solute carrier family 18 member A2

Summary
Gene Symbol
  • SLC18A2
Organism
Homo sapiens (human)
NCBI Gene
6571
KEGG Gene ID
PubChem
6571
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell projection
  • Cytoplasmic vesicle
  • Disease variant
  • Disulfide bond
  • Dystonia
  • Glycoprotein
  • Neurotransmitter transport
  • Parkinsonism
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Synapse
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q05940
  • Solute carrier family 18 member 2
  • Vesicular amine transporter 2
  • Vesicular monoamine transporter 2
Gene Ontology (GO)
GO Hierarchy
Displaying entries 6 - 10 of 17 in total
GO Term Evidence Code PMID
axon
dendrite
dendrite
transport vesicle membrane
secretory granule membrane
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
vesicular acetylcholine transporter
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:14330 Parkinson's disease
DOID:0070490 infantile parkinsonism-dystonia 2
Ortholog
Displaying all 3 entries
Species Gene ID Alliance of Genome Resources
214084 MGI:106677
25549 RGD:3694
180837 WB:WBGene00000295

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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