| Identity |
| ICD-Topo | C420,C421,C424 BLOOD, BONE MARROW, & HEMATOPOIETIC SYS |
| Atlas_Id | 3142 |
| 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 myeloid leukemia, t(9;22) |
| Genes involved and Proteins |
| Gene Name | RCC1 |
| Location | 1p35.3 |
| Gene Name | PICALM |
| Location | 11q14.2 |
| Bibliography |
| Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts |
| Levin JZ, Berger MF, Adiconis X, Rogov P, Melnikov A, Fennell T, Nusbaum C, Garraway LA, Gnirke A |
| Genome Biol 2009;10(10):R115 |
| PMID 19835606 |
| Translocations implicated (Data extracted from papers in the Atlas) |
| t(1;11)(p35;q14) RCC1/PICALM | |
| External links |
| Mitelman database | t(1;11)(p35;q14) |
| 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 18:27:08 CET 2020 |
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