Solute carrier family 18 (vesicular monoamine), member 2

Preferred Label : Solute carrier family 18 (vesicular monoamine), member 2;

Symbol : SLC18A2;

CISMeF acronym : SLC18A2;

Type : Gene;

Alternative titles and symbols : Vesicular amine transporter 2; Vesicular monoamine transporter 2; Synaptic vesicle monoamine transporter, brain; Synaptic vesicle amine transporter, brain; VAT2; VMAT2; SVMT; SVAT;

Ensembl ID : ENSG00000165646;

Prefixed ID : *193001;

Détails

Origin ID

193001;

UMLS CUI

C1420115;

Automatic exact mappings (from CISMeF team)
- SLC18A2 Gene [NCIt concept]
- SLC18A2 wt Allele [NCIt concept]
- Synaptic Vesicular Amine Transporter [NCIt concept]
- solute carrier family 18 member A2 [ORDO Gene]
- solute carrier family 18 member A2 [HGNC gene]
- vesicular monoamine transport proteins [MeSH Descriptor]
- vesicular monoamine transporter 2 [MeSH concept]
HGNC gene
- solute carrier family 18 member A2 [HGNC gene]
NCIt concept(s)
- SLC18A2 Gene [NCIt concept]
- SLC18A2 wt Allele [NCIt concept]
- Synaptic Vesicular Amine Transporter [NCIt concept]
ORDO concept(s)
- solute carrier family 18 member A2 [ORDO Gene]
Phenotypes related
- Parkinsonism-dystonia 2, infantile-onset [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC18A2 Gene [NCIt concept]
- solute carrier family 18 member A2 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

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