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GRB7
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GRB7

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GRB7
Protein GRB7 PDB 1mw4.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases GRB7, entrez:2886, growth factor receptor bound protein 7
External IDs OMIM: 601522 MGI: 102683 HomoloGene: 3881 GeneCards: GRB7
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001030002
NM_001242442
NM_001242443
NM_005310
NM_001330207

NM_010346

RefSeq (protein)

NP_001025173
NP_001229371
NP_001229372
NP_001317136
NP_005301

NP_034476

Location (UCSC) Chr 17: 39.74 – 39.75 Mb Chr 11: 98.34 – 98.35 Mb
PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Growth factor receptor-bound protein 7, also known as GRB7, is a protein that in humans is encoded by the GRB7 gene.

Function

The product of this gene belongs to a small family of adaptor proteins that are known to interact with a number of receptor tyrosine kinases and signaling molecules. This gene encodes a growth factor receptor-binding protein that interacts with epidermal growth factor receptor (EGFR) and ephrin receptors. The protein plays a role in the integrin signaling pathway and cell migration by binding with focal adhesion kinase (FAK). Alternative splicing results in multiple transcript variants encoding different isoforms, although the full-length natures of only two of the variants have been determined to date.

Clinical significance

GRB7 is an SH2-domain adaptor protein that binds to receptor tyrosine kinases and provides the intra-cellular direct link to the Ras proto-oncogene. Human GRB7 is located on the long arm of chromosome 17, next to the ERBB2 (alias HER2/neu) proto-oncogene.

These two genes are commonly co-amplified (present in excess copies) in breast cancers. GRB7, thought to be involved in migration, is well known to be over-expressed in testicular germ cell tumors, esophageal cancers, and gastric cancers.

Interactions

GRB7 has been shown to interact with:

Model organisms

Model organisms have been used in the study of GRB7 function. A conditional knockout mouse line called Grb7tm1b(EUCOMM)Wtsi was generated at the Wellcome Trust Sanger Institute. Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion. Additional screens performed: - In-depth immunological phenotyping

Further reading

External links


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