Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6581
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 22 member 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC22A3
Synonyms (NCBI Gene) Gene synonyms aliases
EMT, EMTH, OCT3
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q25.3
Summary Summary of gene provided in NCBI Entrez Gene.
Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar c
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019444 hsa-miR-148b-3p Microarray 17612493
MIRT021441 hsa-miR-9-5p Microarray 17612493
MIRT022967 hsa-miR-124-3p Microarray 18668037
MIRT639284 hsa-miR-1272 HITS-CLIP 19536157
MIRT639283 hsa-miR-1322 HITS-CLIP 19536157
Transcription factors
Transcription factor Regulation Reference
KLF8 Unknown 17671186
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001692 Process Histamine metabolic process TAS 23505051
GO:0005326 Function Neurotransmitter transmembrane transporter activity IDA 10196521, 16581093, 20858707
GO:0005326 Function Neurotransmitter transmembrane transporter activity IEA
GO:0005326 Function Neurotransmitter transmembrane transporter activity IMP 23505051
GO:0005515 Function Protein binding IPI 17474147
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604842 10967 ENSG00000146477
Protein
UniProt ID O75751
Protein name Solute carrier family 22 member 3 (Extraneuronal monoamine transporter) (EMT) (Organic cation transporter 3) (OCT3)
Protein function Electrogenic voltage-dependent transporter that mediates the transport of a variety of organic cations such as endogenous bioactive amines, cationic drugs and xenobiotics (PubMed:10196521, PubMed:10966924, PubMed:12538837, PubMed:17460754, PubMe
PDB 7ZH0 , 7ZH6 , 7ZHA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 142 485 Major Facilitator Superfamily Family
Tissue specificity TISSUE SPECIFICITY: Expressed in liver (PubMed:10196521, PubMed:9933568). Expressed in intestine (PubMed:16263091, PubMed:20858707). Expressed in kidney in proximal tubular cells (PubMed:10966924). Expressed in placenta (PubMed:10966924, PubMed:9933568).
Sequence
Sequence length 556
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Choline metabolism in cancer   Abacavir transmembrane transport
Organic cation transport
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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
Barrett esophagus Barrett's esophagus N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Coronary artery disease Coronary artery disease N/A N/A GWAS
Coronary Heart Disease Coronary heart disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 17805461
Arsenic Poisoning Associate 36436256
Cap Myopathy Associate 21820706
Carcinoma Hepatocellular Associate 22439694
Cardiovascular Diseases Associate 20665672, 27893421, 37948393
Colorectal Neoplasms Associate 23555006, 30561001, 33976257
Coronary Artery Disease Associate 27893421, 31870308, 32685059
Coronary Artery Disease Autosomal Dominant 1 Associate 22216278
Coronary Disease Associate 25561729
Death Associate 31874997