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FLASH GENE
Symbol PNPLA3 contributors: mct/npt/pgu - updated : 10-06-2011
HGNC name patatin-like phospholipase domain containing 3
HGNC id 18590
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
9 - 2805 52.7 481 - 2008 19029121
EXPRESSION
Type
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Digestiveintestinelarge intestinecolon  
 liver   highly Homo sapiens
Nervousbrain    
Skin/Tegumentskin    
Urinarykidney    
Visualeye    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Connectiveadipose  highly Homo sapiens
Muscularstriatumskeletal  
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • a shared protein domain discovered initially in patatin
  • HOMOLOGY
    interspecies homolog to Drosophila CG5560
    homolog to C.elegans C05D11.7a
    Homologene
    FAMILY
  • IPLA2/lipase family
  • patatin-like phospholipase family
  • CATEGORY enzyme
    SUBCELLULAR LOCALIZATION     plasma membrane
    text
  • strongly associated with membranes and with lipid droplets
  • basic FUNCTION
  • triacylglycerol lipase that mediates triacylglycerol hydrolysis in adipocytes
  • may be involved in the balance of energy usage/storage in adipocytes
  • participating in triacylglycerol hydrolysis and the acyl-CoA independent transacylation of acylglycerols, thereby facilitating energy mobilization and storage in adipocytes
  • lipid hydrolase with an unusual folding topology that differs from classical lipases
  • role for adiponutrin as a susceptibility gene for hepatic dysfunction
  • its function may be related to some regulatory aspect of the pathway of lipogenesis or lipolysis
  • plays a role in the hydrolysis of glycerolipids (
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein interacting with USF2 (USF2 is one of the transcription factors that can regulate adiponutrin promoter activity in the presence of glucose)
    cell & other
    REGULATION
    Other highly regulated by changes in energy balance
    nutritionally regulated, decreasing after fasting and strongly up-regulated by feeding in adipose tissue and liver
    regulated in a coordinated manner with genes involved in lipogenesis
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    constitutional     --low  
    by fasting in adipose tissue
    constitutional     --over  
    in adipose tissue and in liver of obese patients
    constitutional germinal mutation     loss of function
    I148M substitution causes a loss of function in nonalcoholic fatty liver disease
    Susceptibility
  • to nonalcoholic fatty liver disease
  • to obesity
  • to alcoholic liver disease and clinically evident alcoholic cirrhosis
  • to lower HDL cholesterol and a tendency toward lower free fatty acid levels
  • to hepatic steatosis in obese youths
  • to non-alcoholic fatty liver disease
  • Variant & Polymorphism SNP , other
  • variant (rs738409) was strongly associated with hepatic fat content and nonalcoholic fatty liver disease
  • rs738409 variant associated with obesity
  • rs738409 in PNPLA3 is strongly associated with alcoholic liver disease and clinically evident alcoholic cirrhosis
  • GG genotype had significantly lower HDL cholesterol and a tendency toward lower free fatty acid levels
  • common variant of the PNPLA3 gene confers susceptibility to hepatic steatosis in obese youths without increasing the level of hepatic and peripheral insulin resistance
  • PNPLA3 p.I148M variants represent genetic risk factors for non-alcoholic fatty liver disease (NAFLD)
  • Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    obesity  
    potential target for therapies to manage obesity and its associated disorders by controlling its expression or actions
    ANIMAL & CELL MODELS