Sialin

Summary
UniProt ID
Q9NRA2
Gene Symbol
SLC17A5
Gene ID
26503
Organism
Homo sapiens (human)
PubChem
Q9NRA2
The Human Metabolome Database
HMDBP02797
RaftProt
Q9NRA2
Re-Glyco
Q9NRA2
Annotation
Keyword
3D-structure Alternative splicing Amino-acid transport Cell membrane Cytoplasmic vesicle Disease variant Glycoprotein Lysosome Phosphoprotein Proteomics identification Reference proteome Symport Synapse Transmembrane helix
Gene Ontology (GO)
GO Hierarchy
Sequence
MRSPVRDLARNDGEESTDRTPLLPGAPRAEAAPVCCSARYNLAILAFFGFFIVYALRVNLSVALVDMVDSNTTLEDNRTSKACPEHSAPIKVHHNQTGKKYQWDAETQGWILGSFFYGYIITQIPGGYVASKIGGKMLLGFGILGTAVLTLFTPIAADLGVGPLIVLRALEGLGEGVTFPAMHAMWSSWAPPLERSKLLSISYAGAQLGTVISLPLSGIICYYMNWTYVFYFFGTIGIFWFLLWIWLVSDTPQKHKRISHYEKEYILSSLRNQLSSQKSVPWVPILKSLPLWAIVVAHFSYNWTFYTLLTLLPTYMKEILRFNVQENGFLSSLPYLGSWLCMILSGQAADNLRAKWNFSTLCVRRIFSLIGMIGPAVFLVAAGFIGCDYSLAVAFLTISTTLGGFCSSGFSINHLDIAPSYAGILLGITNTFATIPGMVGPVIAKSLTPDNTVGEWQTVFYIAAAINVFGAIFFTLFAKGEVQNWALNDHHGHRH
Glycosylation Sites
Displaying all 3 entries
Position Description PubMed ID GlyTouCan ID Source
71
  • N-linked (GlcNAc...) asparagine
77
  • N-linked (GlcNAc...) asparagine
95
  • N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 4 entries
Pathway Name Organism
Defective SLC17A5 causes Salla disease (SD) and ISSD Homo sapiens
Hyaluronan degradation Homo sapiens
Organic anion transport by SLC5/17/25 transporters Homo sapiens
Sialic acid metabolism Homo sapiens
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:3659 sialuria

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: April 6, 2026