(Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008].
Oppikofer, Sagolla, Haley, Zhang, Kummerfeld, Sudhamsu, Flynn, Bai, Zhang, Ciferri, Cochran: "Non-canonical reader modules of BAZ1A promote recovery from DNA damage." in: Nature communications, Vol. 8, Issue 1, pp. 862, (2018) (PubMed).
Sirbu, McDonald, Dungrawala, Badu-Nkansah, Kavanaugh, Chen, Tabb, Cortez: "Identification of proteins at active, stalled, and collapsed replication forks using isolation of proteins on nascent DNA (iPOND) coupled with mass spectrometry." in: The Journal of biological chemistry, Vol. 288, Issue 44, pp. 31458-67, (2013) (PubMed).
Lu, Meng, Morris, Keating: "A novel human gene, WSTF, is deleted in Williams syndrome." in: Genomics, Vol. 54, Issue 2, pp. 241-9, (1999) (PubMed).