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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

Zinc finger protein 778

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. [provided by RefSeq, Jan 2011] (from NCBI)
Top mentioned proteins: HAD, Tec, M-cadherin, AGE
Papers on ZNF778
Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome.
Tekin et al., Miami, United States. In Am J Med Genet A, 2012
We present a mother and child with a heterozygous 365 Kb deletion at 16q24.3 containing ANKRD11, ZNF778, and SPG7 genes.
Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
GeneRIF
Kleefstra et al., Nijmegen, Netherlands. In Eur J Hum Genet, 2010
ZNF778 is a candidate gene for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
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