HCSGD entry for SUPT5H
1. General information
Official gene symbol | SUPT5H |
---|---|
Entrez ID | 6829 |
Gene full name | suppressor of Ty 5 homolog (S. cerevisiae) |
Other gene symbols | SPT5 SPT5H Tat-CT1 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
This gene isn't in Literature mining network.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000122 | Negative regulation of transcription from RNA polymerase II promoter | IDA | biological_process |
GO:0003682 | Chromatin binding | IEA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005634 | Nucleus | IDA | cellular_component |
GO:0005654 | Nucleoplasm | TAS | cellular_component |
GO:0005730 | Nucleolus | IDA | cellular_component |
GO:0006338 | Chromatin remodeling | NAS | biological_process |
GO:0006354 | DNA-templated transcription, elongation | IDA | biological_process |
GO:0006366 | Transcription from RNA polymerase II promoter | TAS | biological_process |
GO:0006368 | Transcription elongation from RNA polymerase II promoter | IDA TAS | biological_process |
GO:0006370 | 7-methylguanosine mRNA capping | TAS | biological_process |
GO:0007049 | Cell cycle | NAS | biological_process |
GO:0010033 | Response to organic substance | TAS | biological_process |
GO:0010467 | Gene expression | TAS | biological_process |
GO:0016032 | Viral process | TAS | biological_process |
GO:0016239 | Positive regulation of macroautophagy | IMP | biological_process |
GO:0019899 | Enzyme binding | IPI | molecular_function |
GO:0032044 | DSIF complex | IDA | cellular_component |
GO:0032785 | Negative regulation of DNA-templated transcription, elongation | IDA | biological_process |
GO:0032786 | Positive regulation of DNA-templated transcription, elongation | IDA | biological_process |
GO:0039692 | Single stranded viral RNA replication via double stranded DNA intermediate | NAS | biological_process |
GO:0045944 | Positive regulation of transcription from RNA polymerase II promoter | IDA | biological_process |
GO:0046982 | Protein heterodimerization activity | IPI | molecular_function |
GO:0050434 | Positive regulation of viral transcription | TAS | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.0046306599 | 0.9967348961 | 0.1789773862 | 1.0000000000 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Up | 0.4631965990 |
GSE13712_SHEAR | Up | 0.0405740382 |
GSE13712_STATIC | Up | 0.0840909190 |
GSE19018 | Up | 0.1903304177 |
GSE19899_A1 | Up | 0.4165177478 |
GSE19899_A2 | Up | 0.7566247855 |
PubMed_21979375_A1 | Up | 1.3466927812 |
PubMed_21979375_A2 | Up | 2.4727349157 |
GSE35957 | Up | 0.3113537997 |
GSE36640 | Up | 0.3201247724 |
GSE54402 | Up | 0.4619288293 |
GSE9593 | Up | 0.0860320535 |
GSE43922 | Up | 0.3676377594 |
GSE24585 | Up | 0.1561433939 |
GSE37065 | Down | -0.0611404985 |
GSE28863_A1 | Up | 0.0911887025 |
GSE28863_A2 | Up | 0.1523373303 |
GSE28863_A3 | Up | 0.4743159688 |
GSE28863_A4 | Up | 0.1150702157 |
GSE48662 | Up | 0.1186900097 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-155-5p | MIMAT0000646 | MIRT020754 | Proteomics | Functional MTI (Weak) | 18668040 |
hsa-miR-34a-5p | MIMAT0000255 | MIRT025307 | Proteomics | Functional MTI (Weak) | 21566225 |
hsa-miR-26b-5p | MIMAT0000083 | MIRT029450 | Microarray | Functional MTI (Weak) | 19088304 |
hsa-miR-1229-3p | MIMAT0005584 | MIRT036363 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-935 | MIMAT0004978 | MIRT036670 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-93-3p | MIMAT0004509 | MIRT038889 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-92b-3p | MIMAT0003218 | MIRT040704 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-484 | MIMAT0002174 | MIRT042043 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-324-3p | MIMAT0000762 | MIRT042864 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-149-5p | MIMAT0000450 | MIRT045555 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-92a-3p | MIMAT0000092 | MIRT049464 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-16-5p | MIMAT0000069 | MIRT051148 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
No target information from mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 1 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26418880 | In the present study, suppressor of Ty homolog-5 (SPT5), a protein encoded by the SUPT5H gene, was identified as a novel tumor-specific hTERT promoter-binding protein and activator in colon cancer cells |
26418880 | We verified the tumor-specific binding activity of SPT5 to the hTERT promoter in vitro and in vivo and detected high expression levels of SUPT5H in colorectal cancer cell lines and primary human colorectal cancer tissues |
26418880 | SUPT5H was more highly expressed in colorectal cancer cases with distant metastasis than in cases without distant metastasis |
26418880 | Inhibition of endogenous SUPT5H expression by SUPT5H gene-specific short hairpin RNAs effectively attenuated hTERT promoter-driven green fluorescent protein (GFP) expression, whereas no detectable effects on CMV promoter-driven GFP expression in the same cells were observed |
26418880 | In addition, inhibition of SUPT5H expression not only effectively repressed telomerase activity, accelerated telomere shortening, and promoted cell senescence in colon cancer cells, but also suppressed cancer cell growth and migration |
26418880 | Our results demonstrated that SPT5 contributes to the up-regulation of hTERT expression and tumor development, and SUPT5H may potentially be used as a novel tumor biomarker and/or cancer therapeutic target |
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