Atlas of Genetics and Cytogenetics in Oncology and Haematology

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t(12;21)(p13;q22) PDE9A::VWF

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Atlas_Id 3084
Note Non-annotated chromosomal abnormality. Preliminary data :
if you are an author who wish to write a full paper/card on this translocation, go to  How to contribute

Clinics and Pathology

Disease Acute lymphoblastic leukemia/lymphoblastic lymphoma

Genes involved and Proteins

Gene NamePDE9A
Location 21q22.3
Gene NameVWF
Location 12p13.31


Analysis of a breakpoint cluster reveals insight into the mechanism of intrachromosomal amplification in a lymphoid malignancy
Sinclair PB, Parker H, An Q, Rand V, Ensor H, Harrison CJ, Strefford JC
Hum Mol Genet 2011 Jul 1;20(13):2591-602
PMID 21487021

Translocations implicated (Data extracted from papers in the Atlas)

 t(12;21)(p13;q22) PDE9A/VWF

External links

PDE9A (21q22.3) VWF (12p13.31)

Mitelman databaset(12;21)(p13;q22)
COSMICHisto = - Site = haematopoietic_and_lymphoid_tissue (COSMIC)
arrayMap (UZH-SIB Zurich)[select an item]
REVIEW articlesautomatic search in PubMed
Last year articlesautomatic search in PubMed
All articlesautomatic search in PubMed

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indexed on : Fri Oct 8 16:39:41 CEST 2021

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