t(11;14)(q23;q32) IGH/PAFAH1B2

Identity

ICD-Topo	C420,C421,C424 BLOOD, BONE MARROW, & HEMATOPOIETIC SYS
Atlas_Id	3475
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

Mature B-cell neoplasm, NOS

Genes involved and Proteins

Gene Name	IGH
Location	14q32.33

Gene Name

PAFAH1B2

Bibliography

Molecular analysis of an unstable genomic region at chromosome band 11q23 reveals a disruption of the gene encoding the alpha2 subunit of platelet-activating factor acetylhydrolase (Pafah1a2) in human lymphoma

Lecointe N, Meerabux J, Ebihara M, Hill A, Young BD

Oncogene 1999 May 6;18(18):2852-9

PMID 10362256

Translocations implicated (Data extracted from papers in the Atlas)

	t(11;14)(q23;q32) IGH/PAFAH1B2

External links

IGH (14q32.33) PAFAH1B2 ()

Mitelman database	t(11;14)(q23;q32) [Case List]    t(11;14)(q23;q32) [Transloc-MCList] IGH/PAFAH1B2 [Fusion-MCList]
COSMIC	Histo = - Site = haematopoietic_and_lymphoid_tissue (COSMIC)
arrayMap (UZH-SIB Zurich)	[select an item]

REVIEW articles	automatic search in PubMed
Last year articles	automatic search in PubMed
All articles	automatic search in PubMed

© Atlas of Genetics and Cytogenetics in Oncology and Haematology

indexed on : Mon Jul 9 10:15:29 CEST 2018

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