BAZ1B

GENE INFORMATION

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Gene name

BAZ1B (HGNC Symbol)

Synonyms

WBSCR10, WBSCR9, WSTF

Description

Bromodomain adjacent to zinc finger domain, 1B (HGNC Symbol)

Entrez gene summary

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]

Chromosome

7

Cytoband

q11.23

Chromosome location (bp)

73440398 - 73522278

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000009954 (version 78.38)

Entrez gene

9031

UniProt

Q9UIG0 (UniProt - Evidence at protein level)

neXtProt

NX_Q9UIG0

Antibodypedia

BAZ1B antibodies
 

PROTEIN VIEW

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BAZ1B-001
 
BAZ1B-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

BAZ1B-001 ENSP00000342434
ENST00000339594
Q9UIG0
Show all »
Show » Show » 1483 170.9 No 0
BAZ1B-002 ENSP00000385442
ENST00000404251
Q9UIG0
Show all »
Show » Show » 1483 170.9 No 0