ERCC4 is significantly mutated in
(none)
ERCC4 is near significance in
(none)

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

Data details


Mutation list for ERCC4