ERBB2 Exon 20 Insertion Mutation

Preferred Label : ERBB2 Exon 20 Insertion Mutation;

NCIt synonyms : Neu Exon 20 Insertion Mutation; HER2 Exon 20 Insertion Mutation; c-erbB2 Exon 20 Insertion Mutation; HER-2 Exon 20 Insertion Mutation; CD340 Exon 20 Insertion Mutation; HER2/Neu Exon 20 Insertion Mutation; v-Erb-B2 Avian Erythroblastic Leukemia Viral Oncogene Homolog 2 Exon 20 Insertion Mutation; Erb-B2 Receptor Tyrosine Kinase 2 Exon 20 Insertion Mutation;

NCIt definition : A molecular genetic abnormality indicating the presence of an in-frame insertion mutation occurring within exon 20 of the ERBB2 gene.;

NCI Metathesaurus CUI : CL552394;

Details

Origin ID

C150633;

UMLS CUI

C4725889;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- ERBB2 Protein Variant [NCIt concept]
is_target
- EGFR/HER2 Mutant-selective Inhibitor HS-10376 [NCIt concept]
- EGFR/HER2 Mutant-selective Inhibitor STX-721 [NCIt concept]
- HER2 Inhibitor BI 1810631 [NCIt concept]
- HER2 Inhibitor ELVN-002 [NCIt concept]
- Mobocertinib [NCIt concept]
molecular_abnormality_involves_gene
- ERBB2 Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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