AKT Family Gene Mutation

Preferred Label : AKT Family Gene Mutation;

NCIt synonyms : AKT Gene Mutation; AKT Serine/Threonine Kinase Family Gene Mutation; v-akt Murine Thymoma Viral Oncogene Homolog Gene Family Mutation;

NCIt related terms : AKT mutation;

NCIt 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.;

Details

Origin ID

C96865;

UMLS CUI

C3273086;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
related_to_genetic_biomarker
- AKT1 Gene [NCIt concept]
- AKT2 Gene [NCIt concept]
- AKT3 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients