KMT2A-SH3GL1 Fusion Protein Expression

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A molecular abnormality characterized by the expression of a fusion protein that results from chromosomal recombination involving the human genes KMT2A and SH3GL1. This abnormal protein is associated with acute myeloid leukemia.

**Synonyms:** - KMT2A-EEN Fusion Protein Expression - KMT2A/SH3GL1 Fusion Protein Expression - MLL-EEN Fusion Protein Expression - MLL-SH3GL1 Fusion Protein Expression - MLL/EEN Fusion Protein Expression - MLL/SH3GL1 Fusion Protein Expression