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SLC22A1

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Protein-coding gene in the species Homo sapiens
SLC22A1
Identifiers
AliasesSLC22A1, HOCT1, OCT1, oct1_cds, solute carrier family 22 member 1
External IDsOMIM: 602607; MGI: 108111; HomoloGene: 20665; GeneCards: SLC22A1; OMA:SLC22A1 - orthologs
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)
Chromosome 6 (human)Genomic location for SLC22A1Genomic location for SLC22A1
Band6q25.3Start160,121,815 bp
End160,158,718 bp
Gene location (Mouse)
Chromosome 17 (mouse)
Chr.Chromosome 17 (mouse)
Chromosome 17 (mouse)Genomic location for SLC22A1Genomic location for SLC22A1
Band17 A1|17 8.63 cMStart12,867,756 bp
End12,894,716 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lobe of liver

  • cartilage tissue

  • testicle

  • blood

  • granulocyte

  • spleen

  • stromal cell of endometrium

  • left lobe of thyroid gland

  • sural nerve

  • gastrocnemius muscle
Top expressed in
  • right kidney

  • left lobe of liver

  • human kidney

  • proximal tubule

  • Ileal epithelium

  • duodenum

  • atrioventricular valve

  • jejunum

  • Paneth cell

  • gallbladder
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

6580

20517

Ensembl

ENSG00000175003

ENSMUSG00000023829

UniProt

O15245

O08966

RefSeq (mRNA)

NM_003057
NM_153187

NM_009202

RefSeq (protein)

NP_003048
NP_694857

NP_033228

Location (UCSC)Chr 6: 160.12 – 160.16 MbChr 17: 12.87 – 12.89 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 22 member 1 is a protein that in humans is encoded by the gene SLC22A1.

Function

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 cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter.

It is also required for the uptake of metformin by cells.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000175003Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000023829Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Koehler MR, Wissinger B, Gorboulev V, Koepsell H, Schmid M (Jun 1998). "The two human organic cation transporter genes SLC22A1 and SLC22A2 are located on chromosome 6q26". Cytogenetics and Cell Genetics. 79 (3–4): 198–200. doi:10.1159/000134720. PMID 9605850.
  6. ^ "Entrez Gene: SLC22A1 solute carrier family 22 (organic cation transporter), member 1".
  7. Pryor, R; Cabreiro, F; Haberland, G (16 October 2015). "Repurposing metformin: an old drug with new tricks in its binding pockets". Biochemical Journal. 471 (3): 307–322. doi:10.1042/BJ20150497. PMC 4613459. PMID 26475449.
  8. Rosilio, C; Ben-Sahra, I; Bost, F; Peyron, JF (1 May 2014). "Metformin: a metabolic disruptor and anti-diabetic drug to target human leukemia". Cancer Letters. 346 (2): 188–96. doi:10.1016/j.canlet.2014.01.006. PMID 24462823.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Membrane proteins, carrier proteins: membrane transport proteins solute carrier (TC 2A)
By group
SLC1–10
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SLC11–20
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SLC21–30
(21):
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SLC31–40
(31):
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SLC41–48
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SLCO1–4
Ion pumps
Symporter, Cotransporter
Antiporter (exchanger)
see also solute carrier disorders
Categories: