MET Exon 14 Mutation

Preferred Label : MET Exon 14 Mutation;

NCIt synonyms : HGFR Exon 14 Mutation; Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Mutation; c-Met Exon 14 Mutation; MET Proto-Oncogene, Receptor Tyrosine Kinase Exon 14 Mutation;

NCIt definition : A molecular genetic abnormality indicating the presence of a mutation in exon 14 of the MET gene located in the vicinity of 7q31.;

NCIt note : MET exon 14 encodes the juxtamembrane domain of the hepatocyte growth factor receptor protein.;

NCI Metathesaurus CUI : CL508909;

Details

Origin ID

C127129;

UMLS CUI

C4288794;

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]
gene_mutant_encodes_gene_product_sequence_variation
- MET NP_000236.2:p.D1010N [NCIt concept]
- MET NP_000236.2:p.Y1003X [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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