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t(20;21)(q11;q22) RUNX1/NOL4L

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 3173
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 myeloblastic leukemia with maturation (FAB type M2)

Genes involved and Proteins

Gene NameRUNX1
Gene NameNOL4L

Bibliography

CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia
Guastadisegni MC, Lonoce A, Impera L, Di Terlizzi F, Fugazza G, Aliano S, Grasso R, Cluzeau T, Raynaud S, Rocchi M, Storlazzi CT
Leukemia 2010 Aug;24(8):1516-9
PMID 20520637
 


Translocations implicated (Data extracted from papers in the Atlas)

 t(20;21)(q11;q22) RUNX1/NOL4L

External links

RUNX1 () NOL4L ()

Mitelman databaset(20;21)(q11;q22) [Case List]    t(20;21)(q11;q22) [Transloc-MCList] RUNX1/NOL4L [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 : Mon May 14 13:46:03 CEST 2018


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