t(1;11)(p35;q14) RCC1/PICALM

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	13q14.2

Gene Name

PICALM

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

RCC1 (13q14.2) PICALM ()

Mitelman database	t(1;11)(p35;q14) [Case List]    t(1;11)(p35;q14) [Transloc-MCList] RCC1/PICALM [Fusion-MCList]
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 May 14 13:41:46 CEST 2018

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