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FLASH GENE
Symbol DRD2 contributors: mct/pgu - updated : 31-08-2016
HGNC name dopamine receptor D2
HGNC id 3023
ASSOCIATED DISORDERS
corresponding disease(s) MD
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional       loss of function
dysfunction during adolescence impairs neuronal circuits and working memory, and indicate that adolescent interventions to prevent aberrant DRD2 activity protect against cognitive impairment
constitutional       loss of function
is a critical mechanism mediating cocaine-induced glutamate plasticity in ventral tegmental area (VTA) neurons
Susceptibility
  • to opium addiction in Iranian population
  • to schizophrenia
  • to suicide
  • to speech disfluency
  • to nicotine dependence (ND) and alcohol dependence (AD)
  • Variant & Polymorphism SNP , other
  • may be association of the S311C variant with schizophrenia
  • 141C ins/del asociated with schizophrenia and alcoholism
  • allele A1-A1 increases the risk of opium addiction in Iranian population
  • polymorphisms that may be involved in the biological susceptibility to suicide
  • C allele at rs6277 is associated with increased susceptibility to speech disfluency
  • association of DRD2 and its adjacent gene ankyrin repeat and kinase domain containing 1 (ANKK1) with nicotine dependence (ND) and alcohol dependence (AD)
  • Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    psychiatry  
    potential impact of future therapeutic strategies that enhance DRD2 signaling in the nucleus accumbens (NAc)
    tumor  
    DRD2 and SSTR3 seem to be the most promising targets for pharmacological treatment of pituitary adenomas
    ANIMAL & CELL MODELS