ERBB2 erb-b2 receptor tyrosine kinase 2
Gene ID: 2064, updated on 7-Nov-2024Gene type: protein coding
Also known as: NEU; NGL; HER2; TKR1; CD340; HER-2; VSCN2; MLN 19; MLN-19; c-ERB2; c-ERB-2; HER-2/neu; p185(erbB2)
- See all available tests in GTR for this gene
- Go to complete Gene record for ERBB2
- Go to Variation Viewer for ERBB2 variants
Summary
This gene encodes a member of the epidermal growth factor (EGF) receptor family of receptor tyrosine kinases. This protein has no ligand binding domain of its own and therefore cannot bind growth factors. However, it does bind tightly to other ligand-bound EGF receptor family members to form a heterodimer, stabilizing ligand binding and enhancing kinase-mediated activation of downstream signalling pathways, such as those involving mitogen-activated protein kinase and phosphatidylinositol-3 kinase. Allelic variations at amino acid positions 654 and 655 of isoform a (positions 624 and 625 of isoform b) have been reported, with the most common allele, Ile654/Ile655, shown here. Amplification and/or overexpression of this gene has been reported in numerous cancers, including breast and ovarian tumors. Alternative splicing results in several additional transcript variants, some encoding different isoforms and others that have not been fully characterized. [provided by RefSeq, Jul 2008]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Cetuximab response MedGen: CN077967GeneReviews: Not available | See labs |
Gastric cancer | See labs |
Glioma susceptibility 1 | See labs |
Lung cancer | See labs |
Ovarian neoplasm MedGen: C0919267GeneReviews: Not available | See labs |
Panitumumab response MedGen: CN077999GeneReviews: Not available | See labs |
Pertuzumab response MedGen: CN233145GeneReviews: Not available | See labs |
Trastuzumab response MedGen: CN078025GeneReviews: Not available | See labs |
Visceral neuropathy, familial, 2, autosomal recessive | See labs |
Genomic context
- Location:
- 17q12
- Sequence:
- Chromosome: 17; NC_000017.11 (39688094..39728658)
- Total number of exons:
- 35
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for ERBB2 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- Catalogue of Somatic Mutations in Cancer (COSMIC)
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- ERBB2 database
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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