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MIRAGE
solute carrier family 6 member 8

Summary
Gene Symbol
  • SLC6A8
Organism
Homo sapiens (human)
NCBI Gene
6535
PubChem
6535
Alliance of Genome Resources
JoGo
SLC6A8
TogoVar
SLC6A8
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Intellectual disability
  • Metal-binding
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Sodium transport
  • Symport
  • Transmembrane helix
Proteins
Displaying all 3 entries
UniProt Protein Name
P48029
  • Solute carrier family 6 member 8
X5D9C4
Q59EV7
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 9 in total
GO Term Evidence Code PMID
creatine metabolic process
neurotransmitter transport
amino acid transport
muscle contraction
gamma-aminobutyric acid transport
GO Hierarchy
Displaying all 5 entries
GO Term Evidence Code PMID
creatine transmembrane transporter activity
creatine:sodium symporter activity
creatine:sodium symporter activity
creatine:sodium symporter activity
gamma-aminobutyric acid:sodium:chloride symporter activity
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0050800 cerebral creatine deficiency syndrome 1
DOID:1059 intellectual disability
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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: April 6, 2026