BCL6B

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BCL6B
Identifiers
Aliases BCL6B, BAZF, ZBTB28, ZNF62, B-cell CLL/lymphoma 6B
External IDs MGI: 1278332 HomoloGene: 7243 GeneCards: BCL6B
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_181844

NM_007528

RefSeq (protein)

NP_862827
NP_862827.1

NP_031554.1
NP_031554

Location (UCSC) Chr 17: 7.02 – 7.03 Mb Chr 11: 70.22 – 70.23 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

B-cell CLL/lymphoma 6 member B protein is a protein that in humans is encoded by the BCL6B gene.[3][4]

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ Okabe S, Fukuda T, Ishibashi K, Kojima S, Okada S, Hatano M, Ebara M, Saisho H, Tokuhisa T (Jul 1998). "BAZF, a novel Bcl6 homolog, functions as a transcriptional repressor". Molecular and Cellular Biology. 18 (7): 4235–44. PMC 109007Freely accessible. PMID 9632807. 
  4. ^ "Entrez Gene: BCL6B B-cell CLL/lymphoma 6, member B (zinc finger protein)". 

External links[edit]

Further reading[edit]

  • Sakashita C, Fukuda T, Okabe S, Kobayashi H, Hirosawa S, Tokuhisa T, Miyasaka N, Miura O, Miki T (Mar 2002). "Cloning and characterization of the human BAZF gene, a homologue of the BCL6 oncogene". Biochemical and Biophysical Research Communications. 291 (3): 567–73. doi:10.1006/bbrc.2002.6481. PMID 11855826. 
  • Fitzgibbon J, Neat MJ, Jones L, Foot N, Lister TA, Gupta RK (2000). "Assignment of B-cell lymphoma 6, member B (zinc finger protein) gene (BCL6B) to human chromosome 17p13.1 by in situ hybridization". Cytogenetics and Cell Genetics. 89 (3-4): 218–9. doi:10.1159/000015617. PMID 10965127. 
  • Bray P, Lichter P, Thiesen HJ, Ward DC, Dawid IB (Nov 1991). "Characterization and mapping of human genes encoding zinc finger proteins". Proceedings of the National Academy of Sciences of the United States of America. 88 (21): 9563–7. doi:10.1073/pnas.88.21.9563. PMC 52758Freely accessible. PMID 1946370. 
  • Lichter P, Bray P, Ried T, Dawid IB, Ward DC (Aug 1992). "Clustering of C2-H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomes". Genomics. 13 (4): 999–1007. doi:10.1016/0888-7543(92)90013-I. PMID 1505991.