We have a suspicion that you are an automated web bot software, not a real user. To keep our site fast for other users, we have slowed down this page. The slowdown will gradually disappear. If you think this is a mistake, please contact us at genome-www@soe.ucsc.edu. Also note that all data for hgGeneGraph can be obtained through our public MySQL server and all our software source code is available and can be installed locally onto your own computer. If you are unsure how to use these resources, do not hesitate to contact us.
UCSC Genome Browser Gene Interaction Graph
Gene interactions and pathways from curated databases and text-mining

◀ Back to PRKAA2

G6PC — PRKAA2

Pathways - manually collected, often from reviews:

Text-mined interactions from Literome

Mues et al., Horm Metab Res 2009 (Diabetes Mellitus, Type 2) : These data indicate a differential AMPK dependent regulation of G6Pase gene expression by insulin and metformin under basal and dexamethasone/cAMP stimulated conditions
Ota et al., Biochem Biophys Res Commun 2009 : Both metformin and rotenone, an inhibitor of respiratory chain complex I, suppressed glucose-6-phosphatase ( G6pc ), a rate limiting enzyme of liver glucose production, mRNA expression in a rat hepatoma cell line accompanied by a reduction of intracellular ATP concentration and an activation of AMP activated protein kinase (AMPK)
Lee et al., J Biol Chem 2010 : In addition, metformin or overexpression of a constitutively active form of AMPK ( Ad-CA-AMPK ) inhibited S171A mediated PEPCK and G6Pase gene expression, and hepatic glucose production and knockdown of SHP partially relieved the metformin- and Ad-CA-AMPK mediated repression of hepatic gluconeogenic enzyme gene expression in primary rat hepatocytes
Singhal et al., PloS one 2011 (Metabolic Syndrome X) : The ultimate effectors of gluconeogenesis are the three enzymes : PEPCK, F-1,6-BPase, and G6Pase , and their expression is regulated by PPAR? and AMPK