solute carrier family 18 member A2

Summary
Gene Symbol
  • SLC18A2
Organism
Homo sapiens (human)
NCBI Gene
6571
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
  • Reference proteome
  • Synapse
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q05940
  • Monoamine transporter
  • Solute carrier family 18 member 2
  • Vesicular amine transporter 2
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
transporter
Functional Category
  • E: Amino acid transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 9 entries
DO ID Disease Name Source
DOID:0070490 infantile parkinsonism-dystonia 2
DOID:14330 Parkinson's disease
DOID:1440 Machado-Joseph disease
DOID:2030 anxiety disorder
DOID:303 substance-related disorder
DOID:3602 toxic encephalopathy
DOID:670 amphetamine abuse
DOID:809 cocaine abuse
DOID:9744 type 1 diabetes mellitus

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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: December 9, 2024