HCSGD entry for PDXP


1. General information

Official gene symbolPDXP
Entrez ID57026
Gene full namepyridoxal (pyridoxine, vitamin B6) phosphatase
Other gene symbolsCIN PLP dJ37E16.5
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0004647Phosphoserine phosphatase activityIEAmolecular_function
GO:0004721Phosphoprotein phosphatase activityIDAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005829CytosolIDAcellular_component
GO:0005886Plasma membraneIDAcellular_component
GO:0006470Protein dephosphorylationIDAbiological_process
GO:0007088Regulation of mitosisIMPbiological_process
GO:0015629Actin cytoskeletonIDAcellular_component
GO:0030027LamellipodiumIDAcellular_component
GO:0030496MidbodyIDAcellular_component
GO:0030836Positive regulation of actin filament depolymerizationIMPbiological_process
GO:0031072Heat shock protein bindingIDAmolecular_function
GO:0031247Actin rod assemblyIDA IMPbiological_process
GO:0031258Lamellipodium membraneIEAcellular_component
GO:0032154Cleavage furrowIDAcellular_component
GO:0032465Regulation of cytokinesisIMPbiological_process
GO:0032587Ruffle membraneIDAcellular_component
GO:0033883Pyridoxal phosphatase activityIEAmolecular_function
GO:0046872Metal ion bindingIEAmolecular_function
GO:0070938Contractile ringIDAcellular_component
GO:0071318Cellular response to ATPIDAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.36489264090.98673792410.99999024731.0000000000

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

Data sourceUp or downLog 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--
GSE28863_A2--
GSE28863_A3--
GSE28863_A4--
GSE48662Up0.1334066359

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-324-5pMIMAT0000761MIRT043152CLASHFunctional MTI (Weak)23622248
hsa-miR-331-3pMIMAT0000760MIRT043505CLASHFunctional MTI (Weak)23622248
hsa-miR-25-3pMIMAT0000081MIRT050278CLASHFunctional 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: 4 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22092365OBJECTIVES: Chronic idiopathic neutropenia (CIN) is a disorder of granulopoiesis characterized by the presence of activated T-lymphocytes that induce/sustain apoptosis of bone marrow (BM) granulocytic progenitors
22092365T-cell lymphopenia is commonly found in CIN
22092365The aim of the study is to probe the mechanisms underlying T-cell lymphopenia in CIN
22092365RESULTS: Patients with CIN (n = 44) displayed lower proportion of naive CD45RA(+) cells within the CD4(+) and CD8(+) cells compared with controls (n = 15)
22092365The mean relative telomere length of CD4(+) and CD8(+) cells was significantly lower in patients with CIN compared with age-matched controls
22092365CONCLUSIONS: The aberrant T-cell expansions associated with the pathogenesis of CIN result in increased proliferation/apoptosis and possibly exhaustion of peripheral blood T cells which, in association with the inadequate compensatory thymic export of new TREC expressing T cells partially because of IL-7 deficiency, may contribute to lymphopenia in CIN
19686285Malignant glioma (MG) is highly proliferative and invasive, with the malignant characteristics associated with aneuploidy and chromosomal instability (CIN)
19686285These results suggest that GANP protects cells from cellular senescence caused by DNA damage and that a significant decrease in GANP expression leads to malignancy by generating hyperploidy and CIN
18791275Meiotic-like division to a aneuploidy: chromosomal instability (CIN), cell-senescence and cancer
17643075Evidence based on Bub1 mutations in colorectal cancers suggests it might be a driving force in tumorigenesis via generation of chromosomal instability (CIN) and aneuploidy
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