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t(11;21)(p13;q22) RUNX1/KIAA1549L

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 3482
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 without maturation (FAB type M1)

Genes involved and Proteins

Gene NameRUNX1
Location 21q22.12
Gene NameKIAA1549L
Location 11p13

Bibliography

A novel RUNX1-C11orf41 fusion gene in a case of acute myeloid leukemia with a t(11;21)(p14;q22)
Abe A, Katsumi A, Kobayashi M, Okamoto A, Tokuda M, Kanie T, Yamamoto Y, Naoe T, Emi N
Cancer Genet 2012 Nov;205(11):608-11
PMID 23102734
 


Translocations implicated (Data extracted from papers in the Atlas)

 t(11;21)(p13;q22) RUNX1/KIAA1549L

External links

RUNX1 (21q22.12) KIAA1549L (11p13)

Mitelman databaset(11;21)(p13;q22) [Case List]    t(11;21)(p13;q22) [Transloc-MCList] RUNX1/KIAA1549L [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 Nov 6 14:08:09 CET 2018


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