The functional impact of SLC6 transporter genetic variation

Annu Rev Pharmacol Toxicol. 2007;47:401-41. doi: 10.1146/annurev.pharmtox.47.120505.105242.


Solute carrier 6 (SLC6) is a gene family of ion-coupled plasma membrane cotransporters, including transporters of neurotransmitters, amino acids, and osmolytes that mediate the movement of their substrates into cells to facilitate or regulate synaptic transmission, neurotransmitter recycling, metabolic function, and fluid homeostasis. Polymorphisms in transporter genes may influence expression and activity of transporters and contribute to behavior, traits, and disease. Determining the relationship between the monoamine transporters and complex psychiatric disorders has been a particular challenge that is being met by evolving approaches. Elucidating the functional consequences of and interactions among polymorphic sites is advancing our understanding of this relationship. Examining the influence of environmental influences, especially early-life events, has helped bridge the gap between genotype and phenotype. Refining phenotypes, through assessment of endophenotypes, specific behavioral tasks, medication response, and brain network properties has also improved detection of the impact of genetic variation on complex behavior and disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Attention Deficit Disorder with Hyperactivity / genetics
  • Biological Transport / genetics*
  • Depression / genetics
  • Humans
  • Multigene Family / physiology
  • Mutation
  • Plasma Membrane Neurotransmitter Transport Proteins / genetics*
  • Plasma Membrane Neurotransmitter Transport Proteins / physiology
  • Polymorphism, Genetic*


  • Plasma Membrane Neurotransmitter Transport Proteins