t(1;3)(p36.3;q21.3)

Preferred Label : t(1;3)(p36.3;q21.3);

NCIt definition : A chromosomal translocation involving breakpoints within the p36.3 band on the short arm of chromosome 1 and the q21.3 band on the long arm of chromosome 3. This rearrangement may be associated with RPN1-PRDM16 fusion gene expression and various myeloproliferative disorders and leukemias.;

Détails

Origin ID

C217184;

cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 3 [NCIt concept]
molecular_abnormality_involves_gene
- PRDM16 Gene [NCIt concept]
- RPN1 Gene [NCIt concept]

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