HCSGD entry for PAPD7


1. General information

Official gene symbolPAPD7
Entrez ID11044
Gene full namePAP associated domain containing 7
Other gene symbolsLAK-1 LAK1 POLK POLS TRF4 TRF4-1 TRF41 TUTASE5
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0003677DNA bindingIEAmolecular_function
GO:0003887DNA-directed DNA polymerase activityIEAmolecular_function
GO:0004652Polynucleotide adenylyltransferase activityIEAmolecular_function
GO:0005634NucleusIDAcellular_component
GO:0006302Double-strand break repairNASbiological_process
GO:0007062Sister chromatid cohesionTASbiological_process
GO:0007076Mitotic chromosome condensationNASbiological_process
GO:0042493Response to drugIDAbiological_process
GO:0043221SMC family protein bindingTASmolecular_function
GO:0046872Metal ion bindingIEAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.87528920630.01962126820.99999024730.2729747491

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Down-0.3998723683
GSE13712_SHEARDown-0.1361731711
GSE13712_STATICDown-0.2754767728
GSE19018Down-0.7897827784
GSE19899_A1Down-0.6024417459
GSE19899_A2Down-0.4527619881
PubMed_21979375_A1Down-0.0117625789
PubMed_21979375_A2Down-0.3218208097
GSE35957Down-0.6573789802
GSE36640Down-1.0630080185
GSE54402Up0.4591390402
GSE9593Down-0.3569350895
GSE43922Up0.0899342455
GSE24585Down-0.0076834400
GSE37065Up0.1813331279
GSE28863_A1Up0.3679721477
GSE28863_A2Up0.6187921286
GSE28863_A3Down-0.1022683581
GSE28863_A4Down-0.2049120053
GSE48662Down-0.6113922946

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-423-3pMIMAT0001340MIRT016682SequencingFunctional MTI (Weak)20371350
hsa-miR-215-5pMIMAT0000272MIRT024572MicroarrayFunctional MTI (Weak)19074876
hsa-miR-192-5pMIMAT0000222MIRT026248MicroarrayFunctional MTI (Weak)19074876
hsa-miR-32-5pMIMAT0000090MIRT028280SequencingFunctional MTI (Weak)20371350
hsa-miR-106b-3pMIMAT0004672MIRT038569CLASHFunctional MTI (Weak)23622248
hsa-miR-93-5pMIMAT0000093MIRT048855CLASHFunctional 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

20542140In order to achieve this goal, DNA polymerases (Pols) have to faithfully execute DNA synthesis during chromosome replication and repair
20542140However, the conditions under which Pols synthesize DNA are not always optimal; the template DNA can be damaged by various endogenous and exogenous genotoxic agents including reactive oxygen species (ROS), and ROS oxidize dNTPs in the nucleotide pool from which Pols elongate DNA strands
20542140Both damaged DNA and oxidized dNTPs interfere with faithful DNA synthesis by Pols, inducing various cellular abnormalities, such as mutations, cancer, neurological diseases, and cellular senescence
20542140In this review, we focus on the process by which Pols incorporate oxidized dNTPs into DNA and compare the properties of Pols: efficiency, i
20542140In general, Pols involved in chromosome replication, the A- and B-family Pols, are resistant to the incorporation of 8-oxo-dGTP, whereas Pols involved in repair and/or translesion synthesis, the X- and Y-family Pols, incorporate nucleotides in a relatively efficient manner and tend to incorporate it opposite template dA rather than template dC, though there are several exceptions
20542140We discuss the molecular mechanisms by which Pols exhibit different template base preferences for the incorporation of 8-oxo-dGTP and how Pols are involved in the induction of mutations via the incorporation of oxidized nucleotides under oxidative stress
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