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t(9;11)(q34;q23) FBP17/MLL

Identity

Other namesins(11;9)(q23;q34)inv(11)(q13;q23)

Clinics and Pathology

Disease acute non lymphocytic leukemia (ANLL)
Phenotype / cell stem origin one case of M4-ANLL
Epidemiology unknown
Clinics WBC 35 X 109/l
Prognosis poor

Cytogenetics

Cytogenetics Molecular YAC 13HH4; P1 ICRFP700L11103Q5

Genes involved and Proteins

Gene Name FBP17
Location 9q34
Dna / Rna at least 2042 bp
Protein at least 679 amino acids
Gene Name MLL
Location 11q23
Dna / Rna 11910 bp
Protein 3970 amino acids; contains two DNA binding motifs (a AT hook, and Zinc fingers), a DNA methyl transferase motif, a bromodomain; transcriptional regulatory factor; nuclear localisation

Result of the chromosomal anomaly

Hybrid gene
Description 5'-MLL/FBP17-3'
  
Fusion Protein
 
Description Hybrid transcript MLL/FBP17 contains the following domains: from MLL: AT-hook, DNA-Methyltransferase, Zinc-Fingers; from FBP17:cdc15 homology region, putative rho-binding domain, SH3-domain
Oncogenesis unknown
  

External links

Other databaset(9;11)(q34;q23) FBP17/MLL Mitelman database (CGAP - NCBI)
Other databaset(9;11)(q34;q23) FBP17/MLL CancerChromosomes (NCBI)

To be noted

Additional cases are needed to delineate the epidemiology of this rare entity:
you are welcome to submit a paper to our new Case Report section.

Bibliography

The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia.
Fuchs U, Rehkamp G, Haas OA, Slany R, K‰çnig M, Bojesen S, Bohle RM, Damm-Welk C, Ludwig WD, Harbott J, Borkhardt A
Proceedings of the National Academy of Sciences of the United States of America. 2001 ; 98 (15) : 8756-8761.
PMID 11438682
 

Contributor(s)

Written06-2001Uta Fuchs, Arndt Borkhardt

Citation

This paper should be referenced as such :
Fuchs U, Borkhardt A . t(9;11)(q34;q23) FBP17/MLL. Atlas Genet Cytogenet Oncol Haematol. June 2001 .
URL : http://AtlasGeneticsOncology.org/Anomalies/t0911FBPID1205.html

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indexed on : Mon May 12 18:12:44 2008


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