Homo sapiens Protein: BCL7B
Summary
InnateDB Protein IDBP-19938.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BCL7B
Protein Name B-cell CLL/lymphoma 7B
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000223368
InnateDB Gene IDBG-19936 (BCL7B)
Protein Structure
UniProt Annotation
Function May play a role in lung tumor development or progression.
Subcellular Localization
Disease Associations Note=BCL7B is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of BCL7B may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease. {ECO:0000269PubMed:9860302, ECO:0000269PubMed:9931421}.
Tissue Specificity Ubiquitous. {ECO:0000269PubMed:9860302, ECO:0000269PubMed:9931421}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 4 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003779 actin binding
Biological Process
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
Protein Structure and Domains
PDB ID
InterPro IPR006804 BCL7
PFAM PF04714
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9BQE9
PhosphoSite PhosphoSite-Q9BQE9
TrEMBL F2Z3H6
UniProt Splice Variant
Entrez Gene 9275
UniGene Hs.647051
RefSeq NP_001698
HUGO HGNC:1005
OMIM 605846
CCDS CCDS5550
HPRD 05786
IMGT
EMBL AC005089 AJ223979 AK123497 AK290091 BC000956 BC001967 BC009548 BX333744 CH471200 X89985
GenPept AAH00956 AAH01967 AAH09548 BAF82780 CAA11753 CAA62012 EAW69676 EAW69678