Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6570
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 18 member A1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC18A1
Synonyms (NCBI Gene) Gene synonyms aliases
CGAT, VAT1, VMAT1
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p21.3
Summary Summary of gene provided in NCBI Entrez Gene.
The vesicular monoamine transporter acts to accumulate cytosolic monoamines into vesicles, using the proton gradient maintained across the vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2104638 hsa-miR-4778-3p CLIP-seq
MIRT2329112 hsa-miR-3153 CLIP-seq
MIRT2329113 hsa-miR-4505 CLIP-seq
MIRT2329114 hsa-miR-4638-5p CLIP-seq
MIRT2329115 hsa-miR-4646-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005335 Function Serotonin:sodium:chloride symporter activity IBA
GO:0005515 Function Protein binding IPI 32296183
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IDA 16326835
GO:0005789 Component Endoplasmic reticulum membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
193002 10934 ENSG00000036565
Protein
UniProt ID P54219
Protein name Chromaffin granule amine transporter (Solute carrier family 18 member 1) (Vesicular amine transporter 1) (VAT1)
Protein function [Isoform 1]: Electrogenic antiporter that exchanges one cationic monoamine with two intravesicular protons across the membrane of secretory and synaptic vesicles. Uses the electrochemical proton gradient established by the V-type proton-pump ATP
PDB 8TGG , 8TGH , 8TGI , 8TGJ , 8TGK , 8TGL , 8TGM , 8TGN
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 96 433 Major Facilitator Superfamily Family
Tissue specificity TISSUE SPECIFICITY: Expressed primarily in neuroendocrine tissues. Highly expressed in chromaffin cells of the adrenal medulla (at protein level). Detected in peripheral sympathetic ganglia (at protein level). Found in some paracrine cells in stomach and
Sequence
Sequence length 525
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Synaptic vesicle cycle
Serotonergic synapse
Dopaminergic synapse
Parkinson disease
Cocaine addiction
Amphetamine addiction
Alcoholism
  Na+/Cl- dependent neurotransmitter transporters
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 30194079
Alcoholism Associate 26861143
Anxiety Associate 26861143
Anxiety Disorders Associate 26861143
Autistic Disorder Associate 30194079
Bipolar Disorder Associate 16936705, 26861143, 30194079
Carcinoid Tumor Associate 17717663
Carcinoid Tumor Stimulate 18708724
Complement component 5 deficiency Associate 30194079
Depressive Disorder Associate 26861143