Atlas of Genetics and Cytogenetics in Oncology and Haematology


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t(1;3)(p32;p21)

Clinics and Pathology

Disease T-cell ALL

Genes involved and Proteins

Gene Name TAL1
Location 1p32
Dna / Rna complex alternate splicing
Protein contains a basic Helix-Loop-Helix (DNA binding) domain; cforms heterodimers; transcription factor; role in haematopoietic cell differentiation
Gene Name TCTA
Location 3p21
Protein contains a hydrophobic domain; may be a membrane associated protein

Result of the chromosomal anomaly

Hybrid gene
Description TCTA and TAL1 are in opposite direction
  
Fusion Protein
Description it may be that the promoting regions from TCTA disregulate TAL1 expression
  

External links

Other databaset(1;3)(p32;p21) Mitelman database (CGAP - NCBI)
Other databaset(1;3)(p32;p21) CancerChromosomes (NCBI)

Bibliography

Disruption of the SCL gene by a t(1;3) translocation in a patient with T cell acute lymphoblastic leukemia.
Aplan PD, Raimondi SC, Kirsch IR
The Journal of experimental medicine. 1992 ; 176 (5) : 1303-1310.
PMID 1402676
 
Cloning and characterization of TCTA, a gene located at the site of a t(1;3) translocation.
Aplan PD, Johnson BE, Russell E, Chervinsky DS, Kirsch IR
Cancer research. 1995 ; 55 (9) : 1917-1921.
PMID 7728759
 

Contributor(s)

Written03-1998Jean-Loup Huret

Citation

This paper should be referenced as such :
Huret JL . t(1;3)(p32;p21). Atlas Genet Cytogenet Oncol Haematol. March 1998 .
URL : http://AtlasGeneticsOncology.org/Anomalies/t1031108.html

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indexed on : Mon May 12 18:12:55 2008


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