Thread: Chromosomal translocation

t(2;5)(p23;q35) - Anaplastic large cell lymphoma
t(8;14) - Burkitt's lymphoma (c-myc)
t(8;21)(q22;q22) - Acute myeloblastic leukemia with maturation (AML1-ETO)
t(9;22)(q34;q11) - Philadelphia chromosome, CML, ALL
t(11;14) - Mantle cell lymphoma (cyclin D1)
t(11;22)(q24;q11.2-12) - Ewing's sarcoma
t(12;21)(p12;q22) - ALL (TEL-AML1)
t(14;18)(q32;q21) - Follicular lymphoma (Bcl-2)
t(17;22) - DFSP
t(15;17) - Acute promyelocytic leukemia
t(1;12)(q21;p13) - Acute myelogenous leukemia
t(9;12)(p24;p13) - CML, ALL (TEL-JAK2)
t(X;18)(p11.2;q11.2) - Synovial sarcoma
t(1;11)(q42.1;q14.3)- Schizophrenia [3]
t(12;15)(p13;q25) - (TEL-TrkC); acute myeloid leukemia, congenital fibrosarcoma, secretory breast carcinoma

**SPAM**

Chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes. A gene fusion may be created when the translocation joins two otherwise separated genes, the occurrence of which is common in cancer.
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