Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Basic function annotation. > Subcellular Location, Domain and Function > Gene Ontology > KEGG and Reactome Pathway |
Subcellular Location | Cytoplasm Note=Isoform 2 shows a cytoplasmic perinuclear localization in a myoblastic cell line in resting and insulin-stimulated cells. |
Domain |
PF11830 Domain of unknown function (DUF3350) PF00640 Phosphotyrosine interaction domain (PTB/PID) PF00566 Rab-GTPase-TBC domain |
Function |
May act as a GTPase-activating protein for RAB2A, RAB8A, RAB10 and RAB14. Isoform 2 promotes insulin-induced glucose transporter SLC2A4/GLUT4 translocation at the plasma membrane, thus increasing glucose uptake. |
Biological Process |
GO:0006906 vesicle fusion GO:0010639 negative regulation of organelle organization GO:0016050 vesicle organization GO:0031338 regulation of vesicle fusion GO:0031339 negative regulation of vesicle fusion GO:0032868 response to insulin GO:0032869 cellular response to insulin stimulus GO:0043434 response to peptide hormone GO:0044801 single-organism membrane fusion GO:0048284 organelle fusion GO:0051051 negative regulation of transport GO:0060627 regulation of vesicle-mediated transport GO:0061025 membrane fusion GO:0071375 cellular response to peptide hormone stimulus GO:0071417 cellular response to organonitrogen compound GO:0090174 organelle membrane fusion GO:0090630 activation of GTPase activity GO:1901652 response to peptide GO:1901653 cellular response to peptide |
Molecular Function |
GO:0005096 GTPase activator activity GO:0008047 enzyme activator activity GO:0017016 Ras GTPase binding GO:0017137 Rab GTPase binding GO:0030695 GTPase regulator activity GO:0031267 small GTPase binding GO:0051020 GTPase binding GO:0060589 nucleoside-triphosphatase regulator activity |
Cellular Component |
GO:0030659 cytoplasmic vesicle membrane |
KEGG |
hsa04919 Thyroid hormone signaling pathway |
Reactome |
R-HSA-199991: Membrane Trafficking R-HSA-1445148: Translocation of GLUT4 to the plasma membrane R-HSA-5653656: Vesicle-mediated transport |
Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Literatures that report relations between TBC1D4 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. |
There is no record. |
Summary | |
---|---|
Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
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
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Statistical results of TBC1D4 in screening data sets for detecting immune reponses.
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Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
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 |
Points in the above scatter plot represent the expression difference of TBC1D4 in various data sets.
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Points in the above scatter plot represent the mutation difference of TBC1D4 in various data sets.
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Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of TBC1D4. 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. |
Summary | |
---|---|
Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of TBC1D4. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by TBC1D4. > Immunoinhibitor > Immunostimulator > MHC molecule |
Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of TBC1D4. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene. > Chemokine > Receptor |
Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Distribution of TBC1D4 expression across immune and molecular subtypes. > Immune subtype > Molecular subtype |
Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Associations between TBC1D4 and clinical features. > Overall survival analysis > Cancer stage > Tumor grade |
Summary | |
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Symbol | TBC1D4 |
Name | TBC1 domain family, member 4 |
Aliases | KIAA0603; AS160; DKFZp779C0666; Akt substrate of 160 kDa; NIDDM5; TBC (Tre-2, BUB2, CDC16) domain-containing ...... |
Chromosomal Location | 13q22.2 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Drugs targeting TBC1D4 collected from DrugBank database. |
There is no record. |