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Symbol
Name
ID
Slc6a3
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3
MGI:94862
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Hypomimic face
Disease(s) Associated with SLC6A3
classic dopamine transporter deficiency syndrome

Mouse Phenotypes
abnormal tooth morphology
absent teeth
Availability Mouse Genotype
Slc6a3tm1b(KOMP)Wtsi/Slc6a3tm1b(KOMP)Wtsi

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
04/23/2024
MGI 6.23
The Jackson Laboratory