MET Gene Mutation

Preferred Label : MET Gene Mutation;

NCIt synonyms : c-met Gene Mutation; Hepatocyte Growth Factor Receptor Gene Mutation; Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Gene Mutation; MET Proto-Oncogene, Receptor Tyrosine Kinase Gene Mutation; HGFR Gene Mutation;

NCIt related terms : MET Mutation;

NCIt definition : A change in the nucleotide sequence of the MET gene.;

Details

Origin ID

C39788;

UMLS CUI

C1518121;

Molecular abnormality of diseases
- Calcifying Epithelial Odontogenic Tumor [NCIt concept]
- Clear Cell Calcifying Epithelial Odontogenic Tumor [NCIt concept]
- Cystic/Microcystic Calcifying Epithelial Odontogenic Tumor [NCIt concept]
- Non-Calcifying/Langerhans Cell-Rich Calcifying Epithelial Odontogenic Tumor [NCIt concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Lung Squamous Cell Carcinoma and Lung Adenocarcinoma Baseline Form [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- MET NP_000236.2:p.D1010N [NCIt concept]
- MET NP_000236.2:p.Y1003X [NCIt concept]
- MET Protein Variant [NCIt concept]
is_molecular_abnormality_of_disease
- Hereditary Papillary Renal Cell Carcinoma [NCIt concept]
molecular_abnormality_involves_gene
- MET Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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