Browse SOX4

Summary
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
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 Nucleus
Domain PF00505 HMG (high mobility group) box
Function

Transcriptional activator that binds with high affinity to the T-cell enhancer motif 5'-AACAAAG-3' motif.

> Gene Ontology
 
Biological Process GO:0000075 cell cycle checkpoint
GO:0000077 DNA damage checkpoint
GO:0000082 G1/S transition of mitotic cell cycle
GO:0001501 skeletal system development
GO:0001655 urogenital system development
GO:0001678 cellular glucose homeostasis
GO:0001822 kidney development
GO:0001838 embryonic epithelial tube formation
GO:0001841 neural tube formation
GO:0002065 columnar/cuboidal epithelial cell differentiation
GO:0002244 hematopoietic progenitor cell differentiation
GO:0002320 lymphoid progenitor cell differentiation
GO:0002328 pro-B cell differentiation
GO:0002521 leukocyte differentiation
GO:0002790 peptide secretion
GO:0002791 regulation of peptide secretion
GO:0002793 positive regulation of peptide secretion
GO:0003007 heart morphogenesis
GO:0003170 heart valve development
GO:0003171 atrioventricular valve development
GO:0003174 mitral valve development
GO:0003179 heart valve morphogenesis
GO:0003181 atrioventricular valve morphogenesis
GO:0003183 mitral valve morphogenesis
GO:0003205 cardiac chamber development
GO:0003206 cardiac chamber morphogenesis
GO:0003207 cardiac chamber formation
GO:0003208 cardiac ventricle morphogenesis
GO:0003209 cardiac atrium morphogenesis
GO:0003211 cardiac ventricle formation
GO:0003215 cardiac right ventricle morphogenesis
GO:0003230 cardiac atrium development
GO:0003231 cardiac ventricle development
GO:0003279 cardiac septum development
GO:0003281 ventricular septum development
GO:0003283 atrial septum development
GO:0003284 septum primum development
GO:0003289 atrial septum primum morphogenesis
GO:0003357 noradrenergic neuron differentiation
GO:0006417 regulation of translation
GO:0006473 protein acetylation
GO:0006474 N-terminal protein amino acid acetylation
GO:0006611 protein export from nucleus
GO:0006913 nucleocytoplasmic transport
GO:0006977 DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest
GO:0007050 cell cycle arrest
GO:0007093 mitotic cell cycle checkpoint
GO:0007159 leukocyte cell-cell adhesion
GO:0007346 regulation of mitotic cell cycle
GO:0007507 heart development
GO:0009306 protein secretion
GO:0009743 response to carbohydrate
GO:0009746 response to hexose
GO:0009749 response to glucose
GO:0009914 hormone transport
GO:0010001 glial cell differentiation
GO:0010608 posttranscriptional regulation of gene expression
GO:0010817 regulation of hormone levels
GO:0010948 negative regulation of cell cycle process
GO:0014009 glial cell proliferation
GO:0015833 peptide transport
GO:0016055 Wnt signaling pathway
GO:0016331 morphogenesis of embryonic epithelium
GO:0018076 N-terminal peptidyl-lysine acetylation
GO:0018205 peptidyl-lysine modification
GO:0018394 peptidyl-lysine acetylation
GO:0019827 stem cell population maintenance
GO:0021510 spinal cord development
GO:0021515 cell differentiation in spinal cord
GO:0021517 ventral spinal cord development
GO:0021522 spinal cord motor neuron differentiation
GO:0021782 glial cell development
GO:0021915 neural tube development
GO:0021953 central nervous system neuron differentiation
GO:0023061 signal release
GO:0030072 peptide hormone secretion
GO:0030073 insulin secretion
GO:0030098 lymphocyte differentiation
GO:0030111 regulation of Wnt signaling pathway
GO:0030177 positive regulation of Wnt signaling pathway
GO:0030217 T cell differentiation
GO:0030330 DNA damage response, signal transduction by p53 class mediator
GO:0031016 pancreas development
GO:0031018 endocrine pancreas development
GO:0031365 N-terminal protein amino acid modification
GO:0031396 regulation of protein ubiquitination
GO:0031397 negative regulation of protein ubiquitination
GO:0031570 DNA integrity checkpoint
GO:0031571 mitotic G1 DNA damage checkpoint
GO:0031647 regulation of protein stability
GO:0032024 positive regulation of insulin secretion
GO:0032386 regulation of intracellular transport
GO:0032387 negative regulation of intracellular transport
GO:0033157 regulation of intracellular protein transport
GO:0033500 carbohydrate homeostasis
GO:0034248 regulation of cellular amide metabolic process
GO:0034250 positive regulation of cellular amide metabolic process
GO:0034284 response to monosaccharide
GO:0035019 somatic stem cell population maintenance
GO:0035107 appendage morphogenesis
GO:0035108 limb morphogenesis
GO:0035148 tube formation
GO:0035239 tube morphogenesis
GO:0035270 endocrine system development
GO:0035904 aorta development
GO:0035905 ascending aorta development
GO:0035909 aorta morphogenesis
GO:0035910 ascending aorta morphogenesis
GO:0042063 gliogenesis
GO:0042110 T cell activation
GO:0042593 glucose homeostasis
GO:0042769 DNA damage response, detection of DNA damage
GO:0042770 signal transduction in response to DNA damage
GO:0042886 amide transport
GO:0043543 protein acylation
GO:0044770 cell cycle phase transition
GO:0044772 mitotic cell cycle phase transition
GO:0044773 mitotic DNA damage checkpoint
GO:0044774 mitotic DNA integrity checkpoint
GO:0044783 G1 DNA damage checkpoint
GO:0044819 mitotic G1/S transition checkpoint
GO:0044843 cell cycle G1/S phase transition
GO:0045727 positive regulation of translation
GO:0045786 negative regulation of cell cycle
GO:0045787 positive regulation of cell cycle
GO:0045930 negative regulation of mitotic cell cycle
GO:0046822 regulation of nucleocytoplasmic transport
GO:0046823 negative regulation of nucleocytoplasmic transport
GO:0046825 regulation of protein export from nucleus
GO:0046826 negative regulation of protein export from nucleus
GO:0046879 hormone secretion
GO:0046883 regulation of hormone secretion
GO:0046887 positive regulation of hormone secretion
GO:0048483 autonomic nervous system development
GO:0048485 sympathetic nervous system development
GO:0048514 blood vessel morphogenesis
GO:0048736 appendage development
GO:0048844 artery morphogenesis
GO:0050708 regulation of protein secretion
GO:0050714 positive regulation of protein secretion
GO:0050796 regulation of insulin secretion
GO:0050821 protein stabilization
GO:0051047 positive regulation of secretion
GO:0051051 negative regulation of transport
GO:0051168 nuclear export
GO:0051169 nuclear transport
GO:0051222 positive regulation of protein transport
GO:0051224 negative regulation of protein transport
GO:0060070 canonical Wnt signaling pathway
GO:0060173 limb development
GO:0060174 limb bud formation
GO:0060411 cardiac septum morphogenesis
GO:0060412 ventricular septum morphogenesis
GO:0060413 atrial septum morphogenesis
GO:0060562 epithelial tube morphogenesis
GO:0060563 neuroepithelial cell differentiation
GO:0060828 regulation of canonical Wnt signaling pathway
GO:0060840 artery development
GO:0060993 kidney morphogenesis
GO:0070486 leukocyte aggregation
GO:0070489 T cell aggregation
GO:0071156 regulation of cell cycle arrest
GO:0071158 positive regulation of cell cycle arrest
GO:0071322 cellular response to carbohydrate stimulus
GO:0071326 cellular response to monosaccharide stimulus
GO:0071331 cellular response to hexose stimulus
GO:0071333 cellular response to glucose stimulus
GO:0071593 lymphocyte aggregation
GO:0072001 renal system development
GO:0072175 epithelial tube formation
GO:0072331 signal transduction by p53 class mediator
GO:0072395 signal transduction involved in cell cycle checkpoint
GO:0072401 signal transduction involved in DNA integrity checkpoint
GO:0072413 signal transduction involved in mitotic cell cycle checkpoint
GO:0072422 signal transduction involved in DNA damage checkpoint
GO:0072431 signal transduction involved in mitotic G1 DNA damage checkpoint
GO:0090068 positive regulation of cell cycle process
GO:0090087 regulation of peptide transport
GO:0090263 positive regulation of canonical Wnt signaling pathway
GO:0090276 regulation of peptide hormone secretion
GO:0090277 positive regulation of peptide hormone secretion
GO:0090317 negative regulation of intracellular protein transport
GO:0098727 maintenance of cell number
GO:0198738 cell-cell signaling by wnt
GO:1901983 regulation of protein acetylation
GO:1901985 positive regulation of protein acetylation
GO:1901987 regulation of cell cycle phase transition
GO:1901988 negative regulation of cell cycle phase transition
GO:1901990 regulation of mitotic cell cycle phase transition
GO:1901991 negative regulation of mitotic cell cycle phase transition
GO:1902400 intracellular signal transduction involved in G1 DNA damage checkpoint
GO:1902402 signal transduction involved in mitotic DNA damage checkpoint
GO:1902403 signal transduction involved in mitotic DNA integrity checkpoint
GO:1902806 regulation of cell cycle G1/S phase transition
GO:1902807 negative regulation of cell cycle G1/S phase transition
GO:1903320 regulation of protein modification by small protein conjugation or removal
GO:1903321 negative regulation of protein modification by small protein conjugation or removal
GO:1903532 positive regulation of secretion by cell
GO:1903828 negative regulation of cellular protein localization
GO:1904950 negative regulation of establishment of protein localization
GO:1904951 positive regulation of establishment of protein localization
GO:2000045 regulation of G1/S transition of mitotic cell cycle
GO:2000134 negative regulation of G1/S transition of mitotic cell cycle
GO:2000756 regulation of peptidyl-lysine acetylation
GO:2000758 positive regulation of peptidyl-lysine acetylation
GO:2000759 regulation of N-terminal peptidyl-lysine acetylation
GO:2000761 positive regulation of N-terminal peptidyl-lysine acetylation
Molecular Function GO:0000982 transcription factor activity, RNA polymerase II core promoter proximal region sequence-specific binding
GO:0001046 core promoter sequence-specific DNA binding
GO:0001047 core promoter binding
GO:0001076 transcription factor activity, RNA polymerase II transcription factor binding
GO:0001077 transcriptional activator activity, RNA polymerase II core promoter proximal region sequence-specific binding
GO:0001104 RNA polymerase II transcription cofactor activity
GO:0001105 RNA polymerase II transcription coactivator activity
GO:0001190 transcriptional activator activity, RNA polymerase II transcription factor binding
GO:0001191 transcriptional repressor activity, RNA polymerase II transcription factor binding
GO:0001228 transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific binding
GO:0003713 transcription coactivator activity
GO:0046982 protein heterodimerization activity
GO:0098811 transcriptional repressor activity, RNA polymerase II activating transcription factor binding
Cellular Component GO:0005667 transcription factor complex
GO:0044798 nuclear transcription factor complex
> KEGG and Reactome Pathway
 
KEGG -
Reactome R-HSA-3769402: Deactivation of the beta-catenin transactivating complex
R-HSA-162582: Signal Transduction
R-HSA-195721: Signaling by Wnt
R-HSA-201681: TCF dependent signaling in response to WNT
Summary
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between SOX4 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
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
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 SOX4 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: -3.17; FDR: 0.00979 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
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
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 SOX4 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.7080.125
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.6160.785
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.7920.682
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-0.040.915
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590.2410.919
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47-0.3920.9
729033130MelanomaallAnti-PD-1 (nivolumab) 2623-0.0110.982
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 1511-0.0970.96
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 11120.140.946
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 480.1710.907
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 280.8670.668
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 682300.0440.719
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of SOX4 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)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
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of SOX4. 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
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of SOX4. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by SOX4.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of SOX4. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of SOX4 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between SOX4 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolSOX4
NameSRY (sex determining region Y)-box 4
Aliases EVI16; SRY-related HMG-box gene 4; ecotropic viral integration site 16; Transcription factor SOX-4
Chromosomal Location6p22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting SOX4 collected from DrugBank database.
> Drugs from DrugBank database
 

There is no record.