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MIRAGE
Sodium-dependent neutral amino acid transporter SLC6A17

Summary
UniProt ID
Q9H1V8
Gene Symbol
  • NTT4
  • SLC6A17
Gene ID
388662
Organism
Homo sapiens (human)
GlyGen
Q9H1V8
The Human Metabolome Database
HMDBP09075
The O-GlcNAc Database
Q9H1V8
Re-Glyco
Q9H1V8
Annotation
Keyword
  • Amino-acid transport
  • Cell projection
  • Cytoplasmic vesicle
  • Disease variant
  • Glycoprotein
  • Intellectual disability
  • Neurotransmitter transport
  • Phosphoprotein
  • Reference proteome
  • Sodium transport
  • Symport
  • Synapse
  • Transmembrane helix
Gene Ontology (GO)
Displaying all 8 entries
GO Term
plasma membrane
membrane
cell projection
postsynapse
synaptic vesicle
synaptic vesicle membrane
glutamatergic synapse
GABA-ergic synapse
Subcellular Location(GO Annotation)

Subcellular in which this glycoprotein is expressed are highlighted in blue.

Displaying 1 entry
GO Term
symporter activity
Annotation information from UniProt.
Sequence
MPKNSKVTQREHSSEHVTESVADLLALEEPVDYKQSVLNVAGEAGGKQKAVEEELDAEDRPAWNSKLQYILAQIGFSVGLGNIWRFPYLCQKNGGGAYLVPYLVLLIIIGIPLFFLELAVGQRIRRGSIGVWHYICPRLGGIGFSSCIVCLFVGLYYNVIIGWSIFYFFKSFQYPLPWSECPVVRNGSVAVVEAECEKSSATTYFWYREALDISDSISESGGLNWKMTLCLLVAWSIVGMAVVKGIQSSGKVMYFSSLFPYVVLACFLVRGLLLRGAVDGILHMFTPKLDKMLDPQVWREAATQVFFALGLGFGGVIAFSSYNKQDNNCHFDAALVSFINFFTSVLATLVVFAVLGFKANIMNEKCVVENAEKILGYLNTNVLSRDLIPPHVNFSHLTTKDYMEMYNVIMTVKEDQFSALGLDPCLLEDELDKSVQGTGLAFIAFTEAMTHFPASPFWSVMFFLMLINLGLGSMIGTMAGITTPIIDTFKVPKEMFTVGCCVFAFLVGLLFVQRSGNYFVTMFDDYSATLPLTLIVILENIAVAWIYGTKKFMQELTEMLGFRPYRFYFYMWKFVSPLCMAVLTTASIIQLGVTPPGYSAWIKEEAAERYLYFPNWAMALLITLIVVATLPIPVVFVLRHFHLLSDGSNTLSVSYKKGRMMKDISNLEENDETRFILSKVPSEAPSPMPTHRSYLGPGSTSPLETSGNPNGRYGSGYLLASTPESEL
  • N : N-glycosylation Site
  • ___ : Potential Sequon
Glycosylation Sites
Displaying all 4 entries
Position Description PubMed ID GlyTouCan ID Source
186 N-linked (GlcNAc...) asparagine
393 N-linked (GlcNAc...) asparagine
411
418
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:0081212 autosomal recessive intellectual developmental disorder 48
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025