PPARGC1A


Summary: The protein encoded by this gene is a transcriptional coactivator that regulates the genes involved in energy metabolism. This protein interacts with PPARgamma, which permits the interaction of this protein with multiple transcription factors. This protein can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination. This protein may be also involved in controlling blood pressure, regulating cellular cholesterol homoeostasis, and the development of obesity. [provided by RefSeq, Jul 2008].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:604517
PHARMGKB IDPA33558
Map Location4p15.2

GO terms in PPARGC1A


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Term Type
Evidence Type
GO Term ID
GO Des.
MF ISS GO:0003677 DNA binding
MF TAS GO:0003677 DNA binding
MF TAS GO:0003712 transcription coregulator activity
MF IDA GO:0003713 transcription coactivator activity
MF TAS GO:0003723 RNA binding
MF IPI GO:0005515 protein binding
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Gene expression in normal tissue: PPARGC1A

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in PPARGC1A


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Database
Pathway ID
Pathway Des.
pid atf2_pathway ATF-2 transcription factor network
pid hdac_classiii_pathway Signaling events mediated by HDAC Class III
pid mtor_4pathway mTOR signaling pathway
pid p38alphabetadownstreampathway Signaling mediated by p38-alpha and p38-beta
kegg hsa04152 AMPK signaling pathway - Homo sapiens (human)
kegg hsa04211 Longevity regulating pathway - Homo sapiens (human)
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD84 Lovastatin acid 1
iGMDRD307 Manumycin A 7
iGMDRD532 Olaparib 3
iGMDRD79 Gemcitabine 4
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in PPARGC1A

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
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