Summary | |
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Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Basic function annotation. > Subcellular Location, Domain and Function > Gene Ontology > KEGG and Reactome Pathway |
Subcellular Location | Cytoplasm, cytosol Cytoplasm Cell membrane Membrane Peripheral membrane protein Cytoplasmic side Note=Interaction with PKD1 promotes location at the cell membrane (PubMed:10339594). Interaction with RGS7BP promotes location at the cell membrane (PubMed:15897264). |
Domain |
PF00610 Domain found in Dishevelled PF00631 GGL domain PF00615 Regulator of G protein signaling domain |
Function |
Regulates G protein-coupled receptor signaling cascades. Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits, thereby driving them into their inactive GDP-bound form (PubMed:10521509, PubMed:10862767). The RGS7/GNB5 dimer enhances GNAO1 GTPase activity (PubMed:10521509). May play a role in synaptic vesicle exocytosis (PubMed:12659861). Modulates the activity of potassium channels that are activated by GNAO1 in response to muscarinic acetylcholine receptor M2/CHRM2 signaling (PubMed:15897264). |
Biological Process |
GO:0006457 protein folding |
Molecular Function |
GO:0005096 GTPase activator activity GO:0008047 enzyme activator activity GO:0030695 GTPase regulator activity GO:0031681 G-protein beta-subunit binding GO:0060589 nucleoside-triphosphatase regulator activity |
Cellular Component |
GO:0005834 heterotrimeric G-protein complex GO:0009898 cytoplasmic side of plasma membrane GO:0019897 extrinsic component of plasma membrane GO:0019898 extrinsic component of membrane GO:0031234 extrinsic component of cytoplasmic side of plasma membrane GO:0098552 side of membrane GO:0098562 cytoplasmic side of membrane GO:1905360 GTPase complex |
KEGG | - |
Reactome |
R-HSA-390466: Chaperonin-mediated protein folding R-HSA-6814122: Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding R-HSA-418594: G alpha (i) signalling events R-HSA-388396: GPCR downstream signaling R-HSA-392499: Metabolism of proteins R-HSA-391251: Protein folding R-HSA-162582: Signal Transduction R-HSA-372790: Signaling by GPCR |
Summary | |
---|---|
Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Literatures that report relations between RGS7 and anti-tumor immunity. The specific mechanism were also collected if the literature reports that a gene specifically promotes or inhibits the infiltration or function of T/NK cells. |
There is no record. |
Summary | |
---|---|
Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | High-throughput screening data (e.g. CRISPR-Cas9, shRNA and RNAi) for T cell-mediated killing. Genetic screen techniques can identify mechanisms of tumor cell resistance (e.g., PTPN2) and sensitivity (e.g., APLNR) to killing by cytotoxic T cells, the central effectors of anti-tumor immunity. After comprehensively searching, eight groups of screening data sets were collected in the current database. In this tab, users can check whether their selected genes cause resistance or increase sensitivity to T cell-mediated killing in various data sets. |
> High-throughput Screening
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Statistical results of RGS7 in screening data sets for detecting immune reponses.
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Summary | |
---|---|
Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Transcriptomic and genomic profiling of pre-treated tumor biopsies from responders and non-responders to immunotherapy. These data were used to identify signatures and mechanisms of response to checkpoint blockade (e.g., anti-PDL1 and anti-PD1). One example is that mutations in the gene PBRM1 benefit clinical survival of patients with clear cell renal cell carcinoma. After comprehensively searching, we collected 5 and 6 of transcriptomic and genomic data sets, respectively. In this tab, users can check whether their selected genes have significant difference of expression or mutation between responders and non-responders in various data sets. > Expression difference between responders and non-responders > Mutation difference between responders and non-responders |
Points in the above scatter plot represent the expression difference of RGS7 in various data sets.
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Points in the above scatter plot represent the mutation difference of RGS7 in various data sets.
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Summary | |
---|---|
Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of RGS7. The immune-related signatures of 28 TIL types from Charoentong's study, which can be viewed in the download page. For each cancer type, the relative abundance of TILs were inferred by using gene set variation analysis (GSVA) based on gene expression profile. In this tab, users can examine which kinds of TILs might be regulated by the current gene. |
Summary | |
---|---|
Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of RGS7. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by RGS7. > Immunoinhibitor > Immunostimulator > MHC molecule |
Summary | |
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Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of RGS7. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene. > Chemokine > Receptor |
Summary | |
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Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Distribution of RGS7 expression across immune and molecular subtypes. > Immune subtype > Molecular subtype |
Summary | |
---|---|
Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Associations between RGS7 and clinical features. > Overall survival analysis > Cancer stage > Tumor grade |
Summary | |
---|---|
Symbol | RGS7 |
Name | regulator of G-protein signaling 7 |
Aliases | regulator of G-protein signalling 7; regulator of G-protein signaling RGS7 |
Chromosomal Location | 1q43 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Drugs targeting RGS7 collected from DrugBank database. |
There is no record. |