t(8;17)(p11;q11) MYO18A/FGFR1

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA
Written2018-01Jean-Loup Huret, Philippe Dessen

(Note : for Links provided by Atlas : click)

1. Identity

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

2. Clinics and Pathology

Disease Chronic myeloproliferative disorder, NOS

3. Genes involved and Proteins

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

4. 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

5. Translocations implicated (Data extracted from papers in the Atlas)

 t(8;17)(p11;q11) MYO18A/FGFR1

6. 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
All articlesautomatic search in PubMed

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed Nov 28 16:22:21 CET 2018

For comments and suggestions or contributions, please contact us atlasgeneticsoncology@usal.es.