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t(5;17)(q32;p11) SPECC1/PDGFRB

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 3429
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 Juvenile myelomonocytic leukemia

Genes involved and Proteins

Gene NameSPECC1
Location 17p11.2
Gene NamePDGFRB
Location 5q32

Bibliography

HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;p11
Morerio C, Acquila M, Rosanda C, Rapella A, Dufour C, Locatelli F, Maserati E, Pasquali F, Panarello C
2) Cancer Res
PMID 15087372
 


Translocations implicated (Data extracted from papers in the Atlas)

 t(5;17)(q32;p11) SPECC1/PDGFRB

External links

SPECC1 (17p11.2) PDGFRB (5q32)

Mitelman databaset(5;17)(q32;p11) [Case List]    t(5;17)(q32;p11) [Transloc-MCList] SPECC1/PDGFRB [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 18:20:13 CEST 2018


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