SLC1A1 R445W [plasma membrane]

Stable Identifier
R-HSA-5625045
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
EAAC1, EAAT3
Locations in the PathwayBrowser
Expand all
External Reference Information
External Reference
UniProt:P43005 SLC1A1
Gene Names
SLC1A1, EAAC1, EAAT3, HEAAC1
Chain
chain:1-524
Reference Genes
BioGPS Gene:6505 SLC1A1
COSMIC (genes):SLC1A1 SLC1A1
CTD Gene:6505 SLC1A1
dbSNP Gene:6505 SLC1A1
ENSEMBL:ENSG00000106688 SLC1A1
ENSEMBL_homo_sapiens_GENE:ENSG00000106688.12 SLC1A1
HGNC:10939 SLC1A1
KEGG Gene (Homo sapiens):6505 SLC1A1
Monarch:6505 SLC1A1
NCBI Gene:6505 SLC1A1
OMIM:133550 SLC1A1
UCSC:P43005 SLC1A1
Reference Transcript
Other Identifiers
11721351_at
11721352_at
17083261
206396_PM_at
206396_at
213664_PM_at
213664_at
3160659
3160660
3160674
3160684
3160685
3160687
3160688
3160689
3160690
3160691
3160692
3160697
3160699
3160700
3160701
3160705
38267_at
38268_at
6505
8154135
A_14_P105964
A_23_P216468
A_24_P232252
GE58898
GO:0001662
GO:0001932
GO:0001975
GO:0002027
GO:0003013
GO:0005215
GO:0005253
GO:0005313
GO:0005314
GO:0005515
GO:0005576
GO:0005615
GO:0005737
GO:0005768
GO:0005783
GO:0005886
GO:0006575
GO:0006749
GO:0006750
GO:0006790
GO:0006801
GO:0006811
GO:0006836
GO:0006865
GO:0006882
GO:0006886
GO:0007212
GO:0007215
GO:0007268
GO:0007420
GO:0007611
GO:0007613
GO:0007625
GO:0007626
GO:0009410
GO:0009986
GO:0010460
GO:0010467
GO:0010842
GO:0012501
GO:0015108
GO:0015179
GO:0015183
GO:0015293
GO:0015501
GO:0015813
GO:0016020
GO:0016192
GO:0016324
GO:0016595
GO:0019221
GO:0022008
GO:0023052
GO:0030154
GO:0030424
GO:0030425
GO:0030534
GO:0031410
GO:0031901
GO:0031902
GO:0031982
GO:0032279
GO:0033229
GO:0034330
GO:0034599
GO:0035633
GO:0036211
GO:0036293
GO:0042417
GO:0042802
GO:0042883
GO:0043005
GO:0043025
GO:0043083
GO:0043197
GO:0043198
GO:0043204
GO:0043226
GO:0043278
GO:0043524
GO:0043679
GO:0045121
GO:0045184
GO:0045202
GO:0046872
GO:0048514
GO:0048678
GO:0048856
GO:0050808
GO:0050877
GO:0051402
GO:0051938
GO:0055037
GO:0055038
GO:0055065
GO:0055085
GO:0060013
GO:0060041
GO:0060047
GO:0060291
GO:0061744
GO:0070062
GO:0070633
GO:0070777
GO:0070778
GO:0070779
GO:0071242
GO:0071288
GO:0071314
GO:0071407
GO:0071577
GO:0071944
GO:0072347
GO:0090313
GO:0090461
GO:0097049
GO:0097386
GO:0097440
GO:0098685
GO:0098712
GO:0098793
GO:0098877
GO:0099170
GO:0099544
GO:0140009
GO:0140010
GO:0150002
GO:0150104
GO:1902476
GO:1903712
GO:1903926
GO:1990635
GO:1990708
HMNXSV003000939
Hs.91139.1.A1_3p_at
ILMN_1658917
PH_hs_0005070
TC09000029.hg
U08989_at
g4759121_3p_at
Participates
as a member of
Other forms of this molecule
SLC1A1 I395del [plasma membrane]
SLC1A1 84kb_del [plasma membrane]
SLC1A1 [plasma membrane]
Modified Residues
Name
L-asparagine 445 replaced with L-tryptophan
Coordinate
445
PsiMod
L-tryptophan residue [MOD:00027]
A protein modification that effectively converts a source amino acid residue to L-tryptophan.
L-asparagine removal [MOD:01633]
A protein modification that effectively removes or replaces an L-asparagine.
Disease
Name Identifier Synonyms
amino acid metabolic disorder DOID:9252 inborn errors of amino acid metabolism
Cross References
RefSeq
ZINC - World Drugs
Guide to Pharmacology - Targets
870
OpenTargets
ZINC - FDA approved
ZINC - Substances
ZINC - Biogenic
ZINC target
PRO
PDB
ZINC - Metabolites
GeneCards
HPA
Ensembl
Pharos - Targets
ZINC - Predictions - Purchasable
Orphanet
HMDB Protein
Interactors (1)
Cite Us!