HCSGD entry for ICMT


1. General information

Official gene symbolICMT
Entrez ID23463
Gene full nameisoprenylcysteine carboxyl methyltransferase
Other gene symbolsHSTE14 MST098 MSTP098 PCCMT PCMT PPMT
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:0001701In utero embryonic developmentIEAbiological_process
GO:0001889Liver developmentIEAbiological_process
GO:0003880Protein C-terminal carboxyl O-methyltransferase activityTASmolecular_function
GO:0004671Protein C-terminal S-isoprenylcysteine carboxyl O-methyltransferase activityIEAmolecular_function
GO:0005783Endoplasmic reticulumIDAcellular_component
GO:0005789Endoplasmic reticulum membraneIEAcellular_component
GO:0006464Cellular protein modification processTASbiological_process
GO:0006481C-terminal protein methylationTASbiological_process
GO:0006612Protein targeting to membraneTASbiological_process
GO:0008104Protein localizationIEAbiological_process
GO:0008140CAMP response element binding protein bindingIEAmolecular_function
GO:0008284Positive regulation of cell proliferationIEAbiological_process
GO:0016020MembraneTAScellular_component
GO:0016021Integral component of membraneIEAcellular_component
GO:0035264Multicellular organism growthIEAbiological_process
GO:0046578Regulation of Ras protein signal transductionIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.95107630030.09937589380.99999024730.6033847520

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

Data sourceUp or downLog fold change
GSE11954Up0.0268561809
GSE13712_SHEARUp0.0033664129
GSE13712_STATICUp0.0655165952
GSE19018Down-0.0760186185
GSE19899_A1Down-0.2669671617
GSE19899_A2Down-0.1260246419
PubMed_21979375_A1Down-0.4579939585
PubMed_21979375_A2Down-0.3364495347
GSE35957Down-0.1063685123
GSE36640Down-0.3441249630
GSE54402Down-0.3198595049
GSE9593Up0.2798748553
GSE43922Up0.0450058711
GSE24585Down-0.1017301766
GSE37065Down-0.1248916958
GSE28863_A1Down-0.2753056764
GSE28863_A2Up0.3570169371
GSE28863_A3Down-0.3898542536
GSE28863_A4Down-0.2658879972
GSE48662Up0.1280838966

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-130b-3pMIMAT0000691MIRT020175SequencingFunctional MTI (Weak)20371350
hsa-miR-124-3pMIMAT0000422MIRT022702MicroarrayFunctional MTI (Weak)18668037
hsa-miR-93-5pMIMAT0000093MIRT028069SequencingFunctional MTI (Weak)20371350
hsa-miR-26b-5pMIMAT0000083MIRT029560SequencingFunctional MTI (Weak)20371350
hsa-miR-331-3pMIMAT0000760MIRT043333CLASHFunctional MTI (Weak)23622248
hsa-miR-1260bMIMAT0015041MIRT052699CLASHFunctional 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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

11985579These abnormal residues are specifically recognized by the repair enzyme L-isoaspartate (d-aspartate) protein O-methyltransferase (PCMT; EC 2
18647693The enzymatic methyl esterification of proteins, catalyzed by the enzyme S-adenosylmethionine: protein carboxyl-O-methyl transferase (PCMT), has been investigated in two age-related fractions of bovine lenses
18647693The eukaryotic PCMT methyl esterifies peptides and proteins containing altered aspartyl residues, such as D-aspartyls and L-isoaspartyls, which can arise from the age-dependent deamidation of labile Asn residues
186476934, 37 degrees C), in the presence of L-(methyl-(14)C)methionine, the in vivo precursor of the methyl donor substrate S-adenosylmethionine (AdoMet), a significant decrease in the level of protein methyl esterification was observed in the oldest cell fraction compared to the youngest one; in contrast, the in vitro activity of PCMT does not change during cell aging
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