External Ids for ZNF778 Gene
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. [provided by RefSeq, Jan 2011]
GeneCards Summary for ZNF778 Gene
ZNF778 (Zinc Finger Protein 778) is a Protein Coding gene. Diseases associated with ZNF778 include kbg syndrome and 16q24.3 microdeletion syndrome. Among its related pathways are Gene Expression and Gene Expression. An important paralog of this gene is ZNF426.
UniProtKB/Swiss-Prot for ZNF778 Gene
May be involved in transcriptional regulation.