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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

BCL7B Gene

protein-coding   GIFtS: 52
GCID: GC07M072950

B-Cell CLL/Lymphoma 7B

  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

This gene clusters with an RNA gene
Subcategory (RNA class): lncRNA

Quality score for the ORGUL clustered with this gene is 3

Aliases
B-Cell CLL/Lymphoma 7B1 2
B-Cell CLL/Lymphoma 7 Protein Family Member B2
Allergen Hom S 33

External Ids:    HGNC: 10051   Entrez Gene: 92752   Ensembl: ENSG000001066357   OMIM: 6058465   UniProtKB: Q9BQE93   
ORGUL members:         
NONCODE14:n410180      

Export aliases for BCL7B gene to outside databases

Previous GC identifers: GC07M071591 GC07M072348 GC07M072362 GC07M072395 GC07M072588 GC07M068832


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for BCL7B Gene:
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)

GeneCards Summary for BCL7B Gene: 
BCL7B (B-cell CLL/lymphoma 7B) is a protein-coding gene, and is affiliated with the lncRNA class. Diseases associated with BCL7B include burkitt's lymphoma, and supravalvular aortic stenosis. GO annotations related to this gene include actin binding. An important paralog of this gene is BCL7C.

UniProtKB/Swiss-Prot: BCL7B_HUMAN, Q9BQE9
Function: May play a role in lung tumor development or progression




(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000007.13  NC_018918.2  NT_007933.15  NT_079593.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the BCL7B gene promoter:
         E2F-1   E2F   HSF1short   HSF1 (long)   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): BCL7B promoter sequence
   Search SABiosciences Chromatin IP Primers for BCL7B

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat BCL7B


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 7q11.23   Ensembl cytogenetic band:  7q11.23   HGNC cytogenetic band: 7q11.23

BCL7B Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
BCL7B gene location

GeneLoc information about chromosome 7         GeneLoc Exon Structure

GeneLoc location for GC07M072950:  view genomic region     (about GC identifiers)

Start:
72,950,683 bp from pter      End:
72,972,332 bp from pter
Size:
21,650 bases      Orientation:
minus strand

1 alternative location:
Chr7-,CRA_TCAG 72,283,755-72,305,137     

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: BCL7B_HUMAN, Q9BQE9 (See protein sequence)
Recommended Name: B-cell CLL/lymphoma 7 protein family member B  
Size: 202 amino acids; 22195 Da
Allergen: Causes an allergic reaction in human. Binds to IgE from atopic dermatitis (AD) patients. Identified as
an IgE autoantigen in atopic dermatitis (AD) patients with severe skin manifestations
Secondary accessions: A8K226 C9JWD3 D3DXF0 O43769 Q13845 Q6ZW75
Alternative splicing: 4 isoforms:  Q9BQE9-1   Q9BQE9-2   Q9BQE9-3   Q9BQE9-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for BCL7B: NX_Q9BQE9

Explore proteomics data for BCL7B at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9BQE9

  • BCL7B Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    BCL7B Protein Expression
    REFSEQ proteins (2 alternative transcripts): 
    NP_001184173.1  NP_001698.2  

    ENSEMBL proteins: 
     ENSP00000223368   ENSP00000393230   ENSP00000414473   ENSP00000414231   ENSP00000411073  
     ENSP00000406069  

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    Browse Proteins at Cloud-Clone Corp. 

    Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005575cellular_component ND--

    BCL7B for ontologies           About GeneDecksing



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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    1 InterPro protein domain:
     IPR006804 BCL7

    Graphical View of Domain Structure for InterPro Entry Q9BQE9

    ProtoNet protein and cluster: Q9BQE9

    UniProtKB/Swiss-Prot: BCL7B_HUMAN, Q9BQE9
    Similarity: Belongs to the BCL7 family


    BCL7B for domains           About GeneDecksing


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: BCL7B_HUMAN, Q9BQE9
    Function: May play a role in lung tumor development or progression

         Genatlas biochemistry entry for BCL7B:
    putative F-actin cross linking protein 12 homolog,BCL7A family,involved in cellular and developmental
    functions,highly expressed in heart,skeletal muscle and fetal liver,located in the commonly Williams
    region,atopy-related IgE autoantigen,detected in the serum of patients with severe atopic dermatitis,not
    rearranged in lymphoid malignancies

         Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003779actin binding NAS8605326
         
    BCL7B for ontologies           About GeneDecksing


    Phenotypes:
         4 GenomeRNAi human phenotypes for BCL7B:
     Cell division defect  Increased G2M DNA content  Increased gamma-H2AX phosphory  Increased number of mitotic ce 

    Animal Models:
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    SwitchGear 3'UTR luciferase reporter plasmidBCL7B 3' UTR sequence
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for BCL7B

    STRING Interaction Network Preview (showing 3 interactants - click image to see more details)

    3 Interacting proteins for BCL7B (ENSP000002233684) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    HDAC2ENSP000003813314STRING: ENSP00000381331
    TERF1ENSP000002766034STRING: ENSP00000276603
    TERF2IPENSP000003000864STRING: ENSP00000300086
    About this table

    Gene Ontology (GO): 1 biological process term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0008150biological_process ND--

    BCL7B for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for BCL7B

    Search CenterWatch for drugs/clinical trials and news about BCL7B

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for BCL7B gene (3 alternative transcripts): 
    NM_001197244.1  NM_001707.3  NM_138707.1  

    Unigene Cluster for BCL7B:

    B-cell CLL/lymphoma 7B
    Hs.647051  [show with all ESTs]
    Unigene Representative Sequence: NM_001707
    14 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000486818(uc010lbf.2) ENST00000493671 ENST00000223368(uc003tyf.2 uc003tyg.2)
    ENST00000411832 ENST00000482231(uc003tye.2) ENST00000454871 ENST00000463858
    ENST00000448175 ENST00000455335 ENST00000493679 ENST00000464288 ENST00000416906
    ENST00000493592 ENST00000481667
    miRNA
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    8/30 QIAGEN miScript miRNA Assays for microRNAs that regulate BCL7B (see all 30):
    hsa-miR-26a-2* hsa-miR-607 hsa-miR-148b hsa-miR-4318 hsa-miR-486-3p hsa-miR-1297 hsa-miR-3613-3p hsa-miR-558
    SwitchGear 3'UTR luciferase reporter plasmidBCL7B 3' UTR sequence
    Inhib. RNA
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    Additional mRNA sequence: 

    AJ223979.1 AK290091.1 BC000956.2 BC001967.2 BC009548.1 NR_036682.1 X89985.1 

    18 DOTS entries:

    DT.316994  DT.100796404  DT.95337407  DT.99937132  DT.100796406  DT.100796401  DT.100040319  DT.100763178 
    DT.100796402  DT.100796403  DT.95237244  DT.100796405  DT.100796410  DT.100796412  DT.100796414  DT.102821902 
    DT.97769613  DT.100779218 

    24/307 AceView cDNA sequences (see all 307):

    BQ008758 AA598703 AW328570 CR598410 AA835499 AI282698 AI202070 CR598138 
    AL556002 BM695121 CR594296 N26561 CD558272 BQ007860 CR614287 CR620291 
    CD364959 BC001967 BQ961642 BQ109412 AI090381 BU145459 BX116803 AW169595 

    GeneLoc Exon Structure

    5/10 Alternative Splicing Database (ASD) splice patterns (SP) for BCL7B (see all 10)    About this scheme

    ExUns: 1a · 1b ^ 2a · 2b · 2c ^ 3 ^ 4 ^ 5a · 5b ^ 6a · 6b · 6c ^ 7 ^ 8a · 8b · 8c · 8d · 8e · 8f · 8g · 8h · 8i
    SP1:              -     -     -                             -           -                                                               
    SP2:              -     -     -     -                       -           -                                                               
    SP3:                                -                       -           -                                                               
    SP4:              -     -     -     -                       -     -     -                                                               
    SP5:              -     -     -     -           -     -     -           -                                                               


    ECgene alternative splicing isoforms for BCL7B

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    BCL7B expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TTGAATTGAA
    BCL7B Expression
    About this image


    See BCL7B Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for BCL7B

    SOURCE GeneReport for Unigene cluster: Hs.647051

    UniProtKB/Swiss-Prot: BCL7B_HUMAN, Q9BQE9
    Tissue specificity: Ubiquitous

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    In Situ
    Assay Products:
     

     
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    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of animals.

    Orthologs for BCL7B gene from 6/13 species (see all 13)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Bcl7b1 , 5 B cell CLL/lymphoma 7B1, 5 88.45(n)1
    96.04(a)1
      5 (75.04 cM)5
    120541  NM_009745.21  NP_033875.21 
     1351682835 
    chicken
    (Gallus gallus)
    Aves LOC1008578901 B-cell CLL/lymphoma 7 protein family member B-like 78.88(n)
    90.1(a)
      100857890  XM_003643231.1  XP_003643279.1 
    lizard
    (Anolis carolinensis)
    Reptilia BCL7B6
    Uncharacterized protein
    73(a)
    1 ↔ 1
    GL343734.1(214778-219715)
    zebrafish
    (Danio rerio)
    Actinopterygii bcl7ba1 B-cell CLL/lymphoma 7B, a 65.64(n)
    68.21(a)
      406444  NM_213165.1  NP_998330.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta BCL7-like6
    BCL7-like
    34(a)
    1 → many
    X(9250667-9252627)
    worm
    (Caenorhabditis elegans)
    Secernentea C28H8.16
    BCL7-like protein C28H8.1
    32(a)
    1 → many
    III(5926060-5927166)


    ENSEMBL Gene Tree for BCL7B (if available)
    TreeFam Gene Tree for BCL7B (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for BCL7B gene
    BCL7C2  BCL7A2  
    2 SIMAP similar genes for BCL7B using alignment to 4 protein entries:     BCL7B_HUMAN (see all proteins):
    BCL7C    BCL7A

    BCL7B for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/452 SNPs in BCL7B are shown (see all 452)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 7 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs561119291,2
    C--72288257(+) AAAAA-/AA/AAA
            
    GAGTT
    5 -- int1 cds11NA 2
    rs801639921,2
    C--72288258(+) AAAAAA/GAGTTA 3 -- int10--------
    rs113356761,2
    C--72964975(+) TTTTT-/TGTTTG 3 -- int1 trp31Minor allele frequency- T:0.00CSA 2
    rs1489202401,2
    --76475226(+) TTGCTG/TGTCAG 3 -- ds50010--------
    rs1157746941,2
    C,F--76475313(+) ACTGCG/ACCTGG 3 -- ds50011Minor allele frequency- A:0.02WA 118
    rs2004601971,2
    --76475358(+) TAGAT-/AGAG  
            
    ATAGG
    3 -- ds50010--------
    rs1481014951,2
    --76475514(+) GGGAGA/GCTAGA 3 -- ds50010--------
    rs1886328251,2
    --76475525(+) AATCAC/TTGTCA 3 -- ds50010--------
    rs1419125101,2
    --76475576(+) GCCCAC/GAGTGA 3 -- ds50010--------
    rs1932731411,2
    --76475612(+) CCACCA/CCGGCC 3 -- ds50010--------

    HapMap Linkage Disequilibrium report for BCL7B (72950683 - 72972332 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 3 variations for BCL7B:    About this table     
    Variant IDTypeSubtypePubMed ID
    nsv831028CNV Loss17160897
    nsv888369CNV Loss21882294
    dgv7325n71CNV Loss21882294

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 605846    OMIM disorders: --

    UniProtKB/Swiss-Prot: BCL7B_HUMAN, Q9BQE9
  • 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

  • 10 diseases for BCL7B:    About MalaCards
    burkitt's lymphoma    supravalvular aortic stenosis    williams syndrome    hodgkin's lymphoma
    atopic dermatitis    non-hodgkin lymphoma    williams-beuren syndrome    atopy
    dermatitis    leukemia

    1 disease from the University of Copenhagen DISEASES database for BCL7B:
    Supravalvular aortic stenosis

    BCL7B for disorders           About GeneDecksing

    Genetic Association Database (GAD): BCL7B
    Human Genome Epidemiology (HuGE) Navigator: BCL7B (5 documents)

    Export disorders for BCL7B gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for BCL7B gene, integrated from 9 sources (see all 25):
    (articles sorted by number of sources associating them with BCL7B)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Isolation of cDNA clones coding for IgE autoantigens with serum IgE from atopic dermatitis patients. (PubMed id 9806765)1, 2, 3 Natter S.... Valenta R. (1998)
    2. Molecular cloning of complex chromosomal translocation t(8;14;12)(q24.1;q32.3;q24.1) in a Burkitt lymphoma cell line defines a new gene (BCL7A) with homology to caldesmon. (PubMed id 8605326)1, 2, 3 Zani V.J.... Dyer M.J.S. (1996)
    3. The BCL7 gene family: deletion of BCL7B in Williams syndrome. (PubMed id 9931421)1, 2, 9 Jadayel D.M....Dyer M.J. (1998)
    4. Meta-analysis of genome-wide association studies in & gt;80 000 subjects identifies multiple loci for C-reactive protein levels. (PubMed id 21300955)1, 4 Dehghan A....Chasman D.I. (2011)
    5. Evaluating the discriminative power of multi-trait ge netic risk scores for type 2 diabetes in a northern Swedish population. (PubMed id 20571754)1, 4 Fontaine-Bisson B....Franks P.W. (2010)
    6. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. (PubMed id 18193044)1, 4 Kathiresan S....Orho-Melander M. (2008)
    7. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    8. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    9. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes. (PubMed id 9860302)1, 2 Meng X....Keating M.T. (1998)
    10. Genomic study in Mexicans identifies a new locus for t riglycerides and refines European lipid loci. (PubMed id 23505323)1 Weissglas-Volkov D....Pajukanta P. (2013)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 9275 HGNC: 1005 AceView: BCL7B Ensembl:ENSG00000106635 euGenes: HUgn9275
    ECgene: BCL7B H-InvDB: BCL7B

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for BCL7B Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for BCL7B Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for BCL7B gene:
    Search GeneIP for patents involving BCL7B

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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