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

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 2728

Clinics and Pathology

Disease Acute myelomonocytic leukemia (FAB type M4)

Genes involved and Proteins

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

To be noted

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

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) FGFR1/SQSTM1

External links

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

Mitelman databaset(5;8)(q35;p11) [Case List]    t(5;8)(q35;p11) [Transloc-MCList] FGFR1/SQSTM1 [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 : Wed Jan 10 17:21:22 CET 2018


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jlhuret@AtlasGeneticsOncology.org.