ZNF778 Back

zinc finger protein 778

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of ZNF778

The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene.

Community Annotation of ZNF778 Add / Edit ZNF778: Annotations

No community annotations yet for ZNF778.
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

ZNF778 is highly significantly mutated in
(none)
ZNF778 is significantly mutated in
(none)
ZNF778 is near significance in
(none)

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

Data details


Mutation list for ZNF778