HCSGD entry for ACR


1. General information

Official gene symbolACR
Entrez ID49
Gene full nameacrosin
Other gene symbols
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:0002077Acrosome matrix dispersalNASbiological_process
GO:0003677DNA bindingNASmolecular_function
GO:0004040Amidase activityISSmolecular_function
GO:0004252Serine-type endopeptidase activityIDA IEAmolecular_function
GO:0005507Copper ion bindingNASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005537Mannose bindingIDAmolecular_function
GO:0005576Extracellular regionTAScellular_component
GO:0005798Golgi-associated vesicleIEAcellular_component
GO:0006508ProteolysisIEAbiological_process
GO:0007190Activation of adenylate cyclase activityIDAbiological_process
GO:0007338Single fertilizationISS TASbiological_process
GO:0007339Binding of sperm to zona pellucidaIEAbiological_process
GO:0007340Acrosome reactionIMP TASbiological_process
GO:0007341Penetration of zona pellucidaIDAbiological_process
GO:0008144Drug bindingISSmolecular_function
GO:0008270Zinc ion bindingNASmolecular_function
GO:0032504Multicellular organism reproductionTASbiological_process
GO:0042806Fucose bindingISSmolecular_function
GO:0043159Acrosomal matrixTAScellular_component
GO:0043234Protein complexIDAcellular_component
GO:0048545Response to steroid hormoneIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.49168537290.85386486080.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0999315343
GSE13712_SHEARDown-0.2663528969
GSE13712_STATICDown-0.0470356230
GSE19018Up0.0915130594
GSE19899_A1Up0.0145931224
GSE19899_A2Up0.1257896320
PubMed_21979375_A1Up0.3461445878
PubMed_21979375_A2Up0.1297032007
GSE35957Up0.0552981291
GSE36640Down-0.0175864006
GSE54402Down-0.0899523678
GSE9593Down-0.1016566806
GSE43922Up0.1151503011
GSE24585Up0.1022360563
GSE37065Up0.0499373508
GSE28863_A1Up0.0372158044
GSE28863_A2Down-0.1846917153
GSE28863_A3Up0.3687778239
GSE28863_A4Up0.0987399902
GSE48662Up0.1021307587

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-335-5pMIMAT0000765MIRT018926MicroarrayFunctional MTI (Weak)18185580
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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: 3 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25531190In this study, we examined the effects of acrylamide (ACR), a genotoxic carcinogen, on cellular senescence and the molecular mechanisms of ATF3 function in macrophages
25531190Treatment of macrophages with ACR at low concentrations (<1
25531190Exposure of macrophages to ACR led to stress-induced, telomerase-independent senescence
25531190In addition, ACR treatment for 1, 3, or 5 days showed a concentration-dependent increase in ATF3 expression and G0/G1 phase arrest
25531190To better understand the role of ATF3 in controlling the senescence response to ACR, SA-beta-gal activity was examined using ATF3 knockdown and overexpression
25531190ATF3 also played an important role in regulating intracellular reactive oxygen species (ROS) production in response to ACR treatment
20832529BACKGROUND: Late versus early acute antibody-mediated rejection (AAMR) or acute cellular rejection (ACR) episodes are associated with poorer kidney function and graft survival
20832529We explored whether cell senescence upon detection of AAMR +/- ACR contributes to these results
20832529Biopsies performed for acute graft dysfunction from January 2000 to March 2007 were analyzed for morphological criteria of AAMR with or without ACR (n = 17 from 17 patients)
208325293 cells/HPF in 4 of 8 biopsies performed at a median of 23 (range = 4-80) days (early AAMR +/- ACR), and 59
208325293 cells/HPF in 5 of 9 biopsies performed at a median of 1171 (range = 279-3210) days (late AAMR +/- ACR)
17407150This may be partly attributed to age-dependent changes in the lipid peroxidation product acrolein (ACR), which was abundant at older ages in non-administered cells, but scarcely in TocP-administered cells
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