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t(8;17)(p11;q11) MYO18A/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 3443
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 Chronic myeloproliferative disorder, NOS

Genes involved and Proteins

Gene NameMYO18A
Location 17q11.2
Gene NameFGFR1
Location 8p11.23

Bibliography

The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1
Walz C, Chase A, Schoch C, Weisser A, Schlegel F, Hochhaus A, Fuchs R, Schmitt-Gräff A, Hehlmann R, Cross NC, Reiter A
Leukemia 2005 Jun;19(6):1005-9
PMID 15800673
 


Translocations implicated (Data extracted from papers in the Atlas)

 t(8;17)(p11;q11) MYO18A/FGFR1

External links

MYO18A (17q11.2) FGFR1 (8p11.23)

Mitelman databaset(8;17)(p11;q11) [Case List]    t(8;17)(p11;q11) [Transloc-MCList] MYO18A/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
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indexed on : Tue Aug 28 18:20:56 CEST 2018


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