SLCO2A1 G222R [plasma membrane]

Stable Identifier
R-HSA-5661428
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
PGT, Solute carrier organic anion transporter family member 2A1, SO2A1_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
SLCO2A1, OATP2A1, SLC21A2
Chain
chain:1-643
Reference Transcript
Other Identifiers
0000510593
0003120619
11717560_at
11732970_at
11751208_a_at
11756511_a_at
13742
16959382
16959386
204368_at
221175_at
2696105
2696107
2696108
2696110
2696111
2696112
2696114
2696115
2696116
2696117
2696120
2696125
2696129
2696131
2696132
2696133
2696135
2696137
2696141
2696145
2696147
2696148
2696149
2696163
2696167
2696168
2696188
2696189
37919_at
3MRR
6578
80111
8090817
8090823
A_23_P135990
A_23_P92176
A_33_P3238548
AAC09469
AAC62004
AAH41140
AAH51347
AF056719
AF056720
AF056721
AF056722
AF056723
AF056724
AF056725
AF056726
AF056727
AF056728
AF056729
AF056730
AF056731
AF056732
BC041140
BC051347
C3orf36
CCDS3084
CH471052
E7EU40
EAW79156
ENSG00000174640
ENSP00000311291
ENST00000310926
ENST00000310926.9
EntrezGene:6578
EntrezGene:80111
EntrezGene:C3orf36
EntrezGene:SLCO2A1
F8W9W8
g13376565_3p_at
g5032094_3p_at
GE60473
GE83055
GO:0003674
GO:0005215
GO:0005319
GO:0005515
GO:0005575
GO:0005623
GO:0005886
GO:0005887
GO:0006810
GO:0006869
GO:0008150
GO:0015132
GO:0015347
GO:0015732
GO:0016020
GO:0016021
GO:0022857
GO:0043252
GO:0055085
HGNC:10955
HPA013742
ILMN_1705231
ILMN_1795936
ILMN_1819525
IPR002350
IPR004156
IPR020846
IPR036058
IPR036259
MIM:601460
MIM:614441
NM_005630
NP_005621
PF03137
PF07648
PH_hs_0014898
PH_hs_0027721
Q3SXR2
SLCO2A1
SLCO2A1-201
TC03001799.hg
TC03001800.hg
U70867
U70867_at
UPI000013F0AD
XM_017007077
XM_024453721
XP_016862566
XP_024309489
Participant Of
Other forms of this molecule
Modified Residues
Name
glycine 222 replaced with L-arginine
Coordinate
222
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-arginine.
A protein modification that effectively removes or replaces an glycine.
Disease
Name Identifier Synonyms
primary hypertrophic osteoarthropathy 14283 Pachydermoperiostosis of nail [Ambiguous], Pachydermoperiostosis of nail (disorder), Pachydermoperiostosis of nail, Pachydermoperiostosis syndrome (disorder)
Cross References
RefSeq
ZINC - World Drugs
OpenTargets
ZINC - Substances
ZINC - Biogenic
ZINC target
PRO
PDB
ZINC - Investigational
ZINC - Metabolites
GeneCards
Orphanet
ZINC - Predictions - Purchasable
HMDB Protein