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t(1;14)(p35;q32) LAPTM5/IGH

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 1486

Clinics and Pathology

Disease -

Genes involved and Proteins

Gene NameLAPTM5
Location 1p35.2
Gene NameIGH
Location 14q32.33

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

Inactivation of the E3/LAPTm5 gene by chromosomal rearrangement and DNA methylation in human multiple myeloma
Hayami Y, Iida S, Nakazawa N, Hanamura I, Kato M, Komatsu H, Miura I, Dave BJ, Sanger WG, Lim B, Taniwaki M, Ueda R
Leukemia 2003 Aug;17(8):1650-7
PMID 12886255
 


Translocations implicated (Data extracted from papers in the Atlas)

 t(1;14)(p35;q32) LAPTM5/IGH

External links

LAPTM5 (1p35.2) IGH (14q32.33)

Mitelman databaset(1;14)(p35;q32) [Case List]    t(1;14)(p35;q32) [Transloc-MCList] LAPTM5/IGH [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 17:20:46 CET 2018


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jlhuret@AtlasGeneticsOncology.org.