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SNP information rs921451

RS921451

Normal allele: TT

Polymorphism of the dopamine transporter type 1 gene alters response to treatment in Parkinson's disease.

Polymorphism rs921451 is related to topics like this:

Dopamine transporter genes

The membrane-bound protein called the dopamine transporter (DAT), also known as the...


Research and publications:

  15879433   Haplotype analysis indicates an association between the DOPA decarboxylase (DDC) gene and nicotine dependence.

  17184203   DOPA decarboxylase gene is associated with nicotine dependence.

  19184136   Examination of association of genes in the serotonin system to autism

  21143251   A candidate gene association study of alcohol consumption in young women.

  25073638   Polymorphisms in genes implicated in dopamine, serotonin and noradrenalin metabolism suggest association with cerebrospinal fluid monoamine metabolite concentrations in psychosis.

  25545355   Genetic variants and early cigarette smoking and nicotine dependence phenotypes in adolescents.

  27166759   Converging findings from linkage and association analyses on susceptibility genes for smoking and other addictions.

  32736537   Association studies of dopamine synthesis and metabolism genes with multiple phenotypes of heroin dependence.

  24216088   Polymorphism of the dopa decarboxylase gene influences the motor response to L-dopa in Parkinson's disease.

  25805645   Polymorphisms in the dopamine transporter type 1 gene alter response to treatment in Parkinson's disease.

  28927418   A systematic review and integrative approach to decipher the overall molecular link between levodopa response and Parkinson's disease.

  30216543   A functional polymorphism in intron 13 of the monoamine oxidase B gene predicts putamen dopamine turnover in de novo Parkinson's disease.

  30745869   Dopaminergic pathway genes influence adverse events associated with dopaminergic treatment for Parkinson's disease.

  33013295   Contribution of five functional gene loci related to dopamine metabolism to Parkinson's disease and multiple system atrophy in a Chinese population.

  33093598   Population pharmacokinetics of levodopa gel infusion in Parkinson's disease: effects of entacapone infusion and genetic polymorphism.

  33250838   Polymorphism of the dopa decarboxylase gene modifies the motor response to levodopa in Chinese patients with Parkinson's disease.

  35044623   The role of single nucleotide polymorphisms of monoamine oxidase B, dopamine D2 receptor, and DOPA decarboxylase receptors among patients treated for Parkinson's disease.

  35096365   Functional polymorphism in intron 13 of the MAOB gene predicts dyskinesia in Parkinson's disease.

Mitochondria dna

The mitochondria contain circular chromosomes known as mitochondrial DNA and are organelles...

Diseases genetic

Human genetic illnesses stem from mutations in one or more genes and can be classified as occurring...

Type 2 diabetes genetic

Type 2 diabetes is the most prevalent and impactful subtype of diabetes worldwide, affecting around...

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