Slc6a17 - solute carrier family 6 (neurotransmitter transporter), member 17

Predicted to enable symporter activity. Involved in brain development. Predicted to be located in several cellular components, including cell projection; cytoplasmic vesicle; and synapse. Predicted to be integral component of plasma membrane. Predicted to be active in synaptic vesicle. Predicted to be intrinsic component of membrane. Is expressed in several structures, including nervous system. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human SLC6A17 (solute carrier family 6 member 17). [provided by Alliance of Genome Resources, Apr 2022]