Summary | |
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Symbol | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Basic function annotation. > Subcellular Location, Domain and Function > Gene Ontology > KEGG and Reactome Pathway |
Subcellular Location | Secreted. |
Domain |
PF00057 Low-density lipoprotein receptor domain class A PF01823 MAC/Perforin domain PF00084 Sushi repeat (SCR repeat) PF00090 Thrombospondin type 1 domain |
Function |
Constituent of the membrane attack complex (MAC) that plays a key role in the innate and adaptive immune response by forming pores in the plasma membrane of target cells. C7 serves as a membrane anchor. |
Biological Process |
GO:0002250 adaptive immune response GO:0002443 leukocyte mediated immunity GO:0002449 lymphocyte mediated immunity GO:0002455 humoral immune response mediated by circulating immunoglobulin GO:0002460 adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains GO:0002526 acute inflammatory response GO:0002673 regulation of acute inflammatory response GO:0002697 regulation of immune effector process GO:0002920 regulation of humoral immune response GO:0006956 complement activation GO:0006957 complement activation, alternative pathway GO:0006958 complement activation, classical pathway GO:0006959 humoral immune response GO:0016064 immunoglobulin mediated immune response GO:0016485 protein processing GO:0019724 B cell mediated immunity GO:0019835 cytolysis GO:0030449 regulation of complement activation GO:0050727 regulation of inflammatory response GO:0051604 protein maturation GO:0070613 regulation of protein processing GO:0072376 protein activation cascade GO:1903317 regulation of protein maturation GO:2000257 regulation of protein activation cascade |
Molecular Function | - |
Cellular Component |
GO:0005579 membrane attack complex GO:0046930 pore complex |
KEGG |
hsa04610 Complement and coagulation cascades |
Reactome |
R-HSA-166658: Complement cascade R-HSA-168256: Immune System R-HSA-168249: Innate Immune System R-HSA-977606: Regulation of Complement cascade R-HSA-166665: Terminal pathway of complement |
Summary | |
---|---|
Symbol | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Literatures that report relations between C7 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 | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
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 C7 in screening data sets for detecting immune reponses.
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Summary | |
---|---|
Symbol | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
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 C7 in various data sets.
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Points in the above scatter plot represent the mutation difference of C7 in various data sets.
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Summary | |
---|---|
Symbol | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of C7. 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 | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of C7. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by C7. > Immunoinhibitor > Immunostimulator > MHC molecule |
Summary | |
---|---|
Symbol | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of C7. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene. > Chemokine > Receptor |
Summary | |
---|---|
Symbol | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Distribution of C7 expression across immune and molecular subtypes. > Immune subtype > Molecular subtype |
Summary | |
---|---|
Symbol | C7 |
Name | complement component 7 |
Aliases | Complement component C7 |
Chromosomal Location | 5p13.1 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Associations between C7 and clinical features. > Overall survival analysis > Cancer stage > Tumor grade |