| Written | 2018-01 | Jean-Loup Huret, Philippe Dessen |
| Identity |
| ICD-Topo | C420,C421,C424 BLOOD, BONE MARROW, & HEMATOPOIETIC SYS |
| Atlas_Id | 2853 |
| 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 | Acute lymphoblastic leukemia/lymphoblastic lymphoma |
| Genes involved and Proteins |
| Gene Name | JMJD1C |
| Location | 10q21.3 |
| Gene Name | TSN |
| Location | 2q14.3 |
| Bibliography |
| Trisomy 22 in acute myeloid leukemia: a marker for myeloid leukemia with monocytic features and cytogenetically cryptic inversion 16 |
| Wong KF, Kwong YL |
| Cancer Genet Cytogenet 1999 Mar;109(2):131-3 |
| PMID 10087946 |
| Translocations implicated (Data extracted from papers in the Atlas) |
| t(2;10)(q14;q21) JMJD1C/TSN | |
| External links |
| Mitelman database | t(2;10)(q14;q21) |
| 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 : Sun Jul 12 19:47:19 CEST 2020 |
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