Gene and Protein Information
Species	TM	AA	Chromosomal Location	Gene Symbol	Gene Name	Reference
Human	-	1483	7q11.23	BAZ1B	bromodomain adjacent to zinc finger domain 1B
Mouse	-	1479	5 G2	Baz1b	bromodomain adjacent to zinc finger domain, 1B
Rat	-	1476	12q12	Baz1b	bromodomain adjacent to zinc finger domain, 1B

Previous and Unofficial Names

WBSCR10 | WBSCR9 | Williams-Beuren syndrome chromosome region 10 | WSTF | bromodomain adjacent to zinc finger domain, 1B | bromodomain adjacent to zinc finger domain

Database Links
Alphafold	Q9UIG0 (Hs), Q9Z277 (Mm)
CATH/Gene3D	1.10.30.10, 1.20.920.10, 3.30.40.10
ChEMBL Target	CHEMBL3588730 (Hs)
Ensembl Gene	ENSG00000009954 (Hs), ENSMUSG00000002748 (Mm), ENSRNOG00000001453 (Rn)
Entrez Gene	9031 (Hs), 22385 (Mm), 368002 (Rn)
Human Protein Atlas	ENSG00000009954 (Hs)
KEGG Gene	hsa:9031 (Hs), mmu:22385 (Mm), rno:368002 (Rn)
OMIM	605681 (Hs)
Pharos	Q9UIG0 (Hs)
RefSeq Nucleotide	NM_032408 (Hs), NM_011714 (Mm), NM_001191916 (Rn)
RefSeq Protein	NP_115784 (Hs), NP_035844 (Mm), NP_001178845 (Rn)
UniProtKB	Q9UIG0 (Hs), Q9Z277 (Mm)
Wikipedia	BAZ1B (Hs)

Physiological Consequences of Altering Gene Expression
BAZ1B (WSTF)-deficient mice exhibit some of the heart defects and abnormal calcium metabolism observed in Williams syndrome Species:  Mouse Tissue:  In vivo, cardiac tissue Technique:  Gene knockout References:  1

Gene Expression and Pathophysiology
Deletion of BAZ1B has been identified in patients with Williams-Beuren syndrome (WBS) Tissue or cell type:  Pathophysiology:  Williams-Beuren syndrome (WBS) Species:  Human Technique:  Fluorescence in situ hybridization and gene doasge analysis References:  2-3