Symbol
Name
ID

Slc6a3
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3
MGI:94862

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties	Hyperactivity	Attention deficit hyperactivity disorder
Disease(s) Associated with SLC6A3	Feeding difficulties	Hyperactivity	Attention deficit hyperactivity disorder
attention deficit hyperactivity disorder
classic dopamine transporter deficiency syndrome

Mouse Phenotypes

behavior/neurological phenotype

abnormal behavior

abnormal behavioral response to xenobiotic

impaired conditioned place preference behavior

increased exploration in new environment

abnormal spatial learning

abnormal response to novel odor

increased thigmotaxis

abnormal response to novel object

abnormal grooming behavior

abnormal motor coordination/balance

impaired coordination

abnormal locomotor activation

short stride length

decreased vertical activity

increased vertical activity

increased locomotor activity

hyperactivity

increased stereotypic behavior

abnormal maternal nurturing

Availability

Mouse Genotype

Slc6a3^tm1Hhg/Slc6a3^tm1Hhg

Slc6a3^tm1Mca/Slc6a3^tm1Mca

Slc6a3^tm1Rbl/Slc6a3^tm1Rbl

Slc6a3^tm1Wzh/Slc6a3^tm1Wzh

Slc6a3^tm2Mca/Slc6a3^tm2Mca

Slc6a3^tm1(cre)Xz/Slc6a3⁺

Slc6a3^{tm1b(KOMP)Wtsi}/Slc6a3⁺

Slc6a3^tm1Rbl/Slc6a3⁺

Slc6a3^tm2(tTA)Xz/Slc6a3^tm3(tetO)Xz

Aldh1a1^{tm1.1(cre/ERT2)Cai}/Aldh1a1⁺
Slc6a3^{tm1c(KOMP)Wtsi}/Slc6a3^{tm1c(KOMP)Wtsi} (conditional)

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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