Browse NHS

Summary
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
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 Isoform 1: Apical cell membrane; Peripheral membrane protein. Cell projection, lamellipodium. Cell junction, tight junction. Cell junction, focal adhesion. Note=Colocalizes with the tight junction protein TJP1 in epithelial cells. Localizes to the leading edge of lamellipodia in motile cells.; SUBCELLULAR LOCATION: Isoform 3: Cytoplasm.
Domain PF15273 NHS-like
Function

May function in cell morphology by maintaining the integrity of the circumferential actin ring and controlling lamellipod formation. Involved in the regulation eye, tooth, brain and craniofacial development.

> Gene Ontology
 
Biological Process GO:0001654 eye development
GO:0002088 lens development in camera-type eye
GO:0007423 sensory organ development
GO:0043010 camera-type eye development
Molecular Function -
Cellular Component GO:0005923 bicellular tight junction
GO:0005924 cell-substrate adherens junction
GO:0005925 focal adhesion
GO:0016324 apical plasma membrane
GO:0030027 lamellipodium
GO:0030055 cell-substrate junction
GO:0031252 cell leading edge
GO:0043296 apical junction complex
GO:0045177 apical part of cell
GO:0070160 occluding junction
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between NHS 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
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
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 NHS 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
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
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 NHS in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.7180.0262
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.2980.594
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-1.0180.0287
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-0.2190.494
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.4730.82
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470.0980.969
729033130MelanomaallAnti-PD-1 (nivolumab) 26230.1560.771
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 15111.0250.241
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1112-0.8120.389
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 48-0.0070.993
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 280.0640.952
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.4570.00111
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of NHS 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) 277322.21.420.80.00141
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 275922.21.720.50.00342
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21174.85.9-1.11
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)8612.5012.51
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)131109.1-9.10.458
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160001
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470001
1329033130MelanomaallAnti-PD-1 (nivolumab) 38275.305.30.507
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 22134.504.51
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
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of NHS. 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
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of NHS. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by NHS.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of NHS. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of NHS expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between NHS and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolNHS
NameNance-Horan syndrome (congenital cataracts and dental anomalies)
Aliases CTRCT40; CXN; congenital cataracts and dental anomalies protein; Nance-Horan syndrome protein
Chromosomal LocationXp22.3-p21.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting NHS collected from DrugBank database.
> Drugs from DrugBank database
 

There is no record.