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ABCC2 I1173F [plasma membrane]
Stable Identifier
R-HSA-5679030
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
Multidrug resistance-associated protein 2, MRP2_HUMAN
Icon
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Disorders of transmembrane transporters (Homo sapiens)
ABC transporter disorders (Homo sapiens)
Defective ABCC2 causes DJS (Homo sapiens)
Defective ABCC2 does not transport BMG,BDG from cytosol to extracellular region (Homo sapiens)
ABCC2 mutants [plasma membrane] (Homo sapiens)
ABCC2 I1173F [plasma membrane] (Homo sapiens)
External Reference Information
External Reference
UniProt:Q92887 ABCC2
Gene Names
ABCC2, CMOAT, CMOAT1, CMRP, MRP2
Chain
chain:1-1545
Reference Genes
BioGPS Gene:1244 ABCC2
COSMIC (genes):ABCC2 ABCC2
CTD Gene:1244 ABCC2
dbSNP Gene:1244 ABCC2
ENSEMBL:ENSG00000023839 ABCC2
ENSEMBL_homo_sapiens_GENE:ENSG00000023839.12 ABCC2
HGNC:53 ABCC2
KEGG Gene (Homo sapiens):1244 ABCC2
Monarch:1244 ABCC2
NCBI Gene:1244 ABCC2
OMIM:601107 ABCC2
UCSC:Q92887 ABCC2
Reference Transcript
RefSeq:NM_000392.4 ABCC2
Other Identifiers
11730409_at
11759031_at
1244
16708192
206155_PM_at
206155_at
3260448
3260449
3260451
3260452
3260453
3260454
3260456
3260458
3260459
3260461
3260462
3260463
3260464
3260465
3260466
3260467
3260468
3260469
3260472
3260474
3260475
3260476
3260477
3260478
3260480
3260481
3260483
3260484
3260485
3260486
3260487
3260489
3260490
3260492
3260493
3260496
3260497
3260498
3260499
3260500
33721_at
67977_at
7929779
A_14_P113705
A_23_P158976
A_23_P44569
GE62639
GO:0000166
GO:0003013
GO:0003824
GO:0005215
GO:0005515
GO:0005524
GO:0005886
GO:0006805
GO:0006855
GO:0006869
GO:0008514
GO:0008559
GO:0009986
GO:0010629
GO:0015127
GO:0015431
GO:0015721
GO:0015723
GO:0016020
GO:0016324
GO:0016787
GO:0016887
GO:0022857
GO:0042167
GO:0042626
GO:0042910
GO:0043225
GO:0046581
GO:0046618
GO:0055085
GO:0070633
GO:0071716
GO:0098656
GO:0140359
GO:0140657
GO:0150104
GO:1990962
HMNXSV003017571
HMNXSV003037426
ILMN_1676278
PH_hs_0011436
TC10000715.hg
U49248_at
g4557480_3p_s_at
Participates
as a member of
ABCC2 mutants [plasma membrane] (Homo sapiens)
Other forms of this molecule
ABCC2 R768W [plasma membrane]
ABCC2 R1066* [plasma membrane]
ABCC2 R1150H [plasma membrane]
ABCC2 [plasma membrane]
Modified Residues
Name
L-isoleucine 1173 replaced with L-phenylalanine
Coordinate
1173
PsiMod
L-phenylalanine residue [MOD:00023]
A protein modification that effectively converts a source amino acid residue to L-phenylalanine.
L-isoleucine removal [MOD:01640]
A protein modification that effectively removes or replaces an L-isoleucine.
Disease
Name
Identifier
Synonyms
Dubin-Johnson syndrome
DOID:12308
chronic idiopathic jaundice, Dubin Johnson syndrome
Cross References
RefSeq
NP_000383.1
ZINC - World Drugs
MRP2_HUMAN
Guide to Pharmacology - Targets
780
OpenTargets
ENSG00000023839
ZINC - FDA approved
MRP2_HUMAN
ZINC - Substances
MRP2_HUMAN
ZINC target
Q92887
PRO
Q92887
PDB
8JXQ
,
8JY4
,
8JX7
,
8IZR
,
8JXU
,
8JY5
IntEnz
7.6.2.2
HPA
ENSG00000023839-ABCC2
GeneCards
Q92887
Ensembl
ENSP00000497274
,
ENSG00000023839
,
ENST00000647814
Pharos - Targets
Q92887
Orphanet
15054
ZINC - Predictions - Purchasable
MRP2_HUMAN
HMDB Protein
HMDBP01658
Interactors (1)
Accession
#Entities
Entities
Confidence Score
Evidence (IntAct)
UniProt:P19838 NFKB1
8
NFKB1(1-968) [specific granule lumen]
(R-HSA-6799557)
NFKB1(1-968) [extracellular region]
(R-HSA-6806304)
NFKB1(1-968) [secretory granule lumen]
(R-HSA-6801004)
NFKB1(1-433) [cytosol]
(R-HSA-168168)
NFKB1(1-433) [nucleoplasm]
(R-HSA-177655)
NFKB1(1-968) [cytosol]
(R-HSA-451607)
p-S927,S932-NFKB1(1-968) [cytosol]
(R-HSA-451611)
3xUb-p-S927,S932-NFKB1(1-968) [cytosol]
(R-HSA-451619)
0.508
3
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