VOOZH about

URL: https://en.wikipedia.org/wiki/OATP1B1

⇱ Solute carrier organic anion transporter family member 1B1 - Wikipedia


Jump to content
From Wikipedia, the free encyclopedia
(Redirected from OATP1B1)
Protein found in humans
SLCO1B1
Identifiers
AliasesSLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6, solute carrier organic anion transporter family member 1B1
External IDsOMIM: 604843; MGI: 1351899; HomoloGene: 74575; GeneCards: SLCO1B1; OMA:SLCO1B1 - orthologs
Gene location (Human)
👁 Chromosome 12 (human)
Chr.Chromosome 12 (human)[1]
Band12p12.1Start21,131,194 bp[1]
End21,239,796 bp[1]
Gene location (Mouse)
👁 Chromosome 6 (mouse)
Chr.Chromosome 6 (mouse)[2]
Band6 G2|6 72.57 cMStart141,575,244 bp[2]
End141,632,372 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lobe of liver

  • testicle

  • buccal mucosa cell

  • pancreatic ductal cell

  • gallbladder

  • renal cortex

  • cervix

  • canal of the cervix

  • mouth

  • haematopoietic system
Top expressed in
  • left lobe of liver

  • embryo

  • sexually immature organism

  • medial head of gastrocnemius muscle

  • primary visual cortex

  • proximal tubule

  • jejunum

  • thoracic diaphragm

  • pancreas

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

10599

28253

Ensembl

ENSG00000134538

ENSMUSG00000030236

UniProt

Q9Y6L6

Q9JJL3

RefSeq (mRNA)

NM_006446

NM_020495
NM_178235

RefSeq (protein)

NP_006437

NP_065241

Location (UCSC)Chr 12: 21.13 – 21.24 MbChr 6: 141.58 – 141.63 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier organic anion transporter family member 1B1 is a protein that in humans is encoded by the SLCO1B1 gene.[5][6] Pharmacogenomic research indicates that genetic variations in this gene are associated with response to simvastatin.[7] Clinical guidelines exist that can guide dosing of simvastatin based on SLCO1B1 gene variant using genotyping or whole exome sequencing.[8]

See also

[edit]

References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000134538Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030236Ensembl, 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. ^ Abe T, Kakyo M, Tokui T, Nakagomi R, Nishio T, Nakai D, Nomura H, Unno M, Suzuki M, Naitoh T, Matsuno S, Yawo H (Jul 1999). "Identification of a novel gene family encoding human liver-specific organic anion transporter LST-1". J Biol Chem. 274 (24): 17159–63. doi:10.1074/jbc.274.24.17159. PMID 10358072.
  6. ^ "Entrez Gene: SLCO1B1 solute carrier organic anion transporter family, member 1B1".
  7. ^ Carr DF, O'Meara H, Jorgensen AL, Campbell J, Hobbs M, McCann G, van Staa T, Pirmohamed M (2013). "SLCO1B1 Genetic Variant Associated with Statin-Induced Myopathy: A Proof-of-Concept Study Using the Clinical Practice Research Datalink". Clinical Pharmacology & Therapeutics. 94 (6): 695–701. doi:10.1038/clpt.2013.161. PMC 3831180. PMID 23942138.
  8. ^ Huser V, Cimino JJ (2013). "Providing pharmacogenomics clinical decision support using whole genome sequencing data as input". AMIA Summits on Translational Science Proceedings AMIA Summit on Translational Science. 2013: 81. PMID 24303303.

Further reading

[edit]

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