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BCL7B, BAF chromatin remodeling complex subunit BCL7B

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BCL7B, BAF chromatin remodeling complex subunit BCL7B

  • 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]

  • Gene Synonyms (B-cell CLL/lymphoma 7 protein family member B, B-cell CLL/lymphoma 7B, BCL tumor suppressor 7B, BCL7B, BAF complex component,)
  • NCBI Gene ID: 9275
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9BQE9
    UNIPROT ID#>>F2Z3H6
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

BAF chromatin remodeling complex subunit BCL7B interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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