HCSGD entry for TAZ


1. General information

Official gene symbolTAZ
Entrez ID6901
Gene full nametafazzin
Other gene symbolsBTHS CMD3A EFE EFE2 G4.5 LVNCX Taz1
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:0005739MitochondrionIC IDAcellular_component
GO:0005743Mitochondrial inner membraneTAScellular_component
GO:0005886Plasma membraneIDAcellular_component
GO:0006644Phospholipid metabolic processTASbiological_process
GO:0006936Muscle contractionIMPbiological_process
GO:0007507Heart developmentIMPbiological_process
GO:0007519Skeletal muscle tissue developmentIMPbiological_process
GO:0016021Integral component of membraneIEAcellular_component
GO:0016746Transferase activity, transferring acyl groupsIEAmolecular_function
GO:0030097HemopoiesisIMPbiological_process
GO:0032049Cardiolipin biosynthetic processIMPbiological_process
GO:0032981Mitochondrial respiratory chain complex I assemblyIMPbiological_process
GO:0035965Cardiolipin acyl-chain remodelingTASbiological_process
GO:0042407Cristae formationIMPbiological_process
GO:0042775Mitochondrial ATP synthesis coupled electron transportIDAbiological_process
GO:0044281Small molecule metabolic processTASbiological_process
GO:0046474Glycerophospholipid biosynthetic processTASbiological_process
GO:00471841-acylglycerophosphocholine O-acyltransferase activityIDAmolecular_function
GO:0048738Cardiac muscle tissue developmentIMPbiological_process
GO:0060048Cardiac muscle contractionIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.91215798790.39442632120.99999024731.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0624420416
GSE13712_SHEARUp0.0110776708
GSE13712_STATICDown-0.2714543113
GSE19018Up0.0853143021
GSE19899_A1Down-0.1293935838
GSE19899_A2Up0.0356926923
PubMed_21979375_A1Down-0.1827306129
PubMed_21979375_A2Down-0.1098945162
GSE35957Down-0.0324692859
GSE36640Up0.0340925680
GSE54402Up0.0456880437
GSE9593Down-0.1613390578
GSE43922Up0.0552081794
GSE24585Down-0.2026746709
GSE37065Down-0.1217429665
GSE28863_A1Up0.0987556447
GSE28863_A2Up0.0148947702
GSE28863_A3Up0.0327029802
GSE28863_A4Down-0.0496320127
GSE48662Up0.0254134549

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-335-5pMIMAT0000765MIRT017100MicroarrayFunctional MTI (Weak)18185580
hsa-miR-26b-5pMIMAT0000083MIRT029020MicroarrayFunctional MTI (Weak)19088304
hsa-miR-652-3pMIMAT0003322MIRT039496CLASHFunctional MTI (Weak)23622248
hsa-let-7c-5pMIMAT0000064MIRT051742CLASHFunctional 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

27358050LATS-YAP/TAZ controls lineage specification by regulating TGFbeta signaling and Hnf4alpha expression during liver development
27358050Here we report that the Hippo pathway controls liver cell lineage specification and proliferation separately from Notch signalling, using mice and primary hepatoblasts with liver-specific knockout of Lats1 and Lats2 kinase, the direct upstream regulators of YAP and TAZ
27358050During and after liver development, the activation of YAP/TAZ induced by loss of Lats1/2 forces hepatoblasts or hepatocytes to commit to the biliary epithelial cell (BEC) lineage
27358050Notably, oncogenic YAP/TAZ activation in hepatocytes induces massive p53-dependent cell senescence/death
27358050Together, our results reveal that YAP/TAZ activity levels govern liver cell differentiation and proliferation in a context-dependent manner
22068052In addition to acting as a transcriptional cofactor for p53, ASPP1 has been shown to function in the cytoplasm to regulate the nuclear localization and activity of YAP/TAZ
17606438RESULTS: TBI reduced the pool of BM mesenchymal stem/progenitor cells, and altered osteoblast differentiation ability of BM MSC evidenced by changes in TAZ expression
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