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B-ALL Tables: Prognostic Genomic Abnormalities and Recurrent Gene Fusions (view source)
Revision as of 13:15, 22 July 2021
, 13:15, 22 July 2021small style changes
'''B-ALL'''
'''B-ALL'''
| rowspan="12" |'''''[[ABL1]]''''' (9q34)
| rowspan="12" |'''''[[ABL1]]'''''
(9q34)
|''[[CENPC1]]''
|''[[CENPC1]]''
|t(4;9)(q13;q34)
|t(4;9)(q13;q34)
|
|
|-
|-
| rowspan="3" |'''''[[ABL2]]''''' (1q25.2)
| rowspan="3" |'''''[[ABL2]]'''''
(1q25.2)
|''[[PAG1]]''
|''[[PAG1]]''
|t(1;8)(q25.2;q21.1)
|t(1;8)(q25.2;q21.1)
|
|
|-
|-
| rowspan="3" |'''''[[CSF1R]]''''' (5q32)
| rowspan="3" |'''''[[CSF1R]]'''''
(5q32)
|''[[MEF2D]]''
|''[[MEF2D]]''
|t(1;5)(q22;q32)
|t(1;5)(q22;q32)
|On the same chromosome arm; however, a simple deletion cannot cause the fusion due to the orientation of genes
|On the same chromosome arm; however, a simple deletion cannot cause the fusion due to the orientation of genes
|-
|-
| rowspan="22" |'''''[[JAK2]]''''' (9p24.1)
| rowspan="22" |'''''[[JAK2]]'''''
(9p24.1)
|''[[ATF7IP]]''
|''[[ATF7IP]]''
|-
|-
| rowspan="6" |'''''MEF2D-''rearranged B-ALL'''
| rowspan="6" |'''''MEF2D-''rearranged B-ALL'''
| rowspan="6" |'''''[[MEF2D]]''' (1q22)''
| rowspan="6" |'''''[[MEF2D]]'''''
(1q22)
|''[[BCL9]]''
|''[[BCL9]]''
|inv(1)(q21.2q22)
|inv(1)(q21.2q22)