AKT Family Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A molecular genetic abnormality indicating the presence of mutations in the AKT family of genes. This family includes the AKT1, AKT2, and AKT3 genes that are located on chromosomes 14, 19, and 1, respectively.

**Synonyms:** - AKT Gene Mutation - AKT Serine/Threonine Kinase Family Gene Mutation - AKT mutation - v-akt Murine Thymoma Viral Oncogene Homolog Gene Family Mutation