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Gene : BAZ1B Homo sapiens

Name  ? bromodomain adjacent to zinc finger domain 1B Cytological Location  7q11.23
Brief Description  bromodomain adjacent to zinc finger domain 1B
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. [provided by RefSeq, Jul 2008]
  • synonyms:
  • BAZ1B,
  • uc003tyc.4,
  • transcription factor WSTF,
  • WBSCR10,
  • Williams-Beuren syndrome chromosome region 9,
  • WSTF,
  • AF084479,
  • Williams-Beuren syndrome chromosome region 10,
  • WSTF,
  • NM_032408,
  • WBSCR9,
  • HGNC:961,
  • OTTHUMG00000023847,
  • WBSCR10,
  • WBSCR9
  • identifiers:
  • 9031,
  • ENSG00000009954,
  • BAZ1B

Genome feature

Region: gene ? Length: 81888  
Location: 7:73440406-73522293 reverse strand Cyto location: 7q11.23

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Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



468 SN Ps

5 Cross References

17 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results