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.
A synthesized peptide derived from human BCL7C, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human BCL9, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human BCL9, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human BCL9L, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human BCL9L.
A synthesized peptide derived from human BCLAF1, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human BCL-XL, corresponding to a region within N-terminal amino acids.
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