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 16 - 17 of 17 in total
GO Term Evidence Code PMID
clathrin-sculpted monoamine transport vesicle membrane
dopaminergic synapse
GO Hierarchy
GO Hierarchy
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