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GENE INFORMATION

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Gene name

BCL7B

Synonyms

Description

B-cell CLL/lymphoma 7B (HGNC Symbol)

Entrez gene 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]

Chromosome

7 (Chromosome progress)

Cytoband

q11.23

Chromosome location (bp)

72950686 - 72972332

Ensembl

ENSG00000106635 (version 69.37)

Entrez gene

9275

UniProt

Q9BQE9

neXtProt

NX_Q9BQE9

Antibodypedia

BCL7B antibodies
 

PROTEIN VIEW

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BCL7B-001
 
BCL7B-002
 
BCL7B-006
 
BCL7B-007
 
BCL7B-008
 
BCL7B-014
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

BCL7B-001 ENSP00000223368
ENST00000223368
Q9BQE9
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Show » Show » 202 22.2 No 0
BCL7B-002 ENSP00000393230
ENST00000411832
C9JWD3
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145 16 No 0
BCL7B-006 ENSP00000411073
ENST00000455335
F2Z3H6
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30 3.4 No 0
BCL7B-007 ENSP00000414231
ENST00000448175
F8WE18
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78 9 No 0
BCL7B-008 ENSP00000414473
ENST00000454871
F8WDZ4
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88 9.9 No 0
BCL7B-014 ENSP00000406069
ENST00000416906
F2Z3H6
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30 3.4 No 0