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Symbol
Name
ID
Slc6a3
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3
MGI:94862
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Abnormal circulating carboxylic acid concentration
Increased CSF homovanillic acid concentration
Decreased resting energy expenditure
Disease(s) Associated with SLC6A3
classic dopamine transporter deficiency syndrome
obesity

Mouse Phenotypes
decreased susceptibility to dopaminergic neuron neurotoxicity
increased circulating sodium level
decreased dopamine level
increased dopamine level
increased serotonin level
abnormal physiological response to xenobiotic
decreased physiological sensitivity to xenobiotic
Availability Mouse Genotype
Slc6a3tm1.1Jaja/Slc6a3tm1.1Jaja
Slc6a3tm1Hhg/Slc6a3tm1Hhg
Slc6a3tm1Mca/Slc6a3tm1Mca
Slc6a3tm1Rbl/Slc6a3tm1Rbl
Slc6a3tm2Mca/Slc6a3tm2Mca
Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Slc6a3tm2(tTA)Xz/Slc6a3tm3(tetO)Xz

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory