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BAZ1B is 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.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.
BAZ1B; bromodomain adjacent to zinc finger domain 1B; bromodomain adjacent to zinc finger domain protein 1B; bromodomain adjacent to zinc finger domain, 1B; bromodomain adjacent to zinc finger domain, 1B; Williams-Beuren syndrome chromosome region 9 homolog; C87820; hWALp2; transcription factor WSTF; tyrosine-protein kinase BAZ1B; tyrosine-protein kinase BAZ1B; LOW QUALITY PROTEIN: tyrosine-protein kinase BAZ1B; Tyrosine-protein kinase BAZ1B-like protein; WBSC10; WBSCR10; WBSCR9; williams syndrome transcription factor; Williams syndrome transcription factor homolog; williams-Beuren syndrome chromosomal region 10 protein; Williams-Beuren syndrome chromosomal region 9 protein; williams-Beuren syndrome chromosomal region 9 protein homolog; Williams-Beuren syndrome chromosome region 9 homolog; Wstf
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