ABCG5 R419H [plasma membrane]

Stable Identifier
R-HSA-5679073
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
ABCG5
Chain
chain:1-651
Reference Transcript
Other Identifiers
0005860128
11756916_a_at
16897037
220383_at
2550757
2550758
2550759
2550760
2550761
2550762
2550764
2550768
2550771
2550772
2550773
2550775
2550776
2550777
2550778
2550779
2550781
2550783
2550784
2550785
64240
78329_at
8051866
A_23_P119763
GE63172
GO:0000166
GO:0003674
GO:0005515
GO:0005524
GO:0005575
GO:0005886
GO:0005887
GO:0006810
GO:0006869
GO:0007584
GO:0007588
GO:0008150
GO:0010212
GO:0010949
GO:0015918
GO:0016020
GO:0016021
GO:0016324
GO:0016887
GO:0022857
GO:0030299
GO:0032991
GO:0033344
GO:0042493
GO:0042592
GO:0042626
GO:0042632
GO:0043167
GO:0043190
GO:0043235
GO:0045177
GO:0045796
GO:0046872
GO:0046982
GO:0055085
GO:0120020
ILMN_1716592
PH_hs_0007986
TC02001794.hg
g11967968_3p_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-arginine 419 replaced with L-histidine
Coordinate
419
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-histidine.
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
lipid metabolism disorder 3146 dyslipidemia, fatty acid metabolism disorder
Cross References
RefSeq
OpenTargets
GeneCards
PRO
Orphanet
PDB
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