Gene:
SLCO1B1
solute carrier organic anion transporter family, member 1B1

PharmGKB contains no dosing guidelines for this gene. To report known dosing guidelines, or if you are interested in developing guidelines, click here.

PharmGKB contains no drug labels with pharmacogenomic information for this gene. To report a drug label with PGx, click here.

PharmGKB contains no Clinical Variants that meet the highest level of criteria.

To see more Clinical Variants with lower levels of criteria, click the button at the bottom of the table.

Position ? Drug ? Relevance ? Strength of
Evidence ?
rs11045819 more likely to work 2
rs4149056 dose difficult to predict 2
rs4149081 more likely to cause increased clearance of methotrexate & increased gastrointestinal side effects 2
rs11045879 more likely to cause Gi toxicity 2
rs4149015 less likely to work 3
rs2306283 dose difficult to predict 3
rs2306283 dose difficult to predict 3
rs4149056 more likely to work 3
rs4149056 more likely to work 3
rs4149056 No clinical/PGx action 3
rs4149056 more likely to cause myopathy 3

Download a summary of all Clinical Annotations available.

Disclaimer: The PharmGKB's clinical annotations reflect expert consensus based on clinical evidence and peer-reviewed literature available at the time they are written and are intended only to assist clinicians in decision-making and to identify questions for further research. New evidence may have emerged since the time an annotation was submitted to the PharmGKB. The annotations are limited in scope and are not applicable to interventions or diseases that are not specifically identified.

The annotations do not account for individual variations among patients, and cannot be considered inclusive of all proper methods of care or exclusive of other treatments. It remains the responsibility of the health-care provider to determine the best course of treatment for a patient. Adherence to any guideline is voluntary, with the ultimate determination regarding its application to be made solely by the clinician and the patient. PharmGKB assumes no responsibility for any injury or damage to persons or property arising out of or related to any use of the PharmGKB clinical annotations, or for any errors or omissions.

? = Mouse-over for quick help

A non-comprehensive list of genetic tests for specific variants, including descriptions of and links to individual tests; manually curated by PharmGKB. The information listed is provided for educational purposes only and does not constitute an endorsement of any listed test or manufacturer.

PGx Test Variants Assayed Related Drugs?
SLCO1B1 rs2306283, rs2306283, rs4149056, rs4149056, SLCO1B1*1B, SLCO1B1*5, SLCO1B1*15

The table below contains information about pharmacogenomic variants on PharmGKB. Please follow the link in the "Variant" column for more information about a particular variant. Each link in the "Variant" column leads to the corresponding PharmGKB Variant Page. The Variant Page contains summary data, including PharmGKB manually curated information about variant-drug pairs based on individual PubMed publications. The PMIDs for these PubMed publications can be found on the Variant Page.

The tags in the first column of the table indicate what type of information can be found on the corresponding Variant Page.

Links in the "Drugs" column lead to PharmGKB Drug Pages.

Variant?
(build 132)
Alternate Names ? Drugs ? Alleles ? Function ? Amino Acid?
Translation
No VIP available CA VA
rs11045819 SLCO1B1:*4, SLCO1B1:463C>A, c.463C>A, g.14089937C>A, g.50686C>A, p.Pro155Thr C > A Missense Pro155Thr
No VIP available CA VA
rs11045879 OATP1B1: intronic C/T, c.1865+4846T>C, g.103492T>C, g.14142743T>C C/T Not Available
rs2306283 SLCO1B1*1B, c.388A>G, c.388G>A, g.14089862A>G, g.50611A>G, p.Asn130Asp, p.Asp130Asn T > T/C Missense Asn130Asn/Asp
rs4149015 SLCO1B1:11187G>A, SLCO1B1:G-11187A, g.14043446G>A, g.4195G>A A/G Not Available
rs4149056 SLCO1B1*5, c.521T>C, g.14091673T>C, g.52422T>C, p.Val174Ala T > C Missense Val174Ala
No VIP available CA VA
rs4149081 OATP1B1: intronic A/G, c.1865+248G>A, g.14138145G>A, g.98894G>A A/G Not Available
Alleles, Functions, and Amino Acid Translations are all sourced from dbSNP build 132

Overview

Alternate Names:  OATP-2; liver-specific organic anion transporter 1; sodium-independent organic anion-transporting polypeptide 2; solute carrier family 21 (organic anion transporter), member 6; solute carrier family 21 member 6; solute carrier organic anion transporter family member 1B1
Alternate Symbols:  LST-1; LST1; MGC133282; OATP-C; OATP1B1; OATP2; OATPC; SLC21A6
Haplotypes: SLCO1B1*1A; SLCO1B1*1B; SLCO1B1*1C; SLCO1B1*2; SLCO1B1*3; SLCO1B1*4; SLCO1B1*5; SLCO1B1*6; SLCO1B1*7; SLCO1B1*8; SLCO1B1*9; SLCO1B1*10; SLCO1B1*11; SLCO1B1*12; SLCO1B1*13; SLCO1B1*14; SLCO1B1*15; SLCO1B1*16; SLCO1B1*17; SLCO1B1*22; SLCO1B1*23; SLCO1B1*24; SLCO1B1*25; SLCO1B1*26; SLCO1B1*27; SLCO1B1*28; SLCO1B1*29; SLCO1B1*30; SLCO1B1*31; SLCO1B1*32; SLCO1B1*33; SLCO1B1*34; SLCO1B1*35; SLCO1B1*36
PharmGKB Accession Id: PA134865839

Details

Cytogenetic Location: chr12 : p12.2 - p12.1
GP mRNA Boundary: chr12 : 21284137 - 21392730
GP Gene Boundary: chr12 : 21274137 - 21395730
Strand: plus
Product Name: solute carrier family 21 (organic anion transporter), member 6, solute carrier organic anion transporter family, member 1B1
The mRNA boundaries are calculated using the gene's default feature set from NCBI, mapped onto the UCSC Golden Path. PharmGKB sets gene boundaries by expanding the mRNA boundaries by no less than 10,000 bases upstream (5') and 3,000 bases downstream (3') to allow for potential regulatory regions.

All alleles are displayed on the positive chromosomal strand.

Download Haplotype Data (CSV)

Haplotype chr12:21325710 (hg19) chr12:21355487 (hg19) chr12:21392079 (hg19) rs11045819 rs11045852 rs11045853 rs139257324 rs140790673 rs142965323 rs2306283 rs34671512 rs4149015 rs4149056 rs55737008 rs55901008 rs56061388 rs56101265 rs56199088 rs56387224 rs59113707 rs59502379 rs59710386 rs72559745 rs72559748 rs79135870
SLCO1B1*1A G T C C A G C C G A A G T A T T T A A C G A A A A
SLCO1B1*1B G T C C A G C C G G A G T A T T T A A C G A A A A
SLCO1B1*1C G T C C A G C C G A A G T A T T T A A C G A A A A
SLCO1B1*2 G T C C A G C C G A A G T A T T C A A C G A A A A
SLCO1B1*3 G T C C A G C C G A A G T A T C T A A C G A G A A
SLCO1B1*4 G T C A A G C C G A A G T A T T T A A C G A A A A
SLCO1B1*5 G T C C A G C C G A A G C A T T T A A C G A A A A
SLCO1B1*6 G T C C A G C C G A A G T A C T T A A C G A A A A
SLCO1B1*7 G T C C A G C C G A A G T A T T T A G C G A A A A
SLCO1B1*8 G T C C A G C C G A A G T A T T T A A C G A A G A
SLCO1B1*9 G T C C A G C C G A A G T A T T T A A C C A A A A
SLCO1B1*10 G T C C A G C C G A A G T A T T T G A C G A A A A
SLCO1B1*11 G T C C A G C C G A A G T G T T T A A C G A A A A
SLCO1B1*12 G T C C A G C C G A A G T A T T C G A C G A A A A
SLCO1B1*13 G T C C A G C C G A A G T G T C T A A C G A G A A
SLCO1B1*14 G T C A A G C C G G A G T A T T T A A C G A A A A
SLCO1B1*15 G T C C A G C C G G A G C A T T T A A C G A A A A
SLCO1B1*16 G T C C A G C C G G A G C A T T T A A C G C A A A
SLCO1B1*17 G T C C A G C C G G A A C A T T T A A C G A A A A
SLCO1B1*22 G T C C A G C C G A C T A T T T A A C G A A A A
SLCO1B1*23 A T C C A G C C G A A T A T T T A A C G A A A A
SLCO1B1*24 G T C C G G C C G G A T A T T T A A C G A A A A
SLCO1B1*25 G T C A G A C C G G A T A T T T A A C G A A A A
SLCO1B1*26 G T C C A G C C A A A T A T T T A A C G A A A A
SLCO1B1*27 G T C C A G C C G G A T A T T T A A G G A A A A
SLCO1B1*28 G T C C G A C C G G A T A T T T A A C G A A A A
SLCO1B1*29 G T C C A G C T G G A T A T T T A A C G A A A A
SLCO1B1*30 G T C C A G C C G G A T A T T T A A C G A A A G
SLCO1B1*31 G T C C A G C C G G A T A T T T A A C C A A A A
SLCO1B1*32 G T C A G G C C G G A T A T T T A A C G A A A A
SLCO1B1*33 G T C C G A G C G G A T A T T T A A C G A A A A
SLCO1B1*34 G T T C A G C C G A A T A T T T A A C G A A A A
SLCO1B1*35 G T C C A G C C G G C T A T T T A A C G A A A A
SLCO1B1*36 G G C C A G C C G A A T A T T T A A C G A A A A

PharmGKB Curated Pathways

Pathways created internally by PharmGKB based primarily on literature evidence.

  1. Anti-diabetic Drug Nateglinide Pathway, Pharmacokinetics
    Nateglinide metabolism and transport in liver cell.
  1. Anti-diabetic Drug Repaglinide Pathway, Pharmacokinetics
    Repaglinide metabolism and transport in a liver cell.
  1. Atorvastatin/Lovastatin/Simvastatin Pathway, Pharmacokinetics
    Drug-specific representation of the candidate genes involved in transport, metabolism and clearance.
  1. Codeine and Morphine Pathway, Pharmacokinetics
    Representation of the candidate genes involved in metabolism of codeine and morphine.
  1. Fluvastatin Pathway, Pharmacokinetics
    Drug-specific representation of the candidate genes involved in transport, metabolism and clearance.
  1. Irinotecan Pathway, Pharmacokinetics
    Model human liver cell showing blood, bile and intestinal compartments, indicating tissue specific involvement of genes in the irinotecan pathway.
  1. Methotrexate Pathway, Pharmacokinetics
    Diagramatic representation of uptake, transport and elimination of methotrexate.
  1. Pravastatin Pathway, Pharmacokinetics
    Drug-specific representation of the candidate genes involved in transport, metabolism and clearance.
  1. Rosiglitazone Pharmacokinetic Pathway
    Rosiglitazone is transported from hepatic sinusoids into hepatocytes -- a process mediated by the organic anion transporting polypeptide, where is is metabolized by cytochrome p450 2C8 and 2C9.
  1. Rosuvastatin Pathway, Pharmacokinetics
    Drug-specific representation of the candidate genes involved in transport, metabolism and clearance.
  1. Statin Pathway - Generalized, Pharmacokinetics
    Representation of the superset of all genes involved in the transport, metabolism and clearance of statin class drugs.

External Pathways

Links to non-PharmGKB pathways.

  1. Recycling of bile acids and salts - (Reactome via Pathway Interaction Database)

No related genes are available.

Non-Curated Information ?

A list of non-curated publications that mention this gene along with other genes is available.

Curated Information ?

Drug Class Relationship Evidence
hmg coa reductase inhibitors
  • PD
  • PK
Publications, Variants
sulfonamides, urea derivatives
  • PD
  • PK
Publications
Drug Relationship Evidence
acarbose
  • PD
  • PK
Publications
adefovir dipivoxil
  •   
  •   
Publications
arsenic trioxide
  •   
  •   
Publications
atorvastatin
  • PD
  • PK
Publications, Variants
atrasentan
  •   
  • PK
Publications
bosentan
  •   
  • PK
Publications
caspofungin
  •   
  • PK
Publications
cerivastatin
  • PD
  • PK
Publications
chlorpropamide
  • PD
  • PK
Publications
cimetidine
  •   
  •   
Publications
cisplatin
  •   
  •   
Publications
clotrimazole
  •   
  • PK
Publications
codeine
  •   
  • PK
Publications
cyclosporine
  • PD
  • PK
Publications
digoxin
  •   
  • PK
Publications
diltiazem
  •   
  •   
Publications
dinoprostone
  •   
  • PK
Publications
enalapril
  •   
  • PK
Publications
estradiol
  •   
  • PK
Publications
ezetimibe
  • PD
  • PK
Publications
fexofenadine
  •   
  • PK
Publications
fluorouracil
  • PD
  •   
Publications
fluvastatin
  • PD
  • PK
Publications, Variants
gemfibrozil
  •   
  •   
Publications
glibenclamide
  • PD
  • PK
Publications
gliclazide
  • PD
  • PK
Publications
glimepiride
  • PD
  • PK
Publications
glucose
  • PD
  • PK
Publications
grapefruit juice
  •   
  •   
Publications
irinotecan
  • PD
  • PK
Publications
itraconazole
  •   
  •   
Publications
ketoconazole
  •   
  •   
Publications
liothyronine
  •   
  •   
Publications
lopinavir
  •   
  • PK
Publications
lovastatin
  • PD
  • PK
Publications
metformin
  • PD
  • PK
Publications
methotrexate
  • PD
  • PK
Publications, Pathways
miconazole
  •   
  •   
Publications
midazolam
  • PD
  • PK
Publications
mifepristone
  •   
  • PK
Publications
montelukast
  • PD
  • PK
Publications
morphine
  •   
  • PK
Publications
mycophenolate mofetil
  • PD
  • PK
Publications
mycophenolic acid
  • PD
  • PK
Publications
nateglinide
  • PD
  • PK
Publications, Variants
olmesartan
  •   
  • PK
Publications
paclitaxel
  • PD
  • PK
Publications
penicillin g
  •   
  •   
Publications
pioglitazone
  • PD
  • PK
Publications
pitavastatin
  • PD
  • PK
Publications
pravastatin
  • PD
  • PK
Publications, Variants
repaglinide
  • PD
  • PK
Publications, Variants
rifampin
  •   
  • PK
Publications
ritonavir
  •   
  • PK
Publications
rosiglitazone
  • PD
  • PK
Publications
rosuvastatin
  • PD
  • PK
Publications, Variants
simvastatin
  • PD
  • PK
Publications, Variants
sirolimus
  • PD
  • PK
Publications
SN-38
  • PD
  • PK
Publications
tacrolimus
  • PD
  • PK
Publications
terfenadine
  •   
  • PK
Publications
thyroxine
  •   
  •   
Publications
tolbutamide
  • PD
  • PK
Publications
troglitazone
  • PD
  • PK
Publications
valsartan
  •   
  • PK
Publications
verapamil
  •   
  •   
Publications

Non-Curated Information ?

A list of non-curated publications that mention this gene along with other drugs is available.

Curated Information ?

Non-Curated Information ?

A list of non-curated publications that mention this gene along with other diseases is available.

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