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t(11;12)(p15;q13) NUP98/RARG

Written2018-01Jean-Loup Huret, Philippe Dessen

(Note : for Links provided by Atlas : click)

Identity

ICD-Topo C420,C421,C424 BLOOD, BONE MARROW, & HEMATOPOIETIC SYS
Atlas_Id 1600
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 promyelocytic leukemia (FAB type M3)

Genes involved and Proteins

Gene NameNUP98
Location 11p15.4
Gene NameRARG
Location 12q13.13

Bibliography

A novel NUP98/RARG gene fusion in acute myeloid leukemia resembling acute promyelocytic leukemia
Such E, Cervera J, Valencia A, Barragán E, Ibañez M, Luna I, Fuster O, Perez-Sirvent ML, Senent L, Sempere A, Martinez J, Martín-Aragonés G, Sanz MA
Blood 2011 Jan 6;117(1):242-5
PMID 20935257
 


Translocations implicated (Data extracted from papers in the Atlas)

 t(11;12)(p15;q13) NUP98/RARG

External links

NUP98 (11p15.4) RARG (12q13.13)

Mitelman databaset(11;12)(p15;q13) [Case List]    t(11;12)(p15;q13) [Transloc-MCList] NUP98/RARG [Fusion-MCList]
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 : Tue Aug 28 18:21:44 CEST 2018


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