MET Exon 14 Skipping Mutation

Preferred Label : MET Exon 14 Skipping Mutation;

NCIt synonyms : Deletion of c-MET Exon 14; c-MET Exon 14 Splice Mutation; Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Splice Mutation; Loss of c-MET Exon 14; MET Exon 14 Skipping Alteration; HGFR Exon 14 Skipping Alteration; MET Proto-Oncogene, Receptor Tyrosine Kinase Exon 14 Skipping Alteration; c-Met Exon 14 Skipping Alteration; HGFR Exon 14 Skipping Mutation; Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Skipping Alteration; Deletion of MET Exon 14; MET Proto-Oncogene, Receptor Tyrosine Kinase Exon 14 Skipping Mutation; MET Exon 14 Splice Mutation; c-Met Exon 14 Skipping Mutation; Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Skipping Mutation; Loss of MET Exon 14; HGFR Exon 14 Splice Mutation; MET Exon 14 Deletion Mutation; c-MET Exon 14 Deletion Mutation;

NCIt related terms : MET exon 14 deletion detected;

NCIt definition : A molecular genetic abnormality indicating the presence of a splice site mutation that results in a loss of transcription of exon 14 of the MET gene.;

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

NCI Metathesaurus CUI : CL513169;

Details

Origin ID

C131179;

UMLS CUI

C4330599;

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 Disease Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [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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