Human Gene BCL6B (uc002geg.2)
  Description: Homo sapiens B-cell CLL/lymphoma 6, member B (BCL6B), mRNA.
Transcript (Including UTRs)
   Position: hg19 chr17:6,926,422-6,932,961 Size: 6,540 Total Exon Count: 9 Strand: +
Coding Region
   Position: hg19 chr17:6,926,991-6,930,938 Size: 3,948 Coding Exon Count: 8 

Page IndexSequence and LinksUniProtKB CommentsPrimersGenetic AssociationsMalaCards
CTDGene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein Structure
Other SpeciesGO AnnotationsmRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr17:6,926,422-6,932,961)mRNA (may differ from genome)Protein (479 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCLynxMalacardsMGI
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BioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: BCL6B_HUMAN
DESCRIPTION: RecName: Full=B-cell CLL/lymphoma 6 member B protein; AltName: Full=Bcl6-associated zinc finger protein; AltName: Full=Zinc finger protein 62;
FUNCTION: Acts as a sequence-specific transcriptional repressor in association with BCL6. May function in a narrow stage or be related to some events in the early B-cell development.
SUBUNIT: Associates with BCL6 through the BTB domain (By similarity).
SUBCELLULAR LOCATION: Nucleus (By similarity).
TISSUE SPECIFICITY: Ubiquitously expressed with higher expression found in heart and placenta.
SIMILARITY: Contains 1 BTB (POZ) domain.
SIMILARITY: Contains 5 C2H2-type zinc fingers.

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): BCL6B
CDC HuGE Published Literature: BCL6B
Positive Disease Associations: Cholesterol, LDL
Related Studies:
  1. Cholesterol, LDL
    Sekar Kathiresan et al. BMC medical genetics 2007, A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study., BMC medical genetics. [PubMed 17903299]
    Using a 100K genome-wide scan, we have generated a set of putative associations for common sequence variants and lipid phenotypes. Validation of selected hypotheses in additional samples did not identify any new loci underlying variability in blood lipids. Lack of replication may be due to inadequate statistical power to detect modest quantitative trait locus effects (i.e., <1% of trait variance explained) or reduced genomic coverage of the 100K array. GWAS in FHS using a denser genome-wide genotyping platform and a better-powered replication strategy may identify novel loci underlying blood lipids.

-  MalaCards Disease Associations
  MalaCards Gene Search: BCL6B
Diseases sorted by gene-association score: lymphoma (7)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 11.39 RPKM in Lung
Total median expression: 123.70 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -17.6057-0.309 Picture PostScript Text
3' UTR -735.182023-0.363 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR000210 - BTB/POZ-like
IPR011333 - BTB/POZ_fold
IPR013069 - BTB_POZ
IPR007087 - Znf_C2H2
IPR015880 - Znf_C2H2-like
IPR013087 - Znf_C2H2/integrase_DNA-bd

Pfam Domains:
PF00096 - Zinc finger, C2H2 type
PF00651 - BTB/POZ domain
PF12874 - Zinc-finger of C2H2 type
PF13912 - C2H2-type zinc finger

SCOP Domains:
48695 - Multiheme cytochromes
54695 - POZ domain
57667 - C2H2 and C2HC zinc fingers

ModBase Predicted Comparative 3D Structure on Q8N143
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The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
      
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000977 RNA polymerase II regulatory region sequence-specific DNA binding
GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding
GO:0001227 transcriptional repressor activity, RNA polymerase II transcription regulatory region sequence-specific binding
GO:0003676 nucleic acid binding
GO:0003677 DNA binding
GO:0046872 metal ion binding

Biological Process:
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0042092 type 2 immune response
GO:0042127 regulation of cell proliferation
GO:0045595 regulation of cell differentiation
GO:0050727 regulation of inflammatory response

Cellular Component:
GO:0005634 nucleus


-  Descriptions from all associated GenBank mRNAs
  LF213231 - JP 2014500723-A/20734: Polycomb-Associated Non-Coding RNAs.
LF212407 - JP 2014500723-A/19910: Polycomb-Associated Non-Coding RNAs.
LF209162 - JP 2014500723-A/16665: Polycomb-Associated Non-Coding RNAs.
BC059404 - Homo sapiens B-cell CLL/lymphoma 6, member B (zinc finger protein), mRNA (cDNA clone MGC:71775 IMAGE:30342006), complete cds.
AK293102 - Homo sapiens cDNA FLJ77637 complete cds.
AK292878 - Homo sapiens cDNA FLJ77701 complete cds, highly similar to Homo sapiens B-cell CLL/lymphoma 6, member B (zinc finger protein)(BCL6B), mRNA.
AB076580 - Homo sapiens mRNA for BAZF, complete cds.
JD142268 - Sequence 123292 from Patent EP1572962.
AK122893 - Homo sapiens cDNA FLJ16548 fis, clone PLACE7000410, highly similar to B-cell CLL/lymphoma 6 member B protein.
AB463435 - Synthetic construct DNA, clone: pF1KB7726, Homo sapiens BCL6B gene for B-cell CLL/lymphoma 6, member B, without stop codon, in Flexi system.
KJ900516 - Synthetic construct Homo sapiens clone ccsbBroadEn_09910 BCL6B gene, encodes complete protein.
CU687376 - Synthetic construct Homo sapiens gateway clone IMAGE:100021191 5' read BCL6B mRNA.
EU446594 - Synthetic construct Homo sapiens clone IMAGE:100069804; IMAGE:100011803; FLH258534.01L B-cell CLL/lymphoma 6, member B (zinc finger protein) (BCL6B) gene, encodes complete protein.
LF326496 - JP 2014500723-A/133999: Polycomb-Associated Non-Coding RNAs.
LF326495 - JP 2014500723-A/133998: Polycomb-Associated Non-Coding RNAs.
LF326494 - JP 2014500723-A/133997: Polycomb-Associated Non-Coding RNAs.
LF213229 - JP 2014500723-A/20732: Polycomb-Associated Non-Coding RNAs.
JD242232 - Sequence 223256 from Patent EP1572962.
JD223696 - Sequence 204720 from Patent EP1572962.
JD497030 - Sequence 478054 from Patent EP1572962.
JD086588 - Sequence 67612 from Patent EP1572962.
JD306879 - Sequence 287903 from Patent EP1572962.
JD242210 - Sequence 223234 from Patent EP1572962.
AK024695 - Homo sapiens cDNA: FLJ21042 fis, clone CAE11204.
MA562073 - JP 2018138019-A/133999: Polycomb-Associated Non-Coding RNAs.
MA562072 - JP 2018138019-A/133998: Polycomb-Associated Non-Coding RNAs.
MA562071 - JP 2018138019-A/133997: Polycomb-Associated Non-Coding RNAs.
MA448808 - JP 2018138019-A/20734: Polycomb-Associated Non-Coding RNAs.
MA447984 - JP 2018138019-A/19910: Polycomb-Associated Non-Coding RNAs.
MA444739 - JP 2018138019-A/16665: Polycomb-Associated Non-Coding RNAs.
MA448806 - JP 2018138019-A/20732: Polycomb-Associated Non-Coding RNAs.

-  Other Names for This Gene
  Alternate Gene Symbols: AK122893, BAZF, BCL6B_HUMAN, NM_181844, NP_862827, Q6PCB4, Q8N143, ZNF62
UCSC ID: uc002geg.2
RefSeq Accession: NM_181844
Protein: Q8N143 (aka BCL6B_HUMAN or BL6B_HUMAN)
CCDS: CCDS42248.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: AK122893.1
exon count: 9CDS single in 3' UTR: no RNA size: 3576
ORF size: 1440CDS single in intron: no Alignment % ID: 99.94
txCdsPredict score: 3065.00frame shift in genome: no % Coverage: 98.38
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.