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Dopamine transporter

SLC6A3
Dopamine Transporter.jpg
Identifiers
Aliases SLC6A3, solute carrier family 6 (neurotransmitter transporter), member 3, DAT, DAT1, PKDYS, solute carrier family 6 member 3, Dopamine transporter
External IDs OMIM: 126455 MGI: 94862 HomoloGene: 55547 GeneCards: SLC6A3
Targeted by Drug
atomoxetine, bupropion, clomipramine, desvenlafaxine, dextroamphetamine, dexmethylphenidate, gbr-12935, levomilnacipran, mazindol, methylphenidate, nomifensine, phenelzine, sibutramine, trimipramine, WIN35428
RNA expression pattern
PBB GE SLC6A3 206836 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001044

NM_010020

RefSeq (protein)

NP_001035

NP_034150.1
NP_034150

Location (UCSC) Chr 5: 1.39 – 1.45 Mb Chr 13: 73.54 – 73.58 Mb
PubMed search

NM_001044

NM_010020

NP_001035

NP_034150.1
NP_034150

The dopamine transporter (also dopamine active transporter, DAT, SLC6A3) is a membrane-spanning protein that pumps the neurotransmitter dopamine out of the synapse back into cytosol, from which other transporters sequester DA and NE into vesicles for storage and later release. Dopamine reuptake via DAT provides the primary mechanism through which dopamine is cleared from synapses, although there may be an exception in the prefrontal cortex, where evidence points to a possibly larger role of the norepinephrine transporter.

DAT is implicated in a number of dopamine-related disorders, including attention deficit hyperactivity disorder, bipolar disorder, clinical depression, and alcoholism. The gene that encodes the DAT protein is located on human chromosome 5, consists of 15 coding exons, and is roughly 64 kbp long. Evidence for the associations between DAT and dopamine related disorders has come from a type of genetic polymorphism, known as a VNTR, in the DAT gene (DAT1), which influences the amount of protein expressed.


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