Browse EMILIN2

Summary
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
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. Note=Found mainly at the interface between amorphous elastin and microfibrils.
Domain PF00386 C1q domain
PF07546 EMI domain
Function

May be responsible for anchoring smooth muscle cells to elastic fibers, and may be involved not only in the formation of the elastic fiber, but also in the processes that regulate vessel assembly. Has cell adhesive capacity.

> Gene Ontology
 
Biological Process -
Molecular Function GO:0005201 extracellular matrix structural constituent
GO:0030023 extracellular matrix constituent conferring elasticity
GO:0097493 structural molecule activity conferring elasticity
Cellular Component GO:0005578 proteinaceous extracellular matrix
GO:0005581 collagen trimer
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between EMILIN2 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
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
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 EMILIN2 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
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
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 EMILIN2 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.8990.029
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.8820.587
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.9150.467
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-0.3510.387
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.8960.653
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470.3440.898
729033130MelanomaallAnti-PD-1 (nivolumab) 26230.0840.86
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 15110.3820.806
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1112-0.1950.907
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 481.1680.333
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 281.4590.425
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.1730.295
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of EMILIN2 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) 27737.42.74.70.294
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 01407.1-7.11
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27597.41.75.70.231
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)211723.8023.80.0529
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)8612.5012.51
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)131130.8030.80.0983
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160001
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470001
1329033130MelanomaallAnti-PD-1 (nivolumab) 38275.33.71.61
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 22134.57.7-3.21
1529033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 16146.206.21
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
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of EMILIN2. 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
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of EMILIN2. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by EMILIN2.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of EMILIN2. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of EMILIN2 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between EMILIN2 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolEMILIN2
Nameelastin microfibril interfacer 2
Aliases FLJ33200; FOAP-10; EMILIN-2; elastin microfibril interface-located protein 2; extracellular glycoprotein EMI ......
Chromosomal Location18p11.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting EMILIN2 collected from DrugBank database.
> Drugs from DrugBank database
 

There is no record.