SLCO1B3 I562*

Stable Identifier
R-HSA-5661201
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
OATP-8, Solute carrier organic anion transporter family member 1B3
Locations in the PathwayBrowser
Expand all
External Reference Information
External Reference
UniProt:Q9NPD5 SLCO1B3
Gene Names
SLCO1B3, LST2, OATP1B3, OATP8, SLC21A8
Chain
chain:1-702
Reference Genes
BioGPS Gene:28234 SLCO1B3
COSMIC (genes):SLCO1B3 SLCO1B3
CTD Gene:28234 SLCO1B3
dbSNP Gene:28234 SLCO1B3
ENSEMBL:ENSG00000111700 SLCO1B3
ENSEMBL:ENSG00000111700 SLCO1B3
HGNC:10961 SLCO1B3
KEGG Gene (Homo sapiens):hsa:28234 SLCO1B3
Monarch:28234 SLCO1B3
NCBI Gene:28234 SLCO1B3
OMIM:605495 SLCO1B3
UCSC:Q9NPD5 SLCO1B3
Reference Transcript
Other Identifiers
0005130193
11732569_at
16749036
206354_at
28234
3407630
3407631
3407632
3407633
3407639
3407640
3407643
3407644
3407645
3407646
3407649
3407650
3407652
3407653
3407655
3407656
3407657
3407660
3407663
3407666
3407667
3407668
3407686
3407689
3407690
3407693
4943
50892
7954330
A_14_P102835
A_14_P108697
A_14_P133603
A_23_P105475
A_33_P3364089
AAG43445
AAP81212
AAS01768
AC011604
AC087309
AF187815
AJ251506
AJ400763
AJ400764
AJ400765
AJ400766
AJ400767
AJ400768
AJ400769
AJ400770
AJ400771
AJ400772
AJ400773
AJ400774
AJ400775
AJ400776
AY257471
AY442326
CAB96997
CAB97008
CCDS8684
ENSG00000111700
ENSP00000261196
ENSP00000370956
ENST00000261196
ENST00000381545
EntrezGene:28234
g9790232_3p_at
GE82482
GO:0003674
GO:0005215
GO:0005515
GO:0005575
GO:0005623
GO:0005886
GO:0005887
GO:0006810
GO:0006811
GO:0008150
GO:0008514
GO:0015125
GO:0015347
GO:0015711
GO:0015721
GO:0016020
GO:0016021
GO:0016323
GO:0022857
GO:0043252
GO:0055085
HGNC:10961
HPA004943
HPA050892
ILMN_1687319
IPR002350
IPR004156
IPR020846
IPR036058
IPR036259
MIM:237450
MIM:605495
NM_001349920
NM_019844
NP_001336849
NP_062818
PF03137
PF07648
PH_hs_0030139
SLCO1B3
SLCO1B3-201
SLCO1B3-202
TC12002282.hg
uc001rel.5
uc058ltm.1
UPI000013544A
Other forms of this molecule
SLCO1B3 [plasma membrane]
Modified Residues
Name
L-isoleucine 562 replaced with unknown
Coordinate
562
PsiMod HEY
L-isoleucine removal [MOD:01640]
A protein modification that effectively removes or replaces an L-isoleucine.
Disease
Name Identifier Synonyms
bilirubin metabolic disorder 2741 hyperbilirubinemia, hereditary hyperbilirubinemia
Cross References
RefSeq
ZINC - Metabolites
ZINC - World Drugs
ZINC - FDA approved
GeneCards
ZINC - Substances
ZINC - Biogenic
ZINC target
PRO
Orphanet
ZINC - Predictions - Purchasable
HMDB Protein