SLC6A17 solute carrier family 6 member 17 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 388662)
Source: NCBI Gene (ID 388662)
Symbol: SLC6A17
Full name: solute carrier family 6 member 17
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: MRT48; NTT4
Summary: The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse, the strongest expression of this gene was in cortical and hippocampal tissues where expression increased during embryonic brain development and peaked postnatally. Defects in this gene cause a form of autosomal recessive intellectual disability. [provided by RefSeq, Jul 2017]
Expression: Biased expression in brain (RPKM 23.3), adrenal (RPKM 2.5) and 1 other tissue
Orthologs: mouse
Gene size: 51709bp
Exon count: 12