Browse MRC1

Summary
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
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 Endosome membrane Single-pass type I membrane protein Cell membrane Single-pass type I membrane protein
Domain PF00040 Fibronectin type II domain
PF00059 Lectin C-type domain
PF00652 Ricin-type beta-trefoil lectin domain
Function

Mediates the endocytosis of glycoproteins by macrophages. Binds both sulfated and non-sulfated polysaccharide chains.; FUNCTION: (Microbial infection) Acts as phagocytic receptor for bacteria, fungi and other pathogens.; FUNCTION: (Microbial infection) Acts as a receptor for Dengue virus envelope protein E. ; FUNCTION: (Microbial infection) Interacts with Hepatitis B virus envelope protein.

> Gene Ontology
 
Biological Process GO:0002237 response to molecule of bacterial origin
GO:0006898 receptor-mediated endocytosis
GO:0019058 viral life cycle
GO:0030260 entry into host cell
GO:0032496 response to lipopolysaccharide
GO:0034341 response to interferon-gamma
GO:0044409 entry into host
GO:0046718 viral entry into host cell
GO:0051701 interaction with host
GO:0051806 entry into cell of other organism involved in symbiotic interaction
GO:0051828 entry into other organism involved in symbiotic interaction
GO:0070670 response to interleukin-4
GO:0071216 cellular response to biotic stimulus
GO:0071219 cellular response to molecule of bacterial origin
GO:0071222 cellular response to lipopolysaccharide
GO:0071346 cellular response to interferon-gamma
GO:0071353 cellular response to interleukin-4
GO:0071396 cellular response to lipid
Molecular Function GO:0001618 virus receptor activity
GO:0005537 mannose binding
GO:0030246 carbohydrate binding
GO:0048029 monosaccharide binding
Cellular Component GO:0010008 endosome membrane
GO:0044440 endosomal part
> KEGG and Reactome Pathway
 
KEGG hsa04145 Phagosome
Reactome R-HSA-1280218: Adaptive Immune System
R-HSA-1236975: Antigen processing-Cross presentation
R-HSA-983169: Class I MHC mediated antigen processing & presentation
R-HSA-1236978: Cross-presentation of soluble exogenous antigens (endosomes)
R-HSA-168256: Immune System
Summary
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between MRC1 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
 
  Literatures describing the relation between MRC1 and anti-tumor immunity in human cancer.
PMID Cancer type Relation to immunity Evidence sentences
21523763Pleural Malignant MesotheliomaInhibit immunityWithin MPM tumors, macrophages comprised 27% ± 9% of the tumor area and demonstrated an immunosuppressive phenotype with high expression of CD163, CD206, and interleukin-4 receptor α.
23271806Lung Carcinoma; MesotheliomaInhibit immunityRecurrent tumors and draining lymph nodes are infiltrated with M2 (CD11b+F4/80hiCD206hi and CD11b+F4/80hiCD124hi) macrophages and CD4+Foxp3+ regulatory T cells. This complex network of immunosuppression in the surrounding tumor microenvironment explains the resistance of tumor recurrences to conventional cancer vaccines despite small tumor size, an intact antitumor immune response, and unaltered cancer cells.
Summary
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
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 MRC1 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
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
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 MRC1 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.7030.147
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.9080.378
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.5490.491
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160.4370.735
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.0290.989
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 4710.628
729033130MelanomaallAnti-PD-1 (nivolumab) 2623-0.2350.672
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 1511-0.2740.89
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1112-0.220.921
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 4801
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 2801
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.3960.0292
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of MRC1 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) 14170001
225765070Non-small cell lung cancer (NSCLC)smokingAnti-PD-1 (pembrolizumab) 1030001
325765070Non-small cell lung cancer (NSCLC)non-smokingAnti-PD-1 (pembrolizumab) 4140001
426359337MelanomaallAnti-CTLA-4 (ipilimumab) 27733.71.42.30.469
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27593.71.720.532
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21174.85.9-1.11
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)860001
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)13117.79.1-1.41
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160001
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470001
1329033130MelanomaallAnti-PD-1 (nivolumab) 38270001
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 22130001
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
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of MRC1. 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
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of MRC1. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by MRC1.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of MRC1. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of MRC1 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between MRC1 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolMRC1
Namemannose receptor, C type 1
Aliases CLEC13D; CD206; bA541I19.1; CLEC13DL; MRC1L1; mannose receptor, C type 1-like 1; MMRL1; C-type lectin domain ......
Chromosomal Location10p13
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting MRC1 collected from DrugBank database.
> Drugs from DrugBank database
 

  Details on drugs targeting MRC1.
ID Name Drug Type Targets #Targets
DB09266Technetium Tc-99m tilmanoceptSmall MoleculeMRC11