SLC4A1 V488M [plasma membrane]

Stable Identifier
R-HSA-5657845
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Band 3 anion transport protein, B3AT_HUMAN
SLC4A1 V488M [plasma membrane] icon
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
SLC4A1, AE1, DI, EPB3
Chain
chain:1-911
Other Identifiers
0006550039
11726489_at
11726490_a_at
11726491_at
11758430_s_at
1552713_a_at
15584
16845623
1BH7
1BNX
1BTQ
1BTR
1BTS
1BTT
1BZK
1HYN
205592_at
2BTA
2BTB
33336_at
34438
3759020
3759021
3759022
3759023
3759024
3759025
3759026
3759027
3759029
3759032
3759034
3759036
3759037
3759039
3759040
3759042
3759043
3759044
3759045
3759046
3759048
3759049
3759050
3759051
3759053
3759054
3BTB
4KY9
4YZF
63911
6521
8015991
A0A0A0MS98
A_23_P77980
A_23_P89380
A_24_P385190
A_33_P3400217
AAA35514
AAC60608
AAH96106
AAH96107
AAH99628
AAH99629
AAI01571
AAI01575
AAY57324
ABD74692
ADN39420
ADN39421
BC096106
BC096107
BC099628
BC099629
BC101570
BC101574
CAA31128
CAB034438
CCDS11481
CH471178
DQ072115
DQ419529
EAW51614
ENSG00000004939
ENSP00000262418
ENST00000262418
EntrezGene:6521
GE62780
GO:0003674
GO:0005452
GO:0005515
GO:0005575
GO:0005576
GO:0005615
GO:0005622
GO:0005623
GO:0005737
GO:0005856
GO:0005886
GO:0005887
GO:0006810
GO:0006811
GO:0006820
GO:0006821
GO:0006873
GO:0008092
GO:0008150
GO:0008509
GO:0015106
GO:0015108
GO:0015301
GO:0015701
GO:0016020
GO:0016021
GO:0016323
GO:0022857
GO:0030018
GO:0030506
GO:0030863
GO:0042592
GO:0042803
GO:0043226
GO:0043495
GO:0051453
GO:0055085
GO:0070062
GO:0072562
GO:0098656
GO:1902476
GQ981383
GQ981384
HGNC:11027
HPA015584
HPA063911
Hs.185923.0.S2_3p_at
Hs2.185923.1.S1_3p_s_at
ILMN_1772809
ILMN_3217354
ILMN_3285762
IPR001717
IPR002977
IPR003020
IPR011531
IPR013769
IPR016152
IPR018241
M27819
M27819_at
MIM:109270
MIM:110500
MIM:112010
MIM:112050
MIM:166900
MIM:179800
MIM:185020
MIM:601550
MIM:601551
MIM:611162
MIM:611590
MIM:612653
NM_000342
NP_000333
PF00955
PF07565
PH_hs_0025935
PR00165
PR01187
PR01231
S68680
SLC4A1
SLC4A1-201
TC17001577.hg
uc002igf.5
UPI00000375B8
V9H0V9
X12609
X77737_at
XM_005257593
XM_011525129
XM_011525130
XP_005257650
XP_011523431
XP_011523432
Participant Of
Other forms of this molecule
Modified Residues
Name
L-valine 488 replaced with L-methionine
Coordinate
488
PsiMod
A protein modification that effectively removes or replaces an L-valine.
A protein modification that effectively converts a source amino acid residue to L-methionine.
Disease
Name Identifier Synonyms
hereditary spherocytosis 12971 Minkowski Chauffard syndrome, Congenital spherocytic hemolytic anemia, spherocytic anemia
Cross References
OpenTargets
GeneCards
DOCK Blaster
PRO
Orphanet
Interactors (2)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:P42771 CDKN2A  1 0.602 5
 UniProt:P18031 PTPN1  1 0.499 2