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t(5;8)(q35;p11) SQSTM1/FGFR1

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 3226
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 myelomonocytic leukemia (FAB type M4)

Genes involved and Proteins

Gene NameSQSTM1
Location 5q35.3
Gene NameFGFR1
Location 8p11.23

Bibliography

A novel fusion of SQSTM1 and FGFR1 in a patient with acute myelomonocytic leukemia with t(5;8)(q35;p11) translocation
Nakamura Y, Ito Y, Wakimoto N, Kakegawa E, Uchida Y, Bessho M
Blood Cancer J 2014 Dec 12;4:e265
PMID 25501022
 


Translocations implicated (Data extracted from papers in the Atlas)

 t(5;8)(q35;p11) SQSTM1/FGFR1

External links

SQSTM1 (5q35.3) FGFR1 (8p11.23)

Mitelman databaset(5;8)(q35;p11) [Case List]    t(5;8)(q35;p11) [Transloc-MCList] SQSTM1/FGFR1 [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 18:19:59 CEST 2018


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jlhuret@AtlasGeneticsOncology.org.