SLC22A5 R254* [plasma membrane]

Stable Identifier
R-HSA-5625665
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
OCTN2, Organic cation transporter 2, solute carrier family 22 (organic cation transporter), member 5, Solute carrier family 22 member 5, S22A5_HUMAN
SLC22A5 R254* [plasma membrane] icon
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
SLC22A5, OCTN2
Chain
chain:1-557
Other Identifiers
0006980692
11740657_a_at
11740658_a_at
16989018
205074_at
2828521
2828522
2828523
2828531
2828532
2828534
2828536
2828537
2828540
2828543
2828546
2828548
2828549
2828550
2828551
2828552
2828553
2828554
32084_at
4039277
6584
8107920
A_24_P174755
GE54539
GO:0000166
GO:0003674
GO:0005515
GO:0005524
GO:0005575
GO:0005576
GO:0005615
GO:0005622
GO:0005737
GO:0005829
GO:0005886
GO:0006810
GO:0006811
GO:0006814
GO:0008150
GO:0009609
GO:0015226
GO:0015293
GO:0015651
GO:0015697
GO:0015879
GO:0016020
GO:0016021
GO:0016324
GO:0022857
GO:0030165
GO:0031526
GO:0042592
GO:0042910
GO:0043167
GO:0043226
GO:0055085
GO:0060731
GO:0070062
GO:0070715
GO:0150104
GO:1901235
GO:1902270
GO:1902603
GO:1990961
ILMN_1699357
PH_hs_0001461
TC05000635.hg
g4507004_3p_at
g4507004_3p_x_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-arginine 254 replaced with unknown
Coordinate
254
PsiMod
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
systemic primary carnitine deficiency disease 14365 carnitine uptake defect, carnitine transporter deficiency, primary carnitine deficiency, deficiency of plasma-membrane carnitine transporter, renal carnitine transport defect (disorder)
Cross References
OpenTargets
GeneCards
ZINC target
PRO
Orphanet
HMDB Protein
Interactors (6)
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