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The autosomal recessive immunodeficiency, centromeric instability and facial anomalies (ICF) syndrome is a genetically heterogeneous disorder. Despite recent successes in the identification of the underlying gene defects, it is currently unclear how mutations in any of the four known ICF genes cause...
ORGANISM(S): Homo sapiens (Human) 
2020-08-19 | PXD014741 | Pride
ZBTB24, a gene associated with human ICF syndrome, regulates centromeric and pericentrameric heterochromatin formation
ZBTB24 ICF2 model ES study
Structural basis of specific DNA binding by the transcription factor ZBTB24
ZBTB24, encoding a protein of the ZBTB family of transcriptional regulators, is one of four known genes – the other three being DNMT3B, CDCA7 and HELLS – that are mutated in immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome, a genetic disorder characterized by DNA hypome...
ORGANISM(S): Mus musculus 
2019-06-11 | GSE120969 | GEO
ZBTB24 is a transcriptional regulator that coordinates with DNMT3B to control DNA methylation [Infinium]
Effect of Zbtb24-depletion on gene expressions during the activation of peritoneal B1 cells
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