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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
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Figure notes
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Data details