HCSGD entry for TAF9
1. General information
Official gene symbol | TAF9 |
---|---|
Entrez ID | 6880 |
Gene full name | TAF9 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 32kDa |
Other gene symbols | AK6 CGI-137 CINAP CIP MGC:1603 MGC:3647 MGC:5067 TAF2G TAFII31 TAFII32 TAFIID32 hCINAP |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

This gene isn't in PPI subnetwork.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000125 | PCAF complex | IDA | cellular_component |
GO:0002039 | P53 binding | IPI | molecular_function |
GO:0003677 | DNA binding | IDA IEA | molecular_function |
GO:0003713 | Transcription coactivator activity | IDA IMP | molecular_function |
GO:0004402 | Histone acetyltransferase activity | IDA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005634 | Nucleus | IEA | cellular_component |
GO:0005654 | Nucleoplasm | TAS | cellular_component |
GO:0005669 | Transcription factor TFIID complex | IDA | cellular_component |
GO:0006352 | DNA-templated transcription, initiation | IEA | biological_process |
GO:0006366 | Transcription from RNA polymerase II promoter | TAS | biological_process |
GO:0006367 | Transcription initiation from RNA polymerase II promoter | TAS | biological_process |
GO:0006368 | Transcription elongation from RNA polymerase II promoter | TAS | biological_process |
GO:0006974 | Cellular response to DNA damage stimulus | IC | biological_process |
GO:0010467 | Gene expression | TAS | biological_process |
GO:0016032 | Viral process | TAS | biological_process |
GO:0030307 | Positive regulation of cell growth | IMP | biological_process |
GO:0030914 | STAGA complex | IDA | cellular_component |
GO:0032435 | Negative regulation of proteasomal ubiquitin-dependent protein catabolic process | IDA | biological_process |
GO:0033276 | Transcription factor TFTC complex | IDA | cellular_component |
GO:0033613 | Activating transcription factor binding | IPI | molecular_function |
GO:0043066 | Negative regulation of apoptotic process | IMP | biological_process |
GO:0043966 | Histone H3 acetylation | IDA | biological_process |
GO:0044212 | Transcription regulatory region DNA binding | IDA | molecular_function |
GO:0045944 | Positive regulation of transcription from RNA polymerase II promoter | IDA IEA | biological_process |
GO:0046982 | Protein heterodimerization activity | IEA | molecular_function |
GO:0050821 | Protein stabilization | IDA | biological_process |
GO:0060760 | Positive regulation of response to cytokine stimulus | IMP | biological_process |
GO:0070555 | Response to interleukin-1 | IMP | biological_process |
GO:0070742 | C2H2 zinc finger domain binding | IPI | molecular_function |
GO:0070761 | Pre-snoRNP complex | IDA | cellular_component |
GO:0071339 | MLL1 complex | IDA | cellular_component |
GO:1902166 | Negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator | IC | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.9882230576 | 0.2121633031 | 0.9999902473 | 0.8890861805 |
- 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 | - | - |
GSE13712_SHEAR | - | - |
GSE13712_STATIC | - | - |
GSE19018 | - | - |
GSE19899_A1 | - | - |
GSE19899_A2 | - | - |
PubMed_21979375_A1 | - | - |
PubMed_21979375_A2 | - | - |
GSE35957 | - | - |
GSE36640 | - | - |
GSE54402 | - | - |
GSE9593 | - | - |
GSE43922 | - | - |
GSE24585 | - | - |
GSE37065 | - | - |
GSE28863_A1 | Down | -0.1945388323 |
GSE28863_A2 | Up | 0.1381060853 |
GSE28863_A3 | Down | -0.4239348361 |
GSE28863_A4 | Down | -0.0355889481 |
GSE48662 | Down | -0.1225105693 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-421 | MIMAT0003339 | MIRT016116 | Sequencing | Functional MTI (Weak) | 20371350 |
hsa-miR-26b-5p | MIMAT0000083 | MIRT029623 | Microarray | Functional MTI (Weak) | 19088304 |
hsa-miR-16-5p | MIMAT0000069 | MIRT031755 | Proteomics | Functional MTI (Weak) | 18668040 |
hsa-let-7b-5p | MIMAT0000063 | MIRT032332 | Proteomics | Functional MTI (Weak) | 18668040 |
hsa-miR-505-3p | MIMAT0002876 | MIRT040985 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
No target information from mirRecord
- mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 6 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
23645206 | ZNF313 ubiquitinates p21(WAF1) and also destabilizes p27(KIP1) and p57(KIP2), three members of the CDK-interacting protein (CIP)/kinase inhibitor protein (KIP) family of cyclin-dependent kinase inhibitors, whereas it does not affect the stability of the inhibitor of CDK (INK4) family members, such as p16(INK4A) and p15(INK4B) |
17599058 | Cell-cycle inhibitors of the Cip/Kip and INK4 families are involved in cellular senescence and tumor suppression |
16936260 | Cellular senescence of biliary epithelial cells with p16INK4a and p21WAF1/Cip expression in damaged small bile ducts may be critical for progressive bile duct loss in primary biliary cirrhosis |
15685690 | Biliary epithelial cells in small bile ducts in primary biliary cirrhosis, especially those in patients presenting with chronic non-suppurative cholangitis, frequently expressed senescence-associated beta-galactosidase, and senescence-associated p16(INK4) and p21(WAF1/CIP) |
8706801 | Fourteen genes, including 3 cyclin-dependent kinase (CDK) inhibitors (p16INK4, p21SDI/CIP/WAF and p27KIP), 5 cyclins, 4 CDKs, Cdi-1, and PCNA were tested in four primary fibroblast strains |
8706801 | These results corroborate and extend previous observations demonstrating elevated expression of specific cell cycle genes in higher passage cells and suggest that overexpression of the CDK-inhibitors p16INK4 and p21SDI/CIP/WAF, but not p27KIP, may contribute to lower proliferative activity of senescing primary fibroblasts |
7616677 | In addition, the protein levels of CDK2 and cyclin E are also extremely low, with an increased level of the p53-dependent p21 Cip 1 protein which inhibits the kinase activity of cyclins/CDKs by forming complexes |
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