SLC16A1 G472R

Stable Identifier
R-HSA-5624230
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Monocarboxylate transporter 1, MOT1_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
SLC16A1, MCT1
Chain
chain:1-500
Other Identifiers
0005080601
11718656_at
11748355_a_at
1557918_s_at
16691023
17489
202234_s_at
202235_at
202236_s_at
209900_s_at
2428503
2428504
2428505
2428506
2428507
2428508
2428510
2428511
2428516
2428517
2428520
2428521
2428522
2428523
3324
36206_at
49197_at
6566
71055
73253_at
79035
7918622
A0A024R0H1
A_23_P126825
A_33_P3282434
AAC41707
AAH26317
AAH45664
AJ438945
AL158844
AL162079
BC026317
BC045664
CAB017489
CAB82412
CAD27707
CAI21872
CCDS858
CH471122
EAW56552
EAW56553
ENSG00000155380
ENSG00000281917
ENSP00000358640
ENSP00000441065
ENSP00000485688
ENSP00000486000
ENST00000369626
ENST00000538576
ENST00000628110
ENST00000630362
EntrezGene:6566
g4506982_3p_a_at
g7328161_3p_a_at
GE81228
GO:0002376
GO:0003674
GO:0005575
GO:0005576
GO:0005615
GO:0005622
GO:0005623
GO:0005813
GO:0005815
GO:0005856
GO:0005886
GO:0005887
GO:0006090
GO:0006629
GO:0006810
GO:0007010
GO:0007049
GO:0007098
GO:0007267
GO:0008028
GO:0008150
GO:0015129
GO:0015130
GO:0015293
GO:0015718
GO:0015728
GO:0016020
GO:0016021
GO:0022857
GO:0030054
GO:0032094
GO:0035873
GO:0035879
GO:0040011
GO:0042592
GO:0042593
GO:0042803
GO:0043226
GO:0043231
GO:0044281
GO:0048870
GO:0050796
GO:0050900
GO:0051780
GO:0055085
GO:0070062
GO:0071407
GO:0097159
HGNC:10922
HPA003324
HPA071055
Hs.75231.0.S3_3p_at
Hs2.407205.1.S1_3p_s_at
ILMN_1757052
IPR004743
IPR011701
IPR020846
IPR030757
IPR036259
L31801
L31801_at
MIM:245340
MIM:600682
MIM:610021
MIM:616095
NM_001166496
NM_003051
NP_001159968
NP_003042
PF07690
PH_hs_0031315
Q5T8R3
Q5T8R4
Q5T8R5
SLC16A1
SLC16A1-201
SLC16A1-207
SLC16A1-211
SLC16A1-214
TC01003001.hg
uc001ecx.4
uc001ecy.4
UPI00000012F5
XM_011542026
XM_011542027
XP_011540328
XP_011540329
Participant Of
Other forms of this molecule
Modified Residues
Name
glycine 472 replaced with L-arginine
Coordinate
472
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to an L-arginine.
A protein modification that effectively removes or replaces an glycine.
Disease
Name Identifier Synonyms
inherited metabolic disorder 655 Metabolic hereditary disorder, Inborn Errors of Metabolism, inborn metabolism disorder
Cross References
GeneCards
ZINC - Substances
ZINC target
PRO
Orphanet
ZINC - Predictions - Purchasable
HMDB Protein