QuickView for BAZ1B (gene)

Gene Symbol:

BAZ1B Homo sapiens

Full name:

bromodomain adjacent to zinc finger domain 1B

Synonyms:

WBSCR10, WBSCR9, WSTF, tyrosine-protein kinase BAZ1B, hWALp2, transcription factor WSTF, williams syndrome transcription factor, williams-Beuren syndrome chromosomal region 10 protein, williams-Beuren syndrome chromosomal region 9 protein

Genomic Location:

Chr 7: 72492676-72574544

Description:

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.

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.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Gallus gallus ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus ,  Danio rerio

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

GTGCCAT_MIR183 ,  ATGTACA_MIR493 ,  ATCTTGC_MIR31 ,  CACCAGC_MIR138 ,  GGCACTT_MIR519E ,  AGGCACT_MIR5153P ,  ACAGGGT_MIR10A_MIR10B

miRNA binding sites
(Source: TargetScan):

Predicted Gene Targets for miR-10 ,  Predicted Gene Targets for miR-138 ,  Predicted Gene Targets for miR-183 ,  Predicted Gene Targets for miR-324-3p ,  Predicted Gene Targets for miR-370 ,  Predicted Gene Targets for miR-381 ,  Predicted Gene Targets for miR-493-5p

Cytogenetic Map:

7q11.23

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