Homo sapiens Gene: BCL7A
Summary
InnateDB Gene IDBG-62116.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BCL7A
Gene Name B-cell CLL/lymphoma 7A
Synonyms BCL7
Species Homo sapiens
Ensembl Gene ENSG00000110987
Encoded Proteins
B-cell CLL/lymphoma 7A
B-cell CLL/lymphoma 7A
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is directly involved, with Myc and IgH, in a three-way gene translocation in a Burkitt lymphoma cell line. As a result of the gene translocation, the N-terminal region of the gene product is disrupted, which is thought to be related to the pathogenesis of a subset of high-grade B cell non-Hodgkin lymphoma. The N-terminal segment involved in the translocation includes the region that shares a strong sequence similarity with those of BCL7B and BCL7C. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 12:122019422-122062044
Strand Forward strand
Band q24.31
Transcripts
ENST00000261822 ENSP00000261822
ENST00000432926
ENST00000538010 ENSP00000445868
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Experimentally validated
Total 8 [view]
Protein-Protein 8 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0045892 negative regulation of transcription, DNA-templated
Cellular Component
GO:0005575 cellular_component
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
TNFalpha pathway
REACTOME
KEGG
INOH
PID NCI
Cross-References
SwissProt Q4VC05
TrEMBL
UniProt Splice Variant
Entrez Gene 605
UniGene Hs.530970
RefSeq NM_001024808 NM_020993
HUGO HGNC:1004
OMIM 601406
CCDS CCDS53841 CCDS9226
HPRD
IMGT
EMBL AK296159 AK316486 BC094723 BC113627 CH471054 X89984
GenPept AAH94723 AAI13628 BAG58898 BAH14857 CAA62011 EAW98302
RNA Seq Atlas 605