HCSGD entry for EMD


1. General information

Official gene symbolEMD
Entrez ID2010
Gene full nameemerin
Other gene symbolsEDMD LEMD5 STA
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:0000278Mitotic cell cycleTASbiological_process
GO:0003779Actin bindingIDAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005635Nuclear envelopeIDA TAScellular_component
GO:0005637Nuclear inner membraneNAScellular_component
GO:0005640Nuclear outer membraneIDAcellular_component
GO:0005783Endoplasmic reticulumIDAcellular_component
GO:0005874MicrotubuleIEAcellular_component
GO:0006936Muscle contractionTASbiological_process
GO:0007077Mitotic nuclear envelope disassemblyTASbiological_process
GO:0007084Mitotic nuclear envelope reassemblyTASbiological_process
GO:0007517Muscle organ developmentTASbiological_process
GO:0016021Integral component of membraneIEAcellular_component
GO:0031965Nuclear membraneIDAcellular_component
GO:0035414Negative regulation of catenin import into nucleusIMPbiological_process
GO:0035914Skeletal muscle cell differentiationIEAbiological_process
GO:0046827Positive regulation of protein export from nucleusIMPbiological_process
GO:0048147Negative regulation of fibroblast proliferationIMPbiological_process
GO:0048487Beta-tubulin bindingIDAmolecular_function
GO:0060828Regulation of canonical Wnt signaling pathwayIMPbiological_process
GO:0071363Cellular response to growth factor stimulusIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.99077873180.00706734550.99999024730.1677271827

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

Data sourceUp or downLog fold change
GSE11954Down-0.3815113184
GSE13712_SHEARDown-0.6934873074
GSE13712_STATICDown-0.1906425438
GSE19018Down-0.0706754598
GSE19899_A1Down-0.8177651430
GSE19899_A2Down-0.0628717564
PubMed_21979375_A1Up0.2172195619
PubMed_21979375_A2Down-0.8396992734
GSE35957Down-0.2369515899
GSE36640Down-0.4407624706
GSE54402Down-0.0042325372
GSE9593Down-0.1598887287
GSE43922Down-0.1860009637
GSE24585Down-0.5259087350
GSE37065Down-0.4218455765
GSE28863_A1Up0.0312802259
GSE28863_A2Down-0.8232199374
GSE28863_A3Down-0.0421999142
GSE28863_A4Down-0.0716081284
GSE48662Up0.0424348655

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-124-3pMIMAT0000422MIRT022307MicroarrayFunctional MTI (Weak)18668037
hsa-miR-1MIMAT0000416MIRT023624Proteomics;MicroarrayNon-Functional MTI (Weak)18668037
hsa-miR-615-3pMIMAT0003283MIRT040236CLASHFunctional MTI (Weak)23622248
hsa-miR-484MIMAT0002174MIRT041790CLASHFunctional MTI (Weak)23622248
hsa-miR-125b-5pMIMAT0000423MIRT046034CLASHFunctional MTI (Weak)23622248
hsa-miR-92a-3pMIMAT0000092MIRT049830CLASHFunctional MTI (Weak)23622248
hsa-miR-25-3pMIMAT0000081MIRT050333CLASHFunctional 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: 3 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

27268410LARGE SCALE DATA: GEO accession number: GSE81579 STUDY FUNDING AND COMPETING INTERESTS: Funded in part by EMD Serono Grant for Fertility Innovation (GFI)
19589617The organization of both lamin A/C and its inner nuclear membrane partner emerin are altered, eventually showing a honeycomb pattern upon immunofluorescence microscopy
17274801A number of diseases associated with specific tissue degeneration and premature aging have mutations in the nuclear envelope proteins A-type lamins or emerin
17274801Due to various hypothetical roles of nuclear envelope proteins in genome function we investigated whether alterations to normal genomic behaviour are apparent in cells with mutations in A-type lamins and emerin
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