SLC18A1 - solute carrier family 18 member A1 Gene

Homo sapiens

Also known as CGAT; VAT1; VMAT1

Gene ID: 6570 | Gene type: protein coding

About SLC18A1

Cytogenetic location: 8p21.3 Genomic coordinates (GRCh38): 8:20,144,855-20,183,136 (from NCBI)

This gene has 10 transcripts (splice variants), 196 orthologues and 3 paralogues. Biased expression in adrenal (RPKM 13.1), colon (RPKM 1.0) and 1 other tissue.

Summary

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 been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (Peter et al., 1993 [PubMed 7905859]). See also SLC18A2 (MIM 193001).[supplied by OMIM, Mar 2008]

SLC18A1 Products(4)

mRNA	Protein	Name
NM_001135691.3	NP_001129163.1	chromaffin granule amine transporter isoform a
NM_001142324.2	NP_001135796.1	chromaffin granule amine transporter isoform b
NM_001142325.2	NP_001135797.1	chromaffin granule amine transporter isoform c
NM_003053.4	NP_003044.1	chromaffin granule amine transporter isoform a

SLC18A1 Protein Structure

MFS_1

0
100
200
300
400
525 a.a.

Protein Preferred Names

Protein Names

chromaffin granule amine transporter

solute carrier family 18 (vesicular monoamine transporter), member 1

Related Diseases

Diseases

Alias

Barbiturate Abuse

Adrenal Neuroblastoma

Neuroblastoma Of Adrenal Gland	Adrenal Gland Neuroblastoma
Neuroblastoma Nos

Narcolepsy

Paroxysmal Sleep	Gelineau Syndrome
Narcoleptic Syndrome	Narcolepsy-Cataplexy Syndrome
Cataplexy And Narcolepsy	Narcolepsy, Without Cataplexy
Gelineau'S Syndrome	Narcolepsy With Or Without Cataplexy
Narcolepsy Nos

Schizophrenia

SCZD	Schizophrenia With Or Without An Affective Disorder
Schizophrenia 12	Schizophrenia, Susceptibility To
Schizophrenia-1	Dementia Praecox
Schizophrenia 1

Autism

Autistic Disorder	Autism Susceptibility 1
Childhood Autism	Autistic Disorder Of Childhood Onset
Infantile Autism	Kanner'S Syndrome
Autistic

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (2)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13043	SLC18A1 Human Pre-designed siRNA Set A		/	Unkown
HY-RS13046	SLC18B1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	SLC18A1	MGD	MGI:106684
Bos taurus	SLC18A1	VGNC	VGNC:34705
Canis familiaris	SLC18A1	VGNC	VGNC:46255
Felis catus	SLC18A1	VGNC	VGNC:65226
Rattus norvegicus	SLC18A1	RGD	RGD:3693
Macaca mulatta	SLC18A1	VGNC	VGNC:77406

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