GRB10: Growth Factor Receptor Bound Protein 10

A key regulator of insulin and IGF signaling, implicated in growth disorders and cancer.

Gene Information Card

Symbol GRB10
Full Name Growth factor receptor bound protein 10
Gene Type Protein coding
Chromosomal Location 7p12.1
NCBI Gene ID 2887 ncbi.nlm.nih.gov/gene/2887
Ensembl ID ENSG00000106070
UniProt ID Q13322
OMIM ID 601523
HGNC ID 4464
Aliases GRB-IR, Grb-10, IRBP, MEG1, RSS

Description

GRB10 (Growth factor receptor bound protein 10) encodes a member of the GRB7 family of adaptor proteins. It interacts with tyrosine kinase receptors, including insulin receptor (INSR) and insulin-like growth factor 1 receptor (IGF1R), modulating downstream signaling pathways such as PI3K/AKT and MAPK. GRB10 is imprinted, with maternal expression in most tissues, and plays a critical role in growth regulation, metabolism, and cell proliferation. Dysregulation is linked to Silver-Russell syndrome and various cancers.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Silver-Russell syndrome Maternal uniparental disomy of chromosome 7 or GRB10 duplication leads to reduced IGF signaling and growth restriction OMIM #180860
Type 2 diabetes GRB10 overexpression impairs insulin signaling, contributing to insulin resistance PMID: 15616553
Breast cancer GRB10 overexpression promotes IGF1R-mediated cell proliferation and survival PMID: 19029981
Prostate cancer GRB10 amplification enhances androgen receptor and IGF signaling COSMIC: GRB10

Expression Profile

Tissue Expression
Tissue nTPM level
Skeletal muscle 12.5 Medium
Adipose tissue 8.3 Medium
Liver 6.1 Low
Brain 4.2 Low
Pancreas 3.8 Low
Cell Line Expression
Cell Line nTPM Notes
HEK 293 15.2 High expression
MCF7 10.1 Breast cancer cell line
HepG2 7.4 Hepatocellular carcinoma
PC3 9.8 Prostate cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G Missense Rare Potential loss of function
c.214C>T Nonsense Rare Premature truncation
c.1234G>A Missense 0.01% Unknown effect
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations in GRB10 are predicted to cause loss of adaptor function, impairing negative regulation of IGF signaling.

Gain of Function (GOF)

Amplification or overexpression of GRB10 in cancers leads to enhanced IGF1R signaling and cell proliferation.

Dominant Negative (DN)

Certain missense mutations may disrupt GRB10 interaction with receptors, acting in a dominant-negative manner.

Pathways

Insulin signaling pathway (KEGG: hsa04910)
IGF-1 signaling pathway (Reactome: R-HSA-2404192)
PI3K-Akt signaling pathway (KEGG: hsa04151)

Protein Summary

GRB10 is a 594-amino acid adaptor protein containing an N-terminal proline-rich region, a central PH domain, and a C-terminal SH2 domain. It binds phosphorylated tyrosine residues on activated receptors (INSR, IGF1R) and recruits downstream effectors. The protein negatively regulates insulin and IGF signaling by competing with IRS1 and promoting receptor internalization. Isoforms vary due to alternative splicing and imprinting.

Related Products

Product name Cat.No. Species Gene ID
GRB10 Knockout HEK293 Cell Line EDJ-KQ1172 Human 2887 Details Get a Quote
GRB10 Knockout A-549 Cell Line EDJ-KQ20435 Human 2887 Details Get a Quote
GRB10 Knockout HCT 116 Cell Line EDJ-KQ20436 Human 2887 Details Get a Quote
GRB10 Knockout HeLa Cell Line EDJ-KQ20437 Human 2887 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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