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Gene : BCL7B Homo sapiens

Name  ? BAF chromatin remodeling complex subunit BCL7B Cytological Location  7q11.23
Brief Description  BAF chromatin remodeling complex subunit BCL7B
Description  This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2010]
  • synonyms:
  • NM_001707,
  • BCL tumor suppressor 7B,
  • BCL7B, BAF complex component,
  • B-cell CLL/lymphoma 7B,
  • OTTHUMG00000023412,
  • uc003tyf.3,
  • BCL7B,
  • X89985,
  • HGNC:1005
  • identifiers:
  • 9275,
  • ENSG00000106635,
  • BCL7B

Genome feature

Region: gene ? Length: 21335  
Location: 7:73536356-73557690 reverse strand Cyto location: 7q11.23

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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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]


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

3740 SNPs

5 Cross References

16 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results