Browse LY75

Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
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 Membrane Single-pass type I membrane protein
Domain PF00040 Fibronectin type II domain
PF00059 Lectin C-type domain
Function

Acts as an endocytic receptor to direct captured antigens from the extracellular space to a specialized antigen-processing compartment (By similarity). Causes reduced proliferation of B-lymphocytes.

> Gene Ontology
 
Biological Process -
Molecular Function GO:0030246 carbohydrate binding
Cellular Component -
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between LY75 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 LY75 and anti-tumor immunity in human cancer.
PMID Cancer type Relation to immunity Evidence sentences
22397502Breast CarcinomaInhibit immunity (T cell function); immunotherapy targetWe demonstrate that DEC-HER2 fusion mAb, but not Ctrl Ig-HER2, elicits strong, broad and multifunctional CD4+ T cell immunity, CD8+ T cell responses, and humoral immunity specific for HER2 antigen.
Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
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 LY75 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
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
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 LY75 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)14120.2420.577
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)650.60.447
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.020.976
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160.3570.537
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 591.1540.517
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47-0.6450.782
729033130MelanomaallAnti-PD-1 (nivolumab) 26230.4990.361
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 15110.9670.323
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1112-0.0230.983
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 480.8530.381
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 281.2140.372
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.1870.222
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of LY75 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) 27730001
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27590001
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)2117011.8-11.80.193
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)86016.7-16.70.429
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)131109.1-9.10.458
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 91606.2-6.21
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47014.3-14.31
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) 111307.7-7.71
1729301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 610001
1829301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 51208.3-8.31
Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of LY75. 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
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of LY75. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by LY75.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of LY75. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of LY75 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between LY75 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolLY75
Namelymphocyte antigen 75
Aliases DEC-205; CLEC13B; CD205; GP200-MR6; LY-75; C-type lectin domain family 13 member B; CD antigen CD205
Chromosomal Location2q24
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting LY75 collected from DrugBank database.
> Drugs from DrugBank database
 

There is no record.