BCL7B BAF chromatin remodeling complex subunit BCL7B [ Homo sapiens (human) ]
Source: NCBI Gene (ID 9275)
Symbol: BCL7B
Full name: BAF chromatin remodeling complex subunit BCL7B
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: SMARCJ2
Summary: 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]
Expression: Ubiquitous expression in bone marrow (RPKM 30.9), testis (RPKM 18.4) and 25 other tissues
Orthologs: mouse
Gene size: 21335bp
Exon count: 8