ABCG8 Y658* [plasma membrane]

Stable Identifier
R-HSA-5679080
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
ABCG8 Y658* [plasma membrane] icon
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
ABCG8
Chain
chain:1-673
Other Identifiers
0001570717
11737339_at
16879564
231751_at
2479562
2479563
2479565
2479566
2479567
2479568
2479569
2479575
2479576
2479577
2479579
2479581
2479587
2479588
2479589
2479590
2479591
2479592
2479593
2479594
2479595
2479596
2479597
2479598
2479599
2479601
51189_at
61060_at
64241
8041696
A_23_P209251
A_23_P90577
A_32_P96748
A_33_P3361112
GE82687
GO:0003674
GO:0005515
GO:0005524
GO:0005575
GO:0005886
GO:0005887
GO:0006810
GO:0006869
GO:0007165
GO:0007584
GO:0007588
GO:0008150
GO:0010949
GO:0014850
GO:0015914
GO:0015918
GO:0016020
GO:0016021
GO:0016324
GO:0016887
GO:0022857
GO:0030299
GO:0031667
GO:0032991
GO:0033344
GO:0038183
GO:0042493
GO:0042592
GO:0042626
GO:0042632
GO:0043167
GO:0043190
GO:0043235
GO:0045796
GO:0046872
GO:0046982
GO:0055085
GO:0055092
GO:0061024
GO:0070328
GO:0120009
GO:0120020
Hs.302030.0.S1_3p_at
ILMN_1680309
ILMN_1823937
PH_hs_0024962
TC02000272.hg
Participant Of
Other forms of this molecule
Modified Residues
Name
L-tyrosine 658 replaced with unknown
Coordinate
658
PsiMod
A protein modification that effectively removes or replaces an L-tyrosine.
Disease
Name Identifier Synonyms
lipid metabolism disorder 3146 dyslipidemia, fatty acid metabolism disorder
Cross References
OpenTargets
GeneCards
PRO
Orphanet
PDB
Interactors (1)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:Q14696 MESD      0.556 3
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