Browse TRIP13

Summary
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
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 -
Domain PF00004 ATPase family associated with various cellular activities (AAA)
Function

Plays a key role in chromosome recombination and chromosome structure development during meiosis. Required at early steps in meiotic recombination that leads to non-crossovers pathways. Also needed for efficient completion of homologous synapsis by influencing crossover distribution along the chromosomes affecting both crossovers and non-crossovers pathways. Also required for development of higher-order chromosome structures and is needed for synaptonemal-complex formation. In males, required for efficient synapsis of the sex chromosomes and for sex body formation. Promotes early steps of the DNA double-strand breaks (DSBs) repair process upstream of the assembly of RAD51 complexes. Required for depletion of HORMAD1 and HORMAD2 from synapsed chromosomes (By similarity). Plays a role in mitotic spindle assembly checkpoint (SAC) activation (PubMed:28553959).

> Gene Ontology
 
Biological Process GO:0001556 oocyte maturation
GO:0006302 double-strand break repair
GO:0006310 DNA recombination
GO:0007059 chromosome segregation
GO:0007126 meiotic nuclear division
GO:0007127 meiosis I
GO:0007129 synapsis
GO:0007130 synaptonemal complex assembly
GO:0007131 reciprocal meiotic recombination
GO:0007140 male meiosis
GO:0007141 male meiosis I
GO:0007143 female meiotic division
GO:0007144 female meiosis I
GO:0007281 germ cell development
GO:0007283 spermatogenesis
GO:0007286 spermatid development
GO:0007292 female gamete generation
GO:0009994 oocyte differentiation
GO:0021700 developmental maturation
GO:0022412 cellular process involved in reproduction in multicellular organism
GO:0035825 reciprocal DNA recombination
GO:0045132 meiotic chromosome segregation
GO:0045143 homologous chromosome segregation
GO:0048232 male gamete generation
GO:0048469 cell maturation
GO:0048477 oogenesis
GO:0048515 spermatid differentiation
GO:0048599 oocyte development
GO:0051321 meiotic cell cycle
GO:0070192 chromosome organization involved in meiotic cell cycle
GO:0070193 synaptonemal complex organization
GO:0098813 nuclear chromosome segregation
GO:1903046 meiotic cell cycle process
Molecular Function -
Cellular Component GO:0001673 male germ cell nucleus
GO:0043073 germ cell nucleus
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between TRIP13 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
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
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 TRIP13 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 logFC: -2.40; FDR: 0.04630 Resistant to T cell-mediated killing
29301958CRISPR-Cas9 melanomaB16F10OT-1 T cell NA/NS NA/NS
28783722CRISPR-Cas9 melanomaMel6242CT-CRISPR NA/NS NA/NS
28723893CRISPR-Cas9 melanomaB16GVAX+Anti-PD1 NA/NS NA/NS
28723893CRISPR-Cas9 melanomaB16GVAX NA/NS NA/NS
25691366RNAiBreast cancerMCF7Luc-CTL assay NA/NS NA/NS
24476824shRNAmelanomaB16Primary screen NA/NS NA/NS
24476824shRNAmelanomaB16Secondary screen NA/NS NA/NS
Summary
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
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 TRIP13 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.6040.0899
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.1960.891
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.9080.433
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-0.1190.825
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.0510.971
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47-0.2080.901
729033130MelanomaallAnti-PD-1 (nivolumab) 2623-0.0740.849
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 1511-0.5910.648
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 11120.6830.57
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 48-0.5230.427
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 28-0.0350.968
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 682300.4680.0025
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of TRIP13 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) 27737.407.40.0709
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27597.407.40.096
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21170001
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)860001
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)13110001
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 91606.2-6.21
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59011.1-11.11
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
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of TRIP13. 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
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of TRIP13. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by TRIP13.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of TRIP13. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of TRIP13 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between TRIP13 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolTRIP13
Namethyroid hormone receptor interactor 13
Aliases 16E1BP; thyroid receptor interacting protein 13; 16E1-BP; HPV16 E1 protein binding protein; HPV16 E1 protein ......
Chromosomal Location5p15
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting TRIP13 collected from DrugBank database.
> Drugs from DrugBank database
 

There is no record.