Identity |
ICD-Topo | C420,C421,C424 BLOOD, BONE MARROW, & HEMATOPOIETIC SYS |
Atlas_Id | 1668 |
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 | Chronic myeloproliferative disorder, NOS |
Genes involved and Proteins |
Gene Name | TPR |
Location | 1q31.1 |
Gene Name | FGFR1 |
Location | 8p11.23 |
Bibliography |
Identification of a novel partner gene, TPR, fused to FGFR1 in 8p11 myeloproliferative syndrome |
Li F, Zhai YP, Tang YM, Wang LP, Wan PJ |
Genes Chromosomes Cancer 2012 Sep;51(9):890-7 |
PMID 22619110 |
Molecular identification of a TPR-FGFR1 fusion transcript in an adult with myeloproliferative neoplasm, T-lymphoblastic lymphoma, and a t(1;8)(q25;p11 |
Kim SY, Kim JE, Park S, Kim HK |
2) Cancer Genet |
PMID 25037443 |
Translocations implicated (Data extracted from papers in the Atlas) |
t(1;8)(q31;p11) TPR/FGFR1 | |
External links |
Mitelman database | t(1;8)(q31;p11) |
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 Dec 14 18:27:05 CET 2020 |
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