NCBI Description of RNF168
|This gene encodes an E3 ubiquitin ligase protein that contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The protein is involved in DNA double-strand break (DSB) repair. Mutations in this gene result in Riddle syndrome. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.|
Community Annotation of RNF168 Add / Edit RNF168: Annotations
No community annotations yet for RNF168.
• "Mouse over" a mutation to see details.
Click on a tumor type to see its full list of significant genes.