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del(16)(q22q22) CTCF/PARD6A

Written2018-01Jean-Loup Huret, Philippe Dessen

(Note : for Links provided by Atlas : click)

Identity

ICD-Topo C420,C421,C424 BLOOD, BONE MARROW, & HEMATOPOIETIC SYS
Atlas_Id 2635
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 NameCTCF
Location 16q22.1
Gene NamePARD6A
Location 16q22.1

Bibliography

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia
Paulsson K, Lilljebjörn H, Biloglav A, Olsson L, Rissler M, Castor A, Barbany G, Fogelstrand L, Nordgren A, Sjögren H, Fioretos T, Johansson B
Nat Genet 2015 Jun;47(6):672-6
PMID 25961940
 


Translocations implicated (Data extracted from papers in the Atlas)

 del(16)(q22q22) CTCF/PARD6A

External links

CTCF (16q22.1) PARD6A (16q22.1)

Mitelman databasedel(16)(q22q22) [Case List]    del(16)(q22q22) [Transloc-MCList] CTCF/PARD6A [Fusion-MCList]
COSMICHisto = - Site = haematopoietic_and_lymphoid_tissue (COSMIC)
arrayMap (UZH-SIB Zurich)[select an item]
 
 
REVIEW articlesautomatic search in PubMed
Last year articlesautomatic search in PubMed
All articlesautomatic search in PubMed


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indexed on : Tue Aug 28 18:18:30 CEST 2018


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