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MIRAGE
Solute carrier organic anion transporter family member 1B1

Summary
UniProt ID
Q9Y6L6
Gene Symbol
  • LST1
  • OATP1B1
  • OATP2
  • OATPC
  • SLC21A6
  • SLCO1B1
Gene ID
10599
Organism
Homo sapiens (human)
GlyGen
Q9Y6L6
PubChem
Q9Y6L6
The Human Metabolome Database
HMDBP00454
Re-Glyco
Q9Y6L6
Annotation
Keyword
  • 3D-structure
  • Cell membrane
  • Disulfide bond
  • Glycoprotein
  • Ion transport
  • Lipid transport
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
Gene Ontology (GO)
Displaying all 4 entries
GO Term
plasma membrane
membrane
basal plasma membrane
basolateral plasma membrane
Subcellular Location(GO Annotation)

Subcellular in which this glycoprotein is expressed are highlighted in blue.

Annotation information from UniProt.
Sequence
MDQNQHLNKTAEAQPSENKKTRYCNGLKMFLAALSLSFIAKTLGAIIMKSSIIHIERRFEISSSLVGFIDGSFEIGNLLVIVFVSYFGSKLHRPKLIGIGCFIMGIGGVLTALPHFFMGYYRYSKETNINSSENSTSTLSTCLINQILSLNRASPEIVGKGCLKESGSYMWIYVFMGNMLRGIGETPIVPLGLSYIDDFAKEGHSSLYLGILNAIAMIGPIIGFTLGSLFSKMYVDIGYVDLSTIRITPTDSRWVGAWWLNFLVSGLFSIISSIPFFFLPQTPNKPQKERKASLSLHVLETNDEKDQTANLTNQGKNITKNVTGFFQSFKSILTNPLYVMFVLLTLLQVSSYIGAFTYVFKYVEQQYGQPSSKANILLGVITIPIFASGMFLGGYIIKKFKLNTVGIAKFSCFTAVMSLSFYLLYFFILCENKSVAGLTMTYDGNNPVTSHRDVPLSYCNSDCNCDESQWEPVCGNNGITYISPCLAGCKSSSGNKKPIVFYNCSCLEVTGLQNRNYSAHLGECPRDDACTRKFYFFVAIQVLNLFFSALGGTSHVMLIVKIVQPELKSLALGFHSMVIRALGGILAPIYFGALIDTTCIKWSTNNCGTRGSCRTYNSTSFSRVYLGLSSMLRVSSLVLYIILIYAMKKKYQEKDINASENGSVMDEANLESLNKNKHFVPSAGADSETHC
  • N : N-glycosylation Site
  • ___ : Potential Sequon
Glycosylation Sites
Displaying all 8 entries
Position Description PubMed ID GlyTouCan ID Source
8
130 N-linked (GlcNAc...) asparagine
134 N-linked (GlcNAc...) asparagine
250
432 N-linked (GlcNAc...) asparagine
503 N-linked (GlcNAc...) asparagine
516 N-linked (GlcNAc...) asparagine
617 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 5 entries
Pathway Name Organism
Atorvastatin ADME Homo sapiens
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) Homo sapiens
Heme degradation Homo sapiens
Recycling of bile acids and salts Homo sapiens
Transport of organic anions Homo sapiens
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:2741 bilirubin metabolic disorder
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025