* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Leukaemia Section t(3;14)(p14;q32) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Survey
Document related concepts
Point mutation wikipedia , lookup
History of genetic engineering wikipedia , lookup
Genome (book) wikipedia , lookup
Epigenetics of human development wikipedia , lookup
Nutriepigenomics wikipedia , lookup
Polycomb Group Proteins and Cancer wikipedia , lookup
Neuronal ceroid lipofuscinosis wikipedia , lookup
Microevolution wikipedia , lookup
Designer baby wikipedia , lookup
Public health genomics wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Helitron (biology) wikipedia , lookup
Epigenetics of neurodegenerative diseases wikipedia , lookup
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