t(3;11)(p21;q13) NUMA1/SFMBT1

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

NUMA1

Location

11q13.4

Gene name

SFMBT1

Location

3p21.1

Highly cited references

Pubmed IDYearTitleCitations
264321912015LAMTOR1-PRKCD and NUMA1-SFMBT1 fusion genes identified by RNA sequencing in aneurysmal benign fibrous histiocytoma with t(3;11)(p21;q13).4

Article Bibliography

Pubmed IDLast YearTitleAuthors
264321912015LAMTOR1-PRKCD and NUMA1-SFMBT1 fusion genes identified by RNA sequencing in aneurysmal benign fibrous histiocytoma with t(3;11)(p21;q13).Panagopoulos I et al

Citation

Jean-Loup Huret ; Philippe Dessen

t(3;11)(p21;q13) NUMA1/SFMBT1

Atlas Genet Cytogenet Oncol Haematol. 0000-00-00

Online version: http://atlasgeneticsoncology.org/solid-tumor/105570/t(3;11)(p21;q13)-numa1-sfmbt1