t(17;17)(q12;q21) MED1/ACSF2

0000-00-00   Jean-Loup Huret , Philippe Dessen 

(Note: the fusion was discovered by NGS. Many chromosome rearrangement mechanisms such as translocation, inversion,deletion or complex rearrangement may lead to the same fusion)

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 u00a0How to contribute

Summary

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

Genes Involved and Proteins

Gene name

Location

17q12

Gene name

Location

17q21.33

Highly cited references

Pubmed IDYearTitleCitations
275069352016RWCFusion: identifying phenotype-specific cancer driver gene fusions based on fusion pair random walk scoring method.4

Bibliography

Pubmed IDLast YearTitleAuthors
231190972012Reanalysis of RNA-sequencing data reveals several additional fusion genes with multiple isoforms.Kangaspeska S et al

Citation

Jean-Loup Huret ; Philippe Dessen

t(17;17)(q12;q21) MED1/ACSF2

Atlas Genet Cytogenet Oncol Haematol. 0000-00-00

Online version: http://atlasgeneticsoncology.org/solid-tumor/102512/t(17;17)(q12;q21)-med1-acsf2