HCSGD entry for CTRL


1. General information

Official gene symbolCTRL
Entrez ID1506
Gene full namechymotrypsin-like
Other gene symbolsCTRL1
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:0004252Serine-type endopeptidase activityIEAmolecular_function
GO:0005615Extracellular spaceTAScellular_component
GO:0006508ProteolysisIEAbiological_process
GO:0007586DigestionTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.83647699940.46543746820.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.2351516842
GSE13712_SHEARDown-0.0863818171
GSE13712_STATICDown-0.0624403502
GSE19018Down-0.0850612562
GSE19899_A1Up0.0393139260
GSE19899_A2Up0.0981179785
PubMed_21979375_A1Up0.7036882021
PubMed_21979375_A2Up0.2169664630
GSE35957Up0.0072420832
GSE36640Down-0.1596214619
GSE54402Down-0.0479815116
GSE9593Down-0.1666784110
GSE43922Up0.0361767155
GSE24585Down-0.1556591785
GSE37065Up0.1300493213
GSE28863_A1Down-0.0732154594
GSE28863_A2Down-0.1509461217
GSE28863_A3Up0.0477012185
GSE28863_A4Down-0.0307729775
GSE48662Down-0.0283823032

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase
No target information from mirTarBase
  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

18817863Decline in chymotrypsin-like, peptidylglutamyl-peptide hydrolase and trypsin-like activities of the 20S proteasome was detected in aged RPE cells through degradation of fluorogenic substrates
11099467During proliferative senescence, we found a marked decline in all proteasome activities (trypsin-like activity, chymotrypsin-like activity, and peptidyl-glutamyl-hydrolyzing activity) and in lysosomal cathepsin activity
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