Browse COMP

Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Basic function annotation.
> Subcellular Location, Domain and Function
> Gene Ontology
> KEGG and Reactome Pathway
> Subcellular Location, Domain and Function
 
Subcellular Location Secreted, extracellular space, extracellular matrix.
Domain PF11598 Cartilage oligomeric matrix protein
PF07645 Calcium-binding EGF domain
PF02412 Thrombospondin type 3 repeat
PF05735 Thrombospondin C-terminal region
Function

May play a role in the structural integrity of cartilage via its interaction with other extracellular matrix proteins such as the collagens and fibronectin. Can mediate the interaction of chondrocytes with the cartilage extracellular matrix through interaction with cell surface integrin receptors. Could play a role in the pathogenesis of osteoarthritis. Potent suppressor of apoptosis in both primary chondrocytes and transformed cells. Suppresses apoptosis by blocking the activation of caspase-3 and by inducing the IAP family of survival proteins (BIRC3, BIRC2, BIRC5 and XIAP). Essential for maintaining a vascular smooth muscle cells (VSMCs) contractile/differentiated phenotype under physiological and pathological stimuli. Maintains this phenotype of VSMCs by interacting with ITGA7 (By similarity).

> Gene Ontology
 
Biological Process GO:0001501 skeletal system development
GO:0003416 endochondral bone growth
GO:0003417 growth plate cartilage development
GO:0030198 extracellular matrix organization
GO:0035265 organ growth
GO:0043062 extracellular structure organization
GO:0048705 skeletal system morphogenesis
GO:0048736 appendage development
GO:0051216 cartilage development
GO:0060173 limb development
GO:0060348 bone development
GO:0060349 bone morphogenesis
GO:0060350 endochondral bone morphogenesis
GO:0060351 cartilage development involved in endochondral bone morphogenesis
GO:0061448 connective tissue development
GO:0098868 bone growth
Molecular Function GO:0001948 glycoprotein binding
GO:0002020 protease binding
GO:0005201 extracellular matrix structural constituent
GO:0005518 collagen binding
GO:0005539 glycosaminoglycan binding
GO:0008201 heparin binding
GO:0043394 proteoglycan binding
GO:0043395 heparan sulfate proteoglycan binding
GO:1901681 sulfur compound binding
Cellular Component GO:0005578 proteinaceous extracellular matrix
> KEGG and Reactome Pathway
 
KEGG hsa04145 Phagosome
hsa04151 PI3K-Akt signaling pathway
hsa04510 Focal adhesion
hsa04512 ECM-receptor interaction
Reactome R-HSA-3000178: ECM proteoglycans
R-HSA-1474244: Extracellular matrix organization
R-HSA-216083: Integrin cell surface interactions
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between COMP 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.
> Text Mining
 

There is no record.

Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
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
  Statistical results of COMP in screening data sets for detecting immune reponses.
PMID Screening System Cancer Type Cell Line Data Set Statistical Results Relation to immunity
29301958CRISPR-Cas9 melanomaB16F10Pmel-1 T cell NA/NSNA/NS
29301958CRISPR-Cas9 melanomaB16F10OT-1 T cell NA/NSNA/NS
28783722CRISPR-Cas9 melanomaMel6242CT-CRISPR NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX+Anti-PD1 NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX NA/NSNA/NS
25691366RNAiBreast cancerMCF7Luc-CTL assay NA/NSNA/NS
24476824shRNAmelanomaB16Primary screen NA/NSNA/NS
24476824shRNAmelanomaB16Secondary screen NA/NSNA/NS
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
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
> Expression difference between responders and non-responders
 
Points in the above scatter plot represent the expression difference of COMP in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-1.8410.0205
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-1.9410.273
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-1.7410.13
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160.0310.968
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.0870.965
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470.1820.942
729033130MelanomaallAnti-PD-1 (nivolumab) 26230.3260.74
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 15110.2690.857
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 11120.5120.738
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 480.4310.83
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 281.5840.539
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.450.235
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of COMP in various data sets.
No PMID Cancer type Group Drug # Res # NRes % Mut/Res % Mut/NRes % Diff (R vs NR) Pval Anno
125765070Non-small cell lung cancer (NSCLC)allAnti-PD-1 (pembrolizumab) 14177.107.10.452
225765070Non-small cell lung cancer (NSCLC)smokingAnti-PD-1 (pembrolizumab) 103100101
325765070Non-small cell lung cancer (NSCLC)non-smokingAnti-PD-1 (pembrolizumab) 4140001
426359337MelanomaallAnti-CTLA-4 (ipilimumab) 27733.703.70.27
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27593.703.70.314
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21174.804.81
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)860001
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)13117.707.71
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 91611.1011.10.36
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59200200.357
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470001
1329033130MelanomaallAnti-PD-1 (nivolumab) 38272.602.61
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 22134.504.51
1529033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 16140001
1629301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 11130001
1729301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 610001
1829301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 5120001
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of COMP. 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.
> Lymphocyte
 
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of COMP. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by COMP.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of COMP. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of COMP expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between COMP and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolCOMP
Namecartilage oligomeric matrix protein
Aliases THBS5; thrombospondin-5; PSACH; EDM1; EPD1; cartilage oligomeric matrix protein (pseudoachondroplasia, epiph ......
Chromosomal Location19p13.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting COMP collected from DrugBank database.
> Drugs from DrugBank database
 

  Details on drugs targeting COMP.
ID Name Drug Type Targets #Targets
DB01373CalciumSmall MoleculeALPP, AOC1, ATP2C1, BMP4, CACNA1C, CAST, COMP, CP, MGP, PCDH19, PD ......19