Table 1

Genes whose mutations or changes in expression occur recurrently in cytogenetically normal AML and have clinical significance

Gene symbol
 (aliases and previous gene symbols)Gene nameChromosomal location
FLT3 (STK1, FLK2, CD135) Fms-related tyrosine kinase 3 13q12 
NPM1 (B23)* Nucleophosmin (nucleolar phosphoprotein B23, numatrin) 5q35 
MLL (ALL-1, HRX, HTRX1, CXXC7, TRX1, MLL1A) Myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila11q23 
BAALC Brain and acute leukemia gene, cytoplasmic 8q22.3 
CEBPA (CEBP) CCAAT/enhancer binding protein (C/EBP), alpha 19q13.1 
ERG v-ets erythroblastosis virus E26 oncogene-like (avian) 21q22.3 
Gene symbol
 (aliases and previous gene symbols)Gene nameChromosomal location
FLT3 (STK1, FLK2, CD135) Fms-related tyrosine kinase 3 13q12 
NPM1 (B23)* Nucleophosmin (nucleolar phosphoprotein B23, numatrin) 5q35 
MLL (ALL-1, HRX, HTRX1, CXXC7, TRX1, MLL1A) Myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila11q23 
BAALC Brain and acute leukemia gene, cytoplasmic 8q22.3 
CEBPA (CEBP) CCAAT/enhancer binding protein (C/EBP), alpha 19q13.1 
ERG v-ets erythroblastosis virus E26 oncogene-like (avian) 21q22.3 
*

NPM1 has been referred to as NPM in some articles.12,37-40 

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