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Transcript
Atlas of Genetics and Cytogenetics
in Oncology and Haematology
OPEN ACCESS JOURNAL AT INIST-CNRS
Leukaemia Section
Short Communication
t(3;14)(p14;q32)
Jean-Loup Huret
Genetics, Dept Medical Information, UMR 8125 CNRS, University of Poitiers, CHU Poitiers Hospital, F86021 Poitiers, France (JLH)
Published in Atlas Database: July 2005
Online updated version: http://AtlasGeneticsOncology.org/Anomalies/t0314p14q32ID1398.html
DOI: 10.4267/2042/38255
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 2.0 France Licence.
© 2005 Atlas of Genetics and Cytogenetics in Oncology and Haematology
Clinics and pathology
Genes involved and proteins
Disease
FOXP1
Extra-nodal Marginal Zone B-cell lymphoma
(MZBCL) of mucosa-associated lymphoid tissue
(MALT) type, also called MALT lymphoma.
Note
MALT lymphomas without the t(3;14) are frequently
associated
with
either
a
t(1;14)(p22;q32)
(BCL10/IGH), a t(11;18)(q21;q21) (API2/MALT1, or a
t(14;18)(q32;q21) (IGH/MALT1).
Epidemiology
9 cases detected to date.
Clinics
MALT lymphoma is an indolent disease involving
most often the stomach, the lung, the thyroid, the
salivary gland, the orbit, and the skin, with a non
random anatomic distribution according to the
translocation. The t(3;14) is frequently found in MALT
lymphomas of the thyroid, the orbit, and the skin.
Location
3p14.1.
Protein
Transcription factor; member of the FOXP subfamily,
characterized by a DNA binding forkhead.
IGH
Location
14q32.
Result of the chromosomal
anomaly
Hybrid gene
Description
Breakpoint upstream the first 5' non coding exon of
FOXP1.
References
Cytogenetics
Streubel B, Vinatzer U, Lamprecht A, Raderer M, Chott A.
T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel
recurrent chromosomal aberration in MALT lymphoma.
Leukemia. 2005 Apr;19(4):652-8
Additional anomalies
+3 is found in half cases.
This article should be referenced as such:
Huret JL. t(3;14)(p14;q32). Atlas Genet Cytogenet Oncol
Haematol. 2005; 9(4):331.
Atlas Genet Cytogenet Oncol Haematol. 2005; 9(4)
331
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