chromosomal translocation t(X;1)(p11.2;q21.2)

- chromosomal translocation t(X;1)(p11.2;q21.2) involving PRCC & TFE3 may be a cause of papillary renal cell carcinoma

Properties

GENERAL: chromosomal translocation RELATED: renal cell carcinoma FORM: t(X;1)(p11.2;q21.2) LOCUS: human X-chromosome P11 human chromosome-1 Q21.2 SPLICED-GENES: proline-rich protein PRCC transcription factor E3