MET Gene - CISMeF

Preferred Label : MET Gene;

NCIt synonyms : C-MET Gene; MET Proto-Oncogene, Receptor Tyrosine Kinase Gene;

NCIt related terms : MET;

CISMeF acronym : MET;

NCIt definition : This gene plays a regulatory role in the modulation of cell-surface receptors and hepatocyte growth factor interactions.;

Détails

Origin ID

C18325;

UMLS CUI

C1417123;

False automatic mappings
- microscopy, electron, transmission [MeSH Descriptor]
HGNC gene
- MET proto-oncogene, receptor tyrosine kinase [HGNC gene]
OMIM relation
- Met protooncogene, receptor tyrosine kinase [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MET gene [LOINC component]
- MET proto-oncogene, receptor tyrosine kinase [HGNC gene]
- Met protooncogene, receptor tyrosine kinase [OMIM gene]
concept_is_in_subset
- CCPS Genetics Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Reference Gene Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Childhood Cancer Predisposition Study Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Pediatric Oncology Target Genes/Proteins Terminology [NCIt concept]
gene_encodes_gene_product
- Hepatocyte Growth Factor Receptor [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_involved_in_molecular_abnormality
- Activating MET Exon 14 Gene Mutation [NCIt concept]
- Activating MET Exon 14 Skipping Mutation [NCIt concept]
- Activating MET Gene Mutation [NCIt concept]
- Deleterious MET Gene Mutation [NCIt concept]
- MET Codon 1010 Splice Mutation [NCIt concept]
- MET Codon 963 Splice Mutation [NCIt concept]
- MET Exon 14 Mutation [NCIt concept]
- MET Exon 14 Skipping Mutation [NCIt concept]
- MET Gene Deletion [NCIt concept]
- MET Gene Mutation [NCIt concept]
- MET Gene Rearrangement [NCIt concept]
- MET Intron 13 Mutation [NCIt concept]
- MET Intron 14 Mutation [NCIt concept]
- MET NM_000245.3:c.1510G>C [NCIt concept]
- MET NM_000245.3:c.1915A>C [NCIt concept]
- MET NM_000245.3:c.3208G>A [NCIt concept]
- MET NM_000245.3:c.3209T>A [NCIt concept]
- MET NM_000245.3:c.3209T>G [NCIt concept]
- MET NM_000245.3:c.3274G>A [NCIt concept]
- MET NM_000245.3:c.3280C>T [NCIt concept]
- MET NM_000245.3:c.3598T>A [NCIt concept]
- MET NM_000245.3:c.3613T>G [NCIt concept]
- MET NM_000245.3:c.3682G>A [NCIt concept]
- MET NM_000245.3:c.3688T>C [NCIt concept]
- MET NM_000245.3:c.3689A>G [NCIt concept]
- MET NM_000245.3:c.3708T>A [NCIt concept]
- MET NM_000245.3:c.3749T>C [NCIt concept]
- MET NM_000245.4:c.3028G>A [NCIt concept]
- MET NP_000236.2:p.D1010N [NCIt concept]
- MET NP_000236.2:p.D1228N [NCIt concept]
- MET NP_000236.2:p.D1228X [NCIt concept]
- MET NP_000236.2:p.F1200I [NCIt concept]
- MET NP_000236.2:p.H1094Y [NCIt concept]
- MET NP_000236.2:p.I639L [NCIt concept]
- MET NP_000236.2:p.K324M [NCIt concept]
- MET NP_000236.2:p.L1205V [NCIt concept]
- MET NP_000236.2:p.M1250T [NCIt concept]
- MET NP_000236.2:p.Q1276L [NCIt concept]
- MET NP_000236.2:p.S1236R [NCIt concept]
- MET NP_000236.2:p.V1070E [NCIt concept]
- MET NP_000236.2:p.V1070G [NCIt concept]
- MET NP_000236.2:p.V1070M [NCIt concept]
- MET NP_000236.2:p.V1092I [NCIt concept]
- MET NP_000236.2:p.V504L [NCIt concept]
- MET NP_000236.2:p.Y1003X [NCIt concept]
- MET NP_000236.2:p.Y1230C [NCIt concept]
- MET NP_000236.2:p.Y1230H [NCIt concept]
- MET NP_000236.2:p.Y1230X [NCIt concept]
- MET Protein Variant [NCIt concept]
- c-MET Gene Amplification [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Hereditary Papillary Renal Cell Carcinoma [NCIt concept]
gene_mapped_to_disease
- Hereditary Papillary Renal Cell Carcinoma [NCIt concept]
gene_plays_role_in_process
- Cell Proliferation Regulatory Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Phosphorylation Process [NCIt concept]
- Receptor Signaling [NCIt concept]
- Signal Transduction [NCIt concept]
- Tyrosine Phosphorylation [NCIt concept]
genetic_biomarker_related_to
- Elevated MET Protein Expression [NCIt concept]
- Free Hepatocyte Growth Factor Receptor Measurement [NCIt concept]
- Genetic Predisposition to Papillary Renal Cell Carcinoma [NCIt concept]
- Hepatocyte Growth Factor Receptor Measurement [NCIt concept]
- Hereditary Papillary Renal Cell Carcinoma [NCIt concept]
- MET Amplification Status [NCIt concept]
- MET Exon 14 Skipping Mutation Negative [NCIt concept]
- MET Fusion Gene [NCIt concept]
- MET Fusion Protein [NCIt concept]
- MET Gene Alteration Negative [NCIt concept]
- MET Gene Alteration Positive [NCIt concept]
- MET Gene Amplification Negative [NCIt concept]
- MET Gene Amplification in Blood or Tissue by FISH [NCIt concept]
- MET Gene Copy Number/Chromosome 7 Copy Number in Blood or Tissue by FISH [NCIt concept]
- MET Gene Copy Number/Nucleus in Blood or Tissue by FISH [NCIt concept]
- MET Gene Fusion Negative [NCIt concept]
- MET Gene Fusion Positive [NCIt concept]
- MET Gene Mutation Negative [NCIt concept]
- MET Mutation Analysis [NCIt concept]
- MET Mutation Analysis Testing Method [NCIt concept]
- MET Mutation Analysis Was Not Performed [NCIt concept]
- MET Mutation Analysis Was Performed [NCIt concept]
- MET Mutation or Amplification Indicator [NCIt concept]
- MET Overexpression Positive [NCIt concept]
- MET Positive [NCIt concept]
- MET/CEP7 Copy Number Ratio Finding [NCIt concept]
- MET/CEP7 Ratio Greater than or Equal to 4 [NCIt concept]
- MET/Chromosome 7 Copy Number Ratio Finding [NCIt concept]
- Not Known if MET Mutation Analysis Was Performed [NCIt concept]
- Sensitizing MET Gene Mutation Negative [NCIt concept]
- Specify Other MET Exon 14 Mutation [NCIt concept]
- Specify Other MET Intron 13 Mutation [NCIt concept]
- Specify Other MET Intron 14 Mutation [NCIt concept]
- Specify Other MET Mutation [NCIt concept]
- TPR/MET Fusion Gene [NCIt concept]
- TPR/MET Fusion Protein [NCIt concept]
- Was MET Mutation Analysis Performed Question [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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