SLC4A1 V488M [plasma membrane]

Stable Identifier
R-HSA-5657845
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
Band 3 anion transport protein, B3AT_HUMAN
Icon
SLC4A1 V488M [plasma membrane] icon
SLC4A1 V488M [plasma membrane] icon
Locations in the PathwayBrowser
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External Reference Information
External Reference
UniProt:P02730 SLC4A1
Gene Names
SLC4A1, AE1, DI, EPB3
Chain
chain:1-911
Reference Genes
BioGPS Gene:6521 SLC4A1
COSMIC (genes):SLC4A1 SLC4A1
CTD Gene:6521 SLC4A1
dbSNP Gene:6521 SLC4A1
ENSEMBL:ENSG00000004939 SLC4A1
HGNC:11027 SLC4A1
KEGG:hsa:6521 SLC4A1
Monarch:6521 SLC4A1
NCBI Gene:6521 SLC4A1
UCSC:P02730 SLC4A1
Reference Transcript
Other Identifiers
11726489_at
11726490_a_at
11726491_at
11758430_s_at
1552713_PM_a_at
1552713_a_at
16845623
205592_PM_at
205592_at
33336_at
3759020
3759021
3759022
3759023
3759024
3759025
3759026
3759027
3759029
3759032
3759034
3759036
3759037
3759039
3759040
3759042
3759043
3759044
3759045
3759046
3759047
3759048
3759049
3759050
3759051
3759052
3759053
3759054
6521
8015991
A_23_P77980
A_23_P89380
A_24_P385190
A_33_P3400217
GE62780
GO:0003014
GO:0005215
GO:0005452
GO:0005515
GO:0005856
GO:0005886
GO:0006811
GO:0006820
GO:0006821
GO:0006873
GO:0007596
GO:0008092
GO:0008509
GO:0009898
GO:0015075
GO:0015106
GO:0015108
GO:0015297
GO:0015698
GO:0015701
GO:0016020
GO:0016323
GO:0017121
GO:0030018
GO:0030492
GO:0030506
GO:0030863
GO:0034220
GO:0035811
GO:0042803
GO:0043226
GO:0043495
GO:0045852
GO:0048821
GO:0048856
GO:0051453
GO:0055085
GO:0060090
GO:0061024
GO:0070062
GO:0072562
GO:0072659
GO:0098656
GO:0140900
GO:0170014
GO:1902476
GO:1904539
HMNXSV003000115
Hs.185923.0.S2_3p_at
Hs2.185923.1.S1_3p_s_at
ILMN_1772809
M27819_at
PH_hs_0025935
TC17001577.hg
X77737_at
Participates
as a member of
Other forms of this molecule
SLC4A1 [plasma membrane]
SLC4A1 V850del [plasma membrane]
SLC4A1 R589C [plasma membrane]
SLC4A1 S613F [plasma membrane]
SLC4A1 E90K [plasma membrane]
SLC4A1 G701D [plasma membrane]
SLC4A1 R589H [plasma membrane]
Modified Residues
Name
L-valine 488 replaced with L-methionine
Coordinate
488
PsiMod
L-methionine residue [MOD:00022]
A protein modification that effectively converts a source amino acid residue to L-methionine.
L-valine removal [MOD:01650]
A protein modification that effectively removes or replaces an L-valine.
Disease
Name Identifier Synonyms
hereditary spherocytosis DOID:12971 Minkowski Chauffard syndrome, Congenital spherocytic hemolytic anemia, spherocytic anemia
Cross References
Guide to Pharmacology - Targets
904
OpenTargets
ENSEMBL
HPA
PRO
Pharos - Targets
Orphanet
GlyGen
PDB
Interactors (2)
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