chromosomal translocation t(X;X)(p11.2;q13.1) (papillary renal cell carcinoma)

- chromosomal translocation t(X;X)(p11.2;q13.1) involving NONO with TFE3 may be a cause of papillary renal cell carcinoma (PRCC)

Properties

GENERAL: chromosomal translocation RELATED: renal cell carcinoma FORM: t(X;X)(p11.2;q13.1) LOCUS: human X-chromosome P11.2 human X-chromosome Q13.1 PATHOLOGY: acute leukemia SPLICED-GENES: NONO transcription factor E3

References

UniProt :accession Q15233