t(10;17)(q22;p13) YWHAE/NUTM2B

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

17p13.3

Gene name

Location

10q22.3

Bibliography

Pubmed IDLast YearTitleAuthors
222943822012Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney.O'Meara E et al
254817512015Activation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney.Karlsson J et al
265421792016The clinical phenotype of YWHAE-NUTM2B/E positive pediatric clear cell sarcoma of the kidney.Gooskens SL et al

External Links

Citation

Jean-Loup Huret ; Philippe Dessen

t(10;17)(q22;p13) YWHAE/NUTM2B

Atlas Genet Cytogenet Oncol Haematol. 0000-00-00

Online version: http://atlasgeneticsoncology.org/solid-tumor/100397/t(10;17)(q22;p13)-ywhae-nutm2b