Terminology Service for NFDI4Health
AKT Family Gene Mutation
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http://purl.obolibrary.org/obo/NCIT_C96865
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. [ ]
Term info
Label
AKT Family Gene Mutation
Synonyms
- AKT Family Gene Mutation
- AKT Gene Mutation
- AKT Serine/Threonine Kinase Family Gene Mutation
- v-akt Murine Thymoma Viral Oncogene Homolog Gene Family Mutation
Subsets
NCIT_C116977, NCIT_C142800, NCIT_C142799
Contributing Source
CTRP
Display Name
AKT Family Gene Mutation
Preferred Name
AKT Family Gene Mutation
Related To Genetic Biomarker
http://purl.obolibrary.org/obo/NCIT_C18350, http://purl.obolibrary.org/obo/NCIT_C20937, http://purl.obolibrary.org/obo/NCIT_C18352
Semantic Type
Cell or Molecular Dysfunction
UMLS CUI
C3273086
code
C96865