Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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6570 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Solute carrier family 18 member A1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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SLC18A1 |
SynonymsGene synonyms aliases
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CGAT, VAT1, VMAT1 |
ChromosomeChromosome number
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8 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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8p21.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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 |
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Sequence |
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Sequence length |
525 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
18451639 |
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